Sunday, March 29, 2015

Raynaud is not my friend!!

Interestingly enough, I recently discovered that my Mother also has had occasion to meet Raynaud... I'm not sure to what extent.... However, this might have been beneficial to have known along my path.   

Just more evidence that my willingness to compile this info for my kids won't be for not... 

Mom might have thought I knew or that we had talked about or that it shouldn't be talked about (her own private hell) but it wasn't & for whatever reason I had to re-discover along the way, I don't want my kids to relive my struggles... I want them to have an insight; to their own familiall history / medicinal genetics (?) even if they don't understand they need it, just yet.

Because whenever 'mom had polio' was mentioned the conversation simply moved forward. Most of my medicinal journey has been spent excluding her afflictions, or skipping the generation because I mostly resembled Meemaw.   I wonder now if she's meet Raynaud??

Raynaud syndrome is vasospasm of parts of the hand in response to cold or emotional stress, causing reversible discomfort and color changes (pallor, cyanosis, erythema, or a combination) in one or more digits. Occasionally, other acral parts (eg, nose, tongue) are affected. The disorder may be primary or secondary. Diagnosis is clinical; testing focuses on distinguishing primary from secondary disease. Treatment of uncomplicated cases includes avoidance of cold, biofeedback, smoking cessation, and, as needed, vasodilating Ca channel blockers (eg, nifedipine) or prazosin.

Overall prevalence is about 3 to 5%; women are affected more than men, and younger people are affected more than older people. Raynaud syndrome is probably due to an exaggerated α2-adrenergic response that triggers vasospasm; the mechanism is not defined.

Primary Raynaud syndrome is much more common (> 80% of cases) than secondary; it occurs without symptoms or signs of other disorders. In the remaining 20% of patients with Raynaud symptoms, a causative underlying disease (eg, systemic sclerosis) will be evident at initial presentation or diagnosed subsequently.

Secondary Raynaud syndrome accompanies various disorders and conditions, mostly connective tissue disorders (Table 1: Causes of Secondary Raynaud Syndrome).

Table 1

Open table Causes of Secondary Raynaud Syndrome

Cause

Examples

Connective tissue disorders

Mixed or undifferentiated connective tissue disease

Polymyositis/dermatomyositis

RA

Sjögren syndrome

SLE

Systemic sclerosis

Endocrine disorders

Hypothyroidism

Hematologic disorders

Cold agglutinin disease

Polycythemia vera

Neoplastic disorders

Carcinoid

Paraneoplastic syndrome

Neurologic disorders

Carpal tunnel syndrome

Trauma

Frost bite

Vibration

Vascular disorders

Thoracic outlet syndrome

Drugs

β-Blockers

Cocaine

Ergot preparations

Nicotine

Sympathomimetic drugs

Nicotine commonly contributes to it but is often overlooked. Raynaud syndrome may accompany migraine headaches, variant angina, and pulmonary hypertension, suggesting that these disorders share a common vasospastic mechanism.

Symptoms and Signs

Sensations of coldness, burning pain, paresthesias, or intermittent color changes of one or more digits are precipitated by exposure to cold, emotional stress, or vibration. All can be reversed by removing the stimulus. Rewarming the hands accelerates restoration of normal color and sensation.

Color changes are clearly demarcated across the digit. They may be triphasic (pallor, followed by cyanosis and after warming by erythema due to reactive hyperemia), biphasic (cyanosis, erythema), or uniphasic (pallor or cyanosis only). Changes are often symmetric. Raynaud syndrome does not occur proximal to the metacarpophalangeal joints; it most commonly affects the middle 3 fingers and rarely affects the thumb. Vasospasm may last minutes to hours but is rarely severe enough to cause tissue loss in primary Raynaud syndrome.

Raynaud syndrome secondary to a connective tissue disorder may progress to painful digital gangrene; Raynaud syndrome secondary to systemic sclerosis tends to cause extremely painful, infected ulcers on the fingertips.

Diagnosis

Clinical criteria

Examination and testing for underlying disorder

Raynaud syndrome itself is diagnosed clinically. Acrocyanosis (see Acrocyanosis) also causes color change of the digits in response to cold but differs from Raynaud syndrome in that it is persistent, not easily reversed, and does not cause trophic changes, ulcers, or pain.

Primary and secondary forms are distinguished clinically, supported by vascular laboratory studies and blood testing. Vascular laboratory testing includes digital pulse wave forms and pressures. The primary blood testing is the panel for collagen vascular diseases (eg, testing for ESR or C-reactive protein, rheumatoid factor, anti-DNA, antinuclear, and anti-CCP antibodies).

Clinical findings: 

A thorough history and physical examination directed at identifying a causative disorder are helpful but rarely diagnostic.

 

Findings suggesting primary Raynaud syndrome are the following:

 

Age at onset < 40 (in two thirds of cases)

Mild symmetric attacks affecting both hands

No tissue necrosis or gangrene

No history or physical findings suggesting another cause

Findings suggesting secondary Raynaud syndrome are the following:

 

Age at onset > 30

Severe painful attacks that may be asymmetric and unilateral

Ischemic lesions

History and findings suggesting an accompanying disorder

Laboratory testing: 

Blood tests (eg, measurement of ESR, antinuclear antibodies, rheumatoid factor, anticentromere antibody, anti-SCL-70 antibody) are done to detect accompanying disorders.

