Publications by authors named "Barbro Krevers"

In Sweden, efforts to govern end-of-life care through policies have been ongoing since the 1970s. The aim of this study is to analyse how policy narratives on palliative care in Sweden have been formulated and have changed over time since the 1970s up to 2018. We have analysed 65 different policy-documents.

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Introduction: Health care systems around the world are struggling with limited resources, in relation to the prevailing health care need. An accessible primary care is an important part of the solution for how to provide affordable care for the population and reduce pressure on the overall health care system such as unnecessary hospital stays and associated costs. As primary care constitutes an important first line of healthcare, the task of prioritising and deciding what to do and for whom lies in practice, primarily with the primary care professionals.

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Article Synopsis
  • Up to 10% of individuals experiencing bereavement may develop prolonged grief disorder, with a need to better understand the interactions between family member coping and patient-related factors during this process.
  • A study in Sweden involved 99 family members of patients in palliative home care who completed surveys during and after the patient's care to identify risk factors for prolonged grief symptoms.
  • Key findings indicated that both preloss factors, like the family member's stress and attachment security, and postloss factors, such as continuing bonds with the deceased, significantly influenced prolonged grief symptom severity in bereaved family members.
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Objective: To investigate the treatment decision-making process after an anterior cruciate ligament (ACL) injury from patients', orthopaedic surgeons' and physiotherapists' perspectives.

Methods: The study is a part of the NACOX study, which is designed to describe the natural corollaries after ACL injury. For the present study, a subgroup 101 patients were included.

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Article Synopsis
  • The study explores whether antenatal care for low-risk pregnant women can be effectively monitored with fewer in-person visits to a midwife, utilizing virtual visits instead.
  • It employs a non-inferiority trial design in southeastern Sweden, comparing a modified antenatal care (MAC) program with a standard antenatal care (SAC) program, aiming to ensure safety while improving efficiency.
  • The research aims to enhance care for healthy pregnancies by potentially reducing unnecessary in-person appointments, guided by existing evidence and aiming for cost-effective health care.
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Objectives: To examine similarities and dissimilarities in patient and family caregiver dyads in their experience of stress, support, and sense of security.

Methods: 144 patients and their family caregivers participated. Patients were admitted to six Swedish specialist palliative home care units and diagnosed with a non-curable disease with an expected short survival.

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In Sweden, palliative care has, over the past decades, been object to policies and guidelines with focus on how to achieve "good palliative care". The aim of this study has been to analyse how experts make sense of the development and the current state of palliative care. Departing from this aim, focus has been on identifying how personal experiences of 'the self' are intertwined with culturally available meta-level concepts and how experts contribute to construct new scripts on palliative care.

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Background: Priority setting in healthcare that aims to achieve a fair and efficient allocation of limited resources is a worldwide challenge. Sweden has developed a sophisticated approach. Still, there is a need for a more detailed insight on how measures permeate clinical life.

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Objective: The primary purpose of this study was to assess the cost-effectiveness of caries preventive interventions.

Material And Methods: A systematic review was conducted, following the PRISMA Statement. Four electronic databases were searched (final search 16 March 2020).

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Background: Despite evidence that family members' support to each other can be of importance to its members, there are limited studies of factors related to family members' sense of such support during palliative care.

Aim: Based on the family systems approach, we evaluated which factors were associated with family members' sense of support within their closest family in a palliative home care context and developed a model that predicts such sense of support.

Design: A cross-sectional design was used.

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Article Synopsis
  • This study looked into factors affecting health-related quality of life (HRQoL) and the burden on relatives of older individuals with multiple health issues.
  • Analyzing data from 296 patient-relative pairs, researchers identified 16 variables influencing relatives' HRQoL and 15 affecting their burden, highlighting the interconnectedness of both groups.
  • The findings suggest that enhancing relatives’ HRQoL could reduce their burden, emphasizing the need for supportive measures and recognizing the interdependent well-being of older adults and their caregivers.
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Study Design: Qualitative descriptive.

Introduction: Dupuytren's disease (DD) is a chronic hand condition causing impairment in hand function. Research describing persons' experiences of living with DD is limited.

