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1.
BMC Geriatr ; 19(1): 215, 2019 08 07.
Artigo em Inglês | MEDLINE | ID: mdl-31390994

RESUMO

BACKGROUND: URGENT is a comprehensive geriatric assessment (CGA) based nurse-led care model in the emergency department (ED) with geriatric follow-up after ED discharge aiming to prevent unplanned ED readmissions. METHODS: A quasi-experimental study (sequential design with two cohorts) was conducted in the ED of University Hospitals Leuven (Belgium). Dutch-speaking, community-dwelling ED patients aged 70 years or older were eligible for enrolment. Patients in the control cohort received usual care. Patient in the intervention cohort received the URGENT care model. A geriatric emergency nurse conducted CGA and interdisciplinary care planning among older patients identified as at risk for adverse events (e.g. unplanned ED readmission, functional decline) with the interRAI ED Screener© and clinical judgement of ED staff. Case manager follow-up was offered to at risk patients without hospitalization after index ED visit. For inpatients, geriatric follow-up was guaranteed on an acute geriatric ward or by the inpatient geriatric consultation team on a non-geriatric ward if considered necessary. Primary outcome was unplanned 90-day ED readmission. Secondary outcomes were ED length of stay (LOS), hospitalization rate, in-hospital LOS, 90-day higher level of care, 90-day functional decline and 90-day post-hospitalization mortality. RESULTS: Almost half of intervention patients (404/886 = 45.6%) were categorized at risk. These received on average seven advices. Adherence rate to advices on the ED, during hospitalization and in community care was 86.1, 74.6 and 34.1%, respectively. One out of four at risk patients without hospitalization after index ED visit accepted case manager follow-up. Unplanned ED readmission occurred in 170 of 768 (22.1%) control patients and in 205 of 857 (23.9%) intervention patients (p = .11). The intervention group had shorter ED LOS (12.7 h versus 19.1 h in the control group; p < .001), but higher rate of hospitalization (70.0% versus 67.0% in the control group; p = .003). CONCLUSIONS: The URGENT care model shortened ED LOS and increased the hospitalization rate, but did not prevent unplanned ED readmissions. A geriatric emergency nurse could improve in-hospital patient management, but failed to introduce substantial out-hospital case-management. TRIAL REGISTRATION: The protocol of this study was registered retrospectively with ISRCTN ( ISRCTN91449949 ; registered 20 June 2017).


Assuntos
Estudos Controlados Antes e Depois/tendências , Serviços Médicos de Emergência/tendências , Avaliação Geriátrica , Readmissão do Paciente/tendências , Cuidado Transicional/tendências , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Estudos Controlados Antes e Depois/métodos , Serviços Médicos de Emergência/métodos , Serviço Hospitalar de Emergência/tendências , Feminino , Avaliação Geriátrica/métodos , Mortalidade Hospitalar/tendências , Hospitais Universitários/tendências , Humanos , Masculino , Alta do Paciente/tendências , Estudos Prospectivos , Estudos Retrospectivos
2.
BMC Musculoskelet Disord ; 19(1): 148, 2018 May 16.
Artigo em Inglês | MEDLINE | ID: mdl-29769120

RESUMO

BACKGROUND: Clinical evidence shows knee arthroscopy has little benefit for degenerative conditions and considerable variation in the incidence of knee arthroscopy in Australia has been identified. This study aimed to evaluate a clinician-led evidence-based policy which was implemented in one local health district in New South Wales (NSW) in 2012 to reduce the use of knee arthroscopy for patients aged 50 years or over. METHODS: Trends in rates and volume of knee arthroscopy for patients 50 years or over in NSW between 2004 and 2015 by district were examined. Changes at four hospitals that adopted the policy were assessed by a quasi-experimental before and after study design with control groups, using the generalised estimating equations (GEE) Poisson model. Each case hospital was matched with four control hospitals in terms of the volume of knee arthroscopy surgeries performed in the five years prior to the intervention. RESULTS: Between 2004 and 2015, the number of knee arthroscopies in NSW initially increased and then decreased after 2011, with considerable variation across districts. While an overall reducing trend in NSW was observed between 2011 and 2015 (39%), a 58% reduction (95% CI: 55-62%) was found in the intervention district, including the private sector, being the greatest reduction found in all districts. The GEE Poisson results show that, compared with control hospitals, the number of knee arthroscopy was significantly reduced by 56% (95% CI: 11%-79%) at four hospitals that adopted the policy during the follow-up period (p = 0.02). CONCLUSIONS: Clinicians in one local health district initiated a policy to restrict knee arthroscopy for patients aged 50 years or over, which may explain the greater reduction seen in that district compared to all others, despite an overall decrease noted in the state. A significant reduction found at intervened hospitals proved the effect of the policy, suggesting that the implementation of a simple clinical governance process may help reduce inappropriate surgery.


