Failure of ICD-9-CM codes to identify patients with comorbid chronic kidney disease in diabetes.
In addition to increasing the risk of cardiac disease and acute renal failure, CKD in diabetes greatly increases the risk of chronic kidney failure. Although the majority of patients with comorbid CKD and diabetes die prior to reaching end-stage renal disease (ESRD), almost half of the incident cases of ESRD in the U.S. are attributed to diabetes (Keith et al. 2004; USRDS 2004). CKD in diabetes is usually because of diabetic nephropathy. Given that appropriate medical management can slow the progression of established diabetic nephropathy, identifying patients for interventions to slow the rate of loss of glomerular filtration rate (GFR) will be important to forestall the influx of patients into ESRD programs that is predicted by the surge of prevalent diabetes (Lewis et al. 1993, 2001; Brancati et al. 1997; Gaede et al. 1999; Brenner et al. 2001). One-third of adults with type 2 diabetes and comorbid CKD lack proteinuria, which typically characterizes diabetic nephropathy (Kramer et al. 2003). However, even mild renal insufficiency without proteinuria increases the risk for cardiovascular disease in patients with diabetes (Gimeno-Orna et al. 2004). Therefore, better understanding of comorbid CKD of any etiology may inform strategies to prevent cardiovascular disease, acute renal failure, and ESRD in patients with diabetes.
A first step to understanding how CKD in diabetes affects disease outcomes is to develop methods to accurately identify individuals with CKD in patient populations. Investigators in health services research often turn to the International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) diagnosis codes in administrative records to study the effect of health care delivery upon disease outcomes. The ability of administrative records to identify cases is limited by the completeness and accuracy of diagnosis coding, which in turn is limited by the quality of documentation in the medical record (Fisher et al. 1990, 1992; Mitchell et al. 1994; Daley 1997; Iezzoni 1997; Rosamond et al. 2004). Previous work has validated the use of ICD-9-CM codes from administrative records to identify individuals with diabetes (Hebert et al. 1999; Miller, Safford, and Pogach 2004), but no studies have validated the ability of diagnosis codes to identify individuals with CKD. Despite this limitation, investigators have used ICD-9-CM diagnosis codes to define the presence of comorbid CKD as a risk factor for adverse outcomes in cardiovascular surgery (Mack et al. 2004), estimate CKD prevalence in patient populations with diabetes (Young et al. 2004), and make risk adjustments for renal failure in hospital-based quality assessment systems (Goldfield and Villani 1996). However, it is unknown if renal-related diagnosis codes in administrative records completely and specifically identify patients with CKD.
Although a plethora of codes are used to describe various attributes of kidney disease, most do not indicate the severity of kidney dysfunction. Recognizing the need for standards to both define and assess CKD through all stages of severity, the Work Group of the National Kidney Foundation Kidney Disease Outcomes Quality Initiative (K/DOQI) developed a staging classification based on GFR, defining CKD as GFR less than 60 ml/min/1.73 [m.sup.2] for at least 3 months duration (NKF 2002). A predictive equation derived from the Modification of Diet in Renal Disease study has been validated as a measure of estimated GFR (eGFR), and applied to the K/DOQI definition of CKD (Levey et al. 1999; NKF 2002; Levey et al. 2003). The methodology enables investigators to identify cases of CKD in populations where serum creatinine and demographic data are available, with the limitation that individuals with proteinuria and eGFR greater than 59 ml/min/1.73 [m.sup.2] will be misclassified as not having CKD. Therefore, using only an eGFR-based criterion to define CKD will tend to underestimate the prevalence of CKD.
By linking clinical and administrative datasets from the VA and Medicare systems, we determined how completely and accurately ICD-9-CM diagnosis codes from administrative records identify individuals with CKD in a population of patients with diabetes. We defined CKD by eGFR criterion, using definitions set forth by the K/DOQI Work Group.
MATERIALS AND METHODS
Population, Study Sample, and Data Source
The study sample was drawn from the national VA population of 566,509 veterans with diabetes alive on September 30, 1999. A description of the population, and the criteria for defining diabetes, has been described in previous work (Miller, Safford, and Pogach 2004). Patient-level data elements in VA records included demographics, visits and hospitalizations, providers, diagnosis and procedure codes, and values of serum creatinine tests. Medicare records from institutional inpatient and outpatient files (Part A), and physician care (Part B) included the same data elements plus revenue center and beneficiary status codes, but without serum creatinine values. Records were linked for individuals enrolled in both VA and Medicare systems.
We excluded 153,680 individuals who lacked a record of any serum creatinine tests or key demographic variables needed for estimation of GFR. We excluded 143,678 individuals because they either (1) lacked a second serum creatinine value 90 days or more beyond the index creatinine value, or (2) follow-up eGFR was either greater than 89ml/min/1.73 [m.sup.2], or less than 60 ml/min/1.73 [m.sup.2], when the index eGFR was 60-89 ml/min/1.73 [m.sup.2], or (3) follow-up eGFR was greater than 59 ml/min/1.73 [m.sup.2] when the index eGFR was less than 60 ml/min/1.73 [m.sup.2]. The purpose of these exclusions was to ensure that individuals classified as having CKD by index eGFR had chronically low eGFR, as opposed to a transient decrease in eGFR. The exclusions also ensured that individuals classified as having an index eGFR of 60 ml/min/ 1.73 [m.sup.2] or greater maintained a stable eGFR (neither rising nor declining) for at least 3 months duration. Additionally, we excluded 5,421 individuals with indicators for preexisting ESRD. Preexisting ESRD was defined if any one of the following conditions were present within 2 years before the study period:
* Medicare status codes were 11, 21, or 31, indicating ESRD.
