Faculty Opinions recommendation of Off-label use of recombinant factor VIIa in U.S. hospitals: analysis of hospital records.

Author(s):  
A Koneti Rao
Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 67-67
Author(s):  
Aaron C. Logan ◽  
Veronica Yank ◽  
Randall S. Stafford

Abstract Abstract 67 Background: Recombinant factor VIIa (rFVIIa) is FDA-approved for treatment of bleeding due to factor VIII or factor IX inhibitors in the setting of congenital or acquired hemophilia or due to congenital factor VII deficiency. When first introduced into clinical practice in 1999, rFVIIa was used predominantly for these labeled indications. Over the years since it became widely available, rFVIIa has been employed extensively for off-label indications. The data to support these uses are sparse or, in some cases, contradictory. Objective: To estimate patterns of off-label rFVIIa use in United States hospitals. Data source: We evaluated data from the Premier Perspectives database of United States hospitals. This representative sample was used to extrapolate national usage patterns of rFVIIa. For each hospitalization at member institutions, the database includes information on patient demographics, primary and secondary diagnoses, medications dispensed, service items used, and disposition at discharge. We examined data encompassing hospitalizations between January 1, 2000 and December 31, 2008. Results: Use of rFVIIa was reported in 235 of 615 hospitals (38%) in the Premier database. 12,644 hospitalizations involving administration of rFVIIa during the study period were identified. Based on statistical weights for each member hospital, this translates to an estimated 73,747 hospitalizations nationwide during which rFVIIa was employed, 18,311 (25%) of which occurred during 2008. Between 2000 and 2008, off-label use of rFVIIa increased more than 140-fold, such that in 2008, 97% of in-hospital indications were off-label. In contrast, in-hospital use for the hemophilias has increased 3.7-fold since 2000 and appears to have plateaued, such that on-label use accounted for only 4.2% of use overall and 2.7% of use in 2008. We found cardiac surgery (29% of use in 2008), trauma (28%), and intracranial hemorrhage (11%) to be the most common off-label indications for rFVIIa use. Consistent with the growth of these and other off-label indications, there has been a significant increase in the mean age of patients receiving rFVIIa from 3 years in 2000 to 59 years in 2008. Conditions with a prominent proportion of use in the elderly (>65 years) included aortic aneurysm (82%), prostatectomy (66%), brain trauma (64%), intracranial hemorrhage (58%), cardiac surgery (57%), and gastrointestinal bleeding (57%). Across all indications, in-hospital mortality has increased substantially over time from 5% in 2000 to 27% in 2008. The highest in-hospital mortality rates were associated with aortic aneurysm (57%), neonatal use (54%), variceal bleeding (51%), other liver disease (49%), liver biopsy (45%), vascular procedures (43%), intracranial hemorrhage (43%), brain trauma (40%), body trauma (36%), and gastrointestinal bleeding (35%). The population receiving rFVIIa for the most common indication, adult cardiac surgery, experienced 24% in-hospital mortality. Amongst all patients treated with rFVIIa in 2008, 43% were discharged to home. Most of the remaining patients were transferred to other facilities, including nursing homes, rehabilitation hospitals, and other acute care facilities. In contrast, hemophilia patients receiving rFVIIa experienced a 3.8% in-hospital mortality rate, while 85% were discharged directly home. Finally, we identified a significant shift in rFVIIa use from academic hospitals (89% in 2000) to non-academic hospitals (67% in 2008). Conclusions: In hospitalized patients, off-label use of rFVIIa far exceeds use for the small number of licensed indications. Cardiac surgery, trauma, and non-traumatic intracranial hemorrhage represent the top indications for in-hospital rFVIIa use in the United States, together accounting for an estimated 12,448 of 18,311 (68%) uses during 2008. Across all off-label indications, in-hospital mortality is high, suggesting a substantial proportion of 'end-stage' use of rFVIIa. Use in such circumstances raises concerns about efficacy, associated adverse events, and allocation of resources. The marked shift in off-label use from academic to non-academic hospitals suggests wide acceptance despite these concerns. These patterns of expanding use are concerning given the absence of strong and consistent evidence to support the off-label application of rFVIIa. Disclosures: Off Label Use: This work characterizes patterns of off-label use of recombinant factor VIIa in United States hospitals..


2004 ◽  
Vol 32 (Supplement) ◽  
pp. A163
Author(s):  
Robert MacLaren ◽  
Laura A Weber ◽  
Helga Brake ◽  
Julie L Cerese ◽  
Gardner M ◽  
...  

