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The Biopsychosocial Burden of Prostate Biopsy at the Time of Its Indication, Procedure, and Pathological Report

机译:在其指示,程序和病理报告时前列腺活组织检查的活检性沉重

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Purpose. To explore the burden of prostate biopsy at the time of its indication, procedure, and pathological report in the prostate cancer-screening scenario that is neglected and underestimated in the literature. Methods. Prostate biopsy was offered to 47 consecutive patients with prostate-specific antigen (PSA) over 4 ng/dl or suspicious digital rectal examination (DRE) of whom 16 had undergone a biopsy. Comprehensive validated questionnaires at Time 0 (prebiopsy), Time 1 (before diagnosis, 20 days after biopsy), and Time 2 (after diagnosis, 40 days after biopsy) accessed patients' erectile (IIEF-5) and voiding (IPSS) functions, Beck scales measured anxiety (BAI), hopelessness (BHS), and depression (BDI), added to the emotional thermometers including five visual analog scales for distress, anxiety, depression, anger, and need for help. The Mann-Whitney or Friedman tests were obtained among times and studied variables. Results. Prostate biopsy did not significantly impact patients' erectile and voiding functions while a higher Beck anxiety index (BAI) was observed at Time 0 (6.89 ± 6.33) compared to Time 1 (4.83 ± 2.87),p=0.0214, and to Time 2 (4.22 ± 4.98), p=0.0178. At Time 0, patients that experienced a previous biopsy presented higher distress (3.1 ± 3.0 vs. 1.6 ± 2.3), p=0.043, and emotional suffering thermometer scores (2.3 + 3.3 vs. 0.9 ± 2.4) compared to those undergoing the first biopsy, p=0.036. At Time 2, patients with positive biopsies compared with those with negative ones showed no significant difference in outcome scores. The sample power was >90%. Conclusions. To be considered in patients' counseling and care, the current study supports the hypothesis that the peak burden of prostate biopsy occurs at the time of its indication and might be higher for those experiencing rebiopsy, significantly impacting patients' psychosocial domains. Trial Approval. This trial is registered under number NCT03783741.
机译:意图在文献中被忽视和低估的前列腺癌筛查方案中,探讨前列腺活检在适应症、程序和病理报告方面的负担。方法。对47例前列腺特异性抗原(PSA)超过4ng/dl或可疑直肠指检(DRE)的连续患者进行前列腺活检,其中16例进行了活检。时间0(活检前)、时间1(诊断前、活检后20天)和时间2(诊断后、活检后40天)的综合验证问卷评估了患者的勃起(IIEF-5)和排尿(IPSS)功能,贝克量表测量了焦虑(BAI)、绝望(BHS)和抑郁(BDI),添加到情绪温度计中,包括五个视觉模拟痛苦量表,焦虑、抑郁、愤怒和需要帮助。Mann-Whitney或Friedman检验是在时间和研究变量之间进行的。后果前列腺活检对患者的勃起和排尿功能没有显著影响,而与时间1(4.83±2.87)和时间2(4.22±4.98)相比,在时间0(6.89±6.33)观察到更高的贝克焦虑指数(BAI),p=0.0214,p=0.0178。与第一次活检的患者相比,第0次活检的患者表现出更高的痛苦(3.1±3.0 vs.1.6±2.3),p=0.043和情绪痛苦温度计得分(2.3+3.3 vs.0.9±2.4),p=0.036。在时间2,活检阳性的患者与活检阴性的患者在结果评分上没有显著差异。样品功率>90%。结论。为了在患者的咨询和护理中加以考虑,目前的研究支持这样一种假设,即前列腺活检的峰值负担发生在适应症出现时,对于经历再眼压的患者来说可能更高,从而显著影响患者的心理社会领域。试验批准。本试验注册号为NCT03783741。

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