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Choosing the right reference cohort for assessing outcome of venovenous ECMO
Critical Care volume 26, Article number: 17 (2022)
We thank Karagiannidis et al. for reporting important mortality data of COVID-19 patients supported with extracorporeal membrane oxygenation (ECMO) in Germany . The mortality they reported was notably higher than in other large cohorts . The data come from nationwide billing data of all hospitals in Germany; therefore, the risk of selection bias or underreporting of negative results is lower than in previous cohorts.
The authors argue against the unselective use of ECMO in patients who have a high risk of dying during the course of treatment. We agree that ECMO is an expensive and resource-intensive support option. Therefore, it should be used only in selected patients after careful risk–benefit evaluation. This assessment should take into account all available and relevant prognostic information and the (presumed) patient will. During the COVID-19 pandemic, the availability of trained medical staff and the utilization of available intensive care resources must also be taken into consideration .
Yet, one of the major difficulties in patient selection is to predict with sufficient accuracy the prognosis of individual patients. This is true for both patients with ECMO support and without. A more liberal use of ECMO in healthier patients who might have had a favorable outcome even without ECMO improves the survival probability attributed to the procedure, as does a restrained use in very sick and older patients who have a rather poor prognosis with or without ECMO (Fig. 1) [2, 4]. However, in our view, the expansion of the scope of indications may nevertheless be justified or even warranted. This may be the case when experienced physicians base their decisions on a responsible bedside assessment of the individual patient and expect poorer outcome without the use of ECMO. This approach was recently described as “salvage ECMO” .
For a comprehensive appraisal of the role of ECMO for the treatment of severe respiratory failure, we believe that it is not sufficient to look at the survival rates of patients who eventually received ECMO. Instead, the entire cohort of invasively ventilated patients with defined severity criteria must be considered, including patients in whom ECMO was not chosen, both due to futility and based on the assessment that they will recover even without ECMO. Consequently, the approach that achieves the best overall outcome should be considered superior. This way may help us to offer each patient the optimal therapy and improve our algorithms for making decisions for or against the use of ECMO.
Response to Supady et al.
We thank Dr. Supady and colleagues for their thoughtful letter regarding the difficulty with divining who should be placed on ECMO based on our data demonstrating high mortality with the use of ECMO for COVID-19 in Germany . Implicit in their argument is that declaring a mortality rate to be high or low requires that we know what mortality rate should actually be expected without the use of ECMO in COVID-19, an information that uncontrolled observational data cannot provide  . This is an important argument for conducting well-designed randomized clinical trials. However, absent such evidence, how should we proceed? Nonetheless, we believe that the overall mortality rate should be seen as high relative to the investment of resources, suggesting that the use of ECMO in this population may indeed be too liberal.
One further point that merits discussion is that, while Supady et al. use the term “selection” regarding the decision to implement ECMO, we prefer the term “indication.” Indication is based on the careful assessment of the realistic rehabilitation potential of the patient in association with a given intervention (e.g., ECMO) to allow the patient to resume a reasonable quality of life and to achieve a well-defined therapeutic goal in concert with the goals and values of the individual patient . This concept also aims to balance benefit (survival) against harm (invasive treatment, pain, sedation, immobilization and the psychological burden on surrogates). Therefore, the indication for ECMO should be based on several anamnestic, demographic, medical and prognostic parameters in each individual patient to avoid futile treatments as well as high in-hospital mortality. We agree with Dr. Supady’s framing of the balanced and rational use of ECMO; however, the reality in Germany—as expressed in our letter—shows that we are far from the rational use of ECMO. This has also been clearly emphasized by a recent paper showing that 40% of ECMO cases in Germany are performed in hospitals with 2 or fewer cases per year  with no assurances regarding the quality of ECMO delivery, which may reasonably be expected to contribute to high mortality.
For these reasons, we are confident that the high mortality rate in German ECMO patients reflects an opportunity to insist on a more rational ECMO application, to reflect both on the organizational approach to its use and on the indications that should be broadly acceptable.
Availability of data and materials
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Supady, A., Biever, P.M., Staudacher, D.L. et al. Choosing the right reference cohort for assessing outcome of venovenous ECMO. Crit Care 26, 17 (2022). https://doi.org/10.1186/s13054-021-03880-3
- Extracorporeal membrane oxygenation
- Patient selection