Link to article: Prone positioning under
VV-ECMO in SARS-CoV-2-induced acute respiratory distress syndrome
by Bruno Garcia, Nicolas Cousin, Claire Bourel, Mercé
Jourdain, Julien Poissy and Thibault Duburcq
Background
Infection due to severe acute respiratory coronavirus 2
(SARS-CoV-2) may lead to an atypical acute respiratory distress syndrome (ARDS)
[1], requiring in the most severe cases
veno-venous extracorporeal membrane oxygenation (VV-ECMO). The management of
persistent severe hypoxemia under VV-ECMO requires a multi-step clinical
approach including prone positioning (PP), which could improve oxygenation [2].
Methods
We performed a retrospective study of patients with
SARS-CoV-2-induced ARDS submitted to PP during VV-ECMO. We aimed to describe
mechanical ventilation parameters and gas exchanges before and after PP. We
assess the safety of PP and compare patients with PP under ECMO (prone ECMO
group) to those maintained in the supine position (supine ECMO group). Patients
were treated in accordance with the recommendation guidelines on ARDS [3]. During VV-ECMO, PP was considered in
case of severe hypoxemia (PaO2/FiO2 ratio below 80 mmHg) despite FDO2 and
FiO2 both at 100% and in case of extensive lung consolidation (ECL) on
chest imaging (> 50% of lung volume).
Results
We enrolled 208 COVID-19 patients. Among the 125 patients
with ARDS, 25 (20%) required VV-ECMO, and 14 (56%) were placed at least once in
PP for a total of 24 procedures with a median duration of 16 (15–17) h. The
delay from ECMO implantation therapy to PP was 1.5 days [1,2,3]. The resultant changes in
ventilator/ECMO settings and blood gas analysis before and after PP are
displayed in Table 1. The median PaO2/FiO2 ratio
improvement after PP was 28% [2–36]. High responders (increase PaO2/FiO2 ratio
> 20%) were 62.5%, moderate-responders (increase PaO2/FiO2 < 20%)
were 16.7%, and non-responders (decrease PaO2/FiO2) were 20.8%. We did not
observe any major safety concerns but only pressure sores after 6 procedures,
three minor hemorrhages at the injection cannula, and three moderate drops in
VV-ECMO flow requiring fluid resuscitation. Pre-ECMO characteristics,
ventilator/ECMO settings, and outcomes are exposed in Table 2. Patients in the prone ECMO group were
less likely to be weaned from ECMO, and 28-day mortality rate was significantly
higher.
Discussion
We report that during VV-ECMO, PP improved oxygenation
without a change in respiratory system compliance and PaCO2 at constant
levels of minute ventilation and sweep gas flow. This does not suggest lung
recruitment by PP but rather an optimization of ventilation and perfusion
matching. Three explanations could be advanced for the mortality rate in the
prone ECMO group (78.6%). First, prone ECMO patients may be more severe than
supine ECMO patients. As described by Gattinoni et al., worsening patients
progress from type 1 to type 2 (higher percentage of non-aerated tissue) [1],
which is associated with a higher mortality rate [4].
Prone ECMO patients had much more consolidations, obviously because ECL was the
main indication to be prone (n = 10/14). Furthermore, prone ECMO patients need
a higher respiratory rate for a higher sweep gas flow suggesting that they may
be exposed to a higher mechanical power, and they possibly had also a higher
dead space. Second, postmortem biopsies, performed in 6 patients with ECL in
the prone ECMO group, found a fibrin exudative presence both in the alveolar
spaces and bronchioles followed by a fibroblastic phase [5]
and raise the question of the use of corticosteroids (only one patient in the
prone ECMO group). Third, as already described by Zeng et al. [6],
more than half (8/11) of the patients died from septic shock and multiple organ
failure, for which ECMO may be useless.
Conclusion
Prone positioning under VV-ECMO improves oxygenation in
SARS-CoV-2-induced ARDS without compromising the safety of the patients. The
high mortality rate in prone ECMO patients may be explained by the greater
illness severity and the lack of an immunomodulatory therapy such as
corticosteroids.
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