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Does needle calibre affect pain and complication rates in patients undergoing transperineal prostate biopsy? A prospective randomized trial

机译:口径会影响会阴前列腺活检患者的疼痛和并发症发生率吗?前瞻性随机试验

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摘要

Transperineal prostate biopsy is a procedure that can be used to obtain histological samples from the prostate. To improve both the quality of the biopsy core samples and prostate cancer detection, we are currently performing a prospective, randomized trial comparing prostate biopsy samples obtained using an 18 G-needle to those obtained using a 16 G needle. The aim of this preliminary study was to evaluate pain and complication rates in both groups in order to assess whether performing a prostate biopsy with a larger calibre needle is a feasible procedure. One hundred and eighty-seven patients undergoing transperineal prostate biopsy were prospectively evaluated and divided into two groups. The first group (94 patients, Group A) received a transperineal prostate biopsy using a 16 G-needle and the second group (93 patients, Group B) underwent transperineal prostate biopsy with an 18 G-needle. Anaesthesia was obtained with a single perineal injection at the prostatic apex in all subjects. A visual analogue scale (VAS) and facial expression scale (FES) were used to assess pain during multiple steps of the procedure in each group. A detailed questionnaire was used to obtain information about drug use because it could potentially influence the pain and complications that patients experienced. Two weeks after the procedure, early and late complications were evaluated. Statistical analysis was carried out using non-parametric tests. Prostate Specific Antigen (PSA) and drug use were similar at baseline between the two groups. Pain during prostate biopsy, which was measured with both the VAS and FES instruments, did not differ significantly between the 18- and 16 G-needle groups, and no significant differences were found in early or late complication rates between the groups. Transperineal prostate biopsy with a 16 G-needle is a feasible procedure in terms of pain and complication rates. Further studies with larger patient populations are required to assess whether or not this procedure can improve prostate cancer detection rates.
机译:会阴前列腺活检是可用于从前列腺获取组织学样本的程序。为了同时提高活检核心样本和前列腺癌检测的质量,我们目前正在进行一项前瞻性随机试验,将使用18 G针获得的前列腺活检样本与使用16 G针获得的前列腺活检样本进行比较。这项初步研究的目的是评估两组患者的疼痛和并发症发生率,以评估用较大口径的针进行前列腺穿刺活检是否可行。前瞻性评估了187例经会阴前列腺穿刺活检的患者,并将其分为两组。第一组(94例患者,A组)使用16 G针进行了会阴前列腺活检,第二组(93例患者,B组)用18 G针进行了会阴前列腺活检。在所有受试者中,通过一次会阴注射在前列腺尖处获得麻醉。视觉模拟量表(VAS)和面部表情量表(FES)用于评估每组过程中多个步骤的疼痛。详细的调查表用于获得有关药物使用的信息,因为它可能会影响患者经历的疼痛和并发症。手术两周后,评估早期和晚期并发症。使用非参数检验进行统计分析。两组之间的前列腺特异性抗原(PSA)和药物使用情况在基线时相似。用VAS和FES仪器测量的前列腺活检期间的疼痛在18针和16针G组之间没有显着差异,并且两组之间的早期或晚期并发症发生率也没有显着差异。就疼痛和并发症发生率而言,用16 G针进行会阴前列腺活检是可行的方法。需要对更多的患者人群进行进一步的研究,以评估该程序是否可以提高前列腺癌的检出率。

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