Consumo de medicamentos não padronizados na saúde indígena: uso racional? / Consumption of non-standard medication in indigenous health: rational usage?

Resumo O estudo analisou o consumo de medicamentos não padronizados na saúde indígena, enfatizando a racionalidade da farmacoterapia, por meio de um estudo transversal dos dados secundários, de 2018 e 2019, no Distrito Especial Sanitário de Saúde Indígena Minas Gerais/Espírito Santo. Esses medicamentos foram classificados pela Anatomical Therapeutic Chemical Classification. Para a comparação da origem de prescrição e da forma de aquisição, empregaram-se testes não paramétricos, avaliando o acesso a medicamentos. Verificou-se a racionalidade por meio do perfil de consumo e da opção terapêutica na lista de medicamentos padronizados. Foram consumidas 104.928 apresentações farmacêuticas, 66.967 (66%) eram para o trato alimentar e o metabolismo; 17.705 (17%) para o sistema nervoso; 12.961 (12%) para o sistema cardiovascular. Quanto aos medicamentos mais consumidos por regiões, 171 (90%) dos 190 apresentavam opção terapêutica. As prescrições foram mais provenientes do SUS. Encontraram-se diferenças na forma de aquisição dos medicamentos. O estudo apontou importante consumo de medicamentos não padronizados, podendo existir falhas na racionalidade terapêutica. Na saúde indígena, questões etnoculturais e sociais constituem desafios para o acesso aos medicamentos com uso racional.

Abstract The study analyzed the consumption of non-standard medication in the health of indigenous peoples, emphasizing the rationality of pharmacotherapy, by conducting a cross-sectional study of secondary data from 2018 and 2019 in the Minas Gerais/Espírito Santo Special Sanitary Indigenous Health Districts. These medicines were classified by Anatomical Therapeutic Chemical Classification. Non-parametric tests were applied to compare the origin of prescription and the form of acquisition, assessing access to medication. Rationality was verified through the consumption profile and the therapeutic option in the list of standardized medicines. A total of 104,928 pharmaceutical presentations were consumed, 66,967 (66%) for the alimentary tract and metabolism, 17,705 (17%) for the nervous system, and 12,961 (12%) for the cardiovascular system. With respect to medicines consumed per region, 171 (90%) out of 190 had a therapeutic option. Prescriptions were more from the SUS. Differences were found in the way the medicines were acquired. The study pointed to significant consumption of non-standard medicines, and there may be failings in therapeutic rationality. In indigenous health, ethnocultural and social issues are challenges to access to medicines with rational use.

Pattern of antiepileptic drug utilization in epilepsy patients in outpatient departments of a tertiary care hospital

Background: Epilepsy is one of the common neurological disorders diagnosed early in life. Availability of many antiepileptic drugs (AEDs) makes it difficult to choose the appropriate pharmacotherapy. Aim and Objective: Understanding the pattern of AED prescription to evaluate the rationality of AED prescriptions in epileptic patients. Materials and Methods: This was a retrospective, observational study carried out at new civil hospital, Surat for a duration of 6 months. The study involved collecting data from the case files of all the patients irrespective of age or gender diagnosed with epilepsy and undergoing treatment from any of the outpatient departments of the hospital. Demographic details, clinical diagnosis, and detailed data about the prescribed pharmacotherapy were recorded in a pre-approved data sheet. The WHO prescribing indicators were evaluated for each prescription. Descriptive statistics was used. Results: The average age of the patients was 21.64 ± 10.46 years. A total of 1565 drugs were prescribed in the 331 epilepsy patients’ prescriptions. Out of this, 551 drugs (35.21%) were antiepileptics. Most of the patients received monotherapy (75.53%). The most commonly prescribed drug was sodium valproate (46.10%) followed by phenytoin (30.13%) and carbamazepine (10%). The average AED per prescription was 1.70. Majority of the prescriptions (94.63%) used generic names. There were no injectable used and no fixed dose combinations were prescribed in any of the patients. Conclusion: The prescriptions followed the rational prescribing pattern. Treatment of epilepsy is usually by monotherapy with valproate being the most commonly used AED. Prospective studies to evaluate adverse effects and patient compliance will help in efficient policy-making decisions.

Exploring the safe and rational use of Epimedii Folium based on the evolution of efficacy/toxicity records in ancient and modern literature / 药学学报

Epimedii Folium is a traditional non-toxic Chinese herbal medicine. However, liver injury caused by Chinese herb preparations, including Epimedii Folium, is frequently reported over the years. Based on ancient and modern literature, this paper systematically summarized and analyzed the safe application of Epimedii Folium from the perspectives of varieties, processing methods, clinical adverse reactions, pharmacological effects and toxic mechanism. Combined with our team work, we build the comprehensive prevention and control system "human-drug-application", for the safe and rational application of Epimedii Folium. This study is expected to provide support for scientific evaluation and precise prevention and control of the safety risk of Epimedii Folium.

