TIPS, SUPRISES, and RESOURCES

Singapore, officially the Republic of Singapore, is an island country and city-state in Southeast Asia. The country’s territory comprises one main island63 satellite islands and islets, and one outlying islet. It is about one degree of latitude (137 kilometres or 85 miles) north of the equator, off the southern tip of the Malay Peninsula, bordering the Strait of Malacca to the west, the Singapore Strait to the south along with the Riau Islands in Indonesia, the South China Sea to the east, and the Straits of Johor along with the State of Johor in Malaysia to the north.

Singapore has a generally efficient healthcare system, even though health expenditures are relatively low for developed countries.  The World Health Organisation ranks Singapore’s healthcare system as 6th overall in the world in its World Health Report. Singapore has had the lowest infant mortality rates in the world for the past two decades. In 2019, Singaporeans had the longest life expectancy of any country at 84.8 years. Women can expect to live an average of 87.6 years with 75.8 years in good health. The averages are lower for men.[479] Singapore is ranked 1st on the Global Food Security Index.

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

By OnlineMedEd     February 1, 2025

Key Takeaways:

  • Financial Considerations: Medical professionals often face significant student loan debt, which can impact career choices and personal life decisions.
  • Technological Integration: The integration of technology like telemedicine and electronic health records is transforming how doctors provide care and stay updated with medical advancements.
  • Communication In Medicine: Effective communication skills significantly enhance doctor-patient relationships and improve treatment outcomes, emphasizing their importance alongside medical knowledge.

In the fast-paced and ever-evolving world of medicine, doctors and residents commit to a lifelong calling. These dedicated individuals spend countless hours honing their expertise, driven by a deep commitment to patient care and medical excellence. While the white coat and stethoscope symbolize readiness and a passion for their practice, the reality of their journey is far more complex, filled with challenges and responsibilities that often play a crucial role in shaping their careers and the care they provide.

This article goes beyond common perceptions, revealing ten surprising facts about doctors and residents that highlight the depth and complexity of their roles. Whether you’re a medical student preparing for the road ahead, an educator nurturing future providers, or a healthcare professional seeking deeper insight, these realities offer a fresh perspective on the field. 

Understanding these intricacies fosters greater appreciation, resilience, and professional growth, ensuring that the next generation of physicians is equipped not only with medical knowledge but also with the tools to thrive in both their careers and personal well-being.

Fact 1: Many Doctors Face Student Loan Debt Long Into Their Careers

Becoming a doctor is one of the most rewarding professions, but the financial burden is significant. Many physicians graduate with over $200,000 in student loan debt, impacting career choices and personal milestones. Here are ways that student loan debt can impact medical professionals: 

  • Influences Specialty Decisions: Some choose higher-paying fields over passion-driven specialties.
  • Delays Major Life Events: Homeownership, marriage, and family planning may be postponed until studies are completed.
  • Requires Strategic Financial Planning: Understanding repayment options and budgeting is crucial.

Fact 2: Doctors Must Continually Update Their Knowledge

Medicine evolves rapidly, requiring lifelong learning to provide optimal patient care. Continuing education ensures physicians stay updated on the latest research, treatments, and technologies. Here are some reasons why: 

  • USMLE And CME Requirements: Ongoing exams and certifications keep doctors current.
  • Medical Advancements: New treatments, AI tools, and clinical protocols evolve constantly.
  • Efficient Learning Strategies: Consistent review of clinical content allows doctors to maintain their medical mastery and mitigate skill decline.

Fact 3: Technology Is Transforming How Doctors Practice Medicine

Technology is revolutionizing healthcare for the better and improving efficiency. Below are some ways technology is changing the healthcare game: 

  • Electronic Medical Records (EMRs): Digitally store and organize patient health information, improving accessibility, documentation accuracy, and care coordination.
  • Telemedicine: Expands access to remote and underserved populations.
  • AI And Automation: Enhances diagnostics, workflows, and patient care.

Fact 4: Many Doctors Pursue Research Alongside Clinical Practice

For many doctors, the desire to discover new medical knowledge is as strong as the calling to patient care. Many doctors balance clinical work and medical research to push the field forward. 

Medical research:

  • Advances Evidence-Based Medicine: Research findings shape treatment protocols.
  • Improves Patient Outcomes: Clinical trials lead to breakthrough therapies.
  • Strengthens Analytical Skills: Evaluating data sharpens clinical decision-making.

Fact 5: Communication Skills Are As Important As Medical Knowledge

Beyond expertise, strong communication enhances patient trust and treatment outcomes by ensuring clarity, collaboration, and understanding. Below are some communication skills that medical professionals should value: 

  • Clear Explanations: Helps patients make informed decisions.
  • Interdisciplinary Teamwork: Ensures seamless care coordination.
  • Active Listening: Strengthens doctor-patient relationships.

Fact 6: The Number Of Female Physicians Is On The Rise

In recent years, the medical field has witnessed a transformative shift as the number of female physicians steadily increases. Women now make up over 50% of U.S. medical school students, creating a more inclusive healthcare environment. 

This change not only reflects broader societal advancements but also heralds a new era where diverse perspectives lead to more comprehensive patient care. Here are a few reasons why this trend is a positive force in the medical community: 

  • Enhancing Patient Perspectives: Women in medicine improve representation and inclusivity.
  • Expanding Leadership Roles: More female doctors are entering executive positions.
  • Shaping Mentorship And Education: An increasing number of programs support future generations of female physicians.

As more women enter the field, efforts to support career advancement, mentorship, and leadership opportunities continue to grow. These changes contribute to a more balanced healthcare workforce, ensuring that medical education and patient care reflect the diverse needs of the communities they serve.

Fact 7: Residents Are Both Students And Employees

Residents face a tough battle, as they are expected to balance learning with employment. The responsibilities of patient care, combined with a deep, unyielding commitment to mastering the breadth and depth of medical knowledge, create a unique dynamic.

Residents deal with: 

  • Hands-On Experience: Residents manage cases under supervision, participate in medical procedures, and deliver expert care in high-stakes environments.
  • Long Hours And High Stress: Demanding schedules prepare residents for independent practice.
  • Balancing Education And Work: Requires strategic planning and smart time management to stay sharp.

Fact 8: Doctor-Patient Relationships Influence Treatment Outcomes

At the heart of every successful treatment plan lies a strong doctor-patient relationship. This dynamic significantly impacts treatment outcomes, as trust and communication form its foundation. Here’s why this bond is essential to a positive healthcare experience: 

  • Empathy Improves Patient Engagement: Positive experiences with doctors encourage patients to follow treatment plans accordingly.
  • Communication Enhances Understanding: Simplified explanations of medical conditions and solutions lead to informed decisions.
  • Trust Strengthens Compliance: Patients are more likely to return for follow-ups and engage in routine check-ups when they trust their healthcare provider.

Developing effective communication and interpersonal skills allows physicians to foster meaningful connections with their patients. When patients feel understood and respected, they are more likely to adhere to medical advice and treatment plans, ultimately leading to improved health outcomes.

Fact 9: Wellness Programs Are Becoming More Common In Medical Training

The rumors are true: Becoming a doctor is an incredibly long and arduous process. Thankfully, in recent years, wellness programs have been developed to support students and residents with healthy coping mechanisms. These initiatives, including the ones listed below, are a testament to the growing recognition of the demanding pressures faced by medical students and residents and their impact on mental health and overall well-being. 

  • Mental Health Support: Resources such as counseling help prevent burnout.
  • Work-Life Balance Strategies: Encouraging self-care and mindfulness.
  • Peer Support Networks: Strengthening community and resilience.

Fact 10: Global Health Opportunities Are Available To Doctors And Residents

Joining global health initiatives allows medical professionals to see firsthand the different healthcare challenges that occur worldwide. This experience can be pivotal in developing resilience and adaptability, skills that are crucial in any medical setting. For residents, these opportunities can be eye-opening, offering real-world applications of their clinical skills in diverse environments. Here’s why global opportunities can be beneficial for the careers of doctors and residents: 

  • Exposure To Diverse Medical Environments: Broadens clinical expertise and adaptability to different clinical settings.
  • Develops Problem-Solving Skills: Teaches current and aspiring healthcare providers how to work with resource-limited care strategies.
  • Strengthens Public Health Impact: Contributes to underserved communities worldwide.

These opportunities enrich one’s medical expertise and broaden perspectives on health disparities, resource management, and cultural sensitivity. 

Final Thoughts

The road to becoming a doctor is filled with challenges, sacrifices, and unexpected realities, yet it remains one of the most enriching careers. Understanding these crucial facts about doctors fosters greater empathy and appreciation for those dedicated to medicine. While the path is demanding, each step brings the opportunity to grow, refine skills, and make a meaningful impact on patient care.

By embracing a structured and comprehensive approach to medical education, future providers can develop true mastery. Investing in both clinical knowledge and personal well-being ensures not only success in training but also longevity and fulfillment in practice. Whether you’re a medical student, resident, or educator, every effort you make strengthens your ability to provide exceptional, compassionate care, shaping the future of healthcare for the better.

Source: https://www.onlinemeded.com/blog/facts-about-doctors

Benjamin Kheng Nov 28, 2024 #BenjaminKheng #REALLYINLOVE

REALLY IN LOVE Written by: Benjamin Kheng Produced by: Benjamin Kheng, Evan Low Performed by: Benjamin Kheng Mixed & Mastered by: Charlie Kurata Spatial Audio Master by: Luke Nicholas Foo

Elisha Tushara UPDATED Oct 04, 2024, 01:00 PM

SINGAPORE – Her son weighed just 700g when he was born at 24 weeks after she spent the two weeks prior in hospital due to vaginal bleeding and cervix dilation.

Ms So Bee Leng’s son, Ethan Ang, was born in 2017 with multiple disabilities stemming from his extreme prematurity. At seven days old, he underwent his first major surgery when his intestines were operated on.

For the next five years, he underwent four more major operations, which included implanting a cochlear hearing device, laser eye surgery to help with his vision and placing a feeding device through his belly to the stomach.

It is currently a challenge to identify mothers at risk of giving birth to premature babies as the only gauge is when mothers have had previous preterm births, like Ms So, said Professor Teoh Tiong Ghee, director of maternal and child global health and care transformation at KK Women’s and Children’s Hospital (KKH).

To proactively reduce and prevent prematurity, a 10-member team of doctors specialising in newborn care and high-risk pregnancies from KKH and Singapore General Hospital (SGH) will start work on a new Preterm Pregnancy Prevention Programme in October.

The team aims to create a national database of all preterm pregnancies to identify risk factors, and then use this information to develop a screening prediction tool that can accurately assess the risk of preterm pregnancies.

A baby born before 37 full weeks of pregnancy is considered to have been born preterm or prematurely. A preterm baby’s organs may not be fully developed. 

A full-term pregnancy typically lasts about 40 weeks, and babies’ birth weights typically range from 2.5kg to 4.5kg.

Globally, 13.4 million babies – 10 per cent of all births – are born prematurely each year and one million die from preterm complications.

Prematurity is the leading cause of death for children under five.

In 2023, 8.2 per cent of births in Singapore were premature, slightly lower than the 8.8 per cent recorded in 2014.

Recalling the dilemma she faced when told she might deliver early and her baby would develop health complications, Ms So, 38, said: “I was given the choice to either terminate the pregnancy or continue with bed rest in the hospital until I gave birth.

“After weighing the pros and cons, and discussing with my husband, we decided to carry on and accept whatever may come in the future.”

When she conceived again in 2023, her doctor told her she was at risk of another premature delivery. She was referred to the Preterm Birth Clinic at KKH’s Stork Centre, where she was closely monitored.

She underwent a procedure to stitch her cervix – the birth canal opening – when she was 12 weeks along, paving the way for the full-term birth of her daughter, Alysha Ang, at 38 weeks.

Called a cervical cerclage, the procedure is done to help the cervix hold a pregnancy in the womb to prevent preterm birth.

Dr Ilka Tan, a senior consultant at KKH’s department of maternal foetal medicine who oversaw Ms So’s care during her second pregnancy, said that infants are able to survive outside the uterus at 24 weeks.

She added that though there are rare cases of infants surviving when born at 22 or 23 weeks, the “outcome is still not very good” for these babies.

Acknowledging that there have been reports from around the world of some babies born around 22 weeks who have survived, she said: “Those are single anecdotal cases, but it’s not the norm.”

If diagnosed through screening and predictive tests early, mothers who are at risk of preterm births can undergo various treatments to help them bring the pregnancy to term, Dr Tan said.

These include taking the hormone progesterone and getting a cervical cerclage.

The Preterm Pregnancy Prevention Programme will use information collated to study common characteristics among women who deliver prematurely. This in turn can be used to develop a prediction tool to identify expectant mothers who are at risk of preterm births early, so that preventive measures can be taken.

