Evaluation of iron stores in hemodialysis patients on maintenance ferric Carboxymaltose dosing.
Anemia, Iron-Deficiency
/ blood
Dose-Response Relationship, Drug
Drug Monitoring
/ methods
Female
Ferric Compounds
/ administration & dosage
Ferritins
/ blood
Hematinics
/ administration & dosage
Humans
Infusions, Intravenous
/ methods
Iron
/ metabolism
Male
Maltose
/ administration & dosage
Middle Aged
Prospective Studies
Renal Dialysis
/ adverse effects
Renal Insufficiency, Chronic
/ blood
Time Factors
Transferrin
/ analysis
Anemia of chronic kidney disease
Chronic hemodialysis
FCM
Ferric carboxymaltose
Ferritin
Iron
Transferrin saturation
Journal
BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
received:
05
12
2018
accepted:
21
02
2019
entrez:
3
3
2019
pubmed:
3
3
2019
medline:
7
3
2020
Statut:
epublish
Résumé
Iron is administered intravenously (IV) to many dialysis patients at regular intervals and iron stores are evaluated through periodic measurements of ferritin and transferrin saturation (TSAT). In patients without kidney diseases, large single doses of IV iron lead to a transient rise in serum ferritin that does not reflect iron stores. It is not known whether and to what extent smaller IV iron doses used to maintain adequate stores in hemodialysis patients lead to transient spurious elevations of ferritin and TSAT. Ferritin and TSAT were serially determined over four weeks after the administration of ferric carboxymaltose (FCM) in hemodialysis patients on a stable maintenance FCM dosing regimen of 100 mg or 200 mg every four weeks. Ferritin values increased by 113 ± 72.2 μg/l (P < 0.001) from baseline to the peak value and remained significantly elevated until two weeks after the administration of 100 mg FCM (n = 19). After the administration of 200 mg FCM (n = 12), ferritin values increased by 188.5 ± 67.56 μg/l (P < 0.001) and remained significantly elevated by the end of week three. TSAT values increased by 12.0 ± 9.7% (P < 0.001) and 23.1 ± 20.4% (P = 0.002) in patients receiving 100 or 200 mg FCM, respectively, and returned to baseline within four days. IV administration of FCM at doses of 100 or 200 mg in hemodialysis patients leads to dose-dependent transient ferritin elevations of extended duration. Temporal coordination of blood sampling for iron status evaluation with the maintenance IV iron dosing schedule is advisable. ISRCTN12825165 (retrospectively registered 01/02/2019).
Sections du résumé
BACKGROUND
Iron is administered intravenously (IV) to many dialysis patients at regular intervals and iron stores are evaluated through periodic measurements of ferritin and transferrin saturation (TSAT). In patients without kidney diseases, large single doses of IV iron lead to a transient rise in serum ferritin that does not reflect iron stores. It is not known whether and to what extent smaller IV iron doses used to maintain adequate stores in hemodialysis patients lead to transient spurious elevations of ferritin and TSAT.
METHODS
Ferritin and TSAT were serially determined over four weeks after the administration of ferric carboxymaltose (FCM) in hemodialysis patients on a stable maintenance FCM dosing regimen of 100 mg or 200 mg every four weeks.
RESULTS
Ferritin values increased by 113 ± 72.2 μg/l (P < 0.001) from baseline to the peak value and remained significantly elevated until two weeks after the administration of 100 mg FCM (n = 19). After the administration of 200 mg FCM (n = 12), ferritin values increased by 188.5 ± 67.56 μg/l (P < 0.001) and remained significantly elevated by the end of week three. TSAT values increased by 12.0 ± 9.7% (P < 0.001) and 23.1 ± 20.4% (P = 0.002) in patients receiving 100 or 200 mg FCM, respectively, and returned to baseline within four days.
CONCLUSIONS
IV administration of FCM at doses of 100 or 200 mg in hemodialysis patients leads to dose-dependent transient ferritin elevations of extended duration. Temporal coordination of blood sampling for iron status evaluation with the maintenance IV iron dosing schedule is advisable.
TRIAL REGISTRATION
ISRCTN12825165 (retrospectively registered 01/02/2019).
Identifiants
pubmed: 30823916
doi: 10.1186/s12882-019-1263-8
pii: 10.1186/s12882-019-1263-8
pmc: PMC6397449
doi:
Substances chimiques
Ferric Compounds
0
Hematinics
0
Transferrin
0
ferric carboxymaltose
6897GXD6OE
Maltose
69-79-4
Ferritins
9007-73-2
Iron
E1UOL152H7
Banques de données
ISRCTN
['ISRCTN12825165']
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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