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Hipofosfatemia durante la terapia de reemplazo renal y días libres de ventilador: un análisis post-hoc del ensayo
Javier A Neyra1, Melissa Thompson Bastin2, Ehsan Ghamarian3
1Department of Medicine, Division of Nephrology, University of Alabama at Birmingham, Birmingham, Alabama, United States.
Rationale & Objective:
Critically ill patients receiving kidney replacement therapy (KRT), especially continuous KRT (CKRT), have a high risk of hypophosphatemia due to extracorporeal losses, which may contribute to muscle weakness and prolonged respiratory failure. This study evaluated the relationship between incident hypophosphatemia and respiratory function in these patients.
Study Design:
Post hoc observational study of STARRT-AKI trial participants.
Setting & Participants:
Eligible trial participants 1) received continuous kidney replacement therapy (CKRT) >24 hours or intermittent hemodialysis (IHD) or sustained low-efficiency dialysis (SLED) for >1 session, 2) had a serum phosphate ≥0.5 mmol/L on the day of KRT initiation, and 3) had ≥1 serum phosphate measurement during KRT.
Exposures:
Hypophosphatemia (<0.7 mmol/L) and severe hypophosphatemia (<0.5 mmol/L) during KRT.
Outcomes:
Primary outcome was ventilator-free days (VFD) at 28 days of follow-up. Secondary outcomes included mortality and KRT dependence at 90 days.
Analytical Approach:
A truncated hurdle model was fit to describe clinical characteristics associated with hypophosphatemia. Adjusted analyses of VFD utilized an inverse probability weighted zero-inflated negative binomial model and a win-ratio analysis. Secondary outcomes were assessed with logistic regression.
Results:
1,942 trial participants were studied. Among them, 634 (32.6%) developed hypophosphatemia, and 192 (9.9%) developed severe hypophosphatemia. Clinical factors independently associated with incident hypophosphatemia during KRT were female sex, lower body weight, lower serum phosphate levels at KRT initiation, CKRT as the initial KRT modality, and randomization to accelerated KRT initiation. Incident hypophosphatemia and severe hypophosphatemia were associated with fewer VFD at 28 days (β 0.91, 95% CI: 0.87, 0.95 and β 0.87, 95% CI: 0.82, 0.93, respectively, p<0.001 for both). By win-ratio for any random pair of patients, those with incident hypophosphatemia and severe hypophosphatemia had a 27% and 25% lower likelihood of combined 28-day survival and fewer days on the ventilator, respectively. There was no association between hypophosphatemia and 90-day mortality or KRT dependence.
Limitations:
Selection bias and unmeasured confounding.
Conclusions:
Incident hypophosphatemia during KRT was independently associated with fewer VFD at 28 days.
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