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Abstract Number: 0768

Addressing Gaps in Polymyalgia Rheumatica: A Systematic Literature Review

Shelley Fritz1, Angela Degrassi2, Kelly Gavigan2, Ruohan Hong3, Santiago Munoz Perez2, Esteban Rivera4, Erik Stone5, Laura Stradford6, Ambika Vartak2, Anne Sydor2 and Shilpa Venkatachalam3, 1Global Healthy Living Foundation, Kalaheo, HI, 2Global Healthy Living Foundation, Upper Nyack, NY, 3Global Healthy Living Foundation, New York, NY, 4Global Healthy Living Foundation, Long Island City, NY, 5Global Healthy Living Foundation, Upper Nyack, 6Global Healthy Living Foundation, Nyack, NY

Meeting: ACR Convergence 2024

Keywords: corticosteroids, Diagnostic criteria, Polymyalgia Rheumatica (PMR), quality of life, Vasculitis

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Session Information

Date: Saturday, November 16, 2024

Title: Vasculitis – Non-ANCA-Associated & Related Disorders Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: This systematic literature review on polymyalgia rheumatica (PMR) and PMR with giant cell arteritis (GCA) evaluates existing literature on disease burden, management, and treatment efficacy and safety, identifying knowledge gaps affecting patient care and outcomes. Understanding treatments, diagnostic markers, and quality of life (QOL) can improve the patient journey in PMR and GCA.

Methods: Using PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines, a systematic search (PubMed, Embase) from November 16, 2023, to January 24, 2024, included key terms like “polymyalgia rheumatica” and “giant cell arteritis” for English language articles published between 1966-2023. Filters applied were “Clinical Trial”, “Meta-Analysis”, “Randomized Controlled Trial”, and “Systematic Review”. The review focused on symptoms, diagnosis, treatment, prognosis, health disparities, and QOL. Abstracts were reviewed by two individuals, with a third adjudicating disagreements. Two reviewers read and summarized 114 full-text articles, assessing quality while noting methods and results. Articles behind paywalls were excluded. An analysis identified commonalities, discrepancies, and research gaps in PMR and PMR with GCA.

Results: The initial search yielded 371 abstracts; 224 were excluded, and 147 full-text articles were reviewed. Low-quality studies (n=33) were excluded if they did not report results specifically for PMR or GCA, lacked details on identifying or diagnosing patients, or had poorly defined control groups. (Figure 1) The remaining 114 articles were categorized by subtopic (Table 1). Sample sizes ranged from 9 to 1,363 patients, totaling 9,968 patients (PMR: 2,994; GCA: 6,831; PMR and GCA: 143). Less than half (n=52; 45.6%) focused exclusively on PMR. Only two articles (2%) studied patient-reported outcomes (PROs) and QOL. Treatment accounted for 67% of the 114 articles, with diagnosis and clinical presentation comprising 16% and 13%, respectively. Epidemiology, healthcare, prognosis, and public health data made up four percent of all articles. Within treatment, 48% contained data on PMR. Most (83%) treatment articles focused on symptom relief and response; 17% discussed adverse events. Effective treatments (70%) were more common than ineffective (25%) or inconclusive (5%). Main diagnostic biomarkers studied were Fluorodeoxyglucose Positron Emission Tomography (18F-FDG/PET) and Ultrasound/Color Duplex Sonography (Table 2).

Conclusion: The review underscores the need for research addressing gaps in QOL, PROs, diagnosis, and treatment options for PMR. Identifying health disparities is crucial for improving research utility in diverse populations. Low study populations in PMR highlight the need for more research in epidemiology and prognosis. Better diagnostic tools are critical for distinguishing PMR from GCA, enabling prompt and less invasive diagnoses. Monitoring disease activity and PROs, with biomarkers like 18F-FDG/PET, can guide treatment adjustments and improve symptoms. Additional research is vital to enhance patients’ quality of life and longevity. Understanding PMR causes and mechanisms can lead to more effective treatments.

Supporting image 1

Figure 1. PRISMA flow diagram

Supporting image 2

Table 1. Articles on PMR by topic with exclusion details

Supporting image 3

Table 2. Treatment and diagnosis markers


Disclosures: S. Fritz: None; A. Degrassi: None; K. Gavigan: Global Healthy Living Foundation, 3; R. Hong: None; S. Munoz Perez: None; E. Rivera: None; E. Stone: None; L. Stradford: AbbVie, 5, Amgen, 5, BMS, 5, Eli Lilly, 5, Global Healthy Living Foundation, 3, Pfizer, 5; A. Vartak: None; A. Sydor: None; S. Venkatachalam: None.

To cite this abstract in AMA style:

Fritz S, Degrassi A, Gavigan K, Hong R, Munoz Perez S, Rivera E, Stone E, Stradford L, Vartak A, Sydor A, Venkatachalam S. Addressing Gaps in Polymyalgia Rheumatica: A Systematic Literature Review [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/addressing-gaps-in-polymyalgia-rheumatica-a-systematic-literature-review/. Accessed .
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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.

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