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Target e*Studio® – EDC Made Simple
Target Health is pleased to announce that Target e*Studio® Version 1 will be released 21 February 2011. Target e*Studio allows independent programmers and data managers outside of Target Health to configure Target e*CRF® EDC applications. Our estimate is that after the 1-2-week training period, those with the appropriate programming and data management skills will be able to build and release an EDC application in 2-3 weeks or sooner. Most importantly, Target e*Studio will allow programmers to access the forms and database to provide advanced features when necessary. This way, there will be no limit for any EDC application. Target e*Studio Version 1.1 will be released in mid-May and will be showcased at the DIA annual meeting.
Our CRO partner in Korea, LSK Global Pharma Services, led by Dr. Young Jack Lee (formerly of NIH fame), has licensed the software and will be launching their first study in Korea mid-March. Joonhyuk Choi, Director of Application Development at Target Health will be in Korea in February to provide onsite training.
Target e*CRF applications built with Target e*Studio will be fully integrated with Target Encoder®, Target e*CTR® (eClinical Trial Record), Target e*Monitoring and Target e*Pharmacovigilance®.
All Target Health Software Products are reasonably priced and will not “break the bank.” As per Bucky Fuller, you can, “do more with less.”
All Target Health software products Are 21 CFR Part 11 compliant and validated and full documentation is available. There are now 19 approved and marketed products which used Target e*CRF for their pivotal trials including 1 of the 21 drug FDA approvals and 1 PMA diagnostic device approval in 2010. We expect at least 1 drug and 1 PMA approval in 2011.
For more information about Target Health contact Warren Pearlson (212-681-2100 ext. 104). For additional information about software tools for paperless clinical trials, please also feel free to contact Dr. Jules T. Mitchel or Ms. Joyce Hays. Target Health’s software tools are designed to partner with both CROs and Sponsors. Please visit the Target Health Website at www.TargetHealth.com
United States Ranks Seventh in Global Cancer Rates
Countries With the Highest Overall Cancer Rates (per 100,000 Population)
The US has the seventh highest cancer rate in the world, according to new data compiled in January 2011, by the American Institute for Cancer Research (AICR). Of the 50 nations with the highest overall cancer rates in the world, Denmark takes first place and South Africa comes in at number 50.
Overall, the estimates show that high-income countries have significantly higher cancer rates than 1) ___-income ones. The differences in cancer rates among the top 10 nations are relatively small. “But when we look at the top 20 or 25 countries and compare those rates to the lower-income countries, that’s where you really see the differences,” said Alice Bender, of the International Agency for Research on Cancer (AICR), which is part of WHO. “The general idea is that many of these cancers can be prevented by changes in lifestyle and diet,” she said in an interview with Medscape Medical News. “We have very good evidence that a number of our most common cancers can be prevented by being at a healthy weight and being physically 2) ___.”
We can look at these higher rates as being due to some of our 3) ___ issues. For example, people in high-income countries are more likely to be overweight, consume more alcohol, and be inactive. In Denmark, which is at the top of the list, both alcohol and tobacco use are quite 4) ___. Some countries are also better at diagnosing and recording cancer cases; that might play into some of the more subtle differences between the countries on the list. But it is hard to say what exactly is contributing to the subtle differences in ranking.
When broken down by gender, the US comes is ranked 10th for men and 8th women. The 5 most common cancers in the US, are those of the 5) ___, prostate, breast, colorectum, and bladder.
The statistics come from GLOBOCAN, a project from the AICR. Although high-income countries continue to have significantly higher rates of cancer, this disparity is beginning to change. According to 2008 data from GLOBOCAN, more than half of new cancer cases (56%) and deaths (63%) occur in less-developed regions of the world. It takes a few years for these changes to show up, but the pattern is also being seen with other chronic diseases. The increased rates of heart disease and 6) ___ in lower-income countries has some of the same risk factors as other chronic diseases.”
Awareness is an important aspect, and physicians need to realize that, Ms. Bender pointed out. “They do discuss preventing heart disease and diabetes, but they may not spend as much time discussing cancer 7) ___ and what you can do to lower your risk.” Fortunately, many of the recommendations for lowering the risk for other chronic conditions are applicable to reducing the risk for 8) ___. Certainly, there are some cancers that are difficult to prevent, but for many cancers, there are many steps that they can take that will affect their 9) ___.
In the more developed regions, which GLOBOCAN designates as all of Europe plus Northern America, Australia, New Zealand, and Japan, prostate and lung cancer are the most common malignancies found in men. Among women, cancers of the breast and colorectum are the most common. In less developed regions, which include all of Africa, Asia (excluding Japan), Latin America, the Caribbean, Melanesia, Micronesia, and Polynesia, lung and stomach cancer are the most common cancers in men. For women, breast and cervix/uterine cancers are the most common. Source: Medscape.com
ANSWERS: 1) lower; 2) active; 3) lifestyle; 4) high; 5) lung; 6) diabetes; 7) prevention; 8) cancer; 9) risk
Thomas Jefferson Also Supported Government Run Health Care
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FORBES.com, January 30, 2011, by Rick Ungar — In response to Forbes’ earlier piece, “An Act for the Relief of Sick and Disabled Seamen”, the 1798 law revealing that a number of our founders were more supportive of the notion of mandated health coverage and a government run hospital system than some may have imagined, many have noted that it is not surprising that such legislation would have been signed into law by President John Adams, a noted Federalist who serves as a model for much of what today’s Tea Party finds objectionable. Their point is not wholly unreasonable. After all, it was John Adams who brought us the highly objectionable Alien & Sedition Acts.
However, Washington Post blogger, Greg Sargent, today reports that it wasn’t only John Adams who supported the notion of government run health care. According to Georgetown University history professor and noted historian of America’s early days, Adam Rothman, Thomas Jefferson –the iconic hero of the Tea Party – also supported the legislation.
