Acute myocardial infarction in von Willebrand disease: characteristics and outcomes

被引:4
|
作者
Leiva, Orly [1 ]
Connors, Jean M. [2 ]
Connell, Nathan T. [2 ]
Berger, Jeffrey S. [1 ,3 ]
机构
[1] NYU, Dept Med, Leon H Charney Div Cardiol, Grossman Sch Med, New York, NY USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Div Hematol, Dept Med, Boston, MA USA
[3] NYU, Leon H Charney Div Cardiol, Grossman Sch Med, 550 First Ave, New York, NY 10016 USA
关键词
acute myocardial infarction; bleeding; readmission; von Willebrand disease; ACUTE CORONARY SYNDROMES; DIAGNOSIS;
D O I
10.1016/j.rpth.2023.102198
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Von Willebrand disease (VWD) is the most common inherited bleeding disorder. As treatments have improved prognosis of VWD, age-related diseases, including acute myocardial infarction (AMI), have become more prevalent. The treat-ment of AMI includes antithrombotic therapies, which increase the risk of bleeding. Current guidelines suggest weighing risks/benefits of antithrombotic therapy in pa-tients with VWD. However, data to inform these discussions are lacking.Objective: To characterize outcomes of patients with VWD after AMI.Methods: We conducted a retrospective cohort study utilizing the National Read-missions Database of patients with and without VWD admitted with AMI in 2017 and 2018. Primary outcomes were 90-day any-cause, bleeding-related, and arterial thrombosis-related readmissions. Case-control matching was performed for age, sex (male or female), ST-elevation myocardial infarction, percutaneous coronary interven-tion, diabetes, and chronic kidney disease. Time-to-event analysis was performed after matching using Cox proportional hazards regression.Results: A total of 136 patients with VWD were matched with 3400 controls without VWD. At 90 days, there were no differences in all-cause (10.7% vs 11.5%; P = 1.00), arterial thrombosis (1.9% vs 3.1%; P = .77), and bleeding (1.9% vs 0.4%; P = .083) readmission in patients with VWD. VWD was associated with increased risk of 90-day bleeding (hazard ratio [HR], 4.75; 95% CI, 1.05-21.66) but not all-cause (HR, 0.91; 95% CI, 0.50-1.67) or arterial thrombosis (HR, 0.54; 95% CI, 0.39-2.19) readmission.Conclusion: Among patients admitted with AMI, VWD was associated with higher risk of 90-day readmission for bleeding but not any-cause and arterial thrombosis-related readmissions. Further studies are needed to balance bleeding and thrombotic risks post-AMI in patients with VWD.
引用
收藏
页数:5
相关论文
共 50 条
  • [41] Biological therapies for von Willebrand disease
    Favaloro, Emmanuel J.
    Franchini, Massimo
    Lippi, Giuseppe
    EXPERT OPINION ON BIOLOGICAL THERAPY, 2012, 12 (05) : 551 - 564
  • [42] Rethinking the diagnosis of von Willebrand disease
    Favaloro, Emmanuel J.
    THROMBOSIS RESEARCH, 2011, 127 : S17 - S21
  • [43] Predictions and outcomes of atrial fibrillation in the patients with acute myocardial infarction
    Vukmirovic, Mihailo
    Boskovic, Aneta
    Vukmirovic, Irena Tomasevic
    Vujadinovic, Radoje
    Fatic, Nikola
    Bukumiric, Zoran
    Vukmirovic, Filip
    OPEN MEDICINE, 2017, 12 (01): : 115 - 124
  • [44] Advances in diagnosis of von Willebrand disease
    Castaman, Giancarlo
    Linari, Silvia
    EXPERT OPINION ON ORPHAN DRUGS, 2019, 7 (04): : 147 - 155
  • [45] Predictors of von Willebrand disease in children
    Sidonio, Robert F., Jr.
    Gunawardena, Sriya
    Shaw, Peter H.
    Ragni, Margaret
    PEDIATRIC BLOOD & CANCER, 2012, 58 (05) : 736 - 740
  • [46] State of the art: von Willebrand disease
    James, A. H.
    Eikenboom, J.
    Federici, A. B.
    HAEMOPHILIA, 2016, 22 : 54 - 59
  • [47] VON-WILLEBRAND DISEASE IN CHILDHOOD
    SCHNEPPENHEIM, R
    THOMAS, KB
    SUTOR, AH
    SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1995, 21 (03) : 261 - 275
  • [48] Molecular biology of von Willebrand disease
    Melo-Nava, Brenda
    Penaloza, Rosenda
    REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, 2007, 59 (05): : 401 - 408
  • [49] Reduced von Willebrand factor survival in von Willebrand disease: pathophysiologic and clinical relevance
    Castaman, G.
    Tosetto, A.
    Rodeghiero, F.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 : 71 - 74
  • [50] Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate®, a new generation von Willebrand factor/factor VIII concentrate
    Berntorp, E.
    Windyga, J.
    HAEMOPHILIA, 2009, 15 (01) : 122 - 130