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1.
Clin Neuropharmacol ; 47(2): 37-43, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38478363

RESUMEN

OBJECTIVE: Refractory status epilepticus (RSE) treated with anesthetic agents can be associated with complications including respiratory depression and hypotension. Ketamine is an emerging RSE treatment, but optimal dosing and timing are unknown. We studied provider attitudes and practices regarding the use of ketamine for RSE. METHODS: A literature review informed the creation of the survey, developed by professionals in epilepsy, pharmacy, and neurocritical care. The survey was distributed to members of the Critical Care EEG Monitoring and Research Consortium, Neurocritical Care Society, American Academy of Neurology Synapse community, American Epilepsy Society, and the Canadian League Against Epilepsy. Descriptive statistics were calculated. RESULTS: There were 109 respondents. First-line agents for RSE were midazolam (53%), propofol (42%), pentobarbital (2%), and ketamine (1%). Reasons for ketamine use included failure of midazolam/propofol to control seizures (81%) or hypotension on another anesthetic (35%). Perceived contraindications included hypertension (37%), elevated intracranial pressure (24%), and heart failure (18%). Perceived benefits included decreased use of vasopressors (53%) and more rapid RSE control when used adjunctively (49%). Routine ketamine users often treated more than 10 RSE cases per year, worked as intensivists or at academic institutions. Of the respondents, 59% found ketamine useful for RSE and 94% were interested in learning more about its use. CONCLUSIONS: Although most participants found ketamine helpful for RSE, it is mainly used as a second-line agent adjunctively with midazolam or propofol. Perceived ketamine benefits included decreased need for hemodynamic support and more rapid seizure control when used in conjunction with other anesthetics. Perceived contraindications centered on cardiac and intracranial pressure concerns.


Asunto(s)
Epilepsia , Hipotensión , Ketamina , Propofol , Estado Epiléptico , Humanos , Midazolam/uso terapéutico , Ketamina/uso terapéutico , Propofol/uso terapéutico , Anticonvulsivantes/uso terapéutico , Canadá , Estado Epiléptico/tratamiento farmacológico , Convulsiones , Hipotensión/tratamiento farmacológico , Epilepsia/tratamiento farmacológico
2.
Cureus ; 15(5): e39129, 2023 May.
Artículo en Inglés | MEDLINE | ID: mdl-37332441

RESUMEN

This case report details a surgical complication with a delayed presentation in a 23-year-old male with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). MELAS is a rare entity that can complicate the routine medical and surgical management of patients. Without sufficient research and guidelines, decision-making for patients who require time-sensitive care may be difficult. This patient population may require special consideration and preventative measures to maximize safety in their surgical care. This case serves to highlight a surgical complication that MELAS patients may be susceptible to, as well as to detail possible means of prevention and protection.

3.
World Neurosurg ; 161: e289-e294, 2022 05.
Artículo en Inglés | MEDLINE | ID: mdl-35134583

RESUMEN

BACKGROUND: Recent publications on minimally invasive surgery (MIS) for hematoma evacuation have suggested survival benefits in select patients. Since 2015, our center has been performing an MIS technique using continuous irrigation with aspiration through an endoscope (stereotactic intracerebral underwater blood aspiration [SCUBA]). It is unknown how these patient outcomes compare with intracerebral hemorrhage (ICH) score predictions. Our aim is to determine if SCUBA patients had better 30-day mortality than predicted by their presenting ICH score. METHODS: Retrospective review of consecutively admitted patients who underwent SCUBA between December 2015 and March 2019. Operative criteria for MIS evacuation included supratentorial hematoma volume ≥15 mL, age >18, National Institutes of Health Stroke Scale score ≥6, and modified Rankin Scale (mRS) score ≤3. Demographic, radiographic, and clinical data were collected prospectively. The prespecified primary outcome was observed 30-day mortality of SCUBA patients compared with predicted mortality by ICH score on presentation. RESULTS: One-hundred and fifteen patients underwent SCUBA for hematoma evacuation. Initial mean ICH volume was 51.4 mL (standard deviation 33.9 mL), with a median National Institutes of Health Stroke Scale score of 17 and ICH score of 2. At 1 month, 12 of the 115 SCUBA patients had passed away (30-day mortality rate 10.4%). This was significantly lower than the predicted mortality of 35.1% when calculated using the presenting ICH score (χ2 (1, N = 115) = 9.5, P < 0.0001), equating to an absolute risk reduction of 24.7%. CONCLUSIONS: This study suggests that minimally invasive hematoma evacuation with the SCUBA technique for ICH may reduce predicted 30-day mortality, with a number needed to treat of 4 to prevent 1 mortality.


