Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 20 de 27
Filtrer
1.
Artif Organs ; 2024 Aug 03.
Article de Anglais | MEDLINE | ID: mdl-39096053

RÉSUMÉ

BACKGROUND: Pre-left ventricular assist device (LVAD) pectoralis muscle assessment, an estimate of sarcopenia, has been associated with postoperative mortality and gastrointestinal bleeding, though its association with inflammation, endotoxemia, length-of-stay (LOS), and readmissions remains underexplored. METHODS: This was a single-center cohort study of LVAD patients implanted 1/2015-10/2018. Preoperative pectoralis muscle area was measured on chest computed tomography (CT), adjusted for height squared to derive pectoralis muscle area index (PMI). Those with PMI in the lowest quintile were defined as low-PMI cohort; all others constituted the reference cohort. Biomarkers of inflammation (interleukin-6, adiponectin, tumor necrosis factor-α [TNFα]) and endotoxemia (soluble (s)CD14) were measured in a subset of patients. RESULTS: Of the 254 LVAD patients, 95 had a preoperative chest CT (median days pre-LVAD: 7 [IQR 3-13]), of whom 19 (20.0%) were in the low-PMI cohort and the remainder were in the reference cohort. Compared with the reference cohort, the low-PMI cohort had higher levels of sCD14 (2594 vs. 1850 ng/mL; p = 0.04) and TNFα (2.9 vs. 1.9 pg/mL; p = 0.03). In adjusted analyses, the low-PMI cohort had longer LOS (incidence rate ratio 1.56 [95% confidence interval 1.16-2.10], p = 0.004) and higher risk of 90-day and 1-year readmissions (subhazard ratio 5.48 [1.88-16.0], p = 0.002; hazard ratio 1.73 [1.02-2.94]; p = 0.04, respectively). CONCLUSIONS: Pre-LVAD PMI is associated with inflammation, endotoxemia, and increased LOS and readmissions.

2.
Clin Transplant ; 38(7): e15401, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-39023081

RÉSUMÉ

BACKGROUND: The use of glucagon-like-peptide 1 receptor agonists (GLP1-RA) has dramatically increased over the past 5 years for diabetes mellitus type 2 (T2DM) and obesity. These comorbidities are prevalent in adult heart transplant (HT) recipients. However, there are limited data evaluating the efficacy of this drug class in this population. The aim of the current study was to describe cardiometabolic changes in HT recipients prescribed GLP1-RA at a large-volume transplant center. METHODS: We retrospectively reviewed all adult HT recipients who received GLP1-RA after HT for a minimum of 1-month. Cardiometabolic parameters including body mass index (BMI), lipid panel, hemoglobin A1C, estimated glomerular filtration rate (eGFR), and NT-proBNP were compared prior to initiation of the drug and at most recent follow-up. We also evaluated for significant dose adjustments to immunosuppression after drug initiation and adverse effects leading to drug discontinuation. RESULTS: Seventy-four patients were included (28% female, 53% White, 20% Hispanic) and followed for a median of 383 days [IQR 209, 613] on a GLP1-RA. The majority of patients (n = 56, 76%) were prescribed semaglutide. The most common indication for prescription was T2DM alone (n = 33, 45%), followed by combined T2DM and obesity (n = 26, 35%). At most recent follow-up, mean BMI decreased from 33.3 to 31.5 kg/m2 (p < 0.0001), HbA1C from 7.3% to 6.7% (p = 0.005), LDL from 78.6 to 70.3 mg/dL (p = 0.018) and basal insulin daily dose from 32.6 to 24.8 units (p = 0.0002). CONCLUSION: HT recipients prescribed GLP1-RA therapy showed improved glycemic control, weight loss, and cholesterol levels during the study follow-up period. GLP1-RA were well tolerated and were rarely associated with changes in immunosuppression dosing.


