5 results match your criteria: "Los Angeles (KBW); UCLA Semel Institute for Neuroscience and Human Behavior[Affiliation]"
Background: The EXCELLENT registry aimed to evaluate the effectiveness of the EMBOTRAP Revascularization Device in an all-comer population in a real-world setting, with a focus on the composition of retrieved clots.
Methods: EXCELLENT is a prospective, global registry of patients with acute ischemic stroke treated with EMBOTRAP as the first-line mechanical thrombectomy device conducted at 34 sites (25 sites contributing clot) from September 2018 to March 2021, utilizing core imaging and central histology laboratories blinded to clinical data, independent 90-day modified Rankin Scale assessment and Clinical Events Committee.
Results: After screening 3799 patients, a total of 997 subjects (mean age, 70.
Antibiotics (Basel)
December 2021
Summa Health, Akron, OH 44304, USA.
Lefamulin was the first systemic pleuromutilin antibiotic approved for intravenous and oral use in adults with community-acquired bacterial pneumonia based on two phase 3 trials (Lefamulin Evaluation Against Pneumonia [LEAP]-1 and LEAP-2). This pooled analysis evaluated lefamulin efficacy and safety in adults with community-acquired bacterial pneumonia caused by atypical pathogens (, , and ). In LEAP-1, participants received intravenous lefamulin 150 mg every 12 h for 5-7 days or moxifloxacin 400 mg every 24 h for 7 days, with optional intravenous-to-oral switch.
View Article and Find Full Text PDFJ Glob Antimicrob Resist
June 2022
Nabriva Therapeutics US, Inc., Fort Washington, PA, USA.
Objectives: Lefamulin, a pleuromutilin antibiotic approved for community-acquired bacterial pneumonia (CABP), was evaluated for microbiological efficacy in a prespecified pooled analysis of LEAP 1 and 2 phase 3 clinical trial data in patients with CABP.
Methods: In LEAP 1, adults (PORT risk class III‒V) received intravenous (IV) lefamulin 150 mg every 12 h (q12h) for 5‒7 days or moxifloxacin 400 mg every 24 h (q24h) for 7 days, with optional IV-to-oral switch. In LEAP 2, adults (PORT II‒IV) received oral lefamulin 600 mg q12h for 5 days or moxifloxacin 400 mg q24h for 7 days.
J Am Board Fam Med
August 2019
From the VA Health Services Research and Development (HSR&D) Center for the Study of Healthcare Innovation, Implementation, & Policy, Greater Los Angeles VA Healthcare System, Los Angeles, CA (LBL, LVR, KBW); Division of General Internal Medicine and Health Services Research, University of California-Los Angeles (UCLA) David Geffen School of Medicine, Los Angeles (LBL, LVR, JJE); VA Health Economics Resource Center, VA Palo Alto Healthcare System, Menlo Park, CA (JY); Department of General Internal Medicine, University of California-San Francisco School of Medicine, San Francisco, CA (JY); RAND Corporation, Santa Monica, CA (LVR, KBW); UCLA School of Public Health, Los Angeles (LVR, KBW, CAS, JJE); VA Center for Clinical Management Research, Ann Arbor, MI (EPP, MEM); University of Michigan Medical School, Ann Arbor (EPP); UCLA Center for Health Services and Society, Los Angeles (KBW); UCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles (KBW, CAS).
Objective: Aiming to foster timely, high-quality mental health care for Veterans, VA's Primary Care-Mental Health Integration (PC-MHI) embeds mental health specialists in primary care and promotes care management for depression. PC-MHI and patient-centered medical home providers work together to provide the bulk of mental health care for primary care patients with low-to-moderate-complexity mental health conditions. This study examines whether increasing primary care clinic engagement in PC-MHI services is associated with changes in patient health care utilization and costs.
View Article and Find Full Text PDFJ Am Board Fam Med
November 2017
From the Veterans Administration Health Services Research and Development Center for the Study of Healthcare Innovation, Implementation and Policy, Veterans Administration Greater Los Angeles Healthcare System, Sepulveda, CA (CAL); the Departments of Medicine (CAL) and Psychiatry and Biobehavioral Sciences (TRB, KBW), David Geffen School of Medicine, University of California, Los Angeles, Los Angeles (CAL); RAND Corp., Santa Monica, CA (CS, KBW); the Center for Health Services and Society, University of California, Los Angeles, Los Angeles (LT, JM, KBW); the Departments of Biostatistics (TRB) and Health Policy and Management (KBW), Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, Los Angeles; Healthy African American Families II, Los Angeles, CA (PW); the Department of Research, Charles R. Drew University of Medicine and Science, Los Angeles, CA (PW); and the J.D. Pacada Foundation, Los Angeles, CA (AY-B).
Background: Disparities in depression care exist among the poor. Community Partners in Care (CPIC) compared a community coalition model with technical assistance to improve depression services in under-resourced communities. We examine effects on health, social, and utilization outcomes among the poor and, non-poor depressed, and poor subgroups.
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