Gerd Ahlström
Titel
Professor, chef för Vårdalinsitutet
046-2221916
+46702747767
Gerd [dot] Ahlstrom [at] med [dot] lu [dot] se
Publikationer (hämtat ur Lunds universitets publikationsdatabas)
författare
- 2013
- 2012
- Childhood overweight and obesity conceived by Child Health Care nurses: a qualitative study.
- Empowerment Intervention in Outpatient Care of Persons with Chronic Kidney Disease Pre-Dialysis
- Empowerment interventions in outpatient care of patients with chronic kidney disease
- Enjoying Work or Burdened by it? How Personal Assistants Experience and Handle Stress at Work
- Enjoying Work or Burdened by it? How Personal Assistants Experience and Handle Stress at Work.
- Experiences of providing prosthetic and orthotic services in Sierra Leone - the local staff's perspective
- Experiences of providing prosthetic and orthotic services in Sierra Leone – the local staff’s perspective.
- Health-related quality of life in family members of patients with an advanced cancer diagnosis: A one-year prospective study
- Swedish Child Health Care nurses conceptions of overweight in children: a qualitative study
- The experience of empowerment in the patient-staff encounter: the patient's perspective.
- The experience of empowerment in the patient-staff encounter: the patients´ perspective.
- The meaning and validation of social support networks for close family of persons with advanced cancer.
- The patient's view of quality in psychiatric outpatient care.
- The patient’s view of quality in psychiatric out-patient care.
- 2011
- Academic leadership in the field of nursing and health science research
- Empowerment in outpatient care for patients with chronic kidney disease - from the family member's perspective.
- Experiences of relocation in dementia care from the perspective of six care workers.
- Family members' experiences of personal assistance given to a relative with disabilities.
- General practitioners' and district nurses' conceptions of the encounter with obese patients in primary health care.
- Psychometric properties of the Quality in Psychiatric Care - Outpatient (QPC-OP) instrument.
- Quality in Psychiatric Care: a new measuring instrument in three versions based on patient’s experiences.
- Striving to be prepared for the painful: Management strategies following a family member's diagnosis of advanced cancer.
- What next of kin perceive as quality of care in psychiatric care: a phenomenographic interview study.
- 2009
- Research outcomes about Coping in Swedish populations: the Ways of Coping Questionnaire
- Research outcomes about Coping in Swedish populations: the Ways of Coping Questionnaire.
- Subjective quality of life in persons with low-grade glioma and their next of kin.
- The Development of Nursing in the Modern Societies
- 2008
- A cross-cultural comparison of nurses' ethical concerns.
- Chronic sorrow in next of kin of patients with multiple sclerosis.
- Coping with Neuromuscular Disease and the Implications for Interventions
- Coping with Neuromuscular Disease and the Implications for Interventions.
- Falling ill with Guillain-Barré syndrome: patients' experiences during the initial phase.
- ICU patients' recall of emotional reactions in the trajectory from falling critically ill to hospital discharge: follow-ups after 3 and 12 months.
- Integration of health care improvement into professional learning
- Integration of health care improvement into professional learning
- Intentional Partnerships – Creating New Partnerships
- Intentional Partnerships – Creating New Partnerships
- Interprofessional ethics rounds concerning dialysis patients: staff's ethical reflections before and after rounds.
- Learning a way through ethical problems: Swedish nurses' and doctors' experiences from one model of ethics rounds.
- Learning about each other: students’ conceptions before and after interprofessional education on a training ward.
- Managing chronic sorrow: experiences of patients with multiple sclerosis
- Nurses' conceptions of decision making concerning life-sustaining treatment.
- Students’ learning experiences from interprofessional collaboration on a training ward in municipal care.
- Students’ learning experiences from interprofessional collaboration on a training ward in municipal care.
- The patient's perception of having recovered from an eating disorder.
- Workplace distress and ethical dilemmas in neuroscience nursing.
