Showing posts with label health care. Show all posts
Showing posts with label health care. Show all posts

Thursday, April 11, 2024

 

Removing bias from health care AI tools

global faces
Credit: Pixabay/CC0 Public Domain

Rapid advances in artificial intelligence (AI) have opened the way for the creation of a huge range of new health care tools, but to ensure that these tools do not exacerbate preexisting health inequities, researchers urge the use of more representative data in their development.

11 april 2024--Researchers from Oxford University's Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University College London and the Center for Ethnic Health Research, supported by Health Data Research UK, have for the first time studied the full detail of ethnicity data in the NHS. They outline the importance of using representative data in health care provision and have compiled this information into a research-ready database.

The new study, published in Scientific Data, is the first part of a three-phase project that aims to reduce bias in AI health prediction models which are trained on real-world patient data. The project, which addresses ethnicity disparities that were highlighted during the pandemic, is part of the UK Government's COVID-19 Data and Connectivity National Core Study led by Health Data Research UK.

The researchers used de-identified data on ethnicity and other characteristics from general practice and hospital health records, accessed safely within NHS England's Secure Data Environment (SDE) service, via the British Heart Foundation Data Science Center's CVD-COVID-UK/COVID-IMPACT Consortium.

This is the first time that patient ethnicity data has been studied at this depth and breadth for the whole population of England. The researchers were able to combine records to analyze patient self-identified ethnicity recorded through over 489 potential codes.

Researchers analyzed how more than 61 million people in England identified their ethnicity in over 250 different groups. They also looked at the characteristics of those with no record of their ethnicity, and how conflicts in patient ethnicity data can arise. The data, now available for other researchers to use, shows that 1/10 patients lack ethnicity records, and around 12% of patients had conflicting ethnicity codes in their patient records.

Sara Khalid, Associate Professor of Health Informatics and Biomedical Data Science at NDORMS, explained, "Health inequity was highlighted during the COVID19 pandemic, where individuals from ethnically diverse backgrounds were disproportionately affected, but the issue is long-standing and multi-faceted.

"Because AI-based health care technology depends on the data that is fed into it, a lack of representative data can lead to biased models that ultimately produce incorrect health assessments. Better data from real-world settings, such as the data we have collected, can lead to better technology and ultimately better health for all."

Professor Cathie Sudlow, Chief Scientist at Health Data Research UK and Director of its BHF Data Science Center said, "We are delighted to be supporting hundreds of researchers to harness the power of the UK's rich health data. This study on ethnicity recording highlights how different sources of health data from the whole English population can be accessed and analyzed in a safe and secure way, providing insights that are relevant to everyone.

"The findings will empower health professionals, patients, carers and policymakers to make better decisions that will benefit people of all ages, ethnic groups, and social backgrounds across the country."

The study assessed the available detail of ethnicity data in NHS England, including across different types of ethnicity codes. For example, NHS hospitals record patient data via 19 ethnicity codes, while GPs use the globally recognized SNOMED-CT Codes, of which there are 489. However, health researchers lose the finer detail from these recording systems as they typically collapse these groups into just five or six, potentially leading to less accurate research.

The researchers plan to demonstrate the value of these findings in the subsequent phases of the project, which will first focus on using these detailed results on ethnicity data to better describe how different ethnicities were impacted by the COVID-19 pandemic, and then feed into more equitable artificial intelligence and machine learning tools suitable for use by diverse patient groups.

More information: Marta Pineda-Moncusí et al, Ethnicity data resource in population-wide health records: completeness, coverage and granularity of diversity, Scientific Data (2024). DOI: 10.1038/s41597-024-02958-1

Sunday, January 28, 2018

Want a healthier population? Spend less on health care and more on social services

Increased social spending was associated with health improvements at the population level, while health spending increases did not have the same effect, according to a large new Canadian study in CMAJ (Canadian Medical Association Journal).

28 jan 2018--"Spending more on health care sounds like it should improve health, but our study suggests that is not the case and social spending could be used to improve the health of everyone," says Dr. Daniel Dutton, The School of Public Policy, University of Calgary, Calgary, Alberta. "Relative to health care, we spend little on social services per person, so redistributing money to social services from health care is actually a small change in health care spending."
Health care costs are expanding in many developed countries like Canada, and governments are seeking ways to contain costs while maintaining a healthy population. Treating the social determinants of health like income, education, or social and physical living environments through spending on social services can help address the root causes of disease and poor health. However, health spending continues to make up the lion's share of spending.
The study looked at data from 9 of Canada's 10 provinces over 31 years from 1981 to 2011 (Prince Edward Island and the northern territories were not included because of insufficient data) to see if social and health care spending ratios were linked to population health status. The researchers looked at three health outcomes: potentially avoidable mortality, infant mortality, and life expectancy.
Average per capita spending on social services was $930 compared with $2900—almost three times the amount—for health services. Health spending per capita increased 10-fold over the study period compared with social spending. However, increased social spending per dollar spent on health care was associated with improved health outcomes at the population level by province.
"Social spending as a share of health spending is associated with improvements in potentially avoidable mortality and life expectancy," says Dr. Dutton. "If governments spent one cent more on social services per dollar spent on health by rearranging money between the two portfolios, life expectancy could have experienced an additional 5% increase and potentially avoidable mortality could have experienced an additional 3% decrease in one year."
This has implications for the way governments allocate spending.
"If social spending addresses the social determinants of health, then it is a form of preventive health spending and changes the risk distribution for the entire population rather than treating those with disease. Redirecting resources from health to social services, that is, rearranging payment without additional spending, is an efficient way to improve health outcomes," he says.
In a related commentary, Dr. Paul Kershaw, School of Population and Public Health, University of British Columbia, Vancouver, BC, writes that the researchers found that increased healthspending "is associated with lost opportunities to improve life expectancy and prevent avoidable mortality by comparison with a more even distribution between medical and social investments. These results add to evidence that should impel governments to seek better balance between medical and social expenditures."
Governments have increased health spending as the aging population has expanded.
The commentary author suggests governments should allocate social spending fairly for both young and old to ensure that the younger generation is not being shortchanged.

More information: Daniel J. Dutton et al. Effect of provincial spending on social services and health care on health outcomes in Canada: an observational longitudinal study, Canadian Medical Association Journal (2018). DOI: 10.1503/cmaj.170132
Paul Kershaw. The need for health in all policies in Canada, Canadian Medical Association Journal (2018). DOI: 10.1503/cmaj.171530

Provided by Canadian Medical Association Journal

Friday, February 13, 2009

How to help patients make wiser health choices

WASHINGTON, 13 feb 2009– It's one of medicine's uncomfortable truths: That blood test for prostate cancer is far from perfect. Would as many men take a PSA test if they knew? Or consider treatment for early breast cancer: Is saving the breast worth all the extra doctor visits for radiation or would you prefer the whole breast removed in one trip?

There's no single right answer for everyone yet patients often are ill-equipped to weigh increasingly complex medical options. Now there's a small but growing movement to get unbiased reports of the pros and cons of different tests and treatments into patients' hands before they fall back on, "Doc, just tell me what you'd choose."

"No matter how hard I tried" to be objective, "inevitably my personal biases got involved," recalls breast surgeon Dr. Dale Collins of New Hampshire's Dartmouth-Hitchcock Medical Center, which helped pioneer the concept that it calls shared decision-making.

Think of it as "informed consent 2.0," going a step beyond the brief patient education that doctors are required to provide. One state, Washington, has passed a law encouraging the trend. And it may get renewed attention in this era of health care reform because studies suggest that patients who get the full scoop frequently choose more conservative therapy than their doctors initially recommend.

Savvy patients today turn to places like the National Institutes of Health or American Cancer Society for advice. For the less savvy, some medical groups are developing what they call decision aids, plain-English guides that give equal voice to the advantages and disadvantages of options and include real patients explaining why they chose differently. They can be videos or pamphlets, but the goal is for patients to get the guides even before doctor appointments so they come armed with better questions.

Consider that PSA blood test. Most men over 50 have had one even though it's hugely controversial. Why? Most men who undergo a biopsy for an abnormal PSA test don't turn out to have prostate cancer at all. Of those who do, there's no proof yet that the early detection saves lives. But finding an early prostate cancer forces a decision about trying surgery or radiation treatments that can cause incontinence and impotence — known harm for unknown benefit.

In fact, health guidelines issues last year concluded men over age 75 shouldn't get a PSA test while younger men should make an individual choice after hearing the pros and cons.