“What we’re trying to do is to get all these demographics, and use biomarkers from blood and cervical length measurements, to try to predict each woman’s personalised risk so as to target with specific therapy,” said Prof Teoh.

The programme is funded by a $500,000 grant from Far East Organization.

Besides the child potentially suffering long-term health consequences and an increased risk of disability and developmental delays, the parents and the rest of the family experience long-term stress too, Prof Teoh noted.

“Some have to stop work to look after the kid. So not only does it have a psychological impact on the family, it’s got a big financial impact as well,” he added.

Dr Tan also leads the Preterm Birth Clinic at KKH that provides specialised care for women who may have a higher risk of having premature babies.

The clinic began operations in July 2021 and had 100 patients that year. In 2024, 402 patients were referred to the clinic from January to September.

Ms. So said she received personalised care and attention at the Preterm Birth Clinic to help her carry her second child to term.

“I was seen by the same doctor – it wasn’t random. So I felt well-looked after and relieved. I was assured that there was a plan to help me, and that was important.”

Souce:https://www.straitstimes.com/singapore/team-from-kkh-sgh-aims-to-develop-screening-tool-to-identify-women-at-risk-of-premature-births

Credit: Pixabay/CC0 Public Domain

by Erin Digitale    Stanford University     August 7, 2024

Skin-to-skin cuddling with a parent has lasting cognitive benefits for premature babies, according to a new Stanford Medicine study. Preemies who received more skin-to-skin contact, also known as kangaroo care, while hospitalized as newborns were less likely to be developmentally delayed at 1 year of age, the study found.

The research, which was published online July 11 in The Journal of Pediatrics, showed that even small increases in the amount of skin-to-skin time made a measurable difference in the babies’ neurologic development during their first year.

“It’s interesting and exciting that it doesn’t take much to really improve babies’ outcomes,” said the study’s senior author, Katherine Travis, Ph.D., who was an assistant professor at Stanford Medicine when the study was conducted and is now an assistant professor at Weill Cornell Medical School and Burke Neurological Institute.

The study’s first author is Molly Lazarus, a clinical research coordinator in pediatrics previously at Stanford Medicine and now at Weill Cornell Medical School.

The intervention is simple: With the baby only in a diaper, a parent holds the baby on their chest, next to their skin. But because hospitalized preemies are small and fragile, and often hooked to lots of tubes and wires, holding the baby can seem complicated. Parents may need help from their baby’s medical team to get set up. That work is worth it, the study showed.

“It didn’t matter if the baby was from a high- or low-income family; the effects we found were the same. And it didn’t matter if the baby was sicker or less sick—both responded to this treatment,” Travis said.

Neurological complications are challenging

Over the last 50 years, preemies’ survival rates have improved dramatically thanks to better treatments for many of the complications of prematurity, which is defined as being born at least three weeks early. For instance, neonatologists have developed effective approaches to help preemies breathe, even with immature lungs, while in the neonatal intensive care unit.

But premature birth still leaves babies at risk for long-term neurodevelopmental problems, including developmental delays and learning disabilities. Doctors and families have long hoped for treatments they could use during the newborn period to prevent such challenges.

“Ultimately, we want our patients to be healthy kids who can achieve the same milestones as if they didn’t come to the NICU,” said study co-author Melissa Scala, MD, clinical professor of pediatrics. Scala is a neonatologist who cares for preemies at Lucile Packard Children’s Hospital Stanford.

“Our finding legitimizes skin-to-skin care as a vital intervention in the neonatal intensive care unit to support our goal of getting that child out of the hospital, able to learn and develop,” Scala said.

Skin-to-skin care was first used in low-income countries to boost babies’ survival, where it is often used for healthy infants born after full-term pregnancies. In rural or impoverished areas, it is an essential way to keep newborns warm, promote parent-child bonding and facilitate the start of breastfeeding.

It’s been slower to catch on in the United States, especially for premature babies, who generally receive high-tech intensive care. But a growing body of research suggests that the practice has benefits for preemies’ brains, possibly because it could offer some of the same developmental inputs they would have received if they had not been born early.

More skin-to-skin was better

The research team reviewed medical records for infants who were born very prematurely, meaning at least eight weeks early, and were cared for at Lucile Packard Children’s Hospital Stanford between May 1, 2018, and June 15, 2022. Nurses in the hospital’s NICU had begun making notes in patients’ medical charts about developmental care practices, including the amount of time parents held babies skin-to-skin, shortly before the study began.

The study included 181 preemies who did not have genetic or congenital conditions known to affect neurodevelopment and who had received follow-up evaluations after they left the NICU. All very premature babies are eligible for care through California’s High Risk Infant Follow-Up program until age 3. The program provides developmental testing and connects families to appropriate therapists if their children have developmental delays.

The study used records from follow-up evaluations that the babies received at 6 and 12 months’ adjusted age, meaning their ages were corrected to account for how early they were born.

The evaluation included measures of visual-motor problem solving in standard tasks (such as dropping a cube into a cup) and expressive and receptive language skills (such as turning to see where the sound of a bell is coming from).

In addition to accounting for infants’ gestational age (how early they were born), the outcomes were adjusted for families’ socioeconomic status and for four common complications of prematurity: bronchopulmonary dysplasia, a breathing complication; brain hemorrhage, or bleeding; sepsis, an infection of the bloodstream; and necrotizing enterocolitis, an intestinal condition.

The infants in the study were born, on average, at about 28 weeks’ gestation, or about 12 weeks before their due dates. They stayed in the hospital for an average of about two and a half months.

Babies in the study averaged about 17 minutes a day of skin-to-skin care, usually in sessions lasting more than an hour but occurring less than two days per week. Seven percent of families did not do any skin-to-skin care, and 8% did more than 50 minutes per day.

Small increases in the amount of skin-to-skin care were linked to large differences in 12-month neurodevelopmental scores. An average of 20 minutes more per day of skin-to-skin care was associated with a 10-point increase on the scoring scale used for neurodevelopment. Similar to an IQ test, the scale has an average of 100 points; a score of 70 or less suggests significant developmental delays.

The frequency and duration of skin-to-skin contact predicted 12-month cognitive scores even after controlling for possible confounding factors, including the infant’s gestational age and medical complications, and the family’s socioeconomic status and frequency with which they visited the NICU.

How does it work?

Although the study was not set up to explore how skin-to-skin care benefits babies’ brains, the researchers have some educated guesses.

“We think of the womb as our benchmark for preterm babies. In utero, a fetus is physically contained, listening to the maternal heartbeat, hearing Mom’s voice, probably hearing her digest her sandwich,” Scala said. “In the NICU, they’re not next to anybody, and they hear the fan in the incubator; it’s a very different environment. Skin-to-skin care is probably the closest we can get to mimicking the womb.”

Parents can also benefit from skin-to-skin care, and this in turn may benefit their newborns, the research team said.

“The environment of the NICU is very stressful for parents and babies, and skin-to-skin care may buffer that,” Travis said, noting that it is not unusual for parents with a very tiny, sick baby to develop post-traumatic stress disorder.

In addition, many preemies are not developmentally ready to breastfeed, and skin-to-skin care can provide an alternate way to promote bonding between parents and babies.

The researchers hope their findings will motivate medical teams to help parents provide skin-to-skin care in NICUs across the country and will encourage parents by showing them the long-term benefits of this simple but important technique.

Packard Children’s recently expanded its infant developmental care program by hiring neurodevelopmental nurse practitioners, more physical and occupational therapists, a psychologist, and child life and music therapy experts for their NICU and intermediate care nurseries. The expanded team can make customized developmental care plans for high-risk infants.

Scala hopes other hospitals will follow suit.

“I would love for people to see this as part of the medical plan, not just something nice we’re doing, but to be really intentional about it,” Scala said. “Our findings underscore the value of having parents on the intensive care unit, doing this important part of infant care.”

Source:https://scx1.b-cdn.net/csz/news/800a/2024/preterm-infant.jpg

Imagine giving birth at 22 weeks—facing the uncertainty, the emotional rollercoaster, and the challenges of an 8-month NICU stay. For Asma, this journey was life-changing, but it also ignited her passion for advocacy, helping other parents navigate the NICU experience with confidence and strength. Join us as Asma shares: ✅ Her raw & real experience as a NICU mom to baby Cylia Maria ✅ The emotional & logistical challenges of a long NICU stay ✅ The transition home—what she wishes she knew ✅ How sharing her story has fueled her passion for advocacy & parent empowerment ✅ Guidance for parents: questions to ask & how to take an active role in their baby’s care.

International Council of Multiple Birth Organisations / ICOMBO

International Federation of Spina Bifida and Hydrocephalus / IFSBH

International Patient Organistion for Primary Immunodeficiencies / IPOPI

Country Specific Organizations

It can be very stressful having a baby in the NICU. During this time, it is helpful to include siblings as much as possible; to explain in simple terms what is happening with your new baby; to reassure them that they have not caused the baby to be early, sick, or small; and to remind them that they are not the source of your current worries. Most of all, you should reserve special time just for them, and remind them daily of your constant and unconditional love. More than ever, they need to feel secure, valued, safe, and loved by you and others.

Platypus Media is proud to offer a number of NICU sibling support resources. We hope these will be meaningful and useful for families experiencing the difficulty of having a child in the NICU. 

The Come Home Soon coloring book series (available for baby boys and girls, in both English and Spanish) will help you guide your children to an understanding of why their baby sister or brother is in the NICU, and what they can do to help.

Rich and Creamy for Our Preemie, by Naomi Bar-Yam, ACSW, Ph.D., available in English and in Spanish, is a coloring book about how the NICU, milk banks, and families work together to help preemies. 

Here is a list of other NICU sibling support resources: 

  • Hand to Hold sibling support webpage (www.HandToHold.org) offers sample activity pages and NICU video tour.

  • No Bigger than My Teddy Bearby Valerie Pankow describes the NICU experience through the eyes of a new big brother.

  • My Brother is a Preemie/My Sister is a Preemie:A Children’s Guide to the NICU Experienceby Abraham R. Chuzzlewit & Dr. Jos. A. Vitterito II gives a child-friendly introduction to the NICU.

  • The Invisible Stringby Patrice Karst reassures children that even when loved ones are apart, they are always in each other’s hearts.

Keep reading for a list of organizations that help preemie families…

Different Dream serves as a gathering place for parents with special needs children.

Hand to Hold provides resources and support to parents of preemies, babies with special health care needs and new parents who have lost a baby.

Human Milk Banking Association of North American provides information and resources on donor milk banking for parents and health care providers. It also sets safety guidelines for all non-profit mothers’ milk banks in North America.

Kangaroo Mother Care promotes skin-to-skin contact, a universally available and biologically sound method of care for all newborns, and preemies in particular.

La Leche League International is a mother-to-mother breastfeeding support organization. They are a source of information and firsthand accounts related to providing preterm babies with breastmilk.

Managing the Neonatal Intensive Care Unit is an article from the Loyola University of New Orleans’ online nursing resource center. A great resource for students, professionals, and even parents of babies in the NICU.

March of Dimes (MOD) has a wealth of information about the NICU. They support an online community especially for NICU families. March of Dimes NICU Family Support programs operate in many NICUs. (Also available in Spanish.)

National Premature Infant Health Coalition consists of a variety of support organizations focused on improving the lives of parents and their preemies.

NICU Parent Support Site provides information, resources, and encouragement to reassure and support NICU parents.

Prematurity strives to support preemie parents by providing information on prematurity and preemie care.

Preemie Parent Alliance(PPA) represents a number of organizations that help support the parents of preemies and strives to improve the quality of the care they provide.

Preemie World brings together parents and professionals in the NICU. They strive to educate and help make the transition to home easier for everyone.

Ronald McDonald House serves as a home away from home for families with children receiving medical treatment. Families can do laundry, eat freshly cooked meals, sleep in private rooms, and gain/give support with other families.

Supplemental Security Income (SSI) and Medicaid Programs provide financial assistance for NICU medical expenses. Eligibility for assistance is determined by a baby’s birth weight rather than an income. You must apply for these programs shortly after your baby is born. Ask your social worker or care manager for assistance.

WIC (Women, Infants, and Children) provides nutritious foods to supplement diets, information on healthy eating, and referrals to health care for women, infants, and children up to 5 years. Even if you have been denied Medicaid due to financial reasons, you might still qualify for WIC.

This list can be found in the Resource for NICU Families section of our award winning Coloring Book for the Big Brothers and Big Sisters of the NICU.

