Practice of adjunctive treatments in critically ill COVID-19 patients-rational for the multicenter observational PRoAcT-COVID study in The Netherlands

Christel M A Valk, Pien Swart, Leonoor S Boers, Michela Botta, Lieuwe D J Bos, Marcelo Gama de Abreu, Liselotte Hol, Markus W Hollmann, Janneke Horn, Ignacio Martin-Loeches, Guido Mazzinari, Sheila N Myatra, Sunny G Nijbroek, Neeltje M Rosenberg, Willemke Stilma, Anissa M Tsonas, Ward H van der Ven, Ary Serpa Neto, Marcus J Schultz, Frederique Paulus, Christel M A Valk, Pien Swart, Leonoor S Boers, Michela Botta, Lieuwe D J Bos, Marcelo Gama de Abreu, Liselotte Hol, Markus W Hollmann, Janneke Horn, Ignacio Martin-Loeches, Guido Mazzinari, Sheila N Myatra, Sunny G Nijbroek, Neeltje M Rosenberg, Willemke Stilma, Anissa M Tsonas, Ward H van der Ven, Ary Serpa Neto, Marcus J Schultz, Frederique Paulus

Abstract

Background: Patients with coronavirus disease 2019 (COVID-19) may need hospitalization for supplemental oxygen, and some need intensive care unit (ICU) admission for escalation of care. Practice of adjunctive and supportive treatments remain uncertain and may vary widely between countries, within countries between hospitals, and possibly even within ICUs. We aim to investigate practice of adjunctive and supportive treatments, and their associations with outcome, in critically ill COVID-19 patients.

Methods: The 'PRactice of Adjunctive Treatments in Intensive Care Unit Patients with Coronavirus Disease 2019' (PRoAcT-COVID) study is a national, observational study to be undertaken in a large set of ICUs in The Netherlands. The PRoAcT-COVID includes consecutive ICU patients, admitted because of COVID-19 to one of the participating ICUs during a 3-month period. Daily follow-up lasts 28 days. The primary endpoint is a combination of adjunctive treatments, including types of oxygen support, ventilation, rescue therapies for hypoxemia refractory to supplementary oxygen or during invasive ventilation, other adjunctive and supportive treatments, and experimental therapies. We will also collect tracheostomy rate, duration of invasive ventilation and ventilator-free days and alive at day 28 (VFD-28), ICU and hospital length of stay, and the mortality rates in the ICU, hospital and at day 90.

Discussion: The PRoAcT-COVID study is an observational study combining high density treatment data with relevant clinical outcomes. Information on treatment practices, and their associations with outcomes in COVID-19 patients in highly and urgently needed. The results of the PRoAcT-COVID study will be rapidly available, and circulated through online presentations, such as webinars and electronic conferences, and publications in peer-reviewed journals-findings will also be presented at a dedicated website. At request, and after agreement of the PRoAcT-COVID steering committee, source data will be made available through local, regional and national anonymized datasets.

Trial registration: The PRoAcT-COVID study is registered at clinicaltrials.gov (study identifier NCT04719182).

Keywords: Coronavirus disease 2019 (COVID-19); adjunctive treatments; intensive care; mortality; ventilatory support.

Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-21-764). The authors have no conflicts of interest to declare.

2021 Annals of Translational Medicine. All rights reserved.

Figures

Figure 1
Figure 1
Sequence of data collection. ICU, intensive care unit; SAPS II, Simplified Acute Physiology Score II; SOFA score, Sequential Organ Failure Assessment score; ECMO, extracorporeal membrane oxygenation; RASS score, Richmond Agitation-Sedation score; PPI, proton pump inhibitors; AKI, acute kidney injury; RRT, renal replacement therapy; GI, gastrointestinal; VTE, venous thromboembolism; DVT, deep venous thrombosis.

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Source: PubMed

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