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Sleep and Cognition After Ambulatory Hip and Knee Arthroplasty

Sleep and Cognition After Ambulatory Hip and Knee Arthroplasty

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04227873
Enrollment
16
Registered
2020-01-14
Start date
2020-03-31
Completion date
2020-07-31
Last updated
2020-02-18

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

Conditions

Arthroplasty Complications, Delirium, Sleep Disturbance

Brief summary

Sleep and rest are key elements in postoperative rehabilitation and recovery. There are complex relations between major surgery, sleep disturbance and complications. Major surgery leeds to severe postoperative sleep disturbances, initially reducing REM sleep time and disturbing the remaining sleep stages. Major surgery is again a risk factor for postoperative delirium and other cognitive impairment. The underlying mechanisms includes pain, opioid medication, sleep disturbances and neuroinflammation, along with external factors as noise during hospitalisation. The physiologic stress from sleep disturbances and sleep deprivation is associated with blood-brain barrier impairment, inflammation, decreased restitution, altered nociceptive function. Likewise, undiagnosed and untreated sleep apnea is a risk for postoperative complications and is itself affected by anesthesia and some analgesics (i.a. opioids). Fast-track surgery development has led to restitution period shortening, optimized pain management reducing opioid use, postoperative inflammatory stress response reduction and less delirium. Evolution of hip and knee arthroplasty(THA/TKA), organisation, optimized pain management and pharmacologic modification of inflammatory response by high dose steroid has permitted to perform these surgeries in an outpatient setting. Previous studies of fast-track THA/TKA using multimodal opioid-sparring analgesia, however neither using high dose steroids nor in an out patient setting, have demonstrated REM sleep period reduction from a normal range of 18% preoperatively to 1% postoperatively. However, changes in sleep architecture after THA/TKA in at setting attempting to minimise abnormal sleep by means of ambulatory surgery added to perioperative reduction of inflammatory response to surgery, pain and opioid use by high dose steroid, haven't been studied. The purpose of this study is to investigate how much an optimized ambulatory THA/TKA , reducing pain and inflammatory response to surgery and opioid use by high doses steroid can conserve the preoperative sleep architecture.

Interventions

None listed

Sponsors

Kehlet, Henrik, M.D., Ph.D.
CollaboratorINDIV
Nicolai Bang Foss
CollaboratorUNKNOWN
Poul Jenum
CollaboratorUNKNOWN
Anders Troelsen
CollaboratorUNKNOWN
Kirill Gromov
CollaboratorUNKNOWN
Mette Grentoft
CollaboratorUNKNOWN
Henning Piilgaard Hansen
CollaboratorUNKNOWN
Hvidovre University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* ASA classification I or II * Scheduled hospital discharge same day after surgery * Adult person following the patient 24 hours at the patients habitation * Informed consent and signature. * Patient speaks and understands Danish

Exclusion criteria

* Hospital discharge later than same day after surgery * No consent form patient * Alcohol or drug abuse * Anxiolytic og antipsychotic treatment * Preoperative opioid treatment * Soporific treatment

Design outcomes

Primary

MeasureTime frameDescription
Changes in postoperative REM sleep time compared to preoperativeOne night 2 to 4 night preoperatively, and the first and second postoperative night.Polysomnography

Secondary

MeasureTime frameDescription
Presence and severity of postoperative delirium compared to preoperativeOne night 2 to 4 night preoperatively, and after the second postoperative night.Confusion Assessement Method-Severity (CAM-S). High scores, better outcome.
Presence and severity of postoperative cognitive impairment compared to preoperativeOne night 2 to 4 night preoperatively, and after the second postoperative night.Mini Mental State Examination (MMSE), High scores, better outcome.
Changes Remaining sleep stages and sleep variables (i.a. apnea)One night 2 to 4 night preoperatively, and the first and second postoperative night.Polysomnography

Other

MeasureTime frameDescription
Subjective measurement of sleep qualityOne night 2 to 4 night preoperatively, and after the second postoperative night.Pittsburgh Sleep Quality Index. Lower score, better outcome.
Changes in preoperative inflammatory marker level (CRP) compared to postoperative.One night 2 to 4 night preoperatively, and after the second postoperative night.Blod samples
Subjective measurements of pain at rest and after mobilisation.Immediately after surgery, and after the first and second postoperative night.questionnaire. Visual Analogue Scale(VAS). Lower score, better outcome.
Registration of opioid use.Immediately after surgery, and after the first and second postoperative night.questionnaire. Less opioid use, better outcome.
Subjective measurement of tirednessOne night 2 to 4 night preoperatively, and after the second postoperative night.questionnaire. Better sleep, better outcome.

Countries

Denmark

Contacts

Primary ContactAlexandre Garioud, MD
alexandre.garioud@gmail.com+4542705009
Backup ContactHenrik Kehlet, Dr.med,Phd
henrik.kehlet@regionh.dk+ 45 3545 4774

Outcome results

None listed

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