Bingham Brigid A, Huang Steven Y, Chien Pamela L, Ensor Joe E, Gupta Sanjay
The University of Texas MD Anderson Cancer Center, Department of Interventional Radiology, Houston, TX.
The University of Texas MD Anderson Cancer Center, Department of Interventional Radiology, Houston, TX.
Curr Probl Diagn Radiol. 2020 Jan-Feb;49(1):12-16. doi: 10.1067/j.cpradiol.2018.10.007. Epub 2018 Nov 2.
To evaluate the significance of aspirin, as well as, other potential confounding risk factors, on the incidence and volume of pulmonary hemorrhage in patients undergoing percutaneous computed tomography-guided lung biopsy.
This retrospective study was approved by the institutional review board. Between September 2013 and December 2014, 252 patients taking aspirin underwent transthoracic computed tomography-guided lung biopsy. Patient, technical, and lesion-related risk factors were evaluated. Univariate analysis was performed with a Student's t test, chi-square test, or Fisher's exact test, as appropriate followed by multivariate logistic regression.
Of 252 patients, 49 (19.4%) continued or stopped aspirin ≤4 days prior to biopsy and 203 (80.6%) patients stopped aspirin ≥5 days prior to biopsy. Pulmonary hemorrhage occurred in 174 cases (69.0%). The median volume of hemorrhage was 3.74 cm (range, 0-163.5 cm). Multivariate analysis revealed that lesion size (P < 0.0001) and lesion depth (P < 0.0001) were independent risk factors for the incidence of pulmonary hemorrhage, while lesion size (P = 0.0035), transgression of intraparenchymal vessels (P < 0.0001), and lesion depth (P = 0.0047) were independent risk factors for severity of hemorrhage. Aspirin stopped ≤4 days from a percutaneous lung biopsy was not associated with pulmonary hemorrhage.
Aspirin taken concurrently or stopped within 4 days of transthoracic lung biopsy is not an independent risk factor for pulmonary hemorrhage. The incidence of hemorrhage following lung biopsy is associated with lesion size and depth, while the severity of hemorrhage is associated with lesion size, depth, as well as traversal of intraparenchymal vessels.
评估阿司匹林以及其他潜在混杂风险因素对接受经皮计算机断层扫描引导下肺活检患者肺出血发生率和出血量的影响。
本回顾性研究经机构审查委员会批准。2013年9月至2014年12月期间,252例服用阿司匹林的患者接受了经胸计算机断层扫描引导下肺活检。评估了患者、技术和病变相关的风险因素。根据情况,采用学生t检验、卡方检验或Fisher精确检验进行单因素分析,随后进行多因素逻辑回归分析。
252例患者中,49例(19.4%)在活检前≤4天继续服用或停用阿司匹林,203例(80.6%)患者在活检前≥5天停用阿司匹林。174例(69.0%)发生肺出血。出血的中位数体积为3.74 cm(范围为0 - 163.5 cm)。多因素分析显示,病变大小(P < 0.0001)和病变深度(P < 0.0001)是肺出血发生率的独立危险因素,而病变大小(P = 0.0035)、实质内血管侵犯(P < 0.0001)和病变深度(P = 0.0047)是出血严重程度的独立危险因素。经皮肺活检前≤4天停用阿司匹林与肺出血无关。
经胸肺活检同时服用或在活检后4天内停用阿司匹林不是肺出血的独立危险因素。肺活检后出血的发生率与病变大小和深度有关,而出血的严重程度与病变大小、深度以及实质内血管的穿行有关。