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      <title>NACB Blog: Posts</title>
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      <title>Which Is the RIGHT Equation for Calculating eGFR?</title>
      <link>http://www.aacc.org/members/nacb/NACBBlog/Lists/Posts/ViewPost.aspx?ID=82</link>
      <description><![CDATA[<div><b>Body:</b> <div class="ExternalClassB598E221C0F14EA594B376DB1316E4D8"><p>​Which is the RIGHT equation for calculating eGFR?  Unfortunately, the answer may be “that depends”. Creatinine and BUN/Urea have long been used as markers of renal function, though creatinine has more recently gained prominence.  It was recognized a decade ago that there was significant variation in creatinine assay results from different manufacturers (1).  A world-wide effort in the last few years has resulted in the current standardization of almost all creatinine assays being traceable to IDMS, and assay-to-assay recovery differences being significantly reduced if not almost eliminated, though differences in susceptibility to interferences remain (2).</p>
<p>Creatinine measurements still have in vivo variables depending on the patient’s age, gender, race, diet, muscle mass, and a variety of other factors, so relying on broad measures of reference intervals often became misleading.  Thus eGFR equations were developed that could account for at least some of these major influences and provide physicians with a more coherent measure of renal function.</p>
<p>Today, the field is in flux with a variety of eGFR reporting choices:</p>
<p>The MDRD Equation:  The MDRD equation was originally developed as a measure of eGFR before creatinine assays were standardized.  That assay standardization resulted in a 10-25% decrease in many creatinine assays, and a “standardized” MDRD equation was developed that accounted for those assay changes (3).  However, a recent study from CAP showed that perhaps 40% of labs were reporting results using newer creatinine assays but still reporting eGFR with the older, non-adjusted MDRD equation (4).  Was yours one of them?  The MDRD equation has also not been validated for significant groups of patients (the critically ill, extremes of muscle mass or diet, and other conditions), and can give misleading results.  Does your lab report eGFR for all creatinine results?</p>
<p>CKD-EPI Equation:  The CKD-EPI equation was more recently developed and appears to give a more precise eGFR value across a wider range of results.  It is a more complicated set of equations than the MDRD, but may have broader applicability (5, 6).  </p>
<p>Cockcroft-Gault Equation and Drug Dosing:  Certain drugs have narrow windows of renal tolerance, and dosage levels will vary with renal function.  Most of these drugs had their recommended dosages determined by the Cockcroft-Gault equation for eGFR, and this was done before the current era of creatinine assay standardization when recoveries for most assays shifted (7).  Can these differences make significant changes in drug dosing and patient responses to therapy?</p>
<p>Schwarz Equation in Pediatrics: Pediatric patients are a special challenge in many areas of laboratory medicine.  The Schwartz equation was developed, and recently revised, to estimate GFR in pediatrics (6, 8).  Does your lab routinely report GFR in pediatrics?</p>
<p>Cystatin C: Research with Cystatin C has shown it to be a good marker of renal function and prognosis of comorbidities, and is used in distinct equations for eGFR.  It has been hampered by wide variabilities in recovery between assays, but the recent availability of a new reference material should help standardize Cystatin C and allow it into more routine use (6, 9).  Do you use or expect to use Cystatin C in your lab?</p>
<p>What are your challenges with eGFR reporting?  And how do you address them?<br /></p>
<p> </p></div></div>
<div><b>Category:</b> <a onclick="OpenPopUpPage('http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=16&RootFolder=*', RefreshPage); return false;" href="http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=16&RootFolder=*">Renal/GI/Hepatic</a></div>
<div><b>Published:</b> 5/15/2012 9:10 AM</div>
<div><b>PostAuthorName:</b> Jack Zakowski, PhD, FACB</div>
<div><b>PostAuthorLink:</b> <a href="http://www.aacc.org/resourcecenters/AACCBlogs/bios/Pages/Zakowski.aspx#">Jack Zakowski, PhD, FACB</a></div>
<div><b>PostAuthorPic:</b> <a href="http://www.aacc.org/members/nacb/NACBBlog/Lists/Photos/ZAKOWSKI.jpg">Jack Zakowski, PhD, FACB</a></div>
