Difference between revisions of "E9-31216"

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This is an electronic, anotated copy of a document available at:
+
This is an electronic, annotated copy of a document available at:
http://edocket.access.gpo.gov/2010/pdf/E9-31216.pdf
+
http://edocket.access.gpo.gov/2010/pdf/E9-31216.pdf and at
 +
http://edocket.access.gpo.gov/2010/E9-31216.htm
  
 
== Title Page ==
 
== Title Page ==
Line 9: Line 10:
 
  of Standards, Implementation
 
  of Standards, Implementation
 
  Specifications, and Certification Criteria
 
  Specifications, and Certification Criteria
  for Electronic Health Record Technology;
+
  for Electronic Health [[Record~|Record]] Technology;
 
  Interim Final Rule
 
  Interim Final Rule
  
Line 21: Line 22:
 
  RIN 0991–AB58
 
  RIN 0991–AB58
  
Health Information Technology: Initial Set of Standards, Implementation Specifications, and Certification Criteria for Electronic Health Record Technology
+
Health Information Technology: Initial Set of Standards, Implementation Specifications, and Certification Criteria for Electronic Health [[Record~|Record]] Technology
  
 
  AGENCY: Office of the National
 
  AGENCY: Office of the National
Line 27: Line 28:
 
  Technology, Department of Health and
 
  Technology, Department of Health and
 
  Human Services.
 
  Human Services.
  ACTION: Interim final rule.
+
  [[ACTION~|Action]]: Interim final rule.
  
 
== Summary ==
 
== Summary ==
Line 35: Line 36:
 
This interim final rule represents the first step in an incremental approach to adopting standards, implementation specifications, and certification criteria to enhance the interoperability, functionality, utility, and security of health information technology and to support its meaningful use.
 
This interim final rule represents the first step in an incremental approach to adopting standards, implementation specifications, and certification criteria to enhance the interoperability, functionality, utility, and security of health information technology and to support its meaningful use.
  
The certification criteria adopted in this initial set establish the capabilities and related standards that certified electronic health record (EHR) technology will need to include in order to, at a minimum, support the achievement of the proposed meaningful use Stage 1 (beginning in 2011) by eligible professionals and eligible hospitals under the Medicare and Medicaid EHR Incentive Programs.
+
The certification criteria adopted in this initial set establish the capabilities and related standards that certified electronic health [[record~|Record]] (EHR) technology will need to include in order to, at a minimum, support the achievement of the proposed meaningful use Stage 1 (beginning in 2011) by eligible professionals and eligible hospitals under the Medicare and Medicaid EHR Incentive Programs.
  
 
== DATES: ==
 
== DATES: ==
Line 105: Line 106:
 
