bims-cliped Biomed News
on Clinical pediatrics
Issue of 2026–06–07
29 papers selected by
Alyssa M. Portwood, Akron’s Children



  1. Pediatr Res. 2026 May 30.
      Advances in pediatric research have improved the lives of infants, children, adolescents, and society at large. A decade ago the American Academy of Pediatrics identified seven research achievements in the past 40 years that reduced morbidity and mortality worldwide: preventing disease with life-saving immunizations, reducing sudden infant death with "Back to Sleep," curing Acute Lymphoblastic Leukemia, helping premature babies breathe with surfactant, preventing Human Immunodeficiency Virus transmission from mother to baby, increasing life expectancy for children with Sickle Cell Anemia and Cystic Fibrosis, and saving lives with car seats and seat belts. This follow-up article forecasts the next great achievements in pediatric research and highlights what is needed to continue progress. The pediatric scientific community identified 10 areas of high research promise: genomics; mental and behavioral health; vaccines; artificial intelligence and digital health; perinatal health, including fetal medicine; precision and targeted therapeutics; social determinants of health; nutrition; environmental health; and advances in cancer treatment. Advances in each of these areas are already improving health outcomes. Amid increasing public distrust in science, celebrating scientific progress and committing to continued investment are critical to improving the health of children and the adults they will become. IMPACT: Advances in pediatric research have improved the lives of infants, children, adolescents, and society at large. The pediatric scientific community identified 10 exciting pediatric research breakthroughs on the horizon, which are reviewed in this article. Amid increasing public distrust in science, celebrating scientific progress and committing to continued investment are critical to improving the health of children and the adults they will become.
    DOI:  https://doi.org/10.1038/s41390-026-05126-w
  2. Otolaryngol Head Neck Surg. 2026 Jun 03.
       OBJECTIVE: HPV vaccination recommendations have expanded to include both sexes and a broadened age range since approval in 2006. These changes and increasing HPV-related head and neck cancer rates support vaccination of older and male patients, necessitating changes in HPV education. We aim to analyze vaccination trends and to identify opportunities for increasing awareness.
    STUDY DESIGN: Cross-sectional study analyzing vaccination trends between 2007 and 2023.
    SETTING: US hospitals and clinics using Epic.
    METHODS: Using Epic Cosmos, a national database, vaccination trends for patients aged 9 to 45 were stratified by year, demographics, and administering provider specialty.
    RESULTS: 19.6 million HPV vaccinations were administered between 2007 and 2023. The inclusion of males aged 9 to 21 in the recommendations beginning in 2009 corresponded with an 836% increase in vaccinations in this group from 2010 to 2016. Males comprised 49.9% of vaccinated patients aged 9 to 18 in 2023, a percentage that increased annually since 2010. Head and neck cancer prevention became a designated vaccine indication in 2020. Despite broadened indications, total vaccination declined by 47.1% from 2016 to 2023 in patients aged 9 to 26. In 2012, 74.8% of vaccinations were administered in pediatrics and 18.3% in family medicine. In 2023, pediatrics administered 46.6%, family medicine 33.3%, OBGYN 7.1%, and primary care 6.8%.
    CONCLUSION: Expanding guidelines have had inconsistent impacts on vaccination trends, as rates decreased in target populations since 2016. Males contribute equally to pediatric but not adult vaccinations. Departments administering vaccines are diversifying, though pediatrics predominates. Gendered and outdated education and marketing could contribute to disparities and discordance with guidelines.
    Keywords:  HPV vaccination; epidemiology; head and neck cancer; human papillomavirus
    DOI:  https://doi.org/10.1002/ohn.70310
  3. Hosp Pediatr. 2026 Jun 05. pii: e2025008999. [Epub ahead of print]
       BACKGROUND/OBJECTIVES: Pediatric hospital medicine (PHM) is a growing field with a unique scholarly perspective and evolving role in academic leadership. Since the last systematic assessment of PHM research in 2009, predating subspecialty certification in 2016 and fellowship accreditation in 2020, the research infrastructure within PHM has not been reevaluated. We sought to assess the current state of PHM research by assessing the number, scope, and scholarly domains of research faculty, as well as research funding and support.
    METHODS: Using the Pediatrics Research in Inpatient Settings Network, we distributed a cross-sectional survey to PHM group leaders across the United States and Canada. The 16-item instrument, adapted from prior PHM and adult hospital medicine surveys, assessed program demographics, faculty effort allocation, research support, funding, and scholarly domains. Surveys were distributed via REDCap with follow-up reminders. Descriptive statistics were used.
    RESULTS: 49 programs responded (51% response rate), representing 1702 faculty (∼40% of US pediatric hospitalists). Fewer than half of programs (n = 21, 43%) reported faculty with more than 50% research effort. One-hundred and ninety faculty members (11%) had dedicated research time, and 72% of those conducting quality improvement research did so without any protected effort. Most PHM programs (n = 27, 55%) received less than $100 000 in total annual research funding.
    CONCLUSIONS: Despite recent PHM subspecialty designation and pediatric hospitalist desire to conduct research, dedicated time and associated supports are uncommon in PHM groups. Improvements in the PHM research pipeline will require understanding institutional financial constraints and diversifying and strengthening research funding.
    DOI:  https://doi.org/10.1542/hpeds.2025-008999
  4. Pediatrics. 2026 Jun 04. pii: e2025071494. [Epub ahead of print]
    AAP LIGHT Collaborative
       OBJECTIVE: Subthreshold phototherapy use is common in infants with hyperbilirubinemia but leads to overtreatment of safe bilirubin levels. Coincident with publication of the 2022 American Academy of Pediatrics neonatal hyperbilirubinemia guidelines, we formed a quality improvement (QI) collaborative with the aim to reduce inpatient subthreshold phototherapy use to 10% of all phototherapy encounters over 12 months.
    METHODS: Our QI collaborative included 146 hospitals across North America. Sites submitted data from inpatient phototherapy encounters of newborns born at 35 weeks' gestation or more between February 2022-January 2023 (baseline period; 6-month preguideline period, 6-month washout period) and February 2023-January 2024 (intervention period). Interventions included QI coaching, educational webinars, electronic health record tools, clinical algorithms, and communication resources. We analyzed the primary outcome with interrupted time series and balancing measures by statistical process control.
