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1.
Int J Neurosci ; 128(4): 311-317, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28830290

RESUMO

BACKGROUND: A loading dose of antiplatelets reduces in-stent thrombosis after stent implantation. However, whether it is safe in patients undergoing acute stenting after intravenous recombinant tissue plasminogen activator (rt-PA) is unclear. METHODS: A case series of acute ischemic stroke patients treated with intravenous rt-PA followed by emergent stenting were prospectively included in Jinling Hospital Stroke Unit. An emergent loading dose of antiplatelets (aspirin 300 mg and clopidogrel 300 mg) were administered to all patients through a nasogastric tube immediately before stenting. Clinical and angiographic outcomes were evaluated in these patients. RESULTS: A total of 12 patients were included. The median of NIHSS score on admission was 15 points (interquartile range 11-19). The median of time from stroke symptom onset to start IV rt-PA and stent placement was 172 min (interquartile range 123.75-189) and 311.5 min (interquartile range 285.5-349.5), respectively. All patients reached complete or partial recanalization (TICI ≥2a). One patient occurred hemorrhagic transformation at 24 h following the emergent loading dose of antiplatelets. A favorable outcome as defined by mRS ≤2 at 90 days was obtained in 58.3% (7/12) of all patients. CONCLUSION: Our finding preliminary suggested that an emergent loading dose of antiplatelets may be safe and feasible for acute stenting after IV rt-PA.


Assuntos
Isquemia Encefálica/etiologia , Fibrinolíticos/administração & dosagem , Stents , Acidente Vascular Cerebral/complicações , Acidente Vascular Cerebral/terapia , Ativador de Plasminogênio Tecidual/administração & dosagem , Administração Intravenosa , Idoso , Aspirina/uso terapêutico , Clopidogrel , Angiografia por Tomografia Computadorizada , Estudos de Viabilidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Acidente Vascular Cerebral/diagnóstico por imagem , Ticlopidina/análogos & derivados , Ticlopidina/uso terapêutico , Tomógrafos Computadorizados , Resultado do Tratamento
2.
Catheter Cardiovasc Interv ; 88(2): 255-61, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26774257

RESUMO

BACKGROUND: Fractional flow reserve (FFR)-guided revascularization strategy is popular in coronary intervention. However, the feasibility of assessing stenotic severity in intracranial large arteries using pressure gradient measurements still remains unclear. METHODS: Between March 2013 and May 2014, 12 consecutive patients with intracranial large artery stenosis (including intracranial internal carotid artery, middle cerebral M1 segment, intracranial vertebral artery, and basilar artery) were enrolled in this study. The trans-stenotic pressure gradient was measured before and/or after percutaneous transluminal angioplasty and stenting (PTAS), and was then compared with percent diameter stenosis. A Pd /Pa cut-off of ≤0.70 was used to guide stenting of hemodynamically significant stenoses. The device-related and procedure-related serious adverse events and recurrent cerebral ischemic events were recorded. RESULTS: The target vessel could be reached in all cases. No technical complications occurred due to the specific study protocol. Excellent pressure signals were obtained in all patients. For seven patients who performed PTAS, the mean pre-procedural pressure gradient decreased from 59.0 ± 17.2 to 13.3 ± 13.6 mm Hg after the procedure (P < 0.01). Only one patient who refused stenting experienced a TIA event in the ipsilateral MCA territory. No recurrent ischemic event was observed in other patients. CONCLUSION: Mean trans-stenotic pressure gradients can be safely and easily measured with a 0.014-inch fluid-filled guide wire in intracranial large arteries. © 2016 Wiley Periodicals, Inc.


