Discordance between ICD-Coded Myocardial Infarction and Diagnosis according to the Universal Definition of Myocardial Infarction

Author:

Díaz-Garzón Jorge1,Sandoval Yader23,Smith Stephen W4,Love Sara1,Schulz Karen5,Thordsen Sarah E23,Johnson Benjamin K23,Driver Brian4,Jacoby Katherine4,Carlson Michelle D23,Dodd Kenneth W4,Moore Johanna4,Scott Nathaniel L46,Bruen Charles A4,Hatch Ryan5,Apple Fred S15

Affiliation:

1. Department of Laboratory Medicine and Pathology, Hennepin County Medical Center and University of Minnesota, Minneapolis, MN

2. Division of Cardiology, Hennepin County Medical Center, Minneapolis, MN

3. Minneapolis Heart Institute, Abbott Northwestern Hospital, Minneapolis, MN

4. Department of Emergency Medicine, Hennepin County Medical Center and University of Minnesota, Minneapolis, MN

5. Minneapolis Medical Research Foundation, Minneapolis, MN

6. Department of Medicine, Hennepin County Medical Center, Minneapolis, MN

Abstract

Abstract BACKGROUND International Classification of Diseases (ICD) coding is the standard diagnostic tool for healthcare management. At present, type 2 myocardial infarction (T2MI) classification by the Universal Definition of Myocardial Infarction (MI) remains ignored in the ICD system. We determined the concordance for the diagnosis of MI using ICD-9 coding vs the Universal Definition. METHODS Cardiac troponin I (cTnI) was measured by both contemporary (cTnI) and high-sensitivity (hs-cTnI) assays in 1927 consecutive emergency department (ED) patients [Use of TROPonin In Acute coronary syndromes (UTROPIA) cohort] who had cTnI ordered on clinical indication. All patients were adjudicated using both contemporary and hs-cTnI assays. The Kappa index and McNemar test were used to assess concordance between ICD-9 code 410 and type 1 MI (T1MI) and type 2 MI (T2MI). RESULTS Among the 249 adjudicated MIs using the contemporary cTnI, only 69 (28%) were ICD-coded MIs. Of 180 patients not ICD coded as MI, 34 (19%) were T1MI and 146 (81%) were T2MI. For the ICD-coded MIs, 79% were T1MI and 21% were T2MI. A fair Kappa index, 0.386, and a McNemar difference of 0.0892 (P < 0.001) were found. Among the 207 adjudicated MIs using the hs-cTnI assay, 67 (32%) were ICD coded as MI. Of the 140 patients not ICD coded as MI, 27 (19%) were T1MI and 113 (81%) were T2MI. For the ICD-coded MIs, 85% were T1MI and 15% T2MI. A moderate Kappa index, 0.439, and a McNemar difference of 0.0674 (P < 0.001) were found. CONCLUSIONS ICD-9–coded MIs captured only a small proportion of adjudicated MIs, primarily from not coding T2MI. Our findings emphasize the need for an ICD code for T2MI.

Funder

Minneapolis Medical Research Foundation

Abbott Laboratories

Roche Diagnostics

Siemens Healthcare

Alere

Trinity

Nanomix

Becton Dickinson

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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