Showing posts with label heart disease. Show all posts
Showing posts with label heart disease. Show all posts

Sunday, August 17, 2008

Obesity and diabetes increase heart disease risk

People who are both obese and have diabetes are highly likely to develop heart disease during their lifetime, a new study shows.

Researchers found that of more than 3,400 adults in a long-running U.S. heart study, women who were obese and diabetic had a nearly 80 percent chance of developing heart disease at some point. For their male counterparts, that figure was nearly 90 percent.

Lifetime risk was based on the likelihood that a 50-year-old would develop heart disease in the next 30 years.

Obesity and diabetes commonly go hand-in-hand. The new findings, published in the journal Diabetes Care, show that diabetes on its own significantly raises the lifetime risk of heart disease, and that obesity worsens the situation.

Dr. Caroline S. Fox of the National Heart, Lung and Blood Institute in Bethesda, Maryland, and her colleagues the lifetime heart disease risk of normal-weight women who did not have diabetes was 34 percent. The risk for normal-weight women with diabetes was 55 percent.

Among obese women, those who did not have diabetes had a 47 percent chance of developing heart disease, while the risk for those with diabetes was 79 percent.

The pattern was similar for men, with a lifetime heart disease risk of 49 percent among normal-weight, non-diabetic men, and a 77 percent risk for normal-weight men with diabetes. Obese men without diabetes had a 67 percent lifetime heart disease risk, while the risk for obese diabetic men was 87 percent.

The number of Americans with diabetes is expected to rise to 48.3 million by 2050, the researchers note, and heart disease due to diabetes appears to already be on the rise.

"This trend may continue to worsen if current trajectories do not change," they warn.





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Saturday, August 9, 2008

Doctors fall short on heart disease prevention

Some doctors are not making the grade when it comes to helping their patients ward off heart disease, a new survey suggests.

The survey, of nearly 900 U.S. primary care doctors, found that many do not follow practice guidelines on managing patients who are at elevated risk of heart and blood vessel disease.

"Despite the benefits demonstrated for managing cardiovascular risks, gaps remain in primary care practitioners' management of risks according to guideline recommendations," conclude researchers in a report in the journal BMC Family Practice.

"Patients should talk to their physicians about setting goals together for reducing blood pressure and cholesterol and making a plan to achieve the goals," lead researcher Dr. Hamidreza Doroodchi, from Birmingham, Alabama-based Outcomes, Inc., noted in comments to Reuters Health.

Doroodchi and colleagues sent a survey on cardiovascular disease management to a random sample of 12,000 U.S. family physicians and general internists. A total of 888 completed the survey, which contained "case vignettes" for managing adults deemed to be at low or high risk of heart disease.

The study found that in the hypothetical case of a low-risk 45-year-old woman, only 28 percent of family doctors and 37 percent of internists made the "guideline-based preventive choice" of prescribing no aspirin or other antiplatelet therapy -- drugs that help prevent blood clots by keeping platelet blood cells from clumping together. The majority indicated that they would prescribe a daily aspirin for such a patient to reduce the risk of heart attack.

When asked whether they would start drug therapy to combat abnormal cholesterol levels, 51 percent of doctors said they would not do so in this low-risk patient -- which is in accordance with guidelines. On the other hand, 41 percent said they would prescribe a statin.

When it came to basic lifestyle advice, which is appropriate for low- and high-risk patients alike, doctors often fell short.

For example, while experts recommend that all adults limit their intake of artery-clogging trans fats, over one-third of doctors in the survey failed to recommend this measure for the low-risk 45-year-old woman.

For a 50-year-old man at high risk for heart disease, only 59 percent of family doctors and 56 percent of internists correctly identified the guideline-based goal of keeping "bad" LDL cholesterol below 100 milligrams per deciliter.

Similarly, for a 78-year-old woman at high risk for heart disease but no obvious symptoms, only about half of family doctors and internists were in accordance with guidelines to order a stress test should she develop chest pain or shortness of breath.

Doctors in practice for 10 years or less were much more likely than doctors in practice for more than 10 years to make appropriate guideline-based choices for the prevention of heart disease. Younger doctors were also more apt to adhere to guidelines than were more experienced doctors.

Doroodchi and colleagues found it "especially concerning" that doctors who see a greater percentage of patients with high blood pressure and cholesterol abnormalities were significantly less likely to offer guideline-based care.

"Innovative educational approaches," they conclude, "are needed to address barriers, and target specific groups of physicians to facilitate implementation of guideline-based recommendations for cardiovascular management."

The findings should not, however, be taken as a sign that doctors lack concern for their patients, according to Doroodchi.

"Most primary care physicians are concerned about cardiovascular risk in their patients and set goals for their patients to reduce this risk," the researcher said. "Physicians are concerned that their patients do not follow their advice about changes in exercise and diet, and (that) they do not always take the medicine that is prescribed."



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Thursday, August 7, 2008

Cognitive problems cause heart disease

Results of a study in the European Heart Journal indicate an association between heart disease and lower thinking or "cognitive" performance in middle-aged adults.

Using data from the Whitehall II study, Dr. Archana Singh-Manoux, of INSERM, Cedex, France, and colleagues examined the association between heart disease and cognition in 10,308 subjects who were 35 to 55 years of age when the study began in the late 1980s. Heart attacks and other related heart problems were recorded up to 2004, at which point 5837 subjects had completed six cognitive tests.

Men and women who developed heart disease scored lower on a number of cognitive tests, particularly those involving reasoning and vocabulary, than did their peers without heart disease. Moreover, there was evidence, at least in men, that the longer the heart disease was present, the greater the impairment in thinking.

"Our results suggest that even among middle-aged individuals, heart disease is associated with poor cognitive performance with some evidence to suggest a stronger effect among those with longest standing (disease)," Singh-Manoux and colleagues conclude.

However, these findings are unable to answer the question of whether heart disease leads to impaired cognition or vice versa, the authors note.



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Wednesday, July 30, 2008

Garlic helps lower blood pressure

Garlic supplements may lower blood pressure just as effectively as some drugs used to treat hypertension can, according to a new research review.

"Supplementation with garlic preparations may provide an acceptable alternative or complementary treatment option for hypertension," Dr. Karin Ried and colleagues from The University of Adelaide in South Australia write.

Research to date on garlic and blood pressure has had "inconclusive" results, they note, while the last meta-analysis - in which the results of several studies are analyzed collectively -- only included studies done up until 1994.

To provide an updated perspective, Ried and her team included more recently published studies in their analysis, identifying 11 studies in which the patients were randomly assigned to garlic or placebo. In most studies, participants given garlic took it in powdered form, as a standardized supplement. Doses ranged from 600 mg to 900 mg daily, which study participants took for 12 to 23 weeks.

When the researchers pooled the data from the trials, they found that garlic reduced systolic blood pressure (the top number in a blood pressure reading) by 4.6 mm Hg, on average. An analysis limited to people with high blood pressure showed garlic reduced systolic blood pressure by 8.4 mm Hg, on average, and diastolic blood pressure (the bottom number) by 7.3 mm Hg. The higher a person's blood pressure -was at the beginning of the study, the more it was reduced by taking garlic.

The effects were similar to those of widely used drugs for treating hypertension, for example beta blockers, which reduce systolic blood pressure by 5 mm Hg, and ACE inhibitors, which produce an 8 mm Hg average drop in systolic blood pressure, the researchers note.

The 600 mg to 900 mg dosage used in the studies is equivalent to 3.6 mg to 5.4 mg of garlic's active ingredient, allicin, Ried and her team point out. A fresh clove of garlic contains 5 mg to 9 mg of allicin.

In the population as a whole, they note, reducing systolic blood pressure by an average of 4 to 5 points and diastolic blood pressure by 2 to 3 points could cut the risk of heart disease and heart disease-related death by up to 20 percent.

More research is needed to determine whether garlic supplementation might have a long-term effect on heart disease risk, the researchers conclude.



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Unhealthy lipid levels found in heart patients

Many patients with cardiovascular disease fail to achieve recommended levels of "bad" LDL-cholesterol and other lipids (blood fats), according to a report published this month.

Dr. Nathan D. Wong from the University of California, Irvine, and colleagues examined the extent to which recommended levels of lipids were present in a large sample of U.S. adults.

Among individuals free of cardiovascular disease, 85 percent to 89 percent had recommended levels of harmful LDL-cholesterol and triglycerides and healthy or "good" HDL-cholesterol, the researchers report. The same was true for non-HDL-cholesterol.

In contrast, less than 40 percent of patients with cardiovascular disease were at goal for LDL-cholesterol and non-HDL-cholesterol, 35 percent had low levels of healthy HDL-cholesterol, and 44 percent had levels of harmful triglycerides above the recommended level.

Overall, only 17 percent of cardiovascular disease patients were at recommended levels for all lipids, the researchers report in the American Heart Journal.

Just over a third of patients with abnormal lipid levels reported being treated with a lipid-lowering drug, the report indicates, though this ranged from 3 percent in patients aged 20-29 years to 51 percent in patients aged 70-79 years and from 24 percent in those without cardiovascular disease to 63 percent in those with heart and blood vessel disease.

Despite treatment, only 30 percent of these patients (including only 19 percent of patients with cardiovascular disease) were at recommended levels of all three lipids.

The percent of individuals at goal for the various lipids increased between 1988-1994 and 2003-2006, the investigators say, but treatment rates in all groups remained suboptimal.

"Greater use of proven efficacious dosages of lipid-lowering agents as well as intensified consideration of combination therapy to address those with multiple lipid disorders are required, particularly among persons with cardiovascular and related high-risk comorbidities," Wong and colleagues conclude.



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Cholesterol

CHOLESTEROL IS A LIPID, OR FAT-LIKE SUBSTANCE,
made by animal cells. The role of an elevated blood
cholesterol in causing a blockage to arteries by atherosclerosis
and a subsequent myocardial infarction was a
controversial issue from 1900 to 1994. Advice to patients
during those 90 years was often half-hearted. Until recently
we were not able to put the blame firmly on cholesterol
and convince physicians and patients worldwide to
aggressively lower serum cholesterol levels. The key piece
of scientific evidence proving that lowering elevated blood
cholesterol in humans prevents fatal or nonfatal heart
attacks was missing.

I. THE MAGNITUDE OF THE PROBLEM
If cholesterol is the major cause of atheroma that obstructs
the flow of blood in arteries of the heart and brain,
significant morbidity and mortality from cardiovascular
disease would be prevented by the aggressive lowering of
total serum cholesterol and low-density lipoprotein (LDL)
cholesterol. The complete occlusion of a coronary artery or
cerebral artery is virtually always caused by a combination
of atheromatous obstruction of the artery and subsequent
rupture of the plaque of atheroma with thrombus
formation on the ruptured material. Thus, the term
atherothrombosis (see the chapter, Atherosclerosis/Atherothrombosis).
Atherothrombotic cardiovascular disease causes more
than 14 million deaths per year worldwide in a population
of about 6 billion people. This is expected to increase to
more than 25 million deaths by the year 2020 in a
population of about 7.4 billion people. It is estimated
that worldwide interventions could prevent more than
one million deaths annually. The prevention of atheroma
is obviously more important to world health than
the expensive production of so-called left ventricular assist
devices, which are a bridge to heart transplantation.

