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1.
Ter Arkh ; 76(8): 32-6, 2004.
Artículo en Ruso | MEDLINE | ID: mdl-15471393

RESUMEN

AIM: To compare antianginal efficacy and tolerability of propranolol therapy in patients with stable angina pectoris and chronic hypotension (Hpts) and normotensive patients with angina of effort (Npts). MATERIAL AND METHODS: A randomized, single-blind, placebo-controlled study was made in 35 Hpts and 38 Npts was made using bicycle exercise tests, echocardiography, stress myocardial scintigraphy with 77-199. RESULTS: Acute bicycle exercise tests showed high anti-ischemic activity of propranolol in 86% Hpts and 65% Npts. Stable antianginal propranolol effect in 57% Hpts was accompanied with a decrease of myocardial perfusion defect. Secondary resistance or pseudotolerance to an antianginal effect of propranolol was observed in 43% Hpts in 4-12 weeks (vs 0 of Npts; p < 0.01) as evidenced by T-199 stress myocardial scintigraphy. Hpts with secondary resistance and pseudotolerance to propranolol had lower control hypotension and bradicardia (p < 0.05), more anginal attacks (p < 0.001). CONCLUSION: Hpts had rapidly developing secondary resistance and pseudotolerance to propranolol antianginal effect, bad tolerability of the drug.


Asunto(s)
Angina de Pecho/tratamiento farmacológico , Hipotensión/complicaciones , Propranolol/uso terapéutico , Antagonistas Adrenérgicos beta/efectos adversos , Antagonistas Adrenérgicos beta/farmacología , Antagonistas Adrenérgicos beta/uso terapéutico , Angina de Pecho/complicaciones , Presión Sanguínea/efectos de los fármacos , Resistencia a Medicamentos , Tolerancia a Medicamentos , Ventrículos Cardíacos/efectos de los fármacos , Ventrículos Cardíacos/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Propranolol/efectos adversos , Propranolol/farmacología , Método Simple Ciego
2.
Klin Med (Mosk) ; 81(11): 54-8, 2003.
Artículo en Ruso | MEDLINE | ID: mdl-14689713

RESUMEN

A randomized single blind cross-over trial with placebo lead-in has been conducted in 71 anginal patients with arterial hypotension (group 1) and 38 ischemic heart disease patients with normal arterial pressure (group 2) to compare efficacy of therapy with isosorbide dinitrate (ID), sustac-forte (SF), isosorbide dinitrate retard (IDR) and trinitrolong (TN). Paired bicycle exercises revealed that in group 1 patients ID was low effective in 49%, SF--in 61%, IDR was highly effective in 97% and TN--in 96%. In group 1 tolerance to antianginal effect of ID, SF and IDR shown by stress myocardial scintigraphy with Tl-199 developed earlier--in 2-4 weeks in 63-70% patients (versus 22-27% in group 2; p < 0.01). Recovery of ID, SF, IDR effect required prolongation of the drug withdrawal period to 8-16 days (versus 3-5 days in group 2; p < 0.05). TN therapy remained effective for 3 months. Resistance to ID, SF in group 1 was relative and depended on dosage form of nitrates.


Asunto(s)
Angina de Pecho/tratamiento farmacológico , Hipotensión/complicaciones , Isquemia Miocárdica/tratamiento farmacológico , Nitratos/uso terapéutico , Estudios Cruzados , Prueba de Esfuerzo , Humanos , Dinitrato de Isosorbide/administración & dosificación , Dinitrato de Isosorbide/uso terapéutico , Masculino , Persona de Mediana Edad , Nitratos/administración & dosificación , Donantes de Óxido Nítrico/administración & dosificación , Donantes de Óxido Nítrico/uso terapéutico , Nitroglicerina/administración & dosificación , Nitroglicerina/uso terapéutico , Placebos , Factores de Tiempo , Vasodilatadores/administración & dosificación , Vasodilatadores/uso terapéutico
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