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Published on: November 1, 2015
Reporting consistency in systemic lupus erythematosus patients: how reliable are patient histories?
Y Yazici1, D Erkan, M J Harrison
1yaziciy@hss.edu
Insights
Systemic lupus erythematosus (SLE) patients consistently report their medical and social histories. However, family history reporting by SLE patients showed inconsistencies when questioned multiple times.
Area of Science:
- Rheumatology
- Clinical Research
- Patient Reported Outcomes
Background:
- Systemic lupus erythematosus (SLE) management involves frequent patient-physician interactions.
- Patient history is crucial for clinical decision-making in SLE.
- Limited data exists on the consistency of patient-reported histories in SLE.
Purpose of the Study:
- To assess the reporting consistency of specific aspects of patient history in SLE.
- To compare prospective patient-reported history with retrospective chart review data.
Main Methods:
- Administered a nine-item questionnaire to SLE patients twice, 4 months apart.
- Conducted a retrospective chart review to correlate with patient-reported data.
- Analyzed consistency across general medical, SLE-specific, social, and family histories.
Main Results:
- SLE patients demonstrated good reporting consistency for general medical, SLE-specific, and social histories.
- Chart review data generally aligned with prospective patient questioning.
- A notable lack of consistency was observed in family history reporting.
Conclusions:
- SLE patients are generally reliable reporters of their medical and social histories.
- Family history information reported by SLE patients may lack consistency over time.
- Findings highlight potential limitations in relying solely on patient self-reporting for family history in SLE research and databases.
Abstract:
Systemic lupus erythematosus (SLE) patients are frequently seen by multiple physicians and at multiple times. In each instance, most of the information important in clinical decision-making is gathered from the patient. There are no studies looking at reporting consistency of certain aspects of SLE patients' history. We studied this by administering the same nine-item questionnaire 4 months apart to the same cohort of SLE patients. In addition, a retrospective chart review was done to correlate the information obtained by prospective questioning and with that on the charts. Our results showed overall good consistency in the areas of general medical history, SLE-specific history and social history. The information gathered by the chart review, in general, went in parallel with that obtained by prospective questioning. This was also true for the poor correlation observed in the family history questions. Many studies and databases depend rather heavily on patient reporting and the quality of this information is usually not substantiated. Our study suggests that, even though SLE patients are generally consistent reporters of certain aspects of their histories, family history information provided is frequently not consistent with previous reporting.
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