The validity of using ICD-9 codes and pharmacy records to identify patients with chronic obstructive pulmonary disease
© Cooke et al; licensee BioMed Central Ltd. 2011
Received: 30 May 2010
Accepted: 16 February 2011
Published: 16 February 2011
Administrative data is often used to identify patients with chronic obstructive pulmonary disease (COPD), yet the validity of this approach is unclear. We sought to develop a predictive model utilizing administrative data to accurately identify patients with COPD.
Sequential logistic regression models were constructed using 9573 patients with postbronchodilator spirometry at two Veterans Affairs medical centers (2003-2007). COPD was defined as: 1) FEV1/FVC <0.70, and 2) FEV1/FVC < lower limits of normal. Model inputs included age, outpatient or inpatient COPD-related ICD-9 codes, and the number of metered does inhalers (MDI) prescribed over the one year prior to and one year post spirometry. Model performance was assessed using standard criteria.
4564 of 9573 patients (47.7%) had an FEV1/FVC < 0.70. The presence of ≥1 outpatient COPD visit had a sensitivity of 76% and specificity of 67%; the AUC was 0.75 (95% CI 0.74-0.76). Adding the use of albuterol MDI increased the AUC of this model to 0.76 (95% CI 0.75-0.77) while the addition of ipratropium bromide MDI increased the AUC to 0.77 (95% CI 0.76-0.78). The best performing model included: ≥6 albuterol MDI, ≥3 ipratropium MDI, ≥1 outpatient ICD-9 code, ≥1 inpatient ICD-9 code, and age, achieving an AUC of 0.79 (95% CI 0.78-0.80).
Commonly used definitions of COPD in observational studies misclassify the majority of patients as having COPD. Using multiple diagnostic codes in combination with pharmacy data improves the ability to accurately identify patients with COPD.
Chronic obstructive pulmonary disease (COPD) is a significant cause of morbidity and mortality in the United States and throughout the world . COPD consumes substantial healthcare resources and is among the most expensive medical conditions in the United States [2, 3]. Due to the magnitude of the public health and economic burden of COPD, investigators are actively researching all aspects of the genetics, biology, pathophysiology, epidemiology, pharmacotherapy, and healthcare delivery of COPD .
The Global Initiative for Chronic Obstructive Lung Disease (GOLD), a partnership between the World Health Organization (WHO) and the National Heart, Lung and Blood Institute, define COPD as the presence of postbronchodilator airflow limitation documented as a fixed ratio FEV1/FVC < 0.7 on spirometry . However, there continues to be disagreement among professional societies as to the optimal physiologic criteria to define COPD . While investigators have performed spirometry in population samples quantify the prevalence of COPD throughout the world, such studies are expensive and time consuming to conduct [7–9]. The challenges of obtaining spirometry limit the ability of investigators to identify patients with COPD and investigate differences in COPD care practice across broad geographic regions within the United States.
Many investigators combat these issues by utilizing administrative databases to provide information about the epidemiology of and the care delivered to patients with COPD . The literature is replete with examples of the use of COPD International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9) diagnosis codes to identify COPD cases[10–15] and COPD exacerbations [16–18]. Despite the common use of ICD-9 codes to define COPD in the literature, there is limited data on the validity of such codes [16, 19–21]. Prior studies examining the validity of ICD-9 codes utilize medical record review[20, 21] or physician diagnosis as the gold standard for COPD. There is limited data characterizing the performance of ICD-9 codes when spirometry is used as the gold standard .
We sought to develop a predictive model that would best identify COPD patients using administrative data when spirometry was the gold standard. We focused on determining the performance of outpatient and inpatient ICD-9 codes, but evaluated the ability of additional information, such as age, pharmacy records, and smoking status, to improve the performance of ICD-9 codes in identifying patients with COPD.
We conducted a secondary analysis of data collected as part of an observational study of medication adherence among patients with COPD.
Setting and participants
We utilized the Department of Veterans Affairs (VA) inpatient and outpatient databases to screen all patients receiving any inpatient or outpatient care at two VA medical centers in the Pacific Northwest between January, 2003 and December, 2007. We defined the index date when patients entered the sample as the date on which the first pulmonary function test (PFT) including spirometry was performed. We excluded all patients who did not receive postbronchodilator spirometry from our analysis. We also excluded patients with a past or current diagnosis of lung cancer and patients with a BMI < 15 or ≥55 as these patients may have evidence of airflow obstruction for reasons other COPD.
Data Collection and definitions
We collected demographic data, pharmacy records and the primary ICD-9 code for all outpatient and inpatient visits during the exact calendar date one year pre- and one year post the index date utilizing the VA computerized medical record system.
