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Escherichia coli Nissle 1917 as adjuvant therapy in patients with chronic bacterial prostatitis: a non-blinded, randomized, controlled trial.
Manfredi, Celeste; Calace, Francesco P; Fusco, Ferdinando; Quattrone, Carmelo; Giordano, Dario; Crocetto, Felice; Creta, Massimiliano; De Sio, Marco; Arcaniolo, Davide.
Afiliación
  • Manfredi C; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
  • Calace FP; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy. frap.calace@gmail.com.
  • Fusco F; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
  • Quattrone C; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
  • Giordano D; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
  • Crocetto F; Department of Urology, University "Federico II", Naples, Italy.
  • Creta M; Department of Urology, University "Federico II", Naples, Italy.
  • De Sio M; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
  • Arcaniolo D; Urology Unit, Department of Woman Child and of General and Specialist Surgery, University of Campania "Luigi Vanvitelli", Via S. Pansini 5, Naples, 80131, Italy.
World J Urol ; 39(12): 4373-4379, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34213584
ABSTRACT

PURPOSE:

To evaluate the efficacy and safety of Escherichia coli Nissle 1917 (EcN) in association with levofloxacin in patients with chronic bacterial prostatitis (CBP).

METHODS:

Patients with CBP referred to our clinic from September 2017 to July 2019 were enrolled. At baseline, the symptomatology was assessed with the NIH-Chronic Prostatitis Symptom Index (NIH-CPSI), while the Meares-Stamey test was used to diagnose the infection. Patients were randomized (11) in two groups (A and B). All subjects underwent oral administration of Levoxacin® 500 mg once daily for 4 weeks. Only the patients in Group B underwent oral administration of EcN® 320 mg, twice daily for 4 weeks and then once daily for 8 weeks. After 3 months, each patient repeated the NIH-CPSI questionnaire, while the Meares-Stamey test was repeated at 3 and 6 months in patients who reported persistent symptoms. All adverse events (AEs) were recorded.

RESULTS:

A total of 110 patients were enrolled. After 3 months patients in Group B reported a significantly lower NIH-CPSI score (5.85 ± 3.07 vs. 7.64 ± 3.86; p = 0.009) and biological recurrences rate (9.8 vs. 26.9%; p = 0.043). At 6 months the biological recurrences rate was significantly lower in Group B (8.7 vs. 28.9%; p = 0.038). Only three patients in Group A and six in Group B (p = 0.25) complained mild AEs.

CONCLUSIONS:

Combination therapy with EcN and levofloxacin allows a better control of symptoms and biological recurrences in patients with CBP, without worsening the safety of the treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Prostatitis / Infecciones Bacterianas / Escherichia coli / Levofloxacino / Antibacterianos Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: World J Urol Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Prostatitis / Infecciones Bacterianas / Escherichia coli / Levofloxacino / Antibacterianos Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: World J Urol Año: 2021 Tipo del documento: Article País de afiliación: Italia