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	<title>John B. Moeschler Medical Genetics</title>
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		<title>Check lists to improve health care-NYTimes brief interview with Peter Pronovost from Hopkins</title>
		<link>http://negc.wordpress.com/2010/03/10/check-lists-to-improve-health-care-nytimes-brief-interview-with-peter-pronovost-from-hopkins/</link>
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		<pubDate>Wed, 10 Mar 2010 11:15:45 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[General Health Care Policy and Public Health]]></category>

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		<description><![CDATA[Q. WHAT GOT YOU STARTED ON YOUR CRUSADE FOR HOSPITAL SAFETY?
A. My father died at age 50 of cancer. He had lymphoma. But he was diagnosed with leukemia. When I was a first-year medical student here at Johns Hopkins, I took him to one of our experts for a second opinion. 
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			<content:encoded><![CDATA[<p><a href="http://www.nytimes.com/2010/03/09/science/09conv.html?em"></p>
<p>Interview with Pronovost who attracted national attention (see Gawande&#8217;s book &#8220;Checklist Manifesto&#8221;, for example) when he developed a simple procedure checklist for line insertion in ICU&#8217;s which led to immediate and dramatic reductions in infection complication rates, deaths, and cost.</p>
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		<title>Cottage Industry to Postindustrial Care — The Revolution in Health Care Delivery</title>
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		<pubDate>Sat, 30 Jan 2010 20:58:19 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[New from leaders in the field of health care improvement and the problem of systemic improvement in a system that is more like a cottage industry than an integrated system. Note the discussions about the definition of a &#8220;good doctor&#8221;. Published at www.nejm.org January 20, 2010 (10.1056/NEJMp0911199) Cottage Industry to Postindustrial Care — The Revolution [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=53&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>New from leaders in the field of health care improvement and the problem of systemic improvement in a system that is more like a cottage industry than an integrated system. Note the discussions about the definition of a &#8220;good doctor&#8221;.</p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/20089956?log$=activity"></p>
<p>Published at www.nejm.org January 20, 2010 (10.1056/NEJMp0911199)<br />
Cottage Industry to Postindustrial Care — The Revolution in Health Care Delivery</p>
<p>Stephen J. Swensen, M.D., M.M.M., Gregg S. Meyer, M.D., Eugene C. Nelson, D.Sc., M.P.H., Gordon C. Hunt, Jr., M.D., M.B.A., David B. Pryor, M.D., Jed I. Weissberg, M.D., Gary S. Kaplan, M.D., Jennifer Daley, M.D., Gary R. Yates, M.D., Mark R. Chassin, M.D., M.P.P., M.P.H., Brent C. James, M.D., M.Stat., and Donald M. Berwick, M.D., M.P.P.<br />
U.S. health care is broken. Although other industries have transformed themselves using tools such as standardization of value-generating processes, performance measurement, and transparent reporting of quality, the application of these tools to health care is controversial, evoking fears of &#8220;cookbook medicine,&#8221; loss of professional autonomy, a misinformed focus on the wrong care, or a loss of individual attention and the personal touch in care delivery. We believe that public reporting of performance with regard to appropriately designed clinical standards can overcome these concerns. The application of improvement tools is not only essential to modernizing care delivery but also the key to preserving the values to which our current system aspires.</p>
<p>Our current health care system is essentially a cottage industry of nonintegrated, dedicated artisans who eschew standardization. Services are often highly variable, performance is largely unmeasured, care is customized to individual patients, and standardized processes are regarded skeptically. Autonomy is hardwired into the system, because most physicians practice in small groups with limited oversight or coordination. Even those who work in larger groups, including academic medical centers, create individualized care plans that cannot be integrated with care in neighboring &#8220;out-of-network&#8221; facilities; they cannot treat and track patients over space and time. Today&#8217;s system usually pays for volume rather than value, and we get what we pay for: more tests, exams, surgeries, and appointments. &#8220;Good doctors&#8221; are celebrated for their unwavering dedication to doing whatever it takes to care for their individual patients, which often means swimming upstream against the system, rather than relying confidently on it.</p>
