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3.
Nutr Hosp ; 21(5): 581-90, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17044604

RESUMO

OBJECTIVE: To assess the use of oral nutritional supplements analyzing the reason for prescription and its implication in caloric-protein intake. SETTING: study performed at a university hospital of 350 beds with medical and surgical specialties. SUBJECTS, PATIENTS: Patients inclusion was done by selecting all starting oral nutritional supplement prescription. Exclusion criteria were being younger than 18 years, being admitted to the Intensive Care Unit, having cognition or communication impairments, being on concomitant parenteral nutrition or requiring complete enteral diet, and/or using nasogastric tube for feeding. We also excluded special enteral diets, specifically designed for certain conditions. INTERVENTIONS: One-year long prospective study on prescription of oral nutritional supplements. Through clinical chart review and personal interview, we recorded demographic data, nutritional parameters, characteristics of the diet and supplement, and caloricprotein intake prescribed and ingested. The data were introduced in an Access97 database and processed by means of SPSS software for Windows. We performed a descriptive study of quantitative and qualitative variables, a chi2 analysis between qualitative variables, and a comparative analysis between means of all paired data by means of the student's t test, and variance analysis between quantitative variables. The significance level was set at p < 0.05. RESULTS: we were only able to analyze 77 out of 130 prescriptions for nutritional supplements since we could not adequately interview the remaining patients, mainly due to neurological impairments. Mean age was 74.8 years (SD = 12) and 50.6% were women. The departments prescribing the highest number of supplements were hematology (22.1%) and internal medicine (20.8%). GI neoplasm was the most frequent diagnosis at admission (27.3%). The most frequent indication was kwashiorkor (45.5%), with 15.6% of patients being well nourished. Mean therapy duration was 11 days (SD = 11.1), and the main reason for termination was hospital discharge (70.1%). The supplement was concomitantly prescribed with the meals in 70.6% of the cases, and more than half of the patients (70.1%) liked it, the most frequently prescribed was as a cream (61%) and the best accepted being as a liquid (78%). The average daily caloric load ingested with the foods of the hospital diet was similar between the first an third days of supplement prescription (p = 0.879) and the first and seventh days (p = 0.499). So happened when analyzing protein intake. With the supplement administration, there was a significant increase in patients' caloric intake from 310 Kcal at the third day to 337 Kcal at the seventh day (p < 0.0005) in both cases. Similar results were obtained when assessing total protein load ingested (p < 0.0005). CONCLUSIONS: Nutritional supplements are correctly used in most of the cases. They allow for a significant increase in the protein-caloric intake with no modification of hospital diet, becoming an appropriate nutritional source when the diet is insufficient.


Assuntos
Suplementos Nutricionais/estatística & dados numéricos , Nutrição Enteral/estatística & dados numéricos , Idoso , Idoso de 80 Anos ou mais , Ingestão de Energia , Feminino , Humanos , Masculino
4.
Nutr. hosp ; 21(5): 581-590, sept.-oct. 2006. ilus, tab
Artigo em Es | IBECS | ID: ibc-049884

