Archive for the ‘Carolyn Thomas’ Category

Guest Blog: A Second Opinion from Dr. Google

Carolyn Thomas
Monday, April 16th, 2012

Carolyn Thomas is a heart attack survivor and a 2008 graduate of the annual WomenHeart Science and Leadership Symposium at Mayo Clinic in Rochester, Minnesota – the first Canadian invited to attend this prestigious training event.  She was also named by “Our Bodies Ourselves” of Boston in 2009 as one of 20 inductees from seven countries acknowledged as “Women’s Health Heroes” for community activism in promoting women’s health.  You can read more from Carolyn on her two blogs: Heart Sisters and the Ethical Nag.

I’ve often suspected that if only the E.R. doctor who misdiagnosed me with indigestion had bothered to just Google my cardiac symptoms (chest pain, nausea, sweating and pain radiating down my left arm), he and Dr. Google would have almost immediately hit upon my correct diagnosis: myocardial infarction, or heart attack. But instead, he pronounced that I was “in the right demographic” for acid reflux. I was sent home that day feeling horribly embarrassed for having made a fuss over nothing but a case of indigestion. As time went by, however, and my debilitating symptoms became truly unbearable, I turned to Dr. Google.

And that’s why I forced myself, despite my embarrassment, to return to the E.R. – but with the pronouncement of that E.R. doc still ringing in my ears:

“It is NOT your heart!”

Many physicians out there, however, are not happy when their patients consult Dr. Google to research troubling symptoms like mine.

A female heart patient from Wisconsin, for example, shared recently:

“When I first began discussing my condition with my doctor, he said he hadn’t realized I was a doctor. I told him I’m not a doctor, but I am a very good researcher. He gave that small, insulting half-laugh that doctors reserve for this response and said that he wasn’t sure he approved of patients doing research.

“I told him I had no inclination to apologize for it. I said that I knew he was interested in my health, but not nearly as interested as I am.

“It’s his job, but it’s my life.”

Dr. Stuart Foxman of the College of Physicians and Surgeons of Ontario has written about doctors’ reaction to the growing phenomenon of patients who are self-educated “medical Googlers”. On his blog for physicians called DocTalk, he cited a survey of physicians that found many docs rate the know-it-all Googler as somewhere between “frustrating” and “irritating”.

This study noted a number of doctors’ concerns.  Some patients used the information gleaned on their own for self-diagnosis or self-treatment. Some doctors believed that the information caused the patient unnecessary confusion and distress. Dr. Foxman explained:

“All of these seem like legitimate concerns on the part of physicians. The highly curious and informed patients were sometimes perceived as ‘challenging’ with a tendency to test the knowledge of physicians. Some doctors felt that these patients were overly assertive, undermined their authority, and did not show sufficient trust in their health care provider.”

Consider, for example, Dr. Scott Haig‘s classic TIME magazine essay called ‘When The Patient Is A Googler’ - a scathingly arrogant attack that describes  his Googling patients as:

“. . . suspicious and distrustful, their pressured sentences bursting with misused, mispronounced words and half-baked ideas.”

Just a tad oversensitive to having his authority undermined, wouldn’t you say?

The reality, of course, is that, despite doctors like Haig, patients are indeed consulting Dr. Google in growing numbers.  According to the Pew Internet and American Life Project, 80% of us use the internet to “prepare for or recover from” our doctor visits.

Well-known physician blogger Dr. Kevin Pho believes that it’s time to stop debating whether or not patients should research their own symptoms.  It’s happening already, as he warns:

“The medical profession would be better served to handle this new reality.”

My heart sister Laura Haywood-Cory survived a heart attack at the age of 40, caused by Spontaneous Coronary Artery Dissection. She recently explained her own need to seek information and support online in her essay on the Stanford School of Medicine blog, Scope:

“As a patient with a rare condition that most cardiologists have never encountered, I and others like me have had to become our own experts. And since our numbers are small, we aren’t able to gather for support in person; we do it online.

It seems to me that the answer isn’t to discourage people from seeking medical information from Dr. Google, but rather to teach people, starting in school, some critical thinking skills. How to sift the online wheat from the chaff and how to determine which sites have credible information, versus ones that are just selling the latest formula of snake oil.”