Comparison of two analysis methods of opioid consumption sum in medical institutions / 中国药房

OBJECTIVE To compare the similarities and differences of the two methods in analyzing the use of opioids in third grade class A medical institutions and provide a reference for the management of opioids in medical institutions. METHODS Two methods， Defined Daily Dose （DDD） and Oral Morphine Equivalent （OME）， were used to count the opioid prescription data of five comprehensive medical institutions of third grade class A （named H1-H5） in Shanxi province in 2020， calculate consumption sum of opioid， annual per capita consumption sum， patient cost burden and drug consumption sum ratio， compare the index results presented by the two analysis methods， and explore the application scenarios of the advantages of each of the two evaluation methods. RESULTS The ranking of consumption sum of opioid and patient cost burden calculated by the two methods was the same in the five sample medical institutions， but the ranking of per capita consumption sum was different. Taking the 5 medical institutions as a whole， the top 4 rankings of consumption sum ratio for each species of opioid compared by both methods were the same， i. e. remifentanil＞sufentanil＞oxycodone＞morphine. The ratio of remifentanil was close to 50%. When comparing the ranking of consumption sum ratio in each medical institution， the ranking calculated by the two methods was different for those medical institutions except for H1 medical institutions. The consumption sum ratio of fentanyl calculated by DDD method was significantly higher than that of OME method； whereas consumption sum ratio of remifentanil calculated by OME method was significantly higher than that of DDD method. Perioperative patients had the highest consumption sum ratio， about 50%. The consumption sum ratio of critically ill patients in H3 jwsydey@163.com medical institutions and inpatient patients with cancer pain and other patients in H5 medical institutions calculated by DDD method was significantly higher than that by OME method. There were differences in the order of cost burden of different types of patients calculated by two methods. CONCLUSIONS DDD method can accurately reflect the dosage of opioid drugs and facilitate the monitoring and management of the dosage； OME method can more reflect the analgesic effect and compare the cost burden of patients.

Systematic Review on Safety of Chinese Medicines Combined with Tripterygium wilfordii Preparations in Treatment of Rheumatoid Arthritis and Exploration on Underlying Network Regulatory Mechanisms of Enhancing Efficacy and Reducing Toxicity / 中国实验方剂学杂志

ObjectiveTo systematically evaluate the safety of Chinese medicines combined with Tripterygium wilfordii polyglycoside tablets/Tripterygium wilfordii tablets （TWPT/TWT） in the treatment of rheumatoid arthritis （RA）， and to explore the network regulatory mechanisms of enhancing efficacy and reducing toxicity of commonly used combination regimes. MethodThe literature involving the adverse reactions of TWPT/TWT in treating RA was searched and collected from three Chinese databases （CNKI， Wanfang Data， VIP） and three English databases （PubMed， Cochrane Library， Embase） from the inception of the databases to July 2021. All studies were assessed by the Cochrane risk of bias tool， and the data were extracted and analyzed by Stata 15.0. Furthermore， Integrative Pharmacology-based Research Platform of Traditional Chinese Medicine 2.0 （TCMIP v2.0，http：//www.tcmip.cn/） was used to construct a "drug target-symptom gene of efficacy and toxicity" interaction network， to explore the underlying network regulatory mechanisms of enhancing efficacy and reducing toxicity of common T. wilfordii preparation combinations. ResultA total of 2 132 articles on Chinese medicines combined with TWPT/TWT in the treatment of RA were retrieved， and 18 of them were finally included. The systematic review showed that the adverse reactions of TWPT/TWT against RA mainly occurred in the digestive system， blood system， and reproductive system， of which digestive system had the highest incidence of damages. However， the combination with Chinese medicines effectively alleviated the adverse reactions caused by TWPT/TWT ［RR （95% CI）=0.45 （0.30， 0.66）， P<0.01］. In addition， the subgroup analysis indicated that the age of RA patients， course of disease， combination regimen， medication dosage and duration of treatment all affected the occurrence of adverse reactions of TWPT/TWT. It was found in clinical studies that total glucosides of paeony （TGP） and TWPT/TWT was most widely combined， and the effect of TGP in reducing TWPT/TWT-induced hepatotoxicity was also more significant than that of other Chinese medicines. Moreover， taking this combination regime as an example， this paper explored the "efficacy-toxicity" association mechanisms of TGP-TWPT/TWT against RA. The "drug target-symptom gene of efficacy and toxicity" interaction network revealed that the core network targets of TGP-TWPT/TWT enhanced efficacy and reduced toxicity mainly through regulating immunity-inflammation-related pathways， metabolic pathways and cell signal transduction. Especially， interleukin-4 （IL-4） and interleukin-13 （IL-13）， which were involved in the "immunity-inflammation" module， were the common targets of TGP-TWPT/TWT to enhance efficacy and reduce toxicity. The endogenous sterols， bile acids and bile salts， insulin secretion and other metabolic pathways in the "body metabolism" module were closely associated with the mechanisms of TWPT/TWT inducing hepatotoxicity and TGP reducing hepatotoxicity. While cell function regulation pathways， such as stem cell factor （SCF）/tyrosine kinase receptor （KIT） signaling pathway and phosphatidylinositol 3-kinase （PI3K）/protein kinase B （Akt）signaling pathway were involved in both anti-RA effects and hepatotoxicity of TWPT/TWT. ConclusionClinical application of suitable Chinese medicines combined with TWPT/TWT in the treatment of RA can effectively improve the rheumatism and reduce the adverse reactions of TWPT/TWT， and TGP-TWPT/TWT has the most significant toxicity-reducing effect. Further biological network-based investigation indicates that the toxicity-reducing mechanism of TGP-TWPT/TWT may be related to the regulation of interleukin signaling pathway and bile acid metabolism pathway， and the synergistic efficacy-enhancing effect of the combination may be achieved by acting on interleukin signaling pathway and cell function regulation pathway.