Patients with any of the following primary ICD-9 codes were considered to have a COPD-related visit: 491.xx - chronic bronchitis, 492.xx - emphysema, 493.2 - chronic obstructive asthma, 496.xx - chronic airway obstruction, not elsewhere classified. We did not include 490 - Bronchitis, not specified as acute or chronic in our administrative definition of COPD because the definition itself lacks specificity which increases the concern about misclassification [23, 24]. Outpatient primary and secondary ICD-9 codes were those recorded during a patient encounter in any outpatient clinic while inpatient primary ICD-9 codes were those recorded during an admission to the hospital. ICD-9 codes generated during visits to the pulmonary function laboratory were not considered in this analysis. Although secondary ICD-9 codes were considered for defining a COPD-related visit these were uncommonly (<7% of visits) coded by providers. Comorbid conditions relevant to patients with COPD were determined using ICD-9 codes for all previous outpatient visits in the one year period prior to the index date. These included a diagnosis of lung cancer (162.x, 163.x), acute coronary syndrome (410.xx, 411.xx), congestive heart failure (398.91,415.xx, 416.xx,425.x, 428.x), diabetes (250.x), hypertension (401.xx-405.xx), atrial fibrillation (427.xx), depression (311, 300.4, 296.2x, 296.3x), and schizophrenia (295.xx).
Smoking was assessed at the time of spirometry; patients were classified as never/former or current based upon self report. We determined the total number of metered dose inhaler (MDI) canisters prescribed over the two year period to each patient for both albuterol and ipratropium bromide (categorized as: albuterol - 0, 1-5, 6+ MDI; ipratropium - 0, 1-2, 3+) using the Veterans Integrated Service Network (VISN) data warehouse. The VISN data warehouse contains the complete pharmacy records for patients who filled prescriptions within the VISN region. These data include the drug name, class, prescription identification number, prescription fill dates (primary and refills), number of allowable refills, date of next allowable refill, amount dispensed, day supply, unit price of the medication and directions for use. Nebulized medications were not included in the calculation of these totals. Tiotropium was not included in our analysis as it was adopted slowly in the VA because of formulary restriction.
COPD criterion standard
First, we categorized patients using the GOLD criterion: postbronchodilator FEV1/FVC < 0.70 to define COPD. Although experts are actively debating which COPD criterion standard is optimal, GOLD is criticized for identifying false positives among older patients [25, 26]. The second definition used a postbronchodilator FEV1/FVC < lower limit of normal (LLN), where the LLN is defined by the referent equations of Hankinson, et al . At both centers, spirometry was performed in accordance with the ATS guidelines for reproducibility .
Bivariate comparisons utilized the t-test or Χ2 test as appropriate for the distribution of the variable. We considered a p-value < 0.05 statistically significant.
We pre-specified an approach involving the sequential addition of variables to a multiple logistic regression model for each standard. We considered alternative approaches to model development including classification and regression tress (CART) and neural networks, but neither of these approaches has been consistently shown to outperform logistic regression for most classification problems in medicine [29–31]. We first assessed a model containing a single variable representing the presence/absence of ≥1 outpatient COPD-related ICD-9 code. We then increased the number of codes represented by the indicator variable to ≥3 codes. We then evaluated the performance of ≥1 inpatient COPD-related ICD-9 code. Next, we added pharmacy variables and age to the prior models to characterize changes in the performance of the model after such additions. Because smoking status was assessed by interviewing the patient at the time of spirometry, it is not considered an administrative variable. Nevertheless, this variable may be available to investigators when identifying cohorts of patients with COPD so we added it at the last stage of model development.
We stratified all models by age ≥ 65 years by interacting age (≥65 years) with all variables in each model. This approach allowed separate coefficient estimates for patients ≥ 65 and <65 years of age allowing one to apply the model to Medicare and non-Medicare patients, but provides one number for each estimate of model performance (e.g AUC, Hosmer-Lemeshow, etc).
Model performance was assessed by evaluating the sensitivity and specificity of each model (cut point for the predicted probability of COPD = 0.5), and the discrimination and calibration of each model. Discrimination was determined by calculating the area under the receiver operating characteristic curve (AUC or C-statistic). Calibration was assessed using the Hosmer-Lemeshow goodness-of-fit statistic. We calculated the Brier score for each model as an alternative measure of accuracy that incorporates features of discrimination and calibration as a single measure. The Brier score is calculated as the mean squared error of the model and describes the magnitude by which the predicted probability of COPD generated by the model deviates from the true COPD status of the patient. Because model performance rather than parsimony was our primary concern, we did not employ measures such as the Akaike information criteria during the model building process .
