Difference between revisions of "Meaningful Use (WG6)"
From VistApedia
(→'''Discussion of How VistA Meets or Can Meet Meaningful Use 45 CFR Part 170''') |
(→'''Discussion of How VistA Meets or Can Meet Meaningful Use 45 CFR Part 170''') |
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− | + | '''Discussion of How VistA Meets, or Can Meet, <BR>Meaningful Use, Stage 1<BR> ''45 CFR Part 170''''' | |
− | + | [http://edocket.access.gpo.gov/2010/pdf/E9-31216.pdf Official document published in the Federal Register] | |
− | http://edocket.access.gpo.gov/2010/pdf/E9-31216.pdf | + | |
+ | [http://www.cms.hhs.gov/Recovery/11_HealthIT.asp CMS Topical Web Site] | ||
− | == | + | =Background discussion= |
+ | * The texts discusses EHR's as being '''Certified'''. It is not yet clear how this certification status will be awarded. | ||
+ | * The criteria herein are just for Stage 1. Further criteria are likely to be unveiled as the program progresses. | ||
− | + | =All-in-one vs. Composite systems= | |
+ | |||
+ | =Possible $ Bonus amounts= | ||
+ | |||
+ | |||
+ | =Listing of Criteria for Stage 1 of Meaningful Use= | ||
+ | |||
+ | ==Use Computerised Provider Order Entry (CPOE)== | ||
+ | Enable a user to electronically record, store, retrieve and manage, at a minimum, the following order types: | ||
*# Medications | *# Medications | ||
*# Laboratory | *# Laboratory | ||
*# Radiology/Imaging | *# Radiology/Imaging | ||
*# Provider referrals | *# Provider referrals | ||
+ | |||
+ | ==Implement drug-drug, drug-allergy, drug-formulary checks== | ||
+ | ; VistA | ||
+ | : | ||
+ | ==Maintain an up-to-date problem list of current and active diagnoses based on ICD-9-CM or SNOWMED CT== | ||
+ | ; VistA | ||
+ | : | ||
+ | ==Generage and transmit permissible prescriptions electronically (eRx)== | ||
+ | |||
+ | ==Maintain active medication list== | ||
+ | |||
+ | ==Maintain active medication allergy list== | ||
+ | |||
+ | ==Record demographics== | ||
+ | |||
+ | ==Record and chart changes in vital signs== | ||
+ | |||
+ | ==Record smoking status for patients 13 yrs old or older== | ||
+ | |||
+ | ==Incomporate clinical lab-test results into EHR as structured data== | ||
+ | |||
+ | ==Generate lists of patients by specific conditions to use for quality improvement, reduction of disparities and outreach== | ||
+ | |||
+ | ==Report quality measures to CMS or the States== | ||
+ | |||
+ | ==Send reminders to patients per patient preference for preventative/followup care== | ||
+ | |||
+ | ==Implement 5 clinical decision support rules== | ||
+ | |||
+ | ==Check insurance eligibility electronically frompublic and private payers== | ||
+ | |||
+ | ==Submit claims electronically to public and private payers== | ||
+ | |||
+ | ==Provide patients with an electronic copy of their health information upon request== | ||
+ | |||
+ | ==Provide patients with an electronic copy of their discharge instructions and procedures at time of discharge, upon request== | ||
+ | |||
+ | ==Provide patients with timely electronic access to their health information (including lab results, problem lists, medication lists, allergies) within 96 hours of the information being available to the eligible professional== | ||
+ | |||
+ | ==Provide clinical summaries for patients for each office visit== | ||
+ | |||
+ | ==Capability to exchange key clinical information among providers of care and patient authorized entities electronically.== | ||
+ | |||
+ | ==Provide summary care records for each transition of care and referral== | ||
+ | |||
+ | ==Perform medication reconciliation at relevant encounters and each transition of care== | ||
+ | |||
+ | ==Capability to submit electronic data to immunization registries and actual submission where required and accepted.== | ||
+ | |||
+ | ==Capability to provide electronic submission of reportable lab results (as required by state or local law) to public health agencies and actual submission where is can be received== | ||
+ | |||
+ | ==Capability to provide electronic syndromic surveillance data to public health agencies and actual transmission according to applicable law and practice== | ||
+ | |||
+ | ==Protect electronic health information created or maintained by the certified EHR technology through the implementation of appropriate technical capabilities.== |
Revision as of 18:56, 27 January 2010
Discussion of How VistA Meets, or Can Meet,
Meaningful Use, Stage 1
45 CFR Part 170
Official document published in the Federal Register
Contents
- 1 Background discussion
- 2 All-in-one vs. Composite systems
- 3 Possible $ Bonus amounts
- 4 Listing of Criteria for Stage 1 of Meaningful Use
- 4.1 Use Computerised Provider Order Entry (CPOE)
- 4.2 Implement drug-drug, drug-allergy, drug-formulary checks
- 4.3 Maintain an up-to-date problem list of current and active diagnoses based on ICD-9-CM or SNOWMED CT
- 4.4 Generage and transmit permissible prescriptions electronically (eRx)
- 4.5 Maintain active medication list
- 4.6 Maintain active medication allergy list
- 4.7 Record demographics
- 4.8 Record and chart changes in vital signs
- 4.9 Record smoking status for patients 13 yrs old or older
- 4.10 Incomporate clinical lab-test results into EHR as structured data
- 4.11 Generate lists of patients by specific conditions to use for quality improvement, reduction of disparities and outreach
- 4.12 Report quality measures to CMS or the States
- 4.13 Send reminders to patients per patient preference for preventative/followup care
- 4.14 Implement 5 clinical decision support rules
- 4.15 Check insurance eligibility electronically frompublic and private payers
- 4.16 Submit claims electronically to public and private payers
- 4.17 Provide patients with an electronic copy of their health information upon request
- 4.18 Provide patients with an electronic copy of their discharge instructions and procedures at time of discharge, upon request
- 4.19 Provide patients with timely electronic access to their health information (including lab results, problem lists, medication lists, allergies) within 96 hours of the information being available to the eligible professional
- 4.20 Provide clinical summaries for patients for each office visit
- 4.21 Capability to exchange key clinical information among providers of care and patient authorized entities electronically.
- 4.22 Provide summary care records for each transition of care and referral
- 4.23 Perform medication reconciliation at relevant encounters and each transition of care
- 4.24 Capability to submit electronic data to immunization registries and actual submission where required and accepted.
- 4.25 Capability to provide electronic submission of reportable lab results (as required by state or local law) to public health agencies and actual submission where is can be received
- 4.26 Capability to provide electronic syndromic surveillance data to public health agencies and actual transmission according to applicable law and practice
- 4.27 Protect electronic health information created or maintained by the certified EHR technology through the implementation of appropriate technical capabilities.
Background discussion
- The texts discusses EHR's as being Certified. It is not yet clear how this certification status will be awarded.
- The criteria herein are just for Stage 1. Further criteria are likely to be unveiled as the program progresses.
All-in-one vs. Composite systems
Possible $ Bonus amounts
Listing of Criteria for Stage 1 of Meaningful Use
Use Computerised Provider Order Entry (CPOE)
Enable a user to electronically record, store, retrieve and manage, at a minimum, the following order types:
- Medications
- Laboratory
- Radiology/Imaging
- Provider referrals
Implement drug-drug, drug-allergy, drug-formulary checks
- VistA
Maintain an up-to-date problem list of current and active diagnoses based on ICD-9-CM or SNOWMED CT
- VistA