» Articles » PMID: 23282031

SURgical Interventions with FEIBA (SURF): International Registry of Surgery in Haemophilia Patients with Inhibitory Antibodies

Overview
Journal Haemophilia
Specialty Hematology
Date 2013 Jan 4
PMID 23282031
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Factor VIII Inhibitor Bypassing Activity (FEIBA) can effectively achieve haemostasis in haemophilia patients with inhibitors. Further evaluation of FEIBA in surgical settings is of significant interest considering the relatively limited prospective data published to date. The aim of the study is to evaluate the perioperative efficacy and safety of FEIBA in haemophilia patients with inhibitors. Haemophilia patients with inhibitors who underwent surgical procedures and received FEIBA for perioperative haemostatic control were prospectively enrolled in an open-label, noninterventional, postauthorization study [SURgical interventions with FEIBA (SURF)]. Outcome measures included haemostatic efficacy, safety, FEIBA exposure and blood loss associated with the perioperative use of FEIBA. Thirty-five surgical procedures were performed at 19 centres worldwide in patients with congenital haemophilia A, congenital haemophilia B, or acquired haemophilia A. Haemorrhagic risk was severe in 37.1% (13 of 35) of the procedures, moderate in 25.7% (9 of 35) and mild in 37.1% (13 of 35). One moderate risk surgery was excluded from the efficacy analyses because it did not meet all protocol requirements. Haemostasis was judged to be 'good' or 'excellent' in 91.2% (31 of 34) of surgical procedures and 'fair' in 8.8% (3 of 34). Among the 12 adverse events, three were serious adverse events (SAEs), two of which were unrelated to FEIBA therapy; one SAE, a clot in an arteriovenous fistula, was deemed to be possibly related to therapy. This prospective investigation confirms that FEIBA can be safely and effectively used when performing surgical procedures in haemophilia patients with inhibitors.

Citing Articles

Major Orthopaedic Surgery in Persons with Haemophilia A with and without Inhibitors Treated by Emicizumab: A Mid-Term, Large, and Successful Series at a Single Center.

Carulli C, Daniele G, Linari S, Pieri L, Littera M, Mazzetti M J Clin Med. 2024; 13(9).

PMID: 38731175 PMC: 11084841. DOI: 10.3390/jcm13092646.


Real-world data in patients with congenital hemophilia and inhibitors: final data from the FEIBA Global Outcome (FEIBA GO) study.

Ettingshausen C, Hermans C, Holme P, Cid A, Khair K, Oldenburg J Ther Adv Hematol. 2023; 14:20406207231184323.

PMID: 37529276 PMC: 10387704. DOI: 10.1177/20406207231184323.


Management of haemophilia A with inhibitors: A regional cross-talk.

Peyvandi F, Kavakli K, El-Beshlawy A, Rangarajan S Haemophilia. 2022; 28(6):950-961.

PMID: 35868021 PMC: 9796719. DOI: 10.1111/hae.14638.


International consensus recommendations on the management of people with haemophilia B.

Hart D, Matino D, Astermark J, Dolan G, dOiron R, Hermans C Ther Adv Hematol. 2022; 13:20406207221085202.

PMID: 35392437 PMC: 8980430. DOI: 10.1177/20406207221085202.


Origins, Development, Current Challenges and Future Directions with Activated Prothrombin Complex Concentrate for the Treatment of Patients with Congenital Haemophilia with Inhibitors.

Brackmann H, Schramm W, Oldenburg J, Cano V, Turecek P, Negrier C Hamostaseologie. 2020; 40(5):606-620.

PMID: 32717751 PMC: 7772007. DOI: 10.1055/a-1159-4273.