Sargent reprints the following email he received from Prof. Rothan on the subject “Alexander Hamilton supported the establishment of Marine Hospitals in a 1792 Report, and it was a Federalist congress that passed the law in 1798. But Jefferson (Hamilton’s strict constructionist nemesis) also supported federal marine hospitals, and along with his own Treasury Secretary, Albert Gallatin, took steps to improve them during his presidency. So I guess you could say it had bipartisan support.”
Ezra Klein adds to the debate pointing out that “…it was a payroll tax that all sailors on private merchant ships had to pay, and in return, they were basically given access to a small public health-care system. But it was, in essence, a regulation against a form of inactivity: You were not allowed to not do something, in this case, pay for sailor’s health insurance.”
There are those who will continue to argue that these indications of how the founders viewed these issues in their own time do not necessarily resolve the issue as to how we may, Constitutionally speaking, proceed with reforming the health care system of today. They may well be right. But, at the least, can we not agree that the mounting evidence as to how men like Jefferson and Adams perceived the issue should bar the attempt to pin the objections to health care reform on the backs of the nation’s founders? While it may be an effective device to win over the support of a certain segment of American society, throwing the nation’s founders into the stew is really just one more disingenuous and cynical attempt to mislead the debate away from the real issues. Source: FORBES MAGAZINE @ FORBES.com, The Policy Page by Rick Ungar
Identification of ADAMTS7 as a Novel Locus for Coronary Atherosclerosis and Association of ABO with Myocardial Infarction in the Presence of Coronary Atherosclerosis
According to an article published in The Lancet (2011;377:83-392), a study was performed to test whether genetic factors distinctly contribute to either development of coronary atherosclerosis or, specifically, to myocardial infarction in existing coronary atherosclerosis.
The investigation included two genome-wide association studies (GWAS) with coronary angiographic phenotyping in participants of European ancestry. To identify loci that predispose to angiographic coronary artery disease (CAD), the study compared individuals who had this disorder (n=12,393) with those who did not (controls, n=7,383). To identify loci that predispose to myocardial infarction, patients who had angiographic CAD and myocardial infarction (n=5,783) were compared with those who had angiographic CAD but no myocardial infarction (n=3,644).
The study identified a novel locus (the specific location of a gene or DNA sequence on a chromosome), ADAMTS7 (p=4 98×10-13) in patients with angiographic CAD compared to the control group. In the comparison of patients with angiographic CAD who had myocardial infarction versus those with angiographic CAD but no myocardial infarction, the study identified a novel association at the ABO locus (p=7 62×10−9). The ABO association was attributable to the glycotransferase-deficient enzyme that encodes the ABO blood group O phenotype previously proposed to protect against myocardial infarction.
According to the authors, the findings indicate that specific genetic predispositions promote the development of coronary atherosclerosis whereas others lead to myocardial infarction in the presence of coronary atherosclerosis. The authors added that the relation to specific CAD phenotypes might modify how novel loci are applied in personalized risk assessment and used in the development of novel therapies for CAD.
Effects of Vitamin D Supplementation on Bone Density in Healthy Children
According to an article published in the British Medical Journal (2011;342:c7254), a study was performed to determine 1) the effectiveness of vitamin D supplementation for improving bone mineral density in children and adolescents and, 2) if effects vary with factors such as vitamin D dose and vitamin D status. The study involved a systematic review of the literature and meta-analysis.
Data sources included: 1) Cochrane Central Register of Controlled Trials, Medline (1966 to present); 2) Embase (1980 to present); 3) CINAHL (1982 to present); 4) AMED (1985 to present); 5) ISI Web of Science (1945 to present), and 5) manual searching of conference abstracts from key journals.
Study selection included placebo controlled, randomized controlled trials of vitamin D supplementation, for at least three months, in healthy children and adolescents (aged 1 month to <20 years) with bone density outcomes.
Data analyses included mean differences of the percentage change from baseline in bone mineral density of the forearm, hip, and lumbar spine and total body bone mineral content in treatment and control groups. Subgroup analyses were carried out by gender, pubertal stage, dose of vitamin D, and baseline serum vitamin D concentration. Compliance and allocation concealment were also considered as possible sources of heterogeneity.
Six studies, totaling 343 participants receiving placebo and 541 receiving vitamin D, contributed data to the meta-analyses. Results showed that vitamin D supplementation had no statistically significant effects on total body bone mineral content or on bone mineral density of the hip or forearm. There was a trend to a small effect on lumbar spine bone mineral density (mean difference 0.15; P=0.07). Effects were similar in studies of participants with high compared with low serum vitamin D levels, although there was a trend towards a larger effect with low vitamin D for total body bone mineral content (P=0.09 for difference). In studies with low serum vitamin D, significant effects on total body bone mineral content and lumbar spine bone mineral density were roughly equivalent to a 2.6% and 1.7% percentage point greater change from baseline in the supplemented group.
According to the authors, it is unlikely that vitamin D supplements are beneficial in children and adolescents with normal vitamin D levels. However, the planned subgroup analyses by baseline serum vitamin D level suggested that vitamin D supplementation of deficient children and adolescents could result in clinically useful improvements, particularly in lumbar spine bone mineral density and total body bone mineral content. However, this observation requires confirmation using prospective studies.
The Risk of Cancer in Patients with Rheumatoid Arthritis: A Nationwide Cohort Study in Taiwan
The association of rheumatoid arthritis (RA) and malignancy has rarely been explored in Asian populations. As a result, a study published in Arthritis & Rheumatism (2011;63:352–358) was performed to investigate the relative risk of cancer in Taiwanese patients with RA and to identify groups of patients with a high risk of cancer.
The investigation was a nationwide cohort study of the risk of cancer among 23,644 patients with RA who had no history of malignancies. For the study, data were obtained from the National Health Insurance database of Taiwan from 1996 to 2007. Standardized incidence ratios (SIRs) for various cancers were analyzed.
During the course of the study, 935 cancers were observed. Results showed that patients with RA had an increased risk of cancer (SIR 1.23, especially hematologic cancers (SIR 2.74). The relative risk of cancer was higher among younger patients. Most cancer cases were detected within the first year following the diagnosis of RA.
