Division of Epidemiology and Public Health, Nottingham City Hospital, University of Nottingham, Nottingham, United Kingdom.
Gastroenterology. 2010 Oct;139(4):1230-7. doi: 10.1053/j.gastro.2010.06.015. Epub 2010 Jun 12.
BACKGROUND & AIMS: Estimates of complication rates following elective percutaneous liver biopsy vary and might not accurately reflect current practice. We studied mortality and complication rates, by indication, in patients after they underwent liver biopsies.
We performed a study using hospital episode statistics collected by the National Health Service in England from 1998 to 2005 of elective percutaneous liver biopsies; data were linked with those from the Office for National Statistics to determine mortality rates. Using data from 61,187 people who underwent liver biopsies, all-cause mortality at 7 and 30 days after biopsy, 7-day mortality directly related to liver biopsy, and episodes of bleeding up to 7 days after biopsy were determined.
Overall all-cause mortality by 7 days after biopsy was 2 per 1000 biopsies (95% confidence interval, 1.8-2.5); this rate varied markedly by indication for biopsy, with rates as high as 12 per 1000 for patients investigated for cancer. Death within 7 days directly related to liver biopsy occurred, at most, every 1 in 10,000 biopsies in patients investigated for liver disease or abnormal liver function test results. Overall, 6 episodes of major bleeding occurred per 1000 biopsies.
All-cause mortality risk following elective percutaneous liver biopsy is approximately 0.2%, with a higher risk of major bleeding. Deaths directly related to liver biopsy occur approximately 1 in every 10,000 biopsies. This risk is substantially lower than that of previous reports, indicating that the safety of this procedure has improved.
择期经皮肝脏活检后并发症发生率的估计值各不相同,可能无法准确反映当前的实践情况。我们研究了因不同适应证接受肝脏活检的患者的死亡率和并发症发生率。
我们利用英格兰国民保健署(NHS)在 1998 年至 2005 年间收集的住院病例统计数据进行了一项研究,这些数据与国家统计局的数据相关联,以确定死亡率。通过对 61187 例接受肝脏活检的患者进行研究,确定了活检后 7 天和 30 天的全因死亡率、与肝脏活检直接相关的 7 天内死亡率以及活检后 7 天内的出血事件。
活检后 7 天内的全因死亡率为每 1000 例活检 2 例(95%置信区间,1.8-2.5);该比率因活检适应证而异,对癌症进行调查的患者的比率高达每 1000 例 12 例。在因肝脏疾病或异常肝功能检查结果而接受调查的患者中,与肝脏活检直接相关的 7 天内死亡最多每 10000 例发生 1 例。总体而言,每 1000 例活检发生 6 例严重出血事件。
择期经皮肝脏活检后的全因死亡率约为 0.2%,主要出血风险较高。与肝脏活检直接相关的死亡大约每 10000 例活检发生 1 例。与之前的报告相比,该风险显著降低,表明该程序的安全性已得到提高。