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经会阴徒手游离前列腺磁共振成像融合靶向活检术:单中心前瞻性研究中的技术和可行性。

Transperineal Free-hand mpMRI Fusion-targeted Biopsies Under Local Anesthesia: Technique and Feasibility From a Single-center Prospective Study.

机构信息

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza and University of Turin, Turin, Italy.

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza and University of Turin, Turin, Italy.

出版信息

Urology. 2020 Jun;140:122-131. doi: 10.1016/j.urology.2019.11.078. Epub 2020 Feb 13.

Abstract

OBJECTIVE

To evaluate the feasibility of "in-office" TPFBx under local anesthesia (LA).

MATERIALS AND METHODS

We prospectively screened for eligibility data of 724 consecutive men undergoing either TPFBx (target and systematic cores) or TPSBx (systematic cores only) from September 2016 to June 2018 due to suspicion of prostate cancer (CaP), according to predefined exclusion criteria.

RESULTS

We included 459 men (TPFBx n = 279 including n = 338 mpMRI lesions, Pi-RADS 4 in 63.6%; TPSBx n = 180). Median procedural time and maximum pain were 19 minutes and 5 numeric rating scale (NRS) points; pain was highest at the time of LA. Only 1 major complication occurred (Clavien 3a). Hematuria and hematospermia were frequent (72.6% and 54.2%). Vaso-vagal reactions and AUR were rare (0.7% and 0.4%). No cases of UTI and 1 case of fever were recorded. No significant changes in erectile and urinary functions were noted from baseline compared to 40 days after TPFBx (P = .86 and P = .89). In comparison with TPSBx the sole differences were pain during prostatic sampling (P = .03), duration of hematospermia (P <.0001) and procedural time (P <.001) all higher for TPFBx. Clinically significant (cs) CaP was detected in n = 150 (53.8%) patients in the TPFBx group (34.9%, 51.7%, and 75% of Pirads 3, 4, and 5, respectively). Addition of systematic cores detected n = 25 csCaP that were missed by targeted cores (17.4% of all csCaP).

CONCLUSION

TPFBx under LA are feasible, yielding high tolerability, low complications, no impact on erectile and urinary function and good csCaP detection. Addition of systematic to targeted cores remains recommended. Further studies are needed to confirm our findings.

摘要

目的

评估局部麻醉(LA)下门诊经直肠前列腺穿刺活检术(TPFBx)的可行性。

材料与方法

我们前瞻性筛选了 2016 年 9 月至 2018 年 6 月期间因怀疑前列腺癌(CaP)而接受 TPFBx(靶向和系统核心)或 TPSBx(仅系统核心)的 724 例连续男性患者的合格数据,符合预设排除标准。

结果

我们纳入了 459 例男性患者(TPFBx 组 279 例,包括 n=338 例 mpMRI 病变,Pi-RADS 4 级占 63.6%;TPSBx 组 180 例)。中位操作时间和最大疼痛分别为 19 分钟和 5 分数字评分量表(NRS);LA 时疼痛最高。仅发生 1 例严重并发症(Clavien 3a 级)。血尿和血精很常见(分别为 72.6%和 54.2%)。血管迷走神经反应和急性尿潴留罕见(分别为 0.7%和 0.4%)。无尿路感染病例,仅记录到 1 例发热。与 TPFBx 相比,40 天后勃起和尿功能无明显变化(P=0.86 和 P=0.89)。与 TPSBx 相比,仅在前列腺取样期间疼痛(P=0.03)、血精持续时间(P<0.0001)和操作时间(P<0.001)存在差异,TPFBx 更高。TPFBx 组中 n=150 例(53.8%)患者检测到临床显著(cs)CaP(Pirads 3、4 和 5 分别为 34.9%、51.7%和 75%)。靶向核心检测遗漏的 n=25 例 csCaP 通过系统核心检测到(所有 csCaP 的 17.4%)。

结论

LA 下的 TPFBx 是可行的,具有高耐受性、低并发症、对勃起和尿功能无影响和良好的 csCaP 检测能力。建议增加靶向核心至系统核心。需要进一步研究来证实我们的发现。

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