Eur J Pediatr Surg 2018; 28(02): 156-162
DOI: 10.1055/s-0038-1636929
Review Article
Georg Thieme Verlag KG Stuttgart · New York

Perioperative Complications in Neonatal Surgery: Biliary Atresia and Choledochal Malformations

Jim C. H. Wilde
1   Division of Pediatric Surgery, Hopitaux Universitaires de Geneve, Geneva, Switzerland
,
Ana M. Calinescu
1   Division of Pediatric Surgery, Hopitaux Universitaires de Geneve, Geneva, Switzerland
,
Barbara E. Wildhaber
1   Division of Pediatric Surgery, Hopitaux Universitaires de Geneve, Geneva, Switzerland
› Author Affiliations
Further Information

Publication History

29 January 2018

30 January 2018

Publication Date:
06 March 2018 (online)

Abstract

Biliary atresia (BA) and congenital choledochal malformations (CCM) are rare. Both pathologies must (BA) or may (CCM) be operated during the neonatal period or early infancy. We briefly describe the classical operative techniques for both pathologies, followed by the most common and severe perioperative complications encountered during and up to 30 days after surgery in children operated for BA and CCM early in life. For patients with BA, intestinal complications represent the most common and hazardous perioperative surgical complications. Cholangitis is the most frequently encountered medical complication post hepato-porto-enterostomy. For CCM, it seems that neonates encounter little perioperative complications; however, reports are scarce; bile leak and/or cholangitis are the most reported. Overall, for patients with CCM, the literature is ambivalent whether more perioperative complications occur in the younger or in the older patient, and whether these occur more frequently in those symptomatic or asymptomatic at operation. It is difficult to give clear advice for when children with asymptomatic CCM should be operated, and benefits and risks must be carefully counterbalanced. Perioperative mortality for both BA and CCM is low and is reported to be around 1 to 2%.

