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New Mexico Human Services Department Medical Assistance Division Valorie A. Vigil, Staff Manager Idalia Lechuga-Tena, Communications Manager Systems Bureau NM Medicaid EHR Incentive Program Program Year 2014 Stage 2 Meaningful Use for EPs

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New Mexico Human Services Department

Medical Assistance Division

Valorie A. Vigil, Staff Manager

Idalia Lechuga-Tena, Communications Manager

Systems Bureau

NM Medicaid EHR Incentive Program

Program Year 2014

Stage 2 Meaningful Use for EPs

This Webinar will cover the Stage 2 Objectives and Measures

We will walk through the Objectives and Measures as they

will appear in the NM State Level Registry

Only providers who have attested to two years of Stage 1 MU

are eligible to attest to Stage 2 MU

Under the CMS 2014 CEHRT Flexibility Rule, providers will

only be able to attest to AIU if they have fully implemented

2014 Edition CEHRT

2

Before attesting in the NM State Level Registry, providers are

strongly encouraged to attend the webinar: Program Year

2014— CMS 2014 CEHRT Flexibility Rule & NM State Level

Registry Changes

Or view the webinar slides on the State EHR Website under

the General Information tab:

http://www.hsd.state.nm.us/providers/general-

information.aspx

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NEW EHR FINAL RULE

It is critical that providers know the CEHRT Edition,

Vendor Name and Product Version they are using

for the 90-day EHR Reporting Period

Work with your Vendor and IT Staff to determine the

above

Go to the ONC website to get correct EHR CEHRT

number:

http://oncchpl.force.com/ehrcert/CHPLHome

2014 CEHRT FLEXIBILITY = NM SLR CHANGES

Log into PY 2014 Attestation in the NM SLR

Type in ONC CEHRT Number

Provider will get a Set of Attestation Options based

on the CERHT Edition associated with the number

• Choose from MU Options Available

Only 2014 CEHRT Edition will have the Option for AIU

or Stage 2 MU

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2014 CEHRT FLEXIBILITY = NM SLR CHANGES

The NM SLR will Determine the Set of Measures

Based on the Following:

◦ 2014 CEHRT No.—Characters 3-5 are 14E

◦ Combo 2011/2014 CEHRT No.—Characters 3-5 are H13

◦ 2011 CEHRT No.—If Characters 3-5 are any Combination other

than 14E or H13

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The CEHRT number you have entered results in an option for

MU Stage 2 Objectives and Measures

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*Only

providers

that could

not fully

implement

2014

Edition

CEHRT for

the EHR

reporting

period in

2014 due to

delays in

2014

Edition

CEHRT

availability

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NM State Level Registry—Screen when you login

If Invalid CEHRT ID is entered, the SLR will display the following error

message:

• You have entered a number that does not match the EHR Certification ID

format from the ONC CHPL. Please check the number to ensure it is

correct.

• No attestation record is created and the provider may not continue until a

valid number has been entered.

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NM State Level Registry—Screen when you login

Entering a 2014 CEHRT Edition Number allows 3 options;

• When Option 2 (second box) is selected, the SLR will create a set of

Stage 1 or Stage 2 objectives, measures and CQMs based on the

provider’s prior attestations.

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NM State Level Registry—Screen when you login Once an option is

selected, a

confirmation screen

will display the

CEHRT Edition, MU

Stage and Year (MU

criteria) chosen.

When continue is

clicked, the set of

measures is locked

in and cannot be

changed without

deleting the

attestation and

starting over.

Patient Volume Requirements

Step 2 in the State Level Registry

EPs need a minimum 30%

Medicaid PV for all patient

encounters over a continuous 90-

day Representative Period.

EPs may choose a 90-day

Representative Period from either:

the prior calendar year, OR

the preceding 12 months from date

of attestation

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ONC CEHRT Number After login to PY 2014 Attestation

Step 3 in the SLR

Must have ONC CEHRT # each

Payment Year

First Payment Year: Attach

documentation—a vendor contract or

paid invoice on SLR Step 3

Subsequent Payment Years: If ONC

CEHRT # changes from prior year (new

version of EHR), attach vendor

documentation—a vendor contract or

paid invoice on SLR Step 3

PY 2014: Attach screenshot on SLR

Step 3

http://oncchpl.force.com/ehrcert/CHPLHome

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IMPORTANT TO REMEMBER

The same product and version

may be listed under one or more

of the Edition tabs

However, the CEHRT number will

be different under each Edition

as shown on your left

Again, please verify with your

Vendor which CEHRT number

should be used

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All MU data is input at

Step 3. Attestation of

EHR

• EHR Certification No.

• EHR Reporting Period

• MU General

Requirements

• MU – All Core & Menu

Objectives & Measures;

all CQMs

NM State Level Registry Dashboard

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SLR will populate the CEHRT # that was entered at login. Attach

ONC screenshot of CEHRT # and updated vendor documents.

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If the CEHRT # is changed on

Step 3 to a different CEHRT

Edition # that does not match the

CEHRT # entered at the

beginning of the attestation, you

will get an error message as

shown to the right.

NOTE: If the CEHRT Edition #

entered at login is incorrect, the

2014 attestation will have to be

deleted and the provider will

have to start over.

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MU – Two General Requirements

At least 80% of unique patients must have their records

in a certified EHR during the EHR reporting period

Unique Patients = Number of patients seen in the EHR

reporting period. Patients seen more than once count only

once in the denominator.

For EPs who practice at multiple sites, at least 50% of

total patient encounters during the EHR reporting period

must be at location(s) with certified EHR technology

As long as an EP has certified EHR available for 50% or more

of their patient encounters during the EHR reporting period,

the EP only has to include those encounters where certified

EHR is available at the start of the EHR reporting period.

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Option for a different

CQMs EHR

Reporting Period.

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Reporting Requirements

Eligible Professionals

Meaningful Use 20 Objectives

CORE 17 Objectives

MENU 3 of 6

Objectives

Clinical Quality

Measures 9 Objectives

9 CQMs total out of 64

9 adult

9 pediatric

Any 9

2014– Stage 2

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Stage 2 Objectives and Measures

2014 is the first year an EP can attest to Stage 2 MU if the EP

has already attested to two years of Stage 1 MU

Some Objectives have more than one Measure

Stage 2 Measures have higher thresholds than Stage 1

Immunization Measure moves to the Core set

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2014

Stage 2 Core Set

Core Objectives: Must meet measures for all 17 Core Objectives or

meet an exclusion

•13 of the Core Objectives have percentage-based measures that require a

numerator and a denominator

• 4 of the Core Objectives have Y/N responses – did you perform the action

required in the measure?

• 4 of the Core Objectives have multiple measures

•14 of the Core Objectives have exclusion criteria

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2014

Stage 2 Menu Set

Menu Measures: Must meet 3 out of 6 Menu Objectives without an

exclusion, or must attest to all 6 with some exclusions criteria.

•3 of the Menu Objectives have percentage-based measures that require a

numerator and a denominator

•3 of the Menu Objectives have Y/N responses – did you perform the action

required in the measure?

