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Continuing or discontinuing low-dose aspirin before transrectal prostate biopsy: results of a prospective randomized trial.

机译:经直肠前列腺穿刺活检前继续或停药小剂量阿司匹林:一项前瞻性随机试验的结果。

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OBJECTIVES: To determine whether the incidence and duration of bleeding complications after transrectal prostate biopsy (PB) in patients not discontinuing low-dose aspirin (LDA) are greater than in those discontinuing it. METHODS: A total of 200 consecutive subjects taking chronic LDA were enrolled in a prospective trial and were randomly assigned to undergo transrectal PB while continuing LDA (group 1, n = 67), replacing LDA with low-molecular-weight heparin (group 2, n = 67), or discontinuing LDA (group 3, n = 66). The incidence and duration of hematuria, rectal bleeding, and hematospermia for each group were assessed with a self-administered questionnaire. On days 14 and 30 after PB, all men were evaluated with an outpatient visit and a telephone interview, respectively. RESULTS: The cohort comprised 196 assessable subjects. The median number of biopsy cores taken was 10 (range 6 to 10). The overall bleeding rate was 78.5%, 69.7%, and 81.5% in groups 1, 2, and 3, respectively (P = 0.26). No significant difference was found for hematuria, rectal bleeding, or hematospermia among the groups. No severe bleeding complications occurred. The median duration of hematuria and rectal bleeding was significantly greater statistically in groups 1 and 2 compared with group 3 (6, 4, and 2 days versus 3, 2, and 1 days, respectively; P <0.0001). The proportion of men still reporting hematospermia at 30 days after PB was 21.4%, 18.5%, and 9.3% in groups 1, 2, and 3, respectively (P = 0.2). CONCLUSIONS: The continued use of LDA in men undergoing transrectal PB did not increase the incidence of mild bleeding complications, although it prolonged the duration of self-limiting hematuria and rectal bleeding. Its effect, however, on severe bleeding remains to be determined.
机译:目的:确定未停药小剂量阿司匹林(LDA)的患者经直肠前列腺穿刺活检(PB)后出血并发症的发生率和持续时间是否大于那些停药的患者。方法:共有200名连续的接受慢性LDA的受试者参加了一项前瞻性试验,随机分配接受LD的同时继续LDA的经直肠PB(第1组,n = 67),用低分子量肝素代替LDA(第2组)。 n = 67)或停用LDA(第3组,n = 66)。使用自我管理的问卷评估每组的血尿,直肠出血和血精症的发生率和持续时间。在PB后的第14天和第30天,对所有男性分别进行了门诊和电话采访。结果:该队列包括196名可评估受试者。所取活检核心的中位数为10(范围为6至10)。第1、2和3组的总出血率分别为78.5%,69.7%和81.5%(P = 0.26)。各组之间的血尿,直肠出血或血精症没有显着差异。没有发生严重的出血并发症。与第3组相比,第1和第2组的血尿和直肠出血的中位持续时间在统计学上显着更大(分别为6、4和2天,而第3、2和1天; P <0.0001)。第1、2和3组中,PB后30天仍报告有精子症的男性比例分别为21.4%,18.5%和9.3%(P = 0.2)。结论:经直肠PB患者继续使用LDA不会增加轻度出血并发症的发生率,尽管它延长了自限性血尿和直肠出血的持续时间。然而,其对严重出血的作用尚待确定。

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