 
  • References

  • 1 Lakshminarayanan B, Davenport M. Biliary atresia: a comprehensive review. J Autoimmun 2016; 73: 1-9
  • 2 Lenriot JP, Gigot JF, Ségol P, Fagniez PL, Fingerhut A, Adloff M. ; French Associations for Surgical Research. Bile duct cysts in adults: a multi-institutional retrospective study. Ann Surg 1998; 228 (02) 159-166
  • 3 Soares KC, Arnaoutakis DJ, Kamel I. , et al. Choledochal cysts: presentation, clinical differentiation, and management. J Am Coll Surg 2014; 219 (06) 1167-1180
  • 4 She WH, Chung HY, Lan LC, Wong KK, Saing H, Tam PK. Management of choledochal cyst: 30 years of experience and results in a single center. J Pediatr Surg 2009; 44 (12) 2307-2311
  • 5 Chan KW, Lee KH, Tsui SY, Mou JW, Tam YH. Laparoscopic management of antenatally detected choledochal cyst: a 10-year review. Surg Endosc 2016; 30 (12) 5494-5499
  • 6 Blazer S, Zimmer EZ, Bronshtein M. Nonvisualization of the fetal gallbladder in early pregnancy: comparison with clinical outcome. Radiology 2002; 224 (02) 379-382
  • 7 Bronshtein M, Weiner Z, Abramovici H, Filmar S, Erlik Y, Blumenfeld Z. Prenatal diagnosis of gall bladder anomalies--report of 17 cases. Prenat Diagn 1993; 13 (09) 851-861
  • 8 Serinet MO, Wildhaber BE, Broué P. , et al. Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Pediatrics 2009; 123 (05) 1280-1286
  • 9 Stey AM, Kenney BD, Moss RL. , et al. A risk calculator predicting postoperative adverse events in neonates undergoing major abdominal or thoracic surgery. J Pediatr Surg 2015; 50 (06) 987-991
  • 10 Kasai M, Suzuki S. A new operation for non-correctable biliary atresia: hepatic portoenterostomy. Shuiyutsu 1959; 13: 733-739
  • 11 Wildhaber BE. Biliary atresia: 50 years after the first kasai. ISRN Surg 2012; 2012: 132089
  • 12 Ito T, Nagaya M, Ando H, Niinomi N, Iyomasa Y. Modified hepatic portal enterostomy for biliary atresia. Z Kinderchir 1984; 39 (04) 242-245
  • 13 Toyosaka A, Okamoto E, Okasora T, Nose K, Tomimoto Y, Seki Y. Extensive dissection at the porta hepatis for biliary atresia. J Pediatr Surg 1994; 29 (07) 896-899
  • 14 Endo M, Katsumata K, Yokoyama J. , et al. Extended dissection of the portahepatis and creation of an intussuscepted ileocolic conduit for biliary atresia. J Pediatr Surg 1983; 18 (06) 784-793
  • 15 Hashimoto T, Otobe Y, Shimizu Y. , et al. A modification of hepatic portoenterostomy (Kasai operation) for biliary atresia. J Am Coll Surg 1997; 185 (06) 548-553
  • 16 Suzuki T, Hashimoto T, Kondo S, Sato Y, Hussein MH. Evaluating patients' outcome post-Kasai operation: a 19-year experience with modification of the hepatic portoenterostomy and applying a novel steroid therapy regimen. Pediatr Surg Int 2010; 26 (08) 825-830
  • 17 Ando H, Seo T, Ito F. , et al. A new hepatic portoenterostomy with division of the ligamentum venosum for treatment of biliary atresia: a preliminary report. J Pediatr Surg 1997; 32 (11) 1552-1554
  • 18 Nakajo T, Hashizume K, Saeki M, Tsuchida Y. Intussusception-type antireflux valve in the Roux-en-Y loop to prevent ascending cholangitis after hepatic portojejunostomy. J Pediatr Surg 1990; 25 (03) 311-314
  • 19 Saeki M, Nakano M, Hagane K. [Early complications after hepatic porto-jejunostomy in biliary atresia] [Article in Japanese]. Nippon Geka Gakkai Zasshi 1989; 90 (09) 1353-1356
  • 20 Sawaguchi S, Nakajo T, Hori T. , et al. Reconstruction of the biliary tract in biliary atresia using jejunal conduit. J Jpn Slirg Soc 1968; 69: 13-17
  • 21 Suruga K, Miyano T, Kitahara T, Kojima Y, Fukuda Y. Treatment of biliary atresia: a study of our operative results. J Pediatr Surg 1981; 16 (04) (Suppl. 01) 621-626
  • 22 Esteves E, Clemente Neto E, Ottaiano Neto M, Devanir Jr J, Esteves Pereira R. Laparoscopic Kasai portoenterostomy for biliary atresia. Pediatr Surg Int 2002; 18 (08) 737-740
  • 23 Koga H, Miyano G, Takahashi T. , et al. Laparoscopic portoenterostomy for uncorrectable biliary atresia using Kasai's original technique. J Laparoendosc Adv Surg Tech A 2011; 21 (03) 291-294
  • 24 Ure BM, Kuebler JF, Schukfeh N, Engelmann C, Dingemann J, Petersen C. Survival with the native liver after laparoscopic versus conventional kasai portoenterostomy in infants with biliary atresia: a prospective trial. Ann Surg 2011; 253 (04) 826-830
  • 25 Oetzmann von Sochaczewski C, Petersen C, Ure BM. , et al. Laparoscopic versus conventional Kasai portoenterostomy does not facilitate subsequent liver transplantation in infants with biliary atresia. J Laparoendosc Adv Surg Tech A 2012; 22 (04) 408-411
  • 26 Madadi-Sanjani O, Petersen C, Ure B. Minimally invasive hepatobiliary surgery. Clin Perinatol 2017; 44 (04) 805-818
  • 27 Hussain MH, Alizai N, Patel B. Outcomes of laparoscopic Kasai portoenterostomy for biliary atresia: a systematic review. J Pediatr Surg 2017; 52 (02) 264-267
  • 28 Chan KW, Lee KH, Wong HY. , et al. From laparoscopic to open Kasai portoenterostomy: the outcome after reintroduction of open Kasai portoenterostomy in infant with biliary atresia. Pediatr Surg Int 2014; 30 (06) 605-608
  • 29 Kasai M, Suzuki H, Ohashi E, Ohi R, Chiba T, Okamoto A. Technique and results of operative management of biliary atresia. World J Surg 1978; 2 (05) 571-579
  • 30 Odiévre M, Valayer J, Razemon-Pinta M, Habib EC, Alagille D. Hepatic porto-enterostomy or cholecystostomy in the treatment of extrahepatic biliary atresia. A study of 49 cases. J Pediatr 1976; 88 (05) 774-779
  • 31 Madadi-Sanjani O, Carl N, Longerich T, Petersen C, Andruszkow JH. Inguinal hernias represent the most frequent surgical complication after Kasai in biliary atresia infants. BioMed Res Int 2015; 2015: 383791
  • 32 Moon SB, Park KW, Jae HJ, Jung SE. Caudate arterial branch bleeding: a rare complication after a Kasai portoenterostomy. J Pediatr Surg 2009; 44 (07) e27-e30
  • 33 Hernandez-Cano AM, Geis JR, Rumack CH, Stellin GP, Lilly JR. Portal vein dynamics in biliary atresia. J Pediatr Surg 1987; 22 (06) 519-521
  • 34 Ohuchi N, Ohi R, Takahashi T, Kasai M. Postoperative changes of intrahepatic portal veins in biliary atresia–a 3-D reconstruction study. J Pediatr Surg 1986; 21 (01) 10-14
  • 35 Chen CC, Huang SC, Huang SC, Shieh CS. Retrograde intussusception as a complication of Roux-en-Y anastomosis for choledochal cyst--report of one case. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1994; 35 (06) 546-551
  • 36 Li M, Jin Q, Feng J. [Early postoperative complications of choledochal cyst excision and reconstruction of biliary tract] [Article in Chinese]. Zhonghua Wai Ke Za Zhi 2001; 39 (09) 686-689
  • 37 Eberhardt CS, Merlini L, McLin VA, Wildhaber BE. Cholestasis as the leading sign of a transmesenteric hernia in a split-liver transplanted child - a case report and review of literature. Pediatr Transplant 2012; 16 (05) E172-E176
  • 38 Liu CL, Lo CM, Chan SC, Fan ST, Wong J. Internal hernia of the small bowel after right-lobe live donor liver transplantation. Clin Transplant 2004; 18 (02) 211-213
  • 39 Altman RP, Anderson KD. Surgical management of intractable cholangitis following successful Kasai procedure. J Pediatr Surg 1982; 17 (06) 894-900
