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Dartmouth-Hitchcock GreenCare Registry for Total Knee Replacement

The Dartmouth GreenCare Program: Implementation of Shared Decision Making and Patient-reported Outcomes in a Standardized Care Path for Knee Replacement

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02912806
Acronym
GreenCare
Enrollment
545
Registered
2016-09-23
Start date
2013-01-31
Completion date
2016-04-30
Last updated
2016-09-23

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

Conditions

Arthroplasty, Replacement, Knee

Keywords

Knee Arthroplasty, Total knee replacement, Knee osteoarthritis, Patient-Outcomes Measurement Program, Surgical Registries, Shared Decision Making, Patient Reported Outcomes, Patient Experience, Cohort Studies

Brief summary

Evolving reimbursement policies are driving health systems to improve quality and efficiency. Transitioning to an electronic health record (EHR) provided Dartmouth-Hitchcock Medical Center (DHMC) an opportunity to redesign staff roles and care path for Total Knee Replacement (TKR). The organization implemented a coordinated team-based care delivery model that integrated real-time measurement of: (1) compliance with trusted guidelines, (2) process of Shared Decision-Making (SdM), and (3) use of Patient-Reported Outcomes (PROs). The investigators present the implementation protocol and data.

Detailed description

Patient-reported outcome measures were completed 1 month preceding TKR and also at 1 and 12 months following surgery. The primary outcome was change in physical function from baseline to 1-year following surgery in the Physical Component Summary (PCS) of the Veterans-Rand (VR-12) Survey. Preoperative measures were: (1) general demographics (patient age, sex, height, weight, body mass index (BMI); (2) treatments tried before surgery; (3) health habits (tobacco use, alcohol use); (4) pre-existing medical conditions (Charlson score); (5) physical exam findings (knee range of motion, knee laxity); (7) lab tests (hemoglobin); and (7) radiographic measures (severity of osteoarthritis on standing x-rays). Secondary outcomes included Physical Score (PS) of the Patient Reported Outcome Measurement Information System Global Survey (PROMIS-10), knee function (Knee Osteoarthritis Outcome Score, KOOS), safety (reoperations, readmissions, emergency visits, and infection) and measures of patient experience (Clinician Group and Hospital Consumer Assessment of Healthcare Providers and Systems).

Interventions

PROCEDURETotal Knee Replacement

Primary total knee arthroplasty for knee osteoarthritis

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Scheduled TKR * Osteoarthritis of the knee

Exclusion criteria

* previous TKR on the affected knee * diagnosis other than osteoarthritis * age less than 18 years * declined consent

Design outcomes

Primary

MeasureTime frameDescription
Health Gain as measured by the change in Physical Component Summary (PCS) Score1-year following surgeryHealth Gain from baseline to 12 months (from 300 to 400 days following the date) following surgery, as measured by the change in Physical Score based on standardized US adult population benchmarks for the VR12 survey

Secondary

MeasureTime frameDescription
Discharge to homeAcute hospitalizationDisposition at time of discharge from acute hospitalization
Mortality1 year
Range of motion90 daysKnee range of motion measured by a clinician between 60 and 120 days following surgery
Health Gain as measured by the change in Global Physical Health (GPH)1-yearHealth Gain from baseline to 12 months following surgery, as measured by the change in Physical Score based on standardized US adult population benchmarks for the PRIOMIS10 survey
Health Gain as measured by the change in Percentile Rank, TKR age and gender matched1 yearHealth Gain from baseline to 12 months following surgery, as measured by the change in Physical Score Percentile Rank based on age and gender-matched beta distributions for the Dartmouth TKR population, for the PRIOMIS10 or VR12 survey
Emotional Health1 yearMental Component Summary (MCS) Score change from baseline to 12 months following surgery, as measured by the change in Mental Score based on standardized US adult population benchmarks for the PRIOMIS10 or VR12 survey
Knee Osteoarthritis Outcome Score (KOOS)1 yearChange in KOOS score from baseline to 12 months following surgery
Length of hospital stayAcute hospitalizationNumber of days between date of admission and date of discharge
Readmission3 monthsFrom 0 to 90 days following the date of surgery
ER visits after surgery3 monthsFrom 0 to 90 days following the date of surgery
Infection3 monthsFrom 0 to 90 days following the date of surgery
Patient Satisfaction with Hospital1 monthHCAHPS survey in 10% random subsample completed between 20 to 40 days following the date of surgery
Patient Satisfaction with Surgeon10 monthsClinician Group CAHPS survey in 10% random subsample completed between 300 to 400 days following the date of surgery
Cost of care3 monthsEpisode-based costs for 0 to 90 days following the date of surgery, and also per visit outpatient costs
Reoperation3 monthsFrom 0 to 90 days following the date of surgery

Outcome results

None listed

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