•6 of the Menu Objectives have exclusion criteria

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2014—CQMs

Must report on 9 CQMs instead of 6 and choose from:

• 9 CQMs for adult populations; OR

• 9 CQMs for pediatric populations; OR

• 9 CQMs total from a list of 64

9 CQMs must be from 3 of 6 NQS key health care policy domains

1. Patient and Family Engagement

2. Patient Safety

3. Care Coordination

4. Population/Public Health

5. Efficient Use of Healthcare Resources

6. Clinical Process/Effectiveness

Data must be reported directly from information generated by CEHRT

Measure Types

Percentage-based Measures – Have a

Numerator and Denominator

Yes/No Measures

Some measures have exclusions

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Exclusions

Based on all patients seen during the EHR reporting period – not

just those whose records are maintained in CEHRT

True even if the measure for the objective has the option to choose

only records maintained in the CEHRT

A “Yes” answer to a Core Measure exclusion meets the measure

A “No” answer to an exclusion means the EP has to meet the

required threshold for percentage-based measures or say “Yes” to

taking the required action on a “Yes/No” measure

If no exclusion criteria is offered, the EP must meet the measure

There are no exclusions based on provider type

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Text Boxes in the NM SLR

• Require valid information be input

• Some are free text – must type something in

• Some are dropdown menus

• Some measures have more than one text box

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Selection Pages & Detail Pages in the NM SLR

Each group of measures includes a Selection Page

which provides a place to access or select the

measures.

Each measure within a group also includes a Detail

Page where you input the data.

Use the Save & Continue button on each measure

Detail Page to move into the next measure requiring

input, or to the next Selection Page.

Navigation Menu is on left-hand side of each page.

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Navigation Menu

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The left-hand Navigation Menu will contain

page titles that serve as links associated with

the MU pages. The majority of MU pages are

collected in four or five subgroups.

Clicking the name of a subgroup or clicking the

expand icon ( ) will reveal all the pages in the

subgroup, all of which must be completed by the

user.

Once all the pages in a navigation group have

been completed, and all have passed their

validation criteria, then the subgroup will receive

a completed icon ( ). Clicking the collapse icon

( ) will hide the title of the individual pages in a

subgroup.

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NM Medicaid EHR Incentive Payment Program

Stage 2 MU for EPs—2014

Core Objectives

Skip the Import Screen and Click on

MU Core Objectives

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NM Medicaid EHR Incentive Payment Program S2 MU for EPs—2014 Core Objectives

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NM Medicaid EHR Incentive Payment Program S2 MU for EPs—2014 Core Objectives

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Core Objective 1 – CPOE Definitions

Computerized Provider Order Entry (CPOE) – A provider's use of computer assistance to

directly enter medical orders (for example, medications, consultations with other providers,

laboratory services, imaging studies, and other auxiliary services) from a computer or mobile

device.

Laboratory and radiology orders are included as part of Stage 2 for CPOE:

Laboratory Order – Order for any service provided by a laboratory that could not be provided by

a non-laboratory.

Laboratory – A facility for the biological, microbiological, serological, chemical,

immunohematological, hematological, biophysical, cytological, pathological, or other examination

of from the human body for the purpose of providing information for the diagnosis, prevention, or

treatment of any disease or impairment of, or the assessment of the health of, human beings.

These examinations also include procedures to determine, measure, or otherwise describe the

presence or absence of various substances or organisms in the body. Facilities only collecting or

preparing specimens (or both) or only serving as a mailing service and not performing testing are

not considered laboratories.

Radiology Order – Order for any imaging services that uses electronic product radiation. The

EP can include orders for other types of imaging services that do not rely on electronic product

radiation in this definition as long the policy is consistent across all patient and for the entire EHR

reporting period.

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Core Objective 1 – CPOE Definitions Continued

Electronic Product Radiation – Any ionizing or nonionizing electromagnetic or particulate

radiation, or [a]ny sonic, infrasonic, or ultrasonic wave that is emitted from an electronic product

as the result of the operation of an electronic circuit in such product.

Unique Patient – If a patient is seen by an EP more than once during the EHR reporting period,

then for purposes of measurement that patient is only counted once in the denominator for the

measure.

Objective: Use computerized provider order entry (CPOE) for medication, laboratory and radiology orders

directly entered by any licensed healthcare professional who can enter orders into the medical

record per state, local and professional guidelines.

Measure More than 60 percent of medication, 30 percent of laboratory, and 30 percent of radiology orders

created by the EP during the EHR reporting period are recorded using CPOE.

Exclusion Any EP who writes fewer than 100 medication, radiology, or laboratory orders during the EHR

reporting period.

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Core Objective 1 – CPOE

Additional Information The provider is permitted, but not required, to limit the measure of this objective to those patients whose records are

maintained using certified EHR technology (CEHRT).

The CPOE function must be used to create the first record of the order that becomes part of the patient's medical record

and before any action can be taken on the order to count in the numerator.

However, in some situations it may be impossible or inadvisable to wait to initiate an intervention until a record of the order

has been created. For example, situations where an intervention is identified and immediately initiated by the provider, or

initiated immediately after a verbal order by the ordering provider to a licensed healthcare professional under his/her direct

supervision. Therefore in these situations, so long as the order is entered using CPOE by a licensed healthcare

professional or certified medical assistant to create the first record of that order as it becomes part of the patient’s medical

record, these orders would count in the numerator of the CPOE measure.

Any licensed healthcare professionals and credentialed medical assistants, can enter orders into the medical record for

purposes of including the order in the numerator for the objective of CPOE if they can originate the order per state, local

and professional guidelines. Credentialing for a medical assistant must come from an organization other than the

organization employing the medical assistant.

Electronic transmittal of the medication order is not a requirement for meeting the measure of this objective.

CPOE is the entry of the order into the patient's EHR that uses a specific function of CEHRT. It is not how that order is

filled or otherwise carried out.

In order to meet this objective and measure, an EP must use the capabilities and standards of CEHRT at 45 CFR

170.314(a)(1).

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Core Objective 2 – e-Prescribing (eRx) Definitions:

Permissible Prescriptions – The concept of only permissible prescriptions refers to the current

restrictions established by the Department of Justice on electronic prescribing for controlled substances

in Schedule II-V. (The substances in Schedule II-V can be found at

http://www.deadiversion.usdoj.gov/schedules/orangebook/e_cs_sched.pdf ). Any prescription not subject

to these restrictions would be permissible.

Prescription – The authorization by an EP to a pharmacist to dispense a drug that the pharmacist would

not dispense to the patient without such authorization.

Objective:

Generate and transmit permissible prescriptions electronically (eRx).

Measure:

More than 50 percent of all permissible prescriptions, or all prescriptions, written by the EP are queried

for a drug formulary and transmitted electronically using CEHRT.

Exclusions:

Any EP who:

(1) Writes fewer than 100 permissible prescriptions during the EHR reporting period.

(2) Does not have a pharmacy within their organization and there are no pharmacies that accept

electronic prescriptions within 10 miles of the EP's practice location at the start of his/her EHR

reporting period.

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Core Objective 3 – Record Demographics Definitions:

Preferred Language – The language by which the patient prefers to

communicate.

Unique Patient – If a patient is seen by an EP more than once during the EHR

reporting period, then for purposes of measurement that patient is only counted

once in the denominator for the measure. All the measures relying on the term

‘‘unique patient’’ relate to what is contained in the patient’s medical record. Not

all of this information will need to be updated or even be needed by the

provider at every patient encounter. This is especially true for patients whose

encounter frequency is such that they would see the same provider multiple

times in the same EHR reporting period.

Objective:

Record the following demographics: preferred language, sex, race, ethnicity,

date of birth.

Measure:

More than 80 percent of all unique patients seen by the EP have demographics

recorded as structured data.

Exclusion:

No exclusion.

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Core Objective 3 – Record Demographics

Attestation Requirements:

DENOMINATOR: Number of unique patients seen by the EP during the EHR reporting period.

NUMERATOR: The number of patients in the denominator who have all the elements of demographics (or a

specific notation if the patient declined to provide one or more elements or if recording an element is contrary to

state law) recorded as structured data.

THRESHOLD: The resulting percentage must be more than 80 percent in order for an EP to meet this

measure.

