Critical Factors Associated with Morbimortality in COVID-19 Patients Attended at a Brazilian Public Hospital: a Cross-Sectional Study / Fatores Críticos Associados à Morbimortalidade em Pacientes com COVID-19 Atendidos em um Hospital Público Brasileiro: um Estudo Transversal

The association between death from Covid-19 and case management, especially in small and medium-sized municipalities, is still uncertain. To analyze sociodemographic, clinical, and pharmacological factors associated with death in patients with Coronavirus Disease 2019 (COVID-19), from a Brazilian referral public hospital. This is a cross-sectional study, with data from the hospital records of patients (≥ 18 years old) diagnosed with COVID-19, from March 2020 to March 2021. The sample was classified according to the clinical outcome into two groups (death and discharge), among which statistical associations were performed with the variables of interest, with a 5% significance level. Factors such as need for intensive care, use of mechanical ventilation, and total length of hospital stay was related to higher hospital mortality, as well as the permanence of changes in clinical laboratory testing, including lactic acid, D-dimer, markers of hepatic and renal function, C-Reactive protein, anemia, leukocytosis, lymphopenia, thrombocytopenia, pH, and blood oxygen saturation (SpO2) (P < 0.05). Medications used most frequently in the studied hospital for the treatment of COVID-19, such as enoxaparin, dexamethasone, ivermectin, acetylcysteine, chloroquine, and clarithromycin were correlated with morbimortality (P < 0.05). Clinical outcome was influenced by patient-related factors, such as age and comorbidities, however, therapeutic interventions and the choice of medication also impacted morbimortality. These results reinforce the need for preventive actions and adequate clinical protocols in the treatment of hospitalized COVID-19 patients.(AU)

A associação entre o óbito pela Covid-19 e o manejo dos casos, principalmente em municípios de pequeno e médio porte, ainda é incerta. Analisar os fatores sociodemográficos, clínicos e farmacológicos associados à morte em pacientes com a doença do Coronavírus 2019 (COVID-19) em um hospital público brasileiro de referência. Trata-se de um estudo transversal realizado com dados dos prontuários de pacientes (≥ 18 anos) diagnosticados com COVID-19 no período de março de 2020 a março de 2021. A amostra foi classificada de acordo com o desfecho clínico em dois grupos (óbito e alta) e foram realizados testes de associação estatística com as variáveis de interesse com nível de significância de 5%. Fatores como necessidade de terapia intensiva, uso de ventilação mecânica e tempo total de internação estiveram relacionados com maior mortalidade hospitalar, assim como a permanência de alterações nos exames laboratoriais clínicos, incluindo ácido lático, D-dímero, marcadores de função hepática e renal, proteína C reativa, anemia, leucocitose, linfopenia, trombocitopenia, pH e saturação de oxigênio no sangue (SpO2) (P < 0,05). Os medicamentos utilizados com maior frequência no hospital para o tratamento de COVID-19, como enoxaparina, dexametasona, ivermectina, acetilcisteína, cloroquina e claritromicina, foram correlacionados com morbimortalidade (P < 0,05). O desfecho clínico foi influenciado por fatores relacionados ao paciente, como idade e comorbidades, porém as intervenções terapêuticas e a escolha dos medicamentos também impactaram na morbimortalidade. Esses resultados reforçam a necessidade de ações preventivas e protocolos clínicos adequados no tratamento de pacientes hospitalizados com COVID-19.(AU)

The use of an electronic medication organizer device with alarm to improve medication adherence of older adults with hypertension.

OBJECTIVE: To examine whether the use of a monthly electronic medication organizer device equipped with an alarm clock, called Electronic System for Personal and Controlled Use of Medications (Supermed), improves medication adherence of older adults with hypertension. METHODS: This is a quali-quantitative, prospective, before-and-after study performed with 32 older adult patients with diagnosis of hypertension, who were recruited at a Primary Care Unit in Brazil. RESULTS: The main outcome measures were improvement of medication adherence and blood pressure control after intervention with Supermed. Regarding medication adherence, 81.2% of patients were "less adherent" in the pre-intervention period, and 96.9% were "more adherent" in the post-intervention period. This means that 78.1% of patients changed from "less adherent" to "more adherent" after the intervention with Supermed (p<0.001). The mean systolic and diastolic blood pressure differences between intervention day and post-intervention were 18.5mmHg (p<0.0001) and 4.3mmHg (p<0.007), respectively, and the differences between mean systolic and diastolic blood pressure between pre-intervention and post-intervention were 21.6mmHg (p<0.001) and 4.7mmHg (p<0.001) respectively. CONCLUSION: The use of Supermed significantly improved self-reported medication adherence and blood pressure control in a hypertensive older adult population.

