DEPRESSION AND QUALITY OF LIFE IN PATIENTS WITH PEMPHIGUS: A CROSS-SECTIONAL STUDY

M. Maghade, Anand Saoji, Abhishek Somani, Abhijeet Faye
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Abstract

Objective: The objective of the study is (1) to analyze the prevalence and severity of depression in cases of pemphigus and (2) to study the association of demographic factors with the presence of depression in cases with pemphigus. Methods: A cross-sectional single-interview study was carried out on 100 consecutively selected patients with pemphigus attending the dermatology out-patient department in a tertiary care hospital. The assessment was done with semi-structured pro forma, Beck depression inventory (BDI), and quality of life (QoL) measure – Skindex-16. The Statistical Package for the Social Sciences 24.0 was used for statistical analysis and p<0.05 was taken as statistically significant. Results: Out of 100 cases, there were 60 (60%) males and 40 (40%) were females with M: F ratio of 1:0.66. The mean age of male and female patients was found to be comparable with no statistically significant difference (p=0.6061). The majority were married, employed, and from rural backgrounds. 22% satisfied the Diagnostic and Statistical Manual for Mental Disorders 5th edition criteria for major depressive disorder. Assessment using BDI in these patients for severity of depression showed mild depression in 12%, moderate depression in 7%, and severe depression in 3%. Patients having a longer duration of illness and a history of frequent hospitalization were found to have significantly high scores on the subscale for depressive symptoms. QoL assessment using the Skindex-16 scale among these patients showed that they experienced more severe emotional and symptomatic effects due to skin disease compared to functional effects, especially during relapse. Those who had poor QoL showed significantly high scores on the subscale for depressive symptoms. Conclusion: More than 20% of patients of pemphigus had diagnosable depression with significant effects on QoL. Therefore, regular screening for depression is important in pemphigus patients as it will help in planning early intervention.
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丘疹性荨麻疹患者的抑郁和生活质量:横断面研究
研究目的本研究的目的是:(1) 分析丘疹性荨麻疹患者抑郁症的患病率和严重程度;(2) 研究人口统计学因素与丘疹性荨麻疹患者抑郁症的相关性:方法:对一家三级医院皮肤科门诊部连续挑选的 100 名丘疹性荨麻疹患者进行了横断面单一访谈研究。评估采用半结构式问卷、贝克抑郁量表(BDI)和生活质量(QoL)测量方法--Skindex-16。采用社会科学统计软件包 24.0 进行统计分析,P<0.05 为差异有统计学意义:在 100 例患者中,男性 60 例(占 60%),女性 40 例(占 40%),男女比例为 1:0.66。男女患者的平均年龄相当,差异无统计学意义(P=0.6061)。大多数患者已婚,有工作,来自农村。22%的患者符合《精神疾病诊断与统计手册》第五版的重度抑郁障碍标准。使用 BDI 对这些患者的抑郁严重程度进行的评估显示,12% 的患者患有轻度抑郁,7% 的患者患有中度抑郁,3% 的患者患有重度抑郁。病程较长和有频繁住院史的患者在抑郁症状分量表上的得分明显较高。使用 Skindex-16 量表对这些患者进行的 QoL 评估显示,与功能性影响相比,皮肤病对他们的情绪和症状的影响更为严重,尤其是在复发时。QoL 较差的患者在抑郁症状分量表上的得分明显较高:结论:超过 20% 的丘疹性荨麻疹患者可诊断为抑郁症,并对其 QoL 有显著影响。因此,定期对丘疹性荨麻疹患者进行抑郁症筛查非常重要,因为这有助于制定早期干预计划。
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