SIBEN, Key Trends, Insights

Sierra Leone, officially the Republic of Sierra Leone, is a country on the southwest coast of West Africa. It is bordered to the southeast by Liberia and by Guinea to the north. Sierra Leone’s land area is 73,252 km2 (28,283 sq mi). It has a tropical climate and environments ranging from savannas to rainforests. As of the 2023 census, Sierra Leone has a population of 8,460,512.  Freetown is its capital and largest city.

Sierra Leone is a presidential republic, with a unicameral parliament and a directly elected president. It is a secular state. Its constitution provides for the separation of state and religion and freedom of conscienceMuslims constitute three-quarters of the population, and there is a significant Christian minority. Notably, religious tolerance is very high.

Available healthcare and health status in Sierra Leone is rated very poorly. Globally, infant and maternal mortality rates remain among the highest. The major causes of illness within the country are preventable with modern technology and medical advances. Most deaths within the country are attributed to nutritional deficiencies, lack of access to clean water, pneumoniadiarrheal diseasesanemiamalariatuberculosis and HIV/AIDS.

Healthcare in Sierra Leone is generally charged for and is provided by a mixture of government, private and non-governmental organizations (NGOs). There are over 100 NGOs operating in the health care sector in Sierra Leone. The Ministry of Health and Sanitation is responsible for organizing health care and after the end of the civil war the ministry changed to a decentralized structure of health provision to try to increase its coverage.

Source: https://en.wikipedia.org/wiki/Sierra_Leone

Margaret Yainkain Mansaray Becomes First Sierra Leonean to compete in the Africa Prize for Engineering Innovation

Posted on December 1, 2022 by Design in Design Innovation

Sierra Leonean Innovator and CEO of Women in Energy-SL Margaret Yainkain Mansaray became the first Sierra Leonean to be listed among Innovators competing for the Africa Prize for Engineering Innovation 2023. An award organized annually by the Royal Academy of Engineering UK (The United Kingdom’s national academy of engineering). 

Mansaray, who is the only female rising to compete against 14 other innovators from ten countries across Africa was recognized for her invention of a Smart Green Stove. The smart green stove is a fast and efficient non-electric cooking device she designed to reduce greenhouse gas emissions and health risks that greatly affect women and girls in Africa. 

The stove burns briquettes made from recycled local materials such as coconut and jelly shells which are usually discarded. The insulator absorbs most of the heat and makes the stove nearly smokeless, reducing the harmful soot which would otherwise be released into the environment. 

“My team and I are working tirelessly to uplift women and girls by addressing time and energy poverty. I’ve always been the only woman in a room full of men, and so one of my aims is to educate women and girls, specifically on the role engineering can play in improving their lives.”, Mansaray said.

The Africa Prize for Engineering Innovation was launched in 2014 by the Royal Academy of Engineering. An award for ambitious African innovators creating local and scalable solutions to pan-African and international challenges. The innovations shortlisted in 2023 tackle challenges approaching the UN’s Sustainable Development Goals, including clean water and sanitation, sustainable cities and communities, clean energy, good health and well-being, and quality education. 

According to the Royal Academy of Engineering, Innovators shortlisted for the Africa Prize will benefit from a special package of support including business incubation, mentoring, fundraising and communications. The package will also include access to the Academy’s global network of high-profile and highly experienced engineers and business experts in the UK and Africa. Four finalists will be chosen to direct their innovations and business plans to Africa Prize judges at an event in Accra, Ghana, on July 6th, 2023. The winner will have a take-home of £25,000, and three runners-up will win £10,000 each. An additional One-to-Watch award of £5,000 will be given to the most promising entrepreneur from the remaining shortlist.

Mansaray took to her Facebook handle and expressed her joy as she took pride in being that this is the first time Sierra Leone has been shortlisted for the Royal Academy Africa prize. She emphasized that her achievement is a win for the country and especially for vulnerable girls and women. 

“I am happy to share that for the first time Sierra Leone has been shortlisted in the Royal academy Africa prize and I am the only female among 10 African countries.”, Mansaray wrote.

Source: https://dlit.co/margaret-yainkain-mansaray-becomes-first-sierra-leonean-to-compete-in-the-africa-prize-for-engineering-innovation/

🎧 | 2025 SIERRA LEONE MUSIC 🇸🇱 | Music Sparks

Latest Sierra Leone

The song “Waterloo” is amazing! We discovered it through a promotion by Jakey Jake and instantly fell in love. This talented artist, known as Papi J, deserves to be signed to a record label. In this song, Papi J describes his hometown, Waterloo—a place known for its cassava bread, fried fish, and hardworking community.

Jorge Pleitez Navarrete, MD, Carmen Dávila-Aliaga, MD, Lordes Lemus-Varela, MD, María Teresa Montes Bueno MT, Cristian Muñoz, MD, Augusto Sola, MD, Sergio Golombek, MD, and participants of the XIV SIBEN Clinical Consensus of the Iberoamerican Society of Neonatology (SIBEN)

Abstract: A cultural change in Iberoamerican neonatal hospitalization units is imperative to guarantee respect for the rights of newborns and their families during hospitalization, with equity at different levels of care, without differences based on geographic areas or socioeconomic level. It is essential to train and improve the competencies of the health team, from managers to healthcare professionals, to provide transdisciplinary and humanized care (CTH) for newborns and their families. There is sufficient evidence that CTH positively impacts the outcomes of newborns and their families when their families are involved in the care of their hospitalized babies.

This paper summarizes the results of the XIV SIBEN® Clinical Consensus on “Transdisciplinary and humanized care for newborns and their families,” in which 50 SIBEN® members, neonatologists, and nursing graduates from 14 Iberoamerican countries actively participated during 2023, before, during and after the face-to-face meeting held in Mar de Plata, Argentina in November 2023. This article answers questions based on the best available evidence and describes recommendations of clinical significance for truly providing transdisciplinary and humanized care (CTH).

Introduction:

In the 19th century, infant deaths were considered part of the natural order 1. In 1802, the first pediatric hospital, L’Hôpital des Enfants Malades, was founded in Paris, which promoted breastfeeding and the emotional needs of children.

Neonatology emerged in the 20th century owing to technological advances that increased neonatal survival but with reduced parental involvement. Research, such as the “Citizens’ Committee for Children of New York City” and the “Platt Report” in the United Kingdom, influenced the acceptance of parental presence in hospitals, demonstrating that their presence did not increase infection rates. Spitz coined the term “hospitalism” to describe the adverse effects of prolonged hospital confinement . In the 1980s, the family-centered model of neonatal care was introduced, demonstrating its effectiveness in caring for premature infants.

In 1984, the European Parliament approved the Charter of Patients’ Rights. In 1986, it adopted the European Charter for Hospitalized Children, which recognized 23 rights, including the right to be accompanied by their parents or primary caregivers for as long as possible. This charter was adopted by international organizations such as the WHO and UNICEF. Western countries began to ease visitation restrictions on parents as early as 1990.

Not all neonatology units in Ibero-America had adequate conditions to implement CTH by 2016. A study by the Ibero-American Society of Neonatology (SIBEN®)  revealed that 63% of the units offered space for mothers to stay with their infants (27% overnight), and in 60% of cases, there were time restrictions for parental visits. This demonstrates the need for a cultural change in Ibero-American NICUs to guarantee respect for the rights of neonates and their families during hospitalization.

Concept and principles of transdisciplinary humanized care (CTH) for newborns and families

In recent years, different denominations have incorporated families into the care of hospitalized newborns. We consider that this care is provided by many disciplines to the newborn (NB) and its family in an integrated, simultaneous, non-hierarchical, organized manner, according to the needs of the newborn and, above all, in a humanized way; therefore, SIBEN calls this model of care “Transdisciplinary Humanized Care (CTH) for the newborn and its family.”

With a comprehensive approach, the CTH for the NB and its family emphasizes family participation, respect for their needs, and transparent communication . These interventions reduce neonatal stress, favor their development, reinforce the family’s caregiver role, and improve family bonding and quality of care.

The fundamental principles of CTH are respect, honoring families’ diversity, flexibility, exchange of information, no medical terminology, participation and decision-making, collaboration between the patient, family, and health care providers, and family empowerment to discover their strengths.

Levels of Intervention of CTH for the Newborn and Family :

 • First level: Support parents through psychoeducational, communication, and environmental interventions to help them cope with hospitalization and prepare them for the newborn’s follow-up.

 • Second level: Interventions provided by the parents focused on improving the development and recovery of the newborn, with psychological and physical benefits for parents who received education from the clinical team.

• Third level: Collaborative care models, where parents are fully involved in newborn care.

Elements of CTH (12)

According to the currently available scientific evidence, we agree with the following elements:

• Recognition of the family as an important and indispensable part of the care of hospitalized neonates

 • Constant participation of the family in decision-making, as well as the procedures carried out

• Facilitate family/professional collaboration at all levels of care.

• Communication and exchange of information by health personnel at all times with the family.

• Recognition of family diversity, including ethnicity, socioeconomic, educational, racial, geographic, 

   etc., thus avoiding value judgments.

 • Incorporate models that contribute to parents’ learning regarding the care of their children through courses and educational programs.

 • Unrestricted access at all times and the family can always be involved in the care of their child

• Creation of family support networks.

 • Recognize the family’s strengths, feelings, emotions, concerns, and ability to help and contribute,thus validating them as an important, fundamental, and indispensable part of the NB’s care.

• Facilitate the parents’ stay as much as possible by providing a comfortable space for them to be close to their child for as long as possible.

In 2011, the book Neonatal Care, Discovering the Life of a Sick Newborn by Sola, A  introduces and emphasizes the concept that: “parents are not visitors” and that there should not be limited hours for a mother to be with her baby who is in the neonatal intensive care unit (NICU).

Changes, benefits, and tools for performing CTH:

* promote the newborn’s neurological and physical development

*  humanize care

*  reduce stress

*  improve health

*  improve adherence to treatment

* facilitate breastfeeding

 * optimize discharge care and transition to home care

* increase the quality of care

* increase parental satisfaction

The following are some essential strategies to achieve this objective:

1. Information and awareness-raising: Promote the benefits of BFHC through programs aimed at medical teams, families, and public policymakers.

 2. Staff training: Implementation of workshops, courses, and internships to train staff in CTH.

 3. Involve parents from the beginning: Encourage their presence and participation in medical procedures and daily care to strengthen bonding.

4. Empower parents: Provide them with tools and training so that they can actively participate in making decisions about their babies’ health.

5. Adapt physical spaces: Design areas that allow parents to stay close to their children.

 6. Ongoing emotional support: Offer psychological support programs to help families manage stress and emotional difficulties.

 7. Planning and evaluation: Ensure gradual implementation with constant adjustments and collaboration of professionals, parents, and the community to achieve more humane and effective care.

 Some tools to promote parental involvement in neonatal care include:

 a) Welcome Kit: This kit contains educational information on neonatal care, educational resources,and guidance for parental involvement.

b) Skin-to-skin contact: improves thermal stability, facilitates breastfeeding, and reduces stress in parents and infants (7,18)

c) Care diary: Parents record the baby’s daily activities, such as feeding, diaper changes, and procedures, which allows them to feel more engaged in their care and evaluate their progress as caregivers.

d) Medical rounds participation program: Parents can discuss the baby’s condition and treatment, ask questions, and express concerns.

 e) Training classes and workshops: Educational resources on neonatal care and child development are provided.

 f) Mobile applications and online platforms: Allow parents to access up-to-date information on their baby’s condition, schedule visits, and communicate with medical staff.

g) Support groups and counseling: Facilitate mutual support among parents, share experiences, and get involved in their child’s care.

Difficulties or obstacles in the CTH process:

Including the family in the care of the hospitalized neonate is a humanized and recommended practice, although it is not always implemented in all neonatal units. Some professionals consider that the presence of parents is not necessary, arguing that they may generate anxiety, not be prepared for invasive procedures, or that the physical space is insufficient. In addition, lack of knowledge about family-centered care and institutional regulatory barriers negatively affect the care of the infant and family.

Skin to skin contact: Skin-to-skin contact (SSC) has ancestral origins in different cultures and times, and it is a common practice between mothers and their healthy or sick babies. In protocolized form, it began in the 1970s in Bogota, Colombia; the maternal body heat allowed it to stabilize physiologically and provide comfort and security to neonates. Since 1990, the success of this practice has spread, and it has been adopted in several countries as a neonatal care option.

SSC is beneficial for both term and preterm newborns, and it is applied immediately after delivery, during the first hour of postnatal life, during hospitalization, and even at home. It is associated with decreased maternal postpartum depressive symptoms, improved perspective on motherhood, and intrinsic and extrinsic gratification, especially being able to care for her baby. Lower maternal salivary cortisol levels have been reported at one week and one month postpartum.

 In addition, recent studies have shown a significant prolongation of breastfeeding at six months (5.08 months vs. 2.05 months). Other findings highlight additional benefits, such as increased weight gain of the NB, reduction of hospitalization time, strengthening of the mother-child bond, and contribution to the overall development of the NB.

CTH and the advantages of breastfeeding

CTH includes the concept of 24-hour “open-door units” where fathers are encouraged to be present during breastfeeding and participate in feeding, either directly from the breast or by expressed milk. This approach promotes bonding, analgesia, neurodevelopment, milk production, and breastfeeding.

CTH and family satisfaction:

Parents of hospitalized NBs may experience acute or posttraumatic stress, affecting their physical, psychological, and social health, as well as their relationship with their children. Parents’ confidence increases when they know how to act and the impact of their actions on their infant’s health.

When CTHs are established, the family is recognized as a permanent reference in the child’s life, even during hospitalization. Family members become involved in the care, take an early part in it, and participate in decision-making regarding their child, promoting the parent-child bond .

The most important dimensions of neonatal care for parents are safety, care, communication,information, education, environment, monitoring, pain management, and participation .

SIBEN® recommends:

1. Change the paradigm and improve the communication skills of healthcare personnel to meet the family’s needs regarding the illness, treatment, and recovery of the neonate.

2. Encourage empathy, accessibility, and confidentiality in communication with families, increasing their participation in decisions about care and treatment. In addition, family functioning is considered to be crucial support during the newborn’s hospitalization.

3. Apply CTH from the admission of the newborn, integrating the family as active and competent caregivers of their child.

Family satisfaction helps in dealing with grief.

The NICU neonatal health team focuses on preserving the newborn’s life through therapeutic interventions . When parents face the loss of an infant, the grief they experience requires compassionate accompaniment by multidisciplinary teams that pay attention to psychological, emotional, and spiritual aspects of the family and offer empathy and respect for the parents to mitigate their pain .

 Infrastructure to Implement CTH for the Newborn and Family

The World Health Organization (WHO) recommendation of 24-hour parental presence in the NICU has motivated the construction of neonatal units with private rooms, encouraging these indications. The implementation and use of private rooms in the NICU as a recommendation dates back to approximately 1990.

Impact and Advantages of private rooms for the newborn.

 • Reduction of infections. Decreases the spread of nosocomial infections and makes the isolation of patients colonized by potentially pathogenic microorganisms possible.