CAUSES OF HYPERCHOLESTEROLEMIA
A. Familial Hypercholesterolemia
This is a primary genetic abnormality. In very rare cases,
marked elevation of cholesterol (800–1500 mg/dl) is caused
by a genetic defect. A receptor on the surface of cells (LDL
receptors) removes LDL cholesterol from the blood. In
this disorder there is decreased production or function of
the LDL receptor. This autosomal disorder may involve
abnormalities in the synthesis, transport, or clustering of
the LDL receptor.

Homozygous familial hypercholesterolemia fortunately
is rare and occurs in approximately one per million
individuals in the United States. These patients have no
functioning LDL receptors and have markedly elevated
LDL cholesterol as high as 1200 mg/dl (31 mmol/L)
and extensive coronary and peripheral atherosclerosis.
Acute MI may occur within the first one to two years of
childhood.

Heterozygotes have a reduction of 50% of the circulating
LDL receptors and may have serum cholesterol
levels in the range of 300–800 mg/dl and manifest coronary
artery atherothrombosis, peripheral vascular disease,
or atheromatous obstruction to the abdominal aorta in
the third or fourth decade. Racial differences may determine
the number of LDL receptors, and thus the ability
to remove LDL cholesterol gradually from the bloodstream
is affected.

Familial combined hyperlipidemia is a common condition
that occurs in more than 1% of the North American
population. This disorder may cause elevation of total
cholesterol or triglycerides or both.

B. Polygenic Hypercholesterolemia
In this condition there is a genetic predisposition and
dietary factors. In susceptible individuals with a decreased
number of LDL receptors, high saturated fat and
cholesterol intake causes substantial elevation of serum
cholesterol with levels in range of 260–320 mg/dl
(6.5–8.3 mmol/L). Approximately 3% of the population
in the United States appears to be affected. Although
elevation in total cholesterol is less severe than in heterozygous
familial hypercholesterolemia, the elevation of total
and LDL cholesterol increases risk for coronary artery
disease and drug therapy with statins is advisable.
C. Other Causes for Hypercholesterolemia
Type 2 diabetes occurs in approximately 7% of the North
American population and nearly all of these individuals
have some form of dyslipidemia. Their serum cholesterol is
usually in the range of 240–290 mg/dl (6.2–7.5 mmol/L).
Hypothyroidism is a relatively common condition that
decreases the metabolism with increases in serum cholesterol
in the range of 240–320 mg/dl.

Renal disease can also affect cholesterol levels. A form of
glomerulonephritis causes marked loss of protein in the
urine, diffuse edema, and hypercholesterolemia. Biliary
cirrhosis with its prolonged obstructive jaundice causes
marked elevation in serum cholesterol. Other causes include
pancreatitis, monoclonal gammopathy, and porphyria.

IV. TYPES OF CHOLESTEROL
Cholesterol is a member of a class of naturally occurring
compounds called sterols. It is an essential part of the
fatty sheath that insulates nerves and the outer membrane
of all animal cells, and is a component of chemicals that
include steroids (cortisone) and sex hormones such as
androgens and estrogens. Cholesterol acts as a precursor
of bile acids and occurs in high concentrations in the
brain, nerves, and adrenal glands; cholesterol concentration
is greater than 3 g per 100 g in the brain. Body cells
satisfy their cholesterol requirements for maintenance
and growth by intracellular synthesis of cholesterol and
the receptor-mediated uptake from the external medium
of cholesterol-rich LDL particles.

Dietary cholesterol is absorbed from the jejunum in
an unesterified form. Within the small intestine cholesterol
is esterified with fatty acids and incorporated into the
triglyceride core of chylomicrons that are secreted into
the intestinal lymphatics and reach the blood circulation.
Within the bloodstream chylomicrons are converted
into remnant particles through the action of lipoprotein
lipase. Triglycerides are liberated and virtually all the cholesterol
particles are carried to the liver via the portal vein.
Less than half the cholesterol in the diet is absorbed. It is
interesting that after many years intensive drug research,
ezetimibe, the newest agent, has been shown to localize in
the distal and at the brush border cells of the small intestine
and inhibit cholesterol absorption. This drug is,
therefore, an important addition to our therapeutic armamentarium
because it can be combined safety with the
powerful acting statins that interfere with the manufacture
of cholesterol in the liver.

The human body and contains approximately 1 g of
cholesterol per kilogram body weight. About 1 g of cholesterol
is lost from the body by the conversion to bile
acids and steroid hormones. This loss is balanced by endogenous
synthesis from saturated fats and fecal excretion of
unabsorbed dietary cholesterol.

Some of the cholesterol in blood is derived from the
food you eat, but the major part, greater than 70%, is
manufactured in the liver, mainly from saturated fats.
Thus, if we had no cholesterol in the diet, the liver would
manufacture more cholesterol to compensate. Some excess
cholesterol is excreted in the bile. Cholesterol is present
only in foods of animal origin, in particular, eggs, milk,
butter, cheese and meats, and a very high concentration
is present in gland meats, such as liver, brain, kidney,
heart, and sweetbreads. Plant-based foods such as potatoes,
wheat, rice, vegetables, fruits, grains, and beans contain no
cholesterol.

In order to understand the changes that may be required
in your diet, it is important to learn the difference
between the types of cholesterol: total cholesterol, LDL
cholesterol, and HDL cholesterol. Individuals should
become familiar with the different types of fats in foods
such as triglycerides, saturated fats, monounsaturated fats,
and polyunsaturated fats.

A. Total Cholesterol
Cholesterol is a fat (lipid) that is insoluble in water. It is
absorbed by the intestine or released from the liver into
the bloodstream. Cholesterol does not circulate freely in
solution but is attached to a protein carrier, forming a
molecule called a lipoprotein. Lipoproteins vary in size
and density; the smaller the size, the higher the density.
Cholesterol may be transported in a low-density lipoprotein;
thus the term ‘‘low-density lipoprotein (LDL) cholesterol.’’
There is also a high-density lipoprotein (HDL)
cholesterol (see the chapter Dyslipidemia).

When a doctor states that your cholesterol is 250 mg
(6.5 mmol), he is giving you the total amount of cholesterol
in your blood, which includes LDL and HDL
cholesterol. The total figure is not broken down unless
specifically requested by the doctor. The values given in
milligrams are the amount in each 100 ml of blood or
number of millimoles in one liter of blood.

B. Low-Density Lipoprotein (Bad) Cholesterol
The low-density lipoprotein is small and contains most of
the cholesterol that is transported to cells. About 75%
of the blood cholesterol is carried as LDL cholesterol.
The LDL cholesterol particle is the one responsible for
atheroma formation and progression. The higher the level
of LDL cholesterol in the blood, the greater the risk of
coronary heart disease; thus the term ‘‘bad’’ cholesterol.
Oxidation of LDL cholesterol is believed to be an
important process in the formation and progression of
atheroma. It appears that oxidative modification of LDL
causes an increase in foam cell formation and increased
rates of LDL accumulation within developing atheromatous
plaques. In addition, oxidized LDL appears to have
direct cytotoxic effects on the endothelium of arteries at
the site of injury.

Oxidative stress causes oxidation of LDL cholesterol.
Oxidative stress results from the production of reactive
oxygen species, superoxide anion, and hydrogen peroxide
molecules that cause oxidative damage and trigger intracellular
signaling cascades. The constituents of the atheroma
plaque produce and use reactive oxygen species. LDL
cholesterol reduction appears to reduce the production of
deleterious reactive oxygen species.

This author believes that it is unlikely that LDL particles
cause direct injury to normal healthy endothelium,
because the same blood level of LDL cholesterol is present
in veins that virtually never develop atheroma except
when they are exposed to high blood pressure, such as in
severe pulmonary hypertension. It is more likely that shear
stress caused by turbulence of blood at particular focal
points in arteries, particularly at branching areas, and
other factors cause endothelial injury; LDL particles then
just partake in the orchestration of accelerated atheromatous
plaque growth. Increased blood pressure appears
to promote atherogenesis through the mechanical effects
of pulsatile blood flow (see the chapter Atherosclerosis/
Atheroma).

A plasma level of LDL cholesterol greater than
160 mg/dl is associated with a high risk for coronary
artery disease events in susceptible individuals and levels
less than 100 mg/dl confer a low risk. When an individual
is documented as having very-high-risk LDL cholesterol
levels (>200 mg/dl) associated with premature coronary
artery disease, all available first-degree relatives should be
tested.

C. High-Density Lipoprotein (Good)
Cholesterol
Much interest has been focused on HDL cholesterol,
so-called because it is very small in size and very high in
density. HDL cholesterol is believed to carry cholesterol
away from body cells such as the lining of arteries helping
to keep the artery wall clean; thus the term ‘‘good’’
cholesterol.

As discussed earlier most heart attacks occur in individuals
with total cholesterol levels between 210 and 240
mg/dl (5.5 and 6.2 mmol/L), and more than 50% of adult
Americans have cholesterol levels in this range. In these
individuals with borderline high blood cholesterol, a low
level of HDL cholesterol further increases the risk for
coronary artery disease. Figure 1 shows the incidence of
coronary heart disease in four years by HDL cholesterol
and total plasma cholesterol level for men and women
older than 49 and free of cardiovascular disease.

The HDL system comprises a variety of small lipoproteins
smaller than LDL, but both HDL and LDL
particles contain mostly cholesteryl ester. Virtually all HDL
particles contain apoA-1 as their major apolipoprotein and
the particles vary a little in size; the largest particles is HDL
2 and the predominant smaller particle HDL 3.

1. Metabolism
The many steps involved in HDL metabolism are not
fully understood. Small HDL 3 particles accumulate cholesteryl
ester and expand to HDL 2; an important step is
further transformation by interaction with cholesteryl ester
transfer protein (CETP). At each step of the HDL metabolic
cycle some apoA-1 is lost. High levels of CETP turn
up the cycle at a high rate and this diminishes the total
pool size of HDL that is manifested as a lowered HDL
cholesterol level.

It appears that CETP is an important enzyme involved
in HDL biology. Inhibiting this key enzyme that modulates
HDL can raise HDL levels. Vaccines and cardioactive
agents that may increase HDL levels significantly are being
investigated, and there is great hope that major increases in
HDL cholesterol would cause significant protection from
atherothrombosis and its serious impact on morbidity and
mortality worldwide.

2. Effect on Atherosclerosis
Several epidemiologic studies indicate an inverse relationship
between HDL cholesterol levels and risk for coronary
artery disease (see Fig. 1). A low HDL cholesterol level
greater than 35 mg/dl (0.9 mmol/L) has been designated as
a major risk factor for coronary artery disease. It is stated
that every 1% increase in HDL cholesterol decreases coronary
artery disease risk by about 2%, and each 1% reduction
in total cholesterol should produce a 2% reduction in
coronary artery disease risk. In Finland where HDL blood
cholesterol levels are among the highest in the world, the
cardiovascular death rate is the highest of all European
countries (see the chapter Heart Attacks).

Some scientists suggest that HDL promotes reverse
cholesterol transport, that is, the removal of cholesterol
from tissues including removal of unesterified cholesterol
in atheromatous plaques so that it can be transported to
the liver and excreted. But proof is required. Most important,
HDL is believed to prevent LDL from oxidation
and aggregation and thus protect against formation and
progression of atheroma. This important area requires
further intensive investigation for clarification.

3. Variability of HDL Levels
About 25% of blood cholesterol is carried as HDL
cholesterol. People with high levels of HDL cholesterol,
greater than 60 mg (1.6 mmol), appear to live longer and
have less coronary artery disease. People with levels less
than 31 mg (0.8 mmol) have an increased risk of coronary
artery disease. It is not clear why some people should have
high values and others very low. It appears that about half
of the variation in HDL levels in the general population is
explained by genetic factors. Fortunately not all individuals
with low HDL levels get heart attacks.

Nongenetic factors that are known to be associated with
low levels of HDL are diabetes, obesity, smoking, and lack
of exercise.

Most females and males prior to puberty have about the
same cholesterol levels. Boys, however, at puberty have
about a 20% drop in HDL and a rise in LDL cholesterol.
The decrease in HDL cholesterol may be due to an
increase in androgens. In men the HDL level stays fairly
constant up to age 55, then starts to rise between 55–65.
It is possible that this rise might be due to a decrease
of androgens, which occurs during the male climacteric
period. In women there is a gradual rise in HDL cholesterol
from age 25 onward. Women are believed to be
protected until post menopause by this increase in HDL
and by their hormonal status. Why women are protected
from coronary heart disease until menopause and yet not
protected from strokes is not easily explained, especially if
atherosclerosis is the basis of both diseases.
There is a relationship between HDL cholesterol
levels and population groups, foods, alcohol, exercise,
and drugs.

D. Very-Low-Density Lipoprotein
The very-low-density lipoprotein (VLDL) is very large and
low in density. It transports triglycerides, which are used
mainly as a fuel; for example, in exercising muscle. The
evidence linking elevated blood triglyceride levels with
coronary heart disease is very weak and unclear. Thus, an
elevated blood triglyceride level alone is not of importance.
Weight reduction or cessation of alcohol intake always
causes a marked reduction in triglyceride levels but does
not alter LDL cholesterol levels.

V. BLOOD TESTS
A. Total Cholesterol
What is a normal blood cholesterol, and when does the
level produce a risk of coronary heart disease? Blood
cholesterol is not necessarily very high, that is, greater than
265 mg (6.9 mmol), in those who have heart attacks. In
fact, most heart attacks occur in individuals with blood
cholesterol around the average of 220–250 mg (5.7–6.5
mmol). In the LIPID study described above, only 3806
men with a blood cholesterol greater than 265 mg could be
found from a screening of 480,000. The remainder had
cholesterol levels of less than 265 mg and most likely in the
range of 200 to 250 mg.

Between 1970 and 1989, laboratories in North America
reported a normal cholesterol as between 150 (3.9 mmol)
and 250 (6.5 mmol). But it is now established that
individuals with so-called normal cholesterol in the range
of 220–250 are at increased risk, and heart attacks are
common in individuals with such levels. A blood cholesterol
of 220–250 mg (5.7–6.5 mmol) is considered high
by world standards. Most doctors now talk about an
optimal safe total cholesterol level of less than 190 mg/dl
(4.9 mmol/l) or LDL less than 120 mg (3 mmol). Heart
attacks are uncommon in individuals with a cholesterol
level less than 160 mg (4.2 mmol).

If we treat patients with a cholesterol level greater
than 250 mg (6.5 mmol), we will be excluding more than
80% of the population who are at high risk for coronary
heart disease. To reiterate, most heart attacks in North
America occur in people with blood cholesterol between
220 and 260 mg. Individuals with a blood cholesterol
less than 180 mg (4.7 mmol) obviously deal with
cholesterol by their own natural process. They are among
the fortunate; no dietary modification is necessary, and
blood cholesterol only needs to be rechecked about every
five years.

The blood cholesterol measurement gives the total
blood cholesterol, that is, LDL cholesterol plus HDL
cholesterol. Food eaten within hours does not have an
immediate effect on total blood cholesterol and HDL
cholesterol measurements, so fasting is not necessary for
this test. Triglyceride level is not an independent risk
factor and therefore widespread screening for elevated
triglycerides is not warranted. It is also an expensive
investigation. If your doctor thinks that triglyceride determination
is necessary, you must fast for 14 h before
blood is taken. Blood tests for glucose, diabetes, and
triglycerides are the only tests for which it is necessary to
fast for 12–14 h before the test.

B. Blood LDL Cholesterol Levels
Determination of LDL cholesterol is not done routinely,
because it is a difficult, time-consuming, and expensive
technique. It must be done fasting because it is
calculated by a formula that requires a triglyceride blood
level, which must be done after fasting 12 hours. The
formula for calculating the blood LDL cholesterol level
is as follows:
LDL cholesterol
¼ total cholesterol  HDL cholesterol
 ðtriglyceride divided by 5Þ
¼ mg=dl; for the value in mmol=L divide by 2
This formula does not apply if the triglycerides exceed 250
mg/dl.

In individuals age 15–75 optimal LDL cholesterol levels
are less than 115 mg/dl (3 mmol/L). In North America,
the UK, and Europe the vast majority of individuals
have an LDL cholesterol in the range of 130–200 mg/dl
(3.4–5.2 mmol/L). In patients with coronary heart disease,
the level of LDL is of paramount importance and should
be maintained at less than 100 mg/dl (2.6 mmol).

C. HDL Cholesterol Blood Level
Blood testing for HDL cholesterol levels can be done in the
nonfasting state. Levels less than 35 mg/dl (0.9 mmol/L)
are considered low and less than 27 mg/dl (0.7 mmol/L) is
considered unacceptably low. Levels greater than 54 mg/dl
(1.4 mmol/L) are considered optimal.

CORONARY ARTERY DISEASE RISK
A. Based on LDL Cholesterol
A high LDL cholesterol level is considered the most
important major risk factor for coronary artery disease.
The relationship between LDL cholesterol and coronary
artery disease risk is continuous over a broad range of
blood levels from low to high (110 mg/dl to greater than
190 mg/dl) and LDL cholesterol is the primary target of
therapy.

Patients with established coronary artery disease are
considered to have a 10-year risk greater than 20%. It is
expected that more than 20% of such individuals will
develop a recurrent coronary artery disease event within 10
years. In these individuals LDL cholesterol levels greater
than 130 mg/dl greatly increase the risk. Most national
guidelines state that in patients with proven coronary
artery disease or CAD risk equivalent, particularly
diabetes, drug treatment is strongly indicated to maintain
the level to less than 100 mg/dl (2.6 mmol/L).

Individuals without coronary artery disease or evidence
of cardiovascular disease should be assigned a risk based on
the following:
1. Their levels of LDL cholesterol: risk is increased if the
LDL-C is >190 mg/dl, and the goal should be <130
mg/dl (3.5 mmol/L)
2. Presence of diabetes risk score of >20 with a goal LDL
<100 mg/dl
3. Age
4. Family history of premature coronary heart disease
5. HDL cholesterol level
6. Smoking
7. The presence or absence of hypertension

DIETS AND CHOLESTEROL
A. Saturated Fats and Cholesterol
All animal fat is saturated and solid at normal room
temperatures. The degree of hydrogenation of a fat
determines how solid and saturated it is. Saturated fats
are broken down in the body and increase blood cholesterol.
Therefore, the most effective dietary method of
lowering blood cholesterol is to reduce intake of saturated
fats. High-cholesterol foods are few, therefore, we do not
use the term low-cholesterol diet.

Vegetable fats are unsaturated and almost all are liquid
at room temperatures. There are three vegetable oils that
should be avoided: coconut, palm, and peanut. Coconut
oil contains a high amount of saturated fat and is used
for cooking in several countries. It is also used in North
America in nondairy cream substitutes, for example,
coffee cream. Palm oil contains significant amounts of
saturated fat, and peanut oil, though mainly unsaturated,
has certain fatty acids that produce plaques of atheroma
in animals. The only vegetable that contains a little
saturated fat is the avocado; therefore, low-cholesterol,
low-fat diets often recommend that you avoid avocados.
You will note from Table 1, however, that although a large
avocado contains a significant amount of fat, only a little
of it is saturated, and no cholesterol is present. Therefore,
one avocado a week is an excellent food, especially if a
high potassium intake is required.

B. Polyunsaturates and Linolenic Acid
The replacement of some saturated fats in the diet by
polyunsaturated, monounsaturated, and other unsaturated
fats found in abundance in vegetable oil reduces blood
LDL cholesterol. The saturated and polyunsaturated fat
contents of commonly used foods are given in Table 1.
Oils recommended for the preparation of meals include
canola, olive, and soybean because they contain alphalinolenic
acid, very low cholesterol levels, and a minimum
of saturated fat. For example, ‘‘cholesterol-free’’ canola oil
contains 6% saturates and will produce a small amount
of cholesterol in the body. Not all vegetable oils claim to
be cholesterol free but contain significant saturated fats.
Because vegetable margarines contain a small amount of
saturated fat and hydrogenation remains controversial,
they should be used in moderation. Some products may have palm or
coconut oil added to enhance hardening; these two oils are
not recommended. Olive oil is recommended
for salads, but olive oil margarines may contain palm oil
to enhance hardening so read labels carefully. Some margarines
claim that they contain no cholesterol and are
nonhydrogenated yet they contain palm oil.

It is important to note that many recipes developed for
weight reduction diets tend to cut out carbohydrate foods
in order to decrease weight and may even introduce foods
that increase blood clotting and cholesterol. Therefore,
be careful in choosing ‘‘popular’’ weight reduction diets.
Consult Table 4 and the instructions given in the chapter
on Heart Attacks.

C. Nuts and Cholesterol and Risk
Most nuts contain no cholesterol and very little saturated
fats, but the exceptions include coconut and Brazil nuts
which have high saturated fat content and their products
should be avoided (see Table 4). Cashew nuts and peanuts
have significant saturated fats, and although they contain
an adequate amount of monounsaturated and polyunsaturated
fatty acids, they are not recommended and should
be used sparingly. Additionally, it appears that peanuts
may have atherogenic potential. Nuts that contain little
saturated fat and a high amount of monounsaturated fats
include almonds, walnuts, and hazelnuts and their intake
is highly recommended.

D. General Advice on Diets
Diets to reduce atherosclerosis or heart attacks must be
tailored to meet the needs of the individual, because each
family has different eating habits. Special recipes and diet
sheets may be misleading and difficult to follow for a
lifetime and individuals should consult Table 4, or similar
information.

