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	<title>
	Comments on: Response to ASCP/USCAP &#8220;Sleaze&#8221; Meeting Announcement	</title>
	<atom:link href="https://tissuepathology.com/2008/01/14/response-to-asc/feed/" rel="self" type="application/rss+xml" />
	<link>https://tissuepathology.com/2008/01/14/response-to-asc/</link>
	<description>Educational and informative</description>
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		<title>
		By: fred seid		</title>
		<link>https://tissuepathology.com/2008/01/14/response-to-asc/#comment-408</link>

		<dc:creator><![CDATA[fred seid]]></dc:creator>
		<pubDate>Thu, 06 Mar 2008 19:55:05 +0000</pubDate>
		<guid isPermaLink="false">http://tissuepathology.org/posts/pathology-news/response-to-asc/#comment-408</guid>

					<description><![CDATA[I HAVE WASTED MANY HOURS SENDING EMAILS TO ASCP,CAP AND CMS.
TOO MANY BEHIND THE DOOR AGREEMENTS AND PROTECTION OF THE KEY FIGURES IN THIS POD LAB ISSUE.
EVEN AS THEY TALK AND NYSDOH GOES AROUND INSPECTING LABS, THE DOCS SKIRT THE LAW EVEN READING BIOPSIES THROUGH THE WEB AND SENDING RESULTS TO THE POD OR LAB FOR REPORT GENERATION.  THE PATHOLOGISTS ARE HOME READING THE WORK.
PATHOLOGIST CAN HAVE CONNECTIONS TO 5 PODS MAKING SUBSTANDARD SALARIES.
THIS SOUNDS SO FAMILIAR AS WAS DOCUMENTED IN THE PAP FIELD AS &quot;PIECEWORK&quot; PRACTICES.
WHERE IS THE CONTROL?
YOU CANNOT CONTROL GI AND DERM AND UROLOLOGIST WHO JUST WANT TO COVER FINANCIAL AND THINK BY HIRING OUTSIDE PATHOLOGIST WHO DONOT GENERALLY CARE ABOUT MAINTAINING QUALITY BUT CARE ABOUT A LIVING ONLY ,WILL BE ACCURATE IN DOING WORK IN SO MANY PODS TO MAKE UP THE LOSS OF MONEY THEY CANNOT GET IN THE HOSPITAL OR COMMERICAL LAB.
CMS IS JUST CIRCUMVENTING THE STARK LAW AS THE OTHER REGULARTORY AGENCIES THAT ALLOW THIS AND AFRAID TO JUST MAKE A DECISION THAT WILL PROTECT AND SECURE THE QUALITY AND PRIVACY OF THE PATIENTS.
THE ACCURACY THESE REGULATORY AGENCIES CANNOT CONTROL BECAUSE THESE PODS HIRE THE DOCTOR THAT WILL TAKE THE CHEAPER RATES AND THESE FELLOWS CANNOT WORK IN HOSPITALS BECAUSE THEY MAKE TOO MANY ERRORS AND HAVE THE REVIEW BOARDS ON THERE TAILS. MANY OF THEM ARE THE PATHOLOGIST TRAVELING FROM ONE LAB TO ANOTHER MAKING THE SAME ERRORS.
]]></description>
			<content:encoded><![CDATA[<p>I HAVE WASTED MANY HOURS SENDING EMAILS TO ASCP,CAP AND CMS.<br />
TOO MANY BEHIND THE DOOR AGREEMENTS AND PROTECTION OF THE KEY FIGURES IN THIS POD LAB ISSUE.<br />
EVEN AS THEY TALK AND NYSDOH GOES AROUND INSPECTING LABS, THE DOCS SKIRT THE LAW EVEN READING BIOPSIES THROUGH THE WEB AND SENDING RESULTS TO THE POD OR LAB FOR REPORT GENERATION.  THE PATHOLOGISTS ARE HOME READING THE WORK.<br />
PATHOLOGIST CAN HAVE CONNECTIONS TO 5 PODS MAKING SUBSTANDARD SALARIES.<br />
THIS SOUNDS SO FAMILIAR AS WAS DOCUMENTED IN THE PAP FIELD AS &#8220;PIECEWORK&#8221; PRACTICES.<br />
WHERE IS THE CONTROL?<br />
YOU CANNOT CONTROL GI AND DERM AND UROLOLOGIST WHO JUST WANT TO COVER FINANCIAL AND THINK BY HIRING OUTSIDE PATHOLOGIST WHO DONOT GENERALLY CARE ABOUT MAINTAINING QUALITY BUT CARE ABOUT A LIVING ONLY ,WILL BE ACCURATE IN DOING WORK IN SO MANY PODS TO MAKE UP THE LOSS OF MONEY THEY CANNOT GET IN THE HOSPITAL OR COMMERICAL LAB.<br />
CMS IS JUST CIRCUMVENTING THE STARK LAW AS THE OTHER REGULARTORY AGENCIES THAT ALLOW THIS AND AFRAID TO JUST MAKE A DECISION THAT WILL PROTECT AND SECURE THE QUALITY AND PRIVACY OF THE PATIENTS.<br />
THE ACCURACY THESE REGULATORY AGENCIES CANNOT CONTROL BECAUSE THESE PODS HIRE THE DOCTOR THAT WILL TAKE THE CHEAPER RATES AND THESE FELLOWS CANNOT WORK IN HOSPITALS BECAUSE THEY MAKE TOO MANY ERRORS AND HAVE THE REVIEW BOARDS ON THERE TAILS. MANY OF THEM ARE THE PATHOLOGIST TRAVELING FROM ONE LAB TO ANOTHER MAKING THE SAME ERRORS.</p>
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			</item>
		<item>
		<title>
		By: J Oppenheimer		</title>
		<link>https://tissuepathology.com/2008/01/14/response-to-asc/#comment-407</link>