• Increased weight gain. Preterm infants who remained in private rooms with their parents in the short term had a higher rate of weight gain during hospitalization.

 • Less pain, with fewer procedures and lower pain scores in infants in private rooms compared to infants in shared rooms.

 • Better neurobehavioral outcomes. Infants in private rooms had significantly less physiological stress, hypertonicity, and lethargy.

• Lower noise levels. In the shared NICU model, 20 decibels were found to be 20 decibels higher.

• Fewer days of hospitalization. More infants were discharged early.

• Increased breastfeeding. 90% achieved breastfeeding in private rooms compared to only 66% is shared.

 • Fewer episodes of apnea. In the group stratified on the PEMR (Physician’s Estimate of Mortality Risk) scale, there was a 57% decrease in total apnea events in preterm infants.

• Reduction in direct cost.

• Reduction in illumination. Neonates admitted in open and private NICU rooms at Sanford Children’s Hospital in Sioux Falls, USA, were compared, and a reduction in illumination was shown: 48.4 lux and only 6.4 lux in private rooms (p < 0.05), with longer sleep time in neonates.

• Post-discharge: fewer consultations and hospitalizations. Comparing two groups of preterm infants it was found that they had lower rates  of rehospitalization and requests for medical care at discharge.

• Higher cognitive scores. At an 18-month follow-up, Bayley III cognitive language and motor scores were compared in private and shared rooms in preterm infants under 30 weeks of gestational age. Infants with high maternal involvement in both NICUs had improved cognitive scores.

Disadvantages and risks of private rooms

The optimal types and frequencies of stimulation for very preterm brain development are unknown. Still, the isolation of these infants in relatively dark and quiet private rooms may be going in the wrong direction.  However, auditory stimulation, such as parental voices, is considered positive in the NICU environment, being associated with better motor and language outcomes. Therefore, the need for greater parental permanence and involvement in the single-family room is emphasized, as otherwise, this aspect may be considered a disadvantage.

NICU nurses are at greater risk of fatigue, anxiety, and depression than nurses in general wards. Burnout in neonatal nurses continues to be a problem.

 Is family presence during neonatal resuscitation or other invasive procedures advisable? ANSWER: YES. Parents or family members should be welcome to be present during an inpatient procedure and should not be asked to leave the room if they wish to be there.

 SIBEN® Position. There is no scientific evidence to justify separating parents from critically ill NBs or those requiring advanced cardiopulmonary resuscitation. On the contrary, numerous studies report the beneficial effects on the parents, family, and even their approach concerning the care received. They always respect the parents’ decision to participate and are accompanied by health personnel who explain the situation and what they are seeing.

It is advisable, after the presence of the parents during the resuscitation, to carry out a joint analysis with their presence, to provide feedback to explain the procedures performed, to clarify their doubts, and also to consider their observations and concerns to improve the quality of the procedures performed in our units.

A philosophical concept to be taken into account is the following, which establishes a position in this regard: “Thus, from Anthropology, it can be noted that throughout the history of mankind, women have sought assistance at the time of childbirth, while the rest of mammals do it alone. It is considered that this is due to the complexity implied by the bipedestation, the pelvic cavity, and the human cephalic perimeter.”

 Recommendations to implement transdisciplinary care in Neonatal Units:

• The importance of names: the name of the NB and his/ her parents. Knowing and referring to the mother, father, and newborn by name is essential. Never call or refer to the newborn as: “the baby in incubator number such and such”.

The art of communication. The importance of listening and making yourself understood.

Use simple and straightforward language to ensure that what has been expressed has been understood, especially when listening to the family’s concerns and encouraging them to ask questions and express emotions. Respect the family’s cultural and religious beliefs and customs.

 We are part of the same team—”Parents Are Not Visitors”  The importance of encouraging, facilitating, and accompanying the participation of the mother and family. Encourage skin-to-skin contact.

We should also consider the participation of the newborn’s brothers or sisters, grandfathers and grandmothers, or other designated persons, with the authorization of their mothers and/or fathers.

Interpreting beyond words. The importance of feelings and mental health support. Health care professionals should identify situations where the mother expresses fatigue, anguish, hopelessness, sadness, frustration, depression, crying, etc.

 They are not alone. The importance of the peer support network and parent associations (such as FAMISIBEN)

In 2021, SIBEN®, with the FAMISIBEN working group, drafted recommendations for parents of neonates in the NICU. These recommendations are available in digital format on its website, https://sites.google.com/siben.net/famisiben/, free of charge for family members, caregivers, health professionals, and the general public.

Common questions for implementing CTH in the NICU:

  1. Should the pacifier be banned? Answer: NO. Why? Non-nutritive sucking (NNS) is an integral part of infant developmental physiology. Based on the available evidence, the “SIBEN Mini Clinical Consensus / 2021” authors recommend initiating stimulation with a pacifier (NNS) at 28-29 weeks gestational age. Centers that “prohibit or forbid” the use of pacifiers, teats, or whatever it is referred to should review this restriction and know that this is not baby-friendly but quite the opposite.
  • Should the mother be made to feel welcome for 1440 minutes each day? Answer: YES “Parents are not visitors.”  CTH for the family promotes stress reduction for the parents and a more positive relationship between the parents and the newborn.
  •  Can the mother stay 24 hours a day in the hospital where the NICU is located? Answer: YES. We should encourage the mother or father to stay close to the baby even in the NICU; mothers and fathers in single family nurseries care more for their baby, including skin-to-skin contact compared to mothers in the open NICU, improving infant growth and neurodevelopmental outcomes.
  • d. Is there a minimum or maximum length of stay for at least one parent in the NICU? Answer: NO. There is evidence that the separation of hospitalized patients alters the dynamics of parental care and affects all family group members.
  • e. Will the family member (mother, father, or whoever the mother indicates) be able to participate in NICU care? Answer: YES. Family involvement is a key element in all infants’ physical, cognitive and psychosocial development, including those in the NICU.
  • f. What are the benefits of performing a blood sampling, vaccine placement, peripheral vein cannulation, or other pain-generating procedure with the infant nestled, held, and sucking? The SIBEN® Clinical Consensus on the diagnostic and therapeutic approach to pain and stress in the newborn  recommends non-nutritive sucking when performing procedures that cause mild to moderate pain. Breastfeeding is considered the first choice treatment because of its safety, ease of administration, and availability, in addition to its multiple benefits, which have been extensively studied both nutritionally and immunologically.
  •  What is the role of the “schools for parents” in the CTH for the newborn and the family? The schools are a training space for parents whose roles are as follows:

 1. To allow conscious and active participation of parents in neonatal care.

 2. Teach parents about the child’s physiological states, biorhythms, and adaptation mechanisms.

 3. To offer knowledge for post-discharge care of the newborn.

 4. To instruct on the benefits of breastfeeding and newborn feeding.

 5. To teach and promote skin-to-skin contact.

 6. Teach parents about hygiene, care, and medication administration.

 7. To teach warning signs, infection prevention, and infant cardiopulmonary resuscitation.

 8. Provide tools to work on psychomotor development stimulation, forms of stimulation, and

     expected emotions of the newborn in different circumstances to ensure adequate growth and  

     development of children.

     h. What key actions are indispensable and essential for CTH to exist?

1. First and foremost, a paradigm shift is necessary, associated with a theoretical/practical

     educational plan for all personnel, providing them with specific tools and skills to promote

     change.

2. Achieving the multidisciplinary participation of all neonatology staff without dissonant or

     opposing voices (“everyone cooperates”).

 3. It must be recognized that discussing this type of neonatal care is not enough since

     implementing CTH in action requires facing and overcoming many challenges in different areas.

4. Modify the environment: It is essential to have areas, offices, and spaces for private conversations

     with parents and family.

 5. Partnering with health care administrators and financiers in the task

  i. In the NICU of an institution certified as “mother and child friendly,” is CTH practiced for   the care of the newborn and its family? In many NICUs, even in many hospitals certified as “mother friendly”, mothers are still separated from their babies, and there is little or no space for mothers, and a chair or bed is not always provided next to the newborn’s incubator.

 Key points from SIBEN® about CTHs in the NICU:

• The brain’s structural plasticity is in response to maternal auditory stimulation.

• The quality of experience significantly influences the brain and the function and structure of the  

   developing central nervous system

• The presence of the family in neonatal care has beneficial effects, including improved bonding of  

   the NB with the family and improved quality of care.

 • It should be emphasized that “parents are not visitors.”

• Smooth transition from the hospital environment to the home: no rush and no pressure. Ideally,

   this occurs during pre-hospitalization, especially in prolonged hospitalizations of more than three

  weeks.

• Setting concrete, everyday actions and deeds (not just words or documents) into practice, such as  

   those discussed in this manuscript, is very useful in achieving the best results.

• Periodically carry out critical and continuous self-evaluation of the neonatal team.

Source: https://neonatologytoday.net/newsletters/nt-apr25.pdf

International cooperation and solidarity are essential in tackling global challenges, including efforts to ensure the effective realization of the right to health for all nations.

As proclaimed by the United Nations, promoting international cooperation and solidarity is a duty of States.

In this context, we express our profound appreciation, gratitude, and recognition to Cuban health professionals who have provided—and continue to provide—their services in multiple nations.

Since 2019, and with even greater intensity now, a dishonest campaign has been unleashed to discredit Cuba’s international medical cooperation, exert pressure on recipient governments, and deprive populations of essential healthcare services. 

No one with a basic sense of honesty can doubt that this is an attack on multilateralism, a manipulation for political purposes, and a continuation of aggression and hostility against Cuba.

Access to healthcare is a human right, and millions of people cannot be deprived of this inalienable right for political reasons.

Attempts to delegitimize Cuban medical cooperation overlook the fact that the shortage of health professionals is a pressing issue worldwide, whose solution demands greater international cooperation and solidarity, not unfounded attacks.

Cuba has devoted considerable efforts and resources to health care and today has one of the highest ratios of doctors per capita in the world, enabling it to make a significant contribution to global health.

Cuban international medical cooperation has made it possible to provide high-quality health care to millions of people around the world.

Over the past 60 years, more than 605,000 Cuban health collaborators have completed missions in 165 nations.

Their feats are notable in the fight against Ebola in Africa, blindness in Latin America and the Caribbean, cholera in Haiti, and the COVID-19 pandemic. Numerous brigades from the Cuban International Contingent of Doctors Specialized in Disasters and Major Epidemics ‘Henry Reeve’ have carried out humanitarian work in many nations.

Cuban professionals and technicians participating in these programs do so exclusively upon the express request of the concerned countries, offering their expertise and services freely and voluntarily.

Many of them work in remote rural areas to save lives, even at the risk of losing their own. They provide care to all patients without distinction, refraining from getting involved in internal political affairs and strictly respecting the laws and customs of the countries where they work.

Additionally, Cuba has provided free medical training to 43,000 healthcare professionals from 120 nations. In numerous countries, medical faculties have been established with Cuban professors.

It is imperative to defend and recognize the valuable contributions of thousands of Cuban health professionals who, through immense personal sacrifice, continue to offer their cooperation.

Neither discrediting campaigns nor the devastating effects of the intensified economic, commercial, and financial blockade have succeeded in preventing Cuba from continuing to save lives and share its limited resources with other nations in need.

Cuban medical cooperation will remain a symbol of hope, dedication, humanity, and solidarity.

(Cubaminrex-Permanent Mission of Cuba in Geneva)

Source:https://cubaminrex.cu/en/statement-ministers-health-non-aligned-countries-support-cubas-international-medical-cooperation

***The Non-Aligned Movement is a forum of 120 countries that are not formally aligned with or against any major power bloc, and dedicated to representing the interests and aspirations of developing countries. It was established in 1961.

Source: https://dominicanewsonline.com/news/homepage/news/statement-ministers-of-health-of-the-non-aligned-countries-in-support-of-cubas-international-medical-cooperation/

ProgenyHealth Releases 2025 Key Trends and Insights Report on Maternal & Infant Health

ProgenyHealth      Jan 15, 2025

Report identifies 7 of the most pressing industry trends that will shape the months and years ahead

ProgenyHealth, LLC, a recognized national leader in Maternity and NICU Care Management, today announced the release of its 2025 key trends and insights report, “Steep Challenges & Uneven Progress.” This year’s highly anticipated annual report identifies critical areas within maternal and infant health to watch in the year ahead, for health plans, hospitals, and healthcare providers.

The state of maternal and infant health in America remains precarious. By now, the sobering data has become all too familiar – The United States’ mortality rate is the highest of all high-income nations. Tragically, as many as 80% of maternal deaths, many of which occur in the first 42 days after giving birth, are preventable.

“While many challenges exist, there is continued hope on the horizon, as an increasing volume of healthcare-focused experts strategize to turn this situation around—and as new trends emerge to offer fresh opportunities and solutions,” said Linda Genen, Chief Medical Officer, ProgenyHealth. “These shifts promise to upend the present state of maternal and infant health, setting the nation on a new and better path forward.”

Key findings and predictions of the 2025 trends report include:

  • Maternal Decision-Making Will Take Center Stage. The concept of self-determination in the birthing process is being taken more seriously by medical institutions that are piloting programs to create dedicated care teams to listen to, work with and support those going through the birthing process. Research continues to show that providing women with a more empowered birthing experience pays dividends down the road.

  • Neonatology Will Continue to Advance the Viability of Micro Preemies. Until recently, very few infants born before 26 weeks were likely to survive. Today, many infants born as early as 22 weeks are not only surviving but thriving due to medical advancements. These extraordinary advancements have entirely improved the outlook for those born too young and too early.

  • Payers Will Increase Focus on Postpartum Support for Women. Between 2017 and 2019, nearly 30% of pregnancy-related deaths happened in the six weeks to 12 months after women gave birth, CDC data shows. Notably, many of these deaths were tied directly to mental health issues, which tend to go both undetected and untreated in the postpartum period. It is estimated that 50% of all postpartum depression cases go undiagnosed.

  • Amid Rising Costs, Employers Will Demand Alternatives to Standard Insurance Products. Since total birth costs are one of the top cost categories for health coverage, employers will likely begin to focus on proactive managed care partnerships to provide additional support during this complex period.

  • Increased Birth Anomalies Will Require More Complex Care. Congenital anomalies are among the chief causes of infant mortality, and as births increase across the nation—particularly in states with reproductive health restrictions in place—these anomalies are expected to climb. Children born with such anomalies may require surgical intervention, ongoing physical or occupational therapy, long-term educational support, or an array of assistive devices—needs that may evolve and last for life.

  • Whole Genome Sequencing Will Become a Game-Changer for Newborn Care. Rapid Whole Genome Sequencing (rWGS) testing for newborns may soon address this widespread genetic disorder blind spots. This genetic test can be used to identify and diagnose numerous conditions, including developmental delays, seizure disorders, conditions that affect hearing, vision, and immune deficiencies. rWGS is faster and more accurate than other genetic testing and considers a person’s full DNA sequence. While rWGS remains unavailable to many families, that situation is likely to change in the years ahead.

