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Year 2013, Volume: 14 Issue: 1, 17 - 21, 01.04.2013

Abstract

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References

  • Cassinerio E, Roghi A, Pedrotti P, Brevi F, Zanaboni L, Graziadei G et al. Cardiac iron removal and functional cardiac improvement by different iron chelation regimens in thalassemia major patients. Ann Hematol 2012.
  • Kolnagou A, Kleanthous M, Kontoghiorghes GJ. Efficacy, compliance and toxicity factors are affecting the rate of normalization of body iron stores in thalassemia patients using the deferiprone and deferoxamine combination therapy. Hemoglobin 2011;35(3):186-98.
  • Abetz L, Baladi JF, Jones P, Rofail D. The impact of iron overload and its treatment on quality of life: results from a literature review. Health Qual Life Outcomes 2006;4:73.
  • Cappellini MD, Bejaoui M, Agaoglu L, Porter J, Coates T, Jeng M, et al. Prospective evaluation of patient- reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with beta- thalassemia. Clin Ther 2007;29(5):909-17.
  • Nuboer R, Borsboom GJ, Zoethout JA, Koot HM, Bruining J. Effects of insulin pump vs. injection treatment on quality of life and impact of disease in children with type 1 diabetes mellitus in a randomized, prospective comparison. Pediatr Diabetes 2008;9(4 Pt 1):291-6. YAZIÞMA ADRESÝ
  • Uzm. Dr. Vedat UYGUN
  • Akdeniz Üniversitesi Týp Fakültesi, Çocuk
  • Hematoloji-Onkoloji, ANTALYA, TÜRKÝYE E-Posta
  • : vedat@akdeniz.edu.tr Geliþ Tarihi Kabul Tarihi : 01.04.2013

The Effect of Oral Chelators on Major Thalassemia Patients Life Quality

Year 2013, Volume: 14 Issue: 1, 17 - 21, 01.04.2013

Abstract

OBJECTIVE: One of the most factor that decreases the quality of life of thalassemia major patients is the discomfort of long term subcutanous administration of deferoxamine. In this cross sectional study, we analyzed the effect of oral chelator usage on quality of life of beta thalassemia major patients who are 8-18 years old school children. MATERIALS and METHODS: We have studied 32 thalassemia major patients who were under observation for at least one year at the same center. Deferiprone and deferasirox were used in a dose of 40-75 mg/kg/d thrice daily and 10-40 mg/kg/d once daily in the morning, respectively. For the quality of life assessments, PedsQL was used separately for patients and their parents. The statistical analyses were processed for comparing the two groups´ quantitative variables by using the Student t-test or Mann-Whitney U test. Statistically significant meant a p-value of less than 0.05. RESULTS: We determined that oral chelator usage did not effect the overall score of quality of life assessment according to the self reports of children, however according to the parents, the patients using deferasirox had significantly better quality of life than the patients using deferiprone (p=0.019). Higher frequency of transfusion decreased the quality of life scores, however it was not significant. CONCLUSION: Because of the major effect of lifelong treatment to quality of life of thalassemia major, there should be lower frequency of hospital visits and treatments. We determined that children using deferasirox, which has a lower frequency of dosage, has higher quality of life than deferiprone users.

References

  • Cassinerio E, Roghi A, Pedrotti P, Brevi F, Zanaboni L, Graziadei G et al. Cardiac iron removal and functional cardiac improvement by different iron chelation regimens in thalassemia major patients. Ann Hematol 2012.
  • Kolnagou A, Kleanthous M, Kontoghiorghes GJ. Efficacy, compliance and toxicity factors are affecting the rate of normalization of body iron stores in thalassemia patients using the deferiprone and deferoxamine combination therapy. Hemoglobin 2011;35(3):186-98.
  • Abetz L, Baladi JF, Jones P, Rofail D. The impact of iron overload and its treatment on quality of life: results from a literature review. Health Qual Life Outcomes 2006;4:73.
  • Cappellini MD, Bejaoui M, Agaoglu L, Porter J, Coates T, Jeng M, et al. Prospective evaluation of patient- reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with beta- thalassemia. Clin Ther 2007;29(5):909-17.
  • Nuboer R, Borsboom GJ, Zoethout JA, Koot HM, Bruining J. Effects of insulin pump vs. injection treatment on quality of life and impact of disease in children with type 1 diabetes mellitus in a randomized, prospective comparison. Pediatr Diabetes 2008;9(4 Pt 1):291-6. YAZIÞMA ADRESÝ
  • Uzm. Dr. Vedat UYGUN
  • Akdeniz Üniversitesi Týp Fakültesi, Çocuk
  • Hematoloji-Onkoloji, ANTALYA, TÜRKÝYE E-Posta
  • : vedat@akdeniz.edu.tr Geliþ Tarihi Kabul Tarihi : 01.04.2013
There are 9 citations in total.

Details

Other ID JA25TM49BM
Journal Section Research Article
Authors

Vedat Uygun This is me

Funda Tayfun This is me

Mediha Akcan This is me

Gülsün Tezcan Karasu This is me

Alphan Küpesiz This is me

Akif Yeşilipek This is me

Publication Date April 1, 2013
Published in Issue Year 2013 Volume: 14 Issue: 1

Cite

EndNote Uygun V, Tayfun F, Akcan M, Karasu GT, Küpesiz A, Yeşilipek A (April 1, 2013) The Effect of Oral Chelators on Major Thalassemia Patients Life Quality. Meandros Medical And Dental Journal 14 1 17–21.