Reversal of oral anticoagulation in patients with acute intracerebral hemorrhage

被引:0
作者
Joji B. Kuramatsu
Jochen A. Sembill
Hagen B. Huttner
机构
[1] University Hospital Erlangen,Department of Neurology
来源
Critical Care | / 23卷
关键词
Intracerebral hemorrhage; Anticoagulation reversal; Tranexamic acid; Ciraparantag; Desmopressin;
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摘要
In light of an aging population with increased cardiovascular comorbidity, the use of oral anticoagulation (OAC) is steadily expanding. A variety of pharmacological alternatives to vitamin K antagonists (VKA) have emerged over recent years (direct oral anticoagulants, DOAC, i.e., dabigatran, rivaroxaban, apixaban, and edoxaban) which show a reduced risk for the occurrence of intracerebral hemorrhage (ICH). Yet, in the event of ICH under OAC (OAC-ICH), hematoma characteristics are similarly severe and clinical outcomes likewise substantially limited in both patients with VKA- and DOAC-ICH, which is why optimal acute hemostatic treatment in all OAC-ICH needs to be guaranteed. Currently, International Guidelines for the hemostatic management of patients with OAC-ICH are updated as several relevant large-sized observational studies and recent trials have established treatment approaches for both VKA- and DOAC-ICH. While the management of VKA-ICH is mainly based on the immediate reversal of elevated levels of international normalized ratio using prothrombin complex concentrates, hemostatic management of DOAC-associated ICH is challenging requiring specific antidotes, notably idarucizumab and andexanet alfa. This review will provide an overview of the latest studies and trials on hemostatic reversal agents and timing and summarizes the effects on hemorrhage progression and clinical outcomes in patients with OAC-ICH.
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  • [1] Krishnamurthi RV(2013)Global and regional burden of first-ever ischaemic and haemorrhagic stroke during 1990-2010: findings from the Global Burden of Disease Study 2010 Lancet Glob Health 1 e259-e281
  • [2] Feigin VL(2009)Incidence and 10-year survival of intracerebral hemorrhage in a population-based registry Stroke. 40 394-399
  • [3] Forouzanfar MH(2015)Guidelines for the management of spontaneous intracerebral hemorrhage: a guideline for healthcare professionals from the American Heart Association/American Stroke Association Stroke. 46 2032-2060
  • [4] Mensah GA(2017)Severity assessment in maximally treated ICH patients: the max-ICH score Neurology. 89 423-431
  • [5] Connor M(2016)Platelet transfusion versus standard care after acute stroke due to spontaneous cerebral haemorrhage associated with antiplatelet therapy (PATCH): a randomised, open-label, phase 3 trial Lancet. 387 2605-2613
  • [6] Bennett DA(2018)Tranexamic acid for hyperacute primary IntraCerebral Haemorrhage (TICH-2): an international randomised, placebo-controlled, phase 3 superiority trial The Lancet 391 2107-2115
  • [7] Sacco S(2017)Thrombolytic removal of intraventricular haemorrhage in treatment of severe stroke: results of the randomised, multicentre, multiregion, placebo-controlled CLEAR III trial Lancet. 389 603-611
  • [8] Marini C(2013)Early surgery versus initial conservative treatment in patients with spontaneous supratentorial lobar intracerebral haematomas (STICH II): a randomised trial Lancet. 382 397-408
  • [9] Toni D(2019)Management of oral anticoagulation after intracerebral hemorrhage International Journal of Stroke 14 238-246
  • [10] Olivieri L(2015)Anticoagulant reversal, blood pressure levels, and anticoagulant resumption in patients with anticoagulation-related intracerebral hemorrhage JAMA. 313 824-836