Atenção farmacêutica e farmacoterapia do idoso: uma revisão integrativa / Pharmaceutical care and pharmacotherapy for the elderly: an integrative review / Atención farmacéutica y farmacoterapia de las personas mayores: una revisión integradora

Este trabalho tem como objetivo selecionar e sintetizar as evidências da literatura sobre o contexto atual da atenção farmacêutica e farmacoterapia do idoso, considerando os aspectos clínicos e sociais envolvidos. A revisão foi conduzida de acordo com as diretrizes do protocolo PRISMA, que consiste na busca, seleção, avaliação e síntese de estudos relevantes sobre o tema. Foram selecionados 15 artigos que atenderam aos critérios de inclusão e exclusão estabelecidos. A análise dos artigos permitiu identificar que a atenção farmacêutica é um serviço que visa otimizar o uso racional de medicamentos e melhorar a qualidade de vida dos pacientes, especialmente dos idosos, que apresentam maior risco de polifarmácia, interações medicamentosas e reações adversas. A farmacoterapia do idoso envolve aspectos fisiológicos, psicológicos, sociais e econômicos que devem ser considerados na prescrição, dispensação e acompanhamento dos medicamentos. No entanto, ainda há precariedade na integração do farmacêutico nas equipes de saúde. Conclui-se que a atenção farmacêutica é uma estratégia importante a ser implementada em todas as equipes de saúde públicas e privadas, para promover o uso seguro e efetivo dos medicamentos pelos idosos, contribuindo para um envelhecimento saudável e digno.

This paper aims to select and synthesize evidence from the literature on the current context of pharmaceutical care and pharmacotherapy of the elderly, considering the clinical and social aspects involved. The review was conducted according to the guidelines of the PRISMA protocol, which consists of the search, selection, evaluation and synthesis of relevant studies on the topic. Fifteen articles that have met the established inclusion and exclusion criteria were selected. The analysis of the articles allowed the identification that pharmaceutical care is a service that aims to optimize the rational use of medicines and improve the quality of life of patients, especially the elderly, who present a higher risk of polypharmacy, drug interactions, and adverse reactions. The pharmacotherapy of the elderly involves physiological, psychological, social, and economic aspects that must be considered when prescribing, dispensing, and monitoring medications. However, there is still a precariousness in the integration of the pharmacist in health teams. It is concluded that pharmaceutical care is an important strategy to be implemented in all public and private health teams, to promote the safe and effective use of medicines by the elderly, contributing to a healthy and dignified aging.

Este trabajo tiene como objetivo seleccionar y sintetizar la evidencia de la literatura sobre el contexto actual de la atención farmacéutica y la farmacoterapia de las personas mayores, considerando los aspectos clínicos y sociales implicados. La revisión se ha realizado siguiendo las directrices del protocolo PRISMA, que consiste en la búsqueda, selección, evaluación y síntesis de estudios relevantes sobre el tema. Se seleccionaron 15 artículos que cumplieron los criterios de inclusión y exclusión establecidos. El análisis de los artículos permitió identificar que la atención farmacéutica es un servicio que tiene como objetivo optimizar el uso racional de los medicamentos y mejorar la calidad de vida de los pacientes, especialmente de los ancianos, que presentan un mayor riesgo de polifarmacia, interacciones medicamentosas y reacciones adversas. La farmacoterapia del anciano implica aspectos fisiológicos, psicológicos, sociales y económicos que deben ser considerados a la hora de prescribir, dispensar y monitorizar los medicamentos. Sin embargo, todavía existe una precariedad en la integración del farmacéutico en los equipos de salud. Se concluye que la atención farmacéutica es una estrategia importante a ser implementada en todos los equipos de salud públicos y privados, para promover el uso seguro y eficaz de los medicamentos por los ancianos, contribuyendo para un envejecimiento saludable y digno.

Atuação de um centro regional de informação sobre medicamentos na baixada fluminense de 2020 a 2022 / Performance of a regional drug information center in the baixada fluminense from 2020 to 2022 / Acción de un centro regional de información médica en la baja fluminencia de 2020 a 2022

No ano de 2020 observou-se um aumento da divulgação de informações parciais e sem embasamento científico sobre COVID-19. Nesse contexto, o Centro Regional de Informação sobre Medicamentos (CRIM) em uma Universidade Pública, torna-se um importante disseminador de informações referenciadas. Este trabalho foi realizado para identificar, por meio dos dados obtidos nos canais de comunicação em que essas ações virtuais foram desenvolvidas, o alcance atingido por cada publicação e evento. Dentre os materiais produzidos, 38,5% foram relacionados à COVID-19; 26,9% ao uso de medicamentos; 21,1% às datas representativas da área da saúde; e 13,5% às informações sobre doenças. Destacaram-se temas como: "Qual a diferença entre medicamento referência e genérico?"; "A importância de tomar o medicamento com água"; "CAFEÍNA: Uso indiscriminado"; "Interações fármacos x alimentos"; e "Imunização Infantil: Devo vacinar meu filho contra a COVID-19?". As ações de educação continuada, somadas às visualizações dos eventos produzidos totalizaram 5.160 visualizações. Destaca-se o IV Simpósio sobre Uso Racional de Medicamentos (URM) e o I Simpósio de Direitos Humanos e Saúde Mental que, em sua totalidade, somaram 3.459 visualizações. As ações reforçam a necessidade de promover práticas voltadas à informação para garantia do uso eficaz, seguro e racional de medicamentos.

In 2020, there was an increase in the dissemination of partial and scientifically unsupported information about COVID-19. In this context, the Regional Drug Information Center (RDIC) in a Public University becomes an important disseminator of referenced information. This work was carried out to identify, through the data obtained from the communication channels in which these virtual actions were developed, the reach atteined by each publication and event. Amongst the materials produced, 38.5% were related to COVID-19; 26.9% to the use of medication; 21.1% to representative dates in the health area; and 13.5% to information about diseases. Topics such as: "What is the difference between reference and generic medicine?"; "The importance of taking the medicine with water"; "CAFFEINE: Indiscriminate use"; "Drug x food interactions"; and "Childhood Immunization: Should I vaccinate my child against COVID-19?". Continuing education actions, added to the views of the events produced, totaled 5,160 views. We highlight the IV Symposium on Rational Use of Drugs (RUD) and the I Symposium on Human Rights and Mental Health which, in their entirety, totaled 3,459 views. The actions reinforces the need to promote information-oriented practices to ensure the effective, safe and rational use of medicines.

