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Published on: August 4, 2021
Inpatient Transition From Intravenous to Inhaled Treprostinil in a Pediatric Patient
David Procaccini1, Dennis Delany2, Abigail Self2
1Department of Pharmacy (DP), The Johns Hopkins Hospital, Baltimore, MD.
Insights
This study shows a successful transition from intravenous to inhaled treprostinil for a pediatric patient with idiopathic pulmonary arterial hypertension. The patient maintained stable pulmonary hypertension and improved exercise capacity after the switch.
Area of Science:
- Pediatric Cardiology
- Pulmonology
- Pharmacology
Background:
- Idiopathic pulmonary arterial hypertension (IPAH) is a rare and severe condition.
- Intravenous (IV) prostacyclin analogs are a common treatment for IPAH.
- Transitioning patients to alternative delivery methods requires careful management.
Purpose of the Study:
- To describe a successful transition from IV to inhaled treprostinil in a pediatric IPAH patient.
- To evaluate the safety and efficacy of inhaled treprostinil during this transition.
- To assess the patient's clinical status post-transition.
Main Methods:
- A 7-year-old male with IPAH underwent transition from IV treprostinil to inhaled treprostinil.
- The transition occurred during inpatient admission following removal of central venous catheters.
- Clinical, echocardiographic, and biomarker assessments were performed during and after the transition.
Main Results:
- The 4-day transition was completed without clinical, echocardiographic, or biomarker evidence of IPAH worsening.
- The patient was discharged home without complications.
- Three weeks post-discharge, pulmonary hypertension remained well-controlled, with improved 6-minute walk distance.
Conclusions:
- Inhaled treprostinil can be a safe and effective alternative to IV administration in select pediatric IPAH patients.
- Successful transition is feasible even after removal of central venous access.
- This approach may offer improved quality of life and reduced treatment burden.
Abstract:
We report a case of a 7-year old male with idiopathic pulmonary arterial hypertension, successfully transitioned from an intravenous infusion to inhaled treprostinil during inpatient admission, after his intentional removal of multiple central venous catheters. He had no clinical, echocardiographic, or serum biomarker evidence of loss of control of pulmonary arterial hypertension during the 4-day transition. The patient was discharged home without complications, and 3 weeks after discharge the patient's pulmonary hypertension remained well controlled per clinical and echocardiographic evidence, including a significantly improved 6-minute walk distance test.
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