Thromboembolic Risk of 4-Factor Prothrombin Complex Concentrate versus Fresh Frozen Plasma for Urgent Warfarin Reversal in the Emergency Department.


Journal

The western journal of emergency medicine
ISSN: 1936-9018
Titre abrégé: West J Emerg Med
Pays: United States
ID NLM: 101476450

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 14 11 2018
revised: 25 04 2019
accepted: 26 04 2019
entrez: 19 7 2019
pubmed: 19 7 2019
medline: 28 11 2019
Statut: ppublish

Résumé

Warfarin is a potent anticoagulant used for the prevention and treatment of venous and arterial thrombosis. Occasionally, patients require emergent warfarin reversal due to active bleeding, supratherapeutic international normalized ratio, or emergent diagnostic or therapeutic interventions. Various agents can be used for emergent warfarin reversal, including fresh frozen plasma (FFP) and 4-factor prothrombin complex concentrate (4F-PCC). Both FFP and 4F-PCC are generally considered safe; however, both agents contain coagulation factors and have the potential to provoke a thromboembolic event. Although clinical trials have compared the efficacy and safety of FFP and 4F-PCC, data are limited comparing the risk of thromboembolism between the two agents. A retrospective chart review was performed at a single, urban, academic medical center comparing the incidence of thromboembolism with FFP or 4F-PCC for warfarin reversal during a three-year period in the emergency department (ED) at Massachusetts General Hospital. Patients were included in the study if they were at least 18 years of age and were on warfarin per electronic health records. Patients were excluded if they had received both FFP and 4F-PCC during the same visit. The primary outcome was the frequency of thromboembolism within 30 days of 4F-PCC or FFP. Secondary outcomes included time to thromboembolic event and in-hospital mortality. Three hundred and thirty-six patients met the inclusion criteria. Thromboembolic events within 30 days of therapy occurred in seven patients (2.7%) in the FFP group and 14 patients (17.7%) in the 4F-PCC group (p=<0.001). Death occurred in 39 patients (15.2%) who received FFP and 18 patients (22.8%) who received 4F-PCC (p=0.115). Since the 4F-PCC group was treated disproportionately for central nervous system (CNS) bleeding, a subgroup analysis was performed including patients requiring reversal due to CNS bleeds that received vitamin K. The primary outcome remained statistically significant, occurring in four patients (4.1%) in the FFP group and nine patients (14.1%) in the 4F-PCC group (p=0.02). Our study found a significantly higher risk of thromboembolic events in patients receiving 4F-PCC compared to FFP for urgent warfarin reversal. This difference remained statistically significant when controlled for CNS bleeds and administration of vitamin K.

Identifiants

pubmed: 31316701
doi: 10.5811/westjem.2019.4.41649
pii: wjem-20-619
pmc: PMC6625686
doi:

Substances chimiques

Anticoagulants 0
Blood Coagulation Factors 0
prothrombin complex concentrates 37224-63-8
Warfarin 5Q7ZVV76EI

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

619-625

Déclaration de conflit d'intérêts

Conflicts of Interest: By the WestJEM article submission agreement, all authors are required to disclose all affiliations, funding sources and financial or management relationships that could be perceived as potential sources of bias. No author has professional or financial relationships with any companies that are relevant to this study. There are no conflicts of interest or other sources of funding to declare.

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Auteurs

Michelle Maguire (M)

Massachusetts General Hospital, Department of Pharmacy, Boston, Massachusetts.

Lanting Fuh (L)

Massachusetts General Hospital, Department of Pharmacy, Boston, Massachusetts.

Joshua N Goldstein (JN)

Massachusetts General Hospital, Department of Emergency Medicine, Boston, Massachusetts.
Harvard Medical School, Department of Emergency Medicine, Boston, Massachusetts.

Ariela L Marshall (AL)

Mayo Clinic, Division of Hematology, Department of Internal Medicine, Rochester, Minnesota.
Mayo Clinic, Department of Laboratory Medicine and Pathology, Rochester, Minnesota.

Michael Levine (M)

University of Southern California, Department of Emergency Medicine, Department of Medical Toxicology, Los Angeles, California.

Melissa L Howell (ML)

University of the South, The School of Theology, Sewanee, Tennessee.

Blair A Parry (BA)

Massachusetts General Hospital, Department of Emergency Medicine, Boston, Massachusetts.
Massachusetts General Hospital, Center for Vascular Emergencies, Boston, Massachusetts.

Rachel Rosovsky (R)

Massachusetts General Hospital, Division of Hematology, Department of Internal Medicine, Boston, Massachusetts.
Harvard Medical School, Department of Internal Medicine, Boston, Massachusetts.

Bryan D Hayes (BD)

Massachusetts General Hospital, Department of Pharmacy, Boston, Massachusetts.
Harvard Medical School, Department of Emergency Medicine, Boston, Massachusetts.

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Classifications MeSH