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Tailored sedation in critically ill COVID-19 patients based on lung damage, and pharmacokinetic and pharmacodynamic profiles

  • Alfredo Del Gaudio1
  • Giuseppe Mincolelli1
  • Andreaserena Recchia1
  • Elvio De Blasio2
  • Maura C Tracey3
  • Marco Cascella4

1DSC Anestesia e Rianimazione 2, IRCCS Casa Sollievo Della Sofferenza, 71013 San Giovanni Rotondo (FG), Italy

2Multidisciplinary Emergency Unit for COVID-19 Campania, 80100 Naples, Italy

3Scientific Directorate, Istituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, 80133 Naples, Italy

4Division of Anesthesia and Pain Medicine, Istituto Nazionale Tumori-IRCCS-"Fondazione G. Pascale", 80131 Naples, Italy

DOI: 10.22514/sv.2021.115 Vol.17,Issue 6,November 2021 pp.157-161

Submitted: 22 April 2021 Accepted: 31 May 2021

Published: 08 November 2021

*Corresponding Author(s): Marco Cascella E-mail: m.cascella@istitutotumori.na.it

Abstract

In critically ill COVID-19 patients, proper management of sedation is an important issue. Therefore, for this purpose, several strategies and protocols have been proposed. In this paper, we illustrate an approach focused on lung damage, and both the pharmacokinetic and pharmacodynamic profiles of drugs used. In line with this, during high flow nasal (HFN), continuous positive airway pressure, or non-invasive ventilation, dexmedetomidine-based light sedation can be helpful for maintaining the respiratory driving and improving the patient comfort. A worsening in the respiratory clinical picture with mechanical ventilation may require deep sedation with the use of clonidine. The latter may reduce the hypnotic doses, allowing improved hemodynamic stability. When respiratory performance improves, dexmedetomidine can replace clonidine to reduce the time to extubation.


Keywords

COVID-19; Mechanical ventilation; Sedation; Propofol; Dexmedetomidine


Cite and Share

Alfredo Del Gaudio,Giuseppe Mincolelli,Andreaserena Recchia,Elvio De Blasio,Maura C Tracey,Marco Cascella. Tailored sedation in critically ill COVID-19 patients based on lung damage, and pharmacokinetic and pharmacodynamic profiles. Signa Vitae. 2021. 17(6);157-161.

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