Cytological-energy analysis of pleural effusions with predominance of neutrophils
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
32600177
PubMed Central
PMC7328477
DOI
10.1177/1753466620935772
Knihovny.cz E-zdroje
- Klíčová slova
- coefficient of energy balance, complicated exudate, cytology of pleural effusions, empyema, exudate, inflammation, neutrophils, pleural effusions, pneumonia, transudate,
- MeSH
- aspartátaminotransferasy analýza MeSH
- biologické markery analýza MeSH
- empyém pleurální diagnóza imunologie metabolismus MeSH
- energetický metabolismus * MeSH
- hrudní chirurgické výkony škodlivé účinky MeSH
- L-laktátdehydrogenasa analýza MeSH
- lidé MeSH
- neutrofily imunologie metabolismus MeSH
- pleurální výpotek diagnóza imunologie metabolismus MeSH
- pneumonie diagnóza imunologie metabolismus MeSH
- pooperační komplikace diagnóza imunologie metabolismus MeSH
- retrospektivní studie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aspartátaminotransferasy MeSH
- biologické markery MeSH
- L-laktátdehydrogenasa MeSH
BACKGROUND: The predominance of neutrophils in pleural effusions of patients with different serious impairments of the pleural cavity organs is often found. The aim of this study was to identify the type of injury using the cytological-energy analysis of pleural effusions. METHODS: We analysed 635 samples of pleural effusions with predominance of neutrophils. We compared the values of the coefficient of energy balance (KEB), lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) catalytic activities in the following subgroups of patients: with transudative effusions, purulent pneumonia, chest empyema and after chest surgery with and without purulent complications. Statistical analysis was performed using the ANOVA Kruskal-Wallis test (p < 0.05 was considered as significant). RESULTS: We found the lowest KEB values in pleural effusions of patients with chest empyema and their gradual increases in patients with purulent pneumonia and with transudative effusions. We observed the highest LDH and AST enzymes activity in patients with chest empyema and their gradual decrease in patients with purulent pneumonia and with transudative effusions. LDH and AST enzymes activity was significantly higher in pleural effusions of patients after chest surgery with purulent complications compared with non-purulent cases. CONCLUSION: The most intensive inflammation and the most extensive tissue destruction in the pleural cavity were found in patients with chest empyema. Significantly better parameters were observed in patients with purulent pneumonia. The absence of serious inflammation and the absence of tissue destruction were typical for patients with transudative effusions. Finally, our results confirmed an anticipated higher tissue destruction in patients after chest surgery. Significantly worse injury was found in surgical patients with purulent complications compared with non-purulent ones. The reviews of this paper are available via the supplemental material section.
Biomedical Centre Masaryk Hospital in Usti nad Labem Usti nad Labem Czech Republic
Department of Thoracic Surgery Masaryk Hospital in Usti nad Labem Usti nad Labem Czech Republic
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Batra H, Antony VB. Pleural mesothelial cells in pleural and lung diseases. J Thorac Dis 2015; 7: 964–980. PubMed PMC
Charalampidis C, Youroukou A, Lazaridis G, et al. Physiology of the pleural space. J Thorac Dis 2015; 7(Suppl. 1): S33–S37. PubMed PMC
Chinchkar NJ, Talwar D, Jain SK. A stepwise approach to the etiologic diagnosis of pleural effusion in respiratory intensive care unit and short-term evaluation of treatment. Lung India 2015; 32: 107–115. PubMed PMC
Karkhanis VS, Joshi JM. Pleural effusion: diagnosis, treatment, and management. Open Access Emerg Med 2012; 4: 31–52. PubMed PMC
Light RW. Pleural effusion. N Engl J Med 2002; 346: 1971–1977. PubMed
Rosales C. Neutrophil: a cell with many roles in inflammation or several cell types? Front Physiol 2018; 9: 113. PubMed PMC
Teng TS, Ji AL, Ji XY, et al. Neutrophils and immunity: from bactericidal action to being conquered. J Immunol Res 2017; 2017: 9671604. PubMed PMC
Rosales C, Demaurex N, Lowell CA, et al. Neutrophils: their role in innate and adaptive immunity. J Immunol Res 2016; 2016: 1469780. PubMed PMC
Filias A, Theodorou GL, Mouzopoulou S, et al. Phagocytic ability of neutrophils and monocytes in neonates. BMC Pediatr 2011; 11: 29. PubMed PMC
Turvey SE, Broide DH. Innate immunity. J Allergy Clin Immunol 2010; 125(2 Suppl. 2): S24–S32. PubMed PMC
Segal AW. How neutrophils kill microbes. Annu Rev Immunol 2005; 23: 197–223. PubMed PMC
Lee WL, Harrison RE, Grinstein S. Phagocytosis by neutrophils. Microbes Infect 2003; 5: 1299–1306. PubMed
Sattar SBA, Sharma S. Bacterial pneumonia, https://www.ncbi.nlm.nih.gov/books/NBK513321 (2019, accessed 20 December 2019).
