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Freakonomics Radio - Are You Really Allergic to Penicillin_ _Update_

Published Jul 17, 2026 · Duration 1:05:13 · Language en · 7 highlights

Summary

这期《Freakonomics Radio》节目探讨了青霉素过敏被广泛误诊的现象。主持人Stephen Dubner以自己为例:他从小被告知对青霉素过敏,回避了约50年,2024年一场久治不愈的重病后才做检测,结果证明他其实并不过敏。节目指出,约10%的美国人(超过3000万人)以为自己对青霉素过敏,但真正过敏的不到1%,其中约90%实际上完全可以耐受。被错误贴上过敏标签代价高昂:患者被迫使用更贵、副作用更大、更易引发耐药性的替代抗生素,甚至导致更高的手术感染率和14%的全因死亡率上升。几位过敏专科医生(Elena Resnick、Kimberly Blumenthal)介绍了皮肤点刺、皮内试验和口服激发等“去标签”流程,并呼吁把简单检测推广到基层医疗。节目还延伸讨论了食物与环境过敏的上升、“卫生假说/老朋友假说”、蜱虫叮咬引发红肉过敏等前沿话题,以及过敏研究在医学界资金链中被长期忽视的困境。核心结论是:如果你以为自己对青霉素过敏,应该去做检测,因为这个几十年的常识很可能是错的。

Highlights

  1. The studies show that 90% of people who believe that they are allergic to penicillin actually can tolerate it. So that sounds absurd, obviously, that so many people are walking around with this false belief about themselves.

    研究显示,90%自认为对青霉素过敏的人实际上完全可以耐受它。所以这听起来显然很荒谬——竟有这么多人带着这种关于自己的错误认知在生活。

    The central, counterintuitive statistic of the whole episode
  2. I think you were 100% wrong, I'm sorry to say. The other drugs were so lucky to have them, but many of them have much more severe side effect profiles than penicillin does... and in certain cases, for example, vancomycin, they can actually increase the risk of drug resistant bact ...

    很抱歉地说,我认为你百分之百错了。有那些替代药物我们很幸运,但它们中许多的副作用比青霉素严重得多……而且在某些情况下,比如万古霉素,实际上会增加耐药菌的风险。

    Demolishes the common excuse that a penicillin allergy doesn't matter
  3. If I were to see something like five patients for this a week, myself, and I've been doing it for over a decade, we're near 3,000 patients. I've seen probably 20 allergic.

    如果我每周大约看五个这样的患者,而我已经做了十多年,那就接近3000名患者。我大概只见过20个真正过敏的。

    A clinician's firsthand numbers are even more extreme than published stats
  4. My father died of a bee sting. He died from an anaphylactic reaction to bee venom. He had had a reaction in the past, but it was fairly mild just swelling at the site... And he died on the second sting.

    我父亲死于一次蜜蜂蜇伤。他死于对蜂毒的过敏性休克反应。他过去曾有过反应,但相当轻微,只是叮咬处肿胀……而他在第二次被蜇时就去世了。

    A stark personal tragedy that drove a researcher's whole career
  5. We did an all-cause mortality study in a very nicely controlled observational study. 14% increased all-cause mortality.

    我们做了一项设计非常严谨的观察性全因死亡率研究。结果是全因死亡率增加了14%。

    A shocking hard outcome: a mislabel can literally raise your risk of dying
  6. I can tell you with confidence that I was the first penicillin allergy grant that the NIH funded in 30 years... it was very hard to know who takes ownership of something that crosses every single discipline.

    我可以很有把握地告诉你,我拿到的是NIH三十年来资助的第一个青霉素过敏研究项目……很难界定谁该为一个横跨每一个学科的问题负责。

    Reveals how badly this huge public-health issue is underfunded
  7. We published a paper in which we showed that if people watched a screen, they took less deep breaths. If they're reading a book, they still breathe normally. If a child is watching television and you touch their shoulder, they actually jump slightly because they're in a trance.

    我们发表了一篇论文,表明人们盯着屏幕时深呼吸会减少。如果他们在读书,呼吸依然正常。如果一个孩子在看电视,你碰他的肩膀,他会微微一惊,因为他处于一种恍惚状态。

    A wonderfully unorthodox theory linking screens, breathing, and asthma
Full transcript

Hey there, it's Stephen Dubner. Until last year, I believed that I was allergic to penicillin. That belief caused me some unnecessary trouble. And I am not alone. As I learned, 10% of Americans believe they are allergic to penicillin, but true penicillin allergies are much rarer than that. So...

We made an episode about it, which we first published last year. Since then, we have heard from a ton of listeners who checked out their own alleged penicillin allergies. And you may have run across this topic on the HBO medical drama, The Pit.

But many, many people still avoid penicillin based on a faulty diagnosis. So we decided to replay this episode for you today. As always, we have updated facts and figures as needed. All your feedback is welcome. Our email is radio at Freakonomics.com. They say it is always a good idea to express gratitude. So here's what I'm most grateful for right now. My health. For much of 2024, I was sick.

It started in the spring with a cough that turned into a respiratory infection. That turned into a whole other thing, and for a few months I was miserable. It hurt to talk or swallow. Every time I laughed it would trigger a coughing fit, which is a problem because I like to laugh. Thanks to the cough, I couldn't sleep through the night. I also had some ferocious night sweats and crazy dreams.

During the day, my entire body ached like I'd been hit by a car. Also, no appetite, no energy. Physically, it was the worst few months of my life. But at least I got a story out of it. This one. Today's episode is about penicillin. You may remember the famous story of how penicillin was discovered accidentally nearly 100 years ago by Alexander Fleming. This was at St. Mary's Hospital in London. Fleming was just returning from holiday. In his lab he had left behind a Petri dish where he'd been culturing bacteria and he found some mold growing in the dish. Interestingly, where the mold grew the bacteria did not. It turned out that this mold juice, as Fleming called it, could kill many

types of bacteria, not just the one growing in that petri dish. Penicillin was eventually used to treat strep throat, meningitis, dental infections, gonorrhea, and much more. It came to be thought of as something like a miracle drug. The penicillins are in fact a family of antibiotics, including moxicillin, ampicillin, methicillin, and several others.

