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1.
PLoS One ; 19(8): e0308178, 2024.
Article de Anglais | MEDLINE | ID: mdl-39093899

RÉSUMÉ

OBJECTIVE: To construct a stable rat portal vein thrombosis (PVT) model and explore the time window of urokinase thrombolytic therapy on this basis. METHODS: Constructing a rat PVT model by combining anhydrous ethanol disruption of portal endothelium with stasis of blood flow. Forty-eight rats after PVT modeling were divided into control group and experimental group, with 24 rats in each group. The experimental and control groups were given urokinase treatment and saline tail vein injection, respectively. The two groups of rats were observed and compared for PVT formation at 1, 3 and 5 days after modeling, respectively. RESULTS: A stable rat PVT model was successfully constructed. No significant differences were found in PVT length, portal vein wet weight, and percentage of luminal occlusion area in the control rats at 1, 3, and 5 days after successful modeling (P > 0.05). Compared with control rats 1 day after modeling, the percentage of non-organized thrombus luminal area was significantly decreased (P < 0.0001), and the percentage of organized thrombus luminal area was significantly increased (P < 0.0001) in the PVTs of control rats at 3 and 5 days after modeling. After thrombolytic treatment with urokinase, plasma fibrinogen (FBG) levels were significantly decreased in the experimental group of rats compared with the control group (P < 0.0001), and plasma D-dimer (D2D) levels were significantly increased in the experimental group of rats compared with the control group (P < 0.0001). In addition, we observed prolongation of prothrombin time (PT) in the experimental group at 1, 3 and 5 days after modeling compared to the control group (P = 0.0001). Compared with the control group, portal vein wet weight and PVT length were significantly decreased in the experimental group of rats at 1 day after modeling (P < 0.05), whereas these differences were not found in the two groups of rats at 3 and 5 days after modeling (P > 0.05). The percentage of non-organized thrombus area in the experimental group was significantly decreased compared with that in the control group at 1, 3, and 5 days after modeling (P < 0.05), whereas there was no significant difference in the percentage of lumen area of organized thrombus between the two groups (P > 0.05). CONCLUSION: The method of producing a rat PVT model by destroying the endothelium of the portal vein by anhydrous ethanol combined with blood flow stasis is feasible and reproducible. In addition, the optimal time window for thrombolysis in the treatment of PVT in rats using urokinase is the early stage of thrombosis, when the fibrin content is highest.


Sujet(s)
Modèles animaux de maladie humaine , Veine porte , Traitement thrombolytique , Activateur du plasminogène de type urokinase , Thrombose veineuse , Animaux , Veine porte/effets des médicaments et des substances chimiques , Thrombose veineuse/traitement médicamenteux , Rats , Activateur du plasminogène de type urokinase/métabolisme , Traitement thrombolytique/méthodes , Mâle , Rat Sprague-Dawley , Fibrinolytiques/pharmacologie , Fibrinolytiques/usage thérapeutique , Fibrinogène/métabolisme , Produits de dégradation de la fibrine et du fibrinogène/métabolisme
2.
Int J Stroke ; 19(7): 718-726, 2024 Aug.
Article de Anglais | MEDLINE | ID: mdl-39096172

RÉSUMÉ

A decade on from the first positive thrombectomy trials, hyperacute therapies for ischemic stroke continue to rapidly advance. Effective treatments remain limited to reperfusion, although several cytoprotective approaches continue to be investigated. Intravenous fibrinolytics are now demonstrated to be beneficial up to 24 h in patients selected using perfusion imaging, but their role in patients with non-disabling symptoms appears very limited. Tenecteplase is superior to alteplase in meta-analysis of the latest trials, and adjuvant thrombolytics are an area of active investigation. Endovascular thrombectomy is beneficial in a wide range of anterior and posterior circulation large vessel occlusions up to 24 h after onset with the more distal occlusions, mild presentations, and >24 h window being the main frontiers to be tested in ongoing trials. Imaging parameters are prognostic but appear not to modify the relative treatment benefit of thrombectomy versus standard medical care. Therefore, deciding who not to treat with thrombectomy is a key clinical challenge that requires careful but rapid integration of clinical, imaging, and patient preference considerations. Systems of care to accelerate delivery of these highly effective therapies will maximize benefits for the greatest number of patients with stroke.


Sujet(s)
Fibrinolytiques , Accident vasculaire cérébral ischémique , Thrombectomie , Humains , Accident vasculaire cérébral ischémique/thérapie , Accident vasculaire cérébral ischémique/chirurgie , Thrombectomie/méthodes , Fibrinolytiques/usage thérapeutique , Traitement thrombolytique/méthodes , Procédures endovasculaires/méthodes
3.
Eur J Cardiothorac Surg ; 66(1)2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38979769

RÉSUMÉ

OBJECTIVES: Although intrapleural administration of fibrinolytics is an important treatment option for the management of empyema, the addition of fibrinolytics failed to reduce the need for surgery and mortality in previous randomized controlled trials. This study aimed to investigate the effects of administrating fibrinolytics in the early phase (within 3 days of chest tube insertion) of empyema compared with late administration or no administration. METHODS: We used the Japanese Diagnosis Procedure Combination Inpatient Database to identify patients aged ≥16 years who were hospitalized and underwent chest tube drainage for empyema. A 1:2 propensity score matching and stabilized inverse probability of treatment weighting were conducted. RESULTS: Among the 16 265 eligible patients, 3082 and 13 183 patients were categorized into the early and control group, respectively. The proportion of patients who underwent surgery was significantly lower in the early fibrinolytics group than in the control group; the odds ratio (95% confidence interval) was 0.69 (0.54-0.88) in the propensity score matching (P = 0.003) and 0.64 (0.50-0.80) in the stabilized inverse probability of treatment weighting analysis (P < 0.001). All-cause 30-day in-hospital mortality, length of hospital stay, duration of chest tube drainage, and total hospitalization costs were also more favourable in the early fibrinolytics group. CONCLUSIONS: The early administration of fibrinolytics may reduce the need for surgery and death in adult patients with empyema.


