Literature DB >> 19944216

Evaluating mortality and disease severity in congenital diaphragmatic hernia using the McGoon and pulmonary artery indices.

Shigehiro Takahashi1, Yoshihisa Oishi, Naoki Ito, Yukiko Nanba, Keiko Tsukamoto, Tomoo Nakamura, Yushi Ito, Satoshi Hayashi, Haruhiko Sago, Tatsuo Kuroda, Toshiro Honna.   

Abstract

PURPOSE: Lung hypoplasia is associated with mortality in congenital diaphragmatic hernia (CDH). However, the association between lung hypoplasia and disease severity is unclear. Early prediction of disease severity would provide parents with more precise information about the anticipated course of treatment, minimize treatment disruption, and maximize the efficient management of patients with CDH. We aimed at identifying the relationship between McGoon index (MGI) and pulmonary artery index (PAI) scores and disease severity among infants with CDH.
METHODS: We retrospectively reviewed the medical records of 19 high-risk patients with CDH born between January 2006 and December 2007. McGoon index and PAI scores were determined on admission. We evaluated statistically the relationship between these scores and variables representing severity as follows: number of vasodilators, use of inhaled nitric oxide (iNO), closed method of diaphragm, duration of intubation, duration of hospitalization, and use of home oxygen therapy. Statistical significance was P < .05.
RESULTS: Overall median MGI and PAI scores were 1.40 and 108, respectively; scores for nonsurvivors were significantly (P < .05 and P < .01, respectively) lower than those for survivors. Among survivors, PAI scores were significantly (P < .05) lower in infants requiring iNO than in infants not requiring iNO and patch repair. The PAI scores were significantly correlated with the number of vasodilators (r = -0.789; P < .01) and duration of intubation (r = -0.610; P < .05).
CONCLUSIONS: McGoon index (cutoff value, 1.31) and PAI (cutoff value, 90) are reliable indices for predicting mortality in CDH. Pulmonary artery index appears to be more useful than MGI for predicting disease severity among survivors.

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Year:  2009        PMID: 19944216     DOI: 10.1016/j.jpedsurg.2009.05.012

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


  4 in total

1.  Recent advances in the management of congenital diaphragmatic hernia.

Authors:  V Jain; S Agarwala; V Bhatnagar
Journal:  Indian J Pediatr       Date:  2010-06-08       Impact factor: 1.967

Review 2.  Congenital diaphragmatic hernia.

Authors:  Juan A Tovar
Journal:  Orphanet J Rare Dis       Date:  2012-01-03       Impact factor: 4.123

3.  A Case of Fatal Pulmonary Hypoplasia with Congenital Diaphragmatic Hernia, Thoracic Myelomeningocele, and Thoracic Dysplasia.

Authors:  Ai Ito; Hideshi Fujinaga; Sachiko Matsui; Kumiko Tago; Yuka Iwasaki; Shuhei Fujino; Junko Nagasawa; Shoichiro Amari; Masao Kaneshige; Yuka Wada; Shigehiro Takahashi; Keiko Tsukamoto; Osamu Miyazaki; Takako Yoshioka; Akira Ishiguro; Yushi Ito
Journal:  AJP Rep       Date:  2017-12-29

Review 4.  The role of magnetic resonance imaging in the diagnosis and prognostic evaluation of fetuses with congenital diaphragmatic hernia.

Authors:  Ilaria Amodeo; Irene Borzani; Genny Raffaeli; Nicola Persico; Giacomo Simeone Amelio; Silvia Gulden; Mariarosa Colnaghi; Eduardo Villamor; Fabio Mosca; Giacomo Cavallaro
Journal:  Eur J Pediatr       Date:  2022-07-07       Impact factor: 3.860

  4 in total

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