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1.
Cerebrovasc Dis ; 39(5-6): 269-77, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25871403

RESUMEN

BACKGROUND: An increasing number of stroke patients have to be supported by mechanical ventilation in intensive care units (ICU), with a relevant proportion of them requiring gradual withdrawal from a respirator. To date, weaning studies have focused merely on mixed patient groups, COPD patients or patients after cardiac surgery. Therefore, the best weaning strategy for stroke patients remains to be determined. METHODS: Here, we designed a prospective randomized controlled study comparing adaptive support ventilation (ASV), a continuous weaning strategy, with biphasic positive airway pressure (BIPAP) in combination with spontaneous breathing trials, a discontinuous technique, in the treatment of stroke patients. The primary endpoint was the duration of the weaning process. RESULTS: Only the 40 (out of 54) patients failing in an initial spontaneous breathing trial (T-piece test) were included into the study; the failure proportion is considerably larger compared to previous studies. Eligible patients were pseudo-randomly assigned to one of the two weaning groups. Both groups did not differ regarding age, gender, and severity of stroke. The results showed that the median weaning duration was 10.7 days (±SD 7.0) in the discontinuous weaning group, and 8 days (±SD 4.5) in the continuous weaning group (p < 0.05). CONCLUSIONS: To the best of our knowledge, this is the first clinical study to show that continuous weaning is significantly more effective compared to discontinuous weaning in mechanically ventilated stroke patients. We suppose that the reason for the superiority of continuous weaning using ASV as well as the bad performance of our patients in the 2 h T-piece test is caused by the patients' compliance. Compared to patients on surgical and medical ICUs, neurological patients more often suffer from reduced vigilance, lack of adverse-effects reflexes, dysphagia, and cerebral dysfunction. Therefore, stroke patients may profit from a more gradual withdrawal of weaning.


Asunto(s)
Respiración Artificial , Accidente Cerebrovascular/terapia , Desconexión del Ventilador , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Unidades de Cuidados Intensivos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Factores de Tiempo , Resultado del Tratamiento , Desconexión del Ventilador/métodos
2.
Eur J Neurol ; 20(8): 1218-21, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23163829

RESUMEN

BACKGROUND AND PURPOSE: Microembolic signals (MES) are detectable in the middle cerebral artery by transcranial ultrasound downstream to atherosclerotic lesions of the internal carotid artery (ICA) in patients with stroke or transient ischaemic attack. The occurrence of MES predicts future risk of stroke in patients with symptomatic and asymptomatic carotid stenosis. The detection of intra-plaque neo-vascularization by contrast-enhanced ultrasound (CEUS) in atherosclerotic plaques of the ICA is associated with future cardiovascular/cerebrovascular events. We investigated whether there is an association between both surrogate markers of future vascular events. METHODS: Forty-one patients with symptomatic atherosclerotic plaques underwent ipsilateral transcranial ultrasound MES detection for 30 min followed by a CEUS investigation of the plaque. The occurrence and number of MES was documented, and the degree of intra-plaque neo-vascularization was measured semi-quantitatively. RESULTS: During the 30 min investigation, 17 patients had MES and nine of them showed neo-vascularization of the atherosclerotic plaque. The remaining 24 patients did not have MES, and only in four patients of this group could plaque neo-vascularization be demonstrated (P = 0.020). CONCLUSIONS: We found an association between the occurrence of MES and the presence of neo-vascularization in patients with symptomatic atherosclerotic carotid plaque. Therefore, plaque neo-vascularization might also be a surrogate marker of future stroke risk.


Asunto(s)
Estenosis Carotídea/diagnóstico por imagen , Embolia Intracraneal/diagnóstico por imagen , Neovascularización Patológica/diagnóstico por imagen , Placa Aterosclerótica/diagnóstico por imagen , Anciano , Anciano de 80 o más Años , Arteria Carótida Interna/diagnóstico por imagen , Estenosis Carotídea/complicaciones , Femenino , Humanos , Embolia Intracraneal/complicaciones , Ataque Isquémico Transitorio/diagnóstico por imagen , Masculino , Persona de Mediana Edad , Neovascularización Patológica/etiología , Placa Aterosclerótica/complicaciones , Accidente Cerebrovascular/diagnóstico por imagen , Ultrasonografía Doppler Transcraneal
3.
Nervenarzt ; 83(8): 1039-52, 2012 Aug.
Artículo en Alemán | MEDLINE | ID: mdl-22801666

RESUMEN

Stroke units (SU) have been certified for many years by the German Stroke Society (DSG) and the German Stroke Aid Foundation (SDSH). Since 2009 this is now undertaken in the third generation by the LGA InterCert of the Technical Surveillance Society of Rhineland (TÜV Rheinland). This article presents the amended certification criteria which came into effect in 2012. Many criteria and definitions could be further defined and specified and residual grey areas and fields of conflict could be reduced. For the first time a distinction has been made between the minimum requirements relevant for certification and additional recommendations by the SU Commission of the DSG. In this manner the authors are aiming to motivate SU operators not just to align quality assurance measures to the minimum requirements but to deliberately go beyond them. There is a great deal of evidence to indicate that this will not only serve to increase the motivation of personnel and the quality of treatment but simultaneously the economic situation can also be improved.


