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2.
Ann Card Anaesth ; 27(3): 263-265, 2024 Jul 01.
Article de Anglais | MEDLINE | ID: mdl-38963365

RÉSUMÉ

ABSTRACT: Intraoperative aortic dissection is a life-threatening emergency. The prognosis of patients with aortic dissection has markedly improved in recent years due to prompt diagnosis and the institution of effective medical and surgical therapy. Transesophageal echocardiography (TEE) is helpful in the evaluation of this life-threatening disorder.


Sujet(s)
Aorte , , Échocardiographie transoesophagienne , Complications peropératoires , Humains , /chirurgie , /imagerie diagnostique , Échocardiographie transoesophagienne/méthodes , Aorte/chirurgie , Aorte/imagerie diagnostique , Complications peropératoires/imagerie diagnostique , Anévrysme de l'aorte/chirurgie , Anévrysme de l'aorte/imagerie diagnostique , Mâle , Femelle , Adulte d'âge moyen
4.
Ital J Pediatr ; 50(1): 122, 2024 Jun 26.
Article de Anglais | MEDLINE | ID: mdl-38926831

RÉSUMÉ

BACKGROUND: Arterial switch operation (ASO) is the standard surgical choice for D-transposition of great arteries (D-TGA). However, the implications of ASO on pulmonaries, coronaries, and aorta have not been adequately investigated. The current study evaluates arterial morphologic changes post-ASO at intermediate-term surveillance. METHODS: From May 2021 to May 2022, patients with D-TGA who underwent ASO for more than six months were recruited. Preoperative and operative data were collected. Patients were assessed using echocardiography (ECHO) and multislice CT angiography (MSCT) to evaluate pulmonary, coronary, and aortic arterial anatomy. RESULTS: Twenty patients were included with median age of 11 (10-23.25) days at ASO and 14 (7.25-32.75) months on last follow-up. Neo-aortic regurgitation was detected in 12(60%) and neo-pulmonary regurgitation in 3 (15%). Using ECHO, complete evaluation of pulmonary arteries (PAs) was not achieved in 35% and incomplete coronaries assessment in 40% of cases. No stenosis was detected in coronaries using MSCT, although coronary anomalies were found in 9/20 (45%). Dilated Aortic annulus was detected in 16/20 (80%), dilated aortic root in 18/20 (90%), and dilated sinotubular junction in 70%. Right PA stenosis was diagnosed in 10/20 (50%) and left PA(LPA) stenosis in 7/20 (35%). Although Z-score of PAs did not correlate with aortic data, LPA bending angle was positively correlated to neo-aortic root diameter and Z-score (rho = 0.65,p = 0.016; rho = 0.69,p = 0.01), respectively. CONCLUSION: Echocardiography alone is not a conclusive surveillance tool for detecting late post-ASO anatomic changes in D-TGA patients. Cardiac MSCT should be considered for comprehensive evaluation on the intermediate-term follow-up post-ASO to accurately track morphologic abnormalities in the aorta, pulmonary, and coronary arteries.


Sujet(s)
Détransposition artérielle , Échocardiographie , Tomodensitométrie multidétecteurs , Artère pulmonaire , Transposition des gros vaisseaux , Humains , Mâle , Femelle , Transposition des gros vaisseaux/imagerie diagnostique , Transposition des gros vaisseaux/chirurgie , Nourrisson , Nouveau-né , Détransposition artérielle/effets indésirables , Artère pulmonaire/imagerie diagnostique , Enfant d'âge préscolaire , Vaisseaux coronaires/imagerie diagnostique , Aorte/imagerie diagnostique , Études rétrospectives , Angiographie par tomodensitométrie , Études de suivi
5.
Tuberk Toraks ; 72(2): 137-144, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38869206

