What else is there?

This question comes up frequently:

Aren't there any alternatives to heart scans performed on a CT or EBT device?

Yes, there are.

First of all, heart scans are performed best on an electron-beam CT device (EBT) or a 64-slice multi-detector CT (MDCT) device. (While they are also obtainable through less-than-64 slice CT devices (e.g., 16 slices and less), I would advise against it because of the excessive radiation exposure and poor accuracy.) CT heart scans are not to be confused with now more popular CT coronary angiograms, which are performed on the same devices but require intravenous x-ray dye and many times more radiation.(See CT scans and radiation exposure and Heart scan frustration.) Heart scans currently form the basis for the Track Your Plaque program, a program of tracking plaque in the hopes of stopping or reversing the otherwise inevitable 30% per year increase.

Let's confine our discussion to people without symptoms, meaning people like you and me sitting at home, not in an emergency room having chest pain or other similar acute symptomatic presentation.

Among the other ways to uncover hidden coronary plaque:

--Heart catheterization--to yield a coronary angiogram. Yes, this does tell us whether coronary plaque is present. However, it is invasive, expensive, and crude. (I've performed 5000 over my career; they are crude, though useful, tools in acute settings like unstable symptoms or heart attack, a different situation.) Coronary angiography is also non-quantitative. While they provide a value like "40% blockage mid-way in right coronary" or "90% blockage in left anterior descending" they do not provide a trackable lengthwise index of total plaque volume. Identifying severe blockages in people with symptoms leads to stents, bypass surgery and the like, but it is not practical nor of long-term usefulness in apparently, healthy people without symptoms.

--Carotid ultrasound--Here's is where a lot of confusion comes from. Standard carotid ultrasound (U/S) performed in virtually every hospital and many clinics will yield crude qualitative results, e.g., "16-49% stenosis (blockage) in right internal carotid artery". The crude value range is because much of carotid U/S is based on flow velocities, not just direct visualization of the plaque itself ("2-D imaging). However, if carotid stenosis of any degree is identified, the likelihood of silent coronary plaque is much greater.

Limitations: The qualitative, non-quantitative nature of carotid U/S make it difficult to follow long-term in a precise way. Also, this is carotid plaque, not coronary plaque. It makes it very difficult to follow carotid plaque as an indirect means of tracking coronary plaque. The two arterial territories, carotid and coronary, do not track together: there are divergences in many people, with carotid plaque absent in some people with advanced coronary plaque, carotid plaque more susceptible to different risk factors than coronary. So carotid U/S is helpful for its own purposes, but not terribly helpful for coronary tracking.

How about carotid intimal-medial thickness (CIMT) obtained also with carotid U/S? CIMT is a useful index of bodywide atherosclerosis. CIMT is simply a measure not of plaque (and is measured in regions of the carotid artery away from plaque), but of the thickness of the lining of the carotid arteries. Everybody has a measurable CIMT, but it thickens as atherosclerosis grows. CIMT is a radiation-free test that takes several minutes.

Limitations: Hardly anybody does it outside of research protocols. I know of no hospital or clinic in my area that performs CIMT, though it is slowly being adopted in some centers. It is also difficult to rely on repeated tests, because there is substantial variation when one technologist or another performs it. CIMT is also a flawed index of coronary plaque. When CIMT is compared to heart scan scores, CT coronary angiography, or conventional coronary angiography, CIMT correlates about 60-70% with the degree of coronary atherosclerosis.

CIMT is therefore a useful test for research, but a distant 2nd choice--if you can obtain it.

--Ankle-brachial index (ABI)--ABI is a crude measure, simply a comparison of the blood pressure (obtained with a blood pressure cuff) in the legs divided by blood pressure in the arms. The ratio is called ABI. Any ABI <1.0, meaning less pressure in the legs compared to the arms, is indirectly indicative of advanced coronary disease. ABI is, in fact, a very powerful predictor of cardiovascular events. If ABI is <1.0, your future risk for heart attack is very high, even in the absence of symptoms.

Limitations: The vast majority of people with heart disease, even those having undergone stents or bypass surgery, have normal ABI's. Virtually all people with high heart scan scores have normal ABI's. In other words, ABI is a measure of very advanced atherosclerosis only.

