New and Noteworthy Information—March 2014
Patients who are dementia-free but have two parents with late-onset Alzheimer’s disease may show signs of the disease during brain imaging decades before symptoms appear, researchers reported online ahead of print February 12 in Neurology. A total of 52 persons with normal cognition—including four demographically balanced groups with maternal, paternal, and maternal and paternal family history of late-onset Alzheimer’s disease, as well as those with a negative family history—underwent MRI, 11C-Pittsburgh compound B (PiB) PET, and 18F-fluoro-2-deoxyglucose PET. Subjects with both parents with a history of Alzheimer’s disease had more severe abnormalities in all three biomarkers, compared with the other groups, regarding the number of regions affected and magnitude of impairment. PiB retention and hypometabolism were most pronounced in participants with a maternal and paternal history of Alzheimer’s disease, according to the investigators.
Patients with nonvalvular atrial fibrillation are encouraged to take oral anticoagulants to prevent stroke, according to an updated guideline published in the February 25, 2014, issue of Neurology. Treatment with anticoagulants is especially important for people who have already had a stroke or a transient ischemic attack, according to the authors. The current guideline concludes that new anticoagulants such as dabigatran, rivaroxaban, and apixaban are at least as effective as, if not more effective than, warfarin and entail a lower risk of bleeding in the brain. An advantage of the new drugs is that they do not require frequent blood testing as warfarin does. The guideline also recommends new anticoagulants for the elderly, people with mild dementia, and people at moderate risk of falls.
Giving patients medications to lower blood pressure during the first 48 hours after a stroke may not reduce the likelihood of death or major disability, according to research published February 5 in JAMA. Within 48 hours of onset, 4,071 patients with nonthrombolysed ischemic stroke and elevated systolic blood pressure were randomized to receive antihypertensive treatment or to discontinuation of antihypertensive medications. Mean systolic blood pressure was reduced from 166.7 mm Hg to 144.7 mm Hg within 24 hours in the antihypertensive treatment group and from 165.6 mm Hg to 152.9 mm Hg in the control group within 24 hours after randomization. At 14 days or hospital discharge, researchers recorded 683 incidences of death or major disability in the antihypertensive treatment group and 681 incidences in the control group.
The FDA has granted accelerated approval for Northera (droxidopa) capsules for the treatment of neurogenic orthostatic hypotension (NOH) caused by primary autonomic failure (eg, Parkinson’s disease or multiple system atrophy). Accelerated approval is granted to medicines that fill a serious unmet medical need. The capsules have a boxed warning to alert health care professionals and patients about the risk of supine hypertension, which can cause stroke. Two clinical trials involving people with NOH demonstrated droxidopa’s effectiveness over a period of two weeks. The drug, which is manufactured by Chelsea Therapeutics in Charlotte, North Carolina, has not been demonstrated to provide improvement in patient symptoms beyond two weeks. The most common adverse events reported by clinical trial participants taking droxidopa were headache, dizziness, nausea, high blood pressure, and fatigue.
Earlier treatment with an antiepileptic drug (AED) results in a shorter total seizure duration among children with febrile status epilepticus, according to a study published online ahead of print February 6 in Epilepsia. A total of 199 children (ages 1 month to 6 years), were included in the prospective, multicenter study. The median time from seizure onset to first administration of an AED by EMS or emergency department personnel was 30 minutes. The mean seizure duration for children who were given medication before admission to the emergency department was 81 minutes, compared with 95 minutes for those who were not treated beforehand. The median time from first dose of an AED to the end of a seizure was 38 minutes. “Reducing the time from seizure onset to AED initiation was significantly related to shorter seizure duration,” the investigators concluded.
The FDA has granted 510(k) clearance to the Reveal LINQ Insertable Cardiac Monitor (ICM) System. The device is indicated for patients who have symptoms such as dizziness, palpitation, syncope, and chest pain that may suggest a cardiac arrhythmia, and for patients at increased risk for cardiac arrhythmias. The Reveal LINQ ICM is part of a system that allows physicians to monitor a patient’s heart continuously and wirelessly for as long as three years. The system also provides remote monitoring through the Carelink Network, which allows physicians to request notifications to alert them if their patients have had cardiac events. The Reveal LINQ ICM is approximately one-third the size of an AAA battery. The device is manufactured by Medtronic, which is headquartered in Minneapolis.
