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Träfflista för sökning "LAR1:lu ;lar1:(lnu);pers:(Saveman Britt inger)"

Sökning: LAR1:lu > Linnéuniversitetet > Saveman Britt inger

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1.
  • Franzén, Kristofer (current name Årestedt, Kristofer), et al. (författare)
  • Impact of Chronic Heart Failure on Elderly Persons' Daily Life : A Validation Study
  • 2006
  • Ingår i: European Journal of Cardiovascular Nursing. - : Sage Publications. - 1474-5151 .- 1873-1953. ; 5:2, s. 137-145
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Knowledge about how elderly persons perceive the impact of chronic heart failure (CHF) on daily life is important when planning nursing care. For this purpose, disease specific instruments are needed. However, few instruments have been developed or tested specifically on elderly persons.AIM: To validate a Swedish version of the Minnesota Living with Heart Failure Questionnaire (LHFQ) on elderly persons with CHF, and use it to describe the impact of CHF on daily life in the same population.METHODS: The sample comprised of 357 persons, aged between 65 and 99, diagnosed with CHF. A questionnaire including background data, the LHFQ and the SF-12 was used.RESULTS: A factor analysis resulted in four dimensions: physical, emotional, treatment and pleasure. LHFQ showed convergent validity and ability to discriminate between known groups. Cronbach's alpha for the total scale was 0.94. Impairments in the physical dimension were most common, especially fatigue (88%) and shortness of breath (87%).CONCLUSIONS: The LHFQ showed satisfying psychometric properties in an elderly Swedish population with CHF and can, with minor alterations, be recommended for research and clinical use. The impact of chronic heart failure on daily life was mostly physical, but other impairments were also common.
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2.
  • Franzén, Kristofer, et al. (författare)
  • Predictors for health related quality of life in persons 65 years or older with chronic heart failure.
  • 2006
  • Ingår i: European Journal of Cardiovascular Nursing. - : Oxford University Press (OUP). - 1474-5151 .- 1873-1953. ; 6:2, s. 112-120
  • Tidskriftsartikel (refereegranskat)abstract
    • Background A main goal in nursing care of persons with chronic heart failure (HF) is to strengthen their health related quality of life (HRQoL). This presupposes knowledge about the relation between heart failure and HRQoL. Existing studies have shown incongruent results about whether HRQoL is affected differently depending on age or sex of elderly persons with chronic HF. Aim This study aimed to investigate if age, sex, disease severity, comorbidity and living conditions predict health related quality of life among persons 65 years or older with chronic HF. Methods The study included a sample of 357 persons. HRQoL was measured by the Minnesota Living with Heart Failure Questionnaire and the Short Form-12 Health Survey Questionnaire. Multiple regression analyses were performed to analyse the relation between the predictors and HRQoL. Results The main finding was that self-rated disease severity was strongly associated with HRQoL, but also age, sex, diabetes and respiratory diseases was associated with some of the dimensions of HRQoL. Conclusions Interventions aimed at delaying the progress of the disease, assist persons' to cope with the disease and maintain the domains of HRQoL that are still feasible could be important to improve HRQoL in elderly persons with chronic HF.
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3.
  • Nilsson, Gunilla, et al. (författare)
  • Patients' experiences of illness, operation and outcome with reference to gastro-oesophageal reflux disease.
  • 2002
  • Ingår i: Journal of Advanced Nursing. - : Wiley. - 0309-2402 .- 1365-2648. ; 40:3, s. 307-15
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Describing the illness-story from a patient perspective could increase understanding of living with a chronic disease for health professionals and others, facilitate decision-making about treatment and enhance information about the outcome from a patient perspective. AIM: To illuminate patients' illness experiences of having a gastro-oesophageal reflux disease (GORD), going through surgery and the outcome. METHODS: Twelve patients were interviewed 5 years after having had the operation; six patients had had fundoplication via laparoscopy and six via open surgery. Each patient was asked to talk openly about their experiences, thoughts, feelings and consequences of living with the illness, going through surgery and the period from surgery to the day of interview. A qualitative content analysis was performed concerning the context of the data and its meaning. FINDINGS: Three central categories were identified and nine subcategories: living with GORD- symptoms of the disease affecting daily living, taking medicines, work, family and social life; concerns related to surgery- decision-making about the operation, influence by physicians; life after the operation- outcomes and consequences, side-effects and complications of the operation, sick leave, information and sharing experiences with future patients. All patients were free from symptoms of the illness after surgery independent of type of surgery, but side-effects from surgical treatment varied individually. Interviewees would have liked information concerning side-effects after surgery from previous patients. CONCLUSIONS: This study contributes to knowledge about patients' long-term suffering, their control of symptoms and how they have tried to cure themselves, but also about their concerns about surgery and the importance of surgical treatment to their quality of life. They wanted information about treatment, outcome and consequences, not only from a health care perspective but also from previous patients having had the same treatment.
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4.
  • Söderström, Ing-Mari, et al. (författare)
  • Family adaptation in relation to a family member's stay in ICU
  • 2009
  • Ingår i: Intensive & Critical Care Nursing. - : Elsevier BV. - 0964-3397 .- 1532-4036. ; 25:5, s. 250-257
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives: To describe and interpret the family adaptation during the ICU hospitalisation andup to 18 months after discharge.Research methodology/design: A qualitative design was chosen.Main outcome measures: Individual and family interviews with eight families including 31 familymembers. A hermeneutical analysis was performed and paradigm cases were constructed.Results: The result is presented in three themes: striving for endurance, striving for consolationand striving to rebuild life under new conditions. The family adaptation started at the onset ofthe critical incident and continued during the ICU stay and after discharge. The family membersmetaphorically went through peaks and valleys during the whole process of adaptation.Conclusion: Adaptation is an issue for the whole family and is facilitated by being able to stayclose to the patient and receive supportive unambiguous information from the staff both duringthe ICU stay and after discharge.
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