* Diagnosis codes V420, V56, V451, E8791, indicating ESRD, dialysis, or kidney transplant.
* Procedure codes 3993 or 5498, indicating dialysis.
* CPT4 codes 90935, 90937, 90945, 90947, 90989, 90993, 90921, 90925, indicating dialysis or dialysis training.
* VA stop codes 602-611, indicating a visit to the dialysis unit.
* Revenue Center codes 821, 831,841 or 851, indicating outpatient dialysis.
* Revenue Center codes 801, 802, 803 or 804, indicating inpatient dialysis.
The final study sample of 263,730 veterans had an index creatinine value drawn in fiscal year (FY) 1999, and a subsequent creatinine value drawn 90-365 days following. Of this sample, 71 percent were dually enrolled in VA and Medicare systems; of those with index eGFR less than 60ml/min/ 1.73 [m.sup.2], 87 percent were enrolled in both systems.
The study data is stored at the VA New Jersey Health Care System facility. The research has been approved by the VA New Jersey Health Care System Institutional Review Board.
We used the four-variable Modification of Diet in Renal Disease equation to derive an eGFR from VA serum creatinine values (Levey et al. 1999; Lamb et al. 2003).
eGFR = (186) x [(serum creatinine mg/dl).sup.-1.154] x [(age).sup.-0.203] x (1.212 if black) x (0.742 if female)
We defined index eGFR as either (1) the first eGFR in FY 1999, if all subsequent eGFR values were greater than 89ml/min/1.73 [m.sup.2], or (2) the first eGFR value less than 90ml/min/1.73[m.sup.2] occurring in FY 1999. Veterans whose index eGFR was less than 60 ml/min/1.73 [m.sup.2] were classified as having CKD according to the definition of the K/DOQI Work Group (NKF 2002). The index eGFR was used to stage CKD according to K/DOQI guidelines:
Stage 3: Index eGFR 30-59ml/min/1.73[m.sup.2], subsequent eGFR less than 60 ml/min/1.73 [m.sup.2].
Stage 4: Index eGFR 15-29ml/min/1.73[m.sup.2], subsequent eGFR less than 60 ml/min/1.73 [m.sup.2].
Stage 5: Index eGFR less than 15 ml/min/1.73 [m.sup.2], subsequent eGFR less than 60 ml/min/1.73 [m.sup.2].
Veterans whose index eGFR was greater than 59 ml/min/1.73 [m.sup.2] were classified as "no CKD" for the purposes of this study.
From the ICD-9-CM coding manual, we grouped 79 renal-related diagnosis codes into the following seven categories: (A) chronic renal failure, (B) chronic kidney pathophysiology, (C) diabetic nephropathy, (D) acute renal failure and disease, (E) systemic diseases that can cause CKD, (F) kidney or upper urinary tract neoplasm, and (G) kidney or upper urinary tract anatomical abnormalities (Medicode 1999) (Table 1). Codes were initially assigned to groups by the clinical judgment of a nephrologist based on code descriptors. However, if the code had an ambiguous descriptor, the coding practices of a university-affiliated teaching hospital were also used to make group assignment. The groups were empirically ranked by specificity in identifying individuals with low eGFR within the study sample, with Group A being most specific and Group G being least specific. Although all of the renal-related ICD-9-CM codes were assessed for each individual in the study sample over the time span of 1 year, each individual was ultimately assigned to the single, highest ranked (most specific) group according to the codes in their records.
The study design was a cross-sectional analysis over a 1-year time frame. The study period began with the index eGFR, occurring within FY 1999, and ended 365 days later. We searched inpatient and outpatient encounters within both VA and Medicare records for occurrence of renal-related diagnosis codes. Outpatient encounters were limited to physician-attended office visits. The patient was the unit of analysis for determining the sensitivity and specificity of renal-related codes for the presence of CKD. For comparison of VA and Medicare inpatient coding accuracy, the unit of analysis was the hospital episode of care. Because transfers could potentially inflate the number of hospitalizations that were coded for renal-related diagnoses, we excluded 234 hospital stays that were less than or equal to 1 day length of stay, and had a date of admission or discharge that was less than or equal to one day from an adjacent hospitalization.
Crude prevalence of chronic kidney disease by eGFR criterion was calculated as the number of individuals with Stage 3, 4, or 5 CKD divided by the total sample size. The crude prevalence of CKD was standardized to the reference population for age and sex distributions using the direct method. Sensitivity of each code group (A-G) was calculated as the percent of patients with Stage 3, 4, or 5 CKD assigned to the code group. Specificity was calculated as the percent of patients with e GFR greater than 59 ml/min/1.73 [m.sup.2] not assigned to the code group. For hospital episodes of care, Pearson's [chi square] was used to test the association of chronic renal failure codes (Group A), versus Group B-G codes, with low eGFR. The homogeneity of the odds ratios for code assignment in VA versus Medicare-reimbursed facilities was evaluated with the Breslow-Day test. Alpha error was considered significant at less than 0.05, two-tailed. Frequency counts and analyses were run on SAS for Windows V9 (Statistical Analysis Systems, Carey, NC, USA).
