NCI Comorbidity Index Overview
History of the NCI Comorbidity Index
The Charlson Comorbidity Index was first developed in 1987 by Mary Charlson and colleagues as a weighted index to predict risk of death within 1 year of hospitalization for patients with specific comorbid conditions. Nineteen conditions were included in the index. Each condition was assigned a weight from 1 to 6, based on the estimated 1-year mortality hazard ratio from a Cox proportional hazards model. These weights were summed to produce the Charlson comorbidity score. In 1992 and 1993, Richard Deyo and Patrick Romano separately adapted the Charlson index to ICD-9-CM diagnosis and procedure codes and CPT-4 codes so that the index could be calculated using administrative data.
In 2000 Carrie Klabunde and colleagues developed a cancer-specific NCI Comorbidity Index using breast and prostate cancer cases included in the SEER-Medicare data. Klabunde et al used codes on the Medicare data to identify the conditions identified by Charlson et al. The NCI Comorbidity Index excludes solid tumors, leukemias, and lymphomas as comorbid conditions, given that the NCI Comorbidity Index was developed from a cohort of cancer patients. The remaining 16 Charlson index conditions were included in the NCI Comorbidity Index, with further consolidation to 14 conditions. The approach for creating the NCI Comorbidity Index included review of Medicare claims for the year prior to the date of diagnosis, excluding the month of diagnosis. Separate comorbidity indexes were created for hospitalizations (Medicare Part A) and physician claims (Medicare Part B). Conditions ascertained by physician claims were required to occur more than once in a period greater than 30 days to reduce the risk of false positives. These indexes were later combined into a single NCI Comorbidity Index, which allowed for greater efficiency in analysis.
Changes to the NCI Comorbidity Index
In 2014, staff members from the Healthcare Delivery Research Program (formerly the Applied Research Program) and Surveillance Research Program undertook a thorough evaluation of the codes used to define each of the 16 conditions in the NCI comorbidity index as well as the weights associated with each condition. Professional coders reviewed all original codes to confirm that the codes were accurate and relevant to the conditions and procedures listed in the original macro. New codes were added as appropriate. The original and new codes can be found here. A separate technical report summarizes changes made to the weights included in the NCI Comorbidity Index.
A pilot study was performed using the SEER-Medicare data to assess if revising the codes in the NCI Comorbidity Index changed the estimate of the prevalence of comorbid conditions in cancer patients. SEER patients diagnosed with cancer from 1997-2007 were selected if they were age 66 and over, were covered by Medicare Parts A and B without HMO enrollment during the year prior to their cancer diagnosis. Patients were excluded if they were diagnosed by death certificate and autopsy or had a prior cancer. Non-malignant tumors were excluded. Patients were stratified by cancer site, lung, colorectal, prostate, and breast, and other. Comorbid conditions were extracted from the Medicare claims one year prior to diagnosis. Sources of medical claims included the hospital (Medpar), outpatient facility and physician supplier (carrier) Medicare data. ICD-9-CM diagnosis, ICD-9-CM procedure, and CPT procedure codes were used to identify comorbid conditions. Special focus was devoted to CPT-4 codes because these codes change more frequently than do ICD-9 codes and excluding them from the algorithm could improve stability of the definitions over time. Breast cancer patients from 1997-2007 were used to estimate the prevalence of comorbid conditions using two algorithms with old codes and new codes.
As can be seen on the table below, dropping CPT-4 codes from the index had minimal effect on ascertainment of comorbid conditions. Adding new ICD-9 diagnostic and procedure codes increases disease ascertainment, especially for non-surgical PVD and dementia and these results were similar across cancer sites.
|Comorbid Conditions||Frequency (Prevalence*)||Percent Change*
(Revised-Original) / Original
|Original (with CPT-4)||Revised with CPT-4||Revised without CPT-4||Revised with CPT-4||Revised without CPT-4|
|Conditions with CPT-4 codes|
|Moderate/Severe Liver Disease||99 (0%)||114 (0%)||114 (0%)||15%||15%|
|Cerebrovascular Disease (CVD)||5113 (5%)||5784 (5%)||5784 (5%)||13%||13%|
|Peripheral Vascular Disease (surgical)†||137(0%)||133 (0%)||133(0%)||-3%||-3%|
|Conditions with code revisions|
|Renal disease||1924 (2%)||2249 (2%)||2249 (2%)||17%||17%|
|Peripheral Vascular Disease (diagnosis) †||3155 (3%)||7137 (7%)||7137 (7%)||126%||126%|
|Paralysis (Hemiplegia or Paraplegia)||437 (0%)||608 (1%)||608 (1%)||39%||39%|
|Dementia||1582 (2%)||3075 (3%)||3075 (3%)||94%||94%|
|Mild liver disease||365 (0%)||446 (0%)||446 (0%)||22%||22%|
|Congestive heart failure (CHF)||7705 (7%)||8393 (8%)||8393 (8%)||9%||9%|
|Chronic Obstructive Pulmonary Disease (COPD)||10913 (10%)||11453 (11%)||11453 (11%)||5%||5%|
|Diabetes with complications||3377 (3%)||4946 (5%)||4946 (5%)||46%||46%|
|Diabetes||18581 (18%)||18746 (18%)||18746 (18%)||1%||1%|
*Example calculations for Moderate/ severe liver disease, “revised with CPT”
Prevalence: 114 / 105465 = 0.0011 0.0011*100 = 0.11%
Percent Change: (114 – 99) / 99 = 0.1515 0.1515*100 = 15.15%
†PVD surgical and diagnosis conditions were combined into one category for PVD in the final version of the macro. Prevalence rates for PVD combined were similar to PVD diagnosis.
Accessing NCI Comorbidity Index Macros
Software to implement the NCI comorbidity macros are available for download here.
- Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 1987;40(5):373-83. [View Abstract]
- Deyo RA, Cherkin DC, Ciol MA. Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases. J Clin Epidemiol 1992 Jun;45(6):613-9. [View Abstract]
- Romano PS, Roos LL, Jollis JG. Adapting a clinical comorbidity index for use with ICD-9-CM administrative data: differing perspectives. J Clin Epidemiol 1993 Oct;46(10):1075-9; discussion 1081-90. [Look up in PubMed]
- Klabunde CN, Potosky AL, Legler JM, Warren JL. Development of a comorbidity index using physician claims data. J Clin Epidemiol 2000 Dec;53(12):1258-67. [View Abstract]