Showing posts with label research. Show all posts
Showing posts with label research. Show all posts

Monday, May 21, 2012

Gathering together

There are words for groups of things: a murder of crows, a kindle of kittens.

What do you call a gathering of patients who've all experienced the same under-diagnosed heart condition?

I call it a MIRACLE, and it happened in Naperville, Illinois a couple of weeks ago--the first-ever SCAD Reunion and walk for SCAD Research, Inc.

Women and men who survive a spontaneous coronary artery dissection are often left feeling like freaks, because most doctors have never treated one.

To have 25 SCAD survivors all gathered together in one spot, at the same time, for a common purpose?

Another word: POWERFUL.


It's a tremendous experience, I dare call it life-changing--to be able to meet someone else who shares your diagnosis. I'm thrilled to be part of this SCAD patient collective.

Sunday, January 29, 2012

A Zebra Among Horses

Almost three years ago, I had a heart attack at the age of 40, with no family history or elevated risk factors. I'm not diabetic, I don't smoke, my arteries aren't clogged, and at the time, I was training for a triathlon.

I was in shock to wake up one morning with textbook heart attack symptoms -- pain in the center of my chest that radiated down my left arm and up into my neck and jaw, I had cold sweats, I felt nauseated.

My husband drove us to the hospital, where they treated me as if I were having a heart attack--they gave me a nitro patch, an aspirin, drew blood, did a chest X-ray and an EKG--all the while telling me that it wasn't my heart, because I was too young and too female.

Round two of bloodwork proved them wrong, and a pole-axed doctor came to my room that night to tell me that even though he'd put the odds of me having had a heart attack at less than 1 in 100, I had indeed had a heart attack. A cardiac catheterization procedure the next day showed the cause: my right coronary artery had torn in a corkscrew pattern.

I'd experienced a rare thing called a spontaneous coronary artery dissection, or SCAD.

Only a few thousand SCADs happen in the US every year. Mortality rates are on the decline, thanks in part to better, faster treatment, but a SCAD can still be fatal.

Coronary arteries are constructed in three layers; a dissection is when part of the inner layer tears away, and the tear creates a sort of flap where blood gets diverted from where it should be going (to the heart).

It's like when the lining of your favorite coat tears, up near the shoulder, and you accidentally put your arm through the space between the torn lining and the outer layer of fabric, but since the sleeve and lining are still sewn together at the wrist, your arm can't actually come out where it should, at the end of the sleeve.

Your trapped arm is like the blood in a dissected artery that can't get to its destination.

My right coronary artery was repaired with six drug-eluting stents--the stents are pushing that torn inner layer back in place and are holding it in position, keeping the artery open.

After a week in the hospital, I was able to come home. I was referred for 12 weeks of cardiac rehab--a medically supervised exercise program. At first, I saw my cardiologist every six months. Now it's down to once a year.

I realize how extremely fortunate I am. If you and I ran into each other in public, unless you either noticed my medic alert bracelet or ran off with my wallet and saw my stent location cards, you'd never know that there's something wrong with me.

I don't look sick. Most days, I don't feel sick. I take a few pills every morning. Nineteen months after my spontaneous dissection, I finally competed in the triathlon I'd been training for.

I count my blessings and try not to take anything for granted. I feel fortunate to be able to take myself to the bathroom, without calling for help and without towing a metal tower of wires, monitors, and IV drips along with me. I can get out of bed every morning under my own power. I'm usually not in pain. I don't have any restrictions on my activities.

But I think I will always carry the memory of hearing one of the doctors say, during my catheterization, "Has anyone ever seen this before?"

And having no answers as to why this happened and what the odds are of it happening again, can be hard realities to come to terms with.

That’s why I'm so excited that Mayo Clinic is doing not one, but two studies on SCAD, at the instigation of fellow SCAD patient, Katherine Leon. After her own heart attack and SCAD, Katherine wouldn't take "It's a rare condition, there's nothing to research" for an answer.

