WhiteCoat

Archive for March, 2009

Antibiotics More Harm Than Good For Strep Throat?

Thursday, March 19th, 2009

One of EP Monthly’s newest contributors, Dr. David Newman (of the “Hippocrates’ Shadow” fame), sets out a compelling case for why antibiotics may do more harm than good when treating strep throats. The results of the studies showing that antibiotics prevent rheumatic fever may surprise you.

This article is another example of the medical profession needing to examine treatments we consider as “standard of care” to determine whether the treatments are effective and whether the risk of the treatments outweighs the benefit of their use.

Also an interesting discussion in the comments section of the article on whether antibiotics prevent glomerulonephritis or retropharyngeal abscesses. Chris Carpenter, who is an EBM guru, responds to those questions as well.

ER Stories also has some discussion on the topic. Embarassed to say that TK scooped me on an article on my own site.

UPDATE MARCH 22, 2009
Medscape recently published a short article containing updated guidelines for management of streptococcal pharyngitis.
Important points to note include the following:

  • Strep throat is self-limiting and resolves within a few days. [emphasis mine]
  • The rationale for antibiotic treatment is prevention of suppurative infection, prevention of rheumatic fever, and reduction of communicability
  • The antibiotic of choice is penicillin because no increase in resistance has been seen for the past 50 years
  • Despite appropriate antibiotic treatment, chronic strep colonization is common. Children can be chronic “strep” carriers (i.e. strep present on culture without any signs of infection) for up to 1 year after infection, but there is generally no need to treat chronic carriers because they are thought to be at low risk of transmitting disease or developing invasive GABHS infections. [again, emphasis mine]

In summary, strep throat will go away on its own without antibiotic treatment and we only treat to reduce side effects that don’t occur that much to begin with.
In addition, if we swab family members of people who have strep “just to make sure” they don’t have it too, when we give antibiotics to those with positive results, we’re probably treating patients who have been colonized and won’t benefit from antibiotics anyway.
Finally, a question. The article notes that there has been no increase in the resistance of Group A strep to penicillin in 50 years. There is not a consensus on this issue. If we assume that strep has not become resistant to penicillin, could it be that the strep infections we are “treating” with penicillin would just have gone away anyway and that the penicillin is just a “placebo”?
Looks like a great opportunity for a randomized study.

Another recent Medscape article highlights the strep treatment/rheumatic fever reduction issue.

Good Cover

Wednesday, March 18th, 2009

Speaking about the state database of narcotics prescriptions … there was another patient who came in for chronic back pain. He denied being treated for any previous medical problems, but had allergies to anti-inflammatories and to Tramadol, leaving only narcotic medications to treat his back pain. Happened to be from out of town. Several red flags for drug seeking behavior.

When we went to the state database, we found that he had multiple prescriptions for narcotics from multiple different physicians.

I printed out all of his entries and brought them to the room to confront him.

“So, who’s Doctor Painkill?”
“Beats me.”
“How about Doctor Feelgood?”
“I don’t know.”
“How about Dr. Vicodin?”
“I don’t know. Why are you asking me about all these other doctors?”
“Because prescriptions for narcotics written by these physicians have been filled at several different pharmacies under your name in the past few weeks.”
“It wasn’t me.”
“This print out matches your address and your date of birth. Your name isn’t that common, so I doubt that it would be a mistake with so many different doctors.”
“Someone must have stolen my identity.” He appeared stone-cold serious about it.

That one caught me off guard.

“Tell you what, then, I’ll have the police come down and take a report.”
Then he backpedaled.
“No, that’s OK. I’ll stop at the station on the way home.”
“It’s no problem. Besides, I’ll help you out. I’ll make a statement and give the police a copy of the state print-out.”
“That’s OK. I’ll take care of it myself. I don’t want to wait.”

Rrrrrrriiight. You almost had me there.

Then he called back the ED later on and wanted to know how to get a copy of his records for the police.

Not sure what to believe anymore. I gave him the benefit of the doubt and prescribed a few days of narcotics. If he was seeking, at least he knows someone’s checking on him.

Scary that sometimes we have to go to extremes to discourage drug seeking behavior.

