|Recombinant activated clotting factor VII (rFVIIa) in the treatment of surgical and spontaneous bleeding episodes in hemophilic patients.|
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|PMID: 17323597 Owner: NLM Status: MEDLINE|
|Inhibitors against replacement clotting factors occur in approximately 30%-40% of patients with hemophilia A and 1.5%-3% of patients with hemophilia B. In this group of patients, bleeding events are best treated with bypassing agents. Recombinant activated factor VII (rFVIIa) has become the first-line agent in treating surgical and non-surgical bleeding in many centres with efficacy at standard 90 microg/kg doses approaching 90%. The greater efficacy is associated with early initiation of treatment, as well as, possibly larger doses of rFVIIa. A higher concentration appears to be essential in initiating an adequate thrombin burst, which results in a stable clot. Higher dosage regimens, home therapy and continuous infusion regimens are continuously evolving as we strive to define optimal dosing strategies in hemophilia patients. rFVIIa has been a remarkably safe agent for hemophiliacs but with high dosages being advocated and older patients being given such doses outside a trial setting, thromboembolic events remain a concern.|
|Heng Joo Ng; Lai Heng Lee|
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|Type: Journal Article; Review|
|Title: Vascular health and risk management Volume: 2 ISSN: 1176-6344 ISO Abbreviation: - Publication Date: 2006|
|Created Date: 2007-02-27 Completed Date: 2007-03-30 Revised Date: 2009-11-18|
Medline Journal Info:
|Nlm Unique ID: 101273479 Medline TA: Vasc Health Risk Manag Country: New Zealand|
|Languages: eng Pagination: 433-40 Citation Subset: IM|
|Department of Haematology, Singapore General Hospital, Singapore. firstname.lastname@example.org|
|APA/MLA Format Download EndNote Download BibTex|
Coagulants / administration & dosage, adverse effects, immunology, therapeutic use*
Dose-Response Relationship, Drug
Drug Administration Schedule
Factor VII / administration & dosage, adverse effects, immunology, therapeutic use*
Hemophilia A / complications*
Hemorrhage / blood, drug therapy*, etiology
Recombinant Proteins / administration & dosage, adverse effects, immunology, therapeutic use
Surgical Procedures, Operative / adverse effects*
Thromboembolism / chemically induced
Thrombosis / chemically induced
|0/Coagulants; 0/Recombinant Proteins; 0/recombinant FVIIa; 9001-25-6/Factor VII; EC 184.108.40.206/Factor VIIa|
Journal ID (nlm-ta): Vasc Health Risk Manag
Journal ID (publisher-id): Vascular Health and Risk Management
Publisher: Dove Medical Press
? 2006 Dove Medical Press Limited. All rights reserved
Print publication date: Month: 12 Year: 2006
Electronic publication date: Month: 12 Year: 2006
Volume: 2 Issue: 4
First Page: 433 Last Page: 440
PubMed Id: 17323597
|Recombinant activated clotting factor VII (rFVIIa) in the treatment of surgical and spontaneous bleeding episodes in hemophilic patients|
|Heng Joo Ng|
|Lai Heng Lee|
|Department of Haematology, Singapore General HospitalSingapore
|Correspondence: Correspondence: Heng Joo Ng Department of Haematology, Singapore General Hospital, Outram Road, Singapore 169608, Singapore Email email@example.com
The development of alloimmune antibodies against factor VIII has been recognized since the early treatment of hemophilic patients with blood product transfusion many decades ago (Munro and Jones 1943). Highly effective treatment and prophylaxis of bleeding episodes with increasingly purified factor VIII containing products over the years have been negated by development of inhibitors in approximately 30?40% of patients with severe hemophilia A (Ehrenforth et al 1992; Scharrer et al 1999; Kreuz et al 2002). Similar inhibitors have been developed, between 1.5?3% of hemophilia B patients receiving factor IX concentrates (Warrier and Lusher 1998).
To circumvent their devastating effects against replacement factor concentrates, treatment strategies for bleeding episodes are based upon the premise of either saturating inhibitors with excess of clotting factors or bypassing the factor requirement altogether (von Depka 2005). The first strategy can only be attempted in patients with low inhibitor levels (<5 Bethesda Units). Bleeding episodes in patients with high responding inhibitor levels pose a considerable challenge to clinicians and requires the use of bypassing agents such as prothrombin complexes and recombinant activated factor VIIa (rFVIIa, Novo Seven). Hemostasis is not assured despite the use these agents and responses vary between individual patients, with overall costs being potentially prohibitive for many patients (Allen and Aledort 2006).
