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<title>Permanent Internal Medicine Job in Internal Medicine Job In Metro South Carolina * Easy Drive To Charlotte South Carolina with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job In South Carolina *   $190K Salary   Employed With Full Benefits * 1:4 Call Sign On Bonus *   Loan Forgiveness      **Ready Made Practice - Taking Over Existing Patient Base *  ]]></description>
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<item rdf:about="http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_connecticut/page_1.html">
<title>Permanent Internal Medicine Job in Close To New York City &#x26; Boston ** Excellent Earnings ** Partnership Connecticut with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job With   Easy Access To New York City  &amp; Boston    Partnership Opportunity  * 1:4 Call * Great Earnings Employed With Full Benefits Package &amp; Excellent Patient Census    Call ]]></description>
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<title>Permanent Internal Medicine Job in Houston Texas with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job In   Houston Texas   Competitive Starting Salary + Production Incentives Employed or Solo Position With   Partnership Options   Excellent Patient Census * Full Benefits Package ]]></description>
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<title>Permanent Internal Medicine Job in Internal Medicine Job Near Portland Oregon * 4   Day Work Week * 401K Oregon with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_oregon/page_1.html</link>
<description><![CDATA[ Internal Medicine Job  Near Portland Oregon  Competitive Starting Salary * 1:6 Call * Sign On Bonus Excellent Patient Census *  Great Benefits  Package   401k   *  Vacation  * Relocation * Possible  ]]></description>
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<title>Permanent Internal Medicine Job in $210K Starting Salary * Sign On Bonus * Outdoor Enthusiasts Dream Home!! Utah with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job In Utah * Outdoor Paradise  Mountains * Lakes * Flowers * Skiing &amp; More!     $210K Starting Salary    + Production Incentives * 1:4 Call Sign On Bonus * Excellent Benefits Package ]]></description>
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<title>Permanent Internal Medicine Job in GA statewide Georgia with Medical Doctor Associates, Inc.</title>
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<description><![CDATA[IMMEDIATE NEED - AUGUSTA, GEORGIA for a BC/BE INTERNAL MEDICINE PHYSICIAN! 250K Financial Package.  Practice limited to outpatient only. Excellent payor mix (75% private insurance).  Practice opening ]]></description>
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<title>Permanent Internal Medicine Job in TX statewide Texas with Medical Doctor Associates, Inc.</title>
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<description><![CDATA[Personal Visiting Physician -Texas.  Leading House-Call Practice in the USA dedicated to providing house calls to homebound patients, seeks physicians who value spending time with their patients. You ]]></description>
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<title>Permanent Internal Medicine Job in VA statewide Virginia with Medical Doctor Associates, Inc.</title>
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<description><![CDATA[Virginia Community Health Center actively seeking a BC/BE Internal Medicine physician to join their organization. Outpatient and traditional practice opportunities available. Our clients are willing to ]]></description>
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<title>Permanent Internal Medicine Job in Quick Drive To Savannah * $180K Salary + Sign On Bonus Georgia with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job   Near Savannah Georgia   Competitive Starting Salary + Sign On Bonus Employed Opportunity *   Call Our Experts Today!!    Chosen as one of the best 100 small towns in the U.S., ]]></description>
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<title>Permanent Internal Medicine Job in Jackson Mississippi with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_mississippi/page_1.html</link>
<description><![CDATA[ Internal Medicine Job In   Mississippi Metropolitan City     Earn Upwards of $230K   * 1:6 Call * Sign On Bonus Excellent Benefits Package If Employed   401k  * CME * Insurance *  Loan Forgiveness  &amp; ]]></description>
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<title>Permanent Internal Medicine Job in Earn Upwards of $230K * Internal Medicine Job In Mississippi Near Jackson Mississippi with The Curare Group, Inc.</title>
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<description><![CDATA[ Internal Medicine Job  Near Jackson Mississippi    Earn Upwards of $230K   * 1:6 Call * Sign On Bonus Employed Position with Competitive Benefits   Join This Established Group of Physicians Today!!  ]]></description>