Sujet(s)
Drains thoraciques , Drainage , Empyème pleural , Fibrinolytiques , Humains , Mâle , Femelle , Drainage/méthodes , Fibrinolytiques/administration et posologie , Fibrinolytiques/usage thérapeutique , Empyème pleural/chirurgie , Empyème pleural/mortalité , Empyème pleural/traitement médicamenteux , Adulte d'âge moyen , Sujet âgé , Score de propension , Études rétrospectives , Adulte , Japon/épidémiologie , Durée du séjour/statistiques et données numériques , Mortalité hospitalière
4.
Eur J Cardiothorac Surg ; 66(1)2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38991831

RÉSUMÉ

OBJECTIVES: We hypothesized that ultrasound-assisted thrombolysis (USAT) is non-inferior to surgical pulmonary embolectomy (SPE) to improve right ventricular (RV) function in patients with acute pulmonary embolism (PE). METHODS: In a single-centre, non-inferiority trial, we randomly assigned 27 patients with intermediate-high or high-risk acute PE to undergo either USAT or SPE stratified by PE risk. Primary and secondary outcomes were the baseline-to-72-h difference in right-to-left ventricular (RV/LV) ratio and the Qanadli pulmonary occlusion score, respectively, by contrast-enhanced chest-computed tomography assessed by a blinded CoreLab. RESULTS: The trial was prematurely terminated due to slow enrolment. Mean age was 62.6 (SD 12.4) years, 26% were women, and 15% had high-risk PE. Mean change in RV/LV ratio was -0.34 (95% CI -0.50 to -0.18) in the USAT and -0.53 (95% CI -0.68 to -0.38) in the SPE group (mean difference: 0.152; 95% CI 0.032-0.271; Pnon-inferiority = 0.80; Psuperiority = 0.013). Mean change in Qanadli pulmonary occlusion score was -7.23 (95% CI -9.58 to -4.88) in the USAT and -11.36 (95% CI -15.27 to -7.44) in the SPE group (mean difference: 5.00; 95% CI 0.44-9.56, P = 0.032). Clinical and functional outcomes were similar between the 2 groups up to 12 months. CONCLUSIONS: In patients with intermediate-high and high-risk acute PE, USAT was not non-inferior when compared with SPE in reducing RV/LV ratio within the first 72 h. In a post hoc superiority analysis, SPE resulted in greater improvement of RV overload and reduction of thrombus burden.


Sujet(s)
Embolectomie , Embolie pulmonaire , Traitement thrombolytique , Humains , Femelle , Mâle , Embolie pulmonaire/chirurgie , Embolie pulmonaire/thérapie , Adulte d'âge moyen , Traitement thrombolytique/méthodes , Embolectomie/méthodes , Sujet âgé , Échographie interventionnelle/méthodes , Résultat thérapeutique , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/administration et posologie
5.
S D Med ; 77(5): 213-219, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-39012774

RÉSUMÉ

Heart failure (HF) is a common disorder associated with significant morbidity and mortality. It can increase the risk of thromboembolic events, which subsequently lead to increased risk of stroke, ischemic heart disease, thromboembolism, and death. Antithrombotic therapy has been investigated as a potential management strategy for HF patients in sinus rhythm, but its efficacy remains uncertain. Current guidelines do not recommend the routine use of antithrombotics in patients with HF in sinus rhythm without any other indication for their use. Several randomized controlled trials have investigated the efficacy of antithrombotics in HF patients in sinus rhythm. This article provides a concise review of the existing literature to assess the evidence supporting the use of antithrombotics in HF patients in sinus rhythm. The use of warfarin or other anticoagulants has demonstrated a lower risk of stroke but an increased risk of bleeding. The studies demonstrate that anticoagulant therapy in HF patients in sinus rhythm does not provide significant benefits in terms of overall ischemic events or death.


Sujet(s)
Fibrinolytiques , Défaillance cardiaque , Humains , Défaillance cardiaque/traitement médicamenteux , Défaillance cardiaque/complications , Fibrinolytiques/usage thérapeutique , Anticoagulants/usage thérapeutique , Hémorragie/induit chimiquement , Warfarine/usage thérapeutique , Warfarine/effets indésirables , Thromboembolie/prévention et contrôle , Accident vasculaire cérébral/prévention et contrôle , Antiagrégants plaquettaires/usage thérapeutique
6.
Nutrients ; 16(13)2024 Jun 26.
Article de Anglais | MEDLINE | ID: mdl-38999771

RÉSUMÉ

The study aimed to evaluate the antithrombotic action of Acrocomia aculeata pulp oil (AAPO) in natura, in an in vitro experimental model. AAPO was obtained by solvent extraction, and its chemical characterization was performed by gas chromatography coupled to a mass spectrometer (GC-MS). In vitro toxicity was evaluated with the Trypan Blue exclusion test and in vivo by the Galleria mellonella model. ADP/epinephrine-induced platelet aggregation after treatment with AAPO (50, 100, 200, 400, and 800 µg/mL) was evaluated by turbidimetry, and coagulation was determined by prothrombin activity time (PT) and activated partial thromboplastin time (aPTT). Platelet activation was measured by expression of P-selectin on the platelet surface by flow cytometry and intraplatelet content of reactive oxygen species (ROS) by fluorimetry. The results showed that AAPO has as major components such as oleic acid, palmitic acid, lauric acid, caprylic acid, and squalene. AAPO showed no toxicity in vitro or in vivo. Platelet aggregation decreased against agonists using treatment with different concentrations of AAPO. Oil did not interfere in PT and aPTT. Moreover, it expressively decreased ROS-induced platelet activation and P-selectin expression. Therefore, AAPO showed antiplatelet action since it decreased platelet activation verified by the decrease in P-selectin expression as well as in ROS production.


