Form CMS-10519 PQRS Data Validation Electronic Survey

(CMS-10519) Physician Quality Reporting System and the Electronic Prescribing Incentive Program Data Assessment, Accuracy and Improper Payments Identification Support

PQRS Data Validation Electronic Survey - Att-D-Survey_v1.1

PQRS Data Validation Project Electronic Survey

OMB: 0938-1255

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Physician Quality Reporting System (PQRS) and Electronic Prescribing Incentive (eRx) Program Data Assessment, Accuracy and Improper Payments Identification Support Contract













Sponsored by:

U.S. Department of Health and Human Services,

Centers for Medicare & Medicaid Services








Public Burden Statement: According to the Paperwork Reduction Act of 1995, a federal agency may not conduct, and a person is not required to respond to, an information collection request unless it displays a currently valid OMB control number. The valid OMB control number for this information collection is [XXXX-XXXX]. The time required to complete this information collection is estimated to average 15 minutes per respondent, including the time to review instructions and complete and review the information collection. If you have comments concerning the accuracy of this burden estimate or any suggestions for reducing this burden, please write to: CMS, 7500 Security Boulevard, Attn: PRA Reports Clearance Officer, Mail Stop C4-26-05, Baltimore, MD 21244-1850.

OMB No.: [xxxx-xxxx]

Expires: [3 yrs from OMB approval date]




Participation in this Survey


Your participation is requested on an important survey. As a GPRO/Registry that submits data to the Centers for Medicare & Medicaid Services (CMS) as part of the Physician Quality Reporting System (PQRS)/eRx program, we require your assistance in evaluating features of these programs. This survey consists of 43 GPRO questions and 44 Registry questions regarding how GPROs/Registries collect, validate, and submit data that are reported through the PQRS/eRx program. The questions will guide you through a systematic assessment of your data handling practices and help you identify opportunities for improvement and more accurate future reporting. The survey includes both an online and an interview component. We estimate that participation can be accomplished in less than 2 hours, inclusive of minimal time for preparation and follow up.

This is a voluntary survey. It is designed to measure the (1) data handling by GPROs (or Registries) and CMS and its contractors, (2) clinical quality measures results accuracy, and (3) payment error. Information from participating GPROs and Registries will help formulate PQRS program integrity features that could result in clearer information shared by CMS for future reporting periods. We are genuinely interested in your candid observations of the way your program operates today. If you are willing to participate in this activity, please complete this survey by _____, 2014. If you have difficulty or questions when completing this survey, please contact ____________________ or xxx-xxx-xxxx.

The Questions in this Survey

This survey asks how your organization currently manages data errors and, inconsistencies that are due to data handling, program requirements or changes in measures or specifications. The questions are organized into six sections:


Section 1: Corporate Information asks you to identify demographic and organizational characteristics..

Section 2: Training asks what knowledge, skills, behavior or other learned capabilities are required of your staff or presented in structured training programs.

Section 3: Data handling asks you to describes your process for the transfer of data from one system to another, such as from the provider or the intermediary to CMS, or from the provider to the intermediary.

Section 4: Quality Assurance asks you to describe and comment on your quality assurance processes and your approach to improving quality.

Section 5: eRX


Section 6: Feedback: This section was created for you to provide feedback on the program to CMS. Use this section to enter evaluative or corrective comments.



GPRO Survey

The questions for the GPRO Survey appear in Table 1.


GPRO Survey Questions

Item #

Question

Question Type

Corporate Information

Name

Text input

Practice or Company Name

Auto populate

Address

Auto populate

Telephone

Auto populate

E-mail address

Auto populate

GPRO name

Auto populate

GPRO TIN

Auto populate with Last 4 digits of the TIN only

Did you participate as an eRx GPRO?

Auto populate, if possible, otherwise: Yes or No.

If Yes, select the eRx reporting option:

  • Claims

  • Qualified Registry

  • Qualified direct EHR product

  • Qualified EHR data submission vendor

If the EHR reporting option was not selected, please explain why your organization has not used it.

