Key result
Treating native aortic thrombosis in HLHS yields ~56% overall transplant-free survival.
Why the study?
Native aortic thrombosis in hypoplastic left heart syndrome is a relatively unusual complication with variable presentation and unclear optimal diagnosis and management strategies.
What are the clinical presentation, diagnosis, and management outcomes of native aortic thrombosis in patients with hypoplastic left heart syndrome?
Systematic Review (n=32)
What are the clinical presentation, diagnosis, and management outcomes of native aortic thrombosis in patients with hypoplastic left heart syndrome?
Native aortic thrombosis in HLHS can present variably and is diagnosable by echocardiography; anticoagulation is the most common and relatively effective treatment, though the incidence of major events remains high.
Anticoagulation remains first-line yet event-prone in this rare HLHS complication; extends sparse case data while leaving optimal regimens open for prospective study.
We started with the experience of thrombus formation in the native aorta of a 3-year-old male child with hypoplastic left heart syndrome (HLHS) and severely hypoplastic but patent mitral and aortic valves after Glenn palliation, which occurred soon after left heart decompression by percutaneous stenting of the atrial septum. The diagnosis was incidental, with the child completely asymptomatic, and progressively subsided in a few days with heparin infusion and chronic warfarin therapy. We reviewed the incidence, diagnosis, and management of native aortic thrombosis in HLHS after different stages of Fontan palliation through a systematic literature search. In all 32 cases, native aortic thrombosis in HLHS was found. The HLHS anatomic subtypes included mitral stenosis/aortic stenosis (fourteen cases or 45.2%), mitral stenosis/aortic atresia (eleven cases or 35.5%), and mitral atresia/aortic atresia (four cases or 12.9%). The age at diagnosis ranged from 13 days to 18 years. Clinical presentation varied from incidental findings, chest pain and/or electrocardiographic abnormalities, cardiac arrest, and transient ischemic attack. Diagnosis was feasible in most of the cases with only transthoracic echocardiography. Mostly (59.4%), patients were treated with anticoagulation, while others underwent surgical (18.7%), direct (12.5%), or systemic (9.3%) thrombolysis. Transplant-free survival was 56.2%, and fatal events occurred in 25%. Major events occurred in 26.3% of those treated with anticoagulation, in 33.3% of patients treated with surgical/systemic thrombolysis, and in 100% of patients treated with direct thrombolysis. In summary, native aortic thrombosis in HLHS may occur at different ages, with a wide spectrum of presentation from incidental finding to a sudden major event. Diagnosis is feasible with transthoracic echocardiography, and management with anticoagulation is effective despite the incidence of major events remaining high.
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Cantinotti et al. (2023) conducted a systematic review in Native aortic thrombosis in hypoplastic left heart syndrome (HLHS) (n=32). Anticoagulation or thrombolysis was evaluated on Transplant-free survival and major events. In 32 cases of native aortic thrombosis in HLHS, overall transplant-free survival was 56.2%, with major events occurring in 26.3% of patients treated with anticoagulation.
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