TY - JOUR
T1 - Low-Molecular-Weight Heparin vs Warfarin for Thromboprophylaxis in Children With Coronary Artery Aneurysms After Kawasaki Disease
T2 - A Pragmatic Registry Trial
AU - International Kawasaki Disease Registry
AU - Manlhiot, Cedric
AU - Newburger, Jane W.
AU - Low, Tisiana
AU - Dahdah, Nagib
AU - Mackie, Andrew S.
AU - Raghuveer, Geetha
AU - Giglia, Therese M.
AU - Dallaire, Frederic
AU - Mathew, Mathew
AU - Runeckles, Kyle
AU - Pahl, Elfriede
AU - Harahsheh, Ashraf S.
AU - Norozi, Kambiz
AU - de Ferranti, Sarah D.
AU - Friedman, Kevin
AU - Yetman, Anji T.
AU - Kutty, Shelby
AU - Mondal, Tapas
AU - McCrindle, Brian W.
AU - Altman, Carolyn A.
AU - Anderson, Brett R.
AU - Braunlin, Elizabeth
AU - Burns, Jane C.
AU - Carr, Michael R.
AU - Choueiter, Nadine F.
AU - Colyer, Jessica H.
AU - Crean, Andrew
AU - Dempsey, Adam
AU - Desjardins, Laurent
AU - Dillenburg, Rejane
AU - Dionne, Audrey
AU - Ferris, Anna
AU - Gewitz, Michael
AU - Grcic, Michelle M.
AU - Greenway, Steven C.
AU - Hamel-Perrault, Elodie
AU - Harris, Kevin C.
AU - Hayden-Rush, Christina
AU - Hill, Kevin D.
AU - Jain, Supriya
AU - Jone, Pei Ni
AU - Kimball, Thomas R.
AU - Lang, Sean M.
AU - Li, Jennifer S.
AU - Lin, Ming Tai
AU - Mahle, William T.
AU - McHugh, Kimberly E.
AU - Portman, Michael A.
AU - Renaud, Claudia
AU - Sexson Tejitel, S. Kristen
N1 - Publisher Copyright:
© 2020 Canadian Cardiovascular Society
PY - 2020/10
Y1 - 2020/10
N2 - Background: The substantial risk of thrombosis in large coronary artery aneurysms (CAAs) (maximum z-score ≥ 10) after Kawasaki disease (KD) mandates effective thromboprophylaxis. We sought to determine the effectiveness of anticoagulation (low-molecular-weight heparin [LMWH] or warfarin) for thromboprophylaxis in large CAAs. Methods: Data from 383 patients enrolled in the International KD Registry (IKDR) were used. Time-to-event analysis was used to account for differences in treatment duration and follow-up. Results: From diagnosis onward (96% received acetylsalicylic acid concomitantly), 114 patients received LMWH (median duration 6.2 months, interquartile range [IQR] 2.5-12.7), 80 warfarin (median duration 2.2 years, IQR 0.9-7.1), and 189 no anticoagulation. Cumulative incidence of coronary artery thrombosis with LMWH was 5.7 ± 3.0%, with warfarin 6.7 ± 3.7%, and with no anticoagulation 20.6 ± 3.0% (P < 0.001) at 2.5 years after the start of thromboprophylaxis (LMWH vs warfarin HR 1.5, 95% confidence interval [CI] 0.4-5.1; P = 0.56). A total of 51/63 patients with coronary artery thrombosis received secondary thromboprophylaxis (ie, thromboprophylaxis after a previous thrombus): 27 LMWH, 24 warfarin. There were no differences in incidence of further coronary artery thrombosis between strategies (HR 2.9, 95% CI 0.6-13.5; P = 0.19). Severe bleeding complications were generally rare (1.6 events per 100 patient-years) and were noted equally for patients on LMWH and warfarin (HR 2.3, 95% CI 0.6-8.9; P = 0.25). Conclusions: LMWH and warfarin appear to have equivalent effectiveness for preventing thrombosis in large CAAs after KD, although event rates for secondary thromboprophylaxis and safety outcomes were low. Based on our findings, all patients with CAA z-score ≥ 10 should receive anticoagulation, but the choice of agent might be informed by secondary risk factors and patient preferences.
AB - Background: The substantial risk of thrombosis in large coronary artery aneurysms (CAAs) (maximum z-score ≥ 10) after Kawasaki disease (KD) mandates effective thromboprophylaxis. We sought to determine the effectiveness of anticoagulation (low-molecular-weight heparin [LMWH] or warfarin) for thromboprophylaxis in large CAAs. Methods: Data from 383 patients enrolled in the International KD Registry (IKDR) were used. Time-to-event analysis was used to account for differences in treatment duration and follow-up. Results: From diagnosis onward (96% received acetylsalicylic acid concomitantly), 114 patients received LMWH (median duration 6.2 months, interquartile range [IQR] 2.5-12.7), 80 warfarin (median duration 2.2 years, IQR 0.9-7.1), and 189 no anticoagulation. Cumulative incidence of coronary artery thrombosis with LMWH was 5.7 ± 3.0%, with warfarin 6.7 ± 3.7%, and with no anticoagulation 20.6 ± 3.0% (P < 0.001) at 2.5 years after the start of thromboprophylaxis (LMWH vs warfarin HR 1.5, 95% confidence interval [CI] 0.4-5.1; P = 0.56). A total of 51/63 patients with coronary artery thrombosis received secondary thromboprophylaxis (ie, thromboprophylaxis after a previous thrombus): 27 LMWH, 24 warfarin. There were no differences in incidence of further coronary artery thrombosis between strategies (HR 2.9, 95% CI 0.6-13.5; P = 0.19). Severe bleeding complications were generally rare (1.6 events per 100 patient-years) and were noted equally for patients on LMWH and warfarin (HR 2.3, 95% CI 0.6-8.9; P = 0.25). Conclusions: LMWH and warfarin appear to have equivalent effectiveness for preventing thrombosis in large CAAs after KD, although event rates for secondary thromboprophylaxis and safety outcomes were low. Based on our findings, all patients with CAA z-score ≥ 10 should receive anticoagulation, but the choice of agent might be informed by secondary risk factors and patient preferences.
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U2 - 10.1016/j.cjca.2020.01.016
DO - 10.1016/j.cjca.2020.01.016
M3 - Article
C2 - 32621885
AN - SCOPUS:85087402319
SN - 0828-282X
VL - 36
SP - 1598
EP - 1607
JO - Canadian Journal of Cardiology
JF - Canadian Journal of Cardiology
IS - 10
ER -