AHCDC PRACTICE guidelines


AHCDC PUBLICATIONS

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AHCDC JOINT PUBLICATIONS

2008- Publications

1. Biss, T.T., Chan, A.K., Blanchette, V.S., Iwenofu,L.N., McLimont, M. and Carcao, M.D. for the Association of Hemophilia Clinic Directors of Canada (AHCDC) and the Canadian Association of Nurses in Hemophilia Care (CANHC) (including Poon, M-C). The use of prophylaxis in 2663 children and audlts with haemophilia: results of the 2006 Canadian national haemophilia prophylaxis survey. Haemophilia, 14:923-930, 2008

2. Bowen, T., Cicardi, M., Bork,K., Zuraw, B., Frank, M., Ritchie, B., Farkas, H., Varga, L., ] Zingale, L.C., Binkley, K., Wagner, E., Adomaitis, P., Brosz, K., Burnham, J., Warrington, R., alicinsky, C., Mace, S., McCusker, C., Schellenberg, R., Celeste, L., Hebert, J., Valentine, K., Poon, M-C, Pineo, G., Serushago, B., Neurath, D., Yang, W., Lacuesta, G., Issekutz, A., Hamed, A., Kamra, P., Dean, J., Kanani, A., Stark, D., Rivard, G-E., Leith, E., Tsai, E., Waserman, S., Keith, P., Page, D., Marchesin, S. Canadian 2006 International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema. Annals of Allergy, Asthma and Immunology. 100 (Suppl 2): S30–S40, 2008

3.   Hull, R.D., Pineo, G.F., Rant, R., Liang, J., Cook, R., Solymoss, S., Poon, M-C., Raskob, G. for the LITE Trial Investigators. Home treatment with long-term low molecular weight heparin (tinzaparin) versus usual care oral anticoagulation for proximal vein thrombosis: efficacy, safety and impact on patient satisfaction and the post-thrombotic syndrome.  American Journal of Medicine (in press)

4.   Jackson, S., Beck, P., Buret, A.G., O’Conner, P.M., Meddings, J., Pineo, G. and Poon, M-C. Long term platelet responses to Helicobacter pylori eradication in Canadian patients with immune thrombocytopenic purpura. International Journal of Hematology 88:212-21, 2008  

5.   Jackson, S.C., Sinclair, G.D., Cloutier, S., Duan, Z., Rand, M.L. and Poon, M-C. Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation.  Blood (in press, DOI 10.1182 (blood-2008-06-165233).

6.   Moltzan, C.J., Anderson, D.A., Callum, J., Fremes, S., Hume, H., Mazer, D., Poon, M-C., Rivard, G., Rizoli, S. and Robinson, S. The evidence for the use of recombinant factor VIIa in massive bleeding: development of a transfusion policy framework. Transfusion Medicine, 18: 112–120, 2008

7.   Owen, C.J., Toze, C.L., Koochin, A., Forrest, D.L., Smith, C.A., Eaves, C.J., Jackson, S., Poon, M-C., Sinclair, G., Leber, B., Johnson, P.R.E., Macheta, A., Yin, J.A.L., Lister, T.A., Barnett, M.J., Fitzgibbon, J. New cases of familial platelet disorder with propensity to myeloid malignancy (FPD/AML) support the value of RUNX1 screening in MDS/AML. Blood (in press)

8. Préhu, C., Balamitsa, V., Moradkani, K., Luo, H.-Y., Poon, M-C., Chui, D.H., Wajcman, H. and Patrinos, G.P. Mutations in gene paralogues yielding an identical protein: Functional and evolutionary implications. American Journal of Hematology (in press)

9. .Poon, M-C. and Luke, K-H. Haemophilia care in China: achievements of a decade of World Federation of Hemophilia (WFH) Treatment Center Twinning activities. Haemophilia, 14:879-888, 2008

10. Rubinger, M., Lillicrap, D., Rivard, G.E., Teitel, J., Carcao, M., Hensman, C., Walker, I. and the Association of Hemophilia Clinic Directors of Canada (AHCDC) (including Poon, M-C.) A prospective surveillance study of factor VIII inhibitor development in the Canadian haemophilia A population following the switch to a recombinant factor VIII product formulated with sucrose. Haemophilia. (2); 14: 281-286, 2008

11.   Schulman, S., Eelde, A., Holmstrom, M., Stahlberg, G., Odeberg, J.,  Blombacks, M. Validation of a composite score for clinical severity of hemophilia. Journal of Thrombosis and Haemostasis, 2008, 6: 1113-1121

12. Stonebraker, J.S., Bolton-Maggs, P.H.B., Soucie, J., Walker, I., Brooker, M. A study of variations in the reported haemophilia A prevalence around the world. Haemophilia, 2010, 16, 20-32.

