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Biological Impact of Transpulmonary Driving Pressure in Experimental Acute Respiratory Distress Syndrome.

AbstractBACKGROUND:
Ventilator-induced lung injury has been attributed to the interaction of several factors: tidal volume (VT), positive end-expiratory pressure (PEEP), transpulmonary driving pressure (difference between transpulmonary pressure at end-inspiration and end-expiration, ΔP,L), and respiratory system plateau pressure (Pplat,rs).
METHODS:
Forty-eight Wistar rats received Escherichia coli lipopolysaccharide intratracheally. After 24 h, animals were randomized into combinations of VT and PEEP, yielding three different ΔP,L levels: ΔP,LLOW (VT = 6 ml/kg, PEEP = 3 cm H2O); ΔP,LMEAN (VT = 13 ml/kg, PEEP = 3 cm H2O or VT = 6 ml/kg, PEEP = 9.5 cm H2O); and ΔP,LHIGH (VT = 22 ml/kg, PEEP = 3 cm H2O or VT = 6 ml/kg, PEEP = 11 cm H2O). In other groups, at low VT, PEEP was adjusted to obtain a Pplat,rs similar to that achieved with ΔP,LMEAN and ΔP,LHIGH at high VT.
RESULTS:
At ΔP,LLOW, expressions of interleukin (IL)-6, receptor for advanced glycation end products (RAGE), and amphiregulin were reduced, despite morphometric evidence of alveolar collapse. At ΔP,LHIGH (VT = 6 ml/kg and PEEP = 11 cm H2O), lungs were fully open and IL-6 and RAGE were reduced compared with ΔP,LMEAN (27.4 ± 12.9 vs. 41.6 ± 14.1 and 0.6 ± 0.2 vs. 1.4 ± 0.3, respectively), despite increased hyperinflation and amphiregulin expression. At ΔP,LMEAN (VT = 6 ml/kg and PEEP = 9.5 cm H2O), when PEEP was not high enough to keep lungs open, IL-6, RAGE, and amphiregulin expression increased compared with ΔP,LLOW (41.6 ± 14.1 vs. 9.0 ± 9.8, 1.4 ± 0.3 vs. 0.6 ± 0.2, and 6.7 ± 0.8 vs. 2.2 ± 1.0, respectively). At Pplat,rs similar to that achieved with ΔP,LMEAN and ΔP,LHIGH, higher VT and lower PEEP reduced IL-6 and RAGE expression.
CONCLUSION:
In the acute respiratory distress syndrome model used in this experiment, two strategies minimized ventilator-induced lung injury: (1) low VT and PEEP, yielding low ΔP,L and Pplat,rs; and (2) low VT associated with a PEEP level sufficient to keep the lungs open.
AuthorsCynthia S Samary, Raquel S Santos, Cíntia L Santos, Nathane S Felix, Maira Bentes, Thiago Barboza, Vera L Capelozzi, Marcelo M Morales, Cristiane S N B Garcia, Sergio A L Souza, John J Marini, Marcelo Gama de Abreu, Pedro L Silva, Paolo Pelosi, Patricia R M Rocco
JournalAnesthesiology (Anesthesiology) Vol. 123 Issue 2 Pg. 423-33 (Aug 2015) ISSN: 1528-1175 [Electronic] United States
PMID26039328 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Inflammation Mediators
Topics
  • Animals
  • Inflammation Mediators (immunology, metabolism)
  • Lung (immunology, metabolism)
  • Male
  • Positive-Pressure Respiration (adverse effects, methods)
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Respiratory Distress Syndrome (etiology, immunology, metabolism)
  • Respiratory Mechanics (physiology)
  • Tidal Volume (physiology)

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