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Turk J Gastroenterol ; 28(1): 3-11, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-28007678

RESUMEN

BACKGROUND/AIMS: To evaluate the effect of probiotics administered as an adjuvant to sequential Helicobacter pylori (H. pylori) eradication therapy on treatment outcome and patient compliance. MATERIALS AND METHODS: In total, 159 patients with H. pylori infection receiving sequential H. pylori eradication therapy were included in this randomized placebo-controlled study. Starting from day 0 of sequential eradication therapy (ERA), patients in the ERA+probiotic group [n=53, mean (SD) age: 47.7 (14.0) years, 54.7% were females] also received a probiotic supplement with Bifidobacterium animalis subsp. lactis B94 (1 capsule/day), patients in the ERA+placebo group [n=52, mean (SD) age: 46.4 (13.4) years, 51.9% were males] received placebo treatment (1 capsule/day), and patients in the ERA-only group [n=54, mean (SD) age: 46.3 (11.9) years, 55.6% were females] received no additional treatments. Eradication rates, patient compliance, and side effects of eradication therapy were recorded in each treatment group. RESULTS: Significantly higher eradication rates were noted in the ERA+probiotic group (86.8% vs. 70.8%, p=0.025) than in the combined ERA (ERA-only and ERA-placebo) group. Non-compliance with anti-H. pylori treatment was noted in 24 (15.1%) of 159 patients. Lower rates of first week treatment non-compliance due to diarrhea (1.88% vs. 12.26%, p=0.036) were noted in the ERA+probiotic group than in the combined ERA (ERA-only and ERA-placebo) group. Treatment resistance (p: 0.389) was similar between the groups, indicating pure antibiotic resistance without any compliance problems. The number needed to treat for an additional beneficial outcome (NNTB) was 6.2 (CI 95%, 3.5 to 28.9) for probiotic use. CONCLUSION: In conclusion, adjuvant administration of probiotic (B. animalis subsp. lactis) in 2-week sequential H. pylori eradication therapy is associated with a higher H. pylori eradication rate, lower first week diarrhea-related treatment discontinuation rates, less common self-reported side effects, and higher treatment compliance.


Asunto(s)
Antibacterianos/uso terapéutico , Infecciones por Helicobacter/tratamiento farmacológico , Helicobacter pylori , Probióticos/uso terapéutico , 2-Piridinilmetilsulfinilbencimidazoles/uso terapéutico , Dolor Abdominal/etiología , Adulto , Amoxicilina/uso terapéutico , Anorexia/inducido químicamente , Antibacterianos/efectos adversos , Bifidobacterium animalis , Claritromicina/uso terapéutico , Diarrea/inducido químicamente , Mareo/inducido químicamente , Erupciones por Medicamentos/etiología , Resistencia a Medicamentos/efectos de los fármacos , Quimioterapia Combinada , Femenino , Cefalea/inducido químicamente , Humanos , Masculino , Cumplimiento de la Medicación , Metronidazol/uso terapéutico , Persona de Mediana Edad , Náusea/inducido químicamente , Números Necesarios a Tratar , Pantoprazol , Probióticos/efectos adversos , Inhibidores de la Bomba de Protones/uso terapéutico , Evaluación de Síntomas , Resultado del Tratamiento
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