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<title>Permanent Internal Medicine Job in OH statewide Ohio with Medical Doctor Associates, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_ohio/page_1.html</link>
<description><![CDATA[Outpatient Only Primary Care  available statewide.  A Leading Personal Physician Practice in the USA dedicated to providing house calls to the homebound seeks physicians who value spending time with their ]]></description>
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<title>Permanent Internal Medicine Job in FL statewide Florida with Medical Doctor Associates, Inc.</title>
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<description><![CDATA[COASTAL FLORIDA, Premier IM group seeks BC/BE IM due to extreme population growth.  Immediate busy caseload, equity offered.  $200,000 Financial Package.  Realistic opportunity to be in the 90th percentile ]]></description>
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<title>Permanent Internal Medicine Job in SC statewide South Carolina with Medical Doctor Associates, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_south_carolina/page_1.html</link>
<description><![CDATA[Coastal Southeast Internal Medicine Opportunity! Introducing an opportunity to enjoy an Exceptional Practice and an Outstanding Lifestyle!  An excellent opportunity is now available for a BE/BC Internist ]]></description>
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<title>Permanent Internal Medicine Job in $225K Guarantee!!! Internal Medicine Job In Oklahoma * $25K Sign On Bonus Oklahoma with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_oklahoma/page_1.html</link>
<description><![CDATA[ Internal Medicine Job With   $225K Guarantee   Production Incentives * 1:4 Call *  $25K Sign On Bonus  Employed With 7 Physicians * Full Benefits To Include:  Insurance * Pension * Vacation * CME &amp; ]]></description>
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<title>Permanent Internal Medicine Job in Internal Medicine Job In Tennessee * 5 Minuts From Memphis Tennessee with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_tennessee/page_3.html</link>
<description><![CDATA[ Internal Medicine Job   Just 5 Minutes Of Memphis, TN   Competitive Salary *   Sign On Bonus   * Employed Excellent Patient Census * Full Benefits * Flexible Setup  This community is located just outside ]]></description>
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<item rdf:about="http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_virginia/page_2.html">
<title>Permanent Internal Medicine Job in Internal Medicine Job Near Bristol, TN ** Great Earnings + Partnership Virginia with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_virginia/page_2.html</link>
<description><![CDATA[ Internal Medicine Job   Near Bristol, TN     Excellent Earnings + Partnership   * 1:4 Call 24-25 Patients/Day * Employed With Outstanding Group  Located in the highlands of Virginia with miles of hiking ]]></description>
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<item rdf:about="http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_west_virginia/page_4.html">
<title>Permanent Internal Medicine Job in Internal Medicine Job * Easy Drive To Washington D.C. * Bonus Incentives! West Virginia with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_west_virginia/page_4.html</link>
<description><![CDATA[ Internal Medicine Job Within   Easy Driving Distance To Washington D.C.     Excellent Earning Potential   * 1:6 Call * Production Incentives Work From 1 Facility * Great Benefits Package  Paid Vacation, ]]></description>
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<title>Permanent Internal Medicine Job in Upwards of $200K Salary Near Lexington, KY!! Kentucky with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_kentucky/page_3.html</link>
<description><![CDATA[ Internal Medicine Job With   Easy Access To Lexington, KY   Upwards of $200K Salary   * 1:6 Call * Join  4 Physicians  Partnership Opportunity   Call Our Internal Medicine Experts Today To Inquire About ]]></description>
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<item rdf:about="http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_massachusetts/page_1.html">
<title>Permanent Internal Medicine Job in Internal Medicine Job with Very Easy Access Into Boston, MA &#x26; Providence, RI Massachusetts with The Curare Group, Inc.</title>
<link>http://www.physemp.com/physician_jobs/all_internal_medicine_jobs_in_massachusetts/page_1.html</link>
<description><![CDATA[ Internal Medicine Job With Easy Access To    Boston, MA    &amp;    Providence, RI      Competitive Salary + Incentives   * Join 6 Physicians * 1:10 Call Full Benefits Package To Include:  Malpractice ]]></description>
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<title>Breastfeeding and allergies: time for a change in paradigm?.</title>
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Page: 539DOI: 10.1097/MCI.0b013e32831dae43Authors: Duncan, Joanne M;  Sears, Malcolm R

