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PeRSSonalized Medicine: A free tool to track medical information January 31, 2009

Posted by Dr. Bertalan Meskó in eHealth, Health, Health 2.0, Innovation, Medical Search, Medicine, Medicine 2.0, PeRSSonalized Medicine, RSS, Technology, Web 2.0, Webicina.
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12 comments

We’ve recently had a long discussion on Twitter about why many doctors are not open to these web 2.0 tools. There is no question, they don’t have enough time to use these even if they were designed to help them save time and effort.

That’s why we’ve been working hard on Webicina.com to come up with a free tool that helps those users who cannot spend much time online (e.g. medical professionals). PeRSSonalized Medicine helps them track medical journals, blogs, news and web 2.0 services really easily and creates one personalized place where they can follow international medical content without having a clue what RSS is about.

Webicina.Com

Being up-to-date is crucial for medical professionals, but it takes time and effort. Sitting in a library with a few medical papers is not a proper solution any more. Learning to use an RSS reader is not that easy for those who don’t spend much time online.

PeRSSonalized Medicine is a free tool that lets you select your favourite resources and read the latest news and articles in one personalized place. You can create your own “medical journal” and as we are totally open to suggestions, let us add the journals, blogs and websites that you would like to follow.

perssonalized-medicine

Click on “Personalize It” to hide the resources you don’t want to follow.

You don’t have to register to use it, but if you want to make sure it will save your settings, you can register in a few seconds here.

Now you can follow:

  • Medical journals
  • Medical blogs
  • Medical news
  • Medical Media including Youtube channels, Friendfeed rooms or Del.icio.us tags

One more thing. The developer behind PeRSSonalized Medicine and the whole Webicina platform is Gergő Vargyai. Many thanks to him for his ownderful job!

As always, we are open to suggestions so please let us know which resources to add to the database.

Further reading:

Health Blogs Observatory January 31, 2009

Posted by Dr. Bertalan Meskó in Blogging, Health, Health 2.0, Medicine, Medicine 2.0, Web 2.0.
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6 comments

Ivor Kovic, MD is a unique blogger with a deep interest in web 2.0 and medicine. Now he launched the Health Blogs Observatory based on a great idea, to collect all the medical blogs in order to analyze the health blogosphere.

Health Blogs Observatory is an online research lab devoted to examination of the health blogosphere. It was created by the health bloggers and for the health bloggers.

Main goals of the project are:

Two major characteristics of the Health Blogs Observatory are collaboration and openness. This is why I would like to invite all health/medical bloggers to join the community and start contributing to it by adding their blogs to the web directory and participating in the design of the health bloggers survey.

health-blogs-observatory

You can follow the project on Twitter, by RSS or just track the changes of the wiki.

Medical Revolution – From Molecule to Medicine January 31, 2009

Posted by Dr. Bertalan Meskó in Medicine, Ted Talks, Video, Web 2.0.
1 comment so far

The best way to start a nice Saturday is to watch a few interesting videos.

MEDICAL REVOLUTION The Future, is awarded with two GOLD medals for the short film ‘From Molecule to Medicine’ at the New York Festivals’ International Film & Video Awards 2008. The documentary is selected as ‘World’s best work 2007′ in two categories: ‘Health/Medical Issues’ and ‘Health Care Professional Education’.

The movie exists of 2 parts:
From Molecule to Medicine: explaining the various stages for a pharmaceutical researchers to develop new medicines. Why does it take up to 14 years to develop new medicines, what are the challenges, the risks, the innovation behind it.

The second part, The Future, tells us all about the human body being a vulnerable miracle. How researchers discover bit by bit the secrets it keeps inside, by exploring our DNA / genetic structure. It tells about full body scans, DNA arrays and how personalized medicines will be developed giving hope to many of us, hope for a better future.

(Click here to access the video)

(Click here to access the video)

Check the Speaking at TED 2009 page out as well.

Top 50 Genetics Blogs January 30, 2009

Posted by Dr. Bertalan Meskó in Blogging, genetics, List.
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2 comments

Jessica Merritt has recently come up with a huge list of quality blogs dedicated to genetics. Check it out at US PharmD. I’m honored to be included in the list.

If you’re looking for another great genetics blogs, follow the members of the DNA Network.

The DNA Network logo

Image credit: Ricardo Vidal, My Biotech Life

Scienceroll Search: Order by Date and New Resources January 30, 2009

Posted by Dr. Bertalan Meskó in Medical Search, Medicine, Medicine 2.0, Scienceroll, Scienceroll Search, Web 2.0.
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3 comments

Scienceroll Search is a personalized medical search engine powered by PolyMeta search and clustering engine. You can choose which databases to search in and which one to exclude from your list. It works with well-known medical search engines and databases and we’re totally open to add new ones or remove those you don’t really like.

