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Penicillin V four times daily for five days versus three times daily for 10 days in patients with pharyngotonsillitis caused by group A streptococci: randomised controlled, open label, non-inferiority study
Publ Hlth Agcy Sweden, Sweden.
Lundbergsgatan Primary Hlth Care Ctr, Sweden; Lund Univ, Sweden.
Publ Hlth Agcy Sweden, Sweden.
Karolinska Inst, Sweden; Karolinska Univ Hosp, Sweden.
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2019 (English)In: BMJ. British Medical Journal, E-ISSN 1756-1833, Vol. 367, article id l5337Article in journal (Refereed) Published
Abstract [en]

OBJECTIVE To determine whether total exposure to penicillin V can be reduced while maintaining adequate clinical efficacy when treating pharyngotonsillitis caused by group A streptococci. DESIGN Open label, randomised controlled non-inferiority study. SETTING 17 primary healthcare centres in Sweden between September 2015 and February 2018. PARTICIPANTS Patients aged 6 years and over with pharyngotonsillitis caused by group A streptococci and three or four Centor criteria (fever amp;gt;= 38.5 degrees C, tender lymph nodes, coatings of the tonsils, and absence of cough). INTERVENTIONS Penicillin V 800 mg four times daily for five days (total 16 g) compared with the current recommended dose of 1000 mg three times daily for 10 days (total 30 g). MAIN OUTCOMES MEASURES Primary outcome was clinical cure five to seven days after the end of antibiotic treatment. The noninferiority margin was prespecified to 10 percentage points. Secondary outcomes were bacteriological eradication, time to relief of symptoms, frequency of relapses, complications and new tonsillitis, and patterns of adverse events. RESULTS Patients (n=433) were randomly allocated to the five day (n=215) or 10 day (n=218) regimen. Clinical cure in the per protocol population was 89.6% (n=181/202) in the five day group and 93.3% (n=182/195) in the 10 day group (95% confidence interval -9.7 to 2.2). Bacteriological eradication was 80.4% (n=156/194) in the five day group and 90.7% (n=165/182) in the 10 day group. Eight and seven patients had relapses, no patients and four patients had complications, and six and 13 patients had new tonsillitis in the five day and 10 day groups, respectively. Time to relief of symptoms was shorter in the five day group. Adverse events were mainly diarrhoea, nausea, and vulvovaginal disorders; the 10 day group had higher incidence and longer duration of adverse events. CONCLUSIONS Penicillin V four times daily for five days was noninferior in clinical outcome to penicillin V three times daily for 10 days in patients with pharyngotonsillitis caused by group A streptococci. The number of relapses and complications did not differ between the two intervention groups. Five day treatment with penicillin V four times daily might be an alternative to the currently recommended 10 day regimen.

Place, publisher, year, edition, pages
BMJ PUBLISHING GROUP , 2019. Vol. 367, article id l5337
National Category
Cardiac and Cardiovascular Systems
Identifiers
URN: urn:nbn:se:liu:diva-161396DOI: 10.1136/bmj.l5337ISI: 000489776500001PubMedID: 31585944OAI: oai:DiVA.org:liu-161396DiVA, id: diva2:1367459
Note

Funding Agencies|Public Health Agency of Sweden; Healthcare Committee, Region Vastra Gotaland

Available from: 2019-11-04 Created: 2019-11-04 Last updated: 2019-11-04

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