<div><b>Books:</b> <div class="ExternalClassBD2B05BF23BC4C6592AB3E7214D2E626"><p>​References</p>
<p>1. Myers, et al, Clin Chem 2006:52, 5-18.<br />2. Greenberg, et al, Clin Chem 2011:58, 391-401.<br />3. Levey, et al, Clin Chem 2007:53, 766-772.<br />4. <a href="http://www.nkdep.nih.gov/about-nkdep/working-groups/laboratory-working-group/meeting-summaries/07282011_lab_meeting.shtml">National Kidney Disease Education Program, Working Group meeting 2011.</a> </p>
<p>5. Levey, et al, Ann Intern Med 2009:150, 604-612.<br />6. National Kidney Disease Education Program: <a href="http://www.nkdep.nih.gov/lab-evaluation.shtml">Laboratory Evaluation</a>.</p>
<p>7. National Kidney Disease Education Program: <a href="http://nkdep.nih.gov/resources/CKD-drug-dosing.shtml">CKD and Drug Dosing: Information for Providers</a>.</p>
<p>8. Schwartz, et al, J Am Soc Nephrol 2009:20, 629-637.<br />9. Grubb, et al, Clin Chem Lab Med 2010:48, 1619-1621.<br /></p></div></div>
<div><b>MonthYear:</b> May 2012</div>
<div><b>Year:</b> 2012</div>
]]></description>
      <author>Betsy Garman</author>
      <category>Renal/GI/Hepatic</category>
      <pubDate>Wed, 11 Apr 2012 13:27:36 GMT</pubDate>
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      <title>Does Circadian Rhythm Impact Fasting Blood Glucose Testing?</title>
      <link>http://www.aacc.org/members/nacb/NACBBlog/Lists/Posts/ViewPost.aspx?ID=79</link>
      <description><![CDATA[<div><b>Body:</b> <div class="ExternalClass138F7A4E49F2431FA20B32F710383388"><p><span lang="EN">The title of this NACBLOG post is a question that was recently posted on the AACC chemistry list serv. Does Circadian Rhythm Impact Fasting Blood Glucose Testing?</span></p>
<p><span lang="EN">What is your response? Check back for our response on Monday, April 30, 2012. <span lang="EN"><div>Yes, circadian rhythm does impact fasting plasma glucose levels.<br /><br />In an article published in 2000 (JAMA 284:3157, 2000), the frequency of hyperglycemia (glucose =&gt;126 mg/dL) in the study populations was higher when drawn after an overnight fast (2.8%) than when drawn as a fasting afternoon sample (1.4%).<br /><br />Therefore if a fasting plasma glucose measurement is used to screen for diabetes, an overnight fast is preferred to sampling in the afternoon. In the quoted study, the subjects drawn in the AM had fasted for a mean of 13.5 hrs and the subjects drawn in the afternoon had fasted for a mean of 7 hours. </div>
<div> </div></span></span></p>
<p> </p>
<font face="Tahoma" size="2"></font><p> </p></div></div>
<div><b>Category:</b> <a onclick="OpenPopUpPage('http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=17&RootFolder=*', RefreshPage); return false;" href="http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=17&RootFolder=*">Case Study</a></div>
<div><b>Published:</b> 4/24/2012 8:25 AM</div>
<div><b>PostAuthorName:</b> William E. Winter, MD, and Roger L. Bertholf, PhD</div>
<div><b>PostAuthorLink:</b> <a href="http://www.aacc.org/resourcecenters/AACCBlogs/bios/Pages/winterbertholf.aspx#">William E. Winter, MD, and Roger L. Bertholf, PhD</a></div>
<div><b>PostAuthorPic:</b> <a href="http://www.aacc.org/members/nacb/NACBBlog/Lists/Photos/Winter-Bertholf.jpg">William E. Winter, MD, and Roger L. Bertholf, PhD</a></div>
<div><b>MonthYear:</b> April 2012</div>
<div><b>Year:</b> 2012</div>
]]></description>
      <author>AACC\bgarman</author>
      <category>Case Study</category>
      <pubDate>Fri, 09 Mar 2012 19:19:21 GMT</pubDate>
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      <title>Pediatric Reference Intervals: Current Gaps and New Initiatives</title>
      <link>http://www.aacc.org/members/nacb/NACBBlog/Lists/Posts/ViewPost.aspx?ID=81</link>
      <description><![CDATA[<div><b>Body:</b> <div class="ExternalClassE88ED5736749452BA7BBFC04840C90C5"><p>​Pediatric healthcare is critically dependent on availability of accurate and precise laboratory tests/biomarkers of pediatric disease, and on availability of &quot;reference intervals&quot; (or “normal values”) to allow appropriate clinical interpretation. Children are not small adults; child development and growth profoundly influence laboratory test reference intervals. Adult reference intervals cannot be used to interpret laboratory test results in children until they reach adult levels after puberty. Unfortunately, there is a lack of clearly defined pediatric reference intervals for most tests performed in children and adolescents. There is also a paucity of information on the effects of age, gender, BMI, sexual development (Tanner Stage), and ethnic origin on pediatric reference intervals. Most available reference intervals have been determined on Caucasians and do not consider population diversity. These critical gaps seriously compromise the ability of pediatricians to accurately diagnose medical conditions in their patients and significantly increase healthcare costs. It is thus critical and of utmost urgency that the influence of covariates be determined and a comprehensive database of covariate stratified reference intervals be established in the diverse pediatric populations in North America and elsewhere. </p>