Additional Information

If a patient declines to provide all or part of the demographic information, or if capturing a patient’s ethnicity or

race is prohibited by state law, such a notation entered as structured data would count as an entry for purposes

of meeting the measure. In regards to patients who do not know their ethnicity, EPs should treat these patients

the same way as patients who decline to provide race or ethnicity— identify in the patient record that the patient

declined to provide this information.

EPs are not required to communicate with the patient in his or her preferred language in order to meet the

measure of this objective.

The term “gender” in the Stage 1 objective is replaced with the term “sex” for Stage 2.

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Core Objective 4 – Record Vital Signs

Definitions:

Unique Patient – If a patient is seen by an EP more than once during the EHR

reporting period, then for purposes of measurement that patient is only counted

once in the denominator for the measure. All the measures relying on the term

‘‘unique patient’’ relate to what is contained in the patient’s medical record. Not

all of this information will need to be updated or even be needed by the

provider at every patient encounter. This is especially true for patients whose

encounter frequency is such that they would see the same provider multiple

times in the same EHR reporting period.

Objective:

Record and chart changes in the following vital signs: height/length and weight

(no age limit); blood pressure (ages 3 and over); calculate and display body

mass index (BMI); and plot and display growth charts for patients 0-20 years,

including BMI.

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Core Objective 4 – Record Vital Signs

Measure:

More than 80 percent of all unique patients seen by the EP have blood pressure (for patients age 3

and over only) and/or height and weight (for all ages) recorded as structured data.

Exclusion:

Any EP who:

(1) Sees no patients 3 years or older is excluded from recording blood pressure.

(2) Believes that all 3 vital signs of height/length, weight, and blood pressure have no relevance

to their scope of practice is excluded from recording them.

(3) Believes that height/length and weight are relevant to their scope of practice, but blood

pressure is not, is excluded from recording blood pressure.

(4) Believes that blood pressure is relevant to their scope of practice, but height/length and

weight are not, is excluded from recording height/length and weight.

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Core Objective 5 – Record Smoking Status

Definitions:

Unique Patient – If a patient is seen by an EP more than once during the EHR

reporting period, then for purposes of measurement that patient is only counted once in

the denominator for the measure. All the measures relying on the term ‘‘unique patient’’

relate to what is contained in the patient’s medical record. Not all of this information will

need to be updated or even be needed by the provider at every patient encounter. This

is especially true for patients whose encounter frequency is such that they would see

the same provider multiple times in the same EHR reporting period.

Objective:

Record smoking status for patients 13 years old or older.

Measure:

More than 80 percent of all unique patients 13 years old or older seen by the EP have

smoking status recorded as structured data.

Exclusion:

Any EP that neither sees nor admits any patients 13 years old or older.

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NOTE: You must attest YES to meet the

attestation requirements

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Core Objective 6 – Clinical Decision Support Rule

Definitions:

Clinical Decision Support – HIT functionality that builds upon the foundation of an EHR to

provide persons involved in care processes with general and person-specific information,

intelligently filtered and organized, at appropriate times, to enhance health and health care.

Objective:

Use clinical decision support to improve performance on high-priority health conditions.

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Core Objective 6 – Clinical Decision Support Rule

Measure:

Measure 1: Implement five clinical decision support interventions related to four or more clinical

quality measures at a relevant point in patient care for the entire EHR reporting period. Absent four

clinical quality measures related to an EP’s scope of practice or patient population, the clinical

decision support interventions must be related to high-priority health conditions. Must attest YES

to this measure or EP will not meet Meaningful Use.

If none of the CQMs are applicable to an EP's scope of practice, the EP should implement

CDS interventions that he or she believes will drive improvements in the delivery of care for

the high-priority health conditions relevant to their patient population.

CMS will not issue additional guidance on the selection of appropriate clinical decision

support rules for Stage 2 Meaningful Use. This determination is best left to the EP taking into

account their workflow, patient population, and quality improvement efforts.

Measure 2: The EP has enabled and implemented the functionality for drug-drug and drug-allergy

interaction checks for the entire EHR reporting period.

Exclusion:

For the second measure, any EP who writes fewer than 100 medication orders during the EHR

reporting period.

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Core Objective 7 – Clinical Lab-Test Results

Objective:

Incorporate clinical lab-test results into Certified EHR Technology

(CEHRT) as structured data

Measure:

More than 55 percent of all clinical lab tests results ordered by 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

Exclusion:

Any EP who orders no lab tests where results are either in a

positive/negative affirmation or numeric format during the EHR

reporting period.

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Core Objective 7 – Clinical Lab-Test Results Additional Information:

The structured data for the numeric/quantitative test results may include positive or negative affirmations

and/or numerical format that would include a reference range of numeric results and/or ratios.

Structured data does not need to be electronically exchanged in order to qualify for the measure of this

objective. The EP is not limited to only counting structured data received via electronic exchange, but may

count in the numerator all structured data entered through manual entry through typing, option selecting,

scanning, or other means.

Lab results are not limited to any specific type of laboratory or to any specific type of lab test.

The Medicare and Medicaid EHR Incentive Programs do not specify the use of code set standards in

meeting the measure for this objective. However, the Office of the National Coordinator for Health

Information Technology (ONC) has adopted Logical Observation Identifiers Names and Codes (LOINC®)

version 2.27, when such codes were received within an electronic transaction from a laboratory, for the

entry of structured data for this measure and made this a requirement for EHR technology to be certified.

Provided the lab result is recorded as structured data and uses the standards above, there does not need

to be an explicit linking between the lab result and the order placed by the physician in order to be

counted in the numerator.

In order to meet this objective and measure, an EP must use the capabilities and standards of CEHRT at

45 CFR 170.314(b)(5).

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NOTE: You must attest YES to meet the

attestation requirements

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Core Objective 8 – Patient Lists

Definitions:

Specific Conditions – Those conditions listed in the active patient problem

list.

Objective:

Generate lists of patients by specific conditions to use for quality

improvement, reduction of disparities, research, or outreach.

Measure:

Generate at least one report listing patients of the EP with a specific

condition.

Exclusion:

No exclusion.

Attestation Requirements:

Eligible professionals (EPs) must attest YES to having generated at least one

report listing patients of the EP with a specific condition to meet this measure.

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Core Objective 9 – Preventive Care

Definitions:

Patient Preference – The method of communication that patients prefer to

receive their reminders such as (but not limited to) by mail, by phone or by

secure messaging.

Active Patients – Patients with at least two office visits in the last 24 months.

Objective:

Use clinically relevant information to identify patients who should receive

reminders for preventive/follow-up care and send these patients the

reminders, per patient preference.

Measure:

More than 10 percent of all unique patients who have had 2 or more office

visits with the EP within the 24 months before the beginning of the EHR

reporting period were sent a reminder, per patient preference when available.

Exclusion:

Any EP who has had no office visits in the 24 months before the EHR

reporting period.

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OR

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Core Objective 10 – Patient Electronic Access Definitions:

Access – When a patient possesses all of the necessary information needed to view,

download, or transmit their information. This could include providing patients with instructions

on how to access their health information, the website address they must visit for online

access, a unique and registered username or password, instructions on how to create a

login, or any other instructions, tools, or materials that patients need in order to view,

download, or transmit their information.

View – The patient (or authorized representative) accessing their health information online.

Transmission – Any means of electronic transmission according to any transport

standard(s) (SMTP, FTP, REST, SOAP, etc.). However, the relocation of physical electronic

media (for example, USB, CD) does not qualify as transmission although the movement of

the information from online to the physical electronic media will be a download.

