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Simone D., a pseudonym for a psychiatric patient in the Creedmoor Psychiatric Center in New York, [10] who in 2007 won a court ruling which set aside a two-year-old court order to give her electroshock treatment against her will [11] [12] Duplessis Orphans Orphans of the 1950s in the province of Quebec, Canada, endured electroshock.
Patients who received pulsing electrical impulses, as opposed to a steady flow, seemed to incur less memory loss. The vast majority of modern treatment uses brief pulse currents. [ 70 ] A greater number of treatments and higher electrical charges (stimulus charges) have also been associated with a greater risk of memory impairment.
The list of contraindications for receiving ECT is relatively short. Once the decision to undergo ECT is made collaboratively between the patient and physician, the patient is screened for any contraindications. These include a history of cerebral aneurysms, heart attack, emphysema, multiple sclerosis, and muscular dystrophy. [1]
The term has also been applied specifically to the use of electric current to speed up wound healing. The use of electromagnetic stimulation or EMS is also very wide for dealing with muscular pain. [4] Additionally, the term "electrotherapy" or "electromagnetic therapy" has also been applied to a range of alternative medical devices and ...
Deep sleep therapy, introduced in the late 20th century, involved placing patients into a drug-induced coma for extended periods, purportedly to treat various mental illnesses.< [5] This approach to mental health treatment was part of a broader search for effective therapies during a time when the psychiatric field was struggling with managing ...
In the intent-to-treat population, patients treated with TTFields therapy concomitant with gemcitabine and nab-paclitaxel had an mOS of 16.20 months compared to 14.16 months in patients treated ...
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In 2004, a pulsed electromagnetic field system was approved by the FDA as an adjunct to cervical fusion surgery in patients at high risk for non-fusion. [6] On 8/9 September 2020 the FDA recommended to shift PEMF medical devices from the Class 3 category to a Class 2 status. [ 7 ]