== SUPPLEMENTARY INFORMATION: ==
 
== SUPPLEMENTARY INFORMATION: ==
  
=== Acronyms ===
+
{{:E9-31216 Acronyms}}
;AHIC
 
:American Health Information Community
 
;ANSI
 
:American National Standards Institute
 
;ASP
 
:Application Service Provider
 
;CAH
 
:Critical Access Hospital
 
;CCD
 
:Continuity of Care Document
 
;CCHIT
 
:Certification Commission for Health Information Technology
 
;CCR
 
:Continuity of Care Record
 
;CDA
 
:Clinical Document Architecture
 
;CDC
 
:Centers for Disease Control and Prevention
 
;CFR
 
:Code of Federal Regulations
 
;CGD
 
:Certification Guidance Document
 
;CMS
 
:Centers for Medicare & Medicaid Services
 
;CPOE
 
:Computerized Provider Order Entry
 
;EHR
 
:Electronic Health Record
 
;FIPS
 
:Federal Information Processing Standards
 
;GIPSE
 
:Geocoded Interoperable Population Summary Exchange
 
;HHS
 
:Department of Health and Human Services
 
;HIPAA
 
:Health Insurance Portability and Accountability Act of 1996
 
;HIT
 
:Health Information Technology
 
;HITECH
 
:Health Information Technology for Economic and Clinical Health
 
;HITSP
 
:Healthcare Information Technology Standards Panel
 
;HL7
 
:Health Level Seven
 
;ICD
 
:International Classification of Diseases
 
;ICD–9–CM
 
:ICD, 9th Revision, Clinical Modifications
 
;ICD–10–PCS
 
:ICD, 10th Revision, Procedure Coding System
 
;ICD–10–CM
 
:ICD, 10th Revision, Related Health Problems
 
;IHS
 
:Indian Health Service
 
;LOINC
 
:Logical Observation Identifiers Names and Codes
 
;MA
 
:Medicare Advantage
 
;NCPDP
 
:National Council for Prescription Drug Programs
 
;NCVHS
 
:National Committee on Vital and Health Statistics
 
;NLM
 
:National Library of Medicine
 
;NQF
 
:National Quality Forum
 
;OASIS
 
:Organization for the Advancement of Structured Information Standards
 
;OCR
 
:Office for Civil Rights
 
;OIG
 
:Office of Inspector General
 
;OMB
 
:Office of Management and Budget
 
;ONC
 
:Office of the National Coordinator for Health Information Technology
 
;PHSA
 
:Public Health Service Act
 
;PQRI
 
:Physician Quality Reporting Initiative
 
;REST
 
:Representational state transfer
 
;RFA
 
:Regulatory Flexibility Act
 
;SDOs
 
:Standards Development Organizations
 
;SNOMED CT
 
:Systematized Nomenclature of Medicine Clinical Terms
 
;SOAP
 
:Simple Object Access Protocol
 
;UCUM
 
:Unified Code for Units of Measure
 
;UMLS
 
:Unified Medical Language System
 
;UNII
 
:Unique Ingredient Identifier
 
;XML
 
:eXtensible Markup Language
 
  
= Table of Contents =
+
{{:E9-31216 TOC}}
== I. Background ==
 
=== A. ONC Background ===
 
=== B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities ===
 
==== 1. Medicare and Medicaid EHR Incentive Programs Proposed Rule ====
 
==== 2. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy Rule Accounting of Disclosures Regulation ====
 
==== 3. Previous Recognition of Certification Bodies and New Authority Under the HITECH Act ====
 
==== 4. Other HHS Regulatory Actions ====
 
===== a. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Transactions and Code Sets Standards =====
 
===== b. Electronic Prescribing Standards =====
 
=== C. Standards, Implementation Specifications, and Certification Criteria Processes Before and After the HITECH Act ===
 
==== 1. ONC’s Processes Prior to the HITECH Act ====
 
==== 2. HITECH Act Requirements for the Adoption of Standards, Implementation Specifications, and Certification Criteria ====
 
=== D. Future Updates to Standards, Implementation Specifications, and Certification Criteria ===
 
== II. Overview of the Interim Final Rule ==
 
== III. Section-By-Section Description of the Interim Final Rule ==
 
=== A. Applicability ===
 
=== B. Definitions ===
 
==== 1. Definition of Standard ====
 
==== 2. Definition of Implementation Specification ====
 
==== 3. Definition of Certification Criteria ====
 
==== 4. Definition of Qualified Electronic Health Record (EHR) ====
 
==== 5. Definition of EHR Module ====
 
==== 6. Definition of Complete EHR ====
 
==== 7. Definition of Certified EHR Technology ====
 
==== 8. Definition of Disclosure ====
 
=== C. Initial Set of Standards, Implementation Specifications, and Certification Criteria ===
 
==== 1. Adopted Certification Criteria ====
 
==== 2. Adopted Standards ====
 
===== a. Transport Standards =====
 
===== b. Content Exchange and Vocabulary Standards =====
 
====== i. Patient Summary Record ======
 
====== ii. Drug Formulary Check ======
 
====== iii. Electronic Prescribing ======
 
====== iv. Administrative Transactions ======
 
====== v. Quality Reporting ======
 
====== vi. Submission of Lab Results to Public Health Agencies ======
 
====== vii. Submission to Public Health Agencies for Surveillance or Reporting ======
 
