ISO_639-1 en false 2022-04-01 Heather Leslie Atomica Informatics heather.leslie@atomicainformatics.com Vebjørn Arntzen, Oslo universitetssykehus HF, Norway (Nasjonal IKT redaktør) Koray Atalag, University of Auckland, New Zealand Silje Ljosland Bakke, Helse Vest IKT AS, Norway (openEHR Editor) Sistine Barretto-Daniels, Ocean Informatics, Australia Lars Bitsch-Larsen, Haukeland University hospital, Norway Einar Fosse, National Centre for Integrated Care and Telemedicine, Norway Heath Frankel, Ocean Informatics, Australia Sam Heard, Ocean Informatics, Australia Kