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Background
To estimate the minimal detectable change (MDC) for the Patient Health Questionnaire-9 (PHQ-9) and its eight item (PHQ-8) and two item (PHQ-2) versions including differences by participant and study characteristics .
估计患者健康问卷-9(PHQ-9)及其八项(PHQ-8)和两项(PHQ-2)版本的最小可检测变化(MDC),包括参与者和研究特征的差异。
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Methods
Individual participant data meta-analysis .
个体参与者数据的荟萃分析。
data_sources
Medline , Medline In-Process and other non-indexed citations , PsycInfo , and Web of Science , 1 January 2000 to 9 May 2018.
Medline、Medline In-Process 及其他非索引引文、PsycInfo 和 Web of Science,2000年1月1日至2018年5月9日。
eligibility_criteria_for_selecti
Datasets from articles in any language if participants were aged ≥18 years , were recruited from any non-psychiatric setting , and were not recruited because they were seeking mental healthcare .
如果参与者年龄≥18岁,是从任何非精神病学环境中招募的,且并非因为寻求心理健康护理而被招募,则来自任何语言文章的数据集。
Eligible datasets had a classification for major depressive disorder or major depressive episode based on a validated semi-structured or fully structured interview conducted within two weeks of administering the PHQ-9 , PHQ-8 , or PHQ-2 .
符合条件的数据集基于在PHQ-9、PHQ-8或PHQ-2施测两周内进行的经过验证的半结构化或全结构化访谈,对重性抑郁障碍或重性抑郁发作进行了分类。
Results
Pooled MDCs across studies were estimated for the PHQ-9 , PHQ-8 , and PHQ-2 with random effects meta-analysis for 95% (MDC95), 90% (MDC90), and 67% (MDC67) confidence that change beyond measurement error occurred .
通过随机效应元分析估计了PHQ-9、PHQ-8和PHQ-2的合并最小临床差异(MDCs),其中95%(MDC95)、90%(MDC90)和67%(MDC67)置信区间表示测量误差之外的变化。
PHQ-9 , PHQ-8 , and PHQ-2 analyses included 42 548 participants (94 studies ), 42 592 participants (94 studies ), and 44 085 participants (98 studies ), respectively .
PHQ-9、PHQ-8和PHQ-2的分析分别包括了42,548名参与者(94项研究)、42,592名参与者(94项研究)和44,085名参与者(98项研究)。
Mean participant age was 49 years (standard deviation 17), and 60% of participants were women .
参与者的平均年龄为49岁(标准差17),其中60%为女性。
Overall , 10% of participants had major depression (range 1-57% across studies ).
总体而言,10%的参与者患有重度抑郁症(研究间的范围为1-57%)。
MDC 95 was 5.72 points (95% confidence interval (CI) 5.54 to 5.90, 95% prediction interval (PI) 4.00 to 7.44) for the PHQ-9 , 5.51 points (95% CI 5.33 to 5.68, 95% PI 3.87 to 7.15) for the PHQ-8 , and 2.26 points (95% CI 2.15 to 2.37, 95% PI 1.20 to 3.32) for the PHQ-2 .
对于PHQ-9,最小临床差异(MDC95)为5.72分(95%置信区间(CI)5.54至5.90,95%预测区间(PI)4.00至7.44),对于PHQ-8为5.51分(95% CI 5.33至5.68,95% PI 3.87至7.15),对于PHQ-2为2.26分(95% CI 2.15至2.37,95% PI 1.20至3.32)。
For the PHQ-9 , MDC 95 was highest in inpatient healthcare settings at 6.48 (95% CI 6.05 to 6.92) points .
对于PHQ-9,住院医疗环境中MDC95最高,为6.48(95%置信区间6.05至6.92)分。
MDC 95 for the PHQ-9 increased by 0.40 (95% CI 0.25 to 0.55) points for each 10% increase in the proportion of participants with major depression .
对于PHQ-9,每增加10%的主要抑郁症患者比例,MDC95增加0.40(95%置信区间0.25至0.55)分。
Sex and age had minimal or no association .
性别和年龄的关联性最小或没有。
Subgroup and meta-regression findings were similar for the PHQ-8 and PHQ-2 .
PHQ-8和PHQ-2的亚组和元回归分析结果相似。
Conclusions
Based on the pooled estimate , a six point difference on the PHQ-9 , the PHQ version most used in clinical practice , could be an appropriate MDC threshold in general practice .
基于汇总估计,PHQ-9量表上的六分差异,即临床实践中最常用的PHQ版本,可能是在全科医疗中适当的最小临床重要差异(MDC)阈值。
A higher threshold may be preferred in specialty mental healthcare .
在专科精神卫生保健中,可能更倾向于使用更高的阈值。
MDC 67 or MDC 90 thresholds would provide less certainty that change has occurred .
MDC67 或 MDC90 阈值将提供较少的确定性,表明变化已经发生。
Alternative strategies , such as using the upper end of a prediction interval , would provide more certainty but a greater likelihood of not recognising change .
使用预测区间的上限等替代策略将提供更多的确定性,但不识别变化的可能性更大。
study_registration
PROSPERO CRD 42014010673.
PROSPERO CRD42014010673。
本文献翻译由 AI 辅助生成,仅供文献精读与英语学习参考。临床决策请以 PubMed / PMC 原文为准。
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