Source: https://www.platypusmedia.com/resources-for-nicu-families

Fetal heart rate (FHR) patterns are a critical tool for assessing a baby’s well-being during pregnancy and labor. Nurses must understand how to interpret these patterns to ensure safe care. Here are the key takeaways:

  • Baseline FHR: Normal range is 110-160 bpm. Below 110 bpm (bradycardia) or above 160 bpm (tachycardia) may signal distress.
  • Variability:
    • Moderate (6-25 bpm): Healthy oxygenation.
    • Absent or minimal: Potential concern.
    • Marked (>25 bpm): Possible distress.
  • Decelerations:
    • Early: Harmless, mirrors contractions.
    • Late: Indicates uteroplacental issues, requires action.
    • Variable: Linked to cord compression, may need intervention.
  • Three-Tiered Classification:
    • Category I: Normal.
    • Category II: Indeterminate, needs closer monitoring.
    • Category III: Abnormal, requires urgent action.

Nurses must act quickly on abnormal patterns by repositioning the mother, administering oxygen, or preparing for emergency delivery. Accurate monitoring, documentation, and clinical judgment are essential for ensuring the safety of both mother and baby.

Source:https://blog.nursecram.com/nursing-content-reviews-ngn-focused/fetal-heart-rate-patterns-nursing-interpretation-tips/

|@LevelUpRN   

Joseph B. Philips, III, MD

The moonlighter had just returned with our dinners when the code alarm sounded. Almost simultaneously, our pagers went off “Code infant 3312.” We all knew who it was. The 23-week gestation, two-day-old baby had coded earlier in the afternoon and had been doing poorly since. Oxygen saturations were in the low 80s despite maximal support, and blood pressures were marginal on dopamine, dobutamine, and epinephrine drips. Upon entering the room, we found the infant with saturations in the 40s and a heart rate in the 50s. We quickly assumed our positions around the warmer. The resident began chest compressions, the respiratory therapist hand bagged, the fellow at the head of the bed assessed the airway and ordered fluid pushes and medications, the bedside nurse administered the medications, and I, the attending physician, oversaw it all. The nursing staff also rapidly began their roles, one opening the crash cart and drawing up drugs, another charting, and multiple others observing and ready to assist if needed.

We quickly fell into our all-too-familiar routine, counting “one, two, three” for chest compressions, followed by “breath.” Over and over again. “Ten mils normal saline,” said the fellow, followed by “epi, point 0 five” every five minutes. The intern took over the chest compressions after about 10 minutes, but the cadence remained the same. Blood was bubbling up the endotracheal tube, indicating the presence of a pulmonary hemorrhage. A nurse was dispatched to retrieve emergency-release blood from the blood bank. The saturation and heart rate were steadily falling.

The mother was literally rolling on the floor, wailing, “Save my baby! Save my baby!” over and over again.

Despite several rounds of fluids and epinephrine plus a push of the blood, the baby continued to deteriorate. I knelt beside the mother, put my hand on her shoulder, and asked her to listen. She immediately stopped her wailing and looked me in the eye. I told her that her baby was dying, that we were going to stop CPR as it was not working, and that her baby’s brain had been irreversibly damaged. She nodded in agreement.

“Stop,” I said. The scene instantly shifted from the hustle and bustle of a code to a stony silence pierced only by the sobs of the mother whom the nurses had assisted into a recliner chair. The monitor was turned off, the ventilator and lines were disconnected, syringes and other debris were removed from the bed, and the baby was wrapped in a blanket and placed in mom’s arms. The nurses began their familiar postmortem care routine. The fellow auscultated the baby’s chest and confirmed the death.

We returned to the workroom and ate Chinese takeout. I had cashew shrimp. I conducted a debrief during our meal, asking everyone how they felt. The intern was visibly shaken, with a tear trickling down her cheek. It was July, and this was the first death of a patient in her charge since she had become a real doctor. “His life slipped through my hands when you told me to stop,” she said. One of the upper-level female residents hugged her as she sobbed for a while before regaining her composure and resumed picking at her food.

For myself and the fellow, this death was one of many, but each death is new all over again and is a fresh reminder of our human frailty.

Few outside our world would understand a situation like this. We were eating while a baby had just died and a mother was grieving. For her, life had just changed forever. For us, we had to nourish ourselves to have the strength to continue caring for the living. Nothing taught in medical school can prepare one for these moments. They must be experienced first-hand, processed, and reflected upon. Doing so is what gives us the strength to move forward.

Source:https://www.neonatologytoday.net/newsletters/nt-feb25.pdf

Physician Health – By Georgia Garvey, Contributing News Writer  Mar 18, 2025

Good health care leaders realize that physicians need more than free food and thank yous to thrive. Well-meaning expressions of appreciation that do not address the root cause of burnout or stress cannot alleviate physicians’ stress or stave off burnout the way that truly feeling valued can.

But it takes more than knowledge to change a work environment—it takes concrete action.

“Many leaders know the importance of teamwork and communication,” said Jill Jin, MD, MPH, an internist and senior physician adviser for professional satisfaction and practice sustainability at the AMA. “But where they kind of struggle is, how do you actually support the individual at a level that is meaningful for them?”

Dr. Jin discussed “muffin rage,” a phrase that came about as a result of a 2021 Los Angeles Times op-ed by Jillian Horton, MD, when she—deep in the throes of work-related burnout and distress—happened upon a “resident appreciation” event handing out muffins. 

“Muffin rage is what we feel when there is a vast chasm between our actual needs and what another person or an institution thinks we need,” Dr. Horton wrote.

Dr. Jin spoke alongside Jane Fogg, MD, MPH, physician director of organizational transformation for the AMA, in a recent webinar on how health care organizations can make doctors feel valued, which highlighted an AMA STEPS Forward® playbook on the topic.

During the event, Drs. Jin and Fogg touched on some of the ways that health systems, organizations and leaders can take actions that will make physicians feel valued in a way that avoids muffin rage, a crucial effort with implications for physician well-being, burnout and even the quality of patient care.

Understand feeling valued, burnout link

Physician burnout rates have fallen somewhat from their historic highs during the COVID-19 public health emergency, but too many physicians continue to suffer its damaging effects. And when physicians quit or cut back their hours due to overwork and overstress, the impact is felt by patients and colleagues. 

In fact, physician turnover can cost organizations anywhere from $500,000 to $1 million or more for every physician who leaves. 

“Aside from it being the humane thing to do, there is also a financial benefit—a business case—for investing in your people,” Dr. Jin said. 

For those looking to lessen the load on physicians, a key avenue to pursue is helping them understand the crucial role they play in their organization. Dr. Jin pointed out that research shows feeling valued correlates strongly with lower burnout rates, mentioning a 2022 study published in JAMA Health Forum that found physicians who felt valued had a 37% burnout rate, compared with 69% for those who did not.

As the leader in physician well-being, the AMA is reducing physician burnout by removing administrative burdens and providing real-world solutions to help doctors rediscover the Joy in Medicine™.

Help physicians know their worth

Once the importance of feeling valued as a key mitigator for physician burnout has been understood, Drs. Jin and Fogg said, the next step is determining what, exactly, helps physicians know and understand their worth in an organization.

Instead of superficial gestures like the one described in Dr. Horton’s piece, Dr. Jin said there are ways to effectively communicate gratitude to physicians. Those ways have much more to do with actions than with words.

Some key ways to show doctors they are valued, as described by Drs. Jin and Fogg, were to support: 

  • Schedule flexibility and autonomy.
  • Paid time off (PTO).
  • Professional development.
  • Individual resilience and self-care.
  • Care during and after trauma.

Make work-life balance a priority 

Often it can be difficult to justify costly changes aimed at improving physicians’ work conditions, said Dr. Fogg, but overwork and lack of autonomy in matters such as scheduling result in burnout, which is even more expensive. 

“Productivity is a pressure that we often feel because of falling revenues across the health care landscape,” she said. “With pressure to fill our schedules, we can lose valuable time for our continuity patients. This tension between being productive and being available to our own patients often lies in how we design and manage our schedules.” 

The key, Dr. Fogg said, is giving doctors the ability to “co-design the scheduling processes with their operational team. Make sure you partner with operational leaders to have a physician voice in designing the optimal schedule system for patient access, continuity, and work life balance.”

PTO is another area of concern for organizations looking to create a culture of value, Dr. Jin said.

Health care leaders can be role models in taking time off themselves, and organizations can proactively block off vacations, celebrate time off and resist the impulse to praise working while out of the office. Physicians’ responsibilities should also be fully covered when they’re on vacation, and compensation models and appointment schedules should take PTO into account

Support the physician as a person

To show a physician that they are more than just a cog in the machine, their professional development must be supported, recognizing their individual aspirations and passions beyond the clinical practice of medicine. 

“Feeling valued means the people around you—your supervisor in particular—know who you are, what excites you and what makes you passionate” outside the confines of the clinic or hospital corridor, Dr. Fogg said. “Asking physicians about their long-term goals and offering opportunities to get involved in a variety of activities outside of clinical practice can create a stronger sense of feeling valued. Some opportunities for growth include teaching, research, process improvement initiatives, leadership, community engagement and more.

And, said Dr. Jin, while “self-care” is not a replacement for—and should not be the major focus of—systemic efforts to reduce burnout, organizations can support an individual’s resilience by helping physicians set boundaries, prioritize tasks and limit their distractions. Leadership also should provide resources for and support physicians in self-care, promote collegiality and create spaces for breaks.

Health care organizations should address both individual and collective trauma, Dr. Fogg said, by creating peer-support programs and providing confidential mental health services. They should consider developing develop suicide-prevention plans and response teams in some situations.

Additionally, the credentialling process should remove questions about mental health care so they don’t discourage physicians from seeking care if needed. 

“Burnout is not a sign of mental illness, but there is a lot of overlap that happens when we are severely distressed by the way in which we’re practicing and what we’re witnessing in our practices,” she said.

For more information on this and other topics, explore the AMA STEPS Forward open-access toolkits and playbooks, which offer innovative strategies that allow physicians and their staff to thrive in the new health care environment. These resources can help you prevent burnout, create the organizational foundation for joy in medicine and improve practice efficiency. 

Combat physician burnout

Event: American Conference on Physician Health (ACPH) Sept. 11-13, 2025, focusing on steps organizations can take to improve physician well-being

CME: How health systems can reduce physician burnout

Calculate: See the cost of physician burnout to your organization

Video: Latest trends in physician burnout by specialty

Playbook: Wellness-centered leadership

Source: https://www.ama-assn.org/practice-management/physician-health/4-actions-health-leaders-must-take-show-doctors-they-are

Original Investigation  Pediatrics  November 20, 2024

Asma M. Ahmed, PhD, MD, MPH1Sonia M. Grandi, PhD, MSc2Eleanor Pullenayegum, PhD, MA2; et alSarah D. McDonald, MD, MSc3Marc Beltempo, MD, MSc4Shahirose S. Premji, RN, PhD, MScN5Jason D. Pole, PhD, MSc6Fabiana Bacchini, MSS7Prakesh S. Shah, MD, MSc8Petros Pechlivanoglou, PhD, MSc2

JAMA Netw Open. 2024;7(11):e2445871. doi:10.1001/jamanetworkopen.2024.45871

Key Points

Question  Do individuals born preterm have a higher risk of short-term and long-term mortality compared with those born at term?

Findings  In this cohort study of 4 998 560 births, individuals born preterm had a higher risk of mortality from birth to age 36 years, with the highest risk observed from birth through early childhood. The risk of mortality varied by gestational age at birth and was more pronounced at lower gestational ages.

Meaning  The findings of this study suggest that preterm birth is associated with increased risk of death from infancy to adulthood.

Abstract

Importance  Preterm birth (PTB) is a leading cause of neonatal mortality. However, evidence on mortality beyond the neonatal period is limited, especially in North America.

Objective  To examine associations of PTB with all-cause and cause-specific mortality from birth through 23 to 36 years of age.

Design, Setting, and Participants  This population-based matched cohort study of live births in Canada included individuals born between January 1, 1983, and December 31, 1996, and followed up until December 31, 2019. Data were analyzed from June 1, 2023, to April 30, 2024.

Exposure  PTBs, between 24 and 37 weeks’ gestation (with gestational age [GA]-specific subcategories of 24 to 27 weeks, 28 to 31 weeks, 32 to 33 weeks, and 34 to 36 weeks) compared with term births (37-41 weeks’ gestation).

Main Outcomes and Measures  All-cause mortality and cause-specific mortality were the main outcomes. Risk differences (RDs) and risk ratios (RRs) were estimated for all-cause mortality using log-binomial regressions and hazard ratios were estimated for cause-specific mortality using Cox proportional hazards regression models (censoring individuals who died from other causes) within prespecified age intervals (ages 0-11 months and ages 1-5, 6-12, 13-17, 18-28, and 29-36 years). Observed confounding was accounted for using coarsened exact matching on baseline characteristics.