Asunto(s)
Trastornos Respiratorios , Accidente Cerebrovascular , Hemorragia Cerebral/cirugía , Hematoma , Humanos , Imagenología Tridimensional , Estados Unidos
4.
J Neuroeng Rehabil ; 18(1): 121, 2021 07 28.
Artículo en Inglés | MEDLINE | ID: mdl-34321036

RESUMEN

BACKGROUND: Neurorehabilitation engineering faces numerous challenges to translating new technologies, but it is unclear which of these challenges are most limiting. Our aim is to improve understanding of rehabilitation therapists' real-time decision-making processes on the use of rehabilitation technology (RT) in clinical treatment. METHODS: We used a phenomenological qualitative approach, in which three OTs and two PTs employed at a major, technology-encouraging rehabilitation hospital wrote vignettes from a written prompt describing their RT use decisions during treatment sessions with nine patients (4 with stroke, 2 traumatic brain injury, 1 spinal cord injury, 1 with multiple sclerosis). We then coded the vignettes using deductive qualitative analysis from 17 constructs derived from the RT literature and the Consolidated Framework for Implementation Research (CFIR). Data were synthesized using summative content analysis. RESULTS: Of the constructs recorded, the five most prominent are from CFIR determinants of: (i) relative advantage, (ii) personal attributes of the patients, (iii) clinician knowledge and beliefs of the device/intervention, (iv) complexity of the devices including time and setup, and (v) organizational readiness to implement. Therapists characterized candidate RT as having a relative disadvantage compared to conventional treatment due to lack of relevance to functional training. RT design also often failed to consider the multi-faceted personal attributes of the patients, including diagnoses, goals, and physical and cognitive limitations. Clinicians' comfort with RT was increased by their previous training but was decreased by the perceived complexity of RT. Finally, therapists have limited time to gather, setup, and use RT. CONCLUSIONS: Despite decades of design work aimed at creating clinically useful RT, many lack compatibility with clinical translation needs in inpatient neurologic rehabilitation. New RT continue to impede the immediacy, versatility, and functionality of hands-on therapy mediated treatment with simple everyday objects.


Asunto(s)
Actitud del Personal de Salud , Rehabilitación Neurológica , Toma de Decisiones Clínicas , Humanos , Investigación Cualitativa , Tecnología
5.
Pulm Circ ; 11(2): 20458940211019626, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34104425

RESUMEN

Eleven participants with COVID-19 acute respiratory distress syndrome requiring mechanical ventilation underwent pulmonary artery catheterization for clinical indications. Clinical interventions or events concurrent with hemodynamic were recorded. Increased cardiac index was associated with worse hypoxemia. Modulation of cardiac index may improve hypoxemia in patients with COVID-19 acute respiratory distress syndrome.

6.
World Neurosurg ; 148: e390-e395, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33422715

RESUMEN

OBJECTIVE: The impact of interhospital transfer (IHT) on outcomes of patients with intracerebral hemorrhage (ICH) has not been well studied. We seek to describe the protocolized IHT and systems of care approach of a New York City hospital system, where ICH patients undergoing minimally invasive surgery (MIS) are transferred to a dedicated ICH center. METHODS: We retrospectively reviewed 100 consecutively admitted patients with spontaneous ICH. We gathered information on demographics, variables related to IHT, clinical and radiographic characteristics, and details about the clinical course and outpatient follow-up. We grouped patients into 2 cohorts: those admitted through IHT and those directly admitted through the emergency department. Primary outcome was good functional outcome at 6 months, defined as modified Rankin Scale score 0-3. RESULTS: Of 100 patients, 89 underwent IHT and 11 were directly admitted. On multivariable analysis, there were no significant differences in 6-month functional outcome between the 2 cohorts. All transfers were managed by a system-wide transfer center and 24/7 hotline for neuroemergencies. An ICH-specific IHT protocol was followed, in which a neurointensivist provided recommendations for stabilizing patients for transfer. Average transfer time was 199.7 minutes and average distance travelled was 13.6 kilometers. CONCLUSIONS: In our hospital system, a centralized approach to ICH management and a dedicated ICH center increased access to specialist services, including MIS. Most patients undergoing MIS were transferred from outside hospitals, which highlights the need for additional studies and descriptions of experiences to further elucidate the impact of and best protocols for the IHT of ICH patients.


