by Patrick M. Honore, Aude Mugisha, Luc Kugener, Sebastien
Redant, Rachid Attou, Andrea Gallerani and David De Bels
We read with great interest the recent paper by Liang et al.
who conclude that their meta-analysis indicated an association between
metformin (MET) use prior to admission and lower mortality in septic adult
patients with diabetes mellitus [1].
We would like to make some comments. Nearly half of critically ill patients,
especially those with septic shock, have or develop acute kidney injury (AKI),
and 20–25% need renal replacement therapy (RRT) within the first week of their
admission [2].
Because of its low molecular weight and minimal protein binding, metformin is
equally (highly) eliminated by ultrafiltration (convection) and dialysis
(diffusion). Furthermore, its large volume of distribution within a
two-compartment pharmacokinetic model implies that metformin may be more
effectively cleared by prolonged RRT. This was corroborated by Keller et al.,
who showed a dramatic reduction of metabolic acidosis and metformin plasma
concentrations within the first 24 h after initiating CRRT in patients with
MET-induced lactic acidosis, followed by normalization on the second day in all
subjects [3].
Although we do not know the exact rate of CRRT in both arms [1],
it may well be that one group had more CRRT than the other, particularly the
metformin group. For instance, in the study of Doenyas-Barak et al., which had
a huge impact on the conclusions of this meta-analysis, the use of RRT was
higher in the MET-treated population (38.6 vs. 21.2%, p = 0.13) [1, 4].
Accordingly, we suspect that the observed difference in mortality rate may be
due to the more frequent use of RRT in the MET-treated population. A protective
effect of RRT has already been suggested by Peters et al., who found that
despite higher illness severity, the mortality rate in patients with
MET-associated lactic acidosis treated with intermittent hemodialysis (IHD) was
no different to that of non-dialyzed subjects [5].
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