IHE PaLM TF Suppl. APSR 2.0

Aus Hl7wiki
Draft for Public Comment / Implementierungsleitfaden "Pathologiebefund auf der Basis von CDA R2"
Wechseln zu: Navigation, Suche


Abstimmungsdokument 
Version Datum Status Realm
09 2016 Si-draft.svg Entwurf Flag de.svg Deutschland
Document PDF.svg noch kein download verfügbar
Kontributoren 
Logo-Agfa.jpg Agfa HealthCare GmbH Bonn
Logo-vivantes.jpg Vivantes Netzwerk für Gesundheit Berlin
LogoSKDF.GIF Städtisches Klinikum Dresden Friedrichstadt Dresden

Document information

Dieses Material ist Teil des Leitfadens Implementierungsleitfaden.
  • Direkt im Wiki geändert werden sollten Schreibfehler, ergänzende Hinweise.
  • Offene Fragen, die der Diskussionen bedürfen, sollten auf der Diskussionsseite aufgenommen werden.
  • Liste der Seiten dieses Leitfadens: hier, Liste der Seiten, in denen dieses Material verwendet (transkludiert) siehe hier .

Impressum

For the Anatomic Pathology Structured Report Version 2.0 (APSR 2.0), an IHE Project, the existing German "Leitfaden Pathologiebefund" has been modified to an IHE Technical Framework document, starting from the IHE reference text APSR, Trial Implementation, to be linked with Art-Decor for the specification of value sets, terminologies, and templates according HL7/CDA.

Dieser Leitfaden wird von einer Arbeitsgruppe des Interoperabilitätsforum in Kooperation mit dem Berufsverband der Pathologen erstellt. Er basiert auf dem Leitfaden "Arztbrief 2014", der parallel hierzu durch eine Arbeitsgruppe des Interoperabilitätsforums erstellt wird.

Dieses Material ist Teil des Leitfadens Implementierungsleitfaden.
  • Direkt im Wiki geändert werden sollten Schreibfehler, ergänzende Hinweise.
  • Offene Fragen, die der Diskussionen bedürfen, sollten auf der Diskussionsseite aufgenommen werden.
  • Liste der Seiten dieses Leitfadens: hier, Liste der Seiten, in denen dieses Material verwendet (transkludiert) siehe hier .

Contact

  • IHE PaLM, palm@ihe.net
  • Prof.Dr. Gunter Haroske, BVDP, Berlin, haroske@icloud.com
  • Francois Macary, PHAST, Paris, francois.macary@phast.fr
  • Dr. Frank Oemig, Deutsche Telekom Healthcare Solutions GmbH, Bonn, Frank.Oemig@t-systems.de
  • Dr. Kai-Uwe Heitmann, hl7@kheitmann.de
Dieses Material ist Teil des Leitfadens Implementierungsleitfaden.
  • Direkt im Wiki geändert werden sollten Schreibfehler, ergänzende Hinweise.
  • Offene Fragen, die der Diskussionen bedürfen, sollten auf der Diskussionsseite aufgenommen werden.
  • Liste der Seiten dieses Leitfadens: hier, Liste der Seiten, in denen dieses Material verwendet (transkludiert) siehe hier .

Authors and copyrights, terms of use

Copyright permissions

This document has been developed by Agfa HealthCare GbmH, Bonn, in cooperation with the HL7 user group Germany e.V. The claims for use or publication are not restricted.

The content of this specification is public.

It should be noted that parts of this document are based on the reconciliation package 2 of May 17, 2009 and the HL7 version 3 normative edition 2008, for which © Health Level Seven, Inc. applies. For further information see http://www.hl7.de/ and http://www.hl7.org/.

The extension or rejection of the specification, in whole or in part, shall be notified in writing to the board of the user group and to the editors / authors.

All HL7 specifications, adapted and published to national circumstances, can be used in any type of application software without license and usage fees.

Health Level Seven, Inc. has granted permission to the IHE to reproduce tables from the HL7 standard. The HL7 tables in this document are copyrighted by Health Level Seven, Inc. All rights reserved. Material drawn from these documents is credited where used.

