AI Article Synopsis

  • Recommendations for preventing and diagnosing recurrent urinary tract infections (UTIs) vary widely due to low-quality scientific evidence, leading to inconsistent clinical practices.
  • A systematic review of eight clinical practice guidelines (CPGs) published between 2013 and 2021 revealed high scores in some areas but significant weaknesses in development rigor, stakeholder involvement, and applicability.
  • Improvements in these critical areas are essential to enhance the quality of CPGs for recurrent UTIs, and using established checklists may help guideline developers create more effective recommendations.

Article Abstract

Introduction And Hypothesis: Recommendations for preventing and diagnosing recurrent urinary tract infection (UTI) tend to vary between clinical practice guidelines (CPGs) because of low-quality scientific evidence, potentially leading to practice variation and suboptimal care. We assessed the quality of existing CPGs for recurrent UTI.

Methods: A systematic search was performed from January 2000 to June 2021 in PubMed and EMBASE for CPGs on recurrent UTI prevention or hospital diagnostics in Dutch, English, and Spanish. Each CPG was assessed by four appraisers in a multidisciplinary review team, using the Appraisal of Guidelines, Research, and Evaluation II (AGREE II) instrument.

Results: We identified and assessed eight CPGs published between 2013 and 2021. The scope and purpose (mean and standard deviation: 67.3 ± 21.8) and clarity of presentation (74.8 ± 17.6) domains scored highly. However, issues with methods, patient participation, conflict of interests, and facilitators and barriers were common and resulted in lower scores for the rigour of development (56.9 ± 25.9), applicability (19.6 ± 23.4), stakeholder involvement (50.4 ± 24.6), and editorial independence (62.1 ± 23.1) domains. Overall, two CPGs were recommended, three were recommended with modifications, and three were not recommended.

Conclusions: Significant room for improvement exists in the quality of CPGs for recurrent UTI, with most displaying serious limitations in the stakeholder involvement, rigour of development, and applicability domains. These aspects must be improved to decrease diagnostic and therapeutic uncertainty. Developers could benefit from using checklists and following guidelines when developing de novo CPGs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119892PMC
http://dx.doi.org/10.1007/s00192-022-05089-6DOI Listing

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