Interdialytic weight gain of less than 2.5% seems to limit cardiac damage during hemodialysis.

Biocompatibility NT-pro-BNP emboli heart hemodialysis interdialytic weight gain pentraxin troponin

Journal

The International journal of artificial organs
ISSN: 1724-6040
Titre abrégé: Int J Artif Organs
Pays: United States
ID NLM: 7802649

Informations de publication

Date de publication:
Aug 2021
Historique:
pubmed: 20 12 2020
medline: 19 8 2021
entrez: 19 12 2020
Statut: ppublish

Résumé

To investigate if a single low-flux HD induces a rise in cardiac biomarkers and if a change in clinical approach may limit such mechanism. A total of 20 chronic HD patients each underwent three different study-dialyses. Dialyzers (low-flux polysulfone, 1.8 sqm) had been stored either dry or wet (Wet) and the blood level in the venous chamber kept low or high. Laboratory results were measured at baseline, 30 and 180 min, adjusted for the effect of fluid shift. Ultrasound measured microemboli signals (MES) within the return line. Hemodialysis raised cardiac biomarkers ( Hemodialysis, independent of type of dialyzer storage, was associated with raised cardiac biomarkers, more profoundly in patients with higher pre-dialysis values and IDWG. A limitation in IDWG to <2.5% and prolonged ultrafiltration time may limit cardiac strain during HD, especially in patients with cardiovascular risk.

Identifiants

pubmed: 33339470
doi: 10.1177/0391398820981385
pmc: PMC8366174
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

539-550

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Auteurs

Junko Goto (J)

Institute of Public Health and Clinical Medicine, Division of Medicine, Umeå University, Umeå, Sweden.
Department of Emergency and Critical Care Medicine, School of Medicine, University of Yamanashi, Yamanashi, Japan.

Ulf Forsberg (U)

Institute of Public Health and Clinical Medicine, Division of Medicine, Umeå University, Umeå, Sweden.
Department of Internal Medicine, Skellefteå County Hospital, Skellefteå, Sweden.

Per Jonsson (P)

Institute of Public Health and Clinical Medicine, Division of Medicine, Umeå University, Umeå, Sweden.

Kenichi Matsuda (K)

Department of Emergency and Critical Care Medicine, School of Medicine, University of Yamanashi, Yamanashi, Japan.

Bo Nilsson (B)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.

Kristina Nilsson Ekdahl (K)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Linnaeus Centre of Biomaterials Chemistry, Linnaeus University, Kalmar, Sweden.

Michael Y Henein (MY)

Institute of Public Health and Clinical Medicine, Division of Medicine, Umeå University, Umeå, Sweden.

Bernd G Stegmayr (BG)

Institute of Public Health and Clinical Medicine, Division of Medicine, Umeå University, Umeå, Sweden.

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