PMID- 16100159 OWN - NLM STAT- MEDLINE DCOM- 20050906 LR - 20131121 IS - 0012-3692 (Print) IS - 0012-3692 (Linking) VI - 128 IP - 2 DP - 2005 Aug TI - Effects of lipo-prostaglandin E1 on pulmonary hemodynamics and clinical outcomes in patients with pulmonary arterial hypertension. PG - 714-9 AB - OBJECTIVE: To determine whether lipid microspheres containing prostaglandin E1 (lipo-PGE1) improve pulmonary hemodynamics and clinical outcomes in patients with pulmonary arterial hypertension (PAH). METHODS: Forty-nine patients with PAH (8 patients with primary pulmonary hypertension, 21 patients with collagen vascular disease, 20 patients with congenital systemic-to-pulmonary shunts) were randomly classified into a conventional therapy group (n = 22) or a group receiving lipo-PGE1 plus conventional drugs (lipo-PGE1 group; n = 27). Echocardiographic pulmonary parameters, New York Heart Association (NYHA) functional class, and Bruce treadmill test results for exercise capacity were recorded before and after treatment. RESULTS: After 2 weeks of treatment with lipo-PGE1 (10 microg bid for 14 days), there were significant improvements in the values (+/- SD) for systolic pulmonary arterial pressure (SPAP) [76.9 +/- 27.9 mm Hg vs 66.5 +/- 22.8 mm Hg, p < 0.001]; total pulmonary resistance (27.2 +/- 13.3 dyne.s.cm(-5) vs 20.2 +/- 10.7 dyne.s.cm(-5), p < 0.001); left ventricular ejection fraction (58.7 +/- 9.6% vs 64.4 +/- 6.8%, p < 0.001); and cardiac output (3.1 +/- 0.8 L/min vs 3.7 +/- 1.1 L/min, p < 0.01). The NYHA functional class decreased from 3.0 +/- 0.6 to 2.5 +/- 0.6 (p < 0.001), and the exercise capacity increased from 2.8 +/- 1.0 to 4.3 +/- 1.3 metabolic equivalents (MET) [p < 0.001]. Compared with the conventional therapy group, the lipo-PGE(1) group achieved significant reduction of SPAP (10.4 +/- 10.3 mm Hg vs 2.2 +/- 5.6 mm Hg, p = 0.002) and a significant elevation of exercise capacity (1.5 +/- 0.9 MET vs 0.6 +/- 1.1 MET, p = 0.018). CONCLUSION: Lipo-PGE1 can decrease pulmonary artery pressure and increase exercise capacity in patients with PAH. FAU - Shen, Jieyan AU - Shen J AD - Department of Cardiology, Shanghai Second Medical University--Affiliated Renji Hospital, 1630 Dong Fang Rd, Shanghai 200127, Republic of China. Shenjieyan_66@hotmail.com FAU - He, Ben AU - He B FAU - Wang, Binyao AU - Wang B LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PL - United States TA - Chest JT - Chest JID - 0231335 RN - 0 (Lipids) RN - 0 (Vasodilator Agents) RN - F5TD010360 (Alprostadil) SB - IM MH - Alprostadil/*administration & dosage/pharmacology MH - Drug Delivery Systems MH - Female MH - Hemodynamics/*drug effects MH - Humans MH - Hypertension, Pulmonary/*drug therapy/*physiopathology MH - Lipids MH - Male MH - Microspheres MH - Middle Aged MH - Prospective Studies MH - Treatment Outcome MH - Vasodilator Agents/*administration & dosage/pharmacology EDAT- 2005/08/16 09:00 MHDA- 2005/09/07 09:00 CRDT- 2005/08/16 09:00 PHST- 2005/08/16 09:00 [pubmed] PHST- 2005/09/07 09:00 [medline] PHST- 2005/08/16 09:00 [entrez] AID - S0012-3692(15)50417-0 [pii] AID - 10.1378/chest.128.2.714 [doi] PST - ppublish SO - Chest. 2005 Aug;128(2):714-9. doi: 10.1378/chest.128.2.714.