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ehr onc final certification - Department of Health Care Services

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ability <strong>of</strong> CCD and CCR to support the inclusion <strong>of</strong> the discharge summary and the<br />

principle expressed by CMS that we specify a minimum set <strong>of</strong> information in the adopted<br />

<strong>certification</strong> criterion, we believe that in this instance it is appropriate to exclude<br />

discharge summary from the <strong>certification</strong> criterion.<br />

§170.306(g) - Reportable lab results<br />

Meaningful Use<br />

Stage 1<br />

Objective<br />

Capability to<br />

submit electronic<br />

data on reportable<br />

(as required by<br />

state or local law)<br />

lab results to public<br />

health agencies and<br />

actual submission<br />

in accordance with<br />

applicable law and<br />

practice<br />

Meaningful Use Stage 1<br />

Measure<br />

Performed at least one test <strong>of</strong><br />

certified EHR technology’s<br />

capacity to provide electronic<br />

submission <strong>of</strong> reportable lab<br />

results to public health agencies<br />

and follow-up submission if the<br />

test is successful (unless none <strong>of</strong><br />

the public health agencies to<br />

which eligible hospital or CAH<br />

submits such information have<br />

the capacity to receive the<br />

information electronically)<br />

Page 173 <strong>of</strong> 228<br />

Certification Criterion<br />

Interim Final Rule Text:<br />

Electronically record, retrieve, and transmit<br />

reportable clinical lab results to public health<br />

agencies in accordance with the standard<br />

specified in §170.205(f)(1) and, at a minimum,<br />

the version <strong>of</strong> the standard specified in<br />

§170.205(f)(2).<br />

Final Rule Text:<br />

§170.306(g)<br />

Reportable lab results. Electronically record,<br />

modify, retrieve, and submit reportable clinical<br />

lab results in accordance with the standard (and<br />

applicable implementation specifications)<br />

specified in §170.205(c) and, at a minimum, the<br />

version <strong>of</strong> the standard specified in<br />

§170.207(c).<br />

Comment. One commenter requested that we clarify the meaning <strong>of</strong> “LOINC<br />

when LOINC codes have been received from a laboratory.” The commenter questioned<br />

whether the information exchange for which this criterion would apply is solely exchange<br />

within an organization or only between organizations.<br />

Response. For a more detailed response to this request for clarification, we refer<br />

to the relevant comments and responses relating to the “incorporate laboratory test<br />

results” <strong>certification</strong> criterion, where we discuss this issue at length.<br />

Comment. One commenter stated that it believed the standards we have adopted<br />

are too general or at too high a level for vendors to be able to implement them uniformly.<br />

This commenter suggested that we clarify when lab results should be transmitted, for

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