Critical Care volume 29,
Article number: 482 (2025) Published: 11 November 2025
Background
In patients with acute hypoxemic respiratory failure,
spontaneous breathing efforts may contribute to patient self-inflicted lung
injury through increased ventilation inhomogeneity and systemic inflammation.
Whether early transition to controlled mechanical ventilation (CMV) mitigates
these effects remains uncertain.
Methods
This observational, prospective cohort study included 40 ICU
patients with acute hypoxemic respiratory failure who initially breathed
spontaneously. Based on clinical decisions, patients were managed with either
continued spontaneous breathing (SB group, n = 12)
or transitioned to CMV (CMV group, n = 28).
Arterial blood gases, hemodynamics, plasma cytokines (IL-6 and IL-8), and
ventilation distribution via electrical impedance tomography (EIT) were
recorded at baseline and after 24 h. In the
CMV group, intermediate time points (T2, T6, T12) were also assessed after
intubation. The trial was registered in ClinicalTrials.gov (NCT03513809).
Results
In the CMV group, respiratory rate and heart rate decreased
significantly over time. IL-6 levels dropped markedly from 305 ± 938 pg/mL at baseline to 27 ± 58 pg/mL at 24 h (p = 0.0195), accompanied by a
significant improvement in oxygenation (PaO₂/FiO₂ from 140 ± 51 to 199 ± 67, p = 0.0004).
EIT data showed improved ventilation distribution with increased end-expiratory
lung impedance, decreased global inhomogeneity, and a shift in the center of
ventilation toward dorsal regions. In contrast, the SB group showed no
significant changes over 24 h in gas exchange, systemic
inflammation, or EIT-derived parameters.
Conclusions
In patients with acute hypoxemic respiratory failure
initially breathing spontaneously, transition to CMV was associated with
reduced IL-6 levels and improved ventilatory homogeneity over 24 h. These
exploratory findings indicate that connection to controlled mechanical
ventilation was associated with reduced systemic inflammation, a relationship
that warrants confirmation in larger prospective studies.
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