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Anticoagulation and bleeding risk after core needle biopsy.

机译:穿刺针活检后有抗凝和出血风险。

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OBJECTIVE: The objective of our study was to compare the bleeding complication rates after core needle biopsy in patients receiving anticoagulation therapy and those who had not to assess the safety of performing core needle breast biopsy in anticoagulated patients. MATERIALS AND METHODS: Core needle biopsy was performed at 1,144 sites in 1,055 women from August 2004 to May 2007. A retrospective study of these cases was performed. The patient group was composed of 200 women (220 biopsy sites) who were taking anticoagulant therapy daily (180 patients, aspirin; 16 patients, warfarin; and four patients, Excedrin), and the control group was composed of 855 women (924 biopsy sites) who were not receiving daily anticoagulant therapy. Any adverse reactions after core needle biopsy, including the presence and size of bruises or lumps (hematomas), were recorded. RESULTS: There was a statistically significant difference (p = 0.035) in the percentage of bruises between patients receiving anticoagulation therapy and those who were not. Bruising occurred in 68 of the 200 (34%) women in the patient group (anticoagulated), whereas bruising occurred in 227 of the 855 (26.5%) women in the control group (nonanticoagulated). The differences were not statistically significant for hematoma formation (p = 0.274) or bruising with hematoma formation (p = 0.413). Hematoma occurred in 12 of the 200 (6%) anticoagulated patients versus 36 of the 855 (4.2%) patients in the control group. Patients reporting a bruise and lump (hematoma) numbered 10 of 200 (5%) for the anticoagulated group and 32 of 855 (3.7%) for the control group. CONCLUSION: No patients undergoing core needle biopsy reported any clinically important complications. The results of this study confirm that performing core needle biopsy in patients on anticoagulation therapy is safe.
机译:目的:本研究的目的是比较接受抗凝治疗的患者在进行穿刺针活检后的出血并发症发生率,以及未评估抗凝患者进行穿刺针活检的安全性的患者的并发症发生率。材料与方法:从2004年8月至2007年5月,在1,055名妇女的1,144个部位进行了穿刺针活检。对这些病例进行了回顾性研究。患者组由每天进行抗凝治疗的200名妇女(220个活检部位)组成(180例阿司匹林,16名华法林和4例Excedrin),对照组由855名妇女(924个活检部位)组成。 )不接受每日抗凝治疗的人。记录穿刺活检后的任何不良反应,包括瘀伤或肿块(血肿)的存在和大小。结果:接受抗凝治疗的患者与未接受抗凝治疗的患者之间的瘀伤百分比有统计学差异(p = 0.035)。在患者组(抗凝)的200名女性中有68名(34%)发生瘀伤,而在对照组(未抗凝)的855名女性中有227名(26.5%)发生青紫。对于血肿形成(p = 0.274)或血肿形成瘀伤(p = 0.413),差异无统计学意义。在200例抗凝患者中有12例发生血肿(6%),而对照组的855例患者中有36例(4.2%)发生血肿。报告有瘀伤和肿块(血肿)的患者在抗凝组中占200名中的10名(5%),在对照组中占855名中的32名(3.7%)。结论:没有接受过穿刺活检的患者报告有任何重要的临床并发症。这项研究的结果证实,对抗凝治疗的患者进行核心穿刺活检是安全的。

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