Now we added a new funcion. You can sort search results by relevance or by date.

scienceroll-search-date-order

When date is not assigned to a site, it will be listed in the bottom of the list.

We also added two more resources, Google Scholar and the National Library of Medicine.

If you want to add other resources, please let us know.

Guus van den Brekel at DigiCMB just inserted the search widget into his blog.

scienceroll-search-widget

Feel free to do the same on your blog!

Further reading:

Have you used the services of 23andMe, deCODEme, Navigenics, or Knome? January 30, 2009

Posted by Dr. Bertalan Meskó in genetics, Genome.
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Marcie Lambrix (Research Assistant at Case Western University, School of Medicine) asked me to post this announcement:

Early adopters of Direct to Consumer Genome Scans, researchers at Case Western Reserve University want to talk with YOU!

We’re currently conducting in-depth interviews with early-adopter/consumers of such tests to learn more about an individuals’ decision to us Direct to Consumer genome scanning, what they understand to be the benefits and risks of this technology, both for individuals and society. Our interview question will address how the participant learned of whole genome scanning services, why they were interested in trying the technology, how they feel about the results that they have received, what they have done with the results, and if and how they have used the results to inform their individual healthcare decisions.

To learn more about participating in this study, please contact Marcie Lambrix at 216-368-8753 or via email at mal31 at case.edu

babydna40.jpg

Biomedical communities online: 9 new additions January 29, 2009

Posted by Dr. Bertalan Meskó in Community Site, Medicine, Medicine 2.0, science, Web 2.0.
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4 comments

I’ve been updating my extended list of medical community sites for months and here are a few more additions. It means the full list now contains 33 (!) biomedical community sites with descriptions and screenshots. Feel free to drop me a line if you know more.

  • LaboraTree: a social networking tool for scientists and a research management tool. Laboratree allows you to grow your network by joining up with various colleagues, groups, and projects. Laboratree allows you to e-mail or send messages to all parts of your network. Laboratree allows you to manage a personal or group blog. Laboratree’s latest feature allows you to share papers, documents, and other files with other people on Laboratree.

laboratree

  • BioSpace is a social network in biology.  It provides the necessary functionality to allow you to share information between people (within group, friends)

biospace

  • Researcher ID is a global, multi-disciplinary scholarly research community. With a unique identifier assigned to each author in ResearcherID, you can eliminate author misidentification and view an author’s citation metrics instantly. Search the registry to find collaborators, review publication lists and explore how research is used around the world.

reseacrherid

  • PHYZOOM: you can find the physicians in your community who are staying on top of the latest health trends, products and services. In addition, your search options are much more dynamic than your average physician directory available from your local hospitals and health systems.

phyzoom

  • The Science Advisory Board: Voice your opinions on companies, products, protocols and even humor in a lively, real-time, interactive Online Community of over 42,000 life science & medical professionals. Redeem generous rewards for participation in studies, contributing website content and referring colleagues.

sc-adv-board

  • MySDscience: Scientific collaborations, professional development, and science education while raising awareness for the San Diego Science Festival.

mysdscience

  • Web of Medicine: it was created for busy clinicians who want to build and join professional networks of medical colleagues. Users have expressed a clear requirement to connect with colleagues in their own practices and hospitals but also nationally and internationally.

webofmedicine

  • New Media Medicine is an online Social Network of over 42,000 doctors, medical students and pre-med students. It’s like Facebook for medics.

new-media-medicine

  • Asklepios: the social network for physicians created by the Canadian Medical Association. Here you can make new contacts, get advice from colleagues, and collaborate with people all over the country. And it’s exclusively for Canadian physicians, residents and medical students, so you’ll know exactly who you’re connecting with there.

asklepius

Navigenics Interview: Annual Insight January 28, 2009

Posted by Dr. Bertalan Meskó in Genetic testing, genetics, Genome, Innovation, Medicine, Personalized medicine, Pharmacogenomics, science, Web 2.0.
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4 comments

In my post about the predictions for 2009 in genomics, I said Navigenics would rule the market even if its service was more expensive than the kit of 23andMe. Now I had a chance to do an interview about the scientific background of the service and I have already sent my saliva sample back to their lab so the results should arrive soon.

Now, they came up with a totally new website, a new product and a lower price (read the press release). I’m always saying such genetic tests should be ordered by physicians. Well, here is an excerpt from the press release:

Accessible through Navigenics’ website, the secure portal empowers physicians with a suite of tools including a single access point to all of their participating patients’ genomic information, along with learning tools and case studies for integrating genomic information into their clinical practice.

I believe that was a crucial step to make.

navigenics1

1. There are more and more companies offering direct-to-consumer DNA testing. How does Navigenics try to make a difference?

