Surgical treatment of 125 cases of congenital diaphragmatic eventration in a single institution

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RESEARCH ARTICLE

Open Access

Surgical treatment of 125 cases of congenital diaphragmatic eventration in a single institution Shengliang Zhao1,2,3,4, Zhengxia Pan1,2,3,4,5, Yonggang Li1,2,3,4,5, Yong An1,2,3,4,5, Lu Zhao1,2,3,4, Xin Jin1,2,3,4, Jian Fu1,2,3,4 and Chun Wu1,2,3,4,5,6*

Abstract  Background:  This study sought to investigate the clinical characteristics of congenital diaphragmatic eventration (CDE) and to compare the efficacies of thoracoscopy and traditional open surgery in infants with CDE. Methods:  We retrospectively analyzed the clinical data of 125 children with CDE (90 boys, 35 girls; median age: 12.2 months, range: 1 h-7 years; body weight: 1.99–28.5 kg, median body weight: 7.87 ± 4.40 kg) admitted to our hospital in the previous 10 years, and we statistically analyzed their clinical manifestations and surgical methods. Results:  A total of 108 children in this group underwent surgery, of whom 67 underwent open surgery and 41 underwent thoracoscopic diaphragmatic plication. A total of 107 patients recovered well postoperatively, except for 1 patient who died due to respiratory distress after surgery. After 1–9.5 years of follow-up, 107 patients had significantly improved preoperative symptoms. During follow-up, the location of the diaphragm was normal, and no paradoxical movement was observed. Eleven of the 17 children who did not undergo surgical treatment did not have a decrease in diaphragm position after 1–6 years of follow-up. The index data on the operation time, intraoperative blood loss, chest drainage time, postoperative mechanical ventilation time, postoperative hospital stay and postoperative CCU admission time were better in the thoracoscopy group than in the open group. The difference between the two groups was statistically significant (P