Prevalence of CKD by eGFR Criterion
The study sample of 263,730 individuals with diabetes contained the following proportions of individuals by stage of CKD: (No CKD) 68.4 percent; (Stage 3) 28.7 percent; (Stage 4) 2.5 percent; (Stage 5) 0.4 percent. The overall prevalence of CKD, defined in our study as Stages 3, 4, or 5, was 31.6 percent (83,338/263,730) (Table 2). When standardized to the age and sex distribution of the U.S. adult population with diabetes in 1999 (Pleis and Coles 2003), the prevalence of CKD fell to 29.0 percent. Both crude and standardized prevalence increased with age, up to 46.1 and 54.8 percent, respectively, in those 70 years and older. Because urine protein values were not available, individuals with Stage 1 or Stage 2 CKD could not be distinguished from nonproteinuric individuals without CKD. Consequently, all individuals with eGFR greater than 59 ml/min/1.73 [m.sup.2] were combined in the general category of "no CKD."
Ability of Renal ICD-9-CM Coding to Identify Individuals with CKD
Frequency counts for individuals with one, and only one, occurrence of any of the 79 renal-related ICD-9-CM codes, from inpatient and outpatient records combined, were ascertained to determine potential random error rates (Table 3). While 13.3 percent (11,067/83,338) of all individuals with Stage 3, 4, or 5 CKD received a renal-related ICD-9-CM code at one, and only one, encounter, the false positive rate was 3.8 percent (6,843/180,392), suggesting that the majority of these "one-time only" code assignments were not random errors.
The nine codes in the Group A algorithm are the only ICD-9-CM codes specific for chronic renal failure, either as an isolated diagnosis, or combined with hypertension and/or heart failure. Of individuals with Stage 3, 4, or 5 CKD, 20.2 percent (16,864/83,338) were identified by searching all administrative records for codes from the Group A algorithm: this algorithm had the lowest false positive rate of 0.6 percent (1,034/180,392) compared with any other code group algorithm (Table 3). Including additional individuals with codes in Groups B and C increased the sensitivity to 38.7 percent (32,255/ 83,338), but lowered the specificity to 95.5 percent as more individuals with eGFR greater than 59ml/min/1.73[m.sup.2] were included. When all individuals with any possible renal-related ICD-9-CM codes were included (Groups AG), sensitivity increased to 42.4 percent (35,318/83,338), while specificity dropped to 93.2 percent.
Comparing Accuracy of Coding for Inpatient Encounters
We found a renal-related ICD-9-CM diagnosis code contained in the administrative records of 32,529 hospital episodes for 18,755 individuals: 11,253 of these hospitalizations were reimbursed by Medicare, while 21,276 occurred in VA facilities (Table 4). Of hospitalizations occurring in Medicare-reimbursed facilities, 39.6 percent (4,461/11,253) were assigned a Group A code. However, 15.6 percent (233/1,495) of hospitalizations for patients with eGFR greater than 59 ml/min/1.73 [m.sup.2] were incorrectly assigned a Group A code indicative of chronic renal failure in Medicare-reimbursed facilities. In contrast, only 29.0 percent (6,166/21,276) of hospitalizations in VA facilities received a Group A code. Of these, 7.6 percent (116/1,562) of hospitalizations for patients with eGFR greater than 59 ml/min/1.73 [m.sup.2] were incorrectly assigned a Group A code. In the VA, the odds of assigning a Group A code to patients with Stage 3, 4, or 5 CKD was 5.4 (95 percent CI: 4.4-6.5; p<.0001) times greater than the odds of assigning a non-Group A renal-related code to patients with eGFR greater than 59 ml/min/1.73 [m.sup.2]. In contrast, the odds ratio was 4.1 (95 percent CI: 3.6-4.8; p<.0001) among Medicare-reimbursed facilities. Comparing odds ratios, the correct assignment of Group A codes to patients with Stage 3, 4, or 5 CKD was significantly more likely in VA facilities compared with Medicare-reimbursed facilities (Breslow-Day test for homogeneity of odds ratios, p = .0330).
The main finding of this study is that, in adult veterans with diabetes, ICD-9CM diagnosis codes in VA and Medicare administrative records fail to identify the large majority of individuals with comorbid CKD, when CKD is narrowly defined by eGFR criterion as Stage 3, 4, or 5 CKD. Despite each individual having had, at minimum, two opportunities to diagnose chronic kidney disease within a year, a comprehensive search of all VA and Medicare administrative records revealed that only 20.2 percent of individuals with low eGFR received a code specifically indicating chronic renal failure (Group A code). However, if present, a Group A code indicated that the individual had Stage 3, 4, or 5 CKD with 99.4 percent specificity. Extending the algorithm to 17 additional ICD-9-CM codes for chronic kidney disorders that may not necessarily be associated with low eGFR (Groups B and C) increased sensitivity to 38.7 percent, while specificity declined to 95.5 percent. Extending the algorithm to include individuals with Group D codes, indicating acute renal failure and disease, increased the sensitivity to 40.1 percent, while specificity declined to 95.2 percent. Because underlying CKD is a risk factor for acute renal failure, it is not surprising that including diagnosis codes for acute renal failure in the algorithm identified additional individuals with CKD (Mangoset al. 1995; McCullough et al. 1997; Gruberg et al. 2001). Finally, adding 37 renal-related codes (Groups E-G) for kidney disorders that may, or may not, result in chronically low eGFR increased the sensitivity of the coding algorithm to a maximum value of 42.4 percent, but at a cost of further decline in specificity to 93.2 percent.