Assuntos
Artroscopia/tendências , Estudos Controlados Antes e Depois/tendências , Política de Saúde/tendências , Médicos/tendências , Artroscopia/normas , Estudos Controlados Antes e Depois/normas , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , New South Wales/epidemiologia , Osteoartrite do Joelho/epidemiologia , Osteoartrite do Joelho/cirurgia , Médicos/normas
3.
BMC Geriatr ; 18(1): 19, 2018 01 19.
Artigo em Inglês | MEDLINE | ID: mdl-29351772

RESUMO

BACKGROUND: Education of healthcare workers is a core element of multicomponent delirium strategies to improve delirium care and, consequently, patient outcomes. However, traditional educational strategies are notoriously difficult to implement. E-learning is hypothesised to be easier and more cost effective, but research evaluating effectiveness of delirium education through e-learning is scarce at present. Aim is to determine the effect of a nursing e-learning tool for delirium on: (1) in-hospital prevalence, duration and severity of delirium or mortality in hospitalized geriatric patients, and (2) geriatric nurses' knowledge and recognition regarding delirium. METHODS: A before-after study in a sample of patients enrolled pre-intervention (non-intervention cohort (NIC); n = 81) and post-intervention (intervention cohort (IC); n = 79), and nurses (n = 17) of a geriatric ward (university hospital). The intervention included an information session about using the e-learning tool, which consisted of 11 e-modules incorporating development of knowledge and skills in the prevention, detection and management of delirium, and the completion of a delirium e-learning tool during a three-month period. Key patient outcomes included in-hospital prevalence and duration of delirium (Confusion Assessment Method), delirium severity (Delirium Index) and mortality (in-hospital; 12 months post-admission); key nurse outcomes included delirium knowledge (Delirium Knowledge Questionnaire) and recognition (Case vignettes). Logistic regression and linear mixed models were used to analyse patient data; Wilcoxon Signed Rank tests, McNemar's or paired t-tests for nursing data. RESULTS: No significant difference was found between the IC and NIC for in-hospital prevalence (21.5% versus 25.9%; p = 0.51) and duration of delirium (mean 4.2 ± SD 4.8 days versus 4.9 ± SD 4.8 days; p = 0.38). A trend towards a statistically significant lower delirium severity (IC versus NIC: difference estimate - 1.59; p = 0.08) was noted for delirious IC patients in a linear mixed model. No effect on patient mortality and on nurses' delirium knowledge (p = 0.43) and recognition (p = 1.0) was found. CONCLUSION: Our study, the first in its area to investigate effects of delirium e-learning on patient outcomes, demonstrated no benefits on both geriatric patients and nurses. Further research is needed to determine whether delirium e-learning nested within a larger educational approach inclusive of enabling and reinforcing strategies, would be effective. TRIAL REGISTRATION: ISRCTN ( 82,293,702 , 27/06/2017).


Assuntos
Estudos Controlados Antes e Depois/métodos , Delírio/prevenção & controle , Educação a Distância/métodos , Enfermagem Geriátrica/educação , Pessoal de Saúde/educação , Serviços de Saúde para Idosos , Idoso , Estudos de Coortes , Estudos Controlados Antes e Depois/tendências , Delírio/diagnóstico , Delírio/psicologia , Educação a Distância/tendências , Feminino , Pessoal de Saúde/tendências , Serviços de Saúde para Idosos/tendências , Hospitais Universitários/tendências , Humanos , Masculino , Resultado do Tratamento
4.
Nutr. hosp ; 33(4): 983-1000, jul.-ago. 2016.
Artigo em Inglês | IBECS | ID: ibc-154929

RESUMO

Background and aim: Preoperative nutritional status (NS) has consequences on postoperative (POSTOP) recovery. Our aim was to systematically review the nutritional interventions (NI) in fast-track protocols for colorectal cancer surgery and assess morbidity-mortality and patient´s recovery. Method: Systematic review of scientific literature after consulting bibliographic databases: Medline, The Cochrane Library, Scopus, Embase, Web of Science, Institute for Scientific Information, Latin American and Caribbean Health Sciences Literature, The Cumulative Index to Nursing and Allied Health Literature. MeSH Descriptors: ‘colorectal surgery’, ‘fast-track’, ‘perioperative care’, ‘nutrition therapy’ and ‘enhanced recovery programme’. Filters: ‘humans’, adult (19+ years) and ‘clinical trial’. Variables POSTOP outcomes: bowel recovery (BR), hospital stay (HS), complications and death. Results: Selected studies, 27, had good or excellent methodological quality. From 25 to 597 patients were included. Aged between 16-94 years, men were predominant in 66.6%. NS was evaluated in 13 studies; 7 by body mass index while one by subjective global assessment. One presented POSTOP data. Fast-track groups had solids, liquids or supplements (SS) in prior 2-8 hours. SS were high in carbohydrates, immune-nutrients and non-residue. Free liquids, solids and SS intake was allowed in POSTOP. Half traditional groups fasted between 3-12 hours and resumed POSTOP food intake progressively. Conclusions: Fast-track groups had early BR (p < 0.01). Traditional groups had more infections episodes, deaths and a longer HS. Great variability between NI but had a common item; early intake. Although was seen patient’s recovery. Future studies with detailed NI characteristics are need. Nutritional status must be assessed for a higher acknowledgement of NI impact (AU)


