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Dexmedetomidine Supplemented Analgesia and Incidence of Postoperative Delirium

Impact of Dexmedetomidine Supplemented Analgesia on Incidence of Delirium in Elderly Patients After Cancer Surgery: a Multicenter Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03012984
Enrollment
1500
Registered
2017-01-06
Start date
2017-01-06
Completion date
2022-06-11
Last updated
2026-01-08

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

Conditions

Analgesia, Complication, Postoperative, Delirium, Dexmedetomidine, Elderly, Surgery

Keywords

elderly, surgery, analgesia, dexmedetomidine, delirium

Brief summary

Delirium is a frequently occurred cerebral complication in elderly patients after surgery, and its occurrence is associated with worse outcomes. Sleep disturbances is considered to be one of the most important risk factors of postoperative delirium. Previous studies showed that, for elderly patients admitted to the ICU after surgery, low-dose dexmedetomidine infusion improved the quality of sleep and decreased the incidence of delirium. The investigators hypothesize that, for elderly patients after cancer surgery, dexmedetomidine supplemented analgesia can also decrease the incidence of delirium, possibly by improving sleep quality. The purpose of this multicenter, randomized controlled trial is to investigate the impact of dexmedetomidine supplemented analgesia on the incidence of delirium in elderly patients after cancer surgery.

Detailed description

Delirium is a state of acutely occurred and transient cerebral dysfunction. It is a common complication in elderly patients after surgery. A systematic review showed that an average of 36.8% (range 0 to 73.5%) of surgical patients developed postoperative delirium, and its occurrence increased with age. According to our previous studies, postoperative delirium developed in 51.0% of patients after cardiac surgery and in 44.5% of patients after non-cardiac surgery. The occurrence of delirium is associated with worse short-term outcomes, including increased postoperative complications, prolonged hospital stay, and increased in-hospital mortality; it is also associated with worse longterm outcomes, including declined cognitive function, decreased quality of life, and increased post-hospital mortality. Delirium is the result of multiple factors. Studies showed that postoperative pain is an important risk factor of delirium, whereas good postoperative analgesia reduces the incidence of delirium. For postoperative patients, sleep disturbances occurs frequently and increases the risk of delirium, whereas improving sleep quality reduces the incidence of delirium. Furthermore, the studies found that surgery related inflammatory response also plays an important role in the development of delirium. Dexmedetomidine is a highly selective alpha-2 (α2) adrenoreceptor agonist that provides anxiolysis, sedation, hypnosis and analgesia. It exerts the sedative and hypnotic effects by activating the endogenous sleep pathways, and produces a condition similar to phase 2 non-rapid eye movement sleep. For patients undergoing mechanical ventilation in the ICU, dexmedetomidine sedation helps to maintain a normal circadian rhythm of sleep and improves sleep architecture. Dexmedetomidine also provides analgesic effect by activating α2 adrenergic receptors in the dorsal horn of spinal cord. When used as a supplemental drug it decreases intraoperative and postoperative requirement of opioids. Moreover, animal studies showed that dexmedetomidine significantly inhibits the degree of inflammatory response induced by endotoxin or during spinal cord injury. In clinical studies, dexmedetomidine attenuates the degree of inflammatory response following Coronary Artery Bypass Grafting surgery. These effects of dexmedetomidine make it suitable for prevention of postoperative delirium in high-risk patients. Studies have shown that, for ICU patients requiring mechanical ventilation, sedation with dexmedetomidine reduces the incidence of delirium when compared with other sedatives; for postoperative patients, dexmedetomidine administered in combined with opioids improves analgesia and reduces opioid requirements. A recent study showed that, for elderly patients admitted to the ICU after surgery, low-dose dexmedetomidine infusion (at a rate of 0.1 ug/kg/h, for an average of 15 hours) improves analgesia for up to 24 hours, ameliorates subjective sleep quality for up to 3 days, and reduces the incidence of delirium during the first 7 postoperative days. The investigators hypothesized that the use of dexmedetomidine as a supplement to patient-controlled intravenous analgesia may also reduce the incidence of postoperative delirium.

Interventions

Patients in this group will receive patient-controlled intravenous analgesia for 3 days after surgery. The formula is a mixture of dexmedetomidine (1.25 ug/ml) and morphine (0.5 mg/ml), diluted with normal saline to 160 ml. 5-HT3 receptor antagonist is added when necessary. The analgesic pump is set to administer a background infusion at a rate of 1 ml/h, with a bolus dose of 2 ml each time and a lockout time from 6 to 8 minutes according to patients' condition.