All these years later, they are still among the safest, cheapest, and most reliable drugs around. They have saved hundreds of millions of lives. Even with all the new antibiotics since then, penicillin is still prescribed at the highest rate of any antibiotic. But there's one big problem. 10% of Americans, more than 30 million people, are allergic to it. At least that's what the conventional wisdom says. But The new year is also a good time to tear down conventional wisdoms, especially if they are disastrously wrong. And this one is. So today on Freakinomics Radio, why do so many of us think we have this allergy? Huh. This patient told me they were allergic to penicillin. Oh, it's that your mom told you when you were a kid. Well, what happened? Oh, you don't even know what happened? What should be done about all these false positives?

We should be screaming from the rooftops. This is a misdiagnosis. And what about all the other allergy controversy we hear about, like food and environmental allergies? How bad is the confusion there? It's bad. It's one of the reasons I can't tell you how many people actually have an allergy. What can we tell you? A lot. Starting now. This is Freakonomics Radio, the podcast that explores the hidden side of everything with your host, Stephen Dubner.

Okay, here is the startling fact that I recently learned. While it is true that around 10% of Americans believe they are allergic to penicillin, fewer than 1% actually are. How can there be such a huge gap? And what are the costs of that gap, the medical and economic and social costs? Those are some of the questions we will try to answer today, starting with this new friend of mine. Elena Resnick, I'm an allergist and immunologist.

And how does one get interested in allergy and immunology? I always knew I wanted to be a doctor. My dad's a doctor, and there was never any doubt about that. I was lucky to have a lot of great mentors along the way. My mentor in college, Jerry Groupman, who's up at Harvard.

was very instrumental in my choices. I worked in his lab for four years, applied to medical school, thought I wanted to be a hematologist oncologist like him, explored that field. And later into my residency, I explored allergy immunology, which has fascinating medicine and amazing potential to make people feel better. Give me a little bit of fascinating medicine. I find almost every branch of medicine pretty fascinating in part because There's so much mystery still. I mean, as much as we've learned, there's still so much that we don't know. So what was it that really got you hooked there?

The immune system in particular is fascinating because we know so little about it. It's so important, right? We need our immune system to protect us from disease and to fight things off. When it goes haywire, we can end up with autoimmune disease, which is where our own antibodies attack us. Or we can end up with allergic disease, which is when different types of antibodies, IgE antibodies, react against substances that are harmless. But if we make antibodies against them, we can run into big trouble. Define IgE for me? IgE is immunoglobulin E. It's an immunoglobulin that's made by B cells. It probably had more of a function evolutionarily in terms of fighting off parasitic disease, etc.

It certainly was not evolutionarily made to react to peanuts and pollens, but we don't know why in some people those types of antibodies are made that are specific against harmless substances. Peanuts and pollens, milk and eggs, soybeans and shellfish, these are just a few of the most prominent allergies that tens of millions of people report today. Like Resnick says, harmless substances for most people that cause allergic reactions in some.

Given the magnitude of allergies, especially in the US, you might think that there are a million Elena Resnicks out there, but she is one of just 5,000 allergists in the US. If you need an anesthesiologist, there are more than 40,000. If you need a pediatrician, there are 60,000. But I needed an allergist, and Elena Resnick was the one that my primary doctor sent me to. Here's what happened. Like I said earlier, I got sick last year.

It started with a dry cough that wouldn't go away. So I went to my primary doctor, who I've been seeing for years. Her name is Rebecca Kurth. I love Dr. Kurth. She is very smart, a true scientist. She's determined and methodical, but also a friend and an ally. She's taught me to be vigilant about my health without being paranoid, which I think is a good middle ground.

There was one thing she had been wanting me to take care of for a while, but I never did. My medical history says that I'm allergic to penicillin. The first time I saw her, she asked, how do you know? And I told her the story that lives in my memory that I've been allergic since I was a little kid based on what my mother told me, which was based on what our family doctor told her. And that's when Kirk told me that this kind of story is very common.

but that the vast majority of people who think they are allergic to penicillin are in fact not. So at some point, this was still years ago, Dr. Kurth told me I should try to get my penicillin allergy cleared. This was the first I'd ever heard of being cleared of an allergy. It's also called being delabeled. Way back then, she gave me Elena Resnick's phone number, but I never called. It just seemed like a hassle.

time-consuming and expensive. And I didn't see why getting cleared for penicillin was a big deal since there are so many modern antibiotics. So I did not go see the allergist back then. Fast forward to 2024. And here I was, sick with a cough that wouldn't go away.

Dr. Kurth gave me what's called a Z-PAC or azithromycin. That's a short course of antibiotic that's used in a variety of cases, especially for patients allergic to penicillin. The Z-PAC didn't help. I got sicker. The cough got worse. I went to a radiologist and had a lung scan to look for cancer. No cancer. I began to wonder what would happen if I could take penicillin. Would it fix me or would it maybe Kill me. There is a scary sounding word we all think of when we think about allergies, anaphylaxis. Here is Elena Resnick again. It's the most serious type of IgE mediated allergic reaction where the allergy cells explode. They release all sorts of mediators, histamines, triptase, et cetera. And that causes your vessels to vasodilate. Fluid runs in, people get hives, people get swelling, people's throat closes up or your difficulty breathing.

So what's happening when you die from anaphylaxis? Your airway is basically constricted? Exactly. Your airways constrict and because the vessels all over the body are dilating, your blood pressure drops, you can't get blood back up to your heart and you have a cardiac arrest. So what share of people in the U.S., let's say, who believe that they are allergic to penicillin are in fact allergic to penicillin?

The studies show that 90% of people who believe that they are allergic to penicillin actually can tolerate it. So that sounds absurd, obviously, that so many people are walking around with this false belief about themselves. Are there any similar wrongly held beliefs in medicine that you can think of? Oh my gosh. I don't know that I can think of any. I think that the vast majority of people either have or were told that they had some sort of reaction in childhood. So that is the most common history. The story that I told myself my whole life when I was thought to be allergic to penicillin was, well, you know, medical research has been so amazing that there are all these other drugs and like penicillin or the class of drugs called penicillin. It doesn't really matter if I can't have access to them. How wrong was I in that assessment?

I think you were 100% wrong, I'm sorry to say. The other drugs were so lucky to have them, but many of them have much more severe side effect profiles than penicillin does. They can have more serious complications. They're much more expensive. And in certain cases, for example, vancomycin, they can actually increase the risk of drug resistant bacteria. So you can see the problem here. A lot of people who would benefit from penicillin think they are allergic to it and that they might die if they take it. The vast majority of them are not allergic but many of them don't even think to get cleared and doing so takes some effort. It starts with what's called a prick test. Elena Resnick again.

How do we do that? So every good experiment has a control and the controls that we use are saline, which is salt water. Nobody is allergic to that. And histamine, which is the body's allergic chemical. So we prick you. And when I say prick, I mean, we clean off the forearm and then we use tiny needles to introduce just under the surface of the skin, saline, histamine, and our penicillin reagents. So it's four small pricks under the surface of the skin. So you're not giving me enough to hurt me if I am allergic?

Exactly. But if I am allergic, then what happens? If you are allergic, we would expect that where we pricked you with the saline, nothing would happen. Where we pricked you with the histamine, you'll get a red itchy bump. And where we prick you with the penicillin, you will also get a red itchy bump. That's considered a positive test. We say you've tested positive for penicillin allergy. That's it. Go home. Continue to avoid penicillins.

If it's negative, we go on and do the intradermal test, which hurts a little bit more. We're using the same reagents and we're putting them just under the surface of the skin. And again, we look to see, do those bumps get any bigger during the waiting period? And we're comparing them again against saline. If that test is positive, again, you go home. That's it. You're allergic. But if that test is negative, we now have a skin prick and intradermal tests that are both negative. And the studies show that in those cases it's 95% likely that you'll then pass a penicillin challenge. I think in real life it's probably much, much higher than that.

But we go ahead and we do an oral challenge, which is just what it sounds. We give you a dose of a penicillin. We use a moxicillin, which is a common oral penicillin. We give you that dose. We have you wait in the office for about two hours just to make sure that you're fine. And that's the gold standard, right? Tests are tests. But if you take the medication and you're fine, then we know you're not allergic.

This clearing process that Dr. Resnick just described that's what I did in her office a few months ago I did the skin prick test I did the intradermal test both negative and then at a later visit I took a dose of penicillin and I waited in her office for a couple hours to see if I had an allergic response I Did not I could now definitively say that I am not allergic to penicillin probably never was, although it is true that some people grow out of allergies over time, just as some people grow into them. But whatever childhood rash or temperature spike had led our family doctor to declare me allergic to the penicillin he gave me was likely due to something else, perhaps a viral infection rather than a bacterial one. So now I could take penicillin if I needed it and it appeared I might.

because my illness had deepened. I went back to Dr. Kurth's office for another round of tests, and we turned up some interesting evidence this time. By now, I had something called non-group A strep throat, which seemed to be responsible for some of my symptoms, but I also had thyroiditis, an inflamed thyroid gland. This was the first time in my life I'd ever thought about my thyroid gland. I didn't even know where it is. It turns out it's in the front of the neck.

and it's shaped like a butterfly. It is also a quiet superstar of the immune system. The thyroid produces hormones that help regulate everything from brain and muscle function to body temperature and heart rate. It can also pitch in when your immune system is already under attack and that's probably what happened to me. The strep got so bad that the thyroid marched in like some auxiliary army, but without any specific orders, it just started shooting out hormones. So I was a mess, but I was no longer allergic to penicillin.

So I swallowed as much amoxicillin as dr. Curth would allow and even though it took a while the healing began my cough gradually died down my voice started to come back and then my energy too I started sleeping through the night. That was probably the biggest thing for the first time in months. I felt human Could all that suffering have been prevented if I had taken penicillin back when the trouble started It's hard to say for sure, but it's quite possible. Here is another physician who specializes in allergy. Nothing kills bacteria better than these drugs. That is Kimberly Blumenthal. She is an allergist, immunologist and researcher at the Mayo Clinic. When we spoke with her for this episode, she was at Mass General Hospital and Harvard Medical School. Blumenthal has written dozens of papers about penicillins, not just about the allergy confusion, but about their effectiveness.

If your infection is sensitive to these drugs, they are the best drugs out there. From an adverse effect profile, they're also much more benign than other antibiotics. Unless you happen to be allergic. Unless you happen to be allergic. Penicillin allergy was described immediately after penicillin was released and it's the same with all drugs. You release new drugs and we find patients that are allergic.

but antibiotic allergy is misdiagnosed most of the time. Why is that? When we have infections, we get rashes. It's really as simple as that? Yeah, especially in children. Children get rashes when they have infections. Those infections are treated with antibiotics. There's misattribution of allergy. So often it might even not have been a bacterial infection. It might have been a viral infection. Absolutely. For years and years, we have had This idea that an infection requires antibiotics and only like past five, 10 years, we've tried to pull back on that because of antibiotic resistance. So the moral of the story is if your kid is really sick, just let him stew. Is that the moral of the story or not quite? Don't act too fast, right? I think it's good to be a really busy parent and not be on top of it and rushing them in right away.

But to be fair, when the parent rushes them in, then it's the physician's opportunity to slow things down. Yeah, and some people do it better than others. There are these fantastic discharge prescriptions that aren't actual prescriptions. Things like, rest and drink plenty of water and Nana's chicken soup.

take Tylenol or Motrin for fever. And then if things a week later are still in the same place or things worsen, then call me back and then we treat with antibiotics. When Blumenthal was in medical school, she became fascinated by the idea that two patients with the same infection could have entirely different outcomes depending on how they were treated. I really was drawn to the idea of how important the choice of what drug.

was the key decision. What drug is right for this patient? I pretty immediately realized that regardless of what nonspecific garbage was listed on the allergy list, it really changed care. And I just got totally distracted as to like, does it need to change care? Why is there a two-tier system? If you have an allergy, you treat with this, but everyone else who doesn't have an allergy gets this.