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<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00002.htm</link>
<description><![CDATA[
Page: 547DOI: 10.1097/MCI.0b013e32831dae50Authors: Mortz, Charlotte Gotthard;  Andersen, Klaus Ejner

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00003.htm">
<title>Contemporary approaches to the identification of athletes at risk for sudden cardiac death.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00003.htm</link>
<description><![CDATA[
Page: 552DOI: 10.1097/MCI.0b013e32831daee4Authors: Drezner, Jonathan A

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00004.htm">
<title>How to break the vicious circle of antibiotic resistances?.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00004.htm</link>
<description><![CDATA[
Page: 560DOI: 10.1097/MCI.0b013e32831dabd1Authors: Leone, Marc;  Martin, Claude

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00005.htm">
<title>Benefits of high-protein weight loss diets: enough evidence for practice?.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00005.htm</link>
<description><![CDATA[
Page: 566DOI: 10.1097/MCI.0b013e32831daebdAuthors: Brehm, Bonnie J a;  D'Alessio, David A b

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00006.htm">
<title>Chronic pancreatitis.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00006.htm</link>
<description><![CDATA[
Page: 572DOI: 10.1097/MCI.0b013e32831daddaAuthors: Conwell, Darwin L;  Banks, Peter A

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00007.htm">
<title>Heparin-induced thrombocytopenia: some working hypotheses on pathogenesis, diagnostic strategies and treatment.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00007.htm</link>
<description><![CDATA[
Page: 577DOI: 10.1097/MCI.0b013e32831dae94Authors: Alberio, Lorenzo

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00008.htm">
<title>Long-term prognosis after deep venous thrombosis.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00008.htm</link>
<description><![CDATA[
Page: 586DOI: 10.1097/MCI.0b013e32831daea9Authors: Shbaklo, Hadia a;  Kahn, Susan R a,b

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00009.htm">
<title>New advances in Clostridium difficile infection: changing epidemiology, diagnosis, treatment and control.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00009.htm</link>
<description><![CDATA[
Page: 591DOI: 10.1097/MCI.0b013e32831daed2Authors: DuPont, Herbert L a,b,c;  Garey, Kevin b,c,d;  Caeiro, Juan-Pablo b,c;  Jiang, Zhi-Dong a

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00010.htm">
<title>Elevations in serum creatinine with RAAS blockade: why isn&#x27;t it a sign of kidney injury?.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00010.htm</link>
<description><![CDATA[
Page: 599DOI: 10.1097/MCI.0b013e32831daeffAuthors: Ryan, Michael J a;  Tuttle, Katherine R a,b

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00011.htm">
<title>Renin inhibition: should it supplant ACE inhibitors and ARBS in high risk patients?.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00011.htm</link>
<description><![CDATA[
Page: 606DOI: 10.1097/MCI.0b013e32831daf11Authors: Gaddam, Krishna K;  Oparil, Suzanne

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00012.htm">
<title>Diabetic polyneuropathy: an update.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00012.htm</link>
<description><![CDATA[
Page: 613DOI: 10.1097/MCI.0b013e32831dae0bAuthors: Zochodne, Douglas W

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00013.htm">
<title>Drug-induced myopathies.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00013.htm</link>
<description><![CDATA[
Page: 620DOI: 10.1097/MCI.0b013e32831dae1cAuthors: Klopstock, Thomas

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00014.htm">
<title>Evolving epidemiology of malignancies in HIV.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00014.htm</link>
<description><![CDATA[
Page: 626DOI: 10.1097/MCI.0b013e32831dae71Authors: Bonnet, Fabrice a,b,c;  Chene, Genevieve a,b

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00015.htm">
<title>Vaccines against cervical cancer.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00015.htm</link>
<description><![CDATA[
Page: 633DOI: 10.1097/MCI.0b013e32831dae88Authors: Rogers, Linda J;  Eva, Lois J;  Luesley, David Michael

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00016.htm">
<title>Effectiveness and cost effectiveness of thrombolysis in patients with acute pulmonary embolism.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00016.htm</link>
<description><![CDATA[
Page: 638DOI: 10.1097/MCI.0b013e32831dad76Authors: Zamanian, Roham T a,b;  Gould, Michael K a,c

]]></description>
</item>

<item rdf:about="http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00017.htm">
<title>Update on biologics in juvenile idiopathic arthritis.</title>
<link>http://www.co-internalmedicine.com/pt/re/cointernalmed/abstract.00132980-200812000-00017.htm</link>
<description><![CDATA[
Page: 643DOI: 10.1097/MCI.0b013e32831dae32Authors: Ilowite, Norman T

