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Analysis of Platelet Function Testing in Children Receiving Aspirin for Antiplatelet Effects.
Newland, David M; Palmer, Michelle M; Knorr, Lisa R; Pak, Jennifer L; Albers, Erin L; Friedland-Little, Joshua M; Hong, Borah J; Law, Yuk M; Spencer, Kathryn L; Kemna, Mariska S.
Affiliation
  • Newland DM; Department of Pharmacy, Seattle Children's Hospital, 4800 Sandpoint Way NE, Mailstop MB.5.420, Seattle, WA, 98105, USA. David.Newland@seattlechildrens.org.
  • Palmer MM; School of Pharmacy, University of Washington, Seattle, WA, USA. David.Newland@seattlechildrens.org.
  • Knorr LR; Department of Pharmacy, Seattle Children's Hospital, 4800 Sandpoint Way NE, Mailstop MB.5.420, Seattle, WA, 98105, USA.
  • Pak JL; School of Pharmacy, University of Washington, Seattle, WA, USA.
  • Albers EL; Department of Pharmacy, Seattle Children's Hospital, 4800 Sandpoint Way NE, Mailstop MB.5.420, Seattle, WA, 98105, USA.
  • Friedland-Little JM; School of Pharmacy, University of Washington, Seattle, WA, USA.
  • Hong BJ; Department of Pharmacy, Seattle Children's Hospital, 4800 Sandpoint Way NE, Mailstop MB.5.420, Seattle, WA, 98105, USA.
  • Law YM; School of Pharmacy, University of Washington, Seattle, WA, USA.
  • Spencer KL; Pediatric Cardiology, Seattle Children's Hospital, Seattle, WA, USA.
  • Kemna MS; School of Medicine, University of Washington, Seattle, WA, USA.
Pediatr Cardiol ; 45(3): 614-622, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38153548
ABSTRACT
Aspirin (ASA) remains the most common antiplatelet agent used in children. VerifyNow Aspirin Test® (VN) assesses platelet response to ASA, with therapeutic effect defined by the manufacturer as ≤ 549 aspirin reaction units (ARU). Single-center, observational, analysis of 195 children (< 18 years-old) who underwent first VN between 2015 and 2020. Primary outcome was proportion of patients with ASA biochemical resistance (> 549 ARU). Secondary outcomes included incidence of new clinical thrombotic and bleeding events during ≤ 6 months from VN in those who received ASA monotherapy (n = 113). Median age was 1.8 years. Common indications for ASA included cardiac anomalies or dysfunction (74.8%) and ischemic stroke (22.6%). Median ASA dose before VN was 4.6 mg/kg/day. Mean VN was 471 ARU. ASA biochemical resistance was detected in 14.4% (n = 28). Of 113 patients receiving ASA monotherapy, 14 (12.4%) had a thrombotic event and 2 (1.8%) had a bleeding event. Mean VN was significantly higher at initial testing in patients experiencing thrombotic event compared to those without thrombosis (516 vs 465 ARU, [95% CI 9.8, 92.2], p = 0.02). Multivariable analysis identified initial VN ASA result ≥ 500 ARU at initial testing as the only significant independent risk factor for thrombosis (p < 0.01). VN testing identifies ASA biochemical resistance in 14.4% of children. VN ASA ≥ 500 ARU rather than ≥ 550 ARU at initial testing was independently associated with increased odds of thrombosis. Designated cut-off of 550 ARU for detecting platelet dysfunction by ASA may need reconsideration in children.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Aspirin Limits: Adolescent / Child / Humans / Infant Language: En Journal: Pediatr Cardiol Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Aspirin Limits: Adolescent / Child / Humans / Infant Language: En Journal: Pediatr Cardiol Year: 2024 Type: Article Affiliation country: United States