Health-related quality of life (HRQoL) loss associated with self-perceived anxiety/depression in seropositive rheumatoid arthritis.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY Clinical Rheumatology Pub Date : 2024-10-30 DOI:10.1007/s10067-024-07186-x
Diego Fernando Rojas-Gualdrón, Carolina Franco-Salazar, Clara Ángela Gómez-Henck, Maria Camila Manrique-Castrillón, Yennifer Carime Hoyos-Méndez, Susana Vélez-Romero, Juan Camilo Díaz-Coronado
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Abstract

Objective: To analyze the HRQoL loss associated with self-perceived anxiety/depression in patients with seropositive rheumatoid arthritis (RA).

Method: This secondary data analysis is based on a registry-based retrospective follow-up study of patients with seropositive RA treated between August 2014 and January 2023 in ARTMEDICA, Colombia. HRQoL loss and self-perceived anxiety/depression were defined as outcomes. Disease activity (DAS-28) and other patient data were also gathered. Statistical analyses were performed using the ordinal logistic and generalized linear regression models.

Results: A total of 3579 patients with a mean follow-up of 2.9 (SD 2.4) years, 85.6% women with a median age at diagnosis of 48.1 (IQR 37.8-57.5) years, and a median of 6.5 (IQR 1.9-14.7) years living with RA were included. At program admission, the median DAS-28 score was 2.8 (IQR 2.1-4.2), and 6.6% of patients reported extreme anxiety/depression. The average HRQoL loss was 3.4 months per year lived with seropositive AR. Among patients with no pain or discomfort, moderate and extreme anxiety/depression were associated with mean HRQoL losses of 2.2 (95% CI - 2.3 to - 2.2) and 4.1 (95% CI - 4.3 to - 3.8) months. In patients with extreme pain/discomfort, these estimations were 0.8 (95% CI - 0.9 to - 0.7) and 1.9 (95% CI - 2.1 to - 1.7) months, respectively.

Conclusion: Our study adds to the available body of evidence by clarifying the differential impact of anxiety/depression on HRQoL, depending on the severity of pain. These findings highlight the importance of strengthening mental health care and psychological well-being interventions for patients with RA, regardless of pain or disease activity. Key Points • The average HRQoL loss was 3.4 months per year lived with seropositive AR. • Pain/discomfort rather than disease activity explained the severity of anxiety/depression as well as its associated HRQoL loss. • For patients with extreme pain/discomfort and anxiety/depression, the average HRQoL loss was 8.1 months per year lived with the disease compared to 0.4 months for patients without those impacts.

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血清反应阳性类风湿性关节炎患者的健康相关生活质量(HRQoL)损失与自我感觉焦虑/抑郁有关。
目的分析血清反应阳性类风湿性关节炎(RA)患者自我感觉焦虑/抑郁相关的 HRQoL 损失:这项二手数据分析基于一项登记在册的回顾性随访研究,研究对象是2014年8月至2023年1月期间在哥伦比亚ARTMEDICA接受治疗的血清反应阳性RA患者。HRQoL损失和自我感觉焦虑/抑郁被定义为结果。此外,还收集了疾病活动度(DAS-28)和其他患者数据。统计分析采用了序数逻辑和广义线性回归模型:共纳入 3579 名患者,平均随访时间为 2.9 年(SD 2.4),其中 85.6% 为女性,诊断时的中位年龄为 48.1 岁(IQR 37.8-57.5),RA 患者的中位生活年限为 6.5 年(IQR 1.9-14.7)。入院时,DAS-28 评分的中位数为 2.8(IQR 2.1-4.2),6.6% 的患者表示极度焦虑/抑郁。血清反应呈阳性的 AR 患者平均每年在 HRQoL 方面损失 3.4 个月。在无疼痛或不适的患者中,中度和极度焦虑/抑郁与平均 HRQoL 损失 2.2 个月(95% CI - 2.3 至 - 2.2)和 4.1 个月(95% CI - 4.3 至 - 3.8)相关。在极度疼痛/不适的患者中,这些估计值分别为 0.8(95% CI - 0.9 至 - 0.7)个月和 1.9(95% CI - 2.1 至 - 1.7)个月:我们的研究澄清了焦虑/抑郁对 HRQoL 的不同影响(取决于疼痛的严重程度),从而补充了现有的证据。这些发现强调了加强对RA患者的心理保健和心理健康干预的重要性,无论疼痛或疾病活动情况如何。要点--血清反应呈阳性的AR患者平均每年的HRQoL损失为3.4个月。- 焦虑/抑郁的严重程度及其相关的 HRQoL 损失是由疼痛/不适而非疾病活动造成的。- 对于有极度疼痛/不适和焦虑/抑郁的患者,平均每患病一年会损失8.1个月的 HRQoL,而没有这些影响的患者则为0.4个月。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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