The ORBIT bleeding score: a simple bedside score to assess bleeding risk in atrial fibrillation.

dc.contributor.author

O'Brien, Emily C

dc.contributor.author

Simon, DaJuanicia N

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Thomas, Laine E

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Hylek, Elaine M

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Gersh, Bernard J

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Ansell, Jack E

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Kowey, Peter R

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Mahaffey, Kenneth W

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Chang, Paul

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Fonarow, Gregg C

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Pencina, Michael J

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Piccini, Jonathan P

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Peterson, Eric D

dc.coverage.spatial

England

dc.date.accessioned

2017-07-06T15:33:49Z

dc.date.available

2017-07-06T15:33:49Z

dc.date.issued

2015-12-07

dc.description.abstract

BACKGROUND: Therapeutic decisions in atrial fibrillation (AF) are often influenced by assessment of bleeding risk. However, existing bleeding risk scores have limitations. OBJECTIVES: We sought to develop and validate a novel bleeding risk score using routinely available clinical information to predict major bleeding in a large, community-based AF population. METHODS: We analysed data from Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF), a prospective registry that enrolled incident and prevalent AF patients at 176 US sites. Using Cox proportional hazards regression, we identified factors independently associated with major bleeding among patients taking oral anticoagulation (OAC) over a median follow-up of 2 years (interquartile range = 1.6-2.5). We also created a numerical bedside risk score that included the five most predictive risk factors weighted according to their strength of association with major bleeding. The predictive performance of the full model, the simple five-item score, and two existing risk scores (hypertension, abnormal renal/liver function, stroke, bleeding history or predisposition, labile INR, elderly, drugs/alcohol concomitantly, HAS-BLED, and anticoagulation and risk factors in atrial fibrillation, ATRIA) were then assessed in both the ORBIT-AF cohort and a separate clinical trial population, Rivaroxaban Once-daily oral direct factor Xa inhibition compared with vitamin K antagonism for prevention of stroke and embolism trial in atrial fibrillation (ROCKET-AF). RESULTS: Among 7411 ORBIT-AF patients taking OAC, the rate of major bleeding was 4.0/100 person-years. The full continuous model (12 variables) and five-factor ORBIT risk score (older age [75+ years], reduced haemoglobin/haematocrit/history of anaemia, bleeding history, insufficient kidney function, and treatment with antiplatelet) both had good ability to identify those who bled vs. not (C-index 0.69 and 0.67, respectively). These scores both had similar discrimination, but markedly better calibration when compared with the HAS-BLED and ATRIA scores in an external validation population from the ROCKET-AF trial. CONCLUSIONS: The five-element ORBIT bleeding risk score had better ability to predict major bleeding in AF patients when compared with HAS-BLED and ATRIA risk scores. The ORBIT risk score can provide a simple, easily remembered tool to support clinical decision making.

dc.identifier

https://www.ncbi.nlm.nih.gov/pubmed/26424865

dc.identifier

ehv476

dc.identifier.eissn

1522-9645

dc.identifier.uri

https://hdl.handle.net/10161/15004

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Eur Heart J

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10.1093/eurheartj/ehv476

dc.subject

Anticoagulants

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Atrial fibrillation

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Major bleeding

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Risk prediction

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Aged

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Aged, 80 and over

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Anticoagulants

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Atrial Fibrillation

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Female

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Hemorrhage

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Humans

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Male

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Middle Aged

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Point-of-Care Systems

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Prospective Studies

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Registries

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Risk Assessment

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Risk Factors

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Stroke

dc.title

The ORBIT bleeding score: a simple bedside score to assess bleeding risk in atrial fibrillation.

dc.type

Journal article

duke.contributor.orcid

O'Brien, Emily C|0000-0002-8257-7561

duke.contributor.orcid

Pencina, Michael J|0000-0001-5798-8855|0000-0002-1968-2641

duke.contributor.orcid

Piccini, Jonathan P|0000-0003-0772-2404

duke.contributor.orcid

Peterson, Eric D|0000-0002-5415-4721

pubs.author-url

https://www.ncbi.nlm.nih.gov/pubmed/26424865

pubs.begin-page

3258

pubs.end-page

3264

pubs.issue

46

pubs.organisational-group

Basic Science Departments

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Biostatistics & Bioinformatics

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Clinical Science Departments

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Duke

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Duke Clinical Research Institute

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Institutes and Centers

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Medicine

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Medicine, Cardiology

pubs.organisational-group

Medicine, Clinical Pharmacology

pubs.organisational-group

School of Medicine

pubs.publication-status

Published

pubs.volume

36

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