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Advances in Hematology
Volume 2018, Article ID 1858241, 8 pages
https://doi.org/10.1155/2018/1858241
Research Article

Prevalence of Bleeding Symptoms among Adolescents and Young Adults in the Capital City of Saudi Arabia

1Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
2Center of Excellence in Thrombosis and Hemostasis, King Saud University, Riyadh, Saudi Arabia
3Pediatric Hematology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
4Oncology Center, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
5Research Center, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
6Ministry of Education, Riyadh, Saudi Arabia

Correspondence should be addressed to Tarek Owaidah; as.ude.crhsfk@hadiawot

Received 18 February 2018; Accepted 25 March 2018; Published 2 May 2018

Academic Editor: Elvira Grandone

Copyright © 2018 Tarek Owaidah et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. W. F. O. Hemophilia, “World federation of hemophilia report on the annual global survey 2006,” in World Federation of Hemophilia 1425 René Lévesque Boulevard West, Suite 1010, Montreal, Canada.
  2. W. L. Nichols, M. E. Rick, T. L. Ortel et al., “Clinical and laboratory diagnosis of von Willebrand disease: a synopsis of the 2008 NHLBI/NIH guidelines,” American Journal of Hematology, vol. 84, no. 6, pp. 366–370, 2009. View at Publisher · View at Google Scholar · View at Scopus
  3. L. Hallberg, A. M. Högdahl, L. Nilsson, and G. Rybo, “Menstrual blood loss—a population study. Variation at different ages and attempts to define normality,” Acta Obstetricia et Gynecologica Scandinavica, vol. 45, no. 3, pp. 320–351, 1966. View at Publisher · View at Google Scholar · View at Scopus
  4. F. Rodeghiero, G. Castaman, and E. Dini, “Epidemiological investigations of the prevalence of von Willebrand's disease,” Blood, vol. 69, no. 2, pp. 454–459, 1987. View at Google Scholar · View at Scopus
  5. J. E. Sadler, P. M. Mannucci, E. Berntorp et al., “Impact, diagnosis and treatment of von willebrand disease,” Thrombosis and Haemostasis, vol. 84, no. 08, pp. 160–174, 2017. View at Publisher · View at Google Scholar
  6. E. J. Werner, E. H. Broxson, E. L. Tucker, D. S. Giroux, J. Shults, and T. C. Abshire, “Prevalence of von Willebrand disease in children: a multiethnic study,” Journal of Pediatrics, vol. 123, no. 6, pp. 893–898, 1993. View at Publisher · View at Google Scholar · View at Scopus
  7. A. S. Lukes, R. A. Kadir, F. Peyvandi, and P. A. Kouides, “Disorders of hemostasis and excessive menstrual bleeding: prevalence and clinical impact,” Fertility and Sterility, vol. 84, no. 5, pp. 1338–1344, 2005. View at Publisher · View at Google Scholar · View at Scopus
  8. A. F. Fleming, “Ethnic variation in von Willebrand factor levels can influence the diagnosis of von Willebrand disease,” Clinical & Laboratory Haematology, vol. 25, no. 6, p. 413, 2003. View at Publisher · View at Google Scholar · View at Scopus
  9. B. Friberg, A. K. Örnö, A. Lindgren, and S. Lethagen, “Bleeding disorders among young women: a population-based prevalence study,” Acta Obstetricia et Gynecologica Scandinavica, vol. 85, no. 2, pp. 200–206, 2006. View at Publisher · View at Google Scholar · View at Scopus
  10. T. Quiroga, M. Goycoolea, O. Panes et al., “High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls,” Haematologica, vol. 92, no. 3, pp. 357–365, 2007. View at Publisher · View at Google Scholar · View at Scopus
  11. C. Biron-Andréani, B. Mahieu, A. Rochette et al., “Preoperative screening for von Willebrand disease type 1: low yield and limited ability to predict bleeding,” Journal of Laboratory and Clinical Medicine, vol. 134, no. 6, pp. 605–609, 1999. View at Publisher · View at Google Scholar · View at Scopus
  12. M. Bowman, W. M. Hopman, D. Rapson, D. Lillicrap, M. Silva, and P. James, “A prospective evaluation of the prevalence of symptomatic von Willebrand Disease (VWD) in a pediatric primary care population,” Pediatric Blood & Cancer, vol. 55, no. 1, pp. 171–173, 2010. View at Publisher · View at Google Scholar · View at Scopus
  13. D. R. Terrell, L. A. Beebe, S. K. Vesely, B. R. Neas, J. B. Segal, and J. N. George, “The incidence of immune thrombocytopenic purpura in children and adults: a critical review of published reports,” American Journal of Hematology, vol. 85, no. 3, pp. 174–180, 2010. View at Publisher · View at Google Scholar · View at Scopus
  14. G. D'Andrea, M. Chetta, and M. Margaglione, “Inherited platelet disorders: thrombocytopenias and thrombocytopathies,” Blood Transfusion, vol. 7, no. 4, pp. 278–292, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. M. V. Ragni, N. Machin, L. M. Malec et al., “Von Willebrand factor for menorrhagia: a survey and literature review,” Haemophilia, vol. 22, no. 3, pp. 397–402, 2016. View at Publisher · View at Google Scholar · View at Scopus