It is recommended that the general population use foods
that contain a low amount of saturated fat and cholesterol
and make an effort to increase intake of polyunsaturated
and monounsaturated fat, linolenic acid, and foods that
have a favorable effect on blood clotting (see the chapter
Blood Clots). Reduction in the intake of cholesterol
alone is not sufficient because saturated fat is converted
into cholesterol in the body; therefore, reduction in
saturated fat intake is essential. Most important, the
intake of trans fat must be curtailed.

The recommendation made by the American Heart
Association is as follows:
Total fat intake should be reduced from the average
40% of calories to 30%. Polyunsaturated fat should
provide up to 10% of calories and the polyunsaturated
fat to saturated fat (P/S) ratio should be about 1:1.
Carbohydrate intake should be increased from an
average of about 45%–55% to maintain average
body weight, and protein intake should remain at
about 12–14%.
Scotland has not shared, however, in the slight decline
in mortality that has been experienced in Australia,
Belgium, Canada, Finland, Norway, and the United
States. Scotland has moved up in the world league of
coronary deaths to second for men, and Northern Ireland
has moved to third for men and second for women. In the
UK, fat intake has remained the same for the past 30 years
at about 40% of food energy and even increased between
1974 and 1982 to 41% of food energy. The Department
of Health and Social Security made the following
recommendations to physicians and the general public in
the UK:

Reduce the total fat intake to 35% of food energy with
saturated fats making up no more than 11%. Increase
the polyunsaturated to saturated ratio from the present
0.27 to about 0.45. The intake of polyunsaturated
acids presently at 5% of food energy should reach 7%,
which is less than the American and World Health
Organization’s suggestion of 10%.

The UK panel claims that the effects on the population
of a P/S ratio of 1.0 and beyond are unknown. Individuals
who are considered to have a high risk of developing
coronary heart disease are advised to cut fats to 30% of
food energy, with saturated fats contributing no more
than 10%, i.e., identical to the recommendation in the
United States. Thus there is consensus on both sides of the
Atlantic.

A Mediterranean style diet that contains an abundance
of linolenic acids is strongly recommended by the author;
see the chapter Diets and Heart Disease.
The reduction in dietary saturated fat intake as well
as the cessation of smoking by many individuals has provided
a decline in the incidence of coronary heart disease
mortality.

CHOLESTEROL-LOWERING DRUGS
A. HMC-CoA Reductase Inhibitors (Statins)
The statins, atorvastatin, fluvastatin, lovastatin, pravastatin,
and simvastatin, are cholesterol-lowering agents
that are effective and have few side effects. They cause a
20–40% reduction in total, or LDL, cholesterol. They may
cause a small, 1–6%, increase in HDL cholesterol, but
this effect is variable. Clinical trials have shown that these
agents decrease LDL cholesterol levels and reduce the risk
of heart attack and death from heart attacks. The newest
agent, rosuvastatin, is even more powerful than Lipitor
in reducing LDL levels to goal. Randomized clinical trials
that document the effectiveness of these agents are given
the chapter Dyslipidemia.

Mild side effects from statins include headaches, muscle
aches, and pain in the upper abdomen without gastritis,
ulcers, or bleeding. An increase in the liver enzymes may
be detected on blood test, but the risk subsides when the
drug is discontinued. Caution: Do not take with niacin
or fibrates such as gemfibrozil or fenofibrate. Statins are
contraindicated in pregnancy.

1. Atorvastatin
Supplied: Tablets: 10, 20, 40, 60 mg.
Dosage: 10–40 mg once daily; the author’s maximum
dose is 60 mg daily. The 80 mg dose is rarely required and
more adverse effects may occur at the maximal dose of
the drug.
2. Fluvastatin
Supplied: Capsules: 20 mg.
Dosage: 20–40 mg after the evening meal or bedtime.
3. Lovastatin
Supplied: Tablets: 10, 20, 40 mg.
Dosage: 10–40 mg after the evening meal.
4. Pravastatin
Supplied: Tablets: 10, 20, 40 mg.
Dosage: 10–40 mg after the evening meal or bedtime.

5. Rosuvastatin
Supplied: Tablets: 10, 20, 40 mg.
Dosage: 10 mg once daily is more effective in lowering
LDL cholesterol than 40 mg of Lipitor or simvastatin.
It causes a better increase in HDL cholesterol. The author’s
maximum suggested dose is 20 mg daily.
6. Simvastatin
Supplied: Tablets: 5, 10, 20 40, 60 mg.
Dosage: 10–40 mg after the evening meal.
B. Cholesterol Absorption Inhibitors
1. Ezetimibe
Supplied: Tablets 10 mg.
Dosage: 10 mg once daily. This drug has a low side
effect profile and can be combined with a statin.

Resins

1. Cholestyramine
Supplied: Powder in packets or in cans with a scoop.
Dosage: 12–24 g daily in liquid a half hour before to a
half hour after meals. Start with 4 g (one scoop) twice daily
for one week, then 4 g three times daily for one month,
and if necessary, thereafter increase to 8 g three times daily.
Cholestyramine and colestipol are not absorbed from
the gut and act by binding bile salts in the intestine. This
action causes the liver to increase the conversion of
cholesterol to bile acids, which are excreted in the bile.
Cholestyramine has no serious side effects. Constipation,
nausea, bloating, gas, and abdominal cramps may
occur. High doses taken for several years can cause poor
absorption of certain vitamins. It may interfere with the
absorption of digoxin and blood thinners (anticoagulants).
The recent introduction of ezetimibe as an effective drug
will render bile acid resins such as cholestyramine and
colestipol obsolete.

Fibrates
1. Gemfibrozil
Supplied: Capsules: 300 mg.
Dosage: 300 mg taken about a half hour before the
morning and the evening meal for one to two weeks, then
300 mg twice daily.
Gemfibrozil is the first fibrate to be introduced in the
seventies since the discontinuation of clofibrate in the
late sixties. This drug causes a 5–10% reduction in serum
cholesterol, 30% reduction in triglycerides, and a 5–10 %
increase in HDL cholesterol. Side effects include stomach
pain and bloating in less than 5% of patients. Gallstones
may occur.

In the VA-HIT study gemfibrozil caused a 31% decrease
in triglycerides, but only a 6% increase in HDL cholesterol
compared with placebo. This negligible increase in HDL is
claimed to have caused a beneficial reduction in cardiac
events. There was no reduction in all cause mortality or in
total cardiac mortality; there was a small, 22% reduction
in total cardiac death and nonfatal myocardial infarction
(MI) (P<0.05), a low level of significance. Virtually all of
the benefit was due to reduction in nonfatal MIs; a result
similar to that observed for vitamin E in the CHAOS
study.

2. Fenofibrate
Supplied; Tablets 100, 160 mg.
Dosage: 100–200 mg once daily with the main meal,
maximum 100 mg in renal dysfunction.
3. Bezafibrate
Supplied: Tablets 200 mg.
Dosage: Mono formulation once daily in the evening.
E. Niacin (Nicotinic Acid)
This drug is not often used because of prominent side
effects, which include flushing, itching, nausea, abdominal
pain, diarrhea, jaundice, gout, palpitations, and increased
blood sugar in diabetics. This drug should not be used if
you have low blood pressure or have had a heart attack,
heart failure, liver disease, a stomach ulcer, or diabetes. It is
not advisable to combine niacin with statins because severe
damage to muscles and the kidneys may occur.

Combination Therapy
The combination of simvastatin and ezetimibe has been
shown in a clinical trial to be more effective than simvastatin
alone. The combination caused LDL cholesterol
reductions of 44–57% and HDL cholesterol increases of
8%–11%. Ezetimibe 10 mg plus simvastatin 10 mg and
simvastatin 80 mg alone each caused a 44% reduction
in LDL cholesterol. The combination was well tolerated
with the safety profile similar to those of simvastatin and
of placebo.

The combination of rosuvastatin and ezetimibe is
advisable for severe hypercholesterolemia. This is the
most powerful combination available for the reduction
of elevated LDL cholesterol and is a welcome addition to
the clinician’s armamentarium. Caution is required, however,
because liver dysfunction or rhabdomyolysis may be
precipitated at high doses of any statin, particularly if drug
interaction occurs.

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Chagas Disease


I. EPIDEMIOLOGY
The protozoan Trypanosoma cruzi causes Chagas disease,
which affects more than 30 million individuals, with
approximately 100 million at risk in Latin America.
Figure 1 shows the distribution of Chagas disease in the
Americas. This disease is prevalent only in Central and
South America, particularly in Argentina, Chile, Brazil,
and Bolivia. It also occurs in the southern United States,
however, where more than 90,000 Latin Americans are
believed to be infected. The risk of transmission in the
United States is mainly by blood transfusion by this
immigrant population.

A. Transmission
Chagas disease is transmitted to children and young adults
less than age 20 through the bite of a bug (reduviid,
subfamily Triatominae). The bug becomes infected by
feeding on infected animals such as the armadillo,
opossum, raccoon, and skunks. Domestic dogs and cats
also provide an extensive reduviid reservoir for infecting
entire families.

The biting bug unfortunately dwells in the roofs and
walls of houses. During the night the bug drops onto the
sleeping individual and inflicts bites around the eyes.
Infection is transferred when the trypanosomes in the
animals excrement enters the wounded skin or penetrates
the conjunctiva. The protozoa multiplies and then
migrates through most organs of the body including the
myocardium, pericardium, liver, spleen, and brain. Chagas
disease is primarily transmitted through blood transfusions,
and unfortunately screening of blood is financially
not possible in the affected countries. The simple
accomplishment of screening blood, building better
homes, and screening cats and dogs would prevent the
majority of infections.

II. SYMPTOMS AND SIGNS
A. Acute Phase
The bite of the bug around the eyes allows the
trypanosomes to gain entry through the conjunctiva.
This often results in one-sided swelling around the eye
(periorbital edema) and swelling of the eyelid (Romana
sign). If the entry is through the skin, a lesion called a
chagoma appears. The initial lesion may go unrecognized,
however, and no symptoms may appear until after more
than 15 years when symptoms of chronic disease emerge.
In about 10% of infected individuals acute symptoms
such as muscle aches and pains, fever, sweating, and
enlargement of the liver and spleen occur. If the parasitic
infection involves the cardiac muscle, an acute myocarditis
and heart failure may supervene causing death. Lesions
may spread to involve the endocardium and stimulate the
flowing blood to form a clot that may embolize. The
pericardium may be involved causing pericardial effusions.
Young children become more seriously ill than young
adults, and in more than 10% the acute disease is fatal.
Many patients recover, however, and symptoms disappear
over 1–2 years. More than 40% of infected patients after
a relatively symptom-free interval of several years reveal
signs and symptoms of chronic Chagas disease.

B. Latent and Chronic Phase
Cardiac involvement is mainly due to a cardiomyopathy
that manifests about 20 years after the trypanosomal
infection. At this point, the heart muscle is uniformly
destroyed and replaced by fibrous tissue. The weakened
heart muscle is stretched, the left ventricular chamber
dilates, the pumping function is severely deranged, and
heart failure supervenes. Heart failure produces changes
in the heart, circulation, and veins that can be detected
on examination by the physician. A chest x-ray confirms
dilation of the heart and presence of fluid in the
spongework of the lungs and fluid within the pleural
space (pleural effusions).

