Literature DB >> 25051423

Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agents.

Archwin Tanphaichitr1, Thisarat Kusuwan, Siriporn Limviriyakul, Suvajana Atipas, Julaporn Pooliam, Tuangrat Sangpraypan, Voravarn S Tanphaichitr, Vip Viprakasit.   

Abstract

Ototoxicity due to iron chelation therapy, especially deferoxamine (DFO), is frequently observed in patients who have a higher chelation index (>0.025). However, there is limited data on patients who are less well-chelated and on other chelating regimens, including deferiprone (L1), deferasirox (DFX), and a combination of DFO and L1. To determine the incidence of ototoxicity from iron chelators, we retrospectively analyzed our clinical records from January 1997 to December 2010. All transfusion-dependent thalassemia (TDT) patients received iron chelation therapy with mono DFX, DFO, L1, or a combination. All patients underwent routine otolaryngologic examination and pure-tone audiometry before starting each chelation regimen and were regularly followed every 6 months. One hundred thalassemic patients were enrolled and analyzed (48 males and 52 females), with a mean age of 12.11 ± 4.48 years (range 2.5-22.5 years). Total summative duration of iron chelation therapy in all patients was 596.50 years. Nine patients were found to have conductive hearing loss. Sensorineural hearing loss (SNHL) was identified in seven patients but only four were determined to be associated with iron chelators; three patients were detected while undergoing DFO therapy and one patient with L1 therapy. None of patients undergoing DFO therapy had reached over the levels of chelation index. In our resource-limited setting with poor treatment compliance, there was a rather low incidence of ototoxicity after exposure to iron chelators. However, a routine audiometry remains recommended for early detection and intervention since SNHL still develops and results in a long-term morbidity.

Entities:  

Keywords:  Chelation therapy; ototoxicity; sensorineural hearing loss (SNHL); transfusion-dependent thalassemia (TDT)

Mesh:

Substances:

Year:  2014        PMID: 25051423     DOI: 10.3109/03630269.2014.940462

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  3 in total

1.  Sensorineural hearing loss in children with sickle cell disease.

Authors:  Annie N Farrell; April M Landry; Marianne E Yee; Roberta M Leu; Steven L Goudy
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2018-12-05       Impact factor: 1.675

2.  Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia Patients.

Authors:  Muhammad Ali Khan; Mahrukh A Khan; Ahmed M Seedat; Maria Khan; Sana F Khuwaja; Ram Kumar; Syed Muhammad Usama; Sundus Fareed
Journal:  Cureus       Date:  2019-08-22

Review 3.  Hearing loss in Iranian thalassemia major patients treated with deferoxamine: A systematic review and meta-analysis.

Authors:  Gholamreza Badfar; Akram Mansouri; Masoumeh Shohani; Hamid Karimi; Zahra Khalighi; Shoboo Rahmati; Ali Delpisheh; Yousef Veisani; Ali Soleymani; Milad Azami
Journal:  Caspian J Intern Med       Date:  2017
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.