--Stress tests--I lump all stress tests together in their various forms, e.g., stress thallium, stress Cardiolite, stress Myoview, persantine/adenosine Cardiolite, dobutamine echocardiography, etc. Stress tests are tests of coronary blood flow, not of plaque. Stress tests are useful in people with symptoms, like chest pain or breathlessness, since stress tests are provocative tests that can help determine whether reduced coronary blood flow is the cause behind a symptom, or whether hiatal hernia, esophagitis, gallstones, pleurisy, musculoskeletal causes, or some other process is behind symptoms.

Limitations: Stress test are virtually useless in people without symptoms. This is why people like Tim Russert and Bill Clinton, both without symptoms, underwent several (Russert 3, Clinton 5) nuclear stress tests---all normal. You know what happened to them. Stress tests do not reliably uncover hidden coronary plaque in people without symptoms. Stress tests are, like coronary angiograms, non-quantitative. They are normal or abnormal.


Outside of experimental settings, that's it.

You can probably see why I advocate CT heart scans for tracking plaque. I do not advocate heart scans because I sell them (I don't), because scan centers pay me to say these things (they don't, and in fact my relationship with my usual heart scan centers has become deeply contentious, though I still endorse the technology). I say that heart scans are superior because they are, in 2008, the only way to 1) identify and 2) track coronary plaque that is easy, safe, low-radiation, and reasonably priced (<$200 in Milwaukee at 5 centers).

The need for a technology that allows tracking of plaque, not just initial identification, is also an important distinction. People who've had some measure of atherosclerosis all catch on to this eventually. "Can I reverse it?" is an inevitable question once the disease is identified in some way. So a tool for tracking over time to gauge the success or failure of a program of prevention can be assessed.

Perhaps in 10 years, another technology will emerge as the preferred means to do the same, but better. If that proves true, we will convert to that technology. But today heart scans performed on CT heart scans are the only rational way to both detect, then track, coronary atherosclerotic plaque.

Comments (11) -

  • Steve

    9/7/2008 3:29:00 PM |

    is it true that heart scans do not show soft plaque,which minimizes their benefit since soft plaque is the real concern

  • lizzi

    9/7/2008 4:27:00 PM |

    I think that CIMT may be more widely available in different areas of the country.  I practice in Los Angeles and have the luxury of having Dr. Budhoff 15 minutes away.  I like that my referrals for EBT will contribute to a research protochol.  In addition, many internists are purchasing an ultrasound machine, hiring a tech, and providing CIMT for $350.00. There are two approved CIMT protocols, one which requires only a single measure of IMT, the other which requires six measurements.  Guess which one is more accurate? I am also fortunate that the internist next door to me hires an excellent tech and does 6 measurements.

  • lizzi

    9/7/2008 4:46:00 PM |

    Dr. Davis.  Have you seen P Bhaggi's article in Lancet 8/28/08?  His hypothesis is that even "safe" doses of radiation MAY increase CV disease risk. (<5Gy). He sites a linear association between radiation exposure for peptic ulcer disease (1.6 - 3.9 Gy) and CV disease risk.  I don't know how Gy equates to Msv.

  • Bella6

    9/7/2008 6:58:00 PM |

    Bravo!

  • Anonymous

    9/7/2008 8:49:00 PM |

    Any newer technologies that look promising ?

  • MedPathGroup

    9/8/2008 1:28:00 AM |

    Very relevant information about CT Heart Scan and other alternatives to tracking coronary plaque. I will definitely add this to my research. I will keep on visiting your blog site. I've been a reading a lot of your posts and they are really interesting. Keep it up.

  • Anonymous

    9/8/2008 4:53:00 PM |

    in the new york area they do CIMT and use it as a proxy for CAD.  I would say that 60-70% correlation is pretty good and need for heart scan not necessary if CIMT is abnormal.

  • JD

    9/9/2008 1:56:00 PM |

    For Dr. Davis. He probably is aware of this type of study but thought I would post it.

    http://www.sciencedaily.com/releases
    /2008/09/080908085502.htm

    "For the study, researchers used cardiac and CT scans to measure multiple fat depots in 398 white and black participants from Forsyth County, N.C., ages 47-86. They found that the amount of fat a person had deposited around organs and in between muscles (nonsubcutaneous fat) had a direct correlation to the amount of hard, calcified plaque they had."

  • mike V

    9/9/2008 6:07:00 PM |

    Steve:
    See Heart Scan Blog
    Sunday, December 03, 2006
    Calcium reflects total plaque
    MikeV

  • Maureen Zilly

    9/9/2008 6:19:00 PM |

    I think that the Los Angeles Times story “CT scans can be better medicine for doctors than for patients” portrays an inaccurate picture of how physicians use computed tomography to care for their patients.  

