Publications by authors named "Oriol Turro-Garriga"

Introduction: Currently in Catalonia, multiculturalism is increasing, also among older people. However, little is known about the aspects that give meaning to aging or whether there are differences by origin and culture.

Objectives: Identify what it means to age meaningfully for people over 50 years of age from different origins and cultures.

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Objective: To explore the perceptions of elderly people from diverse cultures regarding the factors relevant to aging, identifying similarities and differences, and describing elements that facilitate or hinder this process, with a focus on the impact of care services.

Method: Qualitative study with 48 participants over 50 years old, residing in the Alt Empordà region, Catalonia. Seven focus groups were conducted, including one exploratory multicultural group and six stratified by origin: native, Western Europe, Eastern Europe, Latin America, North Africa, and West Africa.

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Objective: To evaluate the impact of sociodemographic and clinical sex/gender-associated factors on dementia severity at the time of diagnosis.

Methods: Retrospective, cross-sectional study using 2007-2020 data from the Registry of Dementia of Girona (ReDeGi), collecting information from new dementia diagnoses in the seven hospitals of the Health Region of Girona (Northeast region of Catalonia, Spain). Sociodemographic and clinical variables were compared by sex and dementia severity at diagnosis.

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Multimorbidity, the concurrence of several chronic conditions, is a rising concern that increases the years lived with disability and poses a burden on healthcare systems. Little is known on how it interacts with socioeconomic deprivation, previously associated with poor health-related outcomes. We aimed to characterize the association between multimorbidity and these outcomes and how this relationship may change with socioeconomic development of regions.

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Background: The large number of dementia cases produces a great pressure on health and social care services, which requires efficient planning to meet the needs of patients through infrastructure, equipment, and financial, technical, and personal resources adjusted to their demands. Dementia analysis requires studies with a very precise patient characterization of both the disease and comorbidities present, and long-term follow-up of patients in clinical aspects and patterns of resource utilization and costs generated.

Objective: To describe and quantify direct healthcare expenditure and its evolution from three years before and up to ten years after the diagnosis of dementia, compared to a matched group without dementia.

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Background: A sense of coherence (SOC) could help us better understand why there are individuals who cope better than others in similar situations. The study aimed to assess the effect of SOC on the course of burden reports in relatives of persons with dementia.

Methods: This was a prospective cohort study of 156 dementia carers.

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Aim: To determine the perceived needs of carers of non-institutionalized family members that suffer from dementia.

Methods: Two-steps qualitative study by focus groups of relatives in three centres of different characteristics from the Girona Health Region (step 1) and two in-depth interviews with significant professionals in dementia care (step 2). The analysis was performed based on the interpretation of the transcribed data and the bottom-up coding of categories and themes.

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Background: The concurrence of several chronic conditions is a rising concern that poses a serious burden on ageing populations. Analysing how these conditions appear together and how they change through time may provide useful information to design successful multimorbidity-management programs.

Objective: To identify multimorbidity patterns and their related characteristics from a longitudinal perspective.

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Article Synopsis
  • * A total of 475 homeless individuals were analyzed, with 60 deaths recorded, and the average age at death was found to be 49.1 years, much lower than the general population.
  • * Key mortality risk factors included being Spanish-born, type 2 diabetes, alcohol use disorder, and infectious diseases, with Spanish-born individuals exhibiting higher mortality risk despite having better control over chronic diseases.
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Article Synopsis
  • - The study examined how COVID-19 restrictions impacted the lifestyles of 692 individuals in Catalonia, Spain, assessing their mental health through a telephone survey.
  • - Results showed that 12.7% of participants experienced signs of possible depression, linked to factors like job instability, economic fears, and concerns about health.
  • - The lifestyle changes due to confinement accounted for 32% of the differences in depression scores, highlighting the significant mental health effects of pandemic-related restrictions.
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Background: Dementia care is associated with physical, emotional, and monetary impact on the informal carers providing unpaid care. Differences in the personal characteristics of caregivers may help explain the variations in the costs of dementia care.

Objective: The aim of this study was to analyze the effect of caregivers' sense of coherence (SOC) on direct and indirect costs in dementia care.

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With the start of the great economic recession in 2007, homelessness increased fivefold in some regions of southern Europe. Larger numbers of people experiencing homelessness, compounded by a lowered capacity for social and health services to respond to their needs, precipitated an increase in so-called 'chronic homelessness'. The aim of this study was to establish the presence of chronic homelessness in a defined geographical area of Spain, and to determine the prevalence of diagnosed mental disorders within both the chronic and non-chronic homeless population.

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Objective: To determine mortality rates and to rank the causes and predictors of mortality using a wide range of sociodemographic and clinical variables.

Materials And Methods: It is a prospective population-based cohort study of adults living in the community, 2013-15 N = 48,691, age ≥50; deceased = 1,944. Clinical and sociodemographic data were obtained from the Survey of Health, Ageing and Retirement in Europe SHARE: Age, Gender, Marital Status, Years of Schooling, Income, Loneliness, Cognition, Self-Rated Health, Diseases, Activities of daily living ADL, and Frailty.

