Paediatrica Indonesiana (Sep 2016)

The occurrence of pulmonary hypertension in patients with thalassemia major

  • Hasan Basri,
  • Armijn Firman,
  • Kusnandi Rusmil,
  • Eddy Fadlyana

DOI
https://doi.org/10.14238/pi43.5.2003.162-4
Journal volume & issue
Vol. 43, no. 5
pp. 162 – 4

Abstract

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Background The life of patients with thalassemia major depends on blood transfusions, while repeated blood transfusions may cause adverse effects such as iron deposition in various organs, includ- ing heart and lungs, which eventually increases the pulmonary arterial pressure. Objective This study was proposed to know the occurrence of pulmonary hypertension in patients with thalassemia major, mea- sured by echocardiography in the Thalassemia Clinic, Department of Child Health, Medical School, Padjadjaran University/Hasan Sadikin Hospital, Bandung. Methods A descriptive cross-sectional study was carried out on 30 patients with thalassemia major, aged 10-14 year-old who received repeated blood transfusions. The study was conducted from April to May 2002. Subjects were examined right after a blood transfusion completed and the pulmonary arterial pres- sure was assessed using Doppler–echocardiography and 2-D echocardiography. Results Twenty two out of 30 subjects showed pulmonary hyper- tension, with pulmonary arterial pressure ranged between 32.3 to 46.2 mmHg. According to the age group, pulmonary hypertension was found in 12 out of 17 subjects aged 10-12 years old and 10 out of 13 subjects aged 13-14 years old. Conclusion The occurrence of pulmonary hypertension in patients with thalassemia major at Hasan Sadikin Hospital was 22/30 and seemed to increase with the age of the patients

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