Abstract
Introduction: Our aim in this study was to determine whether intravenous immunoglobulin (IVIg) or plasma exchange (PLEx) for treatment of neurologic disease is a trigger for thrombotic events. Methods: Using administrative data from 2005 to 2014, we identified index admissions for thrombotic events. We performed case-crossover analyses for these admissions with previous admissions for neurologic disease with IVIg or PLEx using exposure periods of between 7 and 120 days. Results: We identified 1.9 million admissions for venous thrombosis embolism, myocardial infarction, or acute ischemic stroke. The odds ratio for venous thrombosis embolism within a 30-day window after exposure to IVIg was 3.33 (1.34–8.30, P =.0097) and for PLEx was 4.29 (1.88–9.76, P =.0005). Myocardial infarction and acute ischemic stroke admissions were not associated with exposure to either therapy. Discussion: Patients admitted for venous thrombosis embolism (but not acute ischemic stroke or myocardial infarction) were more likely exposed to either IVIg or PLEx during previous admission for neurologic disease.
Original language | English |
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Pages (from-to) | 327-332 |
Number of pages | 6 |
Journal | Muscle and Nerve |
Volume | 62 |
Issue number | 3 |
DOIs | |
State | Published - 1 Sep 2020 |
Keywords
- IVIg
- PLEx
- adverse events
- therapeutics
- thrombosis
- trigger