Searched over 200M research papers for "vas disease"
10 papers analyzed
These studies suggest that vas disease encompasses a range of conditions including ventricular arrhythmias, vascular anomalies, and systemic vasculitis, with various diagnostic, treatment, and management strategies aimed at improving patient outcomes.
20 papers analyzed
Ventricular arrhythmias (VAs) encompass a range of conditions from benign, asymptomatic cases to severe, life-threatening events such as sudden cardiac death (SCD). The management of VAs requires careful diagnostic testing and treatment strategies tailored to the specific type of arrhythmia and any underlying structural heart disease (SHD). The European Heart Rhythm Association (EHRA), Heart Rhythm Society (HRS), and Asia Pacific Heart Rhythm Society have provided comprehensive guidelines for clinicians, emphasizing the importance of individualized patient care and the potential need for specialized referral.
Vascular anomalies (VAs) are defects in the vascular system that can significantly impact quality of life. Recent advances have identified key molecular pathways, such as PI3K/AKT/mTOR and RAS/BRAF/MAPK/ERK, and gene mutations responsible for these anomalies. Understanding these genetic factors is crucial for accurate diagnosis, classification, and the development of targeted therapies. The genetic heterogeneity of VAs underscores the need for personalized treatment approaches, highlighting the role of geneticists in multidisciplinary care teams.
The COVID-19 pandemic has highlighted the intersection of infectious diseases and vascular health. Patients with vascular disease (VD) or cardiovascular risk factors (VD-CVR) are at increased risk of severe COVID-19 outcomes. The VAS-European Independent Foundation in Angiology/Vascular Medicine recommends a comprehensive strategy for managing these patients, including the use of eHealth technologies, adherence to antithrombotic treatments, and close medical follow-up. For those with VD-CVR and COVID-19, thromboprophylaxis and careful monitoring are essential to mitigate risks of venous thromboembolism (VTE) and other complications.
VEXAS syndrome, a newly identified autoinflammatory condition, is associated with vasculitis and other inflammatory syndromes. This syndrome is linked to somatic mutations in the UBA1 gene, which plays a role in ubiquitylation. Patients with VEXAS syndrome may present with various forms of vasculitis, such as giant cell arteritis and polyarteritis nodosa, making it a critical area for further research and therapeutic development.
Visual analogue scales (VAS) are valuable tools for documenting symptom severity and monitoring chronic diseases like allergic rhinitis (AR) and chronic rhinosinusitis (CRS). VAS scores correlate well with other validated instruments, such as the Sino-Nasal Outcome Test (SNOT)-22, and can be used to assess disease control and guide treatment decisions . The simplicity and effectiveness of VAS make it a practical choice for both clinical and real-life settings, including digital applications like smartphone apps.
Systemic vasculitis (VAs) poses significant economic and societal challenges due to its severity and high healthcare resource consumption. Despite its impact, there is a lack of comprehensive data on the economic burden of these diseases. More research is needed to inform policy makers and healthcare organizations about the cost-effectiveness of new treatments and the overall societal impact of VAs.
The research on vas disease spans a wide range of topics, from the genetic underpinnings of vascular anomalies to the management of VAs in the context of COVID-19. Understanding these diverse aspects is crucial for improving patient outcomes through targeted therapies, comprehensive management strategies, and effective use of diagnostic tools like VAS. Continued research and multidisciplinary collaboration are essential to address the complexities and challenges associated with vas disease.
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