En el año 2020 se produjo un aumento en la difusión de información parcial y no se obtuvo ninguna base científica sobre el COVID-19. En este contexto, el Centro Regional de Información sobre Medicinas (CRM) de una Universidad Pública se convierte en un importante difusor de información referenciada. Este trabajo se llevó a cabo para identificar, mediante los datos obtenidos en los canales de comunicación en los que se desarrollaron estas acciones virtuales, el alcance alcanzado por cada publicación y evento. De los materiales producidos, el 38,5% estaban relacionados con el COVID-19; el 26,9% con el uso de medicamentos; el 21,1% con las fechas representativas del área de salud; y el 13,5% con información sobre enfermedades. Temas como: "¿Cuál es la diferencia entre la medicina de referencia y la genérica?"; "La importancia de tomar el medicamento con agua"; "CAFEÍNA: uso indiscriminado"; "Interacciones medicamentosas versus alimentos"; e "Inmunización infantil: ¿debo vacunar a mi hijo contra COVID-19?". Las acciones de la educación continua, sumadas a las visualizaciones de los eventos producidos, alcanzaron un total de 5.160 visitas. Se destacan el cuarto simposio sobre el uso racional de los medicamentos (UDA) y el primer simposio sobre derechos humanos y salud mental, que en su totalidad sumaron hasta 3.459 visualizaciones. Las medidas adoptadas refuerzan la necesidad de promover prácticas orientadas a la información para garantizar el uso eficaz, seguro y racional de los medicamentos.

Antibiotic safety among neonates and paediatrics in a public hospital: KwaZulu-Natal

Background: The World Health Organization (WHO) guidelines recommend the empiric treatment of infections before definitive treatment begins. However, ethical concerns limit the availability of clinical trials in neonates and paediatrics to fully ascertain the safety profile of antibiotics in these populations. Aim: This study aimed to quantify the use of antibiotics among neonates and paediatrics and commented on the use, rationale and appropriateness of antibiotics prescribed. Setting: A secondary level public sector hospital located in Durban, KwaZulu-Natal. Methods: Demographic and treatment information of neonates and paediatrics were collected retrospectively from January 2022 to June 2022. Data were obtained from patient files and extracted for analysis using Microsoft Excel®. Analytical and descriptive statistics were used to analyse patient demographics and treatment variables. Results: A total of 568 antibiotics, issued to 389 patients, were reviewed. Penicillins (40.1%), aminoglycosides (24.3%) and combination penicillin-beta-lactam inhibitors (23.3%) were identified as the most frequently prescribed antibiotics for inpatients. Most antibiotics prescribed to inpatients were for complications associated with pre-term birth (66.9%). Combination penicillin-beta-lactam inhibitors (34.7%), penicillins (29.5%) and cephalosporins (29.5%) were the most frequently prescribed antibiotics to outpatients. A correlation was found between the route of administration and the duration of therapy; the intravenous route (63.6%) was preferred over the oral route (36.4%) for administration. Conclusion: Many broad-spectrum antibiotics were prescribed, thus increasing the risk of resistance. Antibiotics were being prescribed according to the guidelines; however, there is still a need for therapeutic drug monitoring to ensure the continuation of rational drug use. Contribution: There was evidence of rational use of antibiotics in the public hospital (KwaZulu-Natal), in keeping with economic and availability factors.

Establishment and application of DUE criteria of Dolasetron / 药学实践杂志

Objective To establish the drug use evaluation ( DUE) of Dolasetron, evaluate the rationality of the clinical use of Dolasetron and provide a reference for the rationally clinical use of Dolasetron．Methods On the basis of Dolasetron DUE criteria, a retrospective analysis was made in 794 hospitalized patients from January 2021 to June 2021. Results The drug use evaluation criterion on Dolasetron consisted of drug indications, drug use process, the result of drug use and indication management. Conclusion There are some inappropriate medication problems in Dolasetron utilization in the hospital. The DUE criterion is very practical which could be used to standardize the clinical utilization of Dolasetron.

Framework design of WHO and typical national essential medicine lists and its implications for China / 中国药房

OBJECTIVE To sort out the common presentation forms and components of the framework of domestic and foreign essential medicine lists （EMLs）， in order to provide reference for optimizing the framework of the Chinese EML. METHODS The latest edition of the EMLs of WHO， China， South Africa， India， Malaysia and other typical countries were compared， and the similarities and differences of the presentation form and constituent elements of the list framework were analyzed. RESULTS & CONCLUSIONS The common presentation forms of WHO and typical countries’ EMLs included version， classifications and symbols， of which management ideas， functions， and implementation difficulties varied； common framework elements included target population， hospital levels， drug use conditions， core and supplementary lists and procurement priority. Through comparison， it was found that the information covered by the Chinese EML was relatively thin， and the framework design had not yet fully played the ideal role in guiding clinical rational drug use and optimizing the allocation of health resources， and there was still some room for improvement. It is recommended that China clarify the characteristics and roles of different presentation forms of the EML， and reasonably set the EML framework based on national conditions and development needs； the multi-dimensional drug information should be supplemented， such as clinical use， economy， and policy attributes of drugs in the EML， to ensure the rational use of essential drugs； it is also necessary to add “the level of hospitals” in the framework of the EML， refine the management requirements for the allocation and use of essential medicine， and optimize the resource allocation of hospitals.

