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High Effectiveness of a 14-Day Concomitant Therapy for Helicobacter pylori Treatment in Primary Care. An Observational Multicenter Study.
Olmedo, Llum; Azagra, Rafael; Aguyé, Amada; Pascual, Marta; Calvet, Xavier; Gené, Emili.
Afiliação
  • Olmedo L; ABS Manresa 3, Althaia, Xarxa Assistencial de Manresa, Programa de Doctorado en Ciencias de la Salud, Universitat Internacional de Catalunya, 08243 Barcelona, Spain.
  • Azagra R; Departamento de Medicina, Universitat Internacional de Catalunya, 08195 Sant Cugat, Barcelona, Spain.
  • Aguyé A; Departamento de Medicina, Universitat Internacional de Catalunya, 08195 Sant Cugat, Barcelona, Spain.
  • Pascual M; USR Metropolitana Nord IDIAP Jordi Gol, Departament de Medicina, Universitat Autònoma de Barcelona, 08017 Barcelona, Spain.
  • Calvet X; CAP Badia del Vallés, Institut Català de la Salut, 08214 Badia del Vallés, Barcelona, Spain.
  • Gené E; USR Metropolitana Nord IDIAP Jordi Gol, Departament de Medicina, Universitat Autònoma de Barcelona, 08017 Barcelona, Spain.
J Clin Med ; 9(8)2020 Jul 28.
Article em En | MEDLINE | ID: mdl-32731455
BACKGROUND: The current cure rates with triple therapy combining a proton-pump inhibitor, amoxicillin and clarithromycin are unacceptably low. AIMS: To evaluate the efficacy of a 14-day concomitant therapy as an empirical first-line treatment for curing Helicobacter pylori (Hp) infection in primary care. METHODS: Patients from six primary care centers in Catalonia -Spain- were included consecutively. Hp status pre and post treatment was assessed according to local clinical practice protocol. A 14-day concomitant therapy (amoxicillin 1 g, clarithromycin 500 mg and metronidazole 500 mg plus omeprazole 20 mg, all drugs administered twice daily) was prescribed. Adherence to therapy and adverse events were assessed by personal interview. RESULTS: 112 patients were enrolled. Mean age was 46.7 ± 16.1 years. Main indication for treatment was non-investigated dyspepsia (83%). Hp eradication was achieved in 100 of the 112 patients. Eradication rates were 89.3% (95% CI: 81.7-94.1) by intention-to-treat (ITT) analysis and 91.7% (95% CI; 84.6-95.9) per protocol (PP). No major side effects were reported; 104 (92.8%) patients complete the treatment. Forty-seven patients (42%) complained of mild side effects (metallic taste, nausea). Low adherence to treatment (p = 0.004) and significant adverse events (p = 0.004) were the variables associated with treatment failure. CONCLUSIONS: In primary care, a 14-day concomitant therapy is highly effective and well tolerated.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Espanha País de publicação: Suíça