ST2 predicts mortality and length of stay in a critically ill noncardiac intensive care unit population

Joseph W. Rudolf, Elizabeth L. Lewandrowski, Kent B. Lewandrowski, James L. Januzzi, Ednan K. Bajwa, Jason M. Baron

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Objectives: The biomarker suppression of tumorigenicity 2 (ST2) is a well-established clinical biomarker of cardiac strain and is frequently elevated in a variety of cardiac conditions. Here, we sought to evaluate the prognostic value of ST2 in critically ill medical intensive care unit (MICU) patients without primary cardiac illness. Methods: We measured ST2 and high-sensitivity troponin T (hsTnT) on plasma specimens collected on 441 patients following admission to a noncardiac MICU and evaluated the prognostic power of ST2 both alone and in multivariate models. Results: Of these critically ill patients, 96% exhibited ST2 concentrations above the reference interval. ST2 concentrations were highly predictive of intensive care unit and hospital length of stay, as well as in-hospital mortality, with high concentrations predicting a poor prognosis. Rates of in-hospital mortality were more than four times higher in patients with ST2 concentrations in the highest compared with the lowest quartile. In multivariate analysis, ST2 remained an important predictor of death after adjustment for age, hsTnT, and common diagnoses. Conclusions: ST2 is increased and predictive of prognosis in critically ill patients without primary cardiac disease, suggesting that critically ill patients may often have unrecognized cardiac injury. Clinical decision support algorithms incorporating ST2 and hsTnT results may be useful in patient risk stratification.

Original languageEnglish (US)
Pages (from-to)203-210
Number of pages8
JournalAmerican journal of clinical pathology
Volume145
Issue number2
DOIs
StatePublished - Feb 1 2016

Keywords

  • Cardiac biomarker
  • Clinical decision support
  • High-sensitivity troponin T
  • HsTnT
  • ST2
  • Suppression of tumorigenicity 2

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