If a hospitalized patient is recognized and coded for renal disease, VA hospitals are slightly more accurate than Medicare-reimbursed hospitals in assigning Group A codes, indicating chronic renal failure, to patients with low eGFR. While less likely to assign a Group A code to an individual with low eGFR, VA hospitals were also less likely to assign a Group A code to individuals with eGFR greater than 59ml/min/1.73[m.sup.2]. For a medical coder to assign any of the Group A codes for chronic renal failure to a patient's discharge abstract, the word "failure" must be included in the description of chronic kidney disease within the medical record (AHA 2002). Terminology such as "renal insufficiency, chronic kidney disease, or diabetic nephropathy" cannot be coded as any of the Group A codes. The slightly lower coding accuracy of chronic kidney disease by Medicare providers, combined with the finding that 87 percent of individuals with chronic kidney disease were dually enrolled in Medicare and the VA system suggests that the coding gap for CKD includes providers reimbursed by Medicare as well as the VA health care system. The fact that individuals in the study sample had at least two serum creatinine tests 3-12 months apart supports the inference that the lack of CKD coding was not due simply to lack of patient encounters with the medical care system.
Inaccuracy in coding CKD in hospitalized patients may compromise the validity of risk adjustment systems that depend on case mix of the patient population. The presence of comorbid CKD greatly increases the risk of adverse outcomes in patients with myocardial infarction or cardiovascular procedures (Miettinen et al. 1996; Conlon et al. 1999; Gruberg et al. 2001; Mann et al. 2001; Shlipak et al. 2002; Wright et al. 2002; Callahan et al. 2003). If individuals with underlying CKD in these patient groups are not correctly identified, risk adjustment may lead to biased outcome assessments. The Work Group of K/DOQI has proposed that the stage of CKD should be included routinely with each renal-related ICD-9-CM code to facilitate the use of administrative databases for epidemiological and outcomes surveillance (NKF 2002).
An important secondary finding of this study is that the prevalence of CKD, narrowly defined as Stage 3, 4, or 5 CKD, is quite high (31.2 percent) among the population of veterans with diabetes. By excluding individuals with nonexistent or unstable patterns of eGFR from the sample, we attempted to minimize misclassification in order to maximize the validity of our findings regarding the sensitivity and specificity of renal-related ICD-9-CM codes. However, our methods may have introduced selection bias, in that we excluded veterans who had no serum creatinine tests, or veterans without sequential serum creatinine values. If patients with CKD are more likely to get sequential serum creatinine testing than patients without CKD, the sample for our study could have been enriched with patients with CKD. However, even taking the extreme position that none of the veterans with diabetes that we initially excluded from our study sample had CKD, a minimum of 14.7 percent (83,338/566,509) of the national VA population of patients with diabetes have CKD based solely on low eGFR criterion.
CKD is increasingly recognized as a common comorbid condition in selected patient populations. CKD is present in 60 percent of diabetic and nondiabetic patients discharged from hospitalizations for acute myocardial infarction (Langston et al. 2003). The prevalence of CKD was 13 percent among U.S. adults with type 2 diabetes in the population-based sample from the Third National Health and Nutrition Examination Survey (NHANES III), where CKD was defined as Stage 3, 4 or 5 CKD based on eGFR (Kramer et al. 2003). Although the mean age of our sample of veterans was older (mean age of 65 versus 61 years for NHANES III) and predominantly male, the age and sex standardized prevalence of CKD remained high in our study sample, at 29 percent. The lower prevalence of CKD in NHANES III, compared with our study, may possibly be explained by a lower percent of individuals in NHANES III who had diabetes of long enough duration to develop kidney disease because (1) NHANES III excluded individuals with type 1 diabetes, and (2) NHANES III included individuals with previously undiagnosed type 2 diabetes.
The importance of validating methods to identify patients with CKD is highlighted by contrasting our study results with an earlier study that estimated the prevalence of CKD in veterans with diabetes using ICD-9-CM codes. Young et al. (2004) found the prevalence of CKD in the VA diabetic population to be 6 percent, which is much lower than the prevalence of CKD in our study. Therefore, case identification using only renal-related diagnosis codes in administrative records greatly underestimates the true prevalence of disease.
The high prevalence of CKD in our study sample underscores the need for more research on the quality of care and outcomes of kidney disease within populations of patients with diabetes. The failure to code the majority of CKD cases in patients with diabetes may indicate under-diagnosis. The insensitivity of serum creatinine tests to indicate CKD in older patients is evident in our data, as 43 percent of the patients with Stage 3 CKD had an index creatinine value less than 1.5 mg/dl (data not shown). To aid recognition of CKD in individual patients, the Work Group of K/DOQI has advocated routine laboratory reporting of eGFR with serum creatinine tests (NKF 2002).