But getting upfront objective information is rare, Dr. Michael Barry of Massachusetts General Hospital told a meeting of the nonprofit Foundation for Informed Medical Decision Making last week, where health workers gathered to debate how to spread "informed choice."

In a decision-aid video the foundation sponsored about PSA testing, one doctor says, "Is this a slippery slope that I really want to get on?" He decided not to have his own PSA level checked.

"It's a good way to diagnose a potentially fatal condition," says another physician on the video who did get tested.

At Dartmouth, every woman diagnosed with early-stage breast cancer now sees a similar decision-aid video before meeting a surgeon. They're also quizzed to be sure they understood that survival is equally good regardless of whether they choose removing just the tumor, followed by radiation, or removing the whole breast — but that there are valid reasons for either choice, such as anxiety about keeping the breast, the time radiation requires, how often more surgery is needed.

Patient choice is only one part of good health care; a separate problem is how often doctors fail to offer proven care, such as medications that improve survival after a heart attack.

But many other scenarios — back surgery, knee and hip replacement, enlarged prostates, especially end-of-life care — have no one-size-fits-all guidelines, and Dartmouth research suggests where patients live often is the biggest determinant of what they get. For example, elderly patients with chronic illnesses spend 11 days in the hospital in Bend, Ore., over their last two years of life — while those in Manhattan spend 35 days in the hospital, although the extra care doesn't lengthen life.

A new University of Michigan study of how 3,000 patients made common medical choices suggests patients frequently have misinformation. Fewer than one in five could name the most common side effect of cholesterol-lowering statin drugs they were considering, for example. Moreover, patients said their doctors discussed treatment advantages more than the disadvantages.

Whether decision aids or some other approach truly improves informed choice remains to be seen, but a handful of medical centers are trying the guides.

"You're getting so much information thrown at you at one time, it's hard to assimilate," says Alethea Cassidy, 53, of Erie, Pa., who was diagnosed with early-stage breast cancer in March 2007 and received a similar decision-aid video from Allegheny General Hospital. It helped her decide to keep her breast. "It alleviates any doubts."

Saturday, January 17, 2009

Health Care You Can’t Afford Not to Afford

About one in three Americans say their family has had problems paying medical bills in the past year, according to a recent poll by the Kaiser Family Foundation, a nonprofit research group focused on health care. More alarming, almost half of those surveyed said someone in their family was postponing or cutting back on medical care they said they needed.

If you or your family are forced into this type of economic triage, you’ve got to do it wisely, says Dr. Ted Epperly, the president of the American Academy of Family Physicians.

The truth is, some health care can probably be safely put off until you’re feeling more flush. If you’re due for your annual physical, for instance, and you feel fine, you can wait a few months before forking over that hefty co-payment. Even children, once they are past vaccination age, can skip a check-up or two, as long as they are healthy and at a normal weight.

And while this suggestion is surely controversial, some experts say routine screenings like mammograms for women or PSA tests for men can also be postponed for a few months, as long as the person doesn’t have any symptoms and no family history of health problems in these areas. “The American Cancer Society wouldn’t like me saying so,” Dr. Epperly said, “but you can stretch out those tests when you need to.”

But the things you can safely skip make a far shorter list than the treatments most health care professionals consider mandatory — no matter how cash-strapped you may be. The following three areas of health care are ones you simply can’t afford to ignore, not only for your immediate well-being, but to avoid even more costly crisis care later. Fortunately, as you’ll see below, there are ways to get help paying for the care you need.

1. Your Medicine More than a third of the people in the Kaiser survey said they were splitting pills, skipping doses of medicine or not filling prescriptions in the first place. “If you’re suffering from a chronic illness such as high blood pressure, diabetes or asthma, you already know how important taking your medicine is,” Dr. Epperly said. “You’re on these medications for a reason, and going off without a physician’s advice will almost always make you sicker.” Even seemingly minor illnesses like strep throat or an ear infection can turn into an emergency room visit if left untreated.

What you can do: If you’re having trouble affording your medicine, talk to your doctor immediately. He or she may be able to switch you to a less expensive alternative or a generic version of the drug you’re now taking. “Generics have the advantage of being much cheaper,” said Dr. Sydney Wolfe, the director of health research for the consumer advocacy group Public Citizen. “But they are also often safer than new, brand-name drugs because they have been in use long enough for potential side effects to be known.”

Your doctor may also be able to help you enroll in a prescription drug aid program like the one sponsored by the Partnership for Prescription Assistance, a coalition of pharmaceutical companies and health-care advocates, says Cheryl Fish-Parcham, the deputy director of health policy at Families USA, another consumer advocacy group.

Another good source for help with finding affordable prescriptions (and all types of medical financial assistance) is MedlinePlus, a Web site backed by the National Library of Medicine and the National Institutes of Health.

2. Your Symptoms Delaying care can work for fully healthy people. But the minute you have symptoms or start to feel something is wrong, that all changes, says Dr. Epperly. Skipping tests and treatments is no longer an option. Still, even if the doctor thinks you really do need an expensive diagnostic test, like a CT scan or M.R.I., there may be ways to get it done at reduced cost.

What you can do: Ask your doctor about free screening programs and low-cost clinics in your community that can provide an affordable test. In New York City, organizations like the Community Service Society offer resources for finding low-cost care. Also, if your test or treatment is related to a specific illness like Crohn’s disease or diabetes, look up the Web site for the association or foundation that specializes in that illness, Ms. Fish-Parcham says. These organizations often provide resources for financial assistance to patients in need.

3. Your General Well-Being When you’re feeling out of control financially, it’s easy to let good habits and routines go out the window and resort to a vice or two. But this is not the time to smoke or drink more, Dr. Epperly advises. You could blow the budget and maybe cause real problems down the line.

What you can do: Keep eating a healthy diet, get plenty of exercise and get a good night’s sleep. “All three of these low-cost treatments have proven health benefits for you,” Dr. Epperly said. And all that healthy living may help you relieve some of the stress you’re feeling about money.

Thursday, January 08, 2009

Health-monitoring technology helps seniors live at home longer, MU researchers find

COLUMBIA, Mo., 08 jan 2009 – Many older adults want to remain active and independent for as long as possible. Seniors want to age in their own homes and avoid moving to institutions or nursing homes. University of Missouri researchers are using sensors, computers and communication systems, along with supportive health care services to monitor the health of older adults who are living at home. According to the researchers, motion sensor networks installed in seniors' homes can detect changes in behavior and physical activity, including walking and sleeping patterns. Early identification of these changes can prompt health care interventions that can delay or prevent serious health events.

As part of the "aging in place" research at MU, integrated sensor networks were installed in apartments of residents at TigerPlace, a retirement community that helps senior residents stay healthy and active to avoid hospitalization and relocation. MU researchers collected data from motion and bed sensors that continuously logged information for more than two years. The researchers identified patterns in the sensor data that can provide clues to predict adverse health events, including falls, emergency room visits and hospitalizations.

"The 'aging in place' concept allows older adults to remain in the environment of their choice and receive supportive health services as needed. With this type of care, most people wouldn't need to relocate to a nursing home," said Marilyn Rantz, professor in the MU Sinclair School of Nursing. "Monitoring sensor patterns is an effective and discreet way to ensure the health and privacy of older adults."

In recent evaluations, the sensor networks detected changes in residents' conditions that were not recognized by traditional health care assessments. MU researchers are perfecting the technology infrastructure at TigerPlace as a model, so these technologies and supportive health care services can be made available to seniors throughout the country.

"Our goal is to generate automatic alerts that notify caregivers of changes in residents' conditions that would allow them to intervene and prevent adverse health events," Rantz said. "Additional work is underway to establish these health alerts, improve the reliability and accuracy of the sensor network, implement a video sensor network, and refine a Web-based interface to make it even more user friendly and meaningful to health care providers."

Tiger II, a 22-unit addition to TigerPlace, opened on Jan. 1. TigerPlace community residents receive health and wellness services through TigerCare, a service of the Sinclair School of Nursing. Residents receive care and services when they need them and where they want them - in the privacy of their apartments.

Through its university affiliation, residents can participate in a number of educational, cultural and research projects both on site and on campus that are conducted by the College of Engineering, School of Nursing, Health Professions, and Medicine at MU.