The use of an electronic medication organizer device with alarm to improve medication adherence of older adults with hypertension / Uso de um dispositivo eletrônico organizador de medicamentos com alarme para melhorar a adesão medicamentosa de idosos com hipertensão

ABSTRACT Objective: To examine whether the use of a monthly electronic medication organizer device equipped with an alarm clock, called Electronic System for Personal and Controlled Use of Medications (Supermed), improves medication adherence of older adults with hypertension. Methods: This is a quali-quantitative, prospective, before-and-after study performed with 32 older adult patients with diagnosis of hypertension, who were recruited at a Primary Care Unit in Brazil. Results: The main outcome measures were improvement of medication adherence and blood pressure control after intervention with Supermed. Regarding medication adherence, 81.2% of patients were "less adherent" in the pre-intervention period, and 96.9% were "more adherent" in the post-intervention period. This means that 78.1% of patients changed from "less adherent" to "more adherent" after the intervention with Supermed (p<0.001). The mean systolic and diastolic blood pressure differences between intervention day and post-intervention were 18.5mmHg (p<0.0001) and 4.3mmHg (p<0.007), respectively, and the differences between mean systolic and diastolic blood pressure between pre-intervention and post-intervention were 21.6mmHg (p<0.001) and 4.7mmHg (p<0.001) respectively. Conclusion: The use of Supermed significantly improved self-reported medication adherence and blood pressure control in a hypertensive older adult population.

RESUMO Objetivo: Avaliar se o uso de um dispositivo organizador de medicamentos eletrônico, mensal, equipado com um despertador, chamado Sistema Eletrônico para Uso Personalizado e Controlado de Medicamentos (Supermed), melhora a adesão à medicação de idosos com hipertensão. Métodos: Trata-se de um estudo qualiquantitativo, prospectivo, antes e depois, realizado com 32 pacientes idosos, com diagnóstico de hipertensão, recrutados em uma Unidade Básica de Saúde do Brasil. Resultados: Os principais desfechos foram a melhor adesão à medicação e o controle da pressão arterial após a intervenção com Supermed. Quanto à adesão medicamentosa, 81,2% dos pacientes eram "menos aderentes" no período pré-intervenção, e 96,9% eram "mais aderentes" no período pós-intervenção. Isso significa que 78,1% dos pacientes mudaram de "menos aderentes" para "mais aderentes" após a intervenção com Supermed (p<0,001). As diferenças da pressão arterial sistólica e diastólica média entre o dia da intervenção e pós-intervenção foram 18,5mmHg (p<0,0001) e 4,3mmHg (p<0,007), respectivamente, e as diferenças entre as médias da pressões arteriais sistólica e diastólica entre os períodos pré-intervenção e pós-intervenção foram de 21,6mmHg (p<0,001) e 4,7mmHg (p<0,001), respectivamente. Conclusão: O uso de Supermed melhorou de forma significativa a adesão medicamentosa e o controle da pressão arterial em uma população idosa hipertensa.

Elaboração e validação do protocolo de desprescrição do clonazepam em idosos / Elaboration and validation of clonazepam deprescribing protocol for the elderly / Elaboración y validación del protocolo de desprescripción del clonazepam en ancianos