Business Days – Business days are defined as Monday through Friday excluding federal or

state holidays on which the EP or their respective administrative staffs are unavailable.

Diagnostic Test Results – All data needed to diagnose and treat disease. Examples

include, but are not limited to, blood tests, microbiology, urinalysis, pathology tests, radiology,

cardiac imaging, nuclear medicine tests, and pulmonary function tests.

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Core Objective 10 – Patient Electronic Access Objective:

Provide patients the ability to view online, download and transmit their health information within four

business days of the information being available to the EP.

Measure:

Measure 1: More than 50 percent of all unique patients seen by the EP during the EHR reporting period

are provided timely (available to the patient within 4 business days after the information is available to the

EP) online access to their health information, with the ability to view, download, and transmit to a third

party.

Measure 2: More than 5 percent of all unique patients seen by the EP during the EHR reporting period

(or their authorized representatives) view, download, or transmit to a third party their health information.

Exclusion:

Any EP who:

(1) Neither orders nor creates any of the information listed for inclusion as part of both measures,

except for "Patient name" and "Provider's name and office contact information,” may exclude both

measures.

(2) Conducts 50 percent or more of his or her patient encounters in a county that does not have 50

percent or more of its housing units with 3Mbps broadband availability according to the latest

information available from the FCC on the first day of the EHR reporting period may exclude only the

second measure.

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Core Objective 10 – Patient Electronic Access Additional Information:

The following information must be made available online: Patient name, provider's name and office

contact information, current and past problem list, procedures. laboratory test results, current

medication list and medication history, current medication allergy list and medication allergy

history, vital signs (height, weight, blood pressure, BMI, growth charts), smoking status,

demographic information (preferred language, sex, race, ethnicity, date of birth), care plan field(s),

including goals and instructions, and any known care team members including the primary care

provider (PCP) of record unless the information is not available in certified EHR technology

(CEHRT), is restricted from disclosure due to any federal, state or local law regarding the privacy

of a person’s health information, including variations due to the age of the patient or the provider

believes that substantial harm may arise from disclosing particular health information in this

manner.

Replaces the Stage 1 core objective for EPs of "Provide patients with an electronic copy of their

health information (including diagnostic test results, problem list, medication lists, medication

allergies) upon request" and the Stage 1 menu objective for EPs of "Provide patients with timely

electronic access to their health information (including lab results, problem list, medication lists,

and allergies) within 4 business days of the information being available to the EP."

Both of the measures for this objective must be met using CEHRT.

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Core Objective 11 – Clinical Summaries Definitions:

Clinical Summary – An after-visit summary that provides a patient with relevant and actionable

information and instructions containing in no particular order:

• Patient name. • Provider's name and office contact information.

• Date and location of the visit. • Reason for the office visit.

• Current problem list. • Current medication list.

• Current medication allergy list. • Procedures performed during the visit.

• Laboratory test results. • List of diagnostic tests pending.

• Clinical instructions. • Future appointments.

• Referrals to other providers. • Future scheduled tests.

• Smoking status. • Care plan field(s), including goals and instructions.

• Recommended patient decision aids (if applicable to the visit).

• Demographic information maintained within certified electronic health record technology (CEHRT)

(sex, race, ethnicity, date of birth, preferred language).

• Immunizations or medications administered during the visit.

•Vital signs taken during the visit (or other recent vital signs).

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Core Objective 11 – Clinical Summaries

Definitions Continued:

Office Visit – Office visits include separate, billable encounters that result from evaluation and

management services provided to the patient and include:

(1) Concurrent care or transfer of care visits,

(2) Consultant visits, or

(3) Prolonged Physician Service without Direct (Face-To-Face) Patient Contact (tele-health). A

consultant visit occurs when a provider is asked to render an expert opinion/service for a specific

condition or problem by a referring provider.

Objective:

Provide clinical summaries for patients for each office visit.

Measure:

Clinical summaries provided to patients or patient-authorized representatives within one business day for

more than 50 percent of office visits.

Exclusion:

Any EP who has no office visits during the EHR reporting period.

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Core Objective 11 – Clinical Summaries

Additional Information:

The provision of the clinical summary is limited to the information contained within CEHRT.

The clinical summary can be provided through a PHR, patient portal on the web site, secure e-mail,

electronic media such as CD or USB fob, or printed copy. If the EP chooses an electronic media, they

would be required to provide the patient a paper copy upon request. They may also default to providing

paper copies, in which case an electronic form of the EP’s choice would need to be provided upon

request.

Providers may not charge patients a fee to provide this information.

When a patient visit lasts several days or a patient is seen by multiple EPs, a single clinical summary at

the end of the visit should be counted only once in both the numerator and denominator.

In the event that a clinical summary is offered to and subsequently declined by the patient, that patient

may still be included in the numerator of the measure.

In circumstances where there is no information available to populate one or more of the fields

previously listed, either because the EP can be excluded from recording such information (for example,

vital signs) or because there is no information to record (for example, no medication allergies or

laboratory tests), an indication that the information is not available in the clinical summary would meet

the measure of this objective.

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Core Objective 12 – Patient-Specific Education Resources Definitions:

Patient-Specific Education Resources identified by Certified EHR Technology – Resources

or a topic area of resources identified through logic built into certified EHR technology which

evaluates information about the patient and suggests education resources that would be of

value to the patient.

Unique Patient – If a patient is seen by an EP more than once during the EHR reporting period,

then for purposes of measurement that patient is only counted once in the denominator for the

measure. All the measures relying on the term ‘‘unique patient’’ relate to what is contained in the

patient’s medical record. Not all of this information will need to be updated or even be needed by

the provider at every patient encounter. This is especially true for patients whose encounter

frequency is such that they would see the same provider multiple times in the same EHR

reporting period.

Objective:

Use clinically relevant information from Certified EHR Technology to identify patient-specific

education resources and provide those resources to the patient.

Measure:

Patient-specific education resources identified by Certified EHR Technology are provided to

patients for more than 10 percent of all unique patients with office visits seen by the EP during

the EHR reporting period.

Exclusion:

Any EP who has no office visits during the EHR reporting period.

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Core Objective 12 – Patient-Specific Education Resources Additional Information:

Unique patients with office visits means that to count in the denominator a patient must be seen by the EP for

one or more office visits during the EHR reporting period, but if a patient seen by the EP more than once

during the EHR reporting period, the patient only counts once in the denominator.

Education resources or materials do not have to be stored within or generated by the certified EHR. However,

the provider should utilize certified EHR technology (CEHRT) in a manner where the technology suggests

patient-specific educational resources based on the information stored in the CEHRT. The provider can make

a final decision on whether the education resource is useful and relevant to a specific patient.

While CEHRT must be used to identify patient-specific education resources, these resources or materials do

not have to be stored within or generated by the CEHRT.

Certified EHR technology is certified to use the patient's problem list, medication list, or laboratory test results

to identify the patient-specific educational resources.

The EP may use these elements or additional elements within CEHRT to identify educational resources

specific to patients' needs. The EP can then provide these educational resources to patients in a useful format

for the patient (such as, electronic copy, printed copy, electronic link to source materials, through a patient

portal or PHR).

If resources or topic area of resources are not identified by CEHRT and provided to the patient then it will not

count in the numerator.

The education resources will need to be provided prior to the calculation and subsequent attestation to

meaningful use.

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Core Objective 13 – Use Secure Electronic Messaging

Definitions:

Secure Message – Any electronic communication between a provider and patient that ensures

only those parties can access the communication. This electronic message could be email or the

electronic messaging function of a PHR, an online patient portal, or any other electronic means.

Objective:

Use secure electronic messaging to communicate with patients on relevant health information.