Results  Of 4 998 560 births (54.2% male), 6.9% were born preterm (with GA-specific subcategories of 0.3% born at 24-27 weeks, 0.6% at 28-31 weeks, 0.8% at 32-33 weeks, and 5.1% at 34-36 weeks). During a median of 29 years of follow-up, 72 662 individuals died (14 312 born preterm and 58 350 at term). PTB was associated with an increased risk of death in all age intervals, with the highest RDs and RRs from birth through infancy (ages 0-11 months) (RD, 2.29% [95% CI, 2.23%-2.35%]; RR, 11.61 [95% CI, 11.09-12.15]) and in early childhood (ages 1-5 years) (RD, 0.34% [95% CI, 0.31%-0.36%]; RR, 2.79 [95% CI, 2.61-2.98]) and the lowest RDs and RRs among those between ages 18 and 28 years (RD, 0.07% [95% CI, 0.04%-0.10%]; RR, 1.13 [95% CI, 1.07-1.19]). We identified increased risks of mortality associated with several causes, including respiratory, circulatory, and digestive system disorders; nervous system, endocrine, and infectious diseases; cancers; congenital malformations; and conditions originating in the perinatal period. No associations were found for external causes of deaths. Associations by GA categories suggested lower risks with higher GA.

Conclusions and Relevance  The findings of this population-based matched cohort study suggest that individuals born preterm were at an increased risk of death from birth until their third and fourth decades of life, with higher risks as GA decreased. Some of these associations may have been partly due to underlying health determinants that affected PTB and mortality. These findings suggest that PTB should be recognized as a risk factor for mortality and could inform preventive strategies. 

Source: https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2826512?widget=personalizedcontent&previousarticle=0

EDITORIAL article Front. Pediatr. , 12 January 2025 Volume 13 – 2025 | https://doi.org/10.3389/fped.2025.1552262

This article is part of the Research Topic What is new on the Horizon in Neonatology? Recent Advances

Minesh Khashu1Karel Allegaert2,3,4*

  • 1Department of Neonatology, University Hospitals Dorset NHS Foundation Trust, Dorset, United Kingdom
  • 2Department of Development and Regeneration, KU Leuven, Leuven, Belgium
  • 3Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium
  • 4Department of Hospital Pharmacy, Erasmus MC, Rotterdam, Netherlands

Introduction

Neonates and infants are commonly referred to as “therapeutic orphans” due to the overall scarcity of therapeutic interventions that have been developed and tailored to their needs and specific characteristics (12). This is well known by care providers and researchers active in this field, but is perhaps less on the radar of authorities, funding bodies or the broader public. There is significant health inequity when comparing newborns to other age populations in terms of specific drug and device development and therapeutics (12). In addition there are health inequities in the provision of neonatal care globally which require special attention in terms of improvement (3).

Bronchopulmonary dysplasia, neonatal seizures, poor growth, necrotizing enterocolitis (NEC) and short bowel, hypoxic-ischemic encephalopathy, retinopathy of prematurity (ROP), neonatal infections and sepsis hereby serve as a non-exhaustive list of “orphan conditions” in need of more equity, through adequately and urgently funded research and improvement.

The good news is that there have been increased efforts, in recent years, by researchers and regulatory bodies to focus on the provision of drugs, devices, and treatment modalities tailored for neonatal use, while further advocacy remains an obvious need (245). This brings perspective and explains the initiative taken to organize a focused research topic on what is on the horizon as well as recent advances.

Overview of the topics covered

We targeted emerging or new aspects related to monitoring, diagnostics and therapeutics in neonatal care for the current research topic. Fortunately, this research topic was perceived as very relevant by the research community, as 135 authors expressed their interest as contributors, resulting in 20 accepted papers. This serves as a signal of the importance to continue to work on this topic.

Post-hoc, and in a somewhat arbitrary way (because of overlap in these subcategories) these papers were subdivided by the editors into different subcategories, with focus on (1, 5 papers) perinatal biomarkers in blood and urine and how these relate to or predict outcomes, (2, 6 papers) adaptations of existing and newly emerging equipment in neonatal units, (3, 3 papers) needed advances in pharmacotherapy, (4, 3 papers) machine learning or deep learning applications in neonatal care, and finally, (5, 3 papers) underreported aspects of contemporary NICU care, with a focus on the holistic nature of care for the infant and the family.

Perinatal biomarkers in blood and urine and how these relate to or predict outcomes

Two papers focused on biomarkers related to gestational diabetes, with reflections and data on maternal and neonatal outcomes. Postnatal maternal levels of glycated albumin and hemoglobin A1c in mothers of large-for-gestational-age (LGA) informed us of the relevance of accurate diagnosis during pregnancy. This is because postpartum women without diagnosis during pregnancy had higher glycated albumin values, associated with LGA and associated complications (Železnik et al.). Interestingly and related to this paper, Yin et al. reported on a untargeted metabolomics study in women with gestational diabetes, with the recommendation of a maternal serum metabolite panel to forecast neonatal adverse outcomes (hypoglycemia and macrosomia) (Yin et al.).

Other papers focused on the use of vitamin D, acid-base and biomarkers associated with fetal growth restriction with impaired neurodevelopmental outcome. In a cohort of 217 preterm neonates, a multivariate regression analysis identified antenatal steroids as protective, and lower birth weight, duration of ventilation, sepsis and the serum 25-(OH)D vitamin as risk factors to develop ROP (Yin et al.). Musco et al. reported on a systematic review on blood biomarkers indicating risks of adverse neurodevelopmental outcome in fetal growth restricted infants (Musco et al.). While the authors retrieved some data on neuron specific enolase and S100B, the overall conclusions reflect a call for further research. Finally, an association between lactate levels in umbilical cord blood and cerebral oxygenation in preterm neonates was studied as a secondary outcome analysis (Dusleag et al.). In non-asphyxiated preterm neonates with respiratory support, lactate levels were negatively associated with cerebral and arterial oxygenation. In term neonates without respiratory support, no associations were observed.

Adaptations of existing and newly emerging equipment in our units

In a review on emerging innovations in neonatal monitoring, Krbec et al. concluded that there is an urgent, still unmet need to develop wireless, non- or minimal-contact, non-adhesive technology, capable to integrate multiple signals in a single platform, tailored to neonates (Krbec et al.). Related to this call of action, Svoboda et al. reported on their pilot experience with contactless assessment of heart rate, applying imaging photoplethysmography (Svoboda et al.). Rectal and axillary temperature monitoring on admission were compared in a cohort of preterm (n = 80, <32 weeks gestational age) by Halabi et al., reporting that rectal measurement was likely more reliable in the event of hypothermia (Halabi et al.). Ultrasound-guided measurement of anterior cerebral artery resistive index in the first week of life in 739 preterm neonates (<35 weeks) was not associated with subsequent co-morbidities on admission or during neonatal stay (asphyxia, sepsis, NEC) (Singh Gill et al.). A case series of neurally adjusted ventilatory assist to rescue pulmonary interstitial emphysema in 5 extremely low birth weight infants illustrated the potential value of this ventilatory equipment and strategy and need for further study (Chen et al.). Finally, van Rens et al. compared a conventional to a modified Seldinger technique (a dedicated micro-insertion kit) for peripherally inserted central catheter (PICC) placement, illustrating the relevance of developing “low risk, high benefit” type of medical devices, adapted to the specific needs of neonates (van Rens et al.).

Advances needed in pharmacotherapy

The currently available medicines and dosing regimens in neonatal care are limited and there is an urgent need for improvement in this domain. This was illustrated by articles on sepsis, septic shock and steroids. Inequity in provision of neonatal care across the globe ought to be a major focus of improvement. Gezahegn et al. described the outcome in neonates admitted with sepsis in Harar (Ethiopia). Low white blood cell count, desaturation, preterm birth, absence of prenatal maternal care, and chorioamnionitis were important risk factors for sepsis-related mortality (Gezahegn et al.). Addressing these prognostic factors hold the promise to act as levelers to improve outcomes. A pilot study compared noradrenaline and adrenaline as first line vasopressor for fluid-refractory sepsis shock (Garegrat et al.). Both interventions were comparable to resolve the septic shock, while the overall mortality (13/42, 30%) remained significant, highlighting the need for better diagnostic and therapeutic options. Finally, in a systematic review, outcome of postnatal systemic corticosteroids (hydrocortisone to dexamethasone) were compared as reported in randomized controlled trials (Boscarino et al.). The authors concluded that dexamethasone appeared to be somewhat more effective than hydrocortisone in improving respiratory outcomes, but with inconclusive but relevant concerns on the uncertainties on long-term neurodevelopmental outcome, again highlighting the need for better therapies for prevention and management of chronic lung disease of prematurity.

Machine learning or deep learning applications in neonatal care

Artificial intelligence is a rapidly advancing area with fast evolving clinical applications in healthcare, including in the NICU (6). It is no surprise that the current research topic also contains papers illustrating its relevance to improve our practices and outcomes. Two papers hereby focused on NEC, and a 3rd paper on prediction of significant patent ductus arteriosus (PDA). In a mini-review, Cuna et al. reports on the various pathophysiological processes underlying NEC endotypes, and how artificial intelligence holds the promise to influence further understanding and management (Cuna et al.). An approach to enhance surgical decision making in NEC is illustrated by Wu et al. Based on x-rays from 263 neonates diagnosed with NEC (94 surgical cases), a binary diagnostic tool was trained and validated, with Resnet18 as approach applied (Wu et al.). For PDA, an ultrasound-based assessment of ductus arteriosus intimal thickness in the first 24 h after birth was applied in 105 preterm neonates. A prediction model for closure on day 7 included birth weight, mechanical ventilation, left ventricular end-diastolic diameter, and PDA intimal thickness (Hu et al.). Such models can be considered to better target future study, integrated in a precision medicine approach. Use of AI and big data have the potential to significantly improve our understanding of neonatal conditions and also support neonatal researchers in asking better research questions.

Underreported aspects of contemporary NICU care, holistic care

As part of this research topic, we also accepted papers reporting on the use of music on pain management, on multisensory stimulation to improve maternal milk volume production, and parents’ experiences related to congenital cardiac surgery. All these 3 papers reflect the need for holistic care and to further integrate the perspectives of (former) patients and parents into neonatal practice.

In a systematic review, Ou et al. demonstrated that music is an effective intervention to relief procedural pain (e.g., Premature Infant Pain Profile score) in preterm neonates, as it reduced some markers of stress, and improved blood oxygen saturation (Ou et al.). Multisensory stimulation (audiovisual, or audiovisual + olfactory) compared to a control setting improved maternal milk volume production, with evidence of positive effects of both interventions, even more pronounced if both interventions are combined (Cuya et al.). Finally, a quantitative analysis of parent’s experiences with neonates admitted to NICU with a congenital heart disease reinformed us on the importance of actively focusing on parental experiences of care (Catapano et al.).

From advances in neonatal care to implementation

In our opinion, this research topic nicely illustrates the diversity in ongoing clinical research activities, that all hold the promise to improve our clinical management practices, with the overarching aim to improve neonatal outcomes. There is an urgent need to focus on the current health inequities in the provision of care to neonates (3). The trend towards a “neuro” dedicated NICU care is an illustration on how relevant progress may occur. This progress is based on improved neuromonitoring techniques (7), improved management and precision medicine in the field of anti-epileptic drugs (8), and integrating families as partners in neonatal neuro-critical care and similar improvement programs (9). The good news is that we are already experiencing a shift in the right direction. The neonatal community and all other relevant stakeholders need to work better together to improve the pace and scale of this improvement.

Source: https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2025.1552262/full

Sprecher, Alicia MD; Roeloffs, Kimberly NNP; Czarnecki, Michelle L. APN; Labovsky, Kristen MD; Kissell, Anna PharmD; Hornung, Genesee MSN, RN; Uhing, Michael MD Editor(s): Dudding, Katherine PhD, RN, RNC-NIC, CNE; Nist, Marliese D. PhD, RNC, Section Editors Advances in Neonatal Care 25(1):p 18-27, February 2025. | DOI: 10.1097/ANC.0000000000001234

Abstract

Background: 

Postoperative pain management in the neonatal period is an area of high variability and a source of staff dissatisfaction. Pain management is a key component of high-quality care; however, pain assessment in infants is difficult and analgesics can negatively impact the developing brain.

Purpose: 

We aimed to improve postoperative pain control for infants in our neonatal intensive care unit (NICU), limit variability in the approach to pain management, and increase staff satisfaction.

Methods: 

This project was completed between April 2019 and March 2022 with sustainment tracked through December 2023. Interventions took place in a 70-bed level IV NICU using quality improvement methodology. Interventions included efforts aimed at improving pain assessment as well as development and implementation of a pain management guideline. Outcome measures included frequency of uncontrolled postoperative pain and measures of staff satisfaction. Process measures included compliance with pain assessment cadence and guideline recommendations. Opioid exposure within 24 hours of surgery was included as a balancing measure.

