FREQUENCIES OF BLEEDING DISORDERS IN CHILDREN PRESENTING TO PEDIATRIC DEPARTMENT OF A TERTIARY CARE HOSPITAL
Main Article Content
Keywords
Bleeding disorders, clotting factor defects, vascular wall problems
Abstract
Background: bleeding disorder are very common in children which occurs due to multiple factors.
Objective: the aim of this study was to find out the frequencies of bleeding disorders in children presenting to pediatric Department of a Tertiary Care Hospital.
Material and method: The present study was carried out at the department of Pediatrics Gambat Institute of medical and health sciences from January 2018 to June 2018 after taking approval from the research committee of the hospital. A total of 116 Children and neonates (day 1 to 12) years with a suspected bleeding tendency or a family or personal history of congenital bleeding disorders were included in the study, as confirmed by the relevant laboratory tests. Parents or legal guardians gave their informed permission. A thorough clinical examination and history were documented. All patients had baseline laboratory tests performed on the same day, including complete blood counts, bleeding times, prothrombine times, APTTs, fibrinogen, and blood groupings. A vascular wall defect was thought to be the source of the bleeding if the coagulation profile was determined to be normal. Schonlen Henock A skin biopsy confirmed purpura. The frequencies and percentages of each qualitative characteristic were examined. For quantitative factors such as age, the mean plus standard deviation was computed. Tables were used to display the findings. The statistical software SPSS version 16 for Windows was used to analyze all of the data.
Results: A total 117 individuals with bleeding disorders were examined in this study .the mean age of the study participants was 06.6884 ± 4.4823 (ranged day 1 up to 12) years. Out of the 56(47.86%) patients who had clotting factor defects, the etiology of coagulative disorders revealed that 17 (14.5%) of them had hemorrhagic disease of the newborn, 15 (12.8%) had diarrhea, 5 (4.2%) had liver parenchymal disease, 5 (4.2%) had DIC, 2 (1.7%) had biliary atresia, 6 (5.1%) had hemophilia "A," 3 (2.5%) had von Wille brand disease, and 3 (2.5%) had factor VII deficiency, respectively. 52 (44.4%) patients had bleeding from thrombocytopenia, 21 (17.9%) had aplastic anemia, 11 (9.4%) had idiopathic thrombocytopenic purpura , 9 (7.5%) had acute lymphocytic leukaemia, 7 (5.9%) had megaloblastic anemia, and 4 (3.4%) had infection-induced thrombocytopenia. Nine cases (7.6%) had vessel wall defects.
Conclusion: The current study concluded that among bleeding disorders the most common was clotting factor deficiencies, followed by platelet and vascular wall problems, respectively.
References
2. Laffan MA, Lee CA. Inherited bleeding disorders. In: Hoffbrand AV, Catovsky D, Tuddenham EGD, editors. Postgraduate haematology. 5th ed. 2005. p. 825-41.
3. Hoyer LW. Haemophilia A. N Engl J Med 1994; 330: 38-47.
4. Stanojevic M. Controversies concerning the prevention of hemorrhagic disease newborns Paediatr Today 2008; 3: 11-23.
5. Shearer MJ. Vitamin K. Lancet 1995; 345: 229-34.
6. McNinch AW, Tripp JH. Haemorrhagic disease of the newborn in the British Isles: two year prospective study. BMJ 1991; 303: 1105-9.
7. Autret-Leca E, Jonville-Béra AP. Vitamin K in neonates: how to administer, when and to whom. Paediatr Drugs 2001; 3: 1-8.
8. Ahmed F, Kannan M, Ranjan R, Bajaj J, Choudhary VP, Saxena R. Inherited platelet function disorders verses other inherited bleeding disorders: an Indian overview. Thromb Res 2008; 121: 835-41.
9. Arun B, Kessler C. Inherited Bleeding Disorders: Haemostasis and Thrombosis. 4th ed. Philadelphia: Lippincott Williams and Wilkens; 2001.
10. Margaret ER, Christopher EW, Nigel SK. Congenital bleeding disorders. Hematology ASH. 2003; 559-74. Also available from URL://http://asheducationbook. hematologylibrary.org/cgi/reprint/2003/1/559.
11. Zafar T, Ikram N, Amanat S, Zafar A, Hassan K. Clinicohaematological spectrum of Haemophilia. J Rawal Med Coll 2006; 10: 54-60.
12.Peyvandi F, Cattaneo M, Inbal A, De Moerloose P, Spreafico M. Rare bleeding disorders. Haemophilia 2008; 14: 202-10.
13.Nazir K, Ahmed S, Kamran S, Anwar J. Frequency of bleeding disorders diagnosed at Armed Forces Institute of Pathology, Rawalpindi. Pak Armed Forces Med J 2011; 61: 387-90
14.Khan A, Aqeel M, Khan TA, Munir A. Pattern of hematological diseases in hospitalized paediatric patients based on bone marrow examination. J Postgrad Med Inst 2008; 22: 196-200
15.Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002; 8: 308-21.
16.Ahmed F, Kannan M, Ranjan R, Bajaj J, Choudhary VP, Saxena R. Inherited platelet function disorders versus other inherited bleeding disorders: An Indian overview. Thromb Res 2008; 121: 835-41
17.Park YB, Lee JW, Cho BS, Min WS, Cheung DY, Kim JI, et al. Incidence and etiology of overt gastrointestinal bleeding in adult patients with aplastic anemia. Dig Dis Sci 2010; 55: 73-81
18. Shah M, Khattak IUD, Khattak ST, Ahad A, Mahsud MAJ. Medical conditions associated with prolonged activated partial thromboplastin time in Swat. Gomal J Med Sci 2011; 9: 15-8
19.Committee on Fetus and Newborn, Policy Statement. Controversies concerning vitamin K and the newborn. Pediatrics 2003; 112: 191-2.
20.Kühne T, Imbach P, Bolton-Maggs PH, Berchtold W, Blanchette V, Buchanan GR, et al. Newly diagnosed idiopathic thrombocytopenic purpura in childhood: an observational study. Lancet 2001; 358: 2122-5
21. Karim R, Zaman A, Tasneem K, Syed MA, Zehra M. Frequencies of Bleeding Disorders in Children Presenting To Pediatric Department of a Tertiary Care Hospital At Peshawar. KJMS. 2013 Jul;6(2):267.
 
							