    RESULTS: Final analysis included 33 384 phototherapy encounters (20 018 baseline, 13 366 intervention) from 119 sites. The percentage of encounters initiated at subthreshold bilirubin levels decreased from 48.2% in the preguideline baseline period to 41.1% at the end of intervention. Overall phototherapy encounters demonstrated a relative decrease of 33.3%, with median encounters per site per month declining from 12 during the baseline period to 8 at the end of intervention. Modest increases were seen in percentage of encounters that met escalation-of-care threshold (5.73%-6.32%) and peak bilirubin greater than 25 mg/dL (0.87%-2.12%).
    CONCLUSIONS: Although subthreshold phototherapy decreased, the chosen goal of reducing subthreshold encounters to 10% or less of all phototherapy encounters was not reached after 12 months. Future work is needed to determine barriers to reducing unnecessary treatment for neonatal jaundice.
    DOI:  https://doi.org/10.1542/peds.2025-071494
  5. Obstet Gynecol Clin North Am. 2026 Jun;pii: S0889-8545(26)00006-9. [Epub ahead of print]53(2): 353-364
      Transgender and gender diverse (TGD) youth face significant health disparities, underscoring the critical need for equitable, evidence-based care. Based on substantial evidence, the gender-affirming care model remains the standard of care. TGD youth may seek gynecologic expertize for a variety of reproductive health care concerns. This article outlines essential considerations for clinicians when providing gender-inclusive services to pediatric patients. Key areas addressed include creating a safe clinical environment, managing psychosocial comorbidities, administering gender affirming medical therapy, and addressing gynecologic needs such as menstrual suppression, contraception, sexual health screening, and fertility counseling.
    Keywords:  Adolescent; Gender diverse; Nonbinary; Pediatric; Transgender; Youth
    DOI:  https://doi.org/10.1016/j.ogc.2026.01.006
  6. Hosp Pediatr. 2026 Jun 04. pii: e2025009011. [Epub ahead of print]
       BACKGROUND: Pediatric emergency department (ED) transfers have increased even among hospitals with pediatric admitting capability. We sought to determine whether pediatric subspecialty capability or pediatric intensive care unit (PICU) capability was associated with ED transfers among hospitals with pediatric admitting capability.
    METHODS: This retrospective cross-sectional study included all pediatric ED visits from the Healthcare Cost and Utilization Project Nationwide Emergency Department Sample database resulting in admission or transfer at hospitals with pediatric admitting capability. We compared EDs with and without pediatric subspecialty or PICU capabilities. Pediatric subspecialties included general surgery, orthopedic surgery, and neurology. Transfer rates were calculated as the number of patients transferred among those not discharged. We used logistic regression to evaluate the association of pediatric subspecialty and PICU capabilities with transfer.
    RESULTS: We analyzed 4 468 922 weighted ED visits. The transfer rate was 42.4% for EDs without pediatric subspecialty capability (adjusted odds ratio [aOR], 12.9; 95% CI, 8.5-19.6 compared with EDs with all 3 subspecialties), 12.8% for those with 1 subspecialty (aOR, 3.7; 95% CI, 2.4-5.6), 4.1% for those with 2 (aOR, 1.3; 95% CI, 0.9-2.1), and 2.6% for those with all 3. There was a 41.7% transfer rate for EDs without PICU capability (aOR, 1.6; 95% CI, 1.3-2.0) compared with 7.0% for those with PICU capability.
    CONCLUSION: Among hospitals with pediatric admitting capability, both the need for pediatric subspecialty care and intensive care were associated with increased transfers, and subspecialty capability had a larger association. Interventions to mitigate rising pediatric transfers may consider expanding subspecialty access.
    DOI:  https://doi.org/10.1542/hpeds.2025-009011
  7. Ann Allergy Asthma Immunol. 2026 Jun 03. pii: S1081-1206(26)00258-9. [Epub ahead of print]
       BACKGROUND: Single maintenance and reliever therapy (SMART) is the guideline-recommended treatment for children with moderate-to-severe asthma, yet it is underutilized in pediatric practice.
    OBJECTIVE: To understand barriers and facilitators to SMART adoption within pediatric practice.
    METHODS: We interviewed 52 participants (16 pediatricians, 22 parents, and 16 children). Interviews were conducted until theme saturation, recorded, transcribed, coded and qualitatively analyzed using the Consolidated Framework for Implementation Research.
    RESULTS: We identified barriers, facilitators and potential solutions to SMART implementation. Participants described barriers at the 1) clinic-level which included lack of clinician training and clinical decision support for SMART, 2) at the family-level which included discomfort transitioning away from traditional albuterol and concern about SMART's effectiveness as a rescue medication, at 3) school-and systems-levels which included poor communication and lack of aligned care plans across community settings like schools, and challenges navigating insurance coverage. Facilitators to SMART implementation included acceptance of SMART as a simpler treatment that could improve asthma symptoms. Proposed solutions to barriers included 1) clinic-level trainings and integrated clinical decision support 2) family-level support for reluctant families, and 3) clear communication between clinics and schools, access to SMART-specific medication orders and action plans, and insurance support.
    CONCLUSION: Most pediatricians and families reported that SMART is a favorable, simple and acceptable treatment approach for children with asthma. However, pediatricians and families described significant barriers to using guideline-concordant SMART within routine practice. These results could inform targeted efforts to improve the adoption of SMART within pediatric asthma care.
    Keywords:  Childhood asthma; guideline-based asthma care; implementation science; inhaled corticosteroid-long acting beta agonist; maintenance and reliever therapy (MART); pediatric pulmonology; single maintenance and reliver therapy (SMART)
    DOI:  https://doi.org/10.1016/j.anai.2026.03.030
  8. J Patient Exp. 2026 ;13 23743735261455630
      Pain represents a subjective experience that manifests with emotional and physical discomfort. In pediatric care, pain management is especially complex due to communicative limitations, which creates a unique point of entry for parents to contribute to their child's treatment process. In this study, we explored whether families' perceptions of their child's pain and preferences for treatment were aligned with healthcare providers' pain management decisions. Using narrative-informed techniques in interviews with families and healthcare providers in pediatric care settings, we analyzed areas of concordance and discordance in pain assessment and treatment priorities. Our findings show that trust is built over time through (1) consistent communication and (2) individualized care for their child's unique needs. Contrastingly, when trust is broken, families experience added stress with care. Future research should prioritize developing tools and interventions that support this collaborative model. Ultimately, these efforts aim to equalize power dynamics in the family-provider relationship by emphasizing the value of both parental understanding and medical knowledge in pediatric pain management.
