Abstract
Purpose
According to Kasai’s classification of biliary atresia (BA), type III is diagnosed when micro bile ducts (MBD) cannot be identified macroscopically on the surface of the biliary remnant transected at the porta hepatis. However, during laparoscopic Kasai (lapKasai), magnification produced by a 30° 10 mm scope at a focal length of 5 cm is ×38 and ×100 when zooming, enabling more MBD to be identified than with the naked eye rendering Kasai’s original classification questionable in the laparoscopic era.
Methods
Intraoperative video recordings of 36 consecutive lapKasai cases (2009–2015) were reviewed to confirm MBD visibility. 85 consecutive open Kasai cases examined macroscopically served as controls.
Results
MBD were not visible under regular laparoscopic magnification during lapKasai in 6/36 (lapMBD−; 16.7 %) cases and visible in 30/36 (83.3 %). However, in open cases, MBD could not be identified macroscopically in 77/85 (macroMBD−; 90.6 %), a typical result reported internationally. For our lapKasai cases, jaundice clearance was lower in lapMBD-cases (4/6 = 66.7 % versus 26/30 = 86.7 %), which was not statistically significant (p = 0.26). Conversely, survival with the native liver was significantly lower in lapMBD-cases (4/6 = 66.7 % versus 23/30 = 76.7 %) (p < 0.05).
Conclusions
BA classification may benefit from revision to include laparoscopic findings to categorize BA more comprehensively.
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References
Kasai M, Sawaguchi M, Akiyama T et al (1976) A proposal of new classification of biliary atresia. J Jpn Soc Pediatr Surg 12:327–331
Davenport M (2012) Biliary atresia: clinical aspects. Semin Pediatr Surg 21:175–184
Superina R, Magee JC, Brandt ML, Healey PJ, Tiao G, Ryckman F et al (2011) The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 254:577–585
Vazquez-Estevez J, Stewart B, Shikes RH, Hall RJ, Lilly JR (1989) Biliary atresia: early determination of prognosis. J Pediatr Surg 24:48–50 (discussion 41–50)
Uchida K, Urata H, Suzuki H, Inoue M, Konishi N, Araki T et al (2004) Predicting factor of quality of life in long-term jaundice-free survivors after the Kasai operation. J Pediatr Surg 39:1040–1044
Altman RP, Lilly JR, Greenfeld J, Weinberg A, van Leeuwen K, Flanigan L (1997) A multivariable risk factor analysis of the portoenterostomy (Kasai) procedure for biliary atresia: twenty-five years of experience from two centers. Ann Surg 226:348-353 (discussion 345–353)
Azarow KS, Phillips MJ, Sandler AD, Hagerstrand I, Superina RA (1997) Biliary atresia: should all patients undergo a portoenterostomy? J Pediatr Surg 32:168–172 (discussion 164–172)
Karrer FM, Lilly JR, Stewart BA, Hall RJ (1990) Biliary atresia registry, 1976 to 1989. J Pediatr Surg 25:1076–1080 (discussion 1081)
Koga H, Wada M, Nakamura H, Miyano G, Okawada M, Lane GJ et al (2013) Factors influencing jaundice-free survival with the native liver in post-portoenterostomy biliary atresia patients: results from a single institution. J Pediatr Surg 48:2368–2372
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Nakamura, H., Murase, N., Koga, H. et al. Classification of biliary atresia in the laparoscopic era. Pediatr Surg Int 32, 1209–1212 (2016). https://doi.org/10.1007/s00383-016-3973-3
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DOI: https://doi.org/10.1007/s00383-016-3973-3