Our study has limitations. If veterans with CKD are more likely to get tested for serum creatinine, our study sample may be enriched with individuals with CKD. Such a selection bias could inflate our estimates of the prevalence of CKD in the veteran population, but should not affect our conclusions regarding the insensitivity of diagnosis codes to identify individuals with CKD. Because our data did not include values for urine protein, we were unable to classify individuals with proteinuria and eGFR greater than 59ml/min/ 1.73 [m.sup.2] as having CKD. Therefore, our study may overestimate the sensitivity of diagnosis codes to identify individuals with CKD, while underestimating the specificity. Individuals covered by health care plans in addition to Medicare fee-for-service and VA during the year of the study may have had missing claims, possibly diminishing our ability to find encounters with a renal-related code. Our study sample has a high proportion of older, male patients. Age or gender bias in coding renal diagnoses might alter the sensitivity and specificity of our algorithm to identify younger individuals, or women with diabetes and CKD. However, the concomitant use of Medicare and VA claims records extends the generalizability of our diagnosis code algorithm to male individuals enrolled in either system.
In summary, CKD is a common comorbidity in older, adult patients with diabetes. The ICD-9-CM diagnosis codes in administrative records are an insensitive, although reasonably specific marker for individuals with comorbid CKD. Research focused on health care quality and outcomes in diabetes, or case-mix methodology that adjusts for excess risk imposed by CKD, should use eGFR rather than diagnosis codes to identify individuals with CKD.
The Department of Veterans Affairs, Veterans Health Administration, Veterans Affairs Medical Center at New Jersey supported the research reported in this article, in addition to grants from VA Medical Service Research and VA Grant IIR 04-205-2 (Dr. Miller and Dr. Pogach), VA Health Services Research Quality Enhancement Research Initiative (Dr. Pogach), and the VA HSR&D Center for Quality Improvement Research (Dr. Aron). The authors gratefully acknowledge the help of Susan Weerts in data management and analysis for this study. Dr. Kern was supported as a fellow in the VA National Quality Scholars Program.
AHA. 2002. Coding Clinic for ICD-9-CM: Official Guidelines for Coding and Reporting/ American Hospital Association. Chicago: American Hospital Association.
Anderson, R.J., M. O'Brien, S. MaWhinney, C. B. VillaNueva, T. E. Moritz, G. K. Sethi, W. G. Henderson, K. E. Hammermeister, F. L. Grover, and A. L. Shroyer. 1999. "Renal Failure Predisposes Patients to Adverse Outcome after Coronary Artery Bypass Surgery. VA Cooperative Study #5." Kidney International 55 (3): 1057-62.
Brancati, F. L., P. K. Whelton, B. L. Randall, J. D. Neaton, J. Stamler, and M.J. Klag. 1997. "Risk of End-Stage Renal Disease in Diabetes Mellitus: A Prospective Cohort Study of Men Screened for MRFIT. Multiple Risk Factor Intervention Trial." Journal of the American Medical Association 278 (23): 2069-74.
Brenner, B. M., M. E. Cooper, D. deZeeuw, W. F. Keane, W. E. Mitch, H. H. Parving, G. Remuzzi, S. M. Snapinn, Z. Zhan, and S. Shahinfar. 2001. "Effects of Losartan on Renal and Cardiovascular Outcomes in Patients with Type 2 Diabetes and Nephropathy." New England Journal of Medicine 345 (12): 861-9.
Callahan, M., D. S. Battleman, P. Christos, M. Efimba, and G. Whitelaw. 2003. "Economic Consequences of Renal Dysfunction among Cardiopulmonary Bypass Surgery Patients: A Hospital-Based Perspective." Value Health 6 (2): 137-43.
Conlon, P.J., M. Stafford-Smith, W. D. White, M. F. Newman, S. King, M. P. Winn, and K. Landolfo. 1999. "Acute Renal Failure following Cardiac Surgery." Nephrology, Dialysis, Transplantation 14 (5): 1158-62.
Daley, J. 1997. "Validity of Risk-Adjustment Methods." In Risk Adjustment for Measuring Healthcare Outcomes, 2d Edition, edited by L. I. Iezzoni, pp. 331-63. Chicago: Health Administration Press.
Fisher, E. S., J. A. Baron, D.J. Malenka, J. Barrett, and T. A. Bubolz. 1990. "Overcoming Potential Pitfalls in the Use of Medicare Data for Epidemiologic Research." American Journal of Public Health 80 (12): 1487-90.
Fisher, E. S., F. S. Whaley, W. M. Krushat, D.J. Malenka, C. Fleming, J. A. Baron, and D. C. Hsia. 1992. "The Accuracy of Medicare's Hospital Claims Data: Progress Has Been Made, but Problems Remain." American Journal of Public Health 82 (2): 243-8.
Gaede, P., P. Vedel, H. H. Parving, and O. Pedersen. 1999. "Intensified Multifactorial Intervention in Patients with Type 2 Diabetes Mellitus and Microalbuminuria: The Steno Type 2 Randomised Study." Lancet 353 (9153): 617-22.
Gimeno-Orna, J. A., L. M. Lou-Arnal, B. Boned-Juliani, and E. Molinero-Herguedas. 2004. "Mild Renal Insufficiency as a Cardiovascular Risk Factor in Non-Proteinuric Type II Diabetes." Diabetes Research and Clinical Practice64 (3): 191-9.
Go, A. S., G. M. Chertow, D. Fan, C. E. McCulloch, and C. Y. Hsu. 2004. "Chronic Kidney Disease and the Risks of Death, Cardiovascular Events, and Hospitalization." New England Journal of Medicine 351 (13): 1296-305.
Goldfield, N., and J. Villani. 1996. "The Use of Administrative Data as the First Step in the Continuous Quality Improvement Process." American Journal of Medical Quality 11 (1): S35-8.
