Defining Optimal Respiratory Support for Patients With COVID-19
Noninvasive respiratory support is an essential component of critical care. Both noninvasive ventilation, with its different interface types and modes (including helmet and face masks), and high-flow nasal oxygen (HFNO) are successfully used to manage patients with acute hypoxemic respiratory failur...
Gespeichert in:
Veröffentlicht in: | JAMA : the journal of the American Medical Association 2022-02, Vol.327 (6), p.531-533 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Noninvasive respiratory support is an essential component of critical care. Both noninvasive ventilation, with its different interface types and modes (including helmet and face masks), and high-flow nasal oxygen (HFNO) are successfully used to manage patients with acute hypoxemic respiratory failure. Noninvasive respiratory support can alleviate respiratory distress, improve oxygenation, and possibly reduce the need for invasive mechanical ventilation. Due to known adverse effects associated with invasive mechanical ventilation (eg, sedation, ventilator-induced lung injury, predisposition for infections), it is conceivable that noninvasive respiratory support may reduce mortality through reduction in the need for tracheal intubation. However, noninvasive ventilation may inappropriately delay tracheal intubation and increase patient self-inflicted lung injury, which may occur at varying degrees depending on the type and interface of noninvasive ventilatory support. The intense respiratory efforts by patients who are spontaneously breathing contribute to and exacerbate acute lung injury. Due to the complexity in the causes and presentations of acute respiratory failure, several randomized clinical trials are needed to clarify the specific roles of noninvasive respiratory support. However, the evaluation of respiratory support strategies for acute illness is challenging for several reasons. First, it is difficult to achieve a balance among trial protocol executability, comprehensiveness, and completeness. Second, the concomitant evaluation |
---|---|
ISSN: | 0098-7484 1538-3598 |
DOI: | 10.1001/jama.2022.0067 |