13 results on '"Benjamin L. Walter"'
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2. MRI-based multivariate gray matter volumetric distance for predicting motor symptom progression in Parkinson's disease
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Anupa A. Vijayakumari, Hubert H. Fernandez, and Benjamin L. Walter
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Medicine ,Science - Abstract
Abstract While Parkinson's disease (PD)-related neurodegeneration is associated with structural changes in the brain, conventional magnetic resonance imaging (MRI) has proven less effective for clinical diagnosis due to its inability to reliably identify subtle changes early in the disease course. In this study, we aimed to develop a structural MRI-based biomarker to predict the rate of progression of motor symptoms in the early stages of PD. The study included 88 patients with PD and 120 healthy controls from the Parkinson's Progression Markers Initiative database; MRI at baseline and motor symptom scores assessed using the MDS-UPDRS-III at two time points (baseline and 48 months) were selected. Group-level volumetric analyses at baseline were not associated with the decline in motor functioning. Then, we developed a patient-specific multivariate gray matter volumetric distance and demonstrated that it could significantly predict changes in motor symptom scores (P
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- 2023
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3. Standardizing default electronic health record tools to improve safety for hospitalized patients with Parkinson’s disease
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Allan D. Wu, Benjamin L. Walter, Anne Brooks, Emily Buetow, Katherine Amodeo, Irene Richard, Kelly Mundth, and Hooman Azmi
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electronic health record ,Parkinson’s disease ,hospitalization ,safety ,Epic Systems ,Neurosciences. Biological psychiatry. Neuropsychiatry ,RC321-571 - Abstract
Electronic Health Record (EHR) systems are often configured to address challenges and improve patient safety for persons with Parkinson’s disease (PWP). For example, EHR systems can help identify Parkinson’s disease (PD) patients across the hospital by flagging a patient’s diagnosis in their chart, preventing errors in medication and dosing through the use of clinical decision support, and supplementing staff education through care plans that provide step-by-step road maps for disease-based care of a specific patient population. However, most EHR-based solutions are locally developed and, thus, difficult to scale widely or apply uniformly across hospital systems. In 2020, the Parkinson’s Foundation, a national and international leader in PD research, education, and advocacy, and Epic, a leading EHR vendor with more than 35% market share in the United States, launched a partnership to reduce risks to hospitalized PWP using standardized EHR-based solutions. This article discusses that project which included leadership from physician informaticists, movement disorders specialists, hospital quality officers, the Parkinson’s Foundation and members of the Parkinson’s community. We describe the best practice solutions developed through this project. We highlight those that are currently available as standard defaults or options within the Epic EHR, discuss the successes and limitations of these solutions, and consider opportunities for scalability in environments beyond a single EHR vendor. The Parkinson’s Foundation and Epic launched a partnership to develop best practice solutions in the Epic EHR system to improve safety for PWP in the hospital. The goal of the partnership was to create the EHR tools that will have the greatest impact on outcomes for hospitalized PWP.
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- 2024
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4. Optimization of inpatient medication administration among persons with Parkinson’s disease: recommendations on pharmacy technology and workflow
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Jeryl Ritzi T. Yu, Brent S. Sokola, and Benjamin L. Walter
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Parkinson’s disease ,inpatient ,medication administration ,pharmacy ,recommendations ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Individuals with Parkinson’s disease (PD) are vulnerable during hospitalizations due to the underlying complexities o1f symptoms, and acute illness or medication changes often lead to decompensation. Complications during hospitalizations are often due to worsening motor and nonmotor symptoms and commonly result from inaccurate medication regimens. Although the accuracy of medication administration relies on an interplay of factors, including patient status, transitions of care, coordination between the hospital prescriber and outpatient neurologist, etc., hospital pharmacists play an integral role in pharmacotherapy. The main aspects of pharmacy strategies aim to achieve timely administration of levodopa-containing medications, reduction of substitution and omissions of antiparkinsonian medications, and avoidance of antidopaminergic medications. This paper highlights critical areas for improvement and recommendations to minimize the impact of other factors from the pharmacy standpoint.