RÉSUMÉ

Introduction: This study explores the impact of vascular diameters on mortality risk in Coronavirus disease-2019 (COVID-19) patients. COVID-19, caused by severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2), presents diverse clinical manifestations and is associated with thrombosis. Materials and Methods: In this study, we retrospectively examined the data of patients who were hospitalized and treated in our hospital between September 1, 2020, and November 30, 2020, and whose COVID-19 diagnosis was confirmed by reverse transcriptase polymerase chain reaction (RT-PCR). The diameters of the ascending aorta, main pulmonary artery, and right and left pulmonary arteries were measured from the chest computed tomography (CT) scans taken at the time of admission. The aim of the study was to investigate the impact of vascular diameters on the course of the disease. Result: Of 1.705 patients, 840 were eligible for the study. We concluded that 36 of the patients (4.3%) died, and among the non-survivors patients, 12 (33.3%) were females, and 24 (66.7%) were males. Hospitalization duration was 7.1 ± 3.1 vs. 6.1 ± 2 days (p= 0.004) in surviving and non-surviving patients respectively. On the other hand, we found the mean diameters of the right pulmonary artery in the chest CT of patients to be 2.17 ± 0.35 vs. 2.44 ± 0.29 cm in survivors and non-survivors, respectively (p< 0.001). In addition, we found the mean diameters of the left pulmonary artery 2.12 ± 0.32 vs. 2.34 ± 0.28 cm in survivors and non-survivors, respectively (p< 0.001). Mean diameters of the ascending aorta were 3.53 ± 0.46 vs. 3.72 ± 0.34 cm in survivors and non-survivors, respectively (p= 0.017). Conclusions: The study underscores the potential prognostic value of vascular diameters, especially in the ascending aorta and main pulmonary artery, as indicators of mortality risk in COVID-19 patients. The association between vascular dilation and severity of COVID-19, coupled with elevated D-dimer levels, suggests a link between thrombosis and vascular involvement.


Sujet(s)
Aorte , COVID-19 , Artère pulmonaire , Humains , COVID-19/mortalité , COVID-19/complications , Mâle , Femelle , Artère pulmonaire/imagerie diagnostique , Artère pulmonaire/anatomopathologie , Études rétrospectives , Adulte d'âge moyen , Aorte/imagerie diagnostique , Sujet âgé , SARS-CoV-2 , Durée du séjour/statistiques et données numériques , Tomodensitométrie , Hospitalisation/statistiques et données numériques , Turquie/épidémiologie , Adulte
6.
J Vet Sci ; 25(3): e37, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38834507

RÉSUMÉ

IMPORTANCE: The portal vein to aorta (PV/Ao) ratio is used to assess the clinical significance of extrahepatic portosystemic shunt (EHPSS). Previous studies using computed tomography (CT) were conducted in dogs but not in cats. OBJECTIVE: This study aimed to establish normal reference values for PV indices (PV/Ao ratio and PV diameter) in cats and determine the usefulness of these for predicting symptomatic EHPSS. METHODS: This study included 95 dogs and 114 cats that underwent abdominal CT. The canine normal (CN) group included dogs without EHPSS. The cats were classified into feline normal (FN, 88/114), feline asymptomatic (FA, 16/114), and feline symptomatic (FS, 10/114) groups. The PV and Ao diameters were measured in axial cross-sections. RESULTS: The group FN had a higher PV/Ao ratio than the group CN (p < 0.001). Within the feline groups, the PV indices were in the order FN > FA > FS (both p < 0.001). The mean PV diameter and PV/Ao ratio for group FN were 5.23 ± 0.77 mm and 1.46 ± 0.19, respectively. The cutoff values between groups FN and FS were 4.115 mm for PV diameter (sensitivity, 100%; specificity, 97.7%) and 1.170 for PV/Ao ratio (90%, 92.1%). The cutoff values between group FA and FS were 3.835 mm (90%, 93.8%) and 1.010 (70%, 100%), respectively. CONCLUSIONS AND RELEVANCE: The results demonstrated significant differences in PV indices between dogs and cats. In cats, the PV/Ao ratio demonstrated high diagnostic performance for symptomatic EHPSS. The PV diameter also performed well, in contrast to dogs.


Sujet(s)
Maladies des chats , Veine porte , Tomodensitométrie , Animaux , Chats , Veine porte/imagerie diagnostique , Veine porte/malformations , Maladies des chats/imagerie diagnostique , Mâle , Femelle , Tomodensitométrie/médecine vétérinaire , Chiens , Maladies des chiens/imagerie diagnostique , Valeurs de référence , Aorte/imagerie diagnostique
8.
J Cardiothorac Surg ; 19(1): 346, 2024 Jun 21.
Article de Anglais | MEDLINE | ID: mdl-38907334

