Iron Polymaltose And Pharmacology - In this article, we report on the findings of a study on iron polymaltose and pharmacology. Keep in mind that the materials contained in this article are technical in nature as they pertain to iron polymaltose and pharmacology.
However, due to space constraints we can only provide some basic information on iron polymaltose and pharmacology. If you want more information about iron polymaltose and pharmacology, we suggest you contact the gentleman who conducted the study on iron polymaltose and pharmacology in question.
The study on iron polymaltose and pharmacology was undertaken by S. Karger AG. Here is an overview of the findings:
“many studies of anaemia in patients on chronic haemodialysis have noted a high prevalence of iron deficiency despite oral iron supplementation. Our study examined the effect of intravenous iron given as bolus replacement. As the majority of these patients were not receiving concurrent recombinant human erythropoietin (rhEPO) it allowed an analysis of the safety and efficacy of intravenous iron as a single agent."
“in our unit, 62 out of 80 (77%) patients were considered iron deficient and received IV iron. Ten (10%) were considered to be in iron balance and 8 (10%) had biochemistry suggesting iron overload. None of the patients receiving iron experienced any adverse reactions. At three months a rise in haemoglobin level of at least 1 g/dl was noted in 53% of patients. The response was less in the remainder, but only 2 showed no response. CONCLUSIONS: Low levels of iron deficiency are often unrecognized in chronic haemodialysis patients on conventional therapy including oral iron supplementation. In such patients, the use of total dose infusion of iron polymaltose (dextrin) is a safe and effective method of raising haemoglobin levels. Substantial improvements may be achieved without the concurrent use of rhEPO.”
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