Dr. Michael Lowenstein, co-director of the California-based Waismann Institute, believes that the more educated patients are about their health, the better care they’ll get. He also says patients need to be their own advocates in today’s health care environment. For example:

“There are patients who educate themselves and go to reputable websites that have good information. It makes for an intelligent dialogue between doctor and patient about the medical condition and treatment options.”

Since we know that many patients are already inclined to go online and search for information, physicians should look at this as an opportunity to enhance their own websites, warns Erin Sharaf of Northeastern University.

“It’s smart for medical practices to have a website and steer their patients to better resources. Refer them to other reputable external sites with links from your own website, so that patients know they are credible, respected and have accurate information. It’s also important to both stay up to date with the medical literature as well as the lay press so you know what your patients are reading.”

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Guest Blog: When Patients Demand Treatments That Won’t Work

Carolyn Thomas
Friday, November 4th, 2011

Carolyn Thomas is a heart attack survivor and a 2008 graduate of the annual WomenHeart Science and Leadership Symposium at Mayo Clinic in Rochester, Minnesota – the first Canadian invited to attend this prestigious training event.  She was also named by “Our Bodies Ourselves” of Boston in 2009 as one of 20 inductees from seven countries acknowledged as “Women’s Health Heroes” for community activism in promoting women’s health.  You can read more from Carolyn on her two blogs: Heart Sisters and the Ethical Nag.

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From The Ethical Nag: Marketing Ethics for the Easily Swayed:

When my son Ben came down with another killer sore throat this past summer, he went to his doctor for an antibiotics prescription. He’d suffered this condition in the past, and he knew just what would help ease his painful symptoms. Both he and the doctor agreed this sure sounded like strep, so without even having to wait for the throat swab test results for the group A Streptococcus bacteria that cause strep throat, Ben left the doctor’s office with a prescription for antibiotics in hand.

But were antibiotics the appropriate treatment for Ben’s painful problem?

The virtually universal recommendation for antibiotic drugs to treat strep throat – or increasingly, sore throats of any cause – is not actually founded on scientific evidence, but rather on a small population of employees at Wyoming’s Warren Air Force Base during the 1940s.

For more than a decade, virulent strains of group A Streptococcus caused unprecedented rates of throat infections among the base trainees, and history’s worst epidemic of rheumatic fever.

Dr. David Newman, in his article called Antibiotics for Strep Do More Harm than Good, picks up on this story:

“Military researchers at the base seized the moment, executing a provocative series of trials that tested the potential of antibiotics to prevent post-streptococcal rheumatic fever. Roughly 2% of the trainees given placebo in their studies developed rheumatic fever, while under 1% of trainees given antibiotics experienced the disease. For every 50-60 trainees treated with antibiotics, the researchers had successfully prevented one case of rheumatic fever. It was a small, but decisive victory. Identifying and treating ‘strep throat’ quickly became a staple of medical education, and little has changed since then.”

Trouble is, since the isolated Warren Air Force Base experience, in large recent studies tracking tens of thousands of strep throats in the general population (many of whom received placebos or no treatment at all) there hasn’t been a case of rheumatic fever reported in a study for nearly 50 years. And when the incidence dropped to less than one per million in 1994, the Centers for Disease Control and Prevention stopped even tracking rheumatic fever entirely.

Dr. George Lundberg, MedPage Today’s Editor-at-Large, also wonders why antibiotics for strep throat became and remain the “standard of practice” to prevent rheumatic fever. Indeed, most major hospital-based medical websites still recommend antibiotic therapy for strep throat infections in order to prevent rheumatic fever.

Dr. Lundberg observes that the length of time a person with sore throat is symptomatic prior to recovery is four to seven days, whether or not strep is found and regardless of whether antibiotics are used. Dr. Lundberg warns:

“One million prescriptions for antibiotics for sore throat may prevent one case of rheumatic fever. But they may cause 2,400 cases of significant allergic reactions up to and including anaphylaxis, 50,000 to 100,000 cases of diarrhea, and some 100,000 cases of skin rash.”

