HIS Manual - CMS

1 21244-1850. OMB Control # OMB Control Number 0938-1153 Expiration 02/29/2024 HIS Manual Guidance Manual for Completion of the hospice Item Set (HIS) Centers for Medicare and Medicaid Services hospice quality Reporting Program Effective February 1 6, 2021 According to the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for this information collection is 0938-1153. The time required to complete this information collection is estimated to average 14 minutes per response for the HIS-Admission and 9 minutes per response for the HIS-Discharge, including the time to review instructions, search existing data resources, gather the data needed, and complete and review the information collection.

2 If you have comments concerning the accuracy of the time estimate(s) or suggestions for improving this form, please write to: CMS, 7500 Security Boulevard, Attn: PRA Reports Clearance Officer, Mail Stop C4 -26-05, Baltimore, Maryland 21244-1850. OMB Control # 0938-1153 [This page intentionally left blank.] Page i TABLE OF CONTENTS TABLE OF CONTENTS .. i CHAPTER 1: Background and Overview of the hospice Item Set Manual .. 1-1 Background and Statutory Authority .. 1-1 Manual Overview .. 1-2 HIS Requirements and Reporting Years .. 1-2 Applicable Facilities and Requirements for New Facilities .. 1-5 Applicable Patients.

3 1-5 Record Types and Definitions .. 1-5 Timing and Sequence Policies .. 1-8 Maintenance of HIS Records .. 1-12 Compliance with HQRP Requirements and APU Determinations .. 1-12 CHAPTER 2: Item -Specific Instructions .. 2-1 Overview .. 2-1 HIS Item Completion Conventions .. 2-2 Section A: Administrative Information .. 2A-1 Section F: Preferences .. 2F-1 Section I: Active Diagnoses .. 2I-1 Section J: Health Conditions .. 2J-1 Section N: Medications .. 2N-1 Section Z: Record Administration .. 2Z-1 CHAPTER 3: Submission and Correction of hospice Item Set Records .. 3-1 Submitting HIS Records .. 3-1 Timeliness Criteria .. 3-1 Validation of Records and Files.

4 3-2 HIS Record Correction Policy .. 3-4 Correcting Errors in HIS Records That Have Not Yet Been Accepted into the QIES ASAP System .. 3-5 Correcting Errors in HIS Records That Have Been Accepted into the QIES ASAP System .. 3-5 Special Manual Record Deletion Request .. 3-9 List of Appendices A: Acronyms And Glossary ..A-1 B: C MS hospice quality Reporting Program C: quality measure Logical Specifications .. C-1 D(a): hospice Item Set Admission .. D(a)-1 D(b): hospice Item Set Discharge .. D(b)-1 Effective February 16, 2021 [This page intentionally left blank.] Page 1-1 CHAPTER 1: BACKGROUND AND OVERVIEW OF THE hospice ITEM SET Manual Background and Statutory Authority Section 3004 of the Patient Protection and Affordable Car e Act ( ACA) authorizes the Health and Hum an Services Secretary to establish a quality reporting program for hospices.

5 The ACA specifies that, for fiscal year (FY) 2014 and each subsequent FY, hospice programs shall submit to the Secretary data on quality measures; th e ACA also describes measure endorsement requirements for any measures specified by the Secretary. A hospice is not required to obtain patient consent to collect dat a for quality measures for th e hospice quality Reporting Program (HQRP) because th e Centers for Medicare & Medicaid Services (CMS ) has th e statutory authority to collect quality data for hospices under Secti on 3004(c) of the ACA. CMS established th e HQRP in the FY 2012 hospice Wage Index final rul e (7 6 FR 47318-47324).

6 CMS finalized the requirement for the hospice Item Set (HIS) as part of t he HQRP in the FY 2014 hospice Wag e Index final rul e (78 FR 48255-48262). Medicare-certifi ed hospices (hospices) will submit a HIS -Admission recor d and a HIS -Discharge recor d for each patient admission on or after July 1, 2 014. Hospices will cont inu e to collect and submit HIS data on all patient admissions; HIS data will be submitted to CMS on a regular and ongoing basis from July 1, 2 014, onward. As also required by the ACA, the Secretary is required to establish procedures for making quality data submitted by hospices available to the public.

7 CMS will implement public reporting of quality data through the establishment of a Care Compare website. Policies and procedures for Care Compare will be proposed and finalized by CMS through rulemaking. The HIS is a standardized set of i tems intended to capture patient-level data on each hospice patient admission. quality measures based on the HIS items are described in the HQRP quality Measures (QM) User s Manual , available in the downloads section of the HQRP Current Measures web page: Please note that the HIS is not an assessment instrument and does not replace a thorough and ongoing assessment of e ach patient as required by the Medicare hospice Conditions of P articipation, nor does it r eplace standard clinical practice and judgment.

8 Effective February 16, 2021 HIS Manual Chapter 1: Introduction Page 1-2 Manual Overview The purpose of the HIS Manual is to offer hospices guidance on the collection and submission of HIS data to CMS. The Manual is divided into three chapters and appendices: Chapter 1 Provides an introduction of contextual information, timing and sequence policies, and general guidance. Chapter 2 Contains item-specific guidance for completing each item in the HIS. Chapter 3 Includes information on HIS record submission and correction processes. Appendices Include the HIS -Admission and HIS-Discharge, glossary, and resources. HIS Requirements and Reporting Years Hospices shall submit two HIS records (a HIS -Admission record and a HIS -Discharge record) for each patient admission occurring on or after July 1, 2014.

9 HIS reporting consists of three primary activities: HIS data collection, HIS record conversion, and HIS record submission. See Figure 1. Effective February 16, 2021 HIS Manual Chapter 1: Introduction Page 1-3 Figure 1: Three primary phases of HIS reporting HIS data collection consists of selecting responses to HIS items in conjunction with patient assessment activities or via abstraction from the patient s clinical record. HIS data may be collected on paper forms or using an electronic health record, but prior to submission, HIS data must be converted into the proper electronic file format (XML), which is necessary for successful submission.

10 To convert HIS records into the proper XML file format, providers can use either the hospice Abstraction Reporting Tool (HART) software, which is free to download and use (available at ), or a vendor-designed software. Once HIS records are converted, files are submitted to CMS via the quality Improvement and Evaluation System (QIES) Assessment Submission and Processing (ASAP) system. Records should be completed and submitted according to the time frames outlined in Section , Timing and Sequence Policies. Although this Manual contains general HIS record completion and submission policies, it does not contain detailed information about conversion and submission software and procedures.