成人女性无并发症尿路感染抗生素的使用:SCOUT试验的定性结果。

IF 2 3区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Patient preference and adherence Pub Date : 2025-08-31 eCollection Date: 2025-01-01 DOI:10.2147/PPA.S531582
Berta Munné-Barellas, Ramon Monfà, Carl Llor, Ana Garcia-Sangenís, Cristina Miranda-Jiménez, Rosa Morros, Ana Moragas, Pablo Alvarez-Greciano, Alfonso Leiva, Mª Luisa Lozano-Del Hoyo, Maria Antonia Sánchez-Calavera, Jaime Marín-Cañada, Raquel Sánchez-Ruano
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引用次数: 0

摘要

背景:本文主要研究女性与尿路感染和抗生素使用的主观体验。无并发症尿路感染(UTI)是初级保健中最常见的感染之一,然而,关于这些经历及其抗生素治疗偏好的证据有限。目的:本研究的目的是收集有关抗生素的使用和参与临床试验的经验,信念和态度。方法:本定性子研究是SCOUT项目的一部分,该项目通过临床试验,旨在评估四种短期抗生素方案的有效性(单次3g剂量磷霉素;3g磷霉素2天;400mg哌美西林3天;100mg呋喃妥因5天)。在西班牙的四个地区(加泰罗尼亚N=19, Aragón N=19,马德里N=15,巴利阿里群岛N=15)共进行了68次半结构化访谈。采用目的性和理论性抽样方法。参与者在参加临床试验后被招募。数据收集于2024年3月至7月期间进行,并使用主题分析进行分析。结果:尿路感染没有引起过度关注,除非抗生素无效或参与者过去经历过多次感染。磷霉素是最广泛认可的抗生素,双剂量方案通常被认为易于服用,同时也比单剂量治疗更有效。较长的疗程可能会产生一些副作用,但在某些情况下,它们被认为更有效。参与临床试验被认为是积极的,因为它有助于提高对尿路感染和用于治疗尿路感染的抗生素的总体认识,并确保对每个具体病例进行更密切的监测。结论:本研究收集了与尿路感染、抗生素治疗方案以及参与SCOUT临床试验相关的经验。它强调需要记录尿路感染的现实,以改善未来的临床试验。
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 Antibiotics for Uncomplicated Urinary Tract Infections in Adult Women: Qualitative Findings From the SCOUT Trial.

Background: This paper focuses on women's subjective experiences with UTIs and antibiotic use. Uncomplicated urinary tract infections (UTI) are among the most common infections treated in primary care, however, there is limited evidence regarding the experiences and their antibiotic treatment preferences.

Objective: The aim of this study is to gather experiences, beliefs, and attitudes regarding the use of antibiotics and the participation in the clinical trial.

Methods: This qualitative sub-study is part of the SCOUT project, which, through a clinical trial, aims to assess the effectiveness of four short antibiotic regimens (a single 3g dose of fosfomycin; 3g of fosfomycin for two days; 400mg of pivmecillinam for three days; and 100mg of nitrofurantoin for five days). A total of 68 semi-structured interviews were conducted in four regions of Spain (Catalonia N=19, Aragón N=19, Madrid N=15, and the Balearic Islands N=15). A purposive and theoretical sampling approach was employed. Participants were recruited after taking part in the clinical trial. Data collection took place between March and July 2024 and analysed using Thematic Analysis.

Results: UTI did not cause excessive concern, except in cases where the antibiotic was ineffective or when participants had experienced multiple infections in the past. Fosfomycin was the most widely recognized antibiotic, and the two-dose regimen was generally well-regarded for being easy to take while also being more effective than the single-dose treatment. Longer regimens could cause some side effects, but in certain cases, they were perceived as more effective. Participation in the clinical trial was viewed positively, as it contributed to increasing overall knowledge about UTI and the antibiotics used to treat them, as well as ensuring closer monitoring of each specific case.

Conclusion: This study gathers experiences related to UTI, antibiotic treatment regimens, and participation in the SCOUT clinical trial. It highlights the need to document the realities of UTI in order to improve future clinical trials.

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来源期刊
Patient preference and adherence
Patient preference and adherence MEDICINE, GENERAL & INTERNAL-
CiteScore
3.60
自引率
4.50%
发文量
354
审稿时长
6-12 weeks
期刊介绍: Patient Preference and Adherence is an international, peer reviewed, open access journal that focuses on the growing importance of patient preference and adherence throughout the therapeutic continuum. The journal is characterized by the rapid reporting of reviews, original research, modeling and clinical studies across all therapeutic areas. Patient satisfaction, acceptability, quality of life, compliance, persistence and their role in developing new therapeutic modalities and compounds to optimize clinical outcomes for existing disease states are major areas of interest for the journal. As of 1st April 2019, Patient Preference and Adherence will no longer consider meta-analyses for publication.
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