    Keywords:  healthcare provider-family relationships; individualized care; parental involvement; pediatric pain management
    DOI:  https://doi.org/10.1177/23743735261455630
  9. Pediatr Emerg Care. 2026 Jun 02.
       OBJECTIVE: Unintentional ingestions in children are a common presenting chief complaint in the emergency department (ED). The decision to consult social work or report to Child Protective Services (CPS) relies on the provider's discretion. We sought to investigate the association between race or insurance status and providers' decisions.
    METHODS: A retrospective cross-sectional study of children younger than 6 years of age presenting to 1 of 6 hospitals within the Yale New Haven Health system in 2013 to 2021 with an ICD-9/10 code of poisoning or accidental ingestion. Multivariable logistic regression was used to assess factors associated with social work and CPS consults.
    RESULTS: Among 759 children with unintentional ingestions, there were 467 (48.4%) ingestions of over-the-counter substances, 359 (47.3%) ingestions of prescription medications and 24 (3.2%) ingestions of illicit substances. Medication error by caregiver accounted for 46 cases (6.1%). Social work was consulted in 23% of cases. Factors associated with social work consults were changes in baseline mental status and vital signs (adjusted odds ratio [aOR]=3.35 [95% CI: 1.62-6.92]), requiring inpatient care (aOR=14.3 [8.04-25.6]), PICU admission (aOR=24.5 [5.57-107.9]), and having toxicology tests ordered (aOR=3.2 [1.85-5.51]). Presentation to a general ED decreased the odds of a social work consult (aOR=0.14 [0.08-0.24]). CPS reports were filed in 6.7% of cases. Factors associated with CPS reports were ingestion type (prescription aOR=2.73 [95%CI 1.19-6.27]; substances illegal for a minor [eg, alcohol, nicotine, THC-containing products] aOR=21.8 [6.76-70.4]), change in mental status or vital signs from baseline (aOR=3.18 [1.39-7.26]), requiring inpatient care (aOR=4.17 [1.95-8.91]) PICU (aOR=6.23 [95%CI 1.67-23.3]) and having toxicology tests ordered (aOR=3.6 [1.71-7.57]).
    CONCLUSIONS: In children presenting after unintentional ingestion, involvement of social work or CPS was associated with clinical severity and substance type but not with race or insurance status.
    Keywords:  child protective services; ingestion; pediatric emergency department; poisoning; social work
    DOI:  https://doi.org/10.1097/PEC.0000000000003631
  10. Front Med (Lausanne). 2026 ;13 1799500
      Emergencies in pediatric rheumatology practice are relatively uncommon but rapid diagnosis and treatment are fundamental. Emergencies can be often misdiagnosed but prompt recognition and treatment are fundamental in order to reduce mortality and morbidity. This narrative review is a non-systematic analysis of the literature addressing the main emergencies in pediatric rheumatology. We aim to summarize the most relevant and frequent emergencies in pediatric rheumatology and provide practical guidance for the diagnosis and the management of emergency rheumatic disease in childhood.
    Keywords:  children; emergency; pediatric; pediatric rheumatology; toxicity
    DOI:  https://doi.org/10.3389/fmed.2026.1799500
  11. J Emerg Nurs. 2026 Jun 03. pii: S0099-1767(26)00153-4. [Epub ahead of print]
       INTRODUCTION: Emergency department visits are unpredictable in nature. A nurse's shift can consist of low-acuity patients, with the surprise of an injured or ill patient. This process improvement project aimed to create ease of supply access and subsequently reduce time delay in critical interventions to support patient outcomes.
    METHODS: This project was conducted in a pediatric emergency department in the western United States. An initial review assessed how the baseline stored supplies were used. With these data, supplies were optimized to ensure that the correct supplies were stored following a Lean methodology. Subsequently, the concept of a fixed storage space was used in a systematic manner following the body system groupings used in trauma primary assessments. Team members were educated on the new supply organization and completed a scavenger hunt retrieving several essential supplies. A multiple-timepoint pre-post time trial was conducted on team members' ability to locate numerous supplies during this scavenger hunt.
    RESULTS: The average time required to locate required supplies decreased dramatically. The preintervention period yielded an average time of 4:27 (minutes to seconds) (SD = .051). The final postintervention point had an average time of 2:05 (SD = .017). This decrease was statistically significant (P≤.0001).
    DISCUSSION: Creating an environment in which the care team can efficiently and effectively operate can improve the timeliness of care. Creating a Lean, fixed organizational system is key to creating this space. This organizational project validated the effectiveness of systemic organization of supplies in improving time to care.
    Keywords:  Efficiency; Emergencies; Nursing; Organization; Resuscitation
    DOI:  https://doi.org/10.1016/j.jen.2026.04.026
  12. Sage Open Pediatr. 2026 Jan-Dec;13:13 30502225261451613
      Refractory shock in children carries persistently high mortality, particularly in low-resource settings. It occurs when circulatory failure persists despite adequate fluid resuscitation and vasoactive medications. This review summarizes pathophysiology, recognition, and escalation strategies for pediatric refractory shock, emphasizing early identification in the emergency department. It examines evidence for fluid management, vasoactive therapy, and point-of-care ultrasound in optimizing decision-making, along with second-line options such as corticosteroids, vasopressin, and milrinone. Special attention is given to resource-constrained settings, describing evidence-based adaptations including conservative fluid strategies from the FEAST trial, simplified algorithms, simulation-based training, and telemedicine. Improving outcomes requires rapid recognition, precise hemodynamic phenotyping, and timely evidence-based interventions.