Dr. Ed Pullen of Puyallup, Washington supports this caution when prescribing antibiotics with the example of another common bacterial infection: acute sinusitis.  He writes:

“There is a lot of evidence suggesting that acute sinusitis of less than 10 days duration usually resolves without antibiotic therapy in about the same number of days and with about the same severity of symptoms as with antibiotic therapy.  The outcome of an episode of acute sinusitis that has not been present long is therefore about the same with or without antibiotic therapy.

“But antibiotic therapy itself can lead to significant morbidity, both the individual treated and to the larger community.  Complications like antibiotic resistance and C. difficile-related pseudomembranous colitis is becoming more common. With essentially every antibiotic from amoxicillin to Levaquin, side effects are very common.

“So physicians face the challenge of convincing patients who have been treated for their sinusitis with antibiotics for years and usually get well within days of treatment (as they would usually without treatment) that they are better treated with saline nasal rinse, analgesics and tincture-of-time.“

Rampant antibiotic use is very good news for pharmaceutical companies who manufacture and distribute these prescription drugs. Annual sales of antibiotic medications in North America in all settings last year exceeded $11 billion. But we do know that U.S. states with active appropriate antibiotic use campaigns (e.g. Get Smart: Know When Antibiotics Work) do have lower prescribing rates. And here in British Columbia, our Do Bugs Need Drugs? Campaign resulted in a reported drop of 18% in the overall number of antibiotics prescribed to children under the age of 14 since the program started in 2005. (See more in this 2010 Do Bugs Need Drugs? Evaluation Summary).

In a New York Times piece called Believing in Treatments That Don’t Work, Tara Parker-Pope listed other examples of ailments for which we patients often expect and demand medical interventions that are not actually evidence-based:

  • Recent press reports detailing the dangers of cough syrup for children have noted that cough syrup doesn’t work. True: no cough remedies have ever been proven better than a placebo, either for adults or children. Yet their use is common.
  • Patients with ear infections are more likely to be harmed by antibiotics than helped. While the pills may cause a small decrease in symptoms (for which ear drops work better), the infections typically recede within days regardless of treatment. Unnecessary antibiotics are still given to more than one in seven North Americans each year for these conditions alone, at a cost of more than $2 billion and tens of thousands of serious adverse medication effects requiring treatment.
  • Back surgeries to relieve pain are, in the majority of cases, no better than non-surgical treatment. Yet doctors perform 600,000 of these surgeries each year, at a cost of over $20 billion.
  • More than a half million North Americans per year undergo arthroscopic surgery to correct osteoarthritis of the knee, at a cost of $3 billion. Despite this, studies show the surgery to be no better than sham knee surgery, in which surgeons “pretend” to do surgery while the patient is under light anesthesia. It is also no better than much cheaper, and much less invasive, physical therapy.

And The Times recently ran this observation from Florida sports medicine orthopedist Dr. James Andrews, who is taking a stand against what he sees as the vast overuse of magnetic resonance imaging (MRI) in his surgical specialty:

When a healthy runner goes for a jog, she’ll have evidence of ‘abnormal’ fluid noted in her knee capsule on an MRI scan immediately afterward. But there is no injury. And if you want an excuse to operate on a pitcher’s throwing shoulder, just get an MRI.”

Historically, we know that in the mid-nineteenth century, medical treatment by doctors actually fell out of fashion, explains Dr. Melvin Konner in his book, Becoming a Doctor: A Journey of Initiation in Medical School. The great illumination from this medical revolution was the news that there were many diseases that were essentially self-limited. Dr. Konner writes:

“They would run their predictable course, if left to run that course without meddling, and, once run, they would come to an end and certain patients would recover by themselves.

“Typhoid fever, for example, although an extremely dangerous and potentially fatal illness, would last for five or six weeks of fever and debilitation, but at the end about 70% of the patients would get well again.

“Lobar pneumonia would run for 10-14 days and then, in previously healthy patients, the famous “crisis” would take place and the patients would recover overnight.

“Patients with the frightening manifestations of delirium tremens only needed to be confined to a dark room for a few days, and then were ready to come out into the world and drink again. Some were doomed at the outset, of course, but not all. The new lesson was that treating them made the outcome worse rather than better.”

In modern times, the current fashion is trending towards what’s known as evidence-based medicine, what British Columbia physician and author Dr. Kevin Patterson describes as asserting the supremacy of data over authority and tradition:

“You can’t kick over a bedpan without hearing the phrase ‘evidence-based medicine’ rattle out.

