A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Suboptimal dialysis initiation is associated with comorbidities and uraemia progression rate but not with estimated glomerular filtration rate
Tekijät: Heaf James, Heiro Maija, Petersons Aivars, Vernere Baiba, Povlsen Johan V, Sørensen Anette Bagger, Clyne Naomi, Bumblyte Inga, Zilinskiene Alanta, Randers Else, Løkkegaard Niels, Ots-Rosenberg Mai, Kjellevold Stig, Kampmann Jan Dominik, Rogland Björn, Lagreid Inger, Heimburger Olof, Lindholm Bengt
Kustantaja: OXFORD UNIV PRESS
Julkaisuvuosi: 2021
Journal: Clinical Kidney Journal
Tietokannassa oleva lehden nimi: CLINICAL KIDNEY JOURNAL
Lehden akronyymi: CLIN KIDNEY J
Vuosikerta: 14
Numero: 3
Aloitussivu: 933
Lopetussivu: 942
Sivujen määrä: 10
ISSN: 2048-8505
eISSN: 2048-8513
DOI: https://doi.org/10.1093/ckj/sfaa041
Verkko-osoite: https://academic.oup.com/ckj/article/14/3/933/5821484
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/58623494
Background
Despite early referral of uraemic patients to nephrological care, suboptimal dialysis initiation (SDI) remains a common problem associated with increased morbimortality. We hypothesized that SDI is related to pre-dialysis care.
Methods
In the 'Peridialysis' study, time and reasons for dialysis initiation (DI), clinical and biochemical data and centre characteristics were registered during the pre- and peri-dialytic period for 1583 end-stage kidney disease patients starting dialysis over a 3-year period at 15 nephrology departments in the Nordic and Baltic countries to identify factors associated with SDI.
Results
SDI occurred in 42%. Risk factors for SDI were late referral, cachexia, comorbidity (particularly cardiovascular), hypoalbuminaemia and rapid uraemia progression. Patients with polycystic renal disease had a lower incidence of SDI. High urea and C-reactive protein levels, acidosis and other electrolyte disorders were markers of SDI, independently of estimated glomerular filtration rate (eGFR). SDI patients had higher eGFR than non-SDI patients during the pre-dialysis period, but lower eGFR at DI. eGFR as such did not predict SDI. Patients with comorbidities had higher eGFR at DI. Centre practice and policy did not associate with the incidence of SDI.
Conclusions
SDI occurred in 42% of all DIs. SDI was associated with hypoalbuminaemia, comorbidity and rate of eGFR loss, but not with the degree of renal failure as assessed by eGFR.
Ladattava julkaisu This is an electronic reprint of the original article. |