rFVIIa is the latest among the limited range of currently available bypassing agents. Successful use of plasma derived FVIIa in hemophilia A patients with inhibitors was first reported about 2 decades ago (Hedner and Kiesel 1983). Experience with its recombinant form in hemophiliacs began in the late 1980's (Hedner et al 1988) and represented a major advance in the treatment of patients with inhibitors (Hedner 1990). The US Food and Drug Administration (FDA) approval for use in both hemophilia A and B patients with inhibitors, was attained in 1999. In Europe, the regulatory approvals have been extended to other indications such as acquired hemophilia, factor VII deficiency and Glanzmann's thrombasthenia. The current understanding of its hemostatic action suggests that pharmacologic doses of rFVIIa enhance the thrombin-generating potential of activated platelets and facilitate full activation of thrombin-activatable fibrinolytic inhibitor (TAFI) and factor XIII. The sum result of these processes is the formation of a stable hemostatic plug, which is resistant to premature lysis (Hedner 2006). rFVIIa has a short half-life of 2.9 hours and dosing at intervals of 2?3 hours is necessary to maintain hemostasis (Lindley et al 1994). Significantly faster clearance has been observed in children compared to adults (Villar et al 2004).
In the following sections, we will review various aspects and issues concerning the use of rFVIIa in treating and prophylaxing against bleeding episodes, among both hemophilia A and B patients. Medline and EMBASE electronic databases were comprehensively searched using the following terms: recombinant FVIIa, recombinant activated factor VII, NovoSeven, eptacog alfa and haemophilia/hemophilia. Unless otherwise stated, the studies and reports mentioned include both hemophilia A and B patients with inhibitors
Following the first reported treatment success with rFVIIa (Hedner et al 1988), many case reports and case series were published, reporting mostly successful control or prevention of bleeding in hemophiliacs with inhibitors (Levi et al 2005). Further suggestions of efficacy came from compilation of data and reports derived from the databases of the Compassionate Use Program and later, the Emergency Treatment Study (Bech 1996; Rice and Savidge 1996; Arkin et al 1998; Scharrer 1999; Arkin et al 2000; Ludlam 2002). Under the first program, 260 patients received rFVIIa for more than 1000 bleeding episodes over 8 years. Doses of 60?90 ?g/kg were used with efficacy reported to be between 80%?87% in serious bleeds and 91%?94% in surgical bleeding. In the Emergency Treatment Study, 253 acute bleeding episodes in 127 patients were treated with rFVIIa at 90 ?g/kg, repeated 2-hourly until bleeding stopped. An efficacy rate of 93% was reported. The compassionate use program and emergency use study were however not subjected to the rigorous standards and monitoring of a clinical trial; hence, a potential for biased and unreliable reporting.
There were, however, two randomized, double blind, multicenter dose-finding trials that assessed control of bleeding in non-surgical and surgical bleeding respectively. In the nonsurgical trial (Lusher et al 1998), 84 patients were treated with either 35 ?g/kg or 70 ?g/kg of rFVIIa given 2?3 hourly, for joint, muscle and mucocutaneous bleeding. Both doses were considered to be equally efficacious with excellent or effective response in 71% of patients. The second randomized trial (Shapiro et al 1998) compared a dose of 35 ?g/kg against 90 ?g/kg in the initiation and maintenance therapy for bleeding during and after surgery. Intra-operative hemostasis was achieved in 28 of 29 patients. All 14 high dosed patients and 12 of 15 low-dosed patients had adequate hemostasis during the first 48 hours. The higher dose was adjudged to be more effective.
Accumulated evidence over the years has mostly shown rFVIIa to be effective in the management of bleeding episodes. Alternative bypassing agents are largely preparations of prothrombin complexes in activated or nonactivated forms. Evidence of efficacy for these alternatives is best described for FEIBA (factor eight bypassing activity), an activated prothrombin complex. In a double blind comparison with a non-activated prothrombin complex, effective non-surgical hemostasis was achieved in 64% vs 52% of hemophilia A patients, in favor of FEIBA (Sjamsoedin et al 1981). More recent reports suggest an efficacy rate closer to 80% in both surgical and non-surgical bleeding (Negrier et al 1997; Hilgartner et al 1990). A randomized multi-center equivalence study comparing the efficacy of rFVIIa against FEIBA (FENOC) has also recently been published in abstract form (Berntorp et al 2005). Sixty-six hemophilia A patients were randomized to either one dose of FEIBA or two doses of rFVIIa for bleeding episodes. At 6 hours, 76.1% of FEIBA treated patients reported cessation of bleeding, in comparison to 65.2% receiving rFVIIa (confidence intervals for equivalence ?2.7%, 24.5%). Equivalence could not be concluded for response at 6 hours though they were determined to be of similar efficacy at 24 and 48 hours. Despite these inconsistencies, it appears that the two products may have similar efficacy.
