Burden of potentially avoidable anticoagulant-associated hemorrhagic and thromobembolic events in the elderly

被引:62
作者
van Walraven, Carl [1 ]
Oake, Natalie [1 ]
Wells, Philip S. [1 ]
Forster, Alan J. [1 ]
机构
[1] Ottawa Hosp, Clin Epidemiol Program, Ottawa Hlth Res Inst, Ottawa, ON K1Y 4E9, Canada
关键词
anticoagulation; biostatistics; bleeding; deep venous thrombosis; gastroenterology; pulmonary embolism;
D O I
10.1378/chest.06-2628
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: On average, patients receiving therapy with oral anticoagulants (OACs) in the community are in the therapeutic range only 55% of the time. Anticoagulation control strongly influences the risk of hemorrhagic and thromboembolic events in such patients. However, not all anticoatulation-associated events are attributable to poor anticoagulation control, nor do all hemorrhagic or thromboembolic events occur in anticoagulated patients. Objective: Measure the proportion of serious hemorrhagic and thromboembolic events that would be avoided if anticoagulation control was perfect. Methods: A retrospective cohort study of eastern Ontario using population-based administrative databases. Anticoagulation control was determined for each day of OAC exposure using linear interpolation. Incident hemorrhagic or thromboembolic hospitalizations for control and OAC patients were identified. Hemorrhages and thromboemboli in OAC patients were deemed to be avoidable if they occurred at international normalized ratios of > 3 and < 2, respectively. Results: The study included > 183,000 patient-years of observation with 6,400 patient-years of OAC exposure. Anticoagulation control could be determined for 51.5% of OAC exposure time. Control patients had hemorrhagic and thromboembolic event rates of 1.8% and 1.5% per year, respectively. A total of 10,020 people were exposed to OACs, and spent 14.2% and 26.7% of the time, respectively, with excessively high and low anticoagulation intensity. Excessively high anticoagulation intensity explained 25.6% (95% confidence interval [CI], 19.4 to 31.7) and 2.0% (95% CI, 1.5 to 2.5), respectively, of all serious hemorrhages in the anticoagulated and entire population. Excessively low anticoagulation intensity explained 11.1% (95% CI, 4.4 to 17.7) and 1.1% (95% CI, 0.7 to 1.6) of all thromboemboli, respectively. Conclusions: Our study showed that extreme anticoagulation. intensity significantly impacted the health of the population. Improving anticoagulation control mill have significant effects on the incidence of serious hemorrhagic and thromboembolic events in the both the anticoagulated and entire populations.
引用
收藏
页码:1508 / 1515
页数:8
相关论文
共 38 条
  • [1] Anavekar NS, 2004, NEW ENGL J MED, V351, P1285, DOI 10.1056/NEJMoa041365
  • [2] The pharmacology and management of the vitamin K antagonists
    Ansell, J
    Hirsh, J
    Poller, L
    Bussey, H
    Jacobson, A
    Hylek, E
    [J]. CHEST, 2004, 126 (03) : 204S - 233S
  • [3] Accuracy of coding for possible warfarin complications in hospital discharge abstracts
    Arnason, T.
    Wells, P. S.
    van Walraven, C.
    Forster, A. J.
    [J]. THROMBOSIS RESEARCH, 2006, 118 (02) : 253 - 262
  • [4] Optimal intensity of oral anticoagulant therapy after myocardial infarction
    Azar, AJ
    Cannegieter, SC
    Deckers, JW
    Briet, E
    vanBergen, PFMM
    Jonker, JJC
    Rosendaal, FR
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 27 (06) : 1349 - 1355
  • [5] OPTIMAL ORAL ANTICOAGULANT-THERAPY IN PATIENTS WITH MECHANICAL HEART-VALVES
    CANNEGIETER, SC
    ROSENDAAL, FR
    WINTZEN, AR
    VANDERMEER, FJM
    VANDENBROUCKE, JP
    BRIET, E
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (01) : 11 - 17
  • [6] Casais P, 2000, AM J HEMATOL, V63, P192, DOI 10.1002/(SICI)1096-8652(200004)63:4<192::AID-AJH5>3.0.CO
  • [7] 2-K
  • [8] Comparison of warfarin and aspirin for symptomatic intracranial arterial stenosis
    Chimowitz, MI
    Lynn, MJ
    Howlett-Smith, H
    Stern, BJ
    Hertzberg, VS
    Frankel, MR
    Levine, SR
    Chaturvedi, S
    Kasner, SE
    Benesch, CG
    Sila, CA
    Jovin, TG
    Romano, JG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (13) : 1305 - 1316
  • [9] Fleiss JL, 2003, STAT METHODS RATES P, P340
  • [10] Franke CL, 1997, ANN NEUROL, V42, P857