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Model for End-stage Liver Disease excluding INR (MELD-XI) score in critically ill patients: Easily available and of prognostic relevance

Author

Listed:
  • Bernhard Wernly
  • Michael Lichtenauer
  • Marcus Franz
  • Bjoern Kabisch
  • Johanna Muessig
  • Maryna Masyuk
  • Uta C Hoppe
  • Malte Kelm
  • Christian Jung

Abstract

Purpose: MELD-XI, an adapted version of Model for End-stage Liver Disease (MELD) score excluding INR, was reported to predict outcomes e.g. in patients with acute heart failure. We aimed to evaluate MELD-XI in critically ill patients admitted to an intensive care unit (ICU) for prognostic relevance. Methods: A total of 4381 medical patients (66±14 years, 2862 male) admitted to a German ICU between 2004 and 2009 were included and retrospectively investigated. Admission diagnoses were e.g. myocardial infarction (n = 2034), sepsis (n = 694) and heart failure (n = 688). We divided our patients in two cohorts basing on their MELD-XI score and evaluated the MELD-XI score for its prognostic relevance regarding short-term and long-term survival. Optimal cut-offs were calculated by means of the Youden-Index. Results: Patients with a MELD-XI score >12 had pronounced laboratory signs of organ failure and more comorbidities. Conclusions: The easily calculable MELD-XI score is a robust and reliable tool to predict both intra-ICU and long-term mortality in critically ill medical patients admitted to an ICU. Optimal cut-off values for MELD-XI scores seem to depend on the primary disease and need to be validated in future prospective studies. Compared to SAPS2 and APACHE score, MELD-XI lacks precision but might have comparable and even additive value, as it is easily available and independent of subjective values.

Suggested Citation

  • Bernhard Wernly & Michael Lichtenauer & Marcus Franz & Bjoern Kabisch & Johanna Muessig & Maryna Masyuk & Uta C Hoppe & Malte Kelm & Christian Jung, 2017. "Model for End-stage Liver Disease excluding INR (MELD-XI) score in critically ill patients: Easily available and of prognostic relevance," PLOS ONE, Public Library of Science, vol. 12(2), pages 1-12, February.
  • Handle: RePEc:plo:pone00:0170987
    DOI: 10.1371/journal.pone.0170987
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