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Does experimental pain assessment before biopsy predict for pain during transrectal ultrasound-guided prostate biopsy?

机译:活检前的实验性疼痛评估是否可以预测经直肠超声引导下的前列腺活检期间的疼痛?

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摘要

OBJECTIVES: To evaluate whether assessment of experimental pain perception using the modified tourniquet test before a biopsy procedure could predict the pain scores during transrectal ultrasound-guided prostate biopsy. However, the relationship between the experimental pain assessment before prostate biopsy and the pain scores during the biopsy procedure has not been established. METHODS: A total of 67 men who underwent transrectal ultrasound-guided 12-core prostate biopsy were prospectively enrolled in the study. The day before biopsy, a modified submaximal effort tourniquet test was performed on all patients. During the test, pain scores were recorded at 30, 60, 90, and 120 seconds after inflation of the blood pressure cuff. Pain scores were also recorded during probe introduction into the rectum and prostate biopsy. Pain was assessed using a visual analogue scale (VAS). RESULTS: A significant correlation was found between the VAS scores in the tourniquet test and the VAS scores during probe introduction and the VAS scores during prostate biopsy (P <0.0001). The most significant correlation was found between the VAS scores during prostate biopsy and the VAS 60-second scores during the tourniquet test (P <0.0001, r=0.756). No significant relation was found between the VAS scores and age, prostate volume, or prostate-specific antigen level (P >0.05). CONCLUSIONS: Our results have shown that a simple and quick tourniquet test could be useful in identifying those men who will experience greater pain during transrectal ultrasound-guided prostate biopsy. In the light of these data, additional studies will be planned to evaluate whether experimental pain assessment before the procedure could predict the analgesic potency of pain-relieving treatment during prostate biopsy.
机译:目的:评估在活检程序之前使用改良的止血带测试评估实验性疼痛知觉是否可以预测经直肠超声引导下的前列腺活检过程中的疼痛评分。然而,尚未确定前列腺活检之前的实验性疼痛评估与活检过程中的疼痛评分之间的关​​系。方法:前瞻性纳入了总共67例经直肠超声引导的12芯前列腺穿刺活检的男性。活检前一天,对所有患者进行改良的最大努力止血带测试。在测试期间,在血压袖带充气后30、60、90和120秒记录疼痛评分。在探头插入直肠和前列腺活检过程中还记录了疼痛评分。使用视觉模拟量表(VAS)评估疼痛。结果:在止血带测试中的VAS评分与探针引入期间的VAS评分与前列腺活检期间的VAS评分之间存在显着相关性(P <0.0001)。在前列腺活检期间的VAS评分与止血带测试期间的VAS 60秒评分之间发现了最显着的相关性(P <0.0001,r = 0.756)。在VAS评分与年龄,前列腺体积或前列腺特异性抗原水平之间未发现显着相关性(P> 0.05)。结论:我们的结果表明,简单而快速的止血带测试可能有助于识别那些在经直肠超声引导下的前列腺穿刺活检期间会感到更大疼痛的男性。根据这些数据,将计划进行其他研究,以评估手术前的实验性疼痛评估是否可以预测前列腺活检过程中止痛治疗的镇痛效果。

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