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产后抑郁症经强光疗法治疗后持续缓解:一项随机、安慰剂对照的初步试验。

Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo-controlled trial.

机构信息

Centre for Chronobiology, University of Basel, Basel, Switzerland.

Transfaculty Research Platform Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.

出版信息

Acta Psychiatr Scand. 2022 Oct;146(4):350-356. doi: 10.1111/acps.13482. Epub 2022 Aug 3.

Abstract

OBJECTIVE

Perinatal depression (PND) is a severe complication of pregnancy, affecting both mothers and newborns. Bright light therapy (BLT) has only been tested in a few studies for treating either antenatal or postnatal depression. We conducted a pilot trial to investigate the efficacy and safety of BLT for PND occurring at any time across the perinatal period.

METHODS

A single-blind RCT was carried out in women with an EPDS >12 from the 2nd gestational trimester until 9 months postpartum. Participants received either 30-minutes morning BLT (10'000 lux) or dim red light (DRL, 19 lux) for 6 weeks.

RESULTS

Twenty-two women were randomised to BLT (n = 11) or DRL (n = 11). Among those receiving BLT, 73% achieved remission (improvement ≥50%, EPDS score ≤ 12), in contrast to 27% in the DRL group (p = 0.04). A significant influence of time on EPDS score and group-time interaction emerged, with a greater reduction in the BLT-group across the follow-up period. No women in either group reported major side effects.

CONCLUSION

Morning BLT induced a significant remission from PND as compared to DRL and this effect was maintained across the perinatal period. BLT showed an excellent safety profile and was well-tolerated, thus representing a valid therapeutic strategy in this vulnerable perinatal population.

摘要

目的

围产期抑郁症(PND)是一种严重的妊娠并发症,影响母亲和新生儿。光照疗法(BLT)仅在少数研究中针对产前或产后抑郁症进行了测试。我们进行了一项试点试验,以调查 BLT 治疗围产期任何时间发生的 PND 的疗效和安全性。

方法

一项单盲 RCT 在 EPDS>12 的孕妇中进行,从妊娠第 2 个妊娠期直至产后 9 个月。参与者接受每天 30 分钟的早晨 BLT(10,000 勒克斯)或昏暗的红光(DRL,19 勒克斯)治疗 6 周。

结果

22 名女性被随机分配到 BLT 组(n=11)或 DRL 组(n=11)。在接受 BLT 的患者中,73%达到缓解(改善≥50%,EPDS 评分≤12),而 DRL 组为 27%(p=0.04)。EPDS 评分和组间时间交互作用的时间有显著影响,BLT 组在整个随访期间的降幅更大。两组均无女性报告主要副作用。

结论

与 DRL 相比,早晨 BLT 可显著缓解 PND,且这种效果在围产期持续存在。BLT 表现出极好的安全性和耐受性,因此代表了这一脆弱围产期人群的有效治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e063/9804451/925040c33669/ACPS-146-350-g001.jpg

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