Results: 

Pain management was assessed in 811 infants: 392 prior to guideline implementation, 273 during implementation, and 146 during sustainment period. Uncontrolled postoperative pain decreased from 26% pre-implementation to 18% post implementation and into the sustainment period. Staff satisfaction improved from 67% to 83%. These improvements were associated with decreased variability in postoperative pain management and a decrease in postoperative opioid exposure.

Implications for Practice and Research: 

The use of a postoperative pain management guideline can improve pain control, decrease drug regimen variability, decrease opioid exposure, and increase staff satisfaction.

Source:https://journals.lww.com/advancesinneonatalcare/abstract/2025/02000/a_nicu_postoperative_pain_management_improvement.5.aspx

Health Care Heros – Environmental Service Workers

Healing Forward: Health & Wellness

In Singapore, where skyscrapers rise and medicine meets innovation, a new kind of wellness journey is unfolding—one led by the smallest among us.

Our Womb Warriors who began life in the NICU are not just survivors—they are thrivers, growing through challenges and emerging with strength forged in the most fragile beginnings. Today, health and wellness for these preemie survivors extends far beyond the hospital walls. It means developmental follow-up, skin-to-skin care, nutrition support, and emotional well-being—not just survival, but quality of life.

Singapore’s approach is inspiring. With personalized risk assessments, neurodevelopmental care programs, and parent-empowering tools like kangaroo care, the wellness journey begins from day one. And studies now confirm what many NICU parents already knew in their hearts: the closeness, love, and presence of family are as powerful as any machine.

As our Warriors grow, their wellness becomes more than a checklist—it becomes a rhythm. Physical therapy. Play. Sensory exploration. Nourishment. Love. And for the parents walking beside them? Wellness looks like deep breaths, long walks, and the quiet courage to ask for help.

Whether your little one is a few months or a few years out of the NICU, this season is a reminder: wellness isn’t a destination—it’s a daily act of love.

Spring into Strength

Spring is a season of becoming—of blooming boldly, stretching softly toward the light, and waking up to what’s possible. For our Womb Warriors, it’s also a reminder that wellness is not about perfection—it’s about progress, presence, and power.

Whether you’re a preemie kid discovering new abilities, a teen navigating your story, or an adult survivor reclaiming your narrative, this season invites you to grow on your terms. Your early beginnings may have been fragile—but your spirit is anything but.

Health and wellness don’t have to look the same for everyone. What matters most is listening to your body, honoring your journey, and celebrating how far you’ve come.

🌸 For Kids

  • Make movement magical—build obstacle courses, splash in puddles, or stretch like your favorite animal.
  • Explore foods that help you grow strong: yogurt parfaits, rainbow fruit plates, or protein-packed pancakes.
  • Practice deep breathing with bubbles or belly-breathing “dragon breaths.”

🌱 For Teens

  • Journal your thoughts under a tree or start a mood-boosting playlist for mental clarity.
  • Try out yoga, trail walks, or a new sport—your strength isn’t defined by speed, but by showing up.
  • Fuel yourself with purpose: balanced snacks, hydration, and sleep that heals.

🌞 For Adults

  • Redefine strength: maybe it’s finishing a workout, setting boundaries, or resting when you need to.
  • Revisit your NICU beginnings—use them to empower your healthcare choices and connect with your past.
  • Create a spring ritual: a morning stretch, a quiet walk, or a personal mantra. Wellness isn’t trendy—it’s transformative.

In Singapore, hospitals are leading the way in early screenings and personalized care to help preemies not just survive, but thrive. That same spirit of innovation and renewal lives in each of us.

So here’s to you—this spring, let’s grow wildly. Heal gently. Thrive loudly.
Because once a Neonatal Womb Warrior, always a Warrior—and you are in full bloom.

Wellness is a journey. In this insightful talk, learn about the PATH model: Perception, Analysis, Trial and Error, and Habits, as a framework for achieving personal well-being. This talk empowers audiences to embrace the process and find a path to a healthier, more fulfilling life. Hi everyone, I’m Alysha! I am a student in grade 11 and I’m one of the speakers for TEDEd’s Empowerment event. Having been part of the club since grade 9 and now as president, I’m really excited to share my talk with everyone! I’ll be talking about wellness and taking autonomy over your own mental health. I’m super excited that this is our first charitable event and can’t wait to see you all there!

10-minute guided meditation for kids 🧘 mindfulness for kids 🕊 Bye Bye Worry Balloons🎈 Worry-Free 💛

Relax, breathe, and feel calm with this simple meditation for kids. In this guided meditation for kids, we’ll say ‘bye-bye’ to worries and hello to happy thoughts. ☀️🎈

Mr. Hassell’s Brain Breaks

Exercise your body and mind with this Spring themed brain break! In this fun and engaging workout video, we play a game of “Would You Rather” by picking our favorite Spring choices and performing exercises!! Perfect for a PE warmup, classroom brain break and at home workout!

Written by published children’s author, Jennifer Marino Walters, “Surprising Spring” tells the simple story of the beauty that Spring brings and its many flowering surprises.


[OFW] WAVEHOUSE Sentosa | Surfing in Singapore

5 years ago     Renan El Viajero

Wave House Sentosa located on the sandy beaches of Sentosa is Asia’s only installation in an archipelago of global Wave Houses that stretches from Durban in South Africa, San Diego in California, Santiago in Chile, and Mallorca in Spain. Singapore has long been a crossroads for surfers seeking the perfect waves at beaches around Southeast Asia, however the island itself lacks the giant waves which surfers long for. With its opening, Wave House Sentosa puts Singapore on the global surfer destination map with its perfect and world famous 10′ FlowBarrel wave.  

Horizons, ND Impairment, Parent Personalization

Slovakia,  officially the Slovak Republic,  is a landlocked country in Central Europe. It is bordered by Poland to the north, Ukraine to the east, Hungary to the south, Austria to the west, and the Czech Republic to the northwest. Slovakia’s mostly mountainous territory spans about 49,000 km (19,000 sq mi), hosting a population exceeding 5.4 million. The capital and largest city is Bratislava, while the second largest city is Košice.

Slovakia is a developed country with an advanced high-income economy. The country maintains a combination of a market economy with a comprehensive social security system, providing citizens with universal health carefree education, one of the lowest retirement age in Europe and one of the longest paid parental leaves in the OECD.  Slovakia is a member of the European Union, the Eurozone, the Schengen Area, the United NationsNATOCERN, the OECD, the WTO, the Council of Europe, the Visegrád Group, and the OSCE. Slovakia is also home to eight UNESCO World Heritage Sites. The world’s largest per-capita car producer, Slovakia manufactured a total of 1.1 million cars in 2019, representing 43% of its total industrial output.

Healthcare in Slovakia has features of the Bismarck, the Beveridge and the National health insurance systems. It has public health system paid largely from taxation. The cost of national health insurance is shared between the employees and the employers. The part of these taxes are paid by the employees as a deduction from theirs wages and the remaining part of these taxes is paid as compulsory contribution by employers. Sole traders pay the full amount of these taxes.  

These taxes are managed by health insurance companies. Current healthcare system has 3 health insurance companies, namely Union (12,4%), Dôvera (32,4%) and Všeobecná zdravotná poisťovňa (55,2%)(market share). Všeobecná zdravotná poisťovňa is a state-run insurance company, the other two are private. These insurance companies have contracts with outpatient clinics, hospitals, rehabilitation centres, pharmacies, etc. Despite this, not everywhere and not always the insurance company covers the costs. The costs are not covered for all medicines, or the full price of them. Also, it is not covered dental treatment.

The government pays health insurance for children, students, pensioners, invalids, people performing activities for a church, religious or charitable community, etc.

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

CR’s experts say it’s much safer for children to wear their winter coat backward and on top of their car seat harness.

“You better bundle that baby up or she’s going to catch a cold!” I knew before I turned around what was happening: The well-meaning lady in the grocery store parking lot wanted to know why my child didn’t have a coat on in her car seat, even though it was the middle of winter.

The reason? Because a bulky coat and a child car seat can be a dangerous combination. As a general rule, winter coats should not be worn underneath a car seat harness because that can leave the harness too loose to be effective in a crash. 

Source: https://www.consumerreports.org/babies-kids/car-seats/the-dangers-of-winter-coats-and-car-seats-a5483582251/

Author affiliations – Naomi R Hemy1 Amber Bates1 Belinda Frank2 Anne McKenzie2 Shannon J Simpson1 3

Abstract

Background It is essential to embed patient and public perspectives into every stage of the research journey, including setting the future research agenda. The substantial gaps in our understanding of prematurity-associated lung disease presented a timely opportunity to determine the community’s research priorities.

Objective To conduct a priority setting partnership (PSP) to determine the top 10 research priorities for preterm lung health.

Design We undertook a modified James Lind Alliance methodology comprising three main stages: (1) an idea generating survey with open questions to ascertain the community’s most important ideas for future preterm lung health research, (2) prioritisation survey to distill the main themes into a shortlist of 20 and (3) consensus workshop where participants were tasked with ranking their final top 10. This PSP is reflective of the view of preterm-born individuals, parents of preterm children and healthcare professionals in an Australian healthcare setting.

Results We collated 144 submissions from the idea generating survey from which 27 prioritisation themes were developed. From the 150 prioritisation survey responses, the 20 themes receiving the most votes were taken to the consensus workshop. Participants identified the following top 10: (1) lifelong impacts; (2) interventions, treatments or supports; (3) ongoing lung health follow-up; (4) diagnostic tools, resources and education for primary healthcare providers; (5) resources to inform and empower families; (6) relationship to physical health and developmental issues; (7) preventing and/or treating lung infections; (8) additional supports, resources and research for minority groups; (9) impact on mental well-being; and (10) likelihood of asthma diagnosis.

Conclusion Priorities identified through the PSP will be invaluable in informing future research into prematurity-associated lung disease.

Full Study-https://bmjpaedsopen.bmj.com/content/9/1/e003050

Posted on 27 January 2025 by Keith Barrington

Neonatal Research

Following important research in neonatology / newborn medicine from around the world

I have written frequently about my concerns with “NDI” as an important measure of neonatal outcomes, indeed, it seems to be often thought of as if it were the only important measure. It has very often been included as part of a composite outcome measure “death or NDI”.

So why am I disturbed about the use of NDI as a primary outcome measure? NDI is itself already a composite measurement, including some indicator of delayed development (most commonly one of the various iterations of the Bayley Scales of Infant Development), some severity of motor disorder expected to be permanent, i.e. Cerebral Palsy, some severity of hearing loss, and some severity of visual impairment. It was a composite invented by neonatologists and follow up specialists as a way of trying to quantify the impacts of adverse cerebral impacts of prematurity. There are many problems with this, both in the actual importance of each component of NDI, and also in the permanence of the finding. For example, most infants with low scores on developmental screening tests at 2 years do not have intellectual impairment at follow up. In the follow up of the CAP trial, for example, only 18% of babies who had a low Bayley score at 18 months (version 2 MDI <70) actually had a low IQ at 5 years (WPSII <70). This is unlike CP, for which a diagnosis at 2 years is very accurate (not 100%, but appears to be about 95% PPV) as a predictor of long term motor dysfunction, but the severity of the problem can vary, especially after a diagnosis at 2 to 3 years, where about 1/3 of infants will change their classification on the GMFCS, either to a higher or a lower score. Visual and auditory impairments seem to be more permanent and invariable, but are a much smaller part of the NDI.

And, of course, combining NDI with death as part of a composite outcome implies that they are equally important, and means that an intervention which decreases death may not be found to be significant is there is an increase in low BSID scores in the survivors (for example).

Do parents of babies who are labelled as having NDI think that their infants are impaired? That is the question asked in a new publication from the follow up centres across Canada (Canadian Neonatal Follow-Up Network, CNFUN). Richter LL, et al. Parental and Medical Classification of Neurodevelopment in Children Born Preterm. Pediatrics. 2025. Over 1000 very preterm infants are involved in the study, and their parents were asked if they thought that their child had a developmental impairment when they attended a follow-up clinic appointment, but before they completed the standardised evaluation. They then had their evaluation and were classified as having no NDI or :

“to have a mild-moderate NDI if they had any 1 or more of the following: CP with GMFCS 1 or 2; Bayley-III motor, cognitive, or language composite scores 70 to 84; hearing loss without requirement for hearing devices or unilateral visual impairment. A child was considered to have a severe NDI if they had any 1 or more of the following: CP with GMFCS 3, 4, or 5; Bayley-III motor, cognitive or language composite scores <70; hearing aid or cochlear implant; or bilateral visual impairment.”

As this table shows, there was poor agreement between what the parents thought, and what the standardised evaluation stated. Most of the disagreements were parents considering their infants to not be impaired, or to be less impaired than the standard classification. There were 185 infants with “severe NDI” according to the definition above, only 23 parents thought their child was severely impaired, in contrast, among the 596 with no NDI, there were 11 parents who found their child to have severe impairment, and 104 thought they had mild-moderate impairment.