Asunto(s)
Hemorragia Cerebral/cirugía , Hospitales Urbanos/organización & administración , Procedimientos Neuroquirúrgicos , Transferencia de Pacientes , Anciano , Evaluación de la Discapacidad , Urgencias Médicas , Servicio de Urgencia en Hospital , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Procedimientos Quirúrgicos Mínimamente Invasivos , Ciudad de Nueva York , Admisión del Paciente , Grupo de Atención al Paciente , Estudios Retrospectivos , Técnicas Estereotáxicas , Triaje
7.
Stroke ; 51(9): e215-e218, 2020 09.
Artículo en Inglés | MEDLINE | ID: mdl-32639861

RESUMEN

BACKGROUND AND PURPOSE: Young patients with malignant cerebral edema have been shown to benefit from early decompressive hemicraniectomy. The impact of concomitant infection with coronavirus disease 2019 (COVID-19) and how this should weigh in on the decision for surgery is unclear. METHODS: We retrospectively reviewed all COVID-19-positive patients admitted to the neuroscience intensive care unit for malignant edema monitoring. Patients with >50% of middle cerebral artery involvement on computed tomography imaging were considered at risk for malignant edema. RESULTS: Seven patients were admitted for monitoring of whom 4 died. Cause of death was related to COVID-19 complications, and these were either seen both very early and several days into the intensive care unit course after the typical window of malignant cerebral swelling. Three cases underwent surgery, and 1 patient died postoperatively from cardiac failure. A good outcome was attained in the other 2 cases. CONCLUSIONS: COVID-19-positive patients with large hemispheric stroke can have a good outcome with decompressive hemicraniectomy. A positive test for COVID-19 should not be used in isolation to exclude patients from a potentially lifesaving procedure.


Asunto(s)
Isquemia Encefálica/complicaciones , Isquemia Encefálica/cirugía , Infecciones por Coronavirus/complicaciones , Craniectomía Descompresiva/métodos , Procedimientos Neuroquirúrgicos/métodos , Neumonía Viral/complicaciones , Accidente Cerebrovascular/complicaciones , Accidente Cerebrovascular/cirugía , Adulto , Edema Encefálico/complicaciones , Edema Encefálico/cirugía , Isquemia Encefálica/diagnóstico por imagen , COVID-19 , Causas de Muerte , Toma de Decisiones Clínicas , Cuidados Críticos , Craniectomía Descompresiva/efectos adversos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Monitoreo Fisiológico , Procedimientos Neuroquirúrgicos/efectos adversos , Pandemias , Estudios Retrospectivos , Accidente Cerebrovascular/diagnóstico por imagen , Tomografía Computarizada por Rayos X , Resultado del Tratamiento
9.
J Neurovirol ; 26(5): 797-799, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-32720233

RESUMEN

There is concern that the global burden of coronavirus disease of 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection might yield an increased occurrence of Guillain-Barré syndrome (GBS). It is currently unknown whether concomitant SARS-CoV-2 infection and GBS are pathophysiologically related, what biomarkers are useful for diagnosis, and what is the optimal treatment given the medical comorbidities, complications, and simultaneous infection. We report a patient who developed severe GBS following SARS-CoV-2 infection at the peak of the initial COVID-19 surge (April 2020) in New York City and discuss diagnostic and management issues and complications that may warrant special consideration in similar patients.


Asunto(s)
Betacoronavirus/patogenicidad , Infecciones por Coronavirus/complicaciones , Síndrome de Guillain-Barré/complicaciones , Hiponatremia/complicaciones , Neumonía Viral/complicaciones , Enfermedad Aguda , Anciano , Anticoagulantes/uso terapéutico , COVID-19 , Infecciones por Coronavirus/patología , Infecciones por Coronavirus/terapia , Infecciones por Coronavirus/virología , Progresión de la Enfermedad , Enoxaparina/uso terapéutico , Femenino , Síndrome de Guillain-Barré/patología , Síndrome de Guillain-Barré/terapia , Síndrome de Guillain-Barré/virología , Humanos , Hiponatremia/patología , Hiponatremia/terapia , Hiponatremia/virología , Ciudad de Nueva York , Pandemias , Plasmaféresis , Neumonía Viral/patología , Neumonía Viral/terapia , Neumonía Viral/virología , SARS-CoV-2
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