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https://www.rpr.lib.ok.us/taxonomy/term/7481/all
enEffect of 7 vs 14 Days of Antibiotic Therapy on Resolution of Symptoms Among Afebrile Men With Urinary Tract Infection: A Randomized Clinical Trial
https://www.rpr.lib.ok.us/resource/effect-7-vs-14-days-antibiotic-therapy-resolution-symptoms-among-afebrile-men-urinary-tract
<div class="field field-name-field-artifact-uploaded-date field-type-datetime field-label-inline clearfix">
<div class="field-label">Date Added: </div>
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<div class="field-item even"><span class="date-display-single" property="dc:date" datatype="xsd:dateTime" content="2021-09-23T00:00:00-05:00">September 23, 2021</span></div>
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<div class="field field-name-field-artifact-journal field-type-text field-label-inline clearfix">
<div class="field-label">Journal/Publication: </div>
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<div class="field-item even">JAMA</div>
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<div class="field field-name-field-artifact-published-date field-type-datetime field-label-inline clearfix">
<div class="field-label">Publication Date: </div>
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<div class="field-item even"><span class="date-display-single" property="dc:date" datatype="xsd:dateTime" content="2021-07-27T00:00:00-05:00">July 27, 2021</span></div>
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<div class="field field-name-field-artifact-issue field-type-text field-label-inline clearfix">
<div class="field-label">Issue: </div>
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<div class="field-item even">4</div>
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<div class="field field-name-field-artifact-volume field-type-text field-label-inline clearfix">
<div class="field-label">Volume: </div>
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<div class="field-item even">326</div>
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<div class="field field-name-field-artifact-pages field-type-text field-label-inline clearfix">
<div class="field-label">Pages: </div>
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<div class="field-item even">324-331</div>
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<div class="field field-name-field-artifact-type field-type-taxonomy-term-reference field-label-inline clearfix">
<div class="field-label">Type: </div>
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<div class="field-item even">Clinical Research Results</div>
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<div class="field field-name-field-artifact-doi-1 field-type-text field-label-inline clearfix">
<div class="field-label">DOI (1): </div>
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<div class="field-item even">doi:10.1001/jama.2021.9899</div>
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<div class="field field-name-field-artifact-mesh field-type-taxonomy-term-reference field-label-above">
<div class="field-label">MeSH </div>
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<div class="field-item even"><a href="/mesh/humans" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Humans</a></div>
<div class="field-item odd"><a href="/mesh/male" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">male</a></div>
<div class="field-item even"><a href="/mesh/trimethoprim-sulfamethoxazole-drug-combination" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">trimethoprim, sulfamethoxazole drug combination</a></div>
<div class="field-item odd"><a href="/mesh/ciprofloxacin" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Ciprofloxacin</a></div>
<div class="field-item even"><a href="/mesh/anti-bacterial-agents" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">anti-bacterial agents</a></div>
<div class="field-item odd"><a href="/mesh/duration-therpay" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Duration of Therpay</a></div>
<div class="field-item even"><a href="/mesh/double-blind-method" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">double-blind method</a></div>
<div class="field-item odd"><a href="/mesh/follow-studies" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">follow-up studies</a></div>
<div class="field-item even"><a href="/mesh/veterans" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Veterans</a></div>
<div class="field-item odd"><a href="/mesh/urinary-tract-infections" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">urinary tract infections</a></div>
<div class="field-item even"><a href="/mesh/communicable-diseases" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Communicable Diseases</a></div>
<div class="field-item odd"><a href="/mesh/treatment-adherence-and-compliance" typeof="skos:Concept" property="rdfs:label skos:prefLabel" datatype="">Treatment Adherence and Compliance</a></div>
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<div class="field field-name-field-artifact-editor-note field-type-text-long field-label-hidden">
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<div class="field-item even"><p>This RCT found that 7 days of antibiotics were sufficient for treatment of symptomatic UTI in afebrile men.</p>
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<div class="views-row views-row-1 views-row-odd views-row-first views-row-last">
<a href="https://jamanetwork.com/journals/jama/fullarticle/2782300" class="btn btn-primary" target="_blank">View</a> </div>
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<div class="field field-name-body field-type-text-with-summary field-label-hidden">
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<div class="field-item even" property="content:encoded"><p>Importance Determination of optimal treatment durations for common infectious diseases is an important strategy to preserve antibiotic effectiveness.</p>
<p>Objective To determine whether 7 days of treatment is noninferior to 14 days when using ciprofloxacin or trimethoprim/sulfamethoxazole to treat urinary tract infection (UTI) in afebrile men.</p>
<p>Design, Setting, and Participants Randomized, double-blind, placebo-controlled noninferiority trial of afebrile men with presumed symptomatic UTI treated with ciprofloxacin or trimethoprim/sulfamethoxazole at 2 US Veterans Affairs medical centers (enrollment, April 2014 through December 2019; final follow-up, January 28, 2020). Of 1058 eligible men, 272 were randomized.</p>
<p>Interventions Participants continued the antibiotic prescribed by their treating clinician for 7 days of treatment and were randomized to receive continued antibiotic therapy (n = 136) or placebo (n = 136) for days 8 to 14 of treatment.</p>
<p>Main Outcomes and Measures The prespecified primary outcome was resolution of UTI symptoms by 14 days after completion of active antibiotic treatment. A noninferiority margin of 10% was selected. The as-treated population (participants who took ≥26 of 28 doses and missed no more than 2 consecutive doses) was used for the primary analysis, and a secondary analysis included all patients as randomized, regardless of treatment adherence. Secondary outcomes included recurrence of UTI symptoms and/or adverse events within 28 days of stopping study medication.</p>
<p>Results Among 272 patients (median [interquartile range] age, 69 [62-73] years) who were randomized, 100% completed the trial and 254 (93.4%) were included in the primary as-treated analysis. Symptom resolution occurred in 122/131 (93.1%) participants in the 7-day group vs 111/123 (90.2%) in the 14-day group (difference, 2.9% [1-sided 97.5% CI, –5.2% to ∞]), meeting the noninferiority criterion. In the secondary as-randomized analysis, symptom resolution occurred in 125/136 (91.9%) participants in the 7-day group vs 123/136 (90.4%) in the 14-day group (difference, 1.5% [1-sided 97.5% CI, –5.8% to ∞]) Recurrence of UTI symptoms occurred in 13/131 (9.9%) participants in the 7-day group vs 15/123 (12.9%) in the 14-day group (difference, –3.0% [95% CI, –10.8% to 6.2%]; P = .70). Adverse events occurred in 28/136 (20.6%) participants in the 7-day group vs 33/136 (24.3%) in the 14-day group.</p>
<p>Conclusions and Relevance Among afebrile men with suspected UTI, treatment with ciprofloxacin or trimethoprim/sulfamethoxazole for 7 days was noninferior to 14 days of treatment with regard to resolution of UTI symptoms by 14 days after antibiotic therapy. The findings support the use of a 7-day course of ciprofloxacin or trimethoprim/sulfamethoxazole as an alternative to a 14-day course for treatment of afebrile men with UTI.</p>
<p>Trial Registration ClinicalTrials.gov identifier: NCT01994538</p>
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<div class="field field-name-field-resource-author field-type-taxonomy-term-reference field-label-inline clearfix">
<div class="field-label">Author/s: </div>
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<div class="field-item even">Drekonja, D. M., Trautner, B., Amundson, C.</div>
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Thu, 23 Sep 2021 05:00:00 +0000Bethie Seay1668 at https://www.rpr.lib.ok.us