====== viii. Submission to Immunization Registries ======
 
====== ix. Table 2A ======
 
===== c. Privacy and Security Standards =====
 
==== 3. Adopted Implementation Specifications ====
 
==== 4. Additional Considerations, Clarifications, and Requests for Public Comments ====
 
===== a. Relationship to Other Federal Laws =====
 
===== b. Human Readable Format =====
 
===== c. Certification Criterion and Standard Regarding Accounting of Disclosures =====
 
===== d. Additional Requests for Public Comment =====
 
== IV. Collection of Information Requirements ==
 
== V. Regulatory Impact Analysis ==
 
=== A. Introduction ===
 
=== B. Why Is This Rule Needed? ===
 
=== C. Costs and Benefits ===
 
==== 1. Costs ====
 
==== 2. Benefits ====
 
=== D. Regulatory Flexibility Act Analysis ===
 
=== E. Executive Order 13132—Federalism ===
 
=== F. Unfunded Mandates Reform Act of 1995 Regulation Text ===
 

Latest revision as of 18:07, 29 July 2012

This is an electronic, annotated copy of a document available at: http://edocket.access.gpo.gov/2010/pdf/E9-31216.pdf and at http://edocket.access.gpo.gov/2010/E9-31216.htm

Contents

Title Page

Part III
Department of Health and Human Services
45 CFR Part 170
Health Information Technology: Initial Set
of Standards, Implementation
Specifications, and Certification Criteria
for Electronic Health Record Technology;
Interim Final Rule


Header

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
45 CFR Part 170
RIN 0991–AB58

Health Information Technology: Initial Set of Standards, Implementation Specifications, and Certification Criteria for Electronic Health Record Technology

AGENCY: Office of the National
Coordinator for Health Information
Technology, Department of Health and
Human Services.
Action: Interim final rule.

Summary

The Department of Health and Human Services (HHS) is issuing this interim final rule with a request for comments to adopt an initial set of standards, implementation specifications, and certification criteria, as required by section 3004(b)(1) of the Public Health Service Act.

This interim final rule represents the first step in an incremental approach to adopting standards, implementation specifications, and certification criteria to enhance the interoperability, functionality, utility, and security of health information technology and to support its meaningful use.

The certification criteria adopted in this initial set establish the capabilities and related standards that certified electronic health Record (EHR) technology will need to include in order to, at a minimum, support the achievement of the proposed meaningful use Stage 1 (beginning in 2011) by eligible professionals and eligible hospitals under the Medicare and Medicaid EHR Incentive Programs.

DATES:

Effective Date: This interim final rule is effective February 12, 2010. The incorporation by reference of certain publications listed in the rule is approved by the Director of the Federal Register as of February 12, 2010.

Comment Date: To be assured consideration, written or electronic comments must be received at one of the addresses provided below, no later than 5 p.m. on March 15, 2010.

ADDRESSES:

Because of staff and resource limitations, we cannot accept comments by facsimile (FAX) transmission.

You may submit comments, identified by RIN 0991–AB58, by any of the following methods (please do not submit duplicate comments).

  • Federal eRulemaking Portal:
 Follow the instructions for submitting comments.
 Attachments should be in Microsoft Word, WordPerfect, or Excel;
 however, we prefer Microsoft Word. http://www.regulations.gov.
  • Regular, Express, or Overnight Mail:
 Department of Health and Human Services, 
 Office of the National Coordinator for Health Information Technology, 
 Attention: HITECH Initial Set Interim Final Rule,
 Hubert H. Humphrey Building,
 Suite 729D,
 200 Independence Ave., SW.,
 Washington, DC 20201. 
Please submit one original and two copies.
  • Hand Delivery or Courier:
 Office of the National Coordinator for Health Information Technology,
 Attention: HITECH Initial Set Interim Final Rule,
 Hubert H. Humphrey Building,
 Suite 729D,
 200 Independence Ave., SW.,
 Washington, DC 20201.
Please submit one original and two copies. 
(Because access to the interior of the Hubert H. Humphrey Building is not readily available to persons without federal government identification, commenters are encouraged to leave their comments in the mail drop slots located in the main lobby of the building.)

