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Impact of Peripheral Nerve Blockade on Outcomes After Total Knee Replacement

Impact of Peripheral Nerve Blockade on Outcomes After Total Knee Replacement

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02742961
Enrollment
178214
Registered
2016-04-19
Start date
2002-04-30
Completion date
2014-03-31
Last updated
2016-04-19

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

Conditions

Osteoarthritis, Pain

Keywords

orthopedics, anesthesiology, nerve block, length of stay, Patient readmission

Brief summary

Pain is common after knee replacement surgery and can impact a variety of patient outcomes. Peripheral nerve blocks provide improved pain control and may improve function. However, their impact on other outcomes is poorly described. Therefore, this comparative effectiveness study will estimate the independent association between nerve blocks and health outcomes after knee replacement surgery.

Detailed description

This retrospective, population-based cohort study will evaluate the comparative effectiveness of peripheral nerve blocks on patient and health system outcomes after elective total knee replacement surgery. The investigators will develop a non-parsimonious propensity score to control for potential indication bias and confounding in this observational study. Using the propensity score the investigators will match patients who receive a peripheral nerve block to a patient who did not to estimate the independent association of peripheral nerve blocks with our study outcomes.

Interventions

OTHERPeripheral nerve block

A physician billing code for deposition of a local anesthetic solution around an anatomically defined nerve or nerve plexus

Sponsors

Ottawa Hospital Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* first primary total knee replacement during the study period

Exclusion criteria

* Revision arthroplasty

Design outcomes

Primary

MeasureTime frameDescription
Hospital length of stayDay of surgery to day of discharge, or up to 365 days, whichever comes firstDetermined from the Canadian Institute for Health Information Discharge Abstract Database record for the index hospitalization

Secondary

MeasureTime frameDescription
Hospital readmissionThe outcome ascertainment window starts on the day of discharge and extends up to 30 days after surgery. Any readmission in this time period will be considered an event.Determined from the Canadian Institute for Health Information Discharge Abstract Database through identification of a new record after discharge from the index hospitalization
In-hospital fallhospital admissionDetermined using validated International Classification of Diseases Tenth edition codes for falls from the index hospitalization Discharge Abstract Database record
Emergency department visitThe outcome ascertainment window starts on the day of discharge and extends up to 30 days after surgery. Any emergency department visit in this time period will be considered an event.Defined as the creation of a record in the National Ambulatory Care Reporting System for an emergency department visit that occurs after discharge and before 30 days after discharge

Other

MeasureTime frameDescription
All cause mortalityDay of surgery to 30 days after surgeryIdentified from the Registered Person's Database that records the date of death for all residents of Ontario

Countries

Canada

Outcome results

None listed

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