###

The study, "Using Technology to Enhance Aging in Place," was presented at the 2008 International Conference on Smart homes and health Telematics. It was funded by a grant from the U.S. Administration on Aging and the National Science Foundation ITR grant.

For more information, visit the eldercare and rehabilitation technology Web site: http://eldertech.missouri.edu/

Tuesday, May 27, 2008

In Central Europe, Better Health Care Comes With a Cost

By NICHOLAS KULISH
PRAGUE, 27 may 2008 — In the Czech Republic, you can now see a doctor for about $1.85. A day in the hospital can verge on $4. This is not cause for celebration.
For Czechs, who visit their doctors more often than anyone in Europe, it has led to great outrage. In fact, the idea of charging anything at all for health care can generate significant controversy, not to mention abrupt about-faces in policy, here and in other Central European countries.
In Hungary, health care fees were resoundingly defeated in a nationwide referendum in March, which resulted in the firing of the health minister. Here in the Czech Republic, which began imposing the modest fees at the start of the year, the prime minister himself was forced before the constitutional court in Brno to testify as the court weighs overturning them. It is scheduled to rule on Wednesday.
Countries rich and poor struggle with how best to provide affordable health care to their citizens without breaking the bank. In places like the Czech Republic, there is a sense of betrayal, because the state long took care of them, but also a justified fear for those left behind in the recent years of growth and change. Even in Prague, known as the golden city, new wealth for some — and their rising expectations for top-notch care — has meant only higher prices for those trapped with low salaries or fixed pensions.
“I have to save so I have money for food,” said Kveta Lachoutova, 78, a widow who is a retired statistician. In an interview in the waiting room at her doctor’s office here, she said that she was trying to live on a monthly pension of about $600, while spending close to $400 on rent and utilities. “I don’t buy anything else.”
For healthy people with jobs, the fees are quite literally pocket change, usually paid with the same 10 and 20 crown coins as streetcar tickets in Prague ($1 is worth around 16 crowns). Affluent Czechs will admit privately that they spend far more on veterinary care for their cats and dogs than their own medical care, even with co-payments for some medications.
But many Czechs see it as a matter of principle that health care should be free — though the system is financed in part through payroll deductions — along with a strong sense of solidarity for the poor. “The only analogy I can think of in our political culture is primary schools,” said Marc J. Roberts, a professor of political economy at the Harvard School of Public Health who has worked in Central Europe. “Most people in the United States believe that primary education should be free and open to all and that it shouldn’t be subject to market principles.”
The region has been a laboratory of health care reform in recent years. The effort has been led by free-market advocates from booming Slovakia, which sports a flat tax and scorching economic growth, at a rate of over 10 percent last year.
Slovakia introduced modest payments for doctors’ visits and hospital stays in 2003. But, as would later happen in Hungary, the fees did not last. The left-wing government that came to power in 2006 rolled them back later that year, within just a few months of taking office.
“What we want to achieve in the health system is a higher individual responsibility, making the consumers more responsible for what they consume,” said Peter Pazitny, executive director and one of the founding partners at the Health Policy Institute in Bratislava, and formerly the principal adviser to the Slovakian minister of health.
The need for reform in the region, Mr. Pazitny said, is obvious. Statistics from the Organization for Economic Cooperation and Development show that the Czech, Slovak and Hungarian health care systems rank at or near the bottom of all member countries in life expectancy, as well as mortality rates for strokes, heart disease and cancer.
The Czech government was receptive to the Health Policy Institute’s input and even employs another of Mr. Pazitny’s partners in Prague. But the members of the opposition would prefer that their former countrymen left them — and their health care system — alone.
“I would understand if these Slovak boys would do it as a paper for their seminar at university, but here they are introducing it into real life,” said Michal Hasek, leader of the Social Democratic caucus, the largest opposition party in Parliament.
The Czech Constitution says that “citizens have on the basis of public insurance the right to free medical care and free medical aids under the conditions defined by the law.” The new payments were not only unconstitutional, according to Mr. Hasek, but also causing real pain in some segments of the population. Opponents and the local tabloid news media have made premature babies in incubators, whose parents must pay the hospital fees, into symbols of the new system.
Experts disagree on whether upfront fees to discourage doctors’ visits are a good idea from a public health perspective, and even question whether they create much in the way of savings for the overall health care system. “Most expensive, unnecessary services are not asked for by patients, but suggested by the physicians just to generate more revenue and more income for them,” said Peter Gaal, professor of health policy at Semmelweis University in Budapest.
The fees here, $1.85 for a prescription as well as a doctor’s visit, and twice that for a day in the hospital, are clearly having an effect on Czech behavior. The Health Ministry said the number of prescriptions fell 40 percent in the first quarter, though some of that may have been a result of stockpiling at the end of last year. The government estimated that public insurers had saved more than $100 million in the first quarter compared with the previous year, while providers collected $62 million in fees.
“We try to take out some of the costs that people can pay for themselves from the health care system,” said Tomas Julinek, the Czech health minister, in an interview in his office last week. But there is a cap on payments, set at just over $300 for the year, which Mr. Julinek said would also protect the seriously ill.
Several chronically ill patients said that they were not sure how the cap would work, or exactly which costs would be included. “So far, I see the negatives and I experience the negatives,” said Lenka Vondrackova, a multiple sclerosis patient struggling to get by with her husband and two teenage sons on about $1,200 a month, a combination of his salary and her disability benefits.
They live crammed into a tiny apartment in a Communist-era apartment building in Cerny Most, a neighborhood in the far eastern part of Prague. Her regimen of medications requires five pills in the morning, a nasal spray once a day and three more pills in the evening, along with a shot administered by her husband or one of her sons. Before the reforms, they were able to save a little each month. “Now everything that’s left is taken up by the fees,” said her husband, Pavel.
“I believe that in the future it will become evident that there will be more money for better equipment and medication,” she said, wishing in particular for pills that could take the place of the painful injection she dreaded each night. “If it works out,” she added, looking away, torn between skepticism and hope.

Monday, September 17, 2007

Do We Really Know What Makes Us Healthy?