 

Treatment

Trigger avoidance

Smoking cessation

Ca channel blockers or prazosin

Treatment of the primary form involves avoidance of cold, smoking cessation, and, if stress is a triggering factor, relaxation techniques (eg, biofeedback) or counseling. Drugs are used more often than behavioral treatments because of convenience. Vasodilating Ca channel blockers (extended-release nifedipine

 60 to 90 mg po once/day, amlodipine

 5 to 20 mg po once/day,felodipine

 2.5 to 10 mg po bid, or isradipine

 2.5 to 5 mg po bid) are most effective, followed by prazosin

 1 to 5 mg po once/day or bid. Topical nitroglycerine paste,pentoxifylline

 400 mg po bid or tid with meals, or both may be effective, but no evidence supports routine use. β-Blockers, clonidine

, and ergot preparations are contraindicated because they cause vasoconstriction and may trigger or worsen symptoms.

Treatment of the secondary form focuses on the underlying disorder. Ca channel blockers or prazosin

 is also indicated. Antibiotics, analgesics, and, occasionally, surgical debridement may be necessary for ischemic ulcers. Low-dose aspirin

 may prevent thrombosis but theoretically may worsen vasospasm via prostaglandin inhibition. IV prostaglandins (alprostadil


, epoprostenol

,iloprost

) appear to be effective and may be an option for patients with ischemic digits. However, these drugs are not yet widely available, and their role is yet to be defined. Cervical or local sympathectomy is controversial; it is reserved for patients with progressive disability unresponsive to all other measures, including treatment of underlying disorders. Sympathectomy often abolishes the symptoms, but relief may last only 1 to 2 yr.

Key Points

Raynaud syndrome is reversible vasospasm of parts of the hand in response to cold or emotional stress.

Raynaud syndrome may be primary, or secondary to another disorder, typically one affecting connective tissue.

Primary Raynaud syndrome, unlike the secondary form, rarely causes gangrene or tissue loss.

Diagnose clinically but consider testing to diagnose a suspected cause.

Avoid cold, smoking, and any other triggers.

Give a vasodilating Ca channel blocker or prazosin

.

Last full review/revision May 2014 by John W. Hallett, Jr., MD

Content last modified May 2014

Thursday, March 26, 2015

Opiod.. Allergies


I have had full-on reaction to
Stadol (required intervention)
Morphine (chest&hand rash (mast cell cast off) + BP)
Hydrocodone (nausea/ intolerance)

Am currently using Dilaudid
(initially nose itching -subsided w/benadryl)

From ER physician Monthly

Narcotic “Allergies”

Nice little “clinical pearl” review article from EMedHome.com about opioid allergies. Seems that they aren’t as common as some patients would have us believe.

It would also seem that if the adverse reactions to opioids are due to histamine release that administering the opioids with an antihistamine such as Phenergan, Vistaril, or Benadryl would serve both to stop the “allergic” reaction and to enhance the effect of the pain medication.

Just be careful giving the Phenergan … at least IV. I often have luck giving opioid agonist/antagonist medications such as Nubain, Stadol or Buprenex to patients who describe horrific allergies to every medication except their narcotic du jour.

Opioid Allergy True anaphylactic reactions to opioids are very rare. When patients say they are allergic to an opiod, it is much more likely that the patient has experienced GI upset or a pseudoallergy.

Flushing, itching, hives, and sweating, especially itching or flushing at the injection site only, suggests a pseudoallergy due to histamine release, a pharmacologic side effect of some opioids.

Codeine, morphine, and meperidine are the opioids most commonly associated with pseudoallergy.

Use of a more potent opioid is less likely to result in histamine release. The potency of opioids, from lower to higher: meperidine < codeine < morphine < hydrocodone < oxycodone < hydromorphone < fentanyl

If the patient describes a true allergy to an opiate, then an opioid in a chemical class different from the one to which the patient reacted may be used with close monitoring:

Phenylpiperidines: meperidine (Demerol), fentanyl (Duragesic, Actiq, Sublimaze), sufentanil (Sufenta)

Diphenylheptanes: methadone (Dolophine), propoxyphene (Darvon)

Morphine group: morphine, codeine, hydrocodone (Vicodin, Lorcet), oxycodone (Percocet, OxyContin), oxymorphone (Numorphan), hydromorphone (Dilaudid), nalbuphine (Nubain), butorphanol (Stadol), pentazocine (Talwin)

References: (1) Gilbar PJ, Ridge AM. Inappropriate labeling of patients as opioid allergic. J Oncol Pharm Practice 2004;10:177-82. (2) Middleton RK, Beringer PM. Anaphylaxis and drug allergies. In: Koda-Kimble MA, Young LY, Kradjan WA, et al., eds. Applied Therapeutics: the clinical use of drugs. 8th ed. Philadelphia: Lippincott Williams & Wilkins, 2005. (3) Nutescu E, et al. Multidisciplinary approach to improving allergy documentation. Am J Health-Syst Pharm 1998;55:364-8. (4) VanArsdel PP. Pseudoallergic drug reactions. Introduction and general review. Immunol Allergy Clin North Am 1991;11:635-44.

Wednesday, March 25, 2015

Thank You!!

Beautiful flowers,
What an unexpected surprise!!

Thank You for all your well wishes, prayers, but most importantly the beauty you add to my life each day!!

Yesterday was really rough, felt allot of stiffening in my throat and ache in my jaw like I had had root canal.

