Abstract

BackgroundThe Intermountain Risk Score (IMRS), composed of the complete blood count (CBC) and basic metabolic profile (BMP), predicts mortality and morbidity in medical and general populations. Whether longitudinal repeated measurement of IMRS is useful for prognostication is an important question for its clinical applicability.MethodsFemales (N = 5,698) and males (N = 5,437) with CBC and BMP panels measured 6 months to 2.0 years apart (mean 1.0 year) had baseline and follow-up IMRS computed. Survival analysis during 4.0±2.5 years (maximum 10 years) evaluated mortality (females: n = 1,255 deaths; males: n = 1,164 deaths) and incident major events (myocardial infarction, heart failure [HF], and stroke).ResultsBoth baseline and follow-up IMRS (categorized as high-risk vs. low-risk) were independently associated with mortality (all p<0.001) in bivariable models. For females, follow-up IMRS had hazard ratio (HR) = 5.23 (95% confidence interval [CI] = 4.11, 6.64) and baseline IMRS had HR = 3.66 (CI = 2.94, 4.55). Among males, follow-up IMRS had HR = 4.28 (CI = 3.51, 5.22) and baseline IMRS had HR = 2.32 (CI = 1.91, 2.82). IMRS components such as RDW, measured at both time points, also predicted mortality. Baseline and follow-up IMRS strongly predicted incident HF in both genders.ConclusionsRepeated measurement of IMRS at baseline and at about one year of follow-up were independently prognostic for mortality and incident HF among initially hospitalized patients. RDW and other CBC and BMP values were also predictive of outcomes. Further research should evaluate the utility of IMRS as a tool for clinical risk adjustment.

Highlights

  • The Intermountain Risk Score (IMRS) is a risk prediction tool created in a general medical population and validated in outpatient, inpatient, cardiovascular, and general populations [1]

  • The study of the red cell distribution width (RDW) as a risk predictor arose from the development of IMRS (RDW is a component of IMRS) [3]

  • IMRS is an idealized clinical prediction rule because its components are well-established in medicine, are familiar to clinicians, are commonly ordered clinically, are quantitative assessments of the parameters they measure, can be entered into a risk score calculation outside of the clinic or hospital room (i.e., IMRS can be computed by laboratory equipment and from the hospital electronic medical record), and are relatively inexpensive tests that can be run at almost every medical center in the world [4,5,6]

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Summary

Introduction

The Intermountain Risk Score (IMRS) is a risk prediction tool created in a general medical population and validated in outpatient, inpatient, cardiovascular, and general populations [1]. IMRS has an exceptional ability to predict mortality and has broadened the understanding of the risk information in the complete blood count (CBC) and basic metabolic profile (BMP) [1,2]. IMRS utilizes all risk information from the CBC and the BMP to predict mortality, [1] and predicts morbidities such as myocardial infarction (MI), heart failure (HF), stroke, and chronic obstructive pulmonary disease [2]. The Intermountain Risk Score (IMRS), composed of the complete blood count (CBC) and basic metabolic profile (BMP), predicts mortality and morbidity in medical and general populations. Whether longitudinal repeated measurement of IMRS is useful for prognostication is an important question for its clinical applicability

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