Post Surgical Pain Clinical Trial
Official title:
Characterization of Postoperative Pain in Shoulder Arthroscopy and Knee Arthroscopy and Assessment of the Defense and Veterans Pain Rating Scale for Persistent Post-Surgical Pain
The purpose of this study is to describe the chronology of post operative pain in patients undergoing total knee arthroplasty and total hip arthroplasty. Further, within this population the predictive validity of the Defense and Veterans Pain Rating Scale will be assessed for persistent post surgical pain.
This is a prospective descriptive correlational design looking to characterize postoperative
pain variables across various procedures that historically have significant levels of
persistent post-surgical pain. Further, bivariate correlations at different time points will
be examined to see how DVPRS along with Pain Assessment Screening Tool and Outcomes Registry
(PASTOR) correlates with other measures.
Methodology/Technical Approach A total goal of 250 participants will be queried regarding
their postoperative pain experience following shoulder arthroscopy and knee arthroscopy.
Descriptive multidimensional tools (the DVPRS and the electronic Pain Assessment Screening
Tool and Outcomes Registry (PASTOR)) will be used preoperative either during their
preoperative surgical visit or the day of surgery and extending to 6 months postoperatively.
As these tools have been utilized in previous studies for the prediction of persistent post
surgical pain, the DVPRS will additionally be evaluated for its predictive validity as it is
a short, easy-to-administer, bedside tool.
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