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The prognostic value of early measures of the ventilatory ratio in the ARDS ROSE trial.

TitleThe prognostic value of early measures of the ventilatory ratio in the ARDS ROSE trial.
Publication TypeJournal Article
Year of Publication2022
AuthorsMonteiro ACarolina C, Vangala S, Wick KD, Delucchi KL, Siegel ER, B Thompson T, Liu KD, Sapru A, Sinha P, Matthay MA
Corporate AuthorsNHLBI PETAL Network
JournalCrit Care
Volume26
Issue1
Pagination297
Date Published2022 Sep 29
ISSN1466-609X
KeywordsAPACHE, Humans, Kaplan-Meier Estimate, Neuromuscular Blockade, Prognosis, Respiratory Distress Syndrome
Abstract

BACKGROUND: The ventilatory ratio (VR, [minute ventilation × PaCO]/[predicted body weight × 100 × 37.5]) is associated with mortality in ARDS. The aims of this study were to test whether baseline disease severity or neuromuscular blockade (NMB) modified the relationship between VR and mortality.METHODS: This was a post hoc analysis of the PETAL-ROSE trial, which randomized moderate-to-severe ARDS patients to NMB or control. Survival among patients with different VR trajectories or VR cutoff above and below the median was assessed by Kaplan-Meier analysis. The relationships between single-day or 48-h VR trajectories with 28- or 90-day mortality were tested by logistic regression. Randomization allocation to NMB and markers of disease severity were tested as confounders by multivariable regression and interaction term analyses.RESULTS: Patients with worsening VR trajectories had significantly lower survival compared to those with improving VR (n = 602, p < 0.05). Patients with VR > 2 (median) at day 1 had a significantly lower 90-day survival compared to patients with VR ≤ 2 (HR 1.36, 95% CI 1.10-1.69). VR at day 1 was significantly associated with 28-day mortality (OR = 1.40, 95% CI 1.15-1.72). There was no interaction between NMB and VR for 28-day mortality. APACHE-III had a significant interaction with VR at baseline for the outcome of 28-day mortality, such that the relationship between VR and mortality was stronger among patients with lower APACHE-III. There was a significant association between rising VR trajectory and mortality that was independent of NMB, baseline PaO/FiO ratio and generalized markers of disease severity (Adjusted OR 1.81, 95% CI 1.28-2.84 for 28-day and OR 2.07 95% CI 1.41-3.10 for 90-day mortality). APACHE-III and NMB were not effect modifiers in the relationship between VR trajectory and mortality.CONCLUSIONS: Elevated baseline and day 1 VR were associated with higher 28-day mortality. The relationship between baseline VR and mortality was stronger among patients with lower APACHE-III. APACHE-III was not an effect modifier for the relationship between VR trajectory and mortality, so that the VR trajectory may be optimally suited for prognostication and predictive enrichment. VR was not different between patients randomized to NMB or control, indicating that VR can be utilized without correcting for NMB.

DOI10.1186/s13054-022-04179-7
Alternate JournalCrit Care
PubMed ID36175982
PubMed Central IDPMC9521854
Grant List5T32 HL72752-17 / NH / NIH HHS / United States
5T32GM008440-24 / NH / NIH HHS / United States
3U01HL123009-07S1 / NH / NIH HHS / United States
5R01HD092471-05 / NH / NIH HHS / United States
5R35GM142992-02 / NH / NIH HHS / United States
U01 HL123004 / NH / NIH HHS / United States