2011 ◽  
Vol 183 (1) ◽  
pp. 26-27 ◽  
Author(s):  
P. C. Hebert ◽  
D. Fergusson ◽  
M. B. Stanbrook

Hematology ◽  
2008 ◽  
Vol 2008 (1) ◽  
pp. 36-38 ◽  
Author(s):  
Rachel P. Rosovsky ◽  
Mark A. Crowther

Abstract A 47-year-old man presents with hypovolemic shock. He takes warfarin as a result of a mechanical mitral valve insertion 5 years prior, his INR at presentation is 8.4 and emergent CT reveals a very large retroperitoneal hematoma. Despite aggressive fluid and transfusion support he continues hypotensive, requiring ionotrope support. You are asked if he should receive recombinant factor VIIa.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 1402-1402
Author(s):  
Mayur B. Patel ◽  
Syamal D. Bhattacharya ◽  
Judson B. Williams ◽  
Timothy E. Sweeney ◽  
Steven N. Vaslef ◽  
...  

Abstract Abstract 1402 Objective: Recombinant factor VIIa (rFVIIa) is used for hemophiliac patients with inhibitors against coagulation factor VIII or IX, but there is varied off-label use of rFVIIa for other patients. The aim of the present study was to examine our institution's off-label use of rFVIIa in an adult population. Methods: We performed an IRB-approved retrospective review of rFVIIa administrations since its first use in January 2003 through December 2008. Patients were identified using an inpatient pharmacy database capturing all rFVIIa administrations. Blood product transfusion (packed red blood cells, pRBCs; fresh frozen plasma, FFP; platelets; cryoprecipitate), adjunctive hemostatic agent use (epsilon aminocaproic acid, protamine, desmopressin, estrogen, or vitamin K), and operative or vascular interventional procedures were examined before and after administration. Laboratory data including pH, temperature, prothrombin time (PT/INR), partial thromboplastin time (PTT), and fibrinogen were also collected by chart review. Outcome measures included mortality at 24h, 48h, and 30d, as well as thrombotic complications. Two-tailed paired T-tests were used for statistical comparisons. Results: A total of 256 consecutive adult patients received rFVIIa. Of these, 20 (8%) received rFVIIa for FDA-approved on-label use. Thus, 236 off-label rFVIIa administrations were confirmed, with an average patient age of 58± 19y. The annual number of doses administered increased from 2003 to 2005, after which rFVIIa utilization remained constant (52 ± 5 patients/year from 2005–2008). rFVIIa was administered for head injury or hemorrhagic stroke (41%), cardiothoracic surgery (23%), gastrointestinal bleeding (14%), trauma (10%), off-label hematologic disorders (4%), vascular surgery (4%), transplantation (2%), orthopedics (2%), and obstetrics (2%). Administration locations consisted of the intensive care unit (70%), operating room (20%), emergency room (6%), and ward (2%). Single doses (79 ± 28 mcg/kg) comprised 79% of administrations. Extremely high and low single dose regimens (> ±1 standard deviation) were used in neurologic and cardiothoracic surgical populations. Immediately before rFVIIa administration, temperature was 36.9 ± 1.0 °C, pH 7.38 ± 0.10, platelets 141 ± 101 × 109/L, PT/PTT 2.7/44 s, and fibrinogen 243 ± 131 mg/dL. These parameters did not clinically change at 24h or 48h after rFVIIa administration, though PT/INR stabilized at 1.28 ± 0.80 and 1.32 ± 0.41, respectively. Mortality rates were 13%, 17%, and 38% at 24h, 48h, and 30d respectively. 80% of deaths at 24h were related to either uncontrolled or intracranial hemorrhage. 2 deaths >48h after administration were stroke related in a post-cardiopulmonary bypass setting. 25 thromboembolic complications occurred at any point following administration and through hospital discharge. Greater than 75% of the complications were deep vein thromboses, none resulting in death. Of the 60 patients requiring massive transfusion (>10 pRBCs) in the 24h prior to rFVIIa administration, the pRBC, FFP and platelet usage significantly decreased within 24h (pRBC: 20.6 ± 9.9 to 8.4 ± 8.6; FFP: 12.0 ± 7.3 to 6.9 ± 8.1; platelets: 3.5 ± 2.8 to 2.1 ±2.0, all p<0.0001). 24h after rFVIIa in massively transfused patients, the number of patients requiring operation or vascular intervention procedures decreased from 27 to 14. This was also associated with a 38% decrease for the need of adjunctive hemostatic agents. There were no meaningful changes in laboratory coagulation parameters. Conclusion: Analysis of this large retrospective cohort of single institution rFVIIa administration reveals 92% off-label use. The majority (64%) of indications are for cardiothoracic surgery and intracranial hemorrhage. Although thromboembolism rates are 10%, mortality at 24h does not seem to be associated with thromboembolism. In those requiring a massive transfusion, rFVIIa use may decrease transfusion requirements, need for operative or vascular intervention, and the need for hemostatic adjunct use. Disclosures: Off Label Use: Recombinant factor VIIa and its off-label use in hemostasis. Lawson:Novo Nordisk: Membership on an entity's Board of Directors or advisory committees.


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