Some of the details of the analyses are quite interesting, for example, the small number of infants with serious CP, GMFCS 4 or 5, were mostly considered to have moderate or severe impairment by parents. The cognitive scores of infants who agreed that their infant, with CNFUN defined severe NDI, had at least moderate impairment were lower (median 70) than those who disagreed (median 80).

Many problems faced by families with ex-preterm infants are not captured by “NDI”. This is reflected, I think, by those parents who thought their child was impaired despite not satisfying CNFUN definitions, such infants were much more likely to be using technology at home, and more likely to have been referred for occupational therapy, or to see a psychologist or other therapist. Needing re-hospitalisation also made parent more likely to agree that their infant had an impairment.

Because we haven’t measured some of the things that impact families, such as behavioural disturbances, feeding problems, and sleep disruption, we really don’t know if they are affected by any of our NICU interventions. It wouldn’t surprise me if some interventions, ranging from postnatal steroids to skin-to-skin care or light cycling, might have major impacts on those outcomes. We just don’t know.

What should we do about findings such as these newly published data, and others from the Parents’ Voices project? Defining a single ‘yes or no’ outcome variable is the old-fashioned way of designing research and determining the benefit of an intervention. There are much better ways of comparing outcomes between groups, ways which can take into account the variety of outcomes, and the preferences of parents. It takes some extra work to define the kind of ordinal outcomes which reflect the values of parents and the relative importance of each component, but that is hugely preferable to using composite outcomes which implicitly value each component as being equivalent. Being dead, having a Bayley Cognitive composite of 69, having severe visual loss all qualify as “dead or severe NDI”, but the implications are enormously different.

In the future outcomes we measure should focus on how infants function, and should recognize that the answer to the question “how is your child doing?” is not a dichotomous choice.

Source: https://neonatalresearch.org/2025/01/27/neurodevelopmental-impairment-who-decides-what-it-is/

Subhasish DasThomas McClintock, Barbara E. CormackFrank H. Bloomfield,Jane E. Harding & Luling Lin Pediatric Research volume 97, pages67–80 (2025)

Abstract

Background

Appropriate protein intake is crucial for growth and development in children born preterm. We assessed the effects of high (HP) versus low protein (LP) intake on neurodevelopment, growth, and biochemical anomalies in these children.

Methods

Randomised and quasi-randomised trials providing protein to children born preterm (<37 completed weeks of gestation) were searched following PRISMA guideline in three databases and four registers (PROSPERO registration CRD42022325659). Random-effects model was used for assessing the effects of HP (≥3.5 g/kg/d) vs. LP (<3.5 g/kg/d).

Results

Data from forty-four studies (n = 5338) showed HP might slightly reduce the chance of survival without neurodisability at ≥12 months (four studies, 1109 children, relative risk [RR] 0.95 [95% CI 0.90, 1.01]; P = 0.13; low certainty evidence) and might increase risk of cognitive impairment at toddler age (two studies; 436 children; RR 1.36 [0.89, 2.09]; P = 0.16; low certainty evidence). At discharge or 36 weeks, HP intake might result in higher weight and greater head circumference z-scores. HP intake probably increased the risk of hypophosphatemia, hypercalcemia, refeeding syndrome and high blood urea, but reduced risk of hyperglycaemia.

Conclusions

HP intake for children born preterm may be harmful for neonatal metabolism and later neurodisability and has few short-term benefits for growth.

Impact statement

  • Planned high protein intake after birth for infants born preterm might be harmful for survival, neurodisability and metabolism during infancy and did not improve growth after the neonatal period.
  • Protein intake ≥3.5 g/kg/d should not be recommended for children born preterm.

Conclusion (Full Study)

Planned high protein intake in the first weeks after preterm birth had few benefits and may be harmful for survival, neurodisability and biochemical abnormalities in neonatal care. However, there are few data beyond the toddler period and considerable unexplained heterogeneity. Longer-term follow-up and an individual participant data meta-analysis of existing trials, including data on total energy intake, would be helpful to clarify the effects of high protein intake for children born preterm.

FULL Article:https://www.nature.com/articles/s41390-024-03296-z

Marlyse F. Haward a, Antoine Payot b c, Chris Feudtner d e, Annie Janvier b c

Abstract

Communication with parents is an essential component of neonatal care. For extremely preterm infants born at less than 25 weeks, this process is complicated by the substantial risk of mortality or major morbidity. For some babies with specific prognostic factors, the majority die. Although many of these deaths occur after admission to the intensive care unit, position statements have focused on communication during the prenatal consultation. This review takes a more comprehensive approach and covers personalized and parent-centered communication in the clinical setting during three distinct yet inter-related phases: the antenatal consultation, the neonatal intensive care hospitalization, and the dying process (when this happens). We advocate that a ‘one-size-fits-all’ communication model focused on standardizing information does not lead to partnerships. It is possible to standardize personalized approaches that recognize and adapt to parental heterogeneity. This can help clinicians and parents build effective partnerships of trust and affective support to engage in personalized decision-making. These practices begin with self-reflection on the part of the clinician and continue with practical frameworks and stepwise approaches supporting personalization and parent-centered communication.

Section snippets

Part 1: Antenatal consultation

Current recommendations for the antenatal consultation focus on equalizing knowledge imbalances by providing parents with physician-derived sets of information to facilitate rational, data-driven choices.14 These information sets span short and long-term morbidities, survival and mortality statistics determined by physicians, with little input from parents. Although recommendationssuggest exploring values, they fall short in acknowledging the ‘process’ of relationship building.

Part 2. Communication during the neonatal hospitalization

Parent-centered communications during neonatal hospitalizations follows similar concepts. This section will add how continuity of care and ‘good parenting beliefs’ can help manage uncertainty, hope, and realism. We will consider the case of Ms. Gladwell.

Part 3. Dealing with death: the importance of a stepwise approach

Generally, for babies born at less than 25 weeks, neonatal death occurs relatively early when the infant does not respond to interventions, often within the first 3 days of life for the most immature babies.84 Other babies die when respiratory support is removed after death is judged inevatable, or for quality of life concerns.15 For parents like Ms. Gladwell, when death is not immediate, time permits knowledge to be acquired and values to be clarified influencing how choices are interpreted.

Conclusion

Parents and families will live with these experiences for the rest of their lives. How they remember the communication process and care their infants received depends on their perceptions of the relationships built with clinicians and their ability to ‘justify’ what happened within the context of their values. Behaviors that make them feel disrespected or their infant not valued can leave lasting impressions, whereas trusting partnerships solidifies their roles as parents.

Source:https://www.sciencedirect.com/science/article/abs/pii/S0146000521001658?via%3Dihub

Efficiently Natural    Jan 24, 2021   #medicalschool #residency #doctorcouple

Here’s another video in our Journey Through Medicine series where we talk about what it was like for us to have a child while both completing our medical residencies. There’s never a perfect time to have a child during medical training, but here’s how we made it work. #medicalschool #residency #doctorcouple

NatureNeonatal Neurocritical Care Series 19 December 2023

Abstract

The survival of preterm infants has steadily improved thanks to advances in perinatal and neonatal intensive clinical care. The focus is now on finding ways to improve morbidities, especially neurological outcomes. Although antenatal steroids and magnesium for preterm infants have become routine therapies, studies have mainly demonstrated short-term benefits for antenatal steroid therapy but limited evidence for impact on long-term neurodevelopmental outcomes. Further advances in neuroprotective and neurorestorative therapies, improved neuromonitoring modalities to optimize recruitment in trials, and improved biomarkers to assess the response to treatment are essential. Among the most promising agents, multipotential stem cells, immunomodulation, and anti-inflammatory therapies can improve neural outcomes in preclinical studies and are the subject of considerable ongoing research. In the meantime, bundles of care protecting and nurturing the brain in the neonatal intensive care unit and beyond should be widely implemented in an effort to limit injury and promote neuroplasticity.

Impact

  • With improved survival of preterm infants due to improved antenatal and neonatal care, our focus must now be to improve long-term neurological and neurodevelopmental outcomes.
  • This review details the multifactorial pathogenesis of preterm brain injury and neuroprotective strategies in use at present, including antenatal care, seizure management and non-pharmacological NICU care.
  • We discuss treatment strategies that are being evaluated as potential interventions to improve the neurodevelopmental outcomes of infants born prematurely.

https://www.nature.com/articles/s41390-023-02895-6

Leading Edge Seminars  May 23, 2017

Compassionate Inquiry is a psychotherapeutic method developed by Dr. Gabor Maté that reveals what lies beneath the appearance we present to the world. Using Compassionate Inquiry, the therapist unveils the level of consciousness, mental climate, hidden assumptions, implicit memories and body states that form the real message that words both express and conceal.

Your friend or family has finally brought their preemie baby home from the NICU, and you’re excited to meet their little miracle, but unsure of how to approach the family altogether.

Don’t worry, as long as you stick to these simple do’s and don’ts written by a preemie mom, visiting a premature baby will be a happy and smooth time for everyone!

Do Listen to the Preemie Parents’ Conditions (and Comply)

Before visiting a premature baby, ask the parents if they are ready to receive visits in their home. And under which terms.

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Top of Form

It’s not uncommon that when we take our babies home, the doctors impose a no visit rule until we can complete the first vaccination schemes (which more often than not include at least three shots of the Synagis shot.) The complete process can take up to three months.

We didn’t allow almost any visit from friends or family until my son was around four months old (2 months old adjusted), some of our friends were understanding, and some weren’t.

We knew that we were doing what was best for our son, so we stuck to it!

If your friend says it’s OK to visit their baby, find out if they have any special request for your visit.

Some of the petitions may seem weird but know that they come from a very real place (the NICU), and visiting a premature baby during her first months is much like visiting babies in the NICU: short and strict.

Some parents may ask you to keep your cell phones at the entrance of the house (phones are full of germs),  wash your hands for five minutes, visit straight from home, or tie your hair, take a shower just before visiting, or wear a surgical face mask. Whatever it is, by doing as they say you’ll help protect their baby and their peace of mind.

Do Bring Extra Clean Clothes for Interacting with the Preemie Baby

This is especially true if you are visiting a premature baby after being all day outside of your home.

The street is full of germs and contamination, and we preemie parents tend to develop a germ-vision.

By bringing freshly laundered clothes and changing into them as soon as you arrive at the house you are visiting you will show them that you are on their side, and support their every measure to keep their baby safe.

It is even more likely that they will let you hold the baby if you do this since she won’t be directly exposed to dirty clothes.

Do: Wash your Hands as Soon as you Enter, Wash your hands thoroughly.

Make sure you wash the space between your fingers, your palm, and the back of your hand.

You’ll be amazed to know the number of diseases we can avoid by just washing hands. Simple, right?

Even so, many of us neglect this standard practice.

When a baby is in the NICU, the nurses teach us parents about the importance of hand-washing, the correct techniques to do so, the right moment to do it. We wash our hands so frequently that we get rashes most of the time (since the NICU soap is strong.)

It is second nature to us to wash our hands when visiting babies!

Having said all this, once our babies are bigger and stronger, we’ll be a bit laxer about this. After all, germs do help develop the immune system, we just don’t want to expose our miracles before they are ready for this!

Do Keep the Visit Short and Simple

There will be time for the lengthy visits that you may be dreaming about. In the months and years to come, you’ll be able to kiss and smooch the baby to your heart’s content, and stay during weekends, afternoons, and evenings!

But right now, the preemie family may be in need of some alone time. And though seeing you will surely help them, keep your visit under 30 minutes if possible.

Most breastfeeding moms need time adjusting to… well…breastfeeding, but this is especially the case of us preemie moms. We came from pumping our way in the NICU to actually breastfeeding a baby. That transition takes time to get used to.

Additionally, like all new parents, we are most likely to be sleep-deprived. Partly because our babies wake us up all night and partly because of the monitors beeping or ourselves waking up to check that the babies are doing fine.

Keeping a short visit is a long time investment in your relationship with NICU families.

Don’t Go if You’re Not Feeling Well

If your head hurts, your throat is sore or your nose itches, reprogram your visit.

Even if you are feeling well but visited someone who has had the flu within seven days before your visit you may be carrying the virus, so it’s also best to reprogram.

RSV and pulmonary infections are dangerous for preemies.

Ollie had simple flu when he was 12 months old and turned into pneumonia and bronchiolitis in less than 24 hours. We had to rush him to the ER because he wasn’t breathing. He was in the hospital on oxygen for ten days until he recovered. The younger the baby, the higher the risk of infection.

We limited our visits to non-flu visitors until Ollie was well over 8 months. And, we still ask everyone who may be sick to wear a facemask. We don’t overprotect our son, he goes to crowded places and has had the flu several times by now at 24 months. But we still don’t want to risk it by letting someone with the flu hold him without wearing a facemask.

