I appeared on the Fed Tech Talk radio program on Federal News Radio which aired on WFED 1500 AM in Washington, DC on January 28, 2014. It was a fun discussion with host John Gilroy (check out his blog here) where we discussed the Office of the National Coordinator for Health Information Technology (ONC) Annual Meeting, the historic signing of an MOU between the United States and Great Britain on sharing health IT tools, health information exchange, EHR adoption, the Direct Project, mobile health, and the current state of health IT in the nation.
I gave some background on my involvement in health information technology and an overview of the landscape in health IT and how we are building out an infrastructure to improve our healthcare system. This was a lot of fun, and hopefully helped get the word out that the state of health IT in this country is strong, and we are looking at the best year ever ahead. The bottom line is that it is time to drag the US healthcare system (albeit kicking and screaming) into the 21st century of technology.
These are Brian Ahier's views and information on Healthcare, Technology and Government 2.0 and do not represent any other organization.
Showing posts with label technology. Show all posts
Showing posts with label technology. Show all posts
Tuesday, January 28, 2014
Tuesday, July 13, 2010
A Meaningful Definition
The Office of the National Coordinator for Health Information Technology (ONC) issued a final rule defining meaningful use requirements to qualify for incentive payments under the HITECH portion of the ARRA. The final rule for meaningful use is embedded below (it is temporarily available at the Public Inspection Desk, but this link will expire after the rule is actually published) and it is scheduled to be published in the Federal Register July, 28 2010. The rule definitively outlines all the specifics of Stage 1 meaningful use and clinical quality measure reporting to receive the incentive payments in 2011 and 2012. The final rule builds on the notice of proposed rulemaking (NPRM) released December 30, 2009.
The definition of meaningful use attempts to harmonize criteria across other CMS programs as much as possible and coordinate with quality initiatives. It also is closely linked to the certification standards criteria in development by the Office of the National Coordinator (ONC) and provides a platform for a staged implementation over time. The temporary certification final rule was published in the Federal Register June 24, 2010. The final rule on Initial Set of Standards, Implementation Specifications, and Certification Criteria is below the meaningful use rule.
Initial Set of Standards, Implementation Specifications, and Certification Criteria
The definition of meaningful use attempts to harmonize criteria across other CMS programs as much as possible and coordinate with quality initiatives. It also is closely linked to the certification standards criteria in development by the Office of the National Coordinator (ONC) and provides a platform for a staged implementation over time. The temporary certification final rule was published in the Federal Register June 24, 2010. The final rule on Initial Set of Standards, Implementation Specifications, and Certification Criteria is below the meaningful use rule.
Initial Set of Standards, Implementation Specifications, and Certification Criteria
Friday, July 2, 2010
Health IT After HITECH
On Wednesday, June 23, 2010 the Center for Democracy and Technology held a panel discussion on health information privacy at the San Francisco office of the law firm of Manatt, Phelps & Phillips, LLP. According to Deven McGraw, the Director of the Health Privacy Project at CDT, the lack of a clear health privacy policy framework on innovation was one topic covered. The video is below and then there are slides from Cal OHIII on secondary uses data flow by entity type:
The panel combined both California and national health IT expertise and featured Jonah Frolich, California Deputy Secretary for Health Information Technology; Alex Kam, Acting Director of the California Office of Health Information Integrity (OHIII); David Lansky, President and CEO of the Pacific Business Group on Health; John Mattison, M.D., Chief Medical Information Officer of Kaiser Permanente; Deven McGraw, CDT’s Health Privacy Project Director; and Julie Murchinson, Managing Director of Manatt Health Solutions. Leslie Harris, President and CEO of CDT, moderated a discussion that quickly became an active one among both panelists and attendees.via cdt.org
The focus was initially on California and a recent paper released by CalOHIII largely raising concerns about “secondary” uses of health data (the paper will be available online shortly, check back here for a link). Such uses are often cited as raising greater privacy concerns. Yet the use of data for secondary (beyond individual treatment) purposes – such as for quality measurement and comparative effectiveness research – are key to achieving greater health system reform, raising the question of whether they should be relegated to secondary status.
The panel also spent some time discussing the appropriate role of individual consent in protecting privacy. The CalOHIII paper presents pro and con views on an “opt-in” approach to electronic health information exchange. CDT also has published papers raising doubts about the ability of privacy policy frameworks anchored by “notice and consent” to protect individual privacy.
via ohi.ca.gov
Wednesday, June 30, 2010
HIT Standards Committee Slides
It appears there is temporarily a problem with the links on the ONC web site for the June 30, 2010 HIT Standards Committee meeting materials. http://healthit.hhs.gov/portal/server.pt?open=512&objID=1816&parentname=CommunityPage&parentid=11&mode=2&in_hi_userid=11113&cached=true
I have posted them below:
I have posted them below:
Tuesday, June 29, 2010
Health IT Meets Rocket Science
In thinking about health IT, NASA might be the last federal agency that comes to mind. That’s what makes a seven-year joint venture between the space agency’s Jet Propulsion Laboratory and Childrens Hospital Los Angeles such an unlikely partnership.
