Minimal detectable change of the Patient Health Questionnaire-9, Patient Health Questionnaire-8, and Patient Health Questionnaire-2: individual patient data meta-analysis.
Wang, Y
Wu, Y
González-Domínguez, NP
Boruff, JT
Levis, B
Cuijpers, P
Gilbody, S
Harel, D
Ioannidis, JPA
Markham, S
Patten, SB
Vigod, SN
Ziegelstein, RC
Benedetti, A
Thombs, BD
DEPRESsion Screening Data (DEPRESSD) PHQ Collaboration,
- Publisher:
- BMJ
- Publication Type:
- Journal Article
- Citation:
- BMJ, 2026, 394, pp. e100119
- Issue Date:
- 2026-07-23
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Full metadata record
| Field | Value | Language |
|---|---|---|
| dc.contributor.author | Wang, Y | |
| dc.contributor.author | Wu, Y | |
| dc.contributor.author | González-Domínguez, NP | |
| dc.contributor.author | Boruff, JT | |
| dc.contributor.author | Levis, B | |
| dc.contributor.author | Cuijpers, P | |
| dc.contributor.author | Gilbody, S | |
| dc.contributor.author | Harel, D | |
| dc.contributor.author | Ioannidis, JPA | |
| dc.contributor.author | Markham, S | |
| dc.contributor.author | Patten, SB | |
| dc.contributor.author | Vigod, SN | |
| dc.contributor.author | Ziegelstein, RC | |
| dc.contributor.author | Benedetti, A | |
| dc.contributor.author | Thombs, BD | |
| dc.contributor.author | DEPRESsion Screening Data (DEPRESSD) PHQ Collaboration, | |
| dc.date.accessioned | 2026-08-05T10:34:27Z | |
| dc.date.available | 2026-06-23 | |
| dc.date.available | 2026-08-05T10:34:27Z | |
| dc.date.issued | 2026-07-23 | |
| dc.identifier.citation | BMJ, 2026, 394, pp. e100119 | |
| dc.identifier.issn | 0959-8138 | |
| dc.identifier.issn | 1756-1833 | |
| dc.identifier.uri | http://hdl.handle.net/10453/195941 | |
| dc.description.abstract | OBJECTIVE: 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. DESIGN: Individual participant data meta-analysis. DATA SOURCES: Medline, Medline In-Process and other non-indexed citations, PsycInfo, and Web of Science, 1 January 2000 to 9 May 2018. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: 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. 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. 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. 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. Mean participant age was 49 years (standard deviation 17), and 60% of participants were women. Overall, 10% of participants had major depression (range 1-57% across studies). MDC95 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. For the PHQ-9, MDC95 was highest in inpatient healthcare settings at 6.48 (95% CI 6.05 to 6.92) points. MDC95 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. Sex and age had minimal or no association. Subgroup and meta-regression findings were similar for the PHQ-8 and PHQ-2. 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. A higher threshold may be preferred in specialty mental healthcare. MDC67 or MDC90 thresholds would provide less certainty that change has occurred. Alternative strategies, such as using the upper end of a prediction interval, would provide more certainty but a greater likelihood of not recognising change. STUDY REGISTRATION: PROSPERO CRD42014010673. | |
| dc.language | eng | |
| dc.publisher | BMJ | |
| dc.relation.ispartof | BMJ | |
| dc.relation.isbasedon | 10.1136/bmj-2026-100119 | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | 1103 Clinical Sciences, 1117 Public Health and Health Services | |
| dc.subject.classification | General & Internal Medicine | |
| dc.subject.classification | 32 Biomedical and clinical sciences | |
| dc.subject.classification | 42 Health sciences | |
| dc.subject.classification | 52 Psychology | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Major Depressive Disorder | |
| dc.subject.mesh | Patient Health Questionnaire | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Reproducibility of Results | |
| dc.subject.mesh | Psychometrics | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Major Depressive Disorder | |
| dc.subject.mesh | Patient Health Questionnaire | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Reproducibility of Results | |
| dc.subject.mesh | Psychometrics | |
| dc.subject.mesh | Male | |
| dc.title | Minimal detectable change of the Patient Health Questionnaire-9, Patient Health Questionnaire-8, and Patient Health Questionnaire-2: individual patient data meta-analysis. | |
| dc.type | Journal Article | |
| utslib.citation.volume | 394 | |
| utslib.location.activity | England | |
| utslib.for | 1103 Clinical Sciences | |
| utslib.for | 1117 Public Health and Health Services | |
| pubs.organisational-group | University of Technology Sydney | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Health | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Health/School of Nursing and Midwifery | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups/INSIGHT: Institute for Innovative Solutions for Wellbeing and Health | |
| pubs.organisational-group | University of Technology Sydney/UTS Groups/Stroke Research Collaborative | |
| pubs.organisational-group | University of Technology Sydney/Faculty of Health/School of Nursing and Midwifery/Discipline of Nursing | |
| utslib.copyright.status | open_access | * |
| dc.rights.license | This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by-nc/4.0/ | |
| dc.date.updated | 2026-08-05T10:34:25Z | |
| pubs.publication-status | Published online | |
| pubs.volume | 394 |
Abstract:
OBJECTIVE: 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. DESIGN: Individual participant data meta-analysis. DATA SOURCES: Medline, Medline In-Process and other non-indexed citations, PsycInfo, and Web of Science, 1 January 2000 to 9 May 2018. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: 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. 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. 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. 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. Mean participant age was 49 years (standard deviation 17), and 60% of participants were women. Overall, 10% of participants had major depression (range 1-57% across studies). MDC95 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. For the PHQ-9, MDC95 was highest in inpatient healthcare settings at 6.48 (95% CI 6.05 to 6.92) points. MDC95 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. Sex and age had minimal or no association. Subgroup and meta-regression findings were similar for the PHQ-8 and PHQ-2. 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. A higher threshold may be preferred in specialty mental healthcare. MDC67 or MDC90 thresholds would provide less certainty that change has occurred. Alternative strategies, such as using the upper end of a prediction interval, would provide more certainty but a greater likelihood of not recognising change. STUDY REGISTRATION: PROSPERO CRD42014010673.
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