<p>The Pediatric Focus Group of the Canadian Society of Clinical Chemists (CSCC) has recently initiated a collaborative project among pediatric centers across Canada to address the critical gaps in pediatric reference intervals by determining the influence of key covariates and establishing a national database for Canada-wide communication and knowledge translation. This project has been named: CALIPER, ‘CAnadian Laboratory Initiative on PEdiatric Reference Intervals’ (<a href="http://www.caliperproject.com/">www.caliperproject.com</a>). A major community outreach and recruitment effort has begun, leading to initial collection of over 4500 blood samples from healthy community children in the three Ontario centers. The first major report from the CALIPER initiative has now been published in Clinical Chemistry (<a href="http://www.ncbi.nlm.nih.gov/pubmed/22371482">http://www.ncbi.nlm.nih.gov/pubmed/22371482</a>). Customizable pediatric reference intervals are also now available on the caliper website: <a href="http://www.caliperdatabase.com/">www.caliperdatabase.com</a>.</p>
<p>Although the CALIPER initiative has been welcomed by most, some in the clinical chemistry community have argued that attempts should be made at determining common reference intervals rather than establishing intervals on specific analytical platforms. A number of groups have proposed establishing “common reference intervals” using a multicenter study design. These reference intervals are determined through the collaboration of laboratories from different regions or countries that use analytical methods that are traceable to a reference method. The concept of common reference intervals has been touted to represent, at least in part, “the way forward”. However, the major obstacles to the common reference interval approach are the lack of harmonization of methods by manufacturers and the lack of availability of reference materials and reference methods for the majority of analytes. It also remains to be tested whether common reference intervals are robust when applied to ethnically diverse populations. Until these problems are characterized and resolved, establishing and validating laboratory- specific reference intervals as mandated will remain the status quo for the foreseeable future.<br /></p>
<p> </p></div></div>
<div><b>Category:</b> <a onclick="OpenPopUpPage('http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=1&RootFolder=*', RefreshPage); return false;" href="http://www.aacc.org/members/nacb/NACBBlog/_layouts/listform.aspx?PageType=4&ListId={2D56F20B-3E83-4913-8C03-0273571591F8}&ID=1&RootFolder=*">Special Populations</a></div>
<div><b>Published:</b> 5/8/2012 11:59 AM</div>
<div><b>PostAuthorName:</b> Khosrow Adeli, PhD, FCACB, FACB, DABCC</div>
<div><b>PostAuthorLink:</b> <a href="http://www.aacc.org/resourcecenters/AACCBlogs/bios/Pages/Adeli.aspx#">Khosrow Adeli, PhD, FCACB, FACB, DABCC</a></div>
<div><b>PostAuthorPic:</b> <a href="http://www.aacc.org/members/nacb/NACBBlog/Lists/Photos/Adeli.jpg">Khosrow Adeli, PhD, FCACB, FACB, DABCC</a></div>
<div><b>Books:</b> <div class="ExternalClassF18A67CFA17145C9B08847707E9C062E"><p><a href="http://www.caliperproject.com/caliperproject/">​Caliper Project</a></p>
<p><a href="http://www.caliperdatabase.com/caliperdatabase/">Caliper Database</a></p>
<p>Colantonio DA, Kyriakopoulou L, Chan MK, et al: Closing the Gaps in Pediatric Laboratory Reference Intervals: A CALIPER Database of 40 Biochemical Markers in a Healthy and Multiethnic Population of Children. <a href="http://www.ncbi.nlm.nih.gov/pubmed/22371482">Clin Chem 2012 May;58(5):854-68.</a></p></div></div>
<div><b>MonthYear:</b> May 2012</div>
<div><b>Year:</b> 2012</div>
]]></description>
      <author>Betsy Garman</author>
      <category>Special Populations</category>
      <pubDate>Wed, 11 Apr 2012 13:14:41 GMT</pubDate>
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