Literature DB >> 25126352

Modeling costs and outcomes associated with a treatment algorithm for problem bleeding episodes in patients with severe hemophilia a and high-titer inhibitors.

Patrick Bonnet1, Alessandro Gringeri2, Edward Gomperts3, Cindy Anne Leissinger4, Roseline d'Oiron5, Jerome Teitel6, Guy Young7, Meg Franklin8, Bruce Ewenstein9, Erik Berntorp10.   

Abstract

BACKGROUND: No evidence-based treatment guidelines are currently available for the treatment of problem bleedings in patients with hemophilia who develop clotting factor inhibitors. A treatment algorithm was developed previously to help providers optimize the approach to the treatment of this patient population. The algorithm provides the specific intervals between treatments; however, it does not specify dosing recommendations and does not offer insights into the likelihood of outcome improvements at each time interval.
OBJECTIVE: To develop a model to analyze the impact on patient outcomes and costs of adhering to a current treatment algorithm for the 2 available clotting therapies to treat bleeding episodes in patients with hemophilia who develop clotting factor inhibitors.
METHODS: A simulation model was developed using a modified Delphi method approach based on a consensus opinion of an expert panel. The model was used to analyze the impact of following the available treatment algorithm on patient outcomes and costs. Treatment patterns and the likelihood of a resolved bleeding episode associated with following the treatment algorithm (ie, adherence) were compared with not following the algorithm (ie, nonadherence). This model assumed 2 scenarios in which treatment was initiated with each of the 2 bypassing agents currently available, and clinical and economic outcomes were mapped for adhering to and not adhering to the consensus treatment algorithm.
RESULTS: The simulation model shows that adhering to the treatment algorithm would result in 74.4% of patients improving at 72 hours compared with only 56.7% of patients when not adhering to the algorithm. According to this model, regardless of the bypassing agent used at initiation, adherence to the treatment algorithm would result in fewer patients requiring combined sequential therapy with the 2 bypassing agents for 3 days. In addition, using this analytic model, reducing the percentage of patients with hemophilia who required combined sequential therapy by 17.6% resulted in an average cost-savings of $16,305 per patient.
CONCLUSION: Adherence to an algorithm in which treatment is altered at regular intervals based on a patient's clinical response has the potential to improve patient outcomes and reduce the number of nonresponsive patients requiring sequential therapy in patients with hemophilia who have clotting factor inhibitors and are experiencing problem bleeding episodes. >Adherence to the algorithm would also result in reduced costs to patients and payers.

Entities:  

Year:  2011        PMID: 25126352      PMCID: PMC4125756     

Source DB:  PubMed          Journal:  Am Health Drug Benefits        ISSN: 1942-2962


  20 in total

Review 1.  Inhibitors: resolving diagnostic and therapeutic dilemmas.

Authors:  D Dimichele
Journal:  Haemophilia       Date:  2002-05       Impact factor: 4.287

2.  Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors.

Authors:  N S Key; L M Aledort; D Beardsley; H A Cooper; G Davignon; B M Ewenstein; G S Gilchrist; J C Gill; B Glader; W K Hoots; C T Kisker; J M Lusher; C G Rosenfield; A D Shapiro; H Smith; E Taft
Journal:  Thromb Haemost       Date:  1998-12       Impact factor: 5.249

3.  The use of factor eight inhibitor by-passing activity (FEIBA immuno) product for treatment of bleeding episodes in hemophiliacs with inhibitors.

Authors:  M W Hilgartner; G L Knatterud
Journal:  Blood       Date:  1983-01       Impact factor: 22.113

4.  A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative (FENOC) Study.

Authors:  Jan Astermark; Sharyne M Donfield; Donna M DiMichele; Alessandro Gringeri; Steven A Gilbert; Jennifer Waters; Erik Berntorp
Journal:  Blood       Date:  2006-09-21       Impact factor: 22.113

Review 5.  FEIBA: mode of action.

Authors:  P L Turecek; K Váradi; H Gritsch; H P Schwarz
Journal:  Haemophilia       Date:  2004-09       Impact factor: 4.287

6.  A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors.

Authors:  J Teitel; E Berntorp; P Collins; R D'Oiron; B Ewenstein; E Gomperts; J Goudemand; A Gringeri; N Key; C Leissinger; P Monahan; G Young
Journal:  Haemophilia       Date:  2007-05       Impact factor: 4.287

Review 7.  Diagnosis and treatment of congenital hemophilia with inhibitors a Latin American perspective.

Authors:  Raúl Pérez Bianco; Margareth Castro Ozelo; Paula Ribeiro Villaça; Maria Helena Solano; Guillermo Jimenez Cruze; Carlos Martinez Murillo; Jaime Garcia Chavez; Saul Mendoza; Ismael Rodriguez Grecco; Arlette Ruiz-Saez
Journal:  Medicina (B Aires)       Date:  2008       Impact factor: 0.653

8.  Unresponsiveness to factor VIII inhibitor bypassing agents during haemostatic treatment for life-threatening massive bleeding in a patient with haemophilia A and a high responding inhibitor.

Authors:  T Hayashi; I Tanaka; M Shima; K Yoshida; K Fukuda; Y Sakurai; T Matsumoto; J C Giddings; A Yoshioka
Journal:  Haemophilia       Date:  2004-07       Impact factor: 4.287

9.  Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs.

Authors:  S Ehrenforth; W Kreuz; I Scharrer; R Linde; M Funk; T Güngör; B Krackhardt; B Kornhuber
Journal:  Lancet       Date:  1992-03-07       Impact factor: 79.321

Review 10.  The action of high-dose factor VIIa (FVIIa) in a cell-based model of hemostasis.

Authors:  Maureane Hoffman; Dougald M Monroe
Journal:  Dis Mon       Date:  2003-01       Impact factor: 3.800

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  1 in total

1.  A Delphi Consensus Approach for Difficult-to-Treat Patients with Severe Hemophilia A without Inhibitors.

Authors:  Sreenivas P Veeranki; Priti Pednekar; Marlon Graf; Rifat Tuly; Michael Recht; Katharine Batt
Journal:  J Blood Med       Date:  2021-10-21
  1 in total

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