ESOPHAGEAL ATRESIA: RESULTS OF 108 CASES IN AN 11 YEAR PERIOD

Authors

  • A KHALEGHNEJAD TABARI From the Dept. of Paediaric Surgery, Bristol Royal Hospital for Sick Children, Bristol, England.
  • D FRANK
  • HR NOBLETT
Abstract:

From October 1977 to December 1988, 108 neonates born with esophageal atresia (EA) and/or a tracheoesophageal fistula (TEF) were treated at the Bristol Royal Hospital for Sick Children. An incidence of I :4000-4500 live births was noted. 1I2.4% had the common- type anomaly, 5.5% had pure esophageal atresia, and 6.5% had an H-type anomaly. 2.8% had upper and lower fistulae and 2.8% had upper fistulae. Forty-nine patients (45.3%) had associated anomalies of which the cardiovascular system (16.6%) was the most commom. With consideration of the urogenital system as a unique system, urogenital anomalies were the most common associated anomalies (20.3%). Thirty (27.7%) of lOll neonates had V ACTERL associated anomalies, which were more frequent in the common- type anomaly. Seven of 9 deaths in the VACTERL associated group were because of associated anomalies and cardiac anomalies were a common cause of late death in this study. In full-term and well babies with common-type anomalies, transanastomotic tubes significantly decreased hospital stay. Every effort was made to maintain the neonate's own esophagus, and in pure esophageal atresia 5 of 6 neonates were successfully treated by spontaneous growth and anastomosis and only I neonate underwent gastric- tube formation as an esophageal replacement. Anastomosis was done in one layer by 5/0 silk , and 17.14% developed leak, 29.62% strictures, 1.90% recurrent fistula, and the rate of anastomotic complications was markedly higher in delayed and staged operations. Fifty-three neonates (50.47%) had respiratory complications which were the most common complication. Thirty-three (31.4%) had gastroesophageal reflux (GER), all but one of which were treated medically. The routine policy now is that all babies are put on Gaviscon until the child can adopt an upright position. Low birth weight and pneumonia are not contraindications for surgery, and with the improvement of surgical technique and postoperative care, do not affect survival. There was 12.03% mortality and the main cause of death was associated anomalies.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

esophageal atresia: results of 108 cases in an 11 year period

from october 1977 to december 1988, 108 neonates born with esophageal atresia (ea) and/or a tracheoesophageal fistula (tef) were treated at the bristol royal hospital for sick children. an incidence of i :4000-4500 live births was noted. 1i2.4% had the common- type anomaly, 5.5% had pure esophageal atresia, and 6.5% had an h-type anomaly. 2.8% had upper and lower fistulae and 2.8% had upper fis...

full text

An 8-Year experience of esophageal atresia repair in sarvar children hospital

Intruduction: Esophageal atresia (EA) is a congenital anomaly treated by surgical reconstruction. Some early postoperative complications may be encountered we assessed complications following EA repair in a large number of neonates with EA / TEF. methods: 243 patients with EA / TEF that were treated operatively in Sarvar Children’s Hospital from 2002 to 2010 were studied. Early post-operat...

full text

Plague Convalescence Period. Analysis of 108 Cases

Hospital, between February and July 1897, no patient, except one who deserted on the twentythird day, was discharged until the temperature had remained normal for at least four days. Those discharged in less than ten days from the hospital had either been kept under observation for some time previous to actual entry of their names in the admission and discharge book, or had had plague outside a...

full text

Assessment of Quantitative and Qualitative characteristics of Golestan Province Forests in an 11-year period (Iran)

The assessment of the quantitative and qualitative changes, the result of the impacts imposed by natural factors, and human interventions during specific sampling periods has a substantial influence on nature, management method and tending operation of every region’s forests. The present research was carried out in Golestan province forests (Iran) over an 11- year period and the obtained statis...

full text

An 18-year experience of tracheoesophageal fistula and esophageal atresia

PURPOSE To determine the clinical manifestations and outcomes of patients with tracheoesophageal fistula (TEF) and esophageal atresia (EA) born at a single neonatal intensive care unit. METHODS A retrospective analysis was conducted for 97 patients with confirmed TEF and EA who were admitted to the neonatal intensive care unit between 1990 and 2007. RESULTS The rate of prenatal diagnosis wa...

full text

Three-year follow up of patients with esophageal atresia in Mashhad, Iran

Introduction:  Esophageal atresia is one of the most significant congenital diseases in pediatric surgery. Postoperative complications have become an important issue. Additionally, the little data are about life quality of baby's that had been surgery. The aim of our study was to analyze and evaluating the long- term life quality of subjects. Methods: We performed an observational study of the...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 9  issue 1

pages  1- 11

publication date 1995-05

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023