{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T09:49:07Z","timestamp":1777888147872,"version":"3.51.4"},"reference-count":13,"publisher":"SAGE Publications","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["PRM"],"published-print":{"date-parts":[[2022,6,22]]},"abstract":"<jats:p>PURPOSE: Congenital myotonic dystrophy (CDM) results in hypotonia and acute respiratory distress at birth. Previous studies show that prolonged periods of intubation (&gt;4 weeks) correlate with increased mortality rates. The objective is to describe the use and duration of respiratory support in newborns with CDM and how these relate to mortality. METHODS: A retrospective chart review was performed at a tertiary pediatric hospital among children with confirmed diagnosis of CDM. The main outcome measures were: mortality, duration of invasive mechanical ventilation (IMV) and non-invasive partial pressure ventilation (NIPPV), along with long-term use of respiratory support and equipment. RESULTS: A total of 18 subjects met inclusion criteria, 83%.f which had documented respiratory distress at birth, 39%.equired NIPPV, and 50%.equired intubation in the neonatal period. The earliest NIPPV was initiated at day one of life, and the latest extubation to NIPPV was at 17 days of life. CONCLUSION: This cohort required IMV for shorter periods with earlier transitions to NIPPV which suggests a possible change in practice and earlier transition to NIPPV recently. Further data are needed to determine if there is a possible correlation between the need for NIPPV\/IMV and mortality rates.<\/jats:p>","DOI":"10.3233\/prm-200726","type":"journal-article","created":{"date-parts":[[2021,11,19]],"date-time":"2021-11-19T11:22:59Z","timestamp":1637320979000},"page":"275-279","source":"Crossref","is-referenced-by-count":2,"title":["Respiratory outcomes in children with congenital myotonic dystrophy"],"prefix":"10.1177","volume":"15","author":[{"given":"Jaclyn","family":"Omura","sequence":"first","affiliation":[{"name":"Pediatric Rehabilitation Medicine, Seattle Children\u2019s Hospital, University of Washington School of Medicine, Seattle, WA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maida","family":"Chen","sequence":"additional","affiliation":[{"name":"Pediatric Pulmonology, Seattle Children\u2019s Hospital, Seattle, WA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miriam","family":"Haviland","sequence":"additional","affiliation":[{"name":"Seattle Children\u2019s Research Institute, Seattle, WA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Susan","family":"Apkon","sequence":"additional","affiliation":[{"name":"Pediatric Rehabilitation Medicine, Children\u2019s Hospital Colorado, Denver, CO, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","reference":[{"issue":"1","key":"10.3233\/PRM-200726_ref1","doi-asserted-by":"publisher","first-page":"120","DOI":"10.1016\/j.jpeds.2012.12.070","article-title":"Congenital myotonic dystrophy: Canadian population-based surveillance study","volume":"163","author":"Campbell","year":"2013","journal-title":"J Pediatr"},{"issue":"4","key":"10.3233\/PRM-200726_ref2","doi-asserted-by":"publisher","first-page":"285","DOI":"10.1016\/0887-8994(92)90367-8","article-title":"Clinical features for prediction 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