Sujet(s)
Récepteur du peptide-1 similaire au glucagon , Transplantation cardiaque , Humains , Femelle , Mâle , Études rétrospectives , Adulte d'âge moyen , Récepteur du peptide-1 similaire au glucagon/agonistes , Transplantation cardiaque/effets indésirables , Études de suivi , Pronostic , Diabète de type 2/traitement médicamenteux , Débit de filtration glomérulaire , Hypoglycémiants/usage thérapeutique , Tests de la fonction rénale , Adulte , Complications postopératoires/traitement médicamenteux , Rejet du greffon/étiologie , Rejet du greffon/prévention et contrôle , Rejet du greffon/traitement médicamenteux ,
4.
J Card Fail ; 2024 Apr 13.
Article de Anglais | MEDLINE | ID: mdl-38616005

RÉSUMÉ

BACKGROUND: Sarcopenia is underappreciated in advanced heart failure and is not routinely assessed. In patients receiving a left ventricular assist device, preoperative sarcopenia, defined by using computed-tomography (CT)-derived pectoralis muscle-area index (muscle area indexed to body-surface area), is an independent predictor of postoperative mortality. The association between preoperative sarcopenia and outcomes after heart transplant (HT) is unknown. OBJECTIVES: The primary aim of this study was to determine whether preoperative sarcopenia, diagnosed using the pectoralis muscle-area index, is an independent predictor of days alive and out of the hospital (DAOHs) post-transplant. METHODS: Patients who underwent HT between January, 2018, and June, 2022, with available preoperative chest CT scans were included. Sarcopenia was diagnosed as pectoralis muscle-area index in the lowest sex-specific tertile. The primary endpoint was DAOHs at 1 year post-transplant. RESULTS: The study included 169 patients. Patients with sarcopenia (n = 55) had fewer DAOHs compared to those without sarcopenia, with a median difference of 17 days (320 vs 337 days; P = 0.004). Patients with sarcopenia had longer index hospitalizations and were also more likely to be discharged to a facility other than home. In a Poisson regression model, sarcopenia was a significant univariable and the strongest multivariable predictor of DAOHs at 1 year (parameter estimate = -0.17, 95% CI -0.19 to -14; P = < 0.0001). CONCLUSIONS: Preoperative sarcopenia, diagnosed using the pectoralis muscle-area index, is an independent predictor of poor outcomes after HT. This parameter is easily measurable from commonly obtained preoperative CT scans and may be considered in transplant evaluations.

7.
J Am Coll Cardiol ; 82(2): 128-138, 2023 07 11.
Article de Anglais | MEDLINE | ID: mdl-37306651

RÉSUMÉ

BACKGROUND: Although malnutrition is associated with poor prognosis in several diseases, its prognostic impact in patients with heart failure (HF) and secondary mitral regurgitation (SMR) is not understood. OBJECTIVES: The purpose of this study was to assess the prevalence and impact of malnutrition in HF patients with severe SMR randomized to transcatheter edge-to-edge repair (TEER) with the MitraClip plus guideline-directed medical therapy (GDMT) vs GDMT alone in the COAPT trial. METHODS: Baseline malnutrition risk was calculated using the validated geriatric nutritional risk index (GNRI) score. Patients were categorized as having "malnutrition" (GNRI ≤98) vs "no malnutrition" (GNRI >98). Outcomes were assessed through 4 years. The primary endpoint of interest was all-cause mortality. RESULTS: Among 552 patients, median baseline GNRI was 109 (IQR: 101-116); 94 (17.0%) had malnutrition. All-cause mortality at 4 years was greater in patients with vs those without malnutrition (68.3% vs 52.8%; P = 0.001). Using multivariable analysis, both baseline malnutrition (adjusted-HR [adj-HR]: 1.37; 95% CI: 1.03-1.82; P = 0.03) and randomization to TEER plus GDMT compared with GDMT alone (adj-HR: 0.65; 95% CI: 0.51-0.82; P = 0.0003) were independent predictors of 4-year mortality. In contrast, GNRI was unrelated to the 4-year rate of heart failure hospitalization (HFH), although TEER treatment reduced HFH (adj-HR: 0.46; 95% CI: 0.36-0.56). The reductions in death (adj-Pinteraction = 0.46) and HFH (adj-Pinteraction = 0.67) with TEER were consistent in patients with and without malnutrition. CONCLUSIONS: Malnutrition was present in 1 of 6 patients with HF and severe SMR enrolled in COAPT and was independently associated with increased 4-year mortality (but not HFH). TEER reduced mortality and HFH in patients with and without malnutrition. (Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients With Functional Mitral Regurgitation [The COAPT Trial] and COAPT CAS [COAPT]; NCT01626079).