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- 2023
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5. End of life care of hospitalized patients with Parkinson disease: a retrospective analysis and brief review
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Sakhi Bhansali, Ekhlas Assaedi, Jeryl Ritzi T. Yu, Nymisha Mandava, Claire Sonneborn, Olivia Hogue, Benjamin L. Walter, Renato V. Samala, and Adam Margolius
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parkinsonism ,Parkinson disease ,palliative care ,antipsychotic ,hospice ,DNR ,Neurosciences. Biological psychiatry. Neuropsychiatry ,RC321-571 - Abstract
BackgroundTowards the end of life (EOL), persons with parkinsonism (PwP) have complex needs and can present with unique palliative care (PC) challenges. There are no widely accepted guidelines to aid neurologists, hospitalists, or PC clinicians in managing the symptoms of PwP at EOL. We examined a population of PwP at EOL, aiming to describe trends of in-hospital management and utilization of PC services.MethodsAll PwP admitted to two hospitals during 2018 (N = 727) were examined retrospectively, assessing those who died in hospital or were discharged with hospice (EOL group, N = 35) and comparing them to the main cohort. Their demographics, clinical data, engagement of multidisciplinary and palliative services, code status changes, invasive care, frequency of admissions, and medication administration were assessed.ResultsAmong the EOL group, 8 expired in hospital, and 27 were discharged to hospice. Forty-six percent of EOL patients received a PC consultation during their admission. The median interval from admission to death was 37 days. Seventy-seven percent had a full code status on admission. Compared to hospice patients, those who expired in hospital had higher rates of invasive procedures and intensive care unit transfers (41% vs. 75%, in both variables), and lower rates of PC involvement (52% vs. 25%). The transition of code status change for the EOL group from Full code to Do Not Resuscitate (DNR) occurred at a median 4–5 days from admission. For patients that passed in the hospital, the median days from transition of code status to death was 0(IQR 0–1). Levodopa dose deviations were frequent in both EOL and non-EOL group, but contraindicated medications were infrequently administered (11% in EOL group vs. 9% in non-EOL group).ConclusionOur data suggest a low utilization of PC services and delayed discussions of goals of care. More work is needed to raise awareness of inpatient teams managing PwP regarding the unique but common challenges facing PwP with advanced disease. A brief narrative review summarizing the suggested management of symptoms common to hospitalized PwP near EOL is provided.
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- 2023
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6. The Parkinson’s disease waiting room of the future: measurements, not magazines
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Jay L. Alberts, Umar Shuaib, Hubert Fernandez, Benjamin L. Walter, David Schindler, Mandy Miller Koop, and Anson B. Rosenfeldt
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Parkinson’s disease ,technology enablement ,technology integration ,healthcare transformation ,clinical integration ,Neurology. Diseases of the nervous system ,RC346-429 - Abstract
Utilizing technology to precisely quantify Parkinson’s disease motor symptoms has evolved over the past 50 years from single point in time assessments using traditional biomechanical approaches to continuous monitoring of performance with wearables. Despite advances in the precision, usability, availability and affordability of technology, the “gold standard” for assessing Parkinson’s motor symptoms continues to be a subjective clinical assessment as none of these technologies have been fully integrated into routine clinical care of Parkinson’s disease patients. To facilitate the integration of technology into routine clinical care, the Develop with Clinical Intent (DCI) model was created. The DCI model takes a unique approach to the development and integration of technology into clinical practice by focusing on the clinical problem to be solved by technology rather than focusing on the technology and then contemplating how it could be integrated into clinical care. The DCI model was successfully used to develop the Parkinson’s disease Waiting Room of the Future (WROTF) within the Center for Neurological Restoration at the Cleveland Clinic. Within the WROTF, Parkinson’s disease patients complete the self-directed PD-Optimize application on an iPad. The PD-Optimize platform contains cognitive and motor assessments to quantify PD symptoms that are difficult and time-consuming to evaluate clinically. PD-Optimize is completed by the patient prior to their medical appointment and the results are immediately integrated into the electronic health record for discussion with the movement disorder neurologist. Insights from the clinical use of PD-Optimize has spurred the development of a virtual reality technology to evaluate instrumental activities of daily living in PD patients. This new technology will undergo rigorous assessment and validation as dictated by the DCI model. The DCI model is intended to serve as a health enablement roadmap to formalize and accelerate the process of bringing the advantages of cutting-edge technology to those who could benefit the most: the patient.