Asunto(s)
Certificación/organización & administración , Guías como Asunto , Unidades Hospitalarias/normas , Neurología/normas , Programas Médicos Regionales/normas , Accidente Cerebrovascular/diagnóstico , Accidente Cerebrovascular/terapia , Alemania , Humanos , Programas Nacionales de Salud/normas
4.
Nervenarzt ; 83(6): 759-65, 2012 Jun.
Artículo en Alemán | MEDLINE | ID: mdl-22278124

RESUMEN

BACKGROUND: Acute stroke is a time- and expertise-critical emergency. An immediate and correct diagnosis by emergency medical services (EMS) in the prehospital phase and patient transfer to the nearest adequate hospital with a stroke unit is required for early treatment of acute stroke. PATIENTS AND METHODS: We evaluated all patients who were admitted by the EMS of Münster to one of the two stroke units in the town between October 2008 and December 2010 with a diagnosis of acute stroke. Furthermore all patients were critically analyzed who were admitted without a diagnosis of acute stroke by the EMS but nonetheless had a stroke and the correct diagnosis was not found until examination in the neurological department. RESULTS: We analyzed 615 patients who were admitted to the stroke units with the diagnosis of acute stroke. In 561 cases (91%) this diagnosis could be confirmed, but in 54 patients (9%) the diagnosis by the EMS was incorrect. Epileptic seizure was the most frequent false-positive diagnosis in this group of patients (39%; n = 21). Although the acute symptoms were caused by a stroke, the correct diagnosis was not defined by the EMS in 127 patients. This accounted for 18% of all patients admitted to the emergency departments by the EMS where ultimately a stroke was diagnosed. In 24% of these cases (n = 30) the emergency doctor missed the correct diagnosis, which meant 4% of all patients admitted by the EMS, finally diagnosed with an acute stroke. In all other cases in the group with a false-negative diagnosis (76% or 97 patients) an emergency doctor was not involved in the referral by the EMS. CONCLUSION: Emergency medical services should be involved in the establishment of admission programs for acute stroke patients to provide the fastest means of transportation to a stroke unit. Coma, symptoms of posterior cerebral circulation and epileptic seizures cause difficulties in ensuring an immediate and correct diagnosis. Sending an emergency doctor to the scene increases diagnostic certainty which is essential to initiate early treatment.


Asunto(s)
Errores Diagnósticos/prevención & control , Errores Diagnósticos/estadística & datos numéricos , Accidente Cerebrovascular/diagnóstico , Accidente Cerebrovascular/epidemiología , Adulto , Anciano , Anciano de 80 o más Años , Servicios Médicos de Urgencia , Femenino , Alemania/epidemiología , Asignación de Recursos para la Atención de Salud , Humanos , Masculino , Prevalencia , Garantía de la Calidad de Atención de Salud , Reproducibilidad de los Resultados , Factores de Riesgo , Sensibilidad y Especificidad , Adulto Joven
5.
Nervenarzt ; 82(8): 1043-52, 2011 Aug.
Artículo en Alemán | MEDLINE | ID: mdl-21761183

RESUMEN

Silent brain infarctions are frequently found by modern cerebral imaging. Up to 30% of persons without a clinical history of stroke were found to have silent brain infarction in epidemiological studies. "Silent" refers to ischemic brain lesions for which no matching clinical syndrome can be found based on history or clinical investigation. Age, education, and ethnic background have a strong impact on noticing and reporting stroke symptoms. The current clinical definition of stroke is insensitive for cognitive deficits which can also be caused by brain infarctions. The majority of silent brain infarctions are localized in the subcortical white matter of the brain; however, about 10% of silent brain infarctions are cortical. Silent brain infarctions are strongly associated with stroke risk factors and comorbidities that are known to cause clinically overt stroke. Silent brain infarctions are 5 to 10 times more frequent than clinically overt strokes. Silent brain infarctions as defined by DWI lesions on MRI imaging are a frequent finding during operative or interventional procedures and their monitoring may help improve the respective techniques in order to decrease the risk of periprocedural stroke.


