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Erschienen in: Surgical Endoscopy 5/2011

01.05.2011

Laparoscopic versus Open Roux-en-Y hepatojejunostomy for children with choledochal cysts: intermediate-term follow-up results

verfasst von: Mei Diao, Long Li, Wei Cheng

Erschienen in: Surgical Endoscopy | Ausgabe 5/2011

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Abstract

Background

Laparoscopic hepatojejunostomy (LH) for children with choledochal cysts (CDC) has been gaining popularity recently. However, its safety and efficacy remain unknown. The purpose of this study was to evaluate the intermediate-term results of LH for CDC children.

Methods

We reviewed 218 patients who underwent LH between October 2001 and October 2009 and 200 patients who underwent open hepatojejunostomy (OH) between September 1993 and September 2001. Ultrasonography, upper gastrointestinal contrast studies, and laboratory tests were performed during the follow-up period. Age, operative blood loss, operative time, postoperative hospital stay, time to full feed, duration of drainage, postoperative complications, and perioperative laboratory tests were evaluated in both groups.

Results

The median follow-up periods of the LH and OH groups were 38 and 146 months, respectively. There was no significant difference in age between the two groups. Interestingly, the operative time of the LH group decreased significantly with increasing number of cases (P < 0.01). The most recent operative time of the LH group did not differ from that of the OH group (3.04 vs. 2.95 h, P = 0.557). The operative blood loss of the LH group was significantly less (P < 0.001). The postoperative hospital stay, resumption of alimentation, and duration of drainage in the LH group were significantly shorter (P < 0.001, respectively). Two of 218 (0.9%) LH patients developed bile leak. This was significantly less than 11 of 200 (5.5%) in the OH group (P < 0.01). The morbidities of LH group were significantly lower than those of the OH group. Postoperative liver function tests and serum amylase levels normalized in both groups (P < 0.001).

Conclusions

Laparoscopic hepatojejunostomy is safe and effective. Its intermediate-term results are comparable to open surgery.
Literatur
1.
Zurück zum Zitat Ohi R, Yaoita S, Kamiyama T, Ibrahim M, Hayashi Y, Chiba T (1990) Surgical treatment of congenital dilatation of the bile duct with special reference to late complications after total excisional operation. J Pediatr Surg 25:613–617PubMedCrossRef Ohi R, Yaoita S, Kamiyama T, Ibrahim M, Hayashi Y, Chiba T (1990) Surgical treatment of congenital dilatation of the bile duct with special reference to late complications after total excisional operation. J Pediatr Surg 25:613–617PubMedCrossRef
2.
Zurück zum Zitat Martinez-Ferro M, Esteves E, Laje P (2005) Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 14:206–215PubMedCrossRef Martinez-Ferro M, Esteves E, Laje P (2005) Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 14:206–215PubMedCrossRef
3.
Zurück zum Zitat Lee H, Hirose S, Bratton B, Farmer D (2004) Initial experience with complex laparoscopic biliary surgery in children: biliary atresia and choledochal cyst. J Pediatr Surg 39:804–807; discussion 804–807 Lee H, Hirose S, Bratton B, Farmer D (2004) Initial experience with complex laparoscopic biliary surgery in children: biliary atresia and choledochal cyst. J Pediatr Surg 39:804–807; discussion 804–807
4.
Zurück zum Zitat Aspelund G, Ling SC, Ng V, Kim PC (2007) A role for laparoscopic approach in the treatment of biliary atresia and choledochal cysts. J Pediatr Surg 42:869–872PubMedCrossRef Aspelund G, Ling SC, Ng V, Kim PC (2007) A role for laparoscopic approach in the treatment of biliary atresia and choledochal cysts. J Pediatr Surg 42:869–872PubMedCrossRef
5.
Zurück zum Zitat Miyano T, Li L, Yamataka A (2009) Choledochal cyst. In: Gupta DK, Sharma S, Azizkhan RG (eds) Pediatric surgery, diagnosis and management. Jayee Brothers, New Delhi, India, pp 1013–1025 Miyano T, Li L, Yamataka A (2009) Choledochal cyst. In: Gupta DK, Sharma S, Azizkhan RG (eds) Pediatric surgery, diagnosis and management. Jayee Brothers, New Delhi, India, pp 1013–1025
6.
Zurück zum Zitat Diao M, Li L, Zhang J-Z, Cheng W (2010) A shorter loop in Roux-Y hepatojejunostomy reconstruction for choledochal cysts is equally effective: preliminary results of a prospective randomized study. J Pediatr Surg 45:845–847 Diao M, Li L, Zhang J-Z, Cheng W (2010) A shorter loop in Roux-Y hepatojejunostomy reconstruction for choledochal cysts is equally effective: preliminary results of a prospective randomized study. J Pediatr Surg 45:845–847
7.
Zurück zum Zitat Farello GA, Cerofolini A, Rebonato M, Bergamaschi G, Ferrari C, Chiappetta A (1995) Congenital choledochal cyst: video-guided laparoscopic treatment. Surg Laparosc Endosc 5:354–358PubMed Farello GA, Cerofolini A, Rebonato M, Bergamaschi G, Ferrari C, Chiappetta A (1995) Congenital choledochal cyst: video-guided laparoscopic treatment. Surg Laparosc Endosc 5:354–358PubMed
8.
Zurück zum Zitat Ure BM, Schier F, Schmidt AI, Nustede R, Petersen C, Jesch NK (2005) Laparoscopic resection of congenital choledochal cyst, choledochojejunostomy, and extraabdominal Roux-en-Y anastomosis. Surg Endosc 19:1055–1057PubMedCrossRef Ure BM, Schier F, Schmidt AI, Nustede R, Petersen C, Jesch NK (2005) Laparoscopic resection of congenital choledochal cyst, choledochojejunostomy, and extraabdominal Roux-en-Y anastomosis. Surg Endosc 19:1055–1057PubMedCrossRef
9.
Zurück zum Zitat She WH, Chung HY, Lan LC, Wong KK, Saing H, Tam PK (2009) Management of choledochal cyst: 30 years of experience and results in a single center. J Pediatr Surg 44:2307–2311PubMedCrossRef She WH, Chung HY, Lan LC, Wong KK, Saing H, Tam PK (2009) Management of choledochal cyst: 30 years of experience and results in a single center. J Pediatr Surg 44:2307–2311PubMedCrossRef
Metadaten
Titel
Laparoscopic versus Open Roux-en-Y hepatojejunostomy for children with choledochal cysts: intermediate-term follow-up results
verfasst von
Mei Diao
Long Li
Wei Cheng
Publikationsdatum
01.05.2011
Verlag
Springer-Verlag
Erschienen in
Surgical Endoscopy / Ausgabe 5/2011
Print ISSN: 0930-2794
Elektronische ISSN: 1432-2218
DOI
https://doi.org/10.1007/s00464-010-1435-x

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