RÉSUMÉ

BACKGROUND: Aneurysms of the pulmonary arteries and the ascending aorta are rare, and both bear a high mortality risk if left untreated. In general, these entities are primarily caused by etiologies such as hypertension, pulmonary arterial hypertension, infection or congenital disorders. Treatment requires a rapid diagnostic work-up or even immediate surgical intervention in acute cases. Nevertheless, surgery entails serious perioperative risks, in particular in patients with multiple comorbidities. CASE PRESENTATION: We discuss a 70-year-old woman presented with decompensated heart failure based on severe pulmonary artery hypertension, coincided by a massive pulmonary artery aneurysm with secondary embolism. Additional diagnostic imaging also showed a chronic post-dissection, saccular aneurysm of the ascending aorta. To our knowledge, this simultaneous diagnosis of a saccular aneurysm of the ascending aorta and a large aneurysm of the pulmonary artery with secondary embolism has not yet been described. Nonetheless, conservative treatment was chosen due to extensive pulmonal and cardiovascular comorbidities and the high-risk profile of surgery. CONCLUSIONS: Extensive aneurysmatic disease of the pulmonary arteries and ascending aorta come with a serious burden of disease, especially if coincided by severe pulmonal and cardiovascular comorbidities. Both conditions can be curatively treated by surgical intervention. However, in every case the risk of surgery and the patient's vitality, comorbidities and wishes should be taken into account to formulate an adequate treatment plan. Therefore, shared decision making is of utter importance.


Sujet(s)
, Artère pulmonaire , Humains , Femelle , Artère pulmonaire/chirurgie , Artère pulmonaire/imagerie diagnostique , Sujet âgé , /chirurgie , /complications , Aorte/chirurgie , Aorte/imagerie diagnostique , Anévrysme de l'aorte/chirurgie , Anévrysme de l'aorte/imagerie diagnostique , Anévrysme de l'aorte/complications , Anévrysme/chirurgie , Anévrysme/complications , Anévrysme/imagerie diagnostique
9.
Glob Heart ; 23: 28, 2024.
Article de Anglais | MEDLINE | ID: mdl-38737456

RÉSUMÉ

Background: Patients diagnosed with Marfan syndrome or a related syndrome require frequent aorta monitoring using imaging techniques like transthoracic echocardiography (TTE) and computed tomography (CT). Accurate aortic measurement is crucial, as even slight enlargement (>2 mm) often necessitates surgical intervention. The 2022 ACC/AHA guideline for Aortic Disease Diagnosis and Management includes updated imaging recommendations. We aimed to compare these with the 2010 guideline. Methods: This retrospective study involved 137 patients with Marfan syndrome or a related disorder, undergoing TTE and ECG-triggered CT. Aortic diameter measurements were taken based on the old 2010 guideline (TTE: inner edge to inner edge, CT: external diameter) and the new 2022 guideline (TTE: leading edge to leading edge, CT: internal diameter). Bland-Altman plots compared measurement differences. Results: Using the 2022 guideline significantly reduced differences outside the clinical agreement limit from 49% to 26% for the aortic sinus and from 41% to 29% for the ascending aorta. Mean differences were -0.30 mm for the aortic sinus and +1.12 mm for the ascending aorta using the 2022 guideline, compared to -2.66 mm and +1.21 mm using the 2010 guideline. Conclusion: This study demonstrates for the first time that the 2022 ACC/AHA guideline improves concordance between ECG-triggered CT and TTE measurements in Marfan syndrome patients, crucial for preventing life-threatening aortic complications. However, the frequency of differences >2 mm remains high. Clinical Relevance/Application: Accurate aortic diameter measurement is vital for patients at risk of fatal aortic complications. While the 2022 guideline enhances concordance between imaging modalities, frequent differences >2 mm persist, potentially impacting decisions on aortic repair. The risk of repeat radiation exposure from ECG-triggered CT, considered the 'gold standard', continues to be justified.


Sujet(s)
Échocardiographie , Syndrome de Marfan , Tomodensitométrie , Humains , Syndrome de Marfan/imagerie diagnostique , Syndrome de Marfan/diagnostic , Études rétrospectives , Mâle , Femelle , Échocardiographie/méthodes , Adulte , Tomodensitométrie/méthodes , Adulte d'âge moyen , Guides de bonnes pratiques cliniques comme sujet , États-Unis/épidémiologie , Jeune adulte , Aorte/imagerie diagnostique , Adolescent
10.
Ren Fail ; 46(1): 2355352, 2024 Dec.
Article de Anglais | MEDLINE | ID: mdl-38785291