Another reason I’m getting one of those stamps that say not to fill prescriptions without picture identification. Now if I could only find a way to put a patient’s picture on a prescription …

Or how about a national picture ID card that people have to swipe to receive medical services?

Bow-Wow

Tuesday, March 17th, 2009

These are drugs:

drugs

.

.

.

.

.

.

.

.

This is your brain on drugs.

Any questions?

When the article says that the police “coaxed him out” of the apartment – wouldn’t it make an awesome Beggin Strips commercial?

Massachusetts’ Next Step

Tuesday, March 17th, 2009

According to this article in the NY Times, Massachusetts is getting crushed by health care costs. A vast majority of people in the state have some form of insurance, but the costs of providing health care in Massachusetts is expected to increase by 42% in 2009 alone.

Now Massachusetts is looking at whether it can regulate insurance premiums – i.e. limit what insurers can charge.

Massachusetts is also deciding whether or not to “bundle” payments for health care. In other words, if you need your appendix out, Massachusetts pays the provider one price to take care of you from beginning to end of treatment for that problem. If you get it done cheaper, the provider keeps the change. If there are complications or if expensive testing is needed, the provider pays out of pocket for whatever costs go above and beyond the flat fee. In theory, providers could lose significant amounts of money by treating high-risk patients who are prone to develop complications or bad outcomes.

This prepayment idea was also tossed about by Michael Canon at the CATO Institute.

On its face, the idea sounds good. But underneath the surface, I think that such a system encourages skimpy medical care and encourages cherry-picking of healthy patients.

Remember the HMOs that paid physicians a flat fee for taking care of all the patients? Remember fighting with physicians for appointments and testing because the physicians had to control costs? How will the system proposed in Massachusetts be any different?

In addition, I think there will be a lot of gaming of the system.

I was going to give examples of how the system could be gamed, but will hold off for now until more about the proposal is disclosed.

I continue to think that “prepayment” or “bundled payment” ideas will have an adverse effect on medical care.

Healthcare policy experts interviewed for the article hit the nail on the head:

Changes in payment practices will not be enough to slow the growth in spending, even when combined with other cost-cutting strategies. To truly change course, they say, the state and federal governments may need to place actual limits on health spending, which could lead to rationing of care.

“Really controlling costs requires just stopping spending,” said Stuart H. Altman, a professor of health policy at Brandeis University.

Taking Care of “Them”

Monday, March 16th, 2009

Tummy Time!This is a stream of consciousness post, so I’ll apologize in advance for rambling. As I read through the post, it jumps around a bit, but it really does get to a point … eventually.

I’ve resigned myself to the idea that our medical system is going to become “socialized”. People want change. Our medical system needs change. President Obama has already stated that we’re going to get change.

As I work my shifts in the emergency department, I see a rather perverse distribution of health care in this country. People who work all of their lives contributing to our economy have little or no access to medical care because it is too expensive and they cannot afford insurance premiums. They make too much money to be covered under Medicaid, they don’t have a disability to qualify for Medicare or disability insurance, and they are too young to meet Medicare’s age limits. In an emergency, the people who sustain our economy worry about how they will be able to pay all of the medical bills. Just being in the emergency department and knowing that soon they will receive a huge bill is as traumatic for them as their illness is. I will never forget about one patient complaint I read that said “As soon as I saw the bill for your services [meaning the hospital ED charges], I almost needed your services again.”

Meanwhile, I see many perfectly healthy people who do not work and who contribute little to the economy who are fully entitled to walk into an emergency department and receive millions of dollars in medical care. Expensive evaluation for coughs, runny noses, pregnancy tests, work excuses, prescriptions for Motrin (so it can be picked up a the pharmacy at no charge), sometimes even follow up care – all at no cost to them in the emergency department.

I dislike the idea of a “socialized” system, but I dislike even more the lack of access to medical care that occurs with so many working families solely because their situation isn’t deemed “dire” enough to receive government handouts.

So socialized medicine, you win. We must take care of our own better than we are doing so now.

Then I sit back and try to imagine how future medical care systems in this country will operate.