Introdução: Algumas alterações fisiológicas que ocorrem no indivíduo idoso favorecem o acúmulo e a intoxicação por medicamentos. Dentre estes, podemos citar a classe dos benzodiazepínicos, medicamentos que, apesar de amplamente prescritos, principalmente para tratamento de distúrbios do sono e ansiedade, são considerados potencialmente inapropriados para o uso em idosos. Portanto, a elaboração de protocolos para desprescrição desses medicamentos é estratégia necessária na gestão do cuidado dos pacientes geriátricos. Objetivo: Elaborar e validar um protocolo de desprescrição do clonazepam para idosos que fazem uso deste medicamento para ansiedade ou insônia. Métodos: Estudo metodológico, desenvolvido em duas etapas, sendo elas a elaboração e a validação do protocolo de desprescrição do clonazepam para idosos que fazem uso desse medicamento para ansiedade ou insônia, excetuando-se aqueles que preenchem os critérios de exclusão. A elaboração do protocolo resultou em três produtos: um fluxograma de desprescrição, um folheto sobre higiene do sono e um folheto contendo os benefícios da desprescrição do clonazepam sob supervisão médica. A validação do protocolo foi realizada por médicos especialistas, por meio da Técnica de Delphi. Já na validação dos folhetos, participaram, além dos especialistas, indivíduos com 60 anos ou mais, de ambos os sexos, que não fizessem uso do clonazepam. A partir dos resultados obtidos, foi analisada a concordância da avaliação por meio do Coeficiente de Validade de Conteúdo (CVC), uma vez que essa ferramenta objetiva medir o grau de concordância dos juízes participantes do processo de validação. Resultados: O fluxograma foi considerado validado após a segunda rodada de avaliação, pois todos os itens avaliados obtiveram CVC igual ou superior a 0,8 nesta rodada. Os folhetos foram considerados validados já na primeira rodada de avaliação, pois todos os itens também obtiveram CVC superior a 0,8 durante esta rodada. Conclusão: Considerando os resultados obtidos, o protocolo se apresenta como uma ferramenta importante ao guiar a conduta médica no processo de desprescrição do clonazepam.

Introduction: Some physiological changes that occur in the elderly individual favor the accumulation and intoxication by drugs. Among these, we can mention the class of benzodiazepines, medicines which, although widely prescribed mainly for the treatment of sleep disorders and anxiety, are considered potentially inappropriate for use in the elderly. Therefore, the elaboration of protocols for the deprescribing of those drugs is a necessary strategy in the management of the care of geriatric patient. Objective: To elaborate and validate a protocol for the Deprescribing of clonazepam for the elderly who use this medication for anxiety or insomnia. Methods: Methodological study, developed in two stages ­ elaboration and validation of the protocol of deprescribing of clonazepam for elderly people who use this medication for anxiety or insomnia, except those who meet the exclusion criteria. The elaboration of the protocol resulted in three products: a flowchart of deprescribing, a leaflet of sleep hygiene, and a leaflet containing the benefits of the clonazepam Deprescribing under medical supervision. The validation of the protocol was performed by medical specialists, through the Delphi Technique. In addition to the specialists, individuals of both sexes, aged 60 years or more who did not use clonazepam, took part in the validation of the leaflets. Based on the results obtained, the agreement of the evaluation was analyzed using the Content Validity Coefficient (CVC), since this tool aims to measure the degree of agreement of the judges participating in the validation process. Results: The flowchart was considered validated after the second round of evaluation, since all items assessed had a CVC equal to or greater than 0.8 in this round. The leaflets were considered validated in the first evaluation round, since all items also obtained CVC greater than 0.8 during this round. Conclusion: Considering the results obtained, the protocol presents itself as an important tool in guiding medical conduct in the process of Deprescribing of clonazepam

Introducción: Algunas alteraciones fisiológicas que ocurren en el individuo mayor favorecen el acumulación y la intoxicación por medicamentos. Entre estas, podemos citar la clase de los benzodiazepínicos, medicamentos que, a pesar de ampliamente prescritos, principalmente para el tratamiento de disturbios del sueño y de la ansiedad, son considerados potencialmente inapropiados si usados por personas mayores. Por lo tanto, la elaboración de protocolos para desprescripción de esos medicamentos son estrategias necesarias en la gestión al cuidado de los pacientes geriátricos. Objetivo: Elaborar y validar un protocolo de desprescripción de clonazepam para mayores que hacen uso de esta medicina para ansiedad o insomnio. Métodos: Estudio metodológico, desarrollado en dos etapas, siendo ellas la elaboración y la validación del protocolo de desprescripción del clonazepam para mayores que hacen uso de ese medicamento para ansiedad o insomnio, exceptuando aquellos que cumplen los criterios de exclusión. La elaboración del protocolo resultó en tres productos: un flujograma de desprescripción, un folleto sobre la higiene del sueño y un folleto conteniendo los beneficios de la desprescripción del clonazepam bajo supervisión médica. La validación del protocolo fue realizada por médicos especialistas, por medio de la Técnica de Delphi. Ya en la validación de los folletos, participaron, además de los especialistas, individuos con 60 años o más, de ambos sexos, que no hiciesen uso de clonazepam. A partir de los resultados obtenidos, fue analizada la concordancia de la evaluación por médio del Coeficiente de Validez de Contenido (CVC), una vez que esa herramienta objetiva medir el grado de concordancia de los jueces partícipes del proceso de validación. Resultados: El flujograma fue considerado validado después de la segunda ronda de evaluación, pues todos los ítems evaluados obtuvieron CVC igual o superior a 0,8 en esta rodada. Los folletos fueron considerados validados ya en la primera rodada de evaluación, pues todos los ítems también obtuvieron CVC superior a 0,8 durante esta rodada. Conclusión: Considerando los resultados obtenidos, el protocolo se presenta como una herramienta importante al guiar la conducta médica en el proceso de desprescripción del clonazepam.