For the best performing model containing only administrative variables we determined the sensitivity, specificity, positive and negative predictive values for three cut points (0.25, 0.5 and 0.75) in the model-based predicted probability of COPD. These cut points illustrate the tradeoff in sensitivity and specificity of the model over the range of predicted values. Patients with a model-based probability of COPD greater than the cut point were classified as having COPD. Because the prevalence of COPD in our cohort was high, we also estimated the positive and negative predictive values for the best performing model using prevalence estimates closer to that experienced in the general population (10-20%) [7, 9, 25].
Validation and sensitivity analysis
We utilized the bootstrap (2000 iterations) to internally validate the best performing model. We selected this previously described approach instead of split sample internal validation because it provides an more accurate, unbiased estimate of performance in external cohorts. No external validation was performed.
Finally, we performed two sensitivity analyses to assess the impact of our cohort definition on the results. Because BMI is not captured in most administrative data sources, we re-fit all models after including all patients regardless of BMI. Since the specificity of ICD-9 codes for COPD in younger patients may be low, we also re-fit each model after excluding patients who were < 40 years-old (n = 552).
All analyses were performed using Stata 10.0 (Statacorp, College Station, TX). The institutional review boards for the University of Washington and the participating Veterans Affairs centers approved of the study.
Characteristics of cohort by presence of fixed airflow obstruction (GOLD/ATS/ERS standard)
Cohort (n = 9573)
No fixed obstruction
(FEV1/FVC > 0.70)
(FEV1/FVC ≤ 0.70)
Male, n (%)
Body Mass Index, n (%)
Comorbidities, n (%)
Congestive heart failure
Smoking status, n (%)
FEV1, L, mean (SD)
FEV1, % predicted, mean (SD)
Severity of airflow limitation (FEV1, % predicted), n (%)
GOLD I: Mild (≥80%)
GOLD II: Moderate (50%-79%)
GOLD III: Severe (30%-49%)
GOLD IV: Very severe (<30%)
Number of albuterol MDI, n (%)
Number of ipratroprium MDI, n (%)
Sensitivity (sens), specificity (spec), discriminative performance (AUC) and calibration (Brier score, Hosmer-Lemeshow [H-L] goodness of fit p-value) for models based on two years of administrative data
Standard for diagnosis of COPD
(FEV1/FVC < 0.70)
(FEV1/FVC < LLN)
Sens. (%)/Spec. (%)
Sens. (%)/Spec. (%)
≥1 outpatient ICD-9 code
≥2 outpatient ICD-9 code
≥3 outpatient ICD-9 codes
≥1 inpatient ICD-9 codes
≥1 outpatient ICD-9 codes
≥1 Ipratropium Bromide MDI
≥1 outpatient ICD-9 codes
≥1 albuterol MDI
≥1 outpatient ICD-9 code
≥1 inpatient ICD-9 code
≥3 ipratropium bromide MDI
≥6 albuterol MDI
Model 7 and age
Model 8 and smoking
The best performing model incorporating only administrative data (model 8) for both standards was well calibrated (Hosmer-Lemeshow statistic [GOLD p = 0.86; LLN p = 0.50]). The Brier score was lowest for these models as well (GOLD 0.187; LLN 0.187).
Logistic regression coefficients (beta) for GOLD and LLN diagnostic standard (model 8, table 2)
GOLD diagnostic standard
Age < 65 years
Age ≥ 65 years
≥1 Outpatient ICD-9 visit
≥1 Inpatient ICD-9 visit
≥3 Ipratropium MDI
≥6 Albuterol MDI
Age (per decade)
LLN diagnostic standard
Age < 65 years
Age ≥ 65 years
≥1 Outpatient ICD-9 visit
≥1 Inpatient ICD-9 visit
≥3 Ipratropium MDI
≥6 Albuterol MDI
Age (per decade)
Sensitivity, specificity, PPV, and NPV for various predicted probabilities of COPD from logistic model 8 by diagnostic standard
GOLD diagnostic standard (model 8)
Model-based predicted probability of COPD (95% CI)
Performance characteristic (%)
LLN diagnostic standard (model 8)
Model-based predicted probability of COPD (95% CI)
Performance characteristic (%)
Bootstrap internal validations of all models resulted in insignificant changes in the AUC and are therefore not reported. Inclusion of all patients regardless of BMI resulted in no substantive changes in all models (data not shown). There were no substantive changes in the models' performance when we limited the cohort to patients over 40 years-old (Additional File 3).
