TY - JOUR
T1 - Hemodynamic effect of hydralazine in interstitial lung disease patients with cor pulmonale. Immediate and short-term evaluation at rest and during exercise
AU - Lupi-Herrera, E.
AU - Seoane, M.
AU - Verdejo, J.
AU - Gomez, A.
AU - Sandoval, J.
AU - Barrios, R.
AU - Martinez, W.
PY - 1985
Y1 - 1985
N2 - Hydralazine was administered short-term to 13 patients who had stable interstitial lung disease (ILD), pulmonary arterial hypertension (PAH); mean pulmonary arterial pressure ([PAP] = 26 ± 9 mm Hg), and cor pulmonale (CP). All patients were studied at rest and during exercise. After intravenous hydralazine at rest, there were statistically significant increases in cardiac index (CI) (p<0.001), arterial oxygen saturation (SaO2) (p<0.01), and mixed venous saturation (Sv̄O2) (p<0.01). Pulmonary vascular resistance (Rp) (p<0.005) and systemic resistance (Rs) decreased (p<0.001), and PAP did not change. During exercise, PAP did not change; however, CI (p<0.01), PaO2 (p<0.001), and Sv̄O2 (p<0.01) increased further. The increase in Rp was significantly reduced (p<0.01). After continuation of oral hydralazine therapy in 12 patients for 7 days, PAP at rest was not statistically different from control; Rp and Rs remained decreased (p<0.001). The same results were found for CI, PaO2, Sv̄O2, and Rs during exercise. Although PAP did not change from control values, the drug significantly reduced the increase in Rp ((p<0.005). Vasodilator therapy with hydralazine could be useful in patients with stable ILD who have inflammation with minimal to moderate fibrosis and PAH and might be used as an adjunct to conventional therapy for ILD and CP.
AB - Hydralazine was administered short-term to 13 patients who had stable interstitial lung disease (ILD), pulmonary arterial hypertension (PAH); mean pulmonary arterial pressure ([PAP] = 26 ± 9 mm Hg), and cor pulmonale (CP). All patients were studied at rest and during exercise. After intravenous hydralazine at rest, there were statistically significant increases in cardiac index (CI) (p<0.001), arterial oxygen saturation (SaO2) (p<0.01), and mixed venous saturation (Sv̄O2) (p<0.01). Pulmonary vascular resistance (Rp) (p<0.005) and systemic resistance (Rs) decreased (p<0.001), and PAP did not change. During exercise, PAP did not change; however, CI (p<0.01), PaO2 (p<0.001), and Sv̄O2 (p<0.01) increased further. The increase in Rp was significantly reduced (p<0.01). After continuation of oral hydralazine therapy in 12 patients for 7 days, PAP at rest was not statistically different from control; Rp and Rs remained decreased (p<0.001). The same results were found for CI, PaO2, Sv̄O2, and Rs during exercise. Although PAP did not change from control values, the drug significantly reduced the increase in Rp ((p<0.005). Vasodilator therapy with hydralazine could be useful in patients with stable ILD who have inflammation with minimal to moderate fibrosis and PAH and might be used as an adjunct to conventional therapy for ILD and CP.
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U2 - 10.1378/chest.87.5.564
DO - 10.1378/chest.87.5.564
M3 - Article
C2 - 3987368
AN - SCOPUS:0021918511
SN - 0012-3692
VL - 87
SP - 564
EP - 573
JO - CHEST
JF - CHEST
IS - 5
ER -