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Clinical risk factors for increased respiratory drive in intubated hypoxemic patients

BACKGROUND: There is very limited evidence identifying factors that increase respiratory drive in hypoxemic intubated patients. Most physiological determinants of respiratory drive cannot be directly assessed at the bedside (e.g., neural inputs from chemo- or mechano-receptors), but clinical risk fa...

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Detalles Bibliográficos
Autores principales: Spinelli, Elena, Pesenti, Antonio, Slobod, Douglas, Fornari, Carla, Fumagalli, Roberto, Grasselli, Giacomo, Volta, Carlo Alberto, Foti, Giuseppe, Navalesi, Paolo, Knafelj, Rihard, Pelosi, Paolo, Mancebo, Jordi, Brochard, Laurent, Mauri, Tommaso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088111/
https://www.ncbi.nlm.nih.gov/pubmed/37041553
http://dx.doi.org/10.1186/s13054-023-04402-z
Descripción
Sumario:BACKGROUND: There is very limited evidence identifying factors that increase respiratory drive in hypoxemic intubated patients. Most physiological determinants of respiratory drive cannot be directly assessed at the bedside (e.g., neural inputs from chemo- or mechano-receptors), but clinical risk factors commonly measured in intubated patients could be correlated with increased drive. We aimed to identify clinical risk factors independently associated with increased respiratory drive in intubated hypoxemic patients. METHODS: We analyzed the physiological dataset from a multicenter trial on intubated hypoxemic patients on pressure support (PS). Patients with simultaneous assessment of the inspiratory drop in airway pressure at 0.1-s during an occlusion (P(0.1)) and risk factors for increased respiratory drive on day 1 were included. We evaluated the independent correlation of the following clinical risk factors for increased drive with P(0.1): severity of lung injury (unilateral vs. bilateral pulmonary infiltrates, PaO(2)/FiO(2), ventilatory ratio); arterial blood gases (PaO(2), PaCO(2) and pHa); sedation (RASS score and drug type); SOFA score; arterial lactate; ventilation settings (PEEP, level of PS, addition of sigh breaths). RESULTS: Two-hundred seventeen patients were included. Clinical risk factors independently correlated with higher P(0.1) were bilateral infiltrates (increase ratio [IR] 1.233, 95%CI 1.047–1.451, p = 0.012); lower PaO(2)/FiO(2) (IR 0.998, 95%CI 0.997–0.999, p = 0.004); higher ventilatory ratio (IR 1.538, 95%CI 1.267–1.867, p < 0.001); lower pHa (IR 0.104, 95%CI 0.024–0.464, p = 0.003). Higher PEEP was correlated with lower P(0.1) (IR 0.951, 95%CI 0.921–0.982, p = 0.002), while sedation depth and drugs were not associated with P(0.1). CONCLUSIONS: Independent clinical risk factors for higher respiratory drive in intubated hypoxemic patients include the extent of lung edema and of ventilation-perfusion mismatch, lower pHa, and lower PEEP, while sedation strategy does not affect drive. These data underline the multifactorial nature of increased respiratory drive. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-023-04402-z.