TY - JOUR
T1 - Family caregiver perspectives in caring of stroke patients
T2 - A qualitative study
AU - Tarigan, Rosina Br
AU - Harris, Salim
AU - Dahlia, Debie
AU - Mansyur, Muchtaruddin
N1 - Publisher Copyright:
© 2024, Pakistan Medical Association. All rights reserved.
PY - 2024
Y1 - 2024
N2 - Objective: To explore the perspective of family caregivers who care for stroke patients in North Sumatra Province, Indonesia. Methodology: This qualitative study included 16 family caregivers who were recruited using purposive sampling method. Data were collected from June to August 2022 at Adam Malik Hospital, North Sumatra, Indonesia. We used in-depth semi-structured interviews and interview guidelines. The data were analyzed using thematic content analysis. Results: Three themes and ten sub-themes were as follows: heavy burden (psychological disorders, limited time for rest, change in social activities, and decreased income); need support and information (requires a support system, using non-pharmacological drugs, and using alternative therapies); and lack of knowledge and skills (lack of knowledge on stroke and its management, lack of knowledge on physical mobility and stroke complications, and lack of knowledge on nutrition). Conclusion: Family caregivers of stroke patients experience a heavy burden, need support and information, and have lack of knowledge and skills in carrying out their duties while caring for patients, because there have been changes in lifestyle before becoming a caregiver.
AB - Objective: To explore the perspective of family caregivers who care for stroke patients in North Sumatra Province, Indonesia. Methodology: This qualitative study included 16 family caregivers who were recruited using purposive sampling method. Data were collected from June to August 2022 at Adam Malik Hospital, North Sumatra, Indonesia. We used in-depth semi-structured interviews and interview guidelines. The data were analyzed using thematic content analysis. Results: Three themes and ten sub-themes were as follows: heavy burden (psychological disorders, limited time for rest, change in social activities, and decreased income); need support and information (requires a support system, using non-pharmacological drugs, and using alternative therapies); and lack of knowledge and skills (lack of knowledge on stroke and its management, lack of knowledge on physical mobility and stroke complications, and lack of knowledge on nutrition). Conclusion: Family caregivers of stroke patients experience a heavy burden, need support and information, and have lack of knowledge and skills in carrying out their duties while caring for patients, because there have been changes in lifestyle before becoming a caregiver.
KW - Family caregivers
KW - perspective
KW - qualitative
KW - stroke
UR - http://www.scopus.com/inward/record.url?scp=85210249850&partnerID=8YFLogxK
U2 - 10.5455/rmj.20240805042128
DO - 10.5455/rmj.20240805042128
M3 - Article
AN - SCOPUS:85210249850
SN - 0303-5212
VL - 49
SP - 960
EP - 963
JO - Rawal Medical Journal
JF - Rawal Medical Journal
IS - 4
ER -