Assuntos
Arteriopatias Oclusivas/diagnóstico , Pressão Arterial , Artéria Basilar/fisiopatologia , Determinação da Pressão Arterial , Artéria Carótida Interna/fisiopatologia , Doenças Arteriais Intracranianas/diagnóstico , Artéria Cerebral Média/fisiopatologia , Artéria Vertebral/fisiopatologia , Adulto , Idoso , Angioplastia com Balão/instrumentação , Arteriopatias Oclusivas/fisiopatologia , Arteriopatias Oclusivas/terapia , Determinação da Pressão Arterial/instrumentação , Angiografia Cerebral , Constrição Patológica , Desenho de Equipamento , Estudos de Viabilidade , Feminino , Humanos , Doenças Arteriais Intracranianas/fisiopatologia , Doenças Arteriais Intracranianas/terapia , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Reprodutibilidade dos Testes , Índice de Gravidade de Doença , Stents , Transdutores de Pressão , Resultado do Tratamento
3.
Zhonghua Yi Xue Za Zhi ; 91(19): 1303-7, 2011 May 24.
Artigo em Chinês | MEDLINE | ID: mdl-21756754

RESUMO

OBJECTIVE: To analyze the predictors of Wingspan in-stent restenosis (ISR) for the treatment of symptomatic intracranial arterial stenosis. METHODS: Between January 2007 and November 2009, 42 patients with symptomatic intracranial arterial stenosis registered in Nanjing stroke registry program (NSRP) were treated with Wingspan stent system. Clinical and follow-up results were retrospectively analyzed. They were divided into the non-restenosis and restenosis groups according to their follow-up imaging data. ISR was defined as > 50% stenosis within 5 mm or adjacent to stent or an absolute luminal loss > 20%. The analysis of stepwise multivariate Cox regression was performed to evaluate the independent predictive factors. RESULTS: ISR was found in 15 patients (15/42, 35.7%) with 16 lesions (16/43, 37.2%) at a median follow-up period of 7 months (range: 4 - 23). Diabetes (HR = 0.281; 95%CI = 0.088 - 0.898; P = 0.032) and stent diameter (HR = 0.213; 95%CI = 0.049 - 0.918; P = 0.038) were two independent predictors for ISR. CONCLUSION: Diabetes and stent diameter may be two independent predictors for ISR after a treatment of Wingspan system.


Assuntos
Angioplastia com Balão , Reestenose Coronária/epidemiologia , Oclusão de Enxerto Vascular/epidemiologia , Stents , Adulto , Idoso , Reestenose Coronária/terapia , Diabetes Mellitus/epidemiologia , Feminino , Oclusão de Enxerto Vascular/terapia , Humanos , Arteriosclerose Intracraniana/terapia , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Resultado do Tratamento
4.
Exp Neurol ; 184(2): 746-52, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14769366

RESUMO

The purpose of this study is to discuss an important component-arachidonic acid (AA) cascade of inflammatory reaction in diabetic rats with cerebral ischemia. Using the model of middle cerebral artery occlusion (MCAO), we have compared the expression of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), and measured the levels of their products prostaglandin E2 (PGE(2)) and cysteine-containing leukotrienes (cys-LTs) after different reperfusion periods in diabetic and normal rats. Cerebral ischemia-reperfusion was accompanied by increased expression of COX-2 and release of PGE(2), peaking at 12 h after reperfusion. The expression of COX-2 was maintained at a high level until 24 h after reperfusion, while the levels of PGE(2) were declined rapidly to baseline. The expression of 5-LOX and levels of cys-LTs reached a peak at 6 and 12 h after reperfusion, respectively, and was returned to baseline at 24 h after reperfusion. Compared with normal rats, the expression of COX-2 and 5-LOX as well as release of PGE(2) and cys-LTs was elevated in the brains of diabetic rats, revealing a possible mechanism for hyperglycemia-mediated aggravation of cerebral ischemic injury. A reduction of arachidonic acid metabolites mediated by inhibitors of its metabolites could be helpful in preventing ischemic brain injury in diabetic rats.


Assuntos
Ácido Araquidônico/metabolismo , Isquemia Encefálica/metabolismo , Diabetes Mellitus Experimental/fisiopatologia , Animais , Araquidonato 5-Lipoxigenase/biossíntese , Western Blotting , Isquemia Encefálica/etiologia , Isquemia Encefálica/fisiopatologia , Ciclo-Oxigenase 2 , Cisteína/metabolismo , Diabetes Mellitus Experimental/metabolismo , Dinoprostona/metabolismo , Infarto da Artéria Cerebral Média/complicações , Isoenzimas/biossíntese , Leucotrienos/metabolismo , Masculino , Prostaglandina-Endoperóxido Sintases/biossíntese , Ratos , Ratos Sprague-Dawley , Reperfusão , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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