ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1306

Risk Factors for Pain After Total Joint Replacement in Osteoarthritis: Different Pain Measures, Distinct Predictors?

Joana Barroso1, Kenta Wakaizumi 2, Thomas Schnitzer 1, Vasco Galhardo 3 and Apkar Apkarian 1, 1Northwestern University Feinberg School of Medicine, Chicago, IL, 2Northwestern University, Chicago, IL, 3Porto University, Porto, Portugal

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: pain and Chronic pain, Total joint replacement

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Monday, November 11, 2019

Title: Osteoarthritis – Clinical Poster I

Session Type: Poster Session (Monday)

Session Time: 9:00AM-11:00AM

Background/Purpose: Prognostic factors for pain persistence after total joint replacement (TJR) in osteoarthritis (OA) have been repeatedly proposed. These factors are commonly considered to act independently, unrelated to each other, even with regard to the various pain intensity measures used.  Here, we purpose that pain outcomes post-TJR relate to different aspects of the pain experience and explore how predictive modeling may lead to different results regarding pain persistence risk factors.

Methods: We conducted a prospective longitudinal study of knee and hip OA patients, assessing multiple measures by questionnaires of quality, mood, affect, health and quality of life, together with radiographic evaluation and performance-based tasks before and 6 months after TJR. These factors were firstly used in a principal component analysis (PCA), thus applying a data reduction technique, and then used to build multivariate regression models (stepwise hierarchical regression: α-to-enter 0.05 and α-to-remove 0.10) for four distinct pain intensity outcomes (NRS, BPI Pain, KOOS pain and SF-36 pain). All pain outcomes were modeled at baseline and post-surgery, both as absolute value and also as score change (% residual pain) for the latest.

Results: A total of 84 knee OA and 24 hip OA patients completed the study. For the four pain scales, pairwise comparisons revealed that pain intensity estimates were significantly lower only  for BPI pain severity at baseline (mean differences [SD]: NRS: -1.72 [-2.44, -0.99], KOOS/HOOS: -1.436 [-2.158, -0.71], SF36: -2.06 [-2.78, -1.4], p< 0.001) and higher 6 months post-surgery with SF-36 pain (NRS: 1.038 [0.23,1,81], BPI: 1.354 [0.57,2.14], p< 0.003). The PCA for questionnaire variables identified 5 distinct components, accounting for 70% of the variability of the data. These were labeled accordingly to its factor loadings as pain quality, affect, catastrophizing, health and physical performance (Figure 1). Hierarchical models showed pain quality as the common dominant factor accounting for higher pain intensity throughout all scales pre-surgery, with additional influences for each outcome (Table 1). Different models were elicited for absolute versus relative pain intensity (change in pain vs pre-TJR) after surgery, with the variance explained by each model being overall lower for change in pain. Again, explanatory variables were also distinct considering the four different pain outcome measures (Table 2).

Conclusion: These results demonstrate that different pain scales relate to distinct facts of the pain experience, resulting in defining distinct prognostic factors for persistence of pain post-TJR.  These models allow for distinction between post-TJR absolute pain levels vs degree of improvement from the pre-op state. Structured and comprehensive methodological approaches regarding pain metrics are necessary in order to better understand and derive clinical prognostic factors in post-TJR pain.


Figure 1

Figure 1. Principal component analysis identified five factors characterizing baseline KOA.
a. Correlation matrix ordered based on principal component analysis results -Pearson’s r represented by color bar-. The five identified components were labeled according to membership properties. b. Factor loadings are shown for the five components. 6MWT, six minute walking test; DN4, The Neuropathic Pain 4 questions; HADS-A-, The Hospital Anxiety and Depression Scale, Anxiety; HADS-D-, The Hospital Anxiety and Depression Scale, Depression; KOOS, Knee Injury and Osteoarthritis Outcome Score, -ADL – Function in daily living-, -S -Knee Symptoms-, -SR – Function in sport and recreation-, -QOL – knee related quality of life-; MPQ, McGill Pain Questionnaire, -A – Affective score- -S – Sensory score-; PCS, Pain Catastrophizing Scale, -R – Rumination subscale-, -M – Magnification subscale-, -H – Helplessness subscale-; SF36, Short-form -36- Health Survey, -PF – Physical Functioning-, -PH – physical role functioning-, -EP – emotional role functioning-, -EF – energy/fatigue-, -E – emotional well-being-, -SF – social functioning-, -GH – general health-; TUG, Timed -up and go test.


Table 1

Table 1. Multiple regression models for KOA pain intensity at baseline for four different pain intensity measures.
Displayed statistics are from the final step of each model. b, unstandardized regression coefficient; SE, standard error; β, standardized regression coefficient; F, obtained F-value; t, obtained t-value; R2, proportion of variance explained. * p ≤ 0.05, **p ≤ 0.01. Displayed statistics are from the final step for each dependent variable. BPI Severity, Brief Pain Inventory Pain: severity subscale; HOOS Pain, Hip Injury and Osteoarthritis Outcome Score: pain subscale; NRS, Numeric Rating Scale; SF36 Pain, Short-form -36- Health Survey: pain subscale.


Table 2

Table 2. Multiple regression models for post-surgical KOA pain intensity, and for percentage residual pain at 6-months post-surgery, for four different pain intensity measures.
b, unstandardized regression coefficient; SE, standard error; β, standardized regression coefficient; F, obtain F-value; t, obtained t-value; R2, proportion variance explained. Gender: male coded as 0, female coded as 1. * p ≤ 0.05, **p ≤ 0.01. Displayed statistics are from the final step for each dependent variable.
BPI Severity, Brief Pain Inventory Pain: severity subscale; HOOS Pain, Hip Injury and Osteoarthritis Outcome Score: pain subscale; NRS, Numeric Rating Scale; SF36 Pain, Short-form -36- Health Survey: pain subscale.


Disclosure: J. Barroso, None; K. Wakaizumi, None; T. Schnitzer, AbbVie, 2, Aptinyx, Astellas, Calibr, Eli Lilly and Company, 2, 5, Flexion, 2, Galapagos, 2, GlaxoSmithKline, Grunenthal, 2, Kolon TissueGene, 2, Pfizer, 2, 5, Regeneron, 2, Sanofi, Vertex; V. Galhardo, None; A. Apkarian, None.

To cite this abstract in AMA style:

Barroso J, Wakaizumi K, Schnitzer T, Galhardo V, Apkarian A. Risk Factors for Pain After Total Joint Replacement in Osteoarthritis: Different Pain Measures, Distinct Predictors? [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/risk-factors-for-pain-after-total-joint-replacement-in-osteoarthritis-different-pain-measures-distinct-predictors/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2019 ACR/ARP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/risk-factors-for-pain-after-total-joint-replacement-in-osteoarthritis-different-pain-measures-distinct-predictors/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology