Novel Pharmacologic and Other Somatic Treatment Approaches for Posttraumatic Stress Disorder in Adults: State of the Evidence.
Lauren M. Sippel, Jessica L. Hamblen, Benjamin Kelmendi, Jonathan E. Alpert, Linda L. Carpenter, Adrienne Grzenda, Nina Kraguljac, William M. Mcdonald, Carolyn I. Rodríguez, Alik S. Widge, Charles B. Nemeroff, Paula P. Schnurr, Paul E. Holtzheimer
The American journal of psychiatry December 1, 2024 DOI: 10.1176/appi.ajp.20230950 via PubMed
Summary
AI-generated from the abstractPTSD is common and can become chronic without treatment. First-line treatments are individual trauma-focused psychotherapies, with antidepressants and non-trauma-focused psychotherapies also evidence-based. Many patients do not fully recover, prompting a search for novel treatments. This review critically evaluates emerging pharmacological and somatic interventions, including medication-assisted psychotherapy (e.g., MDMA), novel monotherapies (e.g., ketamine, cannabidiol), and neuromodulation (e.g., transcranial magnetic stimulation), as well as treatments of increasing interest (hyperbaric oxygen, stellate ganglion block, neurofeedback). Evidence for most novel treatments is preliminary and highly variable, though data for transcranial magnetic stimulation are encouraging.
Study at a glance
| Characteristics | Review Peer reviewed |
|---|---|
| Keywords | Behavioral psychotherapy Cognitive psychotherapy Drug psychotherapy combination Evidence-based treatment Pharmacotherapy |
| Citations | 11 |
| Key finding | Evidence for most novel pharmacological and somatic treatments for PTSD is preliminary and highly variable, but data for transcranial magnetic stimulation are encouraging. |
Abstract
Posttraumatic stress disorder (PTSD) is a highly prevalent psychiatric disorder that can become chronic and debilitating when left untreated. The most commonly recommended first-line treatments for PTSD among adults are individual trauma-focused psychotherapies. Other evidence-based treatments include specific antidepressant medications and non-trauma-focused psychotherapies. Despite the effectiveness of these available treatments, many patients' symptoms do not remit. This has led to the search for novel treatments for PTSD. In this review, the authors critically evaluate the data supporting several emerging pharmacological and other somatic interventions in the categories of medication-assisted psychotherapy, novel medication monotherapy strategies, and neuromodulation, selected because of the salience of their mechanisms of action to the pathophysiology of PTSD (e.g., MDMA-assisted psychotherapy, ketamine, cannabidiol, transcranial magnetic stimulation). The authors also evaluate the evidence for treatments that are the focus of increasing scientific or public interest (i.e., hyperbaric oxygen therapy, stellate ganglion block, neurofeedback). To date, the evidence supporting most novel pharmacological and somatic treatments for PTSD is preliminary and highly variable; however, the data for several specific treatments, such as transcranial magnetic stimulation, are encouraging.