By GARY TAUBES
Once upon a time, women took estrogen only to relieve the hot flashes, sweating, vaginal dryness and the other discomforting symptoms of menopause. In the late 1960s, thanks in part to the efforts of Robert Wilson, a Brooklyn gynecologist, and his 1966 best seller, “Feminine Forever,” this began to change, and estrogen therapy evolved into a long-term remedy for the chronic ills of aging. Menopause, Wilson argued, was not a natural age-related condition; it was an illness, akin to diabetes or kidney failure, and one that could be treated by taking estrogen to replace the hormones that a woman’s ovaries secreted in ever diminishing amounts. With this argument estrogen evolved into hormone-replacement therapy, or H.R.T., as it came to be called, and became one of the most popular prescription drug treatments in America.
By the mid-1990s, the American Heart Association, the American College of Physicians and the American College of Obstetricians and Gynecologists had all concluded that the beneficial effects of H.R.T. were sufficiently well established that it could be recommended to older women as a means of warding off heart disease and osteoporosis. By 2001, 15 million women were filling H.R.T. prescriptions annually; perhaps 5 million were older women, taking the drug solely with the expectation that it would allow them to lead a longer and healthier life. A year later, the tide would turn. In the summer of 2002, estrogen therapy was exposed as a hazard to health rather than a benefit, and its story became what Jerry Avorn, a Harvard epidemiologist, has called the “estrogen debacle” and a “case study waiting to be written” on the elusive search for truth in medicine.
Many explanations have been offered to make sense of the here-today-gone-tomorrow nature of medical wisdom — what we are advised with confidence one year is reversed the next — but the simplest one is that it is the natural rhythm of science. An observation leads to a hypothesis. The hypothesis (last year’s advice) is tested, and it fails this year’s test, which is always the most likely outcome in any scientific endeavor. There are, after all, an infinite number of wrong hypotheses for every right one, and so the odds are always against any particular hypothesis being true, no matter how obvious or vitally important it might seem.
In the case of H.R.T., as with most issues of diet, lifestyle and disease, the hypotheses begin their transformation into public-health recommendations only after they’ve received the requisite support from a field of research known as epidemiology. This science evolved over the last 250 years to make sense of epidemics — hence the name — and infectious diseases. Since the 1950s, it has been used to identify, or at least to try to identify, the causes of the common chronic diseases that befall us, particularly heart disease and cancer. In the process, the perception of what epidemiologic research can legitimately accomplish — by the public, the press and perhaps by many epidemiologists themselves — may have run far ahead of the reality. The case of hormone-replacement therapy for post-menopausal women is just one of the cautionary tales in the annals of epidemiology. It’s a particularly glaring example of the difficulties of trying to establish reliable knowledge in any scientific field with research tools that themselves may be unreliable.
What was considered true about estrogen therapy in the 1960s and is still the case today is that it is an effective treatment for menopausal symptoms. Take H.R.T. for a few menopausal years and it’s extremely unlikely that any harm will come from it. The uncertainty involves the lifelong risks and benefits should a woman choose to continue taking H.R.T. long past menopause. In 1985, the Nurses’ Health Study run out of the Harvard Medical School and the Harvard School of Public Health reported that women taking estrogen had only a third as many heart attacks as women who had never taken the drug. This appeared to confirm the belief that women were protected from heart attacks until they passed through menopause and that it was estrogen that bestowed that protection, and this became the basis of the therapeutic wisdom for the next 17 years.
Faith in the protective powers of estrogen began to erode in 1998, when a clinical trial called HERS, for Heart and Estrogen-progestin Replacement Study, concluded that estrogen therapy increased, rather than decreased, the likelihood that women who already had heart disease would suffer a heart attack. It evaporated entirely in July 2002, when a second trial, the Women’s Health Initiative, or W.H.I., concluded that H.R.T. constituted a potential health risk for all postmenopausal women. While it might protect them against osteoporosis and perhaps colorectal cancer, these benefits would be outweighed by increased risks of heart disease, stroke, blood clots, breast cancer and perhaps even dementia. And that was the final word. Or at least it was until the June 21 issue of The New England Journal of Medicine. Now the idea is that hormone-replacement therapy may indeed protect women against heart disease if they begin taking it during menopause, but it is still decidedly deleterious for those women who begin later in life.
This latest variation does come with a caveat, however, which could have been made at any point in this history. While it is easy to find authority figures in medicine and public health who will argue that today’s version of H.R.T. wisdom is assuredly the correct one, it’s equally easy to find authorities who will say that surely we don’t know. The one thing on which they will all agree is that the kind of experimental trial necessary to determine the truth would be excessively expensive and time-consuming and so will almost assuredly never happen. Meanwhile, the question of how many women may have died prematurely or suffered strokes or breast cancer because they were taking a pill that their physicians had prescribed to protect them against heart disease lingers unanswered. A reasonable estimate would be tens of thousands.
The Flip-Flop Rhythm of Science
At the center of the H.R.T. story is the science of epidemiology itself and, in particular, a kind of study known as a prospective or cohort study, of which the Nurses’ Health Study is among the most renowned. In these studies, the investigators monitor disease rates and lifestyle factors (diet, physical activity, prescription drug use, exposure to pollutants, etc.) in or between large populations (the 122,000 nurses of the Nurses’ study, for example). They then try to infer conclusions — i.e., hypotheses — about what caused the disease variations observed. Because these studies can generate an enormous number of speculations about the causes or prevention of chronic diseases, they provide the fodder for much of the health news that appears in the media — from the potential benefits of fish oil, fruits and vegetables to the supposed dangers of sedentary lives, trans fats and electromagnetic fields. Because these studies often provide the only available evidence outside the laboratory on critical issues of our well-being, they have come to play a significant role in generating public-health recommendations as well.
The dangerous game being played here, as David Sackett, a retired Oxford University epidemiologist, has observed, is in the presumption of preventive medicine. The goal of the endeavor is to tell those of us who are otherwise in fine health how to remain healthy longer. But this advice comes with the expectation that any prescription given — whether diet or drug or a change in lifestyle — will indeed prevent disease rather than be the agent of our disability or untimely death. With that presumption, how unambiguous does the evidence have to be before any advice is offered?
The catch with observational studies like the Nurses’ Health Study, no matter how well designed and how many tens of thousands of subjects they might include, is that they have a fundamental limitation. They can distinguish associations between two events — that women who take H.R.T. have less heart disease, for instance, than women who don’t. But they cannot inherently determine causation — the conclusion that one event causes the other; that H.R.T. protects against heart disease. As a result, observational studies can only provide what researchers call hypothesis-generating evidence — what a defense attorney would call circumstantial evidence.
Testing these hypotheses in any definitive way requires a randomized-controlled trial — an experiment, not an observational study — and these clinical trials typically provide the flop to the flip-flop rhythm of medical wisdom. Until August 1998, the faith that H.R.T. prevented heart disease was based primarily on observational evidence, from the Nurses’ Health Study most prominently. Since then, the conventional wisdom has been based on clinical trials — first HERS, which tested H.R.T. against a placebo in 2,700 women with heart disease, and then the Women’s Health Initiative, which tested the therapy against a placebo in 16,500 healthy women. When the Women’s Health Initiative concluded in 2002 that H.R.T. caused far more harm than good, the lesson to be learned, wrote Sackett in The Canadian Medical Association Journal, was about the “disastrous inadequacy of lesser evidence” for shaping medical and public-health policy. The contentious wisdom circa mid-2007 — that estrogen benefits women who begin taking it around the time of menopause but not women who begin substantially later — is an attempt to reconcile the discordance between the observational studies and the experimental ones. And it may be right. It may not. The only way to tell for sure would be to do yet another randomized trial, one that now focused exclusively on women given H.R.T. when they begin their menopause.
A Poor Track Record of Prevention
No one questions the value of these epidemiologic studies when they’re used to identify the unexpected side effects of prescription drugs or to study the progression of diseases or their distribution between and within populations. One reason researchers believe that heart disease and many cancers can be prevented is because of observational evidence that the incidence of these diseases differ greatly in different populations and in the same populations over time. Breast cancer is not the scourge among Japanese women that it is among American women, but it takes only two generations in the United States before Japanese-Americans have the same breast cancer rates as any other ethnic group. This tells us that something about the American lifestyle or diet is a cause of breast cancer. Over the last 20 years, some two dozen large studies, the Nurses’ Health Study included, have so far failed to identify what that factor is. They may be inherently incapable of doing so. Nonetheless, we know that such a carcinogenic factor of diet or lifestyle exists, waiting to be identified.
These studies have also been invaluable for identifying predictors of disease — risk factors — and this information can then guide physicians in weighing the risks and benefits of putting a particular patient on a particular drug. The studies have repeatedly confirmed that high blood pressure is associated with an increased risk of heart disease and that obesity is associated with an increased risk of most of our common chronic diseases, but they have not told us what it is that raises blood pressure or causes obesity. Indeed, if you ask the more skeptical epidemiologists in the field what diet and lifestyle factors have been convincingly established as causes of common chronic diseases based on observational studies without clinical trials, you’ll get a very short list: smoking as a cause of lung cancer and cardiovascular disease, sun exposure for skin cancer, sexual activity to spread the papilloma virus that causes cervical cancer and perhaps alcohol for a few different cancers as well.
Richard Peto, professor of medical statistics and epidemiology at Oxford University, phrases the nature of the conflict this way: “Epidemiology is so beautiful and provides such an important perspective on human life and death, but an incredible amount of rubbish is published,” by which he means the results of observational studies that appear daily in the news media and often become the basis of public-health recommendations about what we should or should not do to promote our continued good health.