Plus was really missing food that wasn't creamy, smooth, or cold.. Kevin was awesome an brought me some won ton soup!! Broth was delish!! And I even accomplished a little LoMain, yummy!!

I woke to take my pill on time last night, thankfully.  However, I awoke this morning to the usual choking and gasping (like pre-surgery)...

Until I expelled what appears to be a large clump of dead tissue... I don't know if it's newly sloughed away or simply missed by suction and now the inflammation has allowed it to loosen and expel..

I am not experiencing breathing difficulty or bleeding so I will take my pain pill a little ahead of schedule and get some rest.

My ENT!!

Joshua D. Levine, MD -
Charlotte Eye Ear Nose & Throat

Click link or copy & paste

http://youtu.be/g03JYH8OA8c

Tuesday, March 24, 2015

Tues 24th

I overslept my alarm for medication... Ugggh!! It was supposed to have been at 12:30 last night..

Kevin was a doll and set my alarms so I wouldn't miss timely dosing but, apparently I muted the volume... Darn!

As a result, I woke at 3am with extreme pain!! You don't realize that the base of your tongue is actually really long, traveling well down into your throat, and is not a lazy muscle!! 

You don't realize how many times saliva must be helped along its path. Amazing the things taken for granted!!

I was already becoming more and more aware of autonomic function and confused sensory perceptions but, to feel difficulty and discomfort from an internal occurrence that was never previously sensed, ... It's too reminiscent of my other diminished functions... I'll be glad to get through this recovery!

Looking forward to focusing on the next item to be addressed on "make it better checklist"

Thanks for thinking of me! & just remember that people dream of having days like these.... 

Tapioca, breakfast in bed, to the sounds of songbirds rising, and the smell of fresh coffee brewing in the air, of a crisp Carolina morning!

Count Your Many Blessings!!

Monday, March 23, 2015

Post Op update ~ Monday

I had previously made application to disability and upon return from surgery there was follow-up mail; a questionnaire for my return.

In my delirium I attempted to ring them yesterday (Sunday).. Duuhh!

Even though I feel like I have lock jaw and every swallow, of simple saliva, feels like razor blades... I had no choice but to call and report my current status (as indicated in their letter)...
Luckily, my call was answered by someone who heard the distress, understood the struggle, & realized how dramatic it was that she could understand me so soon after surgery.

I will still attempt to get paperwork back asap, as vision allows, but for now the alarm for the dilaudid is about to sound and I couldn't be more thrilled!!

Today's menu features primarily Popsicles (orange & red are favs)!! Making a dietary exception - as these Popsicles are no where close to real fruit, much less, organic. But, Feels so good!
And under the heading "who knew _____ tasted so good" please file cream of chicken soup (organic, carton NOT can).. Delicious, soothing, and savory with a little Mrs.Dash!

I resumed hydro-therapy this morning... Really enjoying the herbal addition of rosemary and mint. Right leg exceptionally stiff and painful since all the hospital walking on Friday, thankful for wheelchair service.
Pelvic, Hip, and Low back pain (the mice?) have cranked up a notch as well.

I'll admit it scared me a degree when I saw my mother's shadow as the light in the hospital parking area silhouetted me!
{she suffered Polio}

Sunday, March 22, 2015

Update on my - lingual tonsillectomy

What a wonderful hospital & great care received.. [Even in light of difficulties like it taking 6 RNs over an hour with lots of lidocaine for numbing, and ultimately even the anesthia doc to find a vein before surgery....

and a first for me (which is saying something, in light of all my hospital experience)...
They (the Pre-Op nurses that all took a poke at me) sent a card to my room for speedy recovery & Apologies!! awww..]
at Presbyterian / Novant Hospital downtown Charlotte NC!

I'm pretty sure I should say a big thank you to all those prayer warriors at Meemaw's Stetson Baptist too!! Wish I could hug y'all, keep up the great work!!

The power of the Lord is amazing!!

While I was under care for lingual tonsillectomy (to be sent for lymphoma biopsy)
& coblation / removal of lymphatic tissue at the base of tongue...

It was discovered I walk in Meemaw's footsteps even more.

Diagnosis; (the precursor to her Angina) Myocardia Ischemia ... & although it will get pushed to the top of the list ... It is, after all, just more validation of my family tree studies!

So while I convalesce at home...
I hope to  up-to-date on the daily...

Kevin is an absolute angel; providing for whatever I may need... Even things like; organic cold press apple juice - very soothing!

I continue to take same meds from prior to surgery plus (now) the pain med dilaudid, anti-inflammatory to keep throat tissues from swelling, a little something for nausea, just in case -don't want to vomit.. It needs to try to form a scab in there.

Coblation: a way to remove tissue without traditional cutting/excision. A plasma laser is robotically directed by surgeon - following a field of saltwater irrigation.  (Doc says the technical lingo for that is; Star Trek stuff!) lol
Tissues are COLD seared & suctioned away, leaving nothing to be stitched - left as open wound.

That's my story for today, and I'm sticking to it!

Night y'all & say your prayers!!