Asunto(s)
Infarto Encefálico/diagnóstico , Anciano , Infarto Encefálico/etiología , Trastornos del Conocimiento/diagnóstico , Comorbilidad , Diagnóstico Diferencial , Dominancia Cerebral/fisiología , Femenino , Humanos , Procesamiento de Imagen Asistido por Computador , Embolia Intracraneal/diagnóstico , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Examen Neurológico , Factores de Riesgo , Accidente Cerebrovascular/diagnóstico
6.
Nervenarzt ; 82(6): 778-84, 2011 Jun.
Artículo en Alemán | MEDLINE | ID: mdl-21308358

RESUMEN

The concept of a "comprehensive stroke unit" (in German: Erweiterte Stroke-Unit) is an additional structural option for those stroke units already certified in Germany. Its aim is to complement the semi-intensive management of stroke unit patients in Germany by early mobilisation and neuropsychological rehab procedures. This concept is recommended in many European countries as well. It is based on the proof of efficacy of the combined treatment package in several randomised controlled trials. According to the Helsingborg Declaration, every stroke patient in Europe should have access to a chain of care best provided by a comprehensive stroke unit. Both early mobilisation and rehabilitation treatment can be integrated and continued without creating an interface between the acute stroke unit and the general neurological or medical ward. The monitoring beds of the acute stroke unit and the non-monitoring "enhanced care" beds are located within the same geographical area of the hospital and are run as a comprehensive stroke care entity. Continuous management of the acute stroke patients by the same team on the same unit means an increase in quality of care, better usage of staff resources and an additional gain in time. The scientific background of the advantages of a comprehensive stroke unit is described as are the structural and staff requirements. The clientel particularly benefiting from treatment on wards with enhanced care beds is described, and the spectrum of treatment services is defined. This concept will be used as the basis for an add-on qualification of already certified German stroke units. An important step was to fit the requirements of the comprehensive stroke unit to the already existing facilities and their infrastructures. From an economic point of view, the comprehensive stroke unit is expected to be cost-effective, either balanced or even positive.


Asunto(s)
Departamentos de Hospitales/organización & administración , Neurología/organización & administración , Rehabilitación/organización & administración , Rehabilitación de Accidente Cerebrovascular , Accidente Cerebrovascular/diagnóstico , Alemania , Humanos
7.
Nervenarzt ; 82(10): 1250-63, 2011 Oct.
Artículo en Alemán | MEDLINE | ID: mdl-21479740

RESUMEN

Susac syndrome, named after John Susac, the first to describe this condition, is characterized by the clinical triad of encephalopathy, branch retinal artery occlusion, and sensorineural hearing loss. Although certainly a rare disease, Susac syndrome needs to be considered in the differential diagnosis of a broad variety of diseases. The pathogenesis is not yet clear. Autoimmune processes leading to damage and inflammation-related occlusion of the microvessels in brain, retina, and inner ear are thought to play a causal role. The diagnosis is based primarily on the clinical presentation, the documentation of branch retinal artery occlusion by fluorescence angiography, and characteristic findings on cerebral MRI. Usually, immunosuppressive therapy is required, though controlled therapy trials are missing so far. The intention of this review article is to raise awareness of this disease among neurologists, psychiatrists, ophthalmologists, and ENT specialists as a high number of unreported cases probably exists. Accordingly, the focus is on the clinical presentation and the diagnostic approach.


Asunto(s)
Conducta Cooperativa , Comunicación Interdisciplinaria , Síndrome de Susac/diagnóstico , Cuerpo Calloso/patología , Diagnóstico Diferencial , Imagen de Difusión por Resonancia Magnética , Angiografía con Fluoresceína , Pérdida Auditiva Sensorineural/diagnóstico , Pérdida Auditiva Sensorineural/inmunología , Pérdida Auditiva Sensorineural/terapia , Humanos , Procesamiento de Imagen Asistido por Computador , Inmunosupresores/uso terapéutico , Imagen por Resonancia Magnética , Examen Neurológico , Pronóstico , Oclusión de la Arteria Retiniana/diagnóstico , Oclusión de la Arteria Retiniana/inmunología , Oclusión de la Arteria Retiniana/terapia , Síndrome de Susac/inmunología , Síndrome de Susac/terapia
8.
Nervenarzt ; 81(6): 727-33, 2010 Jun.
Artículo en Alemán | MEDLINE | ID: mdl-20386872

RESUMEN

Virchow-Robin spaces ensheathe the penetrating vessels of the brain. They communicate with the subpial space, are filled with interstitial fluid and contain a specific population of macrophages.Virchow-Robin spaces are a common finding in both CT and MR imaging. Recent radiologic studies have led to a concise definition of Virchow-Robin spaces.Virchow-Robin spaces appear isointense to cerebrospinal fluid on all imaging sequences. They are typically localised in the basal ganglia, subcortically or in the midbrain and pons. Enlarged Virchow-Robin spaces may appear as a single or multiple lesion(s). They may cause hydrocephalus in rare cases. Some studies indicate that enlarged Virchow-Robin spaces occur more frequently in elderly patients, in patients with arterial hypertension or CADASIL.In this review we illustrate the diagnostic criteria of normal and enlarged Virchow-Robin spaces and discuss their clinical relevance. Furthermore, we present an overview of the current knowledge on the anatomy, physiology and pathology of Virchow-Robin spaces.


