Pulmonary support on day of life 30 is a strong predictor of increased 1 and 5-year morbidity in survivors of congenital diaphragmatic hernia

被引:32
作者
Cauley, Ryan P. [1 ]
Potanos, Kristina [1 ]
Fullington, Nora [1 ]
Bairdain, Sigrid [1 ]
Sheils, Catherine A. [2 ]
Finkelstein, Jonathan A. [2 ]
Graham, Dionne A. [3 ]
Wilson, Jay M. [1 ]
机构
[1] Boston Childrens Hosp, Dept Surg, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Dept Med, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Clin Res Ctr, Boston, MA USA
基金
美国医疗保健研究与质量局;
关键词
Extracorporeal membrane oxygenation; Mechanical ventilation; Risk assessment; Congenital anomaly; EXTRACORPOREAL MEMBRANE-OXYGENATION; TERM-FOLLOW-UP; NEURODEVELOPMENTAL OUTCOMES; ESOPHAGEAL ATRESIA; INFANTS; REPAIR; MANAGEMENT; MORTALITY; CHILDREN;
D O I
10.1016/j.jpedsurg.2014.12.007
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Pulmonary support (PS) on day-of-life-30 (DOL-30) has been shown to be the strongest predictor of subsequent morbidity and in-patient mortality in congenital diaphragmatic hernia (CDH). We hypothesized that PS on DOL-30 can also predict long-term outcomes in CDH survivors. Methods: We analyzed records of 201 CDH survivors followed by a single multidisciplinary clinic (1995-2010). Follow-up was 83 and 70% at 1 and 5 years respectively. PS was defined as: (1) invasive support (n=44), (2) noninvasive support (n = 54), or (3) roomair (n = 103). Logistic regression was used to estimate the adjusted association of PS on DOL-30 with outcomes at 1 and 5-years. Results: Use of PS on DOL-30 was significantly associated with pulmonary and developmental morbidities at 1 and 5-years. Even after adjusting for defect-size and presence of ventilation/perfusion mismatch, greater PS on DOL-30 was associated with a significantly increased odds of requiring supplemental oxygen and developmental referral at 1-year, and asthma and developmental referral at 5-years. Conclusion: CDH survivors continue to have significant long-termpulmonary and developmental morbidities. PS on DOL-30 is a strong independent predictor of morbidity at 1 and 5-years and may be used as a simple prognostic tool to identify high-risk infants. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:849 / 855
页数:7
相关论文
共 31 条
[1]   Institutional practice and outcome variation in the management of congenital diaphragmatic hernia and gastroschisis in Canada: a report from the Canadian Pediatric Surgery Network [J].
Baird, Robert ;
Eeson, Gareth ;
Safavi, Arash ;
Puligandla, Pramod ;
Laberge, Jean-Martin ;
Skarsgard, Erik D. .
JOURNAL OF PEDIATRIC SURGERY, 2011, 46 (05) :801-807
[2]   Pulmonary support on Day 30 as a predictor of morbidity and mortality in congenital diaphragmatic hernia [J].
Cauley, Ryan P. ;
Stoffan, Alexander ;
Potanos, Kristina ;
Fullington, Nora ;
Graham, Dionne A. ;
Finkelstein, Jonathan A. ;
Kim, Heung Bae ;
Wilson, Jay M. .
JOURNAL OF PEDIATRIC SURGERY, 2013, 48 (06) :1183-1189
[3]   Long-term functional impact of congenital diaphragmatic hernia repair on children [J].
Chen, Catherine ;
Jeruss, Stefanie ;
Chapman, Jocelyn S. ;
Terrin, Norma ;
Tighiouart, Hocine ;
Glassman, Erik ;
Wilson, Jay M. ;
Parsons, Susan K. .
JOURNAL OF PEDIATRIC SURGERY, 2007, 42 (04) :657-665
[4]   Morbidity and Long-Term Follow-Up in CDH Patients [J].
Chiu, Priscilla P. L. ;
IJsselstijn, Hanneke .
EUROPEAN JOURNAL OF PEDIATRIC SURGERY, 2012, 22 (05) :384-392
[5]   Survival of severe congenital diaphragmatic hernia has morbid consequences [J].
Cortes, RA ;
Keller, RL ;
Townsend, T ;
Harrison, MR ;
Farmer, DL ;
Lee, HM ;
Piecuch, RE ;
Leonard, CH ;
Hetherton, M ;
Bisgaard, R ;
Nobuhara, KK .
JOURNAL OF PEDIATRIC SURGERY, 2005, 40 (01) :36-45
[6]   Long term respiratory outcomes of congenital diaphragmatic hernia, esophageal atresia, and cardiovascular anomalies [J].
Delacourt, Christophe ;
Hadchouel, Alice ;
Toelen, Jaan ;
Rayyan, Maissa ;
de Blic, Jacques ;
Deprest, Jan .
SEMINARS IN FETAL & NEONATAL MEDICINE, 2012, 17 (02) :105-111
[7]   Neurodevelopmental outcomes of congenital diaphragmatic hernia survivors followed in a multidisciplinary clinic at ages 1 and 3 [J].
Friedman, Sandra ;
Chen, Catherine ;
Chapman, Jocelyn S. ;
Jeruss, Stefanie ;
Terrin, Norma ;
Tighiouart, Hocine ;
Parsons, Susan K. ;
Wilson, Jay M. .
JOURNAL OF PEDIATRIC SURGERY, 2008, 43 (06) :1035-1043
[8]   Long-term neurodevelopmental outcomes of congenital diaphragmatic hernia survivors not treated with extracorporeal membrane oxygenation [J].
Frisk, Virginia ;
Jakobson, Lorna S. ;
Unger, Sharon ;
Trachsel, Daniel ;
O'Brien, Karel .
JOURNAL OF PEDIATRIC SURGERY, 2011, 46 (07) :1309-1318
[9]   A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors [J].
Gischler, Saskia J. ;
van der Cammen-van Zijp, Monique H. M. ;
Mazer, Petra ;
Madern, Gerard C. ;
Bax, Nikolaas M. A. ;
de Jongste, Johan C. ;
van Dijk, Monique ;
Tibboel, Dick ;
Ijsselstijn, Hanneke .
JOURNAL OF PEDIATRIC SURGERY, 2009, 44 (09) :1683-1690
[10]   Predicting inadequate long-term lung development in children with congenital diaphragmatic hernia: an analysis of longitudinal changes in ventilation and perfusion [J].
Hayward, Melissa J. ;
Kharasch, Virginia ;
Sheils, Catherine ;
Friedman, Sandra ;
Dunleavy, Mary-Jo ;
Utter, Sherri ;
Zurakowski, David ;
Jennings, Russell ;
Wilson, Jay M. .
JOURNAL OF PEDIATRIC SURGERY, 2007, 42 (01) :112-116