The relative risk of cancer decreased as the duration of observation increased. Among hematologic cancers, the risk of non-Hodgkin’s lymphoma was greatest (SIR 3.54). Among solid tumors, the risk of cancers of the kidney and female reproductive organs was highest. A decreased risk of cancers of the cervix and nonmelanoma skin cancer in patients with RA was also observed.
According to the authors, patients with RA have an increased risk of cancer, especially hematologic and kidney cancers and that the relative risk of cancer in patients with RA decreased with long-term followup. The authors recommended cancer screening with continued vigilance for patients with RA.
TARGET HEALTH excels in Regulatory Affairs and Public Policy issues. Each week we highlight new information in these challenging areas.
FDA to Improve Most Common Review Path for Medical Devices
The U.S. Food and Drug Administration today unveiled a plan containing 25 actions it intends to implement during 2011 to improve the most common path to market for medical devices.
Key actions include:
1. Streamlining the “de novo” review process for certain innovative, lower-risk medical devices
2. Clarifying when clinical data should be submitted in a premarket submission, guidance that will increase the efficiency and transparency of the review process
3. Establishing a new Center Science Council of senior FDA experts to assure timely and consistent science-based decision making
According to FDA, these actions will result in “a smarter medical device program that supports innovation, keeps jobs here at home, and brings important, safe, and effective technologies to patients quickly,” (Jeffrey Shuren, M.D., J.D., Director of CDRH).
Currently, before marketing most lower-risk medical products such as certain catheters or diagnostic imaging devices, manufacturers must provide the FDA with a premarket notification submission. These submissions are known as 510(k)s for the section of the Federal Food, Drug, and Cosmetic Act that describes this notification requirement. Generally, 510(k)s must demonstrate that a proposed product is substantially equivalent to another, legally marketed medical device that is also lower-risk.
In September 2009, CDRH set up two internal working groups to address concerns relating to the premarket notification process – industry argued that the 510(k) process was unpredictable, inconsistent and opaque, while consumers and health care professionals argued that the review process wasn’t robust enough. At the same time, CDRH also asked the independent, nonprofit Institute of Medicine to study the program. That review is still underway.
In a transparent effort, CDRH sought public input during both the development and review of the two internal reports. The center held two public meetings in the Washington area and separate “town hall” meetings in Minneapolis, Boston and Los Angeles. The FDA also received 76 written comments to three public dockets from industry members, health care professional organizations, consumer groups, patient groups, third-party payers, venture capital groups, agency staff, trial lawyers, foreign regulatory bodies, law firms, individual members of the public, consulting firms and academic institutions.
The two working groups issued 55 recommendations in August 2010. After reviewing public comment, CDRH now intends to take 25 actions to improve the 510(k) program in 2011, including new guidance and enhanced staff training. CDRH also is giving the Institute of Medicine an opportunity to provide feedback on seven recommendations before making a final decision and is planning for a public meeting in April to seek additional feedback on two other recommendations.
Medscape.com, by Lisa Nainggolan, January 27, 2011 (Montreal, Quebec City)— Restricting the prescribing of angiotensin-receptor blockers (ARBs) so that they are given only to patients who are intolerant to ACE inhibitors could save millions of dollars in healthcare costs without any adverse effects on cardiovascular health, say Canadian researchers .
In their paper published online January 24, 2011 in CMAJ,Dr Jason R Guertin (University of Montreal, QC) and colleagues explain that one province in Canada, British Columbia, already restricts the use of ARBs in this way; if all Canadian provinces had done this in 2005–2006, they calculate that the savings would have been more than Can$77 million.
Although the savings are diminishing, we could still save $20 million a year from now on and ongoing for several years if we applied this rule now.
“The sad part of the story is that this is a missed opportunity,” senior author Dr Stéphane Rinfret (University Laval, QC) told heartwire . Because some ARBs are now starting to come off patent and therefore are dropping in price, savings would no longer be this large, he said. “However, although the savings are diminishing, we could still save $20 million a year from now on and ongoing for several years if we applied this rule now.”
Calculations Assume Equivalence of ACE Inhibitors and ARBs
However, Dr Franz Messerli (St Luke’s Roosevelt Hospital, New York, NY), who was not involved with this research, told heartwire ,”This is an interesting paper, but the investigators are assuming equal outcomes with ARBs and ACE inhibitors. However, there is only one study–ONTARGET–in which the difference [between ARBs and ACE inhibitors] was not significant.”
For example, says Messerli, there is evidence that ARBs are more effective than ACE inhibitors in reducing stroke and in the prevention of new-onset diabetes, but that ACE inhibitors are better than ARBs at reducing the risk of MI. “Unless we have a thorough head-to-head comparison we cannot make a serious point,” he states.
ACE inhibitors and ARBs are like brothers and sisters; they are interchangeable.
Rinfret says it is true that their calculations assume equivalent outcomes between ACE inhibitors and ARBs, but he stands by this assumption, saying it’s extremely unlikely that they differ based on the bulk of evidence: “There has only been one study showing that ARBs would save lives in patients with hypertension–LIFE–and the comparator was a beta blocker, [and beta blockers] are now in question as first-line therapy for hypertension. There have been multiple small studies, and when they are meta-analyzed, in hypertension or heart failure, there have been absolutely no advantages of ARBs.”
He stresses that he “is not questioning” the use of ARBs when patients genuinely are intolerant to ACE inhibitors or in the rare few patients who might benefit from both medications, but aside from the dry cough that some patients can experience on ACE inhibitors, “to me they are like brothers and sisters; they are interchangeable.”
Hopefully Canada Will Sit Up and Take Notice
The researchers say the cost of cardiovascular drugs increased by more than 200% in Canada from 1996 to 2006, and the use of ARBs in particular grew at “an especially high rate, rising by more than 4000% during that period.”
“Given a future of increasing economic uncertainty complicated by a demographic shift to an older population with a relatively shrinking tax base, measures are needed to deal with rising healthcare costs,” they observe.