The main manifestation of heart failure is increasing
shortness of breath on mild activity and with severe heart
failure, shortness of breath occurs at rest. Heart failure
describes the signs and symptoms that occur when the left
or right ventricles are unable to eject an adequate amount
of blood into the aorta to fulfill the needs of organs and
tissues. Thus blood remains longer in the lungs and salt
and water escapes into the air sacs (the alveoli), causing
oxygen lack and severe shortness of breath. In heart
failure, salt and water are retained by the kidneys as a
compensatory mechanism and extra fluid exudes into
tissues in dependent parts of the legs causing bilateral
leg edema. The legs are not waterlogged, they are brine
logged (see the chapter Heart Failure).

The pathologic findings include hypertrophy and
dilatation of cardiac chambers in keeping with a dilated
cardiomyopathy. The left ventricle apex becomes thin and
bulges into an aneurysm. Clot formation often occurs
within the aneurysm and thromboembolism to other
organs occurs.

The electrical bundles of the heart, particularly the right
bundle branch and the anterior fascicle of the left bundle
branch, are commonly involved by the inflammatory
process causing the ECG to show a typical pattern of
right bundle branch block and left anterior fascicular
block hemiblock. The large left bundle branch is really
involved.

Symptoms of cardiomyopathy include shortness of
breath, chest pain, syncope, and sudden death caused by
heart block due to involvement of the electrical conducting
system. In many patients the left ventricle fails, but
manifestations are mainly of right heart failure. Thus, the
shortness of breath from left ventricular failure may
diminish and signs of right heart failure may become more
prominent. These signs include fluid retention that causes
swelling of the abdomen (ascites) and bilateral leg edema.
The trypanosome in Brazil often involves the esophagus,
stomach, and colon resulting in a dilated esophagus
(megaesophagus and megacolon). This is uncommon in
Central America and Mexico because it is caused by a
different strain of trypanosome.

In the acute phase of the disease, trypanosomes are
found in the cardiac fibers accompanied by marked cellular
infiltrate around cells that have ruptured and released the
parasites. It is not unusual, however, to be unable to find
parasites in the cardiac tissue at autopsy. An autoimmune
mechanism is believed to explain the lack of correlation
of parasitemia with disease severity. T. cruzi antigen is
frequently found in biopsy specimens.

III. DIAGNOSTIC INVESTIGATIONS
A. Chest X-ray
The chest x-ray shows a dilated heart that increases to
severe proportions as the disease progresses. The lungs
may show evidence of fluid accumulation with pleural
effusions, but the lung fields may be relatively clear if
mainly right heart failure occurs.

B. Blood Tests
In Chagas disease the serum aldolase is usually elevated.
A complement fixation test (Machado-Guerreiro test) that
has high specificity and sensitivity is used to identify
chronic Chagas disease. Xenodiagnosis is the preferred test
in endemic areas. With this test reduviid bugs bred in the
laboratory are allowed to bite the patient. The parasites are
then found in the intestine of the insect proving infection
in the patient.

C. Echocardiography
Echocardiography shows enlargement of all four heart
chambers in Chagas patients. There is also a reduction in
the ejection fraction. On echo, the appearance of Chagas is
distinctive: there is hypokinesis, poor contractility of the
left ventricular posterior wall, relatively preserved intraventricular
septal wall motion, and poor movement of the
apical segment of the heart with dilatation and aneurysmal
formation.

IV. MANAGEMENT
A. Prevention
Vector control and interruption of transmission of the
parasites to humans remain crucial. In endemic areas
individuals should avoid having dogs or cats in the home.
Improved housing conditions, repair of walls and ceilings,
and added fresh paint should deter bugs from these areas.
The use of nets for sleeping should prevent bugs from
falling from ceilings onto the exposed face at night.

B. Medications
Antiparasitic agents such as benzimidazole, itraconazole,
and nifurtimox reduce parasitemia in the acute phase, but
they do not have any effect on the autoimmune-mediated
chronic form of the disease. Anticoagulants are necessary in
patients with left ventricular aneurysm or thrombi detected
in the ventricle and those who have sustained embolism.
Arrhythmias often require treatment with antiarrhythmics
such as amiodarone. This drug is used for symptomatic
relief and does not appear to prolong life.

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Cardiopulmonary Resuscitation (CPR)


PERHAPS YOU MAY HAPPEN TO BE NEAR
someone who falls to the ground and stops breathing.
You may be alone or someone summons you to help. Can
you help? If you have never learned how to do CPR, you
will not know what to do to save a life. Thus it is wise for
all individuals to attend a practical course in CPR or at
least read and practice the drill until it becomes automatic.
Since its description more than 43 years ago, the
fundamentals of CPR have undergone minimal changes.
The technique is quite simple. The main goal in applying
CPR is trying to get oxygen to the individual’s brain to
keep it alive until expert help arrives. Mouth-to-mouth
ventilation oxygenates the blood, and chest compressions
cause forward flow of blood, albeit a small flow, that results
in some cardiac output into the circulation so that
oxygenated blood reaches vital organs.

In this chapter the relevant points of CPR are summarized
so that if you are faced with an individual who has
‘‘dropped dead’’ or appears to have lost consciousness in
your presence, you may be able to render assistance.

I. CAUSES OF LOSS OF CONSCIOUSNESS
Patients may lose consciousness and fall because of several
reasons such as syncope, seizure, stroke, or cardiac arrest.
A. Syncope/Fainting
With syncope the patient has a pulse, does not stop breathing,
and has no shaking of the limbs. Simply keeping the
head down, preferably with the individual lying flat, and
raising the legs up in the air above the patient’s hips will
cause blood to flow from the legs. In about one minute the
individual will recover completely.

B. Seizure/Epilepsy
During a seizure the patient’s limbs exhibit jerky, movements,
the limbs get rigid, or there is a combination of
rigidity and jerking of one or more limbs. The patient is
breathing, but saliva and foam bubble from the mouth.
Some individuals pass urine or stool. Recovery is typical.

C. Stroke
During a stroke, circulation to part of the brain is cut off
because of a blood clot in an artery in the brain. Strokes
usually occur in individuals over age 60. It is rare for the
patient to fall suddenly to the floor without some warning.
The patient will have a pulse and breathing will be present.
There is no reason to do CPR because the heartbeat,
circulation, and respirations have not stopped.

D. Cardiac Arrest
During cardiac arrest, the heart stops beating completely
and is at a standstill (asystole) in about 25% of individuals.
In about 60–75%, cardiac arrest is due to ventricular
fibrillation. Ventricular fibrillation can be treated by an
electrical shock, which defibrillates the heart and replaces
the ventricular fibrillation with a normal heartbeat.
In standstill or asystole, there is no electrical current in
the heart, and using electrical shock is of no value. In a few
cases, the heart may commence beating on its own. This
condition is called a Stokes-Adams attack, named after the
doctors who first described it. A few individuals can be
saved by the insertion of a pacemaker if the attack occurs
in the hospital.

It is wise for a family member of a heart patient to know
how to give CPR. It reassures the patient that something
can be done. The knowledgeable individual also feels some
sense of confidence, which promotes hope.
Each year approximately a quarter million individuals
die suddenly in the United States from coronary artery
disease before reaching a hospital; more than half a
million have a cardiac arrest and receive CPR during
hospitalization.
II. CARDIAC ARREST RHYTHMS
There are only two cardiac arrest rhythms to consider:
ventricular fibrillation and pulseless ventricular tachycardia
(VF/VT).

A. Ventricular Fibrillation/Pulseless
Ventricular Tachycardia
VF is defined as a pulseless chaotic disorganized rhythm
with an undulating irregular pattern that varies in size and
shape and has a ventricular waveform greater than 150 beats
per minute. VT is an irregular wide QRS complex tachycardia
(see the chapter Arrhythmias/Palpitations). Patients
with V Tmay remain stable, alert, and have a pulse. Patients
with unstable ventricular tachycardia are hemodynamically
unstable with a blood pressure of less than 90 mmHg, chest
pain, shortness of breath, clouding of consciousness, or
rapid loss of consciousness.

The American Heart Association (AHA) Guidelines
2000 for CPR and emergency cardiovascular care advises
that in patients with cardiac arrest it is advisable to always
assume that the rhythm is VF or pulseless VT. Because
individuals who can be saved from cardiac arrest are
usually in VF or pulseless VT, the earliest possible delivery
of defibrillation is the single most effective intervention.
A recent study in Norway, however, indicates that the use
of three minutes of CPR prior to defibrillation, rather than
immediate defibrillation, resulted in better outcomes
among VF patients who received attention more than
five minutes after symptom onset. In patients who received
defibrillation immediately, 46% achieved a spontaneous
palpable pulse on admission versus 56% of those within
three minutes of CPR. Further studies are necessary to
clarify this finding.

B. Automated External Defibrillator
The distribution of automatic external defibrillators has
been widespread. The AHA recommends that all firstresponding
emergency personnel such as physicians,
nurses, emergency medical technicians, paramedics, firefighters,
and volunteer emergency personnel be trained
and permitted to operate a defibrillator. The defibrillator
should be available in all emergency ambulances that
engage in the care or transit of cardiac patients.
The automated external defibrillator automatically
interprets the cardiac rhythm and, if VF is present, advises
the operator to provide a shock. Because most cardiac
arrests occur in the home, a case can be made for home
defibrillators for patients at high risk. Their size, that of
a notebook laptop computer, and costs of approximately
$3000 should both decrease considerably over the next
decade.

III. CARDIOPULMONARY RESUSCITATION
CPR is only a temporary measure. The aim is to get blood
containing a fresh supply of oxygen to the brain.
Therefore, it is necessary to breathe enough air into the
patient’s lung, then compress the chest to cause the
nonbeating heart to expel blood into the arteries. This
produces circulation of the blood to the brain. Rarely, the
patient may be revived, and the heart begins to beat
spontaneously. In patients with ventricular fibrillation,
death will occur unless the heart is defibrillated. The hope
is that the ambulance has a portable defibrillator and a
team that can defibrillate the patient.

A. How to Recognize Cardiac Arrest
First, the patient’s level of responsiveness must be determined.
If the patient is unresponsive, he is unconscious
and oblivious to shaking or commands. Second, determine
if the patient is breathing. Within 30 seconds you should
have arrived at a conclusion that a cardiac arrest has
occurred. Speed of diagnosis is critical. Within three to
four minutes of cardiac arrest, irreversible brain damage
can occur because of lack of oxygen. The intention is to
provide basic life support until advanced life support in the
form of expert technical help arrives. When CPR is started
within four minutes after collapse, the probability of
survival doubles.

In a King’s County survey, 46% of patients with VF
survived CPR versus only 7% for presumed asystole and
pulseless electrical activity (PEA). The incidence of VF in
that survey was 45% and asystole/PEA 41%. Thus close to
50% of patients with VF can be resuscitated with efficient
CPR, but less than 10% with other rhythms can be
resuscitated.

