G. Fasching1, A. Huber2, E. Uray2, E. Sorantin3, F. Lindbichler3, J. Mayr2
{"title":"Gastroesophageal Reflux and Diaphragmatic Motility after Repair of Congenital Diaphragmatic Hernia","authors":"G. Fasching1, A. Huber2, E. Uray2, E. Sorantin3, F. Lindbichler3, J. Mayr2","doi":"10.1055/s-2008-1072391","DOIUrl":null,"url":null,"abstract":"Summary At the Department of Pediatric Surgery in Graz, 31 boys and 23 girls were operated on for congenital diaphragmatic hernia (CDH) from 1978 to 1994. In 49 patients the defect was on the left, in five on the right side. In 46 cases, the hernia was diag nosed within the first week of life; in eight children at a later date. 19 children (35 %) died. 25 of the 35 survivors (71 %) came to a follow-up examination on average 9.4 (1-17) years after the operation. 24 h pH-monitoring or manometry and Upper G.I. series revealed pathological gastroesophageal reflux (GER) in 16 patients. Nine children were treated conservatively; in seven patients an antireflux procedure was performed. A tho racic position of the stomach or left Iiver lobe, presence of a hernial sac, gestational age, prenatal diagnosis, use of a patch or severity of lung hypoplasia did not significantly influence the incidence of GER. In three patients, a hiatal hernia was found. The motility of the diaphragm was documented with M-mode sonography (n = 18); arestricted motility could be demonstrat ed in five patients. GER is very common in patients after repair of CDH. We recommend long-term follow-up with special inter est in respect of GER.","PeriodicalId":269806,"journal":{"name":"European Journal of Pediatric Surgery (EJPS)","volume":"8 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2000-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"75","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pediatric Surgery (EJPS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-2008-1072391","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 75
Abstract
Summary At the Department of Pediatric Surgery in Graz, 31 boys and 23 girls were operated on for congenital diaphragmatic hernia (CDH) from 1978 to 1994. In 49 patients the defect was on the left, in five on the right side. In 46 cases, the hernia was diag nosed within the first week of life; in eight children at a later date. 19 children (35 %) died. 25 of the 35 survivors (71 %) came to a follow-up examination on average 9.4 (1-17) years after the operation. 24 h pH-monitoring or manometry and Upper G.I. series revealed pathological gastroesophageal reflux (GER) in 16 patients. Nine children were treated conservatively; in seven patients an antireflux procedure was performed. A tho racic position of the stomach or left Iiver lobe, presence of a hernial sac, gestational age, prenatal diagnosis, use of a patch or severity of lung hypoplasia did not significantly influence the incidence of GER. In three patients, a hiatal hernia was found. The motility of the diaphragm was documented with M-mode sonography (n = 18); arestricted motility could be demonstrat ed in five patients. GER is very common in patients after repair of CDH. We recommend long-term follow-up with special inter est in respect of GER.