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1.
Nutr Hosp ; 34(2): 257-263, 2017 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-28421776

RESUMEN

OBJECTIVE: This study aimed to improve knowledge about drug administration through enteral feeding tubes (EFTs) in order to minimize efficacy and safety problems. MATERIAL AND METHODS: The study was performed in a public secondary care hospital with level II accreditation by the National Accreditation Organization (Organização Nacional de Acreditação ONA), in Fortaleza, Ceará, north-eastern Brazil. RESULTS: One hundred and eight oral solid medications that could be administered through EFTs and were not available in liquid forms were evaluated via transformation of their solid dosage forms into liquid forms. Dispersion times and conditions were assessed to determine which medications should be crushed. We compared the use of dispensers and syringes and their connections to enteral feeding tubes and intravenous devices. Medications whose dispersion occurred within 20 minutes and could be visually perceived and whose content could be expelled without occluding the oral syringe were considered "satisfactory". CONCLUSIONS: The dispersion was "satisfactory" in 82 (75.9%) of the medications; they were classified as capable of being dispersed in water in the oral syringe for further administration via EFTs without the need for crushing. Use the dispenser instead of the syringe for drug administration was safer because the dispenser apparatus did not fit into equipment for intravenous drug administration.


Asunto(s)
Nutrición Enteral/efectos adversos , Nutrición Enteral/instrumentación , Preparaciones Farmacéuticas/administración & dosificación , Cápsulas , Formas de Dosificación , Humanos , Pacientes Internos , Seguridad del Paciente , Comprimidos
2.
Nutr. hosp ; 34(2): 257-263, mar.-abr. 2017. tab, ilus
Artículo en Inglés | IBECS | ID: ibc-162424

RESUMEN

Objective: This study aimed to improve knowledge about drug administration through enteral feeding tubes (EFTs) in order to minimize efficacy and safety problems. Material and methods: The study was performed in a public secondary care hospital with level II accreditation by the National Accreditation Organization (Organização Nacional de Acreditação ONA), in Fortaleza, Ceará, north-eastern Brazil. Results: One hundred and eight oral solid medications that could be administered through EFTs and were not available in liquid forms were evaluated via transformation of their solid dosage forms into liquid forms. Dispersion times and conditions were assessed to determine which medications should be crushed. We compared the use of dispensers and syringes and their connections to enteral feeding tubes and intravenous devices. Medications whose dispersion occurred within 20 minutes and could be visually perceived and whose content could be expelled without occluding the oral syringe were considered «satisfactory». Conclusions: The dispersion was «satisfactory» in 82 (75.9%) of the medications; they were classified as capable of being dispersed in water in the oral syringe for further administration via EFTs without the need for crushing. Use the dispenser instead of the syringe for drug administration was safer because the dispenser apparatus did not fit into equipment for intravenous drug administration (AU)


Objetivo: este estudio tuvo como objetivo aumentar el conocimiento de la administración de medicamentos a través de las sondas de nutrición enteral (SNE), con el fin de reducir al mínimo los problemas de eficacia y seguridad inherentes al uso de esta vía. Material y métodos: el estudio se realizó en un hospital público en la atención secundaria, con el nivel II de acreditación por la Organización Nacional de Acreditación (ONA) en Fortaleza, Ceará, noreste de Brasil. Resultados: se evaluaron 108 preparaciones galénicas en forma sólida que podrían administrarse por SNE, no disponibles en forma líquida, mediante su preparación en una dilución. Se evaluaron los tiempos y las condiciones de dispersión para determinar qué medicamentos deberían triturarse. Se comparó el uso de dispositivos de distribución y de jeringas y sus conexiones con las SNE. Los fármacos cuya dispersión se produjo a los 20 minutos, que pudieran percibirse visualmente y cuyo contenido podría ser administrado sin ocluir la jeringa se consideraron de dispersión «satisfactoria». Conclusiones: la dispersión fue «satisfactoria» en 82 (75,9%) de los fármacos y se calificaron como capaces de dispersarse en agua en una jeringa, para la administración posterior a través de SNE, sin necesidad de ser triturados. El uso del dispensador en lugar de la jeringa para la administración enteral de medicamentos se considera más seguro debido a que el dispensador no se ajusta a los conectores utilizados para la administración de fármacos por vía intravenosa (AU)


