Skip to content

Robert A. Schoevers

University Medical Center Groningen

4 papers in the library · 306 citations · publishing 2016-2025

Papers

Adverse events in clinical treatments with serotonergic psychedelics and MDMA: A mixed-methods systematic review

Journal of Psychopharmacology August 26, 2022 Joost J. Breeksema, Bouwe Kuin, Jeanine Kamphuis et al. 171 citations

A systematic review of 44 clinical studies (34 quantitative, 10 qualitative) involving 598 patients treated with MDMA or serotonergic psychedelics (psilocybin, LSD, ayahuasca) found that treatments were generally well tolerated, though adverse events were often not systematically assessed. Common acute adverse events across diagnoses and compounds included nausea, headaches, and anxiety. Late adverse events included headaches (psilocybin, MDMA), fatigue, low mood, and anxiety (MDMA). One serious adverse event occurred during MDMA administration (increased premature ventricular contractions requiring brief hospitalization); no other events required medical intervention. Qualitative studies suggested that psychologically challenging experiences may be therapeutically beneficial. The authors conclude that adverse events are poorly defined and likely underreported due to study design and sample selection.

Oral ketamine for the treatment of pain and treatment-resistant depression

The British Journal of Psychiatry February 1, 2016 Robert A. Schoevers, Tharcila V. Chaves, Sonya M. Balukova et al. 80 citations

A review of 88 articles examined how ketamine is given (oral, intravenous, intranasal, subcutaneous) for treatment-resistant depression and chronic pain. The methodological quality of studies on ketamine's antidepressant effects was low for all routes. Doses used for depression were lower than those for pain. Studies on pain suggest that oral ketamine may be acceptable for depression in terms of tolerability and side-effects, but few studies have systematically examined longer-term negative consequences. The authors conclude that rigorous randomized controlled trials are needed to study short- and longer-term depression outcomes and side-effects.

Patient perspectives and experiences with psilocybin treatment for treatment-resistant depression: a qualitative study

Scientific Reports February 5, 2024 Alistair Niemeijer, Erwin Krediet, Jeanine Kamphuis et al. 50 citations

Patients with treatment-resistant depression who received psilocybin in a clinical trial described challenges with trust-building and expectation management, the need to navigate intense experiences often guided by music, and a desire for a more comprehensive treatment including multiple psilocybin sessions and sustained therapy. Distrust in mental healthcare generally, but trust in study therapists, was a key subtheme. The findings suggest that optimizing psilocybin treatment for this population requires individualized preparation, investment in trust-building, additional sessions, and access to ongoing psychotherapy with trusted therapists.

Concomitant use of antidepressants and classic psychedelics: A scoping review

Journal of Psychopharmacology September 12, 2025 Stephan Tap, Kelan Thomas, Tomáš Páleníček et al. 5 citations

Classic psychedelics like psilocybin are being studied for psychiatric disorders. Current protocols typically require patients to stop antidepressants (ADs) for at least two weeks before psychedelic use to avoid serotonin syndrome and preserve efficacy, but discontinuation can worsen depression and increase suicidal ideation. This scoping review of 18 studies found that using ADs alongside classic psychedelics is generally safe and tolerable, with no increased risk of serotonin syndrome, especially with psilocybin. Some studies showed significant improvements in depression and other symptoms. Although some evidence suggests a potential reduction in acute subjective psychedelic effects, this was not consistent. The authors conclude that maintaining ADs may improve patient access and avoid discontinuation risks.