RESUMO

Objetivo: Evaluar la utilización de suplementos nutricionales orales analizando el motivo de su prescripción y su implicación en el aporte calórico-proteico ingerido. Ámbito: Estudio realizado en un hospital universitario de 350 camas, que dispone de especialidades médicas y quirúrgicas. Sujetos, pacientes: La inclusión de pacientes se realizó mediante selección de todas las prescripciones de inicio de suplemento nutricional oral. Los criterios de exclusión fueron ser menor de 18 años, estar ingresado en la Unidad de Cuidados Intensivos, presentar problemas cognitivos o de comunicación, seguir tratamiento concomitante con nutrición parenteral o precisar dieta enteral completa, y/o ser portador de sonda nasogástrica para alimentación. También se excluyeron las dietas enterales especiales, que están diseñadas específicamente para algunas patologías. Intervenciones: Estudio longitudinal y prospectivo de la prescripción de suplementos nutricionales por vía oral realizado durante un año. Mediante revisión de la historia clínica y entrevista personalizada, se registraron datos demográficos, parámetros nutricionales, características de la dieta y del suplemento, y aporte calórico-proteico prescrito e ingerido. Los datos fueron introducidos en una base de datos Access 97 y procesados mediante el programa SPSS para Windows. Se realizó un estudio descriptivo de las variables cualitativas y cuantitativas, un análisis de χ2 entre variables cualitativas, un análisis de comparación de medias para datos apareados mediante una t Student y un análisis de la varianza entre variables cuantitativas. El nivel de significación establecido fue p < 0,05. Resultados: De 130 prescripciones de suplemento nutricional, se analizaron 77 por la imposibilidad de entrevistar correctamente al resto de pacientes, principalmente por motivos neurológicos. El promedio de edad fue de 74,8 años (DE = 12) y el 50,6% eran mujeres. Los servicios que prescribieron mayor número de suplementos fueron hematología (22,1%) y medicina interna (20,8%).La neoplasia digestiva fue el diagnóstico de ingreso más frecuente (27,3%). La indicación mayoritaria fue el kwashiorkor (45,5%), observándose un 15,6% de pacientes no malnutridos. La duración media del tratamiento fue de 11 días (DE = 11,1) y el principal motivo de fin, el alta hospitalaria (70,1%). El suplemento se prescribió concomitante con las comidas en el 70,6% de los casos y gustó a más de la mitad de los pacientes (70,1%), siendo el de tipo crema el más prescrito (61%) y el líquido el mejor aceptado (78%). El promedio del aporte calórico diario ingerido con los alimentos de la dieta hospitalaria fue similar entre el día de la prescripción del suplemento y el tercer día (p = 0,879), así como entre el primero y el séptimo (p = 0,499). De forma parecida sucedía al valorar la ingesta proteica. Con la administración del suplemento, se produjo un aumento significativo en la ingesta del paciente de 310 kcal a los 3 días y de 337 kcal a la semana (p < 0,0005 en ambos casos).Resultados similares se obtuvieron en la valoración del aporte proteico total ingerido (p < 0,0005). Conclusiones: Los suplementos nutricionales se utilizan correctamente en la mayoría de los casos. Permiten aumentar significativamente el aporte calórico-proteico ingerido, no modificando la ingesta de la dieta hospitalaria, pudiendo ser una fuente nutricional apropiada que complemente a la dieta cuando ésta resulta insuficiente (AU)


Objective: to assess the use of oral nutritional supplements analyzing the reason for prescription and its implication in caloric-protein intake. Setting: study performed at a university hospital of 350 beds with medical and surgical specialties. Subjects, patients: Patients inclusion was done by selecting all starting oral nutritional supplement prescription.Exclusion criteria were being younger than 18 years, being admitted to the Intensive Care Unit, having cognition or communication impairments, being on concomitant parenteral nutrition or requiring complete enteral diet, and/or using nasogastric tube for feeding. We also excluded special enteral diets, specifically designed for certain conditions. Interventions: One-year long prospective study on prescription of oral nutritional supplements. Through clinical chart review and personal interview, we recorded demographic data, nutritional parameters, characteristics of the diet and supplement, and caloricprotein intake prescribed and ingested. The data were introduced in an Access 97 database and processed by means of SPSS software for Windows®.We performed a descriptive study of quantitative and qualitative variables, a χ2 analysis between qualitative variables, and a comparative analysis between means of all paired data by means of the student´s t test, and variance analysis between quantitative variables. The significance level was set at p < 0.05. Results: we were only able to analyze 77 out of 130 prescriptions for nutritional supplements since we could not adequately interview the remaining patients, mainly due to neurological impairments. Mean age was 74.8 years (SD = 12) and 50.6% were women. The departments prescribing the highest number of supplements were hematology (22.1%) and internal medicine (20.8%). GI neoplasm was the most frequent diagnosis at admission (27.3%). The most frequent indication was kwashiorkor (45.5%), with 15.6% of patients being well nourished.Mean therapy duration was 11 days (SD = 11.1), and the main reason for termination was hospital discharge (70.1%). The supplement was concomitantly prescribed with the meals in 70.6% of the cases, and more than half of the patients (70.1%) liked it, the most frequently prescribed was as a cream (61%) and the best accepted being as a liquid (78%). The average daily caloric load ingested with the foods of the hospital diet was similar between the first an third days of supplement prescription (p =0.879) and the first and seventh days (p = 0.499). So happened when analyzing protein intake. With the supplement administration, there was a significant increase in patients´ caloric intake from 310 Kcal at the third day to 337 Kcal at the seventh day (p < 0.0005) in both cases. Similar results were obtained when assessing total protein load ingested (p < 0.0005). Conclusions: Nutritional supplements are correctly used in most of the cases. They allow for a significant increase in the protein-caloric intake with no modification of hospital diet, becoming an appropriate nutritional source when the diet is insufficient (AU)


Assuntos
Masculino , Feminino , Idoso , Idoso de 80 Anos ou mais , Humanos , Suplementos Nutricionais/estatística & dados numéricos , Nutrição Enteral/estatística & dados numéricos , Ingestão de Energia , Estudos Prospectivos , Estudos Longitudinais , Seguimentos
5.
Farm Hosp ; 28(5): 334-48, 2004.
Artigo em Espanhol | MEDLINE | ID: mdl-15504091

