Protocol biopsy of the stable renal transplant:: A multicenter study of methods and complication rates

被引:164
作者
Furness, PN
Philpott, CM
Chorbadjian, MT
Nicholson, ML
Bosmans, JL
Corthouts, BL
Bogers, JJPM
Schwarz, A
Gwinner, W
Haller, H
Mengel, M
Seron, D
Moreso, F
Cañas, C
机构
[1] Leicester Gen Hosp, Clin Sci Labs, Leicester LE5 4PW, Leics, England
[2] Leicester Gen Hosp, Dept Surg, Leicester LE5 4PW, Leics, England
[3] Univ Hosp Antwerpen, Dept Nephrol Hypertens, Edegem, Belgium
[4] Univ Hosp Antwerpen, Dept Radiol, Edegem, Belgium
[5] Univ Hosp Antwerpen, Dept Pathol, Edegem, Belgium
[6] Hannover Med Sch, Dept Nephrol, D-3000 Hannover, Germany
[7] Hannover Med Sch, Dept Pathol, D-3000 Hannover, Germany
[8] Bellvitge Hosp, Dept Nephrol, Barcelona, Spain
[9] Bellvitge Hosp, Dept Radiol, Barcelona, Spain
关键词
D O I
10.1097/01.TP.0000082542.99416.11
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. Clinical trials in renal transplantation must use surrogate markers of long-term graft survival if conclusions are to be drawn at acceptable speed and cost. Morphologic changes in transplant biopsies provide the earliest available evidence of damage, and "protocol" biopsies from stable grafts can be used to reduce the number of patients needed in clinical trials. This approach has been inhibited by concerns over safety, but the risk of biopsy of a stable kidney, with no active inflammation or acute functional impairment, has never been formally estimated. Methods. In accordance with a predefined set of questions, a retrospective audit of a sequential series of protocol biopsies was performed in four major transplant centers. Results. A total of 2,127 biopsy events were assessed for major complications, and 1,486 were assessed for minor ones. There were no deaths. One graft was lost, under circumstances indicating that the loss should have been prevented. Three episodes of hemorrhage required direct intervention. Three further patients required transfusion. There were two episodes of peritonitis, but one was arguably an unrelated event. All serious complications presented within 4 hr of biopsy. Conclusions. The incidence of clinically significant complications after protocol biopsy of a stable renal transplant is low. Direct benefits to the patients concerned (irrespective of the benefit that may accrue in clinical trials) were not formally assessed but seem likely to outweigh the risk of the procedure. We believe that it is ethically justifiable to ask renal transplant recipients to undergo protocol biopsies in clinical trials and routine care.
引用
收藏
页码:969 / 973
页数:5
相关论文
共 16 条
[1]   Fibrous intimal thickening at implantation as a risk factor for the outcome of cadaveric renal allografts [J].
Bosmans, JL ;
Woestenburg, A ;
Ysebaert, DK ;
Chapelle, T ;
Helbert, MJ ;
Corthouts, R ;
Jürgens, A ;
Van Daele, A ;
Van Marck, EA ;
De Broe, ME ;
Verpooten, GA .
TRANSPLANTATION, 2000, 69 (11) :2388-2394
[2]   Chronic allograft nephropathy: What can the biopsy tell us? [J].
Furness, PN .
TRANSPLANTATION PROCEEDINGS, 2001, 33 (7-8) :3357-3358
[3]   International variation in the interpretation of renal transplant biopsies: Report of the CERTPAP Project [J].
Furness, PN ;
Taub, N .
KIDNEY INTERNATIONAL, 2001, 60 (05) :1998-2012
[4]  
Halloran PF, 1999, J AM SOC NEPHROL, V10, P167
[5]  
HUNSICKER LG, 1995, KIDNEY INT, V48, pS120
[6]  
ISONIEMI H, 1994, TRANSPLANTATION, V58, P1195, DOI 10.1097/00007890-199412150-00010
[7]  
Jain S, 2000, Transpl Int, V13 Suppl 1, pS52, DOI 10.1007/s001470050274
[8]  
KASISKE BL, 1995, KIDNEY INT, V48, pS116
[9]   Serial protocol biopsies to quantify the progression of chronic transplant nephropathy in stable renal allografts [J].
Moreso, F ;
Lopez, M ;
Vallejos, A ;
Giordani, C ;
Riera, L ;
Fulladosa, X ;
Hueso, M ;
Alsina, J ;
Grinyó, JM ;
Serón, D .
AMERICAN JOURNAL OF TRANSPLANTATION, 2001, 1 (01) :82-88
[10]   A prospective randomized trial of three different sizes of core-cutting needle for renal transplant biopsy [J].
Nicholson, ML ;
Wheatley, TJ ;
Doughman, TM ;
White, SA ;
Morgan, JDT ;
Veitch, PS ;
Furness, PN .
KIDNEY INTERNATIONAL, 2000, 58 (01) :390-395