Asunto(s)
Encéfalo/irrigación sanguínea , Encéfalo/patología , Arterias Cerebrales/patología , Venas Cerebrales/patología , Trastornos Cerebrovasculares/diagnóstico , Líquido Extracelular , Imagen por Resonancia Magnética , Piamadre/patología , Tomografía Computarizada por Rayos X , Factores de Edad , Anciano , Ganglios Basales/irrigación sanguínea , Ganglios Basales/patología , CADASIL/diagnóstico , CADASIL/patología , Corteza Cerebral/irrigación sanguínea , Corteza Cerebral/patología , Dilatación Patológica , Humanos , Hidrocefalia/patología , Hipertensión/complicaciones , Mesencéfalo/irrigación sanguínea , Mesencéfalo/patología , Puente/irrigación sanguínea , Puente/patología , Espacio Subaracnoideo/patología
9.
J Neurol Neurosurg Psychiatry ; 80(4): 432-6, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19289480

RESUMEN

BACKGROUND: The progression of white-matter changes in a case of posterior cortical atrophy (PCA) was examined over a period of 15 months using diffusion tensor imaging (DTI) and the association with neuropsychological variables was studied. PATIENT AND METHODS: A PCA patient was observed over a period of 15 months. DTI and volumetric magnetic resonance imaging were obtained at visit 1 and 15 months later. Fractional anisotropy (FA) and volumetric changes were compared with findings in a typical case of Alzheimer disease (AD) and in 65 healthy volunteers, and the association of neuropsychological deficits with these changes was studied. RESULTS: Reduction in FA was focused on the occipital lobe in the early stages of PCA. During the 15-month period, the FA values of the PCA patient tended to align with the FA ratios of the AD patient, with a more pronounced FA reduction in the parietal lobes, as opposed to a stable FA level in the occipital lobe. In addition to the DTI changes, clinical and neuropsychological symptoms deteriorated further. Brain volumes (grey matter, white matter and total normalised brain volume) of the PCA patient were substantially decreased compared with the control group, but loss of tissue volumes showed only marginal progression between visit 1 and 2. CONCLUSIONS: The findings suggest that PCA starts as distinct clinical syndrome but in its later course might turn into a final pathway shared with AD. DTI might be helpful in detecting changes in cerebral white matter during disease progression in PCA patients.


Asunto(s)
Encefalopatías/patología , Corteza Cerebral/patología , Anciano , Anisotropía , Atrofia , Encefalopatías/diagnóstico , Encefalopatías/psicología , Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/psicología , Imagen de Difusión por Resonancia Magnética , Humanos , Masculino , Trastornos de la Memoria/etiología , Trastornos de la Memoria/psicología , Pruebas Neuropsicológicas
10.
Acta Neurol Scand ; 120(1): 68-71, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19053954

RESUMEN

BACKGROUND: The first ever diagnosis of multiple sclerosis (MS) requires consideration of both diagnostic criteria and differential diagnosis. Clinicians are particularly challenged by rare conditions which may mimic MS symptoms and relapses. CASE REPORT: We report the case of a young female patient who presented with relapsing left hemispheric symptoms that were highly suspicious of MS but were caused by an idiopathic occlusive angiopathy of the circle of Willis. CONCLUSION: Occlusive disease of the great cerebral arteries in young patients is a rare but important differential diagnosis of MS. It has to be considered in patients presenting with the first symptoms suspicious of MS as substantial treatment consequences will arise.


Asunto(s)
Enfermedades Arteriales Cerebrales/diagnóstico , Círculo Arterial Cerebral/fisiopatología , Esclerosis Múltiple/diagnóstico , Angiografía Cerebral , Diagnóstico Diferencial , Femenino , Humanos , Imagen por Resonancia Magnética , Adulto Joven
11.
J Clin Neurosci ; 16(1): 79-82, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19017557

RESUMEN

The reported sensitivity of neurovascular ultrasound (nUS) for detecting spontaneous cervical artery dissection (sCAD) varies from 80% to 96% in the internal carotid artery (ICA) and from 70% to 86% in the vertebral arteries (VA). The aim of this study was to assess the sensitivity of nUS compared to MRI of the neck and MR angiography for the detection of sCAD. Forty consecutive patients with sCAD proven by 1.5T MRI were investigated by nUS within 48 hours of admission. A total of 52 cases of sCAD were detected by MRI, equally distributed (n=26, 50%) in the ICA and VA territories. Two sCADs affecting the ICA (n=2, 8%) and two sCADs of the VA (n=2, 8%) had normal initial nUS findings. The sensitivity of nUS in detecting sCAD is high, about 92% for both vascular territories. However, intramural hematomas may be missed either when they are located outside the arterial segments directly visible by nUS or if they are too small to cause hemodynamically significant stenosis.