13. Teitel, J.M., Carcao, M., Lillicrap, D., Mulder, K., Rivard, G.E., St-Louis, J., Smith, F., Walker, I., Zourikian, N. Orthopaedic surgery in haemophilia patients with inhibitors:  a practical guide to haemostatic, surgical and rehabilitative care. Hemophilia 2009, 15, 227-239

2007 and prior Publications

  1. A founder von Willebrand factor haplotype association with type 1 von Willebrand disease. On 20 March 2003 an epublication on Blood first edition on line site.

  2. AHCDC (Association of Hemophilia Clinic Directors of Canada) Hemophilia And Von  Willebrands disease: 1. Diagnosis, comprehensive care and assessment. CMAJ  1995;153:19-25.

  3. AHCDC (Association of Hemophilia Clinic Directors of Canada) Hemophilia And Von Willebrands disease: 2. Management. CMAJ 1995;153:147-57.

  4. Arnold D.M, Julian J.A. and Walker I.R, for the Association of Hemophilia Clinic Directors of Canada. Mortality rates and causes of death among all HIV-positive individuals with hemophilia in Canada over 21 years of follow-up. Blood, 15 July 2006, Volume 108, Number 2, pages 460-464

  5. Arnold E, Heddle N, Lane S, Sek J, Almonte T, Walker I.  Handheld computers and paper diaries for documenting the use of factor concentrates used in haemophilia home therapy: a qualitative study. Haemophilia 11:216-226, 2005.

  6. Arnold DM, Webert KE, Carruthers J, Almonte T, Decker K, Seroski W. Reed J. Chan AKC, Pai M, Walker I..  Trends in the utilization and wastage of coagulation factor concentrates: the application of a regional tracking programme.  Haemophilia 13:3 271, 2007.

  7. Association of Hemophilia Clinic Directors of Canada. Causes of Death in Canadians with Hemophilia 1980-95. Hemophilia 1998;4:714-20

  8. Barnes C, Rivard GE, Poon MC, Teitel J, Pai M, Kern M, Blanchette VS, Carcao M; Inhibitor Subcommittee of Association of Hemophilia Clinic Directors of Canada. Canadian multi-institutional survey of immune tolerance therapy (ITT) - experience with the use of recombinant factor VIII for ITT.  Haemophilia. 2006 Jan;12(1):1-6.

  9. Barr RD, Sek J, Horsman J, Furlong W, Saleh M, Pai M, Walker IR.  Health Status and Health-Related Quality of Life Associated with von Willebrand Disease.  American Journal of Hematology 73:108-114, 2003.

  10. Blanchette V, Rivard G,  Israels S, Robinson S, Ali K, Walker I, Stain A.M, and Blanchette V, on behalf of the Association of Hemophilia Clinic Directors of Canada and the Canadian Association of Nurses in Hemophilia Care. A survey of factor prophylaxis in the Canadian haemophilia A population. Hemophilia (2004), 10, 679–68

  11. Blanchette V, Walker I, Gill P, Adams M, Roberts R, Inwood M, Canadian Hemophilia Clinic Directors Group. Hepatitis C Infection in Patients with Hemophilia. Results of a National Survey. Transfusion Medicine Reviews. 1994;8:210-217.

  12. Canadian Hemophilia Clinic Directors Group. Effect of using safer blood products on prevalence of HIV infection in haemophilic Canadians. Brit Med J 306: 306-7, 1993.

  13. Carcao M, St Louis J, Poon MC, Grunebaum E, Lacroix S, Stain AM, Blanchette VS, Rivard GE; Inhibitor Subcommittee of Association of Hemophilia Clinic Directors of Canada. Rituximab for congenital haemophiliacs with inhibitors: a Canadian experience. Haemophilia. 2006 Jan;12(1):7-18.

  14. Feldman BM, Pai M, Rivard GE, Israels S, Poon MC, Demers C, Robinson S, Luke KH, Wu JK, Gill K, Lillicrap D, Babyn P, McLimont M, Blanchette VS; Association of Hemophilia Clinic Directors of Canada Prophylaxis Study Group. Tailored prophylaxis in severe hemophilia A: interim results from the first 5 years of the Canadian Hemophilia Primary Prophylaxis Study. J Thromb Haemost. 2006 Jun;4(6):1228-36.