Here's a scholarly link about lingual tonsillectomy by cold ablation;

http://www.thefreelibrary.com/Lingual+tonsil+hypertrophy+causing+severe+dysphagia%3A+Treatment+with...-a0222558070

(If link not clickable,  copy & paste into browser)

Saturday, March 21, 2015

Coronary Microvascular Dysfunction


The Women's Heart Foundation is a non-governmental organization that designs and implements demonstration projects for the prevention of heart disease. The site includes a cross section of articles on heart disease, a library of downloadable pdfs and an opportunity to ask questions of a nurse. Paramedic to RN.org

When a patients heart stops working properly, paramedics have to act fast to stabilize the patient, often using defibrillators and heart medication to restart the heart and mitigate the damage that can result from even brief cardiac arrest. These pages cover the basics and the in-depth research behind advanced cardiac life support. Episode number: 501
Topics: Heart Disease & Prevention Women's Health Transcript: Coronary Microvascular Disease (transcript)

Research supports that not only do men and women present with heart disease differently, they can also develop it differently. Coronary Microvascular Disease is predominantly a women's heart disease - one that is often overlooked and under-diagnosed. Is it possible to have heart disease and yet appear to have healthy coronary arteries? The surprising answer is a resounding "yes." What is Coronary Microvascular Disease? Up until about a decade ago, patients with cardiovascular disease symptoms, but with no evidence of blockages in their larger coronary arteries, posed a medical mystery for doctors.

Thanks to advances in diagnostic tools, researchers discovered the problem with these patients occurred not because of coronary artery disease (CAD) in the larger coronary arteries, but rather in the smaller coronary arteries. Thus the term "coronary microvascular disease" was born. Your body needs a flow of oxygen-rich blood to nourish it and your heart muscle is no exception. When the heart doesn't get enough oxygen to meet its needs (myocardial ischemia) one of two things can happen. If the deprivation is limited, chest pain or pressure called angina may occur. If the flow of blood is cut off, the result is a heart attack (myocardial infarction or heart muscle death).

Blood flows to the heart muscle first through three large coronary arteries, then through branches of thousands of smaller arteries called arterioles. Healthy arteries are hollow tubes and the inner lining is smooth and elastic, allowing blood to flow freely. When you exercise, a healthy artery can stretch to let more blood flow to your body's tissues. The transition from artery to arteriole is a gradual one, marked by a progressive thinning of the vessel wall and a decrease in the size of the passageway.

The job of the larger arteries is the distribution of blood. They range from 1.0 - 4.0 millimeters in size. The job of the arterioles is both blood distribution and resistance (pressure and flow regulation). Think of the arterioles as "taps" for circulation, turning the flow up or down to match the needs of your body. They range from 0.1 to 0.5 millimeters in size.

Symptoms of Coronary Microvascular Disease
The symptoms of heart disease, in both men and women, often result from traditional coronary artery disease (CAD). With coronary artery disease, the trouble begins when the inner walls of the larger coronary arteries are damaged from issues such as high blood pressure, high cholesterol, smoking and diabetes. When this happens, plaque (a substance made up of excess cholesterol, calcium, and other substances in the blood) starts to build up (atherosclerosis).

Plaque can slow and completely block the flow of blood to the heart muscle. It can also crack, causing blood cells called platelets to clump together and form blood clots. This type of heart disease can be seen with tests such as coronary angiograms and with noninvasive tests such as special CT and MRI scans.

Coronary microvascular disease is an elusive disease. It doesn't show up on many standard tests. When a doctor sees an angiogram with wide open arteries, he or she may assume that symptoms like chest pain, shortness of breath, light-headedness, diffuse discomfort in the chest or unusual exhaustion are caused by something other than heart disease. If the doctor isn't familiar with coronary microvascular disease, it's unlikely that additional tests will be ordered. Even if the large coronary arteries are clear, coronary microvascular disease can still be present. The angiograms of 50% to 60% of women and 20% of men with symptoms of heart disease show clear arteries on an angiogram.

Medical experts believe that the majority of those have coronary microvascular, a disease that's just as dangerous as coronary artery disease. Just like coronary artery disease, it increases the risk of heart attacks and heart failure.

The characteristics of microvascular dysfunction include: A build-up of plaque that spreads evenly throughout the walls of the small arteries. So while there may be no obvious blockages, blood flow to the heart is still low. (Coronary microvascular is also called non-obstructive CAD.) Vessels that don't expand or dilate properly during physical or emotional stress. Vessels that spasm (contract) abnormally. Coronary microvascular disease has some other unique features. Symptoms of angina with coronary microvascular disease may or may not be the typical chest pain seen in coronary artery disease.

Plus, coronary artery disease symptoms often first appear while a person is being physically active, for example while jogging or going up stairs, and coronary microvascular disease signs are often first noticed during routine daily activities and during times of mental stress. Diagnosing Coronary Microvascular Disease Doctors are refining their methods for diagnosing coronary microvascular disease and research is ongoing to find the best preventive strategies and treatments. In the meantime, doctors are following similar approaches to those used to prevent and treat coronary artery disease. Diagnosis remains the biggest hurdle for people with coronary microvascular disease.

Many people spend years going undiagnosed and some never are. If you have recurrent chest pain and your doctor says you're fine because you have clear coronary arteries, don't give up. Sometimes doctors get it wrong. Seek a second opinion and if that doesn't help, seek a third. You're the expert on your own body. When it's trying to tell you something, listen. Most importantly, if you think you're having a heart attack call 9–1–1. Acting fast at the first sign of heart attack symptoms can save your life and limit damage to your heart.
Treatment is most effective when started within 1 hour of the beginning of symptoms.

Quick Facts
• Coronary microvascular disease (MVD) affects the heart's smallest coronary arteries, called arterioles.
• Coronary microvascular disease is more common in women than in men.
• Heart disease, in general, is a different disease for women than it is for men.
• Signs and symptoms of coronary microvascular disease often differ from those of traditional coronary artery disease (CAD).

