How To Test For Heart Failure

by Mike Selvon

Each year, 5 million Americans will suffer from heart failure, a condition in which the heart can't pump blood to other organs in the body. The root cause is not simply a matter of "blocked pipes" or genetics.

Culprits behind this include narrowed arteries, scar tissue, high blood pressure, heart valve disease, cardiomyopathy (disease of the heart muscle itself), congenital heart defects, infection of the valves (endocarditis), infection of the heart (myocarditis), or a combination of factors.

Coronary Artery Disease is the leading cause of heart failure today. CAD is a manifestation of atherosclerosis, which results from smoking, high cholesterol, hypertension (high blood pressure) and diabetes.

Sometimes a viral infection, exposure to toxins like lead or alcohol, or genetics can cause a disease in the actual heart muscle, also known as cardiomyopathy. Diabetes, high salt intake, sustained rapid heart rhythms, alcoholism and marked obesity can all be contributors to chronic failure of the heart.

To check if you may have heart health problems, your general practitioner can run several tests to be sure. Many people avoid getting tested in advance because they fear invasive pokes and prods, but most of these screening tests are very non-invasive. For instance, one test, which is a "stress test," has you walking on a treadmill for a specific interval of time through several intensity levels, while an IV-injected tracer moves through the blood, indicating possible obstructions or strain.

Another test, the EKG, simply monitors your heart rhythms through electrical wires with adhesive ends stuck to your chest, arms and legs. An "Echocardiogram" is simply an ultrasound image taken of your chest, which is as painless as a photograph.

Most people are familiar with the usual hypertension/blood pressure test done with a cuff around your bicep. The most invasive test, which is recommended for people with a genetic predisposition, is the "Catheriterization," which is a small tube inserted into the artery, which may open an obstruction or insert dye to see where the problem spots are.

If you've been diagnosed with heart failure, then you'll need to adjust your diet considerably. An overwhelming amount of evidence suggests the importance of Omega-3 fatty acids, which are found in fish oil supplements. Dr. James O'Keefe of the Mid America Heart Institute in Kansas recommends at least 1 gram of fish oil per day and as much as 4 grams for people with high triglyceride levels.

"Research shows that this dosage lowers triglyceride levels by 20 to 50 percent," he explains. In addition, you'll be trading in eggs for oatmeal, red meat for fish and hummus instead of chip dip.

Angiotensin II antagonism in Congestive Heart Failure

by Andre Garcia

Congestive Heart Failure (CHF) is a clinical syndrome corresponding to the inability of the heart to meet the metabolic requirements of the body at normal filling pressures. Although many times heart failure is mainly precipitated by left ventricular systolic dysfunction, it sometimes also can be secondary to diastolic dysfunction; or a combination of both. CHF is highly prevalent in the USA, Canada, Europe, Australia (corresponding to the "developed countries" as sometimes is told). Mortality, morbidity, direct and indirect costs; all remain being very high yet. The hemodynamic model of CHF has been largely abandoned and replaced by the concept of left ventricular remodeling; which indicates stretching and dilation with subsequent reduction in left ventricular function. Causes include: Coronary Artery Disease (CAD), Myocardial Infarction (MI), hypertension, valvular heart disease, diabetes, congenital heart defects, anemia, and alcoholism. Independently of the precipitating injury, neuro-hormonal mechanisms are activated and promote the remodeling process. These include the Renin-Angiotensin-Aldosterone System (RAAS) and the sympathetic nervous system. A rise in endothelin-1 production, resulting from dysfunctional endothelium, also occurs and contributes to vasoconstriction. Inflammatory markers and cytokines are increased, hence further exacerbating endothelial dysfunction (a "vicious cycle" thereby occurs). A rise in angiotensin II promotes apoptosis (programmed cell death), hypertrophy, and fibrosis. Angiotensin II also causes an increase in aldosterone secretion, which in return augments the harmful effects of angiotensin II on myocardium and promotes adverse remodeling.

Angiotensin-converting enzyme inhibitors (ACEi) were the first class of drugs proved to reduce mortality on patients with CHF. In 1987, NEJM (New England Journal of Medicine) published the results of CONSENSUS (Cooperative North Scandinavian Enalapril Survival Study), showing that enalapril, used at 2.5 to 40mg per day dosage, on patients with severe (class 4) CHF, resulted in a 40% reduction in risk of death (versus placebo). Later, in 1991, NEJM, again, published a new study about enalapril on patients with severe CHF - it was the SOLVD (Studies of Left Ventricular Dysfunction). (Source: N Engl J Med 1991 Aug 1;325(5):293-302 PMID: 2057034, UI: 91278933) SOLVD was focused on the effect of enalapril on mortality and hospitalization in CHF patients with ejection fractions less than 35%. The reduction in risk of death was 22% (versus placebo). This 2 studies were the first giving some good hope in front of a very catastrophic and disastrous clinical picture (CHF) until then. Enalapril was the hero; the angel that saved lives! Next, many, many studies showed (thus confirming) the same idea - ACEi significantly reduced mortality on patients with severe CHF. This became, then, an (almost) unquestionable and irrefutable golden rule/pearl in the treatment of CHF.