Introducción y objetivo: el estado nutricional (NS) preoperatorio tiene consecuencias sobre la recuperación postoperatoria (POSTOP). El objetivo fue revisar sistemáticamente las intervenciones nutricionales (NI) en los protocolos de fast-track en la cirugía de cáncer colorrectal y evaluar la morbilidad-mortalidad y la recuperación del paciente. Método: revisión sistemática de la literatura científica previa consulta a las bases de datos bibliográficas: Medline, Cochrane Library, Scopus, Embase, Web of Science, Latin American and Caribbean Health Sciences Literature (LILACS), The Cumulative Index to Nursing and Allied Health Literature (CINAHL). Descriptores MeSH: ‘colorectal surgery’, ‘fast-track’, ‘perioperative care’, ‘nutrition therapy’ and ‘enhanced recovery programme’. Filtros: ‘humans’, ‘adult (19+ years)’ and ‘clinical trial’. Variables resultados después de la operación: recuperación del intestino (BR), estancia hospitalaria (HS), complicaciones y la muerte. Resultados: los 27 estudios seleccionados tenían buena o excelente calidad metodológica. Incluían desde 25 a 597 pacientes, con edades comprendidas entre 16-94 años; los hombres fueron predominantes en el 66,6%. El estado nutricional se evaluó en 13 estudios; 7 por el índice de masa corporal, mientras que uno lo fue por la evaluación subjetiva general. Uno de ellos presentó datos después de la operación. Los grupos fast-track ingirieron, líquidos o suplementos (SS) en 2-8 horas antes. SS contenían altas cantidades de hidratos de carbono, inmunonutrientes y sin-residuos. En POSTOP se administraron líquidos, sólidos y SS. Los grupos tradicionales estuvieron en ayunas entre 3-12 horas y se reanudó la ingesta de alimentos progresivamente. Conclusiones: los grupos fast-track presentaron BR temprana (p < 0,01), los tradicionales tuvieron más infecciones, muertes y un HS más larga. Se observó gran variabilidad en las NI, pero había un punto común: ingesta temprana. A pesar de que se observó una recuperación del paciente, se necesitan futuros estudios con características de la NI más detalladas. Se debe evaluar el NS para poder reconocer el estado nutricional para un mayor reconocimiento del impacto NI (AU)


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto Jovem , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Neoplasias Colorretais/dietoterapia , Neoplasias Colorretais/epidemiologia , Vigilância Alimentar e Nutricional , Avaliação Nutricional , Estado Nutricional/fisiologia , Dietoterapia/instrumentação , Dietoterapia/métodos , Dietoterapia , Período Pré-Operatório , Estudos Controlados Antes e Depois/métodos , Estudos Controlados Antes e Depois/tendências
5.
Rev. Soc. Esp. Dolor ; 23(3): 135-140, mayo-jun. 2016. tab
Artigo em Espanhol | IBECS | ID: ibc-153263