  15. Giles AR, Rivard GE, Teitel J, Walker I. Surveillance for factor VIII inhibitor development in the Canadian hemophilia population following the widespread introduction of recombinant factor VIII replacement therapy. Transfus Sci 1998; 19:139-147

  16. Giles AR, Verbruggen B, Rivard GE, Teitel J, Walker I and the Association of Hemophilia Centre Directors of Canada on behalf of the SSC Scientific Subcommittee on Factor VIII and Factor IX.A Detailed Comparison of the Performance of the Standard versus the Nijmegen Modification of the Bethesda Assay in Detecting Factor VIII:C Inhibitors in the Haemophilia A Population of Canada. Vol. 79(4), page 872.

  17. James P, Lillicrap D. Genetic testing for von Willebrand disease: the Canadian experience. Semin Thromb Hemost. 2006 Jul;32(5):546-52.

  18. James PD, Notley C, Hegadorn C, Leggo J, Tuttle A, Tinlin S, Brown C, Andrews C, Labelle A, Chirinian Y, O'Brien L, Othman M, Rivard G, Rapson D, Hough C, Lillicrap D. The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study. Blood. 2007 Jan 1;109(1):145-54.

  19. James PD, Paterson AD, Notley C, Cameron C, Hegadorn C, Tinlin S, Brown C, O'Brien L, Leggo J, Lillicrap D; ASSOCIATION OF HEMOPHILIA CLINIC DIRECTORS OF CANADA. Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study. J Thromb Haemost. 2006 Apr;4(4):783-92.

  20. Lane SJ, Heddle NM, Arnold E, Walker I. A review of randomized controlled trials comparing the effectiveness of hand held computers with paper methods for data collection.  BMC Medical Informatics and Decision Making, 6:23, 2006.

  21. O'Brien LA, James PD, Othman M, Berber E, Cameron C, Notley CR, Hegadorn CA, Sutherland JJ, Hough C, Rivard GE, O'Shaunessey D, Lillicrap D; Association of Hemophilia Clinic Directors of Canada. Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease.  Blood. 2003 Jul 15;102(2):549-57.

  22. Ota S, Mclimont M, Carcao MD, Blanchette VS, Graham N, Paradis E, Feldman BM.  Definitions for haemophilia prophylaxis and its outcomes: the Canadian consensus study. Haemophilia. 2007 Jan;13(1):12-20.

  23. James, PD, Notley C, Hegadorn C, Poon MC, Walker I, Rapson D, Association of Hemophilia Clinic Directors of Canada, Lillicrap D; Challenges in defining type 2M von Willebrand disease: resutls from a Canadian cohort study.  Journal of Thrombosis and Haemostasis 2007; 5: 1914-1922.
  24. Poon MC, Lillicrap D, Hensman C, Card R, Scully MF. Recombinant Factor IX Recovery and Inhibitor Safety: A Canadian Post-Licensure Surveillance Study. Thromb Haemost 2002; 87: 431-435

  25. Rubinger M, Lillicrap D, Rivarg GE, Teitel J, Carcao M, Hensman C, Walker I and the Association of Hemophilia Clinic Directors of Canada:  A Prospective Surveillance Study of Factor VIII Inhibitor Development in the Canadian Hemophilia A  Population Following the Switch to a Recombinant Factor VIII Product formulated with Sucrose.  Haemophilia 2008.

  26. Rubinger M, Rivard GE, Teitel J, Walker I. Suggestions for the management of factor VIII inhibitors. Haemophilia 2000, Suppl.1:52-9.

  27. Teitel JM, Card R, Strawczynski H, and the Association of Hemophilia Clinic Directors of Canada. Laboratory and Clinical Markers of HIV Infection in Canadian Hemophiliacs after Two Years Treatment with Recombinant Factor VIII Concentrate. Haemophilia, 4:731-738, 1998.

  28. Walker I.R, Sek J.T, Almonte T.M, Carruthers J.B, Chan A.K.C, Pai M.K, Thibault A. T, and Heddle N.M. Developing a tracking system for coagulation factor concentrates in souther Ontario. Transfusion Volume 43, May 2003, page 556-562.