RÉSUMÉ

Background: Recent studies have shown that the baseline values of absolute aortic root diameter (ARD) and indexed diameter are associated with all-cause mortality and cardiovascular events in the general population, even in the absence of aneurysmal aortic disease. However, there is limited available data on the association between ARD and prognosis in end-stage renal disease (ESRD) patients receiving maintenance hemodialysis (MHD). Accordingly, the purpose of this study is to investigate the predictive value of ARD for all-cause mortality and cardiovascular events in this specific population.Methods: ARD was measured by echocardiography at the level of the sinuses of Valsalva at end diastole and indexed to body surface area (BSA). The primary endpoint was all-cause mortality. The secondary endpoint was major adverse cardiovascular events (MACE), including cardiovascular mortality, myocardial infarction and stroke. Cox proportional hazards models were conducted to evaluate the association between baseline ARD/BSA and clinical outcomes.Results: A total of 391 patients were included in this study. The primary endpoint occurred in 95 (24.3%) patients while the secondary endpoint occurred in 71 (18.2%) patients. Multivariate Cox regression analysis showed that ARD/BSA was an independent prognostic factor for all-cause mortality (HR, per 1-SD increase, 1.403; 95% CI, 1.118-1.761; p = 0.003) as well as MACE (HR, per 1-SD increase, 1.356; 95% CI, 1.037-1.772; p = 0.026).Conclusions: Our results show that ARD/BSA is predictive of all-cause mortality and MACE in MHD patients with ESRD and support the view that assessment of ARD/BSA may refine risk stratification and preventive strategies in this population.


Sujet(s)
Échocardiographie , Défaillance rénale chronique , Dialyse rénale , Humains , Mâle , Défaillance rénale chronique/thérapie , Défaillance rénale chronique/complications , Défaillance rénale chronique/mortalité , Femelle , Adulte d'âge moyen , Pronostic , Sujet âgé , Aorte/imagerie diagnostique , Aorte/anatomopathologie , Études rétrospectives , Modèles des risques proportionnels , Maladies cardiovasculaires/mortalité , Maladies cardiovasculaires/étiologie , Facteurs de risque
11.
Sci Rep ; 14(1): 10409, 2024 05 06.
Article de Anglais | MEDLINE | ID: mdl-38710782

RÉSUMÉ

In transcatheter aortic valve implantation (TAVI), final device position may be affected by device interaction with the whole aortic landing zone (LZ) extending to ascending aorta. We investigated the impact of aortic LZ curvature and angulation on TAVI implantation depth, comparing short-frame balloon-expanding (BE) and long-frame self-expanding (SE) devices. Patients (n = 202) treated with BE or SE devices were matched based on one-to-one propensity score. Primary endpoint was the mismatch between the intended (HPre) and the final (HPost) implantation depth. LZ curvature and angulation were calculated based on the aortic centerline trajectory available from pre-TAVI computed tomography. Total LZ curvature ( k L Z , t o t ) and LZ angulation distal to aortic annulus ( α L Z , D i s t a l ) were greater in the SE compared to the BE group (P < 0.001 for both). In the BE group, HPost was significantly higher than HPre at both cusps (P < 0.001). In the SE group, HPost was significantly deeper than HPre only at the left coronary cusp (P = 0.013). At multivariate analysis, α L Z , D i s t a l was the only independent predictor (OR = 1.11, P = 0.002) of deeper final implantation depth with a cut-off value of 17.8°. Aortic LZ curvature and angulation significantly affected final TAVI implantation depth, especially in high stent-frame SE devices reporting, upon complete release, deeper implantation depth with respect to the intended one.


Sujet(s)
Sténose aortique , Valve aortique , Remplacement valvulaire aortique par cathéter , Remplacement valvulaire aortique par cathéter/méthodes , Humains , Mâle , Femelle , Sujet âgé de 80 ans ou plus , Sujet âgé , Valve aortique/chirurgie , Valve aortique/imagerie diagnostique , Sténose aortique/chirurgie , Tomodensitométrie , Aorte/imagerie diagnostique , Aorte/chirurgie , Résultat thérapeutique , Prothèse valvulaire cardiaque , Études rétrospectives
12.
Int J Cardiol ; 408: 132067, 2024 Aug 01.
Article de Anglais | MEDLINE | ID: mdl-38714235

