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Erschienen in: Surgical Endoscopy 8/2020

04.09.2019

Laparoscopic Kasai portoenterostomy is advantageous over open Kasai portoenterostomy in subsequent liver transplantation

verfasst von: Chiyoe Shirota, Naruhiko Murase, Yujiro Tanaka, Yasuhiro Ogura, Masahiro Nakatochi, Hideya Kamei, Nobuhiko Kurata, Akinari Hinoki, Takahisa Tainaka, Wataru Sumida, Kazuki Yokota, Satoshi Makita, Kazuo Oshima, Hiroo Uchida

Erschienen in: Surgical Endoscopy | Ausgabe 8/2020

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Abstract

Background

Native liver survival after laparoscopic Kasai portoenterostomy (Lap-PE) for biliary atresia (BA) is controversial. We examined whether a jaundice-free native liver survival rate is comparable between conventional Kasai portoenterostomy (Open-PE) and Lap-PE. Then, the impact of the two types of PE on subsequent living-donor liver transplantation (LTx) was addressed in this study.

Methods

The jaundice-free rate in 1- and 2-year-old patients who underwent Open-PE and Lap-PE from January 2006 to December 2017 was investigated. Additionally, perioperative data (duration from the start of surgery to the completion of hepatectomy and others) of patients aged 2 years or younger who underwent LTx after either Open-PE or Lap-PE from 2006 to 2017 were evaluated.

Results

Thirty-one (67%) out of 46 Open-PE patients and 23 (77%) out of 30 Lap-PE patients showed native liver survival with jaundice-free status at 1 year of age (p = 0.384); 29 (63%) out of 46 Open-PE patients and 19 (70%) out of 27 Lap-PE patients showed native liver survival with jaundice-free status at 2 years of age (p = 0.524); there were no significant differences. Additionally, there were 37 LTx cases after PE within 2 years of birth, including 29 Open-PE and 8 Lap-PE cases. The patients in the Lap-PE group had fewer adhesions and significantly shorter durations of surgery up to the completion of the recipient’s hepatectomy and durations of post-LTx hospital stay compared to the Open-PE group. There were no differences in blood loss or duration of stay in intensive care unit between the Lap-PE and Open-PE groups.

Conclusions

Jaundice-free native liver survival rate has been comparable between Open-PE and Lap-PE. Lap-PE resulted in fewer adhesions, contributing to better outcomes of subsequent LTx compared to Open-PE.
Literatur
1.
Zurück zum Zitat van der Zee DC, Gallo G, Tytgat SHA (2015) Thoracoscopic traction technique in long gap esophageal atresia: entering a new era. Surg Endosc 29:3324–3330CrossRef van der Zee DC, Gallo G, Tytgat SHA (2015) Thoracoscopic traction technique in long gap esophageal atresia: entering a new era. Surg Endosc 29:3324–3330CrossRef
2.
Zurück zum Zitat Le DM, Woo RK, Sylvester K, Krummel TM, Albanese CT (2006) Laparoscopic resection of type 1 choledochal cysts in pediatric patients. Surg Endosc 20:249–251CrossRef Le DM, Woo RK, Sylvester K, Krummel TM, Albanese CT (2006) Laparoscopic resection of type 1 choledochal cysts in pediatric patients. Surg Endosc 20:249–251CrossRef
3.
Zurück zum Zitat Ure B, Kuebler J, Schukfeh N, Engelmann C, Dingemann J, Petersen C (2011) Survival with the native liver after laparoscopic versus conventional Kasai portoenterostomy in infants with biliary atresia: a prospective trial. Ann Surg 253:826–830CrossRef Ure B, Kuebler J, Schukfeh N, Engelmann C, Dingemann J, Petersen C (2011) Survival with the native liver after laparoscopic versus conventional Kasai portoenterostomy in infants with biliary atresia: a prospective trial. Ann Surg 253:826–830CrossRef
4.
Zurück zum Zitat Dutta S, Woo R, Albanese C (2007) Minimal access portoenterostomy: advantages and disadvantages of standard laparoscopic and robotic techniques. J Laparoendosc 172:258–264CrossRef Dutta S, Woo R, Albanese C (2007) Minimal access portoenterostomy: advantages and disadvantages of standard laparoscopic and robotic techniques. J Laparoendosc 172:258–264CrossRef
5.
Zurück zum Zitat Murase N, Hinoki A, Shirota C, Tomita H, Shimojima N, Sasaki H, Nio M, Tahara K, Kanamori Y, Shinkai M, Yamamoto H, Sugawara Y, Hibi T, Ishimaru T, Kawashima H, Koga H, Yamataka A, Uchida H (2019) Multicenter, retrospective, comparative study of laparoscopic and open Kasai portoenterostomy in children with biliary atresia from Japanese high-volume centers. J Hepatobiliary Pancreat Sci 26:43–50CrossRef Murase N, Hinoki A, Shirota C, Tomita H, Shimojima N, Sasaki H, Nio M, Tahara K, Kanamori Y, Shinkai M, Yamamoto H, Sugawara Y, Hibi T, Ishimaru T, Kawashima H, Koga H, Yamataka A, Uchida H (2019) Multicenter, retrospective, comparative study of laparoscopic and open Kasai portoenterostomy in children with biliary atresia from Japanese high-volume centers. J Hepatobiliary Pancreat Sci 26:43–50CrossRef
8.
Zurück zum Zitat Nio M, Sasaki H, Wada M, Kazama T, Nishi K, Tanaka H (2010) Impact of age at Kasai operation on short- and long-term outcomes of type III biliary atresia at a single institution. J Pediatr Surg 45:2361–2363CrossRef Nio M, Sasaki H, Wada M, Kazama T, Nishi K, Tanaka H (2010) Impact of age at Kasai operation on short- and long-term outcomes of type III biliary atresia at a single institution. J Pediatr Surg 45:2361–2363CrossRef
9.
Zurück zum Zitat Ibrahim M, Miyano T, Ohi R, Saeki M, Shiraki K, Tanaka K, Kamiyama T, Nio M (1997) Japanese biliary atresia registry, 1989 to 1994. Tohoku J Exp Med 181:85–957CrossRef Ibrahim M, Miyano T, Ohi R, Saeki M, Shiraki K, Tanaka K, Kamiyama T, Nio M (1997) Japanese biliary atresia registry, 1989 to 1994. Tohoku J Exp Med 181:85–957CrossRef
10.
Zurück zum Zitat Toyosaka A, Okamoto E, Okasora T, Nose K, Tomimoto Y (1993) Outcome of 21 patients with biliary atresia living more than 10 years. J Pediatr Surg 28:1498–1501CrossRef Toyosaka A, Okamoto E, Okasora T, Nose K, Tomimoto Y (1993) Outcome of 21 patients with biliary atresia living more than 10 years. J Pediatr Surg 28:1498–1501CrossRef
11.
Zurück zum Zitat Qiao G, Li L, Cheng W, Zhang Z, Ge J, Wang C (2015) Conditional probability of survival in patients with biliary atresia after Kasai portoenterostomy: a Chinese population-based study. J Pediatr Surg 50:1310–1315CrossRef Qiao G, Li L, Cheng W, Zhang Z, Ge J, Wang C (2015) Conditional probability of survival in patients with biliary atresia after Kasai portoenterostomy: a Chinese population-based study. J Pediatr Surg 50:1310–1315CrossRef
12.
Zurück zum Zitat Muraji T, Nishijima E, Higashimoto Y, Tsugawa C (1997) Biliary atresia: current management and outcome. Tohoku J Exp Med 181:155–160CrossRef Muraji T, Nishijima E, Higashimoto Y, Tsugawa C (1997) Biliary atresia: current management and outcome. Tohoku J Exp Med 181:155–160CrossRef
13.
Zurück zum Zitat Hussain MH, Alizai N, Patel B (2017) Outcomes of laparoscopic Kasai portoenterostomy for biliary atresia: a systematic review. J Pediatr Surg 52:264–267CrossRef Hussain MH, Alizai N, Patel B (2017) Outcomes of laparoscopic Kasai portoenterostomy for biliary atresia: a systematic review. J Pediatr Surg 52:264–267CrossRef
14.
Zurück zum Zitat Martinez-Ferro M, Esteves E, Laje P (2005) Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 14:206–215CrossRef Martinez-Ferro M, Esteves E, Laje P (2005) Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 14:206–215CrossRef
15.
Zurück zum Zitat Wong ZH, Davenport M (2019) What happens after Kasai for biliary atresia? A European multicenter survey. Eur J Pediatr Surg 29:1–6CrossRef Wong ZH, Davenport M (2019) What happens after Kasai for biliary atresia? A European multicenter survey. Eur J Pediatr Surg 29:1–6CrossRef
16.
Zurück zum Zitat Oetzmann von Sochaczewski C, Petersen C, Ure BM, Osthaus A, Schubert KP, Becker T, Lehner F, Kuebler JF (2012) Laparoscopic versus conventional Kasai portoenterostomy does not facilitate subsequent liver transplantation in infants with biliary atresia. Laparoendosc Adv Surg Tech 22(4):408–412CrossRef Oetzmann von Sochaczewski C, Petersen C, Ure BM, Osthaus A, Schubert KP, Becker T, Lehner F, Kuebler JF (2012) Laparoscopic versus conventional Kasai portoenterostomy does not facilitate subsequent liver transplantation in infants with biliary atresia. Laparoendosc Adv Surg Tech 22(4):408–412CrossRef
17.
Zurück zum Zitat Murase N, Uchida H, Ono Y, Tainaka T, Yokota K, Tanano A, Shirota C, Shirotsuki R (2015) A new era of laparoscopic revision of Kasai portoenterostomyfor the treatment of biliary atresia. Biomed Res Int 2015:173014CrossRef Murase N, Uchida H, Ono Y, Tainaka T, Yokota K, Tanano A, Shirota C, Shirotsuki R (2015) A new era of laparoscopic revision of Kasai portoenterostomyfor the treatment of biliary atresia. Biomed Res Int 2015:173014CrossRef
18.
Zurück zum Zitat Gallo A, Esquivel CO (2013) Current options for management of biliary atresia. Pediatr Transplant 17:95–98CrossRef Gallo A, Esquivel CO (2013) Current options for management of biliary atresia. Pediatr Transplant 17:95–98CrossRef
19.
Zurück zum Zitat Nakamura H, Koga H, Cazares J, Okazaki T, Lane GJ, Miyano G, Okawada M, Doi T, Urao M, Yamataka A (2016) A comprehensive assessment of prognosis after laparoscopic portoenterostomy for biliary atresia. J Pediatr Surg 32(2):109–112 Nakamura H, Koga H, Cazares J, Okazaki T, Lane GJ, Miyano G, Okawada M, Doi T, Urao M, Yamataka A (2016) A comprehensive assessment of prognosis after laparoscopic portoenterostomy for biliary atresia. J Pediatr Surg 32(2):109–112
20.
Zurück zum Zitat Shirota C, Uchida H, Ono Y, Murase N, Tainaka T, Yokota K, Oshima K, Shirotsuki R, Hinoki A, Ando H (2016) Long-term outcomes after revision of Kasai portoenterostomy for biliary atresia. J Hepatobiliary Pancreat Sci 23:715–720CrossRef Shirota C, Uchida H, Ono Y, Murase N, Tainaka T, Yokota K, Oshima K, Shirotsuki R, Hinoki A, Ando H (2016) Long-term outcomes after revision of Kasai portoenterostomy for biliary atresia. J Hepatobiliary Pancreat Sci 23:715–720CrossRef
21.
Zurück zum Zitat Nio M (2017) Japanese biliary atresia registry. Pediatr Surg Int 33:1319–1325CrossRef Nio M (2017) Japanese biliary atresia registry. Pediatr Surg Int 33:1319–1325CrossRef
22.
Zurück zum Zitat Nio M, Sasaki H, Tanaka H, Okamura A (2013) Redo surgery for biliary atresia. Pediatr Surg Int 29:989–993CrossRef Nio M, Sasaki H, Tanaka H, Okamura A (2013) Redo surgery for biliary atresia. Pediatr Surg Int 29:989–993CrossRef
23.
Zurück zum Zitat Mendoza MM, Chiang JH, Lee SY, Kao CY, Chuang JH, Tiao MM, Hsieh CS (2012) Reappraise the effect of redo-Kasai for recurrent jaundice following Kasai operation for biliary atresia in the era of liver transplantation. Pediatr Surg Int 28:861–864CrossRef Mendoza MM, Chiang JH, Lee SY, Kao CY, Chuang JH, Tiao MM, Hsieh CS (2012) Reappraise the effect of redo-Kasai for recurrent jaundice following Kasai operation for biliary atresia in the era of liver transplantation. Pediatr Surg Int 28:861–864CrossRef
24.
Zurück zum Zitat Sumida W, Uchida H, Tanaka Y, Tainaka T, Shirota C, Murase N, Oshima K, Shirotsuki R, Chiba K (2017) Review of redo-Kasai portoenterostomy for biliary atresia in the transition to the liver transplantation era. Nagoya J Med Sci 79:415–420PubMedPubMedCentral Sumida W, Uchida H, Tanaka Y, Tainaka T, Shirota C, Murase N, Oshima K, Shirotsuki R, Chiba K (2017) Review of redo-Kasai portoenterostomy for biliary atresia in the transition to the liver transplantation era. Nagoya J Med Sci 79:415–420PubMedPubMedCentral
Metadaten
Titel
Laparoscopic Kasai portoenterostomy is advantageous over open Kasai portoenterostomy in subsequent liver transplantation
verfasst von
Chiyoe Shirota
Naruhiko Murase
Yujiro Tanaka
Yasuhiro Ogura
Masahiro Nakatochi
Hideya Kamei
Nobuhiko Kurata
Akinari Hinoki
Takahisa Tainaka
Wataru Sumida
Kazuki Yokota
Satoshi Makita
Kazuo Oshima
Hiroo Uchida
Publikationsdatum
04.09.2019
Verlag
Springer US
Erschienen in
Surgical Endoscopy / Ausgabe 8/2020
Print ISSN: 0930-2794
Elektronische ISSN: 1432-2218
DOI
https://doi.org/10.1007/s00464-019-07108-y

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