Utilizing over 9500 VA patients with postbronchodilator spirometry we determined that ICD-9 codes have a moderate to good ability to discriminate patients who have fixed airflow obstruction from those who do not with outpatient codes offering better performance than inpatient codes. The addition of a patient's age and pharmacy data including the number of MDIs of albuterol and ipratropium bromide to outpatient and inpatient ICD-9 codes improves the sensitivity and specificity and the overall discriminative performance of a model used to identify patients with airflow obstruction. These variables showed similar performance when utilizing GOLD criteria for airflow obstruction compared to the LLN standard for airflow obstruction.
The use of ICD-9 codes to identify cohorts of patient with COPD using administrative data is common [11–18]. Investigators and payers have utilized these codes to describe the epidemiology of COPD[12, 14, 15, 17, 24, 34–36], to evaluate the effectiveness and safety of treatments in COPD[11, 13, 18, 37, 38], and more recently, as a means to assess the quality of care provided to patients with COPD . In fact, the National Committee for Quality Assurance (NCQA) and the Agency for Health Research and Quality (AHRQ) both advocate for use of quality measures relying on ICD-9 code-based COPD case-identification [39, 40]. It is therefore surprising that the validity of both outpatient and inpatient ICD-9 codes for identifying patients with COPD has not been rigorously studied in large populations.
Most prior efforts to establish the validity of ICD-9 codes for COPD utilize chart review or physician consensus as the gold standard. One of the most widely referenced studies, conducted by Rawson and colleagues, utilized the 1987 Saskatchewan health care data files to assess the validity of inpatient COPD ICD-9 codes compared to both the patient's inpatient medical chart and provider service data . Two hundred patient charts were randomly selected from the 4613 hospitalized patients with a primary ICD-9 code for COPD (n = 496). The charted discharge diagnosis from the patient's medical record showed exact agreement for 94.2% of these patients. However, overall concordance between physician documentation of COPD related care and hospital discharge COPD-related ICD-9 codes (490-493, 496) was 68%. An analysis by Ginde and colleagues utilized a similar approach to determine the positive predictive value for principle ICD-9 codes to identify acute exacerbations of COPD in the emergency department . A random sample of 200 patients was taken from all 644 patients with a code for COPD (491.2x, 492.8, 496) at two academic medical centers between 2005 and 2006. Chart review for these patients was used to establish the gold standard for COPD exacerbation which was defined as: 1) the presence of a respiratory infection, 2) change in cough or 3) change in sputum with known physician diagnosed COPD. The overall positive predictive value for the presence of any of the specified codes was 97%. The positive predictive value for a code of 496 alone was 60% (95% CI 32-84%).
Finally, a more recent study using claims in Ontario, Canada examined the combination of ICD-9 outpatient codes and ICD-10 inpatient codes to identify patients with COPD cared for by community providers . The combination of one or more outpatient ICD-9 codes (491.xx, 492.xx, 496.xx) or one or more inpatient ICD-10 codes (J41, J43, J44) had a sensitivity of 85% and specificity of 78.4% among 113 patients with COPD and 329 patients without COPD. An expert panel reviewed each patient's medical record to determine the gold standard for COPD. Spirometry was available in only 180 patients and details about its collection were not reported in the study. The study was further limited by employing ICD-10 codes which have yet to be universally adopted by many countries around the world.
While these studies outlined above suggest that ICD-9 codes can be used to accurately identify physician defined COPD, none universally employed spirometry to define the criterion standard for COPD. Physician diagnosed COPD may not be the optimal gold standard to define COPD. A number of previous studies highlight the difficulty physicians have in correctly indentifying COPD in the absence of spirometry. In North America only 20-30% of patients billed for a COPD-related visit have had spirometry to confirm or refute the diagnosis of COPD [12, 41–43]. Up to 20% of physicians confronted with a standardized patient in a COPD exacerbation fail to correctly identify COPD as the cause of respiratory complaints . These data raise concerns about the validity of the COPD gold standard used in prior studies examining the use of ICD-9 codes to identify patients.
The only study utilizing primarily spirometry to define COPD compared discrimination between patients with asthma versus patients with COPD. The accuracy of ICD-9 codes demonstrated excellent performance (AUC 0.98) for the calculated ratio of total COPD ICD-9 codes to total respiratory ICD-9 codes to differentiate patients with asthma from patients with COPD; however, this comparison cannot develop models to predict patients with COPD as the comparator was patients with asthma. Finally, unlike our study, which included over 9500 patients, this study was limited by its inclusion of only 151 patients with COPD .
Our study has several strengths. Our gold standard for COPD used the most rigorous definition possible - fixed airflow obstruction on spirometry and captures a large number of patients who had clinical indication for spirometry. This is contrast to many of the previous studies highlighted above.
