Abstract
Aim: to evaluate efficiency and safety of the combined antihypertensive drug Lozap Plus (50 mg losartan, 12,5 mg hydrochlorothiazide) in patients with arterial hypertension (AH) of I-III grade with high and very high cardiovascular risk. Material and methods: 30 patients with AH of I-III grade (13 men and 17 women aged 51.9±1.9) were observed. Patients received Lozan Plus (Zentiva, Czech Republic) 1 time in the morning during 12 weeks. Ambulatory blood pressure monitoring (ABPM), echocardiography, biochemical blood analysis were carried out, microalbuminuria (MA) was determined, quality of life was assessed. Results: After 2 weeks of therapy decrease in office systolic blood pressure (BP) was observed, and after 4 weeks - in diastolic BP. After 12 weeks of treatment decrease in BP became more significant. Target systolic and diastolic BP was reached in 83.3% and 90% of patients respectively. Decrease in systolic BP was observed in 24 hrs. (from 141.9±1.9 to 128.6±0.8 mmHg, p<0.001), in daytime (from 146.8±2.6 to 135.8±1.0 mmHg, p<0.01) and in nighttime (from 131.5±1.9 to 118.8±1.9 mmHg, p<0.001). Diastolic BP also decreased: in 24 hrs. (from 91.7±1.8 to 78.7±1.6 mmHg, p<0.05), in daytime (from 94.3±1.3 to 85.0±1.2 mmHg, p<0.05) and in nighttime (from 83.5±2.0 to 71.2±1.7 mmHg, p<0.01). Daily variability of BP, time index of BP and morning BP rise (from 37.6±2.0 to 23.9±1.9 mmHg, p<0.001) reduced. Normalization of daily profile of BP was observed in the majority of patients after 12 weeks of Lozap Plus therapy. Treatment resulted in reduction of number of patients with myocardial hypertrophy (from 50% to 30%, p<0.01), and of patients with diastolic dysfunction of left ventricle (from 43.3% to 30%, p<0.05). Therapy with Lozap Plus during 12 weeks was followed by decrease in MA from 56.7±1.1 mg/l to 9.0±0.5 mg/l. Lozap Plus demonstrated metabolic safety by assessing carbohydrate, lipid, nitric and electrolyte blood parameters. Increase in quality of life was observed by week 12 of treatment. Conclusion: Lozap Plus is efficient antihypertensive drug providing cardio- and nephroprotection, which doesn’t cause metabolic disturbances and improves quality of life of hypertensive patients.
Highlights
Target systolic and diastolic blood pressure (BP) was reached in 83.3% and 90% of patients respectively
Decrease in systolic BP was observed in 24 hrs., in daytime and in nighttime
Normalization of daily profile of BP was observed in the majority of patients after 12 weeks of Lozap Plus therapy
Summary
Оценить эффективность и безопасность комбинированного гипотензивного препарата Лозап Плюс (50 мг лозартана и 12,5 мг гидрохлортиазида) у больных артериальной гипертонией (АГ) I-III степени, имеющих высокий и очень высокий сердечно-сосудистый риск. Обследовано 30 больных АГ I-III степени (13 мужчин и 17 женщин в возрасте 51,9±1,9 лет). В течение 12 недель больные получали Лозап Плюс (Zentiva, Чехия) однократно утром. Проводили суточное мониторирование артериального давления (СМАД), эхокардиографию, биохимическое исследование крови, определяли микроальбуминурию (МА), изучали качество жизни. Лозап Плюс эффективный антигипертензивный препарат, обладающий кардио- и нефропротективным действием, который не вызывает метаболических нарушений и улучшает качество жизни больных АГ. Aim: to evaluate efficiency and safety of the combined antihypertensive drug Lozap Plus (50 mg losartan, 12,5 mg hydrochlorothiazide) in patients with arterial hypertension (AH) of I-III grade with high and very high cardiovascular risk
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