<p>Growing evidence highlights the dangers of continuing to operate in cottage-industry mode. Fragmentation of care has led to suboptimal performance. The gap between established science and current practice is wide. It is well documented that U.S. patients receive only about half of scientifically advisable care; many unnecessary procedures are performed, leading to avoidable complications and costs; safety problems abound; and there are tremendous regional variations in the quality and quantity of care delivered. Moreover, fragmentation makes it more difficult to transform the industry — for example, through the adoption of health information technology.</p>
<p>The value of health care is a function of three elements: its design (the right treatment for the right patient at the right time), its execution (reliably doing it right every time to achieve the best outcomes), and its cost over time. In cottage-industry medicine, the first two elements are custom-crafted for each clinical situation as part of a problem-solving process. Although this approach may offer ideal care for some, it has limited ability to promote continual learning and improvement, because each patient&#8217;s circumstances are unique. Yet with increasing clinical knowledge and expertise, patients&#8217; responses to treatments can often be predicted. In such cases, the elements of care should be standardized, disseminated, monitored, and continuously improved.1 Three key steps — wise standardization, meaningful measurement, and respectful reporting — have transformed other industries, and we believe they can help health care as well.</p>
<p>Too often, U.S. health care overvalues local autonomy and undervalues disciplined science — not because of inattention or incompetence among doctors and nurses but because it is difficult for the human mind to keep up with the explosion of medical knowledge. Providers need help, and guidelines help them. In fact, the use of guidelines often liberates them to devote more time to patients and to challenges that demand their skills.</p>
<p>The massive investment in clinical-guideline development and dissemination is predominantly being made by experienced professionals and researchers who believe that unscientific and clinically unwarranted variation in practice is widespread, injurious, and costly. When properly constructed, guidelines are grounded in science and thoroughly vetted by experts before being adopted. Of course, undiscerning enforcement of even excellent guidelines can be dangerous. Many patients have complex multisystem diseases, allergies, or genetic conditions that are valid contraindications to a given protocol, and guideline-supported care must be tailored to the patient&#8217;s needs. Most patients, however, will benefit from properly vetted and implemented guidelines.</p>
<p>Guidelines must also be tended over time. Advancing knowledge may render even the best guidelines outdated; for example, recent discoveries have necessitated reconsideration of guidelines for very stringent glycemic control. The evolution of scientific knowledge is not grounds for eschewing guidelines; it is a reason to modify and improve them continually. Allowing physicians to make thoughtful exceptions to guidelines but asking them to report why their practice varies can support loops of continuous learning.</p>
<p>Chaos confounds constructive action, whereas wise standardization is a foundation for effective variation, efficiency, reliability, and rapid innovation. After a process is stable, we can more effectively eliminate waste that does not add value. Humans working in a standardized environment are supported in achieving higher reliability. And standardization facilitates the assessment of the comparative effectiveness of interventions by providing a baseline against which potential improvements can be measured.</p>
<p>Reliably delivering the basics of care improves outcomes and saves money. The Premier Hospital Quality Incentive Demonstration project of the Centers for Medicare and Medicaid Services, which involved more than 1 million patients treated in 250 hospitals, raised overall quality by nearly 16% over 3 years through the delivery of 30 standard and widely accepted care measures. These improvements also saved the lives of an estimated 4700 patients with myocardial infarction.2 A high-value care system embraces the appropriate use of scientifically informed guidelines, standard practice, teamwork, checklists, and accountability and welcomes payment for value, not just for volume.</p>
<p>Health care professionals aspire to improve patient outcomes — to reduce mortality, morbidity, hospital-acquired infections, and costs and to improve functional status, patients&#8217; experience, and access. The bureaucracies required to track enough process measures for broad-based transformation of outcomes would be oppressive and expensive. A system that rewards better patient outcomes while encouraging innovation would be more efficient and effective. Furthermore, given that nearly 20% of all medical diagnoses are incorrect,3 rewarding a correct process (possibly for an incorrect diagnosis) makes less sense than recognizing our ultimate goal: superior outcomes for patients.</p>
