2012
DOI: 10.1097/mph.0b013e3182588996
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Reticulocyte Parameters

Abstract: The aim of the present study was to determine the effects of exclusive oral iron supplementation (iron sulphate 2 mg/kg/die) in asymptomatic children with severe iron-deficiency anemia [median hemoglobin (Hb) level before treatment 6.3 g/dL; range 4.5 to 7 g/dL] and to investigate the accuracy of Hb, reticulocyte hemoglobin content (CHr), and absolute reticulocyte count (ARC) as markers for monitoring early response to treatment. The increase in ARC and CHr was statistically significant at day +3. There was a … Show more

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Cited by 27 publications
(13 citation statements)
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“…Similar conclusion regarding response to exclusive oral iron therapy in a small cohort of children with severe iron deficiency anemia had been previously reported by our group [ 9 ]. Main outcome of our preliminary study [ 9 ] was to evaluate if oral iron supplementation should be proposed as first-line treatment in a small cohort of clinically asymptomatic patients with severe iron deficiency anemia.…”
Section: Resultssupporting
confidence: 91%
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“…Similar conclusion regarding response to exclusive oral iron therapy in a small cohort of children with severe iron deficiency anemia had been previously reported by our group [ 9 ]. Main outcome of our preliminary study [ 9 ] was to evaluate if oral iron supplementation should be proposed as first-line treatment in a small cohort of clinically asymptomatic patients with severe iron deficiency anemia.…”
Section: Resultssupporting
confidence: 91%
“…Similar conclusion regarding response to exclusive oral iron therapy in a small cohort of children with severe iron deficiency anemia had been previously reported by our group [ 9 ]. Main outcome of our preliminary study [ 9 ] was to evaluate if oral iron supplementation should be proposed as first-line treatment in a small cohort of clinically asymptomatic patients with severe iron deficiency anemia. These patients, due to their Hb levels (median 6.3 g/dL, range 4.5–7), needed a tight follow-up; for that reason, the kinetic of response was assessed within 48 hours from the onset of iron administration (T1) and our data demonstrated the utility of ARC and CHr as accurate markers for the early detection of patients not responding to oral iron to be quickly switched to other therapies (parenteral iron supplementation or transfusion).…”
Section: Resultssupporting
confidence: 91%
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“… 4 Among the new hematological parameters recently developed to precisely diagnose IDA, CHr has recently gained ample attention in the pediatric clinical settings since it is found to be the strongest predictor of ID and IDA, 2 , 5 , 6 as well as it could be considered an affordable and widely available marker to detect early responders to oral iron therapy and to switch unresponsive children to parenteral iron supplementation or transfusion. 7 Actually, the utility of CHr in the identification of Saudi children with IDA has been evaluated and showed that a CHr cut-off level of 26 pg is considered to be a reasonable indicator of anemic states. Moreover, CHr together with a complete blood count might provide an alternative to the traditional hematologic or biochemical panel for the diagnosis of ID and IDA in young children and it is cost-effective.…”
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confidence: 99%