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- 2023
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7. Author Correction: MRI-based multivariate gray matter volumetric distance for predicting motor symptom progression in Parkinson's disease
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Anupa A. Vijayakumari, Hubert H. Fernandez, and Benjamin L. Walter
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Medicine ,Science - Published
- 2023
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8. Digitizing a Therapeutic: Development of an Augmented Reality Dual-Task Training Platform for Parkinson’s Disease
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Jay L. Alberts, Ryan D. Kaya, Kathryn Scelina, Logan Scelina, Eric M. Zimmerman, Benjamin L. Walter, and Anson B. Rosenfeldt
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Parkinson’s disease (PD) ,dual-task ,augmented reality ,gait ,postural instability ,Chemical technology ,TP1-1185 - Abstract
Augmented reality (AR) may be a useful tool for the delivery of dual-task training. This manuscript details the development of the Dual-task Augmented Reality Treatment (DART) platform for individuals with Parkinson’s disease (PD) and reports initial feasibility, usability, and efficacy of the DART platform in provoking dual-task interference in individuals with PD. The DART platform utilizes the head-mounted Microsoft HoloLens2 AR device to deliver concurrent motor and cognitive tasks. Biomechanical metrics of gait and cognitive responses are automatically computed and provided to the supervising clinician. To assess feasibility, individuals with PD (N = 48) completed a bout of single-task and dual-task walking using the DART platform. Usability was assessed by the System Usability Scale (SUS). Dual-task interference was assessed by comparing single-task walking and walking during an obstacle course while performing a cognitive task. Average gait velocity decreased from 1.06 to 0.82 m/s from single- to dual-task conditions. Mean SUS scores were 81.3 (11.3), which placed the DART in the “good” to “excellent” category. To our knowledge, the DART platform is the first to use a head-mounted AR system to deliver a dual-task paradigm and simultaneously provide biomechanical data that characterize cognitive and motor performance. Individuals with PD were able to successfully use the DART platform with satisfaction, and dual-task interference was provoked. The DART platform should be investigated as a platform to treat dual-task declines associated with PD.
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- 2022
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9. Interim Safety Profile From the Feasibility Study of the BrainGate Neural Interface System
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Daniel B. Rubin, A. Bolu Ajiboye, Laurie Barefoot, Marguerite Bowker, Sydney S. Cash, David Chen, John P. Donoghue, Emad N. Eskandar, Gerhard Friehs, Carol Grant, Jaimie M. Henderson, Robert F. Kirsch, Rose Marujo, Maryam Masood, Stephen T. Mernoff, Jonathan P. Miller, Jon A. Mukand, Richard D. Penn, Jeremy Shefner, Krishna V. Shenoy, John D. Simeral, Jennifer A. Sweet, Benjamin L. Walter, Ziv M. Williams, and Leigh R. Hochberg
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Neurology (clinical) - Abstract
Background and ObjectivesBrain-computer interfaces (BCIs) are being developed to restore mobility, communication, and functional independence to people with paralysis. Though supported by decades of preclinical data, the safety of chronically implanted microelectrode array BCIs in humans is unknown. We report safety results from the prospective, open-label, nonrandomized BrainGate feasibility study (NCT00912041), the largest and longest-running clinical trial of an implanted BCI.MethodsAdults aged 18–75 years with quadriparesis from spinal cord injury, brainstem stroke, or motor neuron disease were enrolled through 7 clinical sites in the United States. Participants underwent surgical implantation of 1 or 2 microelectrode arrays in the motor cortex of the