Asunto(s)
Disección de la Arteria Carótida Interna/diagnóstico por imagen , Arteria Carótida Interna/diagnóstico por imagen , Ultrasonografía Doppler Dúplex/métodos , Disección de la Arteria Vertebral/diagnóstico por imagen , Arteria Vertebral/diagnóstico por imagen , Adulto , Anciano , Disección de la Arteria Carótida Interna/patología , Femenino , Humanos , Angiografía por Resonancia Magnética , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Sensibilidad y Especificidad , Disección de la Arteria Vertebral/patología , Adulto Joven
12.
Int J Stroke ; : 1747493019833017, 2019 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-30873912

RESUMEN

BACKGROUND: Treatment of individuals with asymptomatic carotid artery stenosis is still handled controversially. Recommendations for treatment of asymptomatic carotid stenosis with carotid endarterectomy (CEA) are based on trials having recruited patients more than 15 years ago. Registry data indicate that advances in best medical treatment (BMT) may lead to a markedly decreasing risk of stroke in asymptomatic carotid stenosis. The aim of the SPACE-2 trial (ISRCTN78592017) was to compare the stroke preventive effects of BMT alone with that of BMT in combination with CEA or carotid artery stenting (CAS), respectively, in patients with asymptomatic carotid artery stenosis of ≥70% European Carotid Surgery Trial (ECST) criteria. METHODS: SPACE-2 is a randomized, controlled, multicenter, open study. A major secondary endpoint was the cumulative rate of any stroke (ischemic or hemorrhagic) or death from any cause within 30 days plus an ipsilateral ischemic stroke within one year of follow-up. Safety was assessed as the rate of any stroke and death from any cause within 30 days after CEA or CAS. Protocol changes had to be implemented. The results on the one-year period after treatment are reported. FINDINGS: It was planned to enroll 3550 patients. Due to low recruitment, the enrollment of patients was stopped prematurely after randomization of 513 patients in 36 centers to CEA (n = 203), CAS (n = 197), or BMT (n = 113). The one-year rate of the major secondary endpoint did not significantly differ between groups (CEA 2.5%, CAS 3.0%, BMT 0.9%; p = 0.530) as well as rates of any stroke (CEA 3.9%, CAS 4.1%, BMT 0.9%; p = 0.256) and all-cause mortality (CEA 2.5%, CAS 1.0%, BMT 3.5%; p = 0.304). About half of all strokes occurred in the peri-interventional period. Higher albeit statistically non-significant rates of restenosis occurred in the stenting group (CEA 2.0% vs. CAS 5.6%; p = 0.068) without evidence of increased stroke rates. INTERPRETATION: The low sample size of this prematurely stopped trial of 513 patients implies that its power is not sufficient to show that CEA or CAS is superior to a modern medical therapy (BMT) in the primary prevention of ischemic stroke in patients with an asymptomatic carotid stenosis up to one year after treatment. Also, no evidence for differences in safety between CAS and CEA during the first year after treatment could be derived. Follow-up will be performed up to five years. Data may be used for pooled analysis with ongoing trials.

13.
Stroke ; 39(7): 1966-71, 2008 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-18420948

RESUMEN

BACKGROUND AND PURPOSE: PDE4D was identified as the first novel gene associated with ischemic stroke risk. Replication studies have produced conflicting results, but many have been small and underpowered. Meta-analysis provides a method to combine this data and determine in a larger sample size whether the association with PDE4D can be replicated. METHODS: A meta-analysis of all PDE4D variants investigated in relation to ischemic stroke has been undertaken. Analysis of any variant appearing in 2 or more replication studies was included; this comprised 6 single nucleotide polymorphisms together with allele 0 of minisatellite AC008818 and the G0 haplotype. A total of 16 studies were identified, allowing examination of up to 5216 cases and 6615 controls for a single variant. Analyses were performed including all data, excluding data from the original report (providing true replication data), and for individual stroke subtypes and limited to white ethnicity. RESULTS: No individual single nucleotide polymorphism was associated with all ischemic stroke cases. Allele 0 of AC008818 and haplotype G0 carriers was associated with increased risk (relative risk, 1.12; 95 CI, 1.01 to 1.25; P=0.03 and relative risk, 1.18; 95% CI, 1.05 to 1.33; P=0.007), but these associations became nonsignificant after exclusion of the original study from the analysis (relative risk, 1.06; 95% CI, 0.94 to 1.20; P=0.34 and relative risk, 1.16; 95% CI, 1.00 to 1.34; P=0.06, respectively). Analyzing only whites, the majority of cases studied, did not result in a significant association for any analysis. Few robust associations were found with individual stroke subtypes. CONCLUSIONS: No genetic variant examined in PDE4D showed a robust and reproducible association to ischemic stroke. Any association that may exist is likely to be weak and potentially restricted to specific populations.


