Interações medicamentosas potenciais entre idosos em uso dos anti-hipertensivos da Relação Nacional de Medicamentos Essenciais do Ministério da Saúde do Brasil

O objetivo deste estudo foi estimar a prevalência de interações medicamentosas potenciais entre anti-hipertensivos e outros fármacos. Foi realizado um inquérito domiciliar com pessoas de 60 anos ou mais de idade, residentes no Rio de Janeiro, Brasil. Foram identificadas as interações medicamentosas potenciais entre os anti- hipertensivos com evidência estabelecida, provável ou suspeita e com gravidade moderada ou elevada. Foram entrevistados 577 idosos (média de idade = 72 anos), 45,2% dos quais em uso de anti-hipertensivos, sendo 31,0% deles sujeitos a interações medicamentosas potenciais. A maioria das interações foi moderadamente grave. Comparados aos demais, os sujeitos às interações medicamentosas potenciais têm chance acima de 4 vezes de usar 5 ou mais medicamentos e acima de duas vezes de ter sido hospitalizado no ano anterior. Entre os pares de interações mais frequentes, 75% produzem redução do efeito hipotensivo (65/87), o que pode resultar em baixa efetividade no controle da pressão arterial, prescrição de mais medicamentos e risco de outros efeitos adversos e de interações

Impact of a tailored program on the implementation of evidence-based recommendations for multimorbid patients with polypharmacy in primary care practices — results of a cluster-randomized controlled trial

Background: Multimorbid patients receiving polypharmacy represent a growing population at high risk for negative health outcomes. Tailoring is an approach of systematic intervention development taking account of previously identified determinants of practice. The aim of this study was to assess the effect of a tailored program to improve the implementation of three important processes of care for this patient group: (a) structured medication counseling including brown bag reviews, (b) the use of medication lists, and (c) structured medication reviews to reduce potentially inappropriate medication. Methods: We conducted a cluster-randomized controlled trial with a follow-up time of 9 months. Participants were general practitioners (GPs) organized in quality circles and participating in a GP-centered care contract of a German health insurance. Patients aged >50 years, suffering from at least 3 chronic diseases, receiving more than 4 drugs, and being at high risk for medication-related events according to the assessment of the treating GP were enrolled. The tailored program consisted of a workshop for GPs and health care assistants, educational materials and reminders for patients, and the elaboration of implementation action plans. The primary outcome was the change in the degree of implementation between baseline and follow-up, measured by a summary score of 10 indicators. The indicators were based on structured surveys with patients and GPs. Results: We analyzed the data of 21 GPs (10 - intervention group, 11 - control group) and 273 patients (130 - intervention group, 143 - control group). The increase in the degree of implementation was 4.2 percentage points (95% confidence interval: −0.3, 8.6) higher in the intervention group compared to the control group (p = 0.1). Two of the 10 indicators were significantly improved in the intervention group: medication counseling (p = 0.017) and brown bag review (p = 0.012). Secondary outcomes showed an effect on patients’ self-reported use of medication lists when buying drugs in the pharmacy (p = 0.03). Conclusions: The tailored program may improve implementation of medication counseling and brown bag review whereas the use of medication lists and medication reviews did not improve. No effect of the tailored program on the combined primary outcome could be substantiated. Due to limitations of the study, results have to be interpreted carefully. The factors facilitating and hindering successful implementation will be examined in a comprehensive process evaluation. Trial registration number ISRCTN34664024, assigned 14/08/201