Red cell distribution width improves the simplified acute physiology score for risk prediction in unselected critically ill patients
© Hunziker et al.; licensee BioMed Central Ltd. 2012
Received: 11 January 2012
Accepted: 18 May 2012
Published: 18 May 2012
Recently, red cell distribution width (RDW), a measure of erythrocyte size variability, has been shown to be a prognostic marker in critical illness. The aim of this study was to investigate whether adding RDW has the potential to improve the prognostic performance of the simplified acute physiology score (SAPS) to predict short- and long-term mortality in an independent, large, and unselected population of intensive care unit (ICU) patients.
This observational cohort study includes 17,922 ICU patients with available RDW measurements from different types of ICUs. We modeled the association between RDW and mortality by using multivariable logistic regression, adjusting for demographic factors, comorbidities, hematocrit, and severity of illness by using the SAPS.
ICU-, in-hospital-, and 1-year mortality rates in the 17,922 included patients were 7.6% (95% CI, 7.2 to 8.0), 11.2% (95% CI, 10.8 to 11.7), and 25.4% (95% CI, 24.8 to 26.1). RDW was significantly associated with in-hospital mortality (OR per 1% increase in RDW (95%CI)) (1.14 (1.08 to 1.19), P < 0.0001), ICU mortality (1.10 (1.06 to 1.15), P < 0.0001), and 1-year mortality (1.20 (95% CI, 1.14 to 1.26); P < 0.001). Adding RDW to SAPS significantly improved the AUC from 0.746 to 0.774 (P < 0.001) for in-hospital mortality and 0.793 to 0.805 (P < 0.001) for ICU mortality. Significant improvements in classification of SAPS were confirmed in reclassification analyses. Subgroups demonstrated robust results for gender, age categories, SAPS categories, anemia, hematocrit categories, and renal failure.
RDW is a promising independent short- and long-term prognostic marker in ICU patients and significantly improves risk stratification of SAPS. Further research is needed the better to understand the pathophysiology underlying these effects.
Red cell distribution width (RDW) is a measure of erythrocyte size variability and has been shown to be a prognostic marker for mortality, mainly in patients with cardiovascular disease and in community-dwelling patients, as well as in general in-hospital patients [1–16]. Although the mechanisms linking RDW to adverse patient outcomes remain incompletely understood, potential pathways include chronic inflammation [17, 18], malnutrition [9–11], and anemia of different etiologies [19, 20], among others. The prognostic potential of RDW is of particular interest because it is routinely included in the automated complete blood count (CBC) analyses in hospitalized patients and thus available at no additional cost for clinicians. Recent studies have found RDW to be a prognostic marker for short- and long-term mortality in critically ill patients [21–23]. The first study in critical illness was conducted in a cohort of 602 patients in China and found that RDW is associated with ICU mortality . Recently, a large 10-year retrospective study from two US centers validated these findings and found RDW to be a robust predictor of the risk of all-cause patient mortality and bloodstream infection in the critically ill . Finally, one report found RDW to be a strong outcome predictor in patients with pneumonia . However, from these studies, it remains unclear whether RDW may improve state-of-the-art risk prediction in unselected critically ill patients.
We therefore aimed to investigate whether adding RDW has the potential to improve the prognostic performance of the Simplified Acute Physiology Score (SAPS) to predict short- and long-term mortality in an independent, large, and unselected population of ICU patients.
Materials and methods
This observational study used the prospectively collected Multiparameter Intelligent Monitoring in Intensive Care (MIMIC II) database, a publicly available clinical database developed by the Massachusetts Institute of Technology, Phillips Healthcare, and Beth Israel Deaconess Medical Center (BIDMC) since 2001 . This database is a repository of de-identified physiologic, laboratory, and survival outcome data from more than 30,000 critically ill patients treated in ICUs at BIDMC. These data include clinical variables such as demographics (patient age, gender), highly granular physiologic data captured by the bedside monitors, medications administered and procedures performed, chronic disease diagnoses as represented by International Classification of Diseases (ICD)-9 codes, as well as laboratory results, such as complete blood count, serum chemistries, and microbiologic data. It further includes severity of illness, as assessed with SAPS I, and survival data within both the ICU and the hospital. The SAPS-I score was chosen in MIMIC II for its simplicity, requiring only available clinical laboratory measurements, fluid balance, and vital signs . Finally, survival outcome data after hospital discharge is provided from the Social Security database. Patients included in this analysis were hospitalized between January 2001 and December 2008.
