0000000001040577

AUTHOR

Antonio Di Carlo

showing 2 related works from this author

Variations in acute stroke care and the impact of organised care on survival from a European perspective: the European Registers of Stroke (EROS) inv…

2013

Background The need for stroke care is escalating with an ageing population, yet methods to estimate the delivery of effective care across countries are not standardised or robust. Associations between quality and intensity of care and stroke outcomes are often assumed but have not been clearly demonstrated. Objective To examine variations in acute care processes across six European populations and investigate associations between the delivery of care and survival. Methods Data were obtained from population-based stroke registers of six centres in France, Lithuania, UK, Spain, Poland and Italy between 2004 and 2006 with follow-up for 1 year. Variations in the delivery of care (stroke unit, …

Malemedicine.medical_specialtyPediatricsPopulation ageingMultivariate analysisPopulationPsychological interventionLogistic regressionCase mix indexAcute caremedicineHumansRegistrieseducationStrokeAgededucation.field_of_studybusiness.industryLithuaniamedicine.diseaseUnited KingdomStrokePsychiatry and Mental healthTreatment OutcomeItalySpainMultivariate AnalysisEmergency medicineFemaleSurgeryFrancePolandNeurology (clinical)businessDelivery of Health CareJournal of Neurology, Neurosurgery & Psychiatry
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Patient engagement with research:European population register study

2014

Background Lay involvement in implementation of research evidence into practice may include using research findings to guide individual care, as well as involvement in research processes and policy development. Little is known about the conditions required for such involvement. Aim To assess stroke survivors’ research awareness, use of research evidence in their own care and readiness to be involved in research processes. Methods Cross sectional survey of stroke survivors participating in population-based stroke registers in six European centres. Results The response rate was 74% (481/647). Reasons for participation in register research included responding to clinician request (56%) and to …

Register (sociolinguistics)Malemedicine.medical_specialtyBiomedical ResearchCross-sectional studyPopulationPatient engagementNursingmedicineHumansRegistriesSurvivorseducationStrokeRegister studyAgedResponse rate (survey)Aged 80 and overeducation.field_of_studybusiness.industryPublic Health Environmental and Occupational HealthEuropean populationMiddle Agedmedicine.diseaseEuropeStrokeCross-Sectional StudiesFamily medicineFemalePatient ParticipationbusinessAttitude to HealthOriginal Research Papers
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