  • The Rate of Home Births Will Keep Rising – as Will Insurers’ Potential Role in Covering Them. Given the growing number of home births, some states are now exploring ways in which supporting this birth choice—and making it safer and more routinized, with intervention available in case of emergency—may help to combat certain aspects of the maternal health crisis

Source: https://www.prnewswire.com/news-releases/progenyhealth-releases-2025-key-trends-and-insights-report-on-maternal–infant-health-302349557.html

In 2018, the Global Health Cluster lead by the World Health Organization (WHO) conducted a capacity survey of Global Health Cluster partners to capture information on partners’ self-assessment of their technical, operational, and coordination capacities. The results showed that most international and national partners reported a lack of capacity and expertise to provide maternal and newborn health (MNH) services. Less than half reported an ability to provide Basic Emergency Obstetric and Neonatal Care (BEmONC) and Comprehensive Emergency Obstetric and Neonatal Care (CEmONC) at primary and secondary level respectively, and only 42% of the international partners and 50% of the national partners reported providing Essential Newborn Care (ENC).

To accelerate newborn health services in humanitarian settings, recent global interagency efforts have led to the development of the 2018 Inter-Agency Working Group on Reproductive Health in Crises (IAWG)-endorsed Newborn Health in Humanitarian Settings: Field Guide (NBFG); the Newborn Care Supply Kits for Humanitarian Settings; and a Roadmap to Accelerate Progress for Newborn Heath in Humanitarian Settings: 2020–2024.

In addition, these resource cards were developed to facilitate capacity building of humanitarian stakeholders. To build these cards, a consultant conducted a mapping of key maternal and newborn health trainings across the development and humanitarian sectors using a methodology that included a desk review of existing trainings, stakeholder interviews, and a short online survey delivered to Health Cluster Coordinators. The findings of the mapping exercise were presented and discussed at an experts meeting organized by Laerdal Global Health, Maternity Foundation, and Save the Children in Stavanger, Norway in 2019.

Overall, the mapping identified a great variety of existing training programs, mainly for clinical health care providers, on all aspects of newborn care and at all levels of care provision. Existing trainings for program managers were somewhat scarce, and access to available tools and guidelines could be improved.

Thus, we have packaged these resource tools as a quick pocket reference to aid  program managers and implementers in humanitarian and fragile settings with  identifying and accessing the most relevant trainings, tools, implementation guidance, and clinical guidance

Resource File: https://healthynewbornnetwork.org/hnn-content/uploads/HNN-Resource-Cards_Web.pdfhttps://healthynewbornnetwork.org/resource/2020/newborn-health-resources-trainings-and-tools-for-improving-newborn-health-in-humanitarian-settings/

Rethinking Platelet and Plasma Transfusion Strategies for Neonates: Evidence, Guidelines, and Unanswered Questions

Rozeta Sokou, Eleni A. Gounari, Alexandra Lianou, Andreas G. Tsantes, Daniele Piovani,,Stefanos Bonovas , Nicoletta Iacovidou, Argirios E. Tsantes

Abstract

The transfusion of platelets and fresh frozen plasma (FFP) to critically ill neonates in neonatal intensive care units (NICUs) is a common intervention, yet it is still widely performed without adhering to international guidelines. The guidance itself on the therapeutic management of neonatal coagulation disorders is generally limited due to the absence of strong indications for treatment and is mainly aimed at the prevention of major hemorrhagic events such as intraventricular hemorrhage (IVH) in premature neonates. Historically, the underrepresentation of neonates in clinical studies related to transfusion medicine had led to significant gaps in our knowledge regarding the best transfusion practices in this vulnerable group and to a wide variability in policies among different neonatal units, often based on local experience or guidance designed for older children or adults, and possibly increasing the risk of inappropriate or ineffective interventions. Platelet transfusion and, particularly, FFP administration have been linked to potentially fatal complications in neonates and thus any decision needs to be carefully balanced and requires a thorough consideration of multiple factors in the neonatal population. Despite recent advances toward more restrictive practices, platelet and FFP transfusions are still subject to wide variability in practices.

This review examines the existing literature on platelet and FFP transfusions and on the management of massive hemorrhage in neonates, provides a summary of evidence-based guidelines on these topics, and highlights current developments and areas for ongoing and future research with the aim of improving clinical practices.

Source:https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2601-9364

Connecting with your premature infant in the Neonatal Intensive Care Unit (NICU) may seem overwhelming and complicated. It can be a unique and challenging experience since it involves the emotional well-being of the parents and the development of the baby.

However, with the proper knowledge, resources, and support, bonding with your preemie may be a lovely and joyful experience. With the appropriate guidance and techniques, these may foster a closer relationship with your infant in its new surroundings.

Every baby and every situation is unique. Be patient with yourself and your baby as you navigate the NICU. Understand preemies’ distinct needs and the most significant ways to help them. This article will delve into everything you need to know about bonding with your premature baby in the NICU.

Understanding Preterm Development: How It Helps With Bonding

Preterm and full-term newborns have a developmental trajectory, even if preterm babies grow at a different rate. Premature infants, or preemies, as they’re fondly called, have a distinct development.

A clear understanding of preterm development is critical to the bonding process between parents and their preemies—a great way to get closer to your baby. You can still establish a connection with your preemie while in the NICU by being aware of their developmental milestones.

Parents must understand their unique requirements and developmental stages to effectively care for and support them. Some of these characteristics include:

Small Body, Thin and Delicate Skin

Overall, premature babies have significantly low birth weight; hence, their physical size is relatively small. Additionally, they have thin and delicate skin. These unique features require special care in handling and bathing them.

Sensitivity to Touch

Premature babies learn about the world mainly through touch. More importantly, a sense of touch is the key for parents to bond with them. However, they’re more sensitive to touch than full-term babies, so providing a gentle and comforting touch is critical.

Vulnerability to Overstimulation

Light and noise are two stimuli that easily overwhelm premature babies. It’s best to create a calm and quiet environment that makes them feel more secure and facilitates bonding.

Delayed Bone and Muscle Development

As advised by medical experts, involve your premature infant in gentle exercises and motions to help support their development and create opportunities for bonding.

Premature babies may have delayed physical development, including muscle and bone development. Late preterm babies, born between 34 and 36 weeks, may have fully developed organs but still have changes happening in their brains.

Premature babies born earlier than 28 weeks and babies born with an extremely low birth weight of less than 1 kg have the highest chance of developing problems.

Potential for Neurodevelopmental Challenges

Premature babies may experience long-term effects on their cognitive and neurological development, including learning disabilities, attention-deficit/hyperactivity disorder (ADHD), and difficulties with executive functioning.

Parents must be aware of these developmental challenges; hence, bonding and interaction with their baby should consider these disabilities. 

Needs Specialized Care

Premature babies in the NICU require specialized medical care, which makes it challenging for parents to bond with them. However, being involved in their care, such as participating in diaper changes or helping with feeding, can still contribute to their bonding success.

Potential for Longer Hospital Stays

Premature babies need to stay in the hospital for an extended period, which can be emotionally challenging for parents. Finding ways to stay connected and involved with their care can help maintain the bond during this time.

Understanding these unique characteristics helps parents bond with their premature babies. By being aware of their baby’s needs and sensitivities, parents can provide a comforting and supportive environment that promotes bonding and development.

Bonding with Your Premature Baby in the NICU

Managing the difficulties and uncertainties of having a preemie could be complex. You need to focus on developing a strong bond, even while in the NICU. By prioritizing this bond, you provide your baby with love and encouragement despite hardship.

Maintaining a deep bond with your baby through care and engagement is essential for their development and general well-being throughout their stay in the NICU. Premature infants who receive loving care are more likely to experience favorable developmental outcomes.

Remember that every baby and family’s situation is unique, so it’s important to tailor your approach based on the specific needs and guidelines provided by the NICU staff

There are many ways to develop a bond with your baby. Here are some tips to consider:

1.   Spend quality time.

Find time to visit your baby regularly at the NICU and make the most of the time you have together. Even if your baby is sleeping or connected to monitors, your presence creates a sense of familiarity and constant support.

Your presence alone provides a long-term positive impact on your baby’s development and gives you confidence as a parent too. Spending time with your baby is such an important part of bonding in the NICU.

2.   Learn your baby’s cues.

With your regular visits to your preemie, you take time to learn your baby’s cues. Get involved in their care, especially on how to make your baby comfortable at all times. You may ask the NICU staff for guidance on how to interact with your baby.

3.   Kangaroo care.

Also known as skin-to-skin contact, kangaroo care is highly encouraged and affords numerous benefits to premature babies. This involves holding the baby against your bare chest with only a diaper on for an extended period.

Hold your baby against your chest so they can hear your heart beating. For a premature baby, such moments are crucial for physical and emotional bonding.

This skin-to-skin contact helps regulate the baby’s temperature, heart rate, and oxygen levels, promotes breastfeeding and breathing, and reduces stress for both the parent and baby. It also promotes weight gain and digestion. All these benefits foster bonding with your preemie.

4.   Gentle touch.

Premature babies are sensitive to touch due to their underdeveloped nervous system. Use a light and gentle touch to stroke your baby’s skin, hands, and feet. This tactile stimulation helps promote relaxation and bonding—a soothing effect that helps establish a connection with the parent.

These comforting touches provide reassurance and make the baby feel loved and secure. Your care team will guide you to feel comfortable while touching your baby. They will guide you in specific ways that your baby will be looking for and can tolerate.

Some NICU infants can be held right away, while others may need an alternative approach. Once their condition is stable, massage can also help them relax. They will feel calm, cared for, and supported. You could hold your baby’s hand or stroke their head, for example.

5.   Talk, sing, and read.

Premature babies benefit from hearing their parent’s voices. Even though they may seem too small to understand or respond to, talking, singing, and reading softly to them create a sense of familiarity and connection. It helps them recognize and connect with your voice, promoting bonding.

Engage in gentle conversation and sing lullabies. Your voice will become familiar to them, providing a sense of security. Your baby recognizes your voice from when they were inside the womb, so hearing it can be comforting and soothing—a source of bonding during the NICU stay.

6.   Help with care tasks.

Discuss with the NICU staff if you could participate in your baby’s care routine as much as possible. Changing diapers, feeding if permitted, and bathing your baby enhance your bonding experience and help you feel more connected with your little one.

Other simple tasks could just be providing comfort through swaddling and positioning. These activities help establish a sense of parental responsibility that promotes bonding.

7.   Create a sense of normalcy.

Despite a highly medicalized environment, try to create a sense of normalcy by personalizing the baby’s space. You can bring familiar items, such as a blanket or a small toy, to make the surroundings feel more like home.

8.   Leave your scent.

Check with NICU staff to learn what cloth items are appropriate to place in your baby’s space. Sleep with that item or wear it all day tucked under your clothing, then place it in your baby’s space. In this way, you’re establishing a connection with your baby through your scent.

Sweet premature baby in an incubator with oxygen and unrecognizable mom caressing baby trying to calm him down

9.   Take care of yourself.

Prioritize self-care during this challenging time, taking care of your physical and emotional well-being during this stressful period. Have a balanced diet, get enough rest, and engage in activities that give you joy and relaxation.

When you’re calm and well-rested, it positively impacts your interactions and connection with your baby.

10.  Seek emotional support.

The NICU experience can be emotionally overwhelming and exhausting, especially for moms. It’s essential to seek support from your partner. Also, from healthcare professionals, therapists, family, friends, and support groups specific to parents of premature babies.

Sharing experiences and emotions can help cope with the challenges and strengthen the bond during this critical period. They can provide comfort, understanding, and guidance, which are essential for maintaining a healthy emotional state during this challenging time.

11.  Seek support from NICU staff.

Ask the medical staff for guidance and support on ways to bond with your premature baby. They have experience working with families in similar situations and can offer valuable advice and resources.

12.  Ask questions.

Don’t hesitate to ask questions or seek clarification from the medical team regarding your baby’s condition, progress, and care plan. Being well-informed helps alleviate anxiety and empowers you to initiate more meaningful interactions with your baby.

13.  Celebrate milestones.

Premature babies often reach developmental milestones later than full-term babies. Celebrate each small achievement, such as gaining weight, moving to an open crib, or starting to breastfeed.

These milestones testify to your baby’s progress and strengthen the bond between you and your little one. Maintaining a positive outlook can help strengthen your bond and offer hope during the NICU journey.

Make Bonding Moments with Your Preemie at the NICU

Nothing is as unique as a parent’s and baby’s bond, despite the challenges. Even in the NICU, you can create lasting memories and form a connection that will grow as your baby grows. Understand your baby’s growth and foster a happy atmosphere with your preemie.

Bonding happens over time, and it’s built on everyday moments like smiling at your baby, touching them, using loving words, and responding to their needs. With the strategies outlined in this article, determine which technique works best for you and your baby.

While every baby is different, you may try various approaches. Enjoy every bonding moment. Your preterm baby may be physically small, but they’re strong and have a lifetime of love and opportunity ahead of them.

Our twin pregnancy

In late 2021, I was pregnant with twins, 2 little siblings for my son Rico. The pregnancy was very exciting, and we couldn’t wait to meet them. We wanted to do a gender reveal, but sadly we didn’t get the opportunity.

At 21 weeks, I had a scan which found that my cervix was open. I had to have an emergency cerclage on New Year’s Eve 2021, and was in hospital for 2 weeks.

A week after being sent home, my waters broke. I was 24 weeks pregnant at this point and very scared. I rushed back to hospital where they told me I would remain until the twins were born.  

Giving birth  

10 days later, after multiple scans, I went into labour. My beautiful twins were born at 25 + 6 weeks at 2:03am (Luna) and 2:36am (Luca).

Both babies were transferred to NICU to begin their fight.  

At 4 days old, suddenly and unexpectedly, our baby boy Luca died. We had to wait 6 months for his postmortem results to find out why, which is when we were told he’d died of NEC. Our survivor Luna spent 87 days in NICU before coming home.

How I coped

The early days of grief I just shut myself away from people. I was at the hospital everyday with Luna and I just engrossed myself in caring for her. I had bereavement therapy which didn’t really help me, but what did help immensely was PTSD therapy.

I’ve also used the Facebook community to reach out to other people who have been through similar situations. I’ve made friends through those communities and we regularly message and support each other when things get tough.

Honouring Luca

We miss Luca every day. Having a surviving twin is such a complex mix of emotions – we feel happy and sad at the same time. We honour Luca daily and include him in our family.

We have a garden for him at home and in my parent’s garden. I also wear jewellery to remind me of him, and have lots of little ornaments around the house in his memory. On the twin’s birthday, we had a cake for both of them (pink and blue).

Every year, I try to do something for charity in his name. Last year I raised over a £1000 in a swimming challenge and this year I took part in Tommy’s Walk for Hope and managed to raise £400.

Advice for others

My advice to anyone who loses a twin baby would be:

Embrace the feelings of happiness and sadness. Losing a baby is something that no one should have to go through, but you’re a twin parent and your survivor will always be a twin.

Reach out to support through charities, and take counselling if you can. You will probably be suffering from some form of PTSD and working through that really helped me. 

