From the Departments of Obstetrics and Gynecology.
Urology, Baylor Scott & White Health.
Female Pelvic Med Reconstr Surg. 2021 Jun 1;27(6):371-376. doi: 10.1097/SPV.0000000000000865.
This study aimed to evaluate successful use of a midstream urine collection device in women with lower urinary tract symptoms and to assess specimen contamination.
Nonpregnant women 18 years or older without use of antibiotics in the last 4 weeks were recruited. After using the midstream urine collection device to obtain a specimen in a private restroom, a paired specimen was obtained by transurethral catheterization. Patients completed preference questionnaires. Culture organisms and microscopic urinalysis of paired specimens (device vs catheterized) were compared using the McNemar χ2 test. Bivariate analysis was performed.
Successful use was demonstrated in 54 (77%) of 70. Reasons for failure included inadequate specimen volume and improper device use. Older median age (50 vs 72 years, P = 0.0003) and history of diabetes (7% vs 27%, P = 0.037) were associated with failed use. Organisms were discordant in 21 (41%) of 51 paired urine culture specimens. The device detected 7 (88%) of 8 uropathogens. There were no detectable differences in microscopic urinalysis.
The midstream urine collection device could increase comfort, and many patients prefer it to transurethral catheterization. With proper patient selection and instructions for use, this device could increase satisfaction. Further studies are needed to assess contamination rates with this device.
本研究旨在评估在患有下尿路症状的女性中成功使用中段尿采集装置,并评估标本污染情况。
招募年龄在 18 岁或以上、过去 4 周内未使用抗生素的非妊娠女性。在私人休息室使用中段尿采集装置获得标本后,通过经尿道插管获得配对标本。患者完成偏好问卷。使用 McNemar χ2 检验比较配对标本(装置与经尿道插管)的培养物和显微镜尿分析结果。进行了双变量分析。
在 70 名患者中的 54 名(77%)成功使用了该装置。失败的原因包括标本量不足和装置使用不当。较年长的中位年龄(50 岁比 72 岁,P=0.0003)和糖尿病史(7%比 27%,P=0.037)与使用失败相关。在 51 对配对尿液培养标本中,有 21 对(41%)存在不一致的病原体。该装置检测到 8 种病原体中的 7 种(88%)。显微镜尿分析无明显差异。
中段尿采集装置可提高舒适度,许多患者更喜欢使用该装置而不是经尿道插管。通过适当的患者选择和使用说明,该装置可以提高满意度。需要进一步研究来评估该装置的污染率。