Case report: Stepwise transition from subcutaneous treprostinil to epoprostenol in high-risk pulmonary arterial hypertension

被引:1
|
作者
Laura Mori, Ana [1 ]
Rodriguez, Andrea [1 ]
Alberto Gagliardi, Juan [1 ]
Stewart Harris, Alejandro [2 ]
机构
[1] Hosp Gen Agudos Dr Cosme Argerich, Dept Med, Cardiol Div, Pi y Margall 750 C1155 AHD, Buenos Aires, DF, Argentina
[2] Hosp Gen Agudos Dr Cosme Argerich, Dept Med, Pi y Margall 750 C1155 AHD, Buenos Aires, DF, Argentina
关键词
Case report; Idiopathic pulmonary hypertension; Prostacyclin analogues; Treprostinil; Epoprostenol; INTRAVENOUS EPOPROSTENOL; PROSTACYCLIN;
D O I
10.1093/ehjcr/ytaa578
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Idiopathic pulmonary arterial hypertension is associated with high morbidity and mortality. In recent years, the use of targeted therapies has led to an improvement in prognosis. Prostacyclin analogues treprostinil and epoprostenol require continuous subcutaneous or intravenous infusion and are generally administered in a stepwise approach. However, there are no clear recommendations for transition in high-risk patients requiring high doses of prostacyclin analogues. Case summary In this report, we describe the case of a 20-year-old woman under combined treatment with sitdenafil, macitentan, and treprostinil who required transition from subcutaneous treprostinil therapy to intravenous epoprostenol due to erratic drug absorption and functional class progression. The transition was performed over 48 h in a stepwise approach reducing treprostinil dose Ong/kg/min every 3 h while increasing epoprostenol infusion 2ng/kg/min until achieving a maintenance dose of 32 ng/kg/min. There were no side effects requiring changes in the infusion rate. Discussion Patients with advanced pulmonary arterial hypertension may necessitate switching from subcutaneous treprostinil to epoprostenol. Although many protocols have been used to date, there are no guidelines to direct this process safely. This 48-h scheme based on the pharmacokinetic properties of each drug was successful and well-tolerated.
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