Early experience and dose finding trials of rFVIIa have suggested that a dose of 90?120 ?g/kg confers adequate hemostatic effect for most surgical and non-surgical bleeding. The initial dose should be high enough to maintain a plasma level of FVII-coagulant activity (FVII:C) of >6 U/mL for several hours (Hedner 1996). Dosing intervals of 2 hours are recommended, until hemostasis is achieved, irrespective of bleeding etiology or location. Higher doses of rFVIIa which, supposedly, ensure the generation of a full thrombin burst, have been touted to be more efficacious (Cooper et al 2001). A full thrombin burst is necessary for the formation of a stable hemostatic plug with a tight fibrin structure, and decrease susceptibility to fibrinolysis (Blomback et al 1994). Besides plasma concentration, early administration of rFVIIa is also important for effective control of bleeding (Lusher 2000). Strategies targeting these two areas have been studied to optimize treatment.
Incremental doses of rFVIIa have been investigated by various workers to determine if such a strategy leads to better control of bleeding without a significant increase in cost (Table 1). Kenet and colleagues compared an augmented versus a standard protocol of rFVIIa administration in a small study population. Initial bolus doses were doubled from 90 ?g/kg to 180 ?g/kg with an increase in infusion rates from 15 ?g/kg/h to 30 ?g/kg/h and a reduction in total infusion duration from 12 to 6 hours (Kenet et al 2000). Shorter response time and duration of therapy was demonstrated in the augmented protocol. These two protocols were subsequently compared with a megadose protocol using a single dose of 300 ?g/kg (Kenet et al 2003). Pain relief and response was fastest with the megadose protocol and most preferred by patients. However, it consumed more rFVIIa per bleed than the standard protocol, but less than the augmented protocol. No serious safety issues were observed. The greater efficacy of high dose rFVIIa was also suggested by a retrospective analysis of data from the Haemophilia and Thrombophilia Research Society Registry (Parameswaran et al 2005). Bleeding episodes were grouped according to the bolus rFVIIa dose used (Table 1). The highest efficacy was achieved in the group given >200 ?g/kg (97%, compared with 84% in the 3 lower dose groups, p < 0.001). Doses as high as 346 ?g/kg were used without apparent safety issues.
Two multi-center prospective randomized trials have compared the use of high dose rFVIIa against standard doses for home treatment of hemarthroses. The first study was open-labeled and compared a standard dose of 90 ?g/kg (repeated every 3 hourly if necessary) against a single dose of 270 ?g/kg in a total of 68 bleeding episodes (Santagostino et al 2006). Success rates were identical at all time points (66% for standard dose vs 64% for high dose at 48 hours) as was the total dose of rFVIIa used. The second study was double blinded and used either 3 single doses of 90 ?g/kg or a dose of 270 ?g/kg with two placebo doses, given at 3-hour intervals (Kavakli et al 2006). No significant difference in efficacy was found (65% for high dose versus 70% for standard dose). Both studies did not identify significant safety issues with the high dose regimen. The authors of both papers surmised that high dose treatment may be preferred by patients because of the convenience of single administration, without a significant increase in consumption of rFVIIa. The data on megadosing are, however, immature and need to be further investigated.
Early treatment of bleeding episodes in hemophiliacs is generally accorded with a greater rate of success and a reduction in damage cause by the bleeding. Analysis of experiences from the compassionate use program, dose finding trials as well as the US home treatment study, showed that the highest rate of efficacy and lowest dose requirement of rFVIIa was found in the home treatment group (Lusher 1998). An efficacy rate of 92% with a mean of 2.3 doses was achieved, which was superior to rates achieved when late treatment was given. The interval between the onset of bleeding and administration of rFVIIa appears crucial and various trials have studied early treatment with rFVIIa at home (Ingerslev et al 1998; Key et al 1998; Laurian et al 1998; Santagostino et al 1999; Santagostino et al 2006; Kavakli et al 2006).
Four studies have investigated home treatment with rFVIIA at a standard dose of 90 ?g/kg given repeatedly every 2?4 hours, if necessary, for up to 12 hours (Ingerslev et al 1998; Key et al 1998; Laurian et al 1998; Santagostino et al 1999). Treatment was safe and effective in 79%?93% of bleeding episodes. Santagostino et al demonstrated that the risk for partially effective or ineffective response was smaller for treatment started within 6 hours of the onset of bleeding than for those started later (OR 0.24, 95% CI, 0.09?0.63) (Santagostino et al 1999). Early treatment was also significantly associated with lower rFVIIa usage (median 1.5 doses vs 3, p = 0.07). A significant improvement in response rate and reduction in doses used was associated with early treatment in all the 4 studies.