In January 2001, the British epidemiologists George Davey Smith and Shah Ebrahim, co-editors of The International Journal of Epidemiology, discussed this issue in an editorial titled “Epidemiology — Is It Time to Call It a Day?” They noted that those few times that a randomized trial had been financed to test a hypothesis supported by results from these large observational studies, the hypothesis either failed the test or, at the very least, the test failed to confirm the hypothesis: antioxidants like vitamins E and C and beta carotene did not prevent heart disease, nor did eating copious fiber protect against colon cancer.
The Nurses’ Health Study is the most influential of these cohort studies, and in the six years since the Davey Smith and Ebrahim editorial, a series of new trials have chipped away at its credibility. The Women’s Health Initiative hormone-therapy trial failed to confirm the proposition that H.R.T. prevented heart disease; a W.H.I. diet trial with 49,000 women failed to confirm the notion that fruits and vegetables protected against heart disease; a 40,000-woman trial failed to confirm that a daily regimen of low-dose aspirin prevented colorectal cancer and heart attacks in women under 65. And this June, yet another clinical trial — this one of 1,000 men and women with a high risk of colon cancer — contradicted the inference from the Nurses’s study that folic acid supplements reduced the risk of colon cancer. Rather, if anything, they appear to increase risk.
The implication of this track record seems hard to avoid. “Even the Nurses’ Health Study, one of the biggest and best of these studies, cannot be used to reliably test small-to-moderate risks or benefits,” says Charles Hennekens, a principal investigator with the Nurses’ study from 1976 to 2001. “None of them can.”
Proponents of the value of these studies for telling us how to prevent common diseases — including the epidemiologists who do them, and physicians, nutritionists and public-health authorities who use their findings to argue for or against the health benefits of a particular regimen — will argue that they are never relying on any single study. Instead, they base their ultimate judgments on the “totality of the data,” which in theory includes all the observational evidence, any existing clinical trials and any laboratory work that might provide a biological mechanism to explain the observations.
This in turn leads to the argument that the fault is with the press, not the epidemiology. “The problem is not in the research but in the way it is interpreted for the public,” as Jerome Kassirer and Marcia Angell, then the editors of The New England Journal of Medicine, explained in a 1994 editorial titled “What Should the Public Believe?” Each study, they explained, is just a “piece of a puzzle” and so the media had to do a better job of communicating the many limitations of any single study and the caveats involved — the foremost, of course, being that “an association between two events is not the same as a cause and effect.”
Stephen Pauker, a professor of medicine at Tufts University and a pioneer in the field of clinical decision making, says, “Epidemiologic studies, like diagnostic tests, are probabilistic statements.” They don’t tell us what the truth is, he says, but they allow both physicians and patients to “estimate the truth” so they can make informed decisions. The question the skeptics will ask, however, is how can anyone judge the value of these studies without taking into account their track record? And if they take into account the track record, suggests Sander Greenland, an epidemiologist at the University of California, Los Angeles, and an author of the textbook “Modern Epidemiology,” then wouldn’t they do just as well if they simply tossed a coin?
As John Bailar, an epidemiologist who is now at the National Academy of Science, once memorably phrased it, “The appropriate question is not whether there are uncertainties about epidemiologic data, rather, it is whether the uncertainties are so great that one cannot draw useful conclusions from the data.”
Science vs. the Public Health
Understanding how we got into this situation is the simple part of the story. The randomized-controlled trials needed to ascertain reliable knowledge about long-term risks and benefits of a drug, lifestyle factor or aspect of our diet are inordinately expensive and time consuming. By randomly assigning research subjects into an intervention group (who take a particular pill or eat a particular diet) or a placebo group, these trials “control” for all other possible variables, both known and unknown, that might effect the outcome: the relative health or wealth of the subjects, for instance. This is why randomized trials, particularly those known as placebo-controlled, double-blind trials, are typically considered the gold standard for establishing reliable knowledge about whether a drug, surgical intervention or diet is really safe and effective.
But clinical trials also have limitations beyond their exorbitant costs and the years or decades it takes them to provide meaningful results. They can rarely be used, for instance, to study suspected harmful effects. Randomly subjecting thousands of individuals to secondhand tobacco smoke, pollutants or potentially noxious trans fats presents obvious ethical dilemmas. And even when these trials are done to study the benefits of a particular intervention, it’s rarely clear how the results apply to the public at large or to any specific patient. Clinical trials invariably enroll subjects who are relatively healthy, who are motivated to volunteer and will show up regularly for treatments and checkups. As a result, randomized trials “are very good for showing that a drug does what the pharmaceutical company says it does,” David Atkins, a preventive-medicine specialist at the Agency for Healthcare Research and Quality, says, “but not very good for telling you how big the benefit really is and what are the harms in typical people. Because they don’t enroll typical people.”
These limitations mean that the job of establishing the long-term and relatively rare risks of drug therapies has fallen to observational studies, as has the job of determining the risks and benefits of virtually all factors of diet and lifestyle that might be related to chronic diseases. The former has been a fruitful field of research; many side effects of drugs have been discovered by these observational studies. The latter is the primary point of contention.
While the tools of epidemiology — comparisons of populations with and without a disease — have proved effective over the centuries in establishing that a disease like cholera is caused by contaminated water, as the British physician John Snow demonstrated in the 1850s, it’s a much more complicated endeavor when those same tools are employed to elucidate the more subtle causes of chronic disease.
And even the success stories taught in epidemiology classes to demonstrate the historical richness and potential of the field — that pellagra, a disease that can lead to dementia and death, is caused by a nutrient-deficient diet, for instance, as Joseph Goldberger demonstrated in the 1910s — are only known to be successes because the initial hypotheses were subjected to rigorous tests and happened to survive them. Goldberger tested the competing hypothesis, which posited that the disease was caused by an infectious agent, by holding what he called “filth parties,” injecting himself and seven volunteers, his wife among them, with the blood of pellagra victims. They remained healthy, thus doing a compelling, if somewhat revolting, job of refuting the alternative hypothesis.
Smoking and lung cancer is the emblematic success story of chronic-disease epidemiology. But lung cancer was a rare disease before cigarettes became widespread, and the association between smoking and lung cancer was striking: heavy smokers had 2,000 to 3,000 percent the risk of those who had never smoked. This made smoking a “turkey shoot,” says Greenland of U.C.L.A., compared with the associations epidemiologists have struggled with ever since, which fall into the tens of a percent range. The good news is that such small associations, even if causal, can be considered relatively meaningless for a single individual. If a 50-year-old woman with a small risk of breast cancer takes H.R.T. and increases her risk by 30 percent, it remains a small risk.
The compelling motivation for identifying these small effects is that their impact on the public health can be enormous if they’re aggregated over an entire nation: if tens of millions of women decrease their breast cancer risk by 30 percent, tens of thousands of such cancers will be prevented each year. In fact, between 2002 and 2004, breast cancer incidence in the United States dropped by 12 percent, an effect that may have been caused by the coincident decline in the use of H.R.T. (And it may not have been. The coincident reduction in breast cancer incidence and H.R.T. use is only an association.)
Saving tens of thousands of lives each year constitutes a powerful reason to lower the standard of evidence needed to suggest a cause-and-effect relationship — to take a leap of faith. This is the crux of the issue. From a scientific perspective, epidemiologic studies may be incapable of distinguishing a small effect from no effect at all, and so caution dictates that the scientist refrain from making any claims in that situation. From the public-health perspective, a small effect can be a very dangerous or beneficial thing, at least when aggregated over an entire nation, and so caution dictates that action be taken, even if that small effect might not be real. Hence the public-health logic that it’s better to err on the side of prudence even if it means persuading us all to engage in an activity, eat a food or take a pill that does nothing for us and ignoring, for the moment, the possibility that such an action could have unforeseen harmful consequences. As Greenland says, “The combination of data, statistical methodology and motivation seems a potent anesthetic for skepticism.”
The Bias of Healthy Users
The Nurses’ Health Study was founded at Harvard in 1976 by Frank Speizer, an epidemiologist who wanted to study the long-term effects of oral contraceptive use. It was expanded to include postmenopausal estrogen therapy because both treatments involved long-term hormone use by millions of women, and nobody knew the consequences. Speizer’s assistants in this endeavor, who would go on to become the most influential epidemiologists in the country, were young physicians — Charles Hennekens, Walter Willett, Meir Stampfer and Graham Colditz — all interested in the laudable goal of preventing disease more than curing it after the fact.
When the Nurses’ Health Study first published its observations on estrogen and heart disease in 1985, it showed that women taking estrogen therapy had only a third the risk of having a heart attack as had women who had never taken it; the association seemed compelling evidence for a cause and effect. Only 90 heart attacks had been reported among the 32,000 postmenopausal nurses in the study, and Stampfer, who had done the bulk of the analysis, and his colleagues “considered the possibility that the apparent protective effect of estrogen could be attributed to some other factor associated with its use.” They decided, though, as they have ever since, that this was unlikely. The paper’s ultimate conclusion was that “further work is needed to define the optimal type, dose and duration of postmenopausal hormone use” for maximizing the protective benefit.