]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19567619&#x26;dopt=Abstract">
<title>Rethinking Randomized Clinical Trials for Comparative Effectiveness Research: The Need for Transformational Change.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19567619&#x26;dopt=Abstract</link>
<description><![CDATA[
	Related Articles
        Rethinking Randomized Clinical Trials for Comparative Effectiveness Research: The Need for Transformational Change.
        Ann Intern Med. 2009 Jun 30;
        Authors:  Luce BR, Kramer JM, Goodman SN, Connor J, Tunis S, Whicher D, Schwartz JS
        
        PMID: 19567619 [PubMed - as supplied by publisher]
    ]]></description>
</item>

<item rdf:about="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19567618&#x26;dopt=Abstract">
<title>Comparative Effectiveness Research: A Report From the Institute of Medicine.</title>
<link>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tmpl=NoSidebarfile&#x26;db=PubMed&#x26;cmd=Retrieve&#x26;list_uids=19567618&#x26;dopt=Abstract</link>
<description><![CDATA[
	Related Articles
        Comparative Effectiveness Research: A Report From the Institute of Medicine.
        Ann Intern Med. 2009 Jun 30;
        Authors:  Sox HC, Greenfield S
        
        PMID: 19567618 [PubMed - as supplied by publisher]
    ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1092?rss=1">
<title>ABOUT THIS JOURNAL: About This Journal</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1092?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1094?rss=1">
<title>IN THIS ISSUE OF ARCHIVES OF INTERNAL MEDICINE: In This Issue of Archives of Internal Medicine</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1094?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1095?rss=1">
<title>COMMENTARY: The Silent Dimension: Expressing Humanism in Each Medical Encounter</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1095?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1100?rss=1">
<title>EDITORIAL: Treating Anemia With Erythropoiesis-Stimulating Agents: Effects on Quality of Life</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1100?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1102?rss=1">
<title>EDITORIAL: Cost-effectiveness Analysis of an Established, Effective Procedure</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1102?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1104?rss=1">
<title>REVIEW ARTICLE: The Impact of Selecting a High Hemoglobin Target Level on Health-Related Quality of Life for Patients With Chronic Kidney Disease: A Systematic Review and Meta-analysis</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1104?rss=1</link>
<description><![CDATA[
Background&nbsp; Treatment of anemia in chronic kidney disease (CKD) with erythropoietin-stimulating agents (ESAs) is commonplace. The optimal hemoglobin treatment target has not been established. A clearer understanding of the health-related quality of life (HQOL) impact of hemoglobin target levels is needed. We systematically reviewed the randomized controlled trial (RCT) data on HQOL for patients treated with low to intermediate (9.0-12.0 g/dL) and high hemoglobin target levels (>12.0 g/dL) and performed a meta-analysis of all available 36-item short-form (SF-36) RCT data.
Methods&nbsp; We conducted a search to identify all RCTs of ESA therapy in patients with anemia associated with CKD (1966&ndash;December 2006). Inclusion criteria were (1) 30 or more participants, (2) anemic adults with CKD, (3) epoetin (alfa and beta) or darbepoetin used, (4) a control arm, and (5) reported HQOL using a validated measure. All available SF-36 data underwent meta-analysis using the weighted mean difference.
Results&nbsp; Of 231 full texts screened, 11 eligible studies were identified. The SF-36 was used in 9 trials. Reporting of these data was generally incomplete. Data from each domain of the SF-36 were summarized. Statistically significant changes were noted in the physical function (weighted mean difference [WMD], 2.9; 95% confidence interval [CI], 1.3 to 4.5), general health (WMD, 2.7; 95% CI, 1.3 to 4.2), social function (WMD, 1.3; 95% CI, &ndash;0.8 to 3.4), and mental health (WMD, 0.4; 95% CI, 0.1 to 0.8) domains. None of the changes would be considered clinically significant.
Conclusions&nbsp; Our study suggests that targeting hemoglobin levels in excess of 12.0 g/dL leads to small and not clinically meaningful improvements in HQOL. This, in addition to significant safety concerns, suggests that targeting treatment to hemoglobin levels that are in the range of 9.0 to 12.0 g/dL is preferred.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1113?rss=1">
