Journal of paediatrics and child health最新文献

{"title":"Recent Advances in the Diagnosis and Treatment of Paediatric Endocrine Disorders","authors":"Lara E. Graves, Benjamin Wheeler","doi":"10.1111/jpc.70047","DOIUrl":"10.1111/jpc.70047","url":null,"abstract":"<p>The discovery, synthesis and administration of hormones revolutionised the medical management of endocrine disorders in the first half of the 20th century. Kocher revolutionised thyroid surgery in the late 1800s and early 1900s [<span>1</span>], Banting and Best are credited with the synthesis of insulin in 1920 [<span>2, 3</span>], and steroids were first administered to patients with congenital adrenal hyperplasia (known as adrenogenital syndrome at the time) in the 1950s [<span>4, 5</span>]. Nobel Prizes were awarded for these and other discoveries that furthered endocrinology knowledge and treatment [<span>6</span>]. Although these hormonal replacements were life-saving, clearly further advancements are required to truly manage these conditions.</p><p>Here we present a collection of narrative reviews on recent advances in paediatric endocrinology, including the management of paediatric thyroid cancer, screening for type 1 diabetes and the use of burosumab in X-linked hypophosphataemic rickets.</p><p>The management of paediatric thyroid cancer has traditionally relied on extrapolation from adult data, but childhood disease behaves differently from adult thyroid cancer. Paediatric differentiated thyroid cancers are more widely metastatic at diagnosis than adults; however, the mortality rate is much lower. The first guideline for the management of paediatric thyroid cancer was published by the American Thyroid Association in 2015 [<span>7</span>]. Vanderniet et al.'s review focuses on developments in the understanding and management of paediatric thyroid cancer since the publication of this guideline [<span>8</span>]. Important conclusions are drawn, including the importance of paediatric-specific data, optimal sonographic and cytological diagnostics, use of advanced genomic techniques to prognosticate and make management decisions, consideration of familial cancer syndromes and that management recommendations are rapidly evolving due to the accumulation of new knowledge. Furthermore, interdisciplinary input is required for optimal management of this rare condition and may include paediatric endocrinologists, surgeons, oncologists, geneticists, pathologists, radiologists and nuclear medicine physicians. As we enter the age of advanced therapeutics, there are new targeted molecular therapies available for some forms of paediatric thyroid cancer that can reduce the burden of traditional treatment such as radioactive iodine.</p><p>Approximately 30% of children and adolescents present with diabetic ketoacidosis (DKA) at the diagnosis of type 1 diabetes [<span>9</span>]. There are potential long-term consequences of DKA, in addition to the acute metabolic decompensation. Clinical type 1 diabetes mellitus is defined as a random plasma glucose level ≥ 11.1 mmol/L or a fasting plasma glucose of ≥ 7.0 mmol/L, which signifies irreversible damage to the insulin-producing beta cells. However, it is now well recognised that the onset of beta cell autoimmu","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 5","pages":"664-665"},"PeriodicalIF":1.6,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jpc.70047","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143772010","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Burden of Paediatric Supracondylar Humeral Fractures Admitted Within a Health Region in New Zealand","authors":"Evangeline Liddicoat,&nbsp;Sheena Moosa,&nbsp;Alastair Smith,&nbsp;Grant Christey","doi":"10.1111/jpc.70045","DOIUrl":"10.1111/jpc.70045","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Supracondylar humeral fractures (SCHF) comprise the majority of all paediatric elbow injuries and most require surgical intervention. This study determines the incidence and outcomes of SCHF in children of all injury severities admitted to hospital over 10 years in a health region of Aotearoa New Zealand (AoNZ).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Materials and Methods</h3>\u0000 \u0000 <p>Retrospective data from Te Manawa Taki (TMT) Trauma Registry was extracted for all paediatric trauma hospitalisations (aged 0–14 years) with SCHF from 1 January 2012 to 31 December 2022. Patients with SCHF were identified using the International Classification of Disease-10 primary cause codes. Demographic and injury characteristics with hospital costs were analysed.