Sujet(s)
Défaillance cardiaque , Implantation de valve prothétique cardiaque , Insuffisance mitrale , Humains , Sujet âgé , Insuffisance mitrale/complications , Insuffisance mitrale/épidémiologie , Insuffisance mitrale/chirurgie , Valve atrioventriculaire gauche/chirurgie , Pronostic , , Défaillance cardiaque/complications , Défaillance cardiaque/épidémiologie , Défaillance cardiaque/thérapie , Résultat thérapeutique
9.
Clin Transplant ; 36(12): e14831, 2022 12.
Article de Anglais | MEDLINE | ID: mdl-36271917

RÉSUMÉ

BACKGROUND: Significant weight loss due to cardiac cachexia is an independent predictor of mortality in many heart failure (HF) clinical trials. The impact of significant weight loss while on the waitlist for heart transplant (HT) has yet to be studied with respect to post-transplant survival. METHODS: Adult HT recipients from 2010 to 2021 were identified in the UNOS registry. Patients who experienced an absolute weight change from the time of listing to transplant were included and classified into two groups by percent weight loss from time of listing to time of transplant using a cut-off of 10%. The primary endpoint was 1-year survival following HT. RESULTS: 5951 patients were included in the analysis, of whom 763 (13%) experienced ≥10% weight loss from the time of listing to transplant. Weight loss ≥ 10% was associated with reduced 1-year post-transplant survival (86.9% vs. 91.0%, long-rank p = .0003). Additionally, weight loss ≥ 10% was an independent predictor of 1-year mortality in a multivariable model adjusting for significant risk factors (adjusted HR 1.23, 95% CI 1.04-1.46). In secondary analyses, weight loss ≥ 10% was associated with reduced 1-year survival independent of hospitalized status at time of transplant as well as obesity status at listing (i.e., body mass index [BMI] < 30 kg/m2 and BMI ≥ 30 kg/m2 ). CONCLUSIONS: Preoperative weight loss ≥ 10% is associated with reduced survival in patients listed for HT. Nutrition interventions prior to transplant may prove beneficial in this population.


Sujet(s)
Défaillance cardiaque , Transplantation cardiaque , Adulte , Humains , Études rétrospectives , Obésité/épidémiologie , Perte de poids , Listes d'attente
10.
JACC Case Rep ; 4(7): 433-437, 2022 Apr 06.
Article de Anglais | MEDLINE | ID: mdl-35693901

RÉSUMÉ

We present the case of a woman with upper gastrointestinal bleeding secondary to gastric varices requiring endoscopic cyanoacrylate glue and coil embolization. The procedure was complicated by regular, wide-complex tachycardia, with further investigation revealing cardiopulmonary migration of the glue and coil. (Level of Difficulty: Advanced.).

11.
J Am Coll Cardiol ; 79(16): 1623-1635, 2022 04 26.
Article de Anglais | MEDLINE | ID: mdl-35450580

RÉSUMÉ

Despite the high prevalence of nutrition disorders in patients with heart failure (HF), major HF guidelines lack specific nutrition recommendations. Because of the lack of standardized definitions and assessment tools to quantify nutritional status, nutrition disorders are often missed in patients with HF. Additionally, a wide range of dietary interventions and overall dietary patterns have been studied in this population. The resulting evidence of benefit is, however, conflicting, making it challenging to determine which strategies are the most beneficial. In this document, we review the available nutritional status assessment tools for patients with HF. In addition, we appraise the current evidence for dietary interventions in HF, including sodium restriction, obesity, malnutrition, dietary patterns, and specific macronutrient and micronutrient supplementation. Furthermore, we discuss the feasibility and challenges associated with the implementation of multimodal nutrition interventions and delineate potential solutions to facilitate addressing nutrition in patients with HF.


Sujet(s)
Défaillance cardiaque , Malnutrition , Défaillance cardiaque/complications , Défaillance cardiaque/thérapie , Humains , Malnutrition/prévention et contrôle , Évaluation de l'état nutritionnel , État nutritionnel , Obésité/complications
12.
Rev Endocr Metab Disord ; 23(2): 293-297, 2022 04.
Article de Anglais | MEDLINE | ID: mdl-35233703

RÉSUMÉ

Patients with pre-existing cardiovascular disease (CVD) are at high risk for adverse outcomes with coronavirus disease 2019 (COVID-19). Further, COVID-19 infection is associated with numerous cardiovascular (CV) complications including arrhythmia, myocardial injury, cardiomyopathy, and thrombotic events. Increased susceptibility to COVID-19 and CV complications related to COVID-19 may be in part related to immune dysregulation and inflammation associated with CV disease which is exacerbated with viral infection. Vitamin D plays a major role in immune function and exerts anti-inflammatory effects, which may prove important in the context of CVD and COVID-19. To date, studies have shown minimal benefit for vitamin D supplementation in patients with COVID-19, though there are no studies specific to patients with CVD and related complications. Further, given that vitamin D has important protective effects on the CV system, including augmentation of myocardial contractility and anti-thrombotic effects, it is unknown if supplementation with vitamin D can mitigate CVD complications associated with COVID-19.


