Arrieta-Blanco JJ, Oñate-Sánchez R, Martínez-López F, Oñate-Cabrerizo D, Cabrerizo-Merino MC. Inherited, congenital and acquired disorders by hemostasis (vascular, platelet & plasmatic phases) with repercussions in the therapeutic oral sphere. Med Oral Patol Oral Cir Bucal. 2014 May 1;19 (3):e280-8.

 

 

doi:10.4317/medoral.19560

http://dx.doi.org/doi:10.4317/medoral.19560

 

 

 

1. Adeyemo TA, Adeyemo WL, Adediran A, Akinbami AJ, Akanmu AS. Orofacial manifestations of hematological disorders: anemia and hemostatic disorders. Indian J Dent Res. 2011;22:454-61.
http://dx.doi.org/10.4103/0970-9290.87070

 

2. Murphy WG, Davies MJ, Eduardo A. The haemostatic response to surgery and trauma. Br J Anaesth. 1993;70:205-13.
http://dx.doi.org/10.1093/bja/70.2.205

 

3. Kaushansky K. Historical review: megakaryopoiesis and thrombopoiesis. Blood. 2008;111:981-6.
http://dx.doi.org/10.1182/blood-2007-05-088500

 

4. Jurk K, Kehrel BE. Platelets: physiology and biochemistry. Semin Tromb Hemost. 2005;31:381-92.
http://dx.doi.org/10.1055/s-2005-916671

 

5. Gibbins JM. Platelet adhesion signaling and the regulation of thrombus formation. J Cell Sci. 2004;117:415-25.
http://dx.doi.org/10.1242/jcs.01325

 

6. Savage B, Cattaneo M, Ruggeri ZM. Mechanisms of platelets aggregation. Curr Opin Hematol. 2001;8:270-6.
http://dx.doi.org/10.1097/00062752-200109000-00002

 

7. Pérez-Gómez F, Bover R. The new coagulation cascade and its possible influence on the delicate balance between thrombosis and hemorrhage. Rev Esp Cardiol. 2007;60:1217-9.
http://dx.doi.org/10.1157/13113924

 

8. Seegmiller A, Sarode R. Laboratory Evaluation of platelet function. Hematolog Oncol Clin N Am. 2007;21:731-42.
http://dx.doi.org/10.1016/j.hoc.2007.06.008

 

9. Dyszkiewicz-Korpanty AM, Frenkel EP, Sarode R. Approach to assessment of platelet function: comparison between optical-based platelet-rich plasma and impedence-based whole blood platelet aggregation methods. Clin Appl Thromb Hemost. 2005;11:25-35.
http://dx.doi.org/10.1177/107602960501100103

 

10. Eleftheriou D, Dillon MJ, Brogan PA. Advances in childhood vasculitis. Curr Opin Rheumatol. 2009;21:411-8.
http://dx.doi.org/10.1097/BOR.0b013e32832c49f2

 

11. Valera MC, Kemoun P, Cousty S, Die P, Payrastre B. Inherited platelet disorders and oral health. J Oral Pathol Med. 2013;42:115-24.
http://dx.doi.org/10.1111/j.1600-0714.2012.01151.x

 

12. Nurden AT, Freson K, Seligsohn U. Inherited platelet disorders. Haemophilia. 2012;18 Suppl 4:154-60.
http://dx.doi.org/10.1111/j.1365-2516.2012.02856.x

 

13. Benito Urdaneta M, Benito Urdaneta M, Ferrara Mendez V, Bernardoni Socorro C, Arteaga Vizcaíno M. Evaluating periodontal conditions in patients with von Willebrand's disease in Hospital Universitario de Maracaibo (University Hospital, Maracaibo)-Venezuela. Med Oral Patol Oral Cir Bucal. 2008;13:e303-6.

 

14. Kadir RA, Sharief LA, Lee CA. Inherited bleeding disorder in older women. Maturitas. 2012;72:35-41.
http://dx.doi.org/10.1016/j.maturitas.2012.02.008

 

15. Favaloro EJ, McDonald D, Lippi G. Laboratory investigation of thrombophilia: the good, the bad and the ugly. Semin Thromb Hemost. 2009;35:695-710.
http://dx.doi.org/10.1055/s-0029-1242723

 

16. Zadro R, Herak DC. Inherited prothrombotic risk factors in children with first ischemic stroke. Biochem Med (Zagreb). 2012;22:298-310.
http://dx.doi.org/10.11613/BM.2012.033

 

17. Anderson JA, Weitz JI. Hypercoagulable states. Crit Care Clin. 2011;27:933-52.
http://dx.doi.org/10.1016/j.ccc.2011.09.007

 

18. Bornert F, Clauss F, Gros CI, Faradji A, Schmittbuhl M, Manière MC, et al. Hemostatic management in pediatric patients with type I von Willebrand disease undergoing oral surgery: case report and literature review. J Oral Maxillofac Surg. 2011;69:2086-91.
http://dx.doi.org/10.1016/j.joms.2011.03.073

