Literature DB >> 15136994

Survival rate in congenital diaphragmatic hernia: the experience of the Canadian Neonatal Network.

Patrick J Javid1, Tom Jaksic, Erik D Skarsgard, Shoo Lee.   

Abstract

BACKGROUND/
PURPOSE: The Canadian Neonatal Network prospectively collects data from 17 pediatric hospitals accounting for 75% of all neonatal intensive care unit beds nationwide. The purpose of this study was to (1) analyze the database to compare actual survival rates of neonates with congenital diaphragmatic hernia (CDH) to predicted outcomes and (2) assess whether institutional CDH volume was associated with improved survival rate.
METHODS: Actual survival rates for CDH patients born during a 22-month period were determined from the registry. Predicted survival rates were calculated using the CDH Study Group logistical regression equation. Actual survival rate was compared with predicted using chi2 analysis. Survival rates were stratified by institutional CDH volume and compared using binomial analysis. P value of less than.05 was deemed statistically significant.
RESULTS: Of approximately 20,500 neonatal admissions, 88 cases of CDH were recorded. Seventy-three of 88 (83%) neonates with CDH survived to discharge, whereas the predicted survival rate was 62% (P <.001). Three centers were considered "high-volume" centers with at least 12 CDH diagnoses, and 11 were considered "low-volume" centers. Actual CDH survival was significantly greater at high-versus low-volume centers (90% v 77%; P <.01).
CONCLUSIONS: From these prospective data, survival rates of Canadian neonates with CDH are significantly better than predicted by the CDH Study Group equation. Further, high-volume centers in Canada have a significantly higher CDH survival rate than low-volume centers.

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Mesh:

Year:  2004        PMID: 15136994     DOI: 10.1016/j.jpedsurg.2004.01.022

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  24 in total

1.  Population-Based Validation of a Clinical Prediction Model for Congenital Diaphragmatic Hernias.

Authors:  Daniel P Bent; Jason Nelson; David M Kent; Howard C Jen
Journal:  J Pediatr       Date:  2018-06-25       Impact factor: 4.406

2.  Risk stratification for congenital diaphragmatic hernia by factors within 24 h after birth.

Authors:  K Terui; K Nagata; Y Kanamori; S Takahashi; M Hayakawa; H Okuyama; N Inamura; H Yoshida; T Taguchi; N Usui
Journal:  J Perinatol       Date:  2017-02-23       Impact factor: 2.521

3.  Preliminary observations of the use of high-frequency jet ventilation as rescue therapy in infants with congenital diaphragmatic hernia.

Authors:  Michael A Kuluz; P Brian Smith; Sarah P Mears; Jennifer R Benjamin; Elisabeth T Tracy; W Lee Williford; Ronald N Goldberg; Henry E Rice; C Michael Cotten
Journal:  J Pediatr Surg       Date:  2010-04       Impact factor: 2.545

4.  Treatment evolution in high-risk congenital diaphragmatic hernia: ten years' experience with diaphragmatic agenesis.

Authors:  Kevin P Lally; Pamela A Lally; Krisa P Van Meurs; Desmond J Bohn; Carl F Davis; Bradley Rodgers; Jatinder Bhatia; Golde Dudell
Journal:  Ann Surg       Date:  2006-10       Impact factor: 12.969

5.  Pulmonary Hypertension in Patients with Congenital Diaphragmatic Hernia: Does Lung Size Matter?

Authors:  Arin L Madenci; Joseph T Church; Robert J Gajarski; Kathryn Marchetti; Edwin J Klein; Megan A Coughlin; Jeannie Kreutzmann; Marjorie Treadwell; Maria Ladino-Torres; George B Mychaliska
Journal:  Eur J Pediatr Surg       Date:  2017-10-16       Impact factor: 2.191

Review 6.  Recent advances in congenital diaphragmatic hernia.

Authors:  N P Smith; E C Jesudason; N C Featherstone; H J Corbett; P D Losty
Journal:  Arch Dis Child       Date:  2005-04       Impact factor: 3.791

Review 7.  Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

Authors:  Barbara R Pober
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

8.  Liver-to-thoracic volume ratio: use at MR imaging to predict postnatal survival in fetuses with isolated congenital diaphragmatic hernia with or without prenatal tracheal occlusion.

Authors:  Mieke M Cannie; Anne-Gaël Cordier; Jocelyne De Laveaucoupet; Stéphanie Franchi-Abella; Maud Cagneaux; Olivier Prodhomme; Marie-Victoire Senat; Mostafa Mokhtari; Vinciane Vlieghe; Dorota Nowakowska; Alexandra Benachi; Jacques C Jani
Journal:  Eur Radiol       Date:  2012-12-16       Impact factor: 5.315

Review 9.  Congenital diaphragmatic hernia: current status and review of the literature.

Authors:  Anthony S de Buys Roessingh; Anh Tuan Dinh-Xuan
Journal:  Eur J Pediatr       Date:  2008-12-23       Impact factor: 3.183

10.  Surgical complications, especially gastroesophageal reflux disease, intestinal adhesion obstruction, and diaphragmatic hernia recurrence, are major sequelae in survivors of congenital diaphragmatic hernia.

Authors:  Kazuki Yokota; Hiroo Uchida; Kenichiro Kaneko; Yasuyuki Ono; Naruhiko Murase; Satoshi Makita; Masahiro Hayakawa
Journal:  Pediatr Surg Int       Date:  2014-08-09       Impact factor: 1.827

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