To the Editor
An increasing number of analyses use administrative claims data to study the epidemiology, risk factors, and resource consumption associated with patients with ocular diseases. These sources of voluminous data allow researchers to study common and uncommon conditions and assess care delivered by different providers in various communities. Since claims data are collected primarily for billing, not research purposes, a concern is whether the diagnoses listed in the billing records reflect the actual conditions described in the medical record.1 If claims data were found to inaccurately reflect patients’ conditions, the usefulness of these data for research would be limited. The accuracy of claims data has been examined for selected eye diseases but not for many common ophthalmic conditions.2–4 We examine the accuracy of claims data for five such conditions.
Methods
With Institutional Review Board approval, 982 consecutive billing records of patients coded with the following ocular conditions were identified from two academic medical centers: cataract (International Classification of Disease-9 [ICD-9-CM] codes 366-366.4), glaucoma suspect (365.0), primary open angle glaucoma (OAG) (365.11), proliferative diabetic retinopathy (PDR) (362.02), and nonexudative macular degeneration (NEAMD) (362.51). One abstractor (KWM) reviewed the documentation in the medical record for each billed encounter and scored the billing code as correct or incorrect. An encounter was classified as billed correctly if evidence in the medical record substantiated that the patient had the condition indicated on the billing form. If no such confirmatory evidence was found, the encounter was classified as billed incorrectly.
Results
Of the 982 encounters reviewed, 949 (97%) were coded correctly. The proportion of encounters with correct codes ranged from 92% (NEAMD) to 100% (cataract) (Table 1). The most common reason for incorrect coding was insufficient detail. For example, in 4 of 10 encounters billed as PDR, the impression noted postoperative status but no diagnosis related to the retinal photocoagulation procedure performed. The proportion of encounters billed correctly was similar between the sites (414/430 [96%] vs. 535/552 [97%], p=0.60). In a multivariable logistic regression model including site, provider type, provider subspecialty, patient age, race, and ocular condition, only ocular condition was associated with incongruency between the billed ICD-9-CM code and chart documentation (p<0.0001).
Table 1.
Ocular Condition* | Number of billing records reviewed | Number of correctly coded encounters | Percentage of encounters coded correctly |
---|---|---|---|
Cataract | 220 | 220 | 100 |
Glaucoma Suspect | 200 | 194 | 97 |
Primary Open Angle Glaucoma | 250 | 245 | 98 |
Proliferative Diabetic Retinopathy | 166 | 156 | 94 |
Non-exudative Age-related Macular Degeneration | 146 | 134 | 92 |
International Classification of Disease (ICD-9-CM) codes queried: Cataract 366 - 366.4; Glaucoma Suspect 365.0; Primary Open Angle Glaucoma 365.11; Proliferative Diabetic Retinopathy 362.02; Non-exudative Age-related Macular Degeneration 362.51.
Comment
For 97% of encounters, the medical record documentation supported the ICD-9-CM billing codes used. For all five conditions studied, greater than 92% of encounters were billed accurately. Our findings expand upon the findings of the previous studies of cataract surgery3 and glaucoma.4
This study included records from 67 providers (ophthalmologists, optometrists, generalists, subspecialists) at two institutions. However, the sites, both academic medical centers, may not be fully representative of all eye clinics. Future research should investigate the accuracy of billing codes for additional ocular conditions and the extent by which all diagnoses captured in the medical record are reflected on the billing forms.
Given the strong agreement between billing data and patients’ corresponding medical records, researchers can confidently use administrative claims data to study these ocular conditions.
Acknowledgments
Financial Support: National Eye Institute K23 Mentored Clinician Scientist Award (JDS:1K23EY019511-01); Blue Cross Blue Shield of Michigan Foundation (JDS); Alliance for Vision Research grant (JDS); VA Health Services Research and Development Career Development Award (KWM)
Footnotes
No conflicting relationship exists for any author regarding any material discussed in this manuscript.
Presented at the Association for Research in Vision and Ophthalmology meeting, Ft. Lauderdale, FL, May 7, 2012
References
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