Inspection of Public Comments:

All comments received before the close of the comment period will be available for public inspection, including any personally identifiable or confidential business information that is included in a comment.

Please do not include anything in your comment submission that you do not wish to share with the general public.

Such information includes, but is not limited to: A person’s social security number; date of birth; driver’s license number; state identification number or foreign country equivalent; passport number; financial account number; credit or debit card number; any personal health information; or any business information that could be considered to be proprietary.

We will post all comments received before the close ofthe comment period at http://www.regulations.gov.

Docket:

For access to the docket to read background documents or comments received, go to http:// www.regulations.gov

or

U.S. Department of Health and Human Services,
Office of the National Coordinator for Health Information Technology,
Hubert H. Humphrey Building, Suite 729D,
200 Independence Ave., SW.,
Washington, DC 20201
(call ahead to the contact listed below to arrange for inspection).

FOR FURTHER INFORMATION CONTACT:

Steven Posnack,
Policy Analyst,
202–690–7151.

SUPPLEMENTARY INFORMATION:

Acronyms

AHIC
American Health Information Community
ANSI
American National Standards Institute
ASP
Application Service Provider
CAH
Critical Access Hospital
CCD
Continuity of Care Document
CCHIT
Certification Commission for Health Information Technology
CCR
Continuity of Care Record
CDA
Clinical Document Architecture
CDC
Centers for Disease Control and Prevention
CFR
Code of Federal Regulations
CGD
Certification Guidance Document
CMS
Centers for Medicare & Medicaid Services
CPOE
Computerized Provider Order Entry
EHR
Electronic Health Record
FIPS
Federal Information Processing Standards
GIPSE
Geocoded Interoperable Population Summary Exchange
HHS
Department of Health and Human Services
HIPAA
Health Insurance Portability and Accountability Act of 1996
HIT
Health Information Technology
HITECH
Health Information Technology for Economic and Clinical Health
HITSP
Healthcare Information Technology Standards Panel
HL7
Health Level Seven
ICD
International Classification of Diseases
ICD–9–CM
ICD, 9th Revision, Clinical Modifications
ICD–10–PCS
ICD, 10th Revision, Procedure Coding System
ICD–10–CM
ICD, 10th Revision, Related Health Problems
IHS
Indian Health Service
LOINC
Logical Observation Identifiers Names and Codes
MA
Medicare Advantage
NCPDP
National Council for Prescription Drug Programs
NCVHS
National Committee on Vital and Health Statistics
NLM
National Library of Medicine
NQF
National Quality Forum
OASIS
Organization for the Advancement of Structured Information Standards
OCR
Office for Civil Rights
OIG
Office of Inspector General
OMB
Office of Management and Budget
ONC
Office of the National Coordinator for Health Information Technology
PHSA
Public Health Service Act
PQRI
Physician Quality Reporting Initiative
REST
Representational state transfer
RFA
Regulatory Flexibility Act
SDOs
Standards Development Organizations
SNOMED CT
Systematized Nomenclature of Medicine Clinical Terms
SOAP
Simple Object Access Protocol
UCUM
Unified Code for Units of Measure
UMLS
Unified Medical Language System
UNII
Unique Ingredient Identifier
XML
eXtensible Markup Language

Table of Contents

I. Background

E9-31216 I

A. ONC Background

E9-31216 I A

B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities

B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities

The HITECH Act creates multiple interdependencies between this interim final rule and other regulatory requirements, processes, and programs.