Only after Stampfer and his colleagues published their initial report on estrogen therapy did other investigators begin to understand the nature of the other factors that might explain the association. In 1987, Diana Petitti, an epidemiologist now at the University of Southern California, reported that she, too, had detected a reduced risk of heart-disease deaths among women taking H.R.T. in the Walnut Creek Study, a population of 16,500 women. When Petitti looked at all the data, however, she “found an even more dramatic reduction in death from homicide, suicide and accidents.” With little reason to believe that estrogen would ward off homicides or accidents, Petitti concluded that something else appeared to be “confounding” the association she had observed. “The same thing causing this obvious spurious association might also be contributing to the lower risk of coronary heart disease,” Petitti says today.
That mysterious something is encapsulated in what epidemiologists call the healthy-user bias, and some of the most fascinating research in observational epidemiology is now aimed at understanding this phenomenon in all its insidious subtlety. Only then can epidemiologists learn how to filter out the effect of this healthy-user bias from what might otherwise appear in their studies to be real causal relationships. One complication is that it encompasses a host of different and complex issues, many or most of which might be impossible to quantify. As Jerry Avorn of Harvard puts it, the effect of healthy-user bias has the potential for “big mischief” throughout these large epidemiologic studies.
At its simplest, the problem is that people who faithfully engage in activities that are good for them — taking a drug as prescribed, for instance, or eating what they believe is a healthy diet — are fundamentally different from those who don’t. One thing epidemiologists have established with certainty, for example, is that women who take H.R.T. differ from those who don’t in many ways, virtually all of which associate with lower heart-disease risk: they’re thinner; they have fewer risk factors for heart disease to begin with; they tend to be more educated and wealthier; to exercise more; and to be generally more health conscious.
Considering all these factors, is it possible to isolate one factor — hormone-replacement therapy — as the legitimate cause of the small association observed or even part of it? In one large population studied by Elizabeth Barrett-Connor, an epidemiologist at the University of California, San Diego, having gone to college was associated with a 50 percent lower risk of heart disease. So if women who take H.R.T. tend to be more educated than women who don’t, this confounds the association between hormone therapy and heart disease. It can give the appearance of cause and effect where none exists.
Another thing that epidemiologic studies have established convincingly is that wealth associates with less heart disease and better health, at least in developed countries. The studies have been unable to establish why this is so, but this, too, is part of the healthy-user problem and a possible confounder of the hormone-therapy story and many of the other associations these epidemiologists try to study. George Davey Smith, who began his career studying how socioeconomic status associates with health, says one thing this research teaches is that misfortunes “cluster” together. Poverty is a misfortune, and the poor are less educated than the wealthy; they smoke more and weigh more; they’re more likely to have hypertension and other heart-disease risk factors, to eat what’s affordable rather than what the experts tell them is healthful, to have poor medical care and to live in environments with more pollutants, noise and stress. Ideally, epidemiologists will carefully measure the wealth and education of their subjects and then use statistical methods to adjust for the effect of these influences — multiple regression analysis, for instance, as one such method is called — but, as Avorn says, it “doesn’t always work as well as we’d like it to.”
The Nurses’ investigators have argued that differences in socioeconomic status cannot explain the associations they observe with H.R.T. because all their subjects are registered nurses and so this “controls” for variations in wealth and education. The skeptics respond that even if all registered nurses had identical educations and income, which isn’t necessarily the case, then their socioeconomic status will be determined by whether they’re married, how many children they have and their husbands’ income. “All you have to do is look at nurses,” Petitti says. “Some are married to C.E.O.’s of corporations and some are not married and still living with their parents. It cannot be true that there is no socioeconomic distribution among nurses.” Stampfer says that since the Women’s Health Initiative results came out in 2002, the Nurses’ Health Study investigators went back into their data to examine socioeconomic status “to the extent that we could” — looking at measures that might indirectly reflect wealth and social class. “It doesn’t seem plausible” that socioeconomic status can explain the association they observed, he says. But the Nurses’ investigators never published that analysis, and so the skeptics have remained unconvinced.
The Bias of Compliance
A still more subtle component of healthy-user bias has to be confronted. This is the compliance or adherer effect. Quite simply, people who comply with their doctors’ orders when given a prescription are different and healthier than people who don’t. This difference may be ultimately unquantifiable. The compliance effect is another plausible explanation for many of the beneficial associations that epidemiologists commonly report, which means this alone is a reason to wonder if much of what we hear about what constitutes a healthful diet and lifestyle is misconceived.
The lesson comes from an ambitious clinical trial called the Coronary Drug Project that set out in the 1970s to test whether any of five different drugs might prevent heart attacks. The subjects were some 8,500 middle-aged men with established heart problems. Two-thirds of them were randomly assigned to take one of the five drugs and the other third a placebo. Because one of the drugs, clofibrate, lowered cholesterol levels, the researchers had high hopes that it would ward off heart disease. But when the results were tabulated after five years, clofibrate showed no beneficial effect. The researchers then considered the possibility that clofibrate appeared to fail only because the subjects failed to faithfully take their prescriptions.
As it turned out, those men who said they took more than 80 percent of the pills prescribed fared substantially better than those who didn’t. Only 15 percent of these faithful “adherers” died, compared with almost 25 percent of what the project researchers called “poor adherers.” This might have been taken as reason to believe that clofibrate actually did cut heart-disease deaths almost by half, but then the researchers looked at those men who faithfully took their placebos. And those men, too, seemed to benefit from adhering closely to their prescription: only 15 percent of them died compared with 28 percent who were less conscientious. “So faithfully taking the placebo cuts the death rate by a factor of two,” says David Freedman, a professor of statistics at the University of California, Berkeley. “How can this be? Well, people who take their placebo regularly are just different than the others. The rest is a little speculative. Maybe they take better care of themselves in general. But this compliance effect is quite a big effect.”
The moral of the story, says Freedman, is that whenever epidemiologists compare people who faithfully engage in some activity with those who don’t — whether taking prescription pills or vitamins or exercising regularly or eating what they consider a healthful diet — the researchers need to account for this compliance effect or they will most likely infer the wrong answer. They’ll conclude that this behavior, whatever it is, prevents disease and saves lives, when all they’re really doing is comparing two different types of people who are, in effect, incomparable.
This phenomenon is a particularly compelling explanation for why the Nurses’ Health Study and other cohort studies saw a benefit of H.R.T. in current users of the drugs, but not necessarily in past users. By distinguishing among women who never used H.R.T., those who used it but then stopped and current users (who were the only ones for which a consistent benefit appeared), these observational studies may have inadvertently focused their attention specifically on, as Jerry Avorn says, the “Girl Scouts in the group, the compliant ongoing users, who are probably doing a lot of other preventive things as well.”
How Doctors Confound the Science
Another complication to what may already appear (for good reason) to be a hopelessly confusing story is what might be called the prescriber effect. The reasons a physician will prescribe one medication to one patient and another or none at all to a different patient are complex and subtle. “Doctors go through a lot of different filters when they’re thinking about what kind of drug to give to what kind of person,” says Avorn, whose group at Harvard has spent much of the last decade studying this effect. “Maybe they give the drug to their sickest patients; maybe they give it to the people for whom nothing else works.”
It’s this prescriber effect, combined with what Avorn calls the eager-patient effect, that is one likely explanation for why people who take cholesterol-lowering drugs called statins appear to have a greatly reduced risk of dementia and death from all causes compared with people who don’t take statins. The medication itself is unlikely to be the primary cause in either case, says Avorn, because the observed associations are “so much larger than the effects that have been seen in randomized-clinical trials.”
If we think like physicians, Avorn explains, then we get a plausible explanation: “A physician is not going to take somebody either dying of metastatic cancer or in a persistent vegetative state or with end-stage neurologic disease and say, ‘Let’s get that cholesterol down, Mrs. Jones.’ The consequence of that, multiplied over tens of thousands of physicians, is that many people who end up on statins are a lot healthier than the people to whom these doctors do not give statins. Then add into that the people who come to the doctor and say, ‘My brother-in-law is on this drug,’ or, ‘I saw it in a commercial,’ or, ‘I want to do everything I can to prevent heart disease, can I now have a statin, please?’ Those kinds of patients are very different from the patients who don’t come in. The coup de grâce then comes from the patients who consistently take their medications on an ongoing basis, and who are still taking them two or three years later. Those people are special and unusual and, as we know from clinical trials, even if they’re taking a sugar pill they will have better outcomes.”
The trick to successfully understanding what any association might really mean, Avorn adds, is “being clever.” “The whole point of science is self-doubt,” he says, “and asking could there be another explanation for what we’re seeing.”
H.R.T. and the Plausibility Problem
Until the HERS and W.H.I. trials tested and refuted the hypothesis that hormone-replacement therapy protected women against heart disease, Stampfer, Willett and their colleagues argued that these alternative explanations could not account for what they observed. They had gathered so much information about their nurses, they said, that it allowed them to compare nurses who took H.R.T. and engaged in health-conscious behaviors against women who didn’t take H.R.T. and appeared to be equally health-conscious. Because this kind of comparison didn’t substantially change the size of the association observed, it seemed reasonable to conclude that the association reflected the causal effect of H.R.T. After the W.H.I. results were published, says Stampfer, their faith was shaken, but only temporarily. Clinical trials, after all, also have limitations, and so the refutation of what was originally a simple hypothesis — that H.R.T. wards off heart disease — spurred new hypotheses, not quite so simple, to explain it.
