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. 2021 Feb;37(2):223-228.
doi: 10.1007/s00383-020-04794-x. Epub 2021 Jan 2.

Effect of microscopy-assisted portoenterostomy (MAPE) for biliary atresia

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Effect of microscopy-assisted portoenterostomy (MAPE) for biliary atresia

Takehisa Ueno et al. Pediatr Surg Int. 2021 Feb.

Abstract

Purpose: Portoenterostomy (PE) is the standard treatment for biliary atresia (BA). However, micro-bile ducts are difficult to identify with surgical loupes and dissect systematically. We report the effects of our attempts to dissect hilar tissue using a surgical microscope.

Methods: Microscopy-assisted portoenterostomy (MAPE) was initiated in 2014. Patients born between 2000 and 2013 who underwent PE until day 70 without a surgical microscope for BA were gathered as historical control. MAPE in re-do PE cases (Re-MAPE) was evaluated in the same manner.

Results: Ten patients underwent MAPE for BA during the study period. 17 patients in the conventional PE group were gathered. In the MAPE group, the jaundice clearance rate was 80%, compared with 53% in the conventional PE group. Re-MAPE was performed in four patients, who had a jaundice clearance rate of 75%, essentially identical to the rate with initial MAPE. At age 4 years, the native liver survival rate was 58% in the MAPE group and 38% in the conventional PE group. The native liver survival rate in the Re-MAPE group was 75%.

Conclusion: MAPE is useful for sharing the surgical field during open PE in patients with BA. It may improve the rate of jaundice clearance.

Keywords: Jaundice clearance; Liver transplantation; Micro-bile duct; Native liver survival.

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References

    1. Sasaki H, Tanaka H, Nio M (2017) Current management of long-term survivors of biliary atresia: over 40 years of experience in a single center and review of the literature. Pediatr Surg Int 33:1327–1333. https://doi.org/10.1007/s00383-017-4163-7 - DOI - PubMed
    1. Ueno T, Kodama T, Noguchi Y, Saka R, Takama Y, Tazuke Y, Bessho K, Okuyama H (2018) Clinical implications of serum Mac-2-binding protein (M2BPGi) during regular follow-up of patients with biliary atresia. Pediatr Surg Int 34:1065–1071. https://doi.org/10.1007/s00383-018-4317-2 - DOI - PubMed
    1. Okazaki T, Kobayashi H, Yamataka A, Lane GJ, Miyano T (1999) Long-term postsurgical outcome of biliary atresia. J Pediatr Surg 34:312–315 - DOI
    1. Nio M, Wada M, Sasaki H, Kazama T, Tanaka H, Kudo H (2016) Technical standardization of Kasai portoenterostomy for biliary atresia. J Pediatr Surg 51:2105–2108. https://doi.org/10.1016/j.jpedsurg.2016.09.047 - DOI - PubMed
    1. Yanagi Y, Yoshimaru K, Matsuura T, Shibui Y, Kohashi K, Takahashi Y, Obata S, Sozaki R, Izaki T, Taguchi T (2019) The outcome of real-time evaluation of biliary flow using near-infrared fluorescence cholangiography with Indocyanine green in biliary atresia surgery. J Pediatr Surg 54:2574–2578. https://doi.org/10.1016/j.jpedsurg.2019.08.029 - DOI - PubMed

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