Sujet(s)
Fibrinolytiques , Sélectine P , Huiles végétales , Agrégation plaquettaire , Espèces réactives de l'oxygène , Animaux , Agrégation plaquettaire/effets des médicaments et des substances chimiques , Sélectine P/métabolisme , Humains , Huiles végétales/pharmacologie , Huiles végétales/composition chimique , Espèces réactives de l'oxygène/métabolisme , Fibrinolytiques/pharmacologie , Plaquettes/effets des médicaments et des substances chimiques , Plaquettes/métabolisme , Coagulation sanguine/effets des médicaments et des substances chimiques , Activation plaquettaire/effets des médicaments et des substances chimiques
7.
Ann Afr Med ; 23(3): 328-334, 2024 Jul 01.
Article de Français, Anglais | MEDLINE | ID: mdl-39034555

RÉSUMÉ

INTRODUCTION: The constantly increasing incidence of stroke in Saudi Arabia substantiates an urgent need to elucidate underlying risk factors and etiologies. In terms of improving outcomes, the predictors of functional outcomes need to be identified as well. As posterior circulation strokes (PCS) have not been studied in detail, the current study aimed to identify the risk factors, etiology, and predictors of outcome in PCS. METHODS: This retrospective study included the data for 138 patients with PCS. Demographics, risk factors, clinical signs/symptoms, etiology, and outcome at discharge and 3-month follow-up were recorded. Factors associated with outcomes were identified, and the difference was ascertained using Chi-square, odds ratios, and 95% confidence intervals. RESULTS: The mean participant age was 58 ± 14.8 years with 73% being males. The mean arrival time was 26.5 ± 31.6 h; with a mean National Institute of Health Stroke scale (NIHSS) score of 7.2 ± 5.6. Motor deficit and dysarthria were the most common presentations. Twenty percent of patients received intravenous recombinant tissue plasminogen activator, whereas endovascular thrombectomy was performed in 9 (6.5%). Follow-up outcome at 3 months was available in 113 (81.8%). Male sex, baseline modified Rankin scale of <2, low baseline NIHSS, and stable or improvement in baseline NIHSS during 24 h of admission were documented as predictors of a good outcome, whereas history of atrial fibrillation and prior stroke, high NIHSS at admission and worsening of symptoms during 24 h of admission, as well as bilateral body involvement were associated with poor outcome. CONCLUSION: The functional outcomes and the predictors of functional outcomes did not differ from the previously published literature; however, significant differences were observed in the risk factors and etiological profile in our population. These differences are of potential interest to the researchers and clinicians, as they carry important therapeutic and prognostic implications and need to be verified through large prospective studies.


Résumé Introduction:L'incidence constamment croissante des accidents vasculaires cérébraux en Arabie Saoudite justifie la nécessité urgente d'élucider les facteurs de risque sous-jacents et les étiologies. En termes d'amélioration des résultats, les prédicteurs des résultats fonctionnels doivent également être identifiés. Comme circulation postérieure Les accidents vasculaires cérébraux (PCS) n'ont pas été étudiés en détail, l'étude actuelle visait à identifier les facteurs de risque, l'étiologie et les prédicteurs de l'issue du PCS.Méthodes:Cette étude rétrospective incluait les données de 138 patients atteints de PCS. Données démographiques, facteurs de risque, signes/symptômes cliniques, étiologie, et les résultats à la sortie et au suivi à 3 mois ont été enregistrés. Les facteurs associés aux résultats ont été identifiés et la différence a été déterminé à l'aide du chi carré, des rapports de cotes et des intervalles de confiance à 95 %.Résultats:L'âge moyen des participants était de 58 ± 14,8 ans avec 73 % étant des hommes. L'heure moyenne d'arrivée était de 26,5 ± 31,6 heures; avec un score moyen sur l'échelle NIHSS (National Institute of Health Stroke Scale) de 7,2 ± 5,6. Moteur le déficit et la dysarthrie étaient les présentations les plus courantes. Vingt pour cent des patients ont reçu du plasminogène tissulaire recombinant par voie intraveineuse activateur, alors qu'une thrombectomie endovasculaire a été réalisée dans 9 cas (6,5 %). Le résultat du suivi à 3 mois était disponible chez 113 (81,8 %). Mâle sexe, échelle de Rankin modifiée de base <2, NIHSS de base faible et stabilité ou amélioration du NIHSS de base au cours des 24 heures suivant l'admission. documentés comme prédicteurs d'un bon résultat, alors que des antécédents de fibrillation auriculaire et d'accident vasculaire cérébral antérieur, un NIHSS élevé à l'admission et une aggravation des symptômes au cours des 24 heures suivant l'admission, ainsi qu'une atteinte corporelle bilatérale étaient associés à de mauvais résultats.Conclusion:le fonctionnel les résultats et les prédicteurs des résultats fonctionnels ne différaient pas de la littérature publiée précédemment; cependant, une différence significative ont été observés dans les facteurs de risque et le profil étiologique dans notre population. Ces différences sont potentiellement intéressantes pour les chercheurs et cliniciens, car ils comportent d'importantes implications thérapeutiques et pronostiques et doivent être vérifiés par de vastes études prospectives.


