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Sudden unexpected death with lamotrigine: risk estimate

 

REPORT FROM THE AMERICAN EPILEPSY SOCIETY 65TH ANNUAL MEETING, BALTIMORE, MD, DECEMBER 2-6, 2011 – A Norwegian study estimates that the risk of sudden unexpected death in epilepsy (SUDEP) is 2.5 per 1000 patient-years in female patients receiving lamotrigine compared to 0.5 per 1000 patient-years in women not on lamotrigine (Aurlien et al. AES 2011; abstract 3.205).

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Alemtuzumab: high rate of autoimmune disorders

 

A UK study reports that 22% of patients treated with alemtuzumab developed autoimmune disorders, notably autoimmune thyroiditis, which occurred in 15.7% (Cossburn et al. Neurology 2011; 2011; 77:573-579). Secondary autoimmunity developed most commonly in months 12-18 of treatment and was evident for up to five years. Risk factors included a family history of autoimmune disorders (OR 7.31) and smoking history (OR 3.05).

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ADAPT trial update: NSAIDs in AD

 

The Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT) was launched a decade ago to determine if an NSAID (naproxen 220 mg BID or celecoxib 200 mg BID) could delay the onset of AD (ADAPT Research Group et al. Alzheimers Dement 2009; 5: 93-104; free full text at www.ncbi.nlm.nih.gov/pmc/articles/PMC2866447/pdf/nihms185404.pdf). The trial was suspended in 2004 following the finding from the Adenoma Prevention with Celecoxib (APC) trial of an increased cardiovascular risk with celecoxib (Solomon et al. N Engl J Med 2005; 352: 1071-1080; free full text at www.nejm.org/doi/full/10.1056/NEJMoa050405).

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Indeed, data from ADAPT subsequently suggested an increased cardiovascular and cerebrovascular risk with celecoxib and naproxen (ADAPT Research Group. PLoS Clin Trials 2006; 1: e33; free full text at www.ncbi.nlm.nih.gov/pmc/articles/PMC1851724/pdf/pctr.0010033.pdf).

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