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Journal of pain research

ISSN 1178-7090

7 papers in the library · 52 citations · publishing 2019-2025

Papers

Salvia divinorum: from recreational hallucinogenic use to analgesic and anti-inflammatory action.

Journal of pain research January 1, 2019 Ulises Coffeen, Francisco Pellicer 33 citations

Salvia divinorum, a plant native to southwest Mexico, has been traditionally used for inflammatory conditions and pain. Its main active component, salvinorin A (SA), is a potent hallucinogen that acts on κ opioid and cannabinoid type 1 receptors. Recent research has uncovered the cellular and molecular mechanisms behind SA's anti-inflammatory and analgesic effects. However, due to SA's short duration and hallucinogenic properties, current research aims to develop analogues that provide long-lasting pain relief and reduced inflammation without psychoactive effects. This review examines the roles of S. divinorum, SA, and its analogues, focusing on analgesic and anti-inflammatory properties while also addressing psychoactive effects.

Opioid-Free versus Opioid-Sparing Anesthesia for Postoperative Pain and Early Recovery After Laparoscopic Cholecystectomy: A Randomized Controlled Trial.

Journal of pain research January 1, 2025 Miaomiao Xiong, Yao Liu, Yingsi Liang et al. 6 citations

Opioid-free anesthesia (OFA) is noninferior to opioid-sparing anesthesia (OSA) for managing pain after laparoscopic cholecystectomy, and it leads to faster bowel recovery. In a randomized controlled trial with 81 adults, pain scores over 36 hours were similar between groups (area under the curve 7.3 for OFA vs. 6.9 for OSA; the difference was 0.384, below the noninferiority threshold of 1.0). Although early pain in the first 12 hours after PACU discharge was slightly higher with OFA, overall pain control was sufficient in both groups. Bowel recovery occurred sooner with OFA (13.8 vs. 15.5 hours). Other outcomes, including hemodynamics and patient satisfaction, were comparable.

Development and Initial Validation of Mindfulness-Based Pain Reduction (MBPR) in Patients With Chronic Low Back Pain.

Journal of pain research January 1, 2025 Wolf E Mehling, Carrie E Brintz, Wendy Hartogensis et al. 4 citations

A modified mindfulness program for chronic low back pain, called Mindfulness-Based Pain Reduction (MBPR), was developed and tested in 58 patients. The curriculum added mindful interoceptive exposure to pain, pain neuroscience education, and yoga postures for low back pain. Participants attended 80% of sessions, and two-thirds of those receiving MBPR showed clinically meaningful improvements in pain intensity and interference scores (PEG scores improved >30%). The program was feasible and acceptable, warranting further testing in a randomized controlled trial.

Balanced Opioid-Free Anesthesia on Chronic Postsurgical Pain After Video-Assisted Thoracoscopic Surgery: A Randomized Controlled Trial Protocol.

Journal of pain research January 1, 2025 Wen-Wen Huo, Jia-Yu Qian, Han-Xue Zhao et al. 4 citations

Opioid-free anesthesia (OFA) combining dexmedetomidine, esketamine, and sevoflurane is being compared with opioid-based anesthesia (OBA) using sufentanil and sevoflurane in a randomized trial of 180 adults undergoing video-assisted thoracoscopic surgery lung resection. The primary outcome is the incidence of chronic postsurgical pain at 3 months. Secondary outcomes include acute pain, pain at 1 and 6 months, opioid consumption, adverse events, and quality of recovery. The hypothesis is that OFA will lower chronic pain rates, reduce adverse events, and improve recovery.

Ethical Considerations Regarding Psychedelics for Clinical Pain Research.

Journal of pain research January 1, 2024 Christopher L Robinson, Matthew Slitzky, Michael E Schatman et al. 4 citations

Psychedelics, historically used in cultural and medicinal contexts, are regaining attention in clinical research, especially for psychiatric conditions like refractory depression, despite their Schedule I status. With chronic pain posing a major health problem and few non-opioid treatments available, psychedelics are being explored as alternative therapies. The National Institutes of Health now funds this research, marking a shift from past limited support. Ethical concerns are significant, particularly for vulnerable populations with chronic pain that impairs autonomy. Researchers must navigate complex regulatory landscapes involving the FDA and DEA. Transparent collaboration among patients, researchers, and regulators is essential. The authors propose using principle-based research ethics—autonomy, beneficence, justice, and nonmaleficence—to guide responsible progress, balancing therapeutic promise with ethical integrity.

Exploring Perceived Barriers and Facilitators for Implementing Acute Pain Clinical Trials: A Mixed-Methods Analysis of Ketamine Infusions for Sickle Cell Pain.

Journal of pain research January 1, 2025 Martha O Kenney, Alexander T Limkakeng, Timothy N Ochoa et al. 1 citation

Barriers to a clinical trial of ketamine for acute sickle cell disease pain include lack of standardized protocols (50.6% of clinicians) and provider attitudes about ketamine (32.5%). Patients cited trust in providers and potential health benefits as facilitators but worried about safety, confidentiality, and time commitment. Clinicians showed varied comfort with ketamine, differing between sickle cell and emergency medicine specialists. Successful implementation requires multidisciplinary approaches, transparent communication, strong clinical frameworks, and patient-centered trial designs.

A Multi-Site, Randomized, Parallel-Group, Controlled Trial of Virtually-Delivered Sahaj Samadhi Meditation for the Management of Moderate Depressive Symptoms in Chronic Pain.

Journal of pain research January 1, 2025 Darren K Cheng, Robert Simpson, Rahim Moineddin et al.

A virtual Sahaj Samadhi Meditation program did not significantly outperform an active control (Health Enhancement Program) in reducing depressive symptoms among people with chronic pain and moderate depression. Within the meditation group, depressive symptoms decreased by an average of 3.97 points on the PHQ-9 at 12 weeks and 4.96 points at 24 weeks, both exceeding the minimal clinically important difference, while the control group showed no significant change. The trial enrolled 108 participants, with 89 randomized. The findings suggest potential benefits of the meditation program, but larger trials under non-pandemic conditions are needed to confirm effectiveness.