<p>Until enough outcome measures that are acceptable for use in performance-based payment have been established, we must balance the use of outcome and process measures. Selected process measures (e.g., whether the correct antibiotic was given before surgery) can serve as a bridge. Selecting metrics is a difficult task, full of potential pitfalls, but it should be accomplished through a scientific, not political, process, and a feedback loop that fosters learning should be created. Feedback that is based on the use of measures in pilot tests will identify their limitations, allowing for correction and improvement.</p>
<p>Transparency is fundamental to the integrity and spread of high-value care. A car buyer can easily learn about a car&#8217;s value from numerous credible sources, transparently comparing it with other cars in terms of results of crash tests, resale value, reliability, dealer costs, and owner satisfaction. But patients must choose a hospital, clinic, care team, or treatment option on the basis of relatively little information. Publicly available data are also important in supporting clinicians as they counsel patients regarding treatment choices. Health care professionals should embrace transparency; patients should expect and demand it.</p>
<p>Public reporting may create value by stimulating improvement on the part of medical professionals, but proper reporting demands statistical sophistication. Most publicly reported quality data are not statistically valid for the accurate ranking of physicians or hospitals, yet they are often reported with unwarranted claims of precision. The benefits of transparency outweigh the deficits when measurements are clearly understood.</p>
<p>Although most current measures cannot yet be used to rank hospitals or physicians accurately, they can help us assess, manage, and systematically improve processes. For example, it took only 5 years of national data collection and 3 years of public reporting by the Joint Commission for hospitals to achieve very high levels of performance on key treatment indicators for acute myocardial infarction. In 2007, 96% of hospitals scored above 90% for giving patients aspirin on arrival (up from 88% in 2005), and 94% of hospitals scored above 90% for the provision of beta-blockers on discharge (up from 81% in 2005).4,5</p>
<p>Expert guidelines and meaningful outcome measures will transform us from high-variation clinicians to a more streamlined, consistent community of care, since improvement in care delivery will necessitate integration and cooperation. We see the public reporting of outcomes and adherence to standardized care processes as key tactics for driving health care improvement.</p>
<p>The transformation from cottage industry to postindustrial care will be facilitated by combining the three elements of standardizing care, measuring performance, and transparent reporting. Interoperable electronic data systems will help to facilitate transformation but are insufficient. Our profession should move away from a simplistic &#8220;craft of medicine&#8221; mentality, embrace accountability and transparency, and support the pressing national need for improvement. A transparent, high-value system is a patient-centered way to deliver care and promote health. To achieve this goal, we need to eliminate unwarranted clinical variation, waste, and defects. We need to aspire to deliver the same foundation of evidence-based care, no matter where a patient lives or whom a patient sees.</p>
<p>This shift requires reconsidering the very definition of a &#8220;good doctor.&#8221; In the past, a stereotypical good doctor was independent and always available, had encyclopedic knowledge, and was a master of rescue care. Today, a good doctor must have a solid fund of knowledge and sound decision-making skills but also must be emotionally intelligent, a team player, able to obtain information from colleagues and technological sources, embrace quality improvement as well as public reporting, and reliably deliver evidence-based care, using scientifically informed guidelines in a personal, compassionate, patient-centered manner.</p>
<p>Modern physicians should welcome guidelines covering the basics of evidence-based care, which can free them to focus on the complex issues that require their training and expertise. Effective standard practice will also require interdisciplinary care. An invaluable consequence of fostering interdependence is better teamwork that should lead to safer care (e.g., comfort in speaking up when something seems wrong, as well as better handoffs and communication). Such cooperation will engender employee engagement and improve both the experiences of patients and the financial performance of practices. Today&#8217;s good doctors should see process improvement as part of their core work. Rather than undermining health care, public reporting on the performance of standardized care processes and outcomes will be the key to converting our isolated cottages into integrated, continually improving communities.</p>
