Literature DB >> 21444179

Assessing the quality of sleep in Greek primary caregivers of patients with secondary progressive multiple sclerosis: a cross-sectional study.

Andreas A Argyriou1, Panagiotis Karanasios, Konstantinos Assimakopoulos, Gregoris Iconomou, Alexandra Makridou, Foteini Giannakopoulou, Nicolaos Makris.   

Abstract

CONTEXT: Several studies have investigated the prevalence of sleep disorders in patients suffering from multiple sclerosis (MS) and have shown that up to 54% of patients may have significantly more sleep problems than the general population. To our knowledge, however, no data are available about the quality of sleep of the primary caregivers of patients with MS.
OBJECTIVES: The objectives of the current cross-sectional study were to assess the quality of sleep in Greek primary caregivers of patients with MS and to investigate its relationship with the degree of caregivers' emotional distress.
METHODS: Twenty-two male and 13 female primary caregivers (mean age 47.3±12.4 years) of an equal number of patients with MS, who consented to participate, completed the validated Greek version of the Pittsburgh Sleep Quality Index (PSQI) and the validated Greek version of the Hospital Anxiety and Depression Scale (HADS). Thirty-five age-, gender-, and education-matched healthy controls were used for comparisons.
RESULTS: Caregivers experienced a higher degree of anxiety than depression. The mean score in the seven-item HADS-A subscale was 9.5±4 (range 3-15) and the mean score in the seven-item HADS-D subscale was 7.1±3.1 (range 2-14). The mean scores of caregivers on both HADS-A and HADS-D were significantly higher than those of controls (P<0.001). The PSQI scoring demonstrated that 19 (54.3%) caregivers had poor sleep quality (cut-off value of >5). The mean values of caregivers for the PSQI were 6.0±2.8 (range 2-12) compared with controls, who scored at a significantly lower level (1.5±0.8; P<0.001). Poor quality of sleep was significantly correlated with increased levels of anxiety (r=0.392; P=0.02) and depression (r=0.424; P=0.01). Among the PSQI components, the sleep duration and sleep latency were mostly influenced by the degree of emotional distress.
CONCLUSION: A significant proportion of primary caregivers of MS patients experience poor sleep quality. The degree of their emotional distress appears to significantly influence their quality of sleep. Appropriate psychopharmacological interventions may be required for those individuals.
Copyright © 2011 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21444179     DOI: 10.1016/j.jpainsymman.2011.01.005

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  2 in total

1.  Care Partners and Multiple Sclerosis: Differential Effect on Men and Women.

Authors:  Tamara McKenzie; Mary Elizabeth Quig; Tuula Tyry; Ruth Ann Marrie; Gary Cutter; Edward Shearin; Kamau Johnson; James Simsarian
Journal:  Int J MS Care       Date:  2015 Nov-Dec

2.  Associations of self-reported and objectively measured sleep disturbances with depression among primary caregivers of children with disabilities.

Authors:  Olivia R Orta; Clarita Barbosa; Juan Carlos Velez; Bizu Gelaye; Xiaoli Chen; Lee Stoner; Michelle A Williams
Journal:  Nat Sci Sleep       Date:  2016-06-10
  2 in total

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