Considerations for Acquired and Inherited Blood Disorders

Course Number: 685

References / Additional Resources

  1. Hoyer LH, Hemophilia A. N Engl J Med. 1994. pp. 38–47.

  2. Otto JC. An account of an hemorrhagic disposition existing in certain families. Med Repos. 1803;6:1–4.

  3. A Brief History of Hemophilia Treatment | Hemophilia News Today

  4. Hoyer LH, Hemophilia A. N Engl J Med. 1994. pp. 38–47.

  5. Rogaev EI, Grigorenko AP, Faskhutdinova G, Kittler EL, Moliaka YK. Genotype analysis identifies the cause of the "royal disease". Science. 2009;326:817. doi: 10.1126/science.1180660.

  6. Mannucci PM, Tuddenham EGD. The hemophiliac – from royal genes to gene therapy. N Engl J Med. 2001;344:1773–1779. doi: 10.1056/NEJM200106073442307.

  7. Stevens RF. The history of haemophilia in the royal families of Europe. Br J Haematol. 1999;105:25–32.

  8. James PD, Goodeve AC. von Willebrand disease. Genet Med. 2011 May;13(5):365-76. doi: 10.1097/GIM.0b013e3182035931. PMID: 21289515; PMCID: PMC3832952.

  9. Bleeding Disorders History: 2 AD to Modern Advances | NBDF

  10. Kroner BL, Rosenberg PS, Aledort LM, Alvord WG, Goedert JJ. HIV-1 infection incidence among persons with hemophilia in the United States and Western Europe, 1978-1990. J Acquir Immune Defic Syndr 1994; 7:279-286.

  11. Eyster ME, Diamondstone LS, Lien JM, Ehmann WC, Quan S, Goedert JJ. Natural history of hepatitis C virus infection in multitransfused hemophiliacs: effect of coinfection with human immunodeficiency virus. J Acquir Immune Defic Syndr 1993; 6:602-610.

  12. Bleeding Disorders History: 2 AD to Modern Advances | NBDF

  13. Vanduine, S., Ridley, K., Bashutski, J.D., Snyder, M., Powell, C., & Taichman, S. (2017). Gingival bleeding and oral hygiene in women with von Willebrand Disease (VWD): a pilot study. The Journal of Haemophilia Practice, 4, 49 - 57.

  14. (https://www.bleeding.org/bleeding-disorders-a-z/overview/what-is-a-bleeding-disorder)

  15. Bleeding Disorders - Types | NHLBI, NIH

  16. Sites of initial bleeding episodes, mode of delivery and age of diagnosis in babies with haemophilia diagnosed before the age of 2 years: a report from The Centers for Disease Control and Prevention's (CDC) Universal Data Collection (UDC) project - PubMed (nih.gov)

  17. Dimensions of Dental Hygiene. July/August 2020;18(7):36-39.

  18. Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand’s disease. Blood. 1987 Feb;69(2):454-9.

  19. Werner EJ, Broxson EH, Tucker EL, et al. Prevalence of von Willebrand disease in children: a multiethnic study. J Pediatr 1993 Dec; 123(6): 893-8.

  20. Data and Statistics on von Willebrand Disease | CDC

  21. Paroskie A, Gailani D, DeBaun MR, Sidonio RF, Jr. A cross-sectional study of bleeding phenotype in haemophilia A carriers. Br J Haematol 2015;170:223-8.)

  22. https://www.cdc.gov/ncbddd/hemophilia/data.html

  23. Rare Bleeding Disorders Overview: Symptoms, Treatment | NBDF

  24. Recognizing Types of Bleeds in Bleeding Disorders | NBDF

  25. Brewer, A., & Correa, M. E. (2006). Guidelines for Dental Treatment of Patients with Inherited Bleeding Disorders. Treatment of Hemophilia, No 40. World Federation of Hemophilia

  26. Ljung R, Auerswald G, Benson G, Dolan G, Duffy A, Hermans C, Jiménez-Yuste V, Lambert T, Morfini M, Zupančić-Šalek S, Santagostino E. Inhibitors in haemophilia A and B: Management of bleeds, inhibitor eradication and strategies for difficult-to-treat patients. Eur J Haematol. 2019 Feb;102(2):111-122. doi: 10.1111/ejh.13193. Epub 2018 Dec 6. PMID: 30411401; PMCID: PMC6936224.

  27. World Federation of Hemophilia. Rare Clotting Factor Deficiencies. Accessed May 13, 2024.

  28. CDA Position on Antibiotic Prophylaxis for Dental Patients at Risk. Canadian Dental Association. 2005.

  29. Scully C, Dios PD, Giangrande P. Oral Care for People With Hemophilia or a Hereditary Bleeding Tendency. 2nd ed. Montreal, QC: World Federation of Hemophilia; 2008.

  30. Scully C, Dios PD, Giangrande P. Oral Care for People With Hemophilia or a Hereditary Bleeding Tendency. 2nd ed. Montreal, QC: World Federation of Hemophilia; 2008.

  31. Harrington B. Primary Dental Care of Patients with Hemophilia. Montreal, QC: World Federation of Hemophilia; 2004.

  32. Scully C, Dios PD, Giangrande P. Oral Care for People With Hemophilia or a Hereditary Bleeding Tendency. 2nd ed. Montreal, QC: World Federation of Hemophilia; 2008.

  33. The Hemophilia Handbook, Atlanta, GA; Hemophilia of Georgia; 2007.

  34. Nehring SM, Goyal A, Patel BC. C Reactive Protein. 2023 Jul 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 28722873.