Yet the two have an ongoing common need: to easily share and analyze massive amounts of data across far flung labs and clinics across the nation.
NASA’s research target was planetary science; Childrens Hospital’s was early detection of pediatric cancer. A chance encounter of researchers associated with the two fields at a 2003 conference ultimately led to a project to use grid software developed by JPL to help build a system to support the early detection of pediatric cancer.
(for more see http://www.govhealthit.com/Article.aspx?id=74068
*NOTE ~ This will be presented at O'Reilly OSCON in Portland, Oregon July 22, 2010
Yet the two have an ongoing common need: to easily share and analyze massive amounts of data across far flung labs and clinics across the nation.
NASA’s research target was planetary science; Childrens Hospital’s was early detection of pediatric cancer. A chance encounter of researchers associated with the two fields at a 2003 conference ultimately led to a project to use grid software developed by JPL to help build a system to support the early detection of pediatric cancer.
(for more see http://www.govhealthit.com/Article.aspx?id=74068
*NOTE ~ This will be presented at O'Reilly OSCON in Portland, Oregon July 22, 2010
Monday, June 28, 2010
Enrollment Workgroup 6-28-2010
The Enrollment Workgroup of the HIT Policy and HIT Standards Committees are working to come up with a set of standards which would facilitate enrollment in Federal and state health and human services programs. At their June 28, 2010 meeting they discussed key takeaways from their first meeting and had a general discussion on a base use case of a consumer-facing web portal. This web portal would allow applicants to:
The slides from the meeting are below:
via healthit.hhs.gov
- Identify available services for which they might be eligible
- Conduct initial screening and enrollment checks
- Retrieve electronic verification information from outside sources
- Determine eligibility or forward eligibility “packet” (screening information and verification information) to programs for final determination
- Store and re-use eligibility information
The slides from the meeting are below:
via healthit.hhs.gov
Friday, June 25, 2010
Interoperability Framework Overview
There was a very interesting presentation to the HIT Policy Committee from Douglas Fridsma, MD, PhD the Acting Director of the Office of Interoperability & Standards at ONC. The slides are below:
Tuesday, June 22, 2010
Leveraging the Electronic Health Record for Public Health Alerting
With the passage of the American Recovery and Reinvestment Act and its focus on EHR systems, public health has an unprecedented opportunity to leverage the information, technologies and standards enabled by this effort to support critical public health functions such as alerting and surveillance. Having public health systems interface with EHR might be able to prevent clinicians from being bombarded during health emergencies, as they were during the H1N1 pandemic with multiple sources, some of which provided contradictory information. The CDC hosted a conference call on June 22, 2010 on this subject.
Nedra Garrett, MS, acting director of the CDC's division of informatics practice, policy, and coordination, discussed strategies to increase compliance with public health recommendation and guidelines, and also how improved dissemination of public health information at point of care can lead to more timely patient specific information by utilizing EHR systems. She said some of the challenges are to connect public health alerts and guidance to relevant patient data in the EHR and to make sure systems have a meaningful impact on point-of-care practices, such as ordering lab tests and distributing educational information to patients.
The slides from her presentation are below:
Nedra Garrett, MS, acting director of the CDC's division of informatics practice, policy, and coordination, discussed strategies to increase compliance with public health recommendation and guidelines, and also how improved dissemination of public health information at point of care can lead to more timely patient specific information by utilizing EHR systems. She said some of the challenges are to connect public health alerts and guidance to relevant patient data in the EHR and to make sure systems have a meaningful impact on point-of-care practices, such as ordering lab tests and distributing educational information to patients.
The slides from her presentation are below:
Rule on meaningful use of EHR is coming soon
We are getting very close to having a final rule issued on meaningful use. I believe the final rule will have some significant changes from the proposed rule regarding how high a bar we must reach to qualify for the first year incentive payments. The proposed rule contains 25 measures that providers must use to qualify for federal incentives beginning January 2011. The rule also contains 23 measures through which hospitals must demonstrate meaningful use of healthcare IT for incentives beginning Oct. 1, 2011. I do not think the timelines will change, and I think that the measures are likely to stay basically intact. It is very difficult to substantially change a proposed rule, without requiring a whole new comment period.
So what exactly can they do make the rule more palatable and allow the greatest number of providers and hospitals to participate in incentive payments? It would be a terrible thing to offer a stimulus that few could qualify for... There were many, many comments submitted on the proposed rule, from every area of the industry, and I think most pointed in the same direction. We need to flatten the slope of adoption or we could see some massive failure points, particularly in rural and underserved areas, which actually need the stimulus the most.