Gruberg, L., R. Mehran, G. Dangas, G. S. Mintz, R. Waksman, K. M. Kent, A. D. Pichard, L. F. Satler, H. Wu, and M. B. Leon. 2001. "Acute Renal Failure Requiring Dialysis after Percutaneous Coronary Interventions." Catheterization and Cardiovascular Interventions 52 (4): 409-16.
Harris, M. I., K. M. Flegal, C. C. Cowie, M. S. Eberhardt, D. E. Goldstein, R. R. Little, H. M. Wiedmeyer, and D. D. Byrd-Holt. 1998. "Prevalence of Diabetes, Impaired Fasting Glucose, and Impaired Glucose Tolerance in U.S. Adults. The Third National Health and Nutrition Examination Survey, 1988-1994." Diabetes Care 21 (4): 518-24.
Hebert, P. L., L. S. Geiss, E. F. Tierney, M. M. Engelgau, B. P. Yawn, and A. M. McBean. 1999. "Identifying Persons with Diabetes Using Medicare Claims Data." American Journal of Medical Quality 14 (6): 270-7.
Iezzoni, L. I. 1997. "Risk Adjustment and Current Health Policy Initiatives." In Risk Adjustment for Measuring Healthcare Outcomes, 2d edition, edited by L. I. Iezzoni, pp. 517-95. Chicago: Health Administration Press.
Keith, D. S., G. A. Nichols, C. M. Gullion, J. B. Brown, and D. H. Smith. 2004. "Longitudinal Follow-up and Outcomes among a Population with Chronic Kidney Disease in a Large Managed Care Organization." Archives of Internal Medicine 164 (6): 659-63.
Kramer, H.J., Q. D. Nguyen, G. Curhan, and C. Y. Hsu. 2003. "Renal Insufficiency in the Absence of Albuminuria and Retinopathy among Adults with Type 2 Diabetes Mellitus." Journal of the American Medical Association 289 (24): 3273-7.
Lamb, E. J., M. C. Webb, D. E. Simpson, A. J. Coakley, D. J. Newman, and S. E. O'Riordan. 2003. "Estimation of Glomerular Filtration Rate in Older Patients with Chronic Renal Insufficiency: Is the Modification of Diet in Renal Disease Formula an Improvement?" Journal of the American Geriatrics Society 51 (7): 1012-7.
Langston, R. D., R. Presley, W. D. Flanders, and W. M. McClellan. 2003. "Renal Insufficiency and Anemia Are Independent Risk Factors for Death among Patients with Acute Myocardial Infarction." Kidney International 64 (4): 1398-405.
Levey, A. S., J. P. Bosch, J. B. Lewis, T. Greene, N. Rogers, and D. Roth. 1999. "A More Accurate Method to Estimate Glomerular Filtration Rate from Serum Creatinine: A New Prediction Equation. Modification of Diet in Renal Disease Study Group." Annals of Internal Medicine 130 (6): 461-70.
Levey, A. S., J. Coresh, E. Balk, A. T. Kausz, A. Levin, M. W. Steffes, R. J. Hogg, R. D. Perrone, J. Lau, and G. Eknoyan. 2003. "National Kidney Foundation Practice Guidelines for Chronic Kidney Disease: Evaluation, Classification, and Stratification." Annals of Internal Medicine 139 (2): 137-47.
Lewis, E. J., L. G. Hunsicker, W. R. Clarke, T. Berl, M. A. Pohl, J. B. Lewis, E. Ritz, R. C. Atkins, R. Rohde, and I. Raz. 2001. "Renoprotective Effect of the Angiotensin-Receptor Antagonist Irbesartan in Patients with Nephropathy Due to Type 2 Diabetes." New England Journal of Medicine 345 (12): 851-60.
Lewis, E. J., L. G. Hunsicker, R. P. Bain, and R. D. Rohde. 1993. "The Effect of Angiotensin-Converting-Enzyme Inhibition on Diabetic Nephropathy. The Collaborative Study Group." New England Journal of Medicine 329 (20): 1456-62.
Mack, M. J., P. P. Brown, A. D. Kugelmass, S. L. Battaglia, L. G. Tarkington, A. W. Simon, S. D. Culler, and E. R. Becker. 2004. "Current Status and Outcomes of Coronary Revascularization 1999 to 2002: 148,396 Surgical and Percutaneous Procedures." Annals of Thoracic Surgery 77 (3): 761-6, discussion 66-8.
Mangos, G. J., M. A. Brown, W. Y. Chan, D. Horton, P. Trew, and J. A. Whitworth. 1995. "Acute Renal Failure following Cardiac Surgery: Incidence, Outcomes and Risk Factors." Australian and New Zealand Journal of Medicine 25 (4): 284-9.
Mann, J. F., H. C. Gerstein, J. Pogue, J. Bosch, and S. Yusuf. 2001. "Renal Insufficiency as a Predictor of Cardiovascular Outcomes and the Impact of Ramipril: The Hope Randomized Trial." Annals of Internal Medicine 134 (8): 629-36.
McCullough, P. A., R. Wolyn, L. L. Rocher, R. N. Levin, and W. W. O'Neill. 1997. "Acute Renal Failure after Coronary Intervention: Incidence, Risk Factors, and Relationship to Mortality." American Journal of Medicine 103 (5): 368-75.