Construction and application of rational drug use database for children in our hospital / 中国药房

OBJECTIVE To establish a database of rational drug use for children in our hospital， and to provide reference for ensuring the safety of drug use in children. METHODS The construction and filling of the knowledge base of rational drug use for children were performed by establishing the basic structure of the knowledge base， formulating reference standards for the quality level of pediatric medication evidence， and refining evidence-based evidence of pediatric medication. The rule base of rational drug use for children was designed and built from four aspects： preliminary determination rules for patient information， basic drug information rules， prescription suitability review rules， result labeling and post-processing rules. The database was embedded into prescription review system of our hospital and was applied online to test its effectiveness. RESULTS A set of database containing 672 commonly used pediatric medicines and more than 15 000 rules for rational drug use for children was initially constructed. The average interception rate of unreasonable medical orders for hospitalized children after database application（from December 2021 to May 2022）was 2.03%， and was higher than 0.80% before database application（from June 2021 to November 2021）（χ 2＝5 784.389， P＜0.001）； after post-sampling and prescription review， the average qualified rate of medication orders in discharged medical records for children after the application of the database was 99.10%， and was higher than 94.58% before the application of the database （χ 2＝301.237， P＜0.001）. CONCLUSIONS Self-constructed evidence-based rational drug use database for children is close to the actual clinical needs of pediatrics in medical institutions， which can effectively reduce clinical irrational drug use behaviors in pediatrics， improve the pass rate of prescriptions， and ensure the safety of children’s drug use.

Plan de implementación de Dosis Unitaria en el servicio de neonatología en el Hospital Cochabamba / Plan for the Implementation of the Unit Dose in the Neonatology Service of Cochabamba Hospital / Plano de Implementação de Dose Unitária no Serviço de Neonatologia do Hospital Cochabamba

En la actualidad la sepsis neonatal es uno de los principales diagnósticos en el servicio de Neonatología del Hospital Cochabamba, el medicamento de mayor elección para el tratamiento farmacológico de esta infección es la Amicacina, con la probabilidad de causar hipoacusia neonatal, la hipoacusia o disminución de la percepción auditiva, es un problema de especial importancia durante la infancia, ya que el desarrollo intelectual y social del niño está íntimamente ligado a las aferencias auditivas al sistema nervioso central, cuyo potencial discapacitante y minusvalidante depende en gran medida de la precocidad con que se realice el diagnóstico y se instaure el tratamiento y la rehabilitación. Objetivo. Diseñar un plan de implementación de Dosis Unitaria para contribuir a disminuir la hipoacusia en los pacientes neonatos. Materiales y Métodos se realizó un estudio documental basado en los registros de las Historias clínicas de los pacientes, realizándose un estudio descriptivo y retrospectivo. Se utilizaron los métodos empíricos como la encuesta, la entrevista y la observación científica, con el fin de demostrar y obtener un diagnóstico fidedigno, apoyándose con fuentes y estudios sobre la hipoacusia como sustento teórico. Resultados. Ante la evidencia de la existencia de la hipoacusia neonatal, como posible efecto adverso del uso farmacológico de la amicacina, se obtiene como resultado de la investigación la necesidad imperiosa de un plan de implementación en Dosis Unitaria para el servicio de neonatología del Hospital. Conclusiones. Los pacientes neonatos recibirán una atención segura, eficaz y humanizada con base a una implementación de Dosis Unitaria.

At present, neonatal sepsis is one of the main diagnoses in the Neonatology service of the Cochabamba Hospital, the drug of choice for the pharmacological treatment of this infection is Amicacin, with the probability of causing neonatal hypoacusis, the hypoacusis or decrease in auditory perception, is a problem of special importance during childhood, since the intellectual and social development of the child is intimately linked to the auditory afferents to the central nervous system, whose disabling and handicapping potential depends to a great extent on the precocity with which the diagnosis is made and the treatment and rehabilitation are established. Objective. To design a plan for the implementation of Unit Dose to contribute to the reduction of hearing loss in neonatal patients. Materials and Methods. A documentary study was carried out based on the patients' medical records, performing a descriptive and retrospective study. Empirical methods such as survey, interview and scientific observation were used in order to demonstrate and obtain a reliable diagnosis, supported by sources and studies on hypoacusis as theoretical support. Results. In view of the evidence of the existence of neonatal hypoacusis, as a possible adverse effect of the pharmacological use of amikacin, it is obtained as a result of the research the imperative need of an implementation plan in Unit Dose for the neonatology service of the Hospital. Conclusions. Neonatal patients will receive safe, effective and humanized care based on a Unit Dose implementation.

Atualmente, a sepse neonatal é um dos principais diagnósticos no serviço de Neonatologia do Hospital de Cochabamba. O medicamento de escolha para o tratamento farmacológico desta infecção é a Amicacina, com a probabilidade de causar hipoacusia neonatal, hipoacusia ou diminuição da percepção auditiva, é um problema de especial importância durante a infância, já que o desenvolvimento intelectual e social da criança está intimamente ligado aos aferentes auditivos do sistema nervoso central, cujo potencial incapacitante e deficiente depende em grande parte de quão cedo o diagnóstico é feito e como o tratamento e a reabilitação são estabelecidos. Objetivo. Elaborar um plano para a implementação da Unidade Dose para contribuir para a redução da perda auditiva em pacientes neonatais. Materiais e Métodos. Foi realizado um estudo documental baseado nos registros das histórias clínicas dos pacientes, realizando um estudo descritivo e retrospectivo. Métodos empíricos como pesquisa, entrevista e observação científica foram utilizados para demonstrar e obter um diagnóstico confiável, apoiado por fontes e estudos sobre hipoacusia como suporte teórico. Resultados. Dada a evidência da existência de hipoacusia neonatal, como um possível efeito adverso do uso farmacológico do amikacin, os resultados da pesquisa mostram a necessidade imperativa de um plano de implementação na Unidade Dose para o serviço de neonatologia do Hospital. Conclusões. Os pacientes neonatais receberão um cuidado seguro, eficaz e humanizado com base na implementação de uma dose unitária.