Sujet(s)
Accident vasculaire cérébral , Humains , Mâle , Femelle , Adulte d'âge moyen , Études rétrospectives , Sujet âgé , Facteurs de risque , Arabie saoudite/épidémiologie , Accident vasculaire cérébral/épidémiologie , Résultat thérapeutique , Adulte , Thrombectomie , Activateur tissulaire du plasminogène/usage thérapeutique , Activateur tissulaire du plasminogène/administration et posologie , Indice de gravité de la maladie , Fibrinolytiques/usage thérapeutique , Procédures endovasculaires
8.
Article de Anglais | MEDLINE | ID: mdl-39037060

RÉSUMÉ

BACKGROUND: Management of complicated pleural infections (CPIs) had historically been surgical; however, following the publication of the second multicenter intrapleural sepsis trial (MIST-2), combination tissue plasminogen (tPA) and dornase (DNase) offers a less invasive and effective treatment. Our aim was to assess the quality of life (QOL) and functional ability of patients' recovery from a CPI managed with either intrapleural fibrinolytic therapy (IPFT) or surgery. METHODS: We identified 565 patients managed for a CPI between January 1, 2013 and March 31, 2018. There were 460 patients eligible for contact, attempted through 2 phone calls and one mailer. Two questionnaires were administered: the Short Form 36-Item Health Survey (SF-36) and a functional ability questionnaire. RESULTS: Contact was made in 35% (159/460) of patients, and 57% (90/159) completed the survey. Patients had lower QOL scores compared to average US citizens; those managed with surgery had higher scores in physical functioning (surgery: 80, IPFT: 70, P=0.040) but lower pain scores (surgery: 58, IPFT: 68, P=0.045). Of 52 patients who returned to work, 48% (25) reported an impact on their work effectiveness during recovery, similarly between management strategies (IPFT: 50%, 13/26 vs. surgery: 46%, 12/26; P=0.781). CONCLUSION: Patients with a CPI had a lower QOL compared with average US citizens. Surgically managed patients reported improved physical functioning but worse pain compared with patients managed with IPFT. Patients returned to work within 4 weeks of discharge, and nearly half reported their ability to work effectively was impacted by their recovery. With further research into recovery timelines, patients may be appropriately counselled for expectations.


Sujet(s)
Qualité de vie , Humains , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Récupération fonctionnelle , Enquêtes et questionnaires , Activateur tissulaire du plasminogène/usage thérapeutique , Activateur tissulaire du plasminogène/administration et posologie , Traitement thrombolytique/méthodes , Résultat thérapeutique , Reprise du travail/statistiques et données numériques , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/administration et posologie , Adulte , Maladies de la plèvre/thérapie
9.
Clin Interv Aging ; 19: 1247-1258, 2024.
Article de Anglais | MEDLINE | ID: mdl-39006937

RÉSUMÉ

Purpose: To investigate the benefit (90-day mRS score) and rate of major complications (early symptomatic intracranial hemorrhage-SICH) after reperfusion therapy (RT) (including intravenous thrombolysis -IVT and mechanical thrombectomy -MT) in patients over 80 years with acute ischemic stroke (AIS). Patients and Methods: AIS patients aged over 80 admitted to Huizhou Central People's Hospital from September 2018 to 2023 were included in this study. Data on SICH, NIHSS, and mRS were analyzed. A good prognosis was defined as a mRS ≤ 2 or recovery to pre-stroke status at 90 days. Results: Of 209 patients, 80 received non-RT, 100 received IVT and 29 underwent MT. The non-RT group had the lowest baseline NIHSS while the MT group had the highest (non-RT 6.0 vs IVT 12.0 vs MT 18.0, P <0.001). Higher NIHSS was associated with increased SICH risk (OR 1.083, P=0.032), while RT was not (OR 5.194, P=0.129). The overall SICH rate in the RT group was higher but not significantly different after stratification by stroke severity. Poor prognosis was associated with higher admission NIHSS, stroke due to large artery atherosclerosis (LAA) combined with cardioembolism (CE), and stroke-associated pneumonia (SAP) (OR 0.902, P<0.001; OR 0.297, P=0.029; OR 0.103, P<0.001, respectively). The RT group showed a greater reduction in NIHSS (delta NIHSS) than the non-RT group (non-RT 2.0 vs IVT 4.0 vs MT 6.0, P<0.005). For severe AIS, the IVT group had a better prognosis at 90 days (non-RT 0% vs IVT 38.2%, P=0.039). No 90-day mortality difference was found between groups after stratification. Conclusion: Stroke severity, rather than RT, is an independent risk factor for SICH in AIS patients over 80. RT in severe stroke patients improves NIHSS at 90 days, suggesting RT is safe and effective in this demographic. Further studies with larger samples are required to confirm these findings.


Sujet(s)
Accident vasculaire cérébral ischémique , Thrombectomie , Traitement thrombolytique , Humains , Mâle , Femelle , Accident vasculaire cérébral ischémique/thérapie , Sujet âgé de 80 ans ou plus , Résultat thérapeutique , Études rétrospectives , Pronostic , Reperfusion , Chine , Indice de gravité de la maladie , Hémorragies intracrâniennes , Facteurs de risque , Fibrinolytiques/usage thérapeutique
10.
Neurol India ; 72(3): 632-634, 2024 May 01.
Article de Anglais | MEDLINE | ID: mdl-39041986

RÉSUMÉ

Artery of Percheron (AOP) is an uncommon anatomical variation in the posterior circulation neurovasculature. It is a single artery arising from P1 segment of posterior cerebral artery (PCA) which supplies bilateral paramedian thalami and the rostral midbrain and as a result, occlusion of it leads to bilateral thalamic and mesencephalic infarction. Due to very low incidence (ranges from 0.1% to 2% of all ischemic strokes) and varied presentation, the diagnosis of AOP infarction requires strong clinical and radiological suspicion and hence, AOP infarction is often missed and patients are rarely thrombolysed. Here we discuss a patient with acute altered sensorium who recovered completely in short time following treatment with intra-venous thrombolysis for bilateral medial thalamic ischemic stroke due to AOP occlusion.