- 2007
- Caring and uncaring experiences as narrated by persons with long-term pain after a stroke.
- Chinese nurses’ experiences of ethical dilemmas in a neurological ward.
- Diabetes : a cross-cultural interview study of immigrants from Somalia.
- Ethics rounds or ethics consultation in Sweden? How much input should the ethicist have? - Nurses’ and physicians’ experiences.
- Experiences of loss and chronic sorrow in persons with severe chronic illness.
- Interprofessional education on a training ward for older people: students' conceptions of nurses, occupational therapists and social workers.
- Lifeworld perspectives utilizing assistive devices: individuals, lived experience following a stroke.
- Lived experience of significant others of persons with diabetes.
- Living with Long-Term Pain after a Stroke.
- Living with diabetes: a interview study with immigrants from Somalia.
- Managing chronic sorrow in patients with multiple sclerosis: emotional distress but also personal growth.
- Next of kin’s conceptions of the quality of care in the psychiatric setting: a phenomenographic study.
- Patientens perspektiv på vårdkvalitet inom psykiatrisk vård: ett instrument för förväntningar och upplevelser.
- Patientens perspektiv på vårdkvalitet inom psykiatrisk vård: ett instrument för förväntningar och upplevelser.
- Patients' perceptions of the concept of quality of care in the psychiatric setting: a phenomenographic study. (Response)
- Patterns of and reasons for relocation in dementia care.
- Quality in psychiatric care: an instrument evaluating patients' expectations and experiences.
- The meaning of women’s experience of living with long-term urinary incontinence is powerlessness.
- The presence and meaning of chronic sorrow in patients with multiple sclerosis.
- The value of an outdoor powered wheelchair with regard to the quality of life of persons with stroke.
- The value of an outdoor powered wheelchair with regard to the quality of life of persons with stroke: a follow-up study.
- Workplace Distress and Ethical Dilemmas in Neuroscience Nursing: A qualitative study of Chinese nurses’ experience.
- Workplace distress and ethical dilemmas among Swedish neuroscience nurses.
- 2006
- A comprehensive rehabilitation programme tailored to the needs of adults with muscular dystrophy.
- Being the next of kin of an adult person with muscular dystrophy.
- Cross-cultural interviews studies using interpreters: systematic literature review.
- Emotional distress and coping in the early stage of recovery following acute traumatic hand injury: a questionnaire survey.
- Experiences of onset and diagnosis of low-grade glioma from the patient's perspective.
- From becoming aware of to an everyday life with a hereditary disease.
- From symptom to diagnosis: illness experiences of multiple sclerosis patients.
- Long-term pain conditions after a stroke.
- Nurses and physicians' opinions regarding aggressivnes of care for general ward patients.
- Patients' perceptions of the concept of quality of care in the psychiatric setting: A phenomenographic study.
- Personal assistance for patients living with a severe neurological disorder
- Philosophers leading of ‘Ethics Rounds’ regarding dialysis patients – nurses’ and physicians’ experiences.
- Psychometric Evaluation of the Ways of Coping Questionnaire as applied to Clinical and Non-Clinical Groups.
- Severly ill ICU patients recall of factual events and unreal experiences of hospital admission and ICU stay: 3 and 12 months after discharge.
- Students’ conceptions about their own and others’ profession before and after inter-professional education at a training ward.
- The effect of an outdoor powered wheelchair on activity and participation in users with stroke.
- The impact of a powered wheelchair for outdoor use on activity, participation, and quality of life of users with stroke.
- The relationship between function, quality of life and coping in patients with low-grade gliomas.
- Theoretical model of coping among relatives of patients in intensive care units: a simultaneous concept analysis.
- 2005
- Boendebyte i demensvård: förekomst och orsaker.
- Coping with Long-term Neurological Illness and the Implications for Nursing Interventions.
- Coping with Long-term Neurological illness and the Implications for Nursing Interventions.
