The First Asian Kidney Transplantation Prediction Models for Long-term Patient and Allograft Survival

被引:17
|
作者
Udomkarnjananun, Suwasin [1 ,2 ,3 ,4 ]
Townamchai, Natavudh [1 ,2 ,3 ,4 ]
Kerr, Stephen J. [5 ]
Tasanarong, Adis [6 ]
Noppakun, Kajohnsak [7 ]
Lumpaopong, Adisorn [8 ,9 ]
Prommool, Surazee [10 ]
Supaporn, Thanom [9 ,11 ]
Avihingsanon, Yingyos [1 ,2 ,3 ,4 ]
Praditpornsilpa, Kearkiat [1 ,2 ]
Eiam-ong, Somchai [1 ,2 ]
机构
[1] Chulalongkorn Univ, Fac Med, Dept Med, Div Nephrol, Bangkok 10330, Thailand
[2] King Chulalongkorn Mem Hosp, Bangkok 10330, Thailand
[3] King Chulalongkorn Mem Hosp, Thai Red Cross Soc, Excellence Ctr Organ Transplantat ECOT, Bangkok, Thailand
[4] Chulalongkorn Univ, Fac Med, Renal Immunol & Transplantat Res Unit, Bangkok, Thailand
[5] Chulalongkorn Univ, Fac Med, Res Affairs, Bangkok, Thailand
[6] Thammasat Univ, Dept Med, Fac Med, Div Nephrol, Pathum Thani, Thailand
[7] Chiang Mai Univ, Dept Med, Fac Med, Div Nephrol, Chiang Mai, Thailand
[8] Phramongkutklao Hosp, Dept Pediat, Fac Med, Div Nephrol, Bangkok, Thailand
[9] Coll Med, Bangkok, Thailand
[10] Navamindradhiraj Univ, Vajira Hosp, Fac Med, Div Nephrol,Dept Med, Bangkok, Thailand
[11] Phramongkutklao Hosp, Fac Med, Dept Med, Div Nephrol, Bangkok, Thailand
关键词
CLINICAL-PRACTICE GUIDELINE; CALCINEURIN INHIBITORS; RENAL-TRANSPLANTATION; GRAFT-SURVIVAL; CYCLOSPORINE-A; ORGAN-TRANSPLANTATION; SURVEILLANCE BIOPSY; TACROLIMUS; OUTCOMES; RISK;
D O I
10.1097/TP.0000000000002918
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Several kidney transplantation (KT) prediction models for patient and graft outcomes have been developed based on Caucasian populations. However, KT in Asian countries differs due to patient characteristics and practices. To date, there has been no equation developed for predicting outcomes among Asian KT recipients. Methods. We developed equations for predicting 5- and 10-year patient survival (PS) and death-censored graft survival (DCGS) based on 6662 patients in the Thai Transplant Registry. The cohort was divided into training and validation data sets. We identified factors significantly associated with outcomes by Cox regression. In the validation data set, we also compared our models with another model based on KT in the United States. Results. Variables included for developing the DCGS and PS models were recipient and donor age, background kidney disease, dialysis vintage, donor hepatitis C virus status, cardiovascular diseases, panel reactive antibody, donor types, donor creatinine, ischemic time, and immunosuppression regimens. The C statistics of our model in the validation data set were 0.69 (0.66-0.71) and 0.64 (0.59-0.68) for DCGS and PS. Our model performed better when compared with a model based on US patients. Compared with tacrolimus, KT recipients aged <= 44 years receiving cyclosporine A had a higher risk of graft loss (adjusted hazard ratio = 1.26; P = 0.046). The risk of death was higher in recipients aged >44 years and taking cyclosporine A (adjusted hazard ratio = 1.44; P = 0.011). Conclusions. Our prediction model is the first based on an Asian population, can be used immediately after transplantation. The model can be accessed at www.nephrochula.com/ktmodels.
引用
收藏
页码:1048 / 1057
页数:10
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