“But the problem is that if it makes sense that a treatment will work – or if one stands to make money if a treatment works – then a doctor will, with alarming and disheartening reliability, perceive that it does in fact work.”

But in our current chicken-or-egg dilemma, which comes first?

Is it the medical profession’s unquestioning embrace of a particular (and often profitable) treatment option, or is it the consumer’s demand (fueled by consumer education like those “Ask Your Doctor” direct-to-consumer ads sponsored by those who stand to gain financially by these treatment choices?) that also drive these questionable yet widely accepted practices?

What’s your experience been like?  Do all bugs need drugs?

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Guest Blog: Is it Post-heart Attack Depression – or Just Feeling Sad?

Carolyn Thomas
Thursday, August 4th, 2011

Carolyn Thomas is a heart attack survivor and a 2008 graduate of the annual WomenHeart Science and Leadership Symposium at Mayo Clinic in Rochester, Minnesota – the first Canadian invited to attend this prestigious training event.  She was also named by “Our Bodies Ourselves” of Boston in 2009 as one of 20 inductees from seven countries acknowledged as “Women’s Health Heroes” for community activism in promoting women’s health.  You can read more from Carolyn on her two blogs: Heart Sisters and the Ethical Nag.

One of the small joys of having launched my site is discovering by happy accident the wisdom of other writers – even when they’re writing on unrelated topics not remotely connected to my favourite subject which is, of course, women and heart disease. For example, I happened upon a link to Sandra Pawula‘s lovely blog called Always Well Within. Sandra teaches mindfulness meditation, and she lives in Hawai’i (note her correct spelling).

She also has a hubby and three cats. I don’t even know this woman, but I like her already.  And while scanning through her beautiful site, I was stopped cold by an article she called: “Why Sadness is the Key to True Happiness“.

Something about this title stopped me because for quite some time, I’ve been ruminating (something heart attack survivors are apparently very good at doing!) on whether the word depression is actually the most accurate way to describe what hits many of us survivors following a cardiac event.

Mayo Clinic cardiologists estimate that up to 65% of those living with heart disease exhibit symptoms of depression, yet fewer than 10% are appropriately diagnosed.

Psychologist Dr. Elvira Aletta has instead used the word grief to describe the symptoms experienced by patients newly diagnosed with a chronic illness like heart disease:

“Chronic illness means getting sick and being told it is not going away, and that stinks. Our bodies have suddenly freaked out on us, and we’ve lost control of the one thing we thought we could count on.”

But lately I’ve been mulling over the possibility of pure semantics being the culprit in post-heart attack mental health diagnostics here.

After I started writing recently about medical research on clinical depression, for example, I learned that most studies actually suggest that what we know as depression tends to be a naturally self-limiting mental health condition that generally improves over time with or without the pharmaceutical assistance of antidepressant drugs. For example, University of Connecticut researchers* examined 38 pharmaceutical company-funded studies involving over 3,000 depressed patients and found that those taking antidepressants did improve, but the improvement differences between the medicated and placebo-taking groups were actually described as “miniscule”.

Research reported in the British Journal of Cardiology last July also suggested that interventions for anxiety and depression in heart attack survivors are not particularly successful. Cardiac psychologist Dr. Stephen Parker (and a fellow heart attack survivor himself who blogs at www.heartcurrents.com) believes:

“A supportive strategy is probably more effective, as would be education in anxiety reduction and strategies for the management of depression.

“I think the depression and anxiety following a heart attack are a bit different than the depression and anxiety that most therapists encounter, and both are going to be more resistant to treat because there are damn good reasons to feel anxious and depressed.

“A heart attack is a deeply wounding event, and it is a wound that takes a long time to recover from, whatever the treatment.”

I’m now wondering if Sandra Pawula’s observations about sadness may also be added to that list of alternative descriptions of post-heart attack depression or grief.

Could it be that it’s actually crushing sadness over this “deeply wounding event” that we feel after surviving a catastrophic cardiac event?

In addition, Sandra believes that:

“Sadness is not always as bad as it’s made out to be.  In fact, sadness can be the start of your journey directly to the heart of true happiness.”