Rinfret explains that currently, in BC, “you cannot simply prescribe an ARB without proving that the patient is intolerant to an ACE inhibitor. If this is the case, another step is required–in the form of a fax sent to the public healthcare plan stating this fact–and almost 100% of the time this request is approved,” he points out.
He hopes that this new research will make Canadians sit up and take notice. “We expect in Canada there is going to be some reaction, and maybe some other provinces will want to imitate BC.” He and his colleagues point out that a similar initiative in Sweden, where reimbursement restrictions for ARBs were implemented in 2008, has led to a 24% reduction in the dispensing of ARBs and a drop of 5% in total drug expenditure.
“I think this kind of move is essential; it’s not only specific to ARBs–there are a lot of other drugs in cardiovascular care and other branches of medicine that would benefit from such restriction,” Rinfret observes. “Targeting the expensive drugs that don’t bring any more health value is the way to go in the future if you want to save some money for other, more useful spending.”
But he and his colleagues stress, “Policies can neither be draconian nor take a one-size-fits-all approach. Patient well-being must always come first. We believe that favoring the least expensive medication over others of comparable effectiveness is one way to address future economic challenges without creating social disparities.”
Rinfret has received research grants and consulting fees from Pfizer Canada, Bristol-Myers Squibb, and Sanofi-Aventis. Disclosures for the coauthors are listed in the paper. Messerli is on the speaker’s bureaus of GlaxoSmithKline, Novartis, AstraZeneca, Bayer, Boehringer Ingelheim, Forest, and Sankyo and has received research funding and grants from GlaxoSmithKline, Pfizer, Novartis, and Cardiovascular Therapeutics.
References: Guertin JR, Jackevicius CA, Cox JL, et al. The potential economic impact of restricted access to
angiotensin-receptor blockers. CMAJ 2011; DOI: 10.1503/cmaj.100787ARBs. Available at: http://www.cmaj.ca.
Heart Disease Drugs: Beta Blockers and Calcium Channel Blockers
For heart disease, medication choices abound: ACE inhibitors, angiotensin II receptor blockers, beta blockers, calcium channel blockers. Learn about how each of these medications works, pros and cons, and potential side effects
Medically reviewed by Lindsey Marcellin, MD, MPH
The names ACE inhibitors, angiotensin II receptor blockers (ARBs), beta blockers, and calcium channel blockers may sound familiar: They are all heart medications and they all lower blood pressure, among other effects on the heart.
But they work in different ways and they each have their own side effects. They all also come in many different forms.
Angiotensin-Converting Enzyme (ACE) Inhibitors
ACE inhibitors are medications primarily used to treat hypertension (high blood pressure) and congestive heart failure, a condition in which the heart can’t pump enough blood to the other organs. They are also used to:
- Prevent repeat heart attacks
- Reverse thickening of the heart due to high blood pressure
- Prevent kidney function decline in people with diabetes and high blood pressure
ACE inhibitors help dilate blood vessels by blocking the angiotensin-converting enzyme, which is part of a chain reaction that begins in the kidneys and constricts blood vessels, causing blood pressure to rise.
ACE Inhibitor Generic and Brand Names
Common ACE inhibitors include:
- Benazepril (Lotensin)
- Captopril (Capoten)
- Enalapril (Vasotec)
- Fosinopril (Monopril)
- Lisinopril (Prinivil, Zestril)
- Moexipril (Univasc)
- Perindopril (Aceon)
- Quinapril (Accupril)
- Ramipril (Altace)
- Trandolapril (Mavik)
Pros and Cons of ACE Inhibitors
The pros are considerable. They’ve been in widespread use for more than two decades. Many are available as generics and are, therefore, less expensive. ACE inhibitors can also remodel a weak heart — that is, they can help repair it.
As for the cons: “Not all patients can take ACE inhibitors. About 5 to 10 percent will have side effects,” says Douglas Weaver, MD, head of the division of cardiology and co-director of the Heart and Vascular Institute at Henry Ford Hospital in Detroit.
Side Effects of ACE Inhibitors
Potential side effects of these medications include:
- Decline in kidney function, particularly when taken with diuretics (water pills)
- A persistent dry, hacking cough
- A skin rash
- Altered sense of taste
Some people may feel weak or dizzy when they begin taking ACE inhibitors because it lowers their blood pressure. That’s why some doctors recommend you take ACE inhibitors at night before going to bed — you’ll be lying down soon after.
Angiotensin II Receptor Blockers (ARBs)
Like ACE inhibitors, these medications aim to lower blood pressure by targeting the chemical angiotensin II, which is part of the chain reaction mentioned above. But instead of blocking the production of angiotensin, as ACE inhibitors do, ARBs prevent the chemical, once it’s made, from having an effect on the blood vessels and the heart. Like with ACE inhibitors, the result is the blood vessels dilate and blood pressure lowers.
They are generally prescribed for people who have high blood pressure, and for some people, to reduce the risk of diabetic kidney disease and stroke.
Generic and Brand Names of ARBs
Commonly used ARBs include:
- Valsartan (Diovan)
- Telmisartan (Micardis)
- Irbesartan (Avapro)
- Olmesartan (Benicar)
- Losartan (Cozaar)
- Candesartan (Atacand)
- Eprosartan (Teveten)
Pros and Cons of ARBs
The benefits of ARBs are similar to those for ACE inhibitors, but if you develop a chronic cough as a side effect of an ACE inhibitor, an ARB should be just as effective.
And the negatives: ARBs should not be taken by women who are pregnant or who plan on becoming pregnant, as they could harm a fetus. Also, a recent study suggested that ARBs may be associated with a slightly increased cancer risk. The authors say that more research is needed to draw any conclusions. The U.S. Food and Drug Administration (FDA) is reviewing information related to ARBs, saying that although the agency has not reached the conclusion that ARBs cause an increased risk of cancer, it appears that the benefits of taking ARBs outweigh the possible risks.
