How to pronounce "seatbelts"

This is my great uncle,

my father's father's younger brother.

His name was Joe McKenna.

He was a young husband and a semi-pro basketball player

and a fireman in New York City.

Family history says he loved being a fireman,

and so in 1938, on one of his days off,

he elected to hang out at the firehouse.

To make himself useful that day, he started polishing all the brass,

the railings on the fire truck, the fittings on the walls,

and one of the fire hose nozzles,

a giant, heavy piece of metal,

toppled off a shelf and hit him.

A few days later, his shoulder started to hurt.

Two days after that, he spiked a fever.

The fever climbed and climbed.

His wife was taking care of him,

but nothing she did made a difference, and when they got the local doctor in,

nothing he did mattered either.

They flagged down a cab and took him to the hospital.

The nurses there recognized right away that he had an infection,

what at the time they would have called "blood poisoning,"

and though they probably didn't say it,

they would have known right away

that there was nothing they could do.

There was nothing they could do because the things we use now

to cure infections didn't exist yet.

The first test of penicillin, the first antibiotic,

was three years in the future.

People who got infections either recovered, if they were lucky,

or they died.

My great uncle was not lucky.

He was in the hospital for a week, shaking with chills,

dehydrated and delirious,

sinking into a coma as his organs failed.

His condition grew so desperate

that the people from his firehouse lined up to give him transfusions

hoping to dilute the infection surging through his blood.

Nothing worked. He died.

He was 30 years old.

If you look back through history,

most people died the way my great uncle died.

Most people didn't die of cancer or heart disease,

the lifestyle diseases that afflict us in the West today.

They didn't die of those diseases because they didn't live long enough

to develop them.

They died of injuries --

being gored by an ox,

shot on a battlefield,

crushed in one of the new factories of the Industrial Revolution --

and most of the time from infection,

which finished what those injuries began.

All of that changed when antibiotics arrived.

Suddenly, infections that had been a death sentence

became something you recovered from in days.

It seemed like a miracle,

and ever since, we have been living inside the golden epoch of the miracle drugs.

And now, we are coming to an end of it.

My great uncle died in the last days of the pre-antibiotic era.

We stand today on the threshold of the post-antibiotic era,

in the earliest days of a time when simple infections

such as the one Joe had will kill people once again.

In fact, they already are.

People are dying of infections again because of a phenomenon

called antibiotic resistance.

Briefly, it works like this.

Bacteria compete against each other for resources, for food,

by manufacturing lethal compounds that they direct against each other.

Other bacteria, to protect themselves,

evolve defenses against that chemical attack.

When we first made antibiotics,

we took those compounds into the lab and made our own versions of them,

and bacteria responded to our attack the way they always had.

Here is what happened next:

Penicillin was distributed in 1943,

and widespread penicillin resistance arrived by 1945.

Vancomycin arrived in 1972,

vancomycin resistance in 1988.

Imipenem in 1985,

and resistance to in 1998.

Daptomycin, one of the most recent drugs, in 2003,

and resistance to it just a year later in 2004.

For 70 years, we played a game of leapfrog --

our drug and their resistance,

and then another drug, and then resistance again --

and now the game is ending.

Bacteria develop resistance so quickly that pharmaceutical companies

have decided making antibiotics is not in their best interest,

so there are infections moving across the world

for which, out of the more than 100 antibiotics

available on the market,

two drugs might work with side effects,

or one drug,

or none.

This is what that looks like.

In 2000, the Centers for Disease Control and Prevention, the CDC,

identified a single case

in a hospital in North Carolina

of an infection resistant to all but two drugs.

Today, that infection, known as KPC,

has spread to every state but three,

and to South America, Europe

and the Middle East.

In 2008, doctors in Sweden

diagnosed a man from India with a different infection

resistant to all but one drug that time.

The gene that creates that resistance,

known as NDM, has now spread from India into China, Asia, Africa,

Europe and Canada, and the United States.

It would be natural to hope

that these infections are extraordinary cases,

but in fact,

in the United States and Europe,

50,000 people a year

die of infections which no drugs can help.

A project chartered by the British government

known as the Review on Antimicrobial Resistance

estimates that the worldwide toll right now is 700,000 deaths a year.

That is a lot of deaths,

and yet, the chances are good that you don't feel at risk,

that you imagine these people were hospital patients

in intensive care units

or nursing home residents near the ends of their lives,

people whose infections are remote from us,

in situations we can't identify with.

What you didn't think about, none of us do,

is that antibiotics support almost all of modern life.

If we lost antibiotics,

here's what else we'd lose:

First, any protection for people with weakened immune systems --

cancer patients, AIDS patients,

transplant recipients, premature babies.

Next, any treatment that installs foreign objects in the body:

stents for stroke, pumps for diabetes,

dialysis, joint replacements.

How many athletic baby boomers need new hips and knees?

A recent study estimates that without antibiotics,

one out of ever six would die.

Next, we'd probably lose surgery.

Many operations are preceded

by prophylactic doses of antibiotics.