MIMIC II is a public de-identified ICU database that was developed with funding from the National Institutes of Health and the National Institute of Bio-imaging and Bioengineering. The project had approval from by Institutional Review Boards of both Beth Israel Deaconess Medical Center (Boston, MA, USA) and the Massachusetts Institute of Technology (Cambridge, MA, USA). The requirement for individual patient consent was waived because the study did not affect clinical care, and all protected health information had been deleted.
Patients, outcomes, and covariates
We included all adult patients admitted to ICU floors who had an RDW measured on admission. RDW is routinely measured in admitted patients reported on every CBC and required no separate physician order. All CBCs were conducted on Advia Equipment (Siemens, models 2120 and 120). The normal reference range for RDW at our center is 10.5% to 15.5%. The primary outcome of interest was in-hospital mortality, defined as death before hospital discharge for any reason. The secondary outcomes of interest were ICU mortality, defined as death before ICU discharge and 1-year long-term mortality. The primary predictor of interest was RDW measured on ICU admission. We classified patients' comorbidity status based on the method described by Elixhauser et al. , as implemented by the Agency for Healthcare Research and Quality Comorbidity Software .
First, we used descriptive statistics including mean with standard deviation and frequencies to describe the population, as appropriate. Next, we investigated the association between RDW used as a continuous variable and mortality by using logistic regression analysis and reported odds ratios (ORs) and 95% confidence intervals (CIs). We conducted univariable analysis and a multivariable analysis adjusted for SAPS, age, gender, hematocrit, and different comorbidities (anemia, renal failure, CHF, cardiac arrhythmias, valvular disease, chronic pulmonary disease, lung embolism, pneumonia, peripheral vascular disease, hypertension, paralysis, other neurologic diseases, diabetes, hypothyroidism, liver disease, peptic ulcer, HIV, lymphoma, cancer, rheumatoid arthritis, coagulopathy, obesity, weight loss, electrolyte disturbance, alcohol abuse, drug abuse, psychosis, and depression). To account for potential clustering within ICUs, we performed hierarchic modeling with a generalized estimating equation (GEE) by using an exchangeable variance-covariance structure with compound symmetry. Model discrimination was assessed by calculation of the receiver-operating characteristic (ROC) curves and reporting of the area under the curve (AUC). To assess the fit of the GEE model, we used the Quasi-likelihood under the Independence model Criterion (QIC) statistic, as previously suggested . We also tested for effect modification by using interaction terms, to determine whether the effect of RDW on mortality varied by subgroups.
In addition to ROC analysis, we assessed the effect of adding RDW to risk-adjusted models by using reclassification-analysis methods, as suggested by Pencina . Reclassification analysis is a more modern method that is widely recommended for assessing the incremental contribution of biomarkers to risk prediction. It is also more intuitive than areas under the ROC curve: for example, a net reclassification improvement (NRI) for mortality of 10% means that 10% of patients are more accurately classified by the new algorithm when compared with the old. The analyses used continuous variable information with evaluation of the effects on risk-category reclassification for survivors and nonsurvivors. This approach separately analyzed the reclassification of persons who died and those who did not die during the ICU and hospital course. Reclassification to a higher-risk group was considered upward movement in classification for nonsurvivors. Conversely, reclassification downward was considered a failure for nonsurvivors and vice versa for survivors. Improvement in reclassification was estimated by taking the sum of differences in proportions of individuals reclassified upward minus the proportion reclassified downward for nonsurvivors and the proportion of individuals moving downward minus the proportion moving upward for survivors. For estimating meaningful a priori mortality risk categories, we defined probabilities for mortality as < 2%, 2% to 5%, > 5% to 10%, > 10% to 20%, > 20% to 50%, and > 50%. We calculated the net reclassification improvement (NRI), which assesses improvement in reclassification over risk categories; we also assessed integrated discrimination improvement (IDI), which can be viewed as a continuous version of the NRI without the recourse to a priori defined risk categories.
All reported CIs are two-sided 95% intervals, and tests were performed at the two-sided 5% significance level. All analyses were performed with SAS 9.2.