Source: https://www.tommys.org/baby-loss-support/baby-loss-stories/baby-loss-stories/having-surviving-twin-such-complex-mix

Led by trained PSI facilitators, our online NICU group is intended for parents of babies who are currently or formerly in the NICU. This peer support group is for those with babies up to two years old who experienced a NICU stay for any reason. Connecting with others who have experienced the uniquely stressful environment of a NICU will provide parents with understanding, as well as helpful tools and resources. Whether your baby is currently in the NICU or you have finally returned home, our NICU Postpartum Parents support group is here for you.

Register Here

Note: This group is not for people processing the details and trauma of pregnancy and/or infant loss. Please join one of our Loss and Grief Support Groups for this important support.

PSI Support Groups

All of our groups are FREE and virtual. When registering for Sharewell for the first time, skip the unlimited offer on the payment page.

What to Expect

Our groups are 90 minutes (1.5 hours) in length. The first ~30 minutes is spent providing information, education, and establishing group guidelines. The next ~60 minutes is “talk time,” in which group members share and talk with each other. Group members must be present for the group guidelines before joining in the discussion or “talk time.”

Student and clinical observations are not allowed in our group spaces due to confidentiality and creating a safe space.

  • Cameras are required during introductions for the safety of all group members. Please make sure your technology allows you to turn on your camera at least briefly for this portion of the session.
  • The session will take place via Zoom (from the ShareWell website), so make sure your device is compatible with the Zoom app. This may require updating or downloading the Zoom app.
  •  

Student and clinical observations are not allowed in our group spaces due to confidentiality and creating a safe space.

Registration Information

PSI Support Groups are hosted on ShareWell and are split into different “wells.” Click on the registration link above to go to the Well, which includes support groups in each category.

When signing up for groups and making an account:

  • Skip the unlimited offer on the payment page (all of our groups are free!)
  • Access PSI support groups in each dedicated community
  • Reach out to groups@postpartum.net if you have any questions

In this new platform, we will no longer have a waitlist function. **We will allow up to 16 group members to enter the group, so please arrive on time to get a spot. Once we reach 16 members OR we have started talk time, the group space will be closed.

Source:https://postpartum.net/group/nicu-postpartum-parents/

Key points

  • Parents of sick or premature babies have a lot of stress in the early months of their babies’ lives.
  • Practical help and emotional support from friends and family can help parents cope.
  • It’s good to ask parents exactly how you can help.

Supporting parents of sick or premature babies

Parents of sick or premature babies go through a lot of emotional ups and downs in the early weeks and months of their babies’ lives.

When they get practical help and emotional support from family and friends, parents often cope a lot better with the experience. And when they’re managing well, they’re better able to look after their babies.

Here’s how you can help

  1. Celebrate as you usually would when a baby is born

Offer congratulations, send a card or flowers, and ring the new parents. By celebrating the birth of their baby in this way, you’re helping them celebrate as well. Give a gift if this is what you’d usually do. Small gifts for the parents can help them feel nurtured too.

If you’re thinking of giving clothes for the baby, make sure they’re very easy to put on and take off – loose necklines and armholes are good. If the baby is premature, size 00000 clothes can also be useful, because many parents won’t have bought these smaller sizes. Baby clothes for later are wonderful too, because they help the parents think about the future, when their child is at home.

Another gift could be a voucher for hospital parking. Or you could give a voucher for a restaurant close to the hospital, so that parents can have a meal and some time together but not be far from their baby.

You might be able to contribute to or help the parents organise cultural or religious traditions or ceremonies to celebrate their baby’s birth.

2. Offer practical help

Parents will be visiting the hospital as often and for as long as they can for days, weeks or months to come. This means that everyday chores are hard to fit in or don’t get done, which can be stressful.

Here are helpful things you could offer to do:

  • Mow the lawn or walk the dog.
  • Prepare meals or do the weekly grocery shopping.
  • Take older siblings to preschool or school or look after the other children in the evening.
  • Give parents a lift to the hospital – parking and transport can be very expensive.
  • Set up a messaging group or social media page, so that parents can send updates to just one source.

3. Support parents in whatever way they need

It’s OK to ask parents what they need. Some parents want to shut themselves off and cope with the situation alone or with a few close friends and family. Respect their wishes, but also let them know that you’re thinking of them. You could try to offer help when they seem ready.

Some parents need a lot of people around for support. These parents might love having company at the hospital. You could offer to drive, have lunch or just sit with them. Some parents want to talk about things other than the baby. Parents’ needs can change as their baby grows and changes.

4. Stay in touch with parents

A text message, an email, a quick phone call or voice message, or even an old-fashioned card in the mail – these are simple ways to let parents know you’re thinking of them. They help parents feel supported and remembered.

Try to understand how stressed the parents are and avoid judging them if they forget a birthday, can’t get to a family gathering, or take less interest in what’s happening in your life. It’s not that they don’t care – it’s just that right now, all their energy and focus is on their baby.

5. Say positive things about the baby

You can show your support by saying positive things like ‘Your baby is growing fast already’, or ‘They’re strong just like you’.

Avoid talking about setbacks that might happen or challenges that the baby could face, unless the parents bring it up with you. Also avoid giving advice about the baby.

6. Don’t expect to cuddle the baby

Sick or premature babies are very sensitive to touch, noise, infection and other things in their environment, so cuddling or touching is often limited or not allowed. Parents can also be very protective of their babies.

You might not even be able to see the baby, because there are usually limits on the number of visitors allowed at one time. Often it’s only 2 visitors. Sometimes only family is allowed – often this is only the baby’s parents. Each hospital has its own set of rules. Instead, you could ask to see photos of the baby (if the parent feels up to sharing them) or have a coffee with the parents at the hospital café.

Don’t be surprised if you still can’t have a good cuddle when the baby goes home. Many babies are still easily overwhelmed and might need to be protected from too much handling and too many new people.

If you’re sick, it’s important to avoid visiting a family with a baby in the neonatal intensive care unit (NICU) or the special care nursery. Sick or premature babies can get illnesses and infections very easily.

7. Listen to parents

Parents are likely to have mixed and strong feelings about their sick or premature baby and their experiences of the birth or hospital. These might not surface for weeks, months or even years.

Be open, let them talk and avoid giving advice unless it’s asked for. Avoid comparing them with other parents who’ve had a hard time. If you listen more than talk and follow the lead of the baby’s parents, you’re more likely to be helpful.

8. Keep offering help after the baby comes home

Parents might be tied to the house for some weeks once the baby comes home. Having someone organise shopping or preschool and school runs can really help.

Source: https://raisingchildren.net.au/newborns/premature-babies-sick-babies/neonatal-intensive-care/premature-babies-tips

Premature babies, or “preemies,” are born before 37 weeks gestation.

Hailey Petersburg was born at 24 weeks and five days.

Considered a “micro-preemie” and weighing just one pound and seven ounces, Hailey had a 40% chance of survival and a long road ahead of her in the Neonatal Intensive Care Unit (NICU). She spent 133 days in the NICU, where she underwent multiple surgeries and was treated for anaemia of prematurity. “Every day was a rollercoaster,” said Hailey’s mother and Leidos Data Scientist Allison Petersburg. “She was in a critical stage where her condition changed so rapidly every day.”

Before Hailey even reached what would have been full-term at 40 weeks, she received almost two dozen transfusions, which were crucial to her treatment plan.

Hailey’s tiny body was working as hard as it could, often enduring bradycardic events where her heart was beating too slow. Her medical team provided blood and platelet transfusions to help carry oxygen throughout her body; their impact was immediate, improving Hailey’s health and significantly increasing her vital signs.

In the United States, someone is in need of blood or platelets every two seconds. For many months, Hailey was one of those people. She received blood or platelet transfusions almost daily in the first weeks of her life, decreasing over time as she grew stronger each day. “Throughout the NICU experience of being in day-to-day survival mode, the gift of blood was a vital stability for Hailey,” said Allison.

Blood and platelets can’t be manufactured and must be donated. They also have an expiration date, so there is always a need for more blood donors. Since the beginning of the COVID-19 pandemic, the American Red Cross has seen a decline in blood donations, resulting in a national blood crisis. Between blood, platelets, and plasma, “nearly 16 million blood components are transfused each year in the United States.”

“Whenever Hailey had a transfusion, she would immediately begin breathing better, her heart rate was stable. As she received blood, the bradycardic and oxygen desaturation events decreased and all her vital signs improved,” said Allison. “They were lifesaving.”

After almost four and a half months in the hospital, Hailey Petersburg was ready to go home. Fast forward five years, and now Hailey is a recent preschool graduate, who, according to her mother, “is doing absolutely amazing.”

She’s an active soccer player, swimmer, and dancer, as well as an avid Disney princess fan, currently infatuated with Jasmine from Aladdin. Allison thinks Hailey intuitively knows how hard she had to fight soon after she was born, citing her joie de vivre, “she’s just the happiest little girl.”

Hailey is an example of why it’s so imperative to donate blood if you’re able. With nearly 30,000 units of blood needed each day, the Red Cross is continually in need of donors and one pint of blood can save up to three lives.

Even during a global pandemic, Leidos remained committed to diminishing the national blood crisis, collecting more than 311 units over the past two years. Since 2016, we’ve hosted 23 blood drives at our Global Headquarters in Reston, VA, thanks to 674 donors. Other offices, including our Columbia, MD, and San Diego, CA, locations regularly host blood drives, as well as one of our subsidiaries, QTC. The Columbia Leidos office has collected 125 units of blood since 2017.

Not only is donating blood so important, but the process is very quick, only taking about 20 minutes for the physical donation. For perspective, if just 1% more of all Americans donated, blood shortages “would disappear for the foreseeable future.”

“It was clear that the donated blood Hailey received in her transfusions saved her life,” said Allison. “I don’t know if my daughter would be with us today if not for blood donors.”

Schedule an appointment to donate blood today – and save a life.

Source: https://www.leidos.com/insights/whole-new-world-thanks-blood-transfusions

Editorial

The still predominant siloed, vertical structure of academia, health care systems, funding institutions/mechanisms, and public health organizations around the world pose an important challenge to tackle complex societal and health challenges for people, animals, and ecosystems. Understanding and acknowledging the delicate interdependence between ecosystem, human, and animal health is needed to design and implement comprehensive and holistic health strategies, beyond just human health. Infectious diseases with a zoonotic component have caused widespread human suffering in recent decades, with increased interactions between human and animal populations making people ever more vulnerable to new infections, given the rapidly and constantly changing global ecosystem. Additionally, socio-cultural, political, and economic factors impact the ability of systems to better prevent, detect, and respond to public health challenges at the human, animal, and environmental interface. This complex landscape applies to non-communicable diseases as well, requiring multisectoral approaches well beyond the traditional, narrow biomedical model. Hence, a wholesale shift is needed in how we approach public health. Instead of equating public health only with human health, we need to recognize what it truly is: the inter-related health of the world’s people, animals, and the environments we all share.

The complete interdependence between human, animal, and ecosystem health has been long recognized within Indigenous communities; however, the emergence and rapid expansion of the fields and practice of both One Health (OH) and Planetary Health (PLH) are recent developments in the right direction [1]. While the OH approach has been advocated for mostly in the context of addressing global threats related to zoonotic diseases and antimicrobial resistance, this approach is also relevant for several major public health challenges including pollution management, the environmental/agricultural component of food safety, food security, and nutrition. For example, the OH approach may lead to ecologically sustainable dietary patterns impacting the prevention and management of chronic conditions, such as cardiovascular disease.

The OH/PLH approaches have experienced considerable growth and expansion in academia, and within governmental and non-governmental organizations (NGOs)—with greater traction occurring in the past decade . While OH and PLH are highly complementary approaches based on transdisciplinary, multisectoral, and system-based approaches to health, challenges remain when translating ideas into policy and practice. “Overall, One Health and Planetary Health provide an opportunity to build a stronger research community to collectively address pressing public and global health issues in a truly integrated way”.

In March 2023, the Quadripartite organizations: the Food and Agriculture Organization of the United Nations (FAO), United Nations Environment Programme (UNEP), World Health Organization (WHO), and World Organisation for Animal Health (WOAH), issued an unprecedented call for enhanced global action to use the OH approach to “achieve together what no one sector can achieve alone”, emphasizing the need to translate the OH approach into policy action. Additionally, the Quadripartite institutions, in December 2023, published the One Health Joint Plan of Action with recommendations to implement OH approaches at national levels. Similar movements are occurring within the PLH space. For example, a National Planetary Health Action Plan (NPHAP) is being developed in Malaysia “to mainstream planetary health in all national policies and plans through a holistic and whole-of-nation approach”. Having endorsements from national and international organizations are important; however, there are still elements lacking when considering the implementation of OH/PLH to ensure human, animal, and ecosystem health.

What is next? Local community leadership and involvement is needed to build upon progress to date at the global level. To tackle complex public health challenges, a “bottom-up” approach is needed that complements global and national efforts. An emphasis on local, practical, and feasible solutions are also needed to address complex problems, while engaging local stakeholders and affected communities. A key aspect, however, of implementing OH and PLH approaches into public health strategies is to account for the socio-cultural, religious, and economic factors among local and rural communities. This is especially important when working with those most marginalized, such as Indigenous and rural communities, who are often already closely and directly attached to having strong connections with the ecosystem they inhabit.

Scientific, biomedical, and health knowledge is necessary, but not sufficient alone. Successful public health interventions that work at the human-animal-ecosystem interface require the broad and committed collaboration of members from all levels of society. A coordinated, multisectoral approach that involves animal health and public health authorities, health practitioners, physicians, veterinarians, environmental workers, politicians, researchers, experts in social, cultural, and communication issues, as well as economists, farming and agricultural groups, and local communities is necessary. Importantly, bold and courageous political leadership is essential to co-lead while securing public support for health policy decisions and implementation [5]. It is key to develop a OH/PLH “business case” (e.g. cost-benefit analysis), with governments enabling, facilitating, and supporting implementation processes both financially and within appropriate legal frameworks. This will ensure the recognition for not only the importance of economic benefits derived from reducing a specific health issue, but also for assessing the broader public health and societal benefits and impacts.

While OH and PLH offer a rational systems approach for safeguarding health in an interconnected world, to secure its benefits, public health must do what humans, animals, and plants have always done—evolve!

Source: https://academic.oup.com/eurpub/article/35/1/3/7815848

Comparison of maternal and neonatal outcomes of midwifery-led care with routine midwifery care: a retrospective cohort study

Shirin Shahbazi SighaldehElaheh EskandariShahla KhosraviElham EbrahimiShima Haghani & Fatemeh Shateranni

BMC Nursing volume 24, Article number: 158 (2025)

ABSTRACT

Introduction

Globally, the management of low-risk pregnancies by midwives often leads to a more natural childbirth process, which enhances physical and psychological outcomes for mothers and their babies. Midwives implement various models of maternal care in practice. This study investigates and compares maternal and neonatal outcomes associated with midwifery-led care versus routine midwifery care in private hospitals in Iran.

