Difference between revisions of "Cancer Registry Pathology Report"

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=Introduction=
 
=Introduction=
−
''This is a draft of the Cancer Registry Content Profile (CRC) supplement to the PCC Technical Framework.  This draft is a work in progress, not the official supplement or profile.''
+
''This is a draft of the Cancer Registry Pathology Report Content Profile (CRPR) supplement to the PCC Technical Framework.  This draft is a work in progress, not the official supplement or profile.''
  
 
__TOC__
 
__TOC__
  
 
==Profile Abstract==
 
==Profile Abstract==
−
The Cancer Registry Content Profile (CRC)
+
The Cancer Registry Pathology Report Content Profile (CRPR) defines the the content used in the {{ILink|Cancer Registry Content|PCC-11}} to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.
  
−
This profile defines the implementation of HL7 2.3.1 to create a message from the completed pathology report and transmit it to the Cancer Reistry.
+
==Glossary==
  
−
==Glossary==
+
;International Classification of Diseases for Oncology, 3rd Edition (ICD-O-3)<br>
 +
Classification system for reporting incidences of malignant diseases.
 +
 
 +
;NAACCR
 +
The North American Association of Central Cancer Registries. A collaborative umbrella organization for cancer registries, governmental agencies, professional organizations, and private groups in North America interested in enhancing the quality and use of cancer registry data.
  
−
Refer to the Glossary posted on CDC's National Program of Cancer Registries Modeling Electronic Reporting Project website:  www.cdc.gov/cancer/npcr/informatics/merp/TBD
+
;Pathology Report <br>
 +
The written description of the microscopic examination of a tissue.  The gross description reports the physical characteristics of the tissue:  size, color, and abnormalities visible with the unaided eye.  The microscopic description reports the cellular characteristics aided by the use of a microscope:  what cells are involved, the behavior, and the aggressiveness or grade of any abnormality. The final diagnosis is a summary of the findings and indicates the pathologist’s impression of what was found in concise terms.
  
 
==Issue Log==
 
==Issue Log==
 
===Open Issues===
 
===Open Issues===
 +
 +
# Issue:  Dependencies:  need help understanding this component
 +
#* Depends on Care Management with the V2 option (and by reference ATNA and CT)
 +
# Issue: Modify Actor/Transactions (Keith)
 +
# Issue: Modify Content Module for V2 profiles (Keith)
 +
# Issue: Grouping:  Does this need to be modified for the CRC profile?
 +
#* Yes, not sure how
 +
 +
{{Fixme|Register Pathology Implementation Guide with HL7 Message Profile Registry}}
 +
::In Progress
 +
 +
===Closed Issues===
 
# Issue:  Glossary:  Use MERP glossary document or consolidated glossary tool?
 
# Issue:  Glossary:  Use MERP glossary document or consolidated glossary tool?
 
#* Refer to the existing document
 
#* Refer to the existing document
−
# Issue:  Dependencies:  need help understanding this component
 
−
#* Depends on Care Management with the V2 option (and by reference ATNA and CT)
 
−
# Issue:  Under Profile Name:  Add more information about the adverse effect of not getting full reporting.
 
 
# Issue:  Options:  need help understanding this component
 
# Issue:  Options:  need help understanding this component
−
#* Won't have any.
+
#* Won't have any
−
# Issue:  Groupings:  Does this need to be modified for the CRC profile?
+
#* Added options based on discussion at May f2f meeting.
−
#* Yes, not sure how
 
 
# Issue:  Transaction Definitions:  need help understanding this component
 
# Issue:  Transaction Definitions:  need help understanding this component
 
#* Not relevant to this profile
 
#* Not relevant to this profile
−
# Issue:  What information do we need to include in 3.1.2, 3.1.3, 3.2, 3.3, 3.4?  The  current Content Profile refers the reader to the NAACCR Standard already published.
+
# Issue:  What information do we need to include in 3.1.2, 3.1.3, 3.2, 3.3, 3.4?   
−
#* Just reference the NACCR Documentation on this section.
+
#* Just reference the NAACCR Documentation on this section
−
 
+
# Should we include a sample message? 
−
===Closed Issues===
+
#* include a link to a webpage of a sample message.  There are ways to convert a document to a webpage....
  