    To begin with, the piece overstates the growth and utilization of CT. For example, the story uses GAO statistics to demonstrate an increase in CT scans, but the GAO's recent report on medical imaging did not account for the most recent data available. Had the GAO used the more current 2007 Medicare claims instead, its report would have actually shown a decrease in the growth of medical imaging services in recent years.

    Next, the story presents biased information as fact. Insurance companies are wholly motivated to pay less for health care services, which includes limiting medical imaging scans. In fact, insurers have created a cottage industry, called Radiology Benefit Managers, with the sole purpose of refusing coverage for scans. By citing subjective and unverified insurance company-generated analysis of how many scans are "inappropriate," readers are presented with a skewed view about how and why physicians order scans.  

    Clearly, CT has grown as it's become integral to modern day medicine. From best practices to patient advocate guidelines, CT is a powerful tool for improving patient outcomes. But, the larger issue is ensuring patients have access to the right scan at the right time. In computed tomography this is even more important because of the radiation CT employs to generate what are often life-saving images.    

    That's why it is vital for payers -- both private and Medicare -- to ensure that healthcare decision making remains between the physician and patient. The recent Medicare bill is an important step in the right direction because it embraces both accreditation and appropriateness criteria, and it is approaches such as these that will ensure that each scan ordered is appropriate, effective and safe for patients.

    Lastly, the article also claims that CT angiograms (CTA) are "less accurate" than traditional angiograms, but research has indicated otherwise. A recent study published in the Journal of the American College of Cardiology, for instance, found that CTA was 99 percent as effective in ruling out heart disease as the more expensive and invasive coronary angiography traditionally used by physicians. This CTA study is just one of many peer-reviewed data points demonstrating how medical imaging, and CT specifically, improves health outcomes and reduces overall costs.

    Maureen Zilly
    Medical Imaging & Technology Alliance

  • Anonymous

    9/10/2008 4:43:00 PM |

    Are there any options for young adults with a strong family Hx?  I contacted TYP, but they told me that based on my age, the risk of radiation exposure outweighs the potential benefits of the scans.  I'm a 26 y/o female.

Loading
The rules of reversal

The rules of reversal


For the last few years, most practicing physicians have followed a rough blueprint for cholesterol management provided by the Adult Treatment Panel-III “consensus” guidelines, or ATP-III, a lengthy document last released in 2001, updated in 2004.

For instance, ATP-III suggests reducing LDL cholesterol to 100 mg/dl or less for those deemed to be at high risk for future heart disease, arbitrarily defined as a risk of 20% over a 10-year period. It also suggests that a desirable triglyceride level is no more than 150 mg/dl. The ATP-III guidelines have been the topic of discussion in thousands of medical meetings, editorials, and reports. They have served as the basis for many dinners at nice restaurants, weeks in Vegas or Honolulu, many, many lunches catered by pharmaceutical representatives. For most internists, family doctors, cardiologists, and lipid clinics, ATP-III is the Bible for cholesterol management.

AT-III has also become the de facto standard that could conceivably held up as the prevailing "standard of care" in a court of law in cases of presumed negligence to treat cholesterol values. “Doctor, would you agree that the consensus guidelines issued by the National Institutes of Health and endorsed by the American Heart Association state that LDL cholesterol should be reduced to 100? You do? Then why was Mr. Jones’ LDL not addressed according to these guidelines?”

Who was on the ATP-III panel and on what scientific evidence were the guidelines based? Several problems:

1) Of the 9 physician members of the panel, 8 had ties to industry, some of them quite intimate.

2) The studies upon which the guidelines were based and figure prominently, such as the Heart Protection Study, PROVE IT, and 4S, were all funded by the pharmaceutical industry. Of course, it would be unreasonable to expect anyone other than the pharmaceutical industry to fund drug studies. But prominently neglected or understated in the guidelines are all the other insights and treatments for coronary atherosclerotic risk available that were NOT funded by industry.

Of course, there’s money to be made in reducing LDL cholesterol. Lots of it--$23 billion last year alone, in fact. Just keeping that fact in mind makes the ATP-III guidelines make far better sense.

ATP-III is really not a blueprint for heart disease prevention. It is a blueprint--by industry, for industry--on how and when to treat LDL cholesterol.


