Randomized, placebo-controlled, double-blinded study of prophylactic cranberries use in women with recurrent uncomplicated cystitis

被引:0
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作者
Tsiakoulias, Eleftherios [1 ]
Gravas, Stavros [2 ]
Hadjichristodoulou, Christos [3 ]
Oikonomou, Katerina G. [4 ]
Kyritsi, Maria [3 ]
Dadouli, Katerina [3 ]
Matziri, Alexia [3 ]
Kola, Konstantina [3 ]
Vacthsioli, Evangelia [3 ]
Tsiakoulia, Marianna [5 ]
Gianniou, Michaela [6 ]
Tzortzis, Vassilios [1 ]
机构
[1] Univ Thessaly, Univ Hosp Larissa, Fac Med, Sch Hlth Sci,Dept Urol, Larisa 41110, Greece
[2] Univ Cyprus, Med Sch, Dept Urol, Nicosia, Cyprus
[3] Univ Thessaly, Fac Med, Lab Hyg & Epidemiol, Larisa 41222, Greece
[4] Gen Hosp Larissa, Intens Care Unit, Thessaly 41221, Greece
[5] Melathron Agoniston EOKA, Dept Occupat Therapy, CY-4549 Limassol, Cyprus
[6] Univ Thessaly, Fac Med, Dept Immunol & Histocompatibil, Larisa 41500, Greece
关键词
Recurrent urinary tract infections; Cranberry; Proanthocyanidins; PACs; URINARY-TRACT-INFECTION; JUICE; RISK;
D O I
10.1007/s00345-023-04741-0
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Tau he adherence of p-fimbriated Escherichia coli (E. coli) to urothelial cells leading to recurrent urinary tract infections (rUTIs) may be prevented by proanthocyanidins (PACs) contained in American cranberries.Purpose The purpose of this clinical trial was to assess the clinical utility of prophylactic use of high-dose PACs daily in women with a history of rUTIs.Materials and methods 172 adult women with a history of rUTIs, defined as >= 2 within a 6-month period or >= 3 within a 12-month period were enrolled and randomized in two groups to receive either Cysticlean (TM) 240 mg or placebo for a 12-month period. Urine samples, vaginal and rectal swabs were collected at initial and quarterly study visits. The primary study endpoints were the number of urinary tract infections (UTIs) and changes in Quality of Life (QoL), assessed by the 36-Item Short Form Survey (SF-36) questionnaire.Results 160 adult women of median age 40 years old (range 19-82) were finally analyzed in this randomized, placebo-controlled, double-blinded clinical trial. In response to intervention, the number of UTIs was significantly lower (Incidence rate ratio IRR 0.49, p < 0.001) and QoL was slightly improved. The numbers of E. coli isolates detected in vaginal (IRR 0.71, p value < 0.001) and in rectal swabs (IRR 0.87, p value < 0.001) were also significantly decreased. No adverse events were reported.Conclusion The daily use of Cysticlean (TM) 240 mg was associated with a reduction of UTIs and a prolongation of UTI-free survival compared to placebo treatment, supporting its use as prophylaxis in this patient population.
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页数:8
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