The Impact of Preoperative Chronic Pain on Postoperative Depressive States in Elderly Patients Undergoing Joint Replacement Surgery: A Secondary Analysis Based on Prospective Data
1 other identifier
observational
575
1 country
1
Brief Summary
Background: Postoperative depression is a significant complication that hinders recovery in elderly patients undergoing joint replacement surgery. Although preoperative chronic pain is common in this population and pain and depression frequently coexist, the predictive role and underlying mechanisms of preoperative chronic pain on postoperative depression remain unclear. This study aims to systematically explore the association between the two, providing a basis for optimizing perioperative management and improving patient outcomes. Methods: This study is a secondary analysis of multicenter prospective data, including elderly patients who underwent elective knee or hip replacement surgery between April 2020 and April 2022 from a perioperative database of elderly patients in China. The impact of preoperative chronic pain on the occurrence of depressive states within 7 days after surgery was systematically evaluated using univariate and multivariate logistic regression analysis, propensity score matching, and subgroup analysis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 30, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2024
CompletedFirst Submitted
Initial submission to the registry
February 1, 2026
CompletedFirst Posted
Study publicly available on registry
February 11, 2026
CompletedFebruary 11, 2026
February 1, 2026
2 years
February 1, 2026
February 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence and Severity Classification of Postoperative Depressive States (within 7 days)
Postoperative depressive states were assessed using the Chinese version of the Patient Health Questionnaire-9 (PHQ-9). This scale was administered at bedside within 7 days after surgery by trained researchers. It is a self-reported tool comprising 9 items and is widely used for the efficient screening of clinical depressive symptoms. The assessment results were interpreted as follows: a total score ≥ 5 indicated the presence of a postoperative depressive state, with scores of 5-9 classified as mild, 10-14 as moderate, and 15-27 as moderately severe to severe.
within 7 days after surgery
Eligibility Criteria
This study is a secondary analysis based on a multicenter prospective database. We included 881 elderly patients who underwent elective joint replacement surgery at multiple medical centers between April 2020 and April 2022. The data were sourced from the Perioperative Database of Elderly Patients in China, which is a multicenter prospective study. The primary aim of this parent study was to identify perioperative risk factors in elderly patients undergoing non-cardiac surgery and to establish a targeted risk prevention and management system, utilizing data collected over a two-year period from 19 hospitals across the nation.
You may qualify if:
- Age ≥ 65 years.
- No cognitive impairment or history of mental illness.
- Underwent elective joint replacement surgery.
- Completed postoperative assessments, including questionnaires for depression, anxiety, and delirium.
You may not qualify if:
- Non-general anesthesia.
- Patients admitted to the intensive care unit postoperatively.
- Medical centers with fewer than 50 cases. -
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Anesthesiology, First Medical Center of the People's Liberation Army General Hospital
Beijing, Haidian, 100853, China
Related Publications (3)
Li L, Wu P, Wang Z, Meng X, Zha C, Li Z, Qi T, Zhang Y, Han B, Li S, Jiang C, Zhao Z, Cai J. NoncoRNA: a database of experimentally supported non-coding RNAs and drug targets in cancer. J Hematol Oncol. 2020 Feb 28;13(1):15. doi: 10.1186/s13045-020-00849-7.
PMID: 32111231RESULTNinova M, Ronshaugen M, Griffiths-Jones S. Conserved temporal patterns of microRNA expression in Drosophila support a developmental hourglass model. Genome Biol Evol. 2014 Aug 27;6(9):2459-67. doi: 10.1093/gbe/evu183.
PMID: 25169982RESULTThomson KH, Rantala MH, Viita-Aho TK, Vainio OM, Kaartinen LA. Condition-based use of antimicrobials in cats in Finland: results from two surveys. J Feline Med Surg. 2009 Jun;11(6):462-6. doi: 10.1016/j.jfms.2008.10.005. Epub 2008 Dec 25.
PMID: 19111491RESULT
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Li TONG TONG, PHD
Department of Anesthesiology, The First Medical Center of Chinese PLA General Hospital
- STUDY DIRECTOR
Weidong MI Mi, PHD
Department of Anesthesiology, The First Medical Center of Chinese PLA General Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director of the Department of Anesthesiology, The First Medical Center of Chinese PLA General Hospital
Study Record Dates
First Submitted
February 1, 2026
First Posted
February 11, 2026
Study Start
April 30, 2022
Primary Completion
April 30, 2024
Study Completion
April 30, 2024
Last Updated
February 11, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
The individual participant data (IPD) generated in this study are not planned to be shared publicly. The data contain sensitive personal health information and are subject to confidentiality protections under the ethical approval and data management regulations governing this research. Data access is restricted to the immediate research team for the purposes outlined in the approved study protocol