The risk of major bleeding in patients with suspected heparin-induced thrombocytopenia.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
11 2019
Historique:
received: 22 04 2019
accepted: 22 07 2019
pubmed: 28 7 2019
medline: 1 9 2020
entrez: 28 7 2019
Statut: ppublish

Résumé

The presence of a hypercoagulable disorder such as heparin-induced thrombocytopenia (HIT) may protect against anticoagulant-associated bleeding. To determine the incidence of major bleeding in patients with suspected HIT. We performed a retrospective analysis of 310 patients suspected of having HIT from the Hospital of the University of Pennsylvania and an affiliated community hospital. We compared the cumulative incidence of major bleeding following suspicion for HIT by ultimate HIT status (HIT+ or HIT-) and exposure to an alternative anticoagulant (Tx+ or Tx-). Secondary outcomes included the incidence of new/progressive thrombosis and 30-day mortality. The incidence of major bleeding was high in the HIT+Tx+, HIT- Tx+, and HIT-Tx- groups (35.7%, 44.0%, and 37.3%, respectively). The time to first major bleeding event did not differ between groups (P = .24). Factors associated with increased risk of major bleeding included intensive care unit admission (HR 2.24, 95% CI 1.44-3.47), platelet count < 25 × 10 Among patients with suspected HIT, major bleeding was common regardless of HIT status. Contrary to our hypothesis, HIT+ patients were not protected from major bleeding. A better understanding of bleeding risk is needed to inform management decisions in patients with suspected HIT.

Sections du résumé

BACKGROUND
The presence of a hypercoagulable disorder such as heparin-induced thrombocytopenia (HIT) may protect against anticoagulant-associated bleeding.
OBJECTIVES
To determine the incidence of major bleeding in patients with suspected HIT.
METHODS
We performed a retrospective analysis of 310 patients suspected of having HIT from the Hospital of the University of Pennsylvania and an affiliated community hospital. We compared the cumulative incidence of major bleeding following suspicion for HIT by ultimate HIT status (HIT+ or HIT-) and exposure to an alternative anticoagulant (Tx+ or Tx-). Secondary outcomes included the incidence of new/progressive thrombosis and 30-day mortality.
RESULTS
The incidence of major bleeding was high in the HIT+Tx+, HIT- Tx+, and HIT-Tx- groups (35.7%, 44.0%, and 37.3%, respectively). The time to first major bleeding event did not differ between groups (P = .24). Factors associated with increased risk of major bleeding included intensive care unit admission (HR 2.24, 95% CI 1.44-3.47), platelet count < 25 × 10
CONCLUSIONS
Among patients with suspected HIT, major bleeding was common regardless of HIT status. Contrary to our hypothesis, HIT+ patients were not protected from major bleeding. A better understanding of bleeding risk is needed to inform management decisions in patients with suspected HIT.

Identifiants

pubmed: 31350937
doi: 10.1111/jth.14587
pmc: PMC6913895
mid: NIHMS1043808
pii: S1538-7836(22)02707-6
doi:

Substances chimiques

Anticoagulants 0
Heparin 9005-49-6

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1956-1965

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL142122
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007971
Pays : United States

Informations de copyright

© 2019 International Society on Thrombosis and Haemostasis.

Références

Pharmacoeconomics. 2007;25(11):949-61
pubmed: 17960953
J Thromb Haemost. 2014 Jul;12(7):1044-53
pubmed: 24766902
Crit Care Med. 2002 Apr;30(4):753-6
pubmed: 11940740
Am J Hematol. 2017 Aug;92(8):730-738
pubmed: 28388835
Thromb Haemost. 2011 Dec;106(6):993-4
pubmed: 22012630
Blood Adv. 2018 Nov 27;2(22):3360-3392
pubmed: 30482768
Thromb Haemost. 2005 Jul;94(1):132-5
pubmed: 16113796
J Thromb Thrombolysis. 2012 Nov;34(4):491-8
pubmed: 22743780
Blood. 2012 Nov 15;120(20):4160-7
pubmed: 22990018
Blood. 2012 Mar 8;119(10):2209-18
pubmed: 22246036
Blood Adv. 2018 Nov 27;2(22):3155-3162
pubmed: 30463915
N Engl J Med. 1980 Oct 2;303(14):788-95
pubmed: 7412786
J Thromb Haemost. 2010 Jan;8(1):202-4
pubmed: 19878532
Blood. 2000 Aug 1;96(3):846-51
pubmed: 10910895
J Thromb Thrombolysis. 2015 Nov;40(4):512-4
pubmed: 26036229
J Thromb Haemost. 2005 Nov;3(11):2428-36
pubmed: 16241940
Blood. 2015 Feb 5;125(6):924-9
pubmed: 25515959
Circulation. 2001 Apr 10;103(14):1838-43
pubmed: 11294800
Thromb Res. 2014 Jul;134(1):29-35
pubmed: 24703295
J Thromb Haemost. 2017 Jun;15(6):1203-1212
pubmed: 28374939
J Thromb Haemost. 2017 Feb;15(2):370-374
pubmed: 28012249
Blood. 2003 Jan 1;101(1):31-7
pubmed: 12393689
Med Care. 2017 Jul;55(7):698-705
pubmed: 28498196
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354

Auteurs

Allyson M Pishko (AM)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Daniel S Lefler (DS)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Phyllis Gimotty (P)

Department of Biostatistics and Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Koosha Paydary (K)

Department of Internal Medicine, John H. Stroger Jr. Hospital of Cook County, Chicago, Illinois.

Sara Fardin (S)

Department of Radiology, Tufts Medical Center, Boston, Massachusetts.

Gowthami M Arepally (GM)

Division of Hematology, Department of Medicine, Duke University, Durham, North Carolina.

Mark Crowther (M)

Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Lawrence Rice (L)

Hematology Division, Department of Medicine, Houston Methodist Hospital, Weill Cornell Medical College, Houston, Texas.

Rolando Vega (R)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Douglas B Cines (DB)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

James P Guevara (JP)

Department of Biostatistics and Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Adam Cuker (A)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

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