    Keywords:  POCUS; catecholamine-resistant shock; fluid resuscitation; hemodynamic monitoring; mortality reduction; pediatric refractory shock; resource-limited settings; septic shock; tele-ICU; vasoactive agents
    DOI:  https://doi.org/10.1177/30502225261451613
  13. World J Clin Pediatr. 2026 Jun 09. 15(2): 119843
      Migraine is among the most prevalent neurological disorders in children and adolescents and is a leading cause of functional disability, school absenteeism, and impaired quality of life. Pediatric migraine is not merely a younger manifestation of the adult disease; rather, it exhibits distinct clinical phenotypes, developmental neurobiology, triggers, and treatment responses. The growing recognition of its long-term burden underscores the need for updated, pediatric-focused, evidence-based guidance. This narrative review synthesizes contemporary evidence on pediatric migraine across the lifespan, integrating epidemiology, genetic susceptibility, and age-dependent neurobiological mechanisms. Key clinical features, including migraine equivalents and episodic syndromes associated with migraine, are discussed alongside diagnostic considerations using the International Classification of Headache Disorders, third edition, and validated pediatric disability assessment tools. Acute and preventive management strategies are reviewed in detail, encompassing optimized use of non-steroidal anti-inflammatory drugs and triptans, antiemetics, nerve blocks, neuromodulation devices, and emerging targeted therapies such as calcitonin gene-related peptide monoclonal antibodies and gepants. Evidence-based non-pharmacological interventions, including lifestyle optimization, sleep hygiene, cognitive-behavioral therapy, and comorbidity management, are also integral components of care. Pediatric migraine should be recognized as a chronic, neurodevelopmentally modulated neurological disorder that warrants early diagnosis and a multimodal, individualized treatment approach. Advances in mechanistic understanding, neurostimulation technologies, and targeted biologic therapies are reshaping the therapeutic landscape and hold promise for more precise and effective migraine management in children and adolescents.
    Keywords:  Calcitonin gene-related peptide monoclonal antibodies; Diagnosis; Episodic syndromes; Gepants; Migraine equivalents; Neuromodulation devices; Pediatric migraine
    DOI:  https://doi.org/10.5409/wjcp.v15.i2.119843
  14. Rev Cardiovasc Med. 2026 May;27(5): 48601
      Ambulatory blood pressure monitoring (ABPM) provides a unique opportunity to assess day-night blood pressure (BP) variability. Individuals whose night-time BP is 10-20% lower than the subsequent daytime BP values are defined as dippers, whereas those with a nocturnal BP decrease of <10% are considered non-dippers. A non-dipping (ND) pattern has been shown to occur in a substantial proportion of adults with hypertension and is influenced by age, sex, ethnicity, and comorbidities. More importantly, the ND pattern has been reported to adversely affect hypertension-mediated organ damage (HMOD) and cardiovascular prognosis, due to a greater nighttime pressure overload that promotes more severe cardiovascular damage. Notably, current evidence on alterations in circadian BP rhythm in children and adolescents with hypertension remains scarce. Therefore, this narrative review aimed to analyze the available literature on this important topic and to provide updated, comprehensive information on the prevalence of the ND pattern and its association with cardiac and extracardiac HMOD markers. The prevalence of ND patterns (based on data from 16 studies) ranged from 35% to 72% (mean 59%). Regarding the association between ND and HMOD, particularly echocardiographic left ventricular hypertrophy, results have been mixed, leaving uncertainty about whether a blunted nocturnal BP decline in pediatric hypertension contributes to HMOD. Thus, large prospective studies are needed to improve definitions of the clinical significance of alterations in BP circadian rhythm in children and adolescents with hypertension, focusing on methodological issues not yet fully addressed, such as the use of pediatric diagnostic criteria and the reproducibility of the ND pattern over time.
    Keywords:  ambulatory blood pressure monitoring; child; hypertension; left ventricular hypertrophy
    DOI:  https://doi.org/10.31083/RCM48601
  15. Hosp Pediatr. 2026 Jun 02. pii: e2025009078. [Epub ahead of print]
       OBJECTIVES: Black pediatric patients in the United States experience disproportionate harm from systemic racism in health care. Black LGBTQIA+ (Lesbian, Gay, Bisexual, Transgender Queer, Intersex, Asexual, with the "+" representing additional sexual orientations and gender identities) parents and caregivers, as primary navigators of care for their children, may also encounter homophobia, transphobia, and heteronormative bias. These intersecting biases can shape clinical interactions and influence pediatric care quality yet remain underexamined in health equity research. This study assessed how the intersecting identities of Black LGBTQIA+ caregivers influence their interactions with pediatric clinicians and affect the health care their children receive.
    METHODS: This qualitative study recruited 14 Black LGBTQIA+ parents or caregivers of pediatric patients from 10 families through purposive and snowball sampling. Semistructured interviews were conducted via videoconference in 2023. Data analysis was conducted using a 3-round inductive and deductive thematic coding process to identify barriers to inclusive care and caregiver-informed strategies to advance equity in pediatric settings.
    RESULTS: Six themes were identified. Three themes reflect the unique experiences of Black LGBTQIA+ caregivers in pediatric medicine: (1) lack of awareness or experience with same-sex families, (2) proactive caregiver advocacy, and (3) caregiver-perceived impact of clinician representation. The remaining 3 themes offered actionable recommendations for pediatric clinicians: (4) expansion of clinician understanding of caregiver roles, (5) adaptive communication practices, and (6) inclusive caregiver support.
    CONCLUSION: The intersecting identities of Black LGBTQIA+ caregivers shape pediatric care through systemic barriers and opportunities for better clinician engagement. Inclusive, culturally responsive practices that strengthen family relationships, foster open communication, and recognize all caregivers' roles can build trust, improve outcomes, and advance equity in pediatric care.
    DOI:  https://doi.org/10.1542/hpeds.2025-009078
  16. J Perinatol. 2026 Jun 03.
      The American Board of Pediatrics (ABP) has proposed a competency-based fellowship model offering a 2-year clinical pathway with 18 training blocks and no scholarly requirement. This position statement, representing neonatal-perinatal medicine (NPM) training program directors, division leaders, and key stakeholders, contends that the model is not viable for NPM training. Compressing 18 clinical blocks into 24 months would require approximately 3500 annual training hours, nearly double a sustainable NICU workload, approaching Accreditation Council for Graduate Medical Education duty-hour limits, while reducing didactic education by one-third. Survey data from 110 of 111 NPM programs show 76% opposition. Concerns include trainee wellness, reduction in program complement, workforce and funding implications, and the erosion of scholarly training essential to advancing neonatal care. We propose alternatives, including a 2-year residency + 3-year fellowship (2 + 3) pathway and restructured residency tracks, addressing competency gaps while preserving training quality, duration, and collaborative governance.