  16. P. Noris, G. Biino, A. Pecci et al., “Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders,” Blood, vol. 124, no. 6, pp. e4–e10, 2014. View at Publisher · View at Google Scholar · View at Scopus
  17. C. M. Kirchmaier and D. Pillitteri, “Diagnosis and management of inherited platelet disorders,” Transfusion Medicine and Hemotherapy, vol. 37, no. 5, pp. 237–246, 2010. View at Publisher · View at Google Scholar · View at Scopus
  18. P. Gresele, P. Harrison, L. Bury et al., “Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey,” Journal of Thrombosis and Haemostasis, vol. 12, no. 9, pp. 1562–1569, 2014. View at Publisher · View at Google Scholar · View at Scopus
  19. E. A. El-Bostany, N. Omer, E. E. Salama, E. A. El-Ghoroury, and S. K. Al-Jaouni, “The spectrum of inherited bleeding disorders in pediatrics,” Blood Coagulation & Fibrinolysis, vol. 19, no. 8, pp. 771–775, 2008. View at Publisher · View at Google Scholar · View at Scopus
  20. M. A. M. Ahmed, M. O. Al-Sohaibani, S. A. Al-Mohaya, T. Sumer, E. H. Al-Sheikh, and H. Knox-Macaulay, “Inherited bleeding disorders in the eastern province of saudi arabia,” Acta Haematologica, vol. 79, no. 4, pp. 202–206, 1988. View at Publisher · View at Google Scholar · View at Scopus
  21. F. Z. Al-Sharif, M. D. Aljurf, A. M. Al-Momen et al., “Clinical and laboratory features of congenital factor XIII deficiency,” Saudi Medical Journal, vol. 23, no. 5, pp. 552–554, 2002. View at Google Scholar
  22. I. M. Al-Fawaz, A. M. A. Gader, H. M. Bahakim, F. Al-Mohareb, A. K. Al-Momen, and M. S. Harakati, “Hereditary bleeding disorders in Riyadh, Saudi Arabia,” Annals of Saudi Medicine, vol. 16, no. 3, pp. 257–261, 1996. View at Publisher · View at Google Scholar · View at Scopus
  23. S. I. A. Islam and M. I. Quadri, “Spectrum of hereditary coagulation factor deficiencies in Eastern Province, Saudi Arabia,” Eastern Mediterranean Health Journal, vol. 5, no. 6, pp. 1188–1195, 1999. View at Google Scholar · View at Scopus
  24. M. Bowman, G. Mundell, J. Grabell et al., “Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease,” Journal of Thrombosis and Haemostasis, vol. 6, no. 12, pp. 2062–2066, 2008. View at Publisher · View at Google Scholar · View at Scopus
  25. S. S. Khawar, M. Abu-Riash, and A. Al-Suliman, “Translation and adaptation of english language questionnaire into arabic for implementation of a large survey on assessing the symptoms of bleeding disorders in Saudi Arabia,” Journal of Applied Hematology, vol. 8, no. 4, 2017. View at Google Scholar
  26. S. S. Eid, N. R. Kamal, T. S. Shubeilat, and A. G. Wael, “Inherited bleeding disorders: a 14-year retrospective study,” Clinical Laboratory Science, vol. 21, no. 4, pp. 210–214, 2008. View at Google Scholar
  27. G. M. Mokhtar, A. A. G. Tantawy, A. A. M. Adly, M. A. S. Telbany, S. E. E. Arab, and M. Ismail, “A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience,” Blood Coagulation & Fibrinolysis, vol. 23, no. 5, pp. 411–418, 2012. View at Publisher · View at Google Scholar · View at Scopus
  28. A. S. Awidi, “A study of von Willebrand's disease in Jordan,” Annals of Hematology, vol. 64, no. 6, pp. 299–302, 1992. View at Publisher · View at Google Scholar · View at Scopus
  29. M. Anie, G. Arjun, C. Andrews, and A. Vinayakumar, “Descriptive epidemiology of epistaxis in a tertiary care hospital,” International Journal of Advances in Medicine, vol. 2, no. 3, pp. 255–259, 2015. View at Publisher · View at Google Scholar
  30. A. Asghar, M. A. ul Haq, M. I. Anwar, and M. Awais, “Effects of extreme dry climate of sudan on Pakistani peacekeepers,” Pakistan Armed Forces Medical Journal, vol. 67, no. 1, pp. 166–170, 2017. View at Google Scholar
  31. M. R. Chaaban, D. Zhang, V. Resto, and J. S. Goodwin, “Demographic, seasonal, and geographic differences in emergency department visits for epistaxis,” Otolaryngology—Head and Neck Surgery (United States), vol. 156, no. 1, pp. 81–86, 2017. View at Publisher · View at Google Scholar · View at Scopus
  32. B. Friberg, A. Kristin Örnö, A. Lindgren, and S. Lethagen, “Bleeding disorders among young women: a population-based prevalence study,” Acta Obstetricia et Gynecologica Scandinavica, vol. 85, no. 2, pp. 200–206, 2006. View at Publisher · View at Google Scholar · View at Scopus
  33. T. Gursel, A. Biri, Z. Kaya, S. Sivaslioglu, and M. Albayrak, “The frequency of menorrhagia and bleeding disorders in university students,” Pediatric Hematology and Oncology, vol. 31, no. 5, pp. 467–474, 2014. View at Publisher · View at Google Scholar · View at Scopus