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#06-5558 Accrd Manual V7 - COLA

#06-5558 Accrd Manual V7 - COLA

#06-5558 Accrd Manual V7 - COLA

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CYTOLOGY795. EAre unsatisfactory specimens or slide preparations identified and reported as unsatisfactory?The laboratory must establish and follow criteria for defining specimen adequacy, to include required cellularity,obscuring blood or inflammation, and sampling of the transformation zone (lack of an endocervicalcomponent). See questions 727-729 also.796. EDo the reports contain a narrative description of the nomenclature for all results?Cytology reports should use the terminology of a recognized system of disease nomenclature as establishedby international medical societies and organizations and published in medical journals and medical textbooks.797. EDoes the laboratory notify the patient’s physician and issue amended reports, indicating the basis for the correction,if significant discrepancies are identified upon review of previously reported examinations?The laboratory should have a policy regarding when amended reports are required and a mechanism to documentdiscrepant findings when identified. The survey will assess the laboratory’ adherence to stated policybased on review of discrepancy files.The laboratory shall establish the format of reports.798. EDoes the cytology laboratory meet the general examination report requirements for <strong>COLA</strong> accreditation?The laboratory shall be in compliance with all criteria in this subsection, as well as general <strong>COLA</strong> criteria forLaboratory Reports (PST 3 – PST 16).In addition to the general requirements for the examination report, does the cytology report include at leastthe following required information:799. EAge or birth date?800. EAccession number?801. EName and signature of reporting cytotechnologist, general supervisor, technical supervisor or pathologist?802. EA narrative explanation of the morphologic findings?803. EComments and recommendations as appropriate?804. EIf a computer report is generated with an electronic signature, is the signature authorized by the individual whoperformed the examination and made the diagnosis?If a computer report is generated, the electronic signature must be authorized by the technical supervisorwho performed the review.92. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .FOR MORE INFORMATION CONTACT <strong>COLA</strong> PHONE 800.981.9883 | FAX 410.381.8611 | ON-LINE www.cola.org

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