Rocky Mountain Poison and Drug Center, Denver Health Medical Center, University of Colorado, Denver, Colorado ; Vanderbilt University School of Nursing, Nashville, Tennessee.
West J Emerg Med. 2013 May;14(3):218-26. doi: 10.5811/westjem.2012.4.6885.
There are few reports summarizing the effectiveness of oral and intravenous (IV) acetylcysteine. We determined the proportion of acetaminophen poisoned patients who develop hepatotoxicity (serum transaminase > 1000 IU/L) when treated with oral and IV acetylcysteine.
Studies were double abstracted by trained researchers. We determined the proportions of patients who developed hepatotoxicity for each route using a random effects model. Studies were further stratified by early and late treatment.
We screened 4,416 abstracts; 16 articles, including 5,164 patients, were included in the meta-analysis. The overall rate of hepatotoxicity for the oral and IV routes were 12.6% and 13.2%, respectively. Treatment delays are associated with a higher rate of hepatotoxicity.
Studies report similar rates of hepatotoxicity for oral and IV acetylcysteine, but direct comparisons are lacking. While it is difficult to disentangle the effects of dose and duration from route, our findings suggest that the rates of hepatotoxicity are similar for oral and IV administration.
目前鲜有文献汇总口服和静脉(IV)乙酰半胱氨酸的疗效。我们旨在确定接受口服和 IV 乙酰半胱氨酸治疗的对乙酰氨基酚中毒患者发生肝毒性(血清转氨酶 > 1000IU/L)的比例。
经训练有素的研究人员进行双盲摘要提取。我们使用随机效应模型,针对每条给药途径确定发生肝毒性的患者比例。研究还进一步按早期和晚期治疗进行分层。
我们筛选了 4416 篇摘要;纳入了 16 项研究,共 5164 例患者,进行了荟萃分析。口服和 IV 途径的肝毒性总发生率分别为 12.6%和 13.2%。治疗延迟与更高的肝毒性发生率相关。
目前的研究报告口服和 IV 乙酰半胱氨酸的肝毒性发生率相似,但缺乏直接比较。虽然很难将剂量和持续时间的影响与给药途径分开,但我们的研究结果表明,口服和 IV 给药的肝毒性发生率相似。