1. Medicare and Medicaid EHR Incentive Programs Proposed Rule

E9-31216 I B 1

2. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy Rule Accounting of Disclosures Regulation

E9-31216 I B 2

3. Previous Recognition of Certification Bodies and New Authority Under the HITECH Act

E9-31216 I B 3

4. Other HHS Regulatory Actions

Other HHS Regulatory Actions

a. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Transactions and Code Sets Standards

E9-31216 I B 4 a

b. Electronic Prescribing Standards

E9-31216 I B 4 b

C. Standards, Implementation Specifications, and Certification Criteria Processes Before and After the HITECH Act

1. ONC’s Processes Prior to the HITECH Act

E9-31216 I C 1

2. HITECH Act Requirements for the Adoption of Standards, Implementation Specifications, and Certification Criteria

E9-31216 I C 2

D. Future Updates to Standards, Implementation Specifications, and Certification Criteria

E9-31216 I D

II. Overview of the Interim Final Rule

E9-31216 II

III. Section-By-Section Description of the Interim Final Rule

A. Applicability

A. Applicability--Sec. 170.101

This part establishes the applicable standards, implementation specifications, and certification criteria that must be used to test and certify HIT.

B. Definitions

B. Definitions--Sec. 170.102

1. Definition of Standard

E9-31216 III B 1

2. Definition of Implementation Specification

E9-31216 III B 2

3. Definition of Certification Criteria

E9-31216 III B 3

4. Definition of Qualified Electronic Health Record (EHR)

E9-31216 III B 4

5. Definition of EHR Module

E9-31216 III B 5

6. Definition of Complete EHR

E9-31216 III B 6

7. Definition of Certified EHR Technology

E9-31216 III B 7

8. Definition of Disclosure

E9-31216 III B 8

C. Initial Set of Standards, Implementation Specifications, and Certification Criteria

E9-31216 III C

1. Adopted Certification Criteria

E9-31216 III C 1

2. Adopted Standards

E9-31216 III C 2

a. Transport Standards

E9-31216 III C 2 a

b. Content Exchange and Vocabulary Standards

E9-31216 III C 2 b

i. Patient Summary Record

E9-31216 III C 2 b i

ii. Drug Formulary Check

E9-31216 III C 2 b ii

iii. Electronic Prescribing

E9-31216 III C 2 b iii

iv. Administrative Transactions

E9-31216 III C 2 b iv

v. Quality Reporting

E9-31216 III C 2 b v

vi. Submission of Lab Results to Public Health Agencies

E9-31216 III C 2 b vi

vii. Submission to Public Health Agencies for Surveillance or Reporting

E9-31216 III C 2 b vii

viii. Submission to Immunization Registries

E9-31216 III C 2 b viii

ix. Table 2A

E9-31216 III C 2 b ix

c. Privacy and Security Standards

E9-31216 III C 2 c

3. Adopted Implementation Specifications

E9-31216 III C 3

4. Additional Considerations, Clarifications, and Requests for Public Comments

E9-31216 III C 4

a. Relationship to Other Federal Laws

E9-31216 III C 4 a

b. Human Readable Format

E9-31216 III C 4 b

c. Certification Criterion and Standard Regarding Accounting of Disclosures

E9-31216 III C 4 c

d. Additional Requests for Public Comment

E9-31216 III C 4 d

IV. Collection of Information Requirements

E9-31216 IV

V. Regulatory Impact Analysis

E9-31216 V

A. Introduction

E9-31216 V A

B. Why Is This Rule Needed?

E9-31216 V B

C. Costs and Benefits

E9-31216 V C

1. Costs

E9-31216 V C 1

2. Benefits

E9-31216 V C 2

D. Regulatory Flexibility Act Analysis

E9-31216 V D

E. Executive Order 13132—Federalism

E9-31216 V E

F. Unfunded Mandates Reform Act of 1995 Regulation Text

E9-31216 V F