Ethnic Disparity in the Incidence and Outcome of Biliary Atresia in New Zealand

被引:5
|
作者
Evans, Helen M. [1 ,2 ]
Asher, M. Innes [2 ]
Cameron-Christie, Sophia [3 ]
Farthing, Sonja [1 ]
McCall, John [4 ,5 ]
Robertson, Stephen P. [3 ]
Wong, Hayley [2 ]
Morreau, Philip N. [6 ]
机构
[1] Univ Auckland, Dept Paediat Gastroenterol, Starship Child Hlth, Auckland, New Zealand
[2] Univ Auckland, Dept Pediat Child & Youth Hlth, Auckland, New Zealand
[3] Univ Otago, Dunedin Sch Med, Dept Womens & Childrens Hlth, Dunedin, New Zealand
[4] Auckland City Hosp, New Zealand Liver Transplant Unit, Auckland, New Zealand
[5] Univ Otago, Dept Surg, Dunedin, New Zealand
[6] Starship Child Hlth, Dept Paediat Surg, Auckland, New Zealand
关键词
Kasai portoenterostomy; Maori; Pacific; Polynesian;
D O I
10.1097/MPG.0000000000001781
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To determine incidence and outcome of biliary atresia (BA) between ethnic groups in New Zealand (NZ), a retrospective review was undertaken of children with BA born between 2002 and 2014. Prioritized ethnicity was used to determine ethnicity and was compared to population data. Uni- and multivariate analyses were undertaken to determine demographic and biochemical factors associated with outcome. Overall incidence was 1 in 9181 (Maori 1 in 5285; European 1 in 16,228; P<0.0001). Overall and transplant-free survival rates at 1, 2, and 5 years were 92%, 86%, 82% and 70%, 49%, 30% respectively with Maori having improved transplant-free survival (P<0.05) despite European children undergoing Kasai earlier (49 vs 63 days). BA is more common in NZ than Europe and North America, which is attributable to a higher incidence in Maori but overall outcome is poorer. Maori have improved transplant-free survival compared to NZ European children but the reason is unknown.
引用
收藏
页码:218 / 221
页数:4
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