Methods

This retrospective cohort study was conducted in Iran in 2022. The study population consisted of two groups including 387 women in the Routine Care Group (RCG) and 397 women in the Private Care Group (PCG). Participants were selected through continuous sampling in accordance with the inclusion criteria. The two groups were compared in terms of some maternal and neonatal outcomes. The research data collection tool was a researcher-made checklist with variables adjusted according to the ‘Iman’ system of the Iran Ministry of Health. Based on this tool, the data were extracted from the mentioned system and analyzed with SPSS software.

Findings

The results indicated no significant difference between the two groups in terms of the type of delivery (p = 0.999), the use of forceps or vacuum (P = 0.5) and transferring the mother to the operating room (OR) or the intensive care unit (ICU) immediately after delivery (P = 0.744). However, there was a statistically significant difference between the two groups in terms of labor pain control (P < 0.001), induction of labor (P < 0.001), and the use of episiotomy (P < 0.001). Regarding neonatal outcomes, there was no statistically significant difference between the two groups in relation to the average infant weight (P = 0.46), Apgar score (P = 0.75), need for resuscitation (P = 0.999), skin-to-skin contact (P = 0.626), initiation of breastfeeding (P = 0.241) and admission to the neonatal intensive care units (NICU) (P = 0.66).

Conclusion

Given the positive impact of private care on key maternal outcomes, it is recommended that health policymakers create the conditions necessary for establishing a continuous midwifery care model in both governmental and private hospitals. Besides, more quantitative, qualitative, and especially mixed methods research should be conducted to explore the challenges and facilitators of this model across various settings.

Source: https://bmcnurs.biomedcentral.com/articles/10.1186/s12912-025-02789-4

by European Society of Human Genetics  edited by Sadie Harley, reviewed by Robert Egan

May 24, 2025

Children born before 37 weeks of gestation have a considerably increased risk of dying before they reach the age of five. Predicting the risk of preterm birth (PTB) and hence implementing preventive strategies is complicated by the heterogeneity of the condition, the many unknown mechanisms involved, and the lack of reliable predictive tools.

Now, however, researchers have been able to show that blood cell-free RNA (cfRNA) signatures can predict PTB over four months before delivery date. The research was presented at the annual conference of the European Society of Human Genetics.

Dr. Wen-Jing Wang, an associate researcher at BGI Research in Shenzhen, China, together with team leader Professor Chemming Xu from the Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China, and colleagues analyzed blood plasma samples from 851 pregnancies (299 PTB cases and 552 controls) at about 16 weeks gestation to identify cfRNA markers associated with spontaneous PTB, and found significant alterations in cfRNA between PTB and birth at term.

The study included both preterm births with intact membranes and premature rupture of membranes (when the waters break before labor starts), with fewer than 3% having a prior preterm birth.

“Being able to detect these predictive signals over four months suggests early biological priming for PTB, far earlier than current clinical recognition,” she says. “This extended window could revolutionize prevention strategies.”

Annually, about 13.4 million newborns worldwide are delivered prematurely, accounting for approximately one in 10 of all live births. Nearly one million of these preterm infants die each year, and PTB remains the primary cause of mortality in children under five.

Because children born preterm have immature organs that are not yet prepared for life outside the womb, it means that they will have a far higher risk of complications than those born at term. This can lead to a range of health issues such as respiratory problems, jaundice, feeding difficulties, and infections.

Long-term health problems for these children include cerebral palsy, epilepsy, and blindness, and impose substantial emotional and financial burdens on families.

“Practically, our method uses the same blood draw timing as routine Non-Invasive Prenatal Testing (NIPT), enabling dual testing. Current cfRNA sequencing costs are similar to NIPT pricing, but future optimization using targeted qRT-PCR panels could reduce expenses significantly. This creates a potential route to both monitoring patients at high risk and for wider population-level screening,” says Dr. Wang.

Before this diagnostic technique can be used more widely, the researchers say that standardized protocols for sample handling need to be developed, given RNA’s instability compared with DNA.

Prediction algorithms need to be developed in diverse population studies, and the causes of different PTB subtypes explored to be able to guide targeted interventions. The team is pursuing these goals and seeking to collaborate with other institutions in order to accelerate the use of their findings in clinical practice.

Chair of the conference, Professor Alexandre Reymond, said, “Advances in sequencing and analysis technologies are now offering many new diagnostic possibilities. This is a fascinating example of the use of sequencing readouts to evaluate risk, rather than assessing genetic background to assess predisposition.”

Source: https://medicalxpress.com/news/2025-05-early-preterm-birth-cell-free.html

Saving Tiny Lives: The Critical Need for Blood and Platelet Donations for Preemie Babies Undergoing Surgery

Premature infants, especially those born before 32 weeks of gestation, often face life-threatening challenges that require surgical intervention. These delicate babies are at heightened risk for bleeding complications due to their underdeveloped organs and fragile blood vessels. In fact, studies indicate that platelet transfusions are administered to 5.8%–53.0% of neonates with a gestational age at birth below 32 weeks, underscoring the critical need for these life-saving donations.

When it comes to blood versus platelets, it’s essential to understand the differences. Blood transfusions typically involve the whole blood or red blood cells, which help provide oxygen to the body’s tissues. For preemie babies, blood transfusions are often required to address anemia, a condition where the body doesn’t have enough red blood cells to carry sufficient oxygen. Platelet transfusions, on the other hand, are crucial for babies who are at risk of bleeding or have low platelet counts, which are essential for blood clotting. While blood transfusions address oxygen needs, platelet transfusions play a vital role in preventing severe hemorrhaging in these tiny patients.

The impact of blood and platelet transfusions on preemie babies cannot be overstated. For instance, a study involving neonatal surgeries revealed that 14% of neonates received perioperative red blood cell transfusions. Among those transfused, 30-day mortality rates were significantly higher, and they also experienced increased rates of complications such as wound dehiscence, mechanical ventilation beyond 48 hours, cardiac arrest, and septic shock. Platelet transfusions, however, are often the key to minimizing bleeding risks during surgeries and promoting recovery in fragile babies.

Recognizing the importance of these donations, I recently contributed by donating platelets to support children undergoing cardiac surgery. This experience highlighted the profound difference that blood and platelet donations make in the lives of critically ill children. Each donation has the potential to save lives and improve outcomes for these vulnerable patients. If you’re considering how you can make a tangible impact, donating blood or platelets is a powerful way to help. Your donation could be the one that gives a tiny baby the chance to grow, thrive, and lead a healthy life. To learn more about how you can donate and make a difference, visit your national blood donation agency’s website. Your generosity can be the lifeline these babies desperately need.

Sierra Leone’s beaches and waves make them attractive for surfers. But the country has just one surf club. It tries to get boys and girls off the streets and into the water, despite equipment and personnel being in short supply. Sierra Leone is still infamous for its civil war and poverty. But it’s also incredibly beautiful. Enjoy the breathtaking views from Bureh Beach — a perfect spot for surfing.

NW Warriors – Call to Action!

The Dominican Republic is a North American country located on the island of Hispaniola in the Greater Antilles of the Caribbean Sea in the North Atlantic Ocean. It shares a maritime border with Puerto Rico to the east and a land border with Haiti to the west, occupying the eastern five-eighths of Hispaniola which, along with Saint Martin, is one of only two islands in the Caribbean shared by two sovereign states. In the Antilles, the country is the second-largest nation by area after Cuba at 48,671 square kilometers (18,792 sq mi) and second-largest by population after Haiti with approximately 11.4 million people in 2024, of whom 3.6 million reside in the metropolitan area of Santo Domingo, the capital city.

There are three tiers of healthcare in the country:

  • Subsidized regime, which is financed by the government for unemployed, poor, disabled and indigent people.
  • Contributive regime, which is financed by workers and employers
  • Contributive subsidized regime, which is financed by independent workers, technical workers, and self-employed people, but subsidized by the state[16]

Even those for whom care is supposedly provided may have to pay for medical supplies. However, considerable progress in health and overall development was experienced in the country. For instance, there is a substantial increase in health coverage in the nation that is the health insurance coverage from 23% in 2011 to 65% in 2015 (Centers for Disease Control and Prevention n.p). Significantly, updating the list of beneficiaries was the major challenge since the list based on disease prioritization and financial sustainability. Therefore, the first fitness elements, such as migration, poverty education, and gender-based, should be considered in the strategy of hindrance suites.

Government expenditure on healthcare is about $180 per person per year, slightly more than half the average for the Latin American and Caribbean region.

Essentially, there are steps considered by healthcare in the Republic. Firstly, the sponsored organization that caters to the poor, unemployed, and disabled people. Also, the active personnel contained a contributive establishment. Though the low-classes are dependents, the majority of the population is independent on matters of health, according to the Dominican Republic (World Health Organization n.p). Therefore, government expenditure per person is slightly higher in the Dominican Republic compared to other states.

Source:https://en.wikipedia.org/wiki/Health_in_the_Dominican_Republic

Europe needs new ideas and solutions to address the disparities in the care of preterm and ill babies. The European Standards of Care for Newborn Health project presents such a solution by providing European reference standards for this health care area.

With its transdisciplinary focus and international composition of the working groups, the project sets new benchmarks for the care of preterm and newborn babies and can serve as a role model for countries in Europe and worldwide. About 220 experts from more than 30 countries accepted to dedicate their free time to work on this ambitious project over several years. At the time of the launch of the standards, 108 healthcare societies and associations as well as 50 parent organisations have accepted EFCNI’s invitation to officially support the newly developed standards.

Through its multi-stakeholder approach, the perspective of parents, healthcare professionals, and relevant third parties were equally considered, aiming at identifying current best practice. Industry partners were involved in the project by supporting it financially. Their representatives could join the Chair Committee meetings in an observing role and they were welcome to share their knowledge and expertise without exerting influence. Initiated by patient (parent) representatives for patients, it is a true patient-centred project and, for the first time, patients were involved in absolutely every step in the development of the standards. All project participants work together in an open and respectful partnership to pave the way for change and set newborn health on the international and national agendas.

On a political level, addressing European Standards of Care for Newborn Health will stimulate a new debate that can help questioning existing structures, identify gaps and deficiencies, and advance national healthcare systems. To read the standards and to learn more about their development, please visit our project website European Standards of Care for Newborn Health.

On the project website, you also find further information like a project report, an information brochure or social media graphics.

The European Standards of Care for Newborn Health now available in Italian – Gli Standard Assistenziali Europei per la Salute del Neonato sono disponibili in italiano

The Italian Society of Neonatology (SIN) and Vivere ONLUS, the Italian National Coordination of Parents’ Associations, took the initiative to translate the standards into Italian, with Italy becoming the first European country to make this important document available in their national language. The first two sets of standards can be downloaded from our project page.

Call to Action for Newborn Health in Europe

The UN Convention on the Rights of the Child has been ratified by 196 countries and proclaims that “the child, by reason of his physical and mental immaturity, needs special safeguards and care, including appropriate legal protection, before as well as after birth”.  Article 6 affirms every child has the right to life, survival, and development. Furthermore, children have a right to be cared for by their parents and should not be separated from them, as far as possible (Articles 7 and 9). However, upholding the Rights of the Child in reality remains a major challenge.

The European Standards of Care for Newborn Health help support these rights from the beginning of life by serving as a reference for the development and implementation of binding standards and guidelines on a national and international level. European and national policy makers, hospital administrators, insurers, professional and patient associations, and industry should work together to bring the standards into practice and to ensure quality, equity, and dignity for the smallest.

Download the Call to Action Brochures: The Call to Action is available in about 20 languages and can be downloaded here.

News provided by March of Dimes Inc.   Mar 18, 2025

ARLINGTON, Va., March 18, 2025 /PRNewswire/ — March of Dimes, the leading organization committed to improving the health of moms and babies, has been named the United Food and Commercial Workers International Union’s (UFCW) Labor Partner Charity of Choice for 2025. As UFCW’s designated national charity partner, March of Dimes and UFCW will work together to support and advocate for healthy pregnancies, strong families, and improved maternal and infant health outcomes in the US.

“For more than 85 years, March of Dimes has stood alongside labor unions to champion the health and well-being of working families,” said Cindy Rahman, President and CEO of March of Dimes. “Our partnership with UFCW builds on this proud legacy, strengthening our ability to advocate for policies, provide essential resources, and drive meaningful change to improve maternal and infant health outcomes. We will work together to ensure that every family—no matter where they live or work—has access to the care and support they need for a strong, healthy start.”

The US remains the most dangerous high-income nation for childbirth, earning a D+ for a third consecutive year in March of Dimes’ latest Report Card, which measures the state of maternal and infant health in the US. Through this partnership, UFCW and its more than 1.2 million members will have opportunities to engage in fundraising efforts, volunteer initiatives, and awareness campaigns aimed at addressing this growing crisis.

“The UFCW Charity Foundation is committed to supporting organizations that make a real difference in the lives of working families,” said UFCW International President Marc Perrone. “March of Dimes has led the fight to improve maternal and infant health for decades, and we are proud to stand with them in this important work. By joining forces, we have the opportunity to help even more families access the care and resources they need for healthy pregnancies and strong futures.”

Partnering with labor unions to protect the health of working families is a cornerstone of March of Dimes’ mission. We’re honored to have strong and long-standing national and local partners like UFCW through our Labor of Love movement, which raises critical funds to pioneer research, advocate for change, and pave the way for greater equity to give all families the best possible start.

Before being named UFCW’s Charity of Choice, UFCW members have actively supported March of Dimes, raising over $3 million through golf outings, sporting clay events, auctions, and March for Babies teams. They have also uplifted the voices of their own members, like Daniel Scott of UFCW Local 1996, whose twins spent time in the neonatal intensive care unit (NICU) after a challenging pregnancy. For families like the Scotts, March of Dimes’ work is more than a cause—it’s a lifeline, ensuring that babies born too soon or facing complications receive the critical care they need.

For more information on how to get involved, visit https://www.marchofdimes.org/get-involved/partner/labor-union

About March of Dimes
March of Dimes leads the fight for the health of all moms and babies. We support research, education, and advocacy, and provide programs and services so that every family can get the best possible start. Since 1938, we’ve built a successful legacy to support every pregnant person and every family. Visit marchofdimes.org or nacersano.org for more information. Follow us on social at @marchofdimes.  SOURCE March of Dimes Inc.

Source: https://www.prnewswire.com/news-releases/march-of-dimes-named-2025-labor-partner-charity-of-choice-for-united-food-and-commercial-workers-international-union-302404305.html

Andrew Bush    Anne Greenough    Alvar Agustí 

To the Editor:

Premature birth has consequences across the course of life, including reduced life-expectancy, and the most prematurely born have the worst outcomes [12]. Survivors of prematurity have increased respiratory morbidity and mortality, airflow obstruction, asthma-like symptoms and COPD, and cardiovascular disease [14]. A history of prematurity is often not sought in adult clinics [5]. We hypothesised that the long-term consequences of prematurity are insufficiently appreciated, likely with detriment to patient care.