Sujet(s)
Artère cérébrale postérieure , Traitement thrombolytique , Humains , Traitement thrombolytique/méthodes , Artère cérébrale postérieure/imagerie diagnostique , Mâle , Adulte d'âge moyen , Accident vasculaire cérébral ischémique/traitement médicamenteux , Accident vasculaire cérébral ischémique/imagerie diagnostique , Fibrinolytiques/usage thérapeutique , Thalamus/vascularisation , Thalamus/imagerie diagnostique , Thalamus/anatomopathologie , Résultat thérapeutique , Infarctus du territoire de l'artère cérébrale postérieure/traitement médicamenteux , Infarctus du territoire de l'artère cérébrale postérieure/imagerie diagnostique
12.
Expert Rev Cardiovasc Ther ; 22(7): 339-345, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38949642

RÉSUMÉ

BACKGROUND: Triple antithrombotic therapy (TAT) with aspirin, a P2Y12 inhibitor, and oral anticoagulation in patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) raises concerns about increased bleeding. Regimens incorporating more potent P2Y12 inhibitors over clopidogrel have not been investigated adequately. RESEARCH DESIGN AND METHODS: A retrospective observational study was performed on 387 patients with AF receiving TAT for 1 month (n = 236) or ≤1 week (n = 151) after PCI. Major and clinically relevant non-major bleeding and major adverse cardiac and cerebrovascular events (MACCE) were assessed up to 30 days post-procedure. RESULTS: Bleeding was less frequent with ≤1 week versus 1 month of TAT (3.3 vs 9.3%; p = 0.025) while MACCE were similar (4.6 vs 4.7%; p = 0.998). No differences in bleeding or MACCE were observed between ticagrelor/prasugrel and clopidogrel regimens. For patients receiving ≤1 week of TAT, no excess of MACCE was seen in the subgroup given no further aspirin post-PCI compared with those given aspirin for up to 1 week (3.6 vs 5.2%). CONCLUSIONS: TAT post-PCI for ≤1 week was associated with less bleeding despite greater use of ticagrelor/prasugrel but similar MACCE versus 1-month TAT. These findings support further studies on safety and efficacy of dual therapy with ticagrelor/prasugrel immediately after PCI.


Sujet(s)
Anticoagulants , Acide acétylsalicylique , Fibrillation auriculaire , Clopidogrel , Association de médicaments , Hémorragie , Intervention coronarienne percutanée , Antiagrégants plaquettaires , Antagonistes des récepteurs purinergiques P2Y , Humains , Fibrillation auriculaire/traitement médicamenteux , Fibrillation auriculaire/complications , Intervention coronarienne percutanée/méthodes , Mâle , Femelle , Études rétrospectives , Sujet âgé , Adulte d'âge moyen , Hémorragie/induit chimiquement , Acide acétylsalicylique/administration et posologie , Acide acétylsalicylique/usage thérapeutique , Acide acétylsalicylique/effets indésirables , Clopidogrel/administration et posologie , Clopidogrel/usage thérapeutique , Clopidogrel/effets indésirables , Antiagrégants plaquettaires/administration et posologie , Antiagrégants plaquettaires/effets indésirables , Antiagrégants plaquettaires/usage thérapeutique , Anticoagulants/administration et posologie , Anticoagulants/effets indésirables , Anticoagulants/usage thérapeutique , Antagonistes des récepteurs purinergiques P2Y/administration et posologie , Antagonistes des récepteurs purinergiques P2Y/usage thérapeutique , Antagonistes des récepteurs purinergiques P2Y/effets indésirables , Facteurs temps , Résultat thérapeutique , Fibrinolytiques/administration et posologie , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/effets indésirables , Sujet âgé de 80 ans ou plus , Ticagrélor/administration et posologie , Ticagrélor/usage thérapeutique , Ticagrélor/effets indésirables
13.
Cardiovasc Hematol Agents Med Chem ; 22(2): 230-239, 2024.
Article de Anglais | MEDLINE | ID: mdl-38975619

RÉSUMÉ

BACKGROUND: Plants have been used for ages in traditional medicine, and it is exciting to perceive how recent research has recognized the bioactive compounds liable for their beneficial effects. Green synthesis of metal nanoparticles is a hastily emergent research area in nanotechnology. This study describes the synthesis of silver nanoparticles (AgNPs) using Coriandrum sativum and Murraya koenigii leaf extract and its thrombolytic activity. OBJECTIVE: The aim of the study was to determine the clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles. METHODS: Leaves of Coriandrum sativum and Murraya koenigii were collected. Methanolic extraction of the plant sample was done through a Soxhlet extractor. The methanolic extract obtained from both the leaves was subjected to GC-MS analysis. The synthesized NPs from leaf extracts were monitored for analysis, where the typical X-ray diffraction pattern and its diffraction peaks were identified. 3D image of the NPs was analysed by Atomic Force Microscopy. The surface charge of nanoparticles was identified by Zeta potential. The Clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles were analysed by the modified Holmstorm method. RESULTS: The thrombolytic property of the methanolic extract of plants Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 45.99% activity, and Murraya koenigii extract with 66.56% activity. The nanoparticles (Nps) from Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 58.29% activity, and NPs from Murraya koenigii with 54.04% activity. Coriandrum sativum in GC-MS exhibited 3 peaks, whereas Murraya koenigii extract showed five peaks with notable bioactive compounds. CONCLUSION: These NPs were further used for biomedical applications after being fixed by an organic encapsulation agent. The present research reveals the usefulness of Coriandrum sativum and Murraya koenigii for the environmentally friendly manufacture of silver nanoparticles.