Medicode 1999. International Classification of Diseases, Ninth Revision, Clinical Modification. Physican ICD-9-CM Coding Manual, 5th Edition. Vols. 1 and 2, Physician ICD9-CM Coding Manual. Salt Lake City, UT: Medicode Inc.
Miettinen, H., S. M. Haffner, S. Lehto, T. Ronnemaa, K. Pyorala, and M. Laakso. 1996. "Proteinuria Predicts Stroke and Other Atherosclerotic Vascular Disease Events in Nondiabetic and Non-Insulin-Dependent Diabetic Subjects." Stroke 27 (11): 2033-9.
Miller, D. R., M. M. Safford, and L. M. Pogach. 2004. "Who Has Diabetes? Best Estimates of Diabetes Prevalence in the Department of Veterans Affairs Based on Computerized Patient Data." Diabetes Care 27 (2 suppl): B10-21.
Mitchell, J. B., T. Bubolz, J. E. Paul, C. L. Pashos, J. J. Escarce, L. H. Muhlbaier, J. M. Wiesman, W. W. Young, R. S. Epstein, and J. C. Javitt 1994. "Using Medicare Claims for Outcomes Research." Medical Care 32 (7 suppl): JS38-51.
NKF. 2002. "K/DOQI Clinical Practice Guidelines for Chronic Kidney Disease: Evaluation, Classification, and Stratification." American Journal of Kidney Diseases 39 (2 suppl 1): S1-266.
Pleis, J. R., and R. Coles. 2003. "Summary Health Statistics for U.S. Adults: National Health Interview Survey, 1999." Vital Health Statistics 10 (212): 1-145.
Rosamond, W. D., L. E. Chambless, P. D. Sorlie, E. M. Bell, S. Weitzman, J. C. Smith, and A. R. Folsom. 2004. "Trends in the Sensitivity, Positive Predictive Value, False-Positive Rate, and Comparability Ratio of Hospital Discharge Diagnosis Codes for Acute Myocardial Infarction in Four US Communities, 1987-2000." American Journal of Epidemiology 160 (12): 1137-46.
Shlipak, M. G., P. A. Heidenreich, H. Noguchi, G. M. Chertow, W. S. Browner, and M. B. McClellan. 2002. "Association of Renal Insufficiency with Treatment and Outcomes after Myocardial Infarction in Elderly Patients." Annals of Internal Medicine 137 (7): 555-62.
Szczech, L. A., P. J. Best, E. Crowley, M. M. Brooks, P. B. Berger, V. Bittner, B. J. Gersh, R. Jones, R. M. Califf, H. H. Ting, P.J. Whitlow, K. M. Detre, and D. Holmes. 2002. "Outcomes of Patients with Chronic Renal Insufficiency in the Bypass Angioplasty Revascularization Investigation." Circulation 105 (19): 2253-8.
Thakar, C. V., S. Worley, S. Arrigain, J. P. Yared, and E. P. Paganini. 2005. "Influence of Renal Dysfunction on Mortality after Cardiac Surgery: Modifying Effect of Preoperative Renal Function." Kidney International 67 (3): 1112-9.
Tonelli, M., C. Bohm, S. Pandeya, J. Gill, A. Levin, and B. A. Kiberd. 2001. "Cardiac Risk Factors and the Use of Cardioprotective Medications in Patients with Chronic Renal Insufficiency." American Journal of Kidney Diseases 37 (3): 484-9.
USRDS. 2004. U.S. Renal Data System 2004 Annual Data Report. Atlas of End-Stage Renal Disease in the United States, (Table A.11). Bethesda, MD: National Institutes of Health, National Institute for Diabetes, Digestive, and Kidney Diseases.
Weiner, D. E., H. Tighiouart, M. G. Amin, P. C. Stark, B. MacLeod, J. L. Griffith, D. N. Salem, A. S. Levey, and M. J. Sarnak. 2004. "Chronic Kidney Disease as a Risk Factor for Cardiovascular Disease and All-Cause Mortality: A Pooled Analysis of Community-Based Studies." Journal of the American Society of Nephrology 15 (5): 1307-15.
Wright, R. S., G. S. Reeder, C. A. Herzog, R. C. Albright, B. A. Williams, D. L. Dvorak, W. L. Miller, J. G. Murphy, S. L. Kopecky, and A. S. Jaffe. 2002. "Acute Myocardial Infarction and Renal Dysfunction: A High-Risk Combination." Annals of Internal Medicine 137 (7): 563-70.
Young, B. A., J. A. Pugh, C. Maynard, and G. Reiber. 2004. "Diabetes and Renal Disease in Veterans." Diabetes Care 27 (2 suppl): B45-9.