Systematic review protocol: following PRISMA guide from Cochrane to generate evidence as treatment effect of pharmaceutical care for hypertension in primary care

Pharmaceutical care (PC) is in the implementation process in Brazil and Latin America. Synthesis of evidence has been requested for monitoring and evaluating the process regarding the treatment effect. The objective is to build and disseminate a systematic review protocol to make a standard for updating results from pharmaceutical care for hypertension and for other diseases. This is a protocol for systematic review studies regarding a real example of a protocol reasoned in pharmaceutical care for hypertension in primary care. This protocol was delineated grounded in the Cochrane Handbook. Descriptors and words were defined using MeSH (Medical Subject Headings), DeCS (Descriptors in Health Sciences) and Emtree thesaurus, and the search was performed in English, Spanish and Portuguese, without filters, up to March, 27th, 2017. The results were structured in the PRISMA flowchart. Results found from all databases were: the Cochrane Library (n= 202); PubMed (n= 2608); LILACs (n= 909); Embase (n= 1653); Scopus (n=1298); IPA (n=967); and Web of Sciences (n=435). From these, 1688 were duplicate articles. The content of this paper can aid the constant monitoring of pharmaceutical care implementation and contribute to the improvement of the quality and evidence levels of published studies.

Profile of activities developed by community pharmacists: do they corroborate the precepts of the pharmaceutical profession?

Studies that addressed the profile of pharmaceutical activities and behaviors in community pharmacies in the last decades pointed to a gap between community pharmacy practice and the precepts of the profession. Facing the need to analyze whether the new legislation has impacted this scenario, the objective of this study was to describe the general profile and academic profile of community pharmacists, and the profile of the activities they develop, as well as to know their place of work. This is a descriptive study, to which all pharmacists in charge of community pharmacies in the metropolitan area of ​​Belo Horizonte-MG (n = 1624) were invited. Data collection was performed through a questionnaire validated online, from October to December 2017, via Google Docs®. Responses were obtained from 109 pharmacists, most of them female, aged 31-40 years, being general graduates, and in private institutions. Pharmacotherapeutic follow-up, an activity linked to clinical management, is performed by only 37.60% of pharmacists, evidencing that there is still a lag in relation to the provision of clinical services by community pharmacists. Thus, we emphasize the importance of implementing the precepts established by Brazilian curricular guidelines for undergraduate pharmacy courses which focus on the development of clinical skills, since the insertion of the pharmacist into the health team and the provision of clinical services to the community can add new value to the use of medications, and contribute effectively to their rational use in Brazil.

Analysis of clinical pharmacist interventions in the neurology unit of a Brazilian tertiary teaching hospital.