Asunto(s)
Isquemia Encefálica/diagnóstico , Isquemia Encefálica/genética , Fosfodiesterasas de Nucleótidos Cíclicos Tipo 3/genética , Predisposición Genética a la Enfermedad , Variación Genética , Polimorfismo de Nucleótido Simple , Accidente Cerebrovascular/diagnóstico , Accidente Cerebrovascular/genética , Alelos , Estudios de Casos y Controles , Fosfodiesterasas de Nucleótidos Cíclicos Tipo 4 , Interpretación Estadística de Datos , Haplotipos , Riesgo
14.
J Neurol Neurosurg Psychiatry ; 79(9): 1007-12, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18223019

RESUMEN

BACKGROUND AND AIM: The aetiopathogenesis of spontaneous cervical artery dissection (sCAD) is largely unknown. Electron microscopic (EM) examination of skin biopsies of patients with sCAD revealed very subtle pathological changes of dermal connective tissue in about half of these patients leading to the hypothesis of an underlying connective tissue disorder. However, connective tissue abnormalities did not allow clear discrimination between patients and controls in our hands. Therefore, we sought to establish an objective basis for the assessment of connective tissue abnormalities in patients with sCAD using standardised morphometric assessment of collagen fibrils. METHODS: In this study a blinded examination was performed of collagen in skin biopsies and it sought parameters which are able to discriminate between patients with sCAD and controls. Various morphometric parameters were compared between patients with sCAD (n = 20) and control subjects (n = 18). RESULTS: Previously described "flower-like" collagen fibrils in skin biopsies were extremely rare in patients and controls and did not discriminate between the groups. However, they were abundant in the skin biopsy of a patient with Ehlers-Danlos syndrome type III (EDSIII) used as a reference. Morphometric parameters such as collagen fibril diameter, fibril density and relative fibril area did not discriminate between patients and controls on an individual basis, but the mean diameter of collagen fibrils in the skin was lower in patients with sCAD compared with controls while fibril density was higher resulting in nearly equal fibril areas per unit of area (relative fibril area) comparing both groups as well as individuals. CONCLUSIONS: Blinded pathological and morphometric analysis of collagen fibres in skin biopsies was, in our hands, unable to discriminate reliably between patients with sCAD and controls on an individual basis but did show differences in collagen fibril morphometry on a group basis. Furthermore, systematic and blinded pathological studies of skin biopsies in patients with sCAD and controls are needed.


Asunto(s)
Colágenos Asociados a Fibrillas/metabolismo , Piel/metabolismo , Disección de la Arteria Vertebral/metabolismo , Disección de la Arteria Vertebral/patología , Adulto , Biopsia , Diagnóstico Diferencial , Síndrome de Ehlers-Danlos/diagnóstico , Femenino , Humanos , Masculino , Síndrome de Marfan/diagnóstico , Persona de Mediana Edad , Piel/patología
15.
J Neurol Neurosurg Psychiatry ; 79(7): 829-31, 2008 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-18559462

RESUMEN

Obstructive sleep apnoea (OSA) has previously been described in a large family suffering from Charcot-Marie-Tooth disease type 1 (CMT1). In the present study, we used a case control design to establish whether this suggested link between OSA and CMT1 may also be found when studying genetically non-related patients. 12 patients with CMT1 and 24 control patients matched for age, sex and body mass index (BMI) were included in the study. Neurological disability was graded with a previously established 6 point score. All patients underwent overnight polysomnography. The mean apnoea-hypopnoea index (AHI) of patients with CMT1 was 10.5 (16.3) which was significantly higher than that of the control group (1.5 (1.3)). Five out of 12 patients with CMT1 had an AHI > or =10/h compared with 1 of 24 control patients (p<0.01). In patients with CMT1, a significant correlation between AHI and neurological disability was found (Spearman r = 0.62; p = 0.031) while BMI and age were not related to AHI. CMT1, in particular CMT1A, predisposes with disease progression to the development of OSA. Pathophysiologically, one may assume that CMT1 related pharyngeal neuropathy increases the collapsibility of the upper airway which in turn leads to recurring obstructive respiratory events.


Asunto(s)
Enfermedad de Charcot-Marie-Tooth/complicaciones , Apnea Obstructiva del Sueño/epidemiología , Adulto , Factores de Edad , Índice de Masa Corporal , Estudios de Casos y Controles , Enfermedad de Charcot-Marie-Tooth/fisiopatología , Estudios de Cohortes , Femenino , Humanos , Masculino , Persona de Mediana Edad , Polisomnografía , Factores de Riesgo , Apnea Obstructiva del Sueño/diagnóstico , Apnea Obstructiva del Sueño/fisiopatología
16.
J Neurol Neurosurg Psychiatry ; 79(3): 312-4, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18281449