Nowadays, about ACEi, we know as being Level of Evidence A: *) ACEi are recommended in all patients with CHF and left ventricular dysfunction unless a contraindication exists (ACC/AHA Guidelines). *) ACEi should be used in all patients with a history of MI and asymptomatic reduced left ventricular function irrespective of ejection fraction (ACC/AHA Guidelines).

ACEi, as name suggests, inhibit the angiotensin-converting enzyme, thereby blocking the conversion of angiotensin I to angiotensin II and bradykinin breakdown. However, since there are other angiotensin II generation pathways, even a total (100%) ACE blockade would not put angiotensin II levels on absolute zero. Here, angiotensin-receptor blockers (ARBs) can fit in.

ARBs bind to the type 1 angiotensin II (AT1) receptor and block it, what leads to plasma renin, angiotensin I, and angiotensin II increased levels. Blockade of the AT1 receptor will also result in the stimulation of the AT2 receptor (physiologically paradoxical), what will increase nitric oxide (NO) production and will trigger other molecular actions which mediate vasodilation; inhibition of fibrosis and of apoptosis (hence, less ventricular remodeling will happen; more time patient will be alive). Overall, ACEi are cheaper, older and better known than ARBs. However, ARBs tend to be better tolerated (less side effects; specially - less persistent cough and recurrent angioedema - very probably because bradykinin levels will not be raised). Many studies were then done, aiming to directly compare the efficacy and safety of the yet "newborns" (ARBs) versus their "bigger and older cousins" (ACEi). This would not be an easy task for ARB laboratory producers - ACEi had the "golden crown of king" - the only drug class (before Losartan, the first ARB on the market, on 1997) which until then had proved to reduce mortality on patients with CHF, do you remember? Well, ARBs proved to have an efficacy similar to ACEi in treatment of CHF and also for patients with non-complicated or complicated hypertension; MI; and diabetic nephropathy. Great, isn't it? The list of studies is enormous.

Sometimes you can find results different from what I have just said about ARBs efficacy and safety, but such studies were methodologically incorrect (or "less correct"), so it became consensual to use an ACEi as first option to antagonize angiotensin II (same efficacy, less price), and only switch to an ARB if patient cannot tolerate an ACEi due to its side effects (persistent cough is, by far, the side effect more frequently forcing patients to give up using an ACEi; but angioedema, although rarely, can kill, if it makes airway obstruction). This seems a prudent and intelligent strategy; I agree. But from present, I would like all doctors to think on a question - maybe now is the moment to begin researching a new plan - why not associate a lower-dose of an ACEi with a lower-dose of an ARB? It makes sense to suppose a better efficacy (by synergy) and less side effects (lower-dose of each one). Why not give a try on this hypothesis rather than continue repeating the same type of studies (ACEi versus ARB - who wins? - neither! - it's a draw! - surprised? - no! -I have already read it so many times!!)? Feel free to discuss your point of view about this! ;) Statistical and methodological analysis of Clinical Trials always is a supreme challenge for all MDs ;)

Complete Information on Eisenmenger syndrome with Treatment and Prevention

by Alicia Stock

Eisenmenger syndrome occurs in patients with big inborn cardiac or surgically created extracardiac left-to-right shunts. These shunts initially induce increased pulmonary blood flowing. People who have Eisenmenger's syndrome are normally born with a big hole in the eye. The most common situation is a hole between the two pumping chambers, called a ventricular septal defect. Usually, Eisenmenger syndrome develops while individuals with heart defects are still children, but it may occur in adolescence or young adulthood. A number of congenital heart defects can cause Eisenmenger's syndrome, including atrial septal defects, ventricular septal defects, patent ductus arteriosus, and more complex types of acyanotic heart disease. Eisenmenger syndrome usually develops before puberty but may develop in adolescence and early adulthood.

Eisenmenger's syndrome primarily affects adolescents and adults with sure inborn eye defects that are repaired later or that are never repaired. Because the pressures within the left position of the eye are usually greater than those within the correct position of the eye, a beginning between the left and correct position of the eye will induce blood to flood from the left position of the eye into the correct position. The symptoms of Eisenmenger's syndrome may resemble other medical conditions or heart problems. A cardiac catheterization is an invasive procedure that gives very detailed information about the structures inside the heart. Eisenmenger syndrome specifically refers to the combination of pulmonary hypertension and right-to-left shunting of the blood within the heart. Eisenmenger's syndrome in rare instances may also develop with an atrial septal defect.