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This study aims to analyse the use of an instant messaging app (WhatsApp®) as a means of communication for reaching people who inject drugs. An eight-week prospective longitudinal and observational study with three observations was designed for five addiction centres in Catalonia. The participants were 105 people who inject drugs, distributed in five intervention groups.

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Taking care of people with dementia (PWD) has been associated with some degree of burden. The variability of the carer's burden can be partially explained by their personal characteristics. Antonovsky's model of health defined the resistance resources (RRs) as essential mechanisms to cope with stressors, and to shape the personal sense of coherence (SOC).

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Background: Knowledge on survival after diagnosis is important for all stakeholders. We aimed to estimate the survival and life expectancy after a dementia diagnosis, and to quantify the impact of dementia subtypes on mortality.

Methods: Retrospective matched cohort study using a linkage between a dementia-specific registry and two primary care electronic medical records databases.

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Article Synopsis
  • The study analyzed data from 7,357 newly diagnosed individuals with uncommon dementia subtypes to assess incidence rates based on age and sex.
  • Uncommon dementia subtypes had a total incidence rate of 27.8 cases per 100,000 person-years, with significantly higher rates in older individuals (110.9 cases per 100,000 for those aged 65 and older).
  • Differences were noted in demographic and clinical characteristics among uncommon dementia subtypes, influenced by factors such as age, sex, dementia severity, and existing medical conditions.
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Background: The epidemiology of depressive disorders presents notable differences among European countries. The objectives of the study are to determine the prevalence, incidence, persistence and remission rates of depressive symptoms and to identify risk factors and differences between four European regions.

Method: Prospective cohort design using data from waves 5 and 6 (2013-15) of the Survey of Health, Ageing and Retirement in Europe.

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Article Synopsis
  • * This study analyzed data from over 13,000 caregivers across 12 European countries, focusing on how financial vs. non-financial support influences caregivers' health.
  • * Findings revealed that non-financial support (like emotional help and skills training) has a stronger positive effect on caregivers' health than financial assistance, highlighting the importance of providing free time and emotional support for better caregiving experiences.
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Introduction: The care of dependent persons is arduous, and requires time, energy, and physical effort on the part of caregivers. Personal characteristics, such as the sense of coherence (SOC), can influence the perceived burden and care giving.

Objective: To determine the impact of SOC on the perceived burden and to determine if these characteristics are associated with adherence to a psycho-educational program for informal caregivers.

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Objective: To describe the prevalence and concordance of anticholinergic exposure according to 9 published scales, to quantify the relative weight of the drug subtypes included in each scale, and to identify clinical variables related to anticholinergic exposure.

Methods: Observational and cross-sectional study using 5323 cases of dementia diagnosed in the 7 hospitals of the public health care system of the Health Region of Girona (Spain) between 2007 and 2014 and registered by the Registry of Dementias of Girona (ReDeGi). We used the Pharmacy database that includes all the drugs prescribed by specialist and primary care physicians and dispensed in pharmacies.

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Background: There are several position statements and clinical practice guidelines (CPG) for diagnosing dementia.

Objective: Our aims were to evaluate the adherence to CPG among specialists in the 7 memory clinics included in the Registry of Dementias of Girona (ReDeGi), and to compare the results between 2007-2011 and 2012-2015. We also determined the time and number of visits required to achieve a diagnosis, the supplementary tests ordered, and the drugs prescribed according to dementia subtypes.

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Background: Alzheimer's disease (AD) is the most common neurodegenerative dementia of old age, and the leading chronic disease contributor to disability and dependence among older people worldwide. Clinically, AD is characterized by a progressive cognitive decline that interferes with the ability to perform the activities of daily living. Handwriting and drawing are complex human activities that entail an intricate blend of cognitive, kinesthetic, and perceptual-motor features.

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Article Synopsis
  • Acetylcholinesterase inhibitors (AChEIs) and memantine are commonly prescribed for treating symptoms of Alzheimer’s disease, and this study aimed to analyze how these medications are used among patients over time.
  • A cohort of 2,992 Alzheimer’s patients from a registry was examined to identify characteristics associated with the prescription of these drugs and to track usage trends from 2007 to 2014.
  • Results indicated that a significant majority of patients (70.4%) received antidementia medication at diagnosis, with AChEIs prescribed more frequently than memantine, but the use of AChEIs decreased while memantine use increased as the severity of dementia progressed.
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Objectives: The aims of the study were to identify the clinical characteristics of three groups of caregivers: spouses, live-in adult-child or non-live-in adult-child, and their relation to the degree of perceived burden (Caregiver Burden Interview).

Methods: The sample comprised 275 Alzheimer's disease primary caregivers, with a follow-up of 24 months. Cognitive, functional and behavioural characteristics were evaluated in persons with dementia, whilst sociodemographic data, use of socio-medical resources, physical and mental health and self-perceived burden were assessed in caregivers.

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