Literature DB >> 1374865

Dextran antibodies, complement conversion and circulating immune complexes after intravenous iron dextran therapy in dialysed patients.

L W Fleming1, W K Stewart, D Parratt.   

Abstract

Serum immune complexes, plasma dextran antibodies and percentage conversion of complement have been measured in 20 dialysed patients before and after an intravenous infusion of iron dextran providing 600 mg elemental iron. Complement conversion was unmeasurable and there were no changes in circulating immune complexes. The presence of dextran antibodies in nine patients before the infusion was not related to prior exposure to iron dextran. They became undetectable in these patients within hours after the infusion, reappearing 1 month later in three. Two of three patients reporting mild aches and shivers on the day following the infusion had no detectable dextran antibodies. An adverse reaction involving inflamed joints occurred 1-2 days after a second infusion given to one of the patients studied above. The parameters under study were again measured and did not appear to relate to the reaction. The presence of dextran antibodies does not preclude the giving of iron dextran to patients on dialysis, and the immune complex and complement systems remain undisturbed by iron dextran infusions.

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Year:  1992        PMID: 1374865

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  6 in total

1.  Withdrawal of a monopoly treatment.

Authors:  L W Fleming; I S Henderson; M O Jones; W K Stewart
Journal:  BMJ       Date:  1992-08-01

2.  Comparison of hypersensitivity reactions of intravenous iron: iron isomaltoside-1000 (Monofer® ) versus ferric carboxy-maltose (Ferinject® ). A single center, cohort study.

Authors:  Midas B Mulder; Hester L van den Hoek; Erwin Birnie; Antonie J P van Tilburg; Elsbeth M Westerman
Journal:  Br J Clin Pharmacol       Date:  2018-12-11       Impact factor: 4.335

3.  Hypersensitivity reactions to intravenous iron: guidance for risk minimization and management.

Authors:  David Rampton; Joergen Folkersen; Steven Fishbane; Michael Hedenus; Stefanie Howaldt; Francesco Locatelli; Shalini Patni; Janos Szebeni; Guenter Weiss
Journal:  Haematologica       Date:  2014-11       Impact factor: 9.941

Review 4.  Safety aspects of parenteral iron in patients with end-stage renal disease.

Authors:  G Sunder-Plassmann; W H Hörl
Journal:  Drug Saf       Date:  1997-10       Impact factor: 5.606

Review 5.  Hypersensitivity to intravenous iron: classification, terminology, mechanisms and management.

Authors:  J Szebeni; S Fishbane; M Hedenus; S Howaldt; F Locatelli; S Patni; D Rampton; G Weiss; J Folkersen
Journal:  Br J Pharmacol       Date:  2015-10-25       Impact factor: 8.739

6.  Assessment of Dextran Antigenicity of Intravenous Iron Preparations with Enzyme-Linked Immunosorbent Assay (ELISA).

Authors:  Susann Neiser; Taija S Koskenkorva; Katrin Schwarz; Maria Wilhelm; Susanna Burckhardt
Journal:  Int J Mol Sci       Date:  2016-07-21       Impact factor: 5.923

  6 in total

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