Airway Pressure Release Ventilation Prevents Ventilator-Induced Lung Injury in Normal Lungs

被引:53
|
作者
Emr, Bryanna [1 ]
Gatto, Louis A. [2 ]
Roy, Shreyas [1 ]
Satalin, Joshua [1 ]
Ghosh, Auyon [1 ]
Snyder, Kathy [1 ]
Andrews, Penny [3 ]
Habashi, Nader [3 ]
Marx, William [1 ,4 ]
Ge, Lin [1 ]
Wang, Guirong [1 ]
Dean, David A. [5 ]
Vodovotz, Yoram [6 ]
Nieman, Gary [1 ]
机构
[1] SUNY Upstate Med Univ, Syracuse, NY 13210 USA
[2] SUNY Coll Cortland, Cortland, NY 13045 USA
[3] Univ Maryland, Ctr Shock Trauma, Baltimore, MD 21201 USA
[4] Syracuse VA Med Ctr, Syracuse, NY USA
[5] Univ Rochester, Rochester, NY USA
[6] Univ Pittsburgh, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
RESPIRATORY-DISTRESS-SYNDROME; END-EXPIRATORY PRESSURE; LOWER TIDAL VOLUMES; MECHANICAL VENTILATION; PROTECTIVE VENTILATION; SURFACTANT; PULMONARY; INFLAMMATION; ARDS; PATHOGENESIS;
D O I
10.1001/jamasurg.2013.3746
中图分类号
R61 [外科手术学];
学科分类号
摘要
IMPORTANCE Up to 25% of patients with normal lungs develop acute lung injury (ALI) secondary to mechanical ventilation, with 60% to 80% progressing to acute respiratory distress syndrome (ARDS). Once established, ARDS is treated with mechanical ventilation that can paradoxically elevate mortality. A ventilation strategy that reduces the incidence of ARDS could change the clinical paradigm from treatment to prevention. OBJECTIVES To demonstrate that (1) mechanical ventilation with tidal volume (VT) and positive end-expiratory pressure (PEEP) settings used routinely on surgery patients causes ALI/ARDS in normal rats and (2) preemptive application of airway pressure release ventilation (APRV) blocks drivers of lung injury (ie, surfactant deactivation and alveolar edema) and prevents ARDS. DESIGN, SETTING, AND SUBJECTS Rats were anesthetized and tracheostomy was performed at State University of New York Upstate Medical University. Arterial and venous lines, a peritoneal catheter, and a rectal temperature probe were inserted. Animals were randomized into 3 groups and followed up for 6 hours: spontaneous breathing ventilation (SBV, n = 5), continuous mandatory ventilation (CMV, n = 6), and APRV (n = 5). Rats in the CMV group were ventilated with VT of 10 cc/kg and PEEP of 0.5 cm H2O. Airway pressure release ventilation was set with a P-High of 15 to 20 cm H2O; P-Low was set at 0 cm H2O. Time at PHigh (T-High) was 1.3 to 1.5 seconds and a T-Low was set to terminate at 75% of the peak expiratory flow rate (0.11-0.14 seconds), creating a minimum 90% cycle time spent at PHigh. Bronchoalveolar lavage fluid and lungs were harvested for histopathologic analysis at necropsy. RESULTS Acute lung injury/ARDS developed in the CMV group (mean [SE] PaO2/FiO(2) ratio, 242.96 [24.82]) and was prevented with preemptive APRV (mean [SE] PaO2/FIO2 ratio, 478.00 [41.38]; P <.05). Airway pressure release ventilation also significantly reduced histopathologic changes and bronchoalveolar lavage fluid total protein (endothelial permeability) and preserved surfactant proteins A and B concentrations as compared with the CMV group. CONCLUSIONS AND RELEVANCE Continuous mandatory ventilation in normal rats for 6 hours with VT and PEEP settings similar to those of surgery patients caused ALI. Preemptive application of APRV blocked early drivers of lung injury, preventing ARDS. Our data suggest that APRV applied early could reduce the incidence of ARDS in patients at risk.
引用
收藏
页码:1005 / 1012
页数:8
相关论文
共 50 条
  • [21] APPLICATION OF AIRWAY PRESSURE RELEASE VENTILATION BEFORE LUNG INJURY PREVENTS PROGRESSION TO ARDS
    Kollisch-Singule, Michaela
    Emr, Bryanna
    Jain, Sumeet
    Gatto, Louis
    Marx, William
    Andrews, Penny
    Nieman, Gary
    Habashi, Nader
    CRITICAL CARE MEDICINE, 2014, 42 (12)
  • [22] The role of high airway pressure and dynamic strain on ventilator-induced lung injury in a heterogeneous acute lung injury model
    Jain S.V.
    Kollisch-Singule M.
    Satalin J.
    Searles Q.
    Dombert L.
    Abdel-Razek O.
    Yepuri N.
    Leonard A.
    Gruessner A.
    Andrews P.
    Fazal F.
    Meng Q.
    Wang G.
    Gatto L.A.
    Habashi N.M.
    Nieman G.F.
    Intensive Care Medicine Experimental, 5 (1)
  • [23] Optimal mechanical ventilation strategies to minimize ventilator-induced lung injury in non-injured and injured lungs
    Silva, Pedro L.
    Pelosi, Paolo
    Rocco, Patricia R. M.
    Expert Review of Respiratory Medicine, 2016, 10 (12) : 1243 - 1245
  • [24] Bubble CPAP Support after Discontinuation of Mechanical Ventilation Protects Rat Lungs with Ventilator-Induced Lung Injury
    Wu, Chun Shan
    Chou, Hsiu Chu
    Huang, Liang Ti
    Lin, Yen Kuang
    Chen, Chung Ming
    RESPIRATION, 2016, 91 (02) : 171 - 179
  • [25] Ventilator-induced lung injury and recommendations for mechanical ventilation of patients with ARDS
    Lee, WL
    Slutsky, AS
    SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 22 (03) : 269 - 280
  • [26] History of Mechanical Ventilation From Vesalius to Ventilator-induced Lung Injury
    Slutsky, Arthur S.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191 (10) : 1106 - 1115
  • [27] The use of pulsatile airway reopening to reduce ventilator-induced lung injury
    Gaver, DP
    Zimmer, ME
    Halpern, D
    Williams, HAR
    FASEB JOURNAL, 2002, 16 (04): : A409 - A410
  • [28] Role of Dual Oxidase in Airway Neutrophilia in Ventilator-Induced Lung Injury
    Cagle, L.
    Linderholm, A.
    Franzi, L.
    Harper, R. W.
    Kenyon, N. J.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2018, 197
  • [29] Targeting transpulmonary pressure to prevent ventilator-induced lung injury
    Gattinoni, Luciano
    Giosa, Lorenzo
    Bonifazi, Matteo
    Pasticci, Iacopo
    Busana, Mattia
    Macri, Matteo
    Romitti, Federica
    Vassalli, Francesco
    Quintel, Michael
    EXPERT REVIEW OF RESPIRATORY MEDICINE, 2019, 13 (08) : 737 - 746
  • [30] Neutrophil elastase is needed for neutrophil emigration into lungs in ventilator-induced lung injury
    Kaynar, A. Murat
    Houghton, A. McGarry
    Lum, Esther H.
    Pitt, Bruce R.
    Shapiro, Steven D.
    AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2008, 39 (01) : 53 - 60