Sujet(s)
Traitements médicamenteux de la COVID-19 , COVID-19 , Maladies cardiovasculaires , Carence en vitamine D , COVID-19/complications , Maladies cardiovasculaires/étiologie , Maladies cardiovasculaires/prévention et contrôle , Humains , Vitamine D/physiologie , Vitamine D/usage thérapeutique , Carence en vitamine D/complications , Carence en vitamine D/traitement médicamenteux , Vitamines/usage thérapeutique
13.
Annu Int Conf IEEE Eng Med Biol Soc ; 2021: 7170-7173, 2021 11.
Article de Anglais | MEDLINE | ID: mdl-34892754

RÉSUMÉ

This study presents our recent findings on the classification of mean pressure gradient using angular chest movements in aortic stenosis (AS) patients. Currently, the severity of aortic stenosis is measured using ultra-sound echocardiography, which is an expensive technology. The proposed framework motivates the use of low-cost wearable sensors, and is based on feature extraction from gyroscopic readings. The feature space consists of the cardiac timing intervals as well as heart rate variability (HRV) parameters to determine the severity of disease. State-of-the-art machine learning (ML) methods are employed to classify the severity levels into mild, moderate, and severe. The best performance is achieved by the Light Gradient-Boosted Machine (Light GBM) with an F1-score of 94.29% and an accuracy of 94.44%. Additionally, game theory-based analyses are employed to examine the top features along with their average impacts on the severity level. It is demonstrated that the isovolumetric contraction time (IVCT) and isovolumetric relaxation time (IVRT) are the most representative features for AS severity.Clinical Relevance- The proposed framework could be an appropriate low-cost alternative to ultra-sound echocardiography, which is a costly method.


Sujet(s)
Sténose aortique , Algorithmes , Échocardiographie , Rythme cardiaque , Humains , Respiration
14.
Sci Rep ; 11(1): 23817, 2021 12 10.
Article de Anglais | MEDLINE | ID: mdl-34893693

RÉSUMÉ

Recent research has shown promising results for the detection of aortic stenosis (AS) using cardio-mechanical signals. However, they are limited by two main factors: lacking physical explanations for decision-making on the existence of AS, and the need for auxiliary signals. The main goal of this paper is to address these shortcomings through a wearable inertial measurement unit (IMU), where the physical causes of AS are determined from IMU readings. To this end, we develop a framework based on seismo-cardiogram (SCG) and gyro-cardiogram (GCG) morphologies, where highly-optimized algorithms are designed to extract features deemed potentially relevant to AS. Extracted features are then analyzed through machine learning techniques for AS diagnosis. It is demonstrated that AS could be detected with 95.49-100.00% confidence. Based on the ablation study on the feature space, the GCG time-domain feature space holds higher consistency, i.e., 95.19-100.00%, with the presence of AS than HRV parameters with a low contribution of 66.00-80.00%. Furthermore, the robustness of the proposed method is evaluated by conducting analyses on the classification of the AS severity level. These analyses are resulted in a high confidence of 92.29%, demonstrating the reliability of the proposed framework. Additionally, game theory-based approaches are employed to rank the top features, among which GCG time-domain features are found to be highly consistent with both the occurrence and severity level of AS. The proposed framework contributes to reliable, low-cost wearable cardiac monitoring due to accurate performance and usage of solitary inertial sensors.


Sujet(s)
Sténose aortique/diagnostic , Valve aortique/imagerie diagnostique , Valve aortique/anatomopathologie , Valve aortique/physiopathologie , Rythme cardiaque , Sujet âgé , Sujet âgé de 80 ans ou plus , Algorithmes , Analyse de données , Électrocardiographie , Femelle , Humains , Mâle , Modèles théoriques
15.
Am J Cardiol ; 153: 94-100, 2021 08 15.
Article de Anglais | MEDLINE | ID: mdl-34217433

