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Drug Saf ; 34(8): 683-90, 2011 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-21751828

RESUMO

BACKGROUND: Despite the availability and daily use of computerized drug-drug interaction surveillance systems, exposure to potentially relevant drug-drug interactions (DDIs) continues. DDI management guidelines are often inadequate and clear management options are lacking, which attributes to overriding of DDI signals. Although general criteria for the development and reporting of high-quality clinical practice guidelines have been identified, it appears these have not yet been applied to DDI management guidelines. OBJECTIVES: The aim of the study was to assess the clarity and applicability of guidelines for the management of potentially harmful DDIs. METHODS: We selected 13 DDIs that are potentially harmful for patients and frequently occur in community pharmacy practice in the Netherlands. The clarity and applicability of the management guidelines of these DDIs were appraised using the appropriate two domains - 'Clarity and presentation' and 'Applicability', of the validated Appraisal of Guidelines for Research and Evaluation (AGREE) Instrument. The appraisal was performed by 12 community pharmacists and 12 general practitioners. The standardized domain scores and mean item scores for 'Clarity and presentation' and 'Applicability' were compared. RESULTS: All DDI management guidelines were generally found to score well on 'Clarity and presentation', but poorly with respect to 'Applicability' (standardized domain scores 68.0 vs 26.1%). Within the domain 'Clarity and presentation', the item 'tools for application' received the lowest scores. Within the domain 'Applicability', cost implications, organizational barriers and key review criteria were all poorly documented. All guidelines presented non-directive advice using words such as 'consider' and 'regularly'. CONCLUSIONS: Developers of DDI management guidelines should take the appropriate domains of the AGREE Instrument into consideration in their development processes. The applicability of DDI management guidelines should be pretested before publishing. To improve guideline quality, more attention should particularly be paid to the available tools for applications and cost implications.


Assuntos
Sistemas de Notificação de Reações Adversas a Medicamentos/normas , Serviços Comunitários de Farmácia/estatística & dados numéricos , Interações Medicamentosas , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos , Clínicos Gerais/normas , Farmacêuticos/normas , Guias de Prática Clínica como Assunto/normas , Sistemas de Notificação de Reações Adversas a Medicamentos/economia , Serviços Comunitários de Farmácia/normas , Humanos , Países Baixos , Controle de Qualidade
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