Measure:

A secure message was sent using the electronic messaging function of CEHRT by more than 5

percent of unique patients (or their authorized representatives) seen by the EP during the EHR

reporting period.

Exclusion:

Any EP who has no office visits during the EHR reporting period, or any EP who conducts 50

percent or more of his or her patient encounters in a county that does not have 50 percent or more

of its housing units with 3Mbps broadband availability according to the latest information available

from the FCC on the first day of the EHR reporting period.

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Core Objective 13 – Use Secure Electronic Messaging

Attestation Requirements:

DENOMINATOR: Number of unique patients seen by the EP during the EHR

reporting period.

NUMERATOR: The number of patients or patient-authorized representatives in

the denominator who send a secure electronic message to the EP that is

received using the electronic messaging function of CEHRT during the EHR

reporting period.

THRESHOLD: The resulting percentage must be more than 5 percent in order for

an EP to meet this measure.

EXCLUSION: Any EP who has no office visits during the EHR reporting period, or

any EP who conducts 50 percent or more of his or her patient encounters in a

county that does not have 50 percent or more of its housing units with 3Mbps

broadband availability according to the latest information available from the FCC

on the first day of the EHR reporting period.

Additional Information:

There is not an expectation that the EP must personally respond to electronic

messages to the patient.

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Core Objective 14 – Medication Reconciliation

Definitions:

Medication Reconciliation – The process of identifying the most accurate list of all medications that the

patient is taking, including name, dosage, frequency, and route, by comparing the medical record to an

external list of medications obtained from a patient, hospital, or other provider.

Relevant Encounter – An encounter during which the EP performs a medication reconciliation due to

new medication or long gaps in time between patient encounters or for other reasons determined

appropriate by the EP. Essentially an encounter is relevant if the EP judges it to be so. (Note: Relevant

encounters are not included in the numerator and denominator of the measure for this objective.)

Transition of Care – The movement of a patient from one clinical setting (inpatient, outpatient, physician

office, home health, rehab, long-term care facility, etc.) to another or from one EP to another. At a

minimum, transitions of care include first encounters with a new patient and encounters with existing

patients where a summary of care record (of any type) is provided to the receiving provider. The summary

of care record can be provided either by the patient or by the referring/transiting provider or institution.

Objective: The EP who receives a patient from another setting of care or provider of care or believes an

encounter is relevant should perform medication reconciliation.

Measure: The EP who performs medication reconciliation for more than 50 percent of transitions of care in

which the patient is transitioned into the care of the EP.

Exclusion: Any EP who was not the recipient of any transitions of care during the EHR reporting period.

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Core Objective 14 – Medication Reconciliation

Additional Information:

Only patients whose records are maintained using certified

EHR technology must be included in the denominator for

transitions of care.

In the case of reconciliation following transition of care, the

receiving EP should conduct the medication reconciliation.

The electronic exchange of information is not a requirement for

medication reconciliation.

The measure of this objective does not dictate what information

must be included in medication reconciliation. Information

included in the process of medication reconciliation is

appropriately determined by the provider and patient.

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Core Objective 15 – Summary of Care

Definitions:

Transition of Care – The movement of a patient from one setting of care (hospital, ambulatory primary care

practice, ambulatory, specialty care practice, long-term care, home health, rehabilitation facility) to another.

At a minimum this includes all transitions of care and referrals that are ordered by the EP.

Summary of Care Record – A summary of care record must include the following elements:

•Patient name •Smoking status • Reason for referral

• Procedures •Encounter diagnosis • Current medication list

• Immunizations •Laboratory test results • Current medication allergy list

• Vital signs (height, weight, blood pressure, BMI).

• Functional status, including activities of daily living, cognitive and disability status

• Demographic information (preferred language, sex, race, ethnicity, date of birth).

• Care plan field, including goals and instructions.

• Care team including the primary care provider of record and any additional known

care team members beyond the referring or transitioning provider and the receiving provider.

• Referring or transitioning provider's name and office contact information (EP only).

• Current problem list (EPs may also include historical problems at their discretion).

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Core Objective 15 – Summary of Care

Definitions Continued:

Problem List – At a minimum a list of current, active and historical diagnoses. We

do not limit the EP to just including diagnoses on the problem list.

Active/current medication list – A list of medications that a given patient is

currently taking.

Active/current medication allergy list – A list of medications to which a given

patient has known allergies.

Allergy – An exaggerated immune response or reaction to substances that are

generally not harmful.

Care Plan – The structure used to define the management actions for the various

conditions, problems, or issues. A care plan must include at a minimum the

following components: problem (the focus of the care plan), goal (the target

outcome) and any instructions that the provider has given to the patient. A goal is

a defined target or measure to be achieved in the process of patient care (an

expected outcome).

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Core Objective 15 – Summary of Care

Objective: The EP who transitions their patient to another setting of 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.

Measure:

EPs must satisfy both of the following measures in order to meet the objective:

Measure 1: The EP who transitions or refers their patient to another setting of care or provider of care provides

a summary of care record for more than 50 percent of transitions of care and referrals.

Measure 2: The EP who transitions or refers their patient to another setting of care or provider of care provides

a summary of care record for more than 10 percent of such transitions and referrals either (a) electronically

transmitted using CEHRT to a recipient or (b) where the recipient receives the summary of care record via

exchange facilitated by an organization that is a NwHIN Exchange participant or in a manner that is consistent

with the governance mechanism ONC establishes for the NwHIN.

Measure 3: An EP must satisfy one of the following criteria:

Conducts one or more successful electronic exchanges of a summary of care document, as part of which is

counted in "measure 2" (for EPs the measure at §495.6(j)(14)(ii)(B) with a recipient who has EHR

technology that was developed designed by a different EHR technology developer than the sender's EHR

technology certified to 45 CFR 170.314(b)(2).

Conducts one or more successful tests with the CMS designated test EHR during the EHR reporting period.

Exclusion: Any EP who transfers a patient to another setting or refers a patient to another provider less than 100

times during the EHR reporting period is excluded from all three measures.

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Core Objective 15 – Summary of Care

Additional Information:

Only patients whose records are maintained using certified EHR technology must be included in

the denominator for transitions of care.

The EP that transfers or refers the patient to another setting of care or provider should provide

the summary of care document. It is for this provider that has the most recent information on the

patient that may be crucial to the provider to whom the patient is transferred or referred.

The EP can send an electronic or paper copy of the summary care record directly to the next

provider or can provide it to the patient to deliver to the next provider, if the patient can

reasonably expected to do so and meet Measure 1.

If the provider to whom the referral is made or to whom the patient is transitioned to has access

to the medical record maintained by the referring provider then the summary of care record

would not need to be provided, and that patient must not be included in the denominator for

transitions of care.

To count in the numerator of any measure, the EP must verify these three fields for current

problem list, current medication list, and current medication allergy list are not blank and include

the most recent information known by the EP or hospital as of the time of generating the

summary of care document.

To count in the numerator of measure 2, the summary of care record must be received by the

provider to whom the sending provider is referring or transferring the patient.

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Core Objective 15 – Summary of Care

Additional Information:

To count in the numerator of measure 2, one of the following three transmission approaches must be used:

• Use of the transport standard capability required for certification. As required by ONC to meet the CEHRT

definition, every EP, eligible hospital, and CAH, must have EHR technology that is capable of electronically

transmitting a summary care record for transitions of care and referrals according to the primary Direct Project

specification (the Applicability Statement for Secure Health Transport). Thus, EPs, eligible hospitals, or CAHs

that electronically transmit summary care records using their CEHRT’s “Direct” capability (natively or combined

with an intermediary) would be able to count all such electronic transmissions in their numerator.