B. The Steps of CPR
AHA Guidelines provide the following steps for CPR
(see Fig. 1):
 Check responsiveness
 Open the airway
 Check breathing
 Give two effective breaths
 Access the circulation
 Compress the chest (see Fig. 2)
1. Responsiveness — Airway
CPR should be commenced immediately. First, turn the
victim flat on the back on a hard surface (preferably the
floor). Quickly assess head tilt for responsiveness and loss
of consciousness. Figure 2 shows the use of the head tilt/
chin lift maneuver to open the airway. One hand is placed
on the victim’s forehead and firm backward pressure is
applied with the palm to tilt the head back. The index and
middle finger of the other hand are placed under the bony
parts of the lower jaw. The chin is lifted forward and the
jaw is supported. Avoid pressing the fingers into the soft
tissue under the chin. This maneuver should bring the
teeth almost together and maintain dentures in position.

2. Breathing
Place your ear over the victim’s mouth and nose. If you do
not hear or feel the flow of air escaping and the chest does
not rise and fall, the victim is not breathing. Pinch the
victim’s nostrils closed, using your thumb and index finger
of the hand on the forehead. Then take a deep breath,
make a tight seal over the victim’s mouth with your
mouth, and blow into the victim’s mouth. Blow air into
the victim’s mouth to fill the lungs (ventilate) rapidly two
times allowing the chest to deflate totally between each
breath.

C. Circulation
1. The Pulse
There is no pulse if cardiac arrest has occurred. Check for a
pulse by feeling the carotid artery in the neck. The right
carotid artery is felt one inch from the angle of the jaw.
Place the index finger in a straight line parallel with the
wind pipe (trachea) so that the entire length of the first
finger pad is touching the skin. The tip of the index finger
should be approximately opposite the Adam’s apple. Start
by feeling the most prominent part of the Adam’s apple
with the tips of two fingers, then slide the finger outward
to reach the groove between the hard cartilage of the wind
pipe and the muscle of the neck. The carotid artery lies
only a few millimeters under the skin, and the pulsation is
easily felt. Practice feeding this pulse so that you can find it
in a hurry, taking no more than 10 seconds.

Evidence has accumulated from the European Resuscitation
Council and other international expert panels that
the pulse check is not a good diagnostic test for the
presence or absence of a beating heart. The pulse is not a
satisfactory check for lay responders and they should check
for signs of circulation such as any movement including
swallowing or breathing that consists of more than an
occasional gasp.

2. Chest Compression
Place the heel of one hand over the lower half (see Fig. 1)
of the breastbone, but at least one inch (2 cm or two
fingerbreadths) away from the end of the breastbone
(xiphoid process). Position the heel of your other hand on
the top of the first. Keep the fingers off the rib cage. If your
hands are too high, ineffective chest compression may
result, and fracture of the ribs may occur. Keep your arms
straight at the elbow (locked elbows) and apply pressure as
vertically as possible. Your shoulders should be directly
above the victim’s breastbone. Chest compressions are then
easily carried out by forceful movements of the shoulders
and back, thus the maneuver is less tiring. Depress the
breastbone one to two inches (3–5 cm) toward the spine;
alternately compress and relax.

The compression rate should be about 90–100 compressions
per minute. At the end of the 15th compression
two full breaths are given. CPR should never be interrupted
for more than five seconds, and it should be continued
until skilled help arrives. Endotracheal intubation
should be accomplished within 30 seconds of cessation
of CPR.

Note that the victim’s mouth should be almost completely
closed, however, depress the lower lip a bit so that
the mouth remains slightly open. If dentures cannot be
managed in place, remove them after first giving the very
important first two breaths. You must see the chest rise and
fall. If the first two breaths meet with resistance and the
chest fails to rise when you breathe air into the patient’s
mouth, make sure that the airway is properly opened by
the head tilt/chin lift method and that the seal around the
mouth is airtight. Then clear the airway with your fingers
if necessary. The fact that the patient suddenly dropped to
the ground and was not choking while eating is sufficient
to persuade you not to waste time searching for meat or
vomitus.

IV. DEFIBRILLATION
The first shock setting should be 200 joules followed by
a second shock of 300 joules. One defibrillator paddle
is positioned to the right of the sternum below the clavicle.
The other paddle is placed to the left of the left nipple
with the center of the paddle in the mid-axillary line.
An appropriate gel is one that has a low impedance.
Because gel spreads during chest compression, shocks may
arc across the chest surface thus, the gel must be toweled
off. Conducting gel pads should be used but must be
changed between shocks. Heavy arm pressure should be
applied to each paddle applied to the chest and
defibrillation should take place when the victim’s phase
of ventilation is in full expiration. In the UK the lower
paddle is placed over the points designated as V4 and V5
for the ECG, that is, a little outside the position of the
normal apex beat. The paddle should be placed at least five
inches away from a pacemaker generator.

The area around the patient should be checked so that
no personnel are directly or indirectly in contact with the
patient. The operator must not touch the patient when
the shock is delivered. Deliver countershock by depressing
both paddle discharge buttons simultaneously. If
no skeletal muscle contraction is observed, check the
equipment.

After countershock reassess the cardiac rhythm. If VF
persists repeat the shock as soon as possible and continue
CPR during any delays. If an organized rhythm is restored,
check immediately for a pulse. If no pulse is present
resume CPR.

Ventricular asystole causing cardiac arrest indicates
a poor prognosis. After CPR is initiated epinephrine
is given. Occasionally VF may masquerade as asystole.
The monitoring electrodes should be repeated from the
original positioned to ensure that VF is not present.
Asystole or electromechanical dissociation is usually caused
by irreversible myocardial damage that is extensive with a
poor prognosis.

A. Errors in Defibrillation
Eisenberg and Mengert emphasized the following common
errors in CPR. Defibrillation errors may occur if the
synchronized mode is accidentally selected before defibrillation
is attempted, thus no shock is delivered. Asystole
may be falsely displayed when the selection is set for
paddles and the rescuer believes that rhythm lead II is
being displayed. In addition, if a vast amount of chest hair
is present it should be shaved off where the paddles are to
be placed; smeared gel across the chest should be toweled
off before defibrillation.

Oxygen at 100% concentration is given as soon as
possible through a bag-valve mask or endotracheal tube.
Plastic face masks may provide 50–60% oxygen with an
oxygen flow rate of 10 L/min.

V. DRUGS FOR CARDIAC ARREST
A. Epinephrine (Adrenaline)
For more than 40 years epinephrine has been a key agent
used during cardiac arrest. Epinephrine is both an alphaand
beta-adrenergic agonist; therefore, it stimulates spontaneous
cardiac contractions, increases systemic vascular
resistance resulting in an increased aortic diastolic perfusion
pressure, and improves coronary blood flow. It is
relevant that epinephrine constricts peripheral vessels but
preserves flow to vital organs causing coronary artery
dilation.

Epinephrine is indicated for fine VF, which is rendered
more amenable to removal by countershock and for VF
that does not respond to electrical countershock. Asystole
and pulseless idioventricular rhythms and electromechanical
dissociation may respond to this drug, albeit rarely.
A dose of 1 mg IV push every 3–5 minutes (0.01 mg/kg)
is recommended. A 20-ml IV fluid flush should be administered
to ensure delivery of the drug centrally. A dose of
1 mg/10 ml of a 1:10,000 solution may be given via the
tracheobronchial tube.

A higher dose of epinephrine was advocated by the AHA
in 1992 based on studies. If the 1-mg IV dose was
ineffective, escalating doses of 3 and 5 mg or 5 mg per dose
rather than 1 mg were advised; the result of 8 large
randomized trials in patients with cardiac arrest however,
showed no significant benefit. The higher dose regimen is
no longer recommended.

B. Vasopressin
Vasopressin, a clonal substance antidiuretic hormone,
becomes a powerful vasoconstrictor when used at much
higher doses than normally present in the body. This drug
possesses effects that duplicate the positive effects of
epinephrine, but does not duplicate the adverse effects of
epinephrine. Only one dose of vasopressin is required.
This is less frequent than epinephrine because the 10- to
20-minute half-life of vasopressin is much greater than
the 3- to 5-minute half-life of epinephrine. Vasopressin
is recommended only for VF/VT; there is no evidence to
support its usefulness in asystole or PEA.

Vasopressin is to be administered IV single-dose one
time only. If there is no response 5–10 minutes after a
single dose of vasopressin, it is advisable to resume
epinephrine 1 mg IV push every 3–5 minutes.

C. Amiodarone
Amiodarone is a complex drug which effects sodium,
potassium, and calcium channels as well as alpha- and
beta-adrenergic blocking properties (see the chapter
Arrhythmias/Palpitations). This drug is recommended
after defibrillation and epinephrine in cardiac arrest with
persistent VT or VF.

The recommended dose is 300 mg IV push. If VF/
pulseless VT recurs, consider administration of a second
dose of 150 mg IV.

D. Beta-Adrenergic Blocking Agents
The actions and beneficial effects of beta-blockers are given
in the chapter Beta-blockers. Atenolol, metoprolol, and
propranolol have been shown to reduce the incidence
of VF significantly in post-MI patients who did not
received fibrinolytic agents. Beta-blockers have been shown
to prevent recurrent VF. VF is unique among cardiac
arrhythmias because management with immediate countershock
antifibrillatory drugs can be useful. Beta-blockers
increase VF threshold and have been shown to be useful in
patients who have repetitive VF precipitated by electrocution.
Although these agents have a negative inotropic
effect, they are not helpful in patients in cardiac arrest.
Metoprolol is administered 5 mg by slow IV push
over 5 minutes, at 5-minute intervals for a total 15 mg.
Propranolol has been used worldwide and its use continues
at a dose of 0.1 mg/kg by slow IV push divided into three
equal doses at 2- to 3-minute intervals. The rate of
administration should not exceed 1 mg/minute. Esmolol is
a short-acting beta-blocking agent with a short half-life of
2–9 minutes. The drug is metabolized by erythrocyte
esterases and requires no dose adjustment in patients with
renal or hepatic impairment. The dosing regimen is
complex and requires an IV infusion pump (see the
chapters Beta-Blockers and Arrhythmias/Palpitations).

E. Sodium Bicarbonate
This agent is no longer recommended for routine use
except for pre-existing hyperkalemia. Prompt ventilation of
the lungs is essential for excretion of carbon dioxide and is
the most effective method for combating acidosis.
Sodium bicarbonate may be used to combat bicarbonate
responsive acidosis, tricyclic overdose, and after about 10
minutes of ventilation including intubation, defibrillation,
and use of epinephrine. If CPR is still necessary, sodium
bicarbonate may be used. The drug may also be used on
return of circulation after long cardiac arrest, but its
use should be guided by arterial pH measurements.
The recommended dose is an IV bolus of 1 mEq/kg
( 50 mEq).

F. Atropine
This drug is of value in the management of severe
bradycardia associated with cardiac arrest. Patients with
asystole or PEA may respond to atropine while preparations
are made for pacing. Patients with a high degree
atrioventricular block, slow idioventricular rates, and severe
sinus bradycardia with hypotension should be given a trial
of atropine IV.

