Anesth Analg 2007;104:466-468
© 2007 International Anesthesia Research Society
doi: 10.1213/01.ane.0000253691.32957.8b
LETTER TO THE EDITOR
Section Editor:
Lawrence Saidman
Prone Position in Early and Severe Acute Respiratory Distress Syndrome: A Design for a Definitive Randomized Controlled Trial
Spyros D. Mentzelopoulos, MD, PhD,
Charis Roussos, MD, PhD, and
Spyros G. Zakynthinos, MD, PhD
Department of Intensive Care Medicine; University of Athens Medical School; Evaggelismos Hospital; Athens, Greece; sdm{at}hol.gr
To the Editor:
The physiological rationale for placing patients with either acute respiratory failure (ARF) or acute respiratory distress syndrome (ARDS) in a prone position, rather than in some other position, includes better lung mechanics, better gas exchange, better alveolar ventilation, better lung volumes, homogeneity of lung aeration, increased effectiveness of recruitment maneuvers (i.e., sighs), and avoidance of ventilator-induced lung injury (114). Potential outcome benefits for the prone position may be most evident in patients with severe oxygenation failure (PAo2/inspired O2 fraction <88 mm Hg), simplified acute physiology score
50, and diffuse ARDS (11,12). However, the potential lung-protective effects of the prone position seem more pronounced in lobar ARDS (7).
Four randomized controlled trials (RCTs) concerning the effects of systematic prone positioning on patients with ARF or ARDS failed to definitively demonstrate improvement in survival (1114). Methodological limitations of these studies include insufficient duration of prone position, study enrollment late in the patients ARDS course, absence of ventilation guidelines, use of higher tidal volumes in the prone position group, lack of homogeneity with respect to ARF etiology, and insufficient statistical power (11). Consequently, we propose a new, sufficiently powered, multicenter RCT on prone positioning of an ARDS subgroup. The major methodological points are presented in Table 1. Detection of a 15% decrease (i.e., effect size = 0.15) in severe ARDS mortality (11) by "group x event cross-tabulation" and
and ß values of 0.05 and 0.80, respectively, would require enrollment of 350 patients in a new RCT (G*Power, Duesseldorf University, Germany). I invite investigators interested in participating in this study to contact me directly.
REFERENCES
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