 
=Volume I=
 
=Volume I=
 
<pre>Add the following bullet to the list of profiles</pre>
 
<pre>Add the following bullet to the list of profiles</pre>
−
* Cancer Registry Content - The Cancer Registry Content profile identifies the pathology data to be sent to Cancer Registries
+
* The Cancer Registry Pathology Report Content Profile (CPR) defines the the content used in the {{ILink|Cancer Registry Content|PCC-11}} to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.
  
 
===Dependencies===
 
===Dependencies===
 
<pre>Add the following row(s) to the list of dependencies</pre>
 
<pre>Add the following row(s) to the list of dependencies</pre>
−
{|style='background-color:#7f7f7f;' align='center' border='1' cellspacing='0'
+
{{T|Integration Profile|Dependency|Dependency Type|Purpose|Rows=
−
!Integration Profile
+
{{R|Cancer Registry Pathology Report (CPR)|Care Management (CM)|The Content Creator actor of the CPR profile must be grouped with the Clinical Data Source Actor of the CM profile|The CPR profile defines the content sent in the PCC-11 transaction specified in the CM profile}}
−
!Dependency
+
{{R|Cancer Registry Pathology Report (CPR)|Care Management (CM)|The Content Consumer actor of the CPR profile must be grouped with the Care Manager Actor of the CM profile|The CPR profile defines the content recieved in the PCC-11 transaction specified in the CM profile}}
−
!Dependency Type
+
{{R|Cancer Registry Pathology Report (CPR)|ATNA|Actors the CPR profile shall implement the Secure Node Actor of the ATNA profile|Ensures that transmissions and changes to patient health information are logged in an audit repository, and that communication is secured between nodes.}}
−
!Purpose
+
{{R|Cancer Registry Pathology Report (CPR)|ATNA|Actors the CPR profile shall implement the Time Client Actor of the CT profile|Ensures that concistent time is used in all messages.}}
−
|- style='background-color:#ffffff;' align='center'
+
}}
−
|Cancer Registry Content
+
==Cancer Registry Pathology Report Content ==
−
|Care Management
+
The Cancer Registry Pathology Report Content Profile (CRPR) defines the the content used in the {{ILink|Cancer Registry Content|PCC-11}} to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.
−
ATNA
 
  
−
CT
+
Monitoring the occurence of cancer is a cornerstone of cancer control decision making.  this monitoring, referred to as cancer surveillance, can be used to trigger case investigations, follow trends, evaluate the effectiveness of prevention measures such as screening and early detection programs and suggest public health priorities.  It is vital to identify and registrar all cancer cases.  By not identifying all of the cancer cases, cancer incidence will be underestimated, giving a false impression of the magnitude of the cancer problem in the registry’s population area.  Inaccurate incidence rates can misdirect cancer control efforts, and provide a false picture of the effectiveness of treatment efforts.
−
|
 
−
|
 
−
|-
 
−
|}
 
  
−
==Profile Name==
+
Because most cancers are definitively diagnosed by microscopic examination of tissue, cancer surveillance programs rely on pathology reports to identify new cases and collect further information on cases previously reported.
−
The Cancer Registry Content Profile (CRC)
 
−
 
 
−
Monitoring the occurence of cancer is a cornerstone of cancer control decision making.  this monitoring, referred to as cancer surveillance, can be used to trigger case investigations, follow trends, evaluate the effectiveness of prevention measures such as screening and early detection programs and suggest public health priorities.  Because most cancers are definitively diagnosed by microscopic examination of tissue, cancer surveillance programs rely on pathology reports to identify new cases and collect further information on cases previously reported.
 
  
 
Two challenges relate to pathology laboratory reporting of cancer cases.  Laboratories may photocopy selected pathology reports and mail them to the cancer registry.  This method is labor intensive and prone to missing cases because the laboratory staff is not aware of the full case definition for identifying a cancer case.  Additionally, the cancer registry staff must re-enter the information into the cancer registry with a risk of data entry errors.
 
Two challenges relate to pathology laboratory reporting of cancer cases.  Laboratories may photocopy selected pathology reports and mail them to the cancer registry.  This method is labor intensive and prone to missing cases because the laboratory staff is not aware of the full case definition for identifying a cancer case.  Additionally, the cancer registry staff must re-enter the information into the cancer registry with a risk of data entry errors.
  
 
Alternately, laboratories may choose not to actively report cases, but allow cancer registry personnel to identify and photocopy appropriate pathology reports on site. This is very costly for the registry and has the same risk of data entry errors when the reports are manually entered into the registry database.
 
Alternately, laboratories may choose not to actively report cases, but allow cancer registry personnel to identify and photocopy appropriate pathology reports on site. This is very costly for the registry and has the same risk of data entry errors when the reports are manually entered into the registry database.
 +
 +
Further information on the benefits, challenges and the cancer registry's uses of electronic pathology reporting can be found in the:
 +
: [http://www.naaccr.org/filesystem/pdf/E-Path%20Reporting%20Guidelines_FINAL_01-29-07%20.pdf] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.
 +
  
  
 
===Use Cases===
 
===Use Cases===
−
 
 
;Pre-condition<br>
 
;Pre-condition<br>
−
A woman goes in for a routine mammogram and a suspicious area is noted.  The woman is referred to her family physician who does a biopsy and sends the tissue sample to the pathology laboratory for review and diagnosis.  
+
A woman goes in for a routine mammogram and a suspicious area is noted.  The woman is referred by her family physician to a surgeon who does a biopsy and sends the tissue sample to the pathology laboratory for review and diagnosis.  
  
 
The pathology laboratory receives the specimen, logs it into the laboratory information system (LIS) and prepares the specimen for analysis.  The pathologist analyzes the specimen and dictates his/her findings, which are then transcribed into the LIS.  The pathologist verifies the accuracy of the report and signs the transcribed report. The LIS marks the pathology report as "Final",  triggering the use case events.
 
The pathology laboratory receives the specimen, logs it into the laboratory information system (LIS) and prepares the specimen for analysis.  The pathologist analyzes the specimen and dictates his/her findings, which are then transcribed into the LIS.  The pathologist verifies the accuracy of the report and signs the transcribed report. The LIS marks the pathology report as "Final",  triggering the use case events.
  
 
;Events<br>
 
;Events<br>
−
The LIS gathers information from its database and other appropriate databases to create a message that contains all of the required data elements.  The LIS validates the data to ensure it conforms to the HL7 2.3.1 ORU-RO1 specification and transmits it to the Cancer Registry using a secure connection.
+
;1. Pathology Laboratory Creates Message
 +
 
 +
The LIS identifies that the report matches submission criteria because it is a histopathology test (biopsy) and the diagnosis relates to cancer ("carcinoma").  The LIS gathers information from its database and other appropriate databases to create a message that contains all of the required data elements.  The LIS validates the data to ensure it conforms to the HL7 2.3.1 ORU-RO1 specification and transmits it to the Cancer Registry using a secure connection.
 +
 
 +
[[Image:Prepare_Report_05282008.jpg|frame|center|Pathology Laboratory Process Flow <br>
 +
: [http://www.naaccr.org/filesystem/pdf/E-Path%20Reporting%20Guidelines_FINAL_01-29-07%20.pdf] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.]]
 +
 
 +
;1. Cancer Registry Processes Registration
 +
The Cancer Registry receives the HL7 messages, parses it into the processing database and determines that a cancer diagnosis has been documented.  The Cancer Registry staff codes the medical information. The pathology data and coded information is exported to the Cancer Registry Database and the message is archived.
  
−
The Cancer Registry receives the HL7 messages, parses it into the processing database and determines that a cancer diagnosis has been documented. The registrar codes the medical information. The pathology data and coded information is exported to the Cancer Registry Database and the message is archived.
+
[[Image:Process Report 05282008.jpg|frame|center|Cancer Registry Process Flow <br>
 +
: [http://www.naaccr.org/filesystem/pdf/E-Path%20Reporting%20Guidelines_FINAL_01-29-07%20.pdf] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.]]
  
 
;Post-condition<br>
 
;Post-condition<br>
Line 79: Line 96:
 
The message is available for future use as needed.
 
The message is available for future use as needed.
  
−
The following diagram constrains the scope of the Content Profile.
+
=== Scope ===
−
[[image:IHE-scope-of-profile-fig2.png|640px|thumb|center|Cancer Registry Content Profile Scope of Action Diagram]]
+
The following diagram constrains the scope of the Cancer Registry Pathology Report Content Profile.
 +
[[image:IHE-scope-of-profile-fig2.png|640px|thumb|center|Cancer Registry Pathology Report Content Profile Scope of Action Diagram <br>
 +
: [http://www.naaccr.org/filesystem/pdf/E-Path%20Reporting%20Guidelines_FINAL_01-29-07%20.pdf] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.]]
  
 
===Actors/Transaction===
 
===Actors/Transaction===
−
There are two actors in this profile, the Content Creator and the Content Consumer. Content is created by a Content Creator and is to be consumed by a Content Consumer. The sharing or transmission of content from one actor to the other is addressed by the appropriate use of IHE profiles described below, and is out of scope of this profile. A [[Document Source]] or a [[Portable Media Creator]] may embody the [[Content Creator]] Actor. A [[Document Consumer]], a [[Document Recipient]] or a [[Portable Media Importer]] may embody the [[Content Consumer]] Actor.
+
There are two actors in this profile, the Content Creator and the Content Consumer. Content is created by a Content Creator and is to be consumed by a Content Consumer. The sharing or transmission of content from one actor to the other is addressed by the appropriate use of IHE profiles described below, and is out of scope of this profile.  
−
 
 
−
The sharing or transmission of content or updates from one actor to the other is addressed by the use of appropriate IHE profiles described by section 3.7 Content Bindings with XDS, XDM and XDR found in the [[Frameworks#IHE_Patient_Care_Coordination_Technical_Framework|Patient Care Coordination Technical Framework]]
 
  
−
[[image:cccc.png|frame|center|Cancer Registry Content Actor Diagram]]
+
[[image:cccc.png|frame|center|Cancer Registry Pathology Report Content Actor Diagram]]
−
 
 
−
=== Options ===
 
−
 
−
: Not relevant for the Cancer Registry Content Profile
 
  
 
=== Grouping ===
 
=== Grouping ===
−
==== Content Bindings with XDS, XDM and XDR====
+
==== Care Management (CM) ====
−
It is expected that the transfers of care will occur in an environment where hospitals, pathology laboratories and physician offices have a coordinated infrastructure that serves the information sharing needs of this community of care. Several mechanisms are supported by IHE profiles:
+
The [[Content Creator]] of this profile must be grouped with the [[Clinical Data Source]] of the Care Management profile. The Clinical Data Source actor must implement the V2 Care Management Update Option.
−
* A registry/repository-based infrastructure is defined by the IHE [[Cross Enterprise Document Sharing]] (XDS) and other IHE Integration Profiles such as patient identification (PIX & PDQ), and notification of availability of documents (NAV).
 
−
* A media-based infrastructure is defined by the IHE [[Cross Enterprise Document Media Interchange]] (XDM) profile.
 
−
* A reliable messaging-based infrastructure is defined by the IHE [[Cross Enterprise Document Reliable Interchange]] (XDR) profile.
 
−
* All of these infrastructures support Security and privacy through the use of the [[Consistent Time]] (CT) and [[Audit Trail and Node Authentication]] (ATNA) profiles.
 
−
For more details on these profiles, see the [[Frameworks#IHE_IT Infrastructure_Technical_Framework|IHE IT Infrastructure Technical Framework]].
 
−
 
 
−
Content profiles may impose additional requirements on the transactions used when grouped with actors from other IHE Profiles.
 
−
 
 
−
==== Cross Enterprise Document Sharing, Media Interchange and Reliable Messages ====
 
−
Actors from the ITI XDS, XDM and XDR profiles embody the [[Content Creator]] and [[Content Consumer]] sharing function of this profile. A [[Content Creator]] or [[Content Consumer]] must be grouped with appropriate actors from the XDS, XDM or XDR profiles, and the metadata sent in the document sharing or interchange messages has specific relationships to the content of the clinical document described in the content profile.
 
−
 
 
−
==== [[Notification of Document Availability]] (NAV) ====
 
−
A Document Source should provide the capability to issue a [[Send Notification]] Transaction per the ITI [[Notification of Document Availability]] (NAV) Integration Profile in order to notify one or
 
−
more [[Document Consumer]](s) of the availability of one or more documents for retrieval. One of the Acknowledgement Request options may be used to request from a Document Consumer that
 
−
an acknowledgement should be returned when it has received and processed the notification.
 
−
A Document Consumer should provide the capability to receive a [[Receive Notification]] Transaction per the NAV Integration Profile in order to be notified by Document Sources of the availability of one or more documents for retrieval. The [[Send Acknowledgement]] option may be used to issue a Send Acknowledgement to a [[Document Source]] that the notification was received and processed.
 
−
 
 
−
==== [[Document Digital Signature]] (DSG)====
 
−
When a [[Content Creator]] Actor needs to digitally sign a document in a submission set, it may support the Digital Signature (DSG) Content Profile as a [[Document Source]].
 
−
When a [[Content Consumer]] Actor needs to verify a Digital Signature, it may retrieve the digital signature document and may perform the verification against the signed document content.
 
−
 
 
−
=== Content Modules ===
 
−
Content modules describe the content of a payload found in an IHE transaction. Content profiles are transaction neutral. They do not have dependencies upon the transaction that they appear in.
 
−
 
 
−
==== Content Module 1 ====
 
−
 
 
−
=== Process Flow ===
 
−
[[Image:seq.jpg|frame|center|Cancer Registry Content Pathology Laboratory Process Flow]]
 
−
 
 
−
[[Image:IHE-process diagram fig6.jpg|frame|center|Cancer Registry Content Registry Process Flow]]
 
−
 
 
−
 
 
−
Refer to the North American Association of Central Cancer Registries Electronic Pathology (E-Path) Reporting Guidelines for a description of the business rules.
 
−
 
 
−
== Actor Definitions ==
 
−
; Actor :
 
−
 
 
−
The Content Creator is played by the Laboratory Information System.
 
−
 
 
−
The Content Consumer is played by the Cancer Registry Software System.
 
−
 
 
−
== Transaction Definitions ==
 
−
; Transaction
 
−
: Not relevant for the Cancer Registry Content Profile
 
−
 
 
−
=Volume II=
 
−
===Cancer Registry Content ===
 
−
Consists of the following documents:<br>
 
−
Anatomic Pathology report
 
−
: histopathology
 
−
: flow cytometry
 
−
: cytology
 
−
: autopsy
 
−
: bone marrow
 
−
: peripheral smear
 
−
 
 
−
==== Standards ====
 
−
;Content 
 
−
: [http://www.naaccr.org/filesystem/pdf/Standards%20Volume%20V%20version%202.1_draftB_revised%20Jan%202008_B.pdf] :  North American Association of Central Cancer Registries Standards for Cancer Registries Volume V:  Pathology Laboratory Electronic Reporting; Version 2.1
 
−
:  HL7 2.3.1  ORU - Unsolicited Observation Message (event RO1)
 
−
 
 
−
; Standards for Identifying Pathology Reports
 
−
: NAACCR Search Term List
 
−
: [http://www.naaccr.org/index.asp?Col_SectionKey=7&Col_ContentID=139] 
 
−
 
 
−
; Case Definition
 
−
: Chapter III.  Standards for Tumor Inclusion and Reportability. NAACCR Standards for Cancer Registries Volume II:  Data Standards and Data Dictionary. Twelfth Edition; Record Layout Version 11.2. 
 
−
; [http://www.naaccr.org/filesystem/pdf/Vol_II_draft_board%20-%20Fix%20Pg%2098.pdf]
 
−
 
 
−
; Coding of Medical Information;
 
−
: International Classification of Diseases for Oncology (ICD-0) Third Edition
 
−
: World Health Organization
 
−
 
 
−
==== Data Element Index ====
 
−
Refer to NAACCR Standards for Cancer Registries Volume V:  Pathology Laboratory Electronic Reporting Verison 2.1, Chapter 2.6
 
  
−
==== Document Specification ====
+
The [[Content Consumer]] Actor of this profile must be grouped with the [[Care Manager]] actor of the Care Management profile.
−
Refer to NAACCR Standards for Cancer Registries Volume V:  Pathology Laboratory Electronic Reporting Verison 2.1, Chapter 2.6
 
  
−
==Section Template 1==
+
==== Basic Patient Privacy Consents (BCCP) ====
−
Refer to NAACCR Standards for Cancer Registries Volume V: Pathology Laboratory Electronic Reporting Verison 2.1, Chapter 2.6
+
When patient consent is required (for example, as in the case of Quebec), the Content Creator may be grouped with the Content Consumer Actor of the BPPC profile. When grouped with that actor, the Content Creator shall verify that an appropriate consent has been registered for the patient to share the pathology data prior to sending the message.
  
−
==Header Template 1==
+
== Policy Considerations ==
−
<pre>
+
; Batch or Real Time Reporting
−
<entry>An XML Example</entry>
+
Because the Cancer Registry Pathology Report Content Profile relates to secondary use of data, Batch Reporting with a frequency of every 24 hours is recommended.  
−
</pre>
 
−
=== entry ===
 
−
Description of the entry element.
 
  
−
==Entry Template 1==
+
; Case Selection
−
<pre>
+
A Content Consumer may require that all reports be transmitted, regardless of relevance to cancer, or it may require transmission to be restricted based on specific selection criteria.  This is a policy decision made by the Content Receiver based on state, provincial and fedreal legislations and/or regulations, rules or by operating policy.
−
<entry>An XML Example</entry>
 
−
</pre>
 
−
=== entry ===
 
−
Description of the entry element.
 
  
−
[[Category:PCC]]
+
== Security Considerations ==
−
[[Category:Draft Profile Supplement]]
 
  
−
<!-- {{:Content Profile Supplement Template|Antepartum Record|AR|One sentence||PCC}} -->
+
== Requirements/Capabilities ==
 +
; Case selection
 +
Provide option to select all reports or only those that meet selection criteria.  Refer to Volume II for:
 +
* List of anatomic pathology reports
 +
* Standards for Identifying Pathology Reports
 +
* List of Cancer Medicine [http://www.rapidtest.com/products-elisakits.html Elisa kit]
 +
; Message Conformance
 +
Message can be validated using: <br>
 +
: [http://www.naaccr.org/index.asp?Col_SectionKey=7&Col_ContentID=501] : NAACCR Volume V Messaging Workbench Profile.

Latest revision as of 18:53, 7 December 2009

Introduction

This is a draft of the Cancer Registry Pathology Report Content Profile (CRPR) supplement to the PCC Technical Framework. This draft is a work in progress, not the official supplement or profile.

Profile Abstract

The Cancer Registry Pathology Report Content Profile (CRPR) defines the the content used in the PCC-11 to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.

Glossary

International Classification of Diseases for Oncology, 3rd Edition (ICD-O-3)

Classification system for reporting incidences of malignant diseases.

NAACCR

The North American Association of Central Cancer Registries. A collaborative umbrella organization for cancer registries, governmental agencies, professional organizations, and private groups in North America interested in enhancing the quality and use of cancer registry data.

Pathology Report

The written description of the microscopic examination of a tissue. The gross description reports the physical characteristics of the tissue: size, color, and abnormalities visible with the unaided eye. The microscopic description reports the cellular characteristics aided by the use of a microscope: what cells are involved, the behavior, and the aggressiveness or grade of any abnormality. The final diagnosis is a summary of the findings and indicates the pathologist’s impression of what was found in concise terms.

Issue Log

Open Issues

  1. Issue: Dependencies: need help understanding this component
    • Depends on Care Management with the V2 option (and by reference ATNA and CT)
  2. Issue: Modify Actor/Transactions (Keith)
  3. Issue: Modify Content Module for V2 profiles (Keith)
  4. Issue: Grouping: Does this need to be modified for the CRC profile?
    • Yes, not sure how

This text needs to be fixed-->>Register Pathology Implementation Guide with HL7 Message Profile Registry<<--

In Progress

Closed Issues

  1. Issue: Glossary: Use MERP glossary document or consolidated glossary tool?
    • Refer to the existing document
  2. Issue: Options: need help understanding this component
    • Won't have any
    • Added options based on discussion at May f2f meeting.
  3. Issue: Transaction Definitions: need help understanding this component
    • Not relevant to this profile
  4. Issue: What information do we need to include in 3.1.2, 3.1.3, 3.2, 3.3, 3.4?
    • Just reference the NAACCR Documentation on this section
  5. Should we include a sample message?
    • include a link to a webpage of a sample message. There are ways to convert a document to a webpage....

Volume I

Add the following bullet to the list of profiles
  • The Cancer Registry Pathology Report Content Profile (CPR) defines the the content used in the PCC-11 to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.

Dependencies

Add the following row(s) to the list of dependencies
Integration Profile Dependency Dependency Type Purpose
Cancer Registry Pathology Report (CPR) Care Management (CM) The Content Creator actor of the CPR profile must be grouped with the Clinical Data Source Actor of the CM profile The CPR profile defines the content sent in the PCC-11 transaction specified in the CM profile
Cancer Registry Pathology Report (CPR) Care Management (CM) The Content Consumer actor of the CPR profile must be grouped with the Care Manager Actor of the CM profile The CPR profile defines the content recieved in the PCC-11 transaction specified in the CM profile
Cancer Registry Pathology Report (CPR) ATNA Actors the CPR profile shall implement the Secure Node Actor of the ATNA profile Ensures that transmissions and changes to patient health information are logged in an audit repository, and that communication is secured between nodes.
Cancer Registry Pathology Report (CPR) ATNA Actors the CPR profile shall implement the Time Client Actor of the CT profile Ensures that concistent time is used in all messages.

Cancer Registry Pathology Report Content

The Cancer Registry Pathology Report Content Profile (CRPR) defines the the content used in the PCC-11 to send a completed pathology report to a Cancer Registry using an HL7 Version 2.3.1 ORU message.

Monitoring the occurence of cancer is a cornerstone of cancer control decision making. this monitoring, referred to as cancer surveillance, can be used to trigger case investigations, follow trends, evaluate the effectiveness of prevention measures such as screening and early detection programs and suggest public health priorities. It is vital to identify and registrar all cancer cases. By not identifying all of the cancer cases, cancer incidence will be underestimated, giving a false impression of the magnitude of the cancer problem in the registry’s population area. Inaccurate incidence rates can misdirect cancer control efforts, and provide a false picture of the effectiveness of treatment efforts.

Because most cancers are definitively diagnosed by microscopic examination of tissue, cancer surveillance programs rely on pathology reports to identify new cases and collect further information on cases previously reported.

Two challenges relate to pathology laboratory reporting of cancer cases. Laboratories may photocopy selected pathology reports and mail them to the cancer registry. This method is labor intensive and prone to missing cases because the laboratory staff is not aware of the full case definition for identifying a cancer case. Additionally, the cancer registry staff must re-enter the information into the cancer registry with a risk of data entry errors.