A few thoughts on what may be possible:
This is but a small sampling of what might be in store. There will certainly be some scaling back of the requirements. Hopefully, it will be enough to encourage adoption without making it too difficult in the out years to achieve the later stages. If stage one meaningful use is too far watered down, then it will be a long jump to stages two and three. I think we will see the final rule before the Fourth of July - possibly even this week. You can bet there will be tweets and blog postings galore when this baby drops
;-)
So what exactly can they do make the rule more palatable and allow the greatest number of providers and hospitals to participate in incentive payments? It would be a terrible thing to offer a stimulus that few could qualify for... There were many, many comments submitted on the proposed rule, from every area of the industry, and I think most pointed in the same direction. We need to flatten the slope of adoption or we could see some massive failure points, particularly in rural and underserved areas, which actually need the stimulus the most.
A few thoughts on what may be possible:
- Only require a certain number of measures to be met in the first year and move away from "all or nothing approach" - this will almost certainly happen, and it will be interesting to see how far they are dialed back
- Reduce the number of quality measure reporting requirements by allowing identification of selected clinically relevant measures
- Clearer definition of terms such as "health information" and making "48 hours" something achievable by using business days instead
- Tweaking the definition of a "hospital-based physician" even further than accomplished through recent changes in legislation
- Reduction in administrative burden of reporting computerized physician order entry measures
- Scale back objectives and measures that don't directly apply to EHR adoption, such as checking insurance eligibility electronically
This is but a small sampling of what might be in store. There will certainly be some scaling back of the requirements. Hopefully, it will be enough to encourage adoption without making it too difficult in the out years to achieve the later stages. If stage one meaningful use is too far watered down, then it will be a long jump to stages two and three. I think we will see the final rule before the Fourth of July - possibly even this week. You can bet there will be tweets and blog postings galore when this baby drops
;-)
Monday, June 21, 2010
How to Survive a Medical Malpractice Lawsuit
Below is an excerpt from the new book by Dr. Ilene Brenner, MD, an Emergency Room physician and Adjunct Professor, Emory University, Atlanta, Georgia. She also writes a blog at drbrenner.blogspot.com and tweets @irb123. This is a medical malpractice survival book written by a doctor for doctors in non-legalese language that is easy to understand. It is designed to help navigate through what can be a mysterious and terrifying process.
Using her personal experience and expertise, she offers a glimpse into the medical malpractice process and acts as a guide to help a physician effectively deal with the situation. She leads through the process from the moment they receive a summons, through the trial, and into the appeal process. There is some excellent advice on how to best choose an attorney. She also points out that while good documentation won't necessarily keep you from being sued, it is the cornerstone of a good defense. And there is some very good advice about when to keep your mouth shut:
Ilene has done an excellent job of writing a readable and understandable treatise, which includes great advice on how to respond to a lawsuit, and also how to avoid one in the first place. We live in a very litigious culture and this resource is a must have for any clinicians book shelf.
"That dreaded day arrives. And no it is not just a bad dream. That police officer at your front door is not ringing the doorbell to warn you of a prowler in the neighborhood. He has come to serve you with papers notifying you of a complaint filed by a patient: a patient you may or may not remember seeing. Although anybody who serves you with papers is called a process server, in some jurisdictions, like mine, it is done by a sheriff ’s deputy. The feeling is akin to being hit on the head with a bat, stabbed in the back, and disemboweled, all at the same time. Thoughts run through your mind like, 'Will I lose my job?'; 'Is my money protected?'; 'Am I a bad doctor?'; and 'Is my career over?'
You are justifiably depressed, confused, frustrated, and angry. When you have had a few minutes, hours, or days to assimilate this experience that unfortunately has begun a new chapter in your life, you undoubtedly ask, 'Now what?'
When it happened to me, I called my father. Then again, not everyone has a medical malpractice defense trial attorney for a father. Most physicians do ot have an attorney who is readily available to give appropriate and timely advice to initiate damage control. Through this book I am going to suggest what to do and, equally important, what not to do...
Getting sued can damage your self-confidence. However, do not let fear consume you. Make every effort to continue practicing the good medicine you have been doing for years. It is possible that the lawsuit is a result of your unintentional negligence. If that is the case, realize you are human. We all make mistakes."
Using her personal experience and expertise, she offers a glimpse into the medical malpractice process and acts as a guide to help a physician effectively deal with the situation. She leads through the process from the moment they receive a summons, through the trial, and into the appeal process. There is some excellent advice on how to best choose an attorney. She also points out that while good documentation won't necessarily keep you from being sued, it is the cornerstone of a good defense. And there is some very good advice about when to keep your mouth shut:
"There is a common misconception amongst physicians that if they explain things well, their intelligent responses will prove to the plaintiff’s attorney that the whole thing is a mistake. They may also think that they need to explain their defense clearly and completely to the plaintiff’s attorney. However, as will be detailed later on in the chapter, a general rule is, “the less you say the better.” Since there is the potential to do significant damage to your case, it is critically important that you perform well; otherwise you may be forced to settle an otherwise winnable case."There is an excellent review in Emergency Physicians Monthly by Louise B. Andrew, MD, JD. She points out the need to be careful about differing statutes between states, but overall gives a very positive review. Dr. Andrew basically breaks the book into tow sections. The first is a walk through the process of litigation, the second is a practical discussion n preventative measures and reducing risk.