    DOI:  https://doi.org/10.1038/s41372-026-02743-5
  17. J Hosp Palliat Nurs. 2026 Jun 02.
      Pediatric patients in concurrent hospice and palliative care often face fragmented communication regarding family goals of care during acute hospitalizations. This quality improvement project evaluated clinician and care coordinator experiences with the implementation of the Preference for Acute Rehospitalization Scale at Children's Nebraska. A pre- and postimplementation survey design (n = 41 pre-implementation; n = 35 postimplementation) assessed awareness of family goals, confidence in decision-making, and perceptions of the tool among an interdisciplinary team. While clinicians expressed general openness to standardized communication tools, results showed no statistically significant differences in survey items, highlighting that successful adoption in complex pediatric settings requires sustained education, seamless workflow integration, and robust interdisciplinary engagement to ensure treatment remains aligned with family preferences.
    Keywords:  clinical decision-making; goals of care; hospice care; interdisciplinary communication; palliative care; quality improvement
    DOI:  https://doi.org/10.1097/NJH.0000000000001246
  18. J Trauma Nurs. 2026 Jun 03.
       BACKGROUND: Chest tube management is a high-risk, low-frequency clinical skill requiring prompt nursing assessment, troubleshooting, and escalation to prevent complications. Limited exposure may contribute to variability in nursing confidence. Simulation-based education reinforces pediatric nurses' readiness for chest tube management.
    OBJECTIVE: This quality improvement initiative aimed to implement and evaluate a simulation-based educational intervention to improve pediatric nurses' confidence, anxiety, and knowledge related to chest tube management.
    METHODS: This quality improvement initiative used a single-group pretest-post-test design with delayed follow-up, incorporating 3 assessment time points: preintervention, immediately postintervention, and 2-month follow-up. The study was conducted between July and December 2025 at a Level I pediatric Midwestern US trauma center. Registered nurses participated in a 1-hour simulation with 3 stations focused on chest tube assessment, troubleshooting, and escalation. Pediatric surgery faculty and residents served as facilitators. Surveys assessing confidence, anxiety, and knowledge were administered at all time points. Mean differences, 95% confidence intervals, and effect sizes were calculated.
    RESULTS: Sixty-five nurses completed preintervention and postintervention surveys; 22 completed follow-up. Mean confidence increased from 3.9 to 4.8 (mean difference 0.9; 95% CI, 0.7-1.1; Cohen d = 1.12), anxiety decreased from 2.9 to 1.9 (mean difference -1.0; 95% CI, -1.3 to -0.7; Cohen d = -0.83), and knowledge increased from 5.60/7 to 6.65/7 (mean difference 1.05; 95% CI, 0.84-1.26; Cohen d = 1.99). Improvements were observed at follow-up.
    CONCLUSIONS: Simulation-based education was associated with improved nurse confidence, reduced anxiety, and increased knowledge related to pediatric chest tube management.
    Keywords:  chest tube management; nursing education; patient safety; pediatric nursing; quality improvement; simulation-based education
    DOI:  https://doi.org/10.1097/JTN.0000000000000932
  19. Expert Rev Gastroenterol Hepatol. 2026 Jun 05. 1-13
       INTRODUCTION: Proton pump inhibitors (PPIs) are among the most frequently prescribed medications in pediatric practice. While highly effective in acid-mediated disorders, concerns regarding overuse, inappropriate indications, and potential adverse effects have emerged, particularly in infants and children with nonspecific symptoms.
    AREAS COVERED: This review summarizes the current evidence on the indications, efficacy, and safety of PPIs in the pediatric population. A literature search was performed in PubMed/MEDLINE and Embase, supplemented by landmark earlier studies and current clinical practice guidelines. We discuss guideline recommendations and examine the role of PPIs across different clinical scenarios including gastroesophageal reflux disease, esophagitis, eosinophilic esophagitis and special populations. Particular attention is given to emerging data on adverse outcomes, including infections, microbiome alterations, and long-term safety concerns. Strategies for appropriate prescribing, deprescribing, and individualized patient management are also addressed.
    EXPERT OPINION: PPIs remain overprescribed in pediatrics, often for indications lacking clear benefit. Future efforts should prioritize diagnostic precision, short-term therapeutic trials and systematic deprescribing strategies. A shift toward stewardship-based prescribing, combined with improved clinician education and use of objective diagnostic tools, is essential to optimize outcomes and minimize unnecessary exposure.
    Keywords:  Eosinophilic esophagitis; GERD; Helicobacter pylori; PPI; gastroesophageal reflux; pediatric; proton pump inhibitors; safety
    DOI:  https://doi.org/10.1080/17474124.2026.2683678
  20. J Pediatr Nurs. 2026 Jun 04. pii: S0882-5963(26)00253-8. [Epub ahead of print]90 19-30
       BACKGROUND: Nurses play a central role in health education for children and adolescents, yet traditional didactic approaches often fail to engage young people, prompting growing interest in storytelling as an alternative option.
    OBJECTIVE: To examine the use of storytelling as a health education intervention in children and adolescents to inform nursing practice.
    METHODS: We searched CINAHL, Embase, MEDLINE, PsycINFO, The Cochrane Library and Web of Science for randomised controlled trials involving children (4-18 years) receiving storytelling interventions for health education. Two authors independently screened the title and abstracts and full-papers, extracted the data and assessed the risk of bias for each study. Disagreements were resolved through consultation with the third author. Data were descriptively synthesised.
    RESULTS: Twenty-four studies were included. Twelve studies measured knowledge, with the majority (n = 9, 75%) demonstrating significant gains in knowledge. Across the 19 studies which measured attitudes and behaviour, 89% (n = 17) demonstrated significant short-term benefits across a range of health topics, and of the seven studies which explored the impact on participants' level of anxiety, 71% (n = 5) demonstrated a significant reduction in procedural anxiety.
    CONCLUSIONS: Storytelling interventions demonstrated improvements in health-related knowledge, short-term changes in attitudes and behaviour, and reduced procedural anxiety across a diverse range of health topics. Further research is needed to evaluate long-term outcomes and standardise outcome measures.
    IMPLICATIONS TO PRACTICE: These findings support nurses in incorporating age-appropriate storytelling interventions into health education and procedural preparation to enhance understanding, engagement and short-term behaviour change in children and adolescents.
    Keywords:  Adolescents; Children; Health education; Scoping review; Storytelling
    DOI:  https://doi.org/10.1016/j.pedn.2026.05.047
  21. Pediatr Res. 2026 Jun 02.
       IMPACT: Despite nationwide policies for early autism screening and intervention, many children with ASD still face delays; most are diagnosed after age three and receive considerably fewer therapy hours than recommended by experts. Delays occur for various reasons: parents might miss early signs of ASD, services are often limited to big cities, cultural beliefs slow help-seeking, and there is a lack of trained provider resources. Practical steps like parent education programs, government-funded digital therapies, and improved referral systems can facilitate quicker, more effective care for children, particularly in underserved areas.