Patients in this group will receive patient-controlled intravenous analgesia for 3 days after surgery. The formula is morphine (0.5 mg/ml) diluted with normal saline to 160 ml. 5-HT3 receptor antagonist is added when necessary. The analgesic pump is set to administer a background infusion at a rate of 1 ml/h, with a bolus dose of 2 ml each time and a lockout time from 6 to 8 minutes according to patients' condition.

Sponsors

Affiliated Hospital of Hebei University
CollaboratorOTHER
Qingdao Municipal Hospital
CollaboratorOTHER
The Second Affiliated Hospital of Air Force Medical University
CollaboratorUNKNOWN
Peking University International Hospital
CollaboratorOTHER
Guizhou Provincial People's Hospital
CollaboratorOTHER
The Third Xiangya Hospital of Central South University
CollaboratorOTHER
Shanxi Provincial Cancer Hospital
CollaboratorUNKNOWN
Tianjin Hospital of ITCWM-Nankai Hospital
CollaboratorUNKNOWN
Chongqing University Fuling Hospital
CollaboratorUNKNOWN
The Third Central Hospital of Tianjin
CollaboratorUNKNOWN
Xiyuan Hospital of China Academy of Chinese Medical Sciences
CollaboratorOTHER
Peking University First Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Age \>= 65 years, \< 90 years; * Scheduled to undergo curative resection for primary solid organ cancer under general anesthesia, with an expected duration of surgery \>=2 hours; * Planned to use patient-controlled intravenous analgesia after surgery; * Provide written informed consent.

Exclusion criteria

* Preoperative history of schizophrenia, epilepsy, parkinsonism or myasthenia gravis; * Preoperative radio- or chemotherapy; * Inability to communicate in the preoperative period because of coma, profound dementia or language barrier; * Preoperative obstructive sleep apnea (previously diagnosed as obstructive sleep apnea, or a STOP-Bang score \>= 3 and serum HCO3- \>= 28 mmol/L); * Brain trauma or neurosurgery; * Preoperative left ventricular ejection fraction \< 30%, sick sinus syndrome, severe sinus bradycardia (\< 50 beats per minute), or second-degree or above atrioventricular block without pacemaker; * Severe hepatic dysfunction (Child-Pugh class C) or severe renal dysfunction (requirement of renal replacement therapy before surgery); * ASA classification \>= IV.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of delirium within 5 days after surgeryDuring the first 5 days after surgeryIncidence of delirium within 5 days after surgery

Secondary

MeasureTime frameDescription
Length of stay in hospital after surgeryUp to 30 days after surgeryLength of stay in hospital after surgery
Incidence of non-delirium complications after surgeryUp to 30 days after surgeryIncidence of non-delirium complications after surgery
30-day all-cause mortality after surgeryAt the time of 30 days after surgery30-day all-cause mortality after surgery
Quality of life in survival patients on the 30th day after surgeryOn the 30th day after surgeryAssessed with World Health Organization Quality of Life-Bref (WHOQOL-BREF)
Cognitive function in survival patients on the 30th day after surgeryOn the 30th day after surgeryAssessed with Telephone Interview for Cognitive Status-Modified (TICS-M)
Daily prevalence of delirium during the first 5 postoperative daysDuring the first 5 postoperative daysDaily prevalence of delirium during the first 5 postoperative days

Other

MeasureTime frameDescription
Numeric Rating Scale (NRS) pain score during the first 5 days after surgeryDuring the first 5 days after surgeryNumeric Rating Scale (NRS) pain score during the first 5 days after surgery
Numeric Rating Scale (NRS) sleep quality score during the first 5 days after surgeryDuring the first 5 days after surgeryNumeric Rating Scale (NRS) sleep quality score during the first 5 days after surgery
Cumulative morphine consumption during the first 3 days after surgeryDuring the first 3 days after surgeryCumulative morphine consumption during the first 3 days after surgery
Richmond Agitation-Sedation Scale (RASS) score during the first 5 days after surgeryDuring the first 5 days after surgeryRichmond Agitation-Sedation Scale (RASS) score during the first 5 days after surgery

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026