Continuous infusion (CI) regimens theoretically offer the advantage of avoiding the repeated bolus dosing needed to maintain adequate plasma FVII: C concentrations, with a potential for reduction in overall rFVIIa requirement. Surgical patients could derive most benefit because rFVIIa needs to be given for a few days after surgery. Since the first feasibility study by Schulman and colleagues (1996), there have been various studies on CI of rFVIIa at different infusion rates for surgical procedures and bleeding episodes (Mauser-Bunschoten et al 1998; Montoro et al 1998; Kenet et al 2000; Smith et al 2001; Mauser-Bunschoten et al 2002; Ludlam et al 2003). Several studies use an initial bolus dose of 90?120 ?g/kg followed by CI at a rate of 16.5?18 ?g/kg/h, with subsequent adjustments aiming to achieve a FVII: C level of >10 U/ml (Mauser-Bunschoten et al 1998; Montoro et al 1998; Kenet et al 2000; Mauser-Bunschoten et al 2002). Results have however been inconsistent. Higher infusion rates and augmented regimens to achieve a higher FVII: C level have therefore been investigated. Kenet et al (2000) used an initial dose of 180 ?g/kg followed by an infusion of 30 ?g/kg/h. This was 100% effective in securing hemostasis for surgical intervention and 72% effective for non-surgical bleeding. Ludlam et al (2003) reported on a regimen using 90 ?g/kg as an initial dose, followed by 50 ?g/kg/h for major orthopedic surgery. This achieved a FVII: C of 30 U/mL and appears to provide good hemostatic control. Such augmented dosing may however use substantially more rFVII than conventional CI, standard repeated boluses or even megadosing (Kenet et al 2003).
Despite theoretical advantages, the place of CI therapy and its optimal delivery and cost-effectiveness remains controversial. CI may be considered for surgery, complicated bleeding or delayed treatment, where prolonged therapy may be required (Abshire and Kenet 2004). The current concept which places importance on an adequate thrombin burst to achieve effective hemostasis, will further cloud this picture, as this phenomenon is better achieved with the high plasma concentration of rFVIIa that follows the administration of large bolus doses.
RFVIIa has allowed thousands of inhibitor patients to undergo otherwise high risk elective and emergency surgeries successfully. Both bolus (Ingerslev et al 1996; Lusher et al 1998; Shapiro et al 1998; Hvid and Rodriguez-Merchan 2002) and CI regimens (Schulman et al 1996; Mauser-Bunschoten et al 1998; Montoro et al 1998; Kenet et al 2000; Smith et al 2001; Mauser-Bunschoten et al 2002; Ludlam et al 2003) have been studied in patients undergoing surgery. Lusher et al (1998) analyzed data on 103 surgical procedures with most patients given an initial dose of 90 ?g/kg (range 60?120 ?g/kg). Responses were rated as excellent in 81% of major surgical procedures, 86% of and minor procedures and 92% of dental procedures. In a study by Shapiro et al (1998), bolus doses of 90 ?g/kg were repeated every 2 hours for 48 hours, followed by 2- to 6hour intervals for the next 3 days, and all patients had satisfactory control of bleeding at 48 hours. This regimen was superior to the comparative regimen of 35 ?g/kg and is the most commonly used bolus regimen dose. A recent consensus meeting on inhibitor management strategies in surgeries made the following recommendations (Rodriguez-Merchan et al 2004). For minor procedures, a bolus dose of 90?120 ?g/kg given 2 hourly for up to 4 doses, followed by 3- to 6-hour redosing for 24 hours is recommended. For major surgeries, a starting dose of 120 ?g/kg (150 ?g/kg for pediatrics), followed by 90?120 ?g/kg 2 hourly for the first day, is recommended. Subsequent dosing intervals are 3 hourly for day 2, 4 hourly for days 3?5, and 6 hourly thereafter as necessary.
Rates for continuous infusion are less well defined with limited evidence for more specific recommendations. The same consensus meeting recommended infusion rates ranging from 15?50 ?g/kg/h for up to 14 days. There has also been no direct comparison between bolus dosing regimens against continuous infusion protocols.
Thrombotic concerns are understandable with a pro-hemostatic agent such as rFVIIa and thrombogenic potentials of alternative agents such as FEIBA and other prothrombin complexes have been well described (Kohler 1999, Ehrlich et al 2002). Thrombotic events related to the use of rFVIIa in hemophiliacs and other bleeding conditions have however been low since its first introduction. This is largely attributed to its action on activated platelets at sites of bleeding only, and not systemically. Abshire and Kenet (2004) reviewed 25 reported thrombotic events in hemophiliacs and found that a predisposing cause was found in 15/18 (83%) spontaneously reported cases and 5 of 7 (71%) clinical trial patients. Eleven of the 25 patients had received concomitant therapy with activated prothrombin complexes or antifibrinolytic agents. This is consistent with our experience of a young patient developing deep vein thrombosis following sequential use or rFVIIa and prothrombin complexes (Ng et al 2004).
