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1.
J Stroke Cerebrovasc Dis ; 30(9): 105951, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34298426

RESUMEN

OBJECTIVE: We aim to report the incidence and clinical characteristics of patients who were found to have diffusion restricting lesions of the corpus callosum (CC) on Diffusion-weighted imaging (DWI) on magnetic resonance imaging (MRI) following intracranial hemorrhage (ICH). DESIGN/METHODS: A retrospective cross-sectional analysis was performed of medical records of all adult patients admitted to a single tertiary center with a primary diagnosis of ICH and received nicardipine infusion over a 2-year period. Patients without MRI brain available or patients who underwent digital subtraction angiography (DSA) prior to MRI were excluded. ICH and intraventricular hemorrhage (IVH) volumes and scores were calculated. MRI brain scans were evaluated for presence and locations of DWI lesions. RESULTS: Among 162 patients who met inclusion criteria, 6 patients (4%, median age 53, range 37-71, 100% male, 33% white) were found to have DWI lesions in the CC with a median ICH volume of 17ml (range 1-105ml). The ICH locations were lobar (n=3), deep (n=2) and cerebellum (n=1). All patients (100%) had intraventricular hemorrhage (IVH) with median IVH volume of 25ml (range 2.7-55ml). Four patients were on levetiracetam. No identifiable infections or metabolic abnormalities were found among these patients. All but one patient had normal DSA. Follow up MRI was only available in one patient and showed no reversibility at 14 days. CONCLUSION: Although rare, diffusion restricting corpus callosum lesions can be seen in patients with ICH, especially in patients with IVH. The etiology and clinical significance of these lesions remains unknown and warrant further research.


Asunto(s)
Circulación Cerebrovascular , Cuerpo Calloso/irrigación sanguínea , Cuerpo Calloso/diagnóstico por imagen , Imagen de Difusión por Resonancia Magnética , Hemorragias Intracraneales/diagnóstico por imagen , Imagen de Perfusión , Adulto , Anciano , Angiografía de Substracción Digital , Hemorragia Cerebral Intraventricular/diagnóstico por imagen , Hemorragia Cerebral Intraventricular/epidemiología , Hemorragia Cerebral Intraventricular/fisiopatología , Estudios Transversales , Femenino , Humanos , Incidencia , Hemorragias Intracraneales/epidemiología , Hemorragias Intracraneales/fisiopatología , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Pronóstico , Estudios Retrospectivos
2.
Am J Health Syst Pharm ; 74(18): 1486-1493, 2017 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-28887350

RESUMEN

PURPOSE: The Cleveland Clinic experience with care paths, including their creation and implementation, challenges overcome during development and testing, and outcomes of selected care path evaluations, is described. SUMMARY: Care paths are tools to assist healthcare professionals in practicing evidence-based medicine. The Cleveland Clinic health system has implemented or is developing approximately 100 care paths, including care paths designed to optimize management of sepsis and septic shock and to promote timely use of i.v. tissue plasminogen activator and correct dosing of antithrombotics and statins in patients with stroke. Key steps in successful care path initiatives include (1) identifying key stakeholders, (2) achieving stakeholder consensus on a standardized approach to disease or condition management, (3) cultivating provider awareness of care paths, (4) incorporating care path tools into the electronic health record and workflow processes, and (5) securing the resources to develop, implement, and maintain care paths. Electronic health records facilitate the use of and adherence to care paths. After care path implementation, revisions are typically needed due to unexpected issues not initially identified and to optimize care path features and support resources for clinical practice. Ongoing evaluation is required to determine whether an implemented care path is producing the intended patient and quality performance outcomes. CONCLUSION: Care paths provide a standardized approach to treatment or prevention of a disease or condition, reducing unnecessary variability and expense while promoting optimal, cost-effective patient care.


Asunto(s)
Atención a la Salud/normas , Medicina Basada en la Evidencia/normas , Desarrollo de Programa/normas , Evaluación de Programas y Proyectos de Salud/normas , Mejoramiento de la Calidad/normas , Cuidados Críticos/métodos , Cuidados Críticos/normas , Atención a la Salud/métodos , Prestación Integrada de Atención de Salud/métodos , Prestación Integrada de Atención de Salud/normas , Medicina Basada en la Evidencia/métodos , Humanos , Grupo de Atención al Paciente/normas , Desarrollo de Programa/métodos , Evaluación de Programas y Proyectos de Salud/métodos , Sepsis/terapia
3.
Case Rep Neurol Med ; 2017: 9131579, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28182114