I realized that what we were calling allergy was mostly side effects. So if we're drawing a kind of SAT style analogy and penicillin is to these bacterial infections as a hammer is to a nail, let's say, it's the right tool for the right moment. What would the typical non-penicillin antibiotic, what would that be if one suspects that a patient is allergic to penicillin? Something way too big to hammer in the nail. Some sort of mallet is like, you know, I don't do tools and hardware. Would it be like a leg of lamb perhaps? Sure, maybe could get the job done, but by kind of making a mess. So talk about your own practice as a clinician and tell me roughly if you can, how many people have you tested over your career who

thought they were allergic to penicillin and what share of them actually were. If I were to see something like five patients for this a week, myself, and I've been doing it for over a decade, we're near 3,000 patients. I've seen probably 20 allergic. When you say you've seen 3,000, those are 3,000 who are suspected of being penicillin allergic.

Yeah, they present to my clinic at the suggestion of their primary or their surgeon or themselves. Yeah, I would say it's probably been 3,000 patients that I've seen myself. I know and remember two severe reactions. That's it. The rest have been rashes. It's even worse than most of the published numbers I've seen. Most of the published numbers say that roughly 10% of the US population is thought to be penicillin allergic. But of that 10%, roughly 90% are not. According to you, it sounds like it's more like 99% that are not. 99 in my practice. Can you think about another area of medicine where that rate of false positives exists? No, and this is why we should be screaming from the rooftops is misdiagnosis. This is a missed diagnosis. Everyone has something on their chart that's wrong and nobody is.

screaming about taking it off. We reconcile medicines every visit. I'm taking this, I'm not taking this. We try to take care to make sure what is in the chart is correct. This is something that is not ever addressed and is incorrect in the majority of people. Coming up after the break, we take a look at misdiagnosis around food allergies. He used to fight with people to get them to recognize that their issue is food allergy, and now he fights with people to get them to recognize that their issue is not food allergy. I'm Stephen Dubner. This is Free Economics Radio. We'll be right back. You could imagine that artificial intelligence will soon be helpful in sorting out things like who's allergic to what, but we're not there yet. For now, allergy is often a guessing game, a bit of grasping in the dark. It's estimated that roughly 40% of humans have some kind of allergy.

That's expected to rise to 50% by the next decade. Why? We've already heard from a couple of allergists, but to answer this question, we need someone with a broader view. We need a medical anthropologist. Medical anthropology is looking at all the social and cultural factors involved in healthcare systems. We think about how all those beliefs and politics and economics, how all of that factors into the choices people make about their health and how they view their health. This is Teresa McPhail. I'm associate professor of science and technology studies at Stevens Institute of Technology. McPhail recently published a book called Allergic Our Irritated Bodies in a Changing World. She writes that roughly half a billion people suffer from food allergies alone.

That's been a puzzle as to why an immune cell will take a look at something that is otherwise harmless and decide that it's not and do it after sometimes years of tolerating it just fine and suddenly now it's a problem. Just tell me why and how you became interested in the notion, the big notion of allergy. My father died of a bee sting.

He died from an anaphylactic reaction to bee venom. He had had a reaction in the past, but it was fairly mild just swelling at the site. That's mostly what happens to anyone who gets stung by a venomous insect. And he died on the second sting. We really don't know how many times he was stung because he was a Vietnam vet, so there's a chance that he was stung prior to that. And I got curious about my own...

susceptibility to such things. Years later I was diagnosed with allergies, but I am one of the rare people that do not react to skin or blood tests. I have low levels of IgE, the antibody that is driving the allergic response. So there's no way to tell what I'm allergic to except that clinically you can see the signs and symptoms that I am allergic to something. So what are you allergic to?

I think based on my years of detective work that I'm allergic to grass and probably ragweed and maybe dust mites. Can you just say what an allergy is and what an allergy is not? Oh boy, how much time do we have? This is part of the problem. There's a lot of confusion about what an allergy is and isn't. The easiest answer I can give you is that an allergy is when Your body responds to something that is otherwise harmless and triggers an immune response. If your immune cells are not involved in the response, then it is not an allergy. The classic example is milk allergy versus milk intolerance. On the surface, if you have a mild milk allergy, it's going to look the same perhaps, an upset stomach, feeling kind of gross.

some gassiness, but the difference is with the intolerance there's something else going on. In this case, you're not able to digest lactose because you lack an enzyme. But it's producing symptoms that would seem familiar to someone whose immune cells, whose T cells and B cells are producing antibodies and attacking that milk protein.

except that the allergy can, you know, escalate. You can get a skin rash, you can get wheezing, and you can end up in the ER with a full-on anaphylactic event. That's not going to happen with intolerance. But if you have mild forms of this, you're going to be confused and you might just assume that you have an allergy. And the only way to know for certain is to see an allergist. The problem there is we don't really have enough of them.

They're specialists and you need a referral to see one and so a lot of people are out there self-diagnosing. Are allergic rates rising or is there just more awareness and or diagnosis and or treatment? We think as far as we can tell that they are rising but it's complicated. We know that rates of asthma and hay fever started to rise post-World War II, like 1950s, 1960s, and continued right up until the 1990s. And now they seem to have been flattened, but what has been rising in the wake of that are rates of food allergies. We know this because of several reasons. One is you can look at ER visits. You can see when someone is showing up with asthma or with

a rash, like a very bad eczema, eruption, or they are having anaphylaxis. The other thing that we can track is EpiPen or adrenaline prescriptions. Those raised three to four times from the 1990s to around 2018-2019.

As with penicillin, the discovery and isolation of adrenaline is another great story for medical history. I won't go into the details here, but it's worth reading about if you're so inclined. A dose of adrenaline, or epinephrine, administered in an epi-pen, for instance, is the first-line treatment for anaphylaxis. When Theresa McPhail cites the huge spike in epi-pen prescriptions as evidence of a huge spike in allergies? Well, she also points out that much of the demand was driven by the supplier. Mylan Pharmaceuticals marketed the EpiPen aggressively across many channels. Over one 10-year period, McPhail writes, they hired more lobbyists than any other U.S. company. This led to a relabeling of the drug by the FDA, which made more people eligible to take it.