RÉSUMÉ

AIMS: The aim of this study is to evaluate the effect of beta-blockers and angiotensin receptor blockers in reducing the aortic growth rate in children with bicuspid aortic valve (BAV)-related aortopathy and ascending phenotype. METHODS: Consecutive paediatric patients (≤16 years) with BAV and ascending aorta (AsAo) dilation (z-score > 3) were enrolled in this observational retrospective cohort study. Patients receiving prophylactic treatment with either atenolol (0.5 to 1.0 mg/kg/daily) or losartan (0.7 to 1.4 mg/kg/daily) were compared with those who did not receive medical prophylaxis (control group). The primary outcome of interest was the annual rate of change in maximal AsAo diameter z-score in the treatment and control groups. RESULTS: From a cohort of 1005 patients, 120 (mean age 11.3 ± 4.5 years, 82% males) fulfilled the inclusion criteria and were included in the study. Patients in the treatment and control group had similar age, sex, family history of BAV, BAV morphology, and baseline AsAo diameter. During a median follow-up of 7.1 years (interquartile range 3.8-10.2), no differences were observed in the annual growth rate of aortic diameter z-score between patients on treatment and controls. The prevalence of aortic diameter progression was similar in the treatment and control groups, and treatment with atenolol or losartan was not associated with a lower rate of aortic disease progression. CONCLUSIONS: The findings revealed no significant difference in the annual aortic growth rate between treated and untreated patients. Larger cohort studies or, ideally, randomized clinical controlled trials are needed to validate these findings.


Sujet(s)
Antagonistes bêta-adrénergiques , Valve aortique , Maladie de la valve aortique bicuspide , Humains , Mâle , Femelle , Enfant , Études rétrospectives , Adolescent , Antagonistes bêta-adrénergiques/usage thérapeutique , Valve aortique/malformations , Valve aortique/imagerie diagnostique , Valve aortique/anatomopathologie , Valve aortique/effets des médicaments et des substances chimiques , Antagonistes des récepteurs aux angiotensines/usage thérapeutique , Losartan/usage thérapeutique , Études de suivi , Études de cohortes , Aténolol/usage thérapeutique , Résultat thérapeutique , Aorte/effets des médicaments et des substances chimiques , Aorte/imagerie diagnostique , Maladie de la valve aortique/traitement médicamenteux , Valvulopathies/traitement médicamenteux , Valvulopathies/complications , Antagonistes du récepteur de type 1 de l'angiotensine-II/usage thérapeutique
13.
J Biomech ; 168: 112124, 2024 May.
Article de Anglais | MEDLINE | ID: mdl-38701696

RÉSUMÉ

Congenital arterial stenosis such as supravalvar aortic stenosis (SVAS) are highly prevalent in Williams syndrome (WS) and other arteriopathies pose a substantial health risk. Conventional tools for severity assessment, including clinical findings and pressure gradient estimations, often fall short due to their susceptibility to transient physiological changes and disease stage influences. Moreover, in the pediatric population, the severity of these and other congenital heart defects (CHDs) often restricts the applicability of invasive techniques for obtaining crucial physiological data. Conversely, evaluating CHDs and their progression requires a comprehensive understanding of intracardiac blood flow. Current imaging modalities, such as blood speckle imaging (BSI) and four-dimensional magnetic resonance imaging (4D MRI) face limitations in resolving flow data, especially in cases of elevated flow velocities. To address these challenges, we devised a computational framework employing zero-dimensional (0D) lumped parameter models coupled with patient-specific reconstructed geometries pre- and post-surgical intervention to execute computational fluid dynamic (CFD) simulations. This framework facilitates the analysis and visualization of intricate blood flow patterns, offering insights into geometry and flow dynamics alterations impacting cardiac function. In this study, we aim to assess the efficacy of surgical intervention in correcting an extreme aortic defect in a patient with WS, leading to reductions in wall shear stress (WSS), maximum velocity magnitude, pressure drop, and ultimately a decrease in cardiac workload.


Sujet(s)
Hémodynamique , Modèles cardiovasculaires , Syndrome de Williams , Humains , Syndrome de Williams/physiopathologie , Syndrome de Williams/imagerie diagnostique , Hémodynamique/physiologie , Cardiopathies congénitales/physiopathologie , Cardiopathies congénitales/complications , Cardiopathies congénitales/imagerie diagnostique , Aorte/physiopathologie , Aorte/imagerie diagnostique , Vitesse du flux sanguin/physiologie , Mâle , Femelle , Simulation numérique
15.
BMC Pediatr ; 24(1): 317, 2024 May 08.
Article de Anglais | MEDLINE | ID: mdl-38720245

