Opparounds

Saturday, August 29, 2026

Opparounds

01
๐Ÿ”ฌPsychiatric Research Article

Time Trends in Maternal Attention-Deficit/Hyperactivity Disorder and Medication Use in Pregnancy

Sofie Egsgaard, Hilary K. Brown, Jonathan Zipursky, Trine Munk-Olsen, Amreen Babujee, Aditi Patrikar, Mindy Lu, Simone N. Vigod ยท The Journal of Clinical Psychiatry ยท August 2026

Using health administrative data on 2,327,110 pregnancies in Ontario, Canada from 2002 to 2023, this cross-sectional time-series study tracked how often pregnant patients carried an ADHD diagnosis and how often they filled stimulant prescriptions. The proportion of pregnancies with a maternal ADHD diagnosis rose five-fold, from 0.5% in 2002 to 2.5% in 2023. Among those with ADHD, stimulant use in the year before pregnancy climbed from 21.8% to 39.8% between 2014 and 2023, and use during pregnancy itself rose from 10.1% to 20.9% over the same span, with lisdexamfetamine driving most of the recent increase. About three-quarters of patients on a stimulant discontinued it before or during the first trimester, but that still leaves a growing minority carrying a stimulant across the whole pregnancy.

 
๐Ÿ’ก Why it matters

With one in five ADHD-affected pregnancies now continuing stimulant treatment, a resident needs a working answer for this conversation rather than a reflexive taper -- weighing maternal ADHD control against fetal stimulant exposure is becoming a routine consult, not an exceptional one.

Read the paper โ†’  doi:10.4088/JCP.26m16321

02
๐Ÿ“–Psychotherapy Research Article

Mechanisms of Change in the Treatment of Major Depressive Disorder with Metacognitive Therapy and Behavioral Activation โ€” A Random Intercept Cross-Lagged Panel and Mediation Analyses

Anna Schaich, Marie Antia-Frese, Cora Gebauer, Gitta Schippmann, Nele Assmann, Kamila Jauch-Chara, Daniel Alvarez-Fischer, Jan Philipp Klein, Eva Fassbinder ยท Psychotherapy Research ยท July 2026

Using monthly outcome data from 122 depressed patients randomized to six months of Metacognitive Therapy (MCT) or Behavioral Activation (BA), this study modeled the temporal relationship between proposed treatment mechanisms and depressive symptoms with random intercept cross-lagged panel models. MCT produced larger reductions than BA in rumination time, dysfunctional coping, and negative metacognitions, and mediation analyses showed the mechanism doing the most work for MCT was a drop in time spent ruminating, not any single belief change. Cross-lagged modeling found mechanism variables and symptoms moving bidirectionally -- less depression also fed back into less rumination, not only the reverse.

 
๐Ÿ’ก Why it matters

When choosing between MCT and BA for a ruminative depressed patient, this study's mediation data give MCT's theoretical rationale some empirical teeth -- rumination time itself is worth tracking session-to-session as a marker of whether the treatment is working.

Read the paper โ†’  doi:10.1080/10503307.2025.2530543

03
๐Ÿ’ŠPsychiatric Fact

Not every NSAID does the same thing to a lithium level

Nonsteroidal anti-inflammatories are the interaction most residents already screen for on a lithium panel, but the mechanism explains an exception worth knowing. NSAIDs raise lithium levels by inhibiting renal prostaglandin synthesis, which reduces renal blood flow and increases proximal tubular sodium -- and with it, lithium -- reabsorption; the effect is dose-dependent and shows up with ibuprofen, naproxen, and COX-2 inhibitors at their usual anti-inflammatory doses, typically pushing levels up 25 to 40 percent within days. Low-dose aspirin (81 mg), taken for cardiac prophylaxis, is the exception: at that dose it acts almost entirely on platelet COX-1, with minimal effect on renal prostaglandin production, so it does not meaningfully raise lithium levels the way other NSAIDs do. That distinction only holds at antiplatelet dosing -- full anti-inflammatory aspirin doses (over 3 g/day) behave like any other NSAID. So a lithium patient starting low-dose aspirin for cardioprotection doesn't need a preemptive level check, but the same patient reaching for ibuprofen for a headache does.

04
๐Ÿ›‹๏ธPsychotherapy Teaching Pearl

Reverie isn't empathy -- it's digestion

Bion's model treats the therapist's mind as an organ that can metabolize experience the patient cannot yet think. Raw, unprocessed affect and sensation -- what Bion called beta elements -- arrive in the room via projective identification, evacuated because the patient has no way to hold them. Reverie is the therapist's receptive internal state: tolerating not-knowing long enough to let that raw material sit, rather than acting on the urge to soothe, explain, or redirect it away. Through alpha function, that unprocessed material gets transformed into something that can be thought about and eventually spoken back as an interpretation. This differs from ordinary empathy -- empathy recognizes a feeling that's already formed; reverie does the prior work of turning something formless into a feeling at all. The technical task is staying with your own discomfort long enough for that transformation to happen, instead of discharging it through premature reassurance.

 
๐Ÿ—’๏ธ Vignette

A patient describes a chaotic week -- a fight with a partner, a missed deadline, a canceled plan -- in a flat, itemized voice with no apparent distress. The therapist notices a rising sense of dread that doesn't match anything the patient has said, and the urge to fill the silence with a reassuring comment. Instead, the therapist stays with the dread a few more seconds, then offers: "There's a dread here that doesn't have any words yet." The patient stops, goes quiet, and for the first time names a specific fear -- that the relationship is ending and no one will tell her directly. The therapist's own affect was the only form the fear had taken until that moment.

05
๐Ÿ“ฐIn the News
โ€ข The FDA's July 2026 approval of centanafadine (Simtriyo) -- the first norepinephrine-dopamine-serotonin reuptake inhibitor for ADHD -- gives residents a genuinely new mechanism to know, though DEA scheduling (still pending, expected within three months) means it isn't dispensable yet.  source โ†’
โ€ข The FDA's April 2026 label update for lumateperone (Caplyta) adds relapse-prevention data: a 26-week withdrawal trial cut schizophrenia relapse risk by 63 percent versus placebo -- useful evidence when a stable patient asks about stopping.  source โ†’