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Overview of and topical guide to cardiology From Wikipedia, the free encyclopedia
The following outline is provided as an overview of and topical guide to cardiology, the branch of medicine dealing with disorders of the human heart.[1] The field includes medical diagnosis and treatment of congenital heart defects, coronary artery disease, heart failure, valvular heart disease and electrophysiology. Physicians who specialize in cardiology are called cardiologists.
Cardiology can be described as all of the following:
Heart –
The cardiac physical exam focuses on portions of the physical exam that elucidate information about diseases and disorders outlined below. Clinical judgment, of course, should guide the physical exam but the following are pertinent things related to a general / broad cardiac exam.
Coronary artery disease is not currently reversible and eventually requires surgical management if it progresses.
Various cardiology diagnostic tests and procedures.
There are several classes of pharmaceutical drugs used in cardiology to manage various diseases and many of them have cardiovascular side effects.
Drugs that manipulate the cardiovascular system do so through several ways. The first is ion channels, which are often manipulated to manage arrhythmias. The second is receptors of various types. The third is manipulation of enzymes.
Ion channels are responsible for cell membrane voltage, depolarization, and repolarization. These actions lead to conduction of signals down nerves and contraction of cardiomyocytes. Perhaps the most prominent manipulation of ion channels is through antiarrhythmic agents. These agents are commonly classified by the type of ion they manipulate and named the Vaughan Williams classification:
Specifically, types I, III, & IV manipulate ion channels while the others are not.
The adrenergic receptor is a set of receptors that are commonly manipulated. Four properties of the heart — chronotropy, dromotropy, inotropy, & lusitropy — are manipulated by adrenergic receptors. For example, the β1 receptor increases all four of these properties: chronotropy at the SA node, dromotropy through the AV node, inotropy of the cardiomyocytes through increased calcium, and lusitropy through phosphorylation of phospholamban. Catecholamines are a set of drugs and hormones that manipulate the adrenergic receptors. The natural catecholamines are norepinephrine, epinephrine, and dopamine. There are numerous other drugs (e.g., dobutamine, ephedrine, isoproterenol) that manipulate the adrenergic receptors and have variable specificity for the receptors and are, thus, used for various reasons.
Angiotensin II receptor antagonists (ARBs) block the angiotensin II receptors that are linked to hypertension and heart failure, mainly through vasodilation & heart remodeling inhibition.
ACE inhibitors works upstream from angiotensin II receptor antagonists and have similar effects on management of hypertension and heart failure.
Sodium nitroprusside and nitroglycerin function by causing vasodilation through nitric oxide, which manipulates cGMP levels through guanylate cyclase.
COX inhibitors (namely aspirin), warfarin, direct Xa inhibitors, direct thrombin inhibitors, heparin, low-molecular weight heparins, antibodies (e.g., abciximab), and a few others are used for anticoagulation therapy. This is important in those predisposed to blood clots (e.g., Factor V Leiden) but also for thrombus formation when an atherosclerotic plaque rupture that would, otherwise, lead to myocardial infarction.
Numerous drug classes have well-known cardiovascular side effects.
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