    DOI:  https://doi.org/10.1038/s41390-026-05177-z
  22. Cochrane Database Syst Rev. 2026 Jun 02. 6 CD015264
       RATIONALE: Vitamin B12 deficiency is an important public health problem in children, and has been associated with anaemia and impaired growth, cognition, and development. Vitamin B12 deficiency may develop in children due to lower content in breast milk, low dietary intake, and as requirements increase with age. Vitamin B12 supplementation may confer benefits to child growth and development, due to its role in DNA synthesis and methylation, red blood cell formation, and folate metabolism. However, no systematic reviews have been conducted to examine the effects of vitamin B12 supplementation in children.
    OBJECTIVES: To determine the effects of vitamin B12 supplementation on growth, development, and cognition in children less than 12 years of age.
    SEARCH METHODS: We searched CENTRAL, MEDLINE, Embase, 12 other databases, and two trial registries on 23 September 2025. We screened reference lists of studies.
    ELIGIBILITY CRITERIA: We included randomised controlled trials evaluating the effects of oral vitamin B12 supplementation, alone or in combination with other micronutrients, in children < 12 years of age. We excluded cross-over trials, trials targeting pregnant or breastfeeding women, or participants with critical illnesses, and interventions delivered by intravenous/intramuscular injections.
    OUTCOMES: Critical outcomes were vitamin B12 status, anaemia, haemoglobin, growth, cognitive function, developmental outcomes, and any adverse effects. Important outcomes included megaloblastic anaemia, body composition, health-related quality of life, morbidity, and all-cause mortality.
    RISK OF BIAS: We used Cochrane RoB 2 to evaluate bias.
    SYNTHESIS METHODS: We conducted meta-analyses using fixed-effect models. If there was substantial heterogeneity, we used random-effect models. When meta-analyses were not conducted, we described findings from individual trials, and considered synthesis and presentation of findings using other methods. We used GRADE to evaluate the certainty of evidence for critical outcomes.
    INCLUDED STUDIES: We included 16 trials (4083 children; 2 days to 11 years) in 10 countries, including India, Japan, Thailand, Nepal, United Kingdom, Italy, Spain, the United States, El Salvador, and Guatemala. Follow-up periods for outcomes in most studies ranged from five weeks to 31 months, with one study extending follow-up to nine years. Duration of vitamin B12 supplementation varied, ranging from 28 days to 31 months, with doses from 0.9 µg/day to 150 µg/day. Nine trials, including 2391 children, contributed data to meta-analyses.
    SYNTHESIS OF RESULTS: Supplementation with vitamin B12 alone versus placebo There may be little to no difference between groups in height/length (mean difference (MD) -0.19 cm, 95% confidence interval (CI) -2.44 to 2.06; 2 trials, 143 children; low-certainty evidence). There may be little to no difference between groups in cognitive function (e.g. attention) (standardised mean difference (SMD) 0.09, 95% CI -0.10 to 0.28; 2 trials, 438 children, low-certainty evidence). There may be little to no difference between groups in motor skill development (6 to 9 years, NEuroPSYchological assessment, Second Edition (NEPSY-II); 1 trial, 403 children, low-certainty evidence). Vitamin B12 supplementation in children reduces vitamin B12 deficiency (absolute risk difference (ARD) 56 fewer per 1000, 95% CI 68 fewer to 24 fewer; 1.8% versus 7.6%; risk ratio (RR) 0.27, 95% CI 0.11 to 0.69; 3 trials, 642 children; high-certainty evidence), and probably increases total vitamin B12 concentrations (MD 68.53 pmol/L, 95% CI 41.83 to 95.23; 7 trials, 705 children; moderate-certainty evidence), compared to placebo, with an average increase of 68.5 pmol/L. There may be little to no difference between groups in anaemia (ARD 21 more per 1000, 95% CI 26 fewer to 191 more; 9.1% versus 4.5%; RR 1.48, 95% CI 0.41 to 5.27; 2 trials, 144 children; low-certainty evidence). No trials reported the occurrence of any adverse effects. Supplementation with vitamin B12 alone versus no intervention The evidence is very uncertain about the effects of vitamin B12 on height/length (2 trials, 70 children; very low-certainty evidence), compared to no intervention. No trials reported data for the other critical outcomes. Supplementation with vitamin B12 and other micronutrients, compared to the same formulation without vitamin B12 There may be little to no difference between groups in height/length (MD -0.22 cm, 95% CI -0.65 to 0.20; 2 trials, 608 children; low-certainty evidence). There may be little to no difference between groups in cognitive function (e.g. attention) (SMD 0.00, 95% CI -0.13 to 0.13; 3 trials, 956 children; low-certainty evidence). There may be little to no difference between groups in development outcomes (e.g. motor skill development) (SMD -0.05, 95% CI -0.18 to 0.08; 2 trials, 960 children; low-certainty evidence). Children who received vitamin B12 supplementation and other micronutrients may have little to no difference in vitamin B12 deficiency (ARD 2 fewer per 1000, 95% CI 7 fewer to 32 more; 0.7% versus 0.8%; RR 0.77, 95% CI 0.12 to 5.16; 2 trials, 534 children; low-certainty evidence), or total vitamin B12 concentrations (MD 34.32 pmol/L, 95% CI -31.13 to 99.77; 3 trials, 731 children; low-certainty evidence), compared to supplements without vitamin B12. There may be little to no difference between groups in anaemia (21.7% versus 25.0%; 1 trial, 35 children; low-certainty evidence). There may be little to no difference between groups in any adverse effects (9.2% versus 5.9%; 1 trial, 574 children; low-certainty evidence). The certainty of evidence for critical outcomes ranged from high to very low; we downgraded for imprecision due to small sample sizes or few events, risk of bias in outcome measurement, randomisation methods, selective reporting bias, or inconsistency due to substantial statistical heterogeneity. Few studies reported growth, cognition, development, anaemia, or any adverse effects.