- Experiences of kinship with a person with muscular dystrophy.
- Experiences of kinship with a person with muscular dystrophy.
- Illness-related problems and coping among persons with low-grade glioma.
- Lifeworld perspectives on assistive devices: lived experiences of spouses of persons with stroke.
- Living with a hereditary disease: Person’s with Muscular Dystrophy and their next of kin.
- Living with long-term pain after a stroke.
- Long-term pain after a stroke from a family perspective.
- Patienters uppfattningar av begreppet vårdkvalitet inom psykiatrisk vård: en fenomenografisk studie.
- Patients’ experiences of being informed of the Diagnosis of Multiple Sclerosis.
- Quality of Life and Impairment in Patients with Multiple Sclerosis.
- Quality of Life in patients with Muscular Dystrophy and Their Next of Kin.
- Quality of life and lifestyle changes after coronary angioplasty.
- Relocation within community sheltered housing for demented persons during one year.
- Sickness impact in people with muscular dystrophy: a longitudinal study over 10 years.
- Unaccompanied young adult refugees in Sweden, experiences of their life situation and well-being: a qualitative follow-up study.
- What psychiatric patients think about the concept of quality of care: A phenomenographic interview study.
- 2004
- Coping with long-term pain after a stroke.
- Experiences of Loss and Chronic Sorrow in Persons with Neurological disorders.
- Health-related quality of life in persons with long-term pain after a stroke.
- Is life-sustaining treatment justified? - Nurses and physicians’ opinions regarding general ward patients.
- Living with Neurological Disorders: Illness Experiences, Coping and Coping Resources.
- Living with a deteriorating disease: the trajectory with muscular dystrophy over ten years.
- Nursing diagnoses in patients with acute traumatic hand injuries.
- Problems and coping strategies of people with low-malignancy brain tumours.
- Problems experienced during the first year of an acute traumatic hand injury: a prospective study.
- Psychiatric care staff’s and care associates’ perceptions of the concept of quality of care: A qualitative study.
- Staying put or living somewhere else in dementia care.
- Using a novel exercise program in patients with muscular dystrophy Part I: A qualitative study.
- Using a novel exercise program in patients with muscular dystrophy Part II: A quantitative study.
- 2003
- Better care for patients with brain tumours and their next of kin
- Final report: Looking after patients with glioma in a new, integrated way.
- Follow-up of traumatic experiences in connection with an acute traumatic hand injury.
- From symptom to diagnosis: illness experiences of Multiple Sclerosis patients.
- Lifeworld perspectives on using assistive devices: Lived experiences of persons with stroke.
- Long-term pain after stroke.
- Pitfalls in the assessment of disability in individuals with low-grade gliomas.
- Psychiatric care staff and care associates’ perceptions of the quality of care in psychiatric care.
- Trauma-related distress and mood disorders in the early stage of an acute traumatic hand injury.
- What psychiatric care staff and care associates think about the concept of quality of care: a phenomenographic interview study.
- 2002
- Characteristics in the early stage of acute traumatic hand injury.
- Coping with illness-related stress and events of daily living: the Swedish version of the Ways of Coping Questionnaire.
- Daily life, coping and quality of life in individuals with brain tumour and their next of kin.
- Disabilities after stroke and how long-term pain affects daily life.
- Disability after a stroke and the influence of long-term pain on everyday life.
- Living with a highly malignant brain tumour: the family perspective.
- Living with muscular dystrophy from a family perspective — longitudinal research.
- Long-term pain after stroke
- Long-term pain conditions after a stroke.
- Psychiatric care staff and care associates’ perceptions of the concept of quality of care in psychiatric care: a phenomenographic study.
- Quality of life and impairment in patients with Multiple Sclerosis.
- Rehabilitation of individuals with muscular dystrophy: an intervention study with complementary health methods.