Typical signs and symptoms of cornary artery disease include angina (chest pain), feeling pressure or squeezing in the chest, shortness of breath, excessive sweating, and arm or shoulder pain.
Women with coronary microvascular disease may also have shortness of breath, sleep problems, fatigue (tiredness), and lack of energy.
Symptoms are often first noticed during routine daily activities and times of mental stress.

• Coronary microvascular disease occurs when plaque forms in the arteries, when the arteries spasm (tighten), or when the walls of the arteries are diseased or damaged, preventing enough oxygen-rich blood from getting to the heart muscle.
• In coronary microvascular disease, plaque doesn't always lead to blockages as it does in traditional coronary artery disease (CAD). For this reason, coronary microvascular disease is called non-obstructive coronary artery disease.
• Women with chest pain and other heart symptoms are more likely than men to have clear coronary arteries when diagnostic tests are performed.
• The same cluster of risk factors that cause coronary artery disease may cause coronary microvascular disease. These include unhealthy cholesterol levels, high blood pressure, smoking, insulin resistance, diabetes, overweight and obesity, lack of physical activity, age, and family history of early heart disease.
• Coronary microvascular disease is difficult to diagnose.

Your doctor may start with a questionnaire called the Duke Activity Status Index, which measures how well you're able to do your daily activities.
Other tests include pharmacological stress testing and a special type of coronary angiogram used to measure coronary artery flow reserve.

• If you have coronary microvascular disease, you can take steps to stop it from getting worse. These may include lifestyle changes, medicines, and regular medical care. Ask Your Doctor This list of questions is a good starting point for discussion with your doctor; however, it is not a comprehensive list.
What is my risk for heart disease?
What is my blood pressure, and is it at a healthy level?
What is my blood cholesterol, and is it at a healthy level?
What lifestyle changes (such as diet, exercise, etc.) should I make to prevent heart disease?
Do I need screening tests, even though I don't have heart disease symptoms? What sorts of symptoms should I be watching for? I've noticed these symptoms: . . .
What medical tests should I take to get an accurate diagnosis?
Are the diagnostic tests that are most effective in detecting coronary MVD available locally?
I've heard heart disease is different for women than for men.

What are the differences? What are the differences in how you diagnose and treat coronary MVD versus coronary artery disease (CAD)?

How familiar are you with coronary microvascular disease?
Have you treated other patients with the condition?
Should I be referred to a specialist? If your doctor finds evidence of heart disease: How serious is my condition?
What are the treatment options, and what are their benefits, risks, and side effects?
Am I a candidate for a heart attack, even after taking medication?
When should I suspect that I am having a heart attack?
Should I get involved in a clinical trial? Key Point 1 When it comes to heart disease, not only are the symptoms sometimes different for men and women – but the disease itself may be different.

There's an entertaining theory that men and women are from different planets. It's a not-so entertaining fact that men and women experience heart disease differently. It's not always clear why, but women are less likely to survive a heart attack than men.
Women have a 50 percent greater chance of dying during heart surgery. And, they're more likely than their male counterparts to develop heart failure, a weakening of the heart muscle that can be incapacitating and ultimately fatal.
Heart disease kills 500,000 women every year – ten times more than breast cancer and more than all other cancers combined. It's also a leading cause of disability. Eight million women are currently living with it.
While women develop cardiovascular disease about ten years later than men, it's estimated that one in ten American women 45 to 64 years of age has some form of heart disease, increasing to one in four women over the age of 65.

Historically, studies that set the standard for detection and treatment of heart disease were mostly done on men. But researchers found the results didn't always apply to women. Now, thanks to new research sponsored by National Institutes of Health (NIH) National Heart, Lung, and Blood Institute (NHLBI), more attention is being directed toward a better understanding of the unique features of heart disease in women.
Here's what scientists are finding out about gender differences and heart disease. Women with heart disease may have different symptoms than men. Women may experience the classic symptoms of gripping chest pain, sweating and shortness of breath, but they also may present with vaguer symptoms like generalized discomfort in the chest, breast, back, shoulders, jaw, neck or throat; indigestion; nausea; light-headedness; palpitations; sleep disturbances; and unexplained fatigue.

Tests that reliably pick up signs of heart damage in men don't always work in women. These range from simple blood tests to exercise stress tests to standard angiograms.
Some women don't have the strength to do a full exercise stress test and an incomplete one doesn't work the heart enough to yield truly useful results.
Single-vessel heart disease, which is more common in women than in men, may not be picked up on a routine exercise stress test.
Women with chest pain and other heart symptoms are more likely than men to have coronary microvascular disease even though tests show clear large coronary arteries.
(See More About Women and Coronary MVD below.)

Women tend to have heart attacks later in life. As a result, they're more likely to have other health issues. Symptoms of heart disease might be attributed to existing conditions such as arthritis or diabetes. Problems like high blood pressure, high cholesterol and diabetes may make surgery a riskier proposition for them. Women have smaller hearts and arteries than men.
One reason women haven't fared as well as men after bypass surgery and balloon procedures may be that their smaller vessels clog up again more easily after the procedures. In addition, surgeons performing bypasses in women are less likely to use an artery from inside the chest wall, because it's smaller and harder to work with, even though using the chest artery gives most patients better odds of long-term survival.