RESUMEN

Introduction. Status epilepticus is associated with neuronal breakdown. Radiological sequelae of status epilepticus include diffusion weighted abnormalities and T2/FLAIR cortical hyperintensities corresponding to the epileptogenic cortex. However, progressive generalized cerebral atrophy from status epilepticus is underrecognized and may be related to neuronal death. We present here a case of diffuse cerebral atrophy that developed during the course of super refractory status epilepticus management despite prolonged barbiturate coma. Methods. Case report and review of the literature. Case. A 19-year-old male with a prior history of epilepsy presented with focal clonic seizures. His seizures were refractory to multiple anticonvulsants and eventually required pentobarbital coma for 62 days and midazolam coma for 33 days. Serial brain magnetic resonance imaging (MRI) showed development of cerebral atrophy at 31 days after admission to our facility and progression of the atrophy at 136 days after admission. Conclusion. This case highlights the development and progression of generalized cerebral atrophy in super refractory status epilepticus. The cerebral atrophy was noticeable at 31 days after admission at our facility which emphasizes the urgency of definitive treatment in patients who present with super refractory status epilepticus. Further research into direct effects of therapeutic coma is warranted.

4.
Pharmacotherapy ; 36(11): 1138-1144, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-27726155

RESUMEN

STUDY OBJECTIVE: It is unknown if ß-lactam monotherapy is sufficient for complicated intra-abdominal infections or if broader coverage is required, such as with vancomycin. This study sought to determine the clinical outcomes of piperacillin/tazobactam (PIP/TAZ) monotherapy compared to combination therapy with vancomycin and PIP/TAZ for complicated intra-abdominal infections among patients within a surgical intensive care unit (ICU). DESIGN: Retrospective cohort study. SETTING: Three surgical ICUs at a tertiary academic medical center. PATIENTS: Four hundred seventeen patients with a secondary peritonitis identified by International Classification of Diseases, Ninth Revision codes who received either PIP/TAZ monotherapy (228 patients) or PIP/TAZ and vancomycin combination therapy (189 patients). MEASUREMENTS AND MAIN RESULTS: The primary outcome was day 28 clinical cure; secondary outcomes included day 7 clinical cure, length of stay (LOS), and mortality. There were no statistically significant differences between the monotherapy and combination therapy groups with respect to day 28 clinical cure (33.9% vs 25.5%, p=0.064), day 7 clinical cure (23.6% vs 17.6%, p=0.14), or 28-day mortality (7% vs 7.9%, p=0.72). LOS in the ICU was significantly shorter in the monotherapy group (6 days) compared with the combination therapy group (7 days; p=0.04); however, hospital LOS was not significantly different. CONCLUSIONS: No difference was observed in clinical cure rates at day 28 or day 7 between those who received PIP/TAZ monotherapy compared to PIP/TAZ and vancomycin combination therapy.


Asunto(s)
Antibacterianos/administración & dosificación , Infecciones Intraabdominales/tratamiento farmacológico , Ácido Penicilánico/análogos & derivados , Vancomicina/administración & dosificación , Centros Médicos Académicos , Anciano , Estudios de Cohortes , Quimioterapia Combinada , Femenino , Humanos , Unidades de Cuidados Intensivos , Infecciones Intraabdominales/mortalidad , Tiempo de Internación , Masculino , Persona de Mediana Edad , Ácido Penicilánico/administración & dosificación , Piperacilina/administración & dosificación , Combinación Piperacilina y Tazobactam , Estudios Retrospectivos , Factores de Tiempo , Resultado del Tratamiento
5.
Neurocrit Care ; 24(3): 413-9, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-26545367

