IMS Meaningful Use Webinar
Presented on: May 9 – 11:00am – 12:00pm (PDT) May 13 – 12:00pm – 1:00pm (EST)
This Webinar Will Be Recorded!
Please send questions that you may have after the session to: info@suitemed.com
IMS Meaningful Use Webinar Presented on: May 9 11:00am 12:00pm - - PowerPoint PPT Presentation
IMS Meaningful Use Webinar Presented on: May 9 11:00am 12:00pm (PDT) May 13 12:00pm 1:00pm (EST) This Webinar Will Be Recorded! Please send questions that you may have after the session to: info@suitemed.com Meaningful Use:
This Webinar Will Be Recorded!
Please send questions that you may have after the session to: info@suitemed.com
– Use in a meaningful manner (ex: e-prescribing) – Use for electronic exchange of health information to improve quality of health care – Use to submit clinical quality and other measures
– Stage 1 sets the baseline for electronic data capture and information sharing (2011 and 2012). – Stage 2 (2013) and Stage 3 (2014-15) will continue to expand on this baseline and be developed through future rule making.
(EP), eligible hospitals, and critical access hospitals (CAH) that demonstrate meaningful use (MU) of certified EHR technology.
– Participation can begin as early as 2011 – EP can receive up to $44k over 5 years; additional incentives for Health Professional Shortage Areas – Maximize benefits; begin in 2011 – After 2015, adjusted reimbursements if not successfully demonstrating MU
and CAHs as they adopt, implement, upgrade, or demonstrate MU of certified EHR technology in their first year of participation and demonstrate MU for up to five remaining participation years.
– Voluntarily offered by individual states and territories and may begin as early as 2011, depending on the state. – EP can receive up to $63,750 over the six years that they choose to participate in the program. – There are no payment adjustments under the Medicaid EHR Incentive Program.
installation.)
example, provide staff training or data entry of patient demographic information into EHR.)
certification requirements. (For example, upgrade to certified EHR technology or add new functionality to meet the definition of certified EHR technology.)
Eligibility Requirements for Professionals
eligible professional successfully demonstrates meaningful use of certified EHR technology.
how many practices or locations at which he or she provide services.
more of his or her services are performed in a hospital inpatient (Place Of Service code 21) or emergency room (Place Of Service code 23) setting.
professionals must have Medicare Part B allowed charges and must be enrolled in an “approved status” for Provider Enrollment, Chain and Ownership System (PECOS).
– Doctor of medicine or osteopathy – Doctor of dental surgery or dental medicine – Doctor of podiatry – Doctor of optometry – Chiropractor
incentive payment under the Medicaid EHR Incentive Program, an eligible professional must meet one of the following criteria:
– Have a minimum 30% Medicaid patient volume* – Have a minimum 20% Medicaid patient volume, and is a pediatrician* – Practice predominantly in a Federally Qualified Health Center or Rural Health Center and have a minimum 30% patient volume attributable to needy individuals
– Doctor of medicine or osteopathy – Doctor of dental surgery or dental medicine – Doctor of podiatry – Doctor of optometry – Chiropractor * Children's Health Insurance Program (CHIP) patients do not count toward the Medicaid patient volume criteria.
What if an EP can qualify for Medicare and Medicaid?
must choose which incentive program they wish to participate in when they register. Before 2015, an eligible professional may switch programs only once after the first incentive payment is initiated. Most eligible professionals will maximize their incentive payments by participating in the Medicaid EHR Incentive Program.