  35. Brewer A and Correa ME Guidelines for dental treatment of patients with inherited bleeding disorders 2006 World Federation of Haemophilia , pdf-1190.pdf (wfh.org)

  36. American Academy of Pediatric Dentistry. Periodicity of examination, preventive dental services, anticipatory guidance/ counseling, and oral treatment for infants, children, and adolescents. The Reference Manual of Pediatric Dentistry. Chicago, Ill.: American Academy of Pediatric Dentistry; 2023:288-300.

  37. Brewer A and Correa ME Guidelines for dental treatment of patients with inherited bleeding disorders 2006 World Federation of Haemophilia , pdf-1190.pdf (wfh.org)

  38. Rafique S, Fiske J, Palmer G, Daly B. Special care dentistry, 1: dental management of patients with inherited bleeding disorders. Dent Update. 2013;40(8):613-616, 619-622, 625-626.

  39. Robertson D, Nusstein J, Reader A, Beck M, McCartney M. The anesthetic efficacy of articaine in buccal infiltration of mandibular posterior teeth. J Am Dent Assoc. 2007;138(8):1104-1112.

  40. The use of prophylactic antibiotics prior to dental procedures in patients with prosthetic joints Sollecito, Thomas P. et al.The Journal of the American Dental Association, Volume 146, Issue 1, 11 - 16.e8

  41. Brewer A and Correa ME Guidelines for dental treatment of patients with inherited bleeding disorders 2006 World Federation of Haemophilia , pdf-1190.pdf (wfh.org)

  42. Brewer A and Correa ME Guidelines for dental treatment of patients with inherited bleeding disorders 2006 World Federation of Haemophilia , pdf-1190.pdf (wfh.org)

  43. https://www1.wfh.org/publication/files/pdf-1190.pdf

  44. Orthodontics for Children: Building a Foundation for a Healthy Smile | American Association of Orthodontists (aaoinfo.org)

  45. Norton LA, Assael LA. Orthodontic and temporomandibular joint considerations in treatment of patients with Ehlers-Danlos syndrome. Am J Orthod Dentofacial Orthop. 1997 Jan;111(1):75-84. doi: 10.1016/s0889-5406(97)70305-6. PMID: 9009927.

  46. Scully C, Dios PD, Giangrande P. Oral Care for People With Hemophilia or a Hereditary Bleeding Tendency. 2nd ed. Montreal, QC: World Federation of Hemophilia; 2008.

  47. Hewson ID, Daly J, Hallett KB, et al. Consensus statement by hospital based dentists providing dental treatment for patients with inherited bleeding disorders. Aust Dental J. 2011; 56(2):221-226

  48. Valentino LA, Kapoor M. Central venous access devices in patients with hemophilia. Expert Rev Med Devices. 2005;2:699–711.

  49. Bhagat M, Tapashetti R, Fatima G et.al. Lasers in periodontal therapy. Gal Int J Health Sci Res. 2020; 5(1): 130-139.

  50. Brewer A, Correa ME. Guidelines for Dental Treatment of Patients With Inherited Bleeding Disorders. Montreal, QC: World Federation of Hemophilia; 2006.

  51. Evans RE, Leake D. Bleeding in a hemophiliac after inferior alveolar nerve block. J Am Dent Assoc. 1964;69(3):352-355

  52. Heiland M, Weber M, Schmelzle R. Life-threatening bleeding after dental extraction in a hemophilia A patient with inhibitors to factor VIII: a case report. J Oral Maxillofac Surg. 2003; 61(11):1350-1353.

  53. Brewer A, Correa ME. Guidelines for Dental Treatment of Patients With Inherited Bleeding Disorders. Montreal, QC: World Federation of Hemophilia; 2006.

  54. Brewer A, Correa ME. Guidelines for Dental Treatment of Patients With Inherited Bleeding Disorders. Montreal, QC: World Federation of Hemophilia; 2006.

  55. Baker JR, Crudder SO, Riske B, Bias V, Forsberg A. A model for a regional system of care to promote the health and well-being of people with rare chronic genetic disorders. Am J Public Health 2005; 95:1910-1916.

  56. Hemophilia Treatment Centers (HTCs) | Hemophilia | CDC

  57. von Drygalski A, Kolaitis NA, Bettencourt R, Bergstrom J, Kruse-Jarres R, Quon DV, Wassel C, Li MC, Waalen J, Elias DJ, Mosnier LO, Allison M. Prevalence and risk factors for hypertension in hemophilia. Hypertension. 2013 Jul;62(1):209-15. doi: 10.1161/HYPERTENSIONAHA.113.01174. Epub 2013 Apr 29. PMID: 23630949; PMCID: PMC3850775.

  58. Nieva NR. Obesity and physical exercise in hemophilia. Blood Coagul Fibrinolysis. 2023 Jun 1;34(S1):S33-S34. doi: 10.1097/MBC.0000000000001216. PMID: 37254730.

  59. Herring, S.W., & Liu, Z. (2001). Loading of the Temporomandibular Joint: Anatomical and in vivo Evidence from the Bones. Cells Tissues Organs, 169, 193 - 200.

  60. Hoffmann RG, Kotchen JM, Kotchen TA, Cowley T, Dasgupta M, Cowley AW Jr. Temporomandibular disorders and associated clinical comorbidities. Clin J Pain. 2011 Mar-Apr;27(3):268-74. doi: 10.1097/AJP.0b013e31820215f5. PMID: 21178593.

  61. Iron-Deficiency Anemia - Hematology.org

  62. Anne Marie U, Murererehe J, Rehman M, Chittilla M, Uwambaye P, Razzaque MS. Oral manifestations of iron imbalance. Front Nutr. 2023 Oct 13;10:1272902. doi: 10.3389/fnut.2023.1272902. PMID: 37899821; PMCID: PMC10611504.