Key result
High-dose titration of nifedipine or diltiazem resulted in a >20% reduction in pulmonary artery pressure in 32% of patients and vascular resistance in 40%.
Why the study?
The effectiveness and tolerability of high dose titration of calcium channel blockers in primary pulmonary hypertension patients required evaluation to guide short-term drug testing.
Does high-dose titration of calcium channel blockers (nifedipine or diltiazem) reduce pulmonary artery pressure and pulmonary vascular resistance in patients with primary pulmonary hypertension?
Does high-dose titration of calcium channel blockers (nifedipine or diltiazem) reduce pulmonary artery pressure and pulmonary vascular resistance in patients with primary pulmonary hypertension?
High-dose titration of calcium channel blockers causes substantial reduction in pulmonary artery pressure and vascular resistance in roughly one-third of primary pulmonary hypertension patients, necessitating acute hemodynamic testing to identify responders.
Supports vasodilator testing to guide CCB therapy in primary PH; leaves open outcome benefits without randomized confirmation.
Forty-seven patients with primary pulmonary hypertension were evaluated with a dose titration protocol utilizing nifedipine (20 mg orally) or diltiazem (60 mg orally) given every hour until maximal effectiveness was achieved. Of the patients tested, 15 (32%) had a greater than 20% reduction in pulmonary artery pressure (mean 36.2 +/- 8%, p less than 0.01) and pulmonary vascular resistance (mean 50.2 +/- 7%, p less than 0.01) (pressure responders). Nineteen (40%) had a greater than 20% reduction in pulmonary vascular resistance (mean 25.2 +/- 12%, p less than 0.01), with less than a 20% decrease in pulmonary artery pressure (resistance responders). Ten had no significant change in pulmonary artery pressure or pulmonary vascular resistance (nonresponders), and three were unable to tolerate the calcium channel blocking agents. No hemodynamic profile allowed prediction of the type of response to these agents. No mortality or serious morbidity was associated with the drug testing. These findings indicate that calcium channel blockers, when titrated to maximally effective doses, may cause substantial reductions in pulmonary artery pressure and pulmonary vascular resistance in patients with primary pulmonary hypertension. Testing with hemodynamic monitoring is necessary to ascertain which patients will respond. Patients with primary pulmonary hypertension are able to tolerate short-term administration of high doses of calcium channel blockers.
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Rich et al. (1991) studied Primary pulmonary hypertension (n=47). Nifedipine or Diltiazem was evaluated on Greater than 20% reduction in pulmonary artery pressure (p=<0.01). High-dose titration of nifedipine or diltiazem resulted in a >20% reduction in pulmonary artery pressure in 32% of patients and vascular resistance in 40%.
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