Kevin Klauer, Editor-in-Chief for Emergency Physicians Monthly, interviewed Ilene Brenner and discussed what to do and what not to do when you find yourself in a malpractice suit.
Ilene has done an excellent job of writing a readable and understandable treatise, which includes great advice on how to respond to a lawsuit, and also how to avoid one in the first place. We live in a very litigious culture and this resource is a must have for any clinicians book shelf.
Friday, June 18, 2010
Temporary Certification of Electronic Health Record Systems
Certification of Health IT will provide assurance to purchasers and other users that an EHR system, or other relevant technology, offers the necessary technological capability, functionality, and security to help them meet the meaningful use criteria established for a given phase. Providers and patients must also be confident that the electronic health IT products and systems they use are secure, can maintain data confidentially, and can work with other systems to share information. Confidence in health IT systems is an important part of advancing health IT system adoption and allowing for the realization of the benefits of improved patient care.
Eligible professionals and eligible hospitals who seek to qualify for incentive payments under the Medicare and Medicaid EHR Incentive Programs are required by statute to use Certified EHR Technology. Once certified, Complete EHRs and EHR Modules would be able to be used by eligible professionals and eligible hospitals, or be combined, to meet the statutory requirement for Certified EHR Technology.
The Final Rule on temporary certification program to assure the availability of Certified EHR Technology prior to the date on which health care providers seeking the incentive payments would begin to report demonstrable meaningful use of Certified EHR Technology will be published June 24, 2010. You can learn more about the certification programs here:
http://healthit.hhs.gov/portal/server.pt?open=512&mode=2&objID=1746
The Final Rule is below:
Eligible professionals and eligible hospitals who seek to qualify for incentive payments under the Medicare and Medicaid EHR Incentive Programs are required by statute to use Certified EHR Technology. Once certified, Complete EHRs and EHR Modules would be able to be used by eligible professionals and eligible hospitals, or be combined, to meet the statutory requirement for Certified EHR Technology.
The Final Rule on temporary certification program to assure the availability of Certified EHR Technology prior to the date on which health care providers seeking the incentive payments would begin to report demonstrable meaningful use of Certified EHR Technology will be published June 24, 2010. You can learn more about the certification programs here:
http://healthit.hhs.gov/portal/server.pt?open=512&mode=2&objID=1746
The Final Rule is below:
It's Elementary Doctor Watson
IBM is working on a computing system that can understand and answer complex questions with enough precision and speed to compete against Jeopardy! contestants. The New York Times gives a good overview of the project. Code-named "Watson" after IBM founder Thomas J. Watson, the IBM computing system is designed to rival the human mind's ability to understand the actual meaning behind words, distinguish between relevant and irrelevant content, and ultimately, demonstrate confidence to deliver precise final answers.
“The essence of making decisions is recognizing patterns in vast amounts of data, sorting through choices and options, and responding quickly and accurately,” said Samuel J. Palmisano, IBM Chairman, President and Chief Executive Officer. “Watson is a compelling example of how the planet – companies, industries, cities – is becoming smarter. With advanced computing power and deep analytics, we can infuse business and societal systems with intelligence. This project is the latest example of IBM’s longstanding commitment to fundamental research and to overcoming ‘grand challenges’ in science and technology.”
This challenge is much more than just a game. Jeopardy! demands knowledge of a broad range of topics including history, literature, politics, film, pop culture and science. What's more, Jeopardy! clues involve irony, riddles, analyzing subtle meaning and other complexities at which humans excel and computers traditionally do not. This, along with the speed at which contestants have to answer, makes Jeopardy! an enormous challenge for computing systems. You can play the New York Time's interactive game to get a sense of what Watson is like.
“The essence of making decisions is recognizing patterns in vast amounts of data, sorting through choices and options, and responding quickly and accurately,” said Samuel J. Palmisano, IBM Chairman, President and Chief Executive Officer. “Watson is a compelling example of how the planet – companies, industries, cities – is becoming smarter. With advanced computing power and deep analytics, we can infuse business and societal systems with intelligence. This project is the latest example of IBM’s longstanding commitment to fundamental research and to overcoming ‘grand challenges’ in science and technology.”
This challenge is much more than just a game. Jeopardy! demands knowledge of a broad range of topics including history, literature, politics, film, pop culture and science. What's more, Jeopardy! clues involve irony, riddles, analyzing subtle meaning and other complexities at which humans excel and computers traditionally do not. This, along with the speed at which contestants have to answer, makes Jeopardy! an enormous challenge for computing systems. You can play the New York Time's interactive game to get a sense of what Watson is like.
Thursday, June 17, 2010
Senate Fiddles as Medicare Burns
The Senate voted on June 17, 2010 against postponing a scheduled 21% reduction in Medicare reimbursement to physicians and other health providers, the so-called "doc fix." The 56-40 vote late in the day fell four votes short of the 60 required. Because the "doc fix" was defeated, CMS is ready to authorize its contractors to begin paying physicians at the lower rate.
