Blood Res.  2020 Dec;55(4):213-216. 10.5045/br.2020.2020023.

Mining of mortality-related findings in rare bleeding disorders: a retrospective study from two centers

Affiliations
  • 1Department of Medical Laboratory Sciences, School of Paramedicine, Hamadan University of Medical Sciences, Hamadan, Iran
  • 2Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran
  • 3Central Diagnostic Laboratories, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran

Abstract

Background
Rare bleeding disorders include inherited coagulation disorders except for von Willebrand disease and hemophilia A and B. These disorders affect both men and women worldwide and mainly have an autosomal recessive pattern of inheritance. Given the paucity of cases of rare bleeding disorders, there are limited data regarding some topics among bleeding disorders.
Methods
This retrospective study from 2005‒2019 collected demographic data and the causes of death among cases with rare bleeding disorders from 2 provinces of Iran.
Results
Overall, 5 deaths were reported, including 3 cases with factor V deficiency, a case with factor XIII deficiency, and a case with combined factor V and factor VIII deficiencies. The main causes of death were bleeding in the central nervous system (2 cases; 1 with factor V deficiency and 1 with combined factor XIII deficiency). Post-partum hemorrhage was the cause of death in a woman with factor V deficiency while anaphylaxis shock was the cause of death in the case with combined factor V and factor VIII deficiencies. A woman with factor V deficiency died from an internal bleeding episode.
Conclusion
Gathering data on the causes of death in rare bleeding disorders through worldwide registries can be helpful for the management of this rare group of bleeding disorders.

Keyword

Anaphylactic shock; Central venous system hemorrhage; Death; Post-partum hemorrhage; rare bleeding disorders; Factor XIII deficiency; Factor V deficiency

Reference

1. Peyvandi F, Jayandharan G, Chandy M, et al. 2006; Genetic diagnosis of haemophilia and other inherited bleeding disorders. Haemophilia. 12 Suppl 3:82–9. DOI: 10.1111/j.1365-2516.2006.01263.x. PMID: 16684001.
Article
2. WFH Network. 2014. Rare clotting factor deficiencies. World Federation of Hemophilia;Montréal, Canada: https://elearning.wfh.org/elearning-centres/rare-clotting-factor-deficiencies/. Accessed October 10, 2019.
3. Mansouritorghabeh H, Manavifar L, Banihashem A, et al. 2013; An investigation of the spectrum of common and rare inherited coagulation disorders in north-eastern Iran. Blood Transfus. 11:233–40. DOI: 10.2450/2012.0023-12. PMID: 23114518. PMCID: PMC3626474.
4. Peyvandi F, Palla R, Menegatti M. 2010; European registry of rare bleeding disorders. InEuropean Hematology Association. 4(Suppl):63–8.
5. Soucie JM, McAlister S, McClellan A, Oakley M, Su Y. 2010; The universal data collection surveillance system for rare bleeding disorders. Am J Prev Med. 38(4 Suppl):S475–81. DOI: 10.1016/j.amepre.2009.12.023. PMID: 20331946.
Article
6. Peyvandi F, Palla R, Menegatti M, Mannucci PM. 2009; Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management. general aspects of clinical features, diagnosis, and management. Semin Thromb Hemost. 35:349–55. DOI: 10.1055/s-0029-1225757. PMID: 19598063.
Article
7. Peyvandi F, Bolton-Maggs PH, Batorova A, De Moerloose P. 2012; Rare bleeding disorders. Haemophilia. 18(Suppl 4):148–53. DOI: 10.1111/j.1365-2516.2012.02841.x. PMID: 22726099.
Article
8. Peyvandi F, Palla R, Menegatti M, et al. 2012; Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. J Thromb Haemost. 10:615–21. DOI: 10.1111/j.1538-7836.2012.04653.x. PMID: 22321862.
Article
9. Dorgalaleh A, Rashidpanah J. 2016; Blood coagulation factor XIII and factor XIII deficiency. Blood Rev. 30:461–75. DOI: 10.1016/j.blre.2016.06.002. PMID: 27344554.
Article
10. Palla R, Peyvandi F, Shapiro AD. 2015; Rare bleeding disorders: diagnosis and treatment. Blood. 125:2052–61. DOI: 10.1182/blood-2014-08-532820. PMID: 25712993.
Article
11. Kadir RA, Economides DL, Sabin CA, Owens D, Lee CA. 1998; Frequency of inherited bleeding disorders in women with menorrhagia. Lancet. 351:485–9. DOI: 10.1016/S0140-6736(97)08248-2. PMID: 9482440.
Article
12. James AH. 2005; More than menorrhagia: a review of the obstetric and gynaecological manifestations of bleeding disorders. Haemophilia. 11:295–307. DOI: 10.1111/j.1365-2516.2005.01108.x. PMID: 16011580.
Article
13. Halimeh S. 2015; Menorrhagia and postpartum haemorrhage in women with rare bleeding disorder. Thromb Res. 135(Suppl 1):S34–7. DOI: 10.1016/S0049-3848(15)50438-6. PMID: 25903531.
Article
14. Mansouritorghabeh H. 2015; Clinical and laboratory approaches to hemophilia A. Iran J Med Sci. 40:194–205. PMID: 25999618. PMCID: PMC4430880.
15. Peyvandi F, Kaufman RJ, Seligsohn U, et al. 2006; Rare bleeding disorders. Haemophilia. 12(Suppl 3):137–42. DOI: 10.1111/j.1365-2516.2006.01271.x. PMID: 16684009.
Article
16. Naderi M, Eshghi P, Saneei Moghaddam E, et al. 2013; Safety of human blood products in rare bleeding disorders in southeast of Iran. Haemophilia. 19:e90–2. DOI: 10.1111/hae.12068. PMID: 23216799.
Article
17. Bolton-Maggs PH, Perry DJ, Chalmers EA, et al. 2004; The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia. 10:593–628. DOI: 10.1111/j.1365-2516.2004.00944.x. PMID: 15357789.
18. Mansouritorghabeh H, Rezaieyazdi Z, Bagheri M. 2009; Successful use of factor VIII concentrate and fresh frozen plasma for four dental extractions in an individual with combined factor V and VIII deficiency. Transfus Med Hemother. 36:138–9. DOI: 10.1159/000205405. PMID: 20823995. PMCID: PMC2928828.
Article
19. Mansouritorghabeh H, Rahimi H, Mohades ST, Behboudi M. 2018; Causes of death among 379 patients with hemophilia: a developing country's report. Clin Appl Thromb Hemost. 24:612–7. DOI: 10.1177/1076029617713873. PMID: 28655282. PMCID: PMC6714710.
Article
20. Karimi M, Haghpanah S, Amirhakimi A, Afrasiabi A, Dehbozorgian J, Nasirabady S. 2009; Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory. Blood Coagul Fibrinolysis. 20:642–5. DOI: 10.1097/MBC.0b013e32832f4371. PMID: 19710607.
Article
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