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Laboratory Compliance Insider
 
Each month with Laboratory Compliance Insider you get more of our exclusive working tools: model guidelines, policies, forms, etc., that you can use to comply with OIG and CMS, reduce claim denials, and get paid in full and on time.

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February 2008   (Volume 5, Issue 2) view entire issue
 
Avoid accreditation risks, pay attention to equipment care
Laboratories should not only regularly check and maintain equipment and instruments, they need to document their efforts, too. CLIA requires laboratories to perform regular equipment maintenance and function checks and correct problems that arise. CAP and The Joint Commission (formerly JCAHO) also look for compliance with this requirement during accreditation surveys and inspections. If something falls through the cracks with your instrument/equipment maintenance, function checks, corrective action, or documentation, expect to be cited during an on-site accreditation inspection, says Deborah A. Miller-Jones, MPH, MT(ASCP), senior technical specialist of the Laboratory Accreditation Program at CAP in Northfield, IL.
 
Avoid scrutiny for ESRD claims
An OIG audit recently resulted in a hospital repaying more than $60,000 for laboratory services to end-stage renal disease (ESRD) patients the OIG claimed were improperly billed. Avoid a similar fate by implementing the tips our experts recommend. The hospital's billing errors The OIG said the audited hospital committed the following three errors when billing for laboratory services to ESRD patients
 

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