Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis

Author:

Wilson Richard C123,Arkell Paul23,Riezk Alaa2,Gilchrist Mark123,Wheeler Graham4,Hope William5,Holmes Alison H123,Rawson Timothy M123ORCID

Affiliation:

1. National Institute for Health and Care Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, Imperial College London , Hammersmith Campus, Du Cane Road, London W12 0NN , UK

2. Centre for Antimicrobial Optimisation, Imperial College London, Hammersmith Hospital , Du Cane Road, Acton, London W12 0NN , UK

3. Imperial College Healthcare NHS Trust, Hammersmith Hospital , Du Cane Road, London W12 0HS , UK

4. Imperial Clinical Trials Unit, Imperial College London , Stadium House, Wood Lane, London W12 7RH , UK

5. Centre for Excellence in Infectious Diseases Research (CEIDR), University of Liverpool , Liverpool L7 8TX , UK

Abstract

Abstract Objectives To explore the literature comparing the pharmacokinetic and clinical outcomes from adding probenecid to oral β-lactams. Methods Medline and EMBASE were searched from inception to December 2021 for all English language studies comparing the addition of probenecid (intervention) with an oral β-lactam [flucloxacillin, penicillin V, amoxicillin (± clavulanate), cefalexin, cefuroxime axetil] alone (comparator). ROBINS-I and ROB-2 tools were used. Data on antibiotic therapy, infection diagnosis, primary and secondary outcomes relating to pharmacokinetics and clinical outcomes, plus adverse events were extracted and reported descriptively. For a subset of studies comparing treatment failure between probenecid and control groups, meta-analysis was performed. Results Overall, 18/295 (6%) screened abstracts were included. Populations, methodology and outcome data were heterogeneous. Common populations included healthy volunteers (9/18; 50%) and those with gonococcal infection (6/18; 33%). Most studies were crossover trials (11/18; 61%) or parallel-arm randomized trials (4/18; 22%). Where pharmacokinetic analyses were performed, addition of probenecid to oral β-lactams increased total AUC (7/7; 100%), Cmax (5/8; 63%) and serum t½ (6/8; 75%). Probenecid improved PTA (2/2; 100%). Meta-analysis of 3105 (2258 intervention, 847 control) patients treated for gonococcal disease demonstrated a relative risk of treatment failure in the random-effects model of 0.33 (95% CI 0.20–0.55; I2 = 7%), favouring probenecid. Conclusions Probenecid-boosted β-lactam therapy is associated with improved outcomes in gonococcal disease. Pharmacokinetic data suggest that probenecid-boosted oral β-lactam therapy may have a broader application, but appropriately powered mechanistic and efficacy studies are required.

Funder

Centre for Antimicrobial Optimisation

CAMO

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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