ArticleJournal of thrombosis and thrombolysis2022
Sickle cell disease related chronic thromboembolic pulmonary hypertension: challenging clinical scenario.
Article in Journal of thrombosis and thrombolysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 3 citations in OpenAlex.
- Haemolytic Anaemia-Related Pulmonary Hypertension.Life (Basel, Switzerland) · 2024Article
- Diagnosis and management of chronic thromboembolic pulmonary hypertension (CTEPH) in sickle cell disease: A review.Pulmonary circulation · 2024Article
- Multiparametric Cardiac Magnetic Resonance Assessment in Sickle Beta Thalassemia.Diagnostics (Basel, Switzerland) · 2024Article
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Authors and funding
6 authors at 1 institution in 1 country.
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Abstract
Sickle cell disease (SCD), a haemoglobinopathy characterized by chronic haemolysis with acute exacerbations and vascular occlusion episodes, may be complicated by pulmonary hypertension. The latter may be caused by chronic thromboembolic disease of pulmonary artery branches and its management is not well-defined. Herein, we present a case of SCD complicated by chronic thromboembolic pulmonary hypertension of subsegmental pulmonary artery branches successfully treated with endothelin receptor antagonists, orally administered prostacyclin analogs and balloon pulmonary angioplasty. This challenging case highlights the need for clinical awareness of chronic thromboembolic pulmonary hypertension as a specific and potentially curable form of pulmonary hypertension complicating SCD course that may necessitate combined pharmacologic and interventional management.
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