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1.
Diabet Med ; 31(6): 657-65, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24533786

RESUMEN

AIM: To determine if hospital admission rates for diabetes complications (acute complications, chronic complications, no complications and hypoglycaemia) were associated with primary care diabetes management. METHODS: We performed an observational study in the population in England during the period 2004-2009 (54 741 278 people registered with 8140 general practices). We used multivariable negative binomial regression to model the associations between indirectly standardized hospital admission rates for complications and primary healthcare quality, supply and access indicators, diabetes prevalence and population factors. RESULTS: In multivariate regression models, increasing deprivation (incidence rate ratio: 1.0154; P < 0.001, 95% CI 1.0141-1.0166) and diabetes prevalence (incidence rate ratio: 1.0956; P < 0.001, 95% CI 1.0677-1.1241) were risk factors for admission, while most healthcare covariates, i.e. a larger practice population (incidence rate ratio 0.9999, P = 0.013, 95% CI 0.9999-0.9999), better patient-perceived urgent and non-urgent access to primary care (incidence rate ratio: 0.9989, P = 0.023; 95% CI 0.9979-0.9998 and incidence rate ratio: 0.9988; P = 0.003, 95% CI 0.9980-0.9996, respectively) and better HbA1c target achievement (incidence rate ratio: 0.9971; P < 0.001, 95% CI 0.9958-0.9984), were protective. Diabetes admissions decreased significantly during the period 2004-2009. CONCLUSIONS: After controlling for population factors, better scheduled primary care access and glycaemic control were associated with lower hospital admission rates across most complications. There is little rationale to restrict primary care-sensitive condition definitions to acute complications. They should be revised to improve the usefulness of hospital admission data as an outcome measure, and to facilitate international comparisons. The risk of emergency hospital admission should be monitored routinely.


Asunto(s)
Complicaciones de la Diabetes/terapia , Hospitalización/estadística & datos numéricos , Atención Primaria de Salud/normas , Adulto , Anciano , Anciano de 80 o más Años , Enfermedad Crónica , Inglaterra , Métodos Epidemiológicos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Calidad de la Atención de Salud/normas
3.
J Nutr Health Aging ; 21(1): 92-104, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-27999855

RESUMEN

The Strategic Implementation Plan of the European Innovation Partnership on Active and Healthy Ageing (EIP on AHA) proposed six Action Groups. After almost three years of activity, many achievements have been obtained through commitments or collaborative work of the Action Groups. However, they have often worked in silos and, consequently, synergies between Action Groups have been proposed to strengthen the triple win of the EIP on AHA. The paper presents the methodology and current status of the Task Force on EIP on AHA synergies. Synergies are in line with the Action Groups' new Renovated Action Plan (2016-2018) to ensure that their future objectives are coherent and fully connected. The outcomes and impact of synergies are using the Monitoring and Assessment Framework for the EIP on AHA (MAFEIP). Eight proposals for synergies have been approved by the Task Force: Five cross-cutting synergies which can be used for all current and future synergies as they consider overarching domains (appropriate polypharmacy, citizen empowerment, teaching and coaching on AHA, deployment of synergies to EU regions, Responsible Research and Innovation), and three cross-cutting synergies focussing on current Action Group activities (falls, frailty, integrated care and chronic respiratory diseases).


Asunto(s)
Envejecimiento , Conductas Relacionadas con la Salud , Población Blanca , Accidentes por Caídas/prevención & control , Anciano , Anciano de 80 o más Años , Enfermedad Crónica , Conducta Cooperativa , Europa (Continente) , Anciano Frágil , Humanos , Afecciones Crónicas Múltiples , Innovación Organizacional , Polifarmacia , Encuestas y Cuestionarios
4.
Eur J Intern Med ; 26(3): 203-10, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25765442

RESUMEN

AIM: To identify patterns of health care use among diabetic patients with multimorbidity across primary, specialised, hospital and emergency care, depending on their type of chronic comorbidity. METHODS: Longitudinal study of a population-based retrospective cohort conformed by adult patients with type-2 diabetes assigned to any of the primary care centres in Aragon during 2010 and 2011 (n=65,716). Negative binomial regressions were run to model the effect of the type of comorbidity on the number of visits to each level of care. Comorbidities were classified as concordant, discordant or mental based on expert consensus and depending on whether they shared the same overall pathophysiologic risk profile and disease management plan designed for type-2 diabetes. RESULTS: Mental comorbidity was independently associated with total and unplanned admissions (incidence rate ratio [IRR]:1.25; 95% confidence interval [CI]:1.12-1.39, IRR:1.21; 95% CI:1.06-1.39), average length of stay (IRR:1.47; 95% CI:1.25-1.73), and total and priority emergency room visits (IRR:1.26; 95% CI:1.17-1.35, IRR:1.30; 95% CI:1.18-1.42). Patients with discordant comorbidities showed the strongest associations with the number of visits to specialists (IRR:1.38; 95% CI:1.33-1.43) and to different specialties (IRR:1.36; 95% CI:1.32-1.39). Differences regarding GP visits were lower but still significant for patients with discordant comorbidity (IRR:1.08; 95% CI:1.06-1.11), but especially for those with mental comorbidity (IRR:1.17; 95% CI:1.14-1.21). CONCLUSION: In patients with type-2 diabetes, the coexistence of mental comorbidity significantly increases the use of unplanned hospital services, and discordant comorbidities have an important effect on specialised care use. Differences with respect to primary care use are not as prominent.