dominant cerebral hemisphere. The primary safety outcome was device-related serious adverse events (SAEs) requiring device explantation or resulting in death or permanently increased disability during the 1-year postimplant evaluation period. The secondary outcomes included the type and frequency of other adverse events and the feasibility of the BrainGate system for controlling a computer or other assistive technologies.ResultsFrom 2004 to 2021, 14 adults enrolled in the BrainGate trial had devices surgically implanted. The average duration of device implantation was 872 days, yielding 12,203 days of safety experience. There were 68 device-related adverse events, including 6 device-related SAEs. The most common device-related adverse event was skin irritation around the percutaneous pedestal. There were no safety events that required device explantation, no unanticipated adverse device events, no intracranial infections, and no participant deaths or adverse events resulting in permanently increased disability related to the investigational device.DiscussionThe BrainGate Neural Interface system has a safety record comparable with other chronically implanted medical devices. Given rapid recent advances in this technology and continued performance gains, these data suggest a favorable risk/benefit ratio in appropriately selected individuals to support ongoing research and development.Trial Registration InformationClinicalTrials.gov Identifier:NCT00912041.Classification of EvidenceThis study provides Class IV evidence that the neurosurgically placed BrainGate Neural Interface system is associated with a low rate of SAEs defined as those requiring device explantation, resulting in death, or resulting in permanently increased disability during the 1-year postimplant period.
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- 2023
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10. Oral ENT-01 Targets Enteric Neurons to Treat Constipation in Parkinson Disease
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Michael Camilleri, Thyagarajan Subramanian, Fernando Pagan, Stuart Isaacson, Ramon Gil, Robert A. Hauser, Mary Feldman, Mark Goldstein, Rajeev Kumar, Daniel Truong, Nisha Chhabria, Benjamin L. Walter, Jonathan Eskenazi, Robert Riesenberg, Daniel Burdick, Winona Tse, Eric Molho, Bradley Robottom, Perminder Bhatia, Srinath Kadimi, Kevin Klos, David Shprecher, Otto Marquez-Mendoza, Gonzalo Hidalgo, Stephen Grill, George Li, Howard Mandell, Mary Hughes, Sharisse Stephenson, Joel Vandersluis, Michael Pfeffer, Andrew Duker, Vikram Shivkumar, William Kinney, James MacDougall, Michael Zasloff, and Denise Barbut
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Treatment Outcome ,Double-Blind Method ,Internal Medicine ,Humans ,Parkinson Disease ,Dementia ,General Medicine ,Defecation ,Constipation - Abstract
Parkinson disease (PD) is associated with α-synuclein (αS) aggregation within enteric neurons. ENT-01 inhibits the formation of αS aggregates and improved constipation in an open-label study in patients with PD.To evaluate the safety and efficacy of oral ENT-01 for constipation and neurologic symptoms in patients with PD and constipation.Randomized, placebo-controlled phase 2b study. (ClinicalTrials.gov: NCT03781791).Outpatient.150 patients with PD and constipation.ENT-01 or placebo daily for up to 25 days. After baseline assessment of constipation severity, daily dosing was escalated to the prokinetic dose, the maximum dose (250 mg), or the tolerability limit, followed by a washout period.The primary efficacy end point was the number of complete spontaneous bowel movements (CSBMs) per week. Neurologic end points included dementia (assessed using the Mini-Mental State Examination [MMSE]) and psychosis (assessed using the Scale for the Assessment of Positive Symptoms adapted for PD [SAPS-PD]).The weekly CSBM rate increased from 0.7 to 3.2 in the ENT-01 group versus 0.7 to 1.2 in the placebo group (Longer treatment periods need to be investigated in future studies.ENT-01 was safe and significantly improved constipation.Enterin, Inc.