Don’t Hold the Preemie Baby

Unless the parents ask you to hold their baby, don’t press them into it.

You’ll have plenty of opportunities. Just make them feel comfortable by knowing that you are OK just looking at the baby. If they are comfortable with you holding her, they will let you know.

Also, to keep on the safe side, avoid kissing the baby and holding her hands.

Don’t Compare their Preemie to any Other Baby

As preemie parents, the greatest joy in the world comes with sorrow.

We love our baby and wouldn’t change him for anyone else, nor would we want him to be any different. So we try not to compare our baby to anyone else’s. But, sometimes it is inevitable, and we internally cave in.

My son looked like a newborn during his first four months. He didn’t smile until he was eight months old and had to go through weekly Physical Therapy to move his hands and arms. He is healthy, bright, and has no significant delay. But when the children of my friends were smiling, walking, and talking, he wasn’t, and it’s human nature to worry and to compare them.

It gets even worse when people pity my boy or openly compare him to others. It feels as if they are undermining us as if they don’t know or don’t care about our background.

A few months ago a fellow mom who has a son two months younger than Ollie (but bigger and heavier), raved on and on about how small and fragile my Ollie was. She held him without my permission and said that she remembered the times when her son was smaller. She went as far as to congratulate me for being so chill and not overprotecting him. He was evidently so weak (to her eyes.) She seemed to be following an anti-manual for visiting a premature baby.

Needless to say, I despised every second we spent together, and I’ve never seen her again.

Don’t Talk about other Full-Time Pregnancies

Us moms also grieve about the weeks that we should have been heavily pregnant and weren’t.

Sometimes I see other moms complaining about their heavy wombs. Begging for their babies to come early so that they can stop being feeling uncomfortable. I understand that they don’t know what they are saying, but it hurts.

My son was born at 31 weeks, which means that I missed out on nine weeks of pregnancy. Some women dream about their pregnancies their whole lives. They imagine them picture perfect, so we miss what we didn’t have. And in some cases, what we’ll never have.

So it’s better to play it safe and stay clear of that topic.

That’s a Wrap

I’m sure you’ll love visiting a premature baby. Take it one step at a time and be patient with us preemie parents. We do want what’s best for our children, even if sometimes it is hard to express ourselves.

Most of all, you’ll see how powerful and miraculous a person can be, no matter how small!

Have you visited a preemie recently? Are you planning a preemie visit? Or, are you a preemie parent and would like people to know how to plan their visits? Tell us all about it in the comment section!

Source: https://preemiemomtips.com/visiting-preemie-dos-donts/

By Jessica A. Stern, University of Virginia and Joseph P. Allen, University of Virginia

Posted on January 14, 2025

Empathy — the capacity to identify others’ needs and emotions, and to provide supportive care that meets those needs.

Our recent research shows that parents who express empathy toward their teenagers may give teens a head start in developing the skill themselves. In addition, adolescents who show empathy and support toward their friends are more likely to become supportive parents, which may foster empathy in their own offspring.

How we did our work

The KLIFF/VIDA study at the University of Virginia has tracked 184 adolescents for more than 25 years: from age 13 well into their 30s.

Starting in 1998, teens came to the university every year with their parents and closest friend, and a team of researchers recorded videos of their conversations. Researchers observed how much empathy the mother showed to her 13-year-old when her teen needed help with a problem. We measured empathy by rating how present and engaged mothers were in the conversation, whether they had an accurate understanding of their teen’s problem, and how much help and emotional support they offered.

Then, each year until teens were 19 years old, we observed whether teens showed those same types of empathic behaviors toward their close friends.

A decade later, when some of those same teens were starting to have children of their own, we surveyed them about their own parenting. We also asked them about their young children’s empathy. For example, parents rated how often their child “tries to understand how others feel” and “tries to comfort others.”

We found that the more empathic a mother was toward her teenager at age 13, the more empathic the teen was toward their close friends across the adolescent years. Among teens who later had kids themselves, the ones who had shown more empathy for close friends as adolescents became more supportive parents as adults. In turn, these parents’ supportive responses to their children’s distress were associated with reports of their young children’s empathy.

Why it matters

The ability to empathize with other people in adolescence is a critical skill for maintaining good relationshipsresolving conflict, preventing violent crime and having good communication skills and more satisfying relationships as an adult.

Adults want teens to develop good social skills and moral character, but simply telling them to be kind doesn’t always work.

Our findings suggest that if parents hope to raise empathic teens, it may be helpful to give them firsthand experiences of being understood and supported.

But teens also need opportunities to practice and refine these skills with their peers. Adolescent friendships may be an essential “training ground” for teens to learn social skills such as empathy, how to respond effectively to other people’s suffering, and supportive caregiving abilities that they can put to use as parents. Our lab’s most recent paper presents some of the first evidence that having supportive teenage friendships matters for future parenting.

What’s next

We’re continuing to follow these participants to understand how their experiences with parents and peers during adolescence might play a role in how the next generation develops.

We’re also curious to understand what factors might interrupt intergenerational cycles of low empathy, aggression and harsh parenting. For example, it’s possible that having supportive friends could compensate for a lack of empathy experienced from one’s family.

While it’s true that you can’t choose your family, you can choose your friends. Empowering teens to choose friendships characterized by mutual understanding and support could have long-term ripple effects for the next generation.

Source: https://youthtoday.org/2025/01/a-25-year-study-reveals-how-empathy-is-passed-from-parents-to-teens-to-their-future-children/

*We checked to  confirm these organizations are still active in February, 2025.There was only one resource we were unable to locate. We have also attached the website links!

It really does take a village for preemie parents by Kinsey Gidick Nov.24, 2020

Only the parents of a premature baby can understand the emotional toll it takes to care for such a fragile child. That’s why finding a community of parents and caretakers who have been through similar circumstances is so important. Fortunately, there are many online resources for parents experiencing the challenge of navigating the NICU and raising a premature baby, from preemie support groups to virtual counseling sessions to even social media accounts.

While each is different, the focus is the same: to provide a space where preemie parents can bring their worries, wins, and concerns to each other and get help and feedback from those going through the same situations. 380,000 babies are born before 37 weeks gestation each year in the U.S. per March of Dimes — that’s 1 out of every 10 American babies. That’s a lot of babies receiving extensive medical intervention including respiratory support, invasive treatments, and extended Neonatal Intensive Care Unit stays. In many cases, these spaces are like lifelines for parents who are afraid of not only the unknown, but the known as well.

Rather than shoulder that burden alone, preemie support groups offer all kinds of resources from chat rooms to virtual mentors, podcasts to classes. It’s the kind of care one won’t often find in a clinic or hospital — ongoing assistance a preemie parent can turn to whether a child is 3 weeks or 3 years old.

1. A space for NICU transition support

Graham’s Foundation, a not-for-profit support group based in Ohio, was founded with a mission that no one should experience prematurity alone. To that end, the organization has a number of programs designed to help pre-term birth families including NICU transition to home care packages, preemie parent mentors who can be contacted 24/7, an app called MyPreemie, and many online forums for parents to engage with other preemie families. –https://www.grahamsfoundation.org/

2.A community of peers

Hand to Hold is an organization created to guide preemie families through the long journey from a NICU stay to home, as well as provide comfort and support in times of loss. To do so, the website maintains forums for its 63,000 online community members. But it’s not just for preemie families. There are also resources for NICU professionals including podcasts and an ambassador program of bedside support volunteers who visit NICUs and provide additional help. –https://handtohold.org/

3.A place for bereavement support

Bereavement support is something all too many families of premature babies need. And High Risk Hope is one place they can find it. The 501(c)3 believes that “there is no foot too small that it cannot leave an imprint on this world.” To do so, the Florida-based organization connects families with other organizations to provide ongoing grief support and counseling. –https://highriskhope.org/

4.One-on-one care

Support 4 NICU Parents Support 4 NICU Parents aims to improve psychosocial support for NICU parents and enhance training and support for NICU healthcare providers, ensuring families and babies thrive together.  https://www.pqcnc.org/node/13721

5.Parental Zoom chats

Tiny Miracles is a nonprofit charity based in Fairfield County, Connecticut, that is dedicated to helping families with premature babies. Like many premature baby groups, it offers all kinds of resources for families, but its most popular offerings are free weekly Zoom support chats that anyone can join. Held every Thursday at 8 p.m. EST, they’re a way for people to get to know other parents beyond a virtual chat room or forum.-https://www.projectsweetpeas.com/

6. Material support

Care packages, hospital events, peer-to-peer support, financial aid, educational materials, these are all the work of Project Sweet Peas. Families can reach out directly for all of the above and receive the care they need from this nonprofit. And for those who have simply been touched by a premature birth and want to give back, they can donate to Project Sweet Peas’ effort which has sent 23,126 NICU care packages to families and 4,909 bereavement boxes as well.-https://www.projectsweetpeas.com/

7.Facebook Preemie Page

Social media sites, like Facebook, are a natural home for support groups and the Parents of Preemies/Premature Babies is one of the biggest for this specific demographic. With 15.3K members, it’s a private group you must ask to join. It was started in 2007 when founder Heather Armstrong writes that she couldn’t find a similar support space. It invites members to discuss topics related to the raising of premature children but doesn’t allow fundraising, self-promotion, or requests for medical advice. It includes parents of preemies from around the world.-https://www.facebook.com/groups/2304668997

8. Helping hand from March of Dimes

Not every hospital has a March of Dimes NICU Family Support program, but it’s worth inquiring should a family find itself with a baby in the newborn intensive care unit. The nonprofit that’s committed to improving the health of mothers and babies organized its NICU Family Support program to provide families with essential materials during their child’s NICU stay. Those include things like “keepsake booklets for their NICU baby, a guide for parenting in the NICU, and a NICU guide” according to the organization’s website. For families with an infant having a shorter NICU stay, March of Dimes provides materials as well. There’s also a helpful app where families can explore their questions and concerns.-https://www.marchofdimes.org/find-support/compassbymarchofdimes

9.Support for babies less than 2 pounds

Premature babies are not a monolith. There are varying levels of prematurity and some of the most at-risk children are those born less than 2 pounds and before 27 weeks. That’s why the Micro Preemie Parents Facebook support page exists, to be there for parents of these special children. Only parents of so called “micro preemies” will be accepted to the private page. Once in, they can expect to be able to join conversations specific to this very unique experience with other parents and guardians who understand where they’re coming from. –https://www.facebook.com/groups/micropreemiemoms

10. A Space for Black Preemie Parents

Black Preemie Parents Community is a Facebook group just for Black parents to find “support, advice, share stories, or just vent as you go through your journey.” It’s a small group with less than 400 members providing those who join with an intimate circle of friends to reach out to during challenging times. –https://www.facebook.com/groups/blackpreemieparentscommunity

11. Where to go when they grow

The premature parenting journey doesn’t end when a child leaves the NICU. It’s a lifelong path and one that might find parents looking for support well into their child’s teens and twenties. For that there’s Parents of Older Preemies. Another Facebook group, this 1.5K member page is for “parents to share their stories of their preemie(s) and how far they have come in their lives in a caring and supportive environment. This group shares triumphs, setbacks, frustrations and positive advice to others that are on their continued “preemie journey.”-https://www.facebook.com/groups/276697059074997

12. Visual Support

Preemie baby support isn’t limited to Facebook and nonprofit organizations. Instagram has also become a network where people kind find kinship in navigating life with a preemie. For instance, preemiesupermoms is an Instagram page dedicated to prematurity awareness. The page posts images of premature babies along with inspiring quotes and stories

For families looking for someone to listen or a place to gather strength, these organizations are here to help. All families need to do is ask. –https://www.instagram.com/preemiesupermoms/

Introduction

Neonates and infants are commonly referred to as “therapeutic orphans” due to the overall scarcity of therapeutic interventions that have been developed and tailored to their needs and specific characteristics . This is well known by care providers and researchers active in this field, but is perhaps less on the radar of authorities, funding bodies or the broader public. There is significant health inequity when comparing newborns to other age populations in terms of specific drug and device development and therapeutics . In addition there are health inequities in the provision of neonatal care globally which require special attention in terms of improvement .

Bronchopulmonary dysplasia, neonatal seizures, poor growth, necrotizing enterocolitis (NEC) and short bowel, hypoxic-ischemic encephalopathy, retinopathy of prematurity (ROP), neonatal infections and sepsis hereby serve as a non-exhaustive list of “orphan conditions” in need of more equity, through adequately and urgently funded research and improvement.

The good news is that there have been increased efforts, in recent years, by researchers and regulatory bodies to focus on the provision of drugs, devices, and treatment modalities tailored for neonatal use, while further advocacy remains an obvious need (245). This brings perspective and explains the initiative taken to organize a focused research topic on what is on the horizon as well as recent advances.

