Sigh Ventilation in Patients With Trauma: The SiVent Randomized Clinical Trial

Document Type

Article

Publication Date

11-28-2023

Publication Title

JAMA : the journal of the American Medical Association

Abstract

IMPORTANCE: Among patients receiving mechanical ventilation, tidal volumes with each breath are often constant or similar. This may lead to ventilator-induced lung injury by altering or depleting surfactant. The role of sigh breaths in reducing ventilator-induced lung injury among trauma patients at risk of poor outcomes is unknown.

OBJECTIVE: To determine whether adding sigh breaths improves clinical outcomes.

DESIGN, SETTING, AND PARTICIPANTS: A pragmatic, randomized trial of sigh breaths plus usual care conducted from 2016 to 2022 with 28-day follow-up in 15 academic trauma centers in the US. Inclusion criteria were age older than 18 years, mechanical ventilation because of trauma for less than 24 hours, 1 or more of 5 risk factors for developing acute respiratory distress syndrome, expected duration of ventilation longer than 24 hours, and predicted survival longer than 48 hours.

INTERVENTIONS: Sigh volumes producing plateau pressures of 35 cm H2O (or 40 cm H2O for inpatients with body mass indexes >35) delivered once every 6 minutes. Usual care was defined as the patient's physician(s) treating the patient as they wished.

MAIN OUTCOMES AND MEASURES: The primary outcome was ventilator-free days. Prespecified secondary outcomes included all-cause 28-day mortality.

RESULTS: Of 5753 patients screened, 524 were enrolled (mean [SD] age, 43.9 [19.2] years; 394 [75.2%] were male). The median ventilator-free days was 18.4 (IQR, 7.0-25.2) in patients randomized to sighs and 16.1 (IQR, 1.1-24.4) in those receiving usual care alone (P = .08). The unadjusted mean difference in ventilator-free days between groups was 1.9 days (95% CI, 0.1 to 3.6) and the prespecified adjusted mean difference was 1.4 days (95% CI, -0.2 to 3.0). For the prespecified secondary outcome, patients randomized to sighs had 28-day mortality of 11.6% (30/259) vs 17.6% (46/261) in those receiving usual care (P = .05). No differences were observed in nonfatal adverse events comparing patients with sighs (80/259 [30.9%]) vs those without (80/261 [30.7%]).

CONCLUSIONS AND RELEVANCE: In a pragmatic, randomized trial among trauma patients receiving mechanical ventilation with risk factors for developing acute respiratory distress syndrome, the addition of sigh breaths did not significantly increase ventilator-free days. Prespecified secondary outcome data suggest that sighs are well-tolerated and may improve clinical outcomes.

TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02582957.

Medical Subject Headings

Humans; Male; Adult; Adolescent; Female; Respiration; Ventilators, Mechanical; Inpatients; Respiratory Distress Syndrome; Ventilator-Induced Lung Injury

PubMed ID

37877609

ePublication

ePub ahead of print

Volume

330

Issue

20

First Page

1982

Last Page

1990

Share

COinS