Mylan also lobbied state legislators as a means to get more EpiPens into schools. They also partnered with Disney to produce children's books about allergy sufferers. So how big is the allergy market? The global market for epinephrine is about $2 billion a year with 60% of that sold in the US. If you look at hay fever, one recent study put the cost of treating Americans at over $4 billion a year, more than a billion of which goes to medication. If you look at the entire category of allergy remediation, the global sales of tests and treatments is around $40 billion a year. So how much of the allergy boom has been driven by more allergies versus well-run pharmaceutical campaigns? It's hard to say.

There are a variety of factors that may be driving allergy increase. Some research shows that environmental and chemical disruption may play a big role. I asked Theresa McPhail about some other potential drivers. Many, many, many people have by now heard or read about the notion of allergy rising because we, especially we of the children variety are not exposed to enough things, pathogens or allergens or whatnot that we don't roll around in the dirt and so on. Right. So in the 1980s, this is after the massive rise of asthma, we're starting to see food allergies. An epidemiologist was curious about this and started collecting data on families and realized that older siblings seem to have more allergic disease than younger siblings.

The theory was that older siblings bring home colds and track in bugs to expose their younger siblings. And there was something about that earlier exposure that had somehow protected these younger siblings. It was called the hygiene hypothesis that is morphed over the years to what is now called the old friends hypothesis, which is nice, isn't it? That's a nicer way to put it.

that there's something about getting the right exposures to the right bacteria or the right viruses in fungi that will help train our immune system. You're born with a novice, a naive immune system that hasn't seen anything. And you're born with an innate immune system, which means There are things online from the very beginning that just act as a brute force response to anything that threatens the individual. And then you have an adaptive immune system which involve your T cells and your B cells and your antibodies that remember the things that you've been exposed to. And so the theory is those have to be trained and they have to be trained in the right order and they have to be exposed to the same type of

bugs, microbes, that they would have been evolving with for millennia. The theory is that we've changed so much that some of those are missing. It has confused our immune system to the extent that you're seeing more allergic disease because you're not getting the training. It feels as though every time I go to a restaurant these days, the server will ask, is anyone allergic to anything? Do you know anything about that?

It's basically advocacy. And at the forefront of that is a group called FAIR, which is food, allergy, research, and education. They're privately funded and run by a group of parents. When I started researching the book, one of the first people I sat down with was Helen Jaffe. Her and her husband, David, are some of the founding members of FAIR and they also have helped to fund the Jaffe Center at Mount Sinai for food allergy research. When they started the foundation, it was because two of their children had quite severe food allergies, but it was at a time where no one was doing this. They live here in New York City and they had to take the train down to Johns Hopkins to see Dr. Hugh Sampson

He's a renowned food allergist and researcher, and he has been doing this for over 40 years. But at the time, there were maybe half a dozen people focused on food allergy. And so initially, Helen told me that their focus was really on education and research funding to try to figure out what was going on, why the rates seemed to be rising, figure out more about the biological mechanisms that drove this response.

I spoke with Dr. Hugh Sampson now, we're talking about years later, and he said he used to fight with people to get them to recognize that their issue was food allergy, and now he fights with people to get them to recognize that their issue is not food allergy. Can you explain? I do see on the fair website that 50 to 60% of all blood tests and skin prick tests for food allergy testing will yield a false positive result. Correct. So that sounds absurdly bad. Is it not as bad as it sounds or is it that bad? No, it's bad. It's bad. I mean, diagnostics are one of the sticking points. It's one of the reasons I can't tell you how many people actually have an allergy because we're stuck with primarily the skin tests, which were invented in the

late 1800s by a UK physician, Dr. Charles Blackley. Wait, the late 1800s? Yes. And if I exhumed him and revived him, he would have no problem giving a skin test today. What about false negative? That's what we should be really concerned about. That is the better situation. It's around 95% certain if you do not respond that you are not going to respond in real life. So that's good news, at least.

Yes, that's good news. That's why we still use them because it's almost like a differential diagnosis. We can rule some things out. So you mentioned in the book that your aunt and your grandmother were allergic to penicillin. Yes. Given everything we've discussed about testing or the lack of great testing and the murkiness surrounding this area, do you think that they actually were allergic to penicillin or maybe?

In my grandmother's case, we know because she was in the hospital and had an actual skin eruption and reaction to penicillin. I honestly don't know about my aunt. Sorry if she's listening to this. Because to my knowledge, she's never been tested. So I don't know. She does avoid them though. At the end of the day, I suppose it doesn't matter. I suppose it doesn't matter, Theresa McPhail says.

That's what I used to think, that a penicillin allergy is no big deal since there are other newer antibiotics that do the same thing. But the allergists we heard from earlier, Elena Resnick and Kimberly Blumenthal, they told me that that is simply not accurate. Resnick told me about a pregnant patient of hers who showed up with a penicillin allergy on her chart.

Penicillins are an amazing drug also because we know them to be safe and effective in pregnancy when a pregnant woman goes into deliver if she is colonized with group B strep which is a very common vaginal infection.

she must be given antibiotics before delivery to ensure that the baby is not exposed to the group B strep. So the antibiotic of choice for group B strep is in the penicillin family. Mom comes in, she's ready to deliver, she gets a dose of penicillin, she gets her second dose four hours later, she delivers the baby, everything is fine.

if she is thought to be penicillin allergic, instead she's given vancomycin. Vancomycin dosing interval is every 12 hours. So if she's not dosed appropriately, the baby can be considered inadequately treated, and that leads to all sorts of other potential decisions, maybe getting put on antibiotics, maybe going to the NICU. Again, the complications just from this penicillin label are intense.

