Dental considerations in a patient with haemophilia

1. Zaliuniene R, Peciuliene V, Brukiene V, Aleksejuniene J. Hemophilia and oral health. Stomatologija 2014; 16(4): 127-31.Search in Google Scholar

2. Srivastava A, Brewer AK, Mauser Bunschoten EP et al. Treatment Guidelines Working Group. The World Federation of Hemophilia. Guidelines for the management of hemophilia. Haemophilia 2013; 19: e1V14.10.1111/j.1365-2516.2012.02909.x22776238Open DOISearch in Google Scholar

3. Gupta A, Epstein J B, Cabay RJ. Bleeding disorders of importance in dental care and related patient management. J Can Dent Assoc 2007; 73(1): 77-83.Search in Google Scholar

4. Nickles K, Wohlfeil M, Alesci S, et al. Comprehensive treatment of periodontitis in patients with von Willebrand disease. J Periodontol 2010; 81(10): 1432-40.10.1902/jop.2010.10007620594049Search in Google Scholar

5. Durham TM, Hodges ED, Harper J, et al. Management of traumatic oralfacial injury in the hemophiliac patient with inhibitor: case report. Pediatr Dent 1993; 15(4): 282-7.Search in Google Scholar

6. Hidaka N, Maeda K, Kawakami C, et al. Fibrinolytic activity in periodontal disease. The relationship between fibrinolytic activity and severity of periodontal disease. J Periodontol 1981; 52(4): 181-6.10.1902/jop.1981.52.4.1816453215Open DOISearch in Google Scholar

7. Kumar JN, Kumar RA, Varadarajan R, Sharma N. Specialty dentistry for the hemophiliac: is there a protocol in place? Indian J Dent Res 2007; 18(2): 48-54.Search in Google Scholar

8. Anderson JA, Brewer A, Creagh D, Hook, et al. Guidance on the dental management of patients with haemophilia and congenital bleeding disorders. Br Dent J 2013; 215(10): 497-504.10.1038/sj.bdj.2013.109724264665Search in Google Scholar

9. Gornitsky M, Hammouda W, Rosen H. Rehabilitation of a hemophiliac with implants: a medical perspective and case report. J Oral Maxillofac Surg 2005; 63(5): 592-7.10.1016/j.joms.2005.01.00915883931Search in Google Scholar

10. Franchini M, Rossetti G, Tagliaferri A, et al. Dental procedures in adult patients with hereditary bleeding disorders: 10 years experience in three Italian Hemophilia Centers. Haemophilia 2005; 11(5): 504-9.10.1111/j.1365-2516.2005.01132.x16128895Search in Google Scholar

11. Vassilopoulos P, Palcanis K. Bleeding disorders and periodontology. Periodontol 2000 2007; 44: 211-23. 10.1111/j.1600-0757.2006.00203.x17474935Search in Google Scholar

12. Lockhart PB, Gibson J, Pond SH, Leitch J. Dental management considerations for the patient with an acquired coagulopathy. Part 2: Coagulopathies from drugs. Br Dent J 2003; 195(9): 495-501.10.1038/sj.bdj.481066014610534Search in Google Scholar

13. Hay CR, Laurian Y, Verroust F, Preston FE, Kernoff PB. Induction of immune tolerance in patients with hemophilia A and inhibitors treated with porcine VIIIC by home therapy. Blood 1990; 76(5): 882-6.10.1182/blood.V76.5.882.882Search in Google Scholar

14. Gruppo RA, Valdez LP, Stout RD. Induction of immune tolerance in patients with hemophilia A and inhibitors. Am J Pediatr Hematol Oncol 1992; 14(1): 82-7.10.1097/00043426-199221000-000131550269Open DOISearch in Google Scholar

15. Mariani G, Kroner B. Immune Tolerance Study Group (ITSG). Immune tolerance in hemophilia with factor VIII inhibitors: predictors of success. Haematologica 2001; 86(11): 1186-93.Search in Google Scholar