Asunto(s)
Comorbilidad , Diabetes Mellitus Tipo 2/complicaciones , Servicios Médicos de Urgencia/estadística & datos numéricos , Atención Primaria de Salud/estadística & datos numéricos , Adolescente , Adulto , Anciano , Registros Electrónicos de Salud , Femenino , Hospitalización , Humanos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Análisis de Regresión , Estudios Retrospectivos , Adulto Joven
5.
J Clin Epidemiol ; 50(4): 411-8, 1997 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9179099

RESUMEN

The data reported here document levels of accuracy in reports of blood pressure and identify correlates of inaccurate reporting. The data come from a long-term follow-up of a cohort of African-American women who registered for antepartum care between September, 1967 and June, 1969. At the follow-up interview, these women were asked whether they had ever received a diagnosis of hypertension from a physician. The self-reports of hypertension were compared with information contained in the medical records of these women. Twenty-five percent reported having high blood pressure but 53% of these reports were unconfirmed by their medical records (overall misreporting rates was 15.9% with 2.5% underreporting and 13.4% overreporting). The factors related to misreporting included a psychiatric diagnosis (based on the Diagnostic Interview Schedule) of major depressive disorder or drug and/or alcohol abuse and a small social network. The conjunction of these three variables significantly affected accuracy of reporting (100% misreporting with all three variables). These results suggest that, using currently standard methodology, there is an unreliable subpopulation of respondents in health surveys that may require the collection of data on health status from a second source to confirm data from self-reported health measures.


Asunto(s)
Negro o Afroamericano , Encuestas Epidemiológicas , Hipertensión/epidemiología , Adulto , Negro o Afroamericano/psicología , Depresión/complicaciones , Femenino , Estado de Salud , Humanos , Hipertensión/complicaciones , Hipertensión/psicología , Psicología , Factores Socioeconómicos , Estados Unidos
6.
Gac Sanit ; 7(39): 282-8, 1993.
Artículo en Español | MEDLINE | ID: mdl-8169039

RESUMEN

The best way to estimate non response bias and its potential effect in epidemiological research to know the characteristics of non respondents. The purpose of this study is to analyze what characteristics of those who refused to answer telephone and personal interviews in a follow-up study can predict non-response. As part of the Yale Health and Ageing Project, a follow-up study initiated in 1982 in the USA in a population sample of 2.806 over 65 years of age, the influence of several factors in non-response rate for those who refused to answer the interview was analyzed. A total of 21 variables related to demographic, health, and social characteristics were analyzed. The dependent variable was defined as response/non-response to the interviews. The results did not show significant statistical associations. The only factors that showed specific patterns were housing (in both types of interviews), and education level, cognitive status, and physical disability in personal interview in women, with p values for the Odds Ratios between 0.05 and 0.07. In conclusion, most results of this study do not support the findings already published. A disadvantaged sociodemographic situation was not a predictor factor of non-response, except for the education level of women in personal interviews. In relation to health status only a poor cognitive status, as it has been already reported, seems to induce refusal of women to personal interviews.


Asunto(s)
Anciano/psicología , Sesgo , Estudios de Seguimiento , Envejecimiento , Trastornos del Conocimiento/psicología , Femenino , Encuestas Epidemiológicas , Vivienda , Humanos , Hipertensión/psicología , Entrevistas como Asunto , Masculino , Factores Sexuales , Factores Socioeconómicos
9.
Aten Primaria ; 21(1): 36-42, 1998 Jan.
Artículo en Español | MEDLINE | ID: mdl-9557355

RESUMEN

OBJECTIVES: To study and analyse the Out-Patient Care Groups (OCGs), and evaluate how they affect use of health resources. DESIGN: An observational, retrospective study. SETTING: Ciudad Jardín Health Centre, Málaga. PARTICIPANTS: 2999 patients with a clinical history opened before 31.12.95, chosen from 5 of the 17 medical lists at the Health Centre, were included. RESULTS: The statistical analysis was performed with the SPSS software package of the Calculation Centre at Málaga University. A descriptive test produced the following results: 33% of the patients were classified in OCG 41 (combination of 2 or 3 out-patient diagnosis groups in people over 34); 19% belonged to groups of stable or unstable chronic illnesses (OCGs 8, 9 and 10); and 9% had acute children's diseases. Then multiple regression constructed a model with the OCGs as independent variable and annual visits, further tests performed and referral to specialists as dependent variables. In this model the OCGs were able to explain 20.3% of resource consumption. CONCLUSIONS: In the retrospective study and with a limited sample of 2999 patients, the OCGs are able to explain 20.3% of resource consumption. However, it does seem a valid model for discriminating between normal and over-using patients.


Asunto(s)
Conductas Relacionadas con la Salud , Servicios de Salud/estadística & datos numéricos , Pacientes Ambulatorios , Humanos , Pacientes Ambulatorios/estadística & datos numéricos , Estudios Retrospectivos , España
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