• Use of the SOAP-based optional transport standard capability permitted for certification. As part of certification,

ONC permits EHR technology developers to voluntarily seek certification for their EHR technology’s capability

to perform SOAP-based electronic transmissions. EHR technology developers who take this approach would

enable their customers to also use this approach to meet the measure. Thus, EPs, eligible hospitals, or CAHs

that electronically transmit summary care records using their CEHRT’s “SOAP-based” capability (natively or

combined with an intermediary) would be able to count all of those transmissions in their numerator.

• Use of CEHRT to create a summary care record in accordance with the required standard (i.e., Consolidated

CDA as specified in 45 CFR 170.314(b)(2)), and the electronic transmission is accomplished through the use of

an eHealth Exchange participant who enables the electronic transmission of the summary care record to its

intended recipient. Thus, EPs, eligible hospitals, or CAHs who create standardized summary care records using

their CEHRT and then use an eHealth Exchange participant to electronically transmit the summary care record

would be able to count all of those transmissions in their numerator.

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Core Objective 15 – Summary of Care

CMS 2014 Flexibility Rule—Limited Exception:

The Flexibility Rule allows providers who cannot meet the Stage 2 Summary of Care

measures to attest to Stage 1 Meaningful Use using the 2014 Edition criteria if the following

applies.

• Provider cannot meet the Stage 2 Summary of Care Measures due to the recipient

Summary of Care transmittal being impacted by a 2014 CEHRT issue. The sending

provider may experience significant difficulty meeting the 10% threshold for electronic

transmissions, despite the referring provider’s ability to send the electronic document if

the intermediary or recipient of the transmission or referral is experiencing delays in the

ability to fully implement 2014 Edition CEHRT.

• The Referring Provider under this circumstance may attest to the 2014 Stage 1

Objectives and Measures for the EHR Reporting Period in 2014.

• The Referring Provider must retain documentation demonstrating that s/he was unable

to meet the 10% threshold to Provide and Electronic Summary of Care document for a

Transition or Referral because the Intermediary or Recipient of the Transmission or Referral is experiencing delays in the ability to Fully Implement 2014 Edition CEHRT.

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https://www.nmhit.org/Registration/

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107

On-Boarding Status

Attach NM DOH

https://www.nmhit.org/

screenshot OR DOH email

dated within 60 days of the

start of EHR Reporting

Period

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Core Objective 16 – Immunization Registries Data Submission

Objective: Capability to submit electronic data to immunization registries or immunization information

systems except where prohibited, and in accordance with applicable law and practice.

Measure: Successful ongoing submission of electronic immunization data from CEHRT to an

immunization registry or immunization information system for the entire EHR reporting period.

Exclusions:

Any EP that meets one or more of the following criteria may be excluded from this objective:

(1) the EP does not administer any of the immunizations to any of the populations for which data

is collected by their jurisdiction's immunization registry or immunization information system

during the EHR reporting period;

(2) the EP operates in a jurisdiction for which no immunization registry or immunization

information system is capable of accepting the specific standards required for CEHRT at the

start of their EHR reporting period;

(3) the EP operates in a jurisdiction where no immunization registry or immunization information

system provides information timely on capability to receive immunization data; or

(4) the EP operates in a jurisdiction for which no immunization registry or immunization

information system that is capable of accepting the specific standards required by CEHRT at the

start of their EHR reporting period can enroll additional EPs.

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Core Objective 16 – Immunization Registries Data Submission

Additional Information: The second exclusion does not apply if an entity designated

by the immunization registry or immunization information system can receive electronic

immunization data submissions. For example, if the immunization registry cannot

accept the data directly or in the standards required by CEHRT, but if it has designated

a Health Information Exchange to do so on their behalf and the Health Information

Exchange is capable of accepting the information in the standards required by CEHRT,

the provider could not claim the second exclusion.

In order to meet this objective and measure, an EP must use the capabilities and

standards of CEHRT at 45 CFR 170.314(f)(1) and (f)(2). However, if EPs prior to CY

2014 have achieved successful ongoing submission using EHR technology certified to

the 2011 Edition EHR certification criteria (HL7 2.3.1 only), it is acceptable to continue

this ongoing submission and meet the Stage 2 measure for as long as HL7 2.3.1

continues to be accepted by the immunizations information system or immunization

registry.

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NOTE: You must attest YES to meet the

attestation requirements

112

Core Objective 17 – Protect Electronic Health Information

Objective:

Protect electronic health information created or maintained by the certified

EHR technology (CEHRT) through the implementation of appropriate

technical capabilities.

Measure:

Conduct or review a security risk analysis in accordance with the

requirements under 45 CFR 164.308(a) (1), including addressing the

encryption/security of data stored in CEHRT in accordance with

requirements under 45 CFR 164.312 (a)(2)(iv) and 45 CFR 164.306(d)(3),

and implement security updates as necessary and correct identified

security deficiencies as part of the provider's risk management process for

EPs.

Exclusion:

No exclusion.

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Core Objective 17 – Protect Electronic Health Information

Additional Information:

EPs must conduct or review a security risk analysis of CEHRT including addressing

encryption/security of data, and implement updates as necessary at least once prior

to the end of the EHR reporting period and attest to that conduct or review. The

testing could occur prior to the beginning of the first EHR reporting period. However,

a new review would have to occur for each subsequent reporting period.

The parameters of the security risk analysis are defined 45 CFR 164.308(a)(1) which

was created by the HIPAA Security Rule. Meaningful use does not impose new or

expanded requirements on the HIPAA Security Rule nor does it require specific use

of every certification and standard that is included in certification of EHR technology.

More information on the HIPAA Security Rule can be found at

http://www.hhs.gov/ocr/privacy/hipaa/administrative/securityrule/

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Core Objective 17 – Protect Electronic Health Information

Additional Information:

An EP who is reporting for a 90-day EHR Reporting Period in 2014 may complete the

security risk analysis requirements outside of the this 90-day period as long as it is

completed between January 1st of the EHR reporting year and no later than the date

the eligible professional submits the attestation for that reporting period. If the EP

attests in the grace period, the security analysis must be performed by December 31,

2014.

For more information, read the updated FAQ 10754 at https://questions.cms.gov/

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Core Objective 17 – Protect Electronic Health Information

Attestation—Attach Supporting Documentation

Providers should attach supporting documentation in the NM State Level

Registry at the time of Attestation, including any of the following:

Copy of the security risk analysis or subsequent review

Letter from provider/practice summarizing results of security risk analysis or

subsequent review; note any actions that were taken or will be taken to address

any security issues identified

Letter from contractor who performed the security risk analysis or subsequent

review—summarizing results; note any actions that were taken or will be taken to

address any security issues identified

New Mexico Human Services Department

Reporting Requirements

Eligible Professionals

Meaningful Use 20 Objectives

CORE 17 Objectives

MENU 3 of 6

Objectives

Clinical Quality

Measures 9 Objectives

9 CQMs total out of 64

9 adult

9 pediatric

Any 9

2014

116

117

NM Medicaid EHR Incentive Payment Program

S2 MU for EPs—2014 Menu Objectives

118

Don’t click here…ask Xerox

119

Don’t click here…ask Xerox

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121

https://www.nmhit.org/Registration/

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122

On-Boarding Status

Attach NM DOH

https://www.nmhit.org/

screenshot OR DOH

email dated within 60

days prior to start of

EHR Reporting Period

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Menu Objective 1 – Syndromic Surveillance Data Submission Definition:

Public Health Agency – An entity under the jurisdiction of the U.S. Department of Health and

Human Services, tribal organization, State level and/or city/county level administration that

serves a public health function.