It is estimated that around five to 10.0% of hospital admissions occur due to clinical conditions resulting from pharmacotherapy. Clinical pharmacist's activity can enhance drug therapy's effectiveness and safety through pharmacotherapy interventions (PIs), thus minimizing drug-related problems (DRPs) and optimizing the allocation of financial resources associated with health care. This study aimed to estimate the DRPs prevalence, evaluate PI which were performed by clinical pharmacists in the Neurology Unit of a Brazilian tertiary teaching hospital and to identify factors associated with the occurrence of PI-related DRP. A single-arm trial included adults admitted in the referred Unit from 2012 July to 2015 June. Patients were evaluated during their hospitalization period and PIs were performed based on trigger DRPs that were detected in medication reconciliation (admission or discharge) or during inpatient follow-up. Student's t-test, Chi-square test, Pearson and Multiple logistic regression models to analise the association among age, number of drugs, hospitalization period, and number of diagnoses with occurrence of DRPs. Analyses level of significance was 5%. In total 409 inpatients were followed up [51.1% male, mean age of 49.1 (SD 16.5)]. Patients received, on average, 11.9 (SD 5.8) drugs, ranging from two to 38 drugs per patient, and 54.3% of the sample presented at least one DRP whose most frequent description was "untreated condition". From all 516 performed PIs that resulted from DRPs, 82.8% were accepted and the majority referred to "drug introduction" (27.5%). Multiple logistic regression showed that age, length of hospital stay, number of drugs used, diagnosis of epilepsy, multiple sclerosis and myasthenia gravis would be clinical variables associated with DRP (p < 0,05). Monitoring the use of drugs allowed the clinical pharmacist to detect DRPs and to suggest interventions that promote rational pharmacotherapy.

Pharmacists in dispensing drugs (PharmDisp): protocol for a clinical trial to test the effectiveness of distance education in training pharmacists for dispensing drugs

ABSTRACT Dispensing drug is a moment in which the pharmacist is able to analyze pharmacotherapy and contribute to its rational use. However, research has shown that some pharmacists lack adequate knowledge to perform this service. This study aims to describe a research protocol for a clinical trial to test the effectiveness of a distance learning program to train pharmacists in dispensing drugs. This is a protocol for an open diagnostic, non-randomized, single group clinical trial. A 12-week duration distance learning course was structured on the Moodle platform for training community pharmacists who are registered in the Regional Board of Pharmacy and work as employees or owners in Brazilian community pharmacies. The course curricula involves concepts and practice of dispensing drugs applied to the treatment of hypertension, diabetes mellitus, dyslipidemia and asthma. Pharmacists are divided randomly into groups, to which previously selected tutors give directions to the discussion and clarify questions. A validated questionnaire is being used before and after the course to measure participants' knowledge. Participant satisfaction with the course is also being measured. Pharmacists who work in the study headquarters municipality receive two visits from a mystery shopper, before and after the course, to evaluate their performance in dispensing drugs. The virtual platform and the content of the course material were evaluated by judges. The study has been approved by the Research Ethics Committee of the School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo. The sample size was estimated to provide desired power for testing the significance of the difference between baseline-to-endpoint change scores. Information about the course is being released through channels such as social networks. The results will be submitted for publication in scientific journals, but information enabling the identification of the study subjects will be kept confidential. The trial has been registered in The Brazilian Clinical Trials Registry with number RBR7mbrp3 on January 15th, 2015.

Dificuldades de acesso aos serviços farmacêuticos pelos idosos / Access barriers to pharmaceutical services among the elderly

Analisar o acesso dos idosos aos serviços de assistência farmacêutica oferecidos pelo Sistema Único de Saúde no município de Ribeirão Preto - SP, Brasil, bem como seus conhecimentos sobre a forma correta de uso dos medicamentos prescritos, Estudo transversal realizado com idosos de idade igual ou superior a 60 anos, os quais retiravam seus medicamentos em uma farmácia pública do município de Ribeirão Preto - SP, Um formulário padronizado foi utilizado para a coleta de dados que aconteceu entre novembro de 2008 e maio de 2009, Foram entrevistados 1000 idosos, dos quais menos da metade (46,8%) conseguiram todos os medicamentos contidos na prescrição por meio do Sistema Único de Saúde, Além disso, 31,3% dos sujeitos entrevistados não conseguiram os medicamentos prescritos por falta de pelo menos um deles na lista de medicamentos padronizados do município, Mais de 87,4% dos idosos afirmaram não receber orientações do farmacêutico no momento da dispensação, 37,1% não sabiam a posologia correta dos medicamentos que utilizavam e 62,2% dos idosos entrevistados deixaram de utilizar os medicamentos prescritos alguma vez ao longo do tratamento, Ressalta-se que 15,8% dos entrevistados possuíam plano de saúde privado, As dificuldades de acesso e a falta de conhecimento dos idosos sobre a posologia dos medicamentos prescritos evidenciam as deficiências com relação à assistência farmacêutica oferecida no sistema público de saúde de Ribeirão Preto - SP...