RÉSUMÉ

We aimed to investigate the relationship of modified body mass index (mBMI), the product of BMI and serum albumin, with survival after transcatheter (TAVI) and surgical aortic valve implantation (SAVI). Frailty is associated with poor outcomes after TAVI and SAVI for severe aortic stenosis (AS). However, clinical frailty is not routinely measured in clinical practice due to the cumbersome nature of its assessment. Modified BMI is an easily measurable surrogate for clinical frailty that is associated with survival in elderly cohorts with non-valvular heart disease. We utilized individual patient-level data from a pooled database of the Placement of Aortic Transcatheter Valves (PARTNER) trials from the PARNTER1, PARTNER2 and S3 cohorts. We estimated cumulative mortality at 1 year for quartiles of mBMI with the Kaplan-Meier method and compared them with the log-rank test. We performed Cox proportional hazards modeling to assess the association of mBMI strata with 1-year mortality adjusting for baseline clinical characteristics. A total of 6593 patients who underwent TAVI or SAVI (mean age 83±7.3 years, 57% male) were included. mBMI was independently associated with all-cause one-year mortality with the lowest mBMI quartile as most predictive (HR 2.33, 95% CI 1.80-3.02, p < 0.0001). Notably, mBMI performed as well as clinical frailty index to predict 1-year mortality in this cohort. In conclusion, modified BMI predicts 1-year survival after both TAVI and SAVI. Given that it performed similar to the clinical frailty index, it may be used as a clinical tool for assessment of frailty prior to valve implantation.


Sujet(s)
Sténose aortique/chirurgie , Indice de masse corporelle , Fragilité/épidémiologie , Mortalité , Sérumalbumine/métabolisme , Activités de la vie quotidienne , Atteinte rénale aigüe/épidémiologie , Sujet âgé , Sujet âgé de 80 ans ou plus , Entraînement électrosystolique , Maladies cardiovasculaires/mortalité , Cause de décès , Femelle , Fragilité/diagnostic , Fragilité/métabolisme , Force de la main , Implantation de valve prothétique cardiaque , Hémorragie/épidémiologie , Humains , Estimation de Kaplan-Meier , Mâle , Pacemaker , Réadmission du patient , Complications postopératoires/épidémiologie , Hémorragie postopératoire/épidémiologie , Pronostic , Modèles des risques proportionnels , Accident vasculaire cérébral/épidémiologie , Remplacement valvulaire aortique par cathéter , Vitesse de marche
17.
Amyloid ; 28(1): 30-34, 2021 Mar.
Article de Anglais | MEDLINE | ID: mdl-32814468

RÉSUMÉ

BACKGROUND: Atrial fibrillation (AF) is common in patients with transthyretin cardiac amyloidosis (ATTR-CA). The optimal strategy to prevent strokes in patients with ATTR-CA and AF is unknown. OBJECTIVES: To compare outcomes in patients with ATTR-CA and AF treated with warfarin versus novel oral anticoagulants (NOACs). METHODS: This study was a retrospective analysis of patients with ATTR-CA stratified by presence or absence of AF and anticoagulation therapy. The primary outcome included a time to event analysis for the combined outcomes of stroke, transient ischaemic attack (TIA), major bleed, or death. RESULTS: Of 290 patients, 217 patients (74.8%) had AF. Of those with AF (n = 217), 78 (35.9%) patients received warfarin compared with 116 (53.5%) patients who received NOACs. There were 17 thrombotic events, all in those diagnosed with AF compared with none in the patients without AF (p = .01). Over a mean follow-up of 2.4 years (range 0.1-12) there was no difference in primary outcome between those with AF treated with warfarin compared with NOACs (p = .35). CONCLUSION: Patient with ATTR-CA and AF are at increased risk for stroke compared to patients with ATTR-CA and without AF. Thrombotic events and major bleeds did not differ between those who received warfarin and NOACs.


Sujet(s)
Neuropathies amyloïdes familiales/traitement médicamenteux , Inhibiteurs du facteur Xa/administration et posologie , Hémorragie/traitement médicamenteux , Accident vasculaire cérébral/traitement médicamenteux , Warfarine/administration et posologie , Sujet âgé , Sujet âgé de 80 ans ou plus , Neuropathies amyloïdes familiales/complications , Neuropathies amyloïdes familiales/métabolisme , Neuropathies amyloïdes familiales/anatomopathologie , Fibrillation auriculaire/traitement médicamenteux , Fibrillation auriculaire/étiologie , Fibrillation auriculaire/métabolisme , Fibrillation auriculaire/anatomopathologie , Femelle , Hémorragie/sang , Hémorragie/étiologie , Humains , Accident ischémique transitoire/sang , Accident ischémique transitoire/traitement médicamenteux , Accident ischémique transitoire/anatomopathologie , Accident ischémique transitoire/prévention et contrôle , Mâle , Adulte d'âge moyen , Accident vasculaire cérébral/étiologie , Accident vasculaire cérébral/prévention et contrôle , Thrombose/traitement médicamenteux , Thrombose/anatomopathologie , Thrombose/prévention et contrôle , Warfarine/effets indésirables
19.
Thromb Haemost ; 120(7): 1004-1024, 2020 Jul.
Article de Anglais | MEDLINE | ID: mdl-32473596