– 15 Core Objectives – EP must meet ALL of these to qualify – 10 Menu Objectives – EP must choose 5 from this list to qualify
measures (CQM). EP must report on 6 total clinical quality measures: 3 required core measures (substituting alternate core measures where necessary) and 3 additional measures (selected from a set of 38 clinical quality measures). For more information on CQM, visit: http://www.cms.gov/QualityMeasures/
register at any time
found: http://www.cms.gov/apps/files/statecontacts.pdf
party to register on their behalf*
– If a third party will be registering for one or more EP, they must first create an account at the Identity & Access Management System (I&A) site https://nppes.cms.hhs.gov/NPPES/IASecurityCheck.do
* NOTE: Medicaid third-party registration availability may vary at the state level
Steps to Registration
1. Gather required information ahead of time a) NPI Number b) NPPES Number (also known as PECOS number) c) Payee Tax ID Number (if benefits to be reassigned) d) Payee NPI (if benefits to be reassigned) 2. Decide which program to register for
– Medicare – Review the Medicare EP Registration User Guide – Medicaid – Review the Medicaid EP Registration User Guide
3. Follow the instructions within the appropriate guide above to complete the registration process
be found: http://www.cms.gov/apps/files/statecontacts.pdf
to register on their behalf*
– If a third party will be attesting for one or more EP, they must first create an account at the Identity & Access Management System (I&A) site https://nppes.cms.hhs.gov/NPPES/IASecurityCheck.do
* NOTE: Medicaid third-party attestation may vary at the state level
Medicare – Requirements for Incentive Payment
successfully attest to meeting meaningful use criteria using EHR technology
Medicaid – Requirements for Incentive Payment
specific Attestation System
When to Attest
– In the first year, must have met MU criteria for one consecutive 90-day reporting period – For all subsequent years, attestation must be met for the entire calendar year – IMPORTANT NOTE: If your initial attestation fails in the first year, you may select a different 90-day that may partially overlap a previously reported 90-day period and attest again. (Tip: Plan to attest initially no later than September 15, 2011 to allow 2 weeks to make EHR or clinic process adjustments if needed and still have a full 90-day period for qualification in case overlap is not possible.)
– In the first year, must attest to adopting, implementing or upgrading EHR – Must check at the state level to find out when participation may begin
Steps to Attestation
1. If not yet registered, register for the EHR Incentive Program 2. Thoroughly review the CMS Attestation User Guide
http://www.cms.gov/EHRIncentivePrograms/Downloads/EP_Attestation_User_Guide.pdf
3. Verify that all of the necessary measures to demonstrate MU and qualify for an EHR incentive payment have been met with the CMS MU Attestation Calculator http://www.cms.gov/apps/ehr/ 4. Following CMS Attestation User Guide instructions, EP or designated third-party representative shall complete attestation
General Notes
might not appear in the same order as shown in the IMS Meaningful Use Report. Be mindful of this!!
does not have to be completed in one sitting. Your work will save as you go and you can return to finish later
meets requirements and successfully attests
upgrading EHR technology in their first year
http://www.cms.gov/EHRIncentivePrograms/Downloads/EP-MU-TOC.pdf
CR01: Computerized Provider Order Entry for Medication
medication orders directly entered by any licensed healthcare professional who can enter orders into the medical record per state, local and professional guidelines.
medication in their medication list seen by the EP have at least one medication order entered using CPOE.
the EHR reporting period.
(NOTE: Electronic prescription transmission IS NOT required for this.)
CR01: Computerized Provider Order Entry for Medication
– Current Medications within the Visit Note must include at least one medication – Patient must have been prescribed a medication from within IMS during the reporting period. Chart history should show that a prescription was given to the patient on the specific date. (NOTE: Prescription does not have to be sent electronically to meet this requirement)
CR02: Drug Interaction Checks
reporting period.
CR02: Drug Interaction Checks
– User Parameters for Prescription set to “Yes” for:
– Cross Sensitive Allergy Check – Inactive ingredient based Allergy Check
– Medium Severity Interaction Check – Low Severity Interaction Check
checked)
CR02: Drug Interaction Checks
CR03 – Transmit Permissible Prescriptions Electronically
electronically.
written by the EP are transmitted electronically using certified EHR technology
the EHR reporting period.
NOTE: Please review the “Permissible Prescriptions” and “Additional Information” sections in the following CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/4PermissiblePrescriptions.pdf
CR03 – Transmit Permissible Prescriptions Electronically
– Prescriptions should be sent by the EP to pharmacy electronically when
prescriptions through either New Crop or Surescripts. Objective is achieved when the Rx ID is assigned during the transmission process.
CR04 – Record Demographics
language*; Gender; Race; Ethnicity; Date of birth
have demographics recorded as structured data.
* Preferred language is the language by which the patient prefers to
communicate
CR04 – Record Demographics
– Patient demographics are created for every patient in IMS. Date of Birth (DOB) and Gender are required fields. EP should verify that Race, Ethnicity, and Language have been captured or documented as “Patient declined”.
