Difference between revisions of "Clinical summaries (MU2))"
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==Links== | ==Links== | ||
:*[[OpenEMR Certification Stage II Meaningful Use|OpenEMR Certification Stage II Meaningful Use Main Project Page]] | |||
:*[[Patient Clinical Summaries|Patient Clinical Summaries wiki page for stage I certification]] | |||
[[Category:Certification]][[Category:Certification Stage II]] | [[Category:Certification]][[Category:Certification Stage II]] |
Revision as of 09:03, 10 September 2012
Overview
MU Requirements
Per ONC
- Taken from ONC Final Rule
(2) Ambulatory setting only – clinical summary. (i) Create. Enable a user to create a clinical summary for a patient in human readable format and formatted according to the standards adopted at § 170.205(a)(3). (ii) Customization. Enable a user to customize the data included in the clinical summary. (iii) Minimum data from which to select. EHR technology must permit a user to select, at a minimum, the following data when creating a clinical summary: (A) Common MU Data Set (which, for the human readable version, should be in their English representation if they associate with a vocabulary/code set) (B) The provider’s name and office contact information; date and location of visit; reason for visit; immunizations and/or medications administered during the visit; diagnostic tests pending; clinical instructions; future appointments; referrals to other providers; future scheduled tests; and recommended patient decision aids.