RESUMEN

BACKGROUND: Activated prothrombin complex concentrates factor eight inhibitor bypassing activity (FEIBA) has been recommended for reversing novel oral anticoagulants (NOAC) in the context of intracerebral hemorrhage (ICH), though few clinical studies report its use. METHODS: A prospective study of patients with spontaneous ICH was conducted from May 2013 to May 2015. Hospital complications including hemorrhage (gastrointestinal bleeding, anemia requiring transfusion, and surgical site bleeding) and thrombosis (pulmonary embolus, deep vein thrombosis, ischemic stroke, and myocardial infarction) were recorded. All ICH patients underwent baseline head CT and a follow-up stability scan in 6 h. NOAC taken within 48 h of presentation was reversed with FEIBA (50 u/kg) per protocol. Three-month outcomes were assessed using the modified rankin score (mRS). RESULTS: Of 127 ICH patients enrolled, 6 (5 %) had NOAC-related ICH including: oral factor XA inhibitor N = 5 (4 %; N = 4 rivaroxaban, N = 1 apixaban] and direct thrombin inhibitor N = 1 (0.8 %; dabigatran). The indication for NOAC was atrial fibrillation in all patients and the median CHADS2-VASC score was 4 (range 2-5). The median admission NIHSS was 2 (range 0-14) and the median ICH volume was 8 mL (range 1-20). Five patients (3 rivaroxaban, 1 apixaban, 1 dabigatran) presented within 48 h and received FEIBA within a median of 13 h (range 10-29 h) from their last NOAC dose and 8 h (range 4.5-20) from the time last known well. None of the patients had ICH expansion, hemorrhagic, or thrombotic complications. Three-month median mRS was 1 (range 0-6). CONCLUSION: In this small case series, reversal of NOAC with FEIBA was not associated with ICH expansion or any thrombotic or hemorrhagic complications.


Asunto(s)
Antitrombinas/efectos adversos , Factores de Coagulación Sanguínea/farmacología , Hemorragia Cerebral/inducido químicamente , Hemorragia Cerebral/tratamiento farmacológico , Coagulantes/farmacología , Inhibidores del Factor Xa/efectos adversos , Evaluación de Resultado en la Atención de Salud , Anciano , Anciano de 80 o más Años , Factores de Coagulación Sanguínea/administración & dosificación , Hemorragia Cerebral/diagnóstico por imagen , Coagulantes/administración & dosificación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Evaluación de Resultado en la Atención de Salud/métodos , Estudios Retrospectivos
7.
Handb Clin Neurol ; 120: 675-82, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24365346

RESUMEN

Neurologic complications are common side-effects of immunosuppressive medications used in the prevention of graft rejection after organ transplantation. The medications most commonly encountered include the calcineurin inhibitors and mycophenolate mofetil. Depression is the most commonly encountered neurotoxicity; however, severe but rare adverse neurological effects related to these therapies have been reported. Interferons, ribavirin, and protease inhibitors are therapeutic options commonly encountered in the treatment of hepatitis. Nucleoside analogs such as adefovir dipivoxil and entecavir carry significant risks for the development of lactic acidosis and hepatic dysfunction; however, most common adverse effects to these therapies in general are mild. While the mechanisms of action are poorly elucidated, they are discussed along with treatment strategies.


Asunto(s)
Inmunosupresores/efectos adversos , Síndromes de Neurotoxicidad/etiología , Hepatitis/tratamiento farmacológico , Hepatitis/cirugía , Humanos , Trasplante de Hígado/métodos
9.
J Crit Care ; 25(2): 362.e7-362.e11, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19926252

RESUMEN

PURPOSE: There are little data regarding the discontinuation of vasoactive medications in patients recovering from septic shock. We designed this retrospective cohort study to evaluate the incidence of hypotension based on the order of removal of norepinephrine (NE) and vasopressin (AVP) in patients receiving concomitant NE and AVP infusions for the treatment of septic shock. MATERIALS AND METHODS: Consecutive patients receiving concomitant NE and AVP infusions for septic shock admitted to the intensive care units of a tertiary care academic medical center were evaluated. RESULTS: Of 50 included patients, the first vasoactive medication discontinued was NE in 32 patients and AVP in 18 patients. The groups had similar Acute Physiology and Chronic Health Evaluation II and Sequential Organ Failure Assessment scores at shock onset and at the time of discontinuation of the first agent. Five patients who had NE discontinued first (16%) versus 10 patients who had AVP discontinued first (56%) developed hypotension within 24 hours (unadjusted relative risk, 3.6; 95% confidence interval, 1.5-4.5; P = .008). In a multivariate analysis, only discontinuation of AVP first was independently associated with hypotension (adjusted relative risk, 5.9; 95% confidence interval, 1.7-21.0; P = .006). CONCLUSIONS: Discontinuation of AVP before NE may lead to a higher incidence of hypotension in patients recovering from septic shock receiving concomitant AVP and NE.