Sujet(s)
Coriandrum , Fibrinolytiques , Technologie de la chimie verte , Nanoparticules métalliques , Murraya , Extraits de plantes , Feuilles de plante , Argent , Nanoparticules métalliques/composition chimique , Murraya/composition chimique , Argent/composition chimique , Extraits de plantes/composition chimique , Extraits de plantes/pharmacologie , Coriandrum/composition chimique , Feuilles de plante/composition chimique , Fibrinolytiques/composition chimique , Fibrinolytiques/pharmacologie
14.
BMJ Open ; 14(7): e086413, 2024 Jul 15.
Article de Anglais | MEDLINE | ID: mdl-39009456

RÉSUMÉ

OBJECTIVES: After introducing a team simulation training programme at our hospital, we saw a reduction in door-to-needle times (DNT) for stroke thrombolysis but persisting variability prompting further investigation. Our objective is to examine this gap through assessing: (1) whether there is an association between DNT and the clinical experience of neurology registrars and (2) whether experience influences the benefits from attending simulation. DESIGN: Prospective cohort study. SETTING AND PARTICIPANTS: Patients treated with intravenous thrombolysis between January 2016 and 2020 at a Norwegian stroke centre. PRIMARY AND SECONDARY OUTCOME MEASURES: Using DNT and prior intravenous thrombolysis administrations (case-based definition of clinical experience) as continuous variables, a mixed effects linear regression model was performed to examine the association between clinical experience, DNT and simulation attendance. For dichotomised analyses, neurology registrars with 15 or more prior treatments were defined as experienced. RESULTS: A total of 532 patients treated by 36 neurology registrars from January 2016 to 2020 were included. There was a linear association between clinical experience and DNT (test for non-linearity p=0.479). Each prior intravenous thrombolysis administration was associated with a significant 1.1% decrease in DNT in the adjusted analysis (ΔDNT -1.1%; 95% CI, -2.2% to -0.0%; p=0.048). The interaction between effects of clinical experience and simulation on DNT was not statistically significant (p=0.150). In the dichotomised analysis, experienced registrars had similar gains from attending simulation sessions (mean DNT from 18.5 min to 13.5 min) compared with less experienced registrars (mean DNT from 22.4 min to 17.4 min). CONCLUSIONS: Less experienced registrars had longer DNT in stroke thrombolysis. Attending team simulation training was associated with similar improvements for experienced and inexperienced neurology registrars. We suggest a focus on high-quality onboarding programmes to close the experience-related quality gap. Our findings suggest that both inexperienced and experienced neurology registrars might benefit from team simulation training for stroke thrombolysis.


Sujet(s)
Compétence clinique , Formation par simulation , Accident vasculaire cérébral , Traitement thrombolytique , Délai jusqu'au traitement , Humains , Traitement thrombolytique/méthodes , Études prospectives , Formation par simulation/méthodes , Femelle , Accident vasculaire cérébral/traitement médicamenteux , Accident vasculaire cérébral/thérapie , Mâle , Norvège , Sujet âgé , Adulte d'âge moyen , Équipe soignante , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/administration et posologie
15.
CNS Neurosci Ther ; 30(7): e14868, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-39014552

RÉSUMÉ

BACKGROUND: Systolic blood pressure (SBP) was a predictor of early neurological deterioration (END) in stroke. We performed a secondary analysis of ARAMIS trial to investigate whether baseline SBP affects the effect of dual antiplatelet versus intravenous alteplase on END. METHODS: This post hoc analysis included patients in the as-treated analysis set. According to SBP at admission, patients were divided into SBP ≥140 mmHg and SBP <140 mmHg subgroups. In each subgroup, patients were further classified into dual antiplatelet and intravenous alteplase treatment groups based on study drug actually received. Primary outcome was END, defined as an increase of ≥2 in the NIHSS score from baseline within 24 h. We investigated effect of dual antiplatelet vs intravenous alteplase on END in SBP subgroups and their interaction effect with subgroups. RESULTS: A total of 723 patients from as-treated analysis set were included: 344 were assigned into dual antiplatelet group and 379 into intravenous alteplase group. For primary outcome, there was more treatment effect of dual antiplatelet in SBP ≥140 mmHg subgroup (adjusted RD, -5.2%; 95% CI, -8.2% to -2.3%; p < 0.001) and no effect in SBP <140 mmHg subgroup (adjusted RD, -0.1%; 95% CI, -8.0% to 7.7%; p = 0.97), but no significant interaction between subgroups was found (adjusted p = 0.20). CONCLUSIONS: Among patients with minor nondisabling acute ischemic stroke, dual antiplatelet may be better than alteplase with respect to preventing END within 24 h when baseline SBP ≥140 mmHg.


Sujet(s)
Pression sanguine , Fibrinolytiques , Antiagrégants plaquettaires , Accident vasculaire cérébral , Activateur tissulaire du plasminogène , Humains , Mâle , Femelle , Pression sanguine/effets des médicaments et des substances chimiques , Pression sanguine/physiologie , Sujet âgé , Activateur tissulaire du plasminogène/usage thérapeutique , Activateur tissulaire du plasminogène/administration et posologie , Adulte d'âge moyen , Antiagrégants plaquettaires/usage thérapeutique , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/administration et posologie , Accident vasculaire cérébral/traitement médicamenteux , Accident vasculaire cérébral/complications , Sujet âgé de 80 ans ou plus , Méthode en double aveugle , Accident vasculaire cérébral ischémique/traitement médicamenteux
16.
BMC Emerg Med ; 24(1): 121, 2024 Jul 18.
Article de Anglais | MEDLINE | ID: mdl-39020294

