PREDICTORS OF SURVIVAL FOR INFANTS WITH CONGENITAL DIAPHRAGMATIC-HERNIA

Citation
Ma. Norden et al., PREDICTORS OF SURVIVAL FOR INFANTS WITH CONGENITAL DIAPHRAGMATIC-HERNIA, Journal of pediatric surgery, 29(11), 1994, pp. 1442-1446
Citations number
19
Categorie Soggetti
Pediatrics,Surgery
ISSN journal
00223468
Volume
29
Issue
11
Year of publication
1994
Pages
1442 - 1446
Database
ISI
SICI code
0022-3468(1994)29:11<1442:POSFIW>2.0.ZU;2-D
Abstract
Over the past decade, the survival rate of infants with congenital dia phragmatic hernia (CDH) treated in the intensive care unit of the Roya l Children's Hospital, Melbourne, has remained unchanged at 56% +/- 6% . Newer forms of treatment, such as extracorporeal membrane oxygenatio n (ECMO), high-frequency oscillation, and surfactant and nitric oxide therapy, are now available. The exact role of these therapies in the m anagement of infants with CDH has not been determined. This study exam ines five clinical parameters derived from an infant's best preoperati ve ventilatory and blood gas data in the first 24 hours of life. One h undred twenty-five CDH infants were admitted to the intensive care uni t between January 1, 1981 and December 31, 1991. Criteria for inclusio n in the study were (1) CDH diagnosed within 6 hours of delivery, (2) ventilation before repair, and (3) no associated lethal congenital abn ormality. Of the 90 cases studied in detail, there were 38 deaths (42% mortality rate). All five parameters were analyzed by receiver operat ing curve analysis to determine the optimum value of each parameter in predicting survival. An oxygenation index (MAP x Fio(2)/Pao(2)) of le ss than 0.08 predicted a 94% chance of survival, with a sensitivity of 96% and a specificity of 95%. Similarly, a modified ventilation index (PIP x RR x CO2/1,000) of less than 40 predicted a 91% chance of surv ival, with a sensitivity of 94% and a specificity of 86%. By stratifyi ng each criterion according to outcome, three groups of infants were i dentified according to their response to conventional therapy. There i s a large group of infants that can be expected to survive with conven tional therapy and are likely to have minimal pulmonary hypoplasia. A second group can be expected to die with use of conventional therapy; this group may well represent infants with severe pulmonary hypoplasia who are unlikely to benefit from therapies designed to combat pulmona ry hypertension or minimize lung barotrauma. Between these two groups is a small group of infants whose outcome from conventional therapy is less predictable. We believe that this group may represent infants wi th significant pulmonary hypertension and moderate pulmonary hypoplasi a. These patients may benefit from newer therapies that treat pulmonar y hypertension and minimize lung injury. Copyright (C) 1994 by W.B. Sa unders Company