Side Effects of ARBs
Like all medications, there are potential side effects associated with ARBs, including:
- Low blood pressure
Two Types of Medication that are Commonly Prescribed to Treat Heart Disease
Cardiomyopathy is a disease involving changes in the heart muscle. These changes
may interfere with the heart’s ability to pump effectively, which can lead to a chronic
condition called heart failure. Cardiomyopathy is sometimes associated with other
chronic conditions, such as high blood pressure or heart valve disease.
1) Beta Blockers
Beta blockers are medicines that treat high blood pressure and heart failure. They block signals to the heart that increase heart rate or strength of contractions, Dr. Weaver says. This approach may seem counterintuitive, but research has shown that it has long-term benefits, he says. Beta blockers allow the heart to take a break by lowering the demand on it and lessening the force of its contractions. Beta blockers can have a similar effect on blood pressure. They lower pressure by toning down and slowing the heart’s contractions.
Beta blockers accomplish this by blocking beta-adrenergic receptors in the body, many of which are in the heart. Beta-adrenergic receptors are part of the nervous system that pick up messages to speed the heart or to pump harder. Blocking these can help reduce fatigue by causing the heart to slow down and pump with less force.
Beta Blocker Generic and Brand Names
There are many different beta blockers available, including
- Metoprolol (Lopressor, Toprol XL)
- Atenolol (Tenormin)
- Bisoprolol (Zebeta)
- Propranolol (Inderal)
- Sotalol (Betapace)
- Pindolol (Visken)
- Penbutolol (Levatol)
- Acebutolol (Sectral)
- Timolol (Blocadren)
- Nadolol (Corgard)
- Betaxolol (Kerlone)
Beta blockers are given to people with histories of heart issues, such as:
- High blood pressure, along with another heart condition such as a history of heart attacks or heart failure
- Heart failure
- Coronary artery disease (CAD) and perhaps angina, which is chest pain
- Atrial fibrillation, which is a rapid heartbeat, or atrial flutter
Pros and Cons of Beta Blockers
Many beta blockers have been around for a long time, so they are available as generics. Other welcome news: Weaver says that most people won’t have side effects from beta blockers, but if they do the most common will be fatigue.
On the down side: Because beta blockers slow down the heart’s function, they can worsen heart failure in some people. Also, beta blockers can cause the airways in the lungs to narrow, so patients with asthma, emphysema, and chronic bronchitis should take them with caution.
Possible Side Effects of Beta Blockers
Side effects of these medications may include:
- Erectile dysfunction
- Can worsen other diseases such as asthma or diabetes
- Coldness in hands and feet
2) Calcium Channel Blockers
Calcium channel blockers are often a first-line treatment for high blood pressure, although they are prescribed less often than beta blockers. Indeed, a recent study in the Journal of the American College of Cardiology found that calcium channel blockers may be more effective for treating high blood pressure in some patients than beta blockers.
Calcium channel blockers reduce the amount of calcium moving through cells in the heart muscle and arteries. Blocking calcium channels allows the heart muscle to function more normally and also helps dilate the arteries, lowering blood pressure. They are given to patients with high blood pressure, those with angina, and those with some abnormal heart rhythms, called arrhythmias.
Generic and Brand Names of Calcium Channel Blockers
Calcium channel blockers include:
- Amlodipine (Norvasc)
- Bepridil (Vascor)
- Diltiazem (Cardizem, Dilacor)
- Felodipine (Plendil)
- Isradipine (DynaCirc)
- Nicardipine (Cardene)
- Nifedipine (Adalat, Procardia)
- Nimodipine (Nimotop)
- Nisoldipine (Sular)
- Verapamil (Calan, Isoptin, Verelan)
Pros and Cons of Calcium Channel Blockers
Calcium channel blockers are less likely to cause fatigue as a side effect than other heart medicines. They have fewer side effects than nitrates, which are also used to treat angina, and they are more convenient than nitrates because they can be taken once a day. Also, recent studies have found that calcium channel blockers protect against heart attacks and stroke.
As for the cons, calcium channel blockers should be used with caution in patients with pulmonary arterial hypertension and congestive heart failure. These medicines can also cause constipation and swelling in the ankles and feet.
Side Effects of Calcium Channel Blockers
Besides the side effects already mentioned, other potential side effects include:
- Irregular or slow heartbeat
- Shortness of breath
- Feeling weak or fatigued
Regardless of the heart medications your doctor chooses for you, you can help them work better by watching your diet, maintaining a healthy weight, and getting regular exercise.
More About High Blood Pressure and Heart Disease
Medscape.com, January 27, 2011, Michael O’Riordan
(Miami Beach, Florida) — Should patients at standard risk for adverse events from carotid endarterectomy be treated with carotid artery stenting? That is the question a Food and Drug Administration (FDA) advisory panel grappled with this past Wednesday, as panel members gathered to make recommendations and vote on an expanded indication for the RX Acculink Carotid Stent System (Abbott, Abbott Park, IL) .
Currently, the RX Acculink stent is approved for use in patients requiring carotid revascularization who are at high risk for adverse events from carotid endarterectomy. These high-risk patients must also have a reference vessel diameter ranging from 4.0 mm to 9.0 mm at the target lesion and be symptomatic with a stenosis of the common or internal carotid artery >50%. The stent is also approved in high-risk patients without neurological symptoms but who have a stenosis of the common or internal carotid artery >80%.
Based on data from the Carotid Revascularization Endarterectomy Versus Stenting Trial (CREST), Abbott is looking to expand the indication of the RX Acculink stent to include patients at standard risk for adverse events from carotid surgery. Patients must meet the same criteria as high-risk patients, but the company is also seeking approval for use in asymptomatic patients with a stenosis >70%, as opposed to >80% with the current indication.
We believe there are data suggesting that, in patients in all risk stratifications, stenting is safe and effective.
