Thoracoscopic treatment for delayed presentation of congenital diaphragmatic hernia in the infant - A report of three cases

Citation
F. Becmeur et al., Thoracoscopic treatment for delayed presentation of congenital diaphragmatic hernia in the infant - A report of three cases, SURG ENDOSC, 15(10), 2001, pp. 1163-1166
Citations number
11
Categorie Soggetti
Surgery
Journal title
SURGICAL ENDOSCOPY-ULTRASOUND AND INTERVENTIONAL TECHNIQUES
ISSN journal
09302794 → ACNP
Volume
15
Issue
10
Year of publication
2001
Pages
1163 - 1166
Database
ISI
SICI code
0930-2794(200110)15:10<1163:TTFDPO>2.0.ZU;2-F
Abstract
Background: Delayed presentations of congenital hernia occurring outside of the neonatal period have been reported for all ages. Classically, repair o f the hernia defect involves a transverse subcostal laparotomy in the pedia tric age group and usually a thoracotomy in the adult. The first report des cribing a laparoscopic repair of a congenital diaphragmatic hernia in a 6-m onth-old infant was published in 1995. During the past 25 years, 17 patient s with delayed presentation of congenital diaphragmatic hernias have been m anaged by our pediatric surgery team. The last three patients underwent sur gery thoracoscopically. Patients and Methods: This study involved two boys (ages, 8.3 and 19 months , respectively) and one girl (age, 9 months) weighing 8 to 13 kg. All three infants underwent surgery using a thoracoscopic approach with general anes thesia. A thoracic epidural catheter was placed systematically for postoper ative analgesia during the first 24 hours. Reduction of the hernia contents using one optical trocar and two operating trocars was difficult in the ca se without any hernia sac. In the cases with a hernia sac, reduction was ea sily and quickly obtained with a pleural insufflation of carbon dioxide (si milar to8 mmHg). The hernia defect was repaired using interrupted sutures o f 2/0 Ethibond. For two of the three patients, this repair was reinforced w ith staples in the one case and a nonresorbable mesh in the other case. Results: The mean operative time was 78 min. The chest tube was removed on the first or second postoperative day and the patients were discharged on t he fourth or fifth postoperative day. At the 19-month follow-up assessment in one case, the chest x-ray was perfectly normal and diaphragmatic motion also was confirmed to be normal by ultrasonography. Conclusions: The thoracoscopic approach for the repair of delayed-presentat ion congenital diaphragmatic hernia is feasible. Our results demonstrate th e safety and efficiency of this surgery, as well as a remarkable functional and cosmetic result and a very quick recovery.