But what if ATP-III had been a map for navigating coronary plaque reversal instead? What if it were not obsessed with just reducing LDL cholesterol, but was focused on providing the corner internist, family doctor, or cardiologist a roadmap for navigating the highways and byways of reversal?

That would be interesting. Mainstream reversal. Imagine that.

Among the difficulties is that the path to reversal is not lined with deep pockets. Treat LDL and who gains? That's easy. Reverse heart disease and who gains? Beyond LDL reduction, very few (beyond you and me, of course).

That’s why the call for a new Age of Self-Empowerment in healthcare is necessary now more than ever. In my view, in the foreseeable future, we will not have an ATP-III-like blueprint for heart disease control or reversal, nor will we witness a boom of nationwide appreciation that coronary atherosclerosis is a reversible process.

It’s time to take the control back and put it in our own hands. Don't expect the American Heart Association to do it. Don't expect the pharmaceutical industry to do it. If there's anyone who's going to do it, it's YOU.

Comments (12) -

  • gc

    11/3/2007 11:26:00 PM |

    Man oh man I wish I lived closer and you were my doc!!!!

    I try nicely to get docs to think that low carb and being off insulin is ok, that not being on a statin may be ok even though my ldl goes up but my lipoprotein a is low.....I don't know what to do about this new doc I am seeing as don't want to turn her off but want to turn her onto TYP.

  • G

    11/10/2007 4:05:00 PM |

    Unfortunately we all do have to be our own advocates... thanks for giving us the means and tools to do so for our family and friends (and patients)!

    The article you mentioned about MMPs (tissue metalloproteinases), CRP and D3 deficiency was quite frankly phenomenal.
    Q J Med: 2002;95:787-796.
    Cirgulating MMP9, vit D and variation in the TIMP-1 response with VDR genotype: mechanisms for inflammatory damage in chronic disorders?

    Again, I think you are correct, the implications revealed here and elsewhere are blatant omissions from discussion in the ATP guidelines (the 'bible' when I was in pharmacy school).  

    One-yr Post-supplementation with intra-muscular Vitamin D(from pre-8 to post-14 ng/ml) produced statistically reduced MMP9, as well as decreased CRP (another marker for chronic inflammation). These are all increased in acute MIs and unstable angina and in active arterial plaques. (unfortunately they did not raise the 25(OH)D levels sufficiently 50-70 ng/ml otherwise perhaps they might've seen substantial primary CAD prevention at the 5yr followup -- *bummer!*).

    Thank you for the info on Doxy. I remember reading > 10yrs ago how doxy helped in arithritis.  It makes sense now!!!

    With the role of D3 emerging that it's vital and affects all organ systems, do you think your TYP program is also treating and preventing ALL chronic conditions? Are you aware that you may be creating an immortal human subpopulation *ha haaa haa*. But alas, we are human...

    Do you think that perhaps since D3 is a steroid structure, D3 may be depleted in cortisol-driven activities (ie, chronic stress -- physical, mental, genetic)?  Perhaps a cascade of events occurs, triggered by (let's conjecture) a marginal reduction in sunlight (since we obtain naturally about 99% of D3 activation from sunlight) which leads to broad widespread decline in D3-dependent cellular activities. Unfortunately D3-dependent cell functions appear to me (from your blog and the literature) to be literally ALL functions...

    Immune cells--flu, infections, MS, lupus, asthma/copd, T1DM, RA
    Thyroid & parathyroid--TSH and PTH irregularities (then eventually Graves/Hashimotos), osteoporosis
    Bones/GI system--without D, GI incapable of absorbing calcium (absorb more Hg, Pb? ...autism spectrum?)
    Colon--cancer, mortality
    Cerebral arteries--migraines
    Brain--depression, less euphoria
    Nerve endings--peripheral neuropathy
    Kidney/renin--hypertention, pre-eclampsia (during pregnancy when E2 and P hormone production is ramped up)
    Pancreas/beta-islet--Metabolic Syndrome, glucose intolerance, Type 2 diabetes
    Liver--PPAR changes, high TG/low HDLs (less HDL to scavenge out LDL)
    Adipose--insulin resistance, weight gain
    Coronary arterial plaque--CAD, MI
    Nephrotic atherosclerosis--CKD, dialysis
    Cerebral vasculature--stroke
    Ovary, breast--infertility, PMS, cancer
    Prostate--cancer
    Hair follicles--male pattern baldness(?)
    Overused joints--osteoarithritis

