Transplantation trends in primary biliary cirrhosis

被引:102
作者
Lee, Jarone
Belanger, Adam
Doucette, John T.
Stanca, Carmen
Friedman, Scott
Bach, Nancy
机构
[1] Mt Sinai Med Ctr, Dept Med, Div Liver Dis, Inst Transplantat, New York, NY 10029 USA
[2] Mt Sinai Med Ctr, Div Biostat & Data Management, Dept Community & Prevent Med, New York, NY 10029 USA
关键词
D O I
10.1016/j.cgh.2007.07.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Ursodeoxycholic acid (UDCA) has shown efficacy in primary biliary cirrhosis (PBC), a chronic, slowly progressive disease. We hypothesized that UDCA use would reduce the need for liver transplantation in PBC. Our study's aim was to assess liver transplantation requirements in PBC over a 12-year period. For comparison, we studied patients with primary sclerosing cholangitis (PSC) because it shares similar characteristics to PBC, but with a decreased response to UDCA. Methods: PBC and PSC transplant data of first-time liver recipients from the United Network for Organ Sharing database were collected from 1995 to 2006. Results: The absolute number of liver transplantations in the United States increased an average of 249 transplants per year (P <.001). The absolute number of transplants performed for PBC decreased an average of 5.4 cases per year (P=.004). The absolute number of transplantations for PSC showed no statistical change (P=.621). The trends for the absolute number of individuals added to the transplant waitlist showed a similar pattern: (1) an increase in total listings for transplants of all diagnoses (beta=265; P=.001); (2) a decrease in PBC (beta=-12.1; P <.001); (3) and no change for PSC (beta=-5.434; P=.083). Conclusions: The liver transplantation burden of PBC in the United States decreased between 1995 and 2006. This is despite an increase in total liver transplants and no change in transplant rates for PSC.
引用
收藏
页码:1313 / 1315
页数:3
相关论文
共 12 条
[1]   The effect of ursodeoxycholic acid therapy on the natural course of primary biliary cirrhosis [J].
Corpechot, C ;
Carrat, F ;
Bahr, A ;
Chrétien, Y ;
Poupon, RE ;
Poupon, R .
GASTROENTEROLOGY, 2005, 128 (02) :297-303
[2]   Management of primary biliary cirrhosis [J].
Heathcote, EJ .
HEPATOLOGY, 2000, 31 (04) :1005-1013
[3]   Primary biliary cirrhosis once rare, now common in the United Kingdom? [J].
James, OFW ;
Bhopal, R ;
Howel, D ;
Gray, J ;
Burt, AD ;
Metcalf, JV .
HEPATOLOGY, 1999, 30 (02) :390-394
[4]   Medical progress: Primary biliary cirrhosis [J].
Kaplan, MM ;
Gershwin, ME .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (12) :1261-1273
[5]   Epidemiology and natural history of primary biliary cirrhosis in a US community [J].
Kim, WR ;
Lindor, KD ;
Locke, GR ;
Therneau, TM ;
Homburger, HA ;
Batts, KP ;
Yawn, BP ;
Petz, JL ;
Melton, LJ ;
Dickson, ER .
GASTROENTEROLOGY, 2000, 119 (06) :1631-1636
[6]   Primary sclerosing cholangitis: Summary of a workshop [J].
LaRusso, Nicholas F. ;
Shneider, Benjamin L. ;
Black, Dennis ;
Gores, Gregory J. ;
James, Stephen P. ;
Doo, Edward ;
Hoofnagle, Jay H. .
HEPATOLOGY, 2006, 44 (03) :746-764
[7]   Ursodiol for primary sclerosing cholangitis [J].
Lindor, KD .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (10) :691-695
[8]   Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic acid [J].
Parés, A ;
Caballería, L ;
Rodés, J .
GASTROENTEROLOGY, 2006, 130 (03) :715-720
[9]   Survival after liver transplantation in the United States: A disease-specific analysis of the UNOS database [J].
Roberts, MS ;
Angus, DC ;
Bryce, CL ;
Valenta, Z ;
Weissfeld, L .
LIVER TRANSPLANTATION, 2004, 10 (07) :886-897
[10]   Epidemiology of primary biliary cirrhosis in Victoria, Australia: High prevalence in migrant populations [J].
Sood, S ;
Gow, PJ ;
Christie, JM ;
Angus, PW .
GASTROENTEROLOGY, 2004, 127 (02) :470-475