2017
DOI: 10.7224/1537-2073.2016-058
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Fatigue and Mood States in Nursing Home and Nonambulatory Home-Based Patients with Multiple Sclerosis

Abstract: The nursing home patients with MS were less likely to report fatigue, pessimism, and tension than those receiving home-based care. Further studies should examine ways of facilitating a greater degree of autonomy and decision-making control in MS patients receiving home-based care.

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Cited by 6 publications
(2 citation statements)
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“…Severely-limited (non-ambulatory) pwMS that are living within a structured nursing home environment report significantly lower level of fatigue, pessimism and tension when compared to home-based care. 47 The periodic fluctuations in MS symptoms can also result with different answers on questionnaires depending on the period the pwMS was recruited and administered. For example, heat-sensitive pwMS may report higher levels of fatigability that could be related to the current meteorological temperatures (pwMS interviewed during winter versus summer months).…”
Section: Discussionmentioning
confidence: 99%
“…Severely-limited (non-ambulatory) pwMS that are living within a structured nursing home environment report significantly lower level of fatigue, pessimism and tension when compared to home-based care. 47 The periodic fluctuations in MS symptoms can also result with different answers on questionnaires depending on the period the pwMS was recruited and administered. For example, heat-sensitive pwMS may report higher levels of fatigability that could be related to the current meteorological temperatures (pwMS interviewed during winter versus summer months).…”
Section: Discussionmentioning
confidence: 99%
“…This finding in line with [66] who mentioned that lack of understanding of MS disease, as well as the uncertainty of MS symptoms, all this challenges makes the MS patient difficult to response to treatments, in which an effective communication has a critical role in improving; acceptance of the disease, patients' compliance with chronic treatments and patients' quality of life. [67] added that the demanding need of care in MS patients demonstrates social, psychological, and physical impact not only patients but also their families or caregivers.…”
Section: Discussionmentioning
confidence: 99%