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Otologic Diagnoses Among Patients With Adult-onset and Pediatric-onset Antiphospholipid Syndrome: A Database Study
Tejal Patki1, Aashish Batheja1, Beth Rubinstein2
1Department of Otolaryngology/Head and Neck Surgery, Virginia Commonwealth University School of Medicine.
Insights
Antiphospholipid syndrome (APS) is linked to increased otologic conditions like hearing loss and vertigo in both adults and children. Further research is needed to understand these associations.
Area of Science:
- Otolaryngology
- Rheumatology
- Genetics
Background:
- Antiphospholipid syndrome (APS) is an autoimmune disorder associated with an increased risk of thrombosis and pregnancy complications.
- The otologic manifestations of APS are not well-characterized, particularly in pediatric populations.
Purpose of the Study:
- To investigate the prevalence of otologic diagnoses in adult-onset and pediatric-onset APS.
- To compare the risk of specific otologic conditions in APS patients versus the general population.
Main Methods:
- Retrospective cohort study using the TriNetX US Collaborative network.
- Adult and pediatric APS cohorts were compared with matched general population cohorts.
- Outcomes included sensorineural hearing loss (SNHL), vertigo (central and peripheral), tinnitus, and Ménière's disease.
Main Results:
- Adult APS patients showed higher risks for SNHL, central and peripheral vertigo, tinnitus, and Ménière's disease.
- Pediatric APS patients had a significantly higher risk of bilateral SNHL.
- Relative risks (RR) and 95% confidence intervals (CI) were calculated for each condition.
Conclusions:
- Both adult and pediatric APS are associated with a greater prevalence of various otologic diagnoses compared to the general population.
- Further research is warranted to identify patient-specific factors contributing to these otologic conditions in APS.
Objectives:
The otologic conditions associated with antiphospholipid syndrome (APS) have yet to be fully categorized. The objective of this study is to investigate the prevalence of otologic diagnoses in both adult-onset and pediatric-onset APS.
Methods:
The TriNetX US Collaborative network was utilized to perform a retrospective cohort study. The adult-onset and pediatric-onset APS cohorts included patients with APS diagnosed in adulthood or before 18 years, respectively. Matched comparison cohorts for the general adult and pediatric populations included patients without APS. Outcomes of interest included prevalence of sensorineural hearing loss (SNHL), central and peripheral vertigo, tinnitus, and Ménière's disease.
Results:
The adult-onset APS cohort (n=25,981) had a higher risk of SNHL [relative risk (RR): 1.4, 95% CI: 1.4-1.5], central vertigo (RR: 1.9, 95% CI: 1.4-2.7), peripheral vertigo (RR: 1.2, 95% CI: 1.1-1.3), tinnitus (RR: 1.2, 95% CI: 1.1-1.2), and Ménière's disease (RR: 1.8, 95% CI: 1.4-2.3) compared with the matched general adult cohort (n=25,981). The pediatric-onset APS cohort (n=2409) had a higher risk of bilateral sensorineural hearing loss (RR: ≥2.4, 95% CI: 1.2-5.0) compared with the matched general pediatric cohort (n=2409).
Conclusions:
Both adult-onset and pediatric-onset APS had a greater prevalence of various otologic diagnoses compared with the general population. More research is needed to evaluate unique patient factors that may contribute to the development of these conditions.
Level Of Evidence:
III.
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