RÉSUMÉ

BACKGROUND: Patients with Turner syndrome (TS) face an increased risk of developing aortic dilatation (AD), but diagnosing AD in children presents greater complexity compared to adults. This study aimed to investigate the application of various assessment indicators of AD in Chinese children and adolescents with TS. METHODS: This study included TS patients admitted to Shenzhen Children's Hospital from 2017 to 2022. Cardiovascular lesions were diagnosed by experienced radiologists. Patients without structural heart disease were divided into different body surface area groups, then the Chinese TS population Z-score (CHTSZ-score) of the ascending aorta was calculated and compared with other indicators such as aortic size index (ASI), ratio of the ascending to descending aortic diameter (A/D ratio), and TSZ-score (Quezada's method). RESULTS: A total of 115 TS patients were included, with an average age of 10.0 ± 3.7 years. The incidences of the three most serious cardiovascular complications were 9.6% (AD), 10.4% (coarctation of the aorta, CoA), and 7.0% (bicuspid aortic valve, BAV), respectively. The proportion of developing AD in TS patients aged ≥ 10 years was higher than that in those < 10 years old (16.6% vs. 1.8%, P = 0.009), and the proportion of patients with CoA or BAV who additionally exhibited AD was higher than those without these conditions (31.6% vs. 5.2%, P < 0.001). The ASI, A/D ratio, TSZ-score, and CHTSZ-score of the 11 patients with AD were 2.27 ± 0.40 cm/m2, 1.90 ± 0.37, 1.28 ± 1.08, and 3.07 ± 2.20, respectively. Among the AD patients, only 3 cases had a TSZ-score ≥ 2, and 2 cases had a TSZ-score ≥ 1. However, based on the assessment using the CHTSZ-score, 6 patients scored ≥ 2, and 5 patients scored ≥ 1. In contrast, the TSZ-score generally underestimated the aortic Z-scores in Chinese children with TS compared to the CHTSZ-score. CONCLUSIONS: The applicability of ASI and A/D ratio to children with TS is questionable, and racial differences can affect the assessment of TSZ-score in the Chinese population. Therefore, establishing the CHTSZ-score specifically tailored for Chinese children and adolescents is of paramount importance.


Sujet(s)
Syndrome de Turner , Humains , Syndrome de Turner/complications , Enfant , Adolescent , Femelle , Chine/épidémiologie , Dilatation pathologique/étiologie , Mâle , Études rétrospectives , Aorte/anatomopathologie , Aorte/imagerie diagnostique , Coarctation aortique , Maladie de la valve aortique bicuspide/complications , Enfant d'âge préscolaire , Incidence , Peuples d'Asie de l'Est
16.
J Med Case Rep ; 18(1): 243, 2024 May 11.
Article de Anglais | MEDLINE | ID: mdl-38730499

RÉSUMÉ

BACKGROUND: An ascending aortic thrombus is exceedingly rare. Two instances have been reported in the setting of lung cancer, but only after cisplatin use, which is associated with hypercoagulability. We present the first case of a patient with lung cancer who developed an ascending aortic thrombus without structural risk factors or chemotherapy use. CASE: A 60-year-old white female with significant smoking history presented with several weeks of malaise. A chest computed tomography scan revealed a 2.2-cm right upper lobe mass. As an outpatient, right hilar lymph node immunohistochemistry (IHC) samples via endobronchial ultrasound confirmed thyroid transcription factor-1 adenocarcinoma. After the procedure, the patient endorsed dyspnea and was advised to go to the emergency department. A chest computed tomography angiography identified a new 2.4 × 1.1 × 1.1 cm thrombus within the proximal aortic arch. No pulmonary emboli or intrapulmonary shunts were identified. A hypercoagulable workup was negative. Transthoracic echocardiogram was without left ventricular thrombus, akinesis or hypokinesis, left atrial dilation, or intracardiac shunts. A lower extremity ultrasound was negative for deep vein thrombosis. Given the procedural risk, thrombectomy was deferred. The patient was transitioned to enoxaparin, and a repeat computed tomography for resolution is in process. CONCLUSION: To our knowledge, this is the only case detailing an in situ ascending aortic thrombus in the setting of lung cancer, without structural risk factors, chemotherapy use, or other hypercoagulable comorbidities. Optimal management for an aortic thrombus and malignant disease is less clear. Clinicians should be vigilant for unusual arterial thromboses in patients with high metastatic burden.