  • 40 Houben C, Phelan S, Davenport M. Late-presenting cholangitis and Roux loop obstruction after Kasai portoenterostomy for biliary atresia. J Pediatr Surg 2006; 41 (06) 1159-1164
  • 41 Zani A, Davenport M. Inguinal hernias associated with biliary atresia. Eur J Pediatr Surg 2012; 22 (02) 117-120
  • 42 Joob B, Wiwanitkit V. Biliary atresia and inguinal hernia. Eur J Pediatr Surg 2012; 22 (06) 488-489
  • 43 Luo Y, Zheng S. Current concept about postoperative cholangitis in biliary atresia. World J Pediatr 2008; 4 (01) 14-19
  • 44 Rumsey S, Winders J, MacCormick AD. Diagnostic accuracy of Charcot's triad: a systematic review. ANZ J Surg 2017; 87 (04) 232-238
  • 45 Wildhaber BE, Coran AG, Drongowski RA. , et al. The Kasai portoenterostomy for biliary atresia: a review of a 27-year experience with 81 patients. J Pediatr Surg 2003; 38 (10) 1480-1485
  • 46 Chung PH, Wong KK, Tam PK. Predictors for failure after Kasai operation. J Pediatr Surg 2015; 50 (02) 293-296
  • 47 Decharun K, Leys CM, West KW, Finnell SM. Prophylactic antibiotics for prevention of cholangitis in patients with biliary atresia status post-Kasai portoenterostomy: a systematic review. Clin Pediatr (Phila) 2016; 55 (01) 66-72
  • 48 Lünzmann K, Schweizer P. The influence of cholangitis on the prognosis of extrahepatic biliary atresia. Eur J Pediatr Surg 1999; 9 (01) 19-23
  • 49 Yanchar NL, Shapiro AM, Sigalet DL. Is early response to portoenterostomy predictive of long-term outcome for patients with biliary atresia?. J Pediatr Surg 1996; 31 (06) 774-778
  • 50 Wu ET, Chen HL, Ni YH. , et al. Bacterial cholangitis in patients with biliary atresia: impact on short-term outcome. Pediatr Surg Int 2001; 17 (5-6): 390-395
  • 51 Nio M, Wada M, Sasaki H, Kazama T, Tanaka H, Kudo H. Technical standardization of Kasai portoenterostomy for biliary atresia. J Pediatr Surg 2016; 51 (12) 2105-2108
  • 52 Petrowsky H, Demartines N, Rousson V, Clavien PA. Evidence-based value of prophylactic drainage in gastrointestinal surgery: a systematic review and meta-analyses. Ann Surg 2004; 240 (06) 1074-1084 , discussion 1084–1085
  • 53 Hwang JB, Choi SO, Park WH. Resolution of refractory chylous ascites after Kasai portoenterostomy using octreotide. J Pediatr Surg 2004; 39 (12) 1806-1807
  • 54 Matsuo S, Suita S, Kubota M, Shono K, Kamimura T, Kinugasa Y. Hazards of hepatic portocholecystostomy in biliary atresia. Eur J Pediatr Surg 2001; 11 (01) 19-23
  • 55 Karrer FM, Lilly JR, Stewart BA, Hall RJ. Biliary atresia registry, 1976 to 1989. J Pediatr Surg 1990; 25 (10) 1076-1080
  • 56 Hery G, Gonzales E, Bernard O, Fouquet V, Gauthier F, Branchereau S. Hepatic portocholecystostomy: 97 cases from a single institution. J Pediatr Gastroenterol Nutr 2017; 65 (04) 375-379
  • 57 Gauthier F, Brunelle F, Bernard O, Montupet P, Valayer J. [Choleperitonitis after hepatoportocholecystostomy for atresia of the biliary tract] [Article in French]. Chir Pediatr 1984; 25 (02) 90-94
  • 58 Johnson KN, Koontz CS, Ricketts RR. Role of hepatic portocholecystostomy (‘gallbladder Kasai’) in treating infants with biliary atresia. Am Surg 2010; 76 (08) 883-887
  • 59 Clavien PA, Barkun J, de Oliveira ML. , et al. The Clavien-Dindo classification of surgical complications: five-year experience. Ann Surg 2009; 250 (02) 187-196
  • 60 Todani T, Watanabe Y, Narusue M, Tabuchi K, Okajima K. Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. Am J Surg 1977; 134 (02) 263-269