 

19. Sánchez-Luceros A, Meschengieser SS, Woods AI, Chuit R, Turdó K, Blanco A, et al. Biological and clinical response to desmopressin (DDAVP) in a retrospective cohort study of children with low von Willebrand factor levels and bleeding history. Thromb Haemost. 2010;104:984-9.
http://dx.doi.org/10.1160/TH10-04-0220

 

20. Kitamura A, Yamashita H, Okumura T, Asahina I. Extraction of four wisdom teeth in a patient with congenital factor V deficiency haemophilia. Oral Surg Oral Med Oral Pathol Oral Radiol, Endod. 2011;112:E1-3.
http://dx.doi.org/10.1016/j.tripleo.2011.03.009

 

21. Geddis AF. Inherited thrombocytopenias an approach to diagnosis and management. Int Jnl Lab Hem. 2013;35:14-25.
http://dx.doi.org/10.1111/j.1751-553X.2012.01454.x

 

22. Croom KF, McCormack PL. Recombinant factor VIIa (eptacog alfa): a review of its use in congenital hemophilia with inhibitors, acquired hemophilia, and other congenital bleeding disorders. BioDrugs. 2008;22:121-36.
http://dx.doi.org/10.2165/00063030-200822020-00005

 

23. Boadas A, Fernandez-Palazzi F, De Bosch NB, Cede-o M, Ruiz-Sáez A. Elective surgery in patients with congénital coagulopathies and inhibitors: experience of the national Haemophilia Centre of Venezuela. Haemophilia. 2011;17:422-7.
http://dx.doi.org/10.1111/j.1365-2516.2010.02427.x

 

24. Weeterings C, Lisman T, de Groot PG. Tissue factor-independence effects of recombinant factor VIIa on hemostasis. Semin Hematol. 2008;45:S12-5.
http://dx.doi.org/10.1053/j.seminhematol.2008.03.018

 

25. Hers I, Mumford A. Understanding the therapeutic action of recombinant factor VIIa in platelet disorders. Platelets. 2008;19:571-81.
http://dx.doi.org/10.1080/09537100802406653

 

26. Plugg I, Mauser-Bunschoten EP, Bröker-Vriends AHJT, Ploos van Amstel HK, van der Booms JG, van Diemen-Homan JEM, et al . Bleeding in carriers of haemophilia. Blood. 2006;108:52-6.
http://dx.doi.org/10.1182/blood-2005-09-3879

 

27. Rayen R, Hariharan VS, Elavazhagan N, Kamalendran N, Varadarajan R. Dental management of haemophiliac child under general anesthesia. J Indian Soc Pedod Prev Dent. 2011;29:74-9.
http://dx.doi.org/10.4103/0970-4388.79954

 

28. Nurden P, Nurden AT. Congenital disorders associated with platelet dysfunctions. Thromb Haemost. 2008;99:253-63.

 

29. Lison S, Dietrich W, Spannagl M. Review article: unexpected bleeding in the operating room: the role of acquired von Willebrand disease. Anesth Analg. 2012;114:73-81.
http://dx.doi.org/10.1213/ANE.0b013e318236b16a

 

30. Jover-Cerveró A, Poveda-Roda R, Bagan JV, Jiménez-Soriano Y. Dental treatment of patients with coagulation factors alterations: an update. Med Oral Patol Oral Cir Bucal. 2007;12:e380-7.

 

31. Nurden P, Youlouz-Marfak I, Siberchicot F, Kostrzewa E, Andia I, Anitua E, et al. Use of autologous platelet-rich clots for prevention of local injury bleeding in patients with severe inherited mucocutaneous bleeding disorders. Haemophilia. 2011;17:620-4.
http://dx.doi.org/10.1111/j.1365-2516.2010.02480.x

 

32. Nickles K, Wohlfeil M, Alesci S, Miesbach W, Eickholz P. Comprehensive treatment of periodontitis in patients with von Willebrand disease. J Periodontol. 2010;81:1432-40.
http://dx.doi.org/10.1902/jop.2010.100076

 

33. Seligsohn U. Treatment of inherited platelet disorders. Haemophilia. 2012;18 Suppl 4:161-5.
http://dx.doi.org/10.1111/j.1365-2516.2012.02842.x

 

34. Israels S, Schwetz N, Boyar R, McNicol A. Bleedings disorders: Characterization, dental considerations and managements. J Can Dent Assoc. 2006;72:827-30.

 

35. Kumar NJ, Kumar RA, Varadarajan R, Sharma N. Specialty dentistry for the haemophiliac: is there a protocol in place?. Indian J Dent Res. 2007;18:48-54.
http://dx.doi.org/10.4103/0970-9290.32419

 

36. Chiono O. Dental anesthesia for the hemophilic patient. Anesth Prog. 1968;15:295-8.