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Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women

BACKGROUND: In adults with febrile urinary tract infection (fUTI), data on optimal treatment duration in patients other than non-pregnant women without comorbidities are lacking. METHODS: A randomized placebo-controlled, double-blind, non-inferiority trial among 35 primary care centers and 7 emergen...

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Autores principales: van Nieuwkoop, Cees, van der Starre, Willize E., Stalenhoef, Janneke E., van Aartrijk, Anna M., van der Reijden, Tanny J. K., Vollaard, Albert M., Delfos, Nathalie M., van ’t Wout, Jan W., Blom, Jeanet W., Spelt, Ida C., Leyten, Eliane M. S., Koster, Ted, Ablij, Hans C., van der Beek, Martha T., Knol, Mirjam J., van Dissel, Jaap T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376681/
https://www.ncbi.nlm.nih.gov/pubmed/28366170
http://dx.doi.org/10.1186/s12916-017-0835-3
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author van Nieuwkoop, Cees
van der Starre, Willize E.
Stalenhoef, Janneke E.
van Aartrijk, Anna M.
van der Reijden, Tanny J. K.
Vollaard, Albert M.
Delfos, Nathalie M.
van ’t Wout, Jan W.
Blom, Jeanet W.
Spelt, Ida C.
Leyten, Eliane M. S.
Koster, Ted
Ablij, Hans C.
van der Beek, Martha T.
Knol, Mirjam J.
van Dissel, Jaap T.
author_facet van Nieuwkoop, Cees
van der Starre, Willize E.
Stalenhoef, Janneke E.
van Aartrijk, Anna M.
van der Reijden, Tanny J. K.
Vollaard, Albert M.
Delfos, Nathalie M.
van ’t Wout, Jan W.
Blom, Jeanet W.
Spelt, Ida C.
Leyten, Eliane M. S.
Koster, Ted
Ablij, Hans C.
van der Beek, Martha T.
Knol, Mirjam J.
van Dissel, Jaap T.
author_sort van Nieuwkoop, Cees
collection PubMed
description BACKGROUND: In adults with febrile urinary tract infection (fUTI), data on optimal treatment duration in patients other than non-pregnant women without comorbidities are lacking. METHODS: A randomized placebo-controlled, double-blind, non-inferiority trial among 35 primary care centers and 7 emergency departments of regional hospitals in the Netherlands. Women and men aged ≥ 18 years with a diagnosis of fUTI were randomly assigned to receive antibiotic treatment for 7 or 14 days (the second week being ciprofloxacin 500 mg or placebo orally twice daily). Patients indicated to receive antimicrobial treatment for at least 14 days were excluded from randomization. The primary endpoint was the clinical cure rate through the 10- to 18-day post-treatment visit with preset subgroup analysis including sex. Secondary endpoints were bacteriologic cure rate at 10–18 days post-treatment and clinical cure at 70–84 days post-treatment. RESULTS: Of 357 patients included, 200 were eligible for randomization; 97 patients were randomly assigned to 7 days and 103 patients to 14 days of treatment. Overall, short-term clinical cure occurred in 85 (90%) patients treated for 7 days and in 94 (95%) of those treated for 14 days (difference –4.5%; 90% CI, –10.7 to 1.7; P (non-inferiority) = 0.072, non-inferiority not confirmed). In women, clinical cure was 94% and 93% in those treated for 7 and 14 days, respectively (difference 0.9; 90% CI, –6.9 to 8.7, P (non-inferiority) = 0.011, non-inferiority confirmed) and, in men, this was 86% versus 98% (difference –11.2; 90% CI –20.6 to –1.8, P (superiority) = 0.025, inferiority confirmed). The bacteriologic cure rate was 93% versus 97% (difference –4.3%; 90% CI, –9.7 to 1.2, P (non-inferiority) = 0.041) and the long-term clinical cure rate was 92% versus 91% (difference 1.6%; 90% CI, –5.3 to 8.4; P (non-inferiority) = 0.005) for 7 days versus 14 days of treatment, respectively. In the subgroups of men and women, long-term clinical cure rates met the criteria for non-inferiority, indicating there was no difference in the need for antibiotic retreatment for UTI during 70–84 days follow-up post-treatment. CONCLUSIONS: Women with fUTI can be treated successfully with antibiotics for 7 days. In men, 7 days of antibiotic treatment for fUTI is inferior to 14 days during short-term follow-up but it is non-inferior when looking at longer follow-up. TRIAL REGISTRATION: The study was registered at ClinicalTrials.gov [NCT00809913; December 16, 2008] and trialregister.nl [NTR1583; December 19, 2008]. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-017-0835-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-53766812017-04-07 Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women van Nieuwkoop, Cees van der Starre, Willize E. Stalenhoef, Janneke E. van Aartrijk, Anna M. van der Reijden, Tanny J. K. Vollaard, Albert M. Delfos, Nathalie M. van ’t Wout, Jan W. Blom, Jeanet W. Spelt, Ida C. Leyten, Eliane M. S. Koster, Ted Ablij, Hans C. van der Beek, Martha T. Knol, Mirjam J. van Dissel, Jaap T. BMC Med Research Article BACKGROUND: In adults with febrile urinary tract infection (fUTI), data on optimal treatment duration in patients other than non-pregnant women without comorbidities are lacking. METHODS: A randomized placebo-controlled, double-blind, non-inferiority trial among 35 primary care centers and 7 emergency departments of regional hospitals in the Netherlands. Women and men aged ≥ 18 years with a diagnosis of fUTI were randomly assigned to receive antibiotic treatment for 7 or 14 days (the second week being ciprofloxacin 500 mg or placebo orally twice daily). Patients indicated to receive antimicrobial treatment for at least 14 days were excluded from randomization. The primary endpoint was the clinical cure rate through the 10- to 18-day post-treatment visit with preset subgroup analysis including sex. Secondary endpoints were bacteriologic cure rate at 10–18 days post-treatment and clinical cure at 70–84 days post-treatment. RESULTS: Of 357 patients included, 200 were eligible for randomization; 97 patients were randomly assigned to 7 days and 103 patients to 14 days of treatment. Overall, short-term clinical cure occurred in 85 (90%) patients treated for 7 days and in 94 (95%) of those treated for 14 days (difference –4.5%; 90% CI, –10.7 to 1.7; P (non-inferiority) = 0.072, non-inferiority not confirmed). In women, clinical cure was 94% and 93% in those treated for 7 and 14 days, respectively (difference 0.9; 90% CI, –6.9 to 8.7, P (non-inferiority) = 0.011, non-inferiority confirmed) and, in men, this was 86% versus 98% (difference –11.2; 90% CI –20.6 to –1.8, P (superiority) = 0.025, inferiority confirmed). The bacteriologic cure rate was 93% versus 97% (difference –4.3%; 90% CI, –9.7 to 1.2, P (non-inferiority) = 0.041) and the long-term clinical cure rate was 92% versus 91% (difference 1.6%; 90% CI, –5.3 to 8.4; P (non-inferiority) = 0.005) for 7 days versus 14 days of treatment, respectively. In the subgroups of men and women, long-term clinical cure rates met the criteria for non-inferiority, indicating there was no difference in the need for antibiotic retreatment for UTI during 70–84 days follow-up post-treatment. CONCLUSIONS: Women with fUTI can be treated successfully with antibiotics for 7 days. In men, 7 days of antibiotic treatment for fUTI is inferior to 14 days during short-term follow-up but it is non-inferior when looking at longer follow-up. TRIAL REGISTRATION: The study was registered at ClinicalTrials.gov [NCT00809913; December 16, 2008] and trialregister.nl [NTR1583; December 19, 2008]. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-017-0835-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-03 /pmc/articles/PMC5376681/ /pubmed/28366170 http://dx.doi.org/10.1186/s12916-017-0835-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
van Nieuwkoop, Cees
van der Starre, Willize E.
Stalenhoef, Janneke E.
van Aartrijk, Anna M.
van der Reijden, Tanny J. K.
Vollaard, Albert M.
Delfos, Nathalie M.
van ’t Wout, Jan W.
Blom, Jeanet W.
Spelt, Ida C.
Leyten, Eliane M. S.
Koster, Ted
Ablij, Hans C.
van der Beek, Martha T.
Knol, Mirjam J.
van Dissel, Jaap T.
Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title_full Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title_fullStr Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title_full_unstemmed Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title_short Treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
title_sort treatment duration of febrile urinary tract infection: a pragmatic randomized, double-blind, placebo-controlled non-inferiority trial in men and women
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376681/
https://www.ncbi.nlm.nih.gov/pubmed/28366170
http://dx.doi.org/10.1186/s12916-017-0835-3
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