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Details

Autor(en) / Beteiligte
Titel
Hospitalization and Survival in Patients Using Epoprostenol for Injection in the PROSPECT Observational Study
Ist Teil von
  • Chest, 2015-02, Vol.147 (2), p.484-494
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2015
Quelle
MEDLINE
Beschreibungen/Notizen
  • BACKGROUND Few studies have prospectively reported outcomes in patients with pulmonary arterial hypertension (PAH) treated with epoprostenol in the modern-day era of oral therapy and combination treatments. The Registry to Prospectively Describe Use of Epoprostenol for Injection (Veletri, prolonged room temperature stable-epoprostenol [RTS-Epo]) in Patients with Pulmonary Arterial Hypertension (PROSPECT) was established to prospectively describe the course of PAH in patients prescribed RTS-Epo. METHODS PROSPECT is a multicenter, US-based drug registry of primarily group 1 patients with PAH treated with RTS-Epo who were parenteral-naive or parenteral-transitioned at enrollment. Patients were followed until discontinuation of RTS-Epo, withdrawal, loss to follow-up, death, or end of study (maximum 1 year). One-year freedom from hospitalization (FH) and survival estimates were summarized by prostacyclin history (parenteral-naive or parenteral-transitioned), sex, and chronic renal insufficiency (CRI). RESULTS A total of 336 patients were included. The overall 1-year FH estimate was 51.0% ! 2.8% and was lower in parenteral-naive patients than parenteral-transitioned patients (42.8% ! 4.3% vs 57.1% ! 3.7%, respectively; P = .002). FH estimates were lower in male patients than female patients (38.3% ! 5.9% vs 54.6% ! 3.2%, respectively; P < .015) and in patients with CRI than patients without CRI (17.0% ! 8.4% vs 53.7% ! 2.9%, respectively; P < .001). The overall 1-year survival estimate was 84.0% ! 2.1%. Survival was poorer in parenteral-naive patients, male patients, and patients with CRI. CONCLUSIONS Risk of hospitalization and mortality remain high in patients with PAH. In particular, patients who are parenteral-naive at initiation of RTS-Epo therapy, male patients, and patients with CRI require close monitoring and aggressive clinical management.

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