We used an online survey developed by a panel of neonatologists, paediatricians, allergologists and pulmonologists. The survey included 21 items addressing four main topics: 1) awareness level among respiratory care providers regarding the long-term respiratory risks of premature birth; 2) communication of neonatal information between different medical specialties; 3) healthcare journey of preterm babies to paediatricians and other respiratory care providers; 4) the knowledge gaps and potential solutions. The survey was customised to each specialty: seven items were for neonatologists only; three for paediatricians; one each for allergologists and respiratory consultants; five for paediatricians, allergologists, and respiratory consultants; and four for all specialties.

We invited 14 651 neonatologists, paediatricians, allergologists and respiratory consultants from Australia, France, Germany, Italy, Spain, the UK, and the USA to participate, excluding physicians with less than 2 years’ experience; 1002 (7%) responded. A web link was emailed from listings extracted from Chiesi Farmaceutici S.p.A and from proprietary databases of external healthcare providers. All had previously consented to email contact. Two email reminders were sent and incomplete surveys were rejected.

Sample size was opportunistic in the absence of data enabling a power calculation. The survey results were analysed using Microsoft Excel and Microsoft Power BI. All items involved categorical answers, and absolute and relative frequencies were calculated. All frequencies were treated descriptively. No geographical comparisons were performed due to sample size limitations. The questionnaire is available on request from the corresponding author.

Results are summarised in figure 1. Of the 1002 respondents, 91% had been in practice for more than 5 years, and 62% were practising in an outpatient facility. In terms of specialities, 282 (28%) were neonatologists, 183 (18%) paediatricians, 290 (30%) allergologists, and 247 (24%) were respiratory consultants. Figure 1a shows that neonatologists regarded the presence of respiratory symptoms as being most important in the decision to refer. By contrast, for paediatricians, birth weight was the most important factor, irrespective of respiratory symptoms (figure 1b). All specialists highlighted that the most important gap was lack of clear recommendations for follow-up (figure 1c) and the need for continuing medical education programmes (figure 1d). Most (96%) respondents considered prematurity and bronchopulmonary dysplasia (BPD) risk factors for lung diseases in adulthood. Nevertheless, 74% of respondents perceived only moderate to very low awareness among colleagues. Adult pulmonologists perceived the lowest level (85%) of awareness among the specialties surveyed.

FIGURE 1

Reasons for neonatologists (a) and paediatricians (b) to refer preterm-born patients to a respiratory specialist. The gaps and potential solutions to improve the long-term respiratory care of preterm-born individuals are shown in (c) and (d). The bars show the percentage of participants who selected each option. NICU: neonatal intensive care unit; BPD: bronchopulmonary dysplasia.

Most (77%) paediatricians “always” took a perinatal history, compared with allergologists (34%) and pulmonologists (21%). Irrespective of specialty, the proportion who always took this history increased with increasing years of clinical experience. Most (95%) neonatologists shared information on gestational age, birth weight, need for supplemental oxygen and respiratory support, BPD diagnosis and other lung sequelae of prematurity (>80%), and this was consistently reviewed by paediatricians (83%). This information was mainly through medical records (57%) and by oral communication (52%). Allergologists and respiratory consultants used feedback from other physicians (58% and 37%, respectively) and electronic medical records (43% and 26%, respectively) to gather neonatal information. They reviewed less neonatal information, although BPD diagnosis and lung sequelae were reviewed by 72% and 65% of allergologists and respiratory consultants, respectively.

Most neonatologists (99%) shared information with parents and caregivers, and more than 70% of paediatricians and allergologists received information from the caregivers. Only 59% of adult pulmonologists acknowledged receiving information from parents and caregivers.

Most neonatologists (70%) followed up preterm babies for two years, but 27% for only 1–2 years. Most (>75%) of all those surveyed, believed that premature babies should be followed up lifelong.

Most (>80%) allergologists modified clinical management, at least partially, if they were aware that the patient was born preterm. Only 60% of adult pulmonologists adapted management pathways in preterm survivors.

Most (>60%) respondents considered that preterm-born individuals and their parents and caregivers should be empowered to ensure they receive the best respiratory care. Other suggested initiatives were measuring lung function during follow-up from 5 years of age, streamlining access to the perinatal medical history and the development of a portable record with neonatal information. Going forward, the use of a lifelong electronic patient record, accessible to all who are involved in patient care, would likely greatly facilitate communication between specialist groups.

In summary, there is inadequate awareness of the importance of preterm birth for management across the life course; communication between specialist teams is inadequate; and there is lack of clear guidance as to how to follow-up preterm born survivors.

The European Respiratory Society [6], and the American Thoracic Society [7] have published guidelines with conditional recommendations on low strength evidence. However, the former only covered the follow-up of BPD survivors [6], and the latter were limited to the follow-up of preterm-born children and adolescents with respiratory symptoms [7]. These guidelines are limited, not least because we now know that the risk of compromised lung health later in adulthood exists even for early term born infants [489]. However very few paediatricians actually referred extremely preterm or low birth weight babies to a respiratory specialist. An international consensus on how to structure respiratory follow-up remains an unmet need [110].

Most allergologists (80%) and adult pulmonologists (60%) modified diagnostic pathways and treatment approaches, at least partly, when they were aware the patient was born premature. Lack of appreciation of the implications of prematurity across the life course may lead to wrong treatment being prescribed. For example, school-age wheeze and variable airflow obstruction is common in preterm survivors [11]. Some may respond to treatment with inhaled corticosteroids (ICS) [12] but in others there is no evidence of type 2 inflammation so they should not be treated with ICS [13]. They may have dysanaptic airway growth [14], which is known to be associated with poor outcomes in term-born children [15]. More work is needed to determine disease pathology in preterm survivors and to stimulate new research. Trials to stimulate lung development at birth and control airway inflammation in extremely premature babies are underway with stem cell-based therapies, insulin-like growth factor 1 and intratracheal surfactant/budesonide.

Proposed mitigation strategies to improve the current situation include better continuing medical education. Another is empowering patients and caregivers by supplying accurate information which they can ensure is available to subsequent caregivers, including during transition to adult services.

The main strength of the survey is that it includes >1000 physicians from different specialties and countries. There are some limitations. The overall response rate was relatively low, although similar to the British Thoracic Society survey [5], and there is a risk of selection bias. General practitioners were not invited, and this was a mistake given their role in follow-up care.

In conclusion, we need to increase awareness of the long-term implications of prematurity to ensure optimal follow-up for these babies, and design studies to obtain an evidence base for the development of improved guidelines.

Source:https://publications.ersnet.org/content/erjor/11/1/00643-2024

Juan Luis Guerra 4.40 – El Farolito (Live) (Video Oficial)

Juan Luis Guerra

3 years ago #JuanLuisGuerra #ElFarolito #EntreMaryPalmeras

Juan Luis Guerra 4.40 – El Farolito (Live)

Houda M. Abdelrahman; Suzanne M. Jenkins; Michael P. Feloney.

Last Update: November 12, 2023.

When the hymen, a thin membrane of stratified squamous epithelium circumscribing the vaginal introitus, does not spontaneously rupture during neonatal development, it is referred to as an imperforate hymen. An imperforate hymen is a rare cause of primary amenorrhea and can present with obstructive symptoms of the female genital and urinary tracts during the perinatal, pediatric, or adolescent years. Timely diagnosis and prompt treatment are critical. Specific pediatric and gynecologic knowledge and skills are necessary to provide comprehensive, patient-centered care. In addition to the anatomical and physiological aspects of imperforate hymen, its clinical presentation, and potential complications, the psychological impact on affected individuals must be understood. Best practices will ultimately improve patients’ quality of life and reproductive health outcomes. This activity reviews the evaluation and treatment of imperforate hymen and highlights the role of the interprofessional team in improving care for patients with this condition.

Continue for training and assessment!

Source: https://www.ncbi.nlm.nih.gov/books/NBK560576/

Jun 17, 2023

Spilling the Tea is an educational series for new preemie moms and dads brought to you by TEACUP Preemie Program®. These brief but in-depth videos will explore aspects of prematurity including emotional and mental effects, the NICU environment, breastfeeding & pumping, reclaiming attachment & bonding, and others. Preemie parents share their experiences through intimate video journals, and experts in infant development and prematurity offer guidance and information. Episode 3: Dads in the NICU, takes you through the emotional rollercoaster experienced by Beau, Chris, and Steve, three preemie dads who have been there. Get ready to be moved and inspired by their stories of resilience, love, and the extraordinary bond they formed with their little miracles.

Mitigating the iatrogenic psychological effects of medical care in the Neonatal Intensive Care Unit (NICU) and beyond is a moral and ethical imperative for quality healthcare delivery. Research has long established the lifelong effects of early childhood adversity, toxic stress, and the critical role of pediatric clinicians in addressing these challenges, and most recently, the American Academy of Pediatrics (AAP) published a clinical report and policy recommendations for the adoption of a trauma-informed paradigm across all child health services.  Provenzi and Montirosso  confirm that preterm birth is an early adverse experience characterized by exposure to toxic stress and reduced access to the buffering effects of maternal care. Understanding the concepts of infant medical stress and its association with alterations in brain growth and development highlights the biological relevance of a trauma-informed developmental approach to care in the NICU and beyond.

Early life adversity, often mediated through relationships with caregivers, is associated with attachment disturbances, posttraumatic stress disorder (PTSD), and developmental trauma disorder (DTD) in survivors . Experiences of maternal separation and cumulative toxic stress within the NICU have profound implications for infants, families, and the healthcare team . Adversity during infancy is associated with significantly poorer health outcomes, risky health behaviors, and socioeconomic challenges . Parents, too, experience significant emotional and psychological distress, which can persist for decades, further reinforcing the need for trauma-informed approaches to care).

During sensitive and critical periods of development, the experiences associated with critical illness and hospitalization take on new meaning as they direct and disrupt biological processes in the wake of toxic stress. These biological processes, mediated by epigenetic mechanisms, have lifelong implications for an individual’s physiologic and psychological health and wellbeing . Maternal separation is the most significant trauma experienced by all newborn mammals, and preterm and critically ill newborns are no exception . Separation of mother and infant at just two days of age for 1 hour has been linked to a 176% increase in autonomic reactivity and an 86% reduction in quiet sleep . The experience of maternal separation in the NICU becomes the foundation for cumulative toxic stress exposures, ranging from inappropriate sensory stimuli to hazardous hospital routines that do not honor the personhood of the infant. These early stressors compound, leading to long-term health and developmental challenges.

 Separation also has profound implications on the parent, leading to depression, anxiety, feelings of helplessness, loss of control, and posttraumatic stress, which may last for decades. These feelings can impact parenting behaviors and the capacity to partner with clinicians in caring for their infant. Understanding the interplay of physical and emotional health, economic and social resources, medical systems, and structural inequities is critical for co-creating compassionate, collaborative, and supportive relationships with infants, families, and clinicians in the NICU.

 Trauma-Informed Care:

A trauma-informed approach realizes the pervasiveness of trauma in everyday life, recognizes its signs and symptoms in patients, families, colleagues, and self, and responds to trauma by integrating knowledge and evidence-based best practices that mitigate and prevent trauma into policies, procedures, and language; and resists re-traumatization by ensuring consistency and compassion in service delivery. The core principles of trauma-informed care—safety, trust and transparency, healthy relationships and interactions, empowerment, voice and choice, equity, anti-bias efforts, and cultural/gender affirmation—guide all interactions in the NICU.

Parenting is central to a trauma-informed approach, as caregivers play a fundamental role in mitigating the stress and trauma of early hospitalization. The research underscores the powerful buffering effect of parental presence, engagement, and nurturing care in reducing toxic stress responses and promoting infant resilience . When parents feel supported and empowered in their caregiving role, they experience lower stress levels, increased confidence, and enhanced bonding with their infant. This benefits the family’s emotional well-being during the NICU stay and has lasting implications for child development and attachment security.

The short-term outcomes of a trauma-informed parenting approach include improved neurodevelopmental stability, reduced incidences of apnea and bradycardia, and better weight gain trajectories for preterm infants. Additionally, trauma-informed care has been linked to greater autonomic stability, reduced stress hormone levels, and improved sleep patterns, all contributing to enhanced physiological regulation and early developmental progress . These immediate benefits lay the groundwork for stronger immune function and better feeding outcomes, helping infants build the resilience needed for longterm health and well-being . Parents who are actively involved in their infant’s care through practices such as skin-to-skin contact and responsive caregiving exhibit lower levels of anxiety and depression, leading to a healthier emotional environment for both the child and the family unit .

Long-term, trauma-informed parenting interventions significantly impact developmental trajectories, reducing the risk of cognitive delays, emotional dysregulation, and behavioral challenges in childhood . Secure attachment formed during these early interventions fosters resilience, social-emotional well-being, and stronger parent-child relationships well into adolescence and adulthood. Studies have also linked early trauma-informed care to improved educational outcomes and a reduced risk of mental health disorders later in life .

Providing parents with the knowledge, tools, and emotional support necessary to engage confidently in trauma-informed caregiving is critical in shaping the health and well-being of NICU graduates . By prioritizing the parent-infant dyad and leveraging evidence-based interventions, trauma-informed care offers a transformative model that extends far beyond the NICU walls, laying the foundation for lifelong resilience and well-being. When parents are given the resources to understand their infant’s cues, respond sensitively, and participate actively in care, they develop a sense of mastery and confidence that translates into more substantial, more secure attachments. This engagement benefits the infant’s immediate well-being and fosters a more compassionate, informed approach to parenting that can positively influence future generations.

 Clinical Application of Trauma Informed Care:

Parent-driven interventions in the NICU center include parents as active participants in their baby’s care, fostering attachment and reducing trauma. One such intervention is The Zaky HUG®, a therapeutic device designed to extend the parent’s presence by mimicking their hands’ touch, warmth, and scent (Fig. 1). Created by a Ph.D. engineer and former NICU and kangaroo mother, this tool emerged from a deeply personal experience of neonatal hospitalization and has since been developed to support sleep, neuroprotection, attachment, developmental care, pain management, and parental involvement. This device helps create a comfortable, warm, and predictable environment, allowing infants to rest and sleep more peacefully. It is designed to provide the benefits of multiple tools, including positioning, nesting, soothing, and attachment.

Initially motivated by the need to provide connection, continuous comfort, and reduce the association of touch with pain and her own infant’s stress, the creator of this hand-mimetic device applied principles of ergonomics and safety engineering to design a device that fosters secure attachment, supports positioning, predictable experience for the infant, family, and clinicians.

Protected sleep is critical for neurodevelopment and overall well-being. Sleep is a primary driver of brain maturation, memory consolidation, and emotional regulation in preterm and critically ill infants. Interruptions to sleep can disrupt these critical processes, leading to increased stress responses, metabolic instability, and impaired neurodevelopmental outcomes. Ensuring a supportive sleep environment requires balancing between providing necessary medical interventions and minimizing disruptions to natural sleep cycles. Frequent repositioning, environmental disruptions, and inconsistent containment can negatively impact an infant’s sleep-wake cycles. Research by Russell et al. has shown that because these nurturing devices are versatile and work for positioning, nesting, attachment, soothing, and sleep support, they reduce the need for frequent repositioning, offering a stable, soothing environment that promotes restful sleep both during kangaroo care and while in the incubator or crib. These devices help infants transition between sleep states more smoothly, reducing startle reflexes and excessive wakefulness by providing gentle, consistent containment and proprioceptive support.

