From patients to end users

Quality of online patient networks needs more attention than quality of online health information

Some doctors still tremble in their boots when patients bring in printouts from the internet. If they refuse to read them, their patients may take offence. But if they attempt to review and discuss them, they may precipitate long, inconclusive discussions. And since many internet aware patients bring in information which their doctors know nothing about,1 such discussions can sometimes be embarrassing. Consequently, some doctors have gone so far as to warn their patients, “Whatever you do, don't go on the internet.”

Some studies seem to confirm the wisdom of such advice. A recent literature search turned up 100 studies that attempted to rate the accuracy and completeness of health information on the world wide web. Ratings ranged from about 15% to 85% (Eysenbach G. personal communication). Some doctors have understandably concluded that the healthcare information on the net is not to be trusted.

Our recent surveys at the Pew Internet and American Life Project offer a strikingly different perspective. 2 3 Of adults from the United States who had gone online for health information, 92% said that the last time they went online they found what they were looking for; 81% said they learned something new; 88% said the information they found improved the way they took care of their health. Of those who found health information online, 94% said that it was either “very easy” or “somewhat easy” to do so. And of the 37% who discussed the results of their searches with a health professional, only a tiny minority said that their health professional disagreed with the information they found online.

In explaining this notable difference of opinion between providers and patients, we must remember that it is only systems without their own inherent intelligence that require perfect input to operate effectively. Suppose that we were to subject a dozen randomly chosen printed sources such as textbooks, articles from magazines, newspaper stories, patient handouts to a similar evaluation and found a similar level of variability in quality and completeness. Would we be justified in concluding that healthcare information in printed form is so undependable and unreliable that we should warn our patients against it? I think not. And before we conclude that the information on the net is inadequate, incomplete, and generally scary, we might try comparing it with what the typical doctor tells the typical patient in the typical 10 minute office visit. Medical services provided online should not be held to a higher standard than similar services provided in person.

Online patients do agree with their doctors on one point—that much of what passes for online health information is not to be trusted. Of those with internet access, 82% say that they are concerned about getting online health information from an unreliable source.4 Where professionals and patients differ is in their views of these patients' ability to tell the good from the bad.

The patients that I and my colleagues have studied have proved themselves so unexpectedly capable in this regard that we have been forced to ask ourselves whether we can, in good conscience, continue to use the term “patient” in describing them. They are by no means patients in the usual sense—a person under a doctor's care, an invalid, a sufferer or victim, someone who bears pain and misfortune with fortitude and calm. We are beginning to substitute the term “medical end user” whenever this seems appropriate.

The medical end users we study do much more than just visit a single website and make snap decisions based on what they find. They typically use a search engine to find and review a number of different sites that target their specific concerns. 2 3 And they frequently find or form sophisticated online and offline networks, which can help them deal with the task of interpreting complex medical information (see box).

These person to person interactions provide patients with a valuable source of quality control. As one online self helper recently commented: “Doc, out here on the internet we patients have our own system of peer review.”

We believe that the 21st century will be the age of the net empowered medical end user and that the patient driven online support networks of today will evolve into more robust and capable medical guidance systems that will allow end users to direct and control an ever growing portion of their own medical care. Doctors who continue to believe that their patients are inherently incapable of navigating the plentiful health resources of the internet will find their net savvy patients leaving them for other doctors. By contrast, those wise and caring doctors who realise that we may have just as much to learn from our patients as they have from us should do very well indeed.