Hip Replacement in a High Volume Community Hospital: Effect on Length of Stay and Hospital Cost

December 17, 2014 updated by: Anne Arundel Health System Research Institute

Introduction of the Direct Anterior Approach to Hip Replacement Into a High Volume Community Hospital: Effect on Length of Stay and Hospital Cost

The investigators propose to evaluate and compare the percentage of patients who are able to be discharged in less than 3 days after undergoing total hip arthroscopy through either a direct anterior or posterior approach, utilizing the identical post operative protocol. The investigators also propose to evaluate the costs associated with the two different approaches to hip replacement in the same group of patients. Post operative resource utilization, discharge disposition, and pain medicine requirement will also be evaluated.

Study Overview

Status

Withdrawn

Conditions

Detailed Description

The investigators hypothesize that a higher proportion of patients treated with the direct anterior approach for hip replacement will be able to leave the hospital in less than 3 days when compared with a less invasive posterior approach. Secondly, decreased length of stay associated with the procedure may reduce hospital costs.

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Maryland
      • Annapolis, Maryland, United States, 21401
        • Anne Arundel Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients who have undergone primary uncemented hip replacement at our institution (Anne Arundel Medical Center) through either a posterior approach or direct anterior approach on a fracture table utilizing the identical post operative protocol.

Description

Inclusion Criteria:

  1. Consecutive single surgeon series of patients who have undergone primary uncemented hip replacement at our institution through either a posterior approach or direct anterior approach on a fracture table. Posterior approach patient - most recent patient prior to March, 2010, compared with consecutive recent anterior approach patients with minimum of 6 month follow-up.
  2. Diagnosis of osteoarthritis, inflammatory arthritis, or avascular necrosis.
  3. No previous surgery on affected hip.
  4. Age 40-90 at time of surgery

Exclusion Criteria:

  1. Patient not permitted to bear full weight after the procedure, per post operative instructions
  2. Hip replacement performed for acute fracture.
  3. Previous hip surgery.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Direct Anterior Approach hip replacement
Single surgeon series of 105 consecutive patients who underwent hip replacement via the direct anterior approach on a fracture table
Posterior Approach Hip Replacement
105 consecutive patients previously operated on by a less invasive posterior approach at the same institution. These surgeries occurred prior to March, 2010.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Length of Hospital Stay
Time Frame: Retrospective review of hospital discharge records
The length of stay and proportion of patients who went home in less than 3 days will be determined for each group. To evaluate and compare the percentage of patients who are able to be discharged in less than 3 days after undergoing total hip arthroscopy through either a direct anterior or posterior approach, utilizing the identical post operative protocol.
Retrospective review of hospital discharge records
Hospital cost
Time Frame: Retrospective review of utilization records
Hospital cost analysis will be undertaken for each group.
Retrospective review of utilization records

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post Operative Pain Medication Utilization
Time Frame: After retrospective chart review is complete -- approximately 6 months
Analysis of post operative pain medicine requirement will be compared for the two groups.
After retrospective chart review is complete -- approximately 6 months
Utilization of inpatient physical therapy resources
Time Frame: Retrospective review -- of hospital discharge
Utilization of inpatient physical therapy resources and post hospital discharge disposition will be compared for the two groups.
Retrospective review -- of hospital discharge

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Paul King, M.D., Anne Arundel Medical Center / Anne Arundel Orthopedic Surgeons

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Primary Completion (Actual)

January 1, 2014

Study Registration Dates

First Submitted

May 10, 2013

First Submitted That Met QC Criteria

May 17, 2013

First Posted (Estimate)

May 20, 2013

Study Record Updates

Last Update Posted (Estimate)

December 18, 2014

Last Update Submitted That Met QC Criteria

December 17, 2014

Last Verified

December 1, 2014

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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