There may be fundamental differences in the way women's hearts work. Researchers believe that women have a different intrinsic rhythm to the pacemaker of their hearts, causing them to beat faster. They also hypothesize that it may take a woman's heart longer to relax after each beat. Several recent landmark studies have revealed that more women than men suffer from coronary microvascular disease. It's estimated that of the 8 million women in the U.S. with heart disease, as many as 3 million of them have coronary microvascular disease.
The diagnosis of coronary microvascular disease poses a unique challenge. Chest pain and other symptoms that the heart muscle isn't getting enough blood have traditionally signaled a narrowing or blockage in one or more of the heart's large arteries – a condition that's easily seen on an angiogram. But, in about 50% to 60% of symptomatic women and 20% of men, the problem lies not in the major arteries but in the smaller branches which are virtually invisible on a standard coronary angiogram.

Bottom line, coronary microvascular disease, like traditional coronary artery disease (CAD), increases a woman's chance for a heart attack. Researchers are just beginning to understand coronary microvascular disease. The same risk factors that cause problems with the larger coronary arteries – heredity, age, race, blood pressure, blood cholesterol, obesity and smoking – may also contribute to coronary microvascular disease. Women appear to be more affected by certain factors, such as high blood pressure, smoking and diabetes than men. In addition, there are a host of other risk factors unique to women.

Only women become pregnant, experience menopause and are prescribed contraceptive pills and postmenopausal estrogens. Theories on why the disease may differ in women include the following:
• Low levels of estrogen. Because estrogen plays a role in processing nitric oxide, which helps arteries function properly, the endothelium may suffer when natural estrogen levels wane.
• More inflammation (an overreaction by the immune system). Inflammation stimulates the body to use cholesterol in the bloodstream as a band-aid to cover up irritated areas in the blood vessels.
• Higher incidence of anemia. Anemia is thought to slow the growth of cells needed to repair damaged blood vessels.
• Lower levels of hemoglobin (a protein in red blood cells that carries oxygen). Hemoglobin deficits may starve the heart muscle and also reduce nitric oxide levels.
• Lower HDL ("good" cholesterol) levels. There is evidence that having low HDL is more predictive of the development of coronary heart disease in women than high LDL ("bad" cholesterol) levels are.

Findings so far have raised as many questions as have been answered, but the work represents a good start in zeroing in on ways to tailor diagnosis specifically for women. Progress has already been made in educating doctors about symptoms that, in the past, were under-recognized or misinterpreted in women.

Scientists are now focusing on how diagnostic and treatment techniques may need to be changed to improve women's outcomes.

Key Point 2
Coronary microvascular disease is tough to diagnose.

If you are experiencing symptoms that concern you, don't ignore them. You need to continue a dialog with your doctor until you're both satisfied. If your doctor suspects you are at risk for heart disease, there are a number of traditional diagnostic tests used to look for blockages that affect blood flow in the large coronary arteries (coronary artery disease or CAD).

However, standard tests for cornary artery disease, such as electrocardiograms, exercise stress tests, echocardiograms and angiograms don't always detect coronary microvascular disease (MVD), a disease where the smallest coronary arteries are affected.

For more information about tests to diagnose heart disease, see the Second Opinion episode on Cardiac Breakthroughs
As more is learned about coronary microvascular disease, new protocols and tests are emerging. Since symptoms of coronary microvascular disease often first appear during routine daily tasks, a questionnaire called the Duke Activity Status Index (DASI) that asks about an individual's ability to perform certain daily tasks can prove useful.
It yields information about how well blood is flowing through coronary arteries and also helps doctors select appropriate next steps.

Duke Activity Status Index Activity Points Can you take care of yourself (eating, dressing, bathing, etc.)?
0.8 Can you walk around your house?
0.5 Can you walk a block or two on level ground?
0.8 Can you climb a flight of stairs or walk up a hill?
1.6 Can you run a short distance?
2.3 Can you do light work around the house (washing dishes, etc.)?
0.8 Can you do moderate work around the house (sweeping, carrying groceries, etc.)?
1.0 Can you do heavy work around the house (scrubbing floors, moving heavy furniture, etc.)?
2.3 Can you do yard work (raking leaves, pushing a mower, etc.)?
1.3 Can you have sexual relations?
1.5 Can you participate in moderate recreational activities (golf, dancing, etc.)?
1.7 Can you participate in strenuous sports (swimming, singles tennis, skiing, etc.)?
2.1 Circle the points for a question only if you can answer "Yes, with no difficulty."
Add up the circled points. The lower the score, the greater the risk.
Total scores of 4.7 or below are considered higher risk.

Stress Tests
Stress tests are performed to determine whether there's enough blood flow to the heart during physical activity. They involve performing simple exercise, usually with a treadmill or a stationary bike. Sometimes pharmacological agents are used to simulate the heart's reactions to exercise. Standard stress tests tend not to be as reliable in women as in men, but using imaging such as echocardiograms or nuclear scans in conjunction with an exercise stress tests improves their accuracy.

• Adensosine Coronary Flow Reserve and Acetylcholine Endothelial Function Test with Cardiac Magnetic Resonance Imaging (MRI)

This is a pharmacological stress test. During the two-step test, the drug adenosine, which causes the small vessels of the heart to dilate, is injected into one of the coronary arteries and the amount of blood flow is measured. Next, the drug acetylcholine, which causes dilation in the large arteries, is injected and the amount of blood flow is again measured. The superior resolution of magnetic resonance imaging is used to get images of the beating heart and to look at its structure and function. MRIs can show poor blood supply to the innermost areas of the heart and can detect changes in the small coronary blood vessels. If either test shows decreased blood flow to the heart muscle, a diagnosis of microvascular disease can be made.

