Oral treprostinil in transition or as add-on therapy in pediatric pulmonary arterial hypertension
Autor: | Russel Hirsch, Derek Solum, Mary P. Mullen, Eric D. Austin, Rachel K. Hopper, Uyen Truong, Delphine Yung, Edward C. Kirkpatrick, Jeffrey A. Feinstein, Jeffrey R. Fineman, C Q Deng, D. Dunbar Ivy |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Pulmonary and Respiratory Medicine
lcsh:RC705-779 medicine.medical_specialty lcsh:Diseases of the circulatory (Cardiovascular) system business.industry prostacyclin treprostinil Prostacyclin lcsh:Diseases of the respiratory system Add on therapy pediatric lcsh:RC666-701 Internal medicine pulmonary arterial hypertension medicine Cardiology business Treprostinil medicine.drug Research Article |
Zdroj: | Pulmonary Circulation Pulmonary Circulation, Vol 9 (2019) |
ISSN: | 2045-8940 2045-8932 |
Popis: | Treprostinil, a prostacyclin analogue, is approved for the treatment of pulmonary arterial hypertension (PAH) in adults. Transition from parenteral to oral treprostinil has been successfully accomplished in adults with PAH but not in children. In this multicenter study, pediatric patients treated with parenteral (Cohort 1) or inhaled (Cohort 2) treprostinil were transitioned to oral treprostinil. Prostacyclin-naïve individuals on background oral PAH therapy received oral treprostinil as add-on therapy (Cohort 3). Successful transition was oral treprostinil dose maintenance through week 24. Patients were monitored for adverse events (AEs), 6-min walk distance (6MWD), PAH symptoms, World Health Organization (WHO) Functional Class (FC), cardiac magnetic resonance imaging (cMRI), cardiopulmonary exercise testing (CPET), and quality of life through 24 weeks. A total of 32 patients were enrolled in the study; 23 (72%) were girls (mean age = 12.2 years). All patients were on background oral PAH therapy. Overall, patients (96.9%) maintained transition to oral treprostinil; one patient (Cohort 1) transitioned to oral treprostinil, then back to parenteral after experiencing syncope and WHO FC change from II to III. Cohorts 1, 2, and 3 received a final mean oral treprostinil dose of 5.6, 3.3, and 4.5 mg t.i.d., respectively. All cohorts had variable changes in 6MWD, cMRI, and CPET. Overall, 12 serious AEs were reported. All patients had drug-related AEs including headache (81%), diarrhea (69%), nausea (66%), vomiting (66%), and flushing (56%). Pediatric patients maintained transition to oral treprostinil with preservation of exercise capacity and WHO FC. Prostanoid-related AEs were most common and similar to those reported in adults. |
Databáze: | OpenAIRE |
Externí odkaz: |