Senate Fiddles as Medicare Burns
Statement attributable to:
Cecil B. Wilson, MD
President, American Medical Association
Senate Fiddles as Medicare Burns
“Congress has broken its promise to America’s seniors and military families. Today is the last day that Medicare can hold claims, and it is now 17 days past the Senate’s deadline to stop the cut. Tomorrow, physicians will start seeing a 21 percent cut in Medicare payments that will hurt seniors’ health care as physicians are forced to make difficult practice changes to keep their practice doors open.
“The Senate has been debating this issue for weeks and the latest proposal is a six-month delay of the cut. Delaying the problem is not a solution. Continued short-term actions are creating severe instability that harms seniors as physicians make decisions to protect their practices from Medicare’s volatility. Continuing down this path just slaps a Band-Aid on a problem that needs urgent surgery.
“This week congressional offices are rec eiving hundreds of signed white lab coats from AMA member physicians as a symbolic reminder of the need for quick resolution to the immediate Medicare crisis and the importance of solving the problem through repeal of the broken Medicare physician payment formula.”
Statement attributable to:
Cecil B. Wilson, MD
President, American Medical Association
Privacy & Security Standards Workgroup
The Privacy and Security Standards Workgroup of the HIT Standards Committee met on June 17, 2010.
The following are members of this Workgroup:
The workgroup is tasked with making recommendations to the HIT Standards Committee on specific privacy and security safeguards that should be included in the definition of Meaningful Use, with a specific focus on the eight (8) areas listed in Section 3002(b)(2)(B):
(1) Technologies that protect the privacy of health information and promote security in a qualified electronic health record, including for the segmentation and protection from disclosure of specific and sensitive individually identifiable health information with the goal of minimizing the reluctance of patients to seek care (or disclose information about a condition) because of privacy concerns, in accordance with applicable law, and for the use and disclosure of limited data sets of such information;
(2) A nationwide health information technology infrastructure that allows for the electronic use and accurate exchange of health information;
(3) The utilization of a certified electronic health record for each person in the United States by 2014;
(4) Technologies that as a part of a qualified electronic health record allow for an accounting of disclosures made by a covered entity (as defined for purposes of regulations promulgated under section 264(c) of the Health Insurance Portability and Accountability Act of 1996) for purposes of treatment, payment, and health care operations (as such terms are defined for purposes of such regulations);
(5) The use of certified electronic health records to improve the quality of health care, such as by promoting the coordination of health care and improving continuity of health care among health care providers, by reducing medical errors, by improving population health, by reducing health disparities, by reducing chronic disease, and by advancing research and education;
(6) Technologies that allow individually identifiable health information to be rendered unusable, unreadable, or indecipherable to unauthorized individuals when such information is transmitted in the nationwide health information network or physically transported outside of the secured, physical perimeter of a health care provider, health plan, or health care clearinghouse;
(7) The use of electronic systems to ensure the comprehensive collection of patient demographic data, including, at a minimum, race, ethnicity, primary language, and gender information; and
(8) Technologies that address the needs of children and other vulnerable populations.
Below are the slides from a presentation by Mike Davis and David Staggs of the Department of Veterans Affairs:
This is the video referenced in the presentation above:
Previous Privacy and Security Standards Workgroup meetings:
5.21.2010
5.14.2010
4.1.2010
2.18.2010
1.26.2010
11.19.2009
The following are members of this Workgroup:
- Dixie Baker, Chair, SAIC
- Steve Findlay, Co-Chair, Consumers Union
- Anne Castro, BCBS/South Carolina
- David McCallie, Cerner
- Gina Perez, Delaware HIE
- Wes Rishel, Gartner
- Sharon Terry, Genetic Alliance
- Aneesh Chopra, OSTP/Chief Technology Officer
- John Halamka, Harvard Medical School
- John Moehrke, HITSP
- Ed Larsen, HITSP
- Walter Suarez, Kaiser Permanente
- Andrew McLaughlin, OSTP
The workgroup is tasked with making recommendations to the HIT Standards Committee on specific privacy and security safeguards that should be included in the definition of Meaningful Use, with a specific focus on the eight (8) areas listed in Section 3002(b)(2)(B):
(1) Technologies that protect the privacy of health information and promote security in a qualified electronic health record, including for the segmentation and protection from disclosure of specific and sensitive individually identifiable health information with the goal of minimizing the reluctance of patients to seek care (or disclose information about a condition) because of privacy concerns, in accordance with applicable law, and for the use and disclosure of limited data sets of such information;
(2) A nationwide health information technology infrastructure that allows for the electronic use and accurate exchange of health information;
(3) The utilization of a certified electronic health record for each person in the United States by 2014;
(4) Technologies that as a part of a qualified electronic health record allow for an accounting of disclosures made by a covered entity (as defined for purposes of regulations promulgated under section 264(c) of the Health Insurance Portability and Accountability Act of 1996) for purposes of treatment, payment, and health care operations (as such terms are defined for purposes of such regulations);
(5) The use of certified electronic health records to improve the quality of health care, such as by promoting the coordination of health care and improving continuity of health care among health care providers, by reducing medical errors, by improving population health, by reducing health disparities, by reducing chronic disease, and by advancing research and education;
(6) Technologies that allow individually identifiable health information to be rendered unusable, unreadable, or indecipherable to unauthorized individuals when such information is transmitted in the nationwide health information network or physically transported outside of the secured, physical perimeter of a health care provider, health plan, or health care clearinghouse;
(7) The use of electronic systems to ensure the comprehensive collection of patient demographic data, including, at a minimum, race, ethnicity, primary language, and gender information; and
(8) Technologies that address the needs of children and other vulnerable populations.
