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http://dx.doi.org/10.1016/j.anpede.2023.06.019 | DOI Listing |
Respirol Case Rep
December 2024
Division of Critical Care Medicine, Department of Internal Medicine National Cheng Kung University Hospital Tainan Taiwan.
Anti-Hu antibody-related paraneoplastic neurologic syndrome (PNS), a rare disease primarily associated with small cell lung carcinoma, is characterized by diverse neurologic manifestations. Central sleep apnea, although rare, is specific to anti-Hu antibody-related PNS. Herein, we present a case of out-of-hospital cardiac arrest attributed to hypercapnic central sleep apnea and detail the subsequent workup that revealed anti-Hu brainstem encephalitis.
View Article and Find Full Text PDFPediatr Pulmonol
November 2024
Pediatric Pulmonology and Respiratory Intermediate Care Unit, Sleep and Long-Term Ventilation Unit, Academic Department of Pediatrics, Pediatric Hospital "Bambino Gesù" Research Institute, Rome, Italy.
Objective: This retrospective study aimed to analyze the clinical characteristics, ventilatory strategies, and effectiveness of ventilation in pediatric patients with central apneas treated at the Sleep Medicine and Long-Term Ventilation Unit of the Bambino Gesù Children's Hospital in Rome from 2012 to 2022.
Methods: Among all ventilated patients at our Center from January 2012 to December 2022, we retrospectively included children with a cAHI ≥ 1 events/h on baseline poly(somno)graphic study. Additional parameters assessed included the underlying disease, type of ventilation (non-invasive vs.
Pediatr Pulmonol
December 2024
Centre de Référence Constitutif Maladies respiratoires rares, Hypoventilations alvéolaires rares, Syndrome d'Ondine, Physiology and Paediatric sleep Unit, Robert Debré Hospital, INSERM NeuroDiderot, AP-HP, Université de Paris-Cité, Paris, France.
Orphanet J Rare Dis
July 2024
Service de Physiologie Pédiatrique-Centre du Sommeil, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, CRMR Maladies respiratoires rares - Hypoventilations alvéolaires rares - Syndrome d'Ondine, INSERM NeuroDiderot, Paris, F-75019, France.
Arch Pediatr
April 2024
Université de Paris-Cité, AP-HP, Hôpital Robert Debré, Service de Médecine intensive et réanimation pédiatriques, F-75019 Paris, France; Université de Paris-Cité, AP-HP, Hôpital Robert Debré, INSERM NeuroDiderot, F-75019 Paris, France.
Congenital central hypoventilation syndrome (CCHS) is an autosomal dominant disease that is caused by heterozygous mutations in the paired-like homeobox 2B gene (PHOX2B). Madani et al. described an abnormally high degree of not only central apnea but also obstructive and mixed apnea in Phox2bnewborn mice.
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