Efficacy and safety of lower versus higher CO<sub>2</sub> extraction devices to allow ultraprotective ventilation: secondary analysis of the SUPERNOVA study.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 31409646.
- Also identified by DOI 10.1136/thoraxjnl-2019-213591.
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Abstract
Retrospective analysis of the SUPERNOVA trial exploring the hypothesis that efficacy and safety of extracorporeal carbon dioxide removal (ECCO<sub>2</sub>R) to facilitate reduction of tidal volume (V<sub>T</sub>) to 4 mL/kg in patients with acute respiratory distress syndrome (ARDS) may differ between systems with <i>lower</i> (area of membrane length 0.59 m<sup>2</sup>; blood flow 300-500 mL/min) and <i>higher</i> (membrane area 1.30 m<sup>2</sup>; blood flow between 800 and 1000 mL/min) CO<sub>2</sub> extraction capacity. Ninety-five patients with moderate ARDS were included (33 patients treated with <i>lower</i> and 62 patients treated with <i>higher</i> CO<sub>2</sub> extraction devices). We found that (1) V<sub>T</sub> of 4 mL/kg was reached by 55% and 64% of patients with the lower extraction versus 90% and 92% of patients with higher extraction devices at 8 and 24 hours from baseline, respectively (p<0.001), and (2) percentage of patients experiencing episodes of ECCO<sub>2</sub>R-related haemolysis and bleeding was higher with <i>lower</i> than with <i>higher</i> extraction devices (21% vs 6%, p=0.045% and 27% vs 6%, p=0.010, respectively). Although V <sub>T</sub> of 4 mL/kg could have been obtained with all devices, this was achieved frequently and with a lower rate of adverse events by devices with <i>higher</i> CO<sub>2</sub> extraction capacity.
Medical subject headings
- Carbon Dioxide
- Extracorporeal Membrane Oxygenation
- Positive-Pressure Respiration
- Respiratory Distress Syndrome