A recent review of adverse events reported to the FDA suggests that most thromboembolic events are associated with use of rFVIIa for ?off-label? indications, with serious morbidity and mortality (O?Connell et al 2006). Pre-existing risk factors for thromboembolic events were strongly associated with these events. In the most compelling evidence of possible thromboembolic risk associated with rFVIIa, serious thromboembolic event rates of 7% (mainly myocardial and cerebral infarction) were reported in a randomized placebo controlled study of rFVIIa for intracerebral hemorrhage involving 399 patients (Mayer et al 2005). This was in comparison to 2% in patients receiving the placebo (p = 0.12). While the characteristics of patients with respect to underlying medical conditions were not well defined, it is likely that the subjects (median age in study groups between 64?68 years) in this study represent an ?at risk population?. Furthermore, the incidence of these events, expressed as a percentage of the number of patients in each study group, was highest (10%) in those receiving 160 ?g/kg, the highest dosage used. Using data from the FDA pharmacovigilance program, thrombotic events after rFVIIa have also been compared against FEIBA and appear to be more frequent for rFVIIa (incidence rate ratio, 2.98; CI 1.71?5.52) (Aledort 2004).
As larger doses and more intensified regimens are being studied for hemophiliacs, thrombotic risks with rFVIIa need to be better characterized. It remains to be defined what a ?safe? dosing regimen will be, especially for older patients.
As with the use of clotting factor replacement in the hemophilias, there have been concerns about the possibility of inhibitor development against rVIIa in patients receiving this therapy. This has so far proved unfounded among the hemophiliacs. Nicolaisen followed up a series of 267 patients given rFVIIa, (including 238 hemophiliacs) for over 9 years with no evidence of inhibitor development (Nicolaisen et al 1998). In contrast, antibodies to rFVIIa have been isolated among 6 patients with hemophilia A and B with high responding inhibitors (Astermark et al 2002). Because of multiple exposure to other bypassing and blood products, causality with use of rFVIIa could not be assigned. Other studies and ongoing experience have not unveiled significant development of inhibitors against rFVIIa among hemophiliacs. At this juncture, the potential for development of inhibitors against rFVIIa in hemophiliacs have not been conclusively disproved and vigilance, as in patients with factor VII deficiency, must continue.
As a bypassing agent, rFVIIa does not fully replicate the effectiveness of pure factor replacement therapy for bleeding episodes in hemophiliacs without inhibitors, nor allow prophylaxis against spontaneous bleeding events. Responses, while impressive, are less than universal and remain unpredictable. It has, nonetheless, advanced the treatment of this unfortunate group of patients and allowed them to benefit from many elective and emergency surgical procedures. rFVIIa's success with hemophiliacs has been extrapolated to an increasing number of ?off-label? indications. Exciting work is currently taking shape for these new indications with more randomized well-controlled trials being conducted. Rather than diverting attention away from hemophiliacs, these studies have produced valuable data with respect to many unresolved issues in hemophiliacs, such as improved dosing strategies and safety data. rFVIIa, in combination with normal clotting factor replacement, may even play a role in better controlling difficult bleeding situations in hemophiliacs without inhibitors.
For the present, outstanding issues that can be surmised from this review are as follows: (Table 2)
- Optimal dosing strategies remain inadequately defined. While the trend is towards higher bolus and CI doses, it is likely that the chosen optimal dose will need to be tailored to the individual patient and clinical situation, for this strategy to be cost effective. There will be a limit on the quantum of rFVIIa that can be given, after which no further significant benefit can be derived and safety and cost effectiveness becomes compromised.
- Objective and easily obtainable measures of adequate response, which may be based on thrombin generation, thromboelastography, plasma concentrations, or combinations of these and other surrogate markers, need to be further developed for this issue of optimal dosing to be resolved.
- For a treatment that is extremely expensive, cost-effectiveness remains of utmost importance and must form part of the equation in any true ?optimal dosing?. A greater role for FEIBA in this aspect cannot be ignored.
- There is a place for both bolus dosing and continuous infusion strategies but CI protocols need to be better defined. Efforts should also continue to develop more user-friendly and effective early home treatment strategies, which can provide better outcomes.
- While remarkably safe so far, safety concerns will likely feature more prominently once this agent is extended to a wider spectrum of patients. Current studies that dispel concerns about thromboembolic risks with incremental doses were confined to young subjects. As this dosing strategy becomes more accepted, it is likely that older patients with significant thromboembolic risk factors will be included and challenge this notion of safety.
