Department of Radiology, Mayo Clinic, 200 1st St., SW, Rochester, MN 55905, USA.
AJR Am J Roentgenol. 2010 Mar;194(3):784-9. doi: 10.2214/AJR.08.2122.
The objective of our study was to report the incidence of bleeding after imaging-guided percutaneous core biopsy at a single center using a standardized technique.
We performed a retrospective review of percutaneous core biopsies performed at our institution from January 2002 through February 2008. Data were collected at the time of biopsy, and clinical information was obtained 24 hours and 3 months after the biopsy. The specific information that was collected included the results of coagulation studies, aspirin use, the organ biopsied, the size of the biopsy needle, and the number of needle passes. Bleeding complications were defined using the Common Terminology Criteria for Adverse Events (CTCAE, version 3.0) established by the National Cancer Institute.
Among the 15,181 percutaneous core biopsies performed during the study period, 70 hemorrhages (0.5%) that were CTCAE grade 3 or greater were identified within 3 months of biopsy. The incidence of bleeding in patients taking aspirin within 10 days before biopsy was 0.6% (18/3,195), which was not statistically different compared with the incidence of bleeding in those not taking aspirin (52/11,986, 0.4%; p = 0.34). The incidence of bleeding after liver biopsy was 0.5%; kidney biopsy, 0.7%; lung biopsy, 0.2%; pancreas biopsy, 1.0%; and other biopsy, 0.2%. There were significant associations between major bleeding and serum platelet count and international normalized ratio (p < 0.001), although the association between major bleeding and the size of the biopsy needle was not significant (p = 0.97).
The overall incidence of major bleeding after imaging-guided percutaneous core needle biopsy is low. Recent aspirin therapy does not appear to significantly increase the risk of such bleeding complications.
本研究的目的是报告在使用标准化技术的单中心行影像引导下经皮穿刺活检后发生出血的发生率。
我们对 2002 年 1 月至 2008 年 2 月期间在本机构进行的经皮穿刺活检进行了回顾性研究。在活检时采集数据,并在活检后 24 小时和 3 个月时获取临床信息。收集的具体信息包括凝血研究结果、阿司匹林使用情况、活检器官、活检针的大小和针道数量。出血并发症使用美国国立癌症研究所制定的不良事件通用术语标准(CTCAE,版本 3.0)进行定义。
在研究期间进行的 15181 例经皮穿刺活检中,在活检后 3 个月内发现 70 例(0.5%)符合 CTCAE 分级 3 级或更高级别的出血。在活检前 10 天内服用阿司匹林的患者中出血的发生率为 0.6%(18/3195),与未服用阿司匹林的患者(52/11986,0.4%;p=0.34)相比无统计学差异。肝活检后出血的发生率为 0.5%;肾活检为 0.7%;肺活检为 0.2%;胰腺活检为 1.0%;其他活检为 0.2%。大量出血与血清血小板计数和国际标准化比值显著相关(p<0.001),尽管与大量出血与活检针大小之间的关系不显著(p=0.97)。
影像引导下经皮穿刺活检后发生重大出血的总体发生率较低。近期阿司匹林治疗似乎不会显著增加此类出血并发症的风险。