There's info on the studies here: http://newsblog.mayoclinic.org/2011/08/17/scad-spontaneous-coronary-artery-dissection-studies-at-mayo-clinic/

Inspire hosts an active online patient community for women with heart disease (they also host groups for a vast array of other conditions, some rare, some not): https://www.inspire.com/groups/womenheart/

There are something like 200 SCAD survivors, from all corners of the globe, concentrated in that one spot online. SCAD is under-diagnosed enough that most of us don't know another survivor in person, so being able to connect online has been a real lifesaver for us.

In 2009, when Katherine first approached Dr. Sharonne Hayes about researching SCAD, Katherine was able to point to all the women of this online community who are anxious for answers and motivated to participate in research on our condition, provided we could find some research to take part in.

Dr. Hayes said "Yes" to Katherine and to researching SCAD. The pilot study results came out last year, and that study spawned two new, ongoing ones.

This is the spirit of "Alone, we are rare, but together we are strong," the theme of this year's Rare Disease Awareness Day on Feb. 29th.

You've probably heard the adage, "When doctors hears hoofbeats, they think of horses, not zebras." Those of us with rare diagnoses are zebras.

Most of the time I don't feel sick, and I don't feel like a zebra. What brings it back to my awareness is when someone else, sent home from the hospital after being patted on the head, told how rare her condition is and how lucky she is to have survived, but with precious little other info, shows up in our online community of SCAD survivors--scared, confused, and looking for answers. Then I am reminded that we're not just survivors, we're a herd of zebras.

I had another zebra moment in cardiac rehab, on the day the nurse was giving us a lesson in properly taking our medications. At one point, she paused, looked at all of us, and said, "Let's face it: you all did something to bring yourselves here." I wanted to raise my hand and ask her to explain to me exactly what I'd done to cause my right coronary artery to dissect, but that would've derailed the class, so I kept silent. At that moment, I felt very much alone.

One zebra in a pasture of horses stands out--a freak, an anomaly, a 40-year-old woman in a cardiac rehab class of men in their 70s.

A few miles down the road, though, there's a whole pasture of zebras. Find your pasture. We're here, and we understand.

Tuesday, December 27, 2011

BPA and the Female Heart

BPA, or bisphenol A, is one of the components in hard, clear plastic -- those ubiquitous refillable water bottles and baby bottles, as well as in the linings of canned foods.

Now researchers at the University of Cincinnati, in an NIH-funded study, have shown that BPA affects female hearts: http://www.sciencenews.org/view/generic/id/337035/title/BPA_sends_false_signals_to_female_hearts

What struck me is that the researchers are calling this a "gender-specific vulnerability to arrhythmias."

I'm hoping that this is a positive development in researchers realizing that males and females are not identical and research that just includes males is not automatically applicable to females.

Sunday, October 23, 2011

HHS wants US--patients!--to participate in grant reviews

That's right, patients, everyday, ordinary patients like us--are being asked to join in reviewing grants next year.

e-Patient Dave has a great, non-technical breakdown of the easy application process.

Longtime readers of my blog know that one of my passions is encouraging more women to participate in heart-related research.

This is a step better; it's a chance for patients to actually shape the direction of new research.

We're being invited to the table. The chair's been pulled out for us. Will we sit down and make our voices heard?

Thursday, October 13, 2011

SCAD Ladies Stand Up: Stories of Patient Empowerment

My partner in crime, the other half of our "Dissection Duo," aka my friend Katherine--she and I, and Dr. Hayes (the courageous cardiologist who agreed to take us on as a group and study us--at 100% Katherine's instigation), and several other SCAD survivors tell our stories here:

The SCAD Ladies Stand Up: Stories of Patient Empowerment (note: it's a PDF).

Thanks to John at Inspire, and the whole team, who worked to put this piece together and publish it.