<p>The views expressed in this article are those of the authors and do not represent official policy of any of their organizations.</p>
<p>Financial and other disclosures provided by the authors are available with the full text of this article at NEJM.org.</p>
<p>Source Information</p>
<p>From the Mayo Clinic, Rochester, MN (S.J.S.); the Center for Quality and Safety, Massachusetts General Hospital and Massachusetts General Physicians Organization, Boston (G.S.M.); Dartmouth–Hitchcock Medical Center, Lebanon, NH (E.C.N.); Sutter Health, Sacramento, CA (G.C.H.); Ascension Health, St. Louis (D.B.P.); Kaiser Permanente, Oakland, CA (J.I.W.); Virginia Mason Health System, Seattle (G.S.K.); Partners Community Healthcare, Boston (J.D.); Sentara Healthcare, Norfolk, VA (G.R.Y); the Joint Commission, Oakbrook Terrace, IL (M.R.C.); Intermountain Healthcare, Salt Lake City (B.C.J.); and the Institute for Healthcare Improvement, Cambridge, MA (D.M.B.).</p>
<p>This article (10.1056/NEJMp0911199) was published on January 20, 2010, at NEJM.org.</p>
<p>References</p>
<p>Bohmer RMJ. Designing care: aligning the nature and management of health care. Boston: Harvard Business Press, June 2009.<br />
CMS/Premier Hospital Quality Incentive Demonstration (HQID). (Accessed January 12, 2010, at http://www.premierinc.com/quality-safety/tools-services/p4p/hqi/index.jsp.)<br />
Groopman JE. How doctors think. Boston: Houghton Mifflin, 2007.<br />
The Joint Commission. Improving America&#8217;s hospitals: the Joint Commission&#8217;s annual report on quality and safety: 2008. (Accessed January 12, 2010, at http://www.jointcommissionreport.org/.)<br />
Idem. Improving America&#8217;s hospitals: the Joint Commission&#8217;s annual report on quality and safety: 2006. (Accessed January 12, 2010, at http://www.jointcommissionreport.org/pdf/JC_2006_Annual_Report.pdf.)</p>
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		<title>&#8220;Counsyl Brings Genetic Screening To The Masses&#8221; NYT</title>
		<link>http://negc.wordpress.com/2010/01/29/counsyl-brings-genetic-screening-to-the-masses-nyt/</link>
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		<pubDate>Fri, 29 Jan 2010 20:22:28 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[I read this with interest this morning; I had seen it on Twitter a bit but now this NYT report is way more than 140 characters and lacks the rah-rah of the Twitters and the online go-go proponents/endorsers. In-home genetic testing for carrier state like this company is offering is &#8220;disruptive&#8221;, meaning challenging the status [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=48&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I read this with interest this morning; I had seen it on Twitter a bit but now this NYT report is way more than 140 characters and lacks the rah-rah of the Twitters and the online go-go proponents/endorsers. In-home genetic testing for carrier state like this company is offering is &#8220;disruptive&#8221;, meaning challenging the status quo. I can think of little direct harm that might come from it. Should be interesting to see where this goes. </p>
<p><a href="http://www.nytimes.com/2010/01/29/business/29gene.html?ref=business&amp;pagewanted=all"></a></p>
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		<title>Federal Advisory Committee Recommends SCID for Universal Newborn Screening</title>
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		<pubDate>Thu, 28 Jan 2010 15:27:14 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
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		<description><![CDATA[I attended this meeting as PI of NEGC, not as a Committee member. There indeed was compelling personal stories from families who traveled from Oregon, Wisconsin and NY to make the case that the screening for certain immune deficiency disorders should be added to the recommended panel. One citation from Jennifer Puck might help with [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=46&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I attended this meeting as PI of NEGC, not as a Committee member. There indeed was compelling personal stories from families who traveled from Oregon, Wisconsin and NY to make the case that the screening for certain immune deficiency disorders should be added to the recommended panel. One citation from Jennifer Puck might help with some background:<br />
Development of population-based newborn screening for severe combined immunodeficiency<br />
Journal of Allergy and Clinical Immunology, Volume 115, Issue 2, Pages 391-398<br />
K. Chan, J. Puck<br />
+++++++++++++++++++++++++++++++++++++<br />
