@article{Charoentawornpanich_Komwilaisak_Wiangnon_Panamonta_Jetsrisuparb_2014, title={Treatment Outcomes of Patients with HbE β-Thalassemia in Srinagarind Hospital}, volume={29}, url={https://li01.tci-thaijo.org/index.php/SRIMEDJ/article/view/23641}, abstractNote={<p><strong><span style="text-decoration: underline;">Background</span></strong><span style="text-decoration: underline;"> <strong>and Objectives </strong>:</span>  HbE β-thalassemia<strong> </strong>is genetically inherited hemoglobin disorder resulting in chronic hemolytic anemia. Blood transfusion keeping near normal hemoglobin is proved to correct the ineffective erythropoiesis. This study aim to investigate the treatment outcomes of patients with HbE β-thalassemia<strong>  </strong>in Srinagarind hospital.</p><p><strong><span style="text-decoration: underline;">Patients and Methods:</span></strong><strong> </strong>A retrospective and a cross-sectional studies were done in patients aged under 18 years with at least 1 year follow- up in the pediatric department, Srinagarind hospital. Most of the patients had received regular transfusions to keep near normal hemoglobin and iron chelators were given when serum ferritin was more than 1000 mcg/L.</p><p><strong><span style="text-decoration: underline;">Results</span></strong><span style="text-decoration: underline;">:</span> The total of 66 patients; 28 males and 38 females were included. The mean age was 11 years 5 months. Impaired growth (height < 3<sup>th</sup>  percentile) was found in 11 out of 66 patients (16.9%), AIHA  in 12/66 (18.1%), subclinical hypothyroid  22.5%, 10 % of patients had hypoparathyroid and 16/43 (37.2%) had gallstone. No evidence of chronic leg ulcer and diabetes in all patients. Splenectomy was performed in 20 of 66 patients (30.3%) of whose 20% had post splenectomy thrombosis.</p><p><strong><span style="text-decoration: underline;">Conclusions</span></strong><span style="text-decoration: underline;">:</span>There were still high complications in thlassemia treatment outcomes especially endocrinopathies. Appropriate treatments of HbE β-thalassemia create a major challenge.</p>}, number={4}, journal={Srinagarind Medical Journal}, author={Charoentawornpanich, Parichat and Komwilaisak, Patcharee and Wiangnon, Surapon and Panamonta, Ouyporn and Jetsrisuparb, Arunee}, year={2014}, month={Nov.}, pages={74} }