Wednesday, October 5, 2011

Mayo Clinic's Social Media Summit

In just under two weeks, I will be at Mayo's third annual Social Media Summit. My SCAD-sister Katherine and I, plus the authors of Mayo's pilot study on spontaneous dissections, will be on a panel together.

http://socialmedia.mayoclinic.org/2011/10/04/scad-ladies-highlight-social-media-summit/

I'm slightly nervous but also looking forward to it. I hope it brings more attention to the two new SCAD studies that Mayo is doing, and that we garner more participants in the research.

Tuesday, September 13, 2011

SCAD studies now on clinicaltrials.gov

Longtime readers will know that I love pointing people to clinicaltrials.gov, to seek out research that we can participate in.

It's one of the most comprehensive and reliable sources for that kind of information.

Now Mayo's two SCAD studies are listed on clinicaltrials.gov,

http://clinicaltrials.gov/ct2/show/study/NCT01427179

and

http://clinicaltrials.gov/ct2/show/NCT01429727

This is excellent news, and I hope the listing leads other people -- men and women both -- who've had dissections to participate in the studies.

Tuesday, August 30, 2011

Spontaneous Dissection Study in Wall Street Journal

Another friend referred to this as "my" 15 minutes of fame. No. I'm too introverted; I don't want fame for myself, I want it for SCADs.

Here's today's story on Mayo's new SCAD research and how it happened, from the Wall Street Journal:

http://online.wsj.com/article/SB10001424053111903352704576538754057145360.html

Many thanks to my heart-sister Katherine for encouraging Dr. Hayes to take on this study, and to Dr. Hayes for agreeing to it. This all happened at Katherine's instigation and she gets 100% full credit for talking to Dr. Hayes.

Here's hoping we'll someday have some answers.

And see, this is what I mean when I say that women's heart disease research is so crucial. We're doing our part to add to the medical knowledge about women's heart issues, and I'd encourage other women to participate as well.

Edit: Sorry some people are having trouble with the Wall Street Journal link. Here's an alternate from Forbes.com:
http://www.forbes.com/sites/davidshaywitz/2011/08/30/as-therapeutics-become-personal-patient-social-networks-may-become-essential/

Wednesday, August 17, 2011

Big news! Mayo announces SCAD studies!

I cannot tell you all how excited I am to see this.

Mayo Clinic is now doing two studies on Spontaneous Coronary Artery Dissections.

http://newsblog.mayoclinic.org/2011/08/17/scad-spontaneous-coronary-artery-dissection-studies-at-mayo-clinic/

This is huge. SCADs are so rare and so poorly understood, to have a prestigious institution like Mayo taking an interest and doing studies is fantastic.

Here's to advancing medical knowledge!

Monday, August 15, 2011

Research Studies & Clinical Trials

Today's topic is again research studies and clinical trials.

I've covered this before, but it's important, especially for women, because as far as cardiac research is concerned, only around 27 percent of the participants are female, despite the fact that heart disease kills more women than men every year.

The Clinical Trials.gov website is still one of the best resources for finding studies.

Also, don't be shy about letting your cardiologist know that you're willing to participate in research.

That's how I found out that I'm not a poor Plavix metabolizer. When the news came out early last year that some people may be taking Plavix and not responding to it, I talked to my cardiologist, and he got me into a study that a colleague was conducting.

All it cost me was some time--one appointment, essentially--and a couple of vials of blood, and a week or two later, I found out that I'm not in the 2 percent of Caucasians who are poor metabolizers. And my stats are now in this researcher's database as part of the study.

A lot of studies or trials are more time-intensive than the one above, and if I had been unlucky enough to be a poor metabolizer, my participation in the study would have been more extensive.

I know it's time-consuming to participate. I work about 30 miles from where I live, and the hospital and cardiologist who are following me are about 10 miles in the other direction from my work commute. I lose at least three hours of work every time I see my cardiologist, and as the cliche goes, "time is money."

But where would we be without these studies, without these clinical trials?

Not to go all melodramatic here, but it really is a matter of life and death.

Heart disease is still so poorly understood in women; we need to step up and do our part to help. If not us, then who?





Monday, August 1, 2011

BMI alone is not a good predictor of heart problems

New study out illustrates that Body Mass Index (BMI) alone is not an accurate predictor for cardiac problems:

http://www.ncbi.nlm.nih.gov/pubmed/21397319

They looked at medical information for over 200,000 people.

Their conclusion?

"BMI, waist circumference, and waist-to-hip ratio, whether assessed singly or in combination, do not importantly improve cardiovascular disease risk prediction in people in developed countries when additional information is available for systolic blood pressure, history of diabetes, and lipids."

In plain English: look at the blood work, not the shape of the person. If your numbers--blood pressure, blood sugar, and cholesterol--are good, don't let medical people browbeat you with where you are on the BMI chart.

Now I'm not saying don't eat well and don't exercise, but if you're living a healthy lifestyle and the numbers back you up, don't let anyone make you feel bad if you're not where the BMI says you should be.

That's how I'm reading these results, anyway.

And note, this study wasn't funded by a drug company--it's always important to read the "funding" or "supported by" statements on these things. It was funded by the British Heart Foundation (similar to the AHA in the US) and the UK Medical Research Council (another nonprofit). So there's no hidden shilling for a product.

Tuesday, July 5, 2011

Gender-Based Disparities in Heart Disease Care

New report: Heart disease can sneak up on women in ways that standard cardiac tests can miss.

I volunteer with WomenHeart, running the Chapel Hill in-person support group. I got involved with them in 2009 after my own surprise heart attack at age 40.

Lucky for me, I had more of the "classic" male symptoms, so it was hard for the ER to brush me off when I came in complaining of chest pain that was radiating down my left arm and up into my neck, jaw and ear.

The report the article talks about is called The 2011 10Q Report: Advancing Women's Heart Health Through Improved Research, Diagnosis and Treatment. If you want to read the whole thing, you can download a PDF here:

http://www.womenheart.org/documents/upload/FINAL-TO-PRINTER-6-15-11.pdf

It's a sobering look at the disparities in care that still exist in women's heart disease treatment.

We have to have a multi-pronged approach, not only educating women, but reaching out and educating the medical community as well.

Tuesday, June 28, 2011

Please take the Yale Heart Study

Hey everyone, if you've had a heart attack, the Yale Heart Study would love to hear from you:

http://heartstudy.yale.edu/hacs/

Message from the survey director:

"I am the director of the Yale Heart Study of how people get medical care when they are having symptoms of a heart attack. We are asking people who have had a heart attack to share with us their experiences at our study website: http://heartstudy.yale.edu/hacs/

The goal of this study is to help people get care as quickly as possible when they are having heart attack symptoms.

This survey of heart attack care-seeking is being conducted on the internet and takes about 30 minutes to an hour to complete depending on your experiences.

Participation in this study is completely anonymous.

The study has been approved by the Yale University Institutional Review Board and is funded by the National Institutes of Health. If you have any questions about this study please contact me at heart . study @ yale . edu" (remove the extra spaces in the address before emailing)."

The more people they hear from, the the better.

It took me around 30 minutes to finish, and there's space at the end to add as much info as you'd like about your individual situation.

Wednesday, September 30, 2009

Clinical Trials

One statistic that always leaps out at me is that women only make up around 27% of the participants in heart-related research. I honestly feel like this is one reason why women die more frequently from their heart attacks than men do; there's simply not as much known about heart disease in women.

We can start to change that by participating in clinical trials. Here's a good source of clinical trials:

http://www.clinicaltrials.gov/

In fact, searching that site, I just now found a study that's currently enrolling young women who've had heart attacks. As soon as this post is up, I'm going to email them and sign up, and I would encourage other women to seek out research opportunities as well.