I mentioned previously that once socialized medicine arrives, we’ll have to change the way we think about medical care in this country. Here’s another article about how our values affect medical care. I foresee a system in which futile care won’t be provided unless the patient pays for it. I don’t think that’s a bad thing … except we have to come up with a definition for what care is and is not “futile.” It won’t stop there, though. A lot of expensive care will have to be rationed. If patients want expensive care, they’ll have to pay out of pocket for it. Cancer treatment will be limited. Kidney dialysis will probably also be limited. Advances in HIV treatment will be curtailed – if you want expensive medications that have only a small benefit in outcomes, you’ll need to pay the $12,000 per year out of your own pocket. Ditto for the MRI to find out what’s causing your shoulder pain – just go to a government physical therapy program instead.

One good thing about such a socialized system is that once the government stops paying for expensive testing and treatment, market forces will kick in. If there’s no demand for a service because of high prices and lack of government reimbursement, then the entity providing the service either maintains its high prices and caters to the rich few, goes out of business, or lowers its prices to sell more of its product to the masses at less of a profit. Walmart created billionaires with high volume and low prices, not high profit margins.

A socialized medical system will also restructure the insurance industry. Who’s going to want to pay $1000+ per month for insurance to cover routine medical care when you can get routine medical care for free? Maybe boutique practices will become more common – there patients can pay cash for routine medical care rather than endure the wait for free medical care. Cash-only practices will also give patients a greater chance of maintaining their anonymity if they so choose.
Those who want insurance can purchase it so that they have faster access to major surgeries or more access to specialist care. Everyone will get all their care for free, but in the “fast care, quality care, free care” paradigm, people should be able to purchase a right to faster and higher quality care.

Socialized medicine will inevitably bring up new inequalities and new issues. There will be a fundamental unfairness in access to medical care that is not unlike the system we have now – only in the next iteration, everyone will have the same access to some level of government-sponsored medical care … the care will just be time-rationed. The focus of people’s angst will be on the speed at which those with insurance can access their care while those without insurance are forced to wait.
Civil rights groups will complain, but just as with every other private industry in this country, there is not and should never be an entitlement to the best of any product, whether it is luxury dining, luxury autos, luxury housing, or luxury medical care.

I also think that there will be another shift in focus – one that gives me hope, but that also concerns me.

Doctors and hospitals will no longer play the “bad guy” role. Instead, in almost every scenario, the government will take over the role as the “evil villain” that limits care. If a socialized system will pay hospitals and doctors for everyone’s care, providers will have no incentive to limit testing or treatment. Similarly, if patients are getting the care for free, the patients have no incentive to limit their demands. That leaves the government as the source of cost-containment. No longer will patients become outraged at hospitals and doctors. Instead, patients and the healthcare providers will fight the uncaring government.
As in …
The government wouldn’t pay for treatment and let him die.
The government says that the treatment “isn’t supported by evidence.”
The government “couldn’t afford” a costly cancer medication.

My guess is that the system will pit patients and doctors versus the government bureaucracy. Hopefully doctors and patients will be able to work together more as a team.

“Us” against “them”.

When you think about it, though, just like the identical twins in the picture, “us” and “them” are pretty much the same people. “We” will be fighting against a government comprised of “us” who are there to protect “our” interests.

Who really is the “them” part of this equation, then?

Those who use the most medical resources. The chronically ill. Those with severe illnesses.

All that separates “us” from “them” is a serious medical illness.

This is where “we” have to be very careful in designing a medical system for all of “us.”

Those in the “us” camp want to limit payouts from the system – keeping money away from those sickly “them” people who are disproportionately using the system resources.

The care that “we” agree to provide to “them” now will be the same care that “we” receive if we become one of “them” in the future.

Just how well will “our” new system take care of “them”?

That concerns me.

Chicago Tribune Inflammatory Headlines

Sunday, March 15th, 2009

I get news feeds from many national newspapers and the Chicago Tribune has just gotten on my nerves.

First it’s the story about the University of Chicago allegedly sending away patients with [wink wink] “nonurgent injuries” who are not able to pay their bills.