Asunto(s)
Humanos , Masculino , Femenino , Nutrición Enteral/métodos , Atención Secundaria de Salud/organización & administración , Atención Secundaria de Salud , Preparaciones Farmacéuticas/administración & dosificación , Administración Intravenosa/métodos , Seguridad del Paciente , Métodos de Alimentación/tendencias , Resultado del Tratamiento , Nutrición Parenteral Total , Jeringas
3.
Rev Bras Reumatol Engl Ed ; 57(1): 23-29, 2017.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-28137399

RESUMEN

OBJECTIVE: The aim of this study was to investigate pharmacological treatment adherence of patients with juvenile idiopathic arthritis, attended in an outpatient pharmacy at a tertiary hospital in northeastern Brazil. METHODS: The analysis of adherence was performed along with caregivers, through a structured questionnaire based on Morisky, Green and Levine, which enabled the categorization of adherence in "highest", "moderate" or "low" grades, and through evaluating medication dispensing registers, which classified the act of getting medications at the pharmacy as "regular" or "irregular". Drug Related Problems (DRP) were identified through the narrative of caregivers and classified according to the Second Granada Consensus. Then, a pharmaceutical orientation chart with information about the therapeutic regimen was applied, in order to function as a guide for issues that influenced adherence. RESULTS: A total of 43 patients was included, with a mean age of 11.12 years, and 65.1% (n=28) were female. Applying the questionnaire, it was found "highest" adherence in 46.5% (n=20) patients, "moderate" adherence in 48.8% (n=21), and "low" adherence in 4.7% (n=2). Through an analysis of the medication dispensing registers, a lower level of adherence was observed: only 25.6% (n=11) of the participants received "regularly" the medications. Twenty-six DRP was identified, and 84.6% (n=22) were classified as real. There were no significant associations between socio-demographic variables and adherence, although some caregivers have reported difficulty in accessing the medicines and in understanding the treatment. CONCLUSION: Our findings showed problems in the adherence process related to inattention, forgetfulness and irregularity in getting medicines, reinforcing the need for the development of strategies to facilitate a better understanding of treatment and to ensure adherence.


Asunto(s)
Artritis Juvenil/tratamiento farmacológico , Cuidadores/estadística & datos numéricos , Cumplimiento de la Medicación/estadística & datos numéricos , Aceptación de la Atención de Salud/estadística & datos numéricos , Farmacias , Adolescente , Artritis Juvenil/epidemiología , Artritis Juvenil/psicología , Brasil , Cuidadores/educación , Niño , Revisión de la Utilización de Medicamentos , Femenino , Conocimientos, Actitudes y Práctica en Salud , Investigación sobre Servicios de Salud , Humanos , Masculino , Evaluación de Necesidades , Encuestas y Cuestionarios
4.
Rev. bras. reumatol ; 57(1): 23-29, Jan.-Feb. 2017. tab
Artículo en Inglés | LILACS | ID: biblio-844203

RESUMEN

ABSTRACT Objective: The aim of this study was to investigate pharmacological treatment adherence of patients with juvenile idiopathic arthritis, attended in an outpatient pharmacy at a tertiary hospital in northeastern Brazil. Methods: The analysis of adherence was performed along with caregivers, through a structured questionnaire based on Morisky, Green and Levine, which enabled the categorization of adherence in “highest”, “moderate” or “low” grades, and through evaluating medication dispensing registers, which classified the act of getting medications at the pharmacy as “regular” or “irregular”. Drug Related Problems (DRP) were identified through the narrative of caregivers and classified according to the Second Granada Consensus. Then, a pharmaceutical orientation chart with information about the therapeutic regimen was applied, in order to function as a guide for issues that influenced adherence. Results: A total of 43 patients was included, with a mean age of 11.12 years, and 65.1% (n = 28) were female. Applying the questionnaire, it was found “highest” adherence in 46.5% (n = 20) patients, “moderate” adherence in 48.8% (n = 21), and “low” adherence in 4.7% (n = 2). Through an analysis of the medication dispensing registers, a lower level of adherence was observed: only 25.6% (n = 11) of the participants received “regularly” the medications. Twenty-six DRP was identified, and 84.6% (n = 22) were classified as real. There were no significant associations between socio-demographic variables and adherence, although some caregivers have reported difficulty in accessing the medicines and in understanding the treatment. Conclusion: Our findings showed problems in the adherence process related to inattention, forgetfulness and irregularity in getting medicines, reinforcing the need for the development of strategies to facilitate a better understanding of treatment and to ensure adherence.


