Low hemoglobin at hemodialysis initiation: an international study of anemia management and mortality in the early dialysis period.

anemia chronic kidney disease hemodialysis hemoglobin mortality

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 24 10 2018
accepted: 29 04 2019
entrez: 24 7 2020
pubmed: 24 7 2020
medline: 24 7 2020
Statut: epublish

Résumé

Anemia at hemodialysis (HD) initiation is common. Correcting low hemoglobin (Hgb) before HD initiation may improve survival by avoiding potential harms of chronic anemia, high doses of erythropoiesis-stimulating agents (ESAs) and intravenous (IV) iron in the early HD period, and/or rapid Hgb rise. We included 4604 incident HD patients from 21 countries in the Dialysis Outcomes and Practice Patterns Study Phases 4-5 (2009-15). Because low Hgb at HD start may reflect comorbidity or ESA hyporesponse, we restricted our analysis to the 80% of patients who achieved Hgb ≥10 g/dL 91-120 days after HD start (Month 4). About 53% of these patients had Hgb <10 g/dL in Month 1 (<30 days after HD start); they were younger with a similar comorbidity profile (versus Hgb ≥10 g/dL). Month 1 Hgb was associated with first-year HD mortality (adjusted hazard ratio for 1 g/dL higher Hgb was 0.89; 95% confidence interval: 0.81-0.97), despite minimal differences in Month 4 Hgb. Patients with lower Hgb in Month 1 received higher doses of ESA, but not IV iron, over the first 3 months of HD. Results were consistent when excluding catheter users or adjusting for IV iron and ESA dose over the first 3 months. Even among patients with Hgb ≥10 g/dL 3 months later, anemia at HD initiation was common and associated with elevated mortality. A more proactive approach to anemia management in advanced chronic kidney disease (CKD) may thus improve survival on HD, though long-term prospective studies of non-dialysis CKD patients are needed.

Sections du résumé

BACKGROUND BACKGROUND
Anemia at hemodialysis (HD) initiation is common. Correcting low hemoglobin (Hgb) before HD initiation may improve survival by avoiding potential harms of chronic anemia, high doses of erythropoiesis-stimulating agents (ESAs) and intravenous (IV) iron in the early HD period, and/or rapid Hgb rise.
METHODS METHODS
We included 4604 incident HD patients from 21 countries in the Dialysis Outcomes and Practice Patterns Study Phases 4-5 (2009-15). Because low Hgb at HD start may reflect comorbidity or ESA hyporesponse, we restricted our analysis to the 80% of patients who achieved Hgb ≥10 g/dL 91-120 days after HD start (Month 4).
RESULTS RESULTS
About 53% of these patients had Hgb <10 g/dL in Month 1 (<30 days after HD start); they were younger with a similar comorbidity profile (versus Hgb ≥10 g/dL). Month 1 Hgb was associated with first-year HD mortality (adjusted hazard ratio for 1 g/dL higher Hgb was 0.89; 95% confidence interval: 0.81-0.97), despite minimal differences in Month 4 Hgb. Patients with lower Hgb in Month 1 received higher doses of ESA, but not IV iron, over the first 3 months of HD. Results were consistent when excluding catheter users or adjusting for IV iron and ESA dose over the first 3 months.
CONCLUSIONS CONCLUSIONS
Even among patients with Hgb ≥10 g/dL 3 months later, anemia at HD initiation was common and associated with elevated mortality. A more proactive approach to anemia management in advanced chronic kidney disease (CKD) may thus improve survival on HD, though long-term prospective studies of non-dialysis CKD patients are needed.

Identifiants

pubmed: 32699623
doi: 10.1093/ckj/sfz065
pii: sfz065
pmc: PMC7367115
doi:

Types de publication

Journal Article

Langues

eng

Pagination

425-433

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA.

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Auteurs

Angelo Karaboyas (A)

Arbor Research Collaborative for Health, Ann Arbor, MI, USA.
Department of Epidemiology, University of Michigan, Ann Arbor, MI, USA.

Hal Morgenstern (H)

Department of Epidemiology and Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
Department of Urology, Medical School, University of Michigan, Ann Arbor, MI, USA.

Sandra Waechter (S)

Vifor Pharma Ltd, Glattbrugg, Switzerland.

Nancy L Fleischer (NL)

Department of Epidemiology, University of Michigan, Ann Arbor, MI, USA.

Raymond Vanholder (R)

Department of Nephrology, University Hospital Ghent, Ghent, Belgium.

Stefan H Jacobson (SH)

Karolinska Institutet, Danderyd University Hospital, Stockholm, Sweden.

Manish M Sood (MM)

Department of Medicine, School of Epidemiology and Public Health, The Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

Douglas E Schaubel (DE)

Department of Biostatistics, University of Michigan, Ann Arbor, MI, USA.

Masaaki Inaba (M)

Department of Metabolism, Endocrinology and Molecular Medicine, Osaka City University Graduate School of Medicine, Osaka, Japan.

Ronald L Pisoni (RL)

Arbor Research Collaborative for Health, Ann Arbor, MI, USA.

Bruce M Robinson (BM)

Arbor Research Collaborative for Health, Ann Arbor, MI, USA.
Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.

Classifications MeSH