CONGENITAL DIAPHRAGMATIC-HERNIA - LONG-TERM OUTCOME IN NEONATES TREATED WITH EXTRACORPOREAL MEMBRANE-OXYGENATION

被引:97
作者
VANMEURS, KP
ROBBINS, ST
REED, VL
KARR, SS
WAGNER, AE
GLASS, P
ANDERSON, KD
SHORT, BL
机构
[1] STANFORD UNIV, LUCILE SALTER PACKARD CHILDRENS HOSP, MED CTR, DEPT PEDIAT, STANFORD, CA 94305 USA
[2] UNIV SO CALIF, CHILDRENS HOSP LOS ANGELES, DEPT PEDIAT SURG, LOS ANGELES, CA 90089 USA
[3] GEORGE WASHINGTON UNIV, SCH MED, CHILDRENS NATL MED CTR, DEPT NEONATOL, WASHINGTON, DC 20052 USA
[4] GEORGE WASHINGTON UNIV, SCH MED, CHILDRENS NATL MED CTR, DEPT CARDIOL, WASHINGTON, DC 20052 USA
[5] GEORGE WASHINGTON UNIV, SCH MED, CHILDRENS NATL MED CTR, DEPT CLIN NUTR, WASHINGTON, DC 20052 USA
关键词
D O I
10.1016/S0022-3476(09)90013-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
As more infants with congenital diaphragmatic hernia (CDH) survive with extracorporeal membrane oxygenation (ECMO), it seems prudent to detail the long-term outcome in these medically complex infants. Eighteen children with CDH treated with postoperative ECMO were recruited for participation in this study. The mean duration of ECMO was 193 hours (range 82 to 493 hours), mean time to extubation after ECMO was 142 hours (range 34 to 312 hours), and median duration of hospitalization was 46 days (range 30 to 181 days). Of the 18 infants, 4 (22%) were discharged home requiring oxygen therapy. At follow-up the notable findings were a high incidence of gastroesophageal reflux and failure to thrive. At both 1 and 2 years of age, 50% of infants were at less than the 5th percentile for weight. At 1 and 2 years of age, 39% and 21%, respectively, were at less than the Sth percentile for weight/length ratio. A total of 16 children (89%) had clinical evidence of reflux, and 8 (44%) were discharged home on a regimen of nasogastric feedings. Reherniation occurred in 4 children (22%) and was more frequent when a patch was used. An electrocardiogram showed right ventricular hypertrophy in 6 (43%); oxygen saturation by pulse oximetry was >95% in all children, and pulmonary artery pressure was estimated by Doppler echocardiography to be normal in 12 of 14 children examined. The neurodevelopmental outcome (Bayley Scales or Stanford-Binet scale) at 1 to 4 years of age was not dissimilar from that of other ECMO-treated children. Given the severity of illness in the neonatal period, the general health and development of children with CDH surviving after ECMO are good. Surprisingly few children have long-term respiratory complications related to pulmonary hypoplasia. Follow-up in the first few years should be aimed at aggressive nutritional intervention to prevent the growth failure that appears to be prevalent in these children.
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页码:893 / 899
页数:7
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