In this particular scenario, this mom went in to deliver. She was thought to be penicillin allergic. They gave her vancomycin. She developed red man syndrome from the vancomycin, which is just what it sounds like, where the body becomes completely red and flushed and other medications have to be given. And then she had a wound infection from her C-section because she was still thought to be penicillin allergic. They gave her clindamycin to treat the wound infection and she developed C-diff.

from the clindamycin. And how did that play out? So when you develop C. diff, then you have to be put on oral vancomycin and then treated usually for two weeks. It's just a nightmare. It's one thing after another. And then she came to see me and we were able to clear her of that penicillin allergy. Why did she come to you in the first place?

So her OBGYN, we also rely on the OBGYNs to find people who in their charts have this penicillin allergy. The problem with that is we're not going to test a pregnant woman just on the off chance that she does end up being one of these rare people who's truly allergic. Obviously we don't want to put a pregnant woman into anaphylaxis. So we're sort of stuck with that label, which is hard for the OB because then their patient gets a simple infection. They can't use a penicillin. So a lot of the OBs will say to their patients, before you get pregnant again, better go get cleared of your penicillin allergy. The fact is that a mislabeled penicillin allergy, and as we've established, the vast majority of penicillin allergies are mislabeled. This is a serious thing. The risk of post-surgical infection is much higher. So are your chances of dying. Kimberly Blumenthal from the Mayo Clinic published a study comparing the long-term outcomes of 60,000 patients with a penicillin allergy in their medical record,

versus more than 200,000 patients without. We did an all-cause mortality study in a very nicely controlled observational study. 14% increased all-cause mortality. Wait a minute. If being labeled penicillin allergic is producing that many more deaths, what exactly are the adverse outcomes that you're avoiding if you're able to take penicillin? There's avoiding antibiotic resistance, C. difficileitis.

avoiding too long of hospital stays, avoiding surgical infections if you had needed an operation, and then there's avoiding other adverse events that result from a choice of antibiotic that's just more toxic and by its nature caused more renal failure or caused more diarrhea or whatnot. This may be impossible to say, but let's say there are two observationally equivalent patients. Let's say me and let's say I have a twin.

And one of us has been labeled penicillin allergic. The other hasn't. We have the same medical problem come up. I'll let you pick the problem. One of us receives a penicillin drug. The other is not eligible to do so. Even if his allergy isn't real, we think it's real. How would you think about comparing the medical and economic outcomes of person A and person B?

It's such a no-brainer. I mean, when you give me this description, what comes to mind is two people who have strep throat. Strep throat and a penicillinology label. One person gets penicillin. That's indicated for penicillin. Strep throat goes away. No long-term sequelae. They're fine. It was cheap. And then the other person gets a Z-PAC, a Zithromycin. And it doesn't fully go away. Then they call back and they get another antibiotic. Maybe this time they get...

a bigger antibiotic, and that causes some problem. They might get a tonsillar abscess. They get a quinolone, seprofloxacin unnecessarily, or some other medication. I mean, I don't know what any of those are, but all those syllables sound bad to me. Yeah. There's no rule like the more syllables the antibiotic has, it's worse. I wish it were that simple. Okay, that's not simple, but this is misdiagnosed penicillin allergies.

are costing all of us a lot of suffering and dollars. So why isn't more being done to solve this problem? Because the public doesn't decide which grants get funded. That's coming up after the break. This is Freakin'omics Radio and I'm Stephen Dubner. Once you know about the benefits of penicillin and how millions of people wrongly believe they are allergic, You can't help but think about the costs of this misdiagnosis. Not just the bad health outcomes and the complications, but the financial costs too. That's why some specialists are pushing for more testing and de-labeling of people who think they are allergic. That might cost a lot up front, but when one in ten people think they have a medical handicap and they don't, this actually presents an opportunity to save money.

It might even be worth testing every single person whose medical history says they are allergic. Here again is Kimberly Blumenthal from the Mayo Clinic. We can evaluate for penicillin allergy with simple tests. And these simple tests need to be delivered to that 10% of America and reimbursed appropriately and taught to a non-specialist workforce. Could be a welcome to college visit.

I mean, welcome to Medicare visit. How much money could you save by doing this? Just my healthcare system would be millions. If we evaluated penicillinology, de-labeled the appropriate ones, we would save millions of dollars just my healthcare system. So it must be in the billions. You'd save it how? You save on antibiotic expenditure. Just because penicillins are cheaper than the other antibiotics? Yes.

You'd save on adverse effect avoidance. Meaning penicillins don't cause as many adverse effects as other antibiotics? Yes, and some of these adverse effects lead you to the emergency room and another hospitalization. You would save on surgical infections, a tremendously costly thing. Blumenthal tried to make these cost savings a reality when she worked in the Mass General Hospital system.

In our hospitals without an hour just involved there is sort of algorithmic care that can clear allergy in low risk situations with just a protocol just a little bit more observation you're ready in the hospital you're being observed. Your vital signs are already on record there. Yeah. And is the idea as simple as you feed the key vital signs into.

the allergy algorithm and see if indeed there's a likelihood that that person is not allergic and then maybe do some challenge testing. Is that the way it works? We do it when patients have infections. So we don't do it electively like if you're there for something not related. But if you have an infection that an allergy is getting in the way of best care, we have a two-step drug challenge process. And as long as the patient's healthy enough to do that.

we do it. So we give a small amount, watch the patient, give a full amount, watch the patient. And then if that's the drug that they need to be treated with, they just continue that drug right then and there. Since there is a treatment for the allergic response, but the default is to not give penicillin if there's a suspicion of allergy, what would happen if you just flip the default and said, no, no, no, we're just going to give penicillin. And if they happen to be in the small group of people who are allergic, then we'll watch and we'll treat it. Is that such a terrible idea or would you kill a bunch of people by accident that way? You would kill some people by accident and in America it's just a non-starter. Because we don't want to kill anybody you're saying? Well there's also this doctor first do no harm like the oath we take and it feels wrong to just disregard allergy labels entirely. The hospitals where Blumenthal worked have achieved a 9% de-labeling rate

over a decade. The national delabeling rate is less than 1%. There's something interesting to notice about Blumenthal's approach. Many specialists in many industries are always trying to grow their leverage to become ever more powerful gatekeepers. Blumenthal is moving in the opposite direction. She wants to shift leverage away from the allergists.

