Intravenous iron dextran therapy in patients with iron deficiency and normal renal function who failed to respond to or did not tolerate oral iron supplementation

PURPOSE: To evaluate the safety and effectiveness of using 500-mg doses of iron as intravenous iron dextran after premedication with diphenhydramine, cimetidine, and dexamethasone. SUBJECTS AND METHODS: We treated 135 iron-deficient adults (26 men, 109 women) with normal renal function (serum creati...

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Veröffentlicht in:The American journal of medicine 2000-07, Vol.109 (1), p.27-32
Hauptverfasser: Barton, James C, Barton, Ellen H, Bertoli, Luigi F, Gothard, Charlene H, Sherrer, Jennifer S
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container_issue 1
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container_title The American journal of medicine
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creator Barton, James C
Barton, Ellen H
Bertoli, Luigi F
Gothard, Charlene H
Sherrer, Jennifer S
description PURPOSE: To evaluate the safety and effectiveness of using 500-mg doses of iron as intravenous iron dextran after premedication with diphenhydramine, cimetidine, and dexamethasone. SUBJECTS AND METHODS: We treated 135 iron-deficient adults (26 men, 109 women) with normal renal function (serum creatinine level ≤1.5 mg/dL or blood urea nitrogen level ≤26 mg/dL) who could not be treated adequately with oral iron supplements due to gastrointestinal symptoms (59%), inadequate hematologic response (39%), severe anemia (19%), or noncompliance (4%). Some patients had more than one reason for treatment. Resolution of iron deficiency was defined as the restoration of transferrin saturation, serum ferritin level, anemia, and abnormal erythrocyte indexes to normal or baseline values. RESULTS: Before treatment with iron dextran, patients had a mean (± SD) transferrin saturation of 8% ± 5%, a median serum ferritin level of 11 ng/mL, and a mean hemoglobin level of 10 ± 2 g/dL. Ninety-two percent were anemic; 60% had unrecognized or untreated causes of anemia other than iron deficiency. We administered 285 iron dextran infusions (median 2, mean 2 infusions per patient; range 1 to 7). Eighty-seven percent of patients had no adverse reaction; 13% had mild reactions, especially arthralgias and myalgias. No patient had an anaphylaxis-like reaction. Fifty-four (40%) patients had resolution of iron deficiency, 34 (25%) continue to receive therapy, 36 (27%) returned to the care of their primary physician, and 11 (8%) died before iron repletion could be achieved. CONCLUSIONS: Iron-deficient adults with normal renal function who cannot be treated adequately with oral iron supplements can be treated effectively and safely with this intravenous iron dextran regimen.
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SUBJECTS AND METHODS: We treated 135 iron-deficient adults (26 men, 109 women) with normal renal function (serum creatinine level ≤1.5 mg/dL or blood urea nitrogen level ≤26 mg/dL) who could not be treated adequately with oral iron supplements due to gastrointestinal symptoms (59%), inadequate hematologic response (39%), severe anemia (19%), or noncompliance (4%). Some patients had more than one reason for treatment. Resolution of iron deficiency was defined as the restoration of transferrin saturation, serum ferritin level, anemia, and abnormal erythrocyte indexes to normal or baseline values. RESULTS: Before treatment with iron dextran, patients had a mean (± SD) transferrin saturation of 8% ± 5%, a median serum ferritin level of 11 ng/mL, and a mean hemoglobin level of 10 ± 2 g/dL. Ninety-two percent were anemic; 60% had unrecognized or untreated causes of anemia other than iron deficiency. We administered 285 iron dextran infusions (median 2, mean 2 infusions per patient; range 1 to 7). Eighty-seven percent of patients had no adverse reaction; 13% had mild reactions, especially arthralgias and myalgias. No patient had an anaphylaxis-like reaction. Fifty-four (40%) patients had resolution of iron deficiency, 34 (25%) continue to receive therapy, 36 (27%) returned to the care of their primary physician, and 11 (8%) died before iron repletion could be achieved. CONCLUSIONS: Iron-deficient adults with normal renal function who cannot be treated adequately with oral iron supplements can be treated effectively and safely with this intravenous iron dextran regimen.</description><identifier>ISSN: 0002-9343</identifier><identifier>EISSN: 1555-7162</identifier><identifier>DOI: 10.1016/S0002-9343(00)00396-X</identifier><identifier>PMID: 10936475</identifier><identifier>CODEN: AJMEAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Adults ; Anemia, Iron-Deficiency - blood ; Anemia, Iron-Deficiency - diet therapy ; Anemia, Iron-Deficiency - drug therapy ; Biological and medical sciences ; Clinical trials ; Dietary Supplements ; Drug therapy ; Female ; Ferritins - blood ; General and cellular metabolism. 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We administered 285 iron dextran infusions (median 2, mean 2 infusions per patient; range 1 to 7). Eighty-seven percent of patients had no adverse reaction; 13% had mild reactions, especially arthralgias and myalgias. No patient had an anaphylaxis-like reaction. Fifty-four (40%) patients had resolution of iron deficiency, 34 (25%) continue to receive therapy, 36 (27%) returned to the care of their primary physician, and 11 (8%) died before iron repletion could be achieved. 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SUBJECTS AND METHODS: We treated 135 iron-deficient adults (26 men, 109 women) with normal renal function (serum creatinine level ≤1.5 mg/dL or blood urea nitrogen level ≤26 mg/dL) who could not be treated adequately with oral iron supplements due to gastrointestinal symptoms (59%), inadequate hematologic response (39%), severe anemia (19%), or noncompliance (4%). Some patients had more than one reason for treatment. Resolution of iron deficiency was defined as the restoration of transferrin saturation, serum ferritin level, anemia, and abnormal erythrocyte indexes to normal or baseline values. RESULTS: Before treatment with iron dextran, patients had a mean (± SD) transferrin saturation of 8% ± 5%, a median serum ferritin level of 11 ng/mL, and a mean hemoglobin level of 10 ± 2 g/dL. Ninety-two percent were anemic; 60% had unrecognized or untreated causes of anemia other than iron deficiency. We administered 285 iron dextran infusions (median 2, mean 2 infusions per patient; range 1 to 7). Eighty-seven percent of patients had no adverse reaction; 13% had mild reactions, especially arthralgias and myalgias. No patient had an anaphylaxis-like reaction. Fifty-four (40%) patients had resolution of iron deficiency, 34 (25%) continue to receive therapy, 36 (27%) returned to the care of their primary physician, and 11 (8%) died before iron repletion could be achieved. CONCLUSIONS: Iron-deficient adults with normal renal function who cannot be treated adequately with oral iron supplements can be treated effectively and safely with this intravenous iron dextran regimen.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10936475</pmid><doi>10.1016/S0002-9343(00)00396-X</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Adult
Adults
Anemia, Iron-Deficiency - blood
Anemia, Iron-Deficiency - diet therapy
Anemia, Iron-Deficiency - drug therapy
Biological and medical sciences
Clinical trials
Dietary Supplements
Drug therapy
Female
Ferritins - blood
General and cellular metabolism. Vitamins
Hemoglobins - metabolism
Humans
Infusions, Intravenous
Iron
Iron, Dietary - therapeutic use
Iron-Dextran Complex - therapeutic use
Kidney - physiology
Kidney Function Tests
Male
Medical sciences
Nutrition
Pharmacology. Drug treatments
Transferrin - metabolism
Treatment Failure
title Intravenous iron dextran therapy in patients with iron deficiency and normal renal function who failed to respond to or did not tolerate oral iron supplementation
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