A dose of 1 mg IV repeated in 3–5 minutes is recommended.
If asystole persists, the maximum of 3 mg can be
administered (0.04 mg/kg).
G. Magnesium Sulfate
Magnesium sulfate is reported to expedite ventricular
defibrillation and is indicated for polymorphic ventricular
tachycardia, torsades de pointes, and management of
hypomagnesemia. A dose of 1–2 mg IV is recommended.

H. Bretylium
Bretylium has been dropped from the VF/pulseless VT
algorithm. This drug was used in the 1980s and 1990s for
recurrent VF, but was only partially successful and never
proven. In the late 1990s, severe problems with obtaining
the raw materials curtailed manufacture. The world sources
of bretylium appear to be nearly exhausted. Bretylium has
a high incidence of side effects including hypotension. It
has been replaced by amiodarone and beta-blocking
agents.


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Tuesday, July 29, 2008

Cardiogenic Shock

CARDIOGENIC SHOCK IS CAUSED BY A DECREASED
pumping ability of the heart that results in a shock-like
state with insufficient blood perfusion to organs and
tissues. During cardiogenic shock, systolic blood pressure is
less than 90 mmHg for greater than one hour and not
responsive to IV fluids. The cardiac index is less than
2.2 L/minute/m2, and the pulmonary capillary wedge pressure
is greater than 18 mmHg. Patients usually have
clouded consciousness and cold extremities.

I. CAUSES
Acute myocardial infarction is the most common cause of
cardiogenic shock. Other causes of cardiogenic shock are
given in Table 1. The complete occlusion of a coronary
artery by a clot causes death of an area of heart muscle that
is supplied by that blood vessel and its branches. If a very
large area of heart muscle is involved, the general pumping
capability of the heart is severely compromised. Because
dead myocardium cannot contract, blood cannot be
effectively ejected out of the left ventricle into the aorta
[see Fig. 1 in the chapter Anatomy of the Heart and
Circulation). Blood is held up in the lungs and fluid
accumulates in air sacs causing pulmonary edema which
results in severe shortness of breath. Because blood cannot
be ejected from the heart, the blood pressure falls
drastically. When more than 40% of the heart muscle is
involved, cardiogenic shock often occurs.

II. PATHOPHYSIOLOGY
In general terms shock is a clinical state in which target
organ–tissue perfusion is inadequate to supply vital substrates
and remove the metabolic waste. Inadequate cellular
oxygenation leads to marked generalized impairment of
cellular function and multiorgan failure.
The heart tries to contract more vigorously in the face of
this catastrophic event; the renin–angiotensin–aldosterone
system is activated and causes severe vasoconstriction
in an attempt to increase blood pressure (see Fig. 1 in
the chapter Angiotensin-Converting Enzyme Inhibitors/
Angiotensin Receptor Blockers), but over time the hypercontractility
of the heart ceases. This occurs because there
is utilization of glucose over fatty acids, loss of Krebs
cycle intermediates, and depletion of substrate required for
ATP production.

Figure 1 illustrates the pathophysiology of shock.
Because forward flow of blood is severely retarded, blood
returned to the heart from veins of the body and from the
lungs cannot be accommodated in a heart that is already
full of blood. Blood then backs up into the venous
circulation of the neck and in the lungs. This pressure of
blood returning to the heart is referred to as an increased
filling pressure (Fig. 1). It is easy to visualize that the shock
state may occur if there is no filling pressure as would
occur in severe dehydration or severe blood loss (i.e., the
tank has no gas).

Basically cardiogenic shock results from profound
reduction in cardiac output. This is usually caused by
marked reduction of left or right ventricular systolic function,
despite adequate ventricular filling pressures, and
there is a failure of compensatory vasoconstrictive mechanisms
that are overwhelmed by inappropriate vasodilation
in large, nonvital vascular beds. Thus this deprivescritical
areas like the heart ,brain, and kidney of perfusion.
Hochman points out that data from the shock trial and
registry indicate that cardiogenic shock is often not
simply due to extensive myocardial infarction with pump
failure, ‘‘but also involves inflammatory mediators. These
mediators induce nitric oxide synthase (iNOS) expression,
increasing nitric oxide (NO) and peroxynitrite levels,
resulting which results in further myocardial dysfunction
and failure of an appropriate peripheral circulatory
response.’’

III. MANAGEMENT
Most patients require an intra-aortic balloon pump and
IV vasopressor drugs to support blood perfusion to organs
and tissues. The opening of the obstructed artery using
balloon angioplasty with the insertion of stents has
improved survival. Because approximately 40% of cardiogenic
shock patients have occlusions in three coronary
arteries, emergency coronary artery bypass surgery is the
only measure that has improved survival in this group.
In the SHOCK trial, the overall 30-day mortality rate
was 47% in patients undergoing emergency revascularization
versus 56% in the medical stabilization group.
This improvement was maintained at the six-month
follow up.

IV. PERSPECTIVE AND RESEARCH
IMPLICATIONS
The incidence of cardiogenic shock will not decrease until
the main cause, which is obstruction to coronary arteries
by atheromatous plaque and thrombosis, is arrested.
Thrombolytic therapy is of little value and revascularization
with balloon angioplasty and coronary bypass surgery
can only be undertaken in special centers. The SHOCK
trial only studied 300 patients. More research is required
to assess if we could develop cardioactive agents to protect
the myocardium from necrosis during an occlusion of
a coronary artery.

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Carcinoid Heart Disease

CARCINOID HEART DISEASE MAY OCCUR IN
patients with carcinoid syndrome. The main symptoms
of flushing, diarrhea, and occasional wheezing are caused
mainly by 5-hydroxytryptamine or serotonin, that is liberated
from carcinoid tumors that originate from chromaffin
cells (neuroendocrine cells) of the terminal ileum.
These tumors of the small intestine contain neurosecretory
granules that release a variety of biogenic amines that
include serotonin, histamine, bradykinins, tachykinins,
and prostaglandins. Involvement of the heart occurs in
about half of carcinoid syndrome cases. It is seen mainly in
patients with malignant tumors that have metastasized to
the liver.

I. HEART DAMAGE
Bioactivity amines, principally, serotonin, liberated from a
malignant tumor causes deformation of the tricuspid valve
that leads to tricuspid regurgitation. The pulmonary valve
becomes deformed by the plaque-like material resulting in
a leaky, incompetent valve (pulmonary regurgitation) or
a tight, stenotic valve (pulmonary stenosis). In a clinical
study of carcinoid heart disease, 97% of patients had
right-sided valvular involvement; severe tricuspid valve
regurgitation occurred in all patients and severe pulmonary
valve regurgitation in 72%.

A whitish colored plaque forms mainly on the right side
of the heart and only in less than 3% of cases are the mitral
and aortic valves of the left heart affected. The lesions of
the valves and endocardium are caused by serotonin that
reaches a high concentration in the right heart. Minimal
quantities reach the left side of the heart because
5-hydroxytryptamine is destroyed in the lungs by monoamine
oxidase. Some serotonin is destroyed in the liver
and in the brain.

The anorectic drugs fenfluramine and dexfenfluramine
exert their effects through interference in serotonin metabolism.
It is interesting that they were associated with
lesions identical to that seen in carcinoid syndrome.

II. DIAGNOSIS
Carcinoid tumors are rare. They arise from enterochromaffin
cells typically located in the gastrointestinal tract.
At the time of diagnosis, more than 30% of patients have
disseminated disease characterized by cutaneous vasomotor
flushing, secretory diarrhea, and mild bronchospasm.
In carcinoid heart disease, 5-hydroxytryptamine is metabolized
to 5-hydroxyindoleacetic acid (5-HIAA). Elevated
levels of 5-HIAA in the urine confirm the diagnosis.
Echocardiography confirms thickening of the tricuspid and
pulmonary valves with tricuspid and pulmonary valve
regurgitation and in some cases, pulmonary valve stenosis.
The lesions in the heart may cause right-sided heart failure.
Because the blood cannot be ejected adequately through
the pulmonary valve, the right ventricle work is increased.
Because the tricuspid valve leaks, blood regurgitates into
the veins of the neck and back toward the liver, which
becomes pulsatile with each heartbeat.

The malignant tumor may spread to involve the muscle
of the heart. These metastatic carcinoid tumors of the heart
are about 2 cm and can be detected by echocardiography.

III. TREATMENT
There are no specific treatments for carcinoid heart disease.
The noncardiac symptoms may be controlled with somatostatin,
but the action of this drug is only minutes.
Octreotide has been shown to be much more effective in
reducing flushing diarrhea and urinary levels of 5-HIAA.

IV. CLINICAL STUDY
Moller et al. studied the poorly understood factors
associated with the progression of carcinoid heart disease.
They studied 71 patients who underwent serial echocardiographic
studies performed more than one year apart
and 32 patients referred directly for surgical intervention.
These workers concluded that high serotonin levels are
related to the progression of carcinoid heart disease, and
the risk of progressive heart disease is higher in patients
who receive chemotherapy.

Somatostatin is a potent inhibitor of many processes
including serotonin. In this nonrandomized study it
appears that somatostatin was ineffective in preventing
development of carcinoid heart disease. Findings
suggested that although serotonin is related to development
of carcinoid disease, neither somatostatin therapy
nor hepatic dearterialization prevents the progression of
chronic lesions. Patients in the study who received
cytotoxic chemotherapy had the highest risk of progressive
carcinoid heart disease. The exact mechanism involved
in the progression of carcinoid disease requires further
clarification.

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Calcium Antagonists


I. MECHANISM OF ACTION
Calcium movement into cells is mediated by several
mechanisms. Albrecht Fleckenstein showed that the
calcium channels can be selectively blocked by a class
of agents. He called these agents calcium antagonists.
Calcium movement into the cells is mediated by several
mechanisms. Calcium antagonists act at the plasma
membrane to inhibit calcium entry into cells by blocking
voltage-dependent calcium channels.

Calcium ions play an important role in the contraction
of cardiac, skeletal, and smooth muscle. Myoplasmic
calcium depends on calcium entry into the cell. Calcium
binds to the regulatory protein troponin, removing the
inhibitory action of tropomyosin. In the presence of
adenosine triphosphate this allows the interaction between
myosin and actin with consequent contraction of the
muscle cell.

There are at least three different types of calcium
channels designated as L, T, and N types. The L-type
channels, once activated, remain for a long period of time
and have a large calcium-carrying capacity. The T channels
have a brief opening time and N channels have
characteristics that are neither of the L nor T type. Only
the L-type channels are sensitive to the action of calcium
antagonists. The effect of the calcium antagonists is to
restrict calcium entry, and over a given period of time
fewer calcium ions are available for participation in
intracellular events such as muscle contraction and neuronal
activity. Thus some have labeled these compounds
calcium channel blockers, calcium channel antagonists,
calcium entry blockers, and slow calcium blockers.
Calcium antagonists differ from one another in terms
of their potency, tissue selectivity, and duration of action.
The calcium antagonists available for clinical use are
mainly L-type channel blockers. The T channel appears at
more negative potentials and seems to play a role in the
initial depolarization of the sinus node and atrioventricular
(AV) node tissue. Mibefradil, a T channel blocker, caused
bradycardia and a host of adverse effects that caused the
drug’s premature withdrawal from the market.