<title>ORIGINAL INVESTIGATION: Cost-effectiveness of Total Knee Arthroplasty in the United States: Patient Risk and Hospital Volume</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1113?rss=1</link>
<description><![CDATA[
Background&nbsp; Total knee arthroplasty (TKA) relieves pain and improves quality of life for persons with advanced knee osteoarthritis. However, to our knowledge, the cost-effectiveness of TKA and the influences of hospital volume and patient risk on TKA cost-effectiveness have not been investigated in the United States.
Methods&nbsp; We developed a Markov, state-transition, computer simulation model and populated it with Medicare claims data and cost and outcomes data from national and multinational sources. We projected lifetime costs and quality-adjusted life expectancy (QALE) for different risk populations and varied TKA intervention and hospital volume. Cost-effectiveness of TKA was estimated across all patient risk and hospital volume permutations. Finally, we conducted sensitivity analyses to determine various parameters' influences on cost-effectiveness.
Results&nbsp; Overall, TKA increased QALE from 6.822 to 7.957 quality-adjusted life years (QALYs). Lifetime costs rose from $37&nbsp;100 (no TKA) to $57&nbsp;900 after TKA, resulting in an incremental cost-effectiveness ratio of $18&nbsp;300 per QALY. For high-risk patients, TKA increased QALE from 5.713 to 6.594 QALY, yielding a cost-effectiveness ratio of $28&nbsp;100 per QALY. At all risk levels, TKA was more costly and less effective in low-volume centers than in high-volume centers. Results were insensitive to variations of key input parameters within policy-relevant, clinically plausible ranges. The greatest variations were seen for the quality of life gain after TKA and the cost of TKA.
Conclusions&nbsp; Total knee arthroplasty appears to be cost-effective in the US Medicare-aged population, as currently practiced across all risk groups. Policy decisions should be made on the basis of available local options for TKA. However, when a high-volume hospital is available, TKAs performed in a high-volume hospital confer even greater value per dollar spent than TKAs performed in low-volume centers.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1121?rss=1">
<title>INVITED COMMENTARY: Cost-effectiveness of Total Knee Arthroplasty in the United States--Invited Commentary</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1121?rss=1</link>
<description><![CDATA[ ]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1123?rss=1">
<title>ORIGINAL INVESTIGATION: Frequency of Failure to Inform Patients of Clinically Significant Outpatient Test Results</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1123?rss=1</link>
<description><![CDATA[
Background&nbsp; Failing to inform a patient of an abnormal outpatient test result can be a serious error, but little is known about the frequency of such errors or the processes for managing results that may reduce errors.
Methods&nbsp; We conducted a retrospective medical record review of 5434 randomly selected patients aged 50 to 69 years in 19 community-based and 4 academic medical center primary care practices. Primary care practice physicians were surveyed about their processes for managing test results, and individual physicians were notified of apparent failures to inform and asked whether they had informed the patient. Blinded reviewers calculated a "process score" ranging from 0 to 5 for each practice using survey responses.
Results&nbsp; The rate of apparent failures to inform or to document informing the patient was 7.1% (135 failures divided by 1889 abnormal results), with a range of 0% to 26.2%. The mean process score was 3.8 (range, 0.9-5.0). In mixed-effects logistic regression, higher process scores were associated with lower failure rates (odds ratio, 0.68; P&nbsp;&lt;&nbsp;.001). Use of a "partial electronic medical record" (paper-based progress notes and electronic test results or vice versa) was associated with higher failure rates compared with not having an electronic medical record (odds ratio, 1.92; P&nbsp;=&nbsp;.03) or with having an electronic medical record that included both progress notes and test results (odds ratio, 2.37; P&nbsp;=&nbsp;.007).
Conclusions&nbsp; Failures to inform patients or to document informing patients of abnormal outpatient test results are common; use of simple processes for managing results is associated with lower failure rates.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1130?rss=1">
<title>ORIGINAL INVESTIGATION: Cutaneous Malignancies Among HIV-Infected Persons</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1130?rss=1</link>
<description><![CDATA[