At the moment, at least three plausible explanations exist for the discrepancy between the clinical trial results and those of the Nurses’ Health Study and other observational studies. One is that the associations perceived by the epidemiologic studies were due to healthy-user and prescriber effects and not H.R.T. itself. Women who took H.R.T. had less heart disease than women who didn’t, because women who took H.R.T. are different from women who didn’t take H.R.T. And maybe their physicians are also different. In this case, the trials got the right answer; the observational studies got the wrong answer.
A second explanation is that the observational studies got the wrong answer, but only partly. Here, healthy-user and prescriber effects are viewed as minor issues; the question is whether observational studies can accurately determine if women were really taking H.R.T. before their heart attacks. This is a measurement problem, and one conspicuous limitation of all epidemiology is the difficulty of reliably assessing whatever it is the investigators are studying: not only determining whether or not subjects have really taken a medication or consumed the diet that they reported, but whether their subsequent diseases were correctly diagnosed. “The wonder and horror of epidemiology,” Avorn says, “is that it’s not enough to just measure one thing very accurately. To get the right answer, you may have to measure a great many things very accurately.”
The most meaningful associations are those in which all the relevant factors can be ascertained reliably. Smoking and lung cancer, for instance. Lung cancer is an easy diagnosis to make, at least compared with heart disease. And “people sort of know whether they smoke a full pack a day or half or what have you,” says Graham Colditz, who recently left the Nurses’ study and is now at Washington University School of Medicine in St. Louis. “That’s one of the easier measures you can get.” Epidemiologists will also say they believe in the associations between LDL cholesterol, blood pressure and heart disease, because these biological variables are measured directly. The measurements don’t require that the study subjects fill out a questionnaire or accurately recall what their doctors may have told them.
Even the way epidemiologists frame the questions they ask can bias a measurement and produce an association that may be particularly misleading. If researchers believe that physical activity protects against chronic disease and they ask their subjects how much leisure-time physical activity they do each week, those who do more will tend to be wealthier and healthier, and so the result the researchers get will support their preconceptions. If the questionnaire asks how much physical activity a subject’s job entails, the researchers might discover that the poor tend to be more physically active, because their jobs entail more manual labor, and they tend to have more chronic diseases. That would appear to refute the hypothesis.
The simpler the question or the more objective the measurement the more likely it is that an association may stand in the causal pathway, as these researchers put it. This is why the question of whether hormone-replacement therapy effects heart-disease risk, for instance, should be significantly easier to nail down than whether any aspect of diet does. For a measurement “as easy as this,” says Jamie Robins, a Harvard epidemiologist, “where maybe the confounding is not horrible, maybe you can get it right.” It’s simply easier to imagine that women who have taken estrogen therapy will remember and report that correctly — it’s yes or no, after all — than that they will recall and report accurately what they ate and how much of it over the last week or the last year.
But as the H.R.T. experience demonstrates, even the timing of a yes-or-no question can introduce problems. The subjects of the Nurses’ Health Study were asked if they were taking H.R.T. every two years, which is how often the nurses were mailed new questionnaires about their diets, prescription drug use and whatever other factors the investigators deemed potentially relevant to health. If a nurse fills out her questionnaire a few months before she begins taking H.R.T., as Colditz explains, and she then has a heart attack, say, six months later, the Nurses’ study will classify that nurse as “not using” H.R.T. when she had the heart attack.
As it turns out, 40 percent of women who try H.R.T. stay on it for less than a year, and most of the heart attacks recorded in the W.H.I. and HERS trials occurred during the first few years that the women were prescribed the therapy. So it’s a reasonable possibility that the Nurses’ Health Study and other observational studies misclassified many of the heart attacks that occurred among users of hormone therapy as occurring among nonusers. This is the second plausible explanation for why these epidemiologic studies may have erroneously perceived a beneficial association of hormone use with heart disease and the clinical trials did not.
In the third explanation, the clinical trials and the observational studies both got the right answer, but they asked different questions. Here the relevant facts are that the women who took H.R.T. in the observational studies were mostly younger women going through menopause. Most of the women enrolled in the clinical trials were far beyond menopause. The average age of the women in the W.H.I. trial was 63 and in HERS it was 67. The primary goal of these clinical trials was to test the hypothesis that H.R.T. prevented heart disease. Older women have a higher risk of heart disease, and so by enrolling women in their 60s and 70s, the researchers didn’t have to wait nearly as long to see if estrogen protected against heart disease as they would have if they only enrolled women in their 50s.
This means the clinical trials were asking what happens when older women were given H.R.T. years after menopause. The observational studies asked whether H.R.T. prevented heart disease when taken by younger women near the onset of menopause. A different question. The answer, according to Stampfer, Willett and their colleagues, is that estrogen protects those younger women — perhaps because their arteries are still healthy — while it induces heart attacks in the older women whose arteries are not. “It does seem clear now,” Willett says, “that the observational studies got it all right. The W.H.I. also got it right for the question they asked: what happens if you start taking hormones many years after menopause? But that is not the question that most women have cared about.”
This last explanation is now known as the “timing” hypothesis, and it certainly seems plausible. It has received some support from analyses of small subsets of the women enrolled in the W.H.I. trial, like the study published in June in The New England Journal of Medicine. The dilemma at the moment is that the first two explanations are also plausible. If the compliance effect can explain why anyone faithfully following her doctor’s orders will be 50 percent less likely to die over the next few years than someone who’s not so inclined, then it’s certainly possible that what the Nurses’ Health Study and other observational studies did is observe a compliance effect and mistake it for a beneficial effect of H.R.T. itself. This would also explain why the Nurses’ Health Study observed a 40 percent reduction in the yearly risk of death from all causes among women taking H.R.T. And it would explain why the Nurses’ Health Study reported very similar seemingly beneficial effects for antioxidants, vitamins, low-dose aspirin and folic acid, and why these, too, were refuted by clinical trials. It’s not necessarily true, but it certainly could be.
While Willett, Stampfer and their colleagues will argue confidently that they can reasonably rule out these other explanations based on everything they now know about their nurses — that they can correct or adjust for compliance and prescriber effects and still see a substantial effect of H.R.T. on heart disease — the skeptics argue that such confidence can never be justified without a clinical trial, at least not when the associations being studied are so small. “You can correct for what you can measure,” says Rory Collins, an epidemiologist at Oxford University, “but you can’t measure these things with precision so you will tend to under-correct for them. And you can’t correct for things that you can’t measure.”
The investigators for the Nurses’ Health Study “tend to believe everything they find,” says Barrett-Connor of the University of California, San Diego. Barrett-Connor also studied hormone use and heart disease among a large group of women and observed and published the same association that the Nurses’ Health Study did. She simply does not find the causal explanation as easy to accept, considering the plausibility of the alternatives. The latest variation on the therapeutic wisdom on H.R.T. is plausible, she says, but it remains untested. “Now we’re back to the place where we’re stuck with observational epidemiology,” she adds. “I’m back to the place where I doubt everything.”
What to Believe?
So how should we respond the next time we’re asked to believe that an association implies a cause and effect, that some medication or some facet of our diet or lifestyle is either killing us or making us healthier? We can fall back on several guiding principles, these skeptical epidemiologists say. One is to assume that the first report of an association is incorrect or meaningless, no matter how big that association might be. After all, it’s the first claim in any scientific endeavor that is most likely to be wrong. Only after that report is made public will the authors have the opportunity to be informed by their peers of all the many ways that they might have simply misinterpreted what they saw. The regrettable reality, of course, is that it’s this first report that is most newsworthy. So be skeptical.
If the association appears consistently in study after study, population after population, but is small — in the range of tens of percent — then doubt it. For the individual, such small associations, even if real, will have only minor effects or no effect on overall health or risk of disease. They can have enormous public-health implications, but they’re also small enough to be treated with suspicion until a clinical trial demonstrates their validity.
If the association involves some aspect of human behavior, which is, of course, the case with the great majority of the epidemiology that attracts our attention, then question its validity. If taking a pill, eating a diet or living in proximity to some potentially noxious aspect of the environment is associated with a particular risk of disease, then other factors of socioeconomic status, education, medical care and the whole gamut of healthy-user effects are as well. These will make the association, for all practical purposes, impossible to interpret reliably.
The exception to this rule is unexpected harm, what Avorn calls “bolt from the blue events,” that no one, not the epidemiologists, the subjects or their physicians, could possibly have seen coming — higher rates of vaginal cancer, for example, among the children of women taking the drug DES to prevent miscarriage, or mesothelioma among workers exposed to asbestos. If the subjects are exposing themselves to a particular pill or a vitamin or eating a diet with the goal of promoting health, and, lo and behold, it has no effect or a negative effect — it’s associated with an increased risk of some disorder, rather than a decreased risk — then that’s a bad sign and worthy of our consideration, if not some anxiety. Since healthy-user effects in these cases work toward reducing the association with disease, their failure to do so implies something unexpected is at work.
All of this suggests that the best advice is to keep in mind the law of unintended consequences. The reason clinicians test drugs with randomized trials is to establish whether the hoped-for benefits are real and, if so, whether there are unforeseen side effects that may outweigh the benefits. If the implication of an epidemiologist’s study is that some drug or diet will bring us improved prosperity and health, then wonder about the unforeseen consequences. In these cases, it’s never a bad idea to remain skeptical until somebody spends the time and the money to do a randomized trial and, contrary to much of the history of the endeavor to date, fails to refute it.