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Paediatric SCHF (<i>n</i> = 1563) incidence was 73.7/100 000 (CI 61.5–85.8). Majority (62.8%) were aged 5–9 years with an incidence rate of 131.5/100 000 (CI 104.2–158.8). They were 6.6 and 2.0 times more frequently hospitalised than 10–14 and 0–4 year olds. The most common place for injury was home (40.9%) followed by school, other institution and public administrative area (32.5%). Falls accounted for 91.7% of injuries with most (52.4%) occurring at a height of less than 1 m. The majority (76.2%) of patients spent 1 day in hospital and over three quarters had operative management. Estimated hospital costs were $9 842 587 total with an average cost of $6354 per admission. There was no significant difference in annual incidence over time.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Paediatric SCHF is a significant issue in AoNZ, particularly in those aged 5–9 years. There is a clear need for injury prevention interventions in the home and school to minimise falls and reduce healthcare costs.</p>\u0000 </section>\u0000 </div>","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 6","pages":"919-925"},"PeriodicalIF":1.6,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143764221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Paediatric Emergency Department Mental Health and Behavioural Presentations in Australia Before and After the Onset of the COVID-19 Pandemic: Retrospective Observational Study","authors":"Jackson Newberry-Dupe,&nbsp;Glenn Melvin,&nbsp;Kylie King,&nbsp;Marietta John White,&nbsp;Vicki Anderson,&nbsp;Franz E. Babl,&nbsp;Meredith L. Borland,&nbsp;Stuart R. Dalziel,&nbsp;Harriet Hiscock,&nbsp;Bruce J. Tonge,&nbsp;Paul Buntine,&nbsp;Brooke Charters,&nbsp;Megan Hamilton,&nbsp;Amit Kochar,&nbsp;Alastair Meyer,&nbsp;Viet Tran,&nbsp;Emogene Aldridge,&nbsp;Giles Barrington,&nbsp;Liam Hackett,&nbsp;Nicole Lowry,&nbsp;Joseph Miller,&nbsp;Sebastian Wrobel,&nbsp;Rohan Borschmann,&nbsp;Simon Craig","doi":"10.1111/jpc.70046","DOIUrl":"10.1111/jpc.70046","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>Although child and adolescent mental health and behavioural presentations to hospital emergency departments (EDs) increased during the first 2 years of the COVID-19 pandemic (2020 and 2021), little is known about the characteristics of these presentations. We aimed to compare demographic, clinical and psychosocial profiles of paediatric presentations to Australian EDs before and after the onset of the pandemic.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We conducted a retrospective observational study of 100 randomly sampled presentations by children (6–11-year-olds) and adolescents (12–17-year-olds) to 10 Australian EDs between 1 January and 31 December 2019 (pre-COVID-19) and 1 January and 31 December 2021 (COVID-19). Using a multilevel factor model, we compared the pre-COVID-19 and COVID-19 cohorts regarding demographic characteristics, diagnoses, precipitants, time-to-treatment, length of stay, and discharge disposition.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The COVID-19 period was characterised by increased presentations by adolescents and girls. Compared to the pre-COVID-19 cohort, the COVID-19 cohort experienced increased median waiting times (48 and 72 min, respectively), median length of ED stay (4.7 and 5.4 h), and likelihood of admissions to the ED short stay unit (9.5% and 12.9%). Patients in the COVID-19 cohort were more likely to present with self-harm and suicidal thoughts/behaviours, eating disorders, neurodevelopmental and neurocognitive disorders, and psychosocial stressors, and less likely to have diagnoses of disruptive behaviour, impulse control, and conduct disorders.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Young people presenting to the ED in 2021 for mental health reasons were more likely to wait longer, stay longer, have a diagnosis of intentional self-harm and/or a neurodevelopmental disorder, and report psychosocial stressors.</p>\u0000 </section>\u0000 </div>","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 6","pages":"910-918"},"PeriodicalIF":1.6,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jpc.70046","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143753184","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Impact of Electronic Devices on Children's Behaviour","authors":"Najlaa Ibrahim Al-Sammak,&nbsp;Muhammad Ahmad Younis,&nbsp;Abdulrhman Akram Abdulrhman,&nbsp;Manahil Ammar Thanoon,&nbsp;Ubayda Abdulsattar Salim,&nbsp;Redhaa Muthanna Khalil,&nbsp;Hiba Thamer Muhammed","doi":"10.1111/jpc.70043","DOIUrl":"10.1111/jpc.70043","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Aim</h3>\u0000 \u0000 <p>One of the main advances today is the development of electronic devices and their applications. They eased human life, but adversely impacted their psych and social relationships. Children, the sensitive part of human development, become involved in these quandaries. So, this study aimed to determine the effects of these devices on childhood behaviours in Mosul/Iraq.