Showing posts with label journal of pharmacotherapy. Show all posts
Showing posts with label journal of pharmacotherapy. Show all posts

Wednesday, 24 May 2017

Twelve Month Follow-Up Audit of Nigerian Hypertensives on Back Titration

The question of whether pharmacotherapy for systemic arterial hypertension should be life-long has continued to agitate the mind of care givers and patients alike. Whereas it is possible in some cases tore duce dose or discontinue drug(s) outright, relapse of high blood pressure is known to occur after some time. 

Hypertensives
Hypertensives

All the same, the attitude of step down or outright discontinuation of anti-hypertensive pharmacotherapy appears to be safe provided close monitoring continued. In an audit of hypertension care in a specialized care facility, the author observed that some patients remained controlled despite self-imposed drug holidays or physician initiated dose reduction following therapy induced hypotensive features. Some earlier workers had called for future studies to shed light on how long and intensively hypertensives could be treated before discontinuation of therapy can be embarked upon. Read more>>>>>>>>

Wednesday, 12 October 2016

Reduced Cardiac Performance after Differential Pharmacological Stress in Streptozotocin-Induced Diabetic Rats

Diabetes Mellitus (DM) is a main risk factor for heart failure. A hallmark of this common complication is a disturbed conductibility of the left ventricle (LV). In this regard, diabetic cardiomyopathy is a significant entity, which could manifest as impaired cardiac performance in the absence of coronary artery disease, systemic hypertension or valvular heart disease that result from metabolic derangement present in diabetes. Among others, structural changes in extracellular matrixand myocyte damage contain hallmarks of this disease. Abnormalities in these compartments may result in left ventricular dysfunction (LV).
Cardiovascular  toxicology
The Application of streptozotozin (STZ) to rats is a well established model of type 1 DM. We previously showed in this model severe impaired LV function under basal conditions in a chronic stage of STZ-induced DM. We further identified pathophysiological mechanisms, which could be responsible for this disturbed cardiac phenotype. This includes endothelial dysfuntion, cardiac fibrosis, inflammation and disturbed myocardial calcium regulation as well as neurohumoral activation.Whereas the cardiac phenotype under basal conditions in the chronic stage in STZ rats is well characterized, we analysed in the present study in vivo the time-dependent LV conductibility in this model. Therefore we measured LV function in STZ diabetic rats on two different time points under basal and under different pharmacological stress conditions using invasive LV microconductance catheter technique. Read more................