TY - JOUR
T1 - Iron Administration, Infection, and Anemia Management in CKD
T2 - Untangling the Effects of Intravenous Iron Therapy on Immunity and Infection Risk
AU - Ganz, Tomas
AU - Aronoff, George R.
AU - Gaillard, Carlo A.J.M.
AU - Goodnough, Lawrence T.
AU - Macdougall, Iain C.
AU - Mayer, Gert
AU - Porto, Graça
AU - Winkelmayer, Wolfgang C.
AU - Wish, Jay B.
N1 - Funding Information:
Tomas Ganz, MD, George R. Aronoff, MD, Carlo A.J.M. Gaillard, MD, Lawrence T. Goodnough, MD, Iain C. Macdougall, MD, Gert Mayer, MD, Graça Porto, MD, Wolfgang C. Winkelmayer, MD, ScD, and Jay B. Wish, MD. This article is based on discussions at an international advisory board meeting sponsored by Vifor Fresenius Medical Care Renal Pharma, which manufactures several iron replacement therapies. Vifor Fresenius Medical Care Renal Pharma provided funding for writing and editing services to assist with the preparation of this manuscript. The article sponsor had no role in the collection, analysis, and interpretation of data; writing the report; or the decision to submit the report for publication. The final decision on the main points to be communicated, including the conclusions drawn, was made by consensus of the authors. Dr Aronoff is consultant to Akebia, AstraZeneca, Bayer, Rockwell Medical, and Vifor; owner of Dosis, Inc; and employee of DaVita, Inc. Dr Gaillard received speakers’ fees, honoraria, and consultancy fees from Amgen, Corvidia, Keryx Pharma, Pharmacosmos, Roche, and Vifor Pharma. Dr Ganz is consultant to Akebia, Gilead, Keryx Pharma, La Jolla Pharmaceutical Company, and Vifor; and scientific founder, shareholder, and consultant to Intrinsic LifeSciences and Silarus Pharma. Dr Goodnough is advisory board member for American Reagent. Dr Macdougall received speakers’ fees, honoraria, and consultancy fees from Akebia, AMAG, Amgen, Astellas, Bayer, FibroGen, GlaxoSmithKline, Pharmacosmos, and Vifor Pharma. Dr Mayer is consultant to Amgen, Astellas, AstraZeneca, Boehringer Ingelheim, Gilead, and Vifor. Dr Porto received speakers’ fees and consultancy fees from Novartis, Silence Therapeutics, and Vifor Pharma. Dr Winkelmayer is consultant to Akebia, Amgen, AstraZeneca, Bayer, Daichii Sankyo, Janssen, Relypsa, and Vifor Fresenius Medical Care Renal Pharma. Dr Wish is consultant to Akebia, AstraZeneca, Otsuka, Rockwell Medical, and Vifor and on the speakers bureau for Akebia and AstraZeneca. Assistance with the writing and editing of the manuscript was provided by Adam Perahia, MD, of NorthStar Strategic Consulting, LLC. Received December 12, 2019. Evaluated by 3 external peer reviewers, with direct editorial input from the Editor-in-Chief. Accepted in revised form January 5, 2020.
Publisher Copyright:
© 2020 The Authors
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Patients with chronic kidney disease (CKD) are at increased risk for infection, attributable to immune dysfunction, increased exposure to infectious agents, loss of cutaneous barriers, comorbid conditions, and treatment-related factors (eg, hemodialysis and immunosuppressant therapy). Because iron plays a vital role in pathogen reproduction and host immunity, it is biologically plausible that intravenous iron therapy and/or iron deficiency influence infection risk in CKD. Available data from preclinical experiments, observational studies, and randomized controlled trials are summarized to explore the interplay between intravenous iron and infection risk among patients with CKD, particularly those receiving maintenance hemodialysis. The current evidence base, including data from a recent randomized controlled trial, suggests that proactive judicious use of intravenous iron (in a manner that minimizes the accumulation of non–transferrin-bound iron) beneficially replaces iron stores while avoiding a clinically relevant effect on infection risk. In the absence of an urgent clinical need, intravenous iron therapy should be avoided in patients with active infection. Although serum ferritin concentration and transferrin saturation can help guide clinical decision making about intravenous iron therapy, definition of an optimal iron status and its precise determination in individual patients remain clinically challenging in CKD and warrant additional study.
AB - Patients with chronic kidney disease (CKD) are at increased risk for infection, attributable to immune dysfunction, increased exposure to infectious agents, loss of cutaneous barriers, comorbid conditions, and treatment-related factors (eg, hemodialysis and immunosuppressant therapy). Because iron plays a vital role in pathogen reproduction and host immunity, it is biologically plausible that intravenous iron therapy and/or iron deficiency influence infection risk in CKD. Available data from preclinical experiments, observational studies, and randomized controlled trials are summarized to explore the interplay between intravenous iron and infection risk among patients with CKD, particularly those receiving maintenance hemodialysis. The current evidence base, including data from a recent randomized controlled trial, suggests that proactive judicious use of intravenous iron (in a manner that minimizes the accumulation of non–transferrin-bound iron) beneficially replaces iron stores while avoiding a clinically relevant effect on infection risk. In the absence of an urgent clinical need, intravenous iron therapy should be avoided in patients with active infection. Although serum ferritin concentration and transferrin saturation can help guide clinical decision making about intravenous iron therapy, definition of an optimal iron status and its precise determination in individual patients remain clinically challenging in CKD and warrant additional study.
KW - Chronic kidney disease
KW - hemodialysis
KW - immunity
KW - infection
KW - intravenous iron
KW - iron deficiency
KW - safety
UR - https://www.scopus.com/pages/publications/85083564356
U2 - 10.1016/j.xkme.2020.01.006
DO - 10.1016/j.xkme.2020.01.006
M3 - Review article
C2 - 32734254
AN - SCOPUS:85083564356
VL - 2
SP - 341
EP - 353
JO - Kidney Medicine
JF - Kidney Medicine
IS - 3
ER -