RESUMEN

BACKGROUND: Aspiration is a common complication in acute stroke patients and is strongly associated with a poor outcome. Due to an insufficient sensitivity and specificity of clinical bedside tests, further refinements are needed to improve the accuracy of clinical aspiration screening in acute stroke. OBJECTIVE: To assess the ability of the simple 2-step swallowing provocation test (SPT) to detect aspiration risk in acute stroke patients. METHODS: 100 consecutive patients with first-ever stroke were examined by SPT and fiberoptic endoscopic evaluation of swallowing (FEES) within 72 hours of stroke onset. Using FEES as an objective instrumental technique to evaluate dysphagia, statistical measures representing the ability of SPT to detect aspiration risk were calculated. RESULTS: The incidence of endoscopically proven aspiration risk was 81%. The 1st-step SPT had a sensitivity of 74.1% and a specificity of 100%. Although the 2nd-step SPT showed the same 100% specificity, sensitivity was significantly lower. False-negative results of SPT appeared predominantly in subjects exhibiting leakage of liquids to pyriform sinus without a pronounced delay in swallow onset. CONCLUSIONS: In acute stroke patients with an impairment of the pharyngeal phase of swallowing, 1st-step SPT reliably detects aspiration risk. In patients with a sole or predominant impairment of the oral phase of swallowing and a relatively intact pharyngeal phase, SPT fails to detect aspiration risk sufficiently. In the latter group, FEES or additional clinical features more specifically indicating oral-phase pathology should be considered to accurately judge the patient's aspiration risk.


Asunto(s)
Trastornos de Deglución/diagnóstico , Trastornos de Deglución/epidemiología , Aspiración Respiratoria/diagnóstico , Aspiración Respiratoria/epidemiología , Accidente Cerebrovascular/epidemiología , Anciano , Causalidad , Comorbilidad , Esofagoscopía , Reacciones Falso Negativas , Femenino , Tecnología de Fibra Óptica , Humanos , Masculino , Valor Predictivo de las Pruebas , Sensibilidad y Especificidad
17.
J Neurol Neurosurg Psychiatry ; 79(12): 1339-43, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18586863

RESUMEN

BACKGROUND: Risk stratification can contribute to individualised optimal secondary prevention in patients with cerebrovascular disease. OBJECTIVE: To prospectively investigate the prediction of the Essen Stroke Risk Score (ESRS) and a pathological Ankle Brachial Index (ABI) in consecutive patients hospitalised with acute ischaemic stroke or transient ischaemic attack (TIA) in 85 neurological stroke units throughout Germany. METHODS: 852 patients were prospectively documented on standardised case report forms, including assessment of ESRS and ABI. After 17.5 months, recurrent cerebrovascular events, functional outcome or death could be assessed in 729 patients predominantly via central telephone interview. RESULTS: After discharge from the documenting hospital, recurrent stroke occurred in 41 patients (5.6%) and recurrent TIA in 15 patients (2.1%). 52 patients (7.1%) had died, 33 (4.5%) from cardiovascular causes. Patients with an ESRS > or = 3 (vs <3) had a significantly higher risk of recurrent stroke or cardiovascular death (9.7% vs 5.1%; odds ratio (OR) 2.00, 95% confidence interval (CI) 1.08 to 3.70) and a higher recurrent stroke risk (6.9% vs 3.7%; OR 1.93, 95% CI 0.95 to 3.94). Patients with an ABI < or = 0.9 (vs > 0.9) had a significantly higher risk of recurrent stroke or cardiovascular death (10.4% vs 5.5%; OR 2.00, 95% CI 1.12 to 3.56) and a higher recurrent stroke risk (6.6% vs 4.6%; OR 1.47, 95% CI 0.76 to 2.83). CONCLUSION: Our prospective follow-up study shows a significantly higher rate of recurrent stroke or cardiovascular death and a clear trend for a higher rate of recurrent stroke in patients with acute cerebrovascular events classified as high risk by an ESRS > or = 3 or a pathological ABI.


Asunto(s)
Índice Tobillo Braquial , Índice de Severidad de la Enfermedad , Accidente Cerebrovascular/diagnóstico , Anciano , Enfermedades Cardiovasculares/metabolismo , Trastornos Cerebrovasculares/diagnóstico , Trastornos Cerebrovasculares/patología , Estudios de Seguimiento , Alemania , Hospitales , Humanos , Valor Predictivo de las Pruebas , Estudios Prospectivos , Recurrencia , Riesgo , Accidente Cerebrovascular/patología , Resultado del Tratamiento
18.
J Neurol ; 255(6): 896-902, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18335159