RÉSUMÉ

BACKGROUND: The percentage of elderly trauma patients under anticoagulation and antiplatelet agents has been rising lately. As newer agents are introduced, each comes with its own advantages and precautions. Our study covered elderly patients admitted to the ED with maxillofacial trauma while on anticoagulation (AC) or antiplatelet therapy (APT). We aimed to investigate the demographic characteristics, causes, and types of maxillofacial trauma, along with concomitant injuries, duration of hospitalisation, haemorrhagic complications, and the overall costs of care in the emergency department (ED). METHODS: Data were gathered from the ED of Bern University Hospital. In this retrospective analysis, patients over 65 of age were included, who presented at our ED with maxillofacial trauma between 2013 and 2019 while undergoing treatment with therapeutic AC/APT. RESULTS: The study involved 188 patients with a median age of 81 years (IQR: 81 [74; 87]), of whom 55.3% (n=104) were male. More than half (54.8%, n=103) were aged 80 years or older. Cardiovascular diseases were present in 69.7% (n=131) of the patients, with the most common indications for AC/APT use being previous thromboembolic events (41.5%, n=78) and atrial fibrillation (25.5%, n=48). The predominant cause of facial injury was falls, accounting for 83.5% (n=157) of cases, followed by bicycle accidents (6.9%, n=13) and road-traffic accidents (5.3%, n=10). The most common primary injuries were fractures of the orbital floor and/or medial/lateral wall (60.1%, n=113), zygomatic bone (30.3%, n=57), followed by isolated orbital floor fractures (23.4%, n=44) and nasal bone fractures (19.1%, n=36). Fractures of the mandible occurred in 14.9% (n=28). Facial hematomas occurred in 68.6% of patients (129 cases), primarily in the midface area. Relevant facial bleeding complications were intracerebral haemorrhage being the most frequent (28.2%, n=53), followed by epistaxis (12.2%, n=23) and retrobulbar/intraorbital hematoma (9%, n=17). Sixteen patients (8.5%) experienced heavy bleeding that required emergency treatment. The in-hospital mortality rate was 2.1% (4 cases). CONCLUSIONS: This study indicates that falls are the leading cause of maxillofacial trauma in the elderly, with the most common diagnoses being orbital, zygomatic, and nasal fractures. Haemorrhagic complications primarily involve facial hematomas, especially in the middle third of the face, with intracerebral haemorrhage being the second most frequent. Surgical intervention for bleeding was required in 8.5% of cases. Given the aging population, it is essential to improve prevention strategies and update safety protocols, particularly for patients on anticoagulant/antiplatelet therapy (AC/APT). This can ensure rapid diagnostic imaging and prompt treatment in emergencies.


Sujet(s)
Anticoagulants , Traumatismes maxillofaciaux , Humains , Mâle , Études rétrospectives , Femelle , Anticoagulants/effets indésirables , Anticoagulants/administration et posologie , Sujet âgé de 80 ans ou plus , Sujet âgé , Suisse/épidémiologie , Traumatismes maxillofaciaux/épidémiologie , Service hospitalier d'urgences/statistiques et données numériques , Antiagrégants plaquettaires/administration et posologie , Antiagrégants plaquettaires/effets indésirables , Fibrinolytiques/administration et posologie , Fibrinolytiques/effets indésirables
17.
Bull Exp Biol Med ; 177(1): 63-67, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38954300

RÉSUMÉ

Compound L-36, a new derivative of 6H-1,3,4-thiadiazine, was studied in in vitro and in vivo experiments. This compound exhibits high antiplatelet and antithrombogenic activity. In in vitro experiments, compound L-36 by its antiplatelet activity (by IC50) was superior to acetylsalicylic acid by 9.4 times. In in vivo experiments, compound L-36 by its ED50 value was close to the comparison drug. On the model of pulmonary artery thrombosis, compound L-36 ensured better survival of experimental animals than acetylsalicylic acid. Morphological studies showed that compound L-36 effectively attenuated the thrombosis processes in the pulmonary tissue induced by intravenous injection of a thrombogenic mixture (epinephrine and collagen).


Sujet(s)
Acide acétylsalicylique , Fibrinolytiques , Antiagrégants plaquettaires , Agrégation plaquettaire , Thiadiazines , Animaux , Antiagrégants plaquettaires/pharmacologie , Antiagrégants plaquettaires/composition chimique , Thiadiazines/pharmacologie , Thiadiazines/composition chimique , Fibrinolytiques/pharmacologie , Fibrinolytiques/composition chimique , Agrégation plaquettaire/effets des médicaments et des substances chimiques , Acide acétylsalicylique/pharmacologie , Mâle , Thrombose/traitement médicamenteux , Thrombose/prévention et contrôle , Rats , Artère pulmonaire/effets des médicaments et des substances chimiques , Collagène , Épinéphrine/pharmacologie , Souris , Plaquettes/effets des médicaments et des substances chimiques
18.
J Nippon Med Sch ; 91(3): 307-315, 2024.
Article de Anglais | MEDLINE | ID: mdl-38972743

RÉSUMÉ

BACKGROUND: Antithrombotic therapy (AT) should generally be avoided within 24 hours after recombinant tissue-plasminogen activator (rt-PA) treatment but should be considered in patients with large-artery atherosclerosis (LAA) who undergo concomitant emergent endovascular treatment (EVT). The aim of the present study was to assess the safety of AT within 24 hours after rt-PA treatment in patients with hyperacute ischemic stroke due to LAA who received concomitant EVT. METHODS: From January 2013 through July 2019, consecutive patients with acute ischemic cerebrovascular disease due to LAA who were admitted within 6 hours from symptom onset were recruited. The patients were classified into six groups based on the reperfusion treatment and early (within 24 hours) AT from rt-PA treatment. Safety outcomes were compared among the groups. RESULTS: A total of 155 patients (35 women [23%], median age 74 [IQR 66-79] years; NIHSS score 3 [1-10]) were included in the present study. Of these, 73 (47%) received no reperfusion therapy, 24 (15%) received rt-PA treatment and early AT, seven (6%) received rt-PA without early AT, 26 (17%) received EVT only, six (4%) received both rt-PA and EVT without early AT, and 19 (12%) received rt-PA and EVT with early AT. AT was administered a median of 3.9 (1.6-8.0) hours after rt-PA in patients with rt-PA+EVT with early AT. AT within 24 hours after rt-PA and EVT treatment did not increase hemorrhagic complications (p > 0.05 for all). CONCLUSION: In this retrospective analyses, early AT administration for patients with hyperacute stroke due to LAA treated with rt-PA plus EVT did not increase hemorrhagic events.