Wednesday, August 15, 2007

Google and Microsoft Look to Change Health Care

By STEVE LOHR
In politics, every serious candidate for the White House has a health care plan. So too in business, where the two leading candidates for Web supremacy, Google and Microsoft, are working up their plans to improve the nation’s health care.
By combining better Internet search tools, the vast resources of the Web and online personal health records, both companies are betting they can enable people to make smarter choices about their health habits and medical care.
“What’s behind this is the mass consumerization of health information,” said Dr. David J. Brailer, the former health information technology coordinator in the Bush administration, who now heads a firm that invests in health ventures.
It is too soon to know whether either Google or Microsoft will make real headway. Health care, experts note, is a field where policy, regulation and entrenched interests tend to slow the pace of change, and technology companies have a history of losing patience.
And for most people, typing an ailment into a Web search engine is very different from entrusting a corporate titan with personal information about their health.
Google and Microsoft recognize the obstacles, and they concede that changing health care will take time. But the companies see the potential in attracting a large audience for health-related advertising and services. And both companies bring formidable advantages to the consumer market for such technology.
Microsoft’s software animates more than 90 percent of all personal computers, while Google is the default starting point for most health searches. And people are increasingly turning to their computers and the Web for health information and advice. A Harris poll, published last month, found that 52 percent of adults sometimes or frequently go to the Web for health information, up from 29 percent in 2001.
If the efforts of the two big companies gain momentum over time, that promises to accelerate a shift in power to consumers in health care, just as Internet technology has done in other industries.
Today, about 20 percent of the nation’s patient population have computerized records — rather than paper ones — and the Bush administration has pushed the health care industry to speed up the switch to electronic formats. But these records still tend to be controlled by doctors, hospitals or insurers. A patient moves to another state, for example, but the record usually stays.
The Google and Microsoft initiatives would give much more control to individuals, a trend many health experts see as inevitable. “Patients will ultimately be the stewards of their own information,” said John D. Halamka, a doctor and the chief information officer of the Harvard Medical School.
Already the Web is allowing people to take a more activist approach to health. According to the Harris survey, 58 percent of people who look online for health information discussed what they found with their doctors in the last year.
It is common these days, Dr. Halamka said, for a patient to come in carrying a pile of Web page printouts. “The doctor is becoming a knowledge navigator,” he said. “In the future, health care will be a much more collaborative process between patients and doctors.”
Microsoft and Google are hoping this will lead people to seek more control over their own health records, using tools the companies will provide. Neither company will discuss their plans in detail. But Microsoft’s consumer-oriented effort is scheduled to be announced this fall, while Google’s has been delayed and will probably not be introduced until next year, according to people who have been briefed on the companies’ plans.
A prototype of Google Health, which the company has shown to health professionals and advisers, makes the consumer focus clear. The welcome page reads, “At Google, we feel patients should be in charge of their health information, and they should be able to grant their health care providers, family members, or whomever they choose, access to this information. Google Health was developed to meet this need.”
A presentation of screen images from the prototype — which two people who received it showed to a reporter — then has 17 other Web pages including a “health profile” for medications, conditions and allergies; a personalized “health guide” for suggested treatments, drug interactions and diet and exercise regimens; pages for receiving reminder messages to get prescription refills or visit a doctor; and directories of nearby doctors.
Google executives would not comment on the prototype, other than to say the company plans to experiment and see what people want. “We’ll make mistakes and it will be a long-range march,” said Adam Bosworth, a vice president of engineering and leader of the health team. “But it’s also true that some of what we’re doing is expensive, and for Google it’s not.”
At Microsoft, the long-term goal is similarly ambitious. “It will take grand scale to solve these problems like the data storage, software and networking needed to handle vast amounts of personal health and medical information,” said Steve Shihadeh, general manager of Microsoft’s health solutions group. “So there are not many companies that can do this.”
This year, Microsoft bought a start-up, Medstory, whose search software is tailored for health information, and last year bought a company that makes software for retrieving and displaying patient information in hospitals. Microsoft software is already used in hospitals, clinical laboratories and doctors’ offices, and, Mr. Shihadeh noted, the three most popular health record systems in doctors’ offices are built with Microsoft software and programming tools.
Microsoft will not disclose its product plans, but according to people working with the company the consumer effort will include online offerings as well as software to find, retrieve and store personal health information on personal computers, cellphones and other kinds of digital devices — perhaps even a wristwatch with wireless Internet links some day.
Mr. Shihadeh declined to discuss specifics, but said, “We’re building a broad consumer health platform, and we view this challenge as far bigger than a personal health record, which is just scratching the surface.”
Yet personal health records promise to be a thorny challenge for practical and privacy reasons. To be most useful, a consumer-controlled record would include medical and treatment records from doctors, hospitals, insurers and laboratories. Under federal law, people can request and receive their personal health data within 90 days. But the process is complicated, and the replies typically come on paper, as photocopies or faxes.
The efficient way would be for that data to be sent over the Internet into a person’s digital health record. But that would require partnerships and trust between health care providers and insurers and the digital record-keepers.
Privacy concerns are another big obstacle, as both companies acknowledge. Most likely, they say, trust will build slowly, and the online records will include as much or as little personal information as users are comfortable divulging.
A person might start, for example, by typing in age, gender and a condition, like diabetes, as a way to find more personalized health information. If a person creates a personal health record and later has second thoughts, a simple mouse click should erase it. The promise, the companies say, will be complete consumer control.
There are plenty of competitors these days in online health records and information from start-ups like Revolution Health, headed by AOL’s founder, Stephen M. Case, and thriving profit-makers led by WebMD.
Potential rivals are not underestimating the two technology giants. But the smaller companies have the advantage of being focused entirely on health, and some have been around for years. WebMD, for example, traces its lineage to Healtheon, a fallen star of the dot-com era, founded by the Netscape billionaire Jim Clark.
Google and Microsoft are great companies, said Wayne T. Gattinella, WebMD’s chief executive, but “that doesn’t mean they will be expert in a specific area like health.”
Specialized health search engines — notably Healthline — are gaining ground and adding partners. AOL recently began using Healthline for searches on its health pages, even though Google is a close partner.
Still, 58 percent of people seeking health information online begin with a general search engine, according to a recent Jupiter Research report, and Google dominates the field. “Google is the entry point for most health search, and that is a huge advantage,” said Monique Levy, a Jupiter analyst.
Indeed, it is the market reach and deep pockets that Google and Microsoft can bring to consumer health information that intrigues medical experts, and has lured recruits. Dr. Roni Zeiger, a graduate of Stanford’s School of Medicine, a medical informatics researcher and a former primary care doctor, joined Google last year. The 36-year-old, who still sees patients some evenings and weekends at a nearby clinic, said, “At Google, I can use my expertise and knowledge to potentially help millions of people each day.”