- Showing one’s world – how persons with extensive lasting disabilities understand their life-situation in relation to the ethical principles embodied in the LSS legislation.
- Studies about the meaning of assistive technology devices in daily life.
- The meaning of assistive technology devices in daily life.
- The value of assistive devices in daily life.
- Traumatic stress and coping in the early stage of acute traumatic hand injury.
- 2001
- Activities of daily living and quality of life in persons with muscular dystrophy.
- Assessment of quality of life in persons with severe illness — who has the preferential right of interpretation?
- Chronic pain after a stroke
- Complementary health methods for patients with chronic illness.
- Experienced life-situation in persons with severe chronic illness and injuries. Interviews about loss, problems, coping and quality of life.
- Experiences of loss and chronic sorrow in persons with neurological disorders
- Experiences of working as a personal assistant.
- Living with brain tumour from a family perspective.
- Long-term pain after stroke.
- Loss and chronic sorrow in persons with neurological disorders.
- Quality of life in persons with severe chronic diseases and injuries. From the perspective of the disabled person, relatives and the personal assistant.
- The difficult balancing act —personal assistants’ possibilities of applying the ethical principles embodied in the LSS legislation.
- The illness experience of adult persons with muscular dystrophy.
- Which research is important/essential for the continued development of nursing science?
- 2000
- A model of caring for nursing practice and research.
- Disability and Quality of Life in Individuals with Post-Polio Syndrome.
- Disability, Coping and Quality of Life in Individuals with Muscular Dystrophy: A Prospective Study over Five-Years.
- Illness Narratives of Persons with Post-Polio Syndrome.
- Making the best of the worst – disabled persons’ view of their life- situation.
- Three core narratives – relatives’ opinions about the meaning of assistance for the disabled person and how the ethical principles embodied in the LSS legislation are applied.
- To be visible but yet invisible – personal assistants’ everyday life.
- 1999
- Chronic pain as expressed by persons with late effects of polio.
- Coping with chronic illness: A qualitative study about coping with postpolio syndrome.
- Experience of Social Support in Rehabilitation: A Phenomenological Study.
- Experiences and consequences of chronic pain in persons with post-polio syndrome (PPS).
- Experiences of support in rehabilitation of individuals with muscular dystrophy.
- Learning together – a rehabilitation programme for individuals with advanced multiple sclerosis and their personal assistants.
- Muscular Dystrophy in adults: A five-year follow-up.
- Pain in persons with post-polio: the Swedish version of the Multidimensional Pain Inventory (MPI).
- People with post-polio tell of their experiences of falling ill with polio and of the subsequent adaptation to a new life.
- Problem-focused coping and satisfaction with activities of daily living in individuals with muscular dystrophy and postpolio.
- Rehabilitation programme for individuals with multiple sclerosis (MS) and their personal assistants.
- 1998
- Assessment Instrument for Problem-Focused Coping: reliability test of APC, Part 1.
- Assessment of coping and quality of life in adults with neuromuscular diseases.
- Experiences and consequences of pain in persons with post-polio.
- Problem-Focused coping and satisfaction in daily living in individuals with muscular weakness.
- 1997
- 1996
- Coping with illness-related problems and quality of life in adult individuals with muscular dystrophy.
- Disability and quality of life in individuals with muscular dystrophies.
- Experience from a multidisciplinary rehabilitation programme for individuals with muscular dystrophy described from a psychosocial angle.
- Prevalence of dysarthria in adult myotonic dystrophy (M. Steinert) patients; speech characteristics and intelligibility.
- 1995
- 1994
- Assessment of coping with muscular dystophy: a methodological evaluation.
- New methods for the grading of impairment and disability in individuals with muscular dystrophies and their predictive value regarding experienced quality of life.
- Respiratory function, electrocardiography and quality of life in individuals with muscular dystrophy.
- Respiratory function, electrocardiogrphy and quality of life in individuals with muscular dystrophy.
- 1993
- 1989