Objective: Capability to submit electronic syndromic surveillance data to public health agencies

except where prohibited, and in accordance with applicable law and practice.

Measure: Successful ongoing submission of electronic syndromic surveillance data from CEHRT

to a public health agency for the entire EHR reporting period.

Exclusion:

Any EP that meets one or more of the following criteria may be excluded from this objective:

(1) the EP is not in a category of providers that collect ambulatory syndromic surveillance

information on their patients during the EHR reporting period;

(2) the EP operates in a jurisdiction for which no public health agency is capable of receiving

electronic syndromic surveillance data in the specific standards required by CEHRT at the start

of their EHR reporting period;

(3) the EP operates in a jurisdiction where no public health agency provides information timely

on capability to receive syndromic surveillance data; or

(4) the EP operates in a jurisdiction for which no public health agency that is capable of

accepting the specific standards required by CEHRT at the start of their EHR

reporting period can enroll additional EPs.

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Menu Objective 2 – Electronic Notes

Definition:

Electronic Notes – Defined as electronic progress notes. CMS will rely on

providers own determinations and guidelines defining when progress notes are

necessary to communicate individual patient circumstances and for coordination

with previous documentation of patient observations, treatments and/or results in

the electronic health record.

Objective:

Record electronic notes in patient records.

Measure:.

Enter at least one electronic progress note created, edited and signed by an EP

for more than 30 percent of unique patients with at least one office visit during the

EHR reporting period. The text of the electronic note must be text searchable and

may contain drawings and other content

Exclusion:

Any EP who has no office visits during the EHR reporting period.

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Menu Objective 3 – Imaging Results

Definition:

Imaging – The description of radiology services from the Stage 2 CPOE objective is the minimum

description of imaging. We describe radiologic services as any imaging service that uses electronic product

radiation. Electronic product radiation is defined at 21 CFR 1000.3 as: "any ionizing or nonionizing

electromagnetic or particulate radiation, or [a]ny sonic, infrasonic, or ultrasonic wave that is emitted from

an electronic product as the result of the operation of an electronic circuit in such product." If the provider

desires to include other types of imaging services that do not rely on electronic product radiation they may

do so as long as the policy is consistent across all patients and for the entire EHR reporting period.

Accessible through – Either incorporation of the image and accompanying information into CEHRT or an

indication in CEHRT that the image and accompanying information are available for a giving patient in

another technology and a link to that image and accompanying information.

Incorporation of the Image – The image and accompanying information is stored by the CEHRT.

A Link to the Image and Accompanying Information – A link to where the image and accompanying

information is stored is available in CEHRT. This link must conform to the certification requirements

associated with this objective in the ONC final rule published elsewhere in this issue of the Federal

Register.

No Access – None of the imaging providers used by the EP provide electronic images and any

explanation or other accompanying information that are accessible through their CEHRT at the start of the

EHR reporting period.

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Menu Objective 3 – Imaging Results

Objective:

Imaging results consisting of the image itself and any explanation or other

accompanying information are accessible through CEHRT.

Measure:

More than 10 percent of all tests whose result is one or more images ordered

by the EP during the EHR reporting period are accessible through CEHRT.

Exclusion:

Any EP who orders less than 100 tests whose result is an image during the

EHR reporting period; or any EP who has no access to electronic imaging

results at the start of the EHR reporting period.

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Menu Objective 4 – Family Health History

Definition:

First Degree Relative – A family member who shares about 50 percent of

their genes with a particular individual in a family. First degree relatives include

parents, offspring, and siblings.

Objective:

Record patient family health history as structured data.

Measure:.

More than 20 percent of all unique patients seen by the EP during the EHR

reporting period have a structured data entry for one or more first-degree

relatives.

Exclusion:

Any EP who has no office visits during the EHR reporting period.

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No NM

Public

Health

registry

capable of

receiving

data under

specific

standards.

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133

Cont’d

134

Menu Objective 5—Report Cancer Cases

Objective: Capability to identify and report cancer cases to a public health central cancer

registry, except where prohibited, and in accordance with applicable law and practice.

Measure: Successful ongoing submission of cancer case information from CEHRT to a public

health central cancer registry for the entire EHR reporting period.

Exclusion:

Any EP that meets at least 1 of the following criteria may be excluded from this objective:

(1) The EP does not diagnose or directly treat cancer;

(2) The EP operates in a jurisdiction for which no public health agency is capable of

receiving electronic cancer case information in the specific standards required for

CEHRT at the beginning of their EHR reporting period;

(3) The EP operates in a jurisdiction where no PHA provides information timely on

capability to receive electronic cancer case information; or

(4) The EP operates in a jurisdiction for which no public health agency that is capable of

receiving electronic cancer case information in the specific standards required for

CEHRT at the beginning of their EHR reporting period can enroll additional EPs.

135

No NM

Public

Health

registry

capable of

receiving

data under

specific

standards.

136

137

Cont’d

138

Menu Objective 6—Specialized Registry

Objective: Capability to identify and report specific cases to a specialized registry (other than a

cancer registry), except where prohibited, and in accordance with applicable law and practice.

Measure: Successful ongoing submission of specific case information from CEHRT to a specialized

registry for the entire EHR reporting period.

EPs must attest YES to successfully submitting specific case information from CEHRT to a

specialized registry for the entire reporting period to meet this measure.

Ongoing submission was already achieved for an EHR reporting period in a prior year and

continues throughout the current EHR reporting period.

Registration with the PHA or other body to whom the information is being submitted of intent to

initiate ongoing submission was made by the deadline (within 60 days of the start of the EHR

reporting period) and ongoing submission was achieved.

Registration of intent to initiate ongoing submission was made by the deadline and the EP or

hospital is still engaged in testing and validation of ongoing electronic submission.

Registration of intent to initiate ongoing submission was made by the deadline and the EP or

hospital is awaiting invitation to begin testing and validation.

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Menu Objective 6—Specialized Registry

Exclusions:

Any EP that meets at least 1 of the following criteria may be excluded from this objective:

(1) The EP does not diagnose or directly treat any disease associated with a specialized registry sponsored by a

national specialty society for which the EP is eligible, or the public health agencies in their jurisdiction;

(2) The EP operates in a jurisdiction for which no specialized registry sponsored by a public health agency or by a

national specialty society for which the EP is eligible is capable of receiving electronic specific case information in

the specific standards required by CEHRT at the beginning of their EHR reporting period;

(3) The EP operates in a jurisdiction where no public health agency or national specialty society for which the EP is

eligible provides information timely on capability to receive information into their specialized registries; or

(4) The EP operates in a jurisdiction for which no specialized registry sponsored by a public health agency or by a

national specialty society for which the EP is eligible that is capable of receiving electronic specific case information

in the specific standards required by CEHRT at the beginning of their EHR reporting period can enroll additional EPs.

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Menu Objective 6—Specialized Registry

Definition of Terms

Specialized Registry – Sponsored by national specialty societies and specialized registries maintained by public health agencies.

Additional Information:

The specialized registry cannot be duplicative of any of the other registries included in other

meaningful use objectives and measures. This means that an EP cannot meet the immunization,

syndromic surveillance or cancer objectives and this objective by reporting to the same registry.

In determining whether an EP meets the first exclusion, the registries in question are those

sponsored by the public health agencies with jurisdiction over the area where the EP practices and

national medical societies covering the EP’s scope of practice.

Attestation: Attach Supporting Documentation:

If attesting to a specialized registry sponsored by a national specialty society, attach a letter from

the specialty society stating that the data was received by them, that the data was transmitted from

the provider’s/practice’s CEHRT, and on what date the transmission occurred.