Sandra offers three ways that sadness can help and empower us, and I believe that each applies to the experience of many heart patients:

1.  Sadness Has the Power to Introduce a Crack in Our Idea of Reality

What previously-invincible heart patient cannot relate to the gigantic ‘crack in our idea of reality’ that a cardiac diagnosis brings? We are often in utter shock and denial about the catastrophic experience of surviving a serious cardiac event, as we wail (silently!) “How can this be happening to ME of all people?” Sandra reminds us:

“There is not a single person in this world who can escape from suffering.  Suffering is the fundamental characteristic of the way we lead our lives. There may be transitory moments of happiness when things go our way, but this happiness is not a long-lasting one.

“All the tension of striving for what we want and rejecting everything else just brings more complications and more suffering: ‘I like this.  I don’t like that.  I want this.  I don’t want that.’

“We’re rarely satisfied for more than a moment.  Then we’re on to achieving a new goal, having the next experience, getting a better possession, or finding the right relationship.

“Sadness has the power to introduce a crack in our limited and limiting version of reality.  Maybe life isn’t all about wanting, getting, accomplishing, and possessing.

“Let sadness spark your life with new meaning and purpose.”

2. Let Your Heart Break Into a Million Pieces

Sandra believes that there’s nothing quite like experiencing pain and suffering to be better able to touch or feel the pain and suffering of others. Heart attack survivors have often told me that it’s only after their own cardiac events that they became exquisitely empathetic to others with outwardly-invisible chronic illnesses like heart disease. Sandra observes:

“When sadness breaks open our heart, we become fully human. We see that your suffering and my suffering are the same.  Suffering is a common thread that unites all of humanity.  From recognizing this simple truth, a profound feeling of interconnectedness can arise.  This sense of interconnection can ignite the wish to bring happiness to others.”

3.  Nothing Ever Stays the Same for Even a Moment

Just when we’re feeling pretty cocky about our own Wonder Woman skills at multi-tasking, job-juggling, “having it all“, blahblahblah – we get blind-sided out of the blue by a catastrophic cardiac event, along with all the physical and emotional chaos that this diagnosis entails. Sandra believes that one benefit of sadness is that it can introduce us to the beauty of impermanence while helping us learn to let go:

“Sadness comes when things change – a relationship ends, someone dies, we’re fired from a job, illness descends, a friend is physically hurt, a disaster happens.

“Change is the only constant in life.  Until we learn to accept change gracefully, we’ll always suffer.  There’s a blessing in embracing the beauty of impermanence. Through doing so, we will come to value every precious moment of this life and live in a far saner and more fulfilling ways.”

IMPORTANT NOTE: Make no mistake, dear readers: I would never want to minimize the devastating impact that ongoing feelings of depression, grief and sadness can have while we are recuperating from a cardiac event. Survivors should certainly take whatever steps they can to address severe symptoms, particularly if they continue unchanged for one month. We also know that there is an important link between women’s comparatively poorer outcomes when heart disease is accompanied by undiagnosed mental health issues.

Treatment options should also include physical exercise and talk therapy, both of which have been shown to successfully reduce symptoms for many.

Read Sandra’s original post called Why Sadness is the Key to True Happiness.

Her excerpts here and her three ways that sadness can help and empower us are from her blog Always Well Within,  © Sandra Pawula 2010-11.

See also:

* Kirsch, I., & Sapirstein, G. (1998). Listening to Prozac But Hearing Placebo: A Meta-analysis of Antidepressant Medication. Prevention and Treatment, 1 (Article 0002a).

Better Health’s Grand Rounds Volume 7, Number 44

CFAH Staff
Tuesday, July 26th, 2011

Welcome to Better Health’s Grand Rounds Volume 7, Number 44! This is our second time hosting Grand Rounds and we’re excited about sharing the posts we received.  The theme of this week’s collection came from a recent Health Affairs blog post by CFAH president, Jessie Gruman, Patient Advocates: Flies In The Ointment Of Evidence-Based Care, which addresses a few of the many challenges of basing health care practices, policies, and decisions on evidence of effectiveness.

We have posts that wrestle with conflicts of interest in reporting on evidence, obstacles to the delivery of evidence-based care, using evidence in practice and care decisions, and providing patient-centered care.  We believe this topic is important to all those involved in health care, from patients and doctors to hospital administrators and policy makers.  Thank you to everyone who submitted a post.  We hope you enjoy this week’s collection.

