Continuous hemodialysis with citrate anticoagulation and standard dialysate for managing acute kidney injury in patients with moderate to severe hyponatremia-A retrospective study

dc.contributor.authorHellman Tapio
dc.contributor.authorUusalo Panu
dc.contributor.authorJärvisalo Mikko J
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=koulutuksen toimiala|en=Educational Affairs|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.contributor.organization-code1.2.246.10.2458963.20.53395929457
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.converis.publication-id53978557
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/53978557
dc.date.accessioned2022-10-28T12:31:45Z
dc.date.available2022-10-28T12:31:45Z
dc.description.abstract<b>Background:</b> The safety of continuous veno-venous hemodialysis (CVVHD) with citrate-calcium anticoagulation for acute kidney injury (AKI) with coincident hyponatremia remains unclear. We aimed to explore the feasibility of CVVHD with standard dialysate and citrate-calcium anticoagulation in hyponatremic critically ill AKI patients.<div><b>Methods:</b> Thirty-seven of the 493 critically ill AKI patients requiring CVVHD and admitted to our intensive care unit during a 10-year period had hyponatremia (<130 mmol/L) and were included in this retrospective study. All patients received CVVHD with citrate-calcium anticoagulation and standard commercial dialysate and plasma sodium concentrations were frequently controlled until death or CVVHD discontinuation. Clinical data, mortalities and cases of central pontine myelinolysis within one-year follow-up were recorded.</div><div><b>Results:</b> Median plasma sodium concentration was 127 (IQR 124-129) mmol/L at CVVHD initiation. CVVHD duration was median 3 (IQR 1.5-5.5) days and the mean daily sodium load of the trisodium citrate solution during the first 3 days of CVVHD was 1754 (SD 730) mmol. The plasma sodium concentration increased a median 8 (IQR 5-10) mmol/L during the first 24 hours of CVVHD and excessively high plasma sodium correction (>8 mmol/L/24 h) was observed in 18 (48.6%) patients. However, increased mortality in association to rapid plasma sodium correction was not observed in this study.</div><div><b>Conclusions:</b> CVVHD using standard citrate-calcium anticoagulation effectively increased plasma sodium concentration in this study. However, excessively high plasma sodium correction was observed in half of the patients and the sodium load provided by the standard citrate anticoagulation solutions was substantial.</div>
dc.identifier.eissn1399-6576
dc.identifier.jour-issn0001-5172
dc.identifier.olddbid177065
dc.identifier.oldhandle10024/160159
dc.identifier.urihttps://www.utupub.fi/handle/11111/32837
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/aas.13798
dc.identifier.urnURN:NBN:fi-fe2021050328519
dc.language.isoen
dc.okm.affiliatedauthorHellman, Tapio
dc.okm.affiliatedauthorUusalo, Panu
dc.okm.affiliatedauthorJärvisalo, Mikko
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1111/aas.13798
dc.relation.ispartofjournalActa Anaesthesiologica Scandinavica
dc.source.identifierhttps://www.utupub.fi/handle/10024/160159
dc.titleContinuous hemodialysis with citrate anticoagulation and standard dialysate for managing acute kidney injury in patients with moderate to severe hyponatremia-A retrospective study
dc.year.issued2021

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