  • 61 Soares KC, Goldstein SD, Ghaseb MA, Kamel I, Hackam DJ, Pawlik TM. Pediatric choledochal cysts: diagnosis and current management. Pediatr Surg Int 2017; 33 (06) 637-650
  • 62 Farello GA, Cerofolini A, Rebonato M, Bergamaschi G, Ferrari C, Chiappetta A. Congenital choledochal cyst: video-guided laparoscopic treatment. Surg Laparosc Endosc 1995; 5 (05) 354-358
  • 63 Zhen C, Xia Z, Long L. , et al. Laparoscopic excision versus open excision for the treatment of choledochal cysts: a systematic review and meta-analysis. Int Surg 2015; 100 (01) 115-122
  • 64 Diao M, Li L, Cheng W. Laparoscopic versus Open Roux-en-Y hepatojejunostomy for children with choledochal cysts: intermediate-term follow-up results. Surg Endosc 2011; 25 (05) 1567-1573
  • 65 Ure BM, Schier F, Schmidt AI, Nustede R, Petersen C, Jesch NK. Laparoscopic resection of congenital choledochal cyst, choledochojejunostomy, and extraabdominal Roux-en-Y anastomosis. Surg Endosc 2005; 19 (08) 1055-1057
  • 66 Matsumoto M, Urushihara N, Fukumoto K, Yamoto M, Miyake H, Nakajima H. Laparoscopic management for prenatally diagnosed choledochal cysts. Surg Today 2016; 46 (12) 1410-1414
  • 67 Narayanan SK, Chen Y, Narasimhan KL, Cohen RC. Hepaticoduodenostomy versus hepaticojejunostomy after resection of choledochal cyst: a systematic review and meta-analysis. J Pediatr Surg 2013; 48 (11) 2336-2342
  • 68 Vutskits L, Xie Z. Lasting impact of general anaesthesia on the brain: mechanisms and relevance. Nat Rev Neurosci 2016; 17 (11) 705-717
  • 69 Vutskits L, Davidson A. Update on developmental anesthesia neurotoxicity. Curr Opin Anaesthesiol 2017; 30 (03) 337-342
  • 70 Diao M, Li L, Cheng W. Timing of surgery for prenatally diagnosed asymptomatic choledochal cysts: a prospective randomized study. J Pediatr Surg 2012; 47 (03) 506-512
  • 71 Lee SC, Kim HY, Jung SE, Park KW, Kim WK. Is excision of a choledochal cyst in the neonatal period necessary?. J Pediatr Surg 2006; 41 (12) 1984-1986
  • 72 Lugo-Vicente HL. Prenatally diagnosed choledochal cysts: observation or early surgery?. J Pediatr Surg 1995; 30 (09) 1288-1290
  • 73 Ohtsuka Y, Yoshida H, Matsunaga T, Kouchi K, Okada T, Ohnuma N. Strategy of management for congenital biliary dilatation in early infancy. J Pediatr Surg 2002; 37 (08) 1173-1176
  • 74 Tanaka H, Sasaki H, Wada M. , et al. Postnatal management of prenatally diagnosed biliary cystic malformation. J Pediatr Surg 2015; 50 (04) 507-510
  • 75 Redkar R, Davenport M, Howard ER. Antenatal diagnosis of congenital anomalies of the biliary tract. J Pediatr Surg 1998; 33 (05) 700-704
  • 76 Okada T, Sasaki F, Ueki S. , et al. Postnatal management for prenatally diagnosed choledochal cysts. J Pediatr Surg 2004; 39 (07) 1055-1058
  • 77 van den Eijnden MHA, de Kleine RH, de Blaauw I. , et al; Netherlands Study Group for Choledochus Cysts/Malformations (NeSCHoC). The timing of surgery of antenatally diagnosed choledochal malformations: a descriptive analysis of a 26-year nationwide cohort. J Pediatr Surg 2017; 52 (07) 1156-1160
  • 78 Li MJ, Feng JX, Jin QF. Early complications after excision with hepaticoenterostomy for infants and children with choledochal cysts. Hepatobiliary Pancreat Dis Int 2002; 1 (02) 281-284
  • 79 Vijayaraghavan P, Lal R, Sikora SS, Poddar U, Yachha SK. Experience with choledochal cysts in infants. Pediatr Surg Int 2006; 22 (10) 803-807
  • 80 Chen CJ. Clinical and operative findings of choledochal cysts in neonates and infants differ from those in older children. Asian J Surg 2003; 26 (04) 213-217