Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis
OBJECTIVESTo explore the literature comparing the pharmacokinetic and clinical outcomes from adding probenecid to oral β-lactams. METHODSMedline and EMBASE were searched from inception to December 2021 for all English language studies comparing the addition of probenecid (intervention) with an oral...
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Veröffentlicht in: | Journal of antimicrobial chemotherapy 2022-08, Vol.77 (9), p.2364-2372 |
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creator | Wilson, Richard C Arkell, Paul Riezk, Alaa Gilchrist, Mark Wheeler, Graham Hope, William Holmes, Alison H Rawson, Timothy M |
description | OBJECTIVESTo explore the literature comparing the pharmacokinetic and clinical outcomes from adding probenecid to oral β-lactams. METHODSMedline 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. RESULTSOverall, 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. CONCLUSIONSProbenecid-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. |
doi_str_mv | 10.1093/jac/dkac200 |
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METHODSMedline 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. RESULTSOverall, 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. CONCLUSIONSProbenecid-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.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkac200</identifier><identifier>PMID: 35726853</identifier><language>eng</language><publisher>Oxford University Press</publisher><subject>Editor's Choice ; Systematic Review</subject><ispartof>Journal of antimicrobial chemotherapy, 2022-08, Vol.77 (9), p.2364-2372</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-bfde35244f505f733af66701e9f341c3f63fbc0f6f9ac1dfbad24b9c6c5f286a3</citedby><cites>FETCH-LOGICAL-c358t-bfde35244f505f733af66701e9f341c3f63fbc0f6f9ac1dfbad24b9c6c5f286a3</cites><orcidid>0000-0002-2630-9722</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids></links><search><creatorcontrib>Wilson, Richard C</creatorcontrib><creatorcontrib>Arkell, Paul</creatorcontrib><creatorcontrib>Riezk, Alaa</creatorcontrib><creatorcontrib>Gilchrist, Mark</creatorcontrib><creatorcontrib>Wheeler, Graham</creatorcontrib><creatorcontrib>Hope, William</creatorcontrib><creatorcontrib>Holmes, Alison H</creatorcontrib><creatorcontrib>Rawson, Timothy M</creatorcontrib><title>Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis</title><title>Journal of antimicrobial chemotherapy</title><description>OBJECTIVESTo explore the literature comparing the pharmacokinetic and clinical outcomes from adding probenecid to oral β-lactams. METHODSMedline 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. RESULTSOverall, 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. CONCLUSIONSProbenecid-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.</description><subject>Editor's Choice</subject><subject>Systematic Review</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVkctKAzEUhoMotlZXvkCWgozNZZKZcSGU4g0EN7pyEc7koqkzkzpJK30tH8RncqRFcHX4OR_fOfAjdErJBSUVny5AT807aEbIHhrTXJKMkYruozHhRGRFLvgIHcW4IIRIIctDNOKiYLIUfIxeZsb45EOHg8PLPtS2s9obnAIOPTT4-ytrQCdoMXTJ1z4kr-MlBhw3MdkWhoh7u_b2cwAMbm2CDDpoNtHHY3TgoIn2ZDcn6Pnm-ml-lz083t7PZw-Z5qJMWe2M5YLluRNEuIJzcFIWhNrK8Zxq7iR3tSZOugo0Na4Gw_K60lILx0oJfIKutt7lqm6t0bZLw-tq2fsW-o0K4NX_Teff1GtYq6pglJf5IDjbCfrwsbIxqdZHbZsGOhtWUTFZVIxXkrEBPd-iug8x9tb9naFE_dahhjrUrg7-A8kbgM8</recordid><startdate>20220825</startdate><enddate>20220825</enddate><creator>Wilson, Richard C</creator><creator>Arkell, Paul</creator><creator>Riezk, Alaa</creator><creator>Gilchrist, Mark</creator><creator>Wheeler, Graham</creator><creator>Hope, William</creator><creator>Holmes, Alison H</creator><creator>Rawson, Timothy M</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2630-9722</orcidid></search><sort><creationdate>20220825</creationdate><title>Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis</title><author>Wilson, Richard C ; Arkell, Paul ; Riezk, Alaa ; Gilchrist, Mark ; Wheeler, Graham ; Hope, William ; Holmes, Alison H ; Rawson, Timothy M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-bfde35244f505f733af66701e9f341c3f63fbc0f6f9ac1dfbad24b9c6c5f286a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Editor's Choice</topic><topic>Systematic Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, Richard C</creatorcontrib><creatorcontrib>Arkell, Paul</creatorcontrib><creatorcontrib>Riezk, Alaa</creatorcontrib><creatorcontrib>Gilchrist, Mark</creatorcontrib><creatorcontrib>Wheeler, Graham</creatorcontrib><creatorcontrib>Hope, William</creatorcontrib><creatorcontrib>Holmes, Alison H</creatorcontrib><creatorcontrib>Rawson, Timothy M</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilson, Richard C</au><au>Arkell, Paul</au><au>Riezk, Alaa</au><au>Gilchrist, Mark</au><au>Wheeler, Graham</au><au>Hope, William</au><au>Holmes, Alison H</au><au>Rawson, Timothy M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><date>2022-08-25</date><risdate>2022</risdate><volume>77</volume><issue>9</issue><spage>2364</spage><epage>2372</epage><pages>2364-2372</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>OBJECTIVESTo explore the literature comparing the pharmacokinetic and clinical outcomes from adding probenecid to oral β-lactams. METHODSMedline 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. RESULTSOverall, 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. CONCLUSIONSProbenecid-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.</abstract><pub>Oxford University Press</pub><pmid>35726853</pmid><doi>10.1093/jac/dkac200</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2630-9722</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Editor's Choice Systematic Review |
title | Addition of probenecid to oral β-lactam antibiotics: a systematic review and meta-analysis |
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