RESUMO

Objetivos: Determinar la frecuencia de uso de analgésicos en pacientes terminales atendidos en domicilio, analizando factores que pudieran intervenir en la percepción del dolor, además de las actuaciones llevadas a cabo. Material y métodos: Estudio analítico prospectivo e intervencional con pacientes derivados al Equipo de Soporte para Atención Domiciliaria (ESAD) de Barbastro. Variables estudiadas: edad, sexo, número de visitas, tiempo de seguimiento, presencia de dolor y de otros síntomas concomitantes, Escala Visual Analógica (EVA), diagnóstico, analgésicos previos y post-intervención, dosis media previa de analgésicos y post-intervención. Estudio estadístico con SPSS 15.0. Resultados: n = 638, 53,9 % hombres (n = 344), edad media 79,64 ± 10,8 años, 56 % oncológicos (n = 357), seguimiento medio 56 ± 56,56 días, media de 2,68 ± 2,5 visitas por proceso. Dolor en primera visita 43,3 % (n = 276), EVA media 6,54 ± 1,87, dolor 47,1 % de hombres (n = 162) y 38,8 % de mujeres (n = 114) (p < 0,05), dolor en 56,6 % de oncológicos (n = 202) y en 26,3 % de crónico-dependientes (n = 74) (p < 0,001). No diferencias en EVA entre grupos. Entre analgésicos pautados en pacientes con dolor controlado y sin controlar previa intervención del ESAD encontramos diferencias estadísticamente significativas (p < 0,005) en morfina y tramadol, y con mayor significación (p < 0,001) en fentanilo transdérmico y transmucosa, paracetamol, metamizol y AINE, todos más frecuentes en dolor no controlado. Las dosis medias previas de todos estos fármacos no mostraron diferencias significativas entre los grupos, aunque eran mayores en el grupo de dolor no controlado. En estos, se pautan o modifican analgésicos, encontrándose diferencias estadísticamente significativas pre-post intervención (p < 0,001) en fentanilo transdérmico y transmucosa, tramadol, paracetamol, metamizol, AINE, pregabalina y con p < 0,05 en gabapentina. Se obtiene diferencias (p < 0,05) únicamente en las dosis posteriores a la actuación del ESAD en fentanilo transdérmico y codeína. Obtenemos correlaciones positivas entre dolor y anorexia, ansiedad, depresión e insomnio; en pacientes oncológicos entre dolor y ansiedad e insomnio, y en pacientes crónico-dependientes entre dolor, náuseas y depresión. No diferencias entre grupos en uso previo de benzodiacepinas, antidepresivos y otros tratamientos, aunque sí en clínica de depresión, ansiedad e insomnio. Tras intervención, diferencias significativas en uso de estos tratamientos y de sedación. Conclusiones: Tras la actuación del ESAD se puede apreciar el aumento progresivo de todas las medicaciones analgésicas; se debería realizar una valoración completa de la sintomatología del paciente y un tratamiento de síntomas multifactorial, además de interrogar al paciente de forma adecuada acerca de la presencia de síntomas asociados, dada la elevada correlación de los mismos (AU)


Objectives: To determine the frequency of use of analgesics in terminal patients attended in home, and factors that may be involved in pain perception, in addition to the interventions carried out. Methods: prospective, interventional and analytical study in patients attended to Homecare Support Team (HSCT) of Barbastro. Variables studied: age, sex, number of visits, time tracking, presence of pain and other concomitant symptoms, Visual Analogic Scale (VAS), diagnosis, analgesics previous and post-intervention, previous and post-intervention average dose of analgesics. Statistical study with SPSS 15.0. Results: n = 638, men 53.9 % (n = 344), mean age 10.8 ± 79.64 years, cancer patient 56 % (n = 357), mean follow-up time 56 ± 56.56 days, 2.5 ± 2.68 mean visits per process. Pain in first visit 43.3 % (n = 276), mean VAS 6.54 ± 1.87, pain 47.1 % of men (n = 162) and 38.8 % of women (n = 114) (p < 0.05), pain in oncology 56.6 % (n = 202) and 26.3 % of non-cancer patients (n = 74) (p < 0.001). No differences between groups in VAS. Before intervention by HCST we found statistically significant differences (p < 0.005) on morphine and tramadol, and greater significance (p < 0.001) in transdermal and transmucosal fentanyl, paracetamol, metamizol and NSAIDs, all more common in uncontrolled pain. Previous mean doses of all these drugs showed no significant differences between groups, although they were higher in the group of uncontrolled pain. In these, analgesics were prescribed or modified, being statistically significant difference pre-post-intervention (p < 0.001) in transdermal and transmucosal fentanyl, tramadol, paracetamol, metamizol, NSAIDs, pregabalin and with p < 0.05 in gabapentin. Was obtained difference (p < 0.05) in mean dose only in transdermal fentanyl and codeine dose post-intervention of HCST. We obtain positive correlations between pain and anorexia, anxiety, depression and insomnia; in cancer patients between pain and anxiety and insomnia, and non-cancer patients between pain, nausea and depression. No differences between groups in previous use of benzodiazepines, antidepressants and other treatments; there was differences in depression, anxiety and insomnia. After intervention, we obtain significant differences in use of these treatments and sedation. Conclusions: after intervention of HCST there was gradual increase of all analgesic; it should conduct a full assessment of the patient’s symptoms and treatment of multifactorial symptoms in addition to questioning the patient adequately about the presence of associated symptoms, given the high correlation of them (AU)


Assuntos
Humanos , Masculino , Feminino , Estudos Controlados Antes e Depois/métodos , Estudos Controlados Antes e Depois/tendências , Manejo da Dor/instrumentação , Manejo da Dor/métodos , Manejo da Dor , Analgésicos/uso terapêutico , Percepção da Dor , População Rural/estatística & dados numéricos , Estudos Prospectivos , Assistência Terminal/métodos , Assistência Terminal , Fentanila/uso terapêutico , Acetaminofen/uso terapêutico , Tramadol/uso terapêutico , Dipirona/uso terapêutico
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