RESUMO Objetivo: Investigar a adesão ao tratamento farmacológico de pacientes com artrite idiopática juvenil, atendidos na farmácia ambulatorial de hospital terciário do Nordeste do Brasil. Métodos: A análise da adesão foi feita junto aos cuidadores, por meio de questionário estruturado com base no teste de Morisky, Green e Levine, que viabilizou a categorização da adesão em “máxima”, “moderada” ou “baixa”, e da avaliação dos registros de dispensação dos medicamentos, que classificou a retirada de medicamentos na farmácia como “regular” ou “irregular”. Os problemas relacionados com medicamentos (PRM) foram identificados por meio da narrativa dos cuidadores e classificados conforme o Segundo Consenso de Granada. Em seguida, aplicou-se uma tabela de orientação farmacêutica, que contém informações sobre o esquema terapêutico, de forma a esclarecer questões que influenciavam a adesão. Resultados: Participaram 43 pacientes, com média de 11,12 anos, 65,1%, (n = 28) do sexo feminino. Por meio do questionário, verificou-se adesão “máxima” em 46,5% (n = 20) dos pacientes, “moderada” em 48,8% (n = 21) e “baixa” em 4,7% (n = 2). Pelo registro de dispensação, observou-se um nível de adesão menor: apenas 25,6% (n = 11) dos participantes receberam os medicamentos “regularmente”. Identificaram-se 26 PRM, 84,6% (n = 22) classificados como “reais”. Não foram observadas associações significativas entre as variáveis sociodemográficas e a adesão, embora alguns cuidadores tenham relatado dificuldade de acesso ao medicamento e de compreensão do tratamento. Conclusão: Nossos achados demonstraram falhas no processo de adesão, relacionadas ao descuido, esquecimento e à irregularidade para receber os medicamentos, o que reforça a necessidade de estratégias para facilitar a compreensão do tratamento e garantir a adesão


Asunto(s)
Humanos , Masculino , Femenino , Niño , Adolescente , Farmacias , Artritis Juvenil/tratamiento farmacológico , Aceptación de la Atención de Salud/estadística & datos numéricos , Cuidadores/estadística & datos numéricos , Cumplimiento de la Medicación/estadística & datos numéricos , Artritis Juvenil/psicología , Artritis Juvenil/epidemiología , Brasil , Conocimientos, Actitudes y Práctica en Salud , Encuestas y Cuestionarios , Cuidadores/educación , Revisión de la Utilización de Medicamentos , Evaluación de Necesidades , Investigación sobre Servicios de Salud
5.
Rev Bras Reumatol ; 2016 Mar 08.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-27012520

RESUMEN

OBJECTIVE: The aim of this study was to investigate pharmacological treatment adherence of patients with juvenile idiopathic arthritis, attended in an outpatient pharmacy at a tertiary hospital in northeastern Brazil. METHODS: The analysis of adherence was performed along with caregivers, through a structured questionnaire based on Morisky, Green and Levine, which enabled the categorization of adherence in "highest", "moderate" or "low" grades, and through evaluating medication dispensing registers, which classified the act of getting medications at the pharmacy as "regular" or "irregular". Drug Related Problems (DRP) were identified through the narrative of caregivers and classified according to the Second Granada Consensus. Then, a pharmaceutical orientation chart with information about the therapeutic regimen was applied, in order to function as a guide for issues that influenced adherence. RESULTS: A total of 43 patients was included, with a mean age of 11.12 years, and 65.1% (n=28) were female. Applying the questionnaire, it was found "highest" adherence in 46.5% (n=20) patients, "moderate" adherence in 48.8% (n=21), and "low" adherence in 4.7% (n=2). Through an analysis of the medication dispensing registers, a lower level of adherence was observed: only 25.6% (n=11) of the participants received "regularly" the medications. Twenty-six DRP was identified, and 84.6% (n=22) were classified as real. There were no significant associations between socio-demographic variables and adherence, although some caregivers have reported difficulty in accessing the medicines and in understanding the treatment. CONCLUSION: Our findings showed problems in the adherence process related to inattention, forgetfulness and irregularity in getting medicines, reinforcing the need for the development of strategies to facilitate a better understanding of treatment and to ensure adherence.

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