Characteristics of ICU cohort (n = 17,922)
Age (year), mean, median (SD, IQR)
63.2, 65.2 (± 17.6, 51.3 to 77.6)
Female gender, n (%)
Type of ICU, n (%)
Cardiac Care Unit
Cardiothoracic Surgery Unit
Medical Intensive Care Unit
Surgical Intensive Care Unit
Lab values on admission
Hematocrit (%), mean, median (SD, IQR)
32.3, 32.0 (± 5.6, 28.4 to 36.0)
SAPS on admission, mean, median (SD, IQR)
13.6, 13.0 (± 5.5, 10.0 to 17.0)
Comorbidities, n (%)
Chronic renal failure
Congestive heart failure
Peripheral vascular disease
RDW and in-hospital and ICU mortality
Regression models for short-term mortality
Results from regression analysis
OR (95% CI)
OR (95% CI)
RDW per 1% increase
1.20 (1.16, 1.24)
1.18 (1.14, 1.22)
SAPS per 1-point increase
1.19 (1.15, 1.23)
1.21 (1.18, 1.25)
RDW per 1% increase
1.14 (1.08, 1.19)
1.10 (1.06, 1.15)
SAPS per 1-point increase
1.16 (1.13, 1.18)
1.20 (1.18, 1.22)
Effect on discrimination and reclassification
Reclassification results for in-hospital and ICU mortality
SAPS and RDW
SAPS versus SAPS/RDW
SAPS and RDW
SAPS versus SAPS/RDW
Model χ2 (log likelihoods)
Area under the ROC curve
Net reclassification improvement
0.175 (SE 0.015)
0.090 (SE 0.049)
Integrated discrimination improvement
0.023 (SE 0.001)
0.011 (SE 0.001)
RDW and 1-year survival
In this large cohort of ICU patients, RDW strongly and independently predicted hospital mortality, ICU mortality, and 1-year mortality. As evidenced by improvement in both AUC and net reclassification index, RDW materially improved the prediction of mortality over and above traditional severity of illness, as measured with SAPS. This finding was robust across subgroups (for example, different age and hematocrit categories and comorbidities such as anemia or renal failure, factors that are known to be positively associated with RDW values [12, 19, 20]).
These results are in accordance with previous research showing an association of RDW and long-term mortality risks in different patient populations, such as patients with cardiovascular disease, chronic heart failure, and acute kidney injury treated with continuous renal-replacement therapy [2–16, 30]. Cohort studies using nationally representative samples of the US population (Third National Health and Nutrition Survey (NHANES III)) also reported an association of RDW with long-term outcomes in community-dwelling patients [9–11]. In addition, recent studies have focused on critically ill patients and found RDW to be a prognostic in this setting as well [21–23]. Importantly, our results based on a broad US patient population admitted to different types of ICUs, including medical, cardiac, surgical, and cardiothoracic surgery confirm and expand these previous findings and demonstrate that RDW is a strong outcome predictor and thereby improves risk prediction based on the well-established SAPS score. We found the association of RDW and outcome to be robust when focusing on hospital and 1-year mortality overall and in different subgroups, such as patients with anemia.
Great interest is expressed in finding new prognostic markers in critically ill patients in the ICU setting. Early prognostication potentially helps to improve triage decisions in terms of early discharge of patients, and also with regard to therapeutic interventions. A prognostic marker should be evaluated based on the information it provides, beyond information already available based on clinical information, such as the information incorporated in SAPS. The SAPS system was developed to measure severity of illness in ICU patients, and subsequent research has validated its use to predict outcome in ICU patients . Within our large sample, SAPS showed reasonable discrimination with AUCs between 0.75 and 0.80. Still, adding RDW to the SAPS further improved its discriminatory ability for both hospital mortality and ICU mortality. This was further confirmed when calculating reclassification statistics. For in-hospital mortality, this was mainly due to better classification of nonsurvivors into lower-risk classes, whereas for ICU mortality, RDW improved classification of survivors and nonsurvivors. Importantly, from a cost perspective, it should be noted that RDW is routinely measured in most patients as part of the admission CBC analysis and thus is free of additional costs. It will important for future studies to assess whether more-advanced severity of illness scores (that is, APACHE IV, SAPS III) can still be improved by the addition of RDW.