If the answer is “Yes”, the eRx tab will be accessible. If the answer is “No”, the eRx tab will be inaccessible.

Number of eligible professionals?

Drop down list:

  • 25-99 Eligible Professionals

  • >100 Eligible Professionals

Training

Do you have education and credentialing requirements for staff that perform chart abstraction?

Yes or No.

How do you train staff to understand measures and perform chart abstraction?

Check all that apply:

  • Vendor-supplied training.

  • Group or classroom setting.

  • One-on-one.

  • Virtual class room.

  • Individual online training.

  • If selecting virtual classroom or individual online training, specify name of training program and URL.

  • Other, specify __

  • Do not provide training.

Do you have written processes and procedures for chart abstraction training?

Yes or No.

If Yes, please upload a copy of your training policy and procedure document.

During the training, how do you validate that the chart abstraction done by the trainee is accurate?


Check all that apply:

  • Practice cases performed during training.

  • Abstractor over-reads (i.e., re-review of abstracted data) in the training environment.

  • What percentage of over-reads are performed (numeric input)?

  • What is your organization’s acceptable error rate (numeric input)?

  • How are records selected for over-reads (numeric input)?

  • Other, specify ___

  • None

Do you have written process and procedures for data conversion (e.g. converting data abstracted from paper medical record to GPRO Web Interface) training?

Yes or No.

If Yes, please upload a copy of your training policy and procedure document.

Do you have written processes and procedures for data reporting (e.g. populating the GPRO Web Interface) training?

Yes or No.

If Yes, please upload a copy of your training policy and procedure document.

Do you use any written training material on the eRx Incentive Program?

Yes or No.

If Yes, please upload document.

What training did you provide to eligible professionals/staff on the eRx program requirements (e.g. both the electronic prescribing denominator CPT codes and the numerator G-code (G8553) must be reported and the provider must have adopted a qualified electronic prescribing (eRx) system)?

Check all that apply:

  • Group or classroom setting.

  • One-on-one.

  • Virtual class room.

  • Individual online training.

  • Email.

  • Other, specify __.

  • Do not provide training.

Data Handling

Do you import the beneficiary list from the GPRO web interface to assist with chart abstraction?

Yes or No.


If yes,

Do you convert the XML file to excel?

Yes or No.

Do you verify that the beneficiary assignment matches your information?

Yes or No.

What are your methods of chart abstraction?

Check all that apply:

  • Manual paper chart abstraction

  • Automated EHR query

  • Web portal

  • Medical Record Abstraction Tool

  • Database

  • Other, specify

How many information systems do you need to access for chart abstraction (e.g., EHRs, paper charts, lab systems, registries)?

Insert numeric input ___

Do you use a tool to collect and store abstracted data prior to entering it into the XML file and/or GPRO Web Interface?


a) Electronic tool name (or vendor)

b) Does the tool do validations and calculate performance?

c) For NO, please select how you input abstracted data?



Yes or No. If Yes, continue to question 22a & 22b. If No, continue to:


a)Tool name or vendor __________________.


b)Yes or No

c)Check all that apply

  • Electronically import into XML file

  • Manually key in data into XML file

  • Manually input data into the Web Interface

  • Other

Do you exclude members for any reason other than what is in the technical specifications?

Yes or No.

If Yes, explain by measure your reason for excluding members.

Do you manually enter or upload data into the GRPO Web Interface?

Drop down list

  • Manually enter

  • Upload data

  • Both

If you encounter errors uploading data to the GPRO Web Interface, what type are they?


Input types of errors.

Have you enabled the data validation Errors and Warning in the GPRO Web Interface?


Yes or No


Do you encounter data validation Errors and Warning in the GPRO Web Interface?

Check all that apply:

Populate missing values

Correct reporting period

Investigate inconsistencies between similar elements

Other, please specify

If you have not enabled the data validation Errors and Warning in the GPRO Web Interface, then how do you resolve the error?

Please describe

Are there measures that consistently have Errors and Warning messages in the GPRO Web Interface?