    In the literature, D supplementation (sometimes with calcium, but I don't think it's necessarily relevant) improves all these chronic conditions. Is it all more interconnected then we suspect? I see all these conditions in the primary care setting, and I find that recently I'm giving the same 'dog-and-pony show' to all pts (migraines, perimenopause, T2DM, HTN, CKD, etc). 'fish oils, nuts/seeds, oat bran, relax, exercise, get some sunlight midday, low GI foods, Ezekiel bread, and on and on'.
    I wonder now...wouldn't it be just easier to put 'the D' in the water?  There are so many challenges in overcoming the havoc caused by MMP and other inflammatory constituents(ie,'target organ disease').  The TYP plan truly seems to offer vitality... and immortality! Another medical genius said ( Hippocrates) "your food is your medicine, and your medicine your food."  He was so right, after all these centuries. Keep up the strong work and don't stop the rhetoric!

  • G

    11/10/2007 4:13:00 PM |

    BTW, is there any tissue that is devoid of VDRs (vitamin D receptors)? toenails?  THANKS!!

  • G

    11/10/2007 5:41:00 PM |

    Additionally...i forgot several disease states...so embryonic tissue in utero are affected too. does calcium modulation make such a difference at age 'zero'? there appears to be evidence. perhaps even for heart disease?

    Skin--psoriasis (treated w/Dovonex a D analogue)
    Maternal D nadirs--schizophrenia (in summer babies; see Oprah Nov's issue! *HA HAAA HAA*), Type 1 DM
    Brain--Alzheimers (D improved cognition, cheaper than Aricept)
    Muscles--chronic pain syndromes, fibromyalgia

    do you have a cure for addiction to reading about disease reversal?

  • Dr. Davis

    11/10/2007 11:07:00 PM |

    G--

    I've had the very same thoughts.

    Every day, I witness some new aspect of vitamin D replacement that I had not appreciated before. All of this needs to be systematically recorded and reported. Our first report on the effects of vitamin D, along with the Track Your Plaque program in all other aspects, will be reported next spring in the scientific literature.

    I'm seeing so many fabulous effects. We will follow our initial report with more on these issues, though little by little. That's how it works, though I tell you about these things before the official report hits the press.

  • Dr. Davis

    11/10/2007 11:08:00 PM |

    Curious thing, G: You will see accelerated growth of toenails and fingernails with vitamin D supplementation!

  • Dr. Davis

    11/10/2007 11:10:00 PM |

    LOL!

    Well, the enormous abyss of ignorance among physicians on these issues is a sobering thought.

  • G

    11/13/2007 3:24:00 AM |

    That's funny. You are so right again! I've always noticed my nails always grower faster in the summer!

    Did you get a chance to see Planet Earth on the Discovery channel?  AMAZING! Do you now what they focused on?!!!

    The sun and the earth...'Sunlight is the engine of life... whether on land or sea, sunlight shapes life... it triggers birth and death...'  

    I guess it's NO SURPRISE that VDRs are hinged next to other steroid receptors estrogen, progesterone,  and thyroid receptors (and possibly glucocortocoid and retinoic acid).
    (is that why TAN MUSCULAR athletes probably procreate more than cardiologists and pharmacists? *ha haaa haaa*)

    You notice and document here the tremendous disease reversal with testosterone, E2, vitamin D and DHEA...
    It A-L-L makes sense!!!!!

  • G

    11/13/2007 3:45:00 AM |

    can u translate?  I know this must mean something...

    Heterodimers of Retinoic Acid Receptors and Thyroid Hormone Receptors Display Unique Combinatorial Regulatory Properties
    http://mend.endojournals.org/cgi/content/full/19/4/863

    There is an interesting discussion about PPAR and other nuclear steroid receptors. I think that Actos and Fibrates improve HDLs and TG and hence plaque reversal with their PPAR activities (gamma- and alpha- respectively).  Do you think that are other nuclear steroid receptors that can be explored for plaque reveral and ultimately reduction in chronic inflammation?

    my health food store nutritionist recommends cod liver because it includes Vitamin A which is a cofactor for D (he said) compared with D3 alone. I'm hesitant because I've read that A can block (perhaps through competition) D activity. I had a *bad* reaction with Chicken liver pate once... ate a whole chunk then drank ONE sip of beer and had the WORSE etoh-dehydrogenase reaction!  I worry about vitamin A toxicity... it also had worse mortality for lung CA patients.