in order to help more patients. This would happen through better technology, better training, and better regulation. In some states, pharmacists are now allowed to perform the skin tests for penicillin allergy. Last year, a Republican congressman with Democratic support reintroduced the PAVE Act that stands for penicillin allergy verification and evaluation. It would fold allergy awareness into annual wellness visits and the preventive welcome to Medicare visits that Blumenthal mentioned earlier. So that all sounds good, but let's not get too excited. Overall, the false positive problem in penicillin.

is under-examined and underfunded. I can tell you with confidence that I was the first penicillin allergy grant that the NIH funded in 30 years. Whose area is it? Is infectious disease? Is it allergy? It's multi-disciplinary. Is it surgery? Is it obstetrics? Because penicillins are used by everybody. Dentists, it was very hard to know who takes ownership of something that crosses every single discipline. When disciplines cross, disciplines compete.

Given the cost of medical research, these can be multi-billion dollar competitions. There's a pecking order in medicine. This is Thomas Platsmills. I'm a professor of medicine at the University of Virginia, and I've been studying allergic disease for a long time. And where does allergic disease fall in the pecking order of medical research? It's actually much worse than anything you imagine. Neurosurgeons are at the top, cardiac surgeons.

All these people fight with each other, but they know that at the bottom there are dermatologists and psychiatrists and allergists. I got very little from the university a little bit in the first few years, but then basically in the last years, nothing, we've always had to get our own money. And I was getting NIH money and the NIH has been very generous. This last time, I actually got a one on a grant. It's actually means you're in the top 1%.

And then I got a merit award, and the merit award is absolutely wonderful because from 18 to 28, I'm funded by the NOH. 10 years instead of five, tick bite research is hot. Platt's Mills is a giant in the field of allergy research. Some of his early work was on the connection between asthma and dust mites. More recently, he and his team have found that getting bitten by the Lone Star tick can trigger an allergy to a sugar molecule called alpha-gal, which is found in the blood of mammals, which means the tick bite can therefore render a person allergic to red meat. As Platsmill said, tick bite research is hot. The Congress voted $100 million for it so that we can get tick bite related grants for different aspects of our research, and that's been tremendously helpful.

Why do you think ticks are such a good selling point for voters Congress etc just because that's relatable? Oh come on God had finished making the earth and then the devil reached over and sprinkled ticks all over it You know that now ticks are very interesting the deer are absolutely infested with ticks It is not unusual for hunters to shoot one of our deer and find the thing with so many ticks, they couldn't possibly count them. When you were embarking on the research about the Alpha Gal red meat allergy related to ticks, did your colleagues think or maybe even say that you were bonkers? They always say I'm bonkers. No, no, I've gone away with murder several times. My father taught us that if we think A and the rest of the world thinks

B, that is formal proof that A is correct. Being educated in an environment like that is really extraordinary. It does strike me, and I'd love you to tell me if I'm wrong. But my sense is that when it comes to allergy, the pharmaceutical side of the equation is doing very well. There's a lot of money being made, selling treatments that may or may not work. But on the research and the public health side of the equation, plainly not nearly as robust. And I'm curious why it would be in a case where if you think of just supply and demand, there's plainly a lot of demand for allergy remediation and so on. The public would like to know more, to suffer less and so on. If the split I'm describing is accurate, why do you think there is such a big split? Because the public doesn't decide which grants get funded. The trouble is that the drug companies are so powerful and they advertise so much.

that people just get the idea that that's what it is. And actually the guidelines are warped. I've been on a guideline panel for asthma where we were told that we should focus on large controlled trials published in the last five years. Well, that basically means drug studies. The number of large controlled trials of tick avoidance that are being done is zero. No one could afford to do them.

Companies have a lot of money and they do big well controlled trials, some of which are really important. But many of which are me too, or trying a new drug, which is a very tiny variant of the previous. It's much more important to try and understand what's happened. I've written a history of food allergy and the three forms of food allergy, which are peanut and the other allergens that cause immediate hypersensitivity eosinophilic esophagitis and the alpha-gal syndrome. And why I pull those apart is because they're mechanistically completely different, causally different, and the reasons why they've increased are different. Peanut is probably ridiculous washing of the skin with detergents. EOE, we've just published a hypothesis that the

processing of milk is a major part of that. Instead of pasteurizing milk at 84 degrees centigrade, all the milk you drink is heated to 135 degrees centigrade. It's dead and it's homogenized, which means the particles are all changed. So they're much smaller. And we say weaponized to immunize the esophagus. And the third one, the alpha-gal syndrome, we believe is primarily due to the loss of dogs in the suburban areas. What happened in the early 80s is leash laws and now the dogs can't get together to drive the deer out. And so we all have a herd of deer on our lawn and the deer are covered with ticks. This connection that Platts Mills has drawn between leash laws and a boom in the tick population is not his only unusual theory. I was very well known in the

70s for saying that television had had a major effect on asthma. We published a paper in which we showed that if people watched a screen, they took less deep breaths. If they're reading a book, they still breathe normally. If a child is watching television and you touch their shoulder, they actually jump slightly because they're in a trance. They're not unconscious. They're not asleep.

but they're in a trance and during that time the hypothesis was that that prevents their breathing and the deep breaths are a better bronchodilator than albuterol. What's happened since then, if you want something really silly, is the children no longer watching television because they've got cell phones and the cell phones don't put them into a trance and asthma has actually become less of a problem. The asthma doctors will be horrified if they have anyone suggesting that asthma is anything but the total problem. But actually, peanut allergy has become more of a problem than asthma. But a totally different causal mechanism, yes? Totally different, yes. What are your views on celiac disease and gluten allergy? Yeah, Gideon Lyak, who did the LEAP study, has been looking at celiac and seeing whether natural exposure to wheat in early childhood

would prevent celiac disease. And I think he's got some evidence, but it's not of a level comparable to the Leap Study. The Leap Study was a tremendous breakthrough. This Leap Study that stands for Learning Early About Peanut Allergy was published in 2015 by the pediatric allergist Gideon Lac. It argued that feeding peanuts to babies will actually reduce their risk of a peanut allergy. Much of the evidence came from Israel.

