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The HPS contains the Patient Health Questionnaire-4 (PHQ-4), a well-established and validated screening tool for anxiety and depression.

2024年2月2日 973点热度 0人点赞 0条评论

Outcome
The HPS contains the Patient Health Questionnaire-4 (PHQ-4),
a well-established and validated screening tool for anxiety and
depression.8,13 The screener asks respondents to report the frequency
during which they felt down, worried, generally uninterested,
and anxious over the past 2weeks, as assessed by
a 4-level scale ranging from “not at all” (score, 0) to “nearly
every day” (score, 3).Responses across these 4 questionswere
aggregated to create a continuous 0 to 12 index (the standard
measure of the PHQ-4). Scores ranging from 0 to 2 represent
nosymptomsof anxietyordepression; 3 to5,mild;6to8,moderate;
and 9 to 12, severe.14 A PHQ-4 score of at least 6 typically
indicates need for clinical intervention and is associated with increased health care use, disability days, and functional
impairment.15 The minimal clinically important difference
of the PHQ-4 scale is not known.

JAMA. 2024;331(4):294-301. doi:10.1001/jama.2023.25599

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最后更新:2024年2月2日

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The study used existing publicly available and deidentified data The Stanford institutional review board deemed this study exempt as it uses deidentified, administratively collected data. The HPS contains the Patient Health Questionnaire-4 (PHQ-4), a well-established and validated screening tool for anxiety and depression. HPS public-use files were used to construct the analytic sample. School of Public Health Institutional Review Board deemed this study exempt. Several study limitations should be acknowledged. Ethical approval was not sought as the data were already publicly available online. We checked the robustness of our findings The aim of this study was twofold. This systematic review and meta-analysis includes previously published observational studies. This indicated there was no requirement for proceeding to a full formal ethics and data protection review by the Usher Research Ethics Group. No overall prospective analysis plan was used. Complete case analyses were used. Study approval was received from Institutional Review Boards (IRBs) of the primary research institution These findings must be interpreted in light of several limitations
Several study limitations should be acknowledged. This indicated there was no requirement for proceeding to a full formal ethics and data protection review by the Usher Research Ethics Group. Ethical approval was not sought as the data were already publicly available online. We checked the robustness of our findings This study was exempt from institutional review board approval These new findings should be examined alongside several study limitations. These findings must be interpreted in light of several limitations No protocol approval was needed for this study We excluded those with missing data for the primary exposure The baseline data collection for this study did not require ethical approval. SUDAAN software, version 10.1 (RTI International), which accounts for weighted data and the complex sample design This study is subject to certain limitations. Study approval was received from Institutional Review Boards (IRBs) of the primary research institution HPS public-use files were used to construct the analytic sample. Consistent with those of other studies, our findings show that

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