CR05 - Maintain Problem List
diagnoses.
have at least one entry or an indication that no problems are known for the patient recorded as structured data.
NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/3MaintainProblemList.pdf
CR05 - Maintain Problem List
– Patient Diagnosis must either:
within the “Active Diagnosis” tab in the Diagnosis Visit Note Template and also within Chart View on the Dx tab. Or
the “Mark as No Known Problem” button if the patient does not have any current problems.
CR06 - Active Medication List
have at least one entry (or an indication that the patient is not currently prescribed any medication) recorded as structured data.
CR06 – Active Medication List
– Current Medications within the Visit Note should include the following:
Or
medication.”
CR07 - Medication Allergy List
have at least one entry (or an indication that the patient has no known medication allergies) recorded as structured data.
CR07 - Medication Allergy List
– Drug Allergy within the Visit Note should include the following:
Or
Allergies”
CR08 - Record Vital Signs
Height; Weight; Blood pressure; Calculate and display body mass index (BMI); Plot and display growth charts for children 2-20 years, including BMI
as structured data.
who believes that all three vital signs of height, weight, and blood pressure of their patients have no relevance to their scope of practice.
CR08 - Record Vital Signs
– Vital Signs must be completed for a minimum of Height, Weight and Blood Pressure. If any one or more of the elements are missing, the requirement will not be met.
CR09 – Record Smoking Status
CR09 – Record Smoking Status
– Within the Meaningful Use Report window, ensure that the EP has defined the appropriate Social History value to be recorded as capturing this data. – For all patients over 13 years of age, Social History within the Visit Note should include the following:
Parameter Or
Parameter
CR10 - Clinical Decision Support Rule
specialty or high clinical priority along with the ability to track compliance with that rule.
NOTE: Please review the “Additional Information” section in the following related CMS Guide: http://www.cms.gov/EHRIncentivePrograms/Downloads/11ClinicalDecisionSupportRule.pdf
CR10 – Clinical Decision Support Rule
– Within IMS, there are a number of features available that qualify as clinical decision support rules. Essentially, this means that based on findings during a patient visit, IMS will offer diagnostic or treatment
reference information and other tools to support decisions within clinical workflow.
guidelines or protocols into IMS workflow would also qualify.
CR11 - Clinical Quality Measures (CQMs)
measures selected by CMS in the manner specified by CMS.
NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/10ClinicalQualityMeasures-CQMs.pdf
CR11 - Clinical Quality Measures (CQMs)
– IMS provides a PQRI/NQF reporting tool for tracking of quality
relevant to their specialty for reporting.
PQRI was presented during our March Webinar series. If you were not able to attend, you may view the recorded session by clicking the link
to the recording will appear:
Lunch & Learn Webinar: IMS v14 - PQRI - Physician Quality Reporting Initiative
CR12 - Electronic Copy of Health Information
information (including diagnostic test results, problem list, medication lists, medication allergies) upon request.
electronic copy of patient health information during the EHR reporting period. NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/12ElectronicCopyofHealthInformation.pdf
CR12 - Electronic Copy of Health Information
– EP shall create a Reminder Category specific to this purpose. Reminder Category shall contain all Reminder Tasks that inform staff that patient requires a copy of their health information in electronic format (CD, USB drive, portal, etc). (NOTE:
information request related reminders are stored within this category.) – EP shall create and configure one or more health information request Reminder Tasks assigned to the above category for use specific to these tasks – EP will associate the Reminder Category created to the “Reminder Category for CR12” field within the MU Report “Set Parameter” window – As Patient Reminders are “Set Done”
CR13 - Clinical Summaries
visit.
percent of all office visits within 3 business days.
reporting period.
NOTE: Please review the “Definition of Terms” and “Additional Information” sections in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/13ClinicalSummaries.pdf
CR13 - Clinical Summaries
– EP shall create a Document Sub-Category that will contain all clinical summary letter options. Document Sub-Category can be named “CR13 Clinical Summaries” within IMS for ease of identification. (NOTE: For Meaningful Use, only one sub- category will be reported on, so it is important that ONLY clinical summary letters are stored within this sub-category. It is equally important that ALL are stored within this sub-category. Letters not assigned to this sub-category will not be factored into the objective requirements.) – Within the Meaningful Use Report window, EP will associate the Document Sub- Category as the “Letter Category for CR13” – As EP or clinic staff create and “Save” the Clinical Summary Letter, the Objective will be achieved
CR14 - Electronic Exchange of Clinical Information
example, problem list, medication list, medication allergies, and diagnostic test results), among providers of care and patient authorized entities electronically.
capacity to electronically exchange key clinical information.