Disclaimer

Although this publication has been compiled with the utmost care, neither HL7 Deutschland e.V. nor the companies involved in the creation can assume any liability for direct or indirect damage that could arise through the content of this specification. {DocumentPart}

Authors

  • Francois Macary, PHAST, Paris
  • Dr. Gunter Haroske, Federal Association of German Pathologists, Berlin
  • Dr. Frank Oemig, Deutsche Telekom Healthcare Solutions GmbH, Bonn
  • Dr. Riki Merrick, APHL, San Francisco
  • Dr. Raj Dash, Duke University, Durham

with contributions by

  • Dr. Christel Daniel, Paris (CD)
  • Prof. Dr. Thomas Schrader, Berlin/Brandenburg (TS)
  • Dr. Kai-Uwe Heitmann, Köln (KH)
  • Dr. Jochen Thümmler, Agfa HealthCare GmbH, früher bei Vivantes Netzwerk für Gesundheit, Berlin, (JT)
  • Prof. Dr. Stefan Sabutsch, ELGA, Wien, (SS)
  • Ivonne Riedel, Agfa HealthCare GmbH, Bonn, (IR)


Dieses Material ist Teil des Leitfadens Implementierungsleitfaden.
  • Direkt im Wiki geändert werden sollten Schreibfehler, ergänzende Hinweise.
  • Offene Fragen, die der Diskussionen bedürfen, sollten auf der Diskussionsseite aufgenommen werden.
  • Liste der Seiten dieses Leitfadens: hier, Liste der Seiten, in denen dieses Material verwendet (transkludiert) siehe hier .

Foreword

This is a supplement to the IHE Pathology and Laboratory Medicine Technical Framework V8.0. Each supplement undergoes a process of public comment and trial implementation before being incorporated into the volumes of the Technical Frameworks.

This supplement was published on September 27, 2017 for Public Comment, with a comment period extending to mid-November. The current content is the Trial Implementation version, which has taken in consideration the comments received.

This supplement describes changes to the existing technical framework documents.

“Boxed” instructions like the sample below indicate to the Volume Editor how to integrate the relevant section(s) into the relevant Technical Framework volume.

Replace Section X.X by the following:

Where the amendment adds text, make the added text bold underline. Where the amendment removes text, make the removed text bold strikethrough. When entire new sections are added, introduce with editor’s instructions to “add new text” or similar, which for readability are not bolded or underlined.

General information about IHE can be found at: http://www.ihe.net.

Information about the IHE Pathology and Laboratory Medicine domain can be found at: http://ihe.net/IHE_Domains.

Information about the structure of IHE Technical Frameworks and Supplements can be found at: http://ihe.net/IHE_Process and http://ihe.net/Profiles.

The current version of the IHE Technical Framework (if applicable) can be found at: http://ihe.net/Technical_Frameworks.

Comments may be submitted on IHE Technical Framework templates any time at http://ihe.net/ihetemplates.cfm. Please enter comments/issues as soon as they are found. Do not wait until a future review cycle is announced.

Acknowledgements

Following authors mainly contributed to this document:

  • Francois Macary, PHAST, Paris
  • Dr. Gunter Haroske, Federal Association of German Pathologists, Berlin
  • Dr. Frank Oemig, Deutsche Telekom Healthcare Solutions GmbH, Bonn
  • Dr. Riki Merrick, APHL, San Francisco
  • Dr. Raj Dash, Duke University, Durham

They have to acknowledge the contributions of Dr. Kai U. Heitmann, who managed the cooperation between PaLM and ART-DECOR. It was the very first time that a complete IHE TF document could be developed by means of the ART-DECOR tools and a media wiki.

Introduction to this Supplement

This supplement complements volume 1 of the PaLM technical framework with the description of the APSR 2.0 content profile, and volume 3 with the bindings, content modules and value sets, which specify this profile.

Open Issues and Questions

None yet

Closed Issues

APSR-07 – Representing the hierarchy of specimens in an entry : This APSR supplement enables to represent the hierarchy of specimens at the CDA level 3. The operations on specimen and production of child specimens are tracked in the “Procedure Steps” section, which has a level 3 entry.

APSR-10 – Observation related to multiple specimens: For example tumor staging may require combining data from multiple specimens (e.g., a breast excision with positive margins followed by a re-excision with clear margins – in this case the tumor size may be a composite of measurements from both specimens. Another example is staging of ovarian carcinomas with multiple biopsies of pelvis, peritoneum, nodes, omentum, etc.). To accommodate these use cases, each problem organizer as well as each observation may reference any number of specimens using the <specimen> child element. Each of these references may point to a detailed description of the specimen, in the "procedure steps" section.

APSR-11 – Derivative specimens:Specimens derived from primary specimens for ancillary studies, which may be sent to a reference lab or done in another part of the same institution, are included in the scope of this profile. The results produced on a derived specimen are attached to this specimen in the report.