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Challenges in the Management of Patients with Vascular Ehlers-Danlos Syndrome: Lessons from three Clinical Cases
Lara Alayasa1, Razan Fiala1, Adriana Skafi1
1Al-Quds University, Faculty of Medicine, Abu Dis, Palestine.
Insights
Vascular Ehlers-Danlos syndrome (vEDS) management requires expert multidisciplinary care and strict adherence to therapy to prevent life-threatening vascular events. Despite optimal care, outcomes remain poor, highlighting the need for novel treatments for this severe connective tissue disorder.
Area of Science:
- Genetics and Molecular Biology
- Cardiovascular Medicine
- Rare Diseases
Background:
- Vascular Ehlers-Danlos syndrome (vEDS) is a severe, life-threatening inherited connective tissue disorder.
- Caused by COL3A1 variants, it leads to arterial fragility and high rates of vascular events.
- Current management is complex, balancing intervention risks with complication prevention.
Purpose of the Study:
- To illustrate the complexities of managing patients with genetically confirmed vEDS.
- To emphasize the critical role of expert centers, genetic counseling, and adherence to therapy.
- To highlight the ongoing need for improved therapeutic strategies for vEDS.
Main Methods:
- Case series presentation of three genetically confirmed vEDS patients.
- Review of current evidence-based management strategies, including pharmacological treatments.
- Discussion of conservative versus invasive intervention approaches.
Main Results:
- Patient cases exemplify challenges in vEDS diagnosis and management.
- Therapeutic adherence and long-term surveillance are vital; interruptions can cause severe events.
- Celiprolol and angiotensin receptor blockers show potential, but outcomes remain suboptimal.
Conclusions:
- Early referral to specialized centers with multidisciplinary teams is essential for vEDS patients.
- Strict adherence to evidence-based therapy and structured follow-up are crucial for preventing vascular events.
- Individualized, predominantly conservative management strategies are preferred, with ongoing research needed for better outcomes.
Abstract:
Vascular Ehlers-Danlos syndrome (vEDS) is one of the most severe heritable connective tissue disorders, caused by pathogenic variants in COL3A1 and characterized by arterial fragility, premature mortality, and a high burden of vascular events. Management remains particularly challenging, requiring careful balance between the risks of intervention and the prevention of catastrophic complications. We present three cases of genetically confirmed vEDS that exemplify the complexity of patient care in this setting. These cases underline the importance of early referral to expert centers, where multidisciplinary care, genetic counseling, and structured follow-up can be guaranteed. They also highlight the central role of therapeutic adherence and long-term surveillance, as interruption of validated medical therapy may lead to life-threatening vascular events. Pharmacological treatment with celiprolol remains the first strategy supported by randomized trial evidence, while recent data suggest that the addition of angiotensin receptor blockers may further reduce vascular risk. Nevertheless, outcomes remain poor, and the prognosis of vEDS continues to be dominated by recurrent arterial complications despite optimal management. Conservative strategies are generally preferred, with invasive interventions reserved for life-threatening circumstances and best performed in specialized centers. These cases underscore both the progress made and the unmet need for novel therapeutic options to improve outcomes in this high-risk population.
Learning Points:
Vascular Ehlers-Danlos syndrome (vEDS) is a rare inherited connective tissue disorder marked by extreme arterial fragility, requiring high clinical suspicion to avoid misdiagnosis and inappropriate interventions.Strict adherence to evidence-based pharmacological therapy and structured long-term follow-up are crucial, as treatment discontinuation may lead to rapid and life-threatening vascular events.Management should be centralized in expert centres with a multidisciplinary approach, where individualized and predominantly conservative strategies can optimize outcomes in this high-risk population.
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