P
Peter J. Osmond
Researcher at University at Buffalo
Publications - 19
Citations - 71
Peter J. Osmond is an academic researcher from University at Buffalo. The author has contributed to research in topics: Blood pressure & Valsartan. The author has an hindex of 4, co-authored 17 publications receiving 58 citations. Previous affiliations of Peter J. Osmond include Erie County Medical Center.
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Hemodynamic and central blood pressure differences between carvedilol and valsartan added to lisinopril at rest and during exercise stress.
TL;DR: Adding V or C to an angiotensin-converting enzyme inhibitor reduced cardiac workload by different mechanisms: vasodilation and reduced central blood pressure with V and lower heart rate with C and during exercise, V persistently lowered central systolic pressure, AP, and SVR, whereas C did not.
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Ambulatory 24–hour cardiac oxygen consumption and blood pressure–heart rate variability: effects of nebivolol and valsartan alone and in combination
TL;DR: It is concluded that the rate-slowing effects of NEB cause ambulatory cardiac myocardial oxygen consumption to be lower with NEB monotherapy or NEB/VAL combination therapy than with VAL monotherapy, and NEb/VAL is not superior to NEB alone in controlling heart rate, blood pressure, or ACRPP.
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Differences in mean and variability of heart rate and ambulatory rate-pressure product when valsartan or carvedilol is added to lisinopril.
TL;DR: In this article, a single-blinded, forced-titration, crossover study was conducted in which carvedilol (C, 20 and 40 mg/day) or a control renin-angiotensin blocker, valsartan (V, 160 and 320 mg) were added to L Ambulatory blood pressure (ABP) and heart rate monitoring was performed at the end of each period.
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Decoupling of Heart Rate and Blood Pressure: Hemodynamic Counter-regulatory Mechanisms and their Implications
TL;DR: The classic approach to systemic hemodynamics has been based on a steady-state electrical circuit model, where Blood Pressure (BP) is the product of “total” blood flow (cardiac output) and Systemic Vascular Resistance (SVR).
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Long-term BP control and vascular health in patients with hyperaldosteronism treated with low-dose, amiloride-based therapy.
Joseph L. Izzo,Joseph L. Izzo,Michael Hong,Michael Hong,Tanveer Hussain,Tanveer Hussain,Peter J. Osmond,Peter J. Osmond +7 more
TL;DR: It is concluded that long‐term ENaC blockade can normalize BP and protect macro‐ and microvascular function in patients with chronic hyperaldosteronism and that aldosterone may not play a major BP‐independent role in human macro‐and microcirculatory diseases.