15
Jul
09

Online physicians are a global phenomenon

Manhattan Research reports that physician adoption of Internet resources is global, and in fact, essential. When asked whether they considered the Internet essential to their professional practice, the results were universally high:

  • 89% of online U.S. physicians
  • 88% of online South Korean physicians
  • 87% of online Australian physicians
  • 81% of online European physicians

According to Manhattan Research, physicians use the online information to support clinical decisions, make recommendations to patients and stay up-to-date with the latest medical advances.

08
Jul
09

From Pew: The Social Life of Health Information

The Pew Internet & American Life Project has released a major new study on the impact of the Web on health information uptake by consumers: The Social Life of Health Information. You can review the results online or download a PDF version. Very cool the way they have it set up.

There is far too much to excerpt here but some key stats for the data junkies in the house:

General

  • 74% of American adults go online
  • 57% of American households have broadband connection
  • 61% of American adults look online for health information (Pew calls these people “e-patients”)
  • 52% of all online health inquiries are on behalf of someone other than the person typing in the search terms.

Seeking/sharing health info

  • 41% of e-patients have read someone else’s commentary or experience about health or medical issues on an online news group, website, or blog.
  • 24% of e-patients have consulted rankings or reviews online of doctors, hospitals, or other providers
  • 12% of e-patients use Twitter or another service to share updates about themselves or to see updates about others

Acting on the info

  • 60% say the information found online affected a decision about how to treat an illness or condition.
  • 56% say it changed their overall approach to maintaining their health or the health of someone they help take care of.
  • 53% say it lead them to ask a doctor new questions, or to get a second opinion from another doctor
  • 38% say it changed the way they cope with a chronic condition or manage pain.

Credible or not?

  • 42% of all adults, or 60% of e-patients, say they or someone they know has been helped by following medical advice or health information found on the internet.
  • Just 3% of all adults, or 3% of e-patients, say they or someone they know has been harmed by following medical advice or health information found on the internet
02
Jul
09

Why Dr. Younes uses social media

This is an excellent account of one oncologist’s rationale for using Twitter (excerpt below). Dr. Anas Younes describes the utility of YouTube and Twitter in spreading credible information and enrolling target patients in clinical trials. Enjoy and have a happy 4th.

Two years ago, I decided to experiment with social media. I have a strong interest in the treatment of Hodgkin’s lymphoma, a rare type of human cancer that affects approximately 8,600 patients per year in the United States. With a cure rate of 75%, it was very challenging to get pharmaceutical companies interested in developing new therapies for this small patient population. Furthermore, because of the limited pool of patients who are eligible for experimental therapy, these trials traditionally never enrolled patients in a timely manner.

My challenge was to convince industry sponsors of the unmet medical need opportunity, and to demonstrate that novel clinical trials in this small patient population can indeed enroll patients in a timely manner. To achieve these objectives, my laboratory collaborated with several biotech and pharmaceutical scientists to examine targeted agents in preclinical experiments. These collaborations resulted in designing several clinical trials for patients with relapsed Hodgkin’s lymphoma. So we went from no clinical trials to four IRB-approved studies that ask important scientific and clinical questions. Now, I needed to spread the message to enroll patients.

Initially, I started sending e-mails to colleagues to draw attention to these clinical trials with links to clinicaltrials.gov. However, the results didn’t match the effort. So I had to use other methods of communications. I contacted the staffs of Oncolog and Conquest, two widely circulated M. D. Anderson publications, and explained to them my challenge. They both published stories and a few additional patients told me that they read these articles and that’s why they came to M. D. Anderson.

But ultimately, the biggest impact came from a social media outlet: YouTube. The online version of Conquest included a YouTube video link that covered our clinical and translational efforts to improve the treatment outcome of patients with relapsed Hodgkin’s lymphoma. In a few months, thousands have watched the video, which was associated with a surge in patient referrals to our clinic. Four years ago we used to enroll a maximum of 20 patients per year with relapsed Hodgkin’s lymphoma on clinical trials. We now enroll approximately 80 patients per year, an unprecedented number for any single institution. Results from these trials are rapidly reported in national and international meetings, and all of a sudden a momentum was created that hope is on the horizon for these patients who were neglected for almost three decades.

30
Jun
09

Tweet, tweet

I have a Twitter account and never post. I am not a Twitter-posting kind of person. Anytime I talk to clients about Twitter, the question always comes up: Why do people tweet? What is the point?

twitter_logo_headerI do my best to explain the difference between Twitter and Facebook, LinkedIn, email, et al. I use the Gaza and now Iran examples to showcase one of the best uses of Twitter. But I also point out what I’ve come to believe: there are two kinds of people in the world – those who like to talk about themselves and those who don’t. Me – I’m definitely in the latter camp.

On the other hand, if you purport to be au courant as it relates to social media, then you need to keep tabs on what’s going on. Thus, I follow a bunch of people on Twitter. To be honest, most of the posts are pretty mundane: lots of links to articles or press releases I don’t have time to read or info about one’s day-to-day routine. There is also a fair amount of puffery: tweets about accolades, awards, and exotic or cool locales.

Doctors have taken to Twitter in droves, and they are typically more fun to follow than business people. Perhaps you saw the June 11th article in the NY Times about MD tweeters, “Medicine in the Age of Twitter.” Even better are the comments on the Well blog accompanying the article. Anyhow I’ve been following doctors for a few months and they do say the darndest things. Among my faves: @Doctor_V (Bryan Vartabedian), a pediatrician in Houston who is hilarious and @EndoGoddess (Jen Dyer), an endocrinologist who is funny and loves wine. Others to get you started: @drval, @kevinmd, @drdannysands, @joemd, @mommy_doctor.

How to amass your own MD Twitter list? Add one person and look at whom he or she is following. Do it when you have a few hours because if you’re anything like me you’ll just keep clicking, following, adding.

You can follow me at @bellerin but there’s not a lot to follow…

18
Jun
09

UCB partners with PatientsLikeMe to create epilepsy community; adverse event reporting part of the package

I know that many pharma brand marketers are constrained by their own regulatory people who will not let them participate in social media programs or even monitor the conversation happening all around them. Well here is an example of one company doing just the opposite.

ucbUCB, headquartered in Brussels with a U.S. presence in Georgia, just announced a partnership with PatientsLikeMe (PLM) to create an online epilepsy community that enables patients to track the daily issues they confront living with the disease such as controlling their seizures and achieving treatment goals. The social community aspect should encourage patients, caregivers and researchers to share information with each other and help industry learn more about the disease and treatment experiences.

According to Medical Marketing & Media, UCB and PLM are working cooperatively to create a pharmacovigilance platform that will monitor the site for adverse events (only those associated with UCB products), which will then be reported directly to the FDA. No personal or identifiable information will be sent to either the FDA or UCB without the permission of the patient.

patientslikeme3UCB is the first pharma company to partner with PatientsLikeMe to launch a patient community; the epilepsy community is expected to launch in early 2010

I have often said that it is only when those in the C-suite take social media seriously that things will happen. Kudos to UCB’s CEO who championed this initiative. In the press release announcing the initiative he said, “UCB has a longstanding commitment to improving the lives of people living with severe conditions. This partnership is exciting because for the first time, patients will be able to contribute their experiences and real-world data to ongoing epilepsy research.”