Section of Psychiatry, Department of Medical Sciences of Communication and Behaviour, University of Ferrara, Italy.
Ann Gen Psychiatry. 2010 Jul 29;9:33. doi: 10.1186/1744-859X-9-33.
Factors Influencing Depression Endpoints Research (FINDER) is a 6-month, prospective, observational study carried out in 12 European countries aimed at investigating health-related quality of life (HRQoL) in outpatients receiving treatment for a first or new depressive episode. The Italian HRQoL data at 6 months is described in this report, and the factors associated with HRQoL changes were determined.
Data were collected at baseline, 3 and 6 months of treatment. HRQoL was measured using components of the 36-item Short Form Health Survey (SF-36; mental component summary (MCS), physical component summary (PCS)) and the European Quality of Life-5 Dimensions (EQ-5D; visual analogue scale (VAS) and health status index (HSI)). The Hospital Anxiety and Depression Scale (HADS) was adopted to evaluate depressive symptoms, while somatic and painful physical symptoms were assessed by using the 28-item Somatic Symptom Inventory (SSI-28) and a VAS.
Of the initial 513 patients, 472 completed the 3-month observation and 466 the 6-month observation. The SF-36 and EQ-5D mean (+/- SD) scores showed HRQoL improvements at 3 months and a further smaller improvement at 6 months, with the most positive effects for SF-36 MCS (baseline 22.0 +/- 9.2, 3 months 34.6 +/- 10.0; 6 months 39.3 +/- 9.5) and EQ-5D HSI (baseline 0.4 +/- 0.3; 3 months 0.7 +/- 0.3; 6 months 0.7 +/- 0.2). Depression and anxiety symptoms (HADS-D mean at baseline 13.3 +/- 4.2; HADS-A mean at baseline 12.2 +/- 3.9) consistently decreased during the first 3 months (8.7 +/- 4.3; 7.5 +/- 3.6) and showed a further positive change at 6 months (6.9 +/- 4.3; 5.8 +/- 3.4). Somatic and painful symptoms (SSI and VAS) significantly decreased, with the most positive changes in the SSI-28 somatic item (mean at baseline 2.4 +/- 0.7; mean change at 3 months: -0.5; 95% CI -0.6 to -0.5; mean change at 6 months: -0.7; 95% CI -0.8 to -0.7); in 'interference of overall pain with daily activities' (mean at baseline 45.2 +/- 30.7; mean change at 3 months -17.4; 95% CI -20.0 to -14.8; mean change at 6 months -24.4; 95% CI -27.3 to -21.6) and in 'having pain while awake' (mean at baseline 41.1 +/- 29.0; mean change at 3 months -13.7; 95% CI -15.9 to -11.5; mean change at 6 months -20.2; 95% CI -22.8 to -17.5) domains. The results from linear regression analyses showed that the antidepressant switch within classes was consistently associated with a worsening in SF-36 MCS, EQ-5D VAS and HSI compared to non-switching treatment. Furthermore, between-group antidepressants (AD) switch was associated with a worse SF-36 MCS and EQ-5D HSI. MCS (P = 0.028), PCS (P = 0.036) and HSI (P = 0.002) were inversely related to the number of each previous additional depressive episode. PCS (P = 0.009) and HSI (P = 0.005) were also less improved in patients suffering from a chronic medical condition. Moreover, PCS (P = 0.044) and EQ-5D VAS (P < 0.0001) worsening was consistently associated with the presence of a psychiatric illness in the 24 months before baseline. For every additional point on the SSI-somatic score and on the overall pain VAS score at baseline, HSI score were on average 0.062 (P < 0.001) and 0.001 (P = 0.005) smaller, respectively.
After starting AD treatment, HRQoL improvements at 3 and 6 months were observed. However, several factors can negatively influence HRQoL, such as the presence of somatic and painful symptoms, the presence of any chronic medical condition or previous psychiatric illness.
影响抑郁终点研究(FINDER)是一项为期 6 个月的前瞻性观察性研究,在 12 个欧洲国家进行,旨在调查首次或新发抑郁发作的门诊患者的健康相关生活质量(HRQoL)。本报告描述了意大利在 6 个月时的 HRQoL 数据,并确定了与 HRQoL 变化相关的因素。
在治疗开始时、第 3 个月和第 6 个月收集数据。使用 36 项简短健康调查(SF-36;精神成分摘要(MCS),身体成分摘要(PCS))和欧洲生活质量 5 维度(EQ-5D;视觉模拟量表(VAS)和健康状况指数(HSI))的成分来测量 HRQoL。采用医院焦虑抑郁量表(HADS)评估抑郁症状,而躯体和疼痛性躯体症状则采用 28 项躯体症状清单(SSI-28)和 VAS 进行评估。
在最初的 513 名患者中,472 名完成了 3 个月的观察,466 名完成了 6 个月的观察。SF-36 和 EQ-5D 的平均(+/- SD)评分显示,在 3 个月时 HRQoL 有所改善,6 个月时进一步有所改善,SF-36 MCS(基线 22.0 +/- 9.2,3 个月 34.6 +/- 10.0;6 个月 39.3 +/- 9.5)和 EQ-5D HSI(基线 0.4 +/- 0.3;3 个月 0.7 +/- 0.3;6 个月 0.7 +/- 0.2)的效果最为显著。抑郁和焦虑症状(HADS-D 平均基线值为 13.3 +/- 4.2;HADS-A 平均基线值为 12.2 +/- 3.9)在最初的 3 个月内持续下降(8.7 +/- 4.3;7.5 +/- 3.6),6 个月时进一步呈阳性变化(6.9 +/- 4.3;5.8 +/- 3.4)。躯体和疼痛症状(SSI 和 VAS)明显减轻,其中 SSI-28 躯体项目的变化最为显著(基线均值为 2.4 +/- 0.7;3 个月时的平均变化值为 -0.5;95%CI-0.6 至-0.5;6 个月时的平均变化值为 -0.7;95%CI-0.8 至-0.7);“总体疼痛对日常活动的干扰”(基线均值为 45.2 +/- 30.7;3 个月时的平均变化值为-17.4;95%CI-20.0 至-14.8;6 个月时的平均变化值为-24.4;95%CI-27.3 至-21.6)和“清醒时有疼痛”(基线均值为 41.1 +/- 29.0;3 个月时的平均变化值为-13.7;95%CI-15.9 至-11.5;6 个月时的平均变化值为-20.2;95%CI-22.8 至-17.5)。线性回归分析结果表明,与非转换治疗相比,在同类药物中转换抗抑郁药与 SF-36 MCS、EQ-5D VAS 和 HSI 的恶化呈持续相关。此外,组间抗抑郁药(AD)转换与 SF-36 MCS 和 EQ-5D HSI 较差相关。MCS(P = 0.028)、PCS(P = 0.036)和 HSI(P = 0.002)与既往每次附加抑郁发作的数量呈负相关。PCS(P = 0.009)和 HSI(P = 0.005)在患有慢性疾病的患者中也改善较少。此外,PC(P = 0.044)和 EQ-5D VAS(P < 0.0001)恶化与基线前 24 个月内存在精神疾病持续相关。在基线时,SSI-躯体评分和整体疼痛 VAS 评分每增加一个点,HSI 评分平均降低 0.062(P < 0.001)和 0.001(P = 0.005)。
开始 AD 治疗后,在 3 个月和 6 个月时观察到 HRQoL 的改善。然而,躯体和疼痛症状、任何慢性医疗状况或既往精神疾病的存在等几个因素可能会对 HRQoL 产生负面影响。