    AUTHORS' CONCLUSIONS: Vitamin B12 supplementation (alone or when supplemented with other micronutrients) in children may have little to no effect on growth (i.e. height/length), cognitive function (e.g. attention), development outcomes (e.g. motor skill development), or anaemia, compared to placebo, no intervention, or the same supplements without vitamin B12. Vitamin B12 supplementation in children reduces vitamin B12 deficiency and probably improves total vitamin B12 concentrations, compared to placebo. However, vitamin B12 supplementation with other micronutrients may result in little to no difference in vitamin B12 deficiency and total vitamin B12 concentrations, compared to the same formulation without vitamin B12.
    FUNDING: This review had no dedicated funding.
    REGISTRATION: Protocol available via DOI 10.1002/14651858.CD015264.
    DOI:  https://doi.org/10.1002/14651858.CD015264.pub2
  23. Res Nurs Health. 2026 Jun 01.
      Secondary traumatic stress is a significant occupational concern in pediatric nursing because frequent exposure to traumatic events can compromise nurses' emotional health, increase burnout, and reduce the quality of care. The aim of this integrative review is to synthesize the current evidence on the prevalence and contributing factors of secondary traumatic stress among pediatric nurses. A comprehensive search was conducted in CINAHL, EMBASE, PsycINFO, PubMed, and Web of Science for peer-reviewed articles published in English. A total of 24 studies met the inclusion criteria and were analyzed using Whittemore and Knafl's integrative review methodology. Reported prevalence rates of secondary traumatic stress ranged from 13% to 87%, which were higher than those of other healthcare professionals. Key contributing factors included patient deaths, parental grief, heavy workload, limited organizational support, and insufficient coping strategies. These factors encompassed the individual, work-related, and organizational domains. The review highlights the need for comprehensive strategies to support pediatric nurses' mental health and to develop interventions that address both personal and workplace contributors. Further high-quality research is warranted to deepen the understanding of this phenomenon and inform evidence-based practices that protect both nurse well-being and the quality of care provided to children and their families.
    Keywords:  compassion fatigue; neonatal nurses; pediatric nurses; secondary traumatic stress
    DOI:  https://doi.org/10.1002/nur.70084
  24. Disabil Rehabil. 2026 Jun 02. 1-14
    READY Advisory Board
       PURPOSE: Older children with spina bifida (SB) can experience barriers to care, yet the availability of support for younger children with SB (ages 3-6 years) is largely unknown. This study explored caregiver experiences navigating medical and community-based systems of care for children with SB during early childhood.
    MATERIALS AND METHODS: Twenty-three caregivers (17 mothers, 6 fathers) of 17 children with SB completed both a semi-structured virtual interview and an online survey about resources accessed to promote their child's early development and barriers to care. Interview data were analyzed using content analysis, and survey responses were evaluated using descriptive statistics.
    RESULTS: Caregivers reported having limited resources available in their community to promote their child's early development, with distance of travel and accessibility as frequent barriers to care. Caregivers also valued SB community connections (e.g., SB medical clinics, adaptive sports, disability groups). Furthermore, 87% of caregivers reported barriers to the use of behavioral health services, including concerns regarding physical accessibility, helpfulness of services, and provider characteristics.
    CONCLUSIONS: While caregivers value SB-specific medical, psychological, and community resources, both for their child with SB and for their family systems, significant barriers exist in accessing these supports. Findings support the need for specialized interdisciplinary care.
    Keywords:  Spina bifida; barriers to care; children; disability; qualitative research
    DOI:  https://doi.org/10.1080/09638288.2026.2678714
  25. J Clin Nurs. 2026 Jun 01.
       BACKGROUND: Hospital-at-home (HaH) is becoming more widely available to children with cancer, providing care in a familiar environment while upholding medical safety and quality. Little is known, however, about how these children experience their parents' caregiving in the context of HaH, how they perceive and interpret parental roles, what they require in daily care, and how they communicate these needs.
    METHODS: Seven children aged 7 to 12 years undergoing home-based cancer treatment were interviewed using interpretative phenomenological analysis (IPA). These interviews, conducted via telephone, were open-ended and exploratory, allowing the children to express their experiences freely.
    RESULTS: One major theme-'the child's voice'-emerged, encompassing two interrelated sub-themes: (1) parental presence as a condition of care; and (2) the strategies children use to express their voice. Parental presence was described as essential for emotional security, predictability and meaning, serving as both a psychological anchor and a temporal organiser in the child's daily life. The children expressed their voice through multiple forms-verbal, gestural, symptom-focused or silent-revealing their active participation in care and their capacity to preserve relational and emotional continuity within the family setting.
    CONCLUSIONS: Children with cancer perceive HaH as more than a transfer of hospital treatment; they experience it as a shared relational experience built on parental presence and mutual understanding. Recognising and supporting the child's voice in its various forms is vital for ensuring that HaH becomes not only a site for medical care but also a meaningful space for living.
    RELEVANCE TO CLINICAL PRACTICE: Our findings highlight the need for healthcare teams to take into account the variety of children's voices and grant them a real place in HaH. They are not simply recipients of care, but also active participants in the care relationship, capable of expressing their needs, emotions, and expectations in their own way.
    PATIENT OR PUBLIC CONTRIBUTION: No patient or public contribution.
    Keywords:  child's experience; child's voice; family care; hospital‐at‐home; interpretative phenomenological analysis; paediatric cancer; psychosocial oncology
    DOI:  https://doi.org/10.1111/jocn.70386
  26. J Palliat Med. 2026 May;29(5): 585-593
       BACKGROUND: Being the caregiver of a pediatric patient with a complex or serious illness can be emotionally intense and stressful. Caregiver burden significantly affects the biopsychosocial well-being of both the child and the caregiver. Interventions such as Narrative Medicine (NM) may help alleviate this burden by enhancing emotional resilience and strengthening support networks.
    OBJECTIVES: This review aimed to explore which NM interventions can reduce the emotional burden of caregivers of pediatric patients under the age of 18.
    METHODS: A systematic literature review was conducted to examine the benefits of NM interventions on caregiver well-being. Primary studies were included if they described NM interventions involving active written narration by caregivers (e.g., diaries, digital writing). Studies relying solely on oral storytelling or third-party facilitation (e.g., interviews, dignity therapy) were excluded. Only studies in English or Italian were considered; studies focusing on adult patients or targeting the patient rather than the caregiver were excluded. The review followed PRISMA guidelines. A comprehensive search was conducted in MEDLINE, Embase, CINAHL, Cochrane Library, and APA PsycInfo in July 2024 with no time limits. Study quality was assessed using JBI and NIH tools, and data were synthesized narratively and in tables.
