Morrison D, Goldman S, Alepa F P
Clin Cardiol. 1984 Jan;7(1):49-53. doi: 10.1002/clc.4960070111.
A patient with severe pulmonary hypertension secondary to the CREST syndrome variant of scleroderma is described. Acute reductions in both pulmonary artery pressure and total pulmonary resistance were seen with nifedipine and oxygen administration. Reductions in resistance were maintained for over one month with this combination. These results raise the possibility that some of the pulmonary hypertension seen in this condition is reversible.
本文描述了一名患有硬皮病CREST综合征变异型继发严重肺动脉高压的患者。使用硝苯地平和吸氧后，肺动脉压和总肺阻力均出现急性降低。联合使用这种方法，阻力降低持续了一个多月。这些结果增加了这种情况下部分肺动脉高压是可逆的可能性。