Chen L, Deng H, Cui H, et al. Inflammatory responses and inflammation-associated diseases in organs. Oncotarget 2017; 9: 7204–7218. PubMed PMC
Nguyen GT, Green ER, Mecsas J. Neutrophils to the ROScue: mechanisms of NADPH oxidase activation and bacterial resistance. Front Cell Infect Microbiol 2017; 7: 373. PubMed PMC
Kruger P, Saffarzadeh M, Weber ANR, et al. Neutrophils: between host defence, immune modulation, and tissue injury. PLoS Pathog 2015; 11: e1004651. PubMed PMC
Ahmed O, Zangan S. Emergent management of empyema. Semin Intervent Radiol 2012; 29: 226–230. PubMed PMC
Rosenstengel A. Pleural infection-current diagnosis and management. J Thorac Dis 2012; 4: 186–193. PubMed PMC
Light RW. Parapneumonic effusions and empyema. Proc Am Thorac Soc 2006; 3: 75–80. PubMed
Nathan C. Neutrophils and immunity: challenges and opportunities. Nat Rev Immunol 2006; 6: 173–182. PubMed
Dahlgren C, Karlsson A. Respiratory burst in human neutrophils. J Immunol Methods 1999; 232: 3–14. PubMed
Kelbich P, Malý V, Matuchová I, et al. Cytological-energy analysis of pleural effusions. Ann Clin Biochem 2019; 56: 630–637. PubMed
Kelbich P, Hejčl A, Staněk I, et al. Principles of the cytological-energy analysis of the extravascular body fluids. Biochem Mol Biol J 2017; 3: 1–3.
Kelbich P, Hejčl A, Selke Krulichová I, et al. Coefficient of energy balance, a new parameter for basic investigation of the cerebrospinal fluid. Clin Chem Lab Med 2014; 52: 1009–1017. PubMed
Kelbich P, Slavík S, Jasanská J, et al. Evaluations of the energy relations in the CSF compartment by investigation of selected parameters of the glucose metabolism in the CSF. Klin Biochem Metab 1998; 6: 213–225.
Na MJ. Diagnostic tools of pleural effusion. Tuberc Respir Dis 2014; 76: 199–210. PubMed PMC
Light RW, MacGregor MI, Luchsinger PC, et al. Pleural effusions: the diagnostic separation of transudates and exudates. Ann Intern Med 1972; 77: 507–513. PubMed
Hooper C, Lee YCG, Maskell N. Investigation of a unilateral pleural effusion in adults: British Thoracic Society pleural disease guideline 2010. Thorax 2010; 65(Suppl. 2): ii4–ii17. PubMed
Porcel JM, Light RW. Diagnostic approach to pleural effusion in adults. Am Fam Physician 2006; 73: 1211–1220. PubMed
Dixit R, Agarwal KC, Gokhroo A, et al. Diagnosis and management options in malignant pleural effusions. Lung India 2017; 34: 160–166. PubMed PMC
Villena GV, Cases VE, Fernández VA, et al. Recommendations of diagnosis and treatment of pleural effusion: update. Arch Bronchoneumol 2014; 50: 235–249. PubMed
Brook I. Measurement of lactic acid in pleural fluid. Respiration 1980; 40: 344–348. PubMed
De Long ER, De Long DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics 1988; 44: 837–845. PubMed
Šimundić AM. Measures of diagnostic accuracy: basic definitions. EJIFCC 2009; 19: 203–211. PubMed PMC
Yang W, Zhang B, Zhang ZM. Infectious pleural effusion status and treatment progress. J Thorac Dis 2017; 9: 4690–4699. PubMed PMC
McCauley L, Dean N. Pneumonia and empyema: causal, casual or unknown. J Thorac Dis 2015; 7: 992–998. PubMed PMC
Mayadas TN, Cullere X, Lowell CA. The multifaceted functions of neutrophils. Annu Rev Pathol 2014; 9: 181–218. PubMed PMC
Miller EJ, Idell S. Interleukin-8: an important neutrophil chemotaxin in some cases of exudative pleural effusions. Exp Lung Res 1993; 19: 589–601. PubMed
Gómez H, Kellum JA. Sepsis-induced acute kidney injury. Curr Opin Crit Care 2016; 22: 546–553. PubMed PMC
Ekpe EE, Essien IO, Idongesit U. Significant pleural effusion in congestive heart failure necessitating pleural drainage. Nig J Cardiol 2015; 12: 106–110.
Ahmed AE, Yacoub TE. Empyema thoracis. Clin Med Insights Circ Respir Pulm Med 2010; 4: 1–8. PubMed PMC
Hoste EAJ, De Corte W. Clinical consequences of acute kidney injury. Contrib Nephrol 2011; 174: 56–64. PubMed
Klebanoff SJ, Kettle AJ, Rosen H, et al. Myeloperoxidase: a front-line defender against phagocytosed microorganisms. J Leukoc Biol 2013; 93: 185–198. PubMed PMC
Chen Y, Junger WG. Measurement of oxidative burst in neutrophils. Methods Mol Biol 2012; 844: 115–124. PubMed PMC
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