Long-term mortality risk associated with citric acid- and acetic acid-based bicarbonate haemodialysis: a historical cohort propensity score-matched study in a large, multicentre, population-based study.


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 27 12 2019
accepted: 27 03 2020
pubmed: 4 7 2020
medline: 1 12 2020
entrez: 4 7 2020
Statut: ppublish

Résumé

Citric acid-based bicarbonate dialysate (CiD) is increasingly used in haemodialysis (HD) to improve haemodynamic tolerance and haemocompatibility associated with acetic acid-based bicarbonate dialysate. Safety concerns over CiD have been raised recently after a French ecological study reported higher mortality hazard in HD clinics with high CiD consumption. Therefore, we evaluated the mortality risk associated with various acidifiers (AcD, CiD) of bicarbonate dialysate. In this multicentre, historical cohort study, we included adult incident HD patients (European, Middle-East and Africa Fresenius Medical Care network; 1 January 2014 to 31 October 2018). We recorded acidifiers of bicarbonate dialysis and dialysate composition for each dialysis session. In the primary intention-to-treat analysis, patients were assigned to the exposed group if they received CiD in >70% of sessions during the first 3 months (CiD70%), whereas the non-exposed group received no CiD at all. In the secondary analysis, exposure was assessed on a monthly basis for the whole duration of the follow-up. We enrolled 10 121 incident patients during the study period. Of them, 371 met the criteria for inclusion in CiD70%. After propensity score matching, mortality was 11.43 [95% confidence interval (CI) 8.86-14.75] and 12.04 (95% CI 9.44-15.35) deaths/100 person-years in the CiD0% and CiD70% groups, respectively (P = 0.80). A similar association trend was observed in the secondary analysis. We did not observe evidence of increased mortality among patients exposed to CiD in a large European cohort of dialysis patients despite the fact that physicians were more inclined to prescribe CiD to subjects with worse medical conditions.

Sections du résumé

BACKGROUND
Citric acid-based bicarbonate dialysate (CiD) is increasingly used in haemodialysis (HD) to improve haemodynamic tolerance and haemocompatibility associated with acetic acid-based bicarbonate dialysate. Safety concerns over CiD have been raised recently after a French ecological study reported higher mortality hazard in HD clinics with high CiD consumption. Therefore, we evaluated the mortality risk associated with various acidifiers (AcD, CiD) of bicarbonate dialysate.
METHODS
In this multicentre, historical cohort study, we included adult incident HD patients (European, Middle-East and Africa Fresenius Medical Care network; 1 January 2014 to 31 October 2018). We recorded acidifiers of bicarbonate dialysis and dialysate composition for each dialysis session. In the primary intention-to-treat analysis, patients were assigned to the exposed group if they received CiD in >70% of sessions during the first 3 months (CiD70%), whereas the non-exposed group received no CiD at all. In the secondary analysis, exposure was assessed on a monthly basis for the whole duration of the follow-up.
RESULTS
We enrolled 10 121 incident patients during the study period. Of them, 371 met the criteria for inclusion in CiD70%. After propensity score matching, mortality was 11.43 [95% confidence interval (CI) 8.86-14.75] and 12.04 (95% CI 9.44-15.35) deaths/100 person-years in the CiD0% and CiD70% groups, respectively (P = 0.80). A similar association trend was observed in the secondary analysis.
CONCLUSIONS
We did not observe evidence of increased mortality among patients exposed to CiD in a large European cohort of dialysis patients despite the fact that physicians were more inclined to prescribe CiD to subjects with worse medical conditions.

Identifiants

pubmed: 32617561
pii: 5866678
doi: 10.1093/ndt/gfaa089
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bicarbonates 0
Buffers 0
Calcium Chelating Agents 0
Citric Acid 2968PHW8QP
Acetic Acid Q40Q9N063P

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1237-1244

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

Auteurs

Luca Neri (L)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Francesco Bellocchio (F)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Fatih Kircelli (F)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Tomas Jirka (T)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Martial Levannier (M)

Dialysis Unit of Beziers, Nephrocare, Beziers, France.

Jean Guillaume (J)

Dialysis Unit of Tassin-Charcot, Nephrocare, Tassin-Charcot, France.

David Attaf (D)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Carlo Barbieri (C)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Mario Garbelli (M)

Clinical & Data Intelligence Systems, Fresenius Medical Care Deutschland GmbH, Vaiano Cremasco (CR), Italy.

Stefano Stuard (S)

Dialysis Unit of Tassin-Charcot, Nephrocare, Tassin-Charcot, France.

Bernard Canaud (B)

Fresenius Medical Care, Bad Homburg, Germany.

Charles Chazot (C)

Country Medical Director, NephroCare France, Fresnes, France.

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Classifications MeSH