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A cross-sectional study was applied on parents' of 1102 children whose ages range 1–15 years. They were chosen conveniently from public places in Mosul over a period of 6 months since December 2023. A self-administered questionnaires were filled by those parents taking their opinions about the benefits and drawbacks of electronic devices on their children. The latter were divided into three comparable groups according to the duration of use. The collected data were analysed by SPSS using the Goodness of Fit test for exploring the significance of comparison.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Mean age of studied children was 9.3 years, half of them (50.9%) used devices for three or more years, and another half (49.3%) had three or more hours of daily use. Parents said that their children's language and educational commitments were promoted by electronic devices, but unfortunately, they significantly suffered from anger, stubbornness, aggressiveness and sleep disturbances, especially after prolonged use (<i>p</i> &lt; 0.001) for each variable.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Although digital devices enhanced the learning abilities of children, they impacted their psych and real communication adversely. So, to protect them, children should have limited time and types of applications used in order to positively promote their wellbeing.</p>\u0000 </section>\u0000 </div>","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 6","pages":"905-909"},"PeriodicalIF":1.6,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143730402","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"FeBRILe3: Risk-Stratification and Diagnosis of Serious Bacterial Infections in Febrile Infants Less Than 3 Months Old","authors":"Ariel O. Mace,&nbsp;Jessica Ramsay,&nbsp;James Totterdell,&nbsp;Andrew C. Martin,&nbsp;Julie Barnett,&nbsp;Jade Ferullo,&nbsp;Briony Hazelton,&nbsp;Paul Ingram,&nbsp;Julie A. Marsh,&nbsp;Peter Richmond,&nbsp;Yue Wu,&nbsp;Thomas L. Snelling","doi":"10.1111/jpc.70041","DOIUrl":"10.1111/jpc.70041","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>Evidence-based recommendations exist for early discharge (before 48 h) of young infants with fever without source (FWS) at low risk of serious bacterial infections (SBIs). However, concerns regarding the applicability of international data to local contexts may hinder implementation. We aimed to describe the local epidemiology of FWS and evaluate a newly implemented risk-stratification guideline to support practice change.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Prospective observational study of infants aged &lt; 3 months admitted for investigation and management of FWS to two hospitals in Perth, Western Australia following implementation of an FWS risk-stratification guideline (August 2019–December 2021). We assessed the risk-stratification rule performance and determined the positive/negative likelihood ratios of individual patient characteristics for predicting SBI diagnosis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Five hundred infants were enrolled in the study cohort (median age 34 days, 36% female). SBI was diagnosed in 159 infants (32%), including urinary tract infection (<i>n</i> = 140), bacteraemia (<i>n</i> = 18) and bacterial meningitis (<i>n</i> = 9). Viruses were detected in 174 out of 406 tested infants (43%). Seventy-one infants met low-risk criteria (14%); only 69 out of 360 infants without SBI were classified as low risk (19%). The risk-stratification criteria demonstrated 99% sensitivity and 97% negative predictive value for SBI diagnosis, but only 21% specificity. Patient characteristics associated with a reduced likelihood of SBI diagnosis included female sex, sick contact exposure and virus detection.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Meeting the low-risk criteria successfully excluded most infants with SBI; however, only a small proportion of infants without SBI fulfilled these criteria. Integrating additional patient characteristics into updated risk-stratification algorithms may improve the predictive value of future prediction tools.