Oral Faropenem Sodium – Implications for Antimicrobial Resistance and Treatment Effectiveness

Rising antimicrobial resistance (AMR) is causing therapeutic failures with antibiotics. Inappropriate use is a contributing factor. One such antibiotic on the radar is faropenem, a broad spectrum antibiotic approved in 2005 in India. Recently, faropenem sodium suspension was approved for use in children. There is a potential danger of overuse due to the convenience of oral administration. Other carbapenems such as meropenem are used parenterally. Overuse of faropenem may promote cross-resistance with other carbapenems making them ineffective.

A prospective, questionnaire-based study to evaluate the knowledge, attitude, and practice of rational use of antibiotics among clinical practitioners in a tertiary care hospital

Background: Irrational antibacterial usage leads to emergence of antibiotic resistance. Hence, to ensure rational prescription regular clinical audits are essential in tertiary care hospitals. Aim and Objective: To assess the knowledge, attitude, and perception of clinician抯 on rational use of antibiotics in a tertiary care hospital. Materials and Methods: The prospective, questionnaire-based study was conducted on clinicians in a tertiary care hospital, after getting approval of the Institutional Ethics Committee to obtain information on rational antibiotic usage and was analyzed using descriptive statistics. Results: The study included 100 clinicians. 95% were aware about Rational antibiotic usage, the ingredients, adverse effects, interactions, contraindications, and cost of the drugs they prescribe and they were also analyzing the culture and sensitivity report before prescription of antibiotics, but only 48% of them were prescribing antibiotics from National List of Essential Medicines, 35% were influenced by patient demands. Around 80% agreed with the usefulness of the feedback given by fellow colleagues on antibiotic decisions. Though 98% of them were aware of the hazards of antibiotic resistance only 68% knew about antibiogram and having antibiotic policy at the workplace. In practice, 95% were showing special interest in proper antibiotic usage, 82% knew the new antibiotics available and 91% were providing proper counseling to patients. 95% suggested the need for training on rational use of medicines and antibiotic policy post MBBS. Conclusion: The clinicians recognized the importance of rational antibiotic use in preventing its resistance thus reducing health care burden on the patients.

Rational use of medicines among resident doctors: A cross-sectional study

Background: Irrational use of prescribing medicines is on the rise due to many factors. The Resident doctors are exposed to variety of prescribing patterns in their daily clinical practice. Aim and Objectives: The study was planned to assess the knowledge, attitude, and practice of rational use of medicine among Resident doctors in a tertiary care teaching hospital. Materials and Methods: A cross-sectional questionnaire-based study was conducted among Resident doctors at a tertiary care teaching hospital. Permission was obtained from the Institutional Ethics Committee. The participants were explained about the study and consent was taken. Identity of the residents was kept confidential. Questionnaire was designed to obtain information about the knowledge, attitude, and practice of Rational Use of Medicines (RUM). The data were recorded and analyzed, and the results are explained in frequency and percentage. Results: About 98% were aware about the term RUM and 96% practiced it, only 9% had National List of Essential Medicines of India available at their work place and 68% were able to correctly name the parts of the prescription slip. 88% respondents were aware about Essential Medicines (EM) and 86% prescribed them. Conclusion: In our study, majority of the Resident doctors were aware about EM and their importance. However, the level of understanding related to P-drug concept and existence of Essential Medicine List was limited. Thus, it is necessary to implement institutional guidelines to achieve more appropriate prescribing patterns, to promote prescription based on the list of EM.

Modelo de terapia assistida para dispensação de medicamentos imunobiológicos para artrite reumatoide no Sistema Único de Saúde: uso racional de recursos reduz despesas / Assisted therapy model for dispensing immunobiological drugs for rheumatoid arthritis by the Brazilian Unified Health System: rational use of resources reduces expenses

Objetivo: A incorporação dos imunobiológicos para tratamento da artrite reumatoide (AR) no Sistema Único de Saúde (SUS) representou um avanço significativo, porém teve um impacto importante no orçamento. Como o modelo vigente de dispensação direta ao paciente apresentava deficiências, implementou-se o modelo do CEDMAC de terapia assistida com foco no uso racional, visando minimizar despesas e potencializar o alcance. Entretanto, não há dados que comparem os dois modelos. Assim, esse estudo objetivou comparar o número de frascos efetivamente dispensados pelo modelo do CEDMAC à dispensação direta e avaliar seu impacto financeiro. Métodos: Foram incluídos atendimentos de pacientes com AR no CEDMAC em 2015, cujo imunobiológico foi fornecido pelo Ministério da Saúde. Foram registrados medicamento e dose recebidos, dose prescrita, número de frascos, cancelamentos por contraindicação e faltas. Como comparação, foi estimado o número de frascos que seriam entregues pela dispensação direta. Calculou-se a diferença entre o número total de frascos dispensados pelos dois sistemas e o impacto financeiro pelo valor de aquisição em 2015. Resultados: Em 2015, o CEDMAC realizou 3.784 atendimentos para pacientes com AR. O total de frascos de imunobiológicos prescritos foi de 10.000 frascos e 1.946 (19,5%) não foram utilizados por otimização de frascos, contraindicações ou absenteísmo. Os frascos não utilizados reduziram as despesas em R$ 806.132,62. A expansão do modelo para todo SUS reduziria as despesas em R$ 121.110.388,27. Conclusão: O modelo de terapia assistida do CEDMAC reduz consideravelmente o volume de frascos dispensados e pode trazer uma relevante redução de despesas no fornecimento dos imunobiológicos para AR no SUS.

