FAQ Directory

Here are some of the most frequently asked questions about NCQA’s various programs. If you don’t see what you are looking for in one of the entries below, you can  ask a question through My NCQA.

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9.15.2014 Osteoporosis Management in Women Who Had a Fracture Step 4 states to exclude members who received a dispensed prescription or had an active prescription to treat osteoporosis during the 365 days (12 months) prior to the IESD. Define “active prescription.”

 An “active prescription” means that a member has a surplus of medication to take from a prescription dispensed previously. Therefore, in step 4 (required exclusions), the member is excluded if a prescription was dispensed during the 12 months prior to the IESD, or prior to that time frame if the member has remaining pills to take in the 12 months prior to the IESD.

 

This applies to the following Programs and Years:
HEDIS 2015

9.15.2014 Comprehensive Diabetes Care For the eye exam indicator, is documentation of hypertensive retinopathy treated differently from diabetic retinopathy? If there is documentation that a member was negative for hypertensive retinopathy in the year prior to the measurement year, is this compliant?

 Although the two diagnoses are clinically different, hypertensive retinopathy is not treated differently from diabetic retinopathy for the CDC measure. The intent of the eye exam indicator is to ensure that members with evidence of any type of retinopathy have an eye exam annually, while members who remain free of retinopathy (i.e., the retinal exam was negative for retinopathy) are screened every other year. If it is clear that a retinal or dilated eye exam was performed by an eye care professional in the year prior to the measurement year and there is documentation indicating that the member is negative for hypertensive retinopathy, this can count as compliant.

 

This applies to the following Programs and Years:
HEDIS 2015

9.15.2014 General Guidelines In the draft MY 2014 P4P Manual published in September 2014, there is no mention of whether to apply a “14-day” rule to administrative data for numerators that require more than one service. It does mention to apply this rule in the new HbA1c 2 tests numerator for Diabetes Care. Should we apply this to CIS and HPV for P4P, as we will do for HEDIS 2015?

 
The “14 day” rule was added to the CDC specification because P4P had not adopted HEDIS 2015 General Guideline 44 for the September release of the MY 2014 P4P Manual. The guideline will be adapted for P4P and added to the final version of the MY 2014 P4P Manual, which will be released on December 1, 2014. This guideline, like HEDIS, will also apply to the CIS and HPV P4P measures, along with the Two HbA1c Tests indicator in the CDC measure.

This applies to the following Programs and Years:
IHA P4P

9.15.2014 General Guidelines Should the change to the logic from HEDIS 2015 General Guideline 41 also be applied to IHA measures that require results from the most recent test?

Yes. HEDIS 2015 General Guideline 41 will be adapted for P4P and added to the final version of the MY 2014 P4P Manual, which will be released on December 1, 2014. The guideline, like HEDIS, will apply to the CDC HbA1c control indicators.

This applies to the following Programs and Years:
IHA P4P

9.15.2014 PHQ: Evidence for seeking input from consumer representatives What evidence must an organization provide to meet the requirement for seeking input from consumer representatives?

The organization must provide a documented process for seeking and receiving input from consumers or consumer groups, and provide reports or materials showing that feedback was solicited and received.
The solicitation must address measures included in the program and how information about physicians is reported.
NCQA defines “consumers” as a non-health care professionals who have, or would, utilize health care services. NCQA defines “consumer groups” as organizations that advocate for people who are actual or potential users of health care services.

This applies to the following Programs and Years:
PHQ 2013

9.10.2014 MEM: Clarifying after-hours response turnaround time for MEM3 Element B and MEM 5 Element B What is NCQA's expectation for organizations responding to calls after normal business hours for MEM 3, Element B and MEM 5, Element B?

An organization that does not have a voicemail system should have other means for identifying member calls after normal business hours, and return members’ call on the next business day.​

This applies to the following Programs and Years:

8.18.2014 HP 2014 UM 8E: Federal guidelines and external reviews Does UM 8, Element E apply if an organization follows federal guidelines for external reviews?

Yes. If an organization informs NCQA that it follows the Affordable Care Act requirements for external reviews (PHS Act section 2719), UM 8, Element E applies, even if the state where the organization operates does not comply with federal regulations.

This applies to the following Programs and Years:

8.15.2014 Plan All-Cause Readmissions In the step 5 examples, how do you determine if an acute inpatient stay is excluded? In example 2, why is Stay 1 not excluded?

To determine if a stay should be excluded, identify the index hospitalization and the FIRST readmission (if there is one). If the FIRST readmission was planned for, drop the index.

So, for example 2:

Stay 1. Index hospitalization with unplanned readmission (stay 2): Include as index.
Stay 2. Index hospitalization with planned readmission (stay 3): Drop as index.
Stay 3. Index hospitalization with planned readmission (stay 4): Drop as index.
Stay 4. Index hospitalization with no readmission: Include as index.

Stay 1 is the index. Stay 2 is the first readmission to assess, but because it does not meet criteria for a “planned hospital stay,” stay 1 is not excluded.

 

This applies to the following Programs and Years:
HEDIS 2015

7.15.2014 Controlling High Blood Pressure Is a problem list in an office visit note considered undated?

No, if a problem list is found in an office visit note then it would be considered a dated problem list and the date of the visit must be used. A true problem list is a standalone document in the medical record that records a member’s conditions. It is typically located in a centralized section of the medical record (usually the front of the chart) and lists all diagnoses. In an EHR a problem list is present at all routine office visits.

If the documentation is part of the member’s medical history, progress note or office visit note, the date of the visit must be used as the date of the HTN confirmation and must be on or before June 30 of the measurement year. The representative BP reading must occur after the date when the diagnosis of HTN was confirmed.

 

 

This applies to the following Programs and Years:
HEDIS 2015

5.20.2014 Supplemental Data Guidelines If a patient does not remember the exact date and location of a test or procedure, what is the minimum acceptable documentation for satisfying the supplemental data requirement for this measure? How specific does this information have to be? May member-reported data be entered into a legal health record by staff members?

General Guideline 28 outlines the requirements for using member-reported supplemental data, which may be accepted only when accompanied by proof-of-service documentation from the legal health record. If proof-of-service documentation is not available, member-reported information on services rendered (patient history) are acceptable only if taken by a PCP as part of the member’s history. Information must be signed, dated and maintained in the member’s legal health record. General Guideline 29: Date Specificity addresses measures that include date requirements in order to achieve numerator compliance. Dates must be specific enough to determine that the event occurred during the period specified by the measure. 

 

This applies to the following Programs and Years:
IHA P4P

5.15.2014 MEM exception for members with no financial liability Is there an exception for MEM 3A and MEM 5A, factor 4 if members have no financial liability beyond a flat copay that is always the same fixed dollar amount and is specified on the organization’s Web site?

Yes, if the flat copay amount is specified on the organization’s Web site. Members must have no additional financial liability (i.e. co-insurance, deductibles, charges in excess of allowed amounts, differentials in cost between in-network care and out-of-network care, costs that vary for the formulary) for services and cannot be balance-billed by a practitioner, provider or other party.

This exception does not apply to Element B in MEM 3 and 5.

This applies to the following Programs and Years:

5.15.2014 Marketplace How will HEDIS work with the Marketplace products?

For Marketplace (Exchange) products, HEDIS will follow the federal Marketplace Quality Rating System (QRS). CMS will release QRS measure specifications and reporting guidelines (including HEDIS) in September 2014.

 

This applies to the following Programs and Years:
Exchange 2015