The DEA Wants Five More Tryptamines in Schedule I. Comments Close October 23
A proposed rule would place five tryptamines into Schedule I. It is the second attempt at the same action, and comments close October 23.
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A proposed rule would place five tryptamines into Schedule I. It is the second attempt at the same action, and comments close October 23.
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Diligence is unglamorous. Nine things acquirers actually look at in a ketamine practice, from accrual books and payer contracts to outcomes data and chair utilization.
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A new letter in npj Mental Health Research argues a 2024 meta-analysis compared ketamine and psilocybin with different instruments. Across the same ketamine studies, one scale explains 3 percent of outcomes and another explains 15 percent.
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Higher dissociation scores went with better depression outcomes on subcutaneous esketamine, with derealization driving the difference. The study was small, open label and exploratory.
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Collecting PHQ-9 scores is common. Being able to state a response rate, and send it back to the referring clinician, is not. That gap is where referrals, payer talks and exit value live.
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From FDA's October 5 psychedelics docket to the DEA telehealth expiration and Medicare's 2027 in-person rule, six dates every ketamine clinic should plan around.
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Oxford found ketamine quieted the habenula 24 hours after infusion. A Texas A&M analysis linked 24-hour brain changes in older veterans to day-7 improvement.
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A Center for Health Care Strategies report examines how psychedelic-assisted therapy could reach Medicaid. Some states already cover off-label IV ketamine.
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Johnson & Johnson, Mindbloom and BetterU are all bidding on generic psychedelic search terms. Here is what that does to a local clinic's acquisition cost.
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Bipolar patients are routinely screened out of ketamine treatment over mania risk. A midazolam-controlled trial in JAMA Psychiatry finally tested the question.
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