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Pentraxin-3 as a marker of sepsis severity and predictor of mortality outcomes: A systematic review and meta-analysis.

Authors :
Lee, Yee Ting
Gong, Mengqi
Chau, Alex
Wong, Wing Tak
Bazoukis, George
Wong, Sunny Hei
Lampropoulos, Konstantinos
Xia, Yunlong
Li, Guangping
Wong, Martin C.S.
Liu, Tong
Wu, William K.K.
Tse, Gary
International Heath Informatics Study (IHIS) Network
Source :
Journal of Infection; Jan2018, Vol. 76 Issue 1, p1-10, 10p
Publication Year :
2018

Abstract

<bold>Objectives: </bold>Pentraxin-3 (PTX-3) is a multi-functional pattern recognition molecule produced by various cell types of peripheral tissues in different infections. It is raised in sepsis, but its values in predicting disease severity or mortality outcomes have been controversial. Therefore, we conducted a systematic review and meta-analysis of these associations.<bold>Methods: </bold>PubMed and Embase were searched until July 18, 2017 for studies that evaluated the relationship between PTX-3 levels and disease severity or mortality in sepsis.<bold>Results: </bold>A total of 23 and 10 entries were retrieved from both databases, respectively, of which 16 studies were included in the final meta-analysis. A total of 3001 patients (56% male, mean age 63 ± 15 years; mean follow-up duration of 207 days) were analysed. PTX-3 was significantly higher in patients with more severe sepsis compared to those with less severe sepsis (standard mean difference = 18.5 ng/mL, standard error: 4.5 ng/mL, P < 0.0001) and higher in non-survivors compared to survivors (standard mean difference = 40.3 ng/mL, standard error: 6.8 ng/mL, P < 0.0001). Elevated PTX-3 levels significantly increased the risk of all-cause mortality (hazard ratio: 1.91, 95% CI: 1.53 to 2.46, P < 0.0001).<bold>Conclusions: </bold>PTX-3 significantly predicts disease severity and mortality in sepsis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01634453
Volume :
76
Issue :
1
Database :
Supplemental Index
Journal :
Journal of Infection
Publication Type :
Academic Journal
Accession number :
126870833
Full Text :
https://doi.org/10.1016/j.jinf.2017.10.016