Finding meaning despite anxiety over life and death in amyotrophic lateral sclerosis patients

被引:42
作者
Ozanne, Anneli O. [1 ]
Graneheim, Ulla H. [2 ]
Strang, Susann [3 ]
机构
[1] Sahlgrens Univ Hosp, Inst Neurosci & Physiol, Dept Neurol, S-41345 Gothenburg, Sweden
[2] Umea Univ, Dept Nursing, Umea, Sweden
[3] Sahlgrens Univ Hosp, Inst Hlth & Care Sci, S-41345 Gothenburg, Sweden
关键词
amyotrophic lateral sclerosis; anxiety; meaning; motor neuron disease; nurse; nursing; quality of life; qualitative content analysis; sense of coherence; MOTOR-NEURON DISEASE; QUALITY-OF-LIFE; PALLIATIVE CARE; ALS; EXPERIENCE; SERVICES; PEOPLE; DIAGNOSIS;
D O I
10.1111/jocn.12071
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Aim and objectives To illuminate how people with amyotrophic lateral sclerosis (ALS) create meaning despite the disease. Background Coping strategies for living with ALS have already been investigated. However, there is a lack of studies on how people with the disease find meaning and what helps and hinders this. Design A qualitative descriptive study. Methods Fourteen individual interviews were performed in Spring 2007. The interviews were analysed by qualitative content analysis. Results Two themes emerged to illuminate the complex life situation of the interviewees: experiences of anxiety over life and death and finding meaning despite the illness. It became clear that the uncertain journey towards death was more frightened than death itself. Despite the incurable disease, which brought feelings of life and death anxiety, physical loss, unfairness, guilt, shame and existential loneliness, they also found meaning in life, which strengthened their will to live. Meaning was found through their family and friends, the act of giving and receiving help, the feeling of having a life of their own and accepting the present. The perspective of life was transferred to a deeper view where material things and quarrels were no longer in focus. Conclusions Despite the disease, the participants found meaning in life which strengthened their will to live. Relevance to clinical practiceThe balance between anxiety over life and death and finding meaning in life indicates the importance of support through the whole disease process. Both disease-specific problems and existential questions must be tackled. Nurses and other professionals need to be aware of the patients' existential qualms. There is a need to focus on what is important for the individual, and emphasis must be placed on where that person can find meaning.
引用
收藏
页码:2141 / 2149
页数:9
相关论文
共 30 条
[1]  
Antonovsky A., 1987, Unraveling the Mystery of Health: how People Manage Stress and Stay Well
[2]   Existential Suffering in the Palliative Care Setting: An Integrated Literature Review [J].
Boston, Patricia ;
Bruce, Anne ;
Schreiber, Rita .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2011, 41 (03) :604-618
[4]   How people with motor neurone disease talk about living with their illness: a narrative study [J].
Brown, Janice ;
Addington-Hall, Julia .
JOURNAL OF ADVANCED NURSING, 2008, 62 (02) :200-208
[5]   Prognostic factors in ALS: A critical review [J].
Chio, Adriano ;
Logroscino, Giancarlo ;
Hardiman, Orla ;
Swingler, Robert ;
Mitchell, Douglas ;
Beghi, Ettore ;
Traynor, Bryan G. .
AMYOTROPHIC LATERAL SCLEROSIS, 2009, 10 (5-6) :310-323
[6]   Finding Meaning in Suffering [J].
Deal, Belinda .
HOLISTIC NURSING PRACTICE, 2011, 25 (04) :205-210
[7]   Meaning in life in patients with amyotrophic lateral sclerosis [J].
Fegg, Martin Johannes ;
Koegler, Monika ;
Brandstaetter, Monika ;
Jox, Ralf ;
Anneser, Johanna ;
Haarmann-Doetkotte, Sigrid ;
Wasner, Maria ;
Borasio, Gian Domenico .
AMYOTROPHIC LATERAL SCLEROSIS, 2010, 11 (05) :469-474
[8]   Personal values and individual quality of life in palliative care patients [J].
Fegg, MJ ;
Wasner, M ;
Neudert, C ;
Borasio, GD .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2005, 30 (02) :154-159
[9]   Perceptions of quality of life in people with ALS: Effects of coping and health care [J].
Foley, Geraldine ;
O'Mahony, Paul ;
Hardiman, Orla .
AMYOTROPHIC LATERAL SCLEROSIS, 2007, 8 (03) :164-169
[10]   Experience of Services as a Key Outcome in Amyotrophic Lateral Sclerosis (ALS) Care: The Case for a Better Understanding of Patient Experiences [J].
Foley, Geraldine ;
Timonen, Virpi ;
Hardiman, Orla .
AMERICAN JOURNAL OF HOSPICE & PALLIATIVE MEDICINE, 2012, 29 (05) :362-367