Asunto(s)
Hipotensión/prevención & control , Norepinefrina/administración & dosificación , Choque Séptico/tratamiento farmacológico , Vasopresinas/administración & dosificación , APACHE , Estudios de Cohortes , Esquema de Medicación , Quimioterapia Combinada , Femenino , Humanos , Hipotensión/epidemiología , Hipotensión/etiología , Incidencia , Masculino , Persona de Mediana Edad , Análisis Multivariante , Estudios Retrospectivos , Choque Séptico/complicaciones , Resultado del Tratamiento
10.
IEEE Comput Graph Appl ; 30(6): 16-28, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-24807895

RESUMEN

This article presents a visualization-assisted process that verifies scientific-simulation codes. Code verification is necessary because scientists require accurate predictions to interpret data confidently. This verification process integrates iterative hypothesis verification with comparative, feature, and quantitative visualization. Following this process can help identify differences in cosmological and oceanographic simulations.

11.
Surg Neurol ; 71(3): 311-7, discussion 317-8, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18423529

RESUMEN

BACKGROUND AND PURPOSE: Aneurysmal SAH is often followed by delayed ischemic deficits attributable to cerebral vasospasm. Recent studies suggest a positive impact of statin therapy on the incidence of vasospasm. This study was designed to assess whether a history of prior use of statin therapy was associated with a lower risk of vasospasm in patients with SAH. METHODS: We performed a comprehensive retrospective review of patients with aneurysmal SAH between 1997 and 2004. Clinical demographics and imaging data for all patients were reviewed, and a logistic regression analysis was performed to identify the predictors of cerebral vasospasm, defined as a combination of clinical signs with radiographic confirmation. RESULTS: Three hundred eight patients were included. Mean age was higher in the group receiving statins (64 +/- 12 vs 54 +/- 12 years). Hunt and Hess scores and treatment modality were not significantly different between the groups. Vasospasm was observed in 31% of patients not taking a statin (n = 282) vs 23% taking a statin (n = 26), without achieving statistical significance. Discontinuation of the statin did not affect risk of vasospasm. CONCLUSIONS: Use of a statin prior to an aneurysmal SAH trended to reduce the incidence of subsequent vasospasm, without achieving statistical significance.


Asunto(s)
Isquemia Encefálica/epidemiología , Inhibidores de Hidroximetilglutaril-CoA Reductasas/uso terapéutico , Hemorragia Subaracnoidea/epidemiología , Vasoespasmo Intracraneal/epidemiología , Adulto , Anciano , Isquemia Encefálica/prevención & control , Femenino , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Análisis Multivariante , Estudios Retrospectivos , Factores de Riesgo , Hemorragia Subaracnoidea/cirugía , Vasoespasmo Intracraneal/prevención & control
12.
Psychiatr Serv ; 58(11): 1486-8, 2007 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-17978262

RESUMEN

OBJECTIVE: This study examined whether inpatient psychiatric treatment and forensic treatment and incarceration were reduced among adolescents and young adults with severe and persistent mental illness after they received services in the Program of Assertive Community Treatment (PACT). METHODS: The pre-post evaluation compared length of inpatient treatment and forensic treatment or incarceration for the year before and after PACT enrollment. Participants (N=15) were their own controls. RESULTS: Annual psychiatric hospitalization fell from 66.2 days before enrollment to 8.7 days in the first year of PACT (p=.025, Cohen's d=.54). Similarly, combined days of inpatient psychiatric treatment and forensic treatment or incarceration fell from 104.1 in the year before enrollment to 24.1 days in the year after (p=.015, Cohen's d=.61). CONCLUSIONS: PACT services significantly reduced time in inpatient psychiatric treatment. These preliminary results may have implications for long-term treatment, service delivery, and cost of care for adolescents and young adults with severe and persistent mental illness.


Asunto(s)
Adolescente Hospitalizado/psicología , Trastornos Mentales/terapia , Evaluación de Programas y Proyectos de Salud , Índice de Severidad de la Enfermedad , Adolescente , Adolescente Hospitalizado/estadística & datos numéricos , Servicios Comunitarios de Salud Mental , Femenino , Medicina Legal , Humanos , Masculino , Wisconsin
13.
Crit Care Med ; 33(11): 2507-12, 2005 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-16276174