Objective: The incorporation of immunobiologicals for the treatment of rheumatoid arthritis (RA) in the Brazilian Unified Health System (SUS) represented a significant advance but had an important impact on the budget. As the current model of direct delivery to the patient presented deficiencies, the CEDMAC model of assisted therapy focusing on rational use was implemented to minimize expenses and increase access. However, there is no data comparing the two models. Thus, this study aimed to compare the number of vials effectively dispensed by the CEDMAC model compared to direct delivery and to evaluate its financial impact. Methods: We included RA patients attended at CEDMAC during 2015, whose immunobiological was provided by Ministry of Health. Drug and dose received, prescribed dose, number of vials, cancellations due to contraindication and absences were recorded. As comparison, the number of vials that would be delivered by the direct delivery model were estimated. Savings were calculated by the difference between the total number of vials dispensed by the two systems and the financial impact by acquisition value in 2015. Results: During 2015, CEDMAC performed 3,784 consultations for RA patients. The total number of immunobiological vials prescribed was 10,000 vials and 1,946 (19.5%) were not used for vial optimization, contraindications or absenteeism. Saved vials reduced expenses by R$ 806,132.62. The expansion of the model for all SUS would reduce expenses by R$ 121,110,388.27. Conclusion: CEDMAC's model of assisted therapy considerably reduces the volume of dispensed vials and can bring significant cost offsets in the supply of RA immunobiologicals by SUS.

Assisted therapy model for dispensing immunobiological drugs for rheumatoid arthritis by the Brazilian Unified Health System: rational use of resources reduces expenses

Objective: The incorporation of immunobiological agents for rheumatoid arthritis (RA) treatment at the Brazilian Unified Health System (SUS) represented a significant advance but had an important impact on the budget. As the current model of direct patient delivery had deficiencies, the CEDMAC model of assisted therapy was implemented to focus on rational use to minimize expenses and increase access. However, there is no data to compare the two models. Thus, this study aimed to compare the number of bottles effectively dispensed by the CEDMAC model to direct dispensing and assess its financial impact. Methods: Care of RA patients at CEDMAC in 2015, whose immunobiological drugs were provided by the Ministry of Health, were included. Drug and dose received, prescribed dose, the number of bottles, cancellations due to contraindication, and absences were recorded. As a comparison, the number of bottles that would be delivered by direct dispensing was estimated. The difference between the total number of bottles dispensed by the two systems and the financial impact of the purchase price in 2015 was calculated. Results: In 2015, CEDMAC provided 3,784 consultations for RA patients. The total number of bottles of immunobiological agents prescribed was 10,000 bottles, and 1,946 (19.5%) were not used for bottle optimization, contraindications, or absenteeism. Unused bottles reduced expenses by R$ 806,132.62. The expansion of the model to the entire SUS would reduce costs by R$ 121,110,388.27. Conclusion: The CEDMAC assisted therapy model considerably reduces the volume of dispensed bottles and can significantly reduce expenses in the supply of immunobiological agents for RA at SUS.

Consumo de anticoncepcionais e fatores associados entre estudantes universitários / Contraceptive use and associated factors among university students

Introdução: o uso de anticoncepcionais vem crescendo a cada ano, sendo um dos principais motivos para a redução das taxas de fecundidade total, inclusive na população mais jovem, como a universitária. Objetivo: identificar o consumo de anticoncepcionais hormonais e fatores associados entre estudantes universitárias. Métodos: a população de estudo foi composta por estudantes universitárias matriculadas nos cursos de graduação da Universidade Estadual de Londrina (UEL), em Londrina, estado do Paraná, Brasil, no ano de 2019, integrantes do projeto maior denominado GraduaUEL. As estudantes responderam um instrumento construído em uma plataforma digital on-line. A variável dependente foi o consumo de contraceptivos hormonais, e as variáveis independentes foram aspectos sociodemográficos e hábitos de vida e de saúde. As associações medidas foram verificadas por meio de Regressão de Poisson, com cálculo da Razão de Prevalência (RP) e intervalo de confiança de 95% (IC 95%). Resultados: das 2.221 estudantes avaliadas, identificou-se o consumo de contraceptivos por 13,0%, maior entre mulheres brancas/amarelas, que relataram serem heterossexuais, que apresentavam pais com maior escolaridade, que referiram possuir plano privado de saúde e companheiro, e que praticavam atividade física pelo menos duas vezes na semana. Entretanto, apenas o fato de serem heterossexuais mostrou-se associação significativa após a análise ajustada (RP: 1,865; IC 95%: 1,308-2,659). Conclusões: diante do exposto, fica clara a necessidade de preparar os profissionais de saúde sobre os contraceptivos e seus efeitos adversos; ainda, que questões sociais devem ser consideradas no processo de uso dos contraceptivos, para combater a discriminação e as desigualdades social e econômica quanto ao acesso e uso destes medicamentos.

