Publications by authors named "Rathmell James"

Preoperative negative affect is a risk factor for worse postoperative pain, but research investigating this association among patients undergoing thoracic surgery is inconsistent. Additionally, female patients often report greater negative affect and postoperative pain than males. This prospective observational study investigated the association between preoperative negative affect and postoperative pain after thoracic surgery and whether this association differed by sex.

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  • * This shortage impacts healthcare facilities by increasing costs, contributing to clinician burnout, disrupting surgery schedules, and threatening the education of future anesthesiologists.
  • * Solutions require a comprehensive approach that includes boosting training positions, harnessing new technologies, and addressing financial policies to improve capacity and retention in the anesthesia workforce.
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Background: Adults with refractory, mechanical chronic low back pain associated with impaired neuromuscular control of the lumbar multifidus muscle have few treatment options that provide long-term clinical benefit. This study hypothesized that restorative neurostimulation, a rehabilitative treatment that activates the lumbar multifidus muscles to overcome underlying dysfunction, is safe and provides relevant and durable clinical benefit to patients with this specific etiology.

Materials And Methods: In this prospective five-year longitudinal follow-up of the ReActiv8-B pivotal trial, participants (N = 204) had activity-limiting, moderate-to-severe, refractory, mechanical chronic low back pain, a positive prone instability test result indicating impaired multifidus muscle control, and no indications for spine surgery.

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The federal No Surprises Act (NSA), designed to eliminate surprise medical billing for out-of-network (OON) care for circumstances beyond patients' control, established the independent dispute resolution (IDR) process to settle clinician-payer payment disputes for OON care. The purpose of our study was to assess the fraction of OON claims for which radiologists and other hospital-based specialists can expect to at least break even when challenging payer-determined payments through the NSA IDR process, as a measure of the process's financial viability. This retrospective study extracted claims from a national commercial database (Optum's deidentified Clinformatics Data Mart) for hospital-based specialties occurring on the same day as in-network emergency department (ED) visits or inpatient stays from January 2017 to December 2021.

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  • The study investigates why some women experience more pain and use more opioids after cesarean delivery, aiming for better personalized pain management practices.
  • It compares three different questionnaires (a 3-item, a longer 58-item, and a 19-item) to see which can best explain variations in psychosocial factors affecting pain and opioid use.
  • Results show that both the brief and long questionnaire models are more effective than the 3-item model, revealing important factors like surgical anxiety and expected pain medication needs that influence postoperative pain and opioid consumption.
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A diet supplemented with vitamin D and marine omega-3 fatty acids may prevent and treat painful disorders by promoting the resolution of inflammation. However, large, randomized placebo-controlled trials evaluating the effects of supplementation with omega-3 fatty acids and vitamin D on the presence and severity of pain are lacking. VITamin D and OmegA-3 triaL-Pain (VITAL-Pain) is an ancillary study to the VITAL trial, a large randomized, double-blind, placebo-controlled trial of vitamin D (2000 IU/day) and omega-3 supplementation (1 g/day) over 5.

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Introduction: Cervical radicular pain is pain perceived in the upper limb, caused by irritation or compression of a cervical spine nerve, the roots of the nerve, or both.

Methods: The literature on the diagnosis and treatment of cervical radicular pain was retrieved and summarized.

Results: The diagnosis is made by combining elements from the patient's history, physical examination, and supplementary tests.

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The year 2022 marked the 30th anniversary of the first Accreditation Council for Graduate Medical Education (ACGME) accreditation of pain medicine training programs. Before this, the education of pain medicine practitioners was through primarily an apprenticeship model. Since accreditation, pain medicine education has grown under the national leadership of pain medicine physicians and educational experts from the ACGME, exemplified by the release of Pain Milestones 2.

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Background: Restorative neurostimulation is a rehabilitative treatment for patients with refractory chronic low back pain (CLBP) associated with dysfunction of the lumbar multifidus muscle resulting in impaired neuromuscular control. The ReActiv8-B randomized, sham-controlled trial provided evidence of the effectiveness and safety of an implanted, restorative neurostimulator. The two-year analysis previously published in this journal demonstrated accrual of clinical benefits and long-term durability.

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  • Chronic low back pain (CLBP) is often linked to issues with the multifidus muscle, and a new neurostimulator system (ReActiv8) has shown promise in treating this condition by inducing muscle contractions.
  • The study followed 204 patients over two years, measuring pain, disability, quality of life, and opioid use, showing significant improvements in these areas.
  • After two years, 76% of participants experienced substantial relief in pain and disability, suggesting the neurostimulator's long-term effectiveness for CLBP.
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Chronic low back pain can be caused by impaired control and degeneration of the multifidus muscles and consequent functional instability of the lumbar spine. Available treatment options have limited effectiveness and prognosis is unfavorable. We conducted an international randomized, double-blind, sham-controlled trial at 26 multidisciplinary centers to determine safety and efficacy of an implantable, restorative neurostimulator designed to restore multifidus neuromuscular control and facilitate relief of symptoms (clinicaltrials.

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  • The ReActiv8-A clinical trial aimed to assess the long-term benefits of stimulating the lumbar multifidus muscle for patients with chronic low back pain who have not found relief through other treatments.
  • Conducted across nine sites in the UK, Belgium, and Australia, the trial involved patients who had disabling low back pain and were followed for four years, measuring various pain and disability scores.
  • Results showed significant improvements in pain and disability levels over the follow-up period, with a notable percentage of participants reporting meaningful positive changes in their quality of life and high satisfaction with the treatment.
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Background: For most procedures, there is insufficient evidence to guide clinicians in the optimal timing of advanced analgesic methods, which should be based on the expected time course of acute postoperative pain severity and aimed at time points where basic analgesia has proven insufficient.

Methods: We conducted a systematic search of the literature of analgesic trials for total hip arthroplasty (THA), extracting and pooling pain scores across studies, weighted for study size. Patients were grouped according to basic anaesthetic method used (general, spinal), and adjuvant analgesic interventions such as nerve blocks, local infiltration analgesia, and multimodal analgesia.

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Randomized clinical trials have demonstrated the efficacy of opioid analgesics for the treatment of acute and chronic pain conditions, and for some patients, these medications may be the only effective treatment available. Unfortunately, opioid analgesics are also associated with major risks (eg, opioid use disorder) and adverse outcomes (eg, respiratory depression and falls). The risks and adverse outcomes associated with opioid analgesics have prompted efforts to reduce their use in the treatment of both acute and chronic pain.

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  • This Practice Advisory offers evidence-based recommendations for using contrast media in interventional pain procedures, created by an international panel of experts from various organizations.
  • It highlights significant risks associated with gadolinium-based contrast agents, including nephrogenic systemic fibrosis and potential brain and neurological issues.
  • The advisory also outlines specific guidance for choosing contrast agents for patients with renal problems, those who've had multiple MRIs, and those with varying levels of hypersensitivity reactions to contrast media.
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In 2018, the American Board of Anesthesiology (ABA) became the first US medical specialty certifying board to incorporate an Objective Structured Clinical Examination (OSCE) into its initial certification examination system. Previously, the ABA's staged examination system consisted of 2 written examinations (the BASIC and ADVANCED examinations) and the Standardized Oral Examination (SOE). The OSCE and the existing SOE are now 2 separate components of the APPLIED Examination.

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