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Cranial electrotherapy stimulation

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1269: 1744: 1754: 20: 1281: 168:, i.e., a physician, psychiatrist, nurse practitioner, psychologist, physician assistant, or occupational therapist who has an appropriate electrotherapy license, dependent upon state regulations. The United States requires a prescription for CES devices from a licensed healthcare practitioner. The FDA says that there are 11 CES devices cleared for marketing in the United States. 827: 175:
In December 2019, the FDA announced that there is no valid evidence for CES as a treatment for depression, and request new trials to be made. "FDA concluded that the four studies published after January 1, 2016, through November 1, 2019, did not contribute sufficient information in the form of valid
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studies. CES treatments have been found to induce changes in neurohormones and neurotransmitters that have been implicated in psychiatric disorders: substantial increases in beta endorphins, adrenocorticotrophic hormone, and serotonin; moderate increases in melatonin and norepinephrine, modest or
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In June 2014, the FDA announced that it "has determined that there is sufficient information to establish special controls, and that these special controls, together with general controls, will provide a reasonable assurance of safety and effectiveness for CES devices. In this action, FDA is
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Soroush Zaghi, Mariana Acar, Brittney Hultgren, Paulo S. Boggio, and Felipe Fregni. "Noninvasive Brain Stimulation with Low-Intensity Electrical Currents: Putative Mechanisms of Action for Direct and Alternating Current Stimulation." Neuroscientist. 2010 Jun;16(3):285–307
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in the 1990s, CES was not a well-known treatment for doctors and patients. During the mid-2000s, the combination of pharmaceutical brands becoming generic and Internet advertising caused CES devices to gain popularity. In 2011, the devices received media attention from the
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CES stimulation of 1 mA (milliampere) has shown to reach the thalamic area at a radius of 13.30 mm. CES has shown to induce changes in the electroencephalogram, increasing alpha relative power and decreasing relative power in delta and beta frequencies.
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Rigorous clinical trial evidence is lacking on the use of cranial electrotherapy stimulation (CES) in acute depression. Thus, at present, there is insufficient evidence on which to base decisions for using CES in treatment of acute
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Devices; Reclassification of Cranial Electrotherapy Stimulator Devices Intended To Treat Anxiety and/or Insomnia; Effective Date of Requirement for Premarket Approval for Cranial Electrotherapy Stimulator Devices Intended To Treat
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Shekelle PG, Cook IA, Miake-Lye IM, Booth MS, Beroes JM, Mak S (2018). "Benefits and Harms of Cranial Electrical Stimulation for Chronic Painful Conditions, Depression, Anxiety, and Insomnia: A Systematic Review".
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A 2014 Cochrane review found insufficient evidence to determine whether or not CES with alternating current is safe and effective for treating depression. The FDA came to the same conclusion in December 2019.
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withdrawing the proposed rule and proposed order to call for PMAs for CES devices. FDA plans to issue a proposed order in the future for the reclassification of the CES device into class II."
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Gibson TH, Donald E. O'Hair. Cranial application of low level transcranial electrotherapy vs. relaxation instruction in anxious patients. American Journal of Electromedicine. 1987;4(1):18–21
86:, headache, neuromusculoskeletal pain, degenerative joint pain, depression, or insomnia; low-strength evidence suggests modest benefit in patients with anxiety and depression. 125:
and others in the 18th century. Aldini had experimented with galvanic head current as early as 1794 (upon himself) and reported the successful treatment of patients with
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CES was initially studied for insomnia and called electrosleep therapy; it is also known as cranial-electro stimulation and transcranial electrotherapy.
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Iwanovsky, A., & Dodge, C. H. (1968). Electrosleep and electroanesthesia–theory and clinical experience. Foreign Science Bulletin, 4 (2), 1–64
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Neurological Devices; Withdrawal of Proposed Effective Date of Requirement for Premarket Approval for Cranial Electrotherapy Stimulator Devices
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Low intensity electrical stimulation is believed to have originated in the studies of galvanic currents in humans and animals as conducted by
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Feusner, Jamie D; Madsen, Sarah; Moody, Teena D; Bohon, Cara; Hembacher, Emily; Bookheimer, Susan Y; Bystritsky, Alexander (May 2012).
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scientific evidence to demonstrate that the subjects met the criteria for any recognized depressive disorder, as defined in DSM-5"
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unquantified increases in cholinesterase, gamma-aminobutyric acid, and dehydroepiandrosterone, and moderate reductions in cortisol.
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Kirsch, DL; Nichols, F (March 2013). "Cranial electrotherapy stimulation for treatment of anxiety, depression, and insomnia".
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CES has also shown to reach cortical and subcortical areas of the brain, in electromagnetic tomography and
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A 2018 systematic review found that evidence is insufficient that CES has clinically important effects on
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via electrodes on the head. CES is used with the intention of treating a variety of conditions such as
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Appel, C. P. (1972). Effect of electrosleep: Review of research. Goteborg Psychology Report, 2, 1–24
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Electrodes are placed on the earlobes, maxilla-occipital junction, mastoid processes or temples.
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Despite the long history of CES, its underlying principles and mechanisms are still not clear.
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Due to the rise of pharmaceutical treatments for depression, anxiety and insomnia, such as
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Working Commission to Investigate the Use of Psychiatry for Political Purposes
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FDA Panel Votes to Curtail Cranial Electrotherapy Stimulators
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In the United States, CES technology is classified by the
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Royal Australian and New Zealand College of Psychiatrists
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Taiwanese Society of Child and Adolescent Psychiatry
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American Academy of Child and Adolescent Psychiatry
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Index


neurostimulation
alternating current
anxiety
depression
insomnia
headaches
fibromyalgia
smoking cessation
depression
fibromyalgia
functional MRI
Giovanni Aldini
Alessandro Volta
melancholia
direct
Prozac
Ambien
Food and Drug Administration
healthcare practitioner
Transcranial direct-current stimulation
Transcranial magnetic stimulation
Electroconvulsive therapy




"Somatic treatments for mood disorders"
doi
10.1038/npp.2011.225

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