Clinically important associations of pleurodesis success in malignant pleural effusion: Analysis of the TIME1 data set

胸膜成形术 医学 间皮瘤 外科 恶性胸腔积液 胸痛 内科学 麻醉 胸腔积液 病理
作者
Rachel Mercer,J. Macready,H Jeffries,Nicole Speck,Nikolaos I. Kanellakis,Nick Maskell,Justin Pepperell,Tarek Saba,Alex West,Nabeel Ali,John Corcoran,Rob Hallifax,Ioannis Psallidas,Rachelle Asciak,Maged Hassan,Robert F. Miller,Najib M. Rahman
出处
期刊:Respirology [Wiley]
卷期号:25 (7): 750-755 被引量:14
标识
DOI:10.1111/resp.13755
摘要

ABSTRACT Background and objective Chemical pleurodesis is performed for patients with MPE with a published success rate of around 80%. It has been postulated that inflammation is key in achieving successful pleural symphysis, as evidenced by higher amounts of pain or detected inflammatory response. Patients with mesothelioma are postulated to have a lower rate of successful pleurodesis due to lack of normal pleural tissue enabling an inflammatory response. Methods The TIME1 trial data set, in which pleurodesis success and pain were co‐primary outcome measures, was used to address a number of these assumptions. Pain score, systemic inflammatory parameters as a marker of pleural inflammation and cancer type were analysed in relation to pleurodesis success. Results In total, 285 patients were included with an overall success rate of 81.4%. There was a significantly higher rise in CRP in the Pleurodesis Success group compared with the Pleurodesis Failure group (mean difference: 19.2, 95% CI of the difference: 6.2–32.0, P = 0.004) but no significant change in WCC. There was no significant difference in pain scores or analgesia requirements between the groups. Patients with mesothelioma had a lower rate of pleurodesis success than non‐mesothelioma patients (73.3% vs 84.9%, χ 2 = 5.1, P = 0.023). Conclusion Change in CRP during pleurodesis is associated with successful pleurodesis but higher levels of pain are not associated. Patients with mesothelioma appear less likely to undergo successful pleurodesis than patients with other malignancies, but there is still a significant rise in systemic inflammatory markers. The mechanisms of these findings are unclear but warrant further investigation.
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