کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6123142 1219621 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Soluble ST2 as a prognostic marker in community-acquired pneumonia
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروبیولوژی و بیوتکنولوژی کاربردی
پیش نمایش صفحه اول مقاله
Soluble ST2 as a prognostic marker in community-acquired pneumonia
چکیده انگلیسی


- Suppression of tumorigenicity 2 (ST2) is a receptor for interleukin (IL)-33.
- sST2 is a predictor of all-cause in-hospital mortality of community acquired pneumonia.
- Combination of sST2 plus the Pneumonia Severity Score (PSI) is superior to PSI alone as a mortality predictor.

SummaryObjectivesCommunity-acquired pneumonia (CAP) is associated with high mortality when initial treatment fails. Early identification of these patients allows physicians to modify treatments earlier, increasing survival.MethodsNinety-one hospitalized patients with CAP were studied. Serum soluble ST2 levels were measured at diagnosis and at 3, 7, and 14 days (days 0, 3, 7, and 14) after the initiation of antimicrobial treatment. The predictive value of all-cause in-hospital mortality and the additive effect of soluble ST2 on the pneumonia severity index (PSI) were evaluated.ResultsIn univariate analysis, high serum levels of soluble ST2 at days 0, 3, 7, and 14 were predictive of death (hazard ratios: 3.1, 10.0, 12.0, and 22.6, respectively). In multivariate analysis, a combination of soluble ST2 at day 3 (above 2700 pg/ml) and PSI were predictive of death with higher accuracy than PSI alone (net reclassification improvement, 0.44; integrated discrimination improvement, 0.17; P = 0.001 for both). Specifically, simultaneous presence of high soluble ST2 (day 3) and a PSI of 5 was suggestive of higher mortality risk than a PSI of 5 alone (mortality 78% vs. 39%, respectively).ConclusionsSoluble ST2 is prognostic indicator of CAP and can add to the predictive value of the PSI.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Infection - Volume 70, Issue 5, May 2015, Pages 474-482
نویسندگان
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