Abstract
IntroductionIron deficiency is common in cyanotic congenital heart disease (CHD) and results in reduced exercise tolerance. Currently, iron replacement is advocated with limited evidence in cyanotic CHD. We investigated the safety and efficacy of iron replacement therapy in this population. MethodsTwenty-five iron-deficient cyanotic CHD patients were prospectively studied between August 2008 and January 2009. Oral ferrous fumarate was titrated to a maximum dose of 200mg thrice-daily. The CAMPHOR QoL questionnaire, 6minute walk test (6MWT) and cardiopulmonary exercise testing were conducted at baseline and after 3months of treatment. ResultsMean age was 39.9±10.9years, 80% females. Fourteen had Eisenmenger syndrome, 6 complex cyanotic disease and 5 Fontan circulation. There were no adverse effects necessitating termination of treatment. After 3months of treatment, hemoglobin (19.0±2.9g/dL to 20.4±2.7g/dL, p<0.001), ferritin (13.3±4.7μg/L to 54.1±24.2μg/L, p<0.001) and transferrin saturation (17.8±9.6% to 34.8±23.4%, p<0.001) significantly increased. Significant improvements were also detected in the total CAMPHOR score (20.7±10.9 to 16.2±10.4, p=0.001) and 6MWT distance (371.7±84.7m to 402.8.0±74.9m, p=0.001). Peak VO2 remained unchanged (40.7±9.2% to 43.8±12.4% of predicted, p=0.15). ConclusionThree months of iron replacement therapy in iron-deficient cyanotic CHD patients was safe and resulted in significant improvement in exercise tolerance and quality of life. Identification of iron deficiency and appropriate replacement should be advocated in these patients.
Published Version
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