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A U.S. National Institutes of Health oversight panel will no longer review all applications for gene therapy experiments. Instead

Comments Open on End of NIH Review for Gene Therapy Studies

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NIH oversight panel no longer plans to review all applications for gene therapy experiments
A brain stimulation device to treat obsessive-compulsive disorder has received approval for marketing by the U.S. Food and Drug Administration.

FDA Permits Marketing of Brain Stimulation Device for OCD

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FDA previously approved transcranial magnetic stimulation for major depression, certain migraines
Certain steps should be taken when discharging a patient for failure or inability to meet financial obligations

Steps Provided for Discharging Patient From Practice

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Letter should be sent informing patient of their discharge, providing at least 30 days' notice
Patient portals have not taken off as expected

Patient Portals Don’t Appear to Have Much Traction

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Patients not accessing them, physicians not using full range of features
Opioid dependence is more likely to occur in patients with degenerative spondylolisthesis before surgery than afterward

Opioid Dependence More Common Before Spine Surgery

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Findings based on large study of patients having surgery for degenerative spondylolisthesis
After the expanded coverage provisions of the Affordable Care Act were implemented in 2014

ACA Coverage Gains Include Workers Without Insurance

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Reduction in uninsurance rate among this group larger than that of not-employed adults
Practice names and logos should be carefully designed to emphasize what is unique about a practice

Practice Names, Logos Should Be Carefully Designed

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The logo should be simple and easy to identify, should send a message about the medical practice
Methylphenidate should be considered as a first choice for the treatment of attention-deficit hyperactivity disorder in children and adolescents

Methylphenidate Good First-Choice Pediatric ADHD Drug

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For adults, amphetamines are reasonable first choice to treat attention-deficit hyperactivity disorder
A U.S. National Institutes of Health oversight panel will no longer review all applications for gene therapy experiments

NIH Panel Will No Longer Review Gene Therapy Experiments

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FDA will now assess gene therapy experiments and products as it does with other treatments, drugs
The rate of pediatric emergency medical services transports from ambulatory practices is 42 per 100

Rate of Pediatric Emergencies in Ambulatory Practices Identified

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Most due to respiratory distress, psychiatric/behavioral emergencies, or seizures