FOR IMMEDIATE RELEASE<br />
Wednesday, January 27, 2010</p>
<p>Federal Advisory Committee Recommends SCID for Universal Newborn Screening</p>
<p>WASHINGTON &#8211; January 27, 2010 &#8211; In a historic vote on January 21, 2010, the Secretary&#8217;s Advisory Committee for Heritable Disorders in Newborns and Children (ACHDNC) unanimously agreed to recommend the addition of Severe Combined Immunodeficiency (SCID) to the uniform newborn screening panel. The ACHDNC adopted a list of 29 recommended conditions in September 2005. Since that time, SCID is the first condition to be added to this list for inclusion into mandatory newborn screening conducted by state public health programs.</p>
<p>SCID is a group of disorders characterized by the absence of an immune system, causing infants with SCID to develop recurrent infections, leading to death in early childhood. SCID affects a minimum of one in 100,000 newborns; however, some studies estimate that the actual number is closer to one in 40,000. Treatment in the first months after birth can prolong life and prevent infections. Wisconsin and Massachusetts both developed cost-effective methods for universal screening for SCID, and a number of other states have started to train their laboratory personnel to start screening for SCID.</p>
<p>Dr. Rebecca Buckley of Duke University Medical Center published the first article showing the effectiveness of early bone marrow transplantation as a treatment for SCID in 1999 in The New England Journal of Medicine. After working for 13 years to get SCID added to the recommended panel, the vote came as &#8220;a dream come true.&#8221;</p>
<p>The Chairman of the ACHDNC, Dr. R. Rodney Howell, noted that &#8220;[the Advisory Committee] has carefully reviewed the detailed, updated evidence review for SCID and related T-lymphocyte deficiencies and found the condition(s) ready to be added to the uniform and secondary panel. &#8230; The Advisory Committee, however, understands that there will be additional work from the NIH, HRSA and the CDC to be reported back to the Committee as this newborn screening proceeds.&#8221;</p>
<p>The ACHDNC was established in February 2003 to advise the Secretary of the U.S. Department of Health and Human Services regarding the most appropriate application of universal newborn screening tests, technologies, policies, guidelines and standards for effectively reducing morbidity and mortality in newborns and children having, or at risk for, heritable disorders. There is currently a formal process for individuals or organizations to nominate a heritable disorder to be considered for inclusion in the recommended uniform screening panel (http://www.hrsa.gov/heritabledisorderscommittee/nominate.htm).</p>
<p>&#8220;This recommendation by the [Advisory] Committee is significant for both newborn screening and for the evidence-based process for decision making,&#8221; declared Sharon Terry, president and chief executive officer of Genetic Alliance, who serves as a liaison on the ACHDNC. &#8220;The recommendation includes surveillance, education and quality control, to be contributed by the National Institutes of Health, Health Resources and Services Administration and Centers for Disease Control and Prevention, and thereby supports the development of a systems approach in newborn screening.&#8221;</p>
<p>To date, six conditions have been brought to the Advisory Committee: Fabry Disease, Krabbe Disease, Niemann-Pick Disease, Pompe Disease, Severe Combined Immunodeficiency (SCID), and Spinal Muscular Atrophy (SMA). Thus far, only SCID has been recommended for addition to the uniform screening panel. By law, the Secretary of Health and Human Services must respond to the recommendation within 180 days.</p>
<p>Vicki Modell, co-founder of the Jeffery Modell Foundation, stated that &#8220;[the] unanimous vote to add SCID to the National Newborn Screening Core Panel was a milestone victory. We thank the Committee for their positive decision on behalf of all the babies with SCID that we lost, the babies today who have hope, and for all the future babies yet to be born, who will have a really good chance at life.&#8221;</p>
<p>About Genetic Alliance &#8211; Genetic Alliance transforms health through genetics, promoting an environment of openness centered on the health of individuals, families, and communities. Genetic Alliance brings together diverse stakeholders that create novel partnerships in advocacy; integrates individual, family, and community perspectives to improve health systems; and revolutionizes access to information to enable translation of research into services and individualized decision making. For more information about Genetic Alliance, visit http://www.geneticalliance.org.</p>
<p>For More Information Contact:<br />
Natasha Bonhomme, Vice President of Strategic Development, at nbonhomme@geneticalliance.org or 202. 966.5557 x211</p>
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		<title>Strengthening the Science of Personal Genomics: Caveat Emptor</title>