Consider the Source

Evidence of clinical effectiveness/harm is revealed over time by additional “white-coat” research and via the real-life experiences of patients and clinicians.  Identifying how and by whom evidence is revealed is an important part of evaluating its reliability and accuracy…and towards following the winding path towards effectively applying evidence to practice.

Elaine Schattner, in her post on Medical Lessons, Patients Words, Unfiltered, Medical Journalism and Evidence, shares her concerns that:  1) journalists often select patients’ voices to support pre-determined points of view;  2) making rational decisions based on data is often more complicated than surface appearances; and while 3) evidence should be the foundation of care…we also must acknowledge that outliers exist.

In Direct-to-Consumer Advertising and the Role of Advocacy Organizations: Two Threats to Evidence Based Testing, Josh Freeman, from Medicine and Social Justice, reviews two recent JAMA “commentaries” that addressed challenges to the implementation of evidence-based practice guidelines from two very different but very powerful forces. The marketing of health care technology and treatment directly to consumers and patient activists present both obstacles and opportunities to advance the delivery of evidence-based care.

How did this Heart Drug get Approved in the First Place?, asks Carolyn Thomas, in her post on The Ethical Nag: Marketing Ethics for the Easily Swayed, referring to the drug Nesiritide.  A heart attack survivor, Carolyn “figured the purpose of the drug approval process is to ensure that testing the effects of new drugs on patient outcomes has already been done before approval is granted.”  Pat Salber, of The Doctor Weighs In, also tackles this in her post: Niseritide, the “Lost Decade”, and the Pinto.

Obstacles to Delivering Evidence-based Care

One challenge to the delivery of evidence-based care is the interpretation and application of evidence by individual clinicians.  A Country Doctor, in his post, Patient Centered or Evidence Based Medicine – Can we really have both?, notes that every physician has to evaluate the evidence and determine how to apply it to each patient’s unique situation.

From Joel M. Topf, of Precious Body Fluids, comes, The Problem with Numbers, the Curse of Intermediate End-points, expressing his concern that medical interventions are increasingly oriented around improving the “numbers” – what he defines as intermediate endpoints – rather than real goals of preventing morbidity and mortality in addition to effectively addressing patient concerns and symptoms.  He worries that medications “are pursued and approved only for their ability to fix the numbers.”

The frenzied pace of many medical practices can also be a barrier to providing optimal care, says Steve Wilkins, of Mind the Gap, in Lack of Time and Reimbursement—Is That Why Physicians Don’t Do a Better Job Communicating With Patients? Steve points out that although doctors claim that there is not enough time for patient education, evidence shows that such conversations improve patient outcomes.

InsureBlog‘s Kelley Beloff makes a similar argument in Wait Times in the Medical Office, proposing that patients should consider why doctors run late before making judgments or feeling frustrated.  Kelley writes, “The standard patient appointment time is 15 minutes.  How many of us could do our entire job in 15 minute increments, 25 to 28 times a day?”

Are We Using Evidence Effectively?

Val Jones of Better Health tells us Why She’s Afraid For Anyone to Enter the Healthcare System…Ever.  Val’s post offers resources for patients, caregivers and health care professionals to ensure they are “on the right diagnostic pathway, getting the most appropriate care that suits their needs and preferences, and protecting them from errors and missteps.”

Rheumatologist Irwin Lim, in One Fracture, Two Fracture, Three Fracture…Enough! writes about the need for targeted interventions for high-risk groups…especially patients with osteoporotic fractures that “are getting a surgical fix or a cast, but not assessed and therefore, not treated for osteoporosis…this causes pain, suffering, disability and loss of independence. It also costs….a lot of…money.”

Harold Pollack at Kaiser Health News says in, It’s Not Just About the Money: Cost Control in Cancer Care, that providing evidence-based care is greatly impacted by incentives promoting aggressive care.  He writes that “We all must face these issues to control costs…We can treat our loved ones, and ultimately ourselves, more effectively, more efficiently, and more decently than we often do.”