“The CREST study gave us a tremendous amount of data, some of which will be presented to the FDA,” Dr James Benenati (Baptist Heart and Vascular Institute, Miami, FL), president of the Society of Interventional Radiologists (SIR), told heartwire last week at the International Symposium on Endovascular Therapy (ISET) 2011. “Basically, in carotid stenting in general, we know that for high-risk symptomatic patients, the FDA has approved this procedure. What many of us in the interventional community are looking for is an expansion. We believe there are data suggesting that, in patients in all risk stratifications, stenting is safe and effective, and the differences between endarterectomy and stenting in all patient subgroups are basically very, very small.”
Based on the FDA briefing materials, the hopes of Benenati and others in the interventional community are supported by the agency. According to an executive summary released early by the FDA, the new “proposed indications are supported by a primary analysis of the CREST trial data and by multiple important secondary and tertiary analyses.”
The FDA Circulatory System Devices advisory panel will be chaired by Dr Jeffrey Borer (University of Pennsylvania, PA), who participates in the voting process with 12 other panel members. During the day-long meeting, panel members are expected to discuss the appropriateness of the RX Acculink device in octogenarians and nonoctogenarians and in symptomatic and asymptomatic patients, as well as likely to discuss the relative role of operator experience in achieving favorable results. The briefing documents are available here.
Treating Asymptomatic Patients
Although large portions of the FDA document are blacked out and won’t be made public until Wednesday during the advisory panel meeting, the agency notes that primary-end-point event rates are lower than acceptable event rates proposed by the American Heart Association (AHA) guidelines for carotid revascularization. For example, the combined end point of periprocedural death and stroke in CREST was 5.9% for carotid stenting and 2.4% for carotid endarterectomy in symptomatic patients, lower than the AHA-acceptable standard of 6%, although it’s close to the limit for carotid stenting. In asymptomatic patients, the AHA-proposed limit for periprocedural death and stroke is 3%, and in CREST both the carotid stenting and endarterectomy arms fell below this limit (2.5% vs 1.3%, respectively).
Speaking at ISET last week, however, were some who believed that asymptomatic patients shouldn’t be treated with stents or surgery at all but rather with medical therapy. In an interview with heartwire , Dr Anthony Comerota (University of Michigan, Ann Arbor) said that the “overwhelming majority” of patients in the US who undergo carotid stenting do not have any symptoms. Good medical management–such as high-dose statin therapy, good blood-pressure control, management of diabetes, and good platelet inhibition–can reduce the risk of stroke, and carotid endarterectomy, as well as carotid stenting, should be best left to highly selected patients, said Comerota.
I wouldn’t advocate that everybody gets a carotid stent, nor would I advocate that every carotid stenosis be treated with stent or surgery.
Speaking at ISET, Comerota said that 97% of carotid-etiology strokes occur in patients with symptomatic disease, and yet 2005 data showed that more than 90% of carotid revascularization procedures were performed in asymptomatic patients. The reason this is important is that the biological characteristics of symptomatic and asymptomatic plaque differ significantly, with symptomatic plaque being more unstable, showing evidence of subintimal hemorrhage and thrombus within the lumen.
Benenati agreed, saying that while candidates for surgery should also be candidates for carotid stenting, not every patient is a candidate for revascularization.
“I wouldn’t advocate that everybody gets a carotid stent, nor would I advocate that every carotid stenosis be treated with stent or surgery,” he told heartwire . “One of the great things that all the carotid stent trials have brought to light is that there are some groups of patients that might do better with medical therapy. For example, asymptomatic patients, high- and low-risk, with stenosis less than 70% or 80%, will probably do fine with medical therapy.”
The Primary End Point in CREST
Although the expanded RX Acculink indication is based on data from CREST, Comerota took issue with the study, saying that the design incorporated an “inherent fallacy” that was part of conventional thinking at the time the trial was started. The primary end point was a composite of clinical stroke, MI, or death during the periprocedural period plus ipsilateral stroke on the vessel that was treated, with patients followed out to four years. At the time, perioperative MI was thought to be a very important problem, Comerota told heartwire , one that led to a significantly higher death rate at six months.
So now we have a major trial equating an elevation in cardiac enzymes with stroke or death.
“This has turned out not to be the case,” he said. “An asymptomatic myocardial infarction, a troponin leak, is not associated with an increased mortality risk and is not associated prognostically with an increased mortality risk over the next four or five years. So now we have a major trial equating an elevation in cardiac enzymes with stroke or death. That clearly is inappropriate, but when enthusiasts of carotid angioplasty and stenting want to present their side of the story, they’ll say there is no difference because of the higher myocardial infarction rate [with surgery]. Myocardial infarction didn’t alter the quality of life of patients down the road, whereas stroke, even minor stroke, altered the quality of life significantly.”
In CREST, as reported previously by heartwire , there was no significant difference in the combined end point of stroke, MI, or death within the periprocedural period (7.2% for carotid stenting vs 6.8% for endarterectomy; p=0.51), but stroke rates were higher in the stenting arm, while rates of MI were higher among the surgical patients.
Based on the FDA documents, the advisory panel will discuss the appropriateness of including MI in the primary end point, as well as its definition and impact on the primary end point. In addition, they will debate the clinical significance and severity of cranial nerve injury, which occurred in 5.2% of patients treated with endarterectomy.
First the FDA Hurdle, Next the CMS
At the end of the day, even if the FDA advisory panel votes to approve the expanded indication for the RX Acculink stent to include standard-risk surgical patients, the Centers for Medicare and Medicaid Services (CMS) still need to green-light reimbursement. Currently, Medicare coverage is confined to patients at high risk for carotid endarterectomy who have symptomatic carotid artery stenosis >70%, as long as stenting is performed using FDA-approved systems with embolic-protection devices and at CMS-approved facilities. The CMS also covers carotid stenting in patients if they are a high-risk endarterectomy patient with lesser degrees of symptomatic carotid artery stenosis (50% to 70%) or at high risk for endarterectomy with asymptomatic carotid artery stenosis >80%, but only if they are participating in pre- or postapproval studies.