Background&nbsp; As the life expectancy of persons infected with human immunodeficiency virus (HIV) increases, cancers have become an important cause of morbidity and mortality. Although cutaneous cancers are the most common malignant neoplasms in the general population, little data exist among HIV-positive persons, especially regarding the impact of HIV-specific factors.
Methods&nbsp; We evaluated the incidence rates and factors associated with the development of cutaneous malignancies among HIV-infected persons by examining data that were prospectively collected from a large HIV study that included 4490 participants (1986-2006). Poisson regression and Cox proportional hazards models were performed.
Results&nbsp; Six percent of HIV-infected persons (n&nbsp;=&nbsp;254) developed a cutaneous malignancy during 33&nbsp;760 person-years of follow-up (mean, 7.5 years). Since the advent of highly active antiretroviral therapy (HAART), the incidence rates of cutaneous non&ndash;AIDS-defining cancers (NADCs), in particular basal cell carcinoma, have exceeded the rates of cutaneous AIDS-defining cancers such as Kaposi sarcoma. Factors associated with the development of cutaneous NADCs in the multivariate models included increasing age (hazard ratio [HR], 2.1; 95% confidence interval [CI], 1.7-2.6) and race. Compared with the white/non-Hispanic race, African Americans (HR, 0.03; 95% CI, 0.01-0.14) and other races (HR, 0.14; 95% CI, 0.03-0.57) had a lower risk of cutaneous NADCs. There were no significant associations between cutaneous NADCs and time-updated CD4 lymphocyte counts, HIV RNA levels, or receipt of HAART.
Conclusions&nbsp; At present, the most common cutaneous malignancies among HIV-infected persons are NADCs. Cutaneous NADCs do not appear to be significantly associated with immune function or HAART but rather are related to traditional factors such as aging and skin color.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1139?rss=1">
<title>ORIGINAL INVESTIGATION: Association Between Late-Life Social Activity and Motor Decline in Older Adults</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1139?rss=1</link>
<description><![CDATA[
Background&nbsp; Loss of motor function is a common consequence of aging, but little is known about the factors that predict idiopathic motor decline. Our objective was to test the hypothesis that late-life social activity is related to the rate of change in motor function in old age.
Methods&nbsp; Longitudinal cohort study with a mean follow-up of 4.9 years with 906 persons without stroke, Parkinson disease, or dementia participating in the Rush Memory and Aging Project. At baseline, participants rated the frequency of their current participation in common social activities from which a summary measure of social activity was derived. The main outcome measure was annual change in a composite measure of global motor function, based on 9 measures of muscle strength and 9 motor performances.
Results&nbsp; Mean (SD) social activity score at baseline was 2.6 (0.58), with higher scores indicating more frequent participation in social activities. In a generalized estimating equation model, controlling for age, sex, and education, global motor function declined by approximately 0.05 U/y (estimate, 0.016; 95% confidence interval [CI], &ndash;0.057 to 0.041 [P&nbsp;=&nbsp;.02]). Each 1-point decrease in social activity was associated with approximately a 33% more rapid rate of decline in motor function (estimate, 0.016; 95% CI, 0.003 to 0.029 [P&nbsp;=&nbsp;.02]). The effect of each 1-point decrease in the social activity score at baseline on the rate of change in global motor function was the same as being approximately 5 years older at baseline (age estimate, &ndash;0.003; 95% CI, &ndash;0.004 to &ndash;0.002 [P&lt;.001]). Furthermore, this amount of motor decline per year was associated with a more than 40% increased risk of death (hazard ratio, 1.44; 95% CI, 1.30 to 1.60) and a 65% increased risk of incident Katz disability (hazard ratio, 1.65; 95% CI, 1.48 to 1.83). The association of social activity with the rate of global motor decline did not vary along demographic lines and was unchanged (estimate, 0.025; 95% CI, 0.005 to 0.045 [P&nbsp;=&nbsp;.01]) after controlling for potential confounders including late-life physical and cognitive activity, disability, global cognition depressive symptoms, body composition, and chronic medical conditions.
Conclusion&nbsp; Less frequent participation in social activities is associated with a more rapid rate of motor function decline in old age.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1147?rss=1">
<title>ORIGINAL INVESTIGATION: Nocturnal Arrhythmias Across a Spectrum of Obstructive and Central Sleep-Disordered Breathing in Older Men: Outcomes of Sleep Disorders in Older Men (MrOS Sleep) Study</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1147?rss=1</link>