Additionally, they assist in creating a cocoon-like space that mimics the security of the womb, further enhancing sleep continuity and quality. Further, consensus guidelines advocate for supporting parents in providing frequent, safe, and prolonged skin-to-skin care, reinforcing the role of these interventions in achieving sleep protection . Research has also highlighted that skin-toskin contact improves sleep patterns, stabilizes respiratory rates, and reduces cortisol levels, mitigating the physiological impacts of stress. When infants experience uninterrupted, restorative sleep, they exhibit improved feeding behaviors, enhanced weight gain, and greater autonomic stability, all crucial for their long-term development.

The Pain and Stress Prevention and Management measure prioritizes proactive pain mitigation strategies. By minimizing stress and discomfort, infants can better participate in essential activities of daily living, such as feeding and movement, which further support their growth and development. The integration of non-pharmacologic interventions such as kangaroo care, proprioceptive input, and containment through trauma-informed devices significantly enhances an infant’s ability to self-regulate and cope with stress . Parents play a vital role in this process, providing direct comfort before, during, and after procedures. Studies show that utilizing familiar, comforting sensory stimuli, such as parental scent-infused devices, can effectively minimize procedural stress and discomfort, reinforcing the protective role of parental presence in the NICU.

Activities of Daily Living, including posture, nourishment, and hygiene, are essential to infant development. Establishing predictable and supportive care routines in these areas helps to create a sense of security and stability for infants, reducing stress and promoting optimal development. Ensuring infants receive proper postural support can facilitate musculoskeletal alignment, improve digestion, and reduce discomfort caused by medical interventions. Additionally, consistent caregiving routines help infants develop circadian rhythms, supporting sleep-wake cycles and overall well-being. Kangaroo care safety devices support proper postural alignment, promoting successful breastfeeding and early oral feeding behaviors. One pair of hand mimetic devices further enhances postural stability, allowing for individualized positioning without restricting movement, facilitating optimal comfort and developmental support. These devices can also provide gentle containment, mimicking the boundaries of the womb, which is particularly beneficial for preterm infants adapting to extrauterine life. Furthermore, integrating nurturing devices in caregiving practices encourages parental involvement in routine care activities, reinforcing their role and confidence in caring for their baby even in a high-tech NICU environment.

Finally, Compassionate Collaborative Relationships focus on emotional well-being, self-efficacy, and communication. Clinicians play a vital role in supporting these trauma-informed measures, ensuring that both parents and staff are equipped with the knowledge and tools to facilitate optimal trauma-informed developmental care. These trauma-informed interventions support neurodevelopment and empower parents, reinforcing their role as primary caregivers. By enabling continuous sensory presence and minimizing separation, these devices help establish a sense of predictability, safety, and emotional security for infants and their families. The research underscores the long-term benefits of these interventions, showing reductions in parental stress and anxiety while fostering stronger attachment and advocacy skills.

By integrating trauma-informed devices and caregiving practices, neonatal teams can transform the NICU experience, bridging the gap between medical excellence and human connection. As neonatal care continues to evolve, integrating trauma-informed interventions into everyday practice is not just beneficial—it is imperative for fostering lifelong resilience in the most vulnerable patients. Prioritizing the five core measures for trauma-informed developmental care ensures that every infant and family receives care that is not only evidence-based but also deeply compassionate and developmentally appropriate.

Summary: Recognizing the trauma experienced by babies and families in the NICU is the first step toward transforming and humanizing neonatal care. This recognition must be followed by meaningful action—integrating trauma-informed practices, supporting parental involvement, and embracing innovative, evidence-based products and solutions that prioritize the holistic well-being of infants and their families. Trauma-informed interventions, particularly those that integrate parental involvement and ergonomic design, provide a compassionate, evidence-based approach to mitigating the effects of early life adversity. By centering the voices of parents and clinicians while utilizing trauma-informed tools designed to enhance neurodevelopment and emotional security, we can reshape the NICU experience and the transition to home after discharge into one that fosters healing rather than deepens distress. By leveraging these nurturing strategies, clinicians can enhance infant and family well-being, improve healthcare outcomes and satisfaction, reduce the cost of care, and foster a culture of healing and resilience in the NICU.

This shift requires dedication from institutions, practitioners, and advocates who believe in the profound impact of early experiences. Investing in trauma-informed developmental care is not just a clinical imperative—it is a moral and ethical responsibility that holds the power to transform lives. The NICU should not only be a place of survival but also one of healing, connection, and love. Every baby, every family, and every clinician deserves an environment that nurtures the body and the soul, where science and compassion intersect to create the best possible start for our most vulnerable patients. Through thoughtful, evidence-based approaches, we can transform neonatal care into a support, compassion, and empowerment model for every infant and family. Now is the time to act—to advocate, to innovate, and to implement trauma-informed care that acknowledges the human experience behind every NICU admission. The smallest among us deserve the best care, and it is our collective responsibility to ensure that their earliest moments are filled with safety, love, and hope.

Source: https://neonatologytoday.net/newsletters/nt-mar25.pdf

@HumankindVideos

CanadianPreemies  Jun 25, 2021

The birth of a premature infant has a profound effect on the family and may require a large portion of parental time, attention, finances, and psychological support. During all this time, the sibling may feel confused and left out of the loop and may resent the amount of time the parents are away with the new infant in the NICU. If the preemie is found to have a disability, these issues are compounded as the parents may be grieving and require further time away to attend several appointments. In this session, Dr. Saigal will discuss strategies to support siblings of premature babies. Dr. Saroj Saigal is a neonatologist and a Professor Emerita at McMaster University, Canada. She is internationally recognized for her long-term studies to adulthood which focuses on the quality of life and consequences of having been born extremely prematurely. She has also participated as a collaborator in several multi-center randomized perinatal clinical trials. Dr. Saigal co-founded Adult Born Preterm International Collaboration (APIC) and invited collaborators from around the world who were doing studies on premature infants in adulthood to participate in data sharing. She is the recipient of many awards from the Canadian Pediatric Society and the American Academy of Pediatrics. She was awarded the 2018 Virginia Apgar Award of the American Pediatric Society for distinguished contributions to perinatal medicine. She was also recognized by her alma mater with the McMaster Faculty of Health Sciences Community of Distinction Award, 2018.


What if a single event could sway health, exercise capacity, learning style, social interactions, and even personal identities–yet individuals had no memory of the event? Adults born preterm are an under-recognized and vulnerable population. Multiple studies of individuals born prematurely, including our 35-year longitudinal study, have found important health concerns that adult healthcare providers should consider in their assessments. Concerns include increased rates of cardiovascular disease, metabolic syndrome, depression, anxiety and attention problems, lower educational attainment and frequency of romantic relationships. A Nordic study of over six million individuals found a linear relationship between gestational age and protection against early adult mortality, with preterm individuals showing 1⋅4 times increased likelihood of early mortality as full-term peers.

At the same time, surviving premature birth has become increasingly common. For the last several decades, nearly one in nine U.S. babies is born early, and now more than 95% survive. Global prevalence and survival data indicate more than 15 million preterm birth survivors annually reach adulthood. This suggests a new population of individuals with emerging healthcare needs for adult health providers.

Birth history should be part of every patients’ medical record.5 Due to the varied risks and prevalence of premature birth, all healthcare practitioners should be aware of the potential for long-term effects. With one in ten 30-year-old patients born preterm, clinical specialists who treat long-term complications of prematurity (i.e., neurology, psychiatry, cardiology) may have more preterm-born patients. Recognizing preterm birth as a cumulative, lifelong risk factor is the first step.

As clinicians and researchers, we have observed the medical community, like society at-large, tends to view prematurity as a health event localized to infancy-something kids outgrow. Ironically, some pediatric providers report limited training and understanding of health complications for children born preterm, and little evidence exists regarding adult practitioners’ knowledge to care for these adults. Preliminary adult primary care guidelines were recently created to screen and manage prematurity-related health complications.

Health risks from prematurity are also risks to equality and justice. Women who bear social risk factors are more likely to give birth early. This includes Black women, those living in socio-economically depressed areas, and women with two or more Adverse Childhood Experiences. The many arms of racism and caste-based inequalities can complicate and worsen the health of people already at risk from preterm birth.

Attention also needs to be drawn to the prematurity research community. To date, research has focused on younger age groups and predominantly White populations. Future research needs to seek out ethnically diverse populations and comprehensively examine potential lifecourse complications of early birth. This is especially important when considering how socioeconomic factors may influence the allostatic load of individuals.

For many born preterm, prematurity is not just a health concern, it’s a matter of who they are. Their perception of health over time, or health related quality of life (HRQL), is a critical outcome. To date, this evidence varies with age, degree of prematurity and reporter; clinicians and parents tend to rate HRQL more negatively than survivors. Preterm-born individuals may not have event memories but, early birth repercussions can reverberate through family narratives and unique life experiences. Some identify as typically developed individuals who happen to have been born early, others as functional and well-adapted “preemies”, and others see prematurity as having colored their lives in negative ways. As prematurity researchers, we aim to uncover and bring awareness to the health outcomes and risks from early birth. A critical need exists for more evidence about adult health following preterm birth and yet, how do we protect individuals with statistically increased risk without unnecessarily pathologizing them?

In clinical practice and research settings, we can take the opportunity to listen to people who were too young as patients to speak for themselves but have riveting and complex stories about preterm birth’s effects. We are aware of just one other published qualitative study about the experiences of adults born preterm. Because most adult healthcare providers have yet to acknowledge and factor this experience into patient care, individuals born preterm are finding alternative avenues to be seen. Adults born preterm report seeking online community and support, connecting globally with people over shared early life experiences, while simultaneously making their needs and identities known.

As a research team, we strive to avoid labels for people born early but have nonetheless found that they are, in often subtle ways, a special group. They beat the odds as infants. Their birth and subsequent survival affected their families and communities in unprecedented ways. As clinicians and researchers, we can attend to the health risks of those born premature while acknowledging and celebrating their unique strengths and perspectives, often resulting from their early life experiences.

Source:https://pmc.ncbi.nlm.nih.gov/articles/PMC9186090/

Kevin Kafaja, MS III

As a third-year medical student, I had rotated through cardiac, neuro, and general ICUs. Each one buzzed with alarms and urgency, charged with adrenaline. But the NICU was different. It didn’t scream. It whispered.

My mother is a pediatrician, and I spent much of my childhood in the corners of her clinic—listening in on patient visits and soaking in the soft rhythm of care. I thought I understood Peds. But the NICU was something else entirely. It was intimate. Intentional. There were hours of serenity—gentle beeping monitors, quiet footsteps—but the stillness could break in an instant. A desaturation alarm. A sudden change. A Code White echoed overhead, and then the team would move—fast, focused, all hands in motion.

That’s where I met her—in the corner of the NICU, they lovingly called Toybox Inn 11, home to some of the tiniest, most vulnerable patients. Her crib was tucked neatly within that space, surrounded by soft blankets, daily goal charts, and quiet victories.

She was born on January 9th at just 31 weeks and 1 day, weighing 940 grams. Her mother’s pregnancy had been complicated— monochorionic diamniotic twins, Twin Anemia-Polycythemia Sequence (TAPS), and maternal hyperthyroidism managed with antithyroid medication. She was delivered via C-section under emergent conditions, including ruptured membranes and maternal fever. She required a partial exchange transfusion and respiratory support on 100% FiO₂ shortly after birth.

When I met her on March 5th—Day of Life 55—she had already fought through respiratory distress syndrome, anemia of prematurity, hyperbilirubinemia, and bradycardic spells. She was breathing room air, feeding fully by mouth, and steadily gaining strength. She was growing stronger, one quiet breath at a time.

In my mind, I called her The Little Engine. I loved toy cars growing up—tiny vehicles that raced like giants. She reminded me of that: small but full of force. Her strength wasn’t loud. It was steady. Unshakable.

At first, I was cautious. How do you care for someone so small? But the NICU team showed me—how to cradle her safely, how to monitor her saturation, how to read her tone and anticipate spells. She’d had a few brief episodes—one during a feed, another while asleep—but none in the final 72 hours before discharge.

The Toybox wasn’t just a clinical space. It was a nursery in progress. A pink blanket draped above her crib. A chart titled “My Day” tracked goals and daily wins. Books sat at her bedside— Goodnight Moon and When I Grow Up I Want to Be…, the latter filled with colorful flaps. I’d read it while keeping watch, wondering who she might become and what her future might hold.

Around her were all the quiet markers of care: diapers, wipes, a milk warmer, and an infant stethoscope. Her corner of Toybox Inn 11 was filled with love and progress, written in the smallest details.

Every Wednesday, during interdisciplinary rounds, we reviewed her journey: apnea monitoring, growth tracking, iron and Epoetin for anemia, and feed progression—35 mL of fortified formula every 3 hours. Her hemoglobin held at 9.9, and her reticulocyte count was strong at 5.4. She crossed the 2000-gram milestone. Each marker is a step closer to going home.

Her mother was a constant presence—gentle and calm. Watching her feed and hold her daughter reminded me that medicine begins not with machines but with presence.

She stayed in the NICU for 2 months and 8 days, and on March 18th, she went home—discharged at 40 weeks and 6 days corrected age, weighing 2170 grams. Her final measurements were length 43 cm, head circumference 34 cm, and abdominal girth 27 cm. She left wrapped in pink, lying in her open crib, breathing independently on room air.

Her discharge plan included a high-calorie formula, follow-up with her pediatrician for weight and EPO management, appointments at the High-Risk Infant Clinic, and a referral to the Regional Center within 1–2 months. I was there the day she left. I watched her resting peacefully in her open crib, bundled and ready to go. Her parents arrived later after I had already stepped away. But when I heard she had gone home—to reunite with her twin brother—it felt like a quiet victory. One we all shared.

In The Toybox, I learned that strength doesn’t always shout. Sometimes, it weighs just over two kilograms, sleeps under a pink blanket, and softly breathes while growing stronger every day.

She was my patient. But more than that, she was my teacher. And in that quiet corner of the NICU, I learned that even the smallest hearts can leave the most lasting marks.

Source:https://neonatologytoday.net/newsletters/nt-mar25.pdf

Highlights

– Adults born preterm report experiences of social exclusion such as being bullied

– They report high sensitivity, reduced stress resilience and tire more easily

– Many report that family, peer and mental health support has helped them most

– Prematurity should be recognized as lifelong condition by health professionals

– Many express gratitude for their life and lead a good life

Abstract

Background

Adults born preterm face greater social, cognitive, mental and physical challenges in adulthood than their full term born peers according to longitudinal studies. In contrast, little is known about the lived experiences of adults born preterm.

Objective

The study investigates the lived experiences of adults born preterm across the life course and their views on health care support.

Methods

A qualitative study of 21 participants completing semi structured interviews analyzed through content analysis.