Introduction: the use of contraceptives has been growing every year, being one of the main reasons for the reduction in total fertility rates, including in the younger population, such as university students. Objective: identify the consumption of hormonal contraceptives and associated factors among university students. Methods: the study population consisted of university students enrolled in undergraduate courses at the Universidade Estadual de Londrina (UEL), in Londrina, Paraná state, Brazil, in 2019, members of the larger project called GraduaUEL. The students answered an instrument built on an on-line digital platform. The dependent variable was the consumption of hormonal contraceptives, and the independent variables were sociodemographic aspects, lifestyle and health. Measured associations were verified using Poisson Regression, with calculation of the Prevalence Ratio (PR) and 95% confidence interval (95% CI). Results: of the 2,221 students evaluated, the consumption of contraceptives was identified by 13.0%, higher among white/yellow women, who reported being heterosexual, who had parents with higher education, who reported having a private health plan and partner, and who practiced physical activity at least twice a week. However, only the fact of being heterosexual showed a significant association after the adjusted analysis (PR: 1.865; 95% CI: 1.308-2.659). Conclusions: in light of the above, the need to prepare health professionals about contraceptives and their adverse effects is clear, as well as what social issues should be considered in the process of using contraceptives, to combat discrimination, social and economic inequality regarding access and the use of these medications.

Clinical Evidence of Treatment of Constipation with Oral Chinese Patent Medicine： A Scoping Review / 中国实验方剂学杂志

This study systematically and comprehensively sorted out the application status of Chinese patent medicines for the treatment of constipation in the clinic， to provide scientific evidence for future research directions and clinical drug use in this field. Based on the method of scoping review， the Chinese patent medicines for the treatment of constipation were retrieved from three drug lists to obtain the medicines that needed to be evaluated. A comprehensive and systematic search was carried out on the included studies on the treatment of constipation by Chinese patent medicines through eight Chinese and English databases， and the included studies were integrated and analyzed. The results were displayed in combination with charts. Thirty-four Chinese patent medicines and 118 studies were included in this study. According to the efficacies， Chinese patent medicines were divided into 4 categories， namely eliminating accumulation， purging fire， promoting Qi， and moistening bowels， involving 125 Chinese medicines. The overall attention of constipation research is on the rise. Marenwan （granules or soft capsules） gained the highest attention， with 42 studies， followed by Qirong Runchang oral liquid， with 21 studies， and Biantong tablets （capsules）， with 19 studies. There are 10 studies on Congrong Tongbian oral liquid. Seventeen Chinese patent medicines had no corresponding clinical research. There were 8 study design types， and all drugs were mainly randomized controlled trials except Danggui Longhui pill. Among the intervention types， the comparison between Chinese patent medicines and western medicines was the most. The highest outcome indicators were efficacy， safety evaluation， and main symptoms or scores， and there was a lack of a unified core outcome indicator set. There were few studies on adverse reactions and the economy. Only 11.86% of the studies were funded. Clinically， Chinese patent medicines are widely used in the treatment of constipation， and the amount of related research shows an increasing trend. However， some Chinese patent medicines lack corresponding clinical evidence， and the published research has problems such as unrigorous design， ununified criteria for efficacy evaluation， lack of comprehensive evidence studies， and insufficient funds. It is hoped that more investment will be made in this field in the future， and more attention will be paid to drugs with relatively blank research and constipation syndromes with few treatments. Comprehensive evidence studies such as systematic reviews should be carried out actively. And the study design should be standardized to provide reliable evidence for the treatment of constipation with Chinese patent medicines.

Análise da polifarmácia e de fatores associados ao uso racional de medicamentos em idosos moradores de residência de cuidados de longa permanência / Analysis of polypharmacy and factors associated with the rational use of medicines in elderly residents of long-term care residences

Este trabalho teve por objetivo analisar a polifarmácia e os fatores associados ao uso racional de medicamentos em idosos moradores de residência de cuidado de longa permanência na perspectiva do cuidado nas condições crônicas de saúde. Foi desenvolvido junto a 68 prontuários, prescrições médicas e/ou registros de administração de medicamentos de idosos moradores de um residencial filantrópico do Vale do Paranapanema/São Paulo. A coleta de dados foi realizada por meio de um instrumento com perguntas abertas e fechadas sobre a temática e a análise se deu por meio do cálculo de frequência absoluta e relativa. A polifarmácia fazia parte da vida de grande parte dos idosos. Não foi possível compreender, por falta de sistematização e de controle documental interno, como os responsáveis técnicos do setor administrativo e da saúde adquiriam medicamentos, nem os custos envolvidos com a compra e o desperdício. Os medicamentos e seus resíduos eram descartados no lixo orgânico. Não foi possível também determinar se idosos recebiam o medicamento apropriado às suas necessidades clínicas, na dose e no período adequado às suas condições de saúde. Conclui-se que idosos moradores do residencial estão expostos à polifarmácia e o uso racional de medicamentos não é praticado.

This study aimed to analyze polypharmacy and factors associated with the rational use of medicines in elderly residents of long-term care homes from the perspective of care in chronic health conditions. This study was developed with sixty-eight medical records, medical prescriptions, and/or medication administration records of elderly residents of a philanthropic home, located in a municipality in the Vale do Paranapanema/São Paulo. Data was collected using an instrument with open and closed questions on the theme. The analysis consisted of calculating absolute and relative frequency. Polypharmacy was part of the life of most elderly people. It was not possible to understand, due to the lack of systematization and internal document control, how the technicians responsible for the administrative and health sectors acquired the medicines, nor the costs involved with the purchase and waste. Medicines and their residues were disposed of in organic waste. It was also not possible to determine whether the elderly received medication appropriate to their clinical needs, in the dose and within the appropriate period to their health conditions. Therefore, elderly residents of the residential are exposed to polypharmacy and the rational use of medicines is not practiced.