Conclusion
Postoperative remote lung injury is not an uncommon condition clinically, and it is associated with adverse effects on overall patient survival. The pathological mechanisms are complex, involving cytokines and DAMPs released by injured organs or surgical sites. As a result, the normal function of the respiratory system is compromised, contributing to the development of lung injury. Due to the poor outcome associated with postoperative remote lung injury, predicting the population at risk is critical in order to facilitate lung injury prevention at the incipient stage. Approaches to ameliorate the pathological effects of postoperative remote lung injury are still required and necessitate further investigation, particularly utilizing well-powered, randomized controlled trials.
Abbreviations
ALI: Acute lung injury; ARDS: Acute respiratory distress syndrome; BALF: Bronchoalveolar lavage fluid; CPB: Cardiopulmonary bypass; DAMPs: Damage-associated molecular patterns; HMGB1: High-mobility group box-1; HSP: Heat shock protein; I/R: Ischaemia/reperfusion; IL: Interleukin; NLRP3: NOD-like receptor protein 3; PEEP: Positive end expiratory pressure; PPC: Postoperative pulmonary complication; ROS: Reactive oxygen species; SLIP: Surgical lung injury prediction; SPR: Stress protein response; TLR4: Tolllike receptor 4; TNF-α: Tumor necrosis factor-α; TRALI: Transfusion related acute lung injury; VT: Tidal volume
Acknowledgements
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Funding
The work was supported by the Medical Research Council, The Developmental Pathway Funding Scheme program (project grant G802392), BJA/RCoA Research Fellowship grant, London, UK and the Basic and Frontier Research Fund (DM) and National Natural Science Foundation of China (No. 81671890) (SLY). The funders have no role in regarding study design, data collection, analysis and manuscript preparation.
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BMC Anesthesiol. 2019;19(30) © 2019 BioMed Central, Ltd.