RESUMEN

OBJECTIVE: To determine the effect of a low-calorie parenteral nutrition (PN) regimen on the incidence and severity of hyperglycemia and insulin requirements. DESIGN: Prospective, randomized, clinical trial. SETTING: Urban, university-affiliated, level-I trauma center. PATIENTS: Consecutive surgical patients requiring PN. INTERVENTIONS: Patients were randomized to receive either a low-calorie PN formulation (20 nonprotein kilocalories per kg per day) or a standard PN formulation (30 nonprotein kilocalories per kg per day). Lipid-derived calories were standardized to 1000 kilocalories three times weekly for all patients; consequently, the number of calories varied only by the amount of carbohydrate administered. Protein requirements were individualized on the basis of estimated metabolic stress. Hyperglycemia was defined as a blood glucose level > or = 200 mg/dL. MEASUREMENTS AND MAIN RESULTS: Forty patients were evaluated (low-calorie PN, n = 20; standard PN, n = 20). Demographics of the two groups were similar. The incidence of hyperglycemic events was significantly lower in the low-calorie group (0% [0-0.5] vs. 33.1% [0-58.4]; p = .001]. Additionally, the severity of hyperglycemia was also lower in the low-calorie group (mean glucose area under the curve = 118 +/- 22 [mg x hr]/dL vs. 172 +/- 44 [mg x hr]/dL; p < .001). This resulted in lower average daily insulin requirements (0 [0-0] units vs. 10.9 [0-25.6] units; p < .001.). The only predictor of hyperglycemia was a dextrose administration rate >4 mg/kg/min. CONCLUSIONS: : Administration of a low-calorie PN formulation resulted in fewer and less-severe hyperglycemic events and lower insulin requirements. PN regimens should not exceed a dextrose administration rate of 4 mg/kg/min to avoid hyperglycemic events.


Asunto(s)
Ingestión de Energía , Hiperglucemia/etiología , Nutrición Parenteral/efectos adversos , Área Bajo la Curva , Femenino , Humanos , Hiperglucemia/clasificación , Hiperglucemia/tratamiento farmacológico , Hipoglucemiantes/uso terapéutico , Incidencia , Insulina/uso terapéutico , Masculino , Persona de Mediana Edad , Periodo Posoperatorio , Índice de Severidad de la Enfermedad , Centros Traumatológicos
14.
J Trauma ; 58(3): 646-51, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15761369

RESUMEN

BACKGROUND: Recombinant factor VII (rFVII) is an attractive agent to control refractory, coagulopathic bleeding in patients following major surgery. The purpose of this review is to evaluate the published experiences of rFVII in adult, nonhemophilic, surgical and trauma patients. METHODS: A computerized literature search was conducted to identify articles pertaining to rFVII use for refractory bleeding in adult, nonhemophilic, surgical patients. The selected articles were reviewed and the applicable data was analyzed. RESULTS: A total of 117 patients were found in 8 case series and 24 case reports. Overall, rFVII was effective in restoring hemostasis in 99/117 (85%) patients with 76/99 (77%) surviving to hospital discharge. In trauma patients, hemostasis was achieved in 20/26 (77%) patients and 17/20 (85%) survived. There were 5 (4%) thromboembolic events observed in the 117 cases and much disparity was noted with the initial dose. Severe acidosis affected the activity of rFVII. CONCLUSION: Recombinant factor VII is an effective therapeutic agent for achieving hemostasis in nonhemophilic surgical patients. Published clinical experiences, however, are limited to small case series and case reports.


Asunto(s)
Factor VII/uso terapéutico , Hemorragia/tratamiento farmacológico , Hemorragia/etiología , Heridas y Lesiones/complicaciones , Análisis Costo-Beneficio , Costos de los Medicamentos , Economía Farmacéutica , Transfusión de Eritrocitos , Factor VII/economía , Factor VII/farmacología , Hemorragia/mortalidad , Hemostasis , Humanos , Selección de Paciente , Seguridad , Análisis de Supervivencia , Resultado del Tratamiento
15.
Work ; 21(1): 57-68, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12897391

RESUMEN

This article explains central constructs and definitions underlying the Americans with Disabilities Act (ADA) and discusses their implications for persons with severe and persistent mental illness, as well as for rehabilitation counselors working with this population. Focus is placed upon Title I of the ADA, which prohibits discrimination in employment. The article provides a brief review of legislative history relevant to the integration of people with mental illness into public life. It proceeds with a discussion of definitions under Title I of the ADA. Considerations in applying the ADA to assist persons with severe and persistent mental illness in employment are addressed throughout and are discussed in detail in the final section of the article.


Asunto(s)
Empleo/legislación & jurisprudencia , Personas con Discapacidades Mentales/legislación & jurisprudencia , Personas con Discapacidades Mentales/rehabilitación , Rehabilitación Vocacional , Orientación Vocacional , Humanos , Estados Unidos
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