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Trial Registration</h3>\u0000 \u0000 <p>Australia and New Zealand Clinical Trials Register (ACTRN12619001010189)</p>\u0000 </section>\u0000 </div>","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 6","pages":"894-904"},"PeriodicalIF":1.6,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143730366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Treatment of Lamellar Ichthyosis in a 10-Year-Old Child With Secukinumab","authors":"Roberto Mazzetto,&nbsp;Francesca Caroppo,&nbsp;Elisa Milan,&nbsp;Fortunato Cassalia,&nbsp;Anna Belloni Fortina","doi":"10.1111/jpc.70044","DOIUrl":"10.1111/jpc.70044","url":null,"abstract":"&lt;p&gt;We report a case of a 10-year-old male patient who was born with severe large scaling and erythema, exhibiting a collodion baby presentation, while otherwise being in good general condition. A TGM1 (transglutaminase type 1) heterozygous mutation (c.788G&gt;A and c.1559A&gt;G) was identified. During the medical examination, no signs of erythroderma were noticeable, whereas the presence of large, brownish scales and palmoplantar keratoderma clinically supported the diagnosis of lamellar ichthyosis (LI). Despite the absence of an evident inflammatory component, the patient reported severe itching.&lt;/p&gt;&lt;p&gt;Figure 1 illustrates the congenital phenotype at birth and the clinical presentation at the baseline medical examination.&lt;/p&gt;&lt;p&gt;Ichthyoses are a clinically heterogeneous group of rare genetic skin diseases characterised by an alteration of keratinisation. This condition can manifest in several forms, ranging from dry and scaly skin to thicker plaques and scales [&lt;span&gt;1&lt;/span&gt;].&lt;/p&gt;&lt;p&gt;The patient had previously been treated with various topical agents, including emollients with urea and/or salicylic acid, as well as systemic acitretin. These failed to adequately manage symptoms, as well as leading to abdominal pain as a side effect. The initial Children's Dermatology Life Quality Index (CDLQI) score was 20, the Numerical Rating Scale (NRS) of pruritus was 8 and NRS of pain was 6, indicating a significant impact on the patient's quality of life.&lt;/p&gt;&lt;p&gt;Recent studies have highlighted an increase in Th1, Th2 and Th17 cytokines in patients with certain genodermatoses [&lt;span&gt;2&lt;/span&gt;]. Specifically, elevated expression of Th17-related cytokines has been observed in the keratinocytes and fibroblasts of patients with ichthyosis vulgaris and Netherton syndrome, supporting their pathogenetic role in pruritus [&lt;span&gt;3&lt;/span&gt;].&lt;/p&gt;&lt;p&gt;Given the poor response to conventional therapies and considering the new scientific discoveries on the pathology of this disease [&lt;span&gt;2&lt;/span&gt;], treatment with secukinumab was initiated. The dosing regimen followed the protocol for psoriasis: an initial subcutaneous dose of 75 mg at weeks 0, 1, 2, 3 and 4, followed by monthly maintenance dosing.&lt;/p&gt;&lt;p&gt;The CDLQI improved from 20 to 8 (a 60% reduction) after 3 months, maintaining this improvement for 12 months. NRS of itching reduced from 8 to 4 (a 50% reduction) within 3 months and NRS of pain decreased from 6 to 2 (a 66.7% reduction). However, despite the improvement of symptoms, scaling remained unchanged (Figure 1).&lt;/p&gt;&lt;p&gt;During the treatment, the patient experienced an otitis media that resolved in 10 days with antibiotic therapy and without sequelae.&lt;/p&gt;&lt;p&gt;De Greef [&lt;span&gt;4&lt;/span&gt;], recently published a case of lamellar ichthyosis treated with acitretin and tralokinumab in a man in his 30s, while Taoming et al. reported a pilot study on combination therapy with secukinumab and dupilumab in Netherton syndrome [&lt;span&gt;5&lt;/span&gt;]. These findings suggest a potential role for ot","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 5","pages":"828-830"},"PeriodicalIF":1.6,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jpc.70044","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143730445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"PSANZ 2025 Oral","authors":"","doi":"10.1111/jpc.70008","DOIUrl":"https://doi.org/10.1111/jpc.70008","url":null,"abstract":"","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 S1","pages":"6-40"},"PeriodicalIF":1.6,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"PSANZ 2025 Poster","authors":"","doi":"10.1111/jpc.70011","DOIUrl":"https://doi.org/10.1111/jpc.70011","url":null,"abstract":"","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 S1","pages":"60-179"},"PeriodicalIF":1.6,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Late-Breaking Posters","authors":"","doi":"10.1111/jpc.70029","DOIUrl":"https://doi.org/10.1111/jpc.70029","url":null,"abstract":"","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 S1","pages":"182-185"},"PeriodicalIF":1.6,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"PSANZ 2025 Oral Poster","authors":"","doi":"10.1111/jpc.70009","DOIUrl":"https://doi.org/10.1111/jpc.70009","url":null,"abstract":"","PeriodicalId":16648,"journal":{"name":"Journal of paediatrics and child health","volume":"61 S1","pages":"41-59"},"PeriodicalIF":1.6,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}