Low-Molecular-Weight Heparin Anti-Xa Guided Reversal of Apixaban With Prothrombin Complex Concentrate in a Patient on Hemodialysis

被引:0
|
作者
Brummett, Christina M. [1 ]
Dingman, James S. [1 ]
Philip, George J. [2 ]
Moran, David A. [1 ]
Gilbert, Brian W. [1 ]
机构
[1] Wesley Med Ctr, Dept Pharm, 550 N Hillside, Wichita, KS 67214 USA
[2] Wesley Med Ctr, Dept Acute Care Trauma & Surg, Wichita, KS USA
关键词
anticoagulation; neurology; emergency medicine; critical care;
D O I
10.1177/08971900211044288
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The growing use of oral factor Xa (FXa) inhibitors in patients with chronic kidney disease (CKD), particularly the recent increased use of apixaban in patients with end-stage renal disease (ESRD), has created a new dilemma in the already controversial topic of oral FXa inhibitor reversal. With the limited availability of anti-Xa levels specific to oral FXa inhibitors and even scarcer availability of reversal data for patients on these agents with ESRD, ensuring adequate reversal is currently often solely guided by repeat imaging and changes in clinical status. Low molecular weight heparin (LMWH) anti-Xa levels have been used as a more commonly accessible test to guide the need for and efficacy of reversal of oral FXa inhibitors in patients with normal renal function. However, evidence supporting this technique is again lacking in patients with renal dysfunction. This case report focuses on the use of LMWH anti-Xa levels to guide reversal of apixaban in a patient with ESRD on hemodialysis and correlation of those levels to the patient's clinical status.
引用
收藏
页码:468 / 471
页数:4
相关论文
共 50 条
  • [41] Low-molecular-weight heparin for routine hemodialysis
    Davenport, Andrew
    HEMODIALYSIS INTERNATIONAL, 2008, 12 : S34 - S37
  • [42] Anaphylactoid reaction induced by low-molecular-weight heparin in a hemodialysis patient
    Ueda, A
    Nagase, S
    Morito, N
    Yotsumoto, M
    Ohba, S
    Hasegawa, Y
    Narita, M
    Koyama, A
    NEPHRON, 2001, 87 (01): : 93 - 94
  • [43] Higher Doses of Low-Molecular-Weight Heparin (Enoxaparin) Are Needed to Achieve Target Anti-Xa Concentrations in Critically Ill Children
    Schloemer, Nathan J.
    Abu-Sultaneh, Samer
    Hanson, Sheila J.
    Yan, Ke
    Hoffmann, Raymond G.
    Punzalan, Rowena C.
    Havens, Peter L.
    PEDIATRIC CRITICAL CARE MEDICINE, 2014, 15 (07) : E294 - E299
  • [44] Monitoring of Anti-Xa in Pregnant Patients With Mechanical Prosthetic Valves Receiving Low-Molecular-Weight Heparin: Peak or Trough Levels?
    Goland, Sorel
    Schwartzenberg, Shmuel
    Fan, John
    Kozak, Natasha
    Khatri, Nudrat
    Elkayam, Uri
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS, 2014, 19 (05) : 451 - 456
  • [45] The contribution of anti-Xa and anti-IIa activities to the profibrinolytic activity of low-molecular-weight heparins
    Ammollo, Concetta T.
    Semeraro, Fabrizio
    Semeraro, Nicola
    Colucci, Mario
    THROMBOSIS AND HAEMOSTASIS, 2009, 101 (04) : 782 - 785
  • [46] RELATION BETWEEN ANTI-XA AND ANTI-IIA AMIDOLYTIC ACTIVITIES AND APTT PROLONGATION OF 3 LOW-MOLECULAR-WEIGHT HEPARIN FRACTIONS VERSUS UNFRACTIONATED HEPARIN
    SAMAMA, MM
    VANDREDEN, P
    QUENTIN, G
    ROLAND, N
    COMBOT, C
    THROMBOSIS AND HAEMOSTASIS, 1995, 73 (06) : 969 - 969
  • [47] Clinical Practice Patterns of Anti-Xa Monitoring During Low Molecular Weight Heparin Therapy
    Stutsky, Martha E.
    Reardon, David P.
    Lee, Alfred I.
    BLOOD, 2015, 126 (23)
  • [48] Should low molecular weight heparin dosing be based on anti-Xa assays in antiphospholipid syndrome?
    Thachil, Jecko
    BLOOD COAGULATION & FIBRINOLYSIS, 2013, 24 (01) : 82 - 84
  • [49] Plasma Anti-Xa Monitoring for Low-Molecular-Weight Heparins in Patients with Chronic Kidney Disease
    Gallieni, Maurizio
    Martini, Alma
    Granata, Antonio
    Fusaro, Maria
    CLINICAL PHARMACOKINETICS, 2010, 49 (11) : 773 - 774
  • [50] Plasma Anti-Xa Monitoring for Low-Molecular-Weight Heparins in Patients with Chronic Kidney Disease
    Maurizio Gallieni
    Alma Martini
    Antonio Granata
    Maria Fusaro
    Clinical Pharmacokinetics, 2010, 49 : 773 - 774