Liu Raymond, Nair Deepu, Ix Joachim, Moore Dan H, Bent Stephen
Department of Medicine, University of California, San Francisco, CA, USA.
J Gen Intern Med. 2005 Feb;20(2):193-200. doi: 10.1111/j.1525-1497.2005.30323.x.
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.
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.
Nine randomized controlled trials satisfied all inclusion criteria and were included in the analysis. The difference in mean change in creatinine between the N-acetylcysteine-treated 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%).
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.
造影剂肾病是住院患者急性肾衰竭的常见原因。尽管通常会给患者使用N-乙酰半胱氨酸以预防造影剂导致的肾损伤,但尚无明确指南支持其使用。我们进行了一项系统评价,以确定在使用造影剂前后给予N-乙酰半胱氨酸是否能降低造影剂肾病的风险。
我们检索了MEDLINE、EMBASE、Cochrane协作网数据库、检索文章的参考文献以及会议论文摘要,并咨询专家以确定相关研究。纳入了在接受造影剂的住院患者中进行的N-乙酰半胱氨酸随机对照试验。如果研究未报告48小时时肌酐的变化或造影剂肾病的发生率,则将其排除。
9项随机对照试验符合所有纳入标准并纳入分析。N-乙酰半胱氨酸治疗组与对照组之间肌酐平均变化的差异为-0.27mg/dl(95%置信区间[CI],-0.43至-0.11)。随机接受N-乙酰半胱氨酸治疗的受试者发生造影剂肾病的相对风险为0.43(95%CI,0.24至0.75)。各研究之间存在显著异质性,提示敏感性分析未识别出的患者人群或研究方法存在差异。透析发生率很低(0.2%)。
我们的研究结果表明,N-乙酰半胱氨酸有助于预防肾功能下降和造影剂肾病。虽然N-乙酰半胱氨酸价格低廉且无毒,但坚持至少在造影剂暴露前12小时给药可能会延迟诊断和治疗程序。需要进一步的研究来探讨该药物的长期临床结局和成本效益。