Symptoms related specifically to pulmonary hypertension result from the inability to increase pulmonary blood flow in response to physiological stress. A person with Eisenmenger's syndrome is paradoxically subject to the possibility of both uncontrolled bleeding due to damaged capillaries and high pressure, and random clots due to hyperviscosity and stasis of blood. The syndrome affects both males and females. Eventually, due to increased resistance, pulmonary pressures may increase sufficiently to cause a reversal of blood flow, so blood begins to travel from the right side of the heart to the left side, and the body is supplied with deoxygenated blood, leading to cyanosis and resultant organ damage. Eisenmenger syndrome is first suspected when an individual begins to show symptoms of pulmonary hypertension.

In early childhood, surgical intervention can repair the heart defect, preventing most of the pathogenesis of Eisenmenger's syndrome. Avoid very hot or humid conditions, which may exacerbate vasodilation, causing syncope and increased right-to-left shunting. If treatment has not taken place, heart-lung transplant is required to fully treat the syndrome. If this option is not available, treatment is mostly palliative, using anticoagulants, pulmonary vasodilators such as bosentan, antibiotic prophylaxis to prevent endocarditis, phlebotomy to treat polycythemia, and maintaining proper fluid balance. It is important to eat a nutritious diet and avoid alcohol and salt. Overexertion and smoking also should be avoided. Some patients might benefit from nocturnal supplementation, although it is most useful as a bridge to heart-lung transplant.

Stem cells - The Master Cells of Human Body

by Melvin Ngiam

The Stem cells are predominantly called the "master cells" of the human body because of their ability to create all other tissues, organs, and systems in the body. The stem cells are the building blocks of your blood and immune system. They are the factory of the blood system and continually make new copies of themselves and produce cells that make every other type of blood --Red blood Cells, White Blood Cells and Platelets. There are basically three sources where stem cells can be easily found .

1) Bone Marrow

2) Peripheral Blood and

3) Umbilical Cord Blood

Various researches done in this field suggest that stem cells obtained from cord blood are relatively more advantages over those retrieved from bone marrow or peripheral blood because they are immunologic ally "younger" and appear to be more versatile. They also demonstrate an important characteristic with embryonic stem cells and are able to differentiate into nearly all cell types in the body. Secondly it is easy to get stem cells from cord blood because they are readily obtained from the placenta at the time of delivery. Harvesting stem cells from bone marrow requires a surgical procedure, performed under general anesthesia and can cause post-operative pain or pose a small risk to the donor.

The promise of using stem cells for medical treatments have been the focus of researches various projects that are showing encouraging results.

• Cord blood stem cells help in the treatment of diseases such as Alzheimer's and Parkinson's.
• They have also proven their ability in the treatments for heart disease, allowing patients to essentially "grow their own bypass."
• Stem cells have the potential to help cure many life-threatening ailments like leukemia, non-Hodgkin's lymphoma, anemia, inherited disorders and all other deficiencies of the immune system.
• Lifestyle diseases such as diabetes, liver disorders and heart ailments can also be treated with stem cells.

On the other hand a wider range of recipients can benefit from cord blood stem cells. These can be stored and transplanted back into the donor, to a family member or to an unrelated recipient. For a bone marrow transplantation, there must be a nearly perfect match of certain tissue proteins between the donor and the recipient. When stem cells from cord blood are used, the donor cells appear more likely to "take" or engraft, even when there are partial tissue mismatches.

Certain complications like graft versus host disease (GVHD), in which donor cells can attack the recipient's tissues, are less likely to occur with cord blood than with bone marrow. This may be because cord blood has a muted immune system and certain cells, usually active in an immune reaction, are not yet educated to attack the recipient. A research done in this field revealed that children who received a cord blood transplant from a closely matched sibling were 59 percent less likely to develop GVHD than children who received a bone marrow transplant from a closely matched sibling.

Cord blood also is less likely to contain certain infectious agents, like some viruses, that can pose a risk to transplant recipients .In addition, cord blood may have a greater ability to generate new blood cells than bone marrow. Ounce for ounce, there are nearly 10 times as many blood-producing cells in cord blood. This fact suggests that a smaller number of cord blood cells are needed for a successful transplantation.

With the rapid advancement in Medical Science there has also been a corresponding development in the number of preserved cord blood units being used in regenerative medicine applications. If expectant parents store their baby's cord blood in a family bank, the stem cells are immediately available for use in medical treatments, including future therapies to repair or replace damaged heart tissues. As a result, an infant's cord blood could prove to be a life-saving treatment option if that child is born with a congenital heart defect, or later in life following a sudden and serious heart attack. In regenerative medicine, the latest scientific evidence suggests that using one's own stem cells likely delivers more favorable outcomes.