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Implementing the EXPEDITE parenteral induction protocol: Rapid parenteral treprostinil titration and transition to oral treprostinil.
Kingrey, John F; Miller, Chad E; Franco, Veronica; Smith, Jimmy S; Zolty, Ronald; Oudiz, Ronald J; Elwing, Jean M; Huston, Jessica H; Melendres-Groves, Lana; Ravichandran, Ashwin; Balasubramanian, Vijay; Wu, Benjamin; Hwang, Stephanie; Seaman, Scott; Broderick, Meredith; Rahaghi, Franck F.
Afiliação
  • Kingrey JF; Integris Baptist NZTI Oklahoma City Oklahoma USA.
  • Miller CE; Piedmont Healthcare Atlanta Georgia USA.
  • Franco V; The Ohio State University Wexner Medical Center Columbus Ohio USA.
  • Smith JS; The Ohio State University Wexner Medical Center Columbus Ohio USA.
  • Zolty R; University of Nebraska Medical Center Omaha Nebraska USA.
  • Oudiz RJ; Lundquist Institute at Harbor-UCLA Medical Center Torrance California USA.
  • Elwing JM; University of Cincinnati College of Medicine Cincinnati Ohio USA.
  • Huston JH; UPMC Presbyterian Pittsburgh Pittsburgh Pennsylvania USA.
  • Melendres-Groves L; University of New Mexico School of Medicine Albuquerque New Mexico USA.
  • Ravichandran A; Ascension St. Vincent Indianapolis Indiana USA.
  • Balasubramanian V; Valley Advanced Lung Diseases Institute Fresno California USA.
  • Wu B; United Therapeutics Corporation Research Triangle Park North Carolina USA.
  • Hwang S; United Therapeutics Corporation Research Triangle Park North Carolina USA.
  • Seaman S; United Therapeutics Corporation Research Triangle Park North Carolina USA.
  • Broderick M; United Therapeutics Corporation Research Triangle Park North Carolina USA.
  • Rahaghi FF; Cleveland Clinic Florida Weston Florida USA.
Pulm Circ ; 13(3): e12255, 2023 Jul.
Article em En | MEDLINE | ID: mdl-37497167
ABSTRACT
Treprostinil is a prostacyclin analogue that targets multiple cellular receptors to treat pulmonary arterial hypertension (PAH). In certain scenarios, patients may require aggressive treprostinil titration. Several studies have demonstrated that higher doses of treprostinil lead to greater clinical benefit. Data supports successful transitions from parenteral to oral treprostinil; however, administration routes, transition duration, and transition setting vary in the real-world. The EXPEDITE clinical trial (NCT03497689) prospectively studied whether rapid parenteral treprostinil induction can be used to achieve high doses of oral treprostinil (total daily dose ≥12 mg) in prostacyclin naïve PAH patients. Parenteral prostacyclin induction may be more appropriate for patients who need to reach therapeutic dosing more urgently than longer titration durations reported with conventional de novo oral treprostinil initiation. This summary provides strategies utilized in EXPEDITE. Parenteral treprostinil was initiated at 2 ng/kg/min intravenously or subcutaneously; clinicians determined the frequency and dose increment of up-titration. Two distinct transition schedules from parenteral to oral treprostinil were employed rapid cross-titration in an inpatient setting (median 2 days) or gradual cross-titration in an outpatient setting (median 5 days). Patient status was closely monitored after transition; oral treprostinil dose was titrated to clinical effect and tolerability. Factors considered when individualizing dosing strategies included parenteral and oral treprostinil target doses, nursing support, patient education, medication counseling and adverse events management. EXPEDITE demonstrated the time to a therapeutic dose of oral treprostinil is significantly shorter when utilizing a short-term parenteral induction strategy and may be suitable for patients requiring aggressive titration of oral treprostinil.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pulm Circ Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pulm Circ Ano de publicação: 2023 Tipo de documento: Article