Sujet(s)
Adénocarcinome pulmonaire , Cisplatine , Tumeurs du poumon , Thrombose , Humains , Femelle , Adulte d'âge moyen , Tumeurs du poumon/traitement médicamenteux , Tumeurs du poumon/anatomopathologie , Cisplatine/usage thérapeutique , Thrombose/imagerie diagnostique , Adénocarcinome pulmonaire/traitement médicamenteux , Adénocarcinome pulmonaire/secondaire , Adénocarcinome pulmonaire/complications , Maladies de l'aorte/imagerie diagnostique , Anticoagulants/usage thérapeutique , Adénocarcinome/traitement médicamenteux , Adénocarcinome/complications , Énoxaparine/usage thérapeutique , Antinéoplasiques/usage thérapeutique , Antinéoplasiques/effets indésirables , Angiographie par tomodensitométrie , Aorte/imagerie diagnostique , Aorte/anatomopathologie
18.
Vascul Pharmacol ; 155: 107376, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38692418

RÉSUMÉ

Cardiovascular disease and osteoporosis, major causes of morbidity and mortality, are associated with hyperlipidemia. Recent studies show that empagliflozin (EMPA), an inhibitor of sodium-glucose cotransporter-2 (SGLT2), improves cardiovascular health. In preclinical animal studies, EMPA mitigates vascular calcification in the males but its effects in the females are not known. Thus, we used female mice to test the effects of EMPA on calcification in the artery wall, cardiac function, and skeletal bone. By serial in vivo microCT imaging, we followed the progression of aortic calcification and bone mineral density in young and older female Apoe-/- mice fed a high-fat diet with or without EMPA. The two different age groups were used to compare early vs. advanced stages of aortic calcification. Results show that EMPA treatment increased urine glucose levels. Aortic calcium content increased in both the controls and the EMPA-treated mice, and EMPA did not affect progression of aortic calcium content in both young and older mice. However, 3-D segmentation analysis of aortic calcium deposits on microCT images revealed that EMPA-treated mice had significantly less surface area and volume of calcified deposits as well as fewer numbers of deposits than the control mice. To test for direct effects on vascular cell calcification, we treated murine aortic smooth muscle cells with EMPA, and results showed a slight inhibition of alkaline phosphatase activity and inflammatory matrix calcification. As for skeletal bone, EMPA-treated mice had significantly lower BMD than the controls in both the lumbar vertebrae and femoral bones in both young and older mice. The findings suggest that, in hyperlipidemic female mice, unlike males, SGLT2 inhibition with empagliflozin does not mitigate progression of aortic calcification and may even lower skeletal bone density.


Sujet(s)
Composés benzhydryliques , Densité osseuse , Modèles animaux de maladie humaine , Glucosides , Hyperlipidémies , Souris invalidées pour les gènes ApoE , Inhibiteurs du cotransporteur sodium-glucose de type 2 , Calcification vasculaire , Microtomographie aux rayons X , Animaux , Glucosides/pharmacologie , Composés benzhydryliques/pharmacologie , Femelle , Inhibiteurs du cotransporteur sodium-glucose de type 2/pharmacologie , Calcification vasculaire/anatomopathologie , Calcification vasculaire/traitement médicamenteux , Calcification vasculaire/prévention et contrôle , Calcification vasculaire/métabolisme , Hyperlipidémies/traitement médicamenteux , Densité osseuse/effets des médicaments et des substances chimiques , Aorte/effets des médicaments et des substances chimiques , Aorte/anatomopathologie , Aorte/métabolisme , Aorte/imagerie diagnostique , Aorte/physiopathologie , Maladies de l'aorte/anatomopathologie , Maladies de l'aorte/métabolisme , Maladies de l'aorte/prévention et contrôle , Maladies de l'aorte/traitement médicamenteux , Maladies de l'aorte/physiopathologie , Maladies de l'aorte/imagerie diagnostique , Souris de lignée C57BL , Alimentation riche en graisse , Souris , Facteurs âges , Cellules cultivées
19.
Circulation ; 149(25): 1938-1948, 2024 06 18.
Article de Anglais | MEDLINE | ID: mdl-38804148