The aim of this study was to analyze the access to pharmaceutical services by the elderly provided by the Unified Health System in the municipality of Ribeirão Preto - SP, Brazil, as well as their knowledge about the correct form of using the prescribed medication. A crosssectional study was performed with elderly patients aged 60 years and older in the moment that they withdrawal their medications at a public pharmacy in the municipality of Ribeirão Preto - SP. A standardized form was used for data collection performed between November 2008 and May 2009. We interviewed 1000 elderly, of which less than half (46.8%) acquired all the medications contained in the prescription through the Unified Health System. In addition, 31.3% of the interviewees did not acquired the prescribed medication by a lack of at least one medication in the standardized list of the municipality. More than 87.4% of the elderly claimed they did not receive guidance from the pharmacist in the moment of drug dispensing, 37.1% reported a lack of knowledge of the correct dosage form of the medications used and 62,2% of the elderly interviewed stopped using the prescribed medication once during the treatment period. It is noteworthy that 15.8% of the respondents have also private health insurance. Access barriers to prescribed medication and the lack of knowledge about the dosage highlight deficiencies with respect to pharmaceutical services offered by the Unified Health System of Ribeirão Preto - SP...

Knowledge and conduct of pharmacists for dispensing of drugs in community pharmacies: a cross-sectional study

The objective of the study was to evaluate the knowledge of pharmacists and check their conduct in relation to dispensing of drugs. This is a cross-sectional study performed in four municipalities from South and Southeast of Brazil, which are reference in health national scenario and concentrate 73.6% of national economic activity. Pharmacists who works in community pharmacies were invited to answer a questionnaire prepared by the authors of this study and validated. The main outcome measured was the pharmaceutical knowledge, rated according to the number of correct answers on that questionnaire prepared by the researchers, and professional conduct in relation to dispensing of drugs. The data collection occurred from September to December 2012 and the information obtained were tabulated in duplicate by two independent researchers for later analysis. 486 community pharmacies were visited but only 112 professionals participated in the study. Among the participants, 78.6% (n = 88) did not have adequate knowledge to perform the dispensing of drugs, despite this same number of pharmacists claiming to have participated in conferences and courses after graduation. The main sources of information on drugs used by participants have a low level of scientific evidence. The performance of non-employment related tasks reduces the time available for the care of medication users. In addition, the indiscriminate sale of antimicrobials and the sale of products other than health, mischaracterize the role of the pharmacist in the community pharmacy. There are gaps in the knowledge of professionals, limiting the satisfactory completion of dispensing of drugs. In addition, the excess of other duties and inadequate professional conduct compromise the promotion of the rational use of drugs.

O objetivo do presente estudo foi avaliar o conhecimento de farmacêuticos e verificar suas condutas em relação à dispensação de medicamentos. Trata-se de um estudo transversal realizado em quatro municípios das regiões sul e sudeste do Brasil, que são referência no cenário nacional de saúde e concentram 73,6% da atividade econômica nacional. Farmacêuticos que trabalham em farmácias comunitárias foram convidados a responder um questionário elaborado pelos autores do presente estudo e validado. Os principais desfechos medidos foram o conhecimento farmacêutico, avaliado segundo o número de acertos em um questionário elaborado pelos pesquisadores, e a conduta dos profissionais durante a dispensação de medicamentos. Os dados foram coletados de setembro a dezembro de 2012 e as informações obtidas foram tabuladas em duplicata por dois pesquisadores para posterior análise. 486 farmácias comunitárias foram visitadas, mas apenas 112 profissionais participaram do estudo. Entre os participantes, 78,6% (n = 88) não tinham conhecimento satisfatório para realizar a dispensação de medicamentos, apesar de este mesmo número de farmacêuticos terem afirmado participar de congressos e cursos após a graduação. As principais fontes de informação sobre medicamentos utilizados pelos participantes possuem um baixo nível de evidência científica. A realização de tarefas não diretamente relacionadas à profissão reduz o tempo disponível para o atendimento aos usuários de medicamentos. Além disso, a venda indiscriminada de antibióticos e a comercialização de produtos alheios à saúde descaracterizam o papel do farmacêutico na farmácia comunitária. Existem lacunas no conhecimento dos profissionais, o que limita a realização satisfatória de dispensação de medicamentos. Além disso, o excesso de atribuições e a conduta profissional inadequada comprometem a promoção do uso racional de medicamentos.