Address correspondence to Elizabeth F. O. Kern, M.D., M.S., Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Case Western Reserve University Department of Medicine, Room 437, Basic Science Research Building, Division of Endocrinology, Case Western Reserve University, 10900 Euclid Ave., Cleveland, OH 44106-4951. Miriam Maney, M.A., C.P.H.Q., Chin-Lin Tseng, Dr.P.H., Anjali Tiwari, M.D., Mangala Rajan, M.B.A., and Leonard Pogach, M.D., M.B.A., are with the Department of Veterans Affairs-New Jersey Healthcare System REAP Center for Healthcare Knowledge Management, Newark, NJ. Donald R. Miller, Sc.D., is with the Bedford VA Medical Center for Health Quality Outcomes and Economic Research, Boston University, School of Public Health, Boston, MA. Chin-Lin Tseng, Dr.P.H., is with the Department of Preventive Medicine/New Jersey Medical School--UMDNJ, Newark, NJ. Anjali Tiwari, M.D., is with the Department of Neuroscience/New Jersey Medical School--UMDNJ, Newark, NJ. Leonard Pogach, M.D., M.B.A., is with the Department of Medicine/New Jersey Medical School--UMDNJ, Newark, NJ. David Aron, M.D., M.S., is with the Case Western Reserve University School of Medicine, VA HSR&D Center for Quality Improvement Research, Cleveland, OH.
Table 1: Renal-Related ICD-9-CM Diagnosis Codes, by Common Descriptor Groups Description Group Codes (79) Chronic renal failure A 403.11 403.91 404.12 404.13 585 586 587 Chronic kidney B 274.1 403.10 403.90 404.10 pathophysiology 581 582 583 590.00 753.13 753.14 Diabetic nephropathy C 250.4 Acute renal failure D 403.00 403.01 404.00 404.01 and disease 453.3 580 584 590.1 593.81 866 Systemic disease E 203.0 277.3 287.0 446.0 causing CKD 710.0 710.1 Upper urinary tract F 189.0 189.1 233.9 236.91 neoplasm Anatomic abnormality G 40.1 447.3 589 591 593.0 593.1 593.2 593.3 753.10 753.11 753.15 753.16 Description Codes (79) Chronic renal failure 404.92 404.93 Chronic kidney 404.11 404.90 404.91 pathophysiology 593.60 593.90 753.12 Diabetic nephropathy Acute renal failure 404.02 404.03 405.01 and disease 0.6 590.3 590.8 Systemic disease 446.2 446.4 446.6 causing CKD Upper urinary tract 239.5 neoplasm Anatomic abnormality 593.4 593.5 593.7 592 593.82 593.89 753.0 753.17 753.19 753.2 753.3 ICD-9-CM, International Classification of Diseases, 9th Revision, Clinical Modification; CKD, chronic kidney disease. Table 2: Demographic Characteristics of Veterans in the Study Sample, by CKD * Status All (N = 263,730) N % CKD (N = 83,338) % with CKD Overall 263,730 100 31.6 Men 258,272 97.9 31.5 Women 5,458 2.1 34.3 < 40 years 4,317 1.6 3.8 40-54 years 52,395 19.9 11.0 55-69 years 103,361 39.2 28.7 70+ years 103,657 39.3 46.1 White 191,539 72.6 35.0 African American 42,529 16.1 26.2 Hispanic 8,351 3.2 21.8 Other 5,090 1.9 30.7 Unknown 16,221 6.2 10.9 * CKD is defined as eGFR less than 60 ml/min/1.73 [m.sup.2]. CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate. Table 3: Identifying Individuals with CKD ([dagger]) Using ICD-9-CM Diagnosis Codes from Inpatient and Outpatient Records: 83,338 Individuals with CKD and 180,392 Individuals without CKD ICD-9-CM Diagnosis Sensitivity Sensitivity Code Groups * True+N (%) False+N (%) Individuals with 1, and only 1, code from any group ABCDEFG 11,067 13.3 6,843 96.2 Individuals with at least 1 code from t the groups A 16,864 20.2 1,034 99.4 AB 29,355 35.2 4,168 97.7 ABC 32,255 38.7 8,035 95.5 ABCD 33,454 40.1 8,736 95.2 ABODE 33,884 40.7 9,106 9.5 ABCDEF 34,151 41.0 9,551 93.5 ABCDEFG 35,318 42.4 12,317 93.2 Total Individuals 83,338 180,392 * See Table 1 for individual ICD-9-CM codes contained within Diagnosis Code Groups. ([dagger]) CKD is defined as eGFR less than 60 ml/min/1.73 [m.sup.2]. CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; ICD-9-CM, International Classification of Diseases, 9th Revision, Clinical Modification. Table 4: Accuracy of Inpatient Coding for Chronic Renal Failure (Group A Codes) by Medicare Provider versus VA Provider Medicare All CKD * (%) No CKD (%) Coded as 4,461 4,228 233 group A (39.6) (43.3) (15.6) Coded as 6,792 5,530 1,262 groups B-G (60.4) (56.7) (84.4) Total 11,253 9,758 1,495 Odds ratio 4.1 (3.6-4.8) p < .0001 Breslow-Day test for homogeneity of odds ratios p = .0330 VA All CKD * (%) No CKD (%) Coded as 6,166 6,050 116 group A (29.0) (30.6) (7.6) Coded as 15,110 13,700 1,410 groups B-G (71.0) (69.4) (92.4) Total 21,276 19,750 1,526 Odds ratio 5.4 (4.4-6.5) p <. 0001 Breslow-Day test for homogeneity of odds ratios p = .0330 * CKD is defined as eGFR less than 60 ml/min/1.73 [m.sup.2] CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate.
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|Title Annotation:||health care outcomes in the united states|
|Author:||Kern, Elizabeth F.O.; Maney, Miriam; Miller, Donald R.; Tseng, Chin-Lin; Tiwari, Anjali; Rajan, Mang|
|Publication:||Health Services Research|
|Article Type:||Case study|
|Date:||Apr 1, 2006|
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