Our results also have important implications for clinical investigators and health services and health policy analysts. We present the coefficients for a model incorporating administrative variables that can be used to accurately identify patients with COPD. This equation can be used by investigators to calculate the predicted probability of airflow obstruction within novel cohorts. The sensitivity, specificity, positive and negative predictive values for cut points in the model-based predicted probability of airflow obstruction will allow an investigator to maximize sensitivity or specificity depending on the needs of the study practice. For example, one might select a lower cut point (0.25) in the model-based predicted probability of airflow obstruction if utilizing this model to screen a clinical database to identify candidates for a COPD clinical trial. In this situation, maximizing sensitivity would capture the majority of patients with true COPD but at the cost of a large number of false positives. Study staff could access the medical records of these patients to eliminate people without airflow obstruction on spirometry.
We recognize several limitations to our analysis. First, we did not externally validate our model in alternative cohorts of patients. Model performance will likely drop when our model is applied to different patients as a result of geographic and temporal changes, differences in data definitions and case-mix. We assessed the optimism in the estimated AUC for our model utilizing the bootstrap which resulted in no appreciable change in the AUC, but recognize that external validation is a necessary step prior to widespread use . Second, our model was derived on US veterans that were mostly older white men. This may limit the generalizability of our models if applied outside of the VA. In addition, the primary reason for collection of ICD-9 codes in VA patients is not for billing purposes. Differences in coding practice between the VA and other organizations capturing ICD-9 codes primarily for billing purposes may alter the performance of our models if applied outside the VA. Third, some degree of ascertainment bias is likely present, as we were unable to assess clinic visits and hospital admissions to non-VA facilities. Fourth, we collected ICD-9 codes from the one year pre- and one year post the date of spirometry, a time interval that may have reduced the sensitivity and specificity of the codes for COPD. For example, a provider may provide a COPD code on initial evaluation only to learn that spirometry rules out the diagnosis of COPD. Nevertheless, we believe the time interval we used is appropriate because it approximates how ICD-9 codes are screened in observational research and provides a conservative estimate of their performance.
Finally, we limited our cohort to patients referred for spirometry who received a bronchodilator during their test. This was done to ensure that we had a rigorous gold standard by which we defined COPD, but may limit the applicability of our model to only patients who are clinically referred for spirometry. Given the high prevalence of COPD in this population, and the VA more generally , the positive predictive value of our model will decrease if applied to a broader population. Several studies suggest that the prevalence of physiologically determined COPD is closer to 10-20%[7, 9, 25], which is considerably lower than the 48% prevalence observed in our sample. By limiting our analysis to only patients referred to spirometry we provide a conservative estimate of the models performance if applied to a general population. Discriminating patients with COPD from those without COPD among patients who are ill enough to be referred to spirometry is likely a more difficult task than discriminating COPD patients from those without COPD among all patients in a general population. Nevertheless, the estimates of the positive and negative predictive values will change when applying our model to cohorts with different COPD prevalence. Additional testing of our model in broader populations should be done prior to widespread use.
Administrative data are ubiquitous, are employed in all aspects of healthcare, and are frequently being used to understand the health and healthcare of patients with COPD. Healthcare payers, policy makers, and investigators using administrative data to study COPD rely upon valid assessment of disease status when conducting analyses. Currently used definitions of COPD in observational studies misclassify the majority of patients as having COPD. We determined that ICD-9 codes in combination with pharmacy data can accurately identify patients with COPD. Further validation of our model is required prior to its widespread application.
Agency for health research and quality
American thoracic society
Area under the receiver operating characteristic curve
Body mass index
Classification and regression trees
Chronic obstructive pulmonary disease
European respiratory society
Forced expiratory volume in one second
Forced vital capacity
Global initiative for chronic obstructive lung disease
International classification of disease, 9th revision
Lower limit of normal
Metered dose inhaler
National committee for quality assurance
Pulmonary function test
This study was supported by the Department of Veterans Affairs, Health Services Research and Development (DHA), American Lung Association (CI-51755-N) awarded to DHA, the American Thoracic Society Fellow Career Development Award (CRC), and the Robert Wood Johnson Foundation Clinical Scholar's Program (CRC). The funding bodies had no role in study design analysis, interpretation and writing of the manuscript, and in the decision to submit the manuscript for publication. The authors would also like to acknowledge the referees for their thoughtful contributions to the manuscript.
This article was made available as Open Access with the support of the University of Michigan COPE Fund, http://lib.umich.edu/cope
Disclaimer: The views expressed in this article are those of the authors and do not necessarily reflect the position or policy of the Department of Veterans Affairs or the United States government.
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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6963/11/37/prepub