N-acetylcysteine for the prevention of contrast-induced nephropathy - A systematic review and meta-analysis

被引:80
作者
Liu, R
Nair, D
Ix, J
Moore, DH
Bent, S
机构
[1] San Francisco VA Med Ctr, Vet Affairs PRIME Program, San Francisco, CA 94121 USA
[2] San Francisco VA Med Ctr, Dept Med, San Francisco, CA 94121 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[4] Calif Pacific Med Ctr, Res Inst, San Francisco, CA 94115 USA
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Osher Ctr Integrat Med, San Francisco, CA 94143 USA
关键词
N-acetylcysteine; contrast-induced nephropathy; acute renal failure; kidney disease;
D O I
10.1111/j.1525-1497.2005.30323.x
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
OBJECTIVE: Contrast-induced nephropathy is a common cause of acute renal failure in hospitalized patients. Although patients are often given N-acetylcysteine to prevent renal injury from contrast agents, there are no clear guidelines supporting its use. We conducted a systematic review to determine whether administering N-acetylcysteine around the time of contrast administration reduces the risk of contrast-induced nephropathy. DESIGN: We searched MEDLINE, EMBASE, the Cochrane Collaboration Database, bibliographies of retrieved articles, and abstracts of conference proceedings, and consulted with experts to identify relevant studies. Randomized controlled trials of N-acetylcysteine in hospitalized patients receiving contrast were included. Studies were excluded if they did not report change in creatinine or incidence of contrast-induced nephropathy at 48 hours. MEASUREMENTS AND MAIN RESULTS: Nine randomized controlled trials satisfied all inclusion criteria and were included in the analysis. The difference in mean change in creatinine between the N-acetylcysteinetreated group and controls was - 0.27 mg/dl (95% confidence interval [CI], - 0.43 to -0.11). The relative risk of developing contrast-induced nephropathy was 0.43 (95% CI, 0.24 to 0.75) in subjects randomized to N-acetylcysteine. Significant heterogeneity existed among studies, suggesting differences in patient populations or study methodology not identified by sensitivity analyses. The incidence of dialysis was rare (0.2%). CONCLUSIONS: Our findings suggest that N-acetylcysteine helps prevent declining renal function and contrast-induced nephropathy. While N-acetylcysteine is inexpensive and nontoxic, undeviating insistence for dosing at least 12 hours in advance of contrast exposure may delay diagnostic and therapeutic procedures. Future studies are needed to address the longer-term clinical outcomes and cost-effectiveness of this agent.
引用
收藏
页码:193 / 200
页数:8
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