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Schistosomiasis: A neglected cause of pulmonary arterial hypertension in Brazil.
Bobrovski, Vinícius G; Pinheiro, Alisson L; de-Castro, João A L; Rech, Eduardo B; Zacarkim, Ezequiel V; Dos-S-Reis, Elise S; Eger, Iriane.
Afiliación
  • Bobrovski VG; Department of Medicine, State University of Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, Paraná 84030-900, Brazil. Electronic address: viniciusbobrovski@gmail.com.
  • Pinheiro AL; Department of Medicine, State University of Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, Paraná 84030-900, Brazil.
  • de-Castro JAL; Department of Medicine, State University of Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, Paraná 84030-900, Brazil.
  • Rech EB; Department of Medicine, State University of Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, Paraná 84030-900, Brazil.
  • Zacarkim EV; Department of General Biology, State University of Ponta Grossa, Paraná, Brazil.
  • Dos-S-Reis ES; Department of Medicine, State University of Ponta Grossa, Avenida Carlos Cavalcanti, 4748, Ponta Grossa, Paraná 84030-900, Brazil.
  • Eger I; Department of General Biology, State University of Ponta Grossa, Paraná, Brazil.
Curr Probl Cardiol ; 49(3): 102340, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38103813
ABSTRACT
Schistosomiasis is a prevalent disease in Brazil whose etiological agent is Schistosoma mansoni, the main species associated with pulmonary arterial hypertension (PAH), a serious complication. It is estimated that this complication affects up to 15% of patients with the hepatosplenic form of the disease. Despite being an endemic country, Brazil does not have a screening scheme for cases of PAH associated with schistosomiasis (PAH-Sch), nor protocols for notification and treatment of this vascular complication. The objectives of this literature review are to gather knowledge about the pathophysiology, clinical manifestations, diagnosis and treatment of PAH-Sch and to highlight relevant aspects for the Brazilian reality. The pathophysiology, although lacking information, has proliferative vasculopathy as a central element. The clinical presentation of this disease can be asymptomatic or with nonspecific manifestations. Thus, complementary exams are essential for a confirmatory diagnosis, the gold standard being right heart catheterization, a scarce resource in endemic regions of the country. The treatment of PAH-Sch is similar to that performed for other causes of PAH, but the impact of anthelmintic therapy on the evolution of the vascular pathology is unknown. Therefore, Brazil needs to develop a screening plan for early diagnosis of PAH-Sch and new studies should be carried out to determine a more specific treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquistosomiasis / Hipertensión Arterial Pulmonar / Hipertensión Pulmonar Límite: Humans País/Región como asunto: America do sul / Brasil Idioma: En Revista: Curr Probl Cardiol Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquistosomiasis / Hipertensión Arterial Pulmonar / Hipertensión Pulmonar Límite: Humans País/Región como asunto: America do sul / Brasil Idioma: En Revista: Curr Probl Cardiol Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos