Impacts of chronic illness on families: Experiences of Iranian family of patients with Multiple Sclerosis: A Qualitative Study
Impacts of chronic illness on families: Experiences of Iranian family of patients with Multiple Sclerosis: A Qualitative Study
نویسندگان: حسین ابراهیمی , هادی حسنخانی , حسین نامدار ارشتناب , اسماعیل خدادادی
کلمات کلیدی: Multiple Sclerosis; Family Caregivers; Chronic illness; Disease Burden; Qualitative Research
نشریه: 0 , 5 , 1 , 2017
| نویسنده ثبت کننده مقاله |
اسماعیل خدادادی |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
دانشکده پرستاری و مامائی |
| کد مقاله |
60545 |
| عنوان فارسی مقاله |
Impacts of chronic illness on families: Experiences of Iranian family of patients with Multiple Sclerosis: A Qualitative Study |
| عنوان لاتین مقاله |
Impacts of chronic illness on families: Experiences of Iranian family of patients with Multiple Sclerosis: A Qualitative Study |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
Journal of Research in Medical and Dental Science |
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
https://jrmds.in/index.php/JRMDS/article/view/239 |
| Family members are often the primary healthcare providers and support for patients with a chronic disease such as Multiple Sclerosis
(MS). Families endure and encounter long term difficulties when caring for a person suffering from MS. This study was conducted to
explain the family experiences with multiple sclerosis and their problem and concerns.In a qualitative research, based on conventional
content analysis, 18 family caregivers of patients with MS were selected by using purposive sampling method. Data were collected
through semi-structured and in-depth interviews conducted at the Multiple Sclerosis Society and hospitals of Tabriz in Iran from May to
December of 2015. Data were analyzed according to qualitative content analysis by using the MAXQDA.10 software. Interviews identified
three main categories regarding family caregiver experiences with MS: 1) disease onset crisis, 2) disease burden, and 3) living in the
shadow of death. The results showed that family caregivers of MS patients face numerous problems and they are at risk for depression
and a lower quality of life due to disease burden. Also the results revealed the main concerns of families are financial problems and fear
of paralysis and patient be crippled. Healthcare providers can use these results to better support and care for patients and their family
members in order to improve their quality of life and reduce disease complications. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Esmail Khodadadi-Impacts of chronic illness on families, Journal of Research in Medical and Dental Sciences, 5(1), 13-18.pdf | 1396/02/05 | 785760 | دانلود |
| photo_2017-04-22_09-35-52.jpg | 1396/02/05 | 164354 | دانلود |
| photo_2017-04-22_09-37-29.jpg | 1396/02/05 | 65600 | دانلود |