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Antiplatelet therapy to prevent ischemic events in giant cell arteritis: protocol for a systematic review and meta-analysis.
Makhzoum, Jean-Paul; Baati, Youssef; Tanase, Octavian; Mendel, Arielle; Pagnoux, Christian; Ross, Carolyn.
Affiliation
  • Makhzoum JP; Vasculitis Clinic, Hopital Sacre-Coeur, University of Montreal, Canadian Vasculitis Research Network, 5400 Bd Gouin O, Montreal, QC, H4J1C5, Canada. jean-paul.makhzoum@umontreal.ca.
  • Baati Y; Hopital Sacre-Coeur, University of Montreal, 5400 Bd Gouin O, Montreal, QC, H4J1C5, Canada.
  • Tanase O; Hopital Sacre-Coeur, University of Montreal, 5400 Bd Gouin O, Montreal, QC, H4J1C5, Canada.
  • Mendel A; Vasculitis and Lupus Clinic, McGill University Health Center, McGill University, Canadian Vasculitis Research Network, 1001 Bd Decarie, Montréal, QC, H4A 3J1, Canada.
  • Pagnoux C; Vasculitis Clinic, Mount Sinai Hospital, University of Toronto, Canadian Vasculitis Research Network, 60 Murray St, Toronto, ON, M5T3L9, Canada.
  • Ross C; Vasculitis Clinic, Hopital Sacre-Coeur, University of Montreal, Canadian Vasculitis Research Network, 5400 Bd Gouin O, Montreal, QC, H4J1C5, Canada.
Syst Rev ; 13(1): 173, 2024 Jul 08.
Article in En | MEDLINE | ID: mdl-38978122
ABSTRACT

BACKGROUND:

Giant cell arteritis (GCA) is the most common systemic vasculitis in adults. Presenting features include new-onset headaches, constitutional symptoms, jaw claudication, polymyalgia rheumatica, and visual symptoms. Arterial inflammation with subsequent stenosis and occlusion may cause tissue ischemia, leading to blindness, strokes, and myocardial infarction. Oral antiplatelet therapy has been hypothesized to reduce GCA-related ischemic events. However, previous studies have demonstrated conflicting results regarding the efficacy of antiplatelet agents in GCA. The objective of this systematic review is to assess the safety and efficacy of antiplatelet therapy for the prevention of these events in adults with giant cell arteritis.

METHODS:

In this systematic review, we will include randomized controlled trials (RTCs), quasi-randomized trials, non-randomized intervention studies, cohort studies, and case-control studies on patients with new-onset or relapsing GCA. The intervention of interest will be pre-existing use or initiation of an oral antiplatelet medication (aspirin, clopidogrel, prasugrel, or ticagrelor) at GCA onset or relapse. The comparator of interest will be the absence of antiplatelet therapy. Endpoints will be evaluated after 6 and 12 months of follow-up. The primary outcome will be GCA-related ischemic events, including permanent blindness, stroke, myocardial infarction, and ischemic event-related deaths. Adverse events such as major bleeding and death caused by a bleeding event will be assessed.

DISCUSSION:

GCA-related ischemic events are catastrophic, sudden, often irreversible, and lead to significant morbidity. Antiplatelet agents are affordable, accessible, and could be effective for the prevention of these events. Nevertheless, the potential benefits of platelet aggregation inhibition must be weighed against their associated risk of bleeding. Assessing the efficacy and safety of antiplatelet therapy in GCA is therefore clinically important. SYSTEMATIC REVIEW REGISTRATION Our systematic review protocol was registered with the International Prospective Register of Systematic Reviews (PROSPERO, registration number CRD42023441574.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Giant Cell Arteritis / Platelet Aggregation Inhibitors / Systematic Reviews as Topic Limits: Humans Language: En Journal: Syst Rev Year: 2024 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Giant Cell Arteritis / Platelet Aggregation Inhibitors / Systematic Reviews as Topic Limits: Humans Language: En Journal: Syst Rev Year: 2024 Document type: Article Affiliation country: Canada