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Authors’ reply - ELMO helmet for CPAP to treat COVID-19-related acute hypoxemic respiratory failure outside the ICU: aspects of/comments on its assembly and methodology

Resposta dos autores - Capacete ELMO para CPAP no tratamento da insuficiência respiratória aguda hipoxêmica por COVID-19 fora da UTI: aspectos/comentários sobre sua montagem e metodologia

Betina Santos Tomaz1, Gabriela Carvalho Gomes2, Juliana Arcanjo Lino2, David Guabiraba Abitbol de Menezes2, Jorge Barbosa Soares2, Vasco Furtado3, Luiz Soares Júnior1, Maria do Socorro Quintino Farias4, Debora Lilian Nascimento Lima4, Eanes Delgado Barros Pereira1, Marcelo Alcantara Holanda1,5

We thank the authors for their comments and questions regarding our study entitled “ELMO, a new helmet interface for CPAP to treat COVID-19-related acute hypoxemic respiratory failure outside the ICU: a feasibility study.”
 
Concerning the first point mentioned by the authors, we agree with the observation regarding the coexistence of metabolic alkalosis in at least 8 of the 10 patients whose arterial blood gas analysis at admission, before the use of ELMO, showed base excess values above 2.0 mEq/L. A possible cause would be the pharmacological therapy with corticosteroids routinely used in patients before their inclusion in the study. Therefore, metabolic alkalosis is not related to the sequential application of CPAP with the helmet.
 
The fact that some patients presented with hyperventilation in accordance with the respiratory alkalosis component is compatible with an increase in the respiratory drive, and, yes, that is possibly associated with an increase in transpulmonary pressure, a mechanism related to the occurrence of self-inflicted lung injury. In the absence of transpulmonary pressure measurement, we believe that VT monitoring in devices such as the ELMO can identify those patients with a greater propensity to self-inflicted lung injury. The effects of the application of CPAP by helmet or another interface on VT require investigation in clinical trials in the future, evaluating its relationship with the progression of lung injury or not. It is worth noting that, experimentally, the application of CPAP can attenuate the variation of transpulmonary pressure in ARDS.(1)
 
Concerning the second point, it is worth explaining the following: first, the heat and moisture exchanger filter used in the ELMO inspiratory branch serves only as a “damper” for the noise generated by the high flow of gases and not for its primary function (heat/humidity); second, the gas passage through the unheated jar was just a practical resource to offer the mixture of gases without raising their temperature. We even observed that this fact prevented condensation inside the helmet and, in volunteers, it was associated with a better sensation of comfort during the use of ELMOcpap due to the slightly cooler temperature around the head and face.(2) Because the CPAP mechanism has a continuous flow of gases, there is no occurrence of asynchrony, unlike helmets coupled to mechanical ventilators, and current trigger mechanisms are not designed for this interface.
 
The safety of the interface regarding the diffusibility of the virus was not the object of our study since it has already been reported in the literature(3); the helmet interface has been considered safe and leakage is negligible when compared with face masks. The description of the absence of COVID-19 cases among researchers should not be seen as proof of this concept; however, we thought it best to report the data for recording purposes.
 
We agree with the idea of continuing to improve the design of the ELMO helmet on several fronts, including the improvement of anti-suffocation mechanisms, the coupling of filters in the gas inlet and outlet, the optimization of its internal volume to reduce the predisposition to CO2 rebreathing, the monitoring of respiratory variables, such as RR, VT, and FIo2, as well as of intra-helmet pressure level, humidity, temperature, and others.
 
Given the innovation of the characteristics of that study with this type of device, our group considered that the total time of therapy would be the maximum tolerated by the patient, and, in agreement with the medical team, we alternated it with the only oxygen therapy then available (reservoir mask), because a high-flow nasal cannula was not available. The degree of comfort observed was great, and the large-scale use after the feasibility study revealed cases of continuous use of ELMOcpap for periods as long as 12-24 h (unpublished data), which is in line with other reports in the literature.
 
REFERENCES
 
1.            Yoshida T, Grieco DL, Brochard L, Fujino Y. Patient self-inflicted lung injury and positive end-expiratory pressure for safe spontaneous breathing. Curr Opin Crit Care. 2020;26(1):59-65. https://doi.org/10.1097/MCC.0000000000000691
2.            Holanda MA, Tomaz BS, Menezes DGA, Lino JA, Gomes GC. ELMO 1.0: a helmet interface for CPAP and high-flow oxygen delivery. J Bras Pneumol. 2021;47(3):e20200590. https://doi.org/10.36416/1806-3756/e20200590.
3.            Ferioli M, Cisternino C, Leo V, Pisani L, Palange P, Nava S. Protecting healthcare workers from SARS-CoV-2 infection: practical indications. Eur Respir Rev. 2020;29(155):200068. https://doi.org/10.1183/16000617.0068-2020

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