Lung Inflammation Persists After 27 Hours of Protective Acute Respiratory Distress Syndrome Network Strategy and Is Concentrated in the Nondependent Lung

被引:27
作者
Borges, Joao Batista [1 ,2 ]
Costa, Eduardo L. V. [2 ,3 ]
Bergquist, Maria [4 ]
Lucchetta, Luca [5 ]
Widstrom, Charles [6 ]
Maripuu, Enn [6 ]
Suarez-Sipmann, Fernando [1 ,7 ]
Larsson, Anders [1 ]
Amato, Marcelo B. P. [2 ]
Hedenstierna, Goran [4 ]
机构
[1] Uppsala Univ, Sect Anaesthesiol & Crit Care, Dept Surg Sci, Hedenstierna Lab, Uppsala, Sweden
[2] Univ Sao Paulo, Heart Inst Incor, Cardiopulm Dept, Div Pulm, Sao Paulo, Brazil
[3] Hosp Sirio Libanes, Res & Educ Inst, Sao Paulo, Brazil
[4] Uppsala Univ, Dept Med Sci, Clin Physiol, Hedenstierna Lab, Uppsala, Sweden
[5] Hosp San Matteo, Dept Intens Care, Pavia, Italy
[6] Univ Uppsala Hosp, Dept Med Phys, Uppsala, Sweden
[7] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Resp, Madrid, Spain
基金
瑞典研究理事会; 巴西圣保罗研究基金会;
关键词
F-18]fluoro-2-deoxy-D-glucose; acute pulmonary inflammation; acute respiratory distress syndrome; mechanical ventilation; positron emission tomography; ventilator-induced lung injury; TIDAL-VOLUME VENTILATION; END-EXPIRATORY PRESSURE; HIGH-FREQUENCY OSCILLATION; BRAIN TRANSFER CONSTANTS; MECHANICAL VENTILATION; BLOOD-FLOW; GRAPHICAL EVALUATION; COMPUTED-TOMOGRAPHY; METABOLIC-ACTIVITY; SKELETAL-MUSCLE;
D O I
10.1097/CCM.0000000000000926
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: PET with [F-18]fluoro-2-deoxy-D-glucose can be used to image cellular metabolism, which during lung inflammation mainly reflects neutrophil activity, allowing the study of regional lung inflammation in vivo. We aimed at studying the location and evolution of inflammation by PET imaging, relating it to morphology (CT), during the first 27 hours of application of protective-ventilation strategy as suggested by the Acute Respiratory Distress Syndrome Network, in a porcine experimental model of acute respiratory distress syndrome. Design: Prospective laboratory investigation. Setting: University animal research laboratory. Subjects: Ten piglets submitted to an experimental model of acute respiratory distress syndrome. Interventions: Lung injury was induced by lung lavages and 210 minutes of injurious mechanical ventilation using low positive end-expiratory pressure and high inspiratory pressures. During 27 hours of controlled mechanical ventilation according to Acute Respiratory Distress Syndrome Network strategy, the animals were studied with dynamic PET imaging of [F-18]fluoro-2-deoxy-D-glucose at two occasions with 24-hour interval between them. Measurements and Main Results: [F-18]fluoro-2-deoxy-D-glucose uptake rate was computed for the total lung, four horizontal regions from top to bottom (nondependent to dependent regions) and for voxels grouped by similar density using standard Hounsfield units classification. The global lung uptake was elevated at 3 and 27 hours, suggesting persisting inflammation. In both PET acquisitions, nondependent regions presented the highest uptake (p = 0.002 and p = 0.006). Furthermore, from 3 to 27 hours, there was a change in the distribution of regional uptake (p = 0.003), with more pronounced concentration of inflammation in nondependent regions. Additionally, the poorly aerated tissue presented the largest uptake concentration after 27 hours. Conclusions: Protective Acute Respiratory Distress Syndrome Network strategy did not attenuate global pulmonary inflammation during the first 27 hours after severe lung insult. The strategy led to a concentration of inflammatory activity in the upper lung regions and in the poorly aerated lung regions. The present findings suggest that the poorly aerated lung tissue is an important target of the perpetuation of the inflammatory process occurring during ventilation according to the Acute Respiratory Distress Syndrome Network strategy.
引用
收藏
页码:E123 / E132
页数:10
相关论文
共 68 条
[1]   Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome [J].
Amato, MBP ;
Barbas, CSV ;
Medeiros, DM ;
Magaldi, RB ;
Schettino, GDP ;
Lorenzi, G ;
Kairalla, RA ;
Deheinzelin, D ;
Munoz, C ;
Oliveira, R ;
Takagaki, TY ;
Carvalho, CRR .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (06) :347-354
[2]  
Angus DC, 2013, NEW ENGL J MED, V369, P840, DOI 10.1056/NEJMra1208623
[3]  
ASHBAUGH DG, 1967, LANCET, V2, P319
[4]  
Bellani G, 2011, MINERVA ANESTESIOL, V77, P439
[5]   Lungs of patients with acute respiratory distress syndrome show diffuse inflammation in normally aerated regions: A [18F]-fluoro-2-deoxy-D-glucose PET/CT study [J].
Bellani, Giacomo ;
Messa, Cristina ;
Guerra, Luca ;
Spagnolli, Ester ;
Foti, Giuseppe ;
Patroniti, Nicolo ;
Fumagalli, Roberto ;
Musch, Guido ;
Fazio, Ferruccio ;
Pesenti, Antonio .
CRITICAL CARE MEDICINE, 2009, 37 (07) :2216-2222
[6]   CORRECTION FOR SCATTERED RADIATION IN A RING DETECTOR POSITRON CAMERA BY INTEGRAL TRANSFORMATION OF THE PROJECTIONS [J].
BERGSTROM, M ;
ERIKSSON, L ;
BOHM, C ;
BLOMQVIST, G ;
LITTON, J .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1983, 7 (01) :42-50
[7]   Reversibility of lung collapse and hypoxemia in early acute respiratory distress syndrome [J].
Borges, Joao B. ;
Okamoto, Valdelis N. ;
Matos, Gustavo F. J. ;
Caramez, Maria P. R. ;
Arantes, Paula R. ;
Barros, Fabio ;
Souza, Ciro E. ;
Victorino, Josue A. ;
Kacmarek, Robert M. ;
Barbas, Carmen S. V. ;
Carvalho, Carlos R. R. ;
Amato, Marcelo B. P. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (03) :268-278
[8]  
Borges JB, 2006, NEW ENGL J MED, V355, P319
[9]  
Borges JB, 2008, JAMA-J AM MED ASSOC, V300, P41, DOI 10.1001/jama.300.1.41-a
[10]   Early Inflammation Mainly Affects Normally and Poorly Aerated Lung in Experimental Ventilator-Induced Lung Injury* [J].
Borges, Joao Batista ;
Costa, Eduardo L. V. ;
Suarez-Sipmann, Fernando ;
Widstrom, Charles ;
Larsson, Anders ;
Amato, Marcelo ;
Hedenstierna, Goran .
CRITICAL CARE MEDICINE, 2014, 42 (04) :E279-E287