Consensus position statement on advancing the classification of patients and tests of cure in studies of antibiotic treatment of complicated urinary tract infections
- PMID: 40378860
- DOI: 10.1016/S1473-3099(25)00142-2
Consensus position statement on advancing the classification of patients and tests of cure in studies of antibiotic treatment of complicated urinary tract infections
Abstract
Complicated urinary tract infections denote an important research field for new antibiotics against Gram-negative pathogens. There is, however, increasing concern that this disease entity is too vaguely defined, leading to heterogeneous study populations and risk of bias. We analysed researchers' adherence to the US Food and Drug Administration (FDA) guidance on complicated urinary tract infection and assessed risk of bias using a three-step procedure: literature review of full-text articles on complicated urinary tract infection; assessment of the importance of risk factors for treatment failure, including statistical evaluation of how patients with risk factors might skew treatment effects; and a Delphi consensus process in a multidisciplinary group. Our evaluation showed poor adherence to FDA guidance on complicated urinary tract infection and significant heterogeneity in the reporting of study, patient, and pathogen characteristics, leading to a high risk of bias when interpreting and comparing study findings. We therefore question the concept of complicated urinary tract infection as a meaningful entity with its own study guidance.
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Conflict of interest statement
Declaration of interests AJ has received speaker fees from bioMerieux, Serosep, and The British Medical Journal; consultancy fees from ADVANZ PHARMA, GSK, Pfizer, and Global Access Diagnostics; grants from Pfizer; support for meeting attendance from Eumedica and GSK; and is a trustee for the British Society for Antimicrobial Chemotherapy. AO has participated in advisory boards hosted by ADVANZ PHARMA and received honoraria from ADVANZ PHARMA, MSD, InfectoPharm, and Pfizer. AS reports receiving grants from Pfizer and Gilead Sciences; consulting fees and honoraria for lectures from Pfizer, MSD, Angelini, Shionogi, Gilead, and Menarini; and support for meeting attendance from Pfizer. BK has participated in advisory boards hosted by OM Pharma; is a member of the European Association of Urology Guidelines Panel on Urological Infections; and is an unpaid chair of the UTISOLVE research group. CB has participated in advisory boards hosted by ADVANZ PHARMA, MiP Pharma, and GSK and received honoraria for lectures from GSK and Mundipharma. DML reports grants from Pfizer; personal fees from Adjutec, ADVANZ PHARMA, AstraZeneca, bioMérieux, Centauri, GenPax, ParaPharm, Pfizer, Shionogi, Sumitovant, Summit, Thermofisher, Zambon, and Zuellig; shareholdings or options from GenPax, GSK, Merck, and Revvity; and nominated holdings in Arecor Therapeutics, Celadon Pharmaceuticals, Destiny Pharma, Genedrive, Genincode, Oxford BioDynamics, Optibiotix Health, Probiotix Health, SkinBiotherapeutics, and VericiDx under Enterprise Investment Schemes with no direct authority to trade holdings. FW has participated in advisory boards hosted by VenatoRx and is a member of the UTISOLVE Research Group. ME reports honoraria for ad hoc expertise from ADVANZ PHARMA and CORREVIO and travel grants from ViiV Healthcare, MSD, Pfizer, and Gilead. TEBJ reports consultancy fees from ADVANZ PHARMA (for chairing the cUTI consensus group and research for this manuscript), Sandoz, and Zambon; participation in advisory board meetings for ADVANZ PHARMA and Zambon; and unpaid leadership roles with ESIU/EAU and UTISOLVE. All other authors declare no competing interests.
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