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Predictive value of systemic and local inflammation parameters in talc pleurodesis assessment
P. Habal, N. Omran, K. Jankovicova, J. Krejsek, J. Mandak
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
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from 2001
Free Medical Journals
from 1998
Medline Complete (EBSCOhost)
from 2007-06-01
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from 2001
PubMed
25059234
DOI
10.5507/bp.2014.038
Knihovny.cz E-resources
- MeSH
- C-Reactive Protein metabolism MeSH
- Length of Stay MeSH
- Leukocytes physiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Lymphoma complications MeSH
- Pleural Effusion, Malignant diagnostic imaging etiology therapy MeSH
- Talc administration & dosage adverse effects MeSH
- Neoplasm Metastasis MeSH
- Mesothelioma complications MeSH
- Lung Neoplasms complications MeSH
- Palliative Care methods MeSH
- Pleurisy chemically induced MeSH
- Pleurodesis adverse effects methods MeSH
- Predictive Value of Tests MeSH
- Recurrence MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Body Temperature physiology MeSH
- Thoracoscopy methods MeSH
- Ultrasonography MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: One option for the palliative treatment of recurrent malignant pleural effusion is powdered talc using thoracoscopy. This paper presents the results of selected systemic and local manifestations of the talc-induced inflammatory reaction using a videothoracoscope. METHOD: A total of 114 patients with repeated malignant pleural effusion were treated at the Cardiac Surgery Clinic in Hradec Kralove from January 2010 to December 2012. Those with a life expectancy more than ≥ 3 months were eligible for talcage surgery. The group was retrospectively divided according to treatment results into Group A (N1 = 98 - successful) and Group B (N2 = 16 - relapsing). The pleural effusion was quantified using ultrasound over 1 year at 3-month intervals. Systemic changes due to the inflammatory reaction (body temperature, serum leukocyte and CRP levels) were evaluated. Local indicators of inflammation included changes in the leukocyte cell population in the effusion and changes in the pleural CRP levels. The dynamics of local expression of membrane receptors TLR-2 and CD-64 on granulocyte and monocyte cell populations in the pleural effusion were also evaluated. RESULTS: The reaction after talcage, included a significant increase in axillary temperature and leukocyte count, 12 h after the procedure. The dynamics were different in the two groups. The dynamics of local inflammatory changes were an early increase in the pleural CRP levels in both groups. The time interval of local inflammatory development and duration was related to the treatment efficacy and showed a significant rise 2 h after talcage in Group A. In Group B the local inflammatory reaction was slower and the rise was only observed 24 h after talc application. A decrease in lymphocyte count and an increase in granulocyte count 2 h after talcage were found. After an initial drop in monocyte level, a rise occurred within 24 h after talcage. Changes in the expression of TLR-2 and CD-64 receptors in relation to their cell carriers were observed depending on time after talcage. CONCLUSION: The differences in the serum and pleural effusion CRP levels suggest that the surgical stress manifests itself locally in the pleural space with a lower intensity and time delay. The TLR-2 and CD-64 receptors exhibit different behaviour depending on the type of cell membrane where they are found. The inverse relation between the granulocyte increase and TLR-2 receptor decrease in the membrane immediately after talcage is a new finding. The dynamics of TLR-2 expression on the monocytes demonstrates a direct proportion between the increasing expression of the TLR-2 receptor and increasing percent fraction of the cell carrier.
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