Without that protection,

we'd lose the ability to open the hidden spaces of the body.

So no heart operations,

no prostate biopsies,

no Cesarean sections.

We'd have to learn to fear infections that now seem minor.

Strep throat used to cause heart failure.

Skin infections led to amputations.

Giving birth killed, in the cleanest hospitals,

almost one woman out of every 100.

Pneumonia took three children out of every 10.

More than anything else,

we'd lose the confident way we live our everyday lives.

If you knew that any injury could kill you,

would you ride a motorcycle,

bomb down a ski slope,

climb a ladder to hang your Christmas lights,

let your kid slide into home plate?

After all, the first person to receive penicillin,

a British policeman named Albert Alexander,

who was so ravaged by infection that his scalp oozed pus

and doctors had to take out an eye,

was infected by doing something very simple.

He walked into his garden and scratched his face on a thorn.

That British project I mentioned which estimates that the worldwide toll

right now is 700,000 deaths a year

also predicts that if we can't get this under control by 2050,

not long, the worldwide toll will be 10 million deaths a year.

How did we get to this point

where what we have to look forward to

is those terrifying numbers?

The difficult answer is, we did it to ourselves.

Resistance is an inevitable biological process,

but we bear the responsibility for accelerating it.

We did this by squandering antibiotics

with a heedlessness that now seems shocking.

Penicillin was sold over the counter until the 1950s.

In much of the developing world, most antibiotics still are.

In the United States, 50 percent

of the antibiotics given in hospitals are unnecessary.

Forty-five percent of the prescriptions written in doctor's offices

are for conditions that antibiotics cannot help.

And that's just in healthcare.

On much of the planet, most meat animals get antibiotics every day of their lives,

not to cure illnesses,

but to fatten them up and to protect them against

the factory farm conditions they are raised in.

In the United States, possibly 80 percent

of the antibiotics sold every year go to farm animals, not to humans,

creating resistant bacteria that move off the farm

in water, in dust,

in the meat the animals become.

Aquaculture depends on antibiotics too,

particularly in Asia,

and fruit growing relies on antibiotics

to protect apples, pears, citrus, against disease.

And because bacteria can pass their DNA to each other

like a traveler handing off a suitcase at an airport,

once we have encouraged that resistance into existence,

there is no knowing where it will spread.

This was predictable.

In fact, it was predicted

by Alexander Fleming, the man who discovered penicillin.

He was given the Nobel Prize in 1945 in recognition,

and in an interview shortly after, this is what he said:

"The thoughtless person playing with penicillin treatment

is morally responsible for the death of a man

who succumbs to infection

with a pencillin-resistant organism."

He added, "I hope this evil can be averted."

Can we avert it?

There are companies working on novel antibiotics,

things the superbugs have never seen before.

We need those new drugs badly,

and we need incentives:

discovery grants, extended patents,

prizes, to lure other companies into making antibiotics again.

But that probably won't be enough.

Here's why: Evolution always wins.

Bacteria birth a new generation every 20 minutes.

It takes pharmaceutical chemistry 10 years to derive a new drug.

Every time we use an antibiotic,

we give the bacteria billions of chances

to crack the codes

of the defenses we've constructed.

There has never yet been a drug

they could not defeat.

This is asymmetric warfare,

but we can change the outcome.

We could build systems to harvest data to tell us automatically and specifically

how antibiotics are being used.

We could build gatekeeping into drug order systems

so that every prescription gets a second look.

We could require agriculture to give up antibiotic use.

We could build surveillance systems

to tell us where resistance is emerging next.

Those are the tech solutions.

They probably aren't enough either,

unless we help.

Antibiotic resistance is a habit.

We all know how hard it is to change a habit.

But as a society, we've done that in the past.

People used to toss litter into the streets,

used to not wear seatbelts,

used to smoke inside public buildings.

We don't do those things anymore.

We don't trash the environment

or court devastating accidents

or expose others to the possibility of cancer,

because we decided those things were expensive,

destructive, not in our best interest.

We changed social norms.

We could change social norms around antibiotic use too.

I know that the scale of antibiotic resistance

seems overwhelming,

but if you've ever bought a fluorescent lightbulb

because you were concerned about climate change,

or read the label on a box of crackers

because you think about the deforestation from palm oil,

you already know what it feels like

to take a tiny step to address an overwhelming problem.

We could take those kinds of steps for antibiotic use too.

We could forgo giving an antibiotic if we're not sure it's the right one.

We could stop insisting on a prescription for our kid's ear infection

before we're sure what caused it.

We could ask every restaurant,

every supermarket,

where their meat comes from.

We could promise each other

never again to buy chicken or shrimp or fruit

raised with routine antibiotic use,

and if we did those things,

we could slow down the arrival of the post-antibiotic world.

But we have to do it soon.

Penicillin began the antibiotic era in 1943.

In just 70 years, we walked ourselves up to the edge of disaster.

We won't get 70 years

to find our way back out again.

Thank you very much.

(Applause)