Sujet(s)
Athérosclérose , Procédures endovasculaires , Fibrinolytiques , Protéines recombinantes , Activateur tissulaire du plasminogène , Humains , Femelle , Sujet âgé , Mâle , Activateur tissulaire du plasminogène/effets indésirables , Activateur tissulaire du plasminogène/administration et posologie , Facteurs temps , Fibrinolytiques/effets indésirables , Fibrinolytiques/administration et posologie , Protéines recombinantes/administration et posologie , Protéines recombinantes/effets indésirables , Procédures endovasculaires/méthodes , Procédures endovasculaires/effets indésirables , Accident vasculaire cérébral/étiologie , Accident vasculaire cérébral/traitement médicamenteux , Accident vasculaire cérébral ischémique/traitement médicamenteux , Accident vasculaire cérébral ischémique/étiologie , Résultat thérapeutique , Études rétrospectives
19.
J Cardiothorac Surg ; 19(1): 422, 2024 Jul 04.
Article de Anglais | MEDLINE | ID: mdl-38965617

RÉSUMÉ

OBJECTIVE: Coronary artery bypass grafting (CABG) is associated with antithrombotic therapy in terms of postoperative adverse events; however, it is still unknown whether the early use of such drugs after CABG is safe and effective. In this study, we aim to evaluate the relationship between different postoperative antithrombotic strategies and in-hospital adverse events in patients undergoing isolated coronary artery bypass grafting surgery. METHODS: This was a single-center, retrospective cohort analysis of patients undergoing isolated CABG due to coronary artery disease (CAD) between 2001 and 2012. Data were extracted from the Medical Information Mart for Intensive Care III database. The patients involved were divided into the ASA (aspirin 81 mg per day only) or DAPT (aspirin plus clopidogrel 75 mg per day) group according to the antiplatelet strategy. Patients were also stratified into subgroups based on the type of anticoagulation. The in-hospital risk of bleeding and adverse events was investigated and compared between groups. Propensity score matching (PSM) was performed to reduce the potential effects of a selection bias. RESULTS: A total of 3274 patients were included in this study, with 2358 in the ASA group and 889 in the DAPT group. Following the PSM, no significant difference was seen in the risk of major bleeding between the two groups according to the PLATO, TIMI or GUSTO criteria. There was no difference in the postoperative mortality. In subgroup analysis, patients given anticoagulant therapy had an increased incidence of bleeding-related events. Multivariable analysis revealed that postoperative anticoagulant therapy and the early use of heparin, but not DAPT, were independent predictors of bleeding-related events. CONCLUSIONS: Postoperative DAPT was not associated with an increased occurrence of bleeding-related events in patients undergoing isolated CABG and appears to be a safe antiplatelet therapy. The addition of anticoagulants to antiplatelet therapy increased the risk of bleeding and should be considered cautiously in clinical practice.


Sujet(s)
Pontage aortocoronarien , Fibrinolytiques , Antiagrégants plaquettaires , Études rétrospectives , Études de cohortes , Pontage aortocoronarien/effets indésirables , Période postopératoire , Fibrinolytiques/usage thérapeutique , Clopidogrel/usage thérapeutique , Acide acétylsalicylique/usage thérapeutique , Antiagrégants plaquettaires/usage thérapeutique , Association de médicaments , Hémorragie/prévention et contrôle , Humains , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé
20.
Nagoya J Med Sci ; 86(2): 237-251, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38962406

RÉSUMÉ

The relationship between demographic/clinical characteristics, clinical outcomes and the development of hemorrhagic complications in patients with ischemic stroke who underwent reperfusion therapy has not been studied sufficiently. We have aimed to compare genders and age groups in terms of clinical features and outcome; and types of reperfusion treatments and clinical features regarding the development of hemorrhagic complications in patients with ischemic stroke who underwent recombinant tissue plasminogen activator (rtPA) and/or thrombectomy. Patients with acute ischemic stroke undergoing rtPA and/or thrombectomy were divided into six age groups. Parameters including hemorrhagic complications, anticoagulant and antiaggregant use, hyperlipidemia, smoking status, biochemical parameters, and comorbidities were documented. National Institutes of Health Stroke Scale (NIHSS) scores, modified Rankin Score (mRS) and Glasgow Coma Scale scores were recorded. Etiological classification of stroke was done. These parameters were compared in terms of age groups, genders, and hemorrhagic complications. Significant differences were found between age groups concerning hypertension, coronary artery disease, smoking status, and antiaggregant use. Rate of hemorrhagic complications in rtPA group was significantly lower when compared with other treatment groups. Hemorrhagic complications developed mostly in the rtPA+thrombectomy group. Among the patients who developed hemorrhagic complications, NIHSS scores on admission were found to be significantly lower in men than women. Admission, discharge, and 3rd month mRS values in men were significantly lower than those of women. Knowing demographic and clinical features of patients that may have an impact on the clinical course of ischemic stroke managed with reperfusion therapy will be useful in predicting the hemorrhagic complications and clinical outcomes.


Sujet(s)
Accident vasculaire cérébral ischémique , Thrombectomie , Activateur tissulaire du plasminogène , Humains , Mâle , Femelle , Sujet âgé , Accident vasculaire cérébral ischémique/épidémiologie , Adulte d'âge moyen , Thrombectomie/effets indésirables , Activateur tissulaire du plasminogène/usage thérapeutique , Reperfusion/effets indésirables , Reperfusion/méthodes , Sujet âgé de 80 ans ou plus , Fibrinolytiques/usage thérapeutique , Fibrinolytiques/effets indésirables , Facteurs âges , Facteurs sexuels , Résultat thérapeutique
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