Below are the slides from a presentation by Mike Davis and David Staggs of the Department of Veterans Affairs:
This is the video referenced in the presentation above:
Previous Privacy and Security Standards Workgroup meetings:
5.21.2010
5.14.2010
4.1.2010
2.18.2010
1.26.2010
11.19.2009
Friday, June 11, 2010
RNAi offers hope for drug discovery
As scientists continue to investigate the human genome, where we now have the complete genetic sequence, there have been remarkable developments in the understanding of disease and consequently a large increase in the number of molecular disease targets to impact a broad range of human disease. The discovery of RNAi is a major breakthrough in biology, and this technology has the potential to make a broad and significant impact. A company called Alnylam Pharmaceuticals is leading the effort in translating the science of RNAi into a robust drug discovery capability. With RNAi it is possible to target virtually any gene in the human genome involved in the causal pathway of disease. The possibility of targeting these previously "undruggable" targets with RNAi is transformative for new drug discovery.
I spoke to Alnylam's CEO John Maraganore:
Below is a rough draft transcript of our conversation.
Alnylum is a company that is focused on creating a whole new class of medicines with a new discovery based on a new discovery in biology called RNA interference or RNAi as it's abbreviated and it's a technology and an approach that we think can transform the treatment of many human diseases because we can silence disease causing genes and basically by turning those genes off temporarily, we can make a difference in people's lives by treating their disease in ways that can't be done with today's medicines.
And the other part of the company, which is quite exciting, is that with what we've been doing over the years now, our technology and innovation is now becoming increasingly a game changer in much of a biomedical discovery, both in industry and in academia. So we've got partnerships with companies like Roche and Novartis and Cicada amongst others, Medtronic as well, and we've also been able to work real closely with major academic institutions like MIT and Plank and Stanford and UT Southwestern and work together on our technology. So it's a company that's hopefully what we believe is going to make a big difference in the treatment of disease with the types of approaches that we're taking. And then at the same time we're finding that we're able to work real closely across the entire biomedical world to basically advance our technology.
Q: Tell us about your newest scientific advisory board
That's a group that's focused on are one of the applications of our technology focused on transforming biologics manufacturing. You know, there's a whole range of medicines that are used today that are collectively called the biologic system: includes recombinant proteins like the use of factor eight for hemophilia or monoclonal antibodies like the use of the drug Avastin for cancer. And then also vaccines, and we've recently started up an effort where we're using our technology to fundamentally transform how those types of products are made. And so the group you're referring to was a recent assembly of some world renowned scientists that are going to help advise us on, on our biotherapeutics effort. But Alnylum overall has had a very active scientific advisory board since 2002 with people like a Phil Sharp and Tom and Bob Langer amongst other people that had been advising or company.
One of the fun things and exciting things about what we've done, is that as we've developed our advanced technology, we've also realized that the role of RNA in general in human biology is far broader than we ever expected. And that allowed us to understand more about micro RNA; these are small RNA that are present in all of ourselves and then we figure out the technologies that allow us to either turn up or turn them down. And by what we've been able to learn is that by sometimes turning them down you can treat specific diseases and sometimes by turning them up you can treat other diseases.
And so a company that we've cofounder with Isis called Regulus. This is an exciting effort that's a focused on micro RNA therapeutics and we and Isis both own 50 percent of that company. So we have a high a retention of the ownership there. We're excited about where that's going and there's a lot of interest in the pharmaceutical industry for where that's going as well.
Tuesday, June 1, 2010
Global Health Corps
Global Health Corps (GHC) aims to mobilize a global community of young leaders to build a movement for health equity.
GHC believes that a global movement of individuals and organizations fighting for improved health outcomes and access to healthcare for the poor is necessary in order to change the unacceptable status quo of extreme inequity. hey are working to build this movement by recruiting, training, and supporting the movement's future leaders and by diversifying the pool of young people working in global health. As reported in the San Francisco Chronicle:
Read more: http://www.sfgate.com
Barbara Bush appeared on CNN June 1, 2010 to discuss the organization:
more at politicalticker.blogs.cnn.com
GHC believes that a global movement of individuals and organizations fighting for improved health outcomes and access to healthcare for the poor is necessary in order to change the unacceptable status quo of extreme inequity. hey are working to build this movement by recruiting, training, and supporting the movement's future leaders and by diversifying the pool of young people working in global health. As reported in the San Francisco Chronicle:
When first daughter Jenna Bush attended a Bay Area AIDS summit hosted by Google.org two years ago, some skeptics doubted it would amount to more than a photo op.
