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Evaluation of Anesthetic Techniques in Outpatient Total Joint Replacement Surgery in an Integrated Health Care Delivery System

Evaluation of Anesthetic Techniques in Outpatient Total Joint Replacement Surgery in an Integrated Health Care Delivery System

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04203732
Enrollment
12466
Registered
2019-12-18
Start date
2020-01-01
Completion date
2020-12-31
Last updated
2021-04-09

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

Conditions

Anesthesia Morbidity, Osteoarthritis, Hip, Osteoarthritis, Knee

Keywords

Retrospective Cohort, Anesthetic Technique, Total Joint Arthroplasty

Brief summary

The study is a retrospective cohort study of adult patients undergoing outpatient primary unilateral total knee or total hip replacement surgeries from 2017 to 2019 assessing for difference in anesthetic techniques and outcomes.

Detailed description

The study is a retrospective cohort study of adult patients undergoing outpatient primary unilateral total knee or total hip replacement surgeries from 2017 to 2019. The purpose of the study is to evaluate the effects of anesthetic techniques for primary total joint replacement in Northern California Kaiser Permanente. The primary objective is to determine if there are clinically and statistically significant differences between the outcomes of general anesthesia and neuraxial anesthesia.

Interventions

The anesthetic type either general anesthesia or neuraxial anesthesia is the intervention type for patients undergoing primary total joint arthroplasty of the knee or hip.

Sponsors

Kaiser Permanente
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* ASA 1 - IV patients * Age \> 18 * Primary total hip/knee replacement

Exclusion criteria

* Total joint replacement for oncologic tumors * Emergent surgery * Age \< 17 * Pregnant Female * Neuraxial anesthesia conversion to general anesthesia * Revision total joint replacement * Bilateral total joint replacement

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Morbidity30-day postoperative30-day Postoperative Morbidity including surgical site infection (defined as infection involving the skin or subcutaneous tissue of the incision, deep incisional infection defined as infected tissue below the subcutaneous tissue including fascia and muscle), major coronary events (defined as nonfatal myocardial infarction, heart failure, ventricular tachycardia, cardiac arrest), pneumonia, urinary tract infection, venous thromboembolism, pulmonary embolism, cerebrovascular accident, renal injury/failure (Defined as increase in baseline creatinine 2 fold/3fold respectively).

Secondary

MeasureTime frameDescription
Postoperative Mortality30-day postoperative30-day postoperative mortality - all cause
Postoperative readmission30-day postoperative30-day postoperative readmission - all cause
Intraoperative blood loss and transfusion ratesDay of surgeryMeasurement of blood loss by mL recorded on record. Measurement of packed red blood cells transfused by unit pack.
Intraoperative opioid useDay of surgeryDefined by type of analgesic medication and total morphine equivalence
Postoperative opioid useDay of surgeryDefined by type of analgesic medication and total morphine equivalence
Postoperative Pain ScoresDay of surgeryNumerical Rating Scale of postsurgical pain measured until discharge from hospital. Numerical rating scale for pain is described as a scale from a minimum of 0, associated with no pain, to a maximum of 10, associated with the worst possible pain. A higher number is associated with a worse outcome.
Postoperative nausea and vomitingDay of surgeryRate of PONV after surgery
Length of postsurgical hospital stayDay of surgeryLength of time defined from end of intraoperative time to discharge from hospital time

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026