  29. Walker I. Survey of the Canadian Hemophilia Population. Can J Public Health 1991;82:127 129

  30. Walker I et al. The Canadian Hemophilia Registry as the Basis for a National System for Monitoring the Use of Factor Concentrates. Accepted for Transfusion, July 1995

  31. Walker I, Sigouin C, Sek J, Almonte T, Carruthers J, Chan A, Pai M, Heddle N., Comparing hand-held computers and paper diaries for haemophilia home therapy: A randomized trial.  Haemophilia 10, 1-7, 2004.

  32. Walker I, Poon MC. Recombinant factor VIII concentrate. The MSAC, Canadian Hemophilia Society. Canadian Hemophilia Clinic Directors Group. Lancet.1992; 339:61-2.
  33. Webert KE, Arnold DM, Carruthers J, Molnar L, Amonte T, Decker K, Seroki W, Reed J, Chan A, Pai M and Walker IR. Utilization of recombinant activated factor VII in southern Ontario in 85 patients with and withouth haemophilia. Haemophilia 2007; 13, 528-526.

  34. Young NL, Bradley CS, Wakefield CD, Barnard D, Blanchette VS, McCusker PJ. How well does the Canadian Haemophilia Outcomes-Kids' Life Assessment Tool (CHO-KLAT) measure the quality of life of boys with haemophilia? Pediatr Blood Cancer. 2006 Sep;47(3):305-11.

  35. Young NL, Bradley CS, Blanchette V, Wakefield CD, Barnard D, Wu JK, McCusker PJ. Development of a health-related quality of life measure for boys with haemophilia: the Canadian Haemophilia Outcomes--Kids Life Assessment Tool (CHO-KLAT). Haemophilia. 2004;10 Suppl 1:34-43.

 

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MEETING ABSTRACTS

  1. Walker I, Canadian Hemophilia Clinic Directors Group. Enumeration of the Canadian Hemophilia Population. XIX International Congress of The World Federation of Hemophilia 1990, Washington, DC. Book of Abstracts p.45, 1990.

  2. Walker IR, Canadian Hemophilia Clinic Directors Group. HIV in Canadians with Hemophilia: Prevalence, Mortality and the Impact of Safer Factor Concentrates. XX Congress of the World Federation of Hemophilia, Athens, Greece, October 1992.

  3. Blanchette VS, Walker 1, Inwood M, Adams M, Gill P and the Canadian Hemophilia Clinic Directors Group. Prevalence of Hepatitis C infection in individuals with Hemophilia: Results of a National Study. XX Congress of the World Federation of Hemophilia, Athens, Greece, October 1992.

  4. Walker IR, and the Canadian Hemophilia Clinical Directors Group. Canadian Hemophilia Registry (CHR) - Update and Assessment of Completeness. XXI International Congress of the World Federation of Hemophilia, Mexico City, Mexico. April 1994.

  5. Inwood MJ, Clegg E, Carter S. on behalf of the Canadian Hemophilia Centre Directors and Nurse Coordinators Group. A survey of Central Venous Access Devices (CVAD) in a Canadian Hemophilia Population. Presented at the congress of the World Hemophilia Federation, Mexico City, April 24-9, 1994.

  6. Inwood MJ, Clegg E, Carter S. on behalf of the Canadian Hemophilia Centre Directors and Nurse Coordinators Group. A survey of Pyoarthrosis in a Canadian Hemophilia Population. Presented at the congress of the World Hemophilia Federation, Mexico City, April 24-9, 1994.

  7. Walker I, Association of Hemophilia Clinic Directors of Canada. Liver Disease in Hemophilia: New Directions in Diagnosis, Management and Treatment. National Hemophilia Foundation. Atlanta, Georgia, March 3-5, 1995.

  8. Walker I, Julian J, Association of Hemophilia Clinic Directors of Canada. Causes of Death in Canadians with Hemophilia 1980-1995. XXII Congress of the World Federation of Hemophilia, Dublin, Ireland, May 1996.

  9. Lee DH, Walker IR, Poon MC, Rivard G, Teitel J, Ritchie B, Akabutu J, Sinclair GD, Pai M, Wu J, Reddy S, Crowther MA, Blachman MA. Factor V Leiden Is Not Protective in Severe Hemophilia. Hemophilia 1996;2 supp 1:178.

 

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ahcdc major award recipients

2007

  1. Dr. David Lillicrap - ISTH Bi-Annual Investigator Recognition Award
  2. Dr. Paula James - Bayer Hemophilia Awards Program - Early Career Investigator Award
  3. Dr. Shannon Meeks - Bayer Health Awards Program - Clinical Training Fellowship Award
  4. Dr. Melanie Bodnar - AHCDC - Bayer Fellowship in Hemostasis

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