    RESULTS: The search identified 1078 unique references. After screening, four studies met the inclusion criteria. Interventions ranged from narrative diaries in pediatric intensive care units to online journaling. All studies showed feasibility and acceptability, with reported benefits including emotional expression, perceived support, improved coping, and greater self-reflection. Most participants were women (85%), although the review included all caregivers regardless of gender.
    CONCLUSIONS: In conclusion, NM appears to be a promising tool to support caregivers of pediatric patients with complex or serious conditions. While preliminary findings are encouraging, further research is needed to assess long-term outcomes. Structured workshops and the involvement of NM facilitators may further support caregiver well-being and reduce psychological burden.
    Keywords:  caregiver burden; medical humanities; narrative medicine; pediatrics; serious illness
    DOI:  https://doi.org/10.1177/10966218251410545
  27. SICOT J. 2026 ;12 36
       BACKGROUND: Pediatric distal radius fractures are the most common fractures in children. Management of displaced injuries remains controversial because remodeling capacity varies with skeletal maturity, fracture stability, and fracture subtype. Metaphyseal and physeal fractures differ biologically: metaphyseal injuries are primarily threatened by redisplacement, whereas physeal injuries carry risks of growth disturbance and iatrogenic physeal injury. An evidence-based, maturity- and stability-guided framework is required.
    METHODS: A PRISMA-compliant systematic review and Meta-analysis was performed using PubMed, Embase, Scopus, Web of Science, and the Cochrane Library (inception-2025). Randomized controlled trials and comparative observational studies of pediatric distal radius fractures (0-18 years) treated with cast or splint immobilization, with or without percutaneous Kirschner-wire fixation, were included. Primary outcomes were redisplacement and secondary intervention for metaphyseal fractures; growth disturbance and physeal complications were evaluated separately for physeal injuries. Secondary outcomes included union, functional recovery, complications, and casting quality.
    RESULTS: Forty-five studies (5,340 patients) were included qualitatively; twelve comparative studies (4 RCTs, 8 observational; 1,455 patients) were analyzed quantitatively (853 cast alone; 602 cast + K-wire). In predominantly metaphyseal fractures, redisplacement occurred in 20-35% after casting versus 0-5% after K-wire fixation (pooled OR 0.10), with reduced secondary intervention (OR 0.15). Union approached 100% and long-term functional outcomes were equivalent. In children with substantial remaining growth, including those <11 years with completely displaced metaphyseal fractures, casting without reduction achieved reliable union and remodeling. For physeal injuries, restoration of physeal alignment and longitudinal growth surveillance were prioritized. Cast length and removable splints demonstrated comparable stability when molding was adequate; casting quality indices were variably predictive.
    CONCLUSIONS: Outcomes are excellent when treatment aligns with fracture biology and skeletal maturity. Metaphyseal and physeal injuries require distinct considerations. Nonoperative care - including acceptance of bayonet apposition in young children - is appropriate for many metaphyseal fractures, while K-wire fixation should be selectively reserved for unstable patterns.
    LEVEL OF EVIDENCE: Level II (Systematic review and meta-analysis of Level I-III studies).
    Keywords:  Cast immobilization; Closed reduction; Fracture remodeling; Kirschner wire fixation; Pediatric distal radius fracture; Redisplacement
    DOI:  https://doi.org/10.1051/sicotj/2026032
  28. BMC Health Serv Res. 2026 Jun 03.
       BACKGROUND: The 10th revision of the International Classification of Diseases (ICD-10) allows healthcare professionals to document social needs with ICD-10 Z-codes. Data derived from the documentation of ICD-10 Z-codes can be leveraged to identify at-risk populations for targeted intervention. However, there remains concern for underutilization of these codes, particularly in the pediatric population. We sought to examine the documentation of ICD-10 Z-codes in the pediatric outpatient setting of the largest Connecticut health system by specialty type and age group.
    METHODS: In this cross-sectional study, we examined deidentified electronic health records of pediatric outpatient patients seen within the Yale New Haven Health System in Connecticut from 2019 to 2020. We used descriptive statistics to measure the proportion of patients with at least one social needs-related ICD-10 Z-code. We compared the rates of documentation across different specialty types and age groups. We also identified nine categories of ICD-10 Z-codes and compared differences in the distribution of Z-code categories across age groups.
    RESULTS: A total of 1,164 out of 59,867 pediatric outpatient patients (1.9%) from 2019 to 2020 had at least one documented ICD-10 Z-code. Across all ages, the specialty type with the highest rate of documentation was school-based health centers (10.6%), followed by pediatric primary care (5.3%). Within the pediatric primary care group, we found that patients aged 22 to 30 were significantly more likely than all other age groups to have an ICD-10 Z-code documented.
    CONCLUSIONS: We demonstrate that social needs documentation with ICD-10 Z-codes in the pediatric department of this health system is low overall and likely unreflective of the true social needs of the population. These findings suggest the need for further study of how pediatric social needs are identified, documented, and operationalized within clinical workflows.
    Keywords:  Health system; ICD-10; Pediatric; Social determinants of health; Social needs; Z-code
    DOI:  https://doi.org/10.1186/s12913-026-14758-x
  29. World J Clin Pediatr. 2026 Jun 09. 15(2): 113603
      Pediatric musculoskeletal trauma differs significantly from adult injuries due to the dynamic and evolving nature of the growing skeleton. The presence of open growth plates (physes), secondary ossification centers, and a more elastic bone structure contributes to unique injury patterns and imaging findings in children. Proper interpretation of pediatric imaging requires an in-depth understanding of age-specific anatomy, biomechanics, and normal developmental variants. This review provides a comprehensive overview of pediatric bone physiology and fracture types, including the Salter-Harris classification, special pediatric fractures, elbow ossification, avulsion injuries, and conditions related to repetitive stress. Additionally, we address the critical topic of non-accidental trauma, underscoring the radiologist's role in early detection. Through an anatomical and pathophysiological lens, this paper explores the challenges and strategies for accurate diagnosis in pediatric trauma imaging.
    Keywords:  Children; Computed tomography; Magnetic resonance imaging; Musculoskeletal; Pediatric; Trauma; X-ray
    DOI:  https://doi.org/10.5409/wjcp.v15.i2.113603