To heartwire , Benenati said the day is coming when clinical centers performing carotid stenting will need to receive accreditation. The Intersocietal Commission for the Accreditation of Carotid Stenting Procedures, in support of numerous societies, including SIR, is seeking to establish minimum requirements and recommendations for facilities performing carotid stenting.
“I’m a strong advocate, as is the society, that not every physician who does endovascular therapy should be doing carotid stenting,” said Benenati. “Carotid stenting is a skill that’s learned–it takes repetition and dedicated continuing medical education. Also, the facility where the carotid stenting takes place is critically important, too.”
Benenati reports serving as the chief medical officer of Northpoint Domain and consulting for or serving on the advisory boards of Abbott, Amaranth Medical, Biosphere, Cordis, Endovention, and WL Gore. Comerota reports speaking for or receiving honoraria from Bristol-Myers Squibb, Covidien, Otsuka, Sanofi-Aventis, Servier, ZymoGenetics; consulting for or serving on the advisory boards of Aastrom, AngioDynamics, Convatec, Cook, Covidien, Bristol-Myers Squibb, Talecris; and receiving research support from Aastrom, Abbott Vascular, Baxter, Bristol-Myers Squibb, Boehringer Ingelheim, BSN, Colorado Prevention Center, CVRx, eV3, Johnson & Johnson, Lombard Medical, Medtronic, the National Institutes of Health, Pfizer, Sanofi-Aventis, Schering-Plough, and Talecris.
More About Carotid Stenting
The two common carotid arteries bring oxygenated blood from the heart through the neck to each side of the head. As people age, plaque can build up inside their arteries. Over time, these plaques collect on arterial walls as cholesterol circulates in the blood. As the plaques enlarge, the arteries become narrow and stiff, a process called atherosclerosis, or “hardening of the arteries.”
Blood clots forming on the plaque can cause an occlusion or blockage, preventing the flow of blood to the brain. The blockage can create an ischemia, or lack of oxygen caused by insufficient blood flow, which can cause an ischemic stroke if the blood flow is blocked long enough.
Atherosclerotic plaques in the carotid arteries can also increase a person’s risk of an arterial embolism, the sudden blocking of an artery by a small piece of loose plaque or a loose blood clot.
Carotid stenting is a procedure in which a tiny, slender metal-mesh tube is fitted inside a carotid artery to increase the flow of blood blocked by plaques. The stent is inserted following a procedure called angioplasty, in which the physician guides a balloon-tipped catheter into the blocked artery. The balloon is inflated and presses against the plaque, flattening it and re-opening the artery. The stent acts as scaffolding to prevent the artery from collapsing or being closed by plaque after the procedure is completed.
WHEN IS THE PROCEDURE INDICATED?
Stenting is often recommended for people who are unable to undergo an endarterectomy. Endarterectomy, the surgical removal of plaque from the artery, is the standard treatment for severe buildup of plaque in the carotid artery. For some people, however, endarterectomy may not be appropriate. For example, the procedure is inappropriate for people who are unable to tolerate the side effects of anesthesia.
Common conditions that make endarterectomy high risk include:
- Advanced age or the presence of serious disease, such as cancer;
- Surgically inaccessible atherosclerotic plaques;
- Having undergone a previous endarterectomy;
- Having severe congestive heart failure or unstable angina; and/or
- Problems with other blood vessels in the head.
WHAT TO EXPECT
The goal of angioplasty is the restoration of adequate blood flow (revascularization) through the affected part of the body by enlarging the blood vessel from within.
To place a stent, the physician removes the angioplasty balloon catheter and inserts a new catheter on which a closed stent surrounds a deflated balloon. The stent-carrying catheter is advanced through the artery to the site of the blockage. The balloon is inflated, causing the stent to expand. The balloon is then deflated and the catheter withdrawn, leaving the stent in place. The stent in a carotid artery allows blood to flow to the brain.
The smooth lining of the arterial wall eventually grows back to cover the stent and secure it, so the stent will not dislodge. Stents are left in place permanently, and because they are made from stainless steel or metal alloys, they will not rust or deteriorate.
Risks commonly associated with carotid stenting may include:
- Slight risk of stroke because of a loose piece of plaque or a blood clot blocking an artery during or immediately following surgery;
- Abrupt closure of the artery after surgery;
- Restenosis (the reoccurrence of plaque buildup) that occurs after a stent has been placed in the carotid artery, preventing future endarterectomy; or
- Short periods of reduced blood pressure and heart rate that may occur, which is treated with medications.
Perhaps the most serious potential risks involved with carotid stenting are the risk of a disrupted plaque particle that breaks free from the site, called an embolism, and blocks an artery in the brain, causing a stroke. These risks are minimized using small filters called embolic protection devices in conjunction with angioplasty and stenting.
Hyper perfusion, or the sudden increased blood flow through a previously blocked carotid artery and into the arteries of the brain, may occur after stenting, and can cause a hemorrhagic stroke. While this is a risk of stenting, it is more likely to occur because of more invasive surgical procedures.
Carotid stenting, while generally safe and less invasive than endarterectomy, remains an evolving field. The first randomized controlled trial comparing surgery to carotid angioplasty and stenting was reported at the American Heart Association in November 2002, and showed significant benefits of stenting over surgery in reducing adverse events at one month in ‘high risk’ patients. More complete data and certain refinements of the devices used during the procedure are needed before stenting can be considered the primary treatment for blocked carotid arteries.
Source: NYU Medical Center
Carotid Stents vs Endarterectomy Surgery
For patients with blockages in the carotid artery that supplies blood to the brain, carotid artery stenting (a non-surgical therapy) may be linked to an increased risk of both short- and long-term adverse outcomes when compared with surgical therapy (carotid endarterectomy), as per a meta-analysis of previously published studies that was posted online today and will appear in the February 2011 print issue of Archives of Neurology, one of the JAMA/Archives journals.