RÉSUMÉ

Coronavirus disease 2019 (COVID-19), currently a worldwide pandemic, is a viral illness caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The suspected contribution of thrombotic events to morbidity and mortality in COVID-19 patients has prompted a search for novel potential options for preventing COVID-19-associated thrombotic disease. In this article by the Global COVID-19 Thrombosis Collaborative Group, we describe novel dosing approaches for commonly used antithrombotic agents (especially heparin-based regimens) and the potential use of less widely used antithrombotic drugs in the absence of confirmed thrombosis. Although these therapies may have direct antithrombotic effects, other mechanisms of action, including anti-inflammatory or antiviral effects, have been postulated. Based on survey results from this group of authors, we suggest research priorities for specific agents and subgroups of patients with COVID-19. Further, we review other agents, including immunomodulators, that may have antithrombotic properties. It is our hope that the present document will encourage and stimulate future prospective studies and randomized trials to study the safety, efficacy, and optimal use of these agents for prevention or management of thrombosis in COVID-19.


Sujet(s)
Infections à coronavirus/immunologie , Fibrinolytiques/usage thérapeutique , Inflammation/traitement médicamenteux , Pneumopathie virale/immunologie , Thrombose/traitement médicamenteux , Animaux , Anti-inflammatoires/usage thérapeutique , Anticoagulants/usage thérapeutique , Antiviraux/usage thérapeutique , Betacoronavirus , COVID-19 , Infections à coronavirus/complications , Infections à coronavirus/traitement médicamenteux , Glycosaminoglycanes/usage thérapeutique , Hémostase , Humains , Inflammation/complications , Inflammation/immunologie , Pandémies , Antiagrégants plaquettaires/usage thérapeutique , Pneumopathie virale/complications , Pneumopathie virale/traitement médicamenteux , SARS-CoV-2 , Thrombose/complications , Thrombose/immunologie , Traitements médicamenteux de la COVID-19
20.
J Am Coll Cardiol ; 75(23): 2950-2973, 2020 06 16.
Article de Anglais | MEDLINE | ID: mdl-32311448

RÉSUMÉ

Coronavirus disease-2019 (COVID-19), a viral respiratory illness caused by the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), may predispose patients to thrombotic disease, both in the venous and arterial circulations, because of excessive inflammation, platelet activation, endothelial dysfunction, and stasis. In addition, many patients receiving antithrombotic therapy for thrombotic disease may develop COVID-19, which can have implications for choice, dosing, and laboratory monitoring of antithrombotic therapy. Moreover, during a time with much focus on COVID-19, it is critical to consider how to optimize the available technology to care for patients without COVID-19 who have thrombotic disease. Herein, the authors review the current understanding of the pathogenesis, epidemiology, management, and outcomes of patients with COVID-19 who develop venous or arterial thrombosis, of those with pre-existing thrombotic disease who develop COVID-19, or those who need prevention or care for their thrombotic disease during the COVID-19 pandemic.


Sujet(s)
Anticoagulants/pharmacologie , Betacoronavirus/isolement et purification , Infections à coronavirus , Fibrinolytiques/pharmacologie , Pandémies , Antiagrégants plaquettaires/pharmacologie , Pneumopathie virale , Thromboembolie , COVID-19 , Infections à coronavirus/sang , Infections à coronavirus/complications , Infections à coronavirus/épidémiologie , Infections à coronavirus/thérapie , Humains , Pneumopathie virale/sang , Pneumopathie virale/complications , Pneumopathie virale/épidémiologie , Pneumopathie virale/thérapie , SARS-CoV-2 , Thromboembolie/traitement médicamenteux , Thromboembolie/épidémiologie , Thromboembolie/étiologie , Thromboembolie/physiopathologie , Résultat thérapeutique
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE