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Functional Requirements Description

Public Health Reporting Initiative

Consensus Approved

1

Public Health Reporting

Initiative Functional Requirements Description

9/25/2012

Functional Requirements Description

Public Health Reporting Initiative

Consensus Approved

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Table of Contents 1.0 Preface and Introduction .................................................................................................................. 2

2.0 Initiative Overview ............................................................................................................................ 3

2.1 Initiative Challenge Statement ...................................................................................................... 4

3.0 Use Case Scope ................................................................................................................................. 5

3.1 Background ................................................................................................................................... 6

3.2 In Scope ......................................................................................................................................... 6

3.3 Out of Scope .................................................................................................................................. 7

3.4 Communities of Interest ............................................................................................................... 8

3.5 Actors and Roles ......................................................................................................................... 10

4.0 Public Health Reporting Workflow ................................................................................................. 11

5.0 Functional Requirements ................................................................................................................ 21

5.1 Information Interchange Requirements ..................................................................................... 21

5.2 System Requirements ................................................................................................................. 22

5.3 Triggers ........................................................................................................................................ 23

6.0 Non-Functional Requirements ........................................................................................................ 24

7.0 Dependencies and Future Considerations ...................................................................................... 25

7.1 Dependencies .............................................................................................................................. 25

7.2 Additional Components and Considerations .............................................................................. 26

8.0 Dataset Requirements .................................................................................................................... 27

9.0 Standards Analysis .......................................................................................................................... 28

List of Figures:

Figure 1: Public Health Reporting Workflow ............................................................................................. 14

Figure 2: Public Health Reporting Workflow with Swimlanes .................................................................... 16

List of Tables:

Table 1: Public Health Reporting Communities of Interest ....................................................................... 10

Table 2: Public Health Reporting Actors and Roles .................................................................................... 11

Table 3: Details about Actions in the Public Health Reporting Workflow ................................................. 21

Table 4: Information Interchange Requirements ...................................................................................... 22

Table 5: Public Health Reporting General System Requirements .............................................................. 22

Table 6: Types of Non-Functional Requirements ....................................................................................... 24

Table 7: Types of Dependencies ................................................................................................................. 26

Table 8: Additional Considerations ............................................................................................................. 27

1.0 Preface and Introduction To fully realize the benefits of health IT, the Office of the National Coordinator for Health Information

Technology (ONC), as part of the Standards and Interoperability (S&I) Framework is developing Use

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Cases and associated functional requirements that define the requirements for health care data

exchange. The functional requirements document is used to specify requirements from a broad range of

stakeholders interested in a specific information exchange. Examples of stakeholders include but are

not limited to healthcare providers, EHR system vendors, public health organizations, and federal

agencies.

The functional requirements described in this document pertain to public health reporting data

exchange and help define:

• The operational context for the data exchange

• The stakeholders with an interest in specific user stories

• The information flows that must be supported by the data exchange

• The types of data and their required specifications for data exchange

The document provides the foundation for identifying and specifying the standards required to support

the data exchange, and facilitate development and/or identification of reference implementations and

tools needed to ensure consistent adoption and applicability of the data exchange standards across

user stories. This document is not intended to replace existing functional requirements or

implementation guides currently in use across the various public health reporting functions referenced

in this document.

2.0 Initiative Overview The Public Health Reporting Initiative (PHRI) is a community-led S&I Framework initiative focused on

harmonizing information exchange standards and creating implementation specifications for public

health 1 reporting from healthcare providers to public health agencies. Our goal is to create a

harmonized specification that can be used to help reduce costs and reporting burden of healthcare

providers to public health agencies. The new specification can be used to promote health information

technology (HIT) adoption and facilitate electronic public health reporting from EHR systems for a

variety of reporting scenarios.

The PHRI consolidated use case was derived using a sample of existing public health reporting scenarios

submitted by Public Health Reporting Initiative members. Some of the user stories submitted for this

initiative reflect current workflows and information flows, but others represent a proposed future state.

For this use case, “public health reporting” refers to provider-initiated information exchange between

healthcare providers such as private physician practices and hospitals to a public health agency. In

particular, this use case will address electronic transmission of EHR-generated or assisted healthcare

provider reports, and receipt or retrieval by the public health agency. Report content for this use case is

based upon patient-level EHR data that is extracted and/or reused to create compliant reports that

meet reporting criteria of the representative public health report types (domains) supported in the use

case.

1 The term “public health,” as used in this document, refers to public health and patient safety programs.

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In the short-term, the Initiative seeks to define criteria and requirements for improved data exchange

standards, specifications and validation rules for sending EHR-generated or assisted reports from a

healthcare provider to a public health agency. The long-term goals of the initiative include:

• Reduce variability in data exchange standards supported by different public health agency

systems covering the same or different jurisdictions

• Increase interoperability and data exchange from healthcare providers to public health agencies

• Reduce the burden on senders to create and manage different data exchanges based upon the

use of the same or similar source clinical or administrative data

• Reduce the burden on public health agencies to receive, extract, translate, load, and analyze

information contained in healthcare provider reports.

This document will build upon the existing use case document to define the functional and non-

functional requirements. In addition, this document references a data model and data element

mapping as outputs generated by harmonization of the user stories submitted under this initiative.

2.1 Initiative Challenge Statement Much public health reporting currently relies on paper forms that are mailed, emailed or faxed; thus

necessitating manual data collection and transmission by providers, and/or manual data entry and

coding by the public health agency prior to initiating analysis or follow-up. There is relatively little

nationwide standardization of public health electronic information exchange, although standardization

does seem to be increasing. . Even when reporting is performed electronically, there are multiple

regulatory or statutory requirements and implementation specifications that cover different reporting

activities. Varied reporting requirements and methods impose burdens on both healthcare providers

and public health agencies to support multiple formats and manage competing requirements defined by

mandated or voluntary reporting programs. Additionally, multiple data exchange standards used for

public health reporting (e.g., HL7 Versions 2.x and 3 messages and HL7 Clinical Document Architecture

(CDA)) introduce additional variability across reporting programs because of differences in data

standards adoption and implementation timelines, data elements, terminology and metadata. The need

to accommodate and manage these variations and extensibility of existing data exchanges increases the

costs and barriers for reporting, data sharing and data reuse for both the senders and receivers of public

health reports.

The PHRI aims to reduce the costs associated with the variability of building and maintaining disparate

specifications. In addition, as a complement to this reduction in costs, this initiative aims to simplify

data exchange and improve interoperability across reporting scenarios for both the senders and

receivers of public health reports. The anticipated healthcare benefit of a successful initiative is a more

standardized and efficient set of infrastructure requirements (standards, terminology, specifications and

tools) applicable to multiple types of provider-initiated public health reports which are typically

mandated by law or regulation. The anticipated public health benefit is more timely, reliable, secure,

standardized and efficient public health reporting which can be received and managed by a more

uniform infrastructure. Automated reporting to public health agencies will help streamline both

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manual, paper-based operations and variable electronic requirements and should result in improved

efficiency. By receiving faster and more harmonized reports, public health agencies should be able to

improve their public health surveillance and risk/harm mitigation activities, which should result in

reductions in preventable disease, disability and death.

3.0 Use Case Scope The PHRI Use Case focuses on a provider-initiated report – a report sent from a provider (using an EHR

system) to a public health agency system containing information about a particular public health event.

The report (at a minimum) will contain specific information about what occurred and the relevant

patient-level information. The report will include data elements automatically populated with

information from the patient’s record in the EHR; it may also include additional information manually

entered by healthcare personnel using the EHR interface. The basic reporting transactions covered by

this use case are:

• Send report (EHR System)

• Receive report (Public Health Agency System)

• Send acknowledgement of report receipt (Public Health Agency System)

• Receive acknowledgement of report receipt (EHR system)

The reporting transactions are described by two potential information flows between an EHR system

and a public health agency. The primary report flow (“basic flow”) is the transmission of a report

directly from the provider’s EHR system to the public health agency system. The alternate report flow is

the transmission of the report from the EHR system through an intermediary system, such as a Health

Information Exchange or Incident Reporting System, to a public health agency.

The Initiative recognizes that cases and reportable events may be identified through a variety of means,

including, but not limited to, provider recognition and/or automated EHR detection. The mechanism for

identifying such reportable events is out of scope for the Public Health Reporting Initiative – the scope

of the Initiative is identifying and defining required and optional data elements for an EHR system to

include in a provider-initiated report and sending it to a public health agency system.

Note that it is not the intent of this initiative to circumvent existing public health reporting infrastructure

or supercede existing widely-used implementation guides (such as those cited in Stages 1 or 2 of the

EHR Incentive Program - “Meaningful Use”). Those public health programs with existing information

exchange specifications that satisfy their requirements (e.g. immunization registry reporting; healthcare

acquired infection reporting) may continue to use existing implementation guides to support their

needs. At the same time, the Public Health Reporting Initiative has welcomed participation from

participants in such existing information exchange and recognizes that both new and established forms

of exchange may benefit from our efforts to develop harmonized reporting content and format.

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3.1 Background On February 17, 2009, the President signed the American Recovery and Reinvestment Act of 2009

(ARRA). This statute includes the Health Information Technology for Economic and Clinical Health Act of

2009 (the HITECH Act) that set forth a plan for advancing the Meaningful Use (MU) of health information

technology (HIT) to improve quality of care and establish a foundation for healthcare reform. Two

Federal Advisory Committees, Health IT Policy and Health IT Standards have been established under this

legislation. In 2010 these Committees identified three types of public health reporting that were

adopted for MU Stage 1 of the HITECH-funded Centers for Medicare and Medicaid Services (CMS)

Incentive Program:

• Capability to submit electronic syndromic surveillance data to public health agencies and actual

transmission according to applicable law and practice.

• Capability to submit electronic data to immunization registries of Immunization Information

Systems and actual submission in accordance with applicable law and practice.

• Capability to submit electronic data on reportable (as required by state or local law) lab results

to public health agencies and actual submission in accordance with applicable law and practice.

Both Committees recognize that these three types of public health reporting represent just a few of the

many types of ongoing information exchange between healthcare providers and public health agencies,

and that creating a unique implementation specification for each would impose long-term burdens on

healthcare providers and agencies alike. Both have suggested that simpler approaches to managing

public health reporting be considered for future stages of Meaningful Use 2 .

ONC manages the S&I Framework to leverage existing and new HIT standards and tools, and to

harmonize and implement standards specifications (implementation specifications) in order to promote

electronic health information exchange interoperability nationwide. In 2011, several S&I Framework

Initiatives were established to provide clarification in HIT standards selected for MU and guide

standards-based products and certification including the Laboratory Results Interface (LRI) Workgroup

and its Public Health Laboratory Reporting Workgroup. The Public Health Laboratory Reporting

Workgroup recognized that additional information is needed for prompt assessment and response to

reportable diseases beyond that contained in the MU Stage 1 implementation specification for

laboratory result reporting. Similar types of information are needed for other kinds of public health

reports. During the ONC S&I Framework face-to-face meeting in Washington DC, June 14-15, 2011 the

LRI Public Health Workgroup proposed establishing the Public Health Reporting Initiative within the ONC

S&I Framework to better understand public health reporting needs and define standards-based

interoperability specifications.

3.2 In Scope The following activities are in scope for the PHRI Functional Requirements analysis:

2 Letter of June 16, 2011 from HITPC chairs to the National Coordinator for HIT.

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• Identifying and harmonizing the core reporting data elements required by public health agencies

shared by various types of reportable events

• Identifying and harmonizing (to extent practical) additional data elements required by public

health agencies for specific types of reportable events (e.g., newborn hearing screening or

healthcare associated infections)

• Defining a standard exchange format including structure and content (i.e., vocabulary)

• Defining the requirements for limited bi-directional data exchange between EHR systems and

public health agency systems – sending the report, receiving the report, and transmitting an

acknowledgement of receipt

• Identifying the content requirements to send reports from certified EHR systems (in a variety of

clinical settings where EHR data is used for reporting purposes – for example, inpatient,

outpatient, emergency room, urgent care, etc.) to public health agencies (Note: the initiative

recognizes that other report information (e.g., administrative, laboratory, pharmacy) may be

imported from separate systems into the EHR in order to complete a public health report;

however, the functional requirements for these systems, including the EHR interface

requirements, are not in scope for this use case)

3.3 Out of Scope The following activities are out of scope for the PHRI Functional Requirements analysis:

• Defining specifications and guidelines on reportable event criteria (e.g., defining reportable

conditions) – by law these specifications typically rest with states. This Initiative will enable

healthcare providers to submit a report based on jurisdictionally-defined laws and regulation,

but will not be responsible for actually creating those reporting criteria

• Describing the precise processes for healthcare providers to add information into an EHR

manually or from an auxiliary (e.g., administrative, laboratory, pharmacy, etc.) system, or how

EHRs or providers recognize public health report “triggers”. It is expected that these details

would be defined by an implementation or demonstration project for a specific user story /

public health reporting scenario;

• Describing the process for public health agencies to perform follow-up activities, including case

monitoring

• Defining specifications and guidelines for reporting by other communications methods such as

telephone, web-based data entry, mailed, or faxed reports)

• Describing any additional or extensive bi-directional communication between a public health

agency and a healthcare provider beyond the limited exchange supported by this use case (i.e.,

the sending of a public health report and the acknowledgement of receipt of that report)

• Identifying transport protocols

• Identifying security requirements, methodologies, procedures, and/or protocols

• Identifying information and data stewardship practices and policies

This Initiative acknowledges that all functions supported by current reporting programs are not

addressed in this document; the Initiative focuses on a common functional starting point – the presence

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of key information in an EHR system that is needed to generate a public health report. The Initiative has

identified other use cases that may have similar actors and information requirements, but which are in

some ways distinct and out of scope for this initiative. These out-of-scope use cases include, but are not

limited to, the following:

• Patient referral to a public health agency (e.g., tobacco quit-line) for services. In this scenario,

the initial public health report may not reflect all the necessary information for the referral or

transition of care or all requirements for the bidirectional exchange that would typically follow a

referral

• A request for information initiated by a clinical provider about a patient (or set of patients) and

sent to a public health system (e.g., a request for a complete immunization history from a public

health Immunization Information System.. Again, the content and flow of information may have

requirements that go beyond those of simple provider-initiated public health reports.

• Other Standards and Interoperability Initiatives (e.g. Transitions of Care and Query Health) are

alternate use cases that may (now or in the future) also be used to support public health

surveillance in addition to or as a replacement for Public Health Reporting, and may inform or

be informed by the PHRI content and format specifications.

However, it is likely that the harmonized data elements and specifications produced by this initiative

will also expedite the implementation of these alternate use cases. For example, data elements such as

the contact information for the subject of the report may support follow-up activities of public health

programs. Thus we welcome the participation of persons interested in these use cases in defining the

products of this Initiative. It is also possible that future phases of this initiative may address some

aspects of these other use cases, although they remain are out of scope for the current phase.

3.4 Communities of Interest Member of Communities of Interest Description

Healthcare Provider Any supplier of a healthcare service; person or organization

that furnishes healthcare in the normal course of business.

Includes physicians and healthcare provider staff, as well as

ancillary healthcare personnel.

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.

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Member of Communities of Interest Description

Electronic Health Record (EHR) /

Electronic Medical Record (EMR) /

Personal Health Record (PHR)

Vendors and Suppliers

An EHR is an electronic record of health-related information

on an individual that conforms to nationally recognized

interoperability standards and that can be created, managed,

and consulted by authorized providers and staff across more

than one health care organization. An EMR is an electronic

record of health-related information on an individual that can

be created, gathered, managed, and consulted by authorized

providers and staff within one health care organization. A

PHR is an electronic record of health-related information on

an individual that conforms to nationally recognized

interoperability standards and that can be drawn from

multiple sources while being managed, shared, and controlled

by the individual. A vendor or supplier is a

company/consortium that provides products and/or services.

Public Health Information System

Vendors/Suppliers

Vendors or suppliers of Public Health Information Systems -

applications which may, among other things, receive public

health reports

Standards Development Organizations Organizations key to identifying, balloting, approving, and

maintaining health information exchange standards, including

exchange, terminology, security, and transport protocols.

Health Information Exchange

Organizations

Organizations (including state Designated Entities for Health

Information Exchange, as well as other organizations

managing information exchange among different corporate

entities). Includes Regional Health Information Organizations

(RHIOs).

Intermediary Systems Systems or organizations that support the transmission of

information from an EHR system and/or a public health

agency system. For the purposes of this document, an

intermediary system is any system that serves to transport

information to or from an EHR or public health agency

system.

Patient Safety Organization A group, institution or association that improves medical care

by reducing medical errors

Quality improvement/measurement

organizations

A group of doctors and healthcare experts that evaluate and

seek to improve the care given to people. For

example, Quality Improvement Organizations (QIOs) are key

stakeholders in Hospital Acquired Infection reporting and in a

range of care and transitions of care issues including the

reporting and control of healthcare associated infections.

Accountable Care Organization (ACO) An ACO is an organization of health care providers that agrees

to be accountable for the quality, cost, and overall care of

Medicare beneficiaries who are enrolled in the traditional fee-

for-service program who are assigned to it

Laboratory The laboratory performs laboratory analyses and produces

lab test results (typically as the filler of a lab order by a

licensed health professional).

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Member of Communities of Interest Description

Laboratory Information System (LIS) or

Laboratory Information Management

System (LIMS), Vendors/Suppliers

An application to streamline the management of laboratory

processes including data collection, workflow management,

and report generation. May provide an automatic interface

to laboratory analytical instruments to transfer verified

results to nurse stations, chart carts, and remote physician

offices. Table 1: Public Health Reporting Communities of Interest

3.5 Actors and Roles The table below describes the roles of the actors in the public health reporting workflow. More detail

about each action in the workflow is provided in later sections.

Actor Role

Healthcare Provider • Deliver care to patient

• Enters information into EHR

• If applicable – suspect reportable event to begin

report generation process

• If applicable – send any immediately-required

public health reports

• If applicable – add information, sign, and/or

verify public health report prior to sending

EHR System (healthcare provider system) • Collect, receive, and/or store patient-level data

• Support additional data entry (e.g. populate

data on an electronic form and allow healthcare

provider to add information)

• Generate public health report and make it

available for validation

• Validate public health report based on

implementation-specific business rules when

automation of validation is possible/allowable.

• Send report to public health agency either

directly or through an intermediary

• Receive acknowledgement either directly or

through an intermediary

Public Health Agency System • Receive report from EHR system or intermediary

• Generate acknowledgement from public health

agency

• Send acknowledgement to EHR system either

directly or through an intermediary

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Actor Role

Intermediary Systems, including Incident

Reporting Systems, Health Information

Exchange Systems, Health Information

Networks, etc.

If applicable:

• Receive report from EHR system and send to

public health agency system

• Receive acknowledgement from public health

agency system and send acknowledgement to

EHR system

Note: Intermediary System is a generic term used to

identify HIT systems or networks that are external to

the EHR system and are used to communicate

between EHR systems and public health agency

systems.

Supporting System (e.g., Testing Facility

System, Laboratory System)

If applicable:

• Transmit test results to the provider and/or

provider EHR system for a specific patient

Table 2: Public Health Reporting Actors and Roles

4.0 Public Health Reporting Workflow The following diagrams and tables describe the public health reporting workflow, indicating the roles of

specific actors and whether or not an action is in scope, out of scope, or specific to a particular

implementation. The use case assumes that all information needed to complete a valid public health

report is made available to the EHR system to generate and send a report. The initiative recognizes that

the functions of generating, sending, receiving, and acknowledging a public health report are dependent

upon automated and/or manual process to incorporate relevant clinical, laboratory, and/or

administrative data within the EHR system. The functional requirements for these processes are not

within the scope of the initiative, however, the reporting workflow assumes that these functions will

become available and operational.

The first diagram, “Public Health Reporting Workflow,” illustrates the public health reporting workflow,

calling out actions that are implementation-specific, in scope, or out of scope. It includes paths to

accomodate the ‘basic flow’ – where a report is sent directly from an EHR system to a public health

agency system – and the ‘alternate flow’ – where the report is sent from and EHR system through an

intermediary system to the public health agency. It illustrates the transactions and decisions that are

required to create and send a provider-initiated report.

It is important to note that the following diagrams represent a generic flow of information and

operations based on a provider initiated report to a public health information system, with a simple

acknowledgement of receipt of the specific report. This is a result of considering a broad range of user

stories from across the spectrum of public health responsibilities. This representation of the information

flow does not represent critical components to several public health programs which rely on the

creation of case and patient records based on a care transition, those that are sourced from multiple

data sources, and / or those that require reconciliation / de-duplication of records. However, these

additional operations can and do impact the content requirements, format standards and information

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exchange model. As such, when it comes to system design and implementation of a particular user

story (or set of user stories), these operations and interoperability requirements need to be accounted

for, and may affect information exchange requirements and standards for this initiative, or for

extensions of the use case built on this initiative.

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Figure 1: Public Health Reporting Workflow

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The second diagram, “Public Health Reporting Activity Flow,” includes the same actors and roles as the

first diagram, but is organized along swimlanes to clearly indicate the roles of each actor.

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Figure 2: Public Health Reporting Workflow with Swimlanes

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Additional details about the actions in the public health reporting workflow are presented in the

following table. Actions are not numbered as they are not necessarily sequential steps. Many of the

actions depicted in the workflow have implementation-specific functional requirements that are out of

the scope of the Public Health Reporting Initiative, but should be considered for an implementation.

Action Additional Information

Healthcare Provider - Refers to the healthcare provider and/or associated staff (e.g., administrative

personnel, clinician, physician, nurses, etc.)

Note that defining the actions of the healthcare provider are out of scope for the Initiative.

Deliver care, order tests, treat

patient, etc…

Describes the healthcare provider action at time of patient

encounter. Specific action depends on provider workflow.

Enter information into patient’s

Electronic Health Record

Information about the patient / patient encounter is entered

into the specific record for that patient in the EHR system.

Suspect reportable event The healthcare provider may suspect a reportable event based

on the patient encounter – this action is ‘optional’ and should

occur concurrently with the EHR system detection of a possible

reportable event.

Immediately sends report to public

health agency as jurisdictionally

mandated.

If the EHR system (or provider, depending on specific triggers

and/or workflows) determines that public health must be

immediately notified of the reportable event (based on

jurisdictional regulations), the healthcare provider is

responsible for transmitting the report. Note that depending

on workflow and regulations, this report may be a phone call

and/or may be an instruction to the EHR system to immediately

send the public health report. Depending on the mechanism of

transmission, the mechanism of receipt by the public health

agency may vary – for example, a health official could accept a

phone call report while a system would accept an electronic

report.

Add information, sign, and/or verify

public health report

If manual action by the healthcare provider is required, the

healthcare provider completes the required manual actions,

based on provider workflows and jurisdictional regulations, to

send the public health report.

EHR System – Refers to a healthcare provider’s Electronic Health Record System that manages electronic

health records for patients

Compiles / stores patient information

(e.g., patient encounter information,

test results, transmission log)

Information may be manually entered into the EHR system or

electronically provided from supporting systems. For example,

a healthcare provider may enter patient notes into a patient’s

electronic health record. However, laboratory test results for a

patient may be transmitted to that patient’s electronic health

record from a supporting system. Defining the requirements

associated with this action are out of scope for the Initiative,

but should be considered when identifying data elements for

public health reporting.

Detect possible reportable event Based on defined reporting criteria (dependent on jurisdictional

regulations), the EHR system (or, if applicable, the event

detection rules engine) identifies a possible reportable event

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associated with a patient. Note that defining the specific

reporting criteria and business rules to identify reportable

events is out of scope of the Initiative.

Generate / assemble public health

report

A public health report is generated and populated based on

specific requirements (e.g., data elements, formats, etc.). The

actual mechanism to generate and assemble the information

(e.g., user interface) is out of scope of the Initiative, but

identifying the data elements that should be included in the

public health report is in scope.

Decision: Immediate report required? The EHR system or provider (depending on specific

implementation) determines if an immediate report to public

health is required, based on specific jurisdictional requirements.

If applicable, the EHR system notifies the healthcare provider

that an immediate report is required. Note that depending on

the implementation, an immediate report may be sent via

phone call or other method or from the EHR system at the

discretion of the healthcare provider. These actions are

accounted for in the public health reporting workflow, but out

of scope for the Initiative.

Decision: Manual action required? The EHR system, based on provider-specific workflows,

determines if manual action to continue the public health

reporting process is required. Defining in detail these actions

and business rules are out of scope for the Initiative.

Generate / populate report for

healthcare provider

If a manual action by the healthcare provider is required to

continue the public health reporting process, the EHR system

generates/populates a report for the healthcare provider. Note

that depending on the implementation, this report may be

displayed through a user interface designed for the provider

(e.g., task list, worksheet, form, etc.). This report is not

necessarily in the same structure as the public health report,

but should be built using the same information. Defining the

mechanism to display this user interface is out of scope for the

Initiative.

Verify / validate public health report The EHR system verifies / validates the public health report by

evaluating its compliance with the specific report requirements

and other implementation-specific business rules. Defining

these business rules is out of scope.

Decision: Verified/validated public

health report?

The EHR system determines if the public health report satisfies

the requirements or requires revisions. Note that if the report

fails the verification / validation step, it is returned to the

healthcare provider for revisions based on a workflow designed

by the provider. Defining the specific actions and business rules

associated with this step are out of scope.

Send public health report If the public health report passes the verification / validation

step, the EHR system electronically sends the public health

report containing the appropriate information in the

appropriate format. The public health report may be sent

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either directly to the public health agency or through an

intermediary system, such as an HIE. Defining the data element

and information exchange requirements associated with

sending the report are in scope for the Initiative.

Receive acknowledgement The EHR system receives an acknowledgement that the public

health agency received the public health report. This

acknowledgement may be received directly from the public

health agency system or through an intermediary system, such

as an HIE. The acknowledgement is stored in the EHR system,

based on implementation-specific requirements. The actual

mechanism of receiving and/or storing the acknowledgement is

out of scope.

Public Health Agency System – Refers to a system at a public health agency designed to collect

information on a reportable event.

Receive public health report The public health agency system receives the public health

report. Note that this report may come from the EHR system

directly or through an intermediary system. Additionally, the

public health agency system may receive a report directly from

a healthcare provider (via phone or other mechanism) if

jurisdictional regulations require an immediate report. Finally,

the public health agency system, as part of a separate

workflow, may receive a report from a supporting system, such

as a laboratory system, where jurisdictionally mandated.

Defining the data and structure of the public health report is in

scope for the Initiative.

Send initial acknowledgement Once the public health agency has received a report, an

acknowledgement of receipt is sent to the sending system

(either HIE or EHR system). Note that this acknowledgement is

sent before any evaluation of the public health report is

performed by the public health agency. The acknowledgement

reflects only the fact that the public health agency received a

public health report from a sending system. The actual

mechanism of creating such an acknowledgement is out of

scope for the Initiatve.

Validate / verify report The Public Health Agency will perform implementation-specific

procedures to verify / validate the report received from the EHR

system. Note that defining these procedures is out of scope for

the Initiative.

Decision: Valid report? Based on public health agency business processes and

requirements, the public health agency system evaluates the

validity of the public health report. The outcome of this

decision has no impact on the sending of an initial

acknowledgement of receipt to the sending system, but may

lead to additional actions depending on the implementation.

Note that this action is out of scope for the Public Health

Reporting Initiative.

De-duplicate and merge records Depending on public health agency business processes, any

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record de-duplication and/or merging is performed. Note that

this action is out of scope for the Public Health Reporting

Initiative.

Decision: More data needed? If a report is deemed valid by the public health agency system,

there may be an additional check to determine if more

information is needed to complete or follow-up on the report.

If more information is needed, the public health agency system

will notify the healthcare provider following implementation-

specific workflows. If no additional information is needed, the

process is complete. Additionally, this decision has no impact

on the initial sending of an acknowledgement of receipt by a

public health agency system to a sending system. Note that this

action and decision are out of scope for the Public Health

Reporting Initiative.

Request information If the Public Health Agency determines that the report is not

valid or requires more information, the Public Health Agency

system request additional information from the EHR system,

either directly or through an Intermediary System. Note that

this request is out of scope of the Initiative and depends on

implementation-specific requirements.

Send secondary acknowledgement If the Public Health Agency determines that the report is valid

and requires no additional information, a ‘secondary

acknowledgement’ is sent to the EHR system, either directly or

through an Intermediary System. This ‘secondary

acknowledgement’ serves to notify the EHR system that report

processing from the Public Health Agency is complete and that

the report has been accepted – no further action is required

from the EHR system (or provider) at this time. Note that this

‘secondary acknowledgement’ is out of scope for the initiative

at this time, but should be considered during implementation.

Intermediary System – Refers to a system that enables the exchange of information between healthcare

providers and public health agencies (e.g., Health Information Exchange)

Receive public health report The intermediary system receives the public health report from

the EHR system. Defining the mechanisms and involvement of

an intermediary system is out of scope for the Initiative, beyond

allowing for the use of such a system.

Send public health report The intermediary system sends the public health report to the

public health agency system. Defining the mechanisms and

involvement of an intermediary system is out of scope for the

Initiative, beyond allowing for the use of such a system.

Receive acknowledgement The intermediary system receives an acknowledgement back

from the public health agency system that the report was

received. Defining the mechanisms and involvement of an

intermediary system is out of scope for the Initiative, beyond

allowing for the use of such a system.

Send acknowledgement The intermediary system, depending on implementation, may

send 2 separate acknowledgements to the EHR system:

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• An acknowledgement that the report was received

from the EHR system (prior to sending to public health

agency system)

• An acknowledgement that the report was received by

the public health agency (after receiving the

acknowledgement from the public health agency)

Defining the mechanisms and involvement of an intermediary

system is out of scope for the Initiative, beyond allowing for the

use of such a system.

Supporting System – Refers to a system that provides additional information to the healthcare provider’s

EHR system about a patient. The actions of and transmissions from a supporting system are out of scope

for the Public Health Reporting Initiative; however, information from supporting systems may be

required to complete a public health report.

Conduct tests The supporting system and/or associated staff conduct

appropriate tests as indicated by the healthcare provider.

Examples of tests include hearing screenings, laboratory tests,

etc. Note that the actions of supporting systems are out of

scope for the Public Health Reporting Initiative.

Send test results The supporting system and/or associated staff send test results

to the healthcare provider. These test results are incorporated

into EHR system either by electronic submission or manual data

entry, depending on the provider-specific workflow. Note that

the actions of supporting systems are out of scope for the

Public Health Reporting Initiative.

Decision: Reportable event from test

site?

Depending on jurisdictional regulations, a supporting system

may send a report to a public health agency. Note that the

actions of supporting systems are out of scope for the Public

Health Reporting Initiative. Table 3: Details about Actions in the Public Health Reporting Workflow

5.0 Functional Requirements

5.1 Information Interchange Requirements Initiating

System

(describes

action)

Information

Interchange

Requirement Name

(describes

action)

Receiving System

Electronic

Health Record

System

Send Public Health Report* Receive Public Health Agency System

Public Health

Agency System

Send Acknowledgement Receive Electronic Health Record

System

Alternate flow:

Electronic

Health Record

System

Send Public Health Report Receive Intermediary System

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Alternate flow:

Intermediary

System

Send Public Health Report Receive Public Health Agency System

Alternate flow:

Public Health

Agency System

Send Acknowledgement Receive Electronic Health Record

System

Alternate flow:

Intermediary

System

Send Acknowledgement Receive Electronic Health Record

System

Table 4: Information Interchange Requirements

5.2 System Requirements System requirements provided in the table below refer to the base (direct transmission) and alternate

(transmission through intermediary system) flow requirements and reflect functions needed to support

various scenarios described in the use case. Note that reporting scenarios may or may not include fully

automated functions – for example, integration with a Clinical Decision Support system for managing

reporting criteria and/or triggers. However, the table includes information for both automated and

manual functions that are needed to support the use case.

System System Requirement

Electronic Health Record System Interface with appropriate clinical, administrative,

laboratory, pharmacy or other systems to receive and

store relevant patient information needed to

generate compliant public health reports

Electronic Health Record System Interface with a clinical decision support system to

receive, store and process public health reporting

criteria and/or triggers

Electronic Health Record System Provide a user interface to support manual entry or

updates to public health reporting criteria or triggers

by healthcare providers or other staff.

Electronic Health Record System Extract data (if outside the EHR system) and render

information needed to create a public health report

based on the appropriate jurisdictional reporting

criteria

Electronic Health Record System Render a public health report for subsequent

validation, completion, verification and certification

Healthcare provider interface Renders a report form for completion, verification,

and certification when necessary

EHR / Healthcare provider interface Generates Public Health Report

EHR reporting module Sends public health report to public health agency

receiving system; archives copy of report and data

exchange transmission; receive and archive Public

Health Agency system acknowedgements

Public health agency system Receives EHR public health report; generate and send

report receipt acknowledgements Table 5: Public Health Reporting General System Requirements

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5.3 Triggers A public health event (such as a new diagnosis of tuberculosis) requiring a public health report is

typically defined by criteria established by local, state or federal statutes, regulations or guidelines.

These criteria may be unique to a specific public health agency or surveillance program, and are

essentially defined by the business requirements of public health surveillance and intervention. Some

reportable events may not even involve a diagnosis, for example, childhood blood lead tests or newborn

hearing examinations may be reportable whether or not they are abnormal. Report creation is

dependent upon healthcare provider discovery or identification of a possible public health event of

interest and comparison of that potential event with criteria. Today in most cases, this a manual

process. Event discovery or detection is a result of data from direct patient care encounters or

assessments of other health information, such as results from laboratory test or diagnostic procedures.

However, depending upon the reporting criteria, IT automation can be applied to the event detection or

discovery process such that direct healthcare provider interaction or intervention is reduced or not

required to initiate the reporting process. For example, a single laboratory test result, a single diagnosis

code, or a combination of demographic and diagnostic elements may algorithmically trigger recognition

of a reportable event by an EHR or by a supporting application.

In the context of this use case, the term “trigger” is used to convey automation of one or more event

discovery or detection parameters based upon jurisdictionally defined reporting criteria. Automated

detection and initiation of the reporting process can be programmatically defined in a computer system

(EHR) or supporting application (such as an EHR services platform, or ESP). The initiation of the

reporting process can be triggered by the presence of information contained in the EHR that meets the

jurisdictionally defined reporting criteria that is used to determine if a report should be sent to a public

health agency. Automated triggers are created or programmed using the reporting criteria and can be

based upon several factors that include but are not limited to:

• Mandated reporting criteria specified by jurisdictional (e.g., federal, state, local or territorial)

legislation, statute or regulation.

• Surveillance criteria for voluntary reporting specified by an organization (e.g., public health

agency, healthcare provider, quality improvement organization, registry, etc.)

• Criteria may include observations or assessments made by healthcare providers or other staff,

whether or not they are documented within the EHR. For example, the suspicion of certain

diseases alone may constitute a reportable condition, whether or not it is written as a diagnosis

in the EHR.

• The presence of specific data or documentation, or a combination of items, within an EHR that

meets the reporting criteria.

As EHR public health reporting functions are designed and piloted, implementers will have to consider

these factors, as well as the clinical workflow, clinical / administrative policies, and report validation /

certification processes. Some implementations may depend upon manual processes to initiate and

execute public health reporting, while others may be partially or fully automated based on the functions

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available within a specific EHR product or supporting application like a public health trigger recognition

system (e.g., ESP at Harvard) or a clinical decision support system.

6.0 Non-Functional Requirements Non-functional Requirements are those requirements that reflect required operational needs, rather

than functional information flow operations. Non-functional requirements are generally

implementation-specific and may vary based on healthcare provider workflow, report type, etc.

These requirements include, but are not limited to, the following:

Type Description

Quality Requirements for quality, reliability, performance,

usability, supportability, and/or implementation.

Constraints Requirements related to security, accessibility,

jurisdictional reporting requirements and

operations, operations, interfaces, and other legal

constraints.

Workflow Requirements related to implementation-specific

workflows (e.g., how a healthcare provider adds

information to or signs a public health report

generated by the EHR system)

Timeliness Requirements related to the timeliness of

reporting

Transmission Mode Requirements related to the batching of reports

vs. the submission of a single report

Consent policies Most types of public health reports are mandated

without patient consent (e.g., the report of a

communicable disease). Others may depend on

consent, often depending on jurisdictional laws

(for example, some immunization registries or

developmental disability registries only collect

information with consent). Especially when

intermediary systems are involved, consent

policies need to correspond to public health legal

requirements. For example, an HIE that only

exchanges information by consent would not be

suitable for most public health reporting. Table 6: Types of Non-Functional Requirements

Non-functional requirements may vary based upon the specific public health agency or program’s

policies. For example, timeframe for reporting, (e.g., within 24 hours of event discovery), may have

operational implications for human and system actors supporting the specific reporting scenarios

expected that pilot implementations will provide a greater level of detail concerning the non functional

requirements relevant to their EHR systems, which includes internal IT infrastructure considerations and

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any manual business processes that are needed to facilitate or augment report generation, validation,

completion, verification, certification and transmission.

7.0 Dependencies and Future Considerations

7.1 Dependencies As a secondary user of clinical information, public health programs rely on the security, accessibility,

reliability, consistency, and quality of information from providers and other information sources that are

not under direct management or regulation of public health agencies. As such, there are several

business processes, policy and technical dependencies that must be understood by report senders and

receivers to both enable specific public health reporting exchanges, and to help promote the long term

sustainability of nationwide public health information exchanges.

These dependencies include, but are not limited to, the following:

Type Description

Certification As the functional and data requirements for

certified electronic health record systems and

modules evolve, there may be downsteam impacts

and opportunities for public health agencies,

including the availability of specific data elements

that enable and are required for reporting

purposes.

Value Set maintenance and provisioning Agreed upon vocabulary value sets associated with

public health reporting data elements must be

maintained. These value sets are critical for EHR /

clinical setting data sources, intermediaries (e.g

health information exchanges), and public health

agency receivers for data validation and

translation. Nationwide and local governance and

technical infrastructure are necessary to enable

implementation, adoption, and sustainability.

Health Information Standards Bodies and

Processes

Public health reporting will rely on standardized

information exchange format and content

standards. These base standards rely on balloting

and consensus processes to promote industry

acceptance and adoption. Current and future

public health reporting specifications may be

dependent on these bodies and their associated

consensus building, maintenance, and distribution

processes.

Healthcare Provider and Public Health Agency

Processes, Procedures, and Tools

In order to realize the full potential of the PHRI

specification, it is recognized that short and long

term commitments from vendors is needed. This

involves providing software tools and/or other

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services that can be used to augment or replace

existing processes used to create and send public

health reports. This also implies reciprocal

commitments from healthcare providers and

public health agencies to adopt and use the PHRI

specification. To facilitate this, there is a specific

need to evaluate impacts to augment current

infrastructure and processes to interoperate (or

map) with/to the PHRI specification Table 7: Types of Dependencies

7.2 Additional Components and Considerations Public health reporting relies on a number of operations that are outside the scope of the functional

requirements and information exchange descriptions captured in this document. Capturing additional

components of the overall public health business process and system flows will be important both in the

specific design and exchange serving a specific public health program / jurisdiction. This includes the

sustainability / extensibilty of public health reporting requirements as the public health programs,

policies, systems and infrastructure change over time. These important components and considerations

include, but are not limited to:

Type Description

Reporting criteria Provider-initiated public health reports rely on

specific criteria associated with jurisdictional /

program policies, public health case definitions,

data availability, provider expertise, and other

factors. These report criteria may change over

time or between jurisdictions, and the technical

systems will require a means to understand which

criteria apply and when criteria change (e.g. when

a new reportable event is added, which

sometimes occurs emergently during an outbreak).

Both public health agencies and healthcare

providers need to consider how information about

criteria are made available, updated and how

notification of change is accomplished. When

automated report triggering is used, how might

systems operating such algorithms receive and

implement different criteria across jurisdictions or

over time? A public health reportable condition

knowledge base may help facilitate up-to-date

access.

Reportable event filters and templates As information exchange specifications for each

public health report are developed and

maintained, reporting templates and filters may be

made available to system senders and receivers, to

facilitate and accelerate reporting. A public health

reportable event knowledge base may help

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promote their availability to affected stakeholders.

Security / Trust Reporting to a public health agency will require a

level of trust between the agency and the

reporting party. As security, accessibility, and

privacy policies and infrastructure are developed,

it will be important that public health reporting

specifications account for these needs. An

important component of this trust is accounting

for program jurisdiction in both the data content

and associated data use accessibility requirements,

including requirements for authentication,

authorization, non-repudiation, and attestation of

the report (via electronic signature or other

mechanism).

Validation / data management processes There are multiple types of validation processes

involved in a public health reporting process,

including message / report format conformance,

data / content verification, error handling, and

case de-duplication and record merging. The

requirements for these processes vary between

the policies, capacities, and needs of particular

programs and jurisdictions. Implementations of

specific public health reporting exchanges in

specific jurisdictions should follow the guidance,

recommendations, and best practices advocated

by various stakeholders, which may include

professional associations, patient advocacy

groups, and/or sponsoring federal, state, and local

agency programs. Table 8: Additional Considerations

8.0 Dataset Requirements The PHRI will identify the data elements along with associated value sets and related guidelines that

have been provided by each domain and/or across domains. 3 This task will result in a PHRI Data

Harmonization Profile that will help promote normalized field definitions, vocabulary bindings, and

content requirements to facilitate the analysis of base content exchange (e.g. HL7 2.x, HL7 Clinical

Document Architecture and terminology standards and future standards development harmonization

tasks). This document is available on the Public Health Reporting Initiative wiki, here:

http://wiki.siframework.org/PHRI+-+Data+%26Terminology+Harmonization+Sub-Workgroup.

As described in the Data Harmonization Profile, the data elements for public health reporting can be

broken down into 3 classifications:

3 Note that the data elements and Data Harmonization Profile have not yet been completed or consensus

approved. Once completed, a separate consensus process will determine acceptance and this footnote will be

deleted.

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• Core Common Data Elements – harmonized data elements that are widely shared across several

report types. Expect EHR systems to be able to produce these data elements but public health

systems may choose to receive these elements at their discretion. Identifying and harmonizing

core common data elements are the primary focus of the Data Harmonization Profile.

• Report Type Specific Data Elements – harmonized data elements (although variance is allowed

where necessary) that are broadly required across public health for a specific report type (e.g., a

communicable disease case report, a birth record report, etc.). Special effort is taken to

harmonize elements between different report types, but this is a secondary effort of the PHRI at

this time. Where possible, report type data elements are detailed and harmonized, but future

companion documents and phases of the Public Health Reporting Initiative may be required to

cover data elements for various types of reports.

• Implementation Specific Data Elements – additional, relatively unique, or non-harmonized data

elements required by a particular jurisdiction or public health program (e.g., a TB report in

California). Defining these elements is out of scope for the Data Harmonization Profile and the

Public Health Reporting Initiative at this time.

Specific public health reporting scenarios, either ‘report type-specific’ or ‘implementation-specific’, will

provide their own requirements for optionality but can take advantage of harmonized value sets and

terminology.

9.0 Standards Analysis In the standards analysis phase, the PHRI will analyze the data harmonization profile, as well as review

relevant existing implementation guides, against the requirements described in the functional

requirements documents. This will help the initiative determine the best data exchange specification

and selection of appropriate data elements, terminologies and value sets. It is possible that different

public health reporting user stories and report types will require different specifications as a result of

this analysis. Our approach will identify a uniform set of “common core data elements” valid for many

different types of public health reports, and “extension data elements” that include unique needs for a

particular type of public health report. This information can be used by EHR and other software

vendors and public health agency system support teams to determine gaps and opportunities for

enhancing existing products, tools, services and infrastructure to support testing and adoption of the

PHRI specifications.