Yes or No

If yes, please describe the type of Error and Warnings messages associated with these measures

Quality Assurance

Do you have written processes and procedures to ensure that accurate data is abstracted?

If Yes, is the process followed consistently?

Yes or No.

Yes or No.

If Yes, please upload a copy of your policy and procedure document.

Do you have written processes and procedures to ensure that accurate data is uploaded into the Web Interface?

If, Yes, is the process followed consistently?

Yes or No.

Yes or No.


If Yes, please upload a copy of your policy and procedure document.

Do you have written processes and procedures to ensure that accurate data is reported to CMS?

If, Yes, is the process followed consistently?

Yes or No.

If Yes, please upload a copy of your policy and procedure document.

Is there someone at your practice supporting quality assurance to ensure that the data is validated before transmission to CMS?

Yes or No.

If Yes, what is that person’s position in your practice?

Do you provide any oversight for chart abstraction done in the field?

Check all that apply:

  • Abstractor over-reads (i.e., re-review of abstracted data) in the field.

  • What percentage of over-reads are performed (numeric input)?

  • What is your organization’s acceptable error rate (numeric input)?

  • How are records selected for over-reads (numeric input)?

  • Other, specify ___

  • None.

Describe how you provide technical assistance and/or train staff on how to respond to questions that arise during chart abstraction.


Check all that apply:

  • One-on-one consultation

  • Ask a supervisor or super-user

  • Online training manual

  • Help line

  • Other, specify ___

  • None

eRx

Do you have a process in place to verify that a qualified electronic prescribing (eRx) system was adopted by eligible professionals who report meeting the eRx Incentive Program requirements?

Yes/No

If Yes, please describe your process or upload your document.

Do you have any audit checks in place to ensure that eligible professionals have actually generated and transmitted an electronic prescription when they report G-code G8553?

Yes/No

If Yes, please describe your process or upload your document.

GPRO Feedback

What do you perceive to be the biggest challenge in reporting accurate and complete data to CMS?

Fill in the blank, or upload document.

Describe any process improvement activities used to increase your organization’s reporting accuracy.

Fill in the blank.

Describe the issues you have observed with the feedback reports

Fill in the blank.

Do you find the informal review process beneficial for resolving any issues? If no, describe the difficulties.

Fill in the blank.

Describe the issues and challenges you have faced with the GPRO Web Interface.

Fill in the blank.

Which measures were the most problematic for your chart abstractors?

Check all that apply:

List GPRO measures in drop down list.

Table 1: GPRO Survey Questions



Registry Survey

The questions for the Registry Survey appear in Table 2.


Item #

Question

Question Type


Registry Information


Name

Text input


Practice or Company Name

Auto populate


Address

Auto populate


Telephone

Auto populate


E-mail address

Auto populate


Registry name

Auto populate


Registry TIN

Auto populate with Last 4 digits of the TIN only


Number of eligible providers reporting for PQRS?


Numeric input.


Training Information


How do you train staff to understand clinical measure specifications?

Check all that apply:

  • Group or classroom setting.

  • One-on-one.

  • Virtual class room.

  • Individual online training.

  • If selecting virtual classroom or individual online training, specify name of training program and URL.

  • Other, specify __

  • Do not train staff.


How do you train staff to understand calculated results?

Please describe process or upload document


How do you train staff to transfer data to XML

Please describe process or upload document


Do you have written processes and procedures for training staff to support eligible professionals’ who submit data to your registry?

Yes or No.

If Yes, please upload a copy of your policy and procedure document.


Do you have written process and procedures for calculating performance results using the PQRS measure specifications?

Yes or No.

If Yes, please upload a copy of your training policy and procedure document.


Do you have written processes and procedures for transferring results to XML?

Yes or No.

If Yes, please upload a copy of your training policy and procedure document.


What type of education do you provide to eligible professionals on the clinical measure specifications?

Check all that apply:

  • Group or classroom setting.

  • One-on-one.

  • Virtual class room.

  • Individual online training.

  • If selecting virtual classroom or individual online training, specify name of training program and URL.

