Literature DB >> 9650683

Neurophysiologic evaluation of long-term desferrioxamine therapy in beta-thalassemia patients.

D I Zafeiriou1, A A Kousi, C T Tsantali, E E Kontopoulos, P A Augoustidou-Savvopoulou, P D Tsoubaris, M A Athanasiou.   

Abstract

Forty patients with beta-thalassemia major (BTM), between 11 and 19 years of age and maintained on long-term desferrioxamine (DFO) treatment, were examined by evoked potential and nerve conduction velocity studies to investigate a possible involvement of the auditory, visual, somatosensory, or peripheral nervous pathways. Pathologic findings in brainstem auditory-, visual-, and somatosensory-evoked potentials, and nerve conduction velocity studies were demonstrated in 25%, 15%, 7.5%, and 25% of the patients, respectively, whereas 15% demonstrated involvement of multiple neural pathways. Subclinical involvement of the auditory pathway was statistically associated with higher mean daily DFO dose and longer duration of DFO therapy, whereas abnormalities regarding the somatosensory pathways were related to older age, longer mean duration of DFO therapy, and lower serum copper levels. Involvement of the peripheral nervous system was related to lower serum copper levels. Multiple involvement of neural pathways was related to longer mean duration of DFO therapy. We conclude that risk factors related to long-term DFO treatment are only partly responsible for the subclinical involvement of neural pathways demonstrated in beta-thalassemia major patients.

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Year:  1998        PMID: 9650683     DOI: 10.1016/s0887-8994(98)00004-6

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  4 in total

Review 1.  Ocular abnormalities in beta thalassemia patients: prevalence, impact, and management strategies.

Authors:  Samira Heydarian; Reza Jafari; Kiumars Nowroozpoor Dailami; Hassan Hashemi; Ebrahim Jafarzadehpour; Mohsen Heirani; Abbasali Yekta; Monireh Mahjoob; Mehdi Khabazkhoob
Journal:  Int Ophthalmol       Date:  2019-10-10       Impact factor: 2.031

2.  Impaired gallbladder motility and delayed orocecal transit contribute to pigment gallstone and biliary sludge formation in beta-thalassemia major adults.

Authors:  Piero Portincasa; Antonio Moschetta; Massimo Berardino; Agostino Di-Ciaula; Michele Vacca; Giuseppe Baldassarre; Anna Pietrapertosa; Rosario Cammarota; Nunzia Tannoia; Giuseppe Palasciano
Journal:  World J Gastroenterol       Date:  2004-08-15       Impact factor: 5.742

3.  Polyneuropathy Associated with Severe Iron Overload and Oxidative Stress in β-Thalassemia Patients.

Authors:  Mona H El-Tagui; Khaled M Salama; Mohamed H El-Sabbagh; Eman R Youness; Marwa Ragaey; Amina Abdel-Salam
Journal:  Indian J Hematol Blood Transfus       Date:  2018-11-22       Impact factor: 0.900

4.  Contrast sensitivity in patients with Beta-thalassemia major and sickle cell disease under regular transfusions and treatment with desferrioxamine.

Authors:  Spyridon Gorezis; Ioannis Asproudis; Nikolaos Chalasios; Aikaterini Karali; Elena Tsanou; Dimitrios Peschos; Aikaterini Christodoulou; Miltiadis Aspiotis
Journal:  Open Ophthalmol J       Date:  2010-07-29
  4 in total

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