Then there’s the recent story titled “Pay tuition or go home” about a high school “send[ing] 100 out the door until bills are resolved”

Since when is it a newsworthy event to expect that people pay for the services they receive? Isn’t the free market concept one of the things that separates our economy from socialism?

What’s next?
“Grocery store tells shoppers ‘Pay for food or starve’”?
“Gas station demands payment for gasoline”?

The Tribune charges upwards of $10,000 per day for a full page ad in its newspapers and $50,000 per week for an online advertisement on its home page.

I have the next headlines:

Tribune tells destitute businesses “Pay For Ads or Go Broke”

or how about

“Tribune refuses circulation to homeless Chicagoans”

Can you believe that the Chicago Tribune would try to coerce money out of struggling businesses and would discriminate against indigent Chicago residents in these tough economic times?

Unbelievable.

HuffPo Letter to POTUS

Saturday, March 14th, 2009

Excellent letter in the Huffington Post from the “Healthcare System” to POTUS (President of the United States for those that didn’t get the acronym – don’t feel bad, I didn’t know what it meant until recently, either).

Shows a lot of insightful thinking on how to change the system for the better. Throwing money at the system will not change the lack of healthcare providers, medical errors, avoidable deaths, the horrible medical malpractice system, or the worsening health of our population. Get rid of the bloat. Focus on outcomes that actually matter (and 4 hours to antibiotics isn’t one of them). Pay attention to infrastructure.

I hope that the powers that be incorporate these ideas into whatever new system that is created.

The Bane of Electronic Medical Records

Saturday, March 14th, 2009

Poignant Op-Ed piece in the NY Times a week ago titled “The Computer Will See You Now.”

Comments to the editorial seem to feel the same way as the author.

Apparently, medicine isn’t adopting the computerized record as quickly as everyone would like.

Will care be better when we do so? I’m not so sure.

Interesting that there was another Op-Ed piece by the exact same title written in 2005 by a different author … noting how the computer is depersonalizing medicine.

“I’m Gonna Die”

Friday, March 13th, 2009

There are certain phrases that evoke strong feelings in me when I hear them.

“I’m gonna die” happens to be on that short list. Patients scare the hell out of me when they say they’re going to die and give me that look.

Car accident victims. Patients having heart attacks. One guy who was vomiting and ended up having a massive GI bleed.

All of them gave me the look of death and said “I’m gonna die.”

They were all right. In my experience, more often than not, people who say those words end up being right. One minute they’re looking at you and talking, the next minute, they’re going toward the light.

It’s eerie. Almost seems like people get some sixth sense about when their time is up. Even more scary is that sometimes my face is the last one they see before “crossing over.”

When someone well-known to the staff says those words, it’s almost surreal. You’re so used to dealing with a person, it’s difficult to think of that person not being there anymore.

The Mayor got that feeling not too long ago. His cancer of many years apparently came back with a vengeance. He came in with a new complaint of difficulty breathing a few months back and a chest x-ray showed diffuse lung cancer. Treatments didn’t help. During one of his recent admits, he went around to all the hospital staff telling them “thanks” for taking care of him and saying his “goodbyes.” He felt as if he would die soon. He, too, was right.

This week, the Mayor died.

Going to be strange not fighting with him about why he doesn’t need to be admitted the day after being discharged.

It will be hard to forget his little brown suitcase.

Strange, there has been a noticeable increase in the amount of soda present in the physician’s lounge. I wonder if he …

Nah.

Rest in peace, Mayor.

Help a Kid With Cancer

Thursday, March 12th, 2009

Been busy the past week, so have basically been scheduling posts several days in advance and haven’t been on the internet a whole lot. Unfortunately, I haven’t had a chance to read all my favorite blogs (and working a shift in a couple of hours, so I still haven’t had the chance), but I noted that ShadowFax is getting his head shaved in the name of St. Baldricks – the patron saint of saving kids with cancer.

If you have a few extra dollars left over from your income tax refund, put it to good use. ShadowFax is a member of Nathan’s Network – named after a little boy who died of a brain tumor at age 4.

Oh, I heard that ShadowFax is sending a lock of his hair to anyone that donates $50 or more.

Plus, I read somewhere that anyone who donates goes straight to heaven.

Give it a thought …

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