		<link>http://negc.wordpress.com/2009/08/17/strengthening-the-science-of-personal-genomics-caveat-emptor/</link>
		<comments>http://negc.wordpress.com/2009/08/17/strengthening-the-science-of-personal-genomics-caveat-emptor/#comments</comments>
		<pubDate>Mon, 17 Aug 2009 18:03:02 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Personal Genomics]]></category>

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		<description><![CDATA[Recommendations Released for Strengthening the Science Base of Personal Genomics Professionals from government agencies, academic and research institutions, industry, and consumer groups make recommendations for strengthening the science base for using personal genomics to assess risk and prevent disease. A new paper published this month in Genetics in Medicine outlines these recommendations, which are based [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=37&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p><strong>Recommendations Released for Strengthening the Science Base of Personal Genomics<br />
</strong><br />
Professionals from government agencies, academic and research institutions, industry, and consumer groups make recommendations for strengthening the science base for using personal genomics to assess risk and prevent disease. A new paper published this month in Genetics in Medicine outlines these recommendations, which are based on a personal genomics workshopExternal hosted by CDC and NIH in December 2008. </p>
<p>The report is published in <a href="http://www.ncbi.nlm.nih.gov/pubmed/19617843?ordinalpos=4&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum">Genetics in Medicine</a>. PMID: 19617843.</p>
<p>&#8220;The <strong>clinical validity</strong> and <strong>utility</strong> of personal genomics is a moving target with rapidly developing discoveries but little translation research to close the gap between discoveries and health impact. Workshop participants made recommendations in five domains: (1) developing and applying scientific standards for assessing personal genomic tests; (2) developing and applying a multidisciplinary research agenda, including observational studies and clinical trials to fill knowledge gaps in clinical validity and utility; (3) enhancing credible knowledge synthesis and information dissemination to clinicians and consumers; (4) linking scientific findings to evidence-based recommendations for use of personal genomics; and (5) assessing how the concept of personal utility can affect health benefits, costs, and risks by developing appropriate metrics for evaluation. To fulfill the promise of personal genomics, a rigorous multidisciplinary research agenda is needed.&#8221;</p>
<p>The <strong>science</strong> of personal genomics is behind the &#8220;business&#8221; of personal genomics, as in 23andMe, deCodeMe, and Navigenics. The field of clinical genetics has taken a largely defensive posture with these direct-to-consumer appeals for genetic risk assessment. This is a thoughtful description of what science is needed to address the clinical validity and clinical utility of personal genomic testing. My view is that PG testing is &#8220;not ready for prime time&#8221;.  The utility of such testing is not yet known and, I suspect, doctors and patients will take actions nevertheless&#8211;some of which will be harmful (and expensive). Caveat emptor. </p>
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		<title>Practicing Medicine in Era of Facebook</title>
		<link>http://negc.wordpress.com/2009/08/13/practicing-medicine-in-era-of-facebook/</link>
		<comments>http://negc.wordpress.com/2009/08/13/practicing-medicine-in-era-of-facebook/#comments</comments>
		<pubDate>Thu, 13 Aug 2009 15:18:05 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://negc.wordpress.com/?p=25</guid>
		<description><![CDATA[I read with interest thisNew England Journal of Medicine essay on one physician&#8217;s experience with a patient contacting her on Facebook. Here is an excerpt: &#8220;Practicing Medicine in the Age of Facebook&#8221; Sachin H. Jain, M.D., M.B.A. &#8220;In my second week of medical internship, I received a &#8220;friend request&#8221; on Facebook, the popular social-networking Web [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=25&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I read with interest this<a href="http://content.nejm.org/cgi/content/full/361/7/649">New England Journal of Medicine</a> essay on one physician&#8217;s experience with a patient contacting her on Facebook. </p>
<p>Here is an excerpt:</p>
<p>&#8220;Practicing Medicine in the Age of Facebook&#8221;<br />
Sachin H. Jain, M.D., M.B.A.</p>
<p>&#8220;In my second week of medical internship, I received a &#8220;friend request&#8221; on Facebook, the popular social-networking Web site. The name of the requester was familiar: Erica Baxter. Three years earlier, as a medical student, I had participated in the delivery of Ms. Baxter&#8217;s baby. Now, apparently, she wanted to be back in touch.</p>
