Management of Major Bleeding Events in Atrial Fibrillation Patients Using Pradaxa

Purpose:

Inclusion criteria:

- Greater than or equal to 18 years of age;

- Confirmed diagnosis of non valvular atrial fibrillation (NVAF) (Diagnosis of AF is
considered confirmed if there is medical chart documentation that the patient has
atrial fibrillation or AF or the ICD-9 or ICD-10 code for AF is documented);

- NVAF is defined as follows: nonvalvular atrial fibrillation is restricted to cases in
which the rhythm disturbance occurs in the absence of rheumatic mitral stenosis or a
prosthetic heart valve.

- Documentation that the patient presented to an emergency department/emergency room
(ED/ER) for a major bleeding event (index event);

- Major bleeding is defined by International Society on Thrombosis and Haemostasis
(ISTH) as:

- fatal bleeding and/or

- symptomatic bleeding in a critical area/organ such as intracranial, intraspinal,
intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with
compartment syndrome, and/or

- bleeding causing a fall in hemoglobin of 20g per liter or more, or leading to
transfusion of 2 or more units of whole blood or red blood cells

- Documentation that the index event occurred in a patient who reported having taken at
least one dose of dabigatran within the 5 days prior to the index event.

Exclusion criteria:

- Confirmed diagnosis of valvular AF (Diagnosis of valvular AF is considered confirmed
if there is medical chart documentation that the patient has valvular AF or VAF. In
the absence of documentation to indicate whether the patient has non-valvular or
valvular AF,);

- Documentation that the patient was taking dabigatran with a concomitant anticoagulant
(contemporaneous parenteral anticoagulant or another oral anticoagulant) within 72
hours of the index event;

- The concomitant administration of antiplatelet medications prior to the onset of the
index event is not exclusionary;

- Documentation of the patient receiving thrombolytic therapy within 48 hours of the
onset of the index event;

- Documentation that the patient was enrolled in an interventional investigational or
other BI observational clinical trial at the time of the onset of the index event;

- Medical record was not retrievable, was missing or empty.