Diagnostic codes for sudden cardiac death and ventricular arrhythmia functioned poorly to identify outpatient events
Sean Hennessy1, Charles E Leonard, Cristin M Palumbo
1Center for Clinical Epidemiology & Biostatistics, Department of Biostatistics & Epidemiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6021, USA. hennessy@mail.med.upenn.edu
Insights
Computerized codes for sudden cardiac death and ventricular arrhythmia (SD/VA) hospitalizations in the General Practice Research Database (GPRD) are not reliable for identifying outpatient events. Case-by-case verification is recommended for future studies.
Area of Science:
- Pharmacovigilance
- Cardiology
- Health Informatics
Background:
- The General Practice Research Database (GPRD) is a valuable resource for studying medication effects.
- Accurate identification of adverse events like sudden cardiac death and ventricular arrhythmia (SD/VA) is crucial for drug safety research.
- The validity of using computerized diagnostic codes for SD/VA in the GPRD for outpatient medication studies is uncertain.
Purpose of the Study:
- To assess the accuracy of OXMIS/Read diagnostic codes for hospitalizations due to SD/VA within the GPRD.
- To determine the utility of these codes for research on the arrhythmogenic effects of outpatient medications.
Main Methods:
- Identified patients with putative SD/VA hospitalizations linked to outpatient prescriptions for cisapride, domperidone, or metoclopramide.
- Surveyed general practitioners (GPs) and reviewed hospital discharge summaries.
- Calculated the positive predictive value (PPV) of diagnostic codes for identifying outpatient events precipitating hospitalization.
Main Results:
- Of 84 putative SD/VA events, 30 were confirmed via GP questionnaires (79% response rate).
- The PPV for any SD/VA diagnosis was high at 93% (95% CI, 78-99%).
- However, the PPV for SD/VA originating in an outpatient setting precipitating hospitalization was low at 23% (95% CI, 10-42%), with most codes reflecting in-hospital events.
Conclusions:
- Computerized SD/VA codes show good agreement with physician diagnoses but are poor indicators of outpatient events leading to hospitalization.
- Future research using the GPRD for SD/VA events necessitates individual case verification to ensure accuracy.
Purpose:
To examine the validity of OXMIS/Read diagnoses of hospitalization for sudden cardiac death and ventricular arrhythmia (SD/VA) for use in studies of arrhythmogenic effects of outpatient medications in the General Practice Research Database (GPRD).
Methods:
We identified putative occurrences of hospitalization for SD/VA in patients receiving outpatient prescriptions for cisapride, domperidone, or metoclopramide. We then administered a questionnaire to general practitioners (GPs) caring for these patients, requested hospital discharge consult letters, and examined the positive predictive value (PPV) of diagnostic codes in identifying outpatient events precipitating hospitalization.
Results:
We identified 84 putative events, 38 (45%) of which occurred in patients cared for by GPs participating in the follow-up scheme. Thirty of 38 questionnaires (79%) were completed. The PPV for the occurrence of any SD/VA was 93% (95% CI, 78-99%). However, the PPV for SD/VA occurrence in an outpatient setting precipitating a hospitalization was only 23% (95% CI, 10-42%). The majority of inpatient diagnostic codes reflected events occurring after hospital admission, not precipitating it.
Conclusions:
While computerized codes for SD/VA agreed well with physician diagnosis, they operated poorly to identify events occurring in an outpatient setting. Studies of SD/VA in the GPRD should verify events on a case-by-case basis.
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