The three major calcium antagonists include nifedipine,
diltiazem, and verapamil (see Fig. 1 for their structural
formulas). Dihydropyridine, the prototype of which
is nifedipine, appears to act by plugging the calcium
channels. These agents cause dilation of coronary arteries
and marked peripheral arteriolar dilatation resulting in a
profound fall in blood pressure. There is little or no action
on the sinoatrial (SA) node and conducting tissue.

Verapamil and diltiazem are phenylalkylamines and
benzothiazepines. They cause distortion of calcium channels
and coronary artery dilation, but there are additional
effects on the SA and AV nodes. These agents also have a
negative inotropic effect and decrease myocardial contractility.
Thus, the dihydropyridines, phenylalkylamines, and
benzodiazepines have vastly different actions. For example,
only amlodipine and felodipine, of the dihydropyridine
family, have proved relatively safe in patients with left
ventricular dysfunction and heart failure. Other agents
may precipitate heart failure.

II. AVAILABLE CALCIUM ANTAGONISTS
A. Dihydropyridines
These agents cause dilation of arteries throughout the
body including mild dilatation of coronary arteries. They
also cause a variable decrease in myocardial contractility
that may lead to heart failure in susceptible individuals.
Dihydropyridines include amlodipine, felodipine, and,
nifedipine. They are indicated for the management of
hypertension. They may also be used for the treatment
of stable angina, but only in combination with a betablocking
drug that prevents an increase in heart rate and
the increase in cardiac workload that may be caused by
dihydropyridines. The common adverse effects include
edema of the ankles, flushing, headaches, and rarely,
hypertrophy of the gums. Other dihydropyridines include
isradipine, nicardipine, nimodipine, nitrendipine, and
niludipine.

1. Amlodipine (Norvasc)
This dihydropyridine has a long half-life of 35–50 h and
peak blood levels are reached after 6–12 h. Amlodipine is
an effective antihypertensive agent that is used worldwide.
It has a good safety profile but pulmonary edema (heart
failure) may be precipitated in patients with severe left
ventricular dysfunction and ejection fraction of less than
30%. Edema of the ankles, feet, and lower leg may be
bothersome in about 10% of treated patients. This drug is
often combined with a beta-blocker in the management
of angina. The dose for angina or hypertension is 5–10 mg
once daily.

2. Felodipine (Plendil)
This dihydropyridine has actions, effects, and indications
that are similar to amlodipine. The dose for hypertension
is 2.5–5 mg daily with a maximum dose of 10 mg.

3. Nifedipine (Procardia, Adalat XL)
Nifedipine is the first calcium antagonist used in clinical
practice. It was introduced during the early 1980s for the
management of hypertension, angina, and particularly
coronary artery spasm (variant angina) and is still used
worldwide. The drug is an excellent antihypertensive
agent. Headache, edema of the ankles, and facial flushing
occur in about 15% of patients. Although introduced for
the management of angina, like other dihydropyridines,
the drug should be used only for stable angina in patients
who are also administered a beta-blocker. For the management
of coronary artery spasm (Prinzmetal variant
angina), the drug can be used without beta-blockers, which
are contraindicated in this condition.

Short-acting capsule or tablet formulations of nifedipine
are no longer recommended because an increase in
morbidity and mortality has been reported in patients with
coronary artery disease. The slow-release once daily
formulation is now used worldwide at a dose of 30–60
mg once daily. The maximum dose of 90 mg should be
used with caution.

B. Benzothiazepines
1. Diltiazem
Diltiazem is a mild arteriolar vasodilator. It is a widely used
calcium antagonist because its safety profile is good. The
blood pressure lowering effect of this benzothiazepine is
not as powerful as the dihydropyridines, and a large dose
is usually required to obtain a satisfactory antihypertensive
effect. Diltiazem has a milder action than the dihydropyridines
and causes less vasodilatation of arteries; thus it
is a week antihypertensive agent. The drug causes some
decrease in myocardial contractility and heart failure may
be precipitated in patients with left ventricular dysfunction
or in patients who are administered a beta-blocking drug
concomitantly.

Most important, the drug inhibits electrical conduction
through the AV node. It is useful for the management of
supraventricular tachycardias by slowing rapid heart rates
that may occur with atrial fibrillation.

Unfortunately, this drug causes some suppression of the
sinus node and normal pacemaker activity and may cause
bradycardia. It should be avoided in patients with sick
sinus syndrome and heart failure. Adverse effects include
increased liver function tests, increased transaminases, and
constipation, but headache and edema of the ankles are less
common than with the dihydropyridines.
Important interactions occur with digoxin, and digoxin
levels may be increased by about 33%. Diltiazem combined
with amiodarone may produce deleterious effects
on the sinus pacemaker causing arrest and hypotension.
Interactions have been noted with cyclosporine, cimetidine,
and carbamazepine.

The short-acting tablet formulation of diltiazem is not
recommended. Long-acting and slow-release formulations
are administered 180 mg to a maximum of 300 mg once
daily.

C. Phenylalkylamines
1. Verapamil
Verapamil is a moderately potent vasodilator. Two major
differences between the actions of verapamil and the
dihydropyridines include a major depressant effect on the
AV node and a mild depressant effect on the SA node.
Also, depression of myocardial contractility for verapamil
is considerably more than the maximum effect observed
for dihydropyridines. This marked negative inotropic
effect may precipitate heart failure in patients with left
ventricular dysfunction and an ejection fraction less than
40%. Because of this effect, verapamil should not be
combined with a beta-blocking agent.

The electrophysiologic effect of mild depression of
conduction through the AV node makes the drug effective
in the management of supraventricular tachycardia. Given
intravenously, verapamil was used worldwide for the
management of this condition from 1984 to 1996 and
has now been relegated to second choice behind adenosine.
Verapamil is indicated for the management of hypertension
and for angina, particularly when beta-blockers
are contraindicated. It is also used for the management
of coronary artery spasm. The intravenous preparation
is indicated for supraventricular tachycardia. Doses of
120–240 mg sustained-release, long-acting preparations
are advised once daily.

Verapamil is contraindicated in patients with bradycardia
( a heart rate of <60) style="font-weight: bold;">III. THERAPEUTIC BENEFITS
Calcium antagonists are indicated for the conditions
outlined below.
 Isolated hypertension without organ damage or coexisting
disease benefits from calcium antagonists.
 These agents are particularly useful for isolated
hypertension in older people of African origin and
usually achieve the blood pressure goal; they have been
shown in randomized clinical trials to be more effective
than ACE inhibitors, beta-blockers, and diuretics.
 In younger people of African origin a clinical study
showed that diltiazem was effective in 64% compared
with 47% for atenolol and 40% for diuretics.
 Patients with severe stage II and III hypertension
require the combination of several antihypertensive
agents and calcium antagonists are appropriate except
in patients with left ventricular dysfunction.
 Calcium antagonists are a critical part of combination
therapy in hypertensive patients with a variety of underlying
disorders (comorbidities) in whom blood pressure
control at more aggressive goals has been deemed
essential but remains elusive.
 Calcium antagonists are used to treat hypertension
associated with renal disease or renal failure if ACE
inhibitors are contraindicated or poorly effective.
 Calcium antagonists have shown benefits in hypertensive
diabetic patients; the large SYST-EUR and the
Systolic Hypertension in China (SYST-China) trials
demonstrated more than a 50% reduction in total
mortality in the diabetic subgroup.
 In patients with stable angina the addition of a calcium
antagonist, particularly a dihydropyridine or diltiazem,
has been shown in clinical trials to cause significant
amelioration of recurrent chest pain.
 In patients with severe aortic regurgitation, the
unloading effect of nifedipine has been shown in a
clinical trial to cause significant reversal of the left
ventricular dilatation and hypertrophy, and surgical
therapy may be appropriately delayed from 1 to 2
years.
 Patients with cold fingers and Raynaud’s phenomenon
may find some benefit with calcium antagonists.
 The dihydropyridine nimodipine, in a clinical trial, was
shown to be useful in the management of cerebral
arterial spasm caused by subarachnoid hemorrhage with
controlled blood pressure.
 Following coronary artery bypass graft using the radial
artery as a conduit, dihydropyridine calcium antagonists
are used for an indefinite period to prevent spasm
and occlusion of the arterial graft.

IV. NEXT GENERATION AGENTS
Several dihydropyridine calcium antagonists have been
introduced during the past 25 years. First degeneration
dihydropyridines are the naturally short-acting agents that
include felodipine, isradipine, nifedipine, and nitrendipine.
These rapid-acting vasodilators are powerful antihypertensive
agents, but their fast onset of action results in
marked vasodilation that causes reflex stimulation of the
sympathetic nervous system and hemodynamic adverse
effects that include increased heart rate, increased cardiac
workload, and an increased incidence of heart failure in
patients with left ventricular dysfunction. These adverse
effects have become controversial and the short-acting
formulations of dihydropyridines such as verapamil and
diltiazem are no longer recommended. They have largely
been removed from the marketplace.

Second generation agents such as verapamil SR,
nifedipine XL, felodipine ER, and diltiazem SR and CD
were developed with modified release properties to slow
their onset of action. Adverse effects are still high, particularly
edema and constipation, and heart failure is precipitated,
albeit rarely.

Third generation agents include amlodipine. These
agents have a naturally occurring long plasma half-life
(over 24 h) but are washed out from the receptor relatively
fast. Equilibrium is essentially between the plasma proteinbound
drug and the calcium L channel. Amlodipine moves
quickly onto the calcium channel to provide a quick onset
of action and thus vasodilatation, which results in modest
sympathetic stimulation and unwanted mild tachycardia
or an increase in heart rate of about 10 beats per minute
from baseline. These agents may precipitate pulmonary
edema in patients with left ventricular dysfunction.
Next generation agents include lercanidipine, lacidipine,
and manidipine. These dihydropyridines have important
and subtle differences when compared with second and
third generation dihydropyridine calcium antagonists.
Lercanidipine has been shown to have major advantages
over amlodipine. Because the drug dilates both afferent
and efferent arterioles, the high incidence of peripheral
edema caused by older calcium antagonists is reduced
more than 50%. The balanced effect of lercanidipine and
manidipine on efferent and afferent arterioles is important
in renal protection. The older calcium antagonists listed
above dilate only afferent arterioles. The COHORT study
of elderly hypertensive patients concluded that lercanidipine
and lacidipine are much better tolerated than
amlodipine.

Recent investigations indicate that lercanidipine administered
to hypertensive diabetic patients is more effective
than the angiotensin receptor blocker, losartan, in reducing
left ventricular hypertrophy and left ventricular mass.
These third generation dihydropyridines represent an
important addition to the therapeutic armamentarium.
Their place in clinical practice will increase further if
they are shown to be devoid of the major adverse effect
of all calcium antagonists — the precipitation of
heart failure in patients with significant left ventricular
dysfunction.

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