  • Other, specify __

  • None


What training did you provide to eligible professionals on the eRx program requirements?

Check all that apply:

  • Group or classroom setting

  • One-on-one

  • Virtual class room

  • Individual online training

  • Email

Other, specify __

None


What training did you provide to staff that submit results for the eRx Incentive Program?

Check all that apply:

  • Group or classroom setting

  • One-on-one

  • Virtual class room

  • Individual online training

  • Other, specify __

  • Do not train staff



Data Handling


What type of tool do you use to collect data from eligible professionals?


Check all that apply:

  • Web Interface

  • XML

  • Direct data query

  • EHR

  • Other, specify ___


Do you use a tool to do validation checks and display performance for the eligible professional to confirm that the information is accurate? if no, answer question 20.

Yes or No.


How do you perform validation checks and display performance for the eligible professional to confirm that the information is accurate?

Please describe your process


Did your registry successfully pass use cases for all measures?

Yes or No.

If No, please describe steps taken to address use case errors.


Did your organization use the 2012 SEVT tool to test XML files?

Yes or No.


Are members excluded for any reason other than what is in the technical specifications?

Yes or No.

If Yes, explain by measure your reason for excluding members.


How many different file formats do EPs use to submit data?

Insert numeric input ___


What is the ETL process to aggregate patient level data into XML?

Fill in blank and upload data.


Do you analyze and update the XML specification changes for each program year?

Yes or No.

If yes, upload documentation that describes that process.


Do you analyze and update the measure specification changes for each program year?

Yes or No.

If yes, upload documentation that describes that process.


Quality Assurance


Do you validate accurate data is collected from eligible professionals?

If Yes, is the process followed consistently?

Yes or No.

Yes or No.

If Yes, please upload a copy of your policy and procedure document.


Do you validate that results are calculated correctly using the correct measure specifications?

If Yes, is the process followed consistently?

Yes or No.

If Yes, please upload a copy of your policy and procedure document.


Do you validate that results are accurately transferred to XML?

If Yes, is the process followed consistently?

Yes or No.

If Yes, please upload a copy of your policy and procedure document.


Do you validate to identify anomalies before you submit your data (e.g. numerator is greater than denominator)?

If Yes, is the process followed consistently?

Yes or No.

If Yes, please upload a copy of your policy and procedure document.


Is there someone at your organization who analyzes XML changes?

Yes or No.

If Yes, what is that person’s position in your practice?


Is there someone at your organization supporting quality assurance to ensure that the data is validated before transmission to CMS?

Yes or No.

If Yes, what is that person’s position in your practice?


Do you provide any oversight for calculating and maintaining measure specifications and algorithms?

Yes or No

If Yes, please describe that process.


How do you provide technical assistance and/or train staff on how to respond to questions that arise on measure specifications, measure calculations, and converting results to XML format.



Check all that apply:

  • One-on-one consultation

  • Ask a supervisor or super-user

  • Online training manual

  • Help line

  • Other, specify ___

  • None.


eRx


Do you have a process in place to verify that a qualified electronic prescribing (eRx) system was adopted by eligible professionals who report meeting the eRx Incentive Program requirements?

Yes/No

If Yes, please describe your process or upload your document.


Do you have any audit checks in place to ensure that eligible professionals have actually generated and transmitted an electronic prescription when they report G-code G8553?

Yes/No

If Yes, please describe your process or upload your document.



Registry Feedback

What do you perceive to be the biggest challenge in reporting accurate and complete data to CMS?

Fill in the blank, or upload document.

Describe any process improvement activities used to increase your organization’s reporting accuracy.

Fill in the blank.

Describe the issues you have observed with the feedback reports

Fill in the blank.

Do you find the informal review process beneficial for resolving any issues? If no, describe the difficulties.

Fill in the blank.

Describe the issues and challenges you have faced transferring data to XML.

Fill in the blank.

Which measures did eligible professionals find the most difficult to understand?

Fill in the blank.

Which measures did staff find the most difficult to program?

Fill in the blank.

Table 2: Registry Survey Questions


18


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