<description><![CDATA[
Background&nbsp; Rates of cardiac arrhythmias increase with age and may be associated with clinically significant morbidity. We studied the association between sleep-disordered breathing (SDB) with nocturnal atrial fibrillation or flutter (AF) and complex ventricular ectopy (CVE) in older men.
Methods&nbsp; A total of 2911 participants in the Outcomes of Sleep Disorders in Older Men Study underwent unattended polysomnography. Nocturnal AF and CVE were ascertained by electrocardiogram-specific analysis of the polysomnographic data. Exposures were (1) SDB defined by respiratory disturbance index (RDI) quartile (a major index including all apneas and hypopneas), and ancillary definitions incorporating (2) obstructive events, obstructive sleep apnea (OSA; Obstructive Apnea Hypopnea Index quartile), or (3) central events, central sleep apnea (CSA; Central Apnea Index category), and (4) hypoxia (percentage of sleep time with &lt;90% arterial oxygen percent saturation). Multivariable logistic regression analyses were performed.
Results&nbsp; An increasing RDI quartile was associated with increased odds of AF and CVE (P values for trend, .01 and &lt;.001, respectively). The highest RDI quartile was associated with increased odds of AF (odds ratio [OR], 2.15; 95% confidence interval [CI], 1.19-3.89) and CVE (OR, 1.43; 95% CI, 1.12-1.82) compared with the lowest quartile. An increasing OSA quartile was significantly associated with increasing CVE (P value for trend, .01) but not AF. Central sleep apnea was more strongly associated with AF (OR, 2.69; 95% CI, 1.61-4.47) than CVE (OR, 1.27; 95% CI, 0.97-1.66). Hypoxia level was associated with CVE (P value for trend, &lt;.001); those in the highest hypoxia category had an increased odds of CVE (OR, 1.62; 95% CI, 1.23-2.14) compared with the lowest quartile.
Conclusions&nbsp; In this large cohort of older men, increasing severity of SDB was associated with a progressive increase in odds of AF and CVE. When SDB was characterized according to central or obstructive subtypes, CVE was associated most strongly with OSA and hypoxia, whereas AF was most strongly associated with CSA, suggesting that different sleep-related stresses may contribute to atrial and ventricular arrhythmogenesis in older men.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1156?rss=1">
<title>ORIGINAL INVESTIGATION: The Frequency of Hyperkalemia and Its Significance in Chronic Kidney Disease</title>
<link>http://archinte.ama-assn.org/cgi/content/short/169/12/1156?rss=1</link>
<description><![CDATA[
Background&nbsp; Hyperkalemia is a potential threat to patient safety in chronic kidney disease (CKD). This study determined the incidence of hyperkalemia in CKD and whether it is associated with excess mortality.
Methods&nbsp; This retrospective analysis of a national cohort comprised 2&nbsp;103&nbsp;422 records from 245&nbsp;808 veterans with at least 1 hospitalization and at least 1 inpatient or outpatient serum potassium record during the fiscal year 2005. Chronic kidney disease and treatment with angiotensin-converting enzyme inhibitors and/or angiotensin II receptor blockers (blockers of the renin-angiotensin-aldosterone system [RAAS]) were the key predictors of hyperkalemia. Death within 1 day of a hyperkalemic event was the principal outcome.
Results&nbsp; Of the 66&nbsp;259 hyperkalemic events (3.2% of records), more occurred as inpatient events (n&nbsp;=&nbsp;34&nbsp;937 [52.7%]) than as outpatient events (n&nbsp;=&nbsp;31&nbsp;322 [47.3%]). The adjusted rate of hyperkalemia was higher in patients with CKD than in those without CKD among individuals treated with RAAS blockers (7.67 vs 2.30 per 100 patient-months; P&nbsp;&lt;&nbsp;.001) and those without RAAS blocker treatment (8.22 vs 1.77 per 100 patient-months; P&nbsp;&lt;&nbsp;.001). The adjusted odds ratio (OR) of death with a moderate (potassium, &ge;5.5 and &lt;6.0 mEq/L [to convert to mmol/L, multiply by 1.0]) and severe (potassium, &ge;6.0 mEq/L) hyperkalemic event was highest with no CKD (OR, 10.32 and 31.64, respectively) vs stage 3 (OR, 5.35 and 19.52, respectively), stage 4 (OR, 5.73 and 11.56, respectively), or stage 5 (OR, 2.31 and 8.02, respectively) CKD, with all P&nbsp;&lt;&nbsp;.001 vs normokalemia and no CKD.
Conclusions&nbsp; The risk of hyperkalemia is increased with CKD, and its occurrence increases the odds of mortality within 1 day of the event. These findings underscore the importance of this metabolic disturbance as a threat to patient safety in CKD.
]]></description>
</item>

<item rdf:about="http://archinte.ama-assn.org/cgi/content/short/169/12/1163?rss=1">
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