Alternately, laboratories may choose not to actively report cases, but allow cancer registry personnel to identify and photocopy appropriate pathology reports on site. This is very costly for the registry and has the same risk of data entry errors when the reports are manually entered into the registry database.

Further information on the benefits, challenges and the cancer registry's uses of electronic pathology reporting can be found in the:

[4] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.


Use Cases

Pre-condition

A woman goes in for a routine mammogram and a suspicious area is noted. The woman is referred by her family physician to a surgeon who does a biopsy and sends the tissue sample to the pathology laboratory for review and diagnosis.

The pathology laboratory receives the specimen, logs it into the laboratory information system (LIS) and prepares the specimen for analysis. The pathologist analyzes the specimen and dictates his/her findings, which are then transcribed into the LIS. The pathologist verifies the accuracy of the report and signs the transcribed report. The LIS marks the pathology report as "Final", triggering the use case events.

Events
1. Pathology Laboratory Creates Message

The LIS identifies that the report matches submission criteria because it is a histopathology test (biopsy) and the diagnosis relates to cancer ("carcinoma"). The LIS gathers information from its database and other appropriate databases to create a message that contains all of the required data elements. The LIS validates the data to ensure it conforms to the HL7 2.3.1 ORU-RO1 specification and transmits it to the Cancer Registry using a secure connection.

Pathology Laboratory Process Flow
 : [1] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.
1. Cancer Registry Processes Registration

The Cancer Registry receives the HL7 messages, parses it into the processing database and determines that a cancer diagnosis has been documented. The Cancer Registry staff codes the medical information. The pathology data and coded information is exported to the Cancer Registry Database and the message is archived.

Cancer Registry Process Flow
 : [2] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.
Post-condition

Pathology information has been added to the Cancer Registry Database.
The message is available for future use as needed.

Scope

The following diagram constrains the scope of the Cancer Registry Pathology Report Content Profile.

Cancer Registry Pathology Report Content Profile Scope of Action Diagram
 : [3] : North American Association of Central Cancer Registries (NAACCR) Electronic Pathology (E-Path) Reporting Guidelines, Dec 2006.

Actors/Transaction

There are two actors in this profile, the Content Creator and the Content Consumer. Content is created by a Content Creator and is to be consumed by a Content Consumer. The sharing or transmission of content from one actor to the other is addressed by the appropriate use of IHE profiles described below, and is out of scope of this profile.

Cancer Registry Pathology Report Content Actor Diagram

Grouping

Care Management (CM)

The Content Creator of this profile must be grouped with the Clinical Data Source of the Care Management profile. The Clinical Data Source actor must implement the V2 Care Management Update Option.

The Content Consumer Actor of this profile must be grouped with the Care Manager actor of the Care Management profile.

Basic Patient Privacy Consents (BCCP)

When patient consent is required (for example, as in the case of Quebec), the Content Creator may be grouped with the Content Consumer Actor of the BPPC profile. When grouped with that actor, the Content Creator shall verify that an appropriate consent has been registered for the patient to share the pathology data prior to sending the message.

Policy Considerations

Batch or Real Time Reporting

Because the Cancer Registry Pathology Report Content Profile relates to secondary use of data, Batch Reporting with a frequency of every 24 hours is recommended.

Case Selection

A Content Consumer may require that all reports be transmitted, regardless of relevance to cancer, or it may require transmission to be restricted based on specific selection criteria. This is a policy decision made by the Content Receiver based on state, provincial and fedreal legislations and/or regulations, rules or by operating policy.

Security Considerations

Requirements/Capabilities

Case selection

Provide option to select all reports or only those that meet selection criteria. Refer to Volume II for:

  • List of anatomic pathology reports
  • Standards for Identifying Pathology Reports
  • List of Cancer Medicine Elisa kit
Message Conformance

Message can be validated using:

[5] : NAACCR Volume V Messaging Workbench Profile.
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