NOTE: Please review the “Definition of Terms” and “Additional Information” sections in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/14ElectronicExchangeofClinicalInformation.pdf
CR14 - Electronic Exchange of Clinical Information
– IMS provides functionality for the Import and Export of Continuity of Care Documents (CCD). The Export (CCD) utility provides options for exporting Payer, Diagnosis, Allergy, Vitals, Medication/Rx, Lab Results, Immunization, Procedures, Family History, and Social History information. The file is created in XML format to share with other authorized entities. The Import (CCR) utility allows the EP to import patient information from XML files and then assign to the appropriate patient for view as a Document.
CR15 - Protect Electronic Health Information
by the certified EHR technology through the implementation of appropriate technical capabilities.
the requirements under 45 CFR 164.308(a)(1) and implement security updates as necessary and correct identified security deficiencies as part
NOTE: Please review the “Definition of Terms” and “Additional Information” sections in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/15ProtectElectronicHealthInformation.pdf
CR15 - Protect Electronic Health Information
– Security - Manages access to patient data at a User and Group level. Provides user level access via Username/Password with additional parameters to enforce: 1) minimum characters for password, 2) case sensitivity, 3) enforced alpha-numeric passwords, 4) lockouts after number of failed login attempts, 5) password resets every set number of days and 6) historically unique
– Lock Session – protects data when a user must step away from the workstation – Audit Log - allows the EP to determine when specific patient related data elements were accessed or modified within the database and by which specific user.
– The security within the EHR depends a great deal on the security practices within the clinic
EP requirements outside of the EHR such as defining security management processes, assigning a security official, limiting personnel and information access, providing security awareness training, handling security incidents, establishing contingency plans, and periodically evaluating security policies and procedures.
MN01 - Drug Formulary Checks
least one internal or external formulary for the entire EHR reporting period.
EHR reporting period.
Additional Information
may be an internally developed formulary or an external formulary. The formularies should be relevant for patient care during the prescribing process.
MN01 - Drug Formulary Checks
– Formularies should be setup at the Carrier and/or Plan level in IMS – When prescribing, EP should take action based on formulary specific action specified
MN02 - Clinical Lab Test Results
data.
the EP during the EHR reporting period whose results are either in a positive/negative or numerical format are incorporated in certified EHR technology as structured data.
positive/negative or numeric format during the EHR reporting period.
NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/2ClinicalLabTestResults.pdf
MN02 - Clinical Lab Test Results
– Although incorporation of an HL7 interface with compatible lab companies will help to ensure the successful input of the required Lab Result data, it is not required. Essentially, the EP should ensure that any Labs defined within IMS have results entered as structured data. Linking a faxed results page to a Lab Order will not qualify for this requirement. The EP or a staff member must associate the returned results to the order by entering the values manually.
MN03 - Patient Lists
quality improvement, reduction of disparities, research, or outreach.
specific condition.
MN03 - Patient Lists
– Patient Special Search - Within IMS, the Patient Special Search feature allows real-time generation of patient lists by specific conditions. The Patient Special Search is found within the Utilities menu. – EMR Reports - IMS also provides specific EMR reports that will also generate the conditions requested
MN04 -Patient Reminders
preventive/follow-up care.
years old or younger were sent an appropriate reminder during the EHR reporting period.
technology.
NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/4PatientReminders.pdf
MN04 -Patient Reminders
– EP shall create a Document Sub-Category specific to this purpose that will contain all Patient Reminder letters that apply to the preventative/follow-up needs associated with patients 5 and under or 65 and older. Document Sub-Category can be aptly named “MN04 Patient Preventative Reminder Letters” within IMS for ease of
stored within this sub-category. It is equally important that ALL relevant letters are stored within this sub-category. If the letters are not assigned to this sub-category, they will not be factored into the objective requirements.) – Within the Meaningful Use Report window, EP will associate the Document Sub- Category as the “Letter Category for MN04” – As EP or clinic staff create and “Save” the Patient Reminder Letter, the Objective will be achieved
MN05 - Patient Electronic Access
(including lab results, problem list, medication lists, and allergies) within 4 business days
(available to the patient within four business days of being updated in the certified EHR technology) electronic access to their health information subject to the EP’s discretion to withhold certain information.
contained in the problem list, medication list, medication allergy list (or other information as listed at 45 CFR 170.304(g)) during the EHR reporting period. NOTE: Please review the “Additional Information” section in the following related CMS Guide: http://www.cms.gov/EHRIncentivePrograms/Downloads/5PatientElectronicAccess.pdf
MN05 - Patient Electronic Access
– IMS Patient Portal is designed to meet these requirements. If the EP is not using Patient Portal, this Menu Requirement is not an available option.
MN06 - Patient-specific Education Resources
education resources and provide those resources to the patient if appropriate.
are provided patient-specific education resources.
MN06 - Patient-specific Education Resources
– EP’s who are using the Micromedix companion in conjunction with IMS “Link with” functionality will meet this requirement. With “Link with” technology, care plan information is presented when relevant diagnosis, lab, prescription, examination findings or procedures are encountered during a patient visit. – EP may also use “Educational Handouts” direct to achieve same goal from within Visit Note.
MN07 - Medication Reconciliation
medication reconciliation.
percent of transitions of care in which the patient is transitioned into the care of the EP.
during the EHR reporting period.
MN07 - Medication Reconciliation
– To comply with the Medication Reconciliation requirements, EP must ensure that the referring provider is recorded within the Case associated with the transitioning
recorded within IMS. Although not specifically stated that current medications must be recorded on the first visit, it is highly recommended that the EP do this to ensure the information is in the chart and so that compliance is achieved.
MN08 - Transition of Care Summary
care or provider of care or refers their patient to another provider of care should provide summary care record for each transition of care or referral.
setting of care or provider of care provides a summary of care record for more than 50 percent of transitions of care and referrals.
refers a patient to another provider during the EHR reporting period.
MN08 - Transition of Care Summary
– IMS provides a Referral Tracking utility for this purpose. Within the Referral Tracking utility, the printing or faxing of a letter or form signifies that a Transition
MN09 - Immunization Registries Data Submission
immunization information systems and actual submission according to applicable law and practice.
electronic data to immunization registries and follow up submission if the test is successful (unless none of the immunization registries to which the EP submits such information has the capacity to receive the information electronically).
electronically NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/9ImmunizationRegistriesDataSubmission.pdf
MN09 - Immunization Registries Data Submission
– This menu option is currently not available in all areas. A status of Registries associated with IMS follows:
NYSIIS (New York), and CAIR (California).
(Pennsylvania), AZ-SIIS (Arizona) and Texas.
MN10 - Syndromic Surveillance Data Submission
agencies and actual submission according to applicable law and practice.
electronic syndromic surveillance data to public health agencies and follow-up submission if the test is successful (unless none of the public health agencies to which an EP submits such information can receive information electronically).
patients during the EHR reporting period or does not submit such information to any public health agency that has the capacity to receive the information electronically.
NOTE: Please review the “Additional Information” section in the following related CMS Guide:
http://www.cms.gov/EHRIncentivePrograms/Downloads/10SyndromicSurveillanceDataSubmission.pdf
MN10 - Syndromic Surveillance Data Submission
– Syndromic Surveillance Data Submission is not currently an IMS option available to EP’s.
CMS References and Source of Non-IMS Webinar Material
http://www.cms.gov/EHRIncentivePrograms/20_RegistrationandAttestation.asp#TopOfPage
http://www.cms.gov/EHRIncentivePrograms/30_Meaningful_Use.asp#TopOfPage
http://www.cms.gov/EHRIncentivePrograms/35_Basics.asp#TopOfPage
http://www.cms.gov/EHRIncentivePrograms/40_MedicaidStateInfo.asp#TopOfPage
CMS Meaningful Use Documentation
http://www.cms.gov/EHRIncentivePrograms/Downloads/EHRMedicareEP_RegistrationUserGuide. pdf
http://www.cms.gov/EHRIncentivePrograms/Downloads/EHRMedicaidEP_RegistrationUserGuide. pdf