Finally, with these shortcomings, we should continue our search for the ideal bypassing agent ? one that is universally effective, cheap, easily administered, has a long half-life, suitable for prophylaxis strategies, uniform in dose requirement and, ultimately, safe.
|Abshire T,Kenet G. Recombinant factor VIIa: review of efficacy, dosing regimens and safety in patients with congenital and acquired factor VIII or IX inhibitorsJ Thromb Haemost 2004;2:899–909. [pmid: 15140125]|
|Aledort LM. Comparative thrombotic event incidence after infusion of recombinant factorVIIa versus factor VIII inhibitor bypass activityJ Thromb Haemost 2004;2:1700–8. [pmid: 15456478]|
|Allen G,Aledort L. Therapeutic decision-making in inhibitor patientsAm J Hematol 2006;81:71–2. [pmid: 16369965]|
|Arkin S,Cooper HA,Hutter JJ,et al. Activated recombinant human coagulation factor VII therapy for intracranial hemorrhage in patients with hemophilia A or B with inhibitors. Results of the novoseven emergency-use programHaemostasis 1998;28:93–8. [pmid: 10087434]|
|Arkin S,Blei F,Fetten J,et al. Human coagulation factor FVIIa (recombinant) in the management of limb-threatening bleeds unresponsive to alternative therapies: results from the NovoSeven emergency-use programme in patients with severe haemophilia or with acquired inhibitorsBlood Coagul Fibrinolysis 2000;11:255–9. [pmid: 10870806]|
|Astermark J,Ekman M,Berntorp E. Antibodies to factor VIIa in patients with haemophilia and high-responding inhibitorsBr J Haematol 2002;119:342–7. [pmid: 12406066]|
|Bech RM. Recombinant factor VIIa in joint and muscle bleeding episodesHaemostasis 1996;26(Suppl 1):135–8. [pmid: 8904188]|
|Berntorp E,Donfield S,Waters J,et al. The FEIBA(R) NovoSeven(R) Comparative Study (FENOC)?A Randomized Evaluation of By-Passing Agents in Hemophilia Complicated by InhibitorsASH Annual Meeting Abstracts 2005;106:324.|
|Blomback B,Carlsson K,Fatah K,et al. Fibrin in human plasma: gel architectures governed by rate and nature of fibrinogen activationThromb Res 1994;75:521–38. [pmid: 7992253]|
|Cooper HA,Jones CP,Campion E,et al. Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic proceduresHaemophilia 2001;7:517–22. [pmid: 11554944]|
|Ehrenforth S,Kreuz W,Scharrer I,et al. Incidence of development of factor VIII and factor IX inhibitors in haemophiliacsLancet 1992;339:594–8. [pmid: 1347102]|
|Ehrlich HJ,Henzl MJ,Gomperts ED. Safety of factor VIII inhibitor bypass activity (FEIBA): 10-year compilation of thrombotic adverse eventsHaemophilia 2002;8:83–90. [pmid: 11952842]|
|Hedner U. Factor VIIa in the treatment of haemophiliaBlood Coagul Fibrinolysis 1990;1:307–17. [pmid: 2103315]|
|Hedner U. Dosing and monitoring NovoSeven treatmentHaemostasis 1996;26(Suppl 1):102–8. [pmid: 8904183]|
|Hedner U. Mechanism of action of recombinant activated factor VII: an updateSemin Hematol 2006;43(Suppl 1):S105–7. [pmid: 16427375]|
|Hedner U,Glazer S,Pingel K,et al. Successful use of recombinant factor VIIa in patient with severe haemophilia A during synovectomyLancet 1988;2:1193. [pmid: 2903400]|
|Hedner U,Kisiel W. Use of human factor VIIa in the treatment of two hemophilia A patients with high-titer inhibitorsJ Clin Invest 1983;71:1836–41. [pmid: 6408124]|
|Hilgartner M,Aledort L,Andes A,et al. Efficacy and safety of vapor-heated anti-inhibitor coagulant complex in hemophilia patients. FEIBA Study GroupTransfusion 1990;30:626–30. [pmid: 2402777]|
|Hvid I,Rodriguez-Merchan EC. Orthopaedic surgery in haemophilic patients with inhibitors: an overviewHaemophilia 2002;8:288–91. [pmid: 12010425]|
|Ingerslev J,Freidman D,Gastineau D,et al. Major surgery in haemophilic patients with inhibitors using recombinant factor VIIaHaemostasis 1996;26(Suppl 1):118–23. [pmid: 8904185]|
|Ingerslev J,Thykjaer H,Kudsk Jensen O,et al. Home treatment with recombinant activated factor VII: results from one centreBlood Coagul Fibrinolysis 1998;9(Suppl 1):S107–10. [pmid: 9819039]|
|Kavakli K,Makris M,Zulfikar B,et al. NovoSeven trial (F7HAEM-1510) investigators. Home treatment of haemarthroses using a single dose regimen of recombinant activated factor VII in patients with haemophilia and inhibitors. A multi-centre, randomised, double-blind, cross-over trialThromb Haemost 2006;95:600–5. [pmid: 16601828]|
