Month: <span>October 2025</span>
Month: October 2025

Parental Consent to a Neonatal Clinical Study: The Roles of Uncertainty, Burden of Sample Collection and Societal Expectations

Acta Paediatr. 2025 Oct 6. doi: 10.1111/apa.70333. Online ahead of print. ABSTRACT AIM: Recruiting participants for neonatal clinical studies may be challenging because parental consent …

Neonatal outcomes with regional versus general anesthesia for cesarean delivery: A meta-analysis of randomized controlled trials

Anesthesiology. 2025 Oct 6. doi: 10.1097/ALN.0000000000005785. Online ahead of print. ABSTRACT BACKGROUND: Neonatal outcomes with regional anesthesia (spinal, epidural, or combined spinal-epidural) versus general anesthesia …

Neonatal demise from a complex abdominal wall defect in a low-resource setting: A case study on the consequences of a fractured perinatal care cascade

Radiol Case Rep. 2025 Sep 22;20(12):6117-6120. doi: 10.1016/j.radcr.2025.08.098. eCollection 2025 Dec. ABSTRACT Survival for neonates with abdominal wall defects (AWDs) exceeds 90% in high-income countries, …

Antithrombotic strategies and outcomes in neonates and infants with cardiac shunts: a systematic review and meta-analysis

Res Pract Thromb Haemost. 2025 Aug 26;9(6):103161. doi: 10.1016/j.rpth.2025.103161. eCollection 2025 Aug. ABSTRACT BACKGROUND: Cardiac shunt thrombosis in neonates and infants remains a concern for …

Home-based telerehabilitation for pediatric neurological motor disorders: Current trends and future perspectives. A systematic review and meta-analysis

Digit Health. 2025 Oct 3;11:20552076251357504. doi: 10.1177/20552076251357504. eCollection 2025 Jan-Dec. ABSTRACT OBJECTIVE: Telerehabilitation is a rapidly growing area within telehealth, providing clinical rehabilitation services through …

A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report

Front Pediatr. 2025 Sep 18;13:1666585. doi: 10.3389/fped.2025.1666585. eCollection 2025. ABSTRACT BACKGROUND: Hereditary spherocytosis (HS) is a genetically inherited hemolytic anemia resulting from erythrocyte membrane defects, …

Modern approaches to the diagnosis and treatment of Dravet syndrome in the Russian Federation. (Literature review and resolution of the Expert Council)

Zh Nevrol Psikhiatr Im S S Korsakova. 2025;125(9):103-116. doi: 10.17116/jnevro2025125091103. ABSTRACT Dravet syndrome (DS) is a rare genetic disorder with onset at 1 year of …