But they were wrong. In a conversation with a Google staffer and a Stanford AIDS activist at one session, she helped come up with a big idea: A plan to improve health care access in the poorest parts of the United States and the world. What may have seemed like a pie-in-the-sky plan has morphed into a nongovernmental organization with an impressive roster of donors and more than $1 million in funding. Few may have heard of the Global Health Corps, but as its influence grows, that is likely to change.
"So many ideas come up in group conversations that never get realized," said corps founding director Dave Ryan, who at the time was the executive director for Face AIDS, a nonprofit group that helps Rwandans living with HIV. "But when we all got together, we saw there was something special that could happen."
Having watched friends transition from college into careers through organizations like Teach for America, they wondered whether they could create a similar organization dedicated to health care.
"We felt like there should be a similar program for public health," said Charlie Hale, who works in Google's direct ad sales division and is one of the group's co-founders.
They enlisted an eager group of socially conscious friends and secured $250,000 in seed money from Google.org. Jenna's sister, Barbara Bush, became the president of the organization, after spending time working in Africa with UNICEF and the U.N. World Food Program
Read more: http://www.sfgate.com
Barbara Bush appeared on CNN June 1, 2010 to discuss the organization:
One of former President George W. Bush's daughters is aiming to change the face of global public health and she intends to use members of her generation to do it.
Former first daughter Barbara Bush's new non-profit, Global Health Corps, was inspired by a 2003 trip that she took with her parents to five African countries. The Bush family was in Africa at the time promoting the Bush administration's anti-AIDS initiative.
A visit to a health clinic for people battling HIV opened Barbara Bush's eyes to how she might make a difference in the health field.
"I think that was the first time that – I was not pre-med; I hadn't studied health – that was the first time that I thought well maybe, what am I doing? Maybe I should focus on this," the Bush daughter said in an interview Tuesday on CNN's American Morning. "And I can. You really can work in the health field even if you're not a doctor or a nurse."
Bush decided to take that premise and use it as the foundation of Global Health Corps, a non-profit that recruits young professionals who are age 30 or younger to work for a year in health organizations.
"They're not doctors or nurses. They're filling any needs that the organizations have. And what we've found is all of our partners want people with technology skills. They want program management skills. They want monitoring and evaluation support. They just want general program support – which are skills that tons of people have. They just don't know they can use them in the health field."
For example, Bush said one participant in the non-profit's first crop of fellows is a former Google employee with a background in product management who is now working on health management information systems in Tanzania.
more at politicalticker.blogs.cnn.com
Friday, May 28, 2010
Dartmouth Atlas
The ONC Funding Opportunities Announcement uses the Dartmouth Atlas map below to define a hospital referral region for the purposes of Beacon Communities. I have been fascinated playing around with the map and comparing various areas of the country.
For more than 20 years, the Dartmouth Atlas Project has documented glaring variations in how medical resources are distributed and used in the United States. The project uses Medicare data to provide comprehensive information and analysis about national, regional, and local markets, as well as individual hospitals and their affiliated physicians.
These reports and the research upon which they are based have helped policymakers, the media, health care analysts and others improve their understanding of the efficiency and effectiveness of our health care system. This valuable data forms the foundation for many of the ongoing efforts to improve health and health systems across America.
via dartmouthatlas.org
For more than 20 years, the Dartmouth Atlas Project has documented glaring variations in how medical resources are distributed and used in the United States. The project uses Medicare data to provide comprehensive information and analysis about national, regional, and local markets, as well as individual hospitals and their affiliated physicians.
These reports and the research upon which they are based have helped policymakers, the media, health care analysts and others improve their understanding of the efficiency and effectiveness of our health care system. This valuable data forms the foundation for many of the ongoing efforts to improve health and health systems across America.
via dartmouthatlas.org
Wednesday, May 26, 2010
Healthcare and Government 2.0 with Aneesh Chopra and Tim O'Reilly
Tim O'Reilly snagged a great interview with Aneesh Chopra at the Gov 2.0 Expo. They started off with a strong focus on the intersection of healthcare and gov 2.0 principles. Aneesh gives an overview of the incentive program for meaningful use of EHRs, reveals an interesting perspective of the genesis of the NHIN Direct project, and also talks about the criteria that patients are entitled to an electronic copy of their medical record. From a policy standpoint he wants to create the conditions for data liquidity and provide a platform for innovation.
Sunday, April 18, 2010
SHARP Focus: Indivo Personally Controlled Health Record
Researchers at Children’s Hospital Boston and Harvard Medical School will lead the efforts of a $15 million grant from the Office of the National Coordinator for Health Information Technology to support research and development of a new health information technology infrastructure. The grant is one of the four awarded through the Strategic Health IT Advanced Research Projects (SHARP) program to address key challenges in adoption and meaningful use of health IT. I wrote previously about the University of Texas Health Science Center at Houston research which will focus on Patient-Centered Cognitive Support. Now we will take a look at the Harvard program on new health care application and network-platform architectures.