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- 2022
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11. Directional Stimulation in Parkinson's Disease and Essential Tremor: The Cleveland Clinic Experience
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Binith Cheeran, Richard Rammo, Sarah J. Ozinga, Sean J. Nagel, Srivatsan Pallavaram, Andre G. Machado, Alexandra White, and Benjamin L. Walter
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Male ,medicine.medical_specialty ,Deep brain stimulation ,Parkinson's disease ,Deep Brain Stimulation ,Essential Tremor ,medicine.medical_treatment ,Thalamus ,Stimulation ,03 medical and health sciences ,0302 clinical medicine ,Physical medicine and rehabilitation ,Subthalamic Nucleus ,Humans ,Medicine ,Thalamic stimulator ,Retrospective Studies ,Essential tremor ,business.industry ,Parkinson Disease ,General Medicine ,medicine.disease ,Single segment ,Subthalamic nucleus ,Anesthesiology and Pain Medicine ,Neurology ,Neurology (clinical) ,business ,030217 neurology & neurosurgery - Abstract
OBJECTIVE To assess use of directional stimulation in Parkinson's disease and essential tremor patients programmed in routine clinical care. MATERIALS AND METHODS Patients with Parkinson's disease or essential tremor implanted at Cleveland Clinic with a directional deep brain stimulation (DBS) system from November 2017 to October 2019 were included in this retrospective case series. Omnidirectional was compared against directional stimulation using therapeutic current strength, therapeutic window percentage, and total electrical energy delivered as outcome variables. RESULTS Fifty-seven Parkinson's disease patients (36 males) were implanted in the subthalamic nucleus (105 leads) and 33 essential tremor patients (19 males) were implanted in the ventral intermediate nucleus of the thalamus (52 leads). Seventy-four percent of patients with subthalamic stimulation (65% of leads) and 79% of patients with thalamic stimulation (79% of leads) were programmed with directional stimulation for their stable settings. Forty-six percent of subthalamic leads and 69% of thalamic leads were programmed on single segment activation. There was no correlation between the length of microelectrode trajectory through the STN and use of directional stimulation. CONCLUSIONS Directional programming was more common than omnidirectional programming. Substantial gains in therapeutic current strength, therapeutic window, and total electrical energy were found in subthalamic and thalamic leads programmed on directional stimulation.
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- 2022
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12. Addressing critical care gaps in inpatient Parkinson's care - Minimizing the impact of comorbidities and developing new care delivery models
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Jeryl Ritzi T. Yu and Benjamin L. Walter
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Hospitalization ,Inpatients ,Neurology ,Critical Care ,Humans ,Parkinson Disease ,Neurology (clinical) ,Geriatrics and Gerontology ,Delivery of Health Care - Published
- 2022
13. Can MRI-based multivariate gray matter volumetric distance predict motor progression and classify slow versus fast progressors in Parkinson’s disease?
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Anupa A Vijayakumari, Hubert H Fernandez, and Benjamin L Walter
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IntroductionWhile Parkinson’s disease (PD) related neurodegeneration is associated with structural changes in the brain, magnetic resonance imaging (MRI) has not been helpful in diagnosing PD or predicting the progression of motor symptoms. In this study, we aimed to develop a structural MRI-based biomarker to predict the rate of progression of motor symptoms and to classify patients based on the symptom severity (i.e. slow vs. fast progressors) in the early stages of PD.MethodsThe study included 59 patients with PD (n=40 for the primary analysis, 19 for the validation analysis), and 55 healthy controls with structural MRI from the Parkinson’s Progression Markers Initiative (PPMI) database. We developed a patient-specific multivariate gray matter volumetric distance using Mahalanobis distance (MGMV) to investigate the changes in MGMVover time using longitudinal linear mixed-effect model, its potential as a biomarker to predict the rate of progression of motor function (MDS-UPDRS-part III) using multiple linear regression model, and classification of patients based on symptom severity using machine learning (ML).ResultsMGMVat BL significantly predicted changes in motor severity (pGMVover time (p = 0.09) were noted. We obtained 85% accuracy in discriminating patients according to their symptom severity, and on an independent test cohort, an accuracy of 90% was achieved.ConclusionsWe identified a promising structural MRI-based biomarker for predicting the rate of progression of motor symptoms and classification of patients based on motor symptom severity.
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- 2022
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