• Dipyridamole Positron Emission Tomography (PET) This cardiac PET scan also shows how much blood flow the heart receives at rest and under stress. During the first stage, fluorodeoxyglucose (FDG) is administered while the patient is at rest. The images that are produced from this first PET scan are checked with a second PET scan after the patient is administered dipyridamole, a drug that produces an effect in the body similar to the effects of strenuous exercise. Doppler Wire Coronary Angiogram The most definitive test for microvascular disease is a special type of coronary angiogram used to measure coronary artery flow reserve or coronary reactivity. It involves threading an ultrathin wire with blood-flow sensors at the tip deep into a coronary artery (called cardiac catheterization).

Blood flow in the artery is then measured before and after injections of one or more medications to cause the microvessels to dilate. The smaller the change in pressure and flow, the stiffer the vessels. This test is done only at a small number of cardiac centers in the country. Cardiac catheterization procedures are invasive and expensive, but the risks of doing them have to be weighed against the risks of not being accurately diagnosed. A great deal remains to be learned about coronary MVD, especially in women. In the meantime, there are some basic strategies that you can use to get an accurate diagnosis and the best possible medical care.
Listen to your body and believe in your instincts. If you feel strongly that something is wrong but your doctor can't find a problem, get a second opinion.
Find a specialist who is familiar with coronary MVD.
Ask questions. If you don't fully understand the answers, ask more questions until you do. There's nothing more important than your health.
By balancing assertiveness with respect for your physicians, you can get the information you need.

Key Point 3
If you've been diagnosed with coronary microvascular disease, getting adequate blood flow to your heart is critical.

Lifestyle changes are the most effective treatment. Treatment goals for coronary microvascular disease are three-fold – stop it from getting worse, improve quality of life by relieving symptoms, and prevent a heart attack. Standard invasive treatments for coronary heart disease (CAD), such as angioplasty, stenting and bypass surgery, aren't used to treat coronary microvascular disease. Instead, treatment focuses on reducing risk through managing underlying conditions. Talk to your doctor about your risk factors for heart disease and how to control them. Know your numbers-ask your doctor for these three tests and have the results explained to you. Lipid profile.

This test measures total cholesterol, LDL cholesterol (often called bad cholesterol), HDL cholesterol (often called good cholesterol), and triglycerides (another form of fat in the blood).

Blood pressure. Fasting blood glucose. This test is for diabetes. Know your body mass index (BMI) and waist circumference.

BMI is an estimate of body fat that's calculated from your height and weight. You can use the National Heart, Lung, and Blood Institute'sonline BMI calculator to figure out your BMI.

To measure your waistline, stand and place a tape measure around your middle, just above your hipbones. Measure your waist just after you breathe out. Know your symptoms and how and when to seek medical help.

Be able to describe the usual pattern of your symptoms. Know how to control them.
Know which medicines you take and when and how to take them. K
now the limits of your physical activity. Make heart-healthy lifestyle changes to reduce your risk factors.
You can't control some risk factors of heart disease such as age and family history. However, you can take aggressive steps to lower or control other risk factors such as high blood pressure, overweight and obesity, high blood cholesterol, diabetes and smoking.
Follow a heart healthy eating plan. Two heart healthy eating plans are the Dietary

Approaches to Stop Hypertension (DASH) diet (for people who have high blood pressure) and the Therapeutic Lifestyle Changes (TLC) diet (for people who have high blood cholesterol). Increase your physical activity.
Aim for at least 30 minutes of moderate-intensity activity on most, and preferably, all days of the week.
If you're trying to manage your weight and keep from gaining weight, try to get 60 minutes of moderate-to-vigorous-intensity physical activity on most days of the week.
Quit smoking, if you smoke.
Lose weight, if you're overweight.
Learn ways to avoid or cope with stress Take medicines as your doctor prescribes.
Standard anti-angina drugs that work by relaxing blood vessels, such as nitroglycerin, can help ease symptoms.
Nitroglycerin is prescribed to relax blood vessels, improve blood flow to the heart muscle, and treat chest pain.

High cholesterol and high blood pressure are almost certainly among the causes of microvascular disease. In addition to diet and exercise, lipid-lowering drugs like statins can be used to improve cholesterol levels and beta blockers, calcium-channel blockers or vasodilators to lower blood pressure and decrease the heart's workload.

If you have diabetes, check your blood sugar level every day to make sure your medicines and diet and exercise are working to keep it in a normal range. Two out of three people with diabetes die from heart disease and stroke.

Low-dose aspirin can be used to help prevent blood clots or control inflammation. Other blood clot reducers include anticoagulants and antiplatelets.

Treat anemia. It slows repair of damaged blood vessels. Anemia treatment depends on the cause and can involve iron supplements, folic acid or hormone injections, and blood transfusion, or antiplatelet drugs.

