Interdialytic weight gain of less than 2.5% seems to limit cardiac damage during hemodialysisShow others and affiliations
2021 (English)In: International Journal of Artificial Organs, ISSN 0391-3988, E-ISSN 1724-6040, Vol. 44, no 8, p. 539-550, article id 391398820981385Article in journal (Refereed) Published
Sustainable development
SDG 3: Ensure healthy lives and promote well-being for all at all ages
Abstract [en]
AIMS: 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.
MATERIAL AND METHODS: 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.
RESULTS: = 0.004) correlated with inter-dialytic-weight-gain (IDWG). Biomarkers behaved similarly between the HD modes. The least negative impact was with an IDWG ⩽ 2.5%. Multiple regression analyses of the Wet-High mode does not exclude a relation between increased exposure of MES and factors such as release of Pro-BNP.
CONCLUSION: 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.
Place, publisher, year, edition, pages
Sage Publications, 2021. Vol. 44, no 8, p. 539-550, article id 391398820981385
Keywords [en]
Biocompatibility, NT-pro-BNP, emboli, heart, hemodialysis, interdialytic weight gain, pentraxin, troponin
National Category
Cardiac and Cardiovascular Systems
Research subject
Natural Science, Biomedical Sciences
Identifiers
URN: urn:nbn:se:lnu:diva-102714DOI: 10.1177/0391398820981385ISI: 000657068800001PubMedID: 33339470Scopus ID: 2-s2.0-85097789568Local ID: 2020OAI: oai:DiVA.org:lnu-102714DiVA, id: diva2:1549428
2021-05-052021-05-052022-03-16Bibliographically approved