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142

Reporting Requirements

Eligible Professionals

Meaningful Use 20 Objectives

CORE 17 Objectives

MENU 3 of 6

Objectives

Clinical Quality

Measures 9 Objectives

9 CQMs total out of 64

9 adult

9 pediatric

Any 9

2014 — Stage 2

143

NM Medicaid EHR Incentive Payment Program

S2 MU for EPs—2014 CQMs

144

Clinical Quality Measures

• Specific to Medical

Conditions

• Help evaluate how a

particular medical

condition is treated

4 Components of CQMs

• Initial Patient Population: The group of patients the performance

measure is designed to address. Example: All patients 65 years and

older.

• Denominator: A subset of the initial patient population; in some

measures the denominator may be the same as the initial patient

population. Example: All patients 65 years and older with diabetes.

• Numerator: A subset of the denominator for whom a process or

outcome of care occurs. Example: Patients who had a diabetic foot

exam.

• Exclusions: The mechanism used to exclude patients from the

denominator of a performance measure when a therapy or service

would not be appropriate in instances for which the patient otherwise

meets the denominator criteria. Example: A patient with bilateral

lower extremity amputation is excluded from a measure of foot

exams.

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146

May choose from:

• 9 CQMs for adult populations; OR

• 9 CQMs for pediatric populations; OR

• 9 CQMs total from a list of 64

Data must be reported directly from

information generated by CEHRT

9 CQMs should be individually certified by

the ONC

Report on 9 CQMs with a denominator

greater than zero; attach a copy of CEHRT

report including CQM data

9 CQMs must be from 3 of 6 NQS key health

care policy domains

1. Patient and Family Engagement

2. Patient Safety

3. Care Coordination

4. Population/Public Health

5. Efficient Use of Healthcare

Resources

6. Clinical Process/Effectiveness

Report on 9 out of 64 CQMs

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Electronic CQMs are optional for 2014

Skip Import Screen and Click on CQMs

148

Electronic CQMs are optional for 2014

Skip Import

2014 Edition Stage 1 Only 9 Adult Core CQMs 1. Questionnaire (1 of 9): Controlling High Blood Pressure

2. Questionnaire (2 of 9): Use of High-Risk Medications in the Elderly

3. Questionnaire (3 of 9): Preventive Care and Screening: Tobacco Use: Screening and

Cessation Intervention

4. Questionnaire (4 of 9): Use of Imaging Studies for Low Back Pain

5. Questionnaire (5 of 9): Preventive Care and Screening: Screening for Clinical

Depression and Follow-Up Plan

6. Questionnaire (6 of 9): Documentation of Current Medications in the Medical Record

7. Questionnaire (7 of 9): Preventive Care and Screening: Body Mass Index (BMI)

Screening and Follow-Up

8. Questionnaire (8 of 9): Closing the referral loop: receipt of specialist report

9. Questionnaire (9 of 9): Functional status assessment for complex chronic conditions

https://www.cms.gov/Regulations-and-Guidance/Legislation/EHRIncentivePrograms/2014_ClinicalQualityMeasures.html

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New Mexico Human Services Department

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2014 Edition Stage 1 Only 9 Pediatric Core CQMs

1. Questionnaire (1 of 9): Appropriate Testing for Children with Pharyngitis

2. Questionnaire (2 of 9): Weight Assessment and Counseling for Nutrition and

Physical Activity for Children and Adolescents

3. Questionnaire (3 of 9): Chlamydia Screening for Women

4. Questionnaire (4 of 9): Use of Appropriate Medications for Asthma

5. Questionnaire (5 of 9): Childhood Immunization Status

6. Questionnaire (6 of 9): Appropriate Treatment for Children with Upper Respiratory

Infection (URI)

7. Questionnaire (7 of 9): ADHD: Follow-Up Care for Children Prescribed Attention-

Deficit/Hyperactivity Disorder (ADHD) Medication

8. Questionnaire (8 of 9): Preventive Care and Screening: Screening for Clinical

Depression and Follow-Up Plan

9. Questionnaire (9 of 9): Children who have dental decay or cavities

https://www.cms.gov/Regulations-and-Guidance/Legislation/EHRIncentivePrograms/2014_ClinicalQualityMeasures.html

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2014 Edition Stage 1 Only SELECTION ERROR MESSAGES

• If you select less than 9 CQMs, when you hit Save & Continue, you will get the following error

message at the bottom of the selection page:

• If you select less than 3 domains, when you hit Save & Continue, you will get the following error

message at the bottom of the selection page:

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CMS Links—Stage 2 MU

Stage 2 MU — https://www.cms.gov/Regulations-and-

Guidance/Legislation/EHRIncentivePrograms/Stage_2.html

Table: Core & Menu Set Objectives

http://www.cms.gov/Regulations-and-

Guidance/Legislation/EHRIncentivePrograms/Downloads/Stage2_Mean

ingfulUseSpecSheet_TableContents_EPs.pdf

Core and Menu Set—Zip File: at bottom of Stage 2 MU Page

2014 Clinical Quality Measures Page

http://www.cms.gov/Regulations-and-

Guidance/Legislation/EHRIncentivePrograms/2014_ClinicalQualityMeas

ures.html

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CMS EHR Final Rules Links

EHR Final Rule 2010

http://www.gpo.gov/fdsys/pkg/FR-2010-07-28/pdf/2010-17207.pdf

EHR Stage 2 Final Rule 2012

http://www.gpo.gov/fdsys/pkg/FR-2012-09-04/pdf/2012-21050.pdf

CMS 2014 CEHRT Flexibility Rule - September 2014

http://www.gpo.gov/fdsys/pkg/FR-2014-09-04/pdf/2014-21021.pdf

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https://questions.cms.gov/

Attestation

• Step 4 in the SLR: Print the attestation agreement.

• Attestation must be signed and dated by the Eligible Professional (EP). A practice

representative or MU/EHR coordinator cannot sign on behalf of the EP.

• Upload the signed and dated attestation agreement on Step 4.

• Step 5 in the SLR : Submit the signed and dated agreement electronically.

• Make a copy of the original agreement for your records for audit purposes.

• Mail the original signed and dated attestation to the address on the agreement.

• The Prepayment review process will begin upon receipt of the agreement..

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Save All Documentation for 6 Years

• You will be asked to attach during attestation, or later submit,

documentation supporting the data from any of the sources

used in the Meaningful Use attestation process.

• It is the responsibility of the individual eligible professional to

retain all supporting documents, reports and other

information used in the attestation process for a period of

six years. This is true even if EPs enrolled in the EHR

program through the Group Administrator function or if EPs

change practice locations.

• Work with your EHR vendor to fully understand the capabilities

of your certified EHR technology. For example, if you were

randomly audited eight months after Meaningful Use

attestation, could your certified EHR produce the identical

report for the 90-day EHR reporting period you used for

Meaningful Use attestation? If not, keep an electronic file copy

or a hard copy of the report used for your attestation.

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Group Administrator Webinar

Group Administrator is a “must use” function for any practice or clinic:

• whose EPs choose to use Group Patient Volume as proxy for the EPs

in the group; and/or

• will have one representative entering data in the NM SLR on behalf of

two or more EPs.

Group Administrator is the only approved method by the NM Medicaid EHR

Incentive Program for someone other than the eligible professional to enter

the data for attestation.

Contact [email protected] to schedule a webinar

demonstration customized to your practice or clinic; 505-827-1342.

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New Mexico Program Contacts

Program Registration: Call 1-800-299-7304

Option 6, then 2

Email [email protected]

Policy Questions: Staff Manager

EHR Incentives Program

Phone: 505-827-1321

[email protected]

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QUESTIONS???

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THANK YOU!