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Outcome of congenital diaphragmatic hernia
1Regional Neonatal Unit, Liverpool Women's Hospital, Liverpool, UK.
Insights
Congenital diaphragmatic hernia (CDH) outcomes vary by diagnosis timing and presence of other anomalies. This review offers clinicians data to guide parents on CDH prognosis.
Area of Science:
- Pediatric Surgery
- Neonatology
- Medical Research
Background:
- Congenital diaphragmatic hernia (CDH) presents varied outcomes based on developmental stage.
- Assessing combined data from nonrandomized studies on CDH is challenging.
- Accurate prognosis is crucial for parental counseling in CDH cases.
Purpose of the Study:
- To systematically review the literature on congenital diaphragmatic hernia (CDH) outcomes.
- To provide clinicians with a guide for counseling parents of fetuses/infants with CDH.
- To analyze mortality rates across different CDH diagnostic and treatment stages.
Main Methods:
- Systematic review of 35 studies on CDH outcomes from 1985 to March 1998.
- Utilized a high-sensitivity search strategy, journal hand-searching, and reference reviews.
- Analyzed data based on antenatal diagnosis, live birth, and postoperative stages.
Main Results:
- Overall median mortality for CDH was 58% if diagnosed in utero, 48% if born alive, and 33% postoperatively.
- Diagnosis before 25 weeks gestation had a median mortality of 60%; other anomalies increased mortality to 93%.
- Median mortality in extracorporeal membrane oxygenation (ECMO) centers was 34% for live-born infants and 44% for all ECMO-treated infants.
Conclusions:
- Mortality in congenital diaphragmatic hernia (CDH) is significantly influenced by diagnostic timing, gestational age, presence of other anomalies, and treatment strategies.
- Extracorporeal membrane oxygenation (ECMO) appears to reduce mortality in treated infants.
- This review provides essential data for improving parental counseling regarding CDH prognosis.
Abstract:
The outcome of congenital diaphragmatic hernia (CDH) differs for different stages of the fetus or infant's life (i.e., antenatal, immediate postnatal, and postoperative). Assessing combined data from nonrandomized studies is technically difficult. Following recognized methods of reviewing such trials, we aimed to review the available literature on the outcome of CDH to provide a guide to clinicians when counselling parents who have a fetus/infant with this condition. Thirty-five studies reporting data for CDH from 1985 to March 1998 were identified using a high sensitive search strategy, hand-searching journals, and reviewing references of relevant studies. These were systematically reviewed. The median overall mortality was 58% (interquartile range (IQR), 43-65%) for babies diagnosed in utero, 48% (IQR, 35-55%) if born alive, and 33% (IQR, 18-54%) postoperatively. Diagnosis before 25 weeks of gestation is not a uniformly bad prognostic indicator (median mortality, 60%). Outcome was worse for those fetuses with other anomalies (median mortality, 93%). The median percentage mortality for all infants born alive and treated in extracorporeal membrane oxygenation (ECMO) centers was 34% (IQR, 26-47%). Median percentage mortality for all ECMO-treated infants was 44% (IQR, 35-50%). Different treatment strategies may have a variable impact on outcome. These figures, together with local data, may help in parental counselling on prognosis for fetuses/infants with CDH.
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