“Carotid artery stenting has emerged as an alternative to carotid endarterectomy for the therapy of carotid artery occlusive disease,” the authors write as background information in the article. The treatmentwhich involves threading a catheter through the femoral (groin) artery to the carotid artery, inflating an angioplasty balloon to compress plaque and inserting a stent to keep the artery openis endorsed by the American Heart Association/American Stroke Association guidelines as a reasonable strategy and recommended by the European Society of Vascular Surgery in certain circumstances. However, its safety and efficacy as compared with carotid endarterectomy (surgery to remove the inner lining of the diseased blood vessel) is controversial.
Sripal Bangalore, M.D., M.H.A., of New York University School of Medicine, New York, and Harvard Clinical Research Institute, Boston, and his colleagues conducted a meta-analysis of 13 randomized clinical trials comparing the two therapys conducted through June 2010 and involving 7,477 patients with carotid artery disease. They assessed the risk of death, heart attack (myocardial infarction) and stroke within the periprocedural period (within 30 days of the procedure) as well as intermediate and long-term outcomes.
In the first 30 days, carotid artery stenting was linked to a 65 percent increased risk of death or stroke and a 67 percent increased risk of any stroke. However, the stent procedure was linked to a 55 percent lower risk of heart attack and 85 percent reduction in cranial nerve injury in this timeframe when compared with carotid endarterectomy.
Intermediate- to long-term outcomes were assessed using a composite involving death, any strokes or strokes on the side of the brain with carotid blockage (ipsalateral stroke) within 30 days or thereafter. Carotid artery stenting as compared with carotid endarterectomy was linked to a 19 percent increase in the risk of such an outcome, as well as an increased risk of various combinations of strokes, ipsilateral stroke and death. Stenting was also linked to an 180-percent increase in the risk of restenosis (repeat narrowing of the carotid artery).
“In this largest and most comprehensive meta-analysis to date using outcomes that are standard in contemporary studies, carotid artery stenting was linked to an increased risk of both periprocedural and intermediate to long-term outcomes, but with a reduction in periprocedural myocardial infarction and cranial nerve injury,” the authors conclude. “Strategies are urgently needed to identify patients who are best served by carotid artery stenting vs. carotid endarterectomy”.
(Arch Neurol. Published online October 11, 2010. doi:10.1001/archneurol.2010.262. Available pre-embargo to the media at www.jamamedia.org.).
Editor’s Note: Senior author Dr. Bhatt has received research grants form AstraZeneca, Bristol-Myers Squibb, Eisai, Ethicon, Heartscape, Sanofi Aventis and The Medicines Company. Please see the article for additional information, including other authors, author contributions and affiliations, financial disclosures, funding and support, etc.
Editorial: Meta-Analysis and Other Data Should Guide Personalized Medical Decisions for Each Patient
“What message can doctors take home from the past surgery vs. stenting horse races, from the numerous reports of results in patients not entered in trials, from the meta-analysis in this month’s Archives and from the recently published results of the Carotid Revascularization Endarterectomy vs. Stenting Trial?” write Louis R. Caplan, M.D, of Beth Israel Deaconess Medical Center, Boston, and Thomas G. Brott, M.D., of Mayo Clinic, Jacksonville, Fla., in an accompanying editorial.
“Both therapeutic procedures are effective. Both procedures showed a relatively low rate of serious complications. Surgery is superior concerning some outcomes; stenting seems to have advantages in others,” they write. In addition, “aggressive medical therapy of blood lipids, blood pressure and anti-platelets along with changes in lifestyle appears to be as good as or better than either surgery or stenting at stroke and myocardial infarcts prevention”.
“The past decades have produced three very effective therapysmedical, surgical and interventionalfor individuals with carotid artery disease,” they conclude. “The results and complications of each can be improved. We have learned much from the trials and they are a beacon to engender even further improvements. However, care of individual patients will always rest in the hands of a trained experienced doctor on one end of a stethoscope and a patient on the other end. Trials can enlighten that encounter but never replace it”.
(Arch Neurol. Published online October 11, 2010. doi:10.1001/archneurol.2010.268. Available pre-embargo to the media at www.jamamedia.org.).
Carotid Angiography and Stenting Photo Gallery
Carotid Artery Anatomy with Angiography
In the past, vascular surgery was the standard of care for patients with carotid artery disease. Co-existing health conditions preventing patients to have surgical treatment led to the first carotid angioplasty and carotid stenting in 1994.
A carotid stent is a small wire mesh tube, inserted after angioplasty that acts as a scaffold to provide support inside the artery. Although carotid stenting remains investigational, several types of carotid stents are available to use during this procedure.
Patient post carotid surgery
Patient post carotid angioplasty & stent (no neck incision)
There are a variety of stents used for carotid stenting – below are three examples of carotid stents:
Caution: These devices are investigational in the United States and are limited by U.S. law to investigational use.
Endotex Carotid Stent
SMART Nitinol Stent
Guidant ACCULINK Carotid Stent System
Carotid stenting filter devices
Emboli protection devices have improved the safety of carotid stenting. Strokes that occur during, or in the first few minutes after, carotid angioplasty and stenting are caused by microemboli (tiny particles in the blood) dislodging and traveling to small distal blood vessels in the brain. Filter devices, combined with antiplatelet medication, provide protection against microemboli. The filter device’s microscopic-sized holes allow blood flow to continue as particles are captured in the device. At the end of the procedure, the filter is removed from the carotid artery along with captured debris. The rate of complications, including stroke, myocardial infarction (MI), and death, at the Cleveland Clinic Foundation are about 3 percent.
There are a variety of emboli protection devices (filters) used during carotid stenting – below are three examples:
Caution: These devices are investigational in the United States and are limited by U.S. law to investigational use.
Angioguard Emboli Capture Guidewire System
Guidant ACCUNET™ Embolic Protection System Filter Basket Specifications
FilterWire EX™ Carotid Wallstent® Monorail™
Filter device removed with microemboli captured
Carotid Angioplasty and Stenting – before and after angiography
Carotid angiography at baseline
Carotid angiography post angioplasty and stent
Mid-cerebral artery angioplasty and stenting – before and after angiography
Mid-cerebral artery angiography at baseline
Mid-cerebral artery angiography post angioplasty and stent