富血小板血浆作为一种新的非手术治疗女性压力性尿失禁的方法:一项前瞻性试点研究。

IF 1.4 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Stavros Athanasiou, Christos Kalantzis, Dimitrios Zacharakis, Nikolaos Kathopoulis, Artemis Pontikaki, Themistoklis Grigoriadis
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引用次数: 6

摘要

目的:本研究旨在评价富血小板血浆(PRP)治疗应激性尿失禁(SUI)的有效性和安全性。方法:这是一项在三级转诊单位进行的前瞻性观察性试点研究,纳入了预定进行SUI手术的SUI女性。共有20名连续女性符合纳入标准并参加了所有随访。所有参与者每隔4至6周在阴道前壁的下三分之一处注射2次PRP。在基线时,他们接受尿动力学研究,1小时尿垫试验,并完成失禁国际咨询问卷-女性下尿路症状和King健康问卷。随访(1、3和6个月)时,患者接受1小时尿垫试验,并完成King's健康问卷、失禁国际咨询问卷-女性下尿路症状和患者总体印象改善量表。主要结局是评价治疗后SUI。次要结果包括评估患者报告的问卷,评估尿量(1小时尿垫试验)和注射期间的不适程度(视觉模拟量表评分)。分别在PRP前和末次治疗后1、3、6个月进行统计学分析。结果:治疗3个月后SUI症状明显改善,6个月时进一步改善。在1小时尿垫试验中,尿丢失平均减少50.2%。在6个月的随访中,80.0%的女性报告至少有所改善。未观察到不良反应。结论:富血小板血浆注射至少在短期内是有效和安全的,可以作为治疗SUI的一种替代门诊手术。然而,这些令人鼓舞的发现值得进一步的随机对照试验研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Use of Platelet-rich Plasma as a Novel Nonsurgical Treatment of the Female Stress Urinary Incontinence: A Prospective Pilot Study.

Objectives: The aim of the study was to evaluate the efficacy and safety of platelet-rich plasma (PRP) for the treatment of stress urinary incontinence (SUI).

Methods: This was a prospective observational pilot study conducted in a tertiary referral unit, enrolling women with SUI booked for SUI surgery. A total of 20 consecutive women met the inclusion criteria and attended all follow-ups. All participants underwent 2 PRP injections into the lower one third of the anterior vaginal wall at 4- to 6-week intervals. At baseline, they underwent urodynamic studies, a 1-hour pad test, and completed the International Consultation on Incontinence Questionnaire-Female Lower Urinary Tract Symptoms and King's Health Questionnaire. At follow-up visits (1, 3, and 6 months), patients underwent the 1-hour pad test and completed the King's Health Questionnaire, International Consultation on Incontinence Questionnaire-Female Lower Urinary Tract Symptoms, and Patient Global Impression Scale of Improvement. Primary outcome was to evaluate posttreatment SUI. Secondary outcomes included assessment of patient-reported questionnaires, assessment of urine loss (1-hour pad test), and the level of discomfort during injections (visual analog scale score). Statistical analysis was performed before PRP and 1, 3, and 6 months after the last treatment.

Results: A significant improvement in SUI symptoms was observed 3 months after treatment with a further improvement at 6 months. A mean reduction of 50.2% in urine loss was observed in the 1-hour pad test. At the 6-month follow-up, 80.0% of women reported to be at least improved. No adverse effects were observed.

Conclusions: Platelet-rich plasma injections were both effective and safe at least in the short term and could be offered as an alternative outpatient procedure for the treatment of SUI. However, these encouraging findings warrant further investigation with randomized controlled trials.

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来源期刊
CiteScore
2.10
自引率
12.50%
发文量
228
期刊介绍: Female Pelvic Medicine & Reconstructive Surgery, official journal of the American Urogynecologic Society, is a peer-reviewed, multidisciplinary journal dedicated to specialists, physicians and allied health professionals concerned with prevention, diagnosis and treatment of female pelvic floor disorders. The journal publishes original clinical research, basic science research, education, scientific advances, case reports, scientific reviews, editorials and letters to the editor.
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