|Kenet G,Lubetsky A,Gitel S,et al. Treatment of bleeding episodes in patients with hemophilia and an inhibitor: comparison of two treatment protocols with recombinant activated factor VIIBlood Coagul Fibrinolysis 2000;11(Suppl 1):S35–8. [pmid: 10850562]|
|Kenet G,Lubetsky A,Luboshitz J,et al. A new approach to treatment of bleeding episodes in young hemophilia patients: a single bolus megadose of recombinant activated factor VII (NovoSeven)J Thromb Haemost 2003;1:450–5. [pmid: 12871449]|
|Key NS,Aledort LM,Beardsley D,et al. Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitorsThromb Haemost 1998;80:912–8. [pmid: 9869160]|
|Kohler M. Thrombogenicity of prothrombin complex concentratesThromb Res 1999;95(4 Suppl 1):S13–7. [pmid: 10499904]|
|Kreuz W,Ettingshausen CE,Zyschka A,et al. Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant productsSemin Thromb Hemost 2002;28:285–90. [pmid: 12098090]|
|Laurian Y,Goudemand J,Negrier C,et al. Use of recombinant activated factor VII as first line therapy for bleeding episodes in haemophiliacs with factor VIII or IX inhibitorsBlood Coagul Fibrinolysis 1998;9:155–156.|
|Levi M,Peters M,Buller HR. Efficacy and safety of recombinant factor VIIa for treatment of severe bleeding: a systematic reviewCrit Care Med 2005;33:883–90. [pmid: 15818119]|
|Lindley CM,Sawyer WT,Macik BG,et al. Pharmacokinetics and pharmacodynamics of recombinant factor VIIaClin Pharmacol Ther 1994;55:638–48. [pmid: 8004880]|
|Ludlam CA. The evidence behind inhibitor treatment with recombinant factor VIIaPathophysiol Haemost Thromb 2002;32(Suppl 1):13–8. [pmid: 12214140]|
|Ludlam CA,Smith MP,Morfini M,et al. A prospective study of recombinant activated factor VII administered by continuous infusion to inhibitor patients undergoing elective major orthopaedic surgery: a pharmacokinetic and efficacy evaluationBr J Haematol 2003;120:808–13. [pmid: 12614214]|
|Lusher JM. Early treatment with recombinant factor VIIa results in greater efficacy with less productEur J Haematol Suppl 1998;63:7–10. [pmid: 9882925]|
|Lusher JM. Acute hemarthroses: the benefits of early versus late treatment with recombinant activated factor VIIBlood Coagul Fibrinolysis 2000;11(Suppl 1):S45–9. [pmid: 10850564]|
|Lusher JM. First and second generation recombinant factor VIII concentrates in previously untreated patients: recovery, safety, efficacy, and inhibitor developmentSemin Thromb Hemost 2002;28:273–6. [pmid: 12098088]|
|Lusher JM,Roberts HR,Davignon G,et al. A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors. rFVIIa Study GroupHaemophilia 1998;4:790–8. [pmid: 10028299]|
|Mauser-Bunschoten EP,de Goede-Bolder A,Wielenga JJ,et al. Continuous infusion of recombinant factor VIIa in patients with haemophilia and inhibitors. Experience in The Netherlands and BelgiumNeth J Med 1998;53:249–55. [pmid: 9883002]|
|Mauser-Bunschoten EP,Koopman MM,Goede-Bolder AD,et al. Recombinant Factor VIIa Data Collection Group. Efficacy of recombinant factor VIIa administered by continuous infusion to haemophilia patients with inhibitorsHaemophilia 2002;8:649–56. [pmid: 12199674]|
|Mayer SA,Brun NC,Begtrup K,et al. Recombinant Activated Factor VII Intracerebral Hemorrhage Trial Investigators. Recombinant activated factor VII for acute intracerebral hemorrhageN Engl J Med 2005;352:777–85. [pmid: 15728810]|
|Montoro JB,Altisent C,Pico M,et al. Recombinant factor VIIa in continuous infusion during central line insertion in a child with factor VIII high-titre inhibitorHaemophilia 1998;4:762–5. [pmid: 9873885]|
|Munro FL,Jones HW. The detrimental effect of frequent transfusions in the treatment of a patient with hemophiliaAm J M Sc 1943;206:107.|
|Negrier C,Goudemand J,Sultan Y,et al. Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing ActivityThromb Haemost 1997;77:1113–9. [pmid: 9241742]|
|Ng HJ,Loh SM,Tan DC,et al. Thrombosis associated with the use of recombinant activated factor VII:profiling two eventsThromb Haemost 2004;92:1448–9. [pmid: 15624250]|
|Nicolaisen EM. Antigenicity of activated recombinant factor VII followed through nine years of clinical experienceBlood Coagul Fibrinolysis 1998;9(Suppl 1):S119–23. [pmid: 9819042]|
|O?Connell KA,Wood JJ,Wise RP,et al. Thromboembolic adverse events after use of recombinant human coagulation factor VIIaJAMA 2006;295:293–8. [pmid: 16418464]|