RESUMEN

BACKGROUND: We performed a prospective study on patients with middle cerebral artery(MCA) ischemic stroke to evaluate the accuracy of perfusion-CT imaging(PCT) to predict the development of malignant brain infarction (MBI). METHODS: 106 patients(women 37 %, mean age 65 years)underwent native cranial computed tomography (CCT), CT angiography(CTA) and PCT after a median of 2 h after stroke onset. We assessed the patency of the MCA and the area of tissue ischemia (AIT)according to cerebral blood flow(CBF), cerebral blood volume (CBV) and time-to-peak (TTP)maps. Optimum sensitivity, specificity,positive (PPV) and negative predictive values (NPV) were calculated for the end-point MBI (= midline shift > 5 mm or decompressive surgery) by means of receiver operating characteristics(ROC). RESULTS: 20 patients (19 %)developed a MBI. In these patients,a larger AIT was found in all perfusion maps as compared to the remaining patients (p < 0.001). All perfusion maps had a very high NPV (95.4-98.4 %), a high sensitivity (85-95 %) and specificity (71.6-77.9 %) and only a moderate PPV (44-47.4 %). Best prediction was found for CBF maps with AIT of > 27.9 % of the hemisphere. CONCLUSION: PCT allows the discrimination of patients without a relevant risk for MBI from those having a 50 % risk of MBI development. Due to the high sensitivity and specificity, PCT is a reliable tool in detecting MBI. Because of PCT's better availability, it is the method of choice at present for an early risk stratification of acute stroke patients.


Asunto(s)
Infarto Encefálico/diagnóstico por imagen , Infarto Encefálico/patología , Angiografía Cerebral/estadística & datos numéricos , Infarto de la Arteria Cerebral Media/diagnóstico por imagen , Infarto de la Arteria Cerebral Media/patología , Tomografía Computarizada por Rayos X/estadística & datos numéricos , Adulto , Anciano , Encéfalo/irrigación sanguínea , Encéfalo/diagnóstico por imagen , Encéfalo/patología , Infarto Encefálico/fisiopatología , Angiografía Cerebral/métodos , Circulación Cerebrovascular/fisiología , Medios de Contraste , Diagnóstico Diferencial , Femenino , Humanos , Procesamiento de Imagen Asistido por Computador , Infarto de la Arteria Cerebral Media/fisiopatología , Masculino , Persona de Mediana Edad , Arteria Cerebral Media/diagnóstico por imagen , Arteria Cerebral Media/patología , Arteria Cerebral Media/fisiopatología , Valor Predictivo de las Pruebas , Pronóstico , Factores de Riesgo , Tomografía Computarizada por Rayos X/métodos
19.
J Clin Neurosci ; 15(6): 650-3, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18400501

RESUMEN

Ehlers-Danlos syndrome (EDS) is a hereditary connective tissue disorder. One important clinical characteristic of classical type EDS is skin hyperextensibility. Examination of clinical evidence and electron microscopic views of skin biopsies suggest that connective tissue abnormalities resembling very mild EDS are present in a sizable proportion of patients with spontaneous cervical artery dissection (sCAD). Manual assessment of skin extensibility is difficult. Therefore, non-invasive machine-aided measurement of skin extensibility was used and compared with manual assessment of skin extensibility and joint hyperextensibility. Patients with classical EDS, vascular-type EDS, sCAD and healthy patients were evaluated. Skin extensibility was measurably and palpably elevated in all patients with classical type EDS but not in sCAD patients or patients with vascular-type EDS compared to healthy control individuals. Our method is able to measure the increased skin extensibility in classical type EDS. Increased skin extensibility is not present in sCAD patients.


Asunto(s)
Síndrome de Ehlers-Danlos/complicaciones , Síndrome de Ehlers-Danlos/patología , Inestabilidad de la Articulación/etiología , Piel/patología , Disección de la Arteria Vertebral/complicaciones , Disección de la Arteria Vertebral/patología , Adolescente , Adulto , Anciano , Análisis de Varianza , Niño , Diagnóstico Diferencial , Síndrome de Ehlers-Danlos/clasificación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Reproducibilidad de los Resultados
20.
Nat Neurosci ; 5(7): 695-9, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12055632

RESUMEN

Language is considered a function of either the left or, in exceptional cases, the right side of the brain. Functional imaging studies show, however, that in the general population a graded continuum from left hemispheric to right hemispheric language lateralization exists. To determine the functional relevance of lateralization differences, we suppressed language regions using transcranial magnetic stimulation (TMS) in healthy human subjects who differed in lateralization of language-related brain activation. Language disruption correlated with both the degree and side of lateralization. Subjects with weak lateralization (more bilaterality) were less affected by either left- or right-side TMS than were subjects with strong lateralization to one hemisphere. Thus in some people, language processing seems to be distributed evenly between the hemispheres, allowing for ready compensation after a unilateral lesion.


Asunto(s)
Encéfalo/fisiología , Susceptibilidad a Enfermedades , Lateralidad Funcional/fisiología , Lenguaje , Adulto , Encéfalo/anatomía & histología , Mapeo Encefálico , Estimulación Eléctrica/instrumentación , Campos Electromagnéticos , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Ultrasonografía Doppler Transcraneal
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