Our results provide an important target for future translational research. Why is RDW associated with increased mortality? The underlying mechanism is still unclear and represents an important avenue for future "bedside-to-bench" research. RDW can be increased in anemia or hemoglobinopathies, hemolysis, or after blood transfusions [19, 20]. Yet, in our study and in the literature, the association of RDW and mortality was independent of anemia, and no evidence was found for effect modification by anemia and hematocrit levels [9–11, 13]. Another possible pathophysiologic explanation is that RDW is a surrogate of inflammation, which is known to increase RDW. Several studies found RDW to be associated with blood markers of inflammation, such as interleukin-6, C-reactive protein (CRP) , as well as impaired iron mobilization . Also, oxidative stress has been shown to increase anisocytosis by disrupting erythropoiesis, and to alter blood cell membrane deformability and red blood cell circulation half-life, ultimately leading to increased RDW [9, 11, 19]. Again, previous research found that adjusting for inflammation (for example, CRP) did not substantially reduce the prognostic value of RDW, demonstrating its effect beyond these factors [9–11, 22]. In our cohort, we were not able to adjust the analysis for inflammatory markers, as these are not routinely measured on admission.
RDW may also reflect the patient's degree of physiological reserve, one of three main determinants of clinical outcome, as suggested by Bion . The physiological reserve represents cellular response to acute stress and the resultant tissue hypoxia. Ischemia activates cellular systems that would reduce oxygen demand and physiologic processes that would improve tissue oxygen delivery, such as increased production and release of mature red cells into the peripheral bloodstream. How well this process of reactive erythropoiesis is carried out under oxidative stress may represent the patient's ability to handle acute physiological insult. Release of large immature red cells with poor oxygen-binding capacity, which results in an increased RDW, implies suboptimal response to oxidative stress. This may explain why the association between RDW and clinical outcome is independent of the severity of acute illness as well as the degree of inflammation. It may well represent the genetic factors that determine how well the body withstands physiological stress, whether from a severe infection, multitrauma, burns, or acute pancreatitis.
Strengths of this study are the large number of patients across different types of ICUs and the availability of a rich annotation of the physiological and clinical context, which allowed rigorous adjustment for severity of acute illness and subgroup analyses with high statistical power. We also included 1-year survival data on all the patients.
This study has limitations; as it was a retrospective, observational study, we were not able to assess causes for mortality and/or for elevated RDW. Also, our data provide no additional information about inflammation and oxidative stress. These pieces of information would be necessary to understand better the pathophysiology underlying the observed effects. Also, only admission RDW levels were considered, and it remains unclear whether changes over time of RDW may provide additional prognostic information. Importantly, we used SAPS, and more recent severity-of-illness scores (such as SAPS III or APACHE IV) have shown superior accuracy for outcome prediction; thus, future studies should address whether RDW has the potential also to improve these severity-of-illness scores. We calculated multivariable regression models, including important demographics and different comorbidities, to investigate the independent association of RDW and outcome; yet, co-linearity and missing clinical information on some important patient-history items (that is, transfusion) may limit the interpretation of the models.
This analysis validated previous studies and found RDW to be a promising independent short- and long-term prognostic marker in ICU patients, which significantly improved the SAPS for risk stratification of patients. This was also true within several subgroups, including patients with anemia. If confirmed in future studies and with updated severity-of-illness scores (such as SAPS III or APACHE IV), RDW may help to improve current prediction scores at little or no additional costs for improved decision-making in ICU patients. Further studies should be conducted to understand better the mechanism linking RDW to these adverse outcomes.
Red cell distribution width (RDW), a measure of erythrocyte size variability, is a promising independent short- and long-term prognostic marker in ICU patients
In this large U.S. cohort study including 17,922 patients from different types of ICUs, RDW was a strong and independent outcome predictor for ICU-, in-hospital, and 1-year mortality
RDW further improved the prognostic accuracy of the SAPS score
Area under the curve
Beth Israel Deaconess Medical Center
chronic obstructive pulmonary disease
complete blood count
generalized estimating equation
integrated discrimination improvement
International Classification of Diseases
- MIMIC II:
Multiparameter Intelligent Monitoring in Intensive Care
net reclassification improvement
Quasi-likelihood under the Independence model Criterion
receiver-operating characteristic curves
red cell distribution width
Simplified Acute Physiology Score
SH was support by an unrestricted research grant from the Swiss National Foundation (SNF PBBSP3-128266) and from the University of Basel, Switzerland. JL and LAC were supported by grant R01 EB001659 from the National Institute of Biomedical Imaging and Bioengineering. MH is partly supported by the Physician Faculty Scholars Program of the Robert Wood Johnson Foundation (grant 66350, to MDH).
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