This four-year project will be led by Isaac Kohane, MD, PhD, and Kenneth Mandl, MD, MPH, of the Children’s Hospital Informatics Program and Harvard Medical School, and will investigate, evaluate, and prototype approaches to achieving an “iPhone-like” health information technology platform model, as was first described by Mandl and Kohane in a March 2009 Perspectives article in The New England Journal of Medicine.
The platform architecture, described as a “SMArt” (Substitutable Medical Applications, reusable technologies) architecture, will provide core services and support extensively networked data from across the health system, as well as facilitate substitutable applications – enabling the equivalent of the iTunes App Store for health. This will stand in stark contrast to the way health information systems have been designed and implemented to date, and will encourage evolution, competition, innovation and efficiency in health care and technology.
The SMArt platform will provide a common interface to the “App Store” for the Indivo open source personally controlled health record platform developed by the CHIP team more than a decade ago and is the codebase behind Dossia. The work will also include open source platforms created by other subcontractors on the ONC grant: Partners HealthCare System’s i2b2 analytic platform and the Regenstrief Institute’s CareWeb EHR.
This is going to be very important because there will be certification of EHR modules, but as yet there is no data exchange and workflow integration between modules. So hopefully this research will provide some solutions for this difficulty. Also there will eventually be a common platform upon which most personal health applications will need to be built. The dominant platform may eventually be Microsoft HealthVault, Google Health, or perhaps something from the Mirth, NHIN Direct or CONNECT projects. But the Indivo X project appears to me to be an important component of the future of the health Internet.
some material provided by harvard.edu
This four-year project will be led by Isaac Kohane, MD, PhD, and Kenneth Mandl, MD, MPH, of the Children’s Hospital Informatics Program and Harvard Medical School, and will investigate, evaluate, and prototype approaches to achieving an “iPhone-like” health information technology platform model, as was first described by Mandl and Kohane in a March 2009 Perspectives article in The New England Journal of Medicine.
The platform architecture, described as a “SMArt” (Substitutable Medical Applications, reusable technologies) architecture, will provide core services and support extensively networked data from across the health system, as well as facilitate substitutable applications – enabling the equivalent of the iTunes App Store for health. This will stand in stark contrast to the way health information systems have been designed and implemented to date, and will encourage evolution, competition, innovation and efficiency in health care and technology.
The SMArt platform will provide a common interface to the “App Store” for the Indivo open source personally controlled health record platform developed by the CHIP team more than a decade ago and is the codebase behind Dossia. The work will also include open source platforms created by other subcontractors on the ONC grant: Partners HealthCare System’s i2b2 analytic platform and the Regenstrief Institute’s CareWeb EHR.
This is going to be very important because there will be certification of EHR modules, but as yet there is no data exchange and workflow integration between modules. So hopefully this research will provide some solutions for this difficulty. Also there will eventually be a common platform upon which most personal health applications will need to be built. The dominant platform may eventually be Microsoft HealthVault, Google Health, or perhaps something from the Mirth, NHIN Direct or CONNECT projects. But the Indivo X project appears to me to be an important component of the future of the health Internet.
some material provided by harvard.edu
Friday, April 16, 2010
Eligible provider fix along with temporary SGR fix
The president has signed H.R. 4851 into law. The bill was approved by the Senate on a 59-38 vote and by the House on a 289-122 vote. This will provide a temporary delay on a 21% cut in Medicare physician payments until June.
There is an important section on clarification of the definition of an eligible provider (which was a serious flaw in the NPRM) being able to participate in Medicare incentive payments for achieving meaningful use. I am very please to see this language clarified so that we do not need to rely on the rule making process for this to fixed, since it is now handled legislatively. The section pertaining to eligible providers is:
There is an important section on clarification of the definition of an eligible provider (which was a serious flaw in the NPRM) being able to participate in Medicare incentive payments for achieving meaningful use. I am very please to see this language clarified so that we do not need to rely on the rule making process for this to fixed, since it is now handled legislatively. The section pertaining to eligible providers is:
SEC. 5. EHR CLARIFICATION.
(a) Qualification for Clinic-based Physicians-
(1) MEDICARE- Section 1848(o)(1)(C)(ii) of the Social Security Act (42 U.S.C. 1395w-4(o)(1)(C)(ii)) is amended by striking `setting (whether inpatient or outpatient)' and inserting `inpatient or emergency room setting'.
(2) MEDICAID- Section 1903(t)(3)(D) of the Social Security Act (42 U.S.C. 1396b(t)(3)(D)) is amended by striking `setting (whether inpatient or outpatient)' and inserting `inpatient or emergency room setting'.
(b) Effective Date- The amendments made by subsection (a) shall be effective as if included in the enactment of the HITECH Act (included in the American Recovery and Reinvestment Act of 2009 (Public Law 111-5)).
(c) Implementation- Notwithstanding any other provision of law, the Secretary of Health and Human Services may implement the amendments made by this section by program instruction or otherwise.
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