RESUMO

OBJECTIVE: To establish a method for evaluating, in a systematic and periodic way, the degree of compliance with the protocols currently being used in the hospital. MATERIALS AND METHOD: Experts from the hospital designed 6 protocols which were later approved by consensus by several committees and agreed by Medical Direction. The doctors were informed of the new protocols by means of info-sessions and printed materials. In order to evaluate to what extent the protocols were complied with, we carried out a number of longitudinal and cross-sectional studies depending on how often the protocols are used. RESULTS: The study involved 2,190 patients. Cross-sectional studies. Surgical antimicrobial prophylaxis protocol: compliance with the application forms was 83.3% and for surgical interventions it was 64.3%. It should be noted that adherence improved with time. Sliding-scale insulin therapy: compliance improved during the observation period from 54 to 71.1%. Prevention of NSAID induced gastropathy: after 6 months a significant improvement was observed in relation to the previous phase. Pain treatment: of the 117 analgesics prescribed on-demand in the previous phase, 27.3% were administered, as well as 68.4% of a total of 95 fixed prescriptions. In the phases previous to setting up these protocols, adherence ranged from 0 to 68.4%. One year later, adhesion has improved significantly for all the evaluated protocols. Longitudinal studies. Community acquired pneumonia: adhesion was 60.8%, while non significant differences were observed according to severity. Transitory ischemic accident: compliance evaluation showed an adherence value of 81.8%. CONCLUSIONS: When the degree of compliance is high, follow-up studies may be spaced out in time. If not, the reasons for this low compliance must be identified and measures must be taken. Follow-up studies must be carried out more often when protocols have just been set up and less frequently as adherence improves.


Assuntos
Revisão de Uso de Medicamentos , Fidelidade a Diretrizes/normas , Hospitais Universitários/normas , Serviço de Farmácia Hospitalar/normas , Estudos Transversais , Fidelidade a Diretrizes/estatística & dados numéricos , Hospitais Universitários/estatística & dados numéricos , Humanos , Estudos Longitudinais , Serviço de Farmácia Hospitalar/estatística & dados numéricos , Avaliação de Programas e Projetos de Saúde , Garantia da Qualidade dos Cuidados de Saúde/métodos
6.
Farm. hosp ; 28(5): 334-348, sept.-oct. 2004.
Artigo em Es | IBECS | ID: ibc-36071

RESUMO

Objetivo: Establecer un método que permita evaluar, de forma sistemática y periódica, el grado de cumplimiento de los protocolos instaurados en el hospital.Material y método: Expertos del hospital elaboraron 6 protocolos, los consensuaron diferentes Comités y los validó la Dirección Médica. Se difundieron a los facultativos empleando métodos de difusión escrita (material impreso) y orales (sesiones informativas).Para evaluar el cumplimiento se realizaron estudios epidemiológicos longitudinales o transversales según su prevalencia de utilización.Resultados: Se evaluaron 2.190 pacientes.Estudios transversales. Protocolo de profilaxis antibiótica en cirugía: el cumplimiento de los impresos de solicitud fue del 83,3 por ciento y de las intervenciones quirúrgicas del 64,3 por ciento, observándose que la adherencia mejoraba con el tiempo. Pauta móvil de insulina rápida: se observó una mejora a lo largo del tiempo del 54 al 71,1 por ciento. Profilaxis de gastropatía por AINE: a los 6 meses se observó una mejora significativa respecto a la fase previa. Tratamiento del dolor: en la fase previa, de los 117 analgésicos prescritos a demanda se administró el 27,3 por ciento y de las 95 pautas fijas el 68,4 por ciento. En las fases previas a la implantación de estos protocolos se observaron resultados que oscilan entre el 0 y el 68,4 por ciento de adherencia. Al año, la adherencia mejora significativamente en todos los protocolos evaluados.Estudios longitudinales. Neumonía adquirida en la comunidad: la adhesión fue del 60,8 por ciento, observándose diferencias no significativas según la gravedad. Accidente isquémico transitorio: el análisis del cumplimiento mostró una adherencia del 81,8 por ciento.Conclusiones: Cuando se consigue un alto nivel de cumplimiento, los estudios de seguimiento pueden hacerse espaciados; si estos no son aceptables, deben buscarse los motivos y tomar las medidas para mejorarlos. El seguimiento debe hacerse más a menudo al implantar los protocolos y espaciar los intervalos a medida que mejora la adherencia (AU)


Assuntos
Humanos , Revisão de Uso de Medicamentos , Estudos Longitudinais , Garantia da Qualidade dos Cuidados de Saúde , Serviço de Farmácia Hospitalar , Hospitais Universitários , Estudos Transversais , Fidelidade a Diretrizes , Avaliação de Programas e Projetos de Saúde
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