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1.
Hemoglobin ; 45(5): 296-302, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-34758688

RESUMO

Deferiprone (DFP) and deferasirox (DFX) are the most well-known, efficacious and safe chelators to reduce the serum ferritin (SF) level in multi transfused thalassemic children, although there are few reports available for assessing the efficacy between DFP and DFX. We compared the efficacy of DFP vs. DFX as iron chelating drugs in ß-thalassemia major (ß-TM) patients. Pediatric patients diagnosed to carry ß-TM, aged between 2 and 10 years, were recruited. A suitable data collection form and questionnaire were used. Paired and unpaired t-tests were used to compare the safety and efficacy of the chelating drugs DFP and DFX. The mean SF level at the 12th month was found to be 3016.73 ± 670.04 ng/mL (p = 0.002) in the DFX-treated group, which was quite significant in contrast to DFP response, where the value was 3204.06 ± 690.15 ng/mL (p = 0.14). There is no statistically significant (p = 0.15) difference on relative changes of the left ventricular ejection fraction (LVEF), between these two groups. The adverse effects were transient and none of them required stoppage of therapy. Deferasirox is more effective when compared to DFP in reducing chelating drug-related complications and iron overload specially in multiple transfusion dependent ß-TM patients.


Assuntos
Deferasirox , Deferiprona , Quelantes de Ferro , Sobrecarga de Ferro , Talassemia beta , Criança , Pré-Escolar , Deferasirox/efeitos adversos , Deferasirox/uso terapêutico , Deferiprona/efeitos adversos , Deferiprona/uso terapêutico , Ferritinas , Humanos , Quelantes de Ferro/efeitos adversos , Quelantes de Ferro/uso terapêutico , Sobrecarga de Ferro/complicações , Sobrecarga de Ferro/etiologia , Volume Sistólico , Função Ventricular Esquerda , Talassemia beta/tratamento farmacológico
2.
J Indian Assoc Pediatr Surg ; 19(3): 175-7, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25197199

RESUMO

Medium chain triglyceride (MCT)-based diet, total parenteral nutrition (TPN) and repeated paracentesis are considered as supportive management for congenital chylous ascites (CCA). TPN is considered where therapy with oral MCT is poorly tolerated by the patient especially young infant with unstable hemodynamic. Surgery is recommended when medical therapy fails. Herein, we report a 2½-month-old infant with CCA, treated successfully with octreotide intravenous infusion after the initial failure to response to conventional conservative therapy with MCT-enriched formula and paracentesis.

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