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Article Synopsis
  • - The study aimed to investigate factors that contribute to family members feeling secure during palliative care, create a model of that security, and assess its impact on their well-being after a loved one’s death.
  • - Conducted with 227 family members in Sweden, the research identified 16 variables influencing feelings of security, with top factors being family members' mastery, stress levels, and self-efficacy, among others.
  • - Results indicated that a strong sense of security during palliative care correlates with better psychological well-being, reduced grief complications, and improved quality of life for family members one year after their loss.
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Background: The prevalence of multimorbidity is increasing worldwide, and older people with multimorbidity are frequent users of health care services. Since multimorbidity has a significant negative impact on Health-related Quality of Life (HrQoL) and is more common in older age it would be expected that factors related to HrQoL in this group might have been thoroughly researched, but this is not the case. Furthermore, it is important to look at old people living at home, considering the shift from residential to home-based care.

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The importance for governments of establishing ethical principles and criteria for priority setting in line with social values, has been emphasised. The risk of such criteria not being operationalised and instead replaced by de-contextualised priority-setting tools, has been noted. The aim of this article was to compare whether citizenś views are in line with how a criterion derived from parliamentary-decided ethical principles have been interpreted into a framework for evaluating severity levels, in resource allocation situations in Sweden.

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Objectives: Demographic change has led to an increase of older people in need of long-term care in nearly all European countries. Informal carers primarily provide the care and support needed by dependent people. The supply and willingness of individuals to act as carers are critical to sustain informal care resources as part of the home health care provision.

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Purpose: To explore and describe clients' needs during a surgical intervention process for Dupuytren's disease.

Materials And Methods: Design: Interview study with 21 men undergoing surgical intervention for Dupuytren's disease. Qualitative content analysis was performed with the model of Patient Evaluation Process as a theoretical framework.

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Background: In order to improve attendance at exercise-based cardiac rehabilitation (CR), a greater insight into patients' perspectives is necessary. The aim of the study was to explore aspects that influence patients' attendance at exercise-based CR after acute coronary artery disease (CAD) and the role of the physiotherapist in patients' attendance at exercise-based CR.

Methods: A total of 16 informants, (5 women; median age 64.

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Purpose: To explore patients' perspectives on surgical intervention for Dupuytren's disease (DD), focusing on patients' appraisal of results, involving previous experiences, expectations and patient characters.

Method: The participants were 21 men, mean age 66 years, scheduled for DD surgery. Qualitative interviews were conducted 2-4 weeks before surgery and 6-8 months after surgery.

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Objective: To compare the effects of care based on comprehensive geriatric assessment (CGA) as a complement to usual care in an outpatient setting with those of usual care alone. The assessment was performed 36 months after study inclusion.

Design: Randomized, controlled, assessor-blinded, single-center trial.

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Background: Primary care is increasingly being encouraged to integrate healthy lifestyle promotion in routine care. However, implementation has been suboptimal. Coordinated care could facilitate lifestyle promotion practice but more empirical knowledge is needed about the implementation process of coordinated care initiatives.

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This study compared the caring situation, health, self-efficacy, and stress of young (16-25) informal carers (YICs) supporting a family member with mental illness with that of YICs supporting a friend. A sample of 225 carers, assigned to a family group (n = 97) or a friend group (n = 128) completed the questionnaire. It was found that the family group experiences a lower level of support and friends experienced a lower positive value of caring.

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Study Design: Prospective cohort study.

Introduction: The evidence of the relationship between functional recovery and impairment after surgery and hand therapy are inconsistent.

Purpose Of The Study: To explore factors that were most related to functional recovery as measured by DASH in patients with Dupuytren's disease.

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Objectives: To examine costs and effects of care based on comprehensive geriatric assessment (CGA) provided by an ambulatory geriatric care unit (AGU) in addition to usual care.

Design: Assessor-blinded, single-center randomized controlled trial.

Setting: AGU in an acute hospital in southeastern Sweden.

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Background: Non-communicable diseases are a leading cause of death and can largely be prevented by healthy lifestyles. Health care organizations are encouraged to integrate healthy lifestyle promotion in routine care. This study evaluates the impact of a team initiative on healthy lifestyle promotion in primary care.

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