|Parameswaran R,Shapiro AD,Gill JC,et al. HTRS Registry Investigators. Dose effect and efficacy of rFVIIa in the treatment of haemophilia patients with inhibitors: analysis from the Hemophilia and Thrombosis Research Society RegistryHaemophilia 2005;11:100–6. [pmid: 15810910]|
|Rice KM,Savidge GF. NovoSeven (recombinant factor VIIa) in central nervous systems bleedsHaemostasis 1996;26(Suppl 1):131–4. [pmid: 8904187]|
|Rodriguez-Merchan EC,Rocino A,Ewenstein B,et al. Consensus perspectives on surgery in haemophilia patients with inhibitors: summary statementHaemophilia 2004;10(Suppl 2):50–2. [pmid: 15385047]|
|Santagostino E,Gringeri A,Mannucci PM. Home treatment with recombinant activated factor VII in patients with factor VIII inhibitors: the advantages of early interventionBr J Haematol 1999;104:22–6. [pmid: 10027707]|
|Santagostino E,Mancuso ME,Rocino A,et al. A prospective randomized trial of high and standard dosages of recombinant factor VIIa for treatment of hemarthroses in hemophiliacs with inhibitorsJ Thromb Haemost 2006;4:367–71. [pmid: 16420567]|
|Scharrer I. Recombinant factor VIIa for patients with inhibitors to factor VIII or IX or factor VII deficiencyHaemophilia 1999;5:253–9. [pmid: 10469179]|
|Scharrer I,Bray GL,Neutzling O. Incidence of inhibitors in haemophilia A patients a review of recent studies of recombinant and plasma-derived factor VIII concentratesHaemophilia 1999;5:145–54. [pmid: 10444280]|
|Schulman S,Bech Jensen M,et al. Feasibility of using recombinant factor VIIa in continuous infusionThromb Haemost 1996;75:432–6. [pmid: 8701403]|
|Shapiro AD,Gilchrist GS,Hoots WK,et al. Prospective, randomised trial of two doses of rFVIIa (NovoSeven) in haemophilia patients with inhibitors undergoing surgeryThromb Haemost 1998;80:773–8. [pmid: 9843170]|
|Sjamsoedin LJ,Heijnen L,Mauser-Bunschoten EP,et al. The effect of activated prothrombin-complex concentrate (FEIBA) on joint and muscle bleeding in patients with hemophilia A and antibodies to factor VIII. A double-blind clinical trialN Engl J Med 1981;305:717–21. [pmid: 6790990]|
|Smith MP,Ludlam CA,Collins PW,et al. Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII: plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleedingThromb Haemost 2001;86:949–53. [pmid: 11686351]|
|Villar A,Aronis S,Morfini M,et al. Pharmacokinetics of activated recombinant coagulation factor VII (NovoSeven) in children vs. adults with haemophilia AHaemophilia 2004;10:352–9. [pmid: 15230949]|
|von Depka M. Managing acute bleeds in the patient with haemophilia and inhibitors: options, efficacy and safetyHaemophilia 2005;11(Suppl 1):18–23. [pmid: 16219045]|
|Warrier I,Lusher JM. Development of anaphylactic shock in haemophilia B patients with inhibitorsBlood Coagul Fibrinolysis 1998;9(Suppl 1):S125–8. [pmid: 9819043]|
Efficacy of rFVIIa at different bolus dose regimens for the treatment of acute non-surgical bleeding in hemophilia A and B patients with inhibitors
|Study||Type of bleeding||Number of episodes (no. of patients, where available)||Dose (?g/kg)||Number of doses used per bleed||Effective response (%)|
|Lusher et al 1998RCT||Joint/muscle/mucocutaneous||Joint?59 Muscle?15||35||Joint?2.7 Muscle?3.5||71 53|
|Lusher et al 1998RCT||Joint/muscle/mucocutaneous||Joint?85 Muscle?14||70||Joint?3.1 Muscle?3.6||71 72|
|Bech 1996a||Joints/muscle||494(111)||60?120||11?65||Joints?79 Muscle?65|
|Rice and Savidge 1996a||Central nervous system (CNS)||29 (21)||80?100||2?332||84|
|Arkin et al 1998a||Intracranial||13 (12)||90||96.9||83|
|Scharrer 1999a||Joints and other sites||45(23)||90||46.8||69|
|Kenet et al 2003||Joints and others||114 (3)||300||1||83b|
|Parameswaran et al 2005||Joint/muscle/mucocutaneous||146||<100||4.3||85|
|Santagostino et al 2006RCT||Joints||36(18)||270||1||64b|
|Kavakli et al 2006RCT||Joints||20(20)||270||1||65b|
aStudies include non-hemophilic patients and were part of the Compassionate Use Program and Emergency Use Study.
bResults of efficacy was analyzed after single dose of rFVIIa (as allowed by protocols).
Abbreviations: RCT, randomized controlled trials.
Unresolved issues with recombinant activated factor VII use in hemophiliacs
Keywords: recombinant activated factor VII, hemophilia, inhibitors, bleeding.
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