Center for Depression Research and Clinical Care, Department of Psychiatry, UT Southwestern Medical Center, Dallas, TX, United States; Peter O'Donnell Jr. Brain Institute, UT Southwestern Medical Center, Dallas, TX, United States.
Center for Depression Research and Clinical Care, Department of Psychiatry, UT Southwestern Medical Center, Dallas, TX, United States; Peter O'Donnell Jr. Brain Institute, UT Southwestern Medical Center, Dallas, TX, United States; Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, United States.
Gen Hosp Psychiatry. 2022 Jan-Feb;74:1-8. doi: 10.1016/j.genhosppsych.2021.11.001. Epub 2021 Nov 11.
This report from VitalSign project describes treatment selection, follow-up rates and remission outcomes by initial depression severity using the PCP-FIRST model.
This retrospective analysis included 32,106 patients aged ≥12 years screened with the Patient Health Questionnaire 2-item (PHQ-2) from November 2016 to July 2019 across 37 primary care clinics. PHQ-2 positive-screen patients (PHQ-2 ≥ 3) received 9-item PHQ (PHQ-9) and 7-item Generalized Anxiety Disorder scales, clinician assessments, and evaluation for pharmacotherapy management with measurement-based care (MBC).
Of PHQ-2 screened patients, 18.7% (5994/32,106) were positive and received a PHQ-9. Of 5994 patients with PHQ-9, 2571 received a clinical diagnosis of depression of whom, 333 had none-mild depression (PHQ-9 < 10) and 2238 had moderate-severe depression (PHQ-9 ≥ 10). Of the 333 patients with none-mild depression and 2238 patients with moderate-severe depression, 266 and 1929 had at least 18 weeks of data available. Of these, 54.9% (146/266) with none-mild depression and 69.1% (1332/1929) with moderate-severe depression were started on pharmacotherapy. Of the 1478 patients with clinical diagnosis of depression, initiated on pharmacotherapy, 1046 returned for ≥1 follow-up and 616 returned for ≥3 follow-ups over 18 weeks. Of the 1046 patients with ≥1 follow-up visit within 18 weeks, remission rates for patients with mild depression, moderate-severe depression, and overall were 55.6% (66/99), 30% (282/941), and 32.4% (338/1040) respectively.
Despite this being a real-world, usual care sample, remission outcomes exceed real world remission rate expectations of 6% in primary care.
本项 VitalSign 项目报告采用 PCP-FIRST 模型,根据初始抑郁严重程度描述了治疗选择、随访率和缓解结局。
本回顾性分析纳入了 2016 年 11 月至 2019 年 7 月期间,37 家初级保健诊所使用患者健康问卷 2 项(PHQ-2)筛选出的 32106 例年龄≥12 岁的患者。PHQ-2 阳性筛查患者(PHQ-2≥3)接受 9 项 PHQ(PHQ-9)和 7 项广泛性焦虑症量表、临床医生评估,以及基于测量的护理(MBC)的药物治疗管理评估。
在 PHQ-2 筛查患者中,18.7%(5994/32106)呈阳性并接受了 PHQ-9 检查。在 5994 例 PHQ-9 患者中,2571 例患者被临床诊断为抑郁症,其中 333 例患者为无轻度抑郁(PHQ-9<10),2238 例患者为中重度抑郁(PHQ-9≥10)。在 333 例无轻度抑郁和 2238 例中重度抑郁患者中,266 例和 1929 例至少有 18 周的可用数据。在这些患者中,无轻度抑郁的患者中有 54.9%(146/266),中重度抑郁的患者中有 69.1%(1332/1929)开始接受药物治疗。在 1478 例临床诊断为抑郁症且开始接受药物治疗的患者中,有 1046 例在 18 周内至少进行了 1 次随访,有 616 例在 18 周内至少进行了 3 次随访。在 1046 例 18 周内至少有 1 次随访的患者中,轻度抑郁、中重度抑郁和总体患者的缓解率分别为 55.6%(66/99)、30%(282/941)和 32.4%(338/1040)。
尽管这是一个真实世界的常规护理样本,但缓解结局超过了初级保健中 6%的实际缓解率预期。