  • Dr. Davis

    11/13/2007 4:04:00 AM |

    I wasn't aware of the proximity of those genes. Thanks, G.

  • Dr. Davis

    11/13/2007 4:07:00 AM |

    Hi, G-

    I'm afraid you've exceeded my scope of experience with that one.

    However, I know of no such vit A/vit D interaction. I prefer single supplement preparations, in general, because it allows independent adjustment of doses.

  • G

    11/13/2007 7:28:00 PM |

    I think you'll like this.  Bruce Ames discusses keeping mitochrondria happy (and preventing DNA damage and antagonistic pleiotropy). Vitamin D deficiency is mentioned as well.

    http://www.pnas.org/cgi/content/short/0608757103v1?rss=1

    Low micronutrient intake may accelerate the degenerative diseases of aging through allocation of scarce micronutrients by triage

    Bruce N. Ames *
    Nutrition and Metabolism Center, Children's Hospital of Oakland Research Institute, 5700 Martin Luther King Jr. Way, Oakland, CA 94609



    Contributed by Bruce N. Ames, October 6, 2006 (sent for review September 20, 2006)

    Inadequate dietary intakes of vitamins and minerals are widespread, most likely due to excessive consumption of energy-rich, micronutrient-poor, refined food. Inadequate intakes may result in chronic metabolic disruption, including mitochondrial decay. Deficiencies in many micronutrients cause DNA damage, such as chromosome breaks, in cultured human cells or in vivo. Some of these deficiencies also cause mitochondrial decay with oxidant leakage and cellular aging and are associated with late onset diseases such as cancer. I propose DNA damage and late onset disease are consequences of a triage allocation response to micronutrient scarcity. Episodic shortages of micronutrients were common during evolution. Natural selection favors short-term survival at the expense of long-term health. I hypothesize that short-term survival was achieved by allocating scarce micronutrients by triage, in part through an adjustment of the binding affinity of proteins for required micronutrients. If this hypothesis is correct, micronutrient deficiencies that trigger the triage response would accelerate cancer, aging, and neural decay but would leave critical metabolic functions, such as ATP production, intact. Evidence that micronutrient malnutrition increases late onset diseases, such as cancer, is discussed. A multivitamin-mineral supplement is one low-cost way to ensure intake of the Recommended Dietary Allowance of micronutrients throughout life.

Loading
My heart scan was wrong!

My heart scan was wrong!



Tom came into the office ready for a confrontation.

Tom's wife insisted that he see me to discuss the implications of his CT heart scan score of 459. At age 50, this was clearly bad news that placed Tom in the 99th percentile (worst 1% of men in his age group).

But Tom had already undergone a stress test. There had apparently been a small abnormality, and a heart catheterization had been performed by another cardiologist. "They told me they didn't need to do anything. No stent, no ballon, no bypass, nothing!"

I asked, "Did they tell you that there was any plaque or blockages seen?"

"Yeah, but he said it was nothing. So the heart scan was wrong!"

I've been here many times before. I explained to Tom that, no, his heart scan was not wrong. All the tests he'd undergone siimply provided a different perspective on the same disease. You could say:

--The stress test, being a test of blood flow, may have been abnormal because of the abnormal constrictive behavior of arteries containing plaque, known as "endothelial dysfunction", because the inner lining of arteries (the endothelium) control the tone of the artery. Abnormal constriction in arteries with plaque is quite common.

--The catheterization simply showed that no plaque had collected in a configuration to block flow, thus no stent, etc., since flow was normal. But there was indeed plaque.

All three tests were right; none were wrong. They all provided a little different perspective on the same process. Of course, I favor the heart scan as the means to identify, precisely measure, and track the atherosclerotic plaque in your arteries. The stress test is too crude and only measures flow, the catheterization is not something you'd want to undergo year after year. Catheterization also is too crude a measure to precisely track plaque growth or reversal.

So I explained to Tom that, even though a stent or similar procedure was unnecessary, he remained at substantial risk for heart attack due to plaque "rupture". In fact, Tom's heart attack risk was 5% per year, or approximately 50% over the next decade. That is, indeed, substantial. In fact, you might say that, of the three tests Tom underwent, only the heart scan revealed his true risk.
Loading