Home mechanical ventilation in childhood-onset hereditary neuromuscular diseases: 13 years' experience at a single center in Korea

• Published in: PloS one 2015-03, Vol.10 (3), p.e0122346-e0122346
• Main Authors: Han, Young Joo, Park, June Dong, Lee, Bongjin, Choi, Yu Hyeon, Suh, Dong In, Lim, Byung Chan, Chae, Jong-Hee
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Age; Air leakage; Analysis; Atrophy; Child; Child, Preschool; Childhood; Children; Clinical trials; Congenital diseases; Diagnosis; Extubation; Female; Genetic aspects; Guidelines; Home Care Services; Hospitalization; Hospitals; Humans; Hypoxia; Infant; Male; Mechanical ventilation; Medical records; Medicine; Mental disorders; Morbidity; Mortality; Neuromuscular diseases; Neuromuscular Diseases - mortality; Neurosciences; Noninvasive Ventilation - methods; Ostomy; Patients; Pediatrics; Quality of life; Republic of Korea; Respiration, Artificial - methods; Respiratory failure; Respiratory Insufficiency - mortality; Respiratory tract; Retrospective Studies; Review boards; Secretions; Spinal muscular atrophy; Ventilation; Ventilators; Young Adult
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0122346

Children with hereditary neuromuscular diseases (NMDs) are at a high risk of morbidity and mortality related to respiratory failure. The use of home mechanical ventilation (HMV) has saved the lives of many children with NMD but, due to a lack of studies, dependable guidelines are not available. We drew upon our experience to compare the various underlying NMDs and to evaluate HMV with regard to respiratory morbidity, the proper indications and timing for its use, and to develop a policy to improve the quality of home noninvasive ventilation (NIV). We retrospectively analyzed the medical records of 57 children with childhood-onset hereditary NMDs in whom HMV was initiated between January 2000 and May 2013 at Seoul National University Children's Hospital. The degree of respiratory morbidity was estimated by the frequency and duration of hospitalizations caused by respiratory distress. The most common NMD was spinal muscular atrophy (SMA, n = 33). Emergent mechanical ventilation was initiated in 44% of the patients before the confirmed diagnosis, and the indicators of pre-HMV respiratory morbidity (e.g., extubation trials, hypoxia, hospitalizations, and intensive care unit stay) were greater in these patients than in others. The proportion of post-HMV hospitalizations (range, 0.00-0.52; median, 0.01) was lower than that of pre-HMV hospitalizations (0.02-1.00; 0.99) (P < 0.001). Eight patients were able to maintain home NIV. The main causes of NIV failure were air leakage and a large amount of airway secretions. The application of HMV helped reduce respiratory morbidity in children with childhood-onset hereditary NMD. Patients with SMA type I can benefit from an early diagnosis and the timely application of HMV. The choice between invasive and noninvasive HMV should be based on the patient's age and NIV trial tolerance. Systematic follow-up guidelines provided by a multidisciplinary team are needed.