Overview of the topics covered

We targeted emerging or new aspects related to monitoring, diagnostics and therapeutics in neonatal care for the current research topic. Fortunately, this research topic was perceived as very relevant by the research community, as 135 authors expressed their interest as contributors, resulting in 20 accepted papers. This serves as a signal of the importance to continue to work on this topic.

Post-hoc, and in a somewhat arbitrary way (because of overlap in these subcategories) these papers were subdivided by the editors into different subcategories, with focus on (1, 5 papers) perinatal biomarkers in blood and urine and how these relate to or predict outcomes, (2, 6 papers) adaptations of existing and newly emerging equipment in neonatal units, (3, 3 papers) needed advances in pharmacotherapy, (4, 3 papers) machine learning or deep learning applications in neonatal care, and finally, (5, 3 papers) underreported aspects of contemporary NICU care, with a focus on the holistic nature of care for the infant and the family.

Perinatal biomarkers in blood and urine and how these relate to or predict outcomes

Two papers focused on biomarkers related to gestational diabetes, with reflections and data on maternal and neonatal outcomes. Postnatal maternal levels of glycated albumin and hemoglobin A1c in mothers of large-for-gestational-age (LGA) informed us of the relevance of accurate diagnosis during pregnancy. This is because postpartum women without diagnosis during pregnancy had higher glycated albumin values, associated with LGA and associated complications (Železnik et al.). Interestingly and related to this paper, Yin et al. reported on a untargeted metabolomics study in women with gestational diabetes, with the recommendation of a maternal serum metabolite panel to forecast neonatal adverse outcomes (hypoglycemia and macrosomia) (Yin et al.).

Other papers focused on the use of vitamin D, acid-base and biomarkers associated with fetal growth restriction with impaired neurodevelopmental outcome. In a cohort of 217 preterm neonates, a multivariate regression analysis identified antenatal steroids as protective, and lower birth weight, duration of ventilation, sepsis and the serum 25-(OH)D vitamin as risk factors to develop ROP (Yin et al.). Musco et al. reported on a systematic review on blood biomarkers indicating risks of adverse neurodevelopmental outcome in fetal growth restricted infants (Musco et al.). While the authors retrieved some data on neuron specific enolase and S100B, the overall conclusions reflect a call for further research. Finally, an association between lactate levels in umbilical cord blood and cerebral oxygenation in preterm neonates was studied as a secondary outcome analysis (Dusleag et al.). In non-asphyxiated preterm neonates with respiratory support, lactate levels were negatively associated with cerebral and arterial oxygenation. In term neonates without respiratory support, no associations were observed.

Adaptations of existing and newly emerging equipment in our units

In a review on emerging innovations in neonatal monitoring, Krbec et al. concluded that there is an urgent, still unmet need to develop wireless, non- or minimal-contact, non-adhesive technology, capable to integrate multiple signals in a single platform, tailored to neonates (Krbec et al.). Related to this call of action, Svoboda et al. reported on their pilot experience with contactless assessment of heart rate, applying imaging photoplethysmography (Svoboda et al.). Rectal and axillary temperature monitoring on admission were compared in a cohort of preterm (n = 80, <32 weeks gestational age) by Halabi et al., reporting that rectal measurement was likely more reliable in the event of hypothermia (Halabi et al.). Ultrasound-guided measurement of anterior cerebral artery resistive index in the first week of life in 739 preterm neonates (<35 weeks) was not associated with subsequent co-morbidities on admission or during neonatal stay (asphyxia, sepsis, NEC) (Singh Gill et al.). A case series of neurally adjusted ventilatory assist to rescue pulmonary interstitial emphysema in 5 extremely low birth weight infants illustrated the potential value of this ventilatory equipment and strategy and need for further study (Chen et al.). Finally, van Rens et al. compared a conventional to a modified Seldinger technique (a dedicated micro-insertion kit) for peripherally inserted central catheter (PICC) placement, illustrating the relevance of developing “low risk, high benefit” type of medical devices, adapted to the specific needs of neonates (van Rens et al.).

Advances needed in pharmacotherapy

The currently available medicines and dosing regimens in neonatal care are limited and there is an urgent need for improvement in this domain. This was illustrated by articles on sepsis, septic shock and steroids. Inequity in provision of neonatal care across the globe ought to be a major focus of improvement. Gezahegn et al. described the outcome in neonates admitted with sepsis in Harar (Ethiopia). Low white blood cell count, desaturation, preterm birth, absence of prenatal maternal care, and chorioamnionitis were important risk factors for sepsis-related mortality (Gezahegn et al.). Addressing these prognostic factors hold the promise to act as levelers to improve outcomes. A pilot study compared noradrenaline and adrenaline as first line vasopressor for fluid-refractory sepsis shock (Garegrat et al.). Both interventions were comparable to resolve the septic shock, while the overall mortality (13/42, 30%) remained significant, highlighting the need for better diagnostic and therapeutic options. Finally, in a systematic review, outcome of postnatal systemic corticosteroids (hydrocortisone to dexamethasone) were compared as reported in randomized controlled trials (Boscarino et al.). The authors concluded that dexamethasone appeared to be somewhat more effective than hydrocortisone in improving respiratory outcomes, but with inconclusive but relevant concerns on the uncertainties on long-term neurodevelopmental outcome, again highlighting the need for better therapies for prevention and management of chronic lung disease of prematurity.

Machine learning or deep learning applications in neonatal care

Artificial intelligence is a rapidly advancing area with fast evolving clinical applications in healthcare, including in the NICU (6). It is no surprise that the current research topic also contains papers illustrating its relevance to improve our practices and outcomes. Two papers hereby focused on NEC, and a 3rd paper on prediction of significant patent ductus arteriosus (PDA). In a mini-review, Cuna et al. reports on the various pathophysiological processes underlying NEC endotypes, and how artificial intelligence holds the promise to influence further understanding and management (Cuna et al.). An approach to enhance surgical decision making in NEC is illustrated by Wu et al. Based on x-rays from 263 neonates diagnosed with NEC (94 surgical cases), a binary diagnostic tool was trained and validated, with Resnet18 as approach applied (Wu et al.). For PDA, an ultrasound-based assessment of ductus arteriosus intimal thickness in the first 24 h after birth was applied in 105 preterm neonates. A prediction model for closure on day 7 included birth weight, mechanical ventilation, left ventricular end-diastolic diameter, and PDA intimal thickness (Hu et al.). Such models can be considered to better target future study, integrated in a precision medicine approach. Use of AI and big data have the potential to significantly improve our understanding of neonatal conditions and also support neonatal researchers in asking better research questions.

Underreported aspects of contemporary NICU care, holistic care

As part of this research topic, we also accepted papers reporting on the use of music on pain management, on multisensory stimulation to improve maternal milk volume production, and parents’ experiences related to congenital cardiac surgery. All these 3 papers reflect the need for holistic care and to further integrate the perspectives of (former) patients and parents into neonatal practice.

In a systematic review, Ou et al. demonstrated that music is an effective intervention to relief procedural pain (e.g., Premature Infant Pain Profile score) in preterm neonates, as it reduced some markers of stress, and improved blood oxygen saturation (Ou et al.). Multisensory stimulation (audiovisual, or audiovisual + olfactory) compared to a control setting improved maternal milk volume production, with evidence of positive effects of both interventions, even more pronounced if both interventions are combined (Cuya et al.). Finally, a quantitative analysis of parent’s experiences with neonates admitted to NICU with a congenital heart disease reinformed us on the importance of actively focusing on parental experiences of care (Catapano et al.).

From advances in neonatal care to implementation

In our opinion, this research topic nicely illustrates the diversity in ongoing clinical research activities, that all hold the promise to improve our clinical management practices, with the overarching aim to improve neonatal outcomes. There is an urgent need to focus on the current health inequities in the provision of care to neonates (3). The trend towards a “neuro” dedicated NICU care is an illustration on how relevant progress may occur. This progress is based on improved neuromonitoring techniques (7), improved management and precision medicine in the field of anti-epileptic drugs (8), and integrating families as partners in neonatal neuro-critical care and similar improvement programs (9). The good news is that we are already experiencing a shift in the right direction. The neonatal community and all other relevant stakeholders need to work better together to improve the pace and scale of this improvement.

Source:https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2025.1552262/full

Abstract

Background

The prenatal shunt, ductus arteriosus (DA), typically closes during the cardio-pulmonary transition at birth. We evaluated maternal and neonatal factors associated with delayed closure of DA in term-born neonates.

Method

We conducted a retrospective cohort study that included full-term neonates from the prospective observational Copenhagen Baby Heart cohort study. We assessed the association between maternal and neonatal factors and delayed ductal closure.

 Results

We included 19,566 neonates, of whom 48% were female. Echocardiography was performed at a median age of 12 (IQR:9-15) and eight (IQR:2-13) days for neonates with no DA and an open DA, respectively. Associations with delayed ductal closure included maternal obesity adjusted risk ratio=2 (95%CI:1-3.8), maternal hypothyroidism during pregnancy aRR=2.02 (95%CI:1.2-3.4), low Apgar 2.6 (95%CI:1.2-6), high weight aRR=1.81(95%CI:1.2-2.6), and length at birth aRR=1.7(95%CI:1.1-2.6).

Conclusion:

The identified risk factors for delayed ductal closure in term-born neonates may help increase clinical attention and improve neonatal care.

Source:https://karger.com/neo/article/doi/10.1159/000543915/921437/Maternal-and-Neonatal-Factors-Associated-with

17 February 2025

Prospects for Children in 2025: Building Resilient Systems for Children’s Futures is the latest edition of Global Outlook, a series of reports produced each year by United Nations Children’s Fund (UNICEF) Innocenti – Global Office of Research and Foresight, which look at the key trends affecting children and young people over the following 12 months and beyond.

In this new report, new and intensifying crises for children – including climate change, conflict and economic instability – are shown to be closely interconnected.

For instance, climate change is disrupting the water cycle, leading to widespread water scarcity, threatening food production and livelihoods across the economy. This disruption poses direct and indirect risks to children, as it impacts the availability of safe water, food, and family income.

The report also notes that debt burdens are forcing governments to cut essential public services, including those related to water, sanitation, and hygiene. These challenges are compounded by a lack of investment in long-term development.

According to UNICEF, rising geopolitical tensions and competition among nations are hindering the implementation of solutions that will protect young people’s lives and build more resilient futures for them.

The report calls for resilient national systems that prioritize children’s health, education and wellbeing, and emphasizes the importance of including children’s rights in climate action.

Download the report here.-https://www.unwater.org/news/unicef-2025-global-outlook-prospects-children-2025-building-resilient-systems-children%E2%80%99s

Hey, Neonatal Warriors!

Empathy and compassion is the foundation of the powerful bond we share as a community. It’s more than just understanding the struggles of others—it’s about truly connecting with their experiences and emotions. As we continue on our journey from the neonatal unit to where we are today, empathy strengthens our resilience and fosters a sense of unity. This connection gives us the strength to support one another, celebrate our victories, and face challenges together.

In the video you’re about to watch, we’ll dive deeper into how our shared experiences and collective empathy can empower us to not only overcome adversity but also to thrive. It highlights the importance of understanding and supporting each other, offering both comfort and encouragement in meaningful ways. Through storytelling and the exchange of our journeys, we create a community that is stronger, more resilient, and ready to face whatever challenges come our way.

I wanted to share this video because it perfectly encapsulates the power of empathy and how, together, we can elevate each other. It’s a reminder that even in difficult times, we are never alone—our shared experiences and collective strength can light the way forward.

Let’s continue to harness the power of empathy as we watch and reflect on the message in this video. Together, we are unstoppable.

What Is The Difference Between Empathy, Sympathy, and Compassion

The Power of Emotional Competency

Expert Reveals the Truth About Empathy, Sympathy and Compassion | Doug Noll

This video shows you the difference between empathy, sympathy, and compassion

 • Sympathy is pity-based and is selfish

• Empathy is a learned skill

• Compassion is empathy with an impulse to relieve distress

This video is for our younger friends to help them understand empathy, which means caring about how others feel and being kind to them. Mark Ruffalo and Murray Monster from Sesame Street will show us what empathy is and give fun examples of how we can be kind and helpful to others. I wanted to share this video because it’s a great way for younger kids to learn how to show empathy and support for their friends and family. Let’s watch and see how we can all use empathy to make the world a kinder place! Enjoy watching!

Sesame Street – Empathy With Mark Ruffalo

This video is perfect for helping young students understand what empathy is. Murray Monster and Mark Ruffalo talk about what empathy means and go through several examples. Use this helpful video for introducing important social skills to your K-2 students!

SnowboardZezula      Jul 11, 2022

Mrkni na report z Quiksilver & Roxy Czech and Slovak Surfing Championship 2022

👉 https://snbz.cz/report-surfchamp-2022