Saturday, October 17, 2026
The AI Psych Brief
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01
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๐ฌ Section 1
Psychiatric Research Article
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Characterizing Artificial Intelligence Psychosis in a Large Medical Setting
Bergson Z, Vassall SG, Wright A, McCoy AB, Schafer KM, Achee MC, Sheffield JM ยท JAMA Psychiatry ยท October 2026
Vanderbilt investigators searched behavioral-health progress notes (December 2022 to April 2026) for AI-related keywords, kept only patients with a documented psychotic disorder, and had two raters sort each case into neutral chatbot use, "AI psychosis" (chatbot use that worsened psychosis), or AI appearing in delusional content without documented use. Across roughly 216,000 patients they found 28 cases of AI psychosis, about 0.013% of those in mental health care. Most were young (median age 27.5) and 60.7% were in their first psychotic episode, far more than in the comparison groups. The chatbot most often acted as an amplifier that validated existing distorted ideas (64%), less often as the object of the delusion (21%) or a catalyst for new symptoms (11%); 86% of cases were documented after the May 2024 GPT-4o release.
The design is retrospective and single-site, depends on what clinicians happened to write down, and cannot establish causation.
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๐ก Why it matters
Ask every patient with psychosis, especially in a first episode, what they talk to chatbots about and how often; the commonest pattern here was a chatbot agreeing with an idea the patient already held, which is easy to miss unless you ask. |
Read the paper โ doi:10.1001/jamapsychiatry.2026.2923
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02
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๐ Section 2
Psychotherapy Research Article
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Shedding light on the efficacy of psychodynamic treatment targeting depression for patients with comorbid narcissistic personality disorder
Mansour M, Kivity Y, Zilcha-Mano S ยท Psychotherapy Research ยท October 2026
This secondary analysis drew on a randomized trial of 100 adults with major depression who received short-term supportive or supportive-expressive (psychodynamic) therapy; 14 met SCID criteria for comorbid narcissistic personality disorder. Depression was tracked on the Hamilton scale across treatment with multilevel models. Patients with comorbid NPD showed greater depressive symptom reduction than those without it. Their NPD diagnostic status, however, did not change significantly over the course of therapy.
The NPD subgroup is small, so the finding is a signal rather than a settled moderator effect.
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๐ก Why it matters
Comorbid narcissistic personality is often treated as a reason to expect a poor depression outcome; this trial suggests a brief psychodynamic course can still lift the depression, provided you set the goal as treating the depression rather than expecting the personality structure to shift in 16 weeks. |
Read the paper โ doi:10.1080/10503307.2026.2738631
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03
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๐ Section 3
Psychiatric Fact
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Thiazides raise lithium within days; ACE inhibitors can take weeks
Thiazides cause mild volume contraction, and the proximal tubule responds by reabsorbing more sodium. It cannot tell sodium from lithium, so lithium is reabsorbed too. Steady-state levels typically rise 25 to 40 percent, and the change shows up within about a week. If a thiazide is unavoidable, reduce the lithium dose pre-emptively and recheck the level in five to seven days. Loop diuretics act downstream of where most lithium is reabsorbed, so they cause smaller and less predictable rises. They still need a level check, mainly because of dehydration.
ACE inhibitors and ARBs are the slower trap. They lower GFR and aldosterone-driven sodium retention gradually, so toxicity can appear three to five weeks after starting, often in an older patient whose first level came back normal. NSAIDs vary widely: indomethacin and diclofenac raise levels substantially, while low-dose aspirin and sulindac matter little. One normal level after any new antihypertensive does not end the monitoring.
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04
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๐๏ธ Section 4
Psychotherapy Teaching Pearl
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A silence has a transference before it has a meaning
Residents tend to treat silence as a pause, either a gap to fill or a technique to hold. Dynamically, silence is a relational event, and it carries a transference before it carries any particular content. The useful question is not "what is the patient not saying?" but "who am I to the patient while we are silent?" The same quiet minute can be felt as an attentive parent's presence, a withholding judge's scrutiny, or an abandonment. Which one it is decides whether the silence helps or harms.
For a patient with a stable enough internal object, a held silence lets associations come forward. For a patient who experiences you as critical or absent, an unaddressed silence repeats the trauma instead of opening it. The technical move is to read the countertransference pressure first (do you feel waited on, shut out, or tested?), then address the experience of the silence before asking what it contains.
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๐๏ธ Vignette
A 34-year-old graduate student in weekly dynamic therapy falls silent after mentioning her advisor's lukewarm email. Two minutes pass. The resident notices he is composing a reassuring comment and feels faintly guilty, as if he has failed her. Rather than reassure her or ask "what are you thinking?", he says: "I wonder what it's been like sitting here quietly with me just now." She says she was waiting for him to say her work was fine, and that when he didn't, she assumed he agreed with the advisor. The silence had turned him into a second withholding evaluator. Naming that, before the email's content, opened the transference and led to the session's real material: her conviction that silence means a verdict. |
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05
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๐ฐ Section 5
In the News
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| โ | The FDA's October 9, 2026 approval of Teva's Weltruza, a once-monthly subcutaneous olanzapine LAI for schizophrenia (318/425/531 mg โ 10/15/20 mg oral), needs no loading dose, oral overlap, or post-injection monitoring, unlike the intramuscular pamoate's REMS and 3-hour observation. That removes a major barrier to olanzapine depots in community clinics; the label still carries a PDSS warning. source โ |
| โ | In September 2026 the FDA gave MindMed's DT120 (lysergide ODT) a second Breakthrough Therapy designation, this time for major depressive disorder, on the strength of the phase 3 Emerge trial: an 8.1-point placebo-adjusted MADRS improvement at week 6 that held to week 12. Patients will ask about it; it is not yet approved. source โ |