Results

Over half of adults born preterm report trauma and feeling of otherness since early childhood, high sensitivity to the environment, higher introversion/shyness and social or performance related anxiety. Over half reported that their parents were traumatized by the preterm birth and tried to compensate by overprotective parenting that, however, stifled them becoming independent. Over half experienced bullying victimization and many have continuing mental health problems. Overload by demands in school or work is a consistent theme that makes it hard to have the energy to socialize. Many received physical therapy in childhood and most had psychotherapy in adulthood. Many feel that health professionals trivialize the long-term effects of prematurity and most find support from their parents or peer network.

Conclusions

Prematurity has significantly shaped the life of adults born preterm. Greater awareness and recognition of the unique needs of this group are essential to provide adequate support. Existing services fail to address these needs highlighting an urgent demand for enhanced social and psychological services for educational and workplace settings.

Source: https://www.sciencedirect.com/science/article/pii/S0378378225000581

Magdalena Sroka, Content Writer   30.08.2024

Neonatology startups aim to take care of newborns, especially premature babies. These highly vulnerable beings require exceptional care, as even the smallest changes can significantly impact their health and development. Sometimes, even the experience and knowledge of doctors aren’t enough to save the little one. Therefore, in a world where technology plays an increasingly vital role, neonatology startups become invaluable support for medical care. By combining advanced technology with specialized knowledge, it is possible to provide newborns, particularly those born prematurely, with the best care and a chance for a healthy start in life.

Necessity is the mother of invention. When designing medical devices for newborns, it is crucial to remember that they will serve the most fragile patients. This often requires an unconventional and comprehensive approach to problem-solving. In this article, we present 10 neonatology startups, whose innovative ideas have the potential to transform this field of medicine.

Neonatology Startups Which Can Shape The Future

  1. AMNION LIFE
    Amnion Life is working on an advanced incubator called AmnioBed, designed to replicate the conditions inside the womb. The goal is to support the development of premature infants by regulating temperature, protecting the skin, and managing fluids. The device is intended to provide warmth, humidity, and protection to newborns in a way that prevents hypothermia and water loss.
  • PRAPELA
    Founded in 2018, Prapela is a startup developing a device that uses vibrations to improve breathing patterns and sleep in newborns. This is aimed at helping stabilize breathing and oxygenation, particularly in infants suffering from apnea, intermittent hypoxemia, and neonatal opioid withdrawal syndrome (NOWS).
  • PEDIAFEED
    PediaFeed’s mission is to improve the feeling process for newborns who struggle with it. The company is developing a special type of tube for neonatology and pediatric patients, which minimizes the risk of tube displacement. It is also designed to be easy to insert and remove both in hospitals and at home, while causing minimal discomfort to the baby. Without proper nutrition it is hard to provide a healthy development.
  • PREGANBIT PRO
    This startup has developed a telemedical device for monitoring fetal well-being through cardiotocography (CTG). The portable device enables remote diagnostics and allows regular monitoring of the health of both mother and baby, including fetal heart rate and uterine contractions. Thanks to this technology, women can perform tests at home between medical visits, with results being transmitted and analyzed by doctors. Pregnabit Pro aims to enhance early detection of potential risks, increase pregnancy safety, and provide peace of mind to expectant mothers.
  • ZOUNDREAM
    Zoundream utilizes artificial intelligence and sound recognition to develop technology that can identify and interpret different types of newborn’s cries. The technology not only focuses on distinguishing the baby’s needs (hunger, tiredness) but is also capable of alerting parents to potential pathologies or developmental disorders. Zoundream’s goal is to provide a tool that enables faster responses to an infant’s needs while offering better support for parents.
  • VENTORA
    Ventora aims to create a device that allows precise real-time monitoring of airway pressure in newborns. The company is working on a solution that improves the process of mechanical ventilation while minimizing the risk of complications associated with traditional ventilation. Additionally, Ventora’s device is designed to assist in selecting the best therapy for the youngest patients.
  • OTONEXUS
    OtoNexus is a startup developing a diagnostic device (in the form of an otoscope) to detect middle ear infections and distinguish their origins in children and infants. The technology behind it is based on ultrasound, which enables quick and precise diagnosis, helping doctors make informed treatment decisions. Moreover, this approach could reduce the number of misdiagnosed and unnecessary antibiotic treatments.
  • BAMBI MEDICAL
    Bambi Medical has developed a wireless system for monitoring the vital signs of newborns, such as breathing, pulse, and temperature. Their solution replaces traditional invasive methods that rely on wires and cables. This provides greater comfort and freedom of movement for preterm infants, and is also gentler on the skin. The device sends data to the NICU monitor and alarm system, collected via a silicone strap placed on the baby’s chest, and alerts when apnea occurs.
  • PREEMIE SENSOR
    Preemie Sensor is working on an advanced device to analyze breast milk for nutrient content, specifically measuring fat, protein, and caloric value. The sensor is paired with software, allowing for the monitoring and optimization of nutrient intake by babies. Ensuring proper nutrition reduces the likelihood of complications associated with prematurity.
  1. OWLET BABY CARE
    Owlet Baby Care is a startup specializing in the creation of smart devices for supervising the vital signs of infants, such as heart rate and blood oxygen levels. The data is collected via socks worn on the baby’s foot and then displayed in a mobile app. This technology provides continuous monitoring, giving parents peace of mind and a chance to feel less stressed and anxious.

Summary

The solutions developed by these neonatology startups not only make it easier to monitor and manage the health of the youngest patients, but also enhance the safety and comfort of both children and their parents. Although not all devices are available on the market yet. Some are awaiting certification, yet they offer hope for saving more premature babies. Thanks to these innovations, the future of neonatal care is becoming increasingly promising, bringing relief and peace of mind to families around the world. Good job startupers! 🫶

If you’re interested in supporting or helping shape the future of neonatal care, don’t hesitate and get in touch with us!

Source:https://consonance.tech/blog/top-10-neonatology-startups-medical-devices/

New evidence from a world-leading Victorian study following premature babies into adulthood shows that babies born before 28 weeks’ gestation are doing surprisingly well as young adults in their twenties.

In a paper published in PEDIATRICS, new data released from the Victorian Infant Collaborative Study (VICS) 1991-92 cohort reveals insights from the 25-year point of the long-term study.

The study, co-led by the Royal Women’s Hospital and Murdoch Children’s Research Institute (MCRI), shows that extremely prematurely born adults are just as likely to have completed secondary school, be in paid work, and be in a romantic relationship, compared to their peers born at full term.

Dr Lauren Pigdon, Research Officer at MCRI, analysed the new data from the unique Australian geographic cohort who were recruited at birth and followed for 25 years.

“A strength of this study is that it represents the earliest survivors of the post-surfactant era to navigate the transition into adulthood and fills a gap in knowledge,” Dr Pigdon said.

The introduction of exogenous surfactant in the early 1990s was a game changer in treating respiratory distress syndrome in newborn intensive care. Since then, there has been a dramatic rise in survival of infants born extremely preterm (younger than 28 weeks’ gestation) or with extremely low birthweight (less than 1000g).

With increased survival rates of even the tiniest babies, concerns arose that these tiny babies might have increased chances of health and developmental problems as children and adults. And that this may in turn have an impact on their transition into adult life. But is this true?

“Our data paints a positive and encouraging picture,” Dr Pigdon said. “There were minimal group differences in self-reported general interpersonal relationships, satisfaction with different aspects of life, and current smoking behaviour.”

However, Professor Jeanie Cheong, Consultant Neonatologist at the Women’s and Co-Group Leader of the Victorian Infant Brain Studies group at MCRI, said there were some differences between the groups.

“More adults born extremely preterm had their main income source from government financial assistance and more had not yet moved out of the parental home compared with their peers born full term,” Professor Cheong said.

“Data from the past 25 years has allowed us to look at how, over time, care has improved for Victoria’s youngest and most vulnerable patients,” Professor Cheong said.

“While survival rates have gone up, we now also know that these babies have the chance to become fully functional members of our society.

“Findings from our study are relevant when counselling families after their baby is born, to put into perspective what the long-term outcomes may mean for their child.”

Meet Duane:

Duane has certainly grown up since he was born extremely premature at 26 weeks’ gestation in March 1992. He weighed only 886 grams at birth.

“I was so tiny that my father’s wedding ring could fit all the way up my arm to my shoulder,” Duane remembers.

After a happy and normal childhood, Duane completed high school and became a competitive slalom skier, trying out for the Australian National Team. While he is an experienced downhill racer avoiding major obstacles, Duane faced a few health issues and injuries in his early 20s.

Duane is now a professional skiing and snowboard instructor. He follows the snow seasons and enjoys living and working abroad. He spent a long time in Austria, where he completed a sports diploma in Innsbruck, and now speaks German fluently.

Currently, Duane is keen for his torn ACL in the knee to heal. Then he plans to hit the slopes again and has offers to work in the USA, Japan and Europe.

Source:https://www.thewomens.org.au/news/prem-babies-become-capable-adults-when-grown-up-new-study-confirms

British Association of General Paediatrics

Bushra Rafique1, Hamid Idriss2, Rajesh Bagtharia3, Premilla Kollipara3, Geeta Subramanian3

Abstract

Objectives: Imperforate hymen (IH) is one of the most common obstructive congenital anomalies of the female genital tract. In this condition the hymen occludes the vaginal opening obstructing effluent discharge. Early diagnosis is possible, as new-born vaginal secretions stimulated by maternal oestrogen cause hymenal bulge, which is an abnormal finding.

The aim of this abstract is to highlight potentially missed opportunities for a neonatal diagnosis of IH. Delayed presentations are associated with significant morbidity such as chronic and severe abdominal pain, acute urinary retention, obstructive uropathy and endometriosis.

A full physical examination of the new-born within 72 hours after delivery is the required standard of the New-born and Infant Physical Examination Screening Programme (NIPE) and National Institute of clinical Excellence (NICE) quality standard 37, statement 7. This includes anogenital examination looking at patency of orifices at birth and at 6 weeks check.

Methods: We conducted a survey, using Survey Monkey portal with the objective to review current clinical practice in postnatal examination. The link was distributed via WhatsApp and email to paediatric trainees, general practice trainees and clinical fellows at our trust and London wide.

Responses were collected over 12 weeks. Following questions were asked looking for a yes or no response.

– Do you perform a genital examination in NIPE?

– Are you aware that NIPE recommends complete examination of the genitals to check for normal

  appearance and patency?

– Do you examine for hymenal opening in female babies by separating labia?

– Are you aware of the findings in imperforate hymen?

– Are you aware of the consequences of delayed diagnosis of imperforate hymen?

– Have you ever picked up an imperforate hymen in neonatal examination?

Results: Out of 220 doctors, 132 responded to the survey questions which resulted in a 60% response rate.87.8% performed a genital examination as a part of NIPE.78.7% were aware that normal patency and appearance of the genitals must be checked. Only 25.7% were examining hymenal opening by separating the labia majora and 35.6% were aware of the findings of IH. 7 out of 132 doctors had made a diagnosis in the neonatal examination. 60% were aware of consequences of a delayed diagnosis.

Conclusion: Our survey highlights insufficiencies in female new-born genital examination. There is a need for increased awareness amongst clinicians about this condition, as there exists a window of opportunity to make an early diagnosis and minimise suffering and morbidity.

Source: https://adc.bmj.com/content/108/Suppl_2/A103.2

Preemie Power: Global Voices, Lasting Impact

🌍 WARRIORS: A Global Conversation for Preemie Survivors

Premature birth doesn’t end at discharge—it echoes throughout life. As survivors, we are not defined by our early start—we are defined by our strength, our resilience, and the legacy we choose to build. From the NICU to adulthood, our stories carry both scars and strength. And now, more than ever, the world needs our voices.

The NW Warriors community reflects a growing global collective—of preemie survivors, families, clinicians, researchers, and advocates—who recognize that prematurity is not a condition left behind in infancy. It is a thread woven into identity, healthcare, and social equity across the lifespan. Whether you were born early, raised a NICU warrior, or cared for one—you are part of a movement greater than any diagnosis.


💥 Why the Warrior Movement Matters

Prematurity is not just a medical event—it’s a lifelong journey. Survivors grow into athletes, educators, scientists, artists, and caregivers. Some carry physical or emotional complications. Others carry memories of separation, struggle, or stigma. All carry a story of endurance.

This is a historic moment. For the first time, the world is witnessing a full generation of NICU survivors reaching adulthood in global numbers. Their experiences bring urgency to overlooked conversations—on trauma-informed care, long-term health, and identity. Their insights are reshaping how neonatal care is defined, not just in the early days, but across the life course.

We are not just patients.
We are architects of change.
We are storytellers.
We are warriors.


🌐 A Growing Global Dialogue

Across countries and cultures, NICU survivors and neonatal communities are coming together. We are asking new questions:

  • What does it mean to be born too soon—and grow into your power?
  • How can we center survivor experiences in clinical and policy conversations?
  • What role does memory, trauma, or advocacy play in healing?
  • How do we recognize preterm birth not just as a medical statistic, but as a lived reality that shapes lives and futures?

There is no single answer. But there is space for all of us here. Some find their power through writing, art, research, or mentorship. Others speak through quiet acts of presence and parenting. Some fight for structural change. Others simply want to be heard, held, and understood.

What unites us is this:
We were born into adversity—and we rise with intention.


🛡️ Rewriting the Narrative

As adults born preterm, or as families and clinicians who lived that journey, we are no longer hidden in hospital charts or lost in long-term data. We are here—visible, vocal, and unafraid to lead.

This movement doesn’t require permission. It begins in honest conversations, in shared memory, in reclaiming our stories from silence. It grows as we listen to each other, uplift survivor narratives, and demand that care systems honor the full trajectory of human life.

We are not asking for pity. We are offering power.
We are not defined by fragility. We are evidence of strength.
We are not waiting. We are rising.


Join the Conversation

Wherever you are—in policy, in practice, in healing, in hope—this conversation is yours. The warrior journey is not just about what we survived. It’s about what we build next.

#NWWarriors #PreemieStrong #GlobalNICU #BornToLead #EchoesOfPrematurity

With love, Kathryn

Building Community: Mohamed Anowar´s Youth Environment

The World Around

MEET THE YOUNG CLIMATE PRIZE COHORT! After Mohammed Anowar fled Myanmar with his family to a refugee camp in Bangladesh, he saw hundred of trees being cut down and decided to start a climate hub. The Community Climate Action Initiative aims to tackle pressing climate challenges such as heatwaves, landslides, and flooding through a multifaceted approach. The project includes a Tree Planting Campaign designed to combat deforestation and mitigate heat impacts by increasing local green cover. Complementing this, Climate Awareness Sessions are held to educate community members in the Kutupalong refugee camp about climate change and effective resilience strategies. Additionally, Youth Leadership Training is provided to equip young leaders with the skills needed to advocate for climate action and promote sustainable practices. The initiative is expected to yield a range of positive outcomes, including an improved local environment, heightened climate awareness, and a cadre of empowered youth spearheading climate resilience efforts in the community.

I Am We, A Book of Community

Renee Walters