Reducing antibiotic use for uncomplicated urinary tract infection in general practice by treatment with uva-ursi (REGATTA) - a double-blind, randomized, controlled comparative effectiveness trial

被引:19
作者
Afshar, Kambiz [1 ]
Fleischmann, Nina [2 ]
Schmiemann, Guido [3 ]
Bleidorn, Jutta [1 ]
Hummers-Pradier, Eva [2 ]
Friede, Tim [4 ]
Wegscheider, Karl [5 ]
Moore, Michael [6 ]
Gagyor, Ildiko [7 ]
机构
[1] Hannover Med Sch, Inst Gen Practice, Carl Neuberg Str 1, D-30625 Hannover, Germany
[2] Univ Med Ctr Gottingen, Dept Gen Practice, Humboldtallee 38, D-37073 Gottingen, Germany
[3] Univ Bremen, Inst Publ Hlth & Nursing Res, Dept Hlth Serv Res, Bremen, Germany
[4] Univ Med Ctr Gottingen, Dept Med Stat, Humboldtallee 32, D-37073 Gottingen, Germany
[5] Univ Med Ctr Hamburg Eppendorf, Dept Med Biometry & Epidemiol, Martinistr 52, D-20246 Hamburg, Germany
[6] Univ Southampton, Aldermoor Hlth Ctr, Primary Care & Populat Sci, Fac Med, Southampton SO16 5ST, Hants, England
[7] Univ Klinikum Wurzburg, Dept Gen Practice, Josef Schneider Str 2-D7, D-97080 Wurzburg, Germany
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2018年 / 18卷
关键词
Comparative effectiveness design; Arctostaphylos uva-ursi; Antibiotic prescription; General practice; Herbal remedy; SINGLE-DOSE FOSFOMYCIN; WOMEN; MANAGEMENT; IBUPROFEN; SYMPTOMS; NITROFURANTOIN; CYSTITIS; PROTOCOL;
D O I
10.1186/s12906-018-2266-x
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Uncomplicated urinary tract infections (UTI) are common in general practice and usually treated with antibiotics. This contributes to increasing resistance rates of uropathogenic bacteria. A previous trail showed a reduction of antibiotic use in women with UTI by initial symptomatic treatment with ibuprofen. However, this treatment strategy is not suitable for all women equally. Arctostaphylos uva-ursi (UU, bearberry extract arbutin) is a potential alternative treatment. This study aims at investigating whether an initial treatment with UU in women with UTS can reduce antibiotic use without significantly increasing the symptom burden or rate of complications. Methods: This is a double-blind, randomized, and controlled comparative effectiveness trial. Women between 18 and 75 yeais with suspected UTI and at least two of the symptoms dysuria, urgency, frequency or lower abdominal pain will be assessed for eligibility in general practice and enrolled into the trial. Participants will receive either a defined daily dose of 3 x 2 arbutin 105 mg for 5 days (intervention) or fosfomycin 3 g once(control). Antibiotic therapy will be provided in the intervention group only if needed, i.e. for women with worsening or persistent symptoms. Two co-primary outcomes are the number of all antibiotic courses regardless of the medical indication from day 0-28, and the symptom burden, defined as a weighted sum of the daily total symptom scores from day 0-7. The trial result is considered positive if superiority of initial treatment with UU is demonstrated with reference to the co-primary outcome number of antibiotic courses and non-inferiority of initial treatment with UU with reference to the co-primary outcome symptom burden. Discussion: The trial's aim is to investigate whether initial treatment with UU is a safe and effective alternative treatment strategy in women with UTI. In that case, the results might change the existing treatment strategy in general practice by promoting delayed prescription of antibiotics and a reduction of antibiotic use in primary care.
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页数:8
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