Although a great deal of new knowledge about coronary MVD has been uncovered in the last decade, more work needs to be done. Watch for new findings from the federally funded Women's Ischemia Syndrome Evaluation (WISE) study Medline Plus Conduct an off-site search for Coronary Microvascular Disease information from MedlinePlus

The material on this Web site is provided for general information only and is not intended to contain or convey medical advice or instruction. Always consult with your physician or other appropriate health care professionals before making any changes in diet, physical activity and/or drug therapy. If you think you may have a medical emergency, call your doctor or 911 immediately. Do not use this Web site for medical emergencies. WXXI did not create and does not recommend or endorse any specific opinions or other information that may be mentioned or referenced on this Web site.  RELIANCE ON ANY INFORMATION ON THIS WEB SITE IS SOLELY AT YOUR OWN RISK. Sponsor Copyright 2014 WXXI - All Rights Reserved

Myocardial Ischemia

NEWS & PERSPECTIVE › MULTISPECIALTY Diagnosis and Management of Myocardial Ischemia (Angina) in the Elderly Patient

Donald D. Tresch, MD, Haritha R. Alla, MD, Medical College of Wisconsin, Division of Cardiology and Geriatrics, Milwaukee, WI Disclosures Am J Geriatr Cardiol. 2001;10(6)

An acute MI may be the initial clinical manifestation of CAD in elderly persons, although many elderly persons experience myocardial ischemia for years prior to an acute MI.

Unfortunately, due to the absence of symptoms and the atypical presentation of myocardial ischemia in elderly persons, CAD will not be diagnosed in many of these patients until an acute MI occurs. Numerous studies[4-6] have shown that 20%-50% of patients 65 years or older demonstrate silent myocardial ischemia upon stress testing or ambulatory electrocardiographic (EKG) monitoring.

Moreover, silent myocardial ischemia is a marker for future coronary events in these patients. Nonfatal MI and death are two to three times more common in patients with silent myocardial ischemia than in those without silent ischemia. The event rate is even higher if, in addition to ischemia, abnormal LV function[4,5,7] or ventricular tachyarrhythmias[8,9] are present.

Therefore, detection of silent myocardial ischemia in elderly persons is important. Some authors have concluded that performing stress testing in persons at the time of their retirement would be more cost effective than the usual practice of stress testing the 50-year-old junior executive. Symptoms in elderly patients with myocardial ischemia may be so atypical, compared to younger patients, that the symptoms may be misdiagnosed as being caused by another disorder or as related merely to aging.

Exertional angina pectoris is commonly the first manifestation of CAD in middle-aged persons, and is usually easily recognized due to its typical features. For elderly persons, however, this may not be the case. Due to limited physical exertion, many elderly persons with CAD will not experience exertional angina. Instead of angina, myocardial ischemia in elderly patients is commonly manifested as dyspnea.

Not infrequently, the dyspnea occurs in combination with angina, although the angina is frequently mild and is of little concern to the patients. In other elderly patients, myocardial ischemia appears as shoulder or back pain and may be misdiagnosed as degenerative joint disease; if the pain is localized in the epigastric area, it may be ascribed to peptic ulcer disease.
Positional postprandial epigastric discomfort that is burning in quality is often attributed to hiatal hernia or esophageal reflux, rather than myocardial ischemia.

Moreover, the frequent presence of comorbid conditions in elderly patients adds to the confusion and may lead to a misdiagnosis of symptoms that are actually due to myocardial ischemia.

Myocardial ischemia may be manifested as acute LV failure in elderly patients, with some patients presenting with acute pulmonary edema.[10-13] Chest pain may not be present, although the myocardial ischemia is severe enough to produce diastolic and/or systolic LV dysfunction. Many of these elderly patients are unaware of having CAD until the onset of the acute heart failure.

A history of hypertension is common and the patient's EKG and echocardiogram will demonstrate LV hypertrophy. Three-vessel CAD is usually found, but ventricular systolic function is only mildly depressed. With revascularization, these patients do well.
Cardiac arrhythmias can be another clinical manifestation of myocardial ischemia in elderly patients. Patients with myocardial ischemia may experience chest palpitations caused by ventricular premature beats.

Unfortunately, in other elderly patients, the arrhythmias may be ventricular tachycardia or fibrillation leading to sudden cardiac death. Prior to sudden death, these patients may be asymptomatic, with no awareness of the presence of CAD.

The initial evaluation of an elderly patient with myocardial ischemia should begin with a thorough history and complete physical examination, and determination of the coronary risk factors and comorbid illnesses. In addition, early assessment of clinical stability, with stratification into a high- or low-risk group, is necessary.[14]

In addition to advanced age, mortality and morbidity in elderly patients with myocardial ischemia are directly related to LV function, the extent of CAD, and the presence of comorbidity. Stress testing is important in stratification of elderly patients with myocardial ischemia, especially in asymptomatic patients (Table I).

The goals of treatment in elderly patients with myocardial ischemia are 1) to relieve symptoms, if present, and to stabilize the acute pathophysiologic process; 2) to prevent recurrence or new onset of symptoms; and 3) to prevent progression and induce regression of the underlying pathophysiology to reduce future coronary events, including death.
The specific management of elderly patients with myocardial ischemia consists of 1) treatment of associated disorders that can precipitate or worsen ischemia; 2) reduction of coronary risk factors; and 3) use of pharmacologic agents. In high-risk elderly patients, coronary angiography is necessary, if there are no contraindications to revascularization.

Wednesday, March 4, 2015

Jacquelyn Kelsey..

Remember we talked about Accessory Tragus... Mine are outties, Yours innie..
Follow link (or copy/paste into browser) for details & images (your brachial cyst)

http://www.newyorkentspecialist.com/blog/tag/first-branchial-cleft