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Quality of life, depression, and sexual dysfunction in spouses of female patients with fibromyalgia

机译:女性纤维肌痛患者配偶的生活质量,抑郁和性功能障碍

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The aim of this study was to investigate the effects of the quality of life and psychological condition of female patients with fibromyalgia and their spouses on sexual function. A total of 32 female patients diagnosed with fibromyalgia and their spouses were analyzed. Thirty married couples were included in the study as the control group. The demographic data of the fibromyalgia patients were recorded, a visual analog scale was used to evaluate the level of pain, and the Fibromyalgia Impact Questionnaire was used to evaluate the impact of the symptoms on the quality of life of the patients. The quality of life of both the patients and the control group were evaluated using the Short Form 36 (SF-36), and psychological variables were evaluated using the Beck Depression Inventory (BDI) and Beck Anxiety Inventory. Sexual function was assessed using the Female Sexual Function Index for female participants and the International Index of Erectile Function (IIEF) for male participants. The IIEF erectile dysfunction scores were significantly lower in the spouses of female patients with fibromyalgia than in the control group (p < 0.05), and the BDI scores were significantly higher in the spouses of the female patients with fibromyalgia (p < 0.05). Among the SF-36 scores, the emotional and physical roles were significantly lower in the spouses of the female patients with fibromyalgia (p = 0.003 and p = 0.004, respectively). In all spouses of FMS patients and controls, there was a significantly negative correlation between erectile function, the BDI score, and to be married with FMS patient and positive correlations between erectile function and emotional role, social function, mental health, SF-36 pain score, and general health (p < 0.05 for all). In a linear regression model, BDI, to be married with FMS patient and general health were found to affect erectile function (beta regression coefficient = -0.572, SE = 0.082, p = 0.001; beta regression coefficient = -0.332, SE = 1.619, p = 0.007; beta regression coefficient = 0.445, SE = 0.065, p = 0.005, respectively). Being a spouse of a patient with fibromyalgia might significantly interfere with quality of life and lead to a high rate of sexual dysfunction. Spouses of patients with fibromyalgia might also be investigated for sexual dysfunction and quality of life. Treatment programs for this group should be considered.
机译:这项研究的目的是调查女性纤维肌痛患者及其配偶的生活质量和心理状况对性功能的影响。总共分析了32名诊断为纤维肌痛的女性患者及其配偶。该研究包括三十对已婚夫妇作为对照组。记录纤维肌痛患者的人口统计数据,使用视觉模拟量表评估疼痛程度,并使用纤维肌痛影响问卷评估症状对患者生活质量的影响。使用简短表格36(SF-36)评估患者和对照组的生活质量,并使用贝克抑郁量表(BDI)和贝克焦虑量表评估心理变量。使用女性参与者的女性性功能指数和男性参与者的国际勃起功能指数(IIEF)评估性功能。女性纤维肌痛患者配偶的IIEF勃起功能障碍评分显着低于对照组(p <0.05),女性纤维肌痛患者配偶的BDI评分显着较高(p <0.05)。在SF-36评分中,患有纤维肌痛的女性患者的配偶的情感和生理作用明显较低(分别为p = 0.003和p = 0.004)。在FMS患者和对照组的所有配偶中,勃起功能,BDI评分以及与FMS患者结婚之间均存在显着的负相关,而勃起功能与情绪角色,社交功能,心理健康,SF-36疼痛之间呈正相关得分和总体健康状况(对于所有患者,p <0.05)。在线性回归模型中,发现BDI与FMS患者结婚并影响整体健康(β回归系数= -0.572,SE = 0.082,p = 0.001;β回归系数= -0.332,SE = 1.619, p = 0.007;β回归系数分别为0.445,SE = 0.065,p = 0.005)。作为纤维肌痛患者的配偶可能会严重影响生活质量,并导致极高的性​​功能障碍。纤维肌痛患者的配偶也可能进行性功能障碍和生活质量调查。应考虑该组的治疗方案。

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