One-year follow-up of endodontic retreatment in a patient with severe Hemophilia A

Submitted: 24 December 2021
Accepted: 17 March 2022
Published: 2 May 2022
Abstract Views: 839
PDF: 565
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Aim: To describe the clinical management of a patient diagnosed with severe Hemophilia A presenting an endodontically treated tooth (ETT) with a persistent periapical radiolucent lesion.

Summary: This case report has been written according to Preferred Reporting Items for Case reports in Endodontics (PRICE) 2020 guidelines. Inherited bleeding disorders (IBDs) are a heterogeneous group of genetic conditions in which missing or defective clotting factors prevent normal blood clotting from occurring. Among those conditions, Hemophilia A (deficiency of factor VIII) is the most prevalent, representing about 85% of all inherited bleeding disorders. A 21-years-old male was referred to our service to retreat a left mandibular first molar. At clinical examination, the ETT showed signs of persistent symptomatic apical periodontitis, confirmed by the radiographic exam. After reviewing the risks and benefits, written informed consent was obtained from the patient, and then, non-surgical root canal retreatment was performed on the tooth under dental operating microscopy. Reciproc R25 NiTi file was used to remove the previous fillings and reprepare the root canal system, and Bio-C Sealer was the chosen sealer to obturate the root canals. The entire retreatment procedure was performed in a single-visit. At the subsequent follow-up visits one year later, the periapical radiograph suggests a successful outcome with periapical repair, a substantial improvement in bone density, and the patient reported that he was free of symptoms and using the tooth as usual.

Key learning points

• Although no complications or excessive bleeding was observed, proper multidisciplinary planning must be carried when treating patients with inherited bleeding disorders.

• All efforts should be made to avoid intraoperative complications or multiple sessions that also require multiple clotting factor infusions, and

• further clinical investigations should focus on the need for prophylactic protocols in order to safely perform endodontic treatment on patients diagnosed with different severity levels of IBDs.

Dimensions

Altmetric

PlumX Metrics

Downloads

Download data is not yet available.

Citations

Peyvandi F, Duga S, Akhavan S, Mannucci PM. Rare coagulation deficiencies. Haemophilia 2002;8(3):308-321.
Srivastava A, Santagostino E. WFH Guidelines for the Management of Hemophilia, 3rd edition. 2020;26 Suppl 6:1-158.
Chen SL. Economic costs of hemophilia and the impact of prophylactic treatment on patient management. The American journal of managed care 2016;22(5 Suppl):s126-133.
Hewson ID, Daly J, Hallett KB, Liberali SA, Scott CL, Spaile G, et al. Consensus statement by hospital based dentists providing dental treatment for patients with inherited bleeding disorders. Aust Dent J 2011;56(2):221-226.
Berntorp E, Shapiro AD. Modern haemophilia care. Lancet 2012;379(9824):1447-1456.
Brewer AK, Roebuck EM, Donachie M, Hazard A, Gordon K, Fung D, et al. The dental management of adult patients with haemophilia and other congenital bleeding disorders. Haemophilia 2003;9(6):673-677.
Leeb IJ. Severe hemorrhage as an endodontic complication. J Endod 1977;3(12):465-467.
Vire DE, Barrett KC. Endodontic Rx for the von Willebrand patient. J Endod 1982;8(11):514-516.
Marashdeh MQ, Friedman S, Lévesque C, Finer Y. Esterases affect the physical properties of materials used to seal the endodontic space. Dent Mater 2019;35(8):1065-1072.
Nagendrababu V, Chong BS, McCabe P, Shah PK, Priya E, Jayaraman J, et al. PRICE 2020 guidelines for reporting case reports in Endodontics: a consensus-based development. Int Endod J 2020;53(5):619-626.
Castellanos-Cosano L, Machuca-Portillo G, Sanchez-Dominguez B, Torres-Lagares D, Lopez-Lopez J, Segura-Egea JJ. High prevalence of radiolucent periapical lesions amongst patients with inherited coagulation disorders. Haemophilia 2013;19(3):e110-115.
Schaffer R, Duong MT, Wachter B, Arana E, Frances D. Access to dental care for people with bleeding disorders: survey results of hemophilia treatment centers in the U.S. Spec Care Dentist 2016;36(6):295-299.
Ng YL, Mann V, Gulabivala K. A prospective study of the factors affecting outcomes of non-surgical root canal treatment: part 2: tooth survival. Int Endod J 2011;44(7):610-625.
Kinalski MA, Sarkis-Onofre R, dos Santos MBF. Inherited bleeding disorders in oral procedures. Assessment of prophylactic and therapeutic protocols: a scoping review. Australian Dental Journal 2020;[epub ahead of print].
Pasi KJ, Collins PW, Keeling DM, Brown SA, Cumming AM, Dolan GC, et al. Management of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctor's Organization. Haemophilia 2004;10(3):218-231.
Zandi H, Petronijevic N, Mdala I, Kristoffersen AK, Enersen M, Rocas IN, et al. Outcome of Endodontic Retreatment Using 2 Root Canal Irrigants and Influence of Infection on Healing as Determined by a Molecular Method: A Randomized Clinical Trial. J Endod 2019;45(9):1089-1098 e1085.
Ferreira AA, Brum IV, Souza JVdL, Leite ICG. Cost analysis of hemophilia treatment in a Brazilian public blood center. Cadernos Saúde Coletiva 2020;28:556-566.

Supporting Agencies

Coordination for the Improvement of Higher Education Personnel (CAPES)

How to Cite

Peixoto de Araújo, L., de Azevedo Kinalski, M., Pinto Carpena, L., Randi Ferraz, C. C., & Bertolini Fernandes dos Santos, M. (2022). One-year follow-up of endodontic retreatment in a patient with severe Hemophilia A. Giornale Italiano Di Endodonzia, 36(1). https://doi.org/10.32067/GIE.2021.35.02.53