by Patrick M. Honore, David De Bels, Sebastien Redant and
Kianoush Kashani
We enthusiastically read the recently published
retrospective study by Chen et al. [1]
who demonstrated that simultaneous use of intra-aortic balloon pumping (IABP)
together with veno-arterial extracorporeal membrane oxygenation (VA-ECMO) in
postcardiotomy cardiogenic shock (PCS) patients improved short-term survival
and reduced peripheral perfusion complications. In this study, 42 (28%)
patients were on concomitant IABP and VA-ECMO [1].
While the study adds substantial value to the current knowledge, the current
literature about the concomitant use of VA-ECMO and IABP remains controversial
[2].
A more mechanical and pragmatic approach would be to state that VA-ECMO
increases left ventricular (LV) afterload and decreases the blood flow in the
coronary arteries due to retrograde blood flow, which can potentially
deteriorate cardiac function while IABP could reduce these effects. Reduced LV
afterload and increased blood flow in the coronary arteries by IABP
theoretically promote myocardial recovery and could potentially improve
survival (although improved survival was never shown) [2, 3].
In the baseline characteristics of patients before VA-ECMO implantation among
the non-survivors, they were significantly more hypertension (35 vs. 15%; P < .004),
secondary thoracotomies (39 vs. 19%; P < .007), cardiac arrests (34 vs.
11%; P < .001), bedside implantations 42 vs. 11%; P < .0001)
and significantly less concomitant insertions of VA-ECMO and IABP (22 vs.
41%; P < .025) when compared with the study survivors [1].
All mentioned variables are well-described risk factors for increased mortality
[3].
It is also reported that brain and kidney blood flow improves with concurrent
initiation of IABP with ECMO [1].
Therefore, the question would be to find the mechanism by which concurrent
initiation could reduce the need for continuous renal replacement therapy
(CRRT) and decrease neurological complications [1].
Strategies aiming to prevent acute kidney injury (AKI) by increasing global
blood flow to the kidneys have failed [4]
as increasing blood flow mostly impacts the cortex while medulla remains
hypoperfused. Therefore, it remains unclear why the use of IABP added to
VA-ECMO in order to improve renal blood flow could significantly reduce the
need for CRRT [1, 3, 4].
In order to decrease the chances of bias in the reported findings, the
traditional AKI risk factors like diabetes mellitus, contrast exposure, the
presence of shock and need for inotropes should be included in the comparison
of these groups (VA-ECMO alone vs. VA-ECMO plus IABP) [1].
Adding IABP to VA-ECMO was not reported to increase limb ischemia [1].
This is in contradiction with a recent study by Yang et al. [5]
which stated major vascular complications (MVCs) to be common and associated
with higher in-hospital mortality among adult PCS patients receiving peripheral
VA-ECMO support. Previously, obesity, concomitant IABP/ECMO, SOFA score at
24 h post-ECMO, and bleeding disorders were reported as independent risk
factors for MVCs [5].
In conclusion and according to our interpretation, this very interesting study
does not definitively show that adding IABP is improving short-term survival as
many confounders could explain the observed difference in mortality.
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