RÉSUMÉ

BACKGROUND: Ascending aorta dilation and aortic valve degeneration are common complications in patients with bicuspid aortic valve. Several retrospective studies have suggested the benefit of statins in reducing these complications. This study aimed to determine whether atorvastatin treatment is effective in reducing the growth of aortic diameters in bicuspid aortic valve and if it slows the progression of valve calcification. METHODS: In a randomized clinical trial, 220 patients with bicuspid aortic valve (43 women; 46±13 years of age) were included and treated with either 20 mg of atorvastatin per day or placebo for 3 years. Inclusion criteria were ≥18 years of age, nonsevere valvular dysfunction, nonsevere valve calcification, and ascending aorta diameter ≤50 mm. Computed tomography and echocardiography studies were performed at baseline and after 3 years of treatment. RESULTS: During follow-up, 28 patients (12.7%) discontinued medical treatment (15 on atorvastatin and 13 taking placebo). Thus, 192 patients completed the 36 months of treatment. Low-density lipoprotein cholesterol levels decreased significantly in the atorvastatin group (median [interquartile range], -30 mg/dL [-51.65 to -1.75 mg/dL] versus 6 mg/dL [-4, 22.5 mg/dL]; P<0.001). The maximum ascending aorta diameter increased with no differences between groups: 0.65 mm (95% CI, 0.45-0.85) in the atorvastatin group and 0.74 mm (95% CI, 0.45-1.04) in the placebo group (P=0.613). Similarly, no significant differences were found for the progression of the aortic valve calcium score (P=0.167) or valvular dysfunction. CONCLUSIONS: Among patients with bicuspid aortic valve without severe valvular dysfunction, atorvastatin treatment was not effective in reducing the progression of ascending aorta dilation and aortic valve calcification during 3 years of treatment despite a significant reduction in low-density lipoprotein cholesterol levels. REGISTRATION: URL: https://www.clinicaltrialsregister.eu; Unique identifier: 2015-001808-57. URL: https://www.clinicaltrials.gov; Unique identifier: NCT02679261.


Sujet(s)
Valve aortique , Atorvastatine , Maladie de la valve aortique bicuspide , Calcinose , Évolution de la maladie , Valvulopathies , Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase , Humains , Atorvastatine/usage thérapeutique , Femelle , Mâle , Adulte d'âge moyen , Valve aortique/imagerie diagnostique , Valve aortique/anatomopathologie , Valve aortique/malformations , Valve aortique/effets des médicaments et des substances chimiques , Calcinose/traitement médicamenteux , Calcinose/imagerie diagnostique , Calcinose/anatomopathologie , Maladie de la valve aortique bicuspide/imagerie diagnostique , Maladie de la valve aortique bicuspide/traitement médicamenteux , Valvulopathies/traitement médicamenteux , Valvulopathies/imagerie diagnostique , Valvulopathies/anatomopathologie , Adulte , Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase/usage thérapeutique , Dilatation pathologique/traitement médicamenteux , Études de suivi , Méthode en double aveugle , Résultat thérapeutique , Aorte/imagerie diagnostique , Aorte/anatomopathologie , Aorte/effets des médicaments et des substances chimiques , Maladie de la valve aortique/traitement médicamenteux , Sténose aortique
20.
Am J Hypertens ; 37(8): 604-611, 2024 Jul 15.
Article de Anglais | MEDLINE | ID: mdl-38693860

RÉSUMÉ

BACKGROUND: Aortic diameters are related to age, sex, and body size. There is a scarcity of data on the long-term sequelae of a hypertensive response to exercise (HRE) on aortic diameters. In this retrospective cohort study, we aimed to evaluate the relationship between the growth rates of the aorta in individuals with a HRE. METHODS: Our analysis included follow-up data of 649 patients recruited between January 2009 and December 2014 with a HRE. Participants with known connective tissue disease or a history of acute aortic syndrome were excluded. Sinus of Valsalva (SoV) and ascending aorta (AscAo) diameters were measured by transthoracic echocardiography using leading edge to leading edge convention at end-diastole. RESULTS: At baseline, median age, maximum systolic blood pressure (BP), body mass index (BMI), diameter of the SoV, and AscAo were 62 years, 208 mm Hg, 26.9 kg/m2, 35 mm, and 35 mm respectively. 32% of patients were female and 67% had hypertension. After a median follow-up of 7.1 years, mean yearly growth rates (±SD) of the SoV and AscAo were 0.09 (0.41) mm and 0.13 (0.56) mm, respectively. No significant associations were observed between growth rates of aortic diameters and maximum systolic and diastolic BP or when considering only individuals with a baseline diameter >40 mm. CONCLUSIONS: In this large cohort study, maximum systolic and diastolic BP during exercise showed no association with growth rates of aortic diameters. Furthermore, the mean growth rates of aortic diameters in this population were in line with growth rates in a normal population.


Sujet(s)
Aorte , Pression sanguine , Exercice physique , Hypertension artérielle , Humains , Femelle , Mâle , Adulte d'âge moyen , Études rétrospectives , Hypertension artérielle/physiopathologie , Exercice physique/physiologie , Sujet âgé , Pression sanguine/physiologie , Aorte/imagerie diagnostique , Aorte/croissance et développement , Aorte/physiopathologie , Échocardiographie , Sinus de l'aorte/imagerie diagnostique , Sinus de l'aorte/croissance et développement , Sinus de l'aorte/physiopathologie , Facteurs temps
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