Family physician Ed Pullen at DrPullen.com struggles with how to best reduce morbidity risks when facing contradictory recommendations for care.  For example, he wonders how to weigh concerns about PSA screening asking “Is there more morbidity related to treating cancer long before symptoms develop, or is there more morbidity from treating cancer after symptoms appear?”

On Pizaazz, Glenn Laffel argues that while no one would dispute screening and prevention as potentially useful tools in the effort to improve the quality of care and reduce unnecessary costs, not all such programs actually work.  Screening for prostate cancer, spiral CT screening for lung cancer, colonoscopies, and ECG screening for high school students, to name a few.  He says, “Some screening and prevention programs are not effective at all.  Others are effective, but prohibitively expensive.”

Gary Schwitzer, of HealthNewsReview, in two posts about using robotics for surgical procedures, raises questions about its use despite many questions about its benefits, harms, and increased costs.  Gary asks, “How are patients to make informed health care decisions and weigh evidence fairly if the information presented is not whole?”

Alexander Friedman adds in his post, My Patient Needed to be Delivered, that cesarean section rates are on the rise due to standard use of fetal heart monitors.  Friedman says that although it’s an “appallingly poor test,” nearly all American mothers are monitored during labor.  Yet, in his experience, almost every time he performs a C-section based on the warnings of distress from the monitor, the baby is delivered “pink, healthy, and a little bit angry…our medical culture prizes technology and tests, even if they don’t work and can cause harm.”

With several recent deaths in Oregon from attempting at-home breech deliveries, Jonie Dawning, an experienced midwife, believes that too many midwives are unaware of the potential risks involved.  In her letter to the Oregon State Legislature, she makes the case for an evidence-based care and policy approach.

Wilderness medicine expert Paul S. Auerbach acknowledges that antibiotics are overused to treat childhood ear infections. But when in an outdoor or wilderness setting, where there is no medical professional to help make the decision, he advises that it is certainly reasonable to administer antibiotics.

Using Evidence for End of Life Care Decisions

In response to a recent NYTimes piece on rising Medicare hospice costs and the role of fraud in the phenomenon, Chris Langston, of The John A. Hartford Foundation HealthAGEnda blog, offers a primer on hospice in the first of a two-part series. With the current budget-cutting environment, Langston “worries that we will make a mistake that will deprive people at the end of their lives of valuable services and that we could even unintentionally increase total health care costs while trying to lower them.”

On GeriPal, Eric Widera shares that “despite a lack of evidence to show any benefits to prevent aspiration pneumonias or pressure ulcers, improving comfort, or prolonging life, feeding tubes are still inserted in patients with advanced dementia.” Widera wonders if family members have unreasonable expectations about the benefits of feeding tubes and specifically if they know that “40 percent of tube fed individuals must be restrained to keep feeding tubes in place.”

Ryan DuBosar, on ACP Hospitalist blog, highlights a recent report from the Center to Advance Palliative Care, noting that nearly two-thirds of all hospitals now have a palliative care program and larger hospitals have even more access. These palliative care teams can help patients and their caregivers when facing a serious illness and making difficult choices.

Receiving Patient-Centered Care…Not Always as Expected

Clinicians, family members and sometimes even strangers can all play a role in providing patient-centered care.  Sometimes you get the support you need…at other times, there is a gap between what you need and what you receive.

Amy Berman, of the John A Hartford Foundation HealthAGEnda blog, shares her experience with what she believes was an overly aggressive treatment recommendation in Can Good Care Produce Bad Health?.  She says, “It doesn’t matter if care is cutting-edge and technologically advanced; if it doesn’t take the patient’s goals into account, it may not be worth doing.”

Posting a sick kid’s photo on Facebook led to the swift diagnosis of a dangerous, fast-moving illness. David E. Williams, in the Health Business Blog, explores the role of social media and crowd-sourcing in his post, Diagnosing an Illness with Facebook.

Beth L. Gainer, of Calling the Shots, recognizes the compassion and support she received from unexpected sources after she received her breast cancer diagnosis and during her treatment in her post, Heroic Moments.

We hope you enjoyed this week’s Grand Rounds.  It was wonderful to read so many posts related to such an important and lasting issue.  Thank you to everyone who submitted a post and to those whose posts we happened upon and included above.  Please be sure to check out next week’s host, James Logan, MD at http://jamesloganmd.com.