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Intraoperative Dexmedetomidine Use, MMP-8, and Postoperative Delirium After Cardiac Surgery With Cardiopulmonary Bypass

Association of Intraoperative Dexmedetomidine Use and Perioperative Plasma MMP-8 Dynamics With Postoperative Delirium in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07759297
Enrollment
5688
Registered
2026-08-12
Start date
2023-04-01
Completion date
2024-10-15
Last updated
2026-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Delirium

Keywords

Cardiac Surgery, Dexmedetomidine, Cardiopulmonary Bypass, Matrix Metalloproteinase 8, MMP-8

Brief summary

This observational study evaluated the association between intraoperative dexmedetomidine use and postoperative delirium (POD) in adults undergoing cardiac surgery with cardiopulmonary bypass (CPB). The study included two linked clinical components. First, routinely collected clinical data from patients undergoing cardiac surgery with CPB at three campuses of Tongji Hospital between January 2015 and December 2022 were analyzed to evaluate the dexmedetomidine-POD association. Second, perioperative plasma samples and clinical data from a prospective observational cohort enrolled between April 2023 and September 2024 were used to characterize perioperative matrix metalloproteinase-8 (MMP-8) dynamics and their associations with intraoperative dexmedetomidine use and POD. Dexmedetomidine administration was determined by the attending anesthesiologist according to clinical judgment and routine anesthetic practice and was not assigned by the study protocol.

Detailed description

This hospital-based observational study comprised two linked clinical components designed to evaluate the association between intraoperative dexmedetomidine use and postoperative delirium (POD) after cardiac surgery with cardiopulmonary bypass (CPB) and to explore the clinical relevance of perioperative matrix metalloproteinase-8 (MMP-8) responses. The first component was a retrospective multicampus cohort study using routinely collected clinical data from three campuses of Tongji Hospital. Adult patients undergoing cardiac surgery with CPB between January 2015 and December 2022 were screened according to predefined eligibility criteria. The primary exposure was intraoperative dexmedetomidine administration by continuous intravenous infusion, ascertained from anesthesia records. Dexmedetomidine administration was determined by the attending anesthesiologist according to clinical judgment and routine anesthetic practice and was not assigned by the study protocol. The primary outcome was POD occurring within 7 days after surgery. Documented POD diagnoses were accepted as confirmed events; when no explicit diagnosis was documented, postoperative medical and nursing records were retrospectively reviewed by trained anesthesiologists and intensivists blinded to intraoperative dexmedetomidine exposure. Secondary outcomes included in-hospital mortality and hospital length of stay. Multivariable regression, propensity score matching, subgroup and interaction analyses, and E-value analysis were used to evaluate the robustness of the dexmedetomidine-POD association. The second component used archived plasma samples and linked clinical data from a previously established prospective observational cohort of adults undergoing cardiac surgery with CPB who were enrolled between April 2023 and September 2024. In the original cohort, intraoperative dexmedetomidine use was determined by the treating anesthesiologist and was not influenced by the study investigators. POD within 7 days after surgery was prospectively assessed, and participants were followed until hospital discharge. Plasma samples had been collected preoperatively, at the end of surgery, and 24 h postoperatively and stored for subsequent analyses. The original prospective cohort enrollment and perioperative biospecimen collection were approved by the Medical Ethics Committee of Tongji Hospital under Approval No. TJ-IRB20231224. The current study, including secondary analyses of archived clinical data and plasma samples, was subsequently approved under Approval No. TJ-IRB202603077. Archived plasma samples were analyzed for MMP-8, and perioperative MMP-8 levels and changes were evaluated in relation to dexmedetomidine exposure and POD. Additional analyses assessed the discriminatory value of perioperative MMP-8 measures for POD and their potential statistical mediating role in the association between intraoperative dexmedetomidine use and POD.

Interventions

DRUGDexmedetomidine

Intraoperative dexmedetomidine administration during cardiac surgery with cardiopulmonary bypass was an observed clinical exposure. The decision to administer dexmedetomidine, including its dose, timing, and duration, was made by the treating anesthesiologist according to clinical judgment and routine anesthetic practice and was not assigned or standardized by the study protocol.

Sponsors

Shusheng Li
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years or older. * Patients undergoing cardiac surgery with cardiopulmonary bypass (CPB). * For the retrospective cohort, eligible patients undergoing cardiac surgery with CPB at the three participating campuses of Tongji Hospital between January 2015 and December 2022. * For the prospective biomarker cohort, eligible participants enrolled between April 2023 and September 2024 with archived plasma samples collected preoperatively, at the end of surgery, and 24 h postoperatively, together with linked clinical data.

Exclusion criteria

* Conditions precluding dexmedetomidine use, including second- or third-degree atrioventricular block without a pacemaker, uncontrolled hypotension, acute cerebrovascular disease, or known hypersensitivity to dexmedetomidine. * Severe neurological or psychiatric disorders, including a history of treatment for severe mental illness. * Inability to communicate effectively because of severe hearing, visual, or speech impairments. * Pregnancy or breastfeeding. * Emergency surgery.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Postoperative DeliriumFrom the end of surgery through postoperative day 7The number and proportion of participants who experienced at least one episode of postoperative delirium within 7 days after surgery. In the retrospective cohort, POD was ascertained from postoperative medical and nursing records using adapted DSM-5 criteria, with blinded review when no explicit diagnosis was documented. In the prospective cohort, POD was assessed prospectively by trained anesthesiologists and intensivists using the CAM-ICU.

Secondary

MeasureTime frameDescription
Hospital Length of StayFrom hospital admission through hospital discharge during the index hospitalization, an average of approximately 3 weeks.The number of calendar days from hospital admission to hospital discharge during the index hospitalization.
In-Hospital All-Cause MortalityFrom the end of surgery until death or hospital discharge, whichever occurred first, an average of approximately 3 weeks.The number and proportion of participants who died from any cause during the index hospitalization after cardiac surgery.

Countries

China

Contacts

PRINCIPAL_INVESTIGATORQin Zhang

Tongj Hospital, Tongji Medical College, Huazhong University of Science and Technology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026