where babies routinely eat bomba, a puffy peanut butter flavored snack. Full disclosure, some adults also love bomba. Given what we've been hearing about allergies these past few decades, especially peanut allergies, you can imagine that many parents would be terrified to let their baby get anywhere near a peanut snack. Once a conventional wisdom is established, it can be hard to dislodge.

which gets us back to the allergy with which we began this episode. The whole generation of doctors were trained thinking that penicillin allergy was very dangerous. And very common. And very common. And it isn't. When I got here in 82, I already was saying things that, no, you don't need to worry about it as much as this. You need to ask the question and take precautions and be sensible. If someone had no history in 15 years, the chances that they're penicillinologic are very small. So what are some solutions? Can you talk about clearing people of penicillinology, for instance? By the way, the reason we're doing this episode is this is something that happened with me. I was told as a child I was allergic to penicillin. I avoided it for approximately 50 years. My current doctor, she said, you know, we should test. So I did. And you were negative.

I was negative, but I had to go through this, you know, two-day first the test and then the challenge test where you actually get a little bit of it. And it's plainly something that's not scalable right now. So I'm curious what you think are solutions. I'm waking my head. People have been trying for a long time. I can't tell you how many of the residents who apply for our fellowship have been doing a study on de-labeling penicillin. So this is not something that people are ignoring.

Can you explain why it's so difficult? Because as much as medical technology has changed, I mean, everything from time-release medicines to the mRNA vaccine, I mean, there's so much technology that has accelerated discovery in medicine. Why is it so hard in this case to come up with a, let's say, cheaper, faster, more scalable way to clear people? Well, there's quite a lot of literature that says you can't quite rely on a blood test.

We should have a simple blood test for IgE to penicillin that absolutely solves the problem. Kimberly Blumenthal is one of the people who has been working on a better blood test for penicillin allergy. We were trying so hard. I was working with Thermo Fisher Scientific. They have developed a blood test panel and they wanted to see if it worked in allergic individuals from America.

We identified in the Boston area, everyone that reacted to penicillin in front of our faces in the last few years. We sent them the blood of these individuals, and I think it picked up like three. It was like three of 20. It didn't pick it up yet. What makes it so hard? The conclusion was, well, they were allergic.

in the last five, 10 years, maybe they weren't allergic now. So I have to bring them back, retest them. And then these patients, they're like needles and haystacks, right? We combed the records of all Mass General Brigham to find these 22 penicillin allergics. We really need to say, okay, you reacted to penicillin in front of my face today, grab your blood and then send it to be able to know that they were true positives. But you're making progress, it sounds like. Slowly.

I mean, by the time you're 600 years old, this problem will be solved. One of my mentors said to me, if you do your job well, you have no job. And I'm like, I just don't think that's going to happen. There's always something else. We need better tests now, back to the basic science in the lab. And then on the population level, we're thinking about implementing penicillinology evaluation in primary care. We just created a measure of de-labeled patients in our healthcare system. And even just now that I can measure it, I can measure it in this clinic and that clinic. And I can see what types of interventions move the needle towards a higher percentage of de-labeled patients. So what would your message be to anyone who believes that they are allergic to penicillin now? Get tested, get tested. If we were to jump ahead 20, 30, 50 years or something, I would imagine

that given the benefits of gene sequencing and machine learning and artificial intelligence, it would be pretty simple at birth to either understand everything that a given person might be susceptible to allergy-wise or just correct it. I think it's possible and it's also possible that we could alter our drugs to be less allergenic. How would you do that? Oh goodness. We'd have to know what metabolite of the drug is.

forming bonds in our body to make the allergen. And so it requires a lot of combined intelligence from different people. I realized though as I asked that question that it's a little touchy for you because I'd be putting you out of business. You okay with that?

Yeah, I would stop happy if we have some sort of way that like everybody knows if they can or cannot have penicillin or any drug or they're going to be allergic or not. If we were able to correct the 30 million mislabels in just America, I'm happy. I'm retired. And you just open a florist shop or something like that and be okay? I do like floral design. Well, there you go. I would like to thank Kimberly Blumenthal for the good conversation today as well as Thomas Platsmills, Teresa McPhail, and Alina Resnick. Thanks also to Dr. Resnick for clearing my stupid penicillin allergy label. And thanks to Becky Kurth, Dr. Deb Jones, Dr. Leni Hurst, and all the other medical professionals who helped turn me from a bone-tired coughing machine into, well, back into me, I am grateful. Making this episode was a good reminder of how much I love physicians.

drive their curiosity, their willingness to admit what they don't know yet and then to work ridiculously hard to find out more. We reached out to Dr. Blumenthal to see how she's been doing since we spoke with her in 2024. She wrote, came to me after being prescribed clindamycin for a dental infection and that had led to a lot of problems with her GI tract and she was very grateful to leave my office de-labeled and able to take a moxicillin next time. That's it for today's episode. Also, we have just launched a new show in addition to Freakonomics Radio. It's a video talk show called Better in Person and I think you will love it. If Freakonomics

is about how things work better in person is about how people work. You can watch it on the Freakonomics YouTube channel. I do hope you will watch it and leave adoring reviews and tell all your friends, can even tell your enemies. And we will be back right here next week with a new episode of Freakonomics Radio. Until then, take care of yourself. And if you can, someone else too. Freakonomics Radio is produced by Renbud Radio. You can find our entire archive on any podcast app.

It's also at Freakonomics.com, where we publish transcripts and show notes. This episode was originally produced and updated by Dalvin Abouaji. It was edited by Gabriel Roth and mixed by Eleanor Osborne. The Freakonomics radio network staff also includes Augusta Chapman, Ellen Frankman, Elsa Hernandez, Alaria Montenacourt, Jake Loomis, Jeremy Johnston, Mandy Gorinstein, Pete Madden, and Theo Jacobs. Our theme song is Mr. Fortune by the Hitchhikers and our composer is Luis Guerra. As always, thanks for listening.

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