  • Navigenics focuses exclusively on providing genetic information for health conditions – all of which can be delayed, prevented or diagnosed early.
  • We offer two DNA testing experiences that provide different levels of premium analysis and service to best meet your needs. With both, you’ll get relevant health information and the support to help you share your results with your doctor effectively.
  • We are the only personalized genetic testing company that provides the support of board-certified genetic
  • ounselors, to help you understand your results and take action.
  • We use only government-certified laboratories.
  • Our results are based on science of the highest possible caliber. We only report on genetic markers that have met stringent criteria developed by our team of Ph.D. geneticists.
  • Privacy is our priority. Your results are kept private and secure, so the only person who has access to your results is you.
  • Navigenics is committed to research and we serve as a leader and collaborator to advance the science of genetics. We collaborate with some of the best medical institutions in the world.

2. So far, the terms of service of Navigenics have stated the results shouldn’t be used for healthcare decisions. Will it change in the near future?

Our Terms and Conditions indicate that our services are not intended to substitute for professional medical advice, diagnosis or treatment, and we have always encouraged customers to work with their physician before taking any steps after receiving their Navigenics results. As our service offerings evolve and more physicians incorporate our services into their practice, we will consider whether that necessitates any changes or clarifications to our Terms and Conditions of service .

3. The new Annual Insight provides a genetic check up for 9 common medical conditions. Personalized genetic services usually analyze more than 20 conditions. What is the reason behind the decision to analyze only 9?

The Navigenics Annual Insight service offers a highly focused snapshot of your genetic predisposition to nine select health conditions. We use a customized test for each marker in order to gather 100% of the genetic information needed to give you a highly targeted analysis of your risk information for those health conditions . By focusing on 10 common conditions, you get a targeted look at some of the most common causes of disease and disability in the U.S. today.

4. What is the genetic background of the analysis? Do you use SNP chips to determine personal risks?

I have attached a detailed white paper that addresses this – please review and let me know if you have further questions. (Access to the pdf file: Applying Preventive Genomic Medicine in Clinical Practice)

5. How accurate do you think SNP analysis is nowadays? Of course, as science is moving forward, it can change, but do you think patients understand the scientific background? Can they make health decisions based on SNP studies?

Again, we encourage our customers to work with their physician before making any changes in their healthcare strategy after they receive their Navigenics results.

6. Are you open to use the tools of telemedicine or patients will have to meet genetic counselors in person? How do you ensure security?

Currently our genetic counseling sessions are conducted by phone. We have found this to be an effective and convenient means of providing professional support to those who engage in our testing services.

Navigenics adheres to rigid security standards throughout the genetic testing process. All of our Genetic Counselors are board-certified professionals who adhere to a code of ethics that includes maintaining the highest levels of privacy and confidentiality.

Navigenics is committed to protecting your privacy. You own your genetic data, and it is our responsibility to safeguard your genetic information. Using the most advanced data protection systems available, we:

  • Anonymize all member profiles to assure data security
  • Capture the minimum account information necessary for transactions.
  • Encrypt all your personal genomic data
  • Generate your genetic risk assessment reports on demand so they exist only as you view them
  • Maintain multiple layers of physical and electronic security measures.
  • Constantly monitor all relevant processes to ensure your genetic test results are not compromised
  • Have our operational, infrastructure and applications procedures independently audited.
  • Have a sophisticated customer identification process and authenticate all transactions.

Thank you for the answers!

What I especially liked on the new portal is the Genetic testing: Myths and truths section.

navigenics2

What do you think? Could Navigenics make the important steps regarding lower prices and more serious physician involvement?

Hope Leman reviews Scienceroll Search January 28, 2009

Posted by Dr. Bertalan Meskó in Interview, Medical Search, Medicine, Medicine 2.0, Scienceroll, Scienceroll Search, Web 2.0.
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3 comments

Scienceroll Search is a personalized medical search engine powered by PolyMeta search and clustering engine. You can choose which databases to search in and which one to exclude from your list. It works with well-known medical search engines and databases and we’re totally open to add new ones or remove those you don’t really like.

Now Hope Leman reviews it on AltSearchEngines.com.

altsearchengines

scienceroll-search

Further reading:

What’s on the web? (28 January 2009) January 28, 2009

Posted by Dr. Bertalan Meskó in What's on the web?, Wikipedia.
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encyc-britannica

Though there are an estimated 234 million operations performed annually worldwide, surgical complications are common and often preventable.  The WHO has developed the ‘Surgical Safety Checklist’, in an effort to help surgical teams confirm that critical safety steps are completed before an operation proceeds.

Prompted by a recent scholarly article that shows a reduction in post-surgical death by more than 40%, this critical research has been adapted into an ‘App’ or software application for the Apple iPhone.

researchblogging-logo

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