<p>Despite certain reservations, I clicked &#8220;confirm,&#8221; and Ms. Baxter joined my list of Facebook &#8220;friends.&#8221; I was curious to hear about the progress of her baby girl, but I wondered about the appropriateness of this interaction. Was Ms. Baxter simply a grateful patient interested in sharing news about her child — as a follow-up to our professional interaction — or did she have other motives that weren&#8217;t apparent to me? In confirming this patient as my &#8220;friend&#8221; on Facebook, I was merging my professional and personal lives. From my Facebook page, Ms. Baxter could identify and reach anyone in my network of friends, view an extensive collection of personal photographs, read my personal blog, and review notations that others had left on my &#8220;wall.&#8221; The anxiety I felt about crossing boundaries is an old problem in clinical medicine, but it has taken a different shape as it has migrated to this new medium.&#8221;</p>
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		<title>NEGC Collaborative Council meeting today</title>
		<link>http://negc.wordpress.com/2009/08/12/negc-collaborative-council-meeting-today/</link>
		<comments>http://negc.wordpress.com/2009/08/12/negc-collaborative-council-meeting-today/#comments</comments>
		<pubDate>Wed, 12 Aug 2009 11:18:05 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[The CC of NEGC is meeting in Durham today. Notes from the meeting and agenda to be posted on our website later.<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=23&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>The CC of NEGC is meeting in Durham today. Notes from the meeting and agenda to be posted on our <a href="http://www.negenetics.org">website</a> later.</p>
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		<title>Health care reform</title>
		<link>http://negc.wordpress.com/2009/08/11/health-care-reform/</link>
		<comments>http://negc.wordpress.com/2009/08/11/health-care-reform/#comments</comments>
		<pubDate>Tue, 11 Aug 2009 19:12:47 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[I am reading a new report from Kaiser Family Foundation on the current health care reform proposals in Congress.<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=17&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>I am reading a <a href="http://tinyurl.com/qyajn9">new report</a> from Kaiser Family Foundation on the current health care reform proposals in Congress.</p>
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		<title>Family History meeting at NIH</title>
		<link>http://negc.wordpress.com/2009/08/10/family-history-meeting-at-nih/</link>
		<comments>http://negc.wordpress.com/2009/08/10/family-history-meeting-at-nih/#comments</comments>
		<pubDate>Mon, 10 Aug 2009 18:31:11 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Clinical Genetics Health Care Improvement]]></category>
		<category><![CDATA[family history]]></category>

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		<description><![CDATA[On August 24-26, 2009, the National Institutes of Health will hold the first Family History State-of-the-Science Conference in Bethesda, Maryland to assess the available scientific evidence related to the use and effectiveness of family history information for predicting and improving patient health outcomes<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=11&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>On August 24-26, 2009, the National Institutes of Health will hold the first Family History State-of-the-Science <a href="http://consensus.nih.gov/2009/familyhistory.htm">Conference in Bethesda</a>, Maryland to assess the available scientific evidence related to the use and effectiveness of family history information for predicting and improving patient health outcomes</p>
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			<media:title type="html">John</media:title>
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		<title>Welcome!</title>
		<link>http://negc.wordpress.com/2009/06/04/welcome/</link>
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		<pubDate>Thu, 04 Jun 2009 16:40:59 +0000</pubDate>
		<dc:creator>John Moeschler</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

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		<description><![CDATA[to an experiment in increasing the flow of information on medical genetics in New England.<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=negc.wordpress.com&amp;blog=8035172&amp;post=8&amp;subd=negc&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>to an experiment in increasing the flow of information on medical genetics in New England.</p>
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			<media:title type="html">John</media:title>
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