		<dc:creator><![CDATA[J Oppenheimer]]></dc:creator>
		<pubDate>Sun, 03 Feb 2008 19:32:51 +0000</pubDate>
		<guid isPermaLink="false">http://tissuepathology.org/posts/pathology-news/response-to-asc/#comment-407</guid>

					<description><![CDATA[With decreasing reimbursements for surgery and increased office staff and capital expenses, clinicians are increasingly looking at the revenues generated by pathology to make ends meet. Reselling pathology services is easy, since it requires no work from the urologist other than adding additional CPT codes when billing the payor, but it is legal in only some states and does not allow the collection of specimens from Medicare patients.
The TC/PC (Technical Component/ Professional Component) allows the clinician (usually urologist or gasteroenterologist) to collect from all payors. In this model, the clinician hires a pathologist as a part-time employee to come to his office and read the biopsies (as well as cytology and FISH cases). The clinician uses the -26 professional component modifier to bill for the pathologist’s services. Medicare pays an average of $36 for each 88305-26 and $41 for each 88342-26 so a twelve specimen biopsy case (as is the norm with prostate biopsies) with a triple stain generates $555 in professional fees. If the pathologist is paid $500/hr and reads four such cases in that time he pockets the $500 while generating $2220 minus $500 or $1720 for the urologist. Meanwhile the laboratory generates $3200 in 88305-TC and $660 in 88342-TC for a total of $3860. Both clinician and pathologist benefit.
But why should the lab make $3860 and the clinician only half as much? This can be remedied by bringing the technical component in-house as some of the larger clinical group have done and many more are planning. Is it possible that the more one profits by doing an activity the more such activity is undertaken?  By comparing the amount of billable biopsy specimens obtained by those clinicians who do not profit from pathology with the amount of billable biopsy specimens obtained by those clinicians who do profit, it has been my experience that this is certainly the case. One can even compare the amount of specimens submitted by the same clinician both before and after they started to profit from such activity.
Each laboratory needs to foster a relationship with the clinician who supplies specimens. The desire for a lasting relationship encourages competing laboratories to kick-back as much of their excess profits as necessary to form and retain this relationship. Supplying attractive sales reps (who routinely make over $150K, and often over $250K/yr)  with company credit cards for expensive meals and fishing/golfing outings  ease the relationship as do charitable donations, reimbursements for expensive computer systems, payments to office staff, in-office placement of nurses and phlebotomists, free office and medical supplies, continuing education credits, free management and recruiting services, etc. The cost of these perks is considerable and can only be generated by performing unnecessary medical tests (excessive IHC stains including triple prostate stains on multiple cores, Giemsa staining of urine cytology, routine FISH Urovysion testing and addition to urine cytology, etc.
]]></description>
			<content:encoded><![CDATA[<p>With decreasing reimbursements for surgery and increased office staff and capital expenses, clinicians are increasingly looking at the revenues generated by pathology to make ends meet. Reselling pathology services is easy, since it requires no work from the urologist other than adding additional CPT codes when billing the payor, but it is legal in only some states and does not allow the collection of specimens from Medicare patients.<br />
The TC/PC (Technical Component/ Professional Component) allows the clinician (usually urologist or gasteroenterologist) to collect from all payors. In this model, the clinician hires a pathologist as a part-time employee to come to his office and read the biopsies (as well as cytology and FISH cases). The clinician uses the -26 professional component modifier to bill for the pathologist’s services. Medicare pays an average of $36 for each 88305-26 and $41 for each 88342-26 so a twelve specimen biopsy case (as is the norm with prostate biopsies) with a triple stain generates $555 in professional fees. If the pathologist is paid $500/hr and reads four such cases in that time he pockets the $500 while generating $2220 minus $500 or $1720 for the urologist. Meanwhile the laboratory generates $3200 in 88305-TC and $660 in 88342-TC for a total of $3860. Both clinician and pathologist benefit.<br />
But why should the lab make $3860 and the clinician only half as much? This can be remedied by bringing the technical component in-house as some of the larger clinical group have done and many more are planning. Is it possible that the more one profits by doing an activity the more such activity is undertaken?  By comparing the amount of billable biopsy specimens obtained by those clinicians who do not profit from pathology with the amount of billable biopsy specimens obtained by those clinicians who do profit, it has been my experience that this is certainly the case. One can even compare the amount of specimens submitted by the same clinician both before and after they started to profit from such activity.<br />
Each laboratory needs to foster a relationship with the clinician who supplies specimens. The desire for a lasting relationship encourages competing laboratories to kick-back as much of their excess profits as necessary to form and retain this relationship. Supplying attractive sales reps (who routinely make over $150K, and often over $250K/yr)  with company credit cards for expensive meals and fishing/golfing outings  ease the relationship as do charitable donations, reimbursements for expensive computer systems, payments to office staff, in-office placement of nurses and phlebotomists, free office and medical supplies, continuing education credits, free management and recruiting services, etc. The cost of these perks is considerable and can only be generated by performing unnecessary medical tests (excessive IHC stains including triple prostate stains on multiple cores, Giemsa staining of urine cytology, routine FISH Urovysion testing and addition to urine cytology, etc.</p>
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