Observational studyPediatric surgery international2017
Impact of fetal counseling on outcome of antenatal congenital surgical anomalies.
Observational study in Pediatric surgery international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The trial behind it
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Who cites it
8 citing papers in PubMed.
- Management, Outcome, Risk, and Expectation classification for structural fetal anomalies to aid antenatal counseling: a prospective validation study.Pediatric surgery international · 2025Article
- Surgically Correctable Congenital Anomalies: Reducing Morbidity and Mortality in the First 8000 Days of Life.World journal of surgery · 2023Review
- Spiritual care in neonatology: analysis of emergency baptisms in an Irish neonatal unit over 15 years.Irish journal of medical science · 2019Article
- Antenatally Diagnosed Surgical Conditions: Fetus As Our Patient.Indian journal of pediatrics · 2018Review
- 'Mutiny on the crown': two cases of rare cephalic malformations.BMJ case reports · 2017Article
- Fetal Malformations and the Pediatric Surgeon.Journal of Indian Association of Pediatric SurgeonsArticle
- Application of Management, Outcome, Risk, and Expectation Classification for Antenatally Suspected Structural Anomalies: A Multidisciplinary Experience.Journal of Indian Association of Pediatric SurgeonsArticle
- Management, Outcome, Risk, and Expectation Classification for Structural Fetal Anomalies to Aid Antenatal Counseling: A Systematic Review.Journal of Indian Association of Pediatric SurgeonsReview
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
aimTo analyze the impact of counseling on antenatal congenital surgical anomalies (ACSA).
methodsCases presenting with ACSA for fetal counseling and those presenting in post-natal period following diagnosis of ACSA (PACSA) for surgical opinion were analyzed for spectrum, presentation and outcome.
results117 cases including ACSA(68);PACSA(49) were analyzed. Gestational age at diagnosis of ACSA;PACSA was 17-37;17-39 weeks (median 24;32 weeks). Diagnoses in ACSA;PACSA included urological (26;31), neurological (10;5), congenital diaphragmatic hernia (CDH)(5;1), gastrointestinal (5;5), lung and chest anomalies (5;1), intraabdominal cysts (4;1), abdominal wall defects (4;0), tumors (3;3), limb anomaly (1;1), esophageal atresia (1;1), conjoint twins (1;0), hepatomegaly (1;0), and major cardiac anomalies (2;0). Two antenatal interventions were done for ACSA; vesicoamniotic shunt and amnioinfusion for oligohydramnios. 17;24 ACSA;PACSA required early surgical intervention in post-natal period. Nine ACSA underwent medical termination of pregnancy and 4 had intrauterine demise. Nine ACSA babies died including two CDH, one gastroschisis, one duodenal atresia, one conjoint twins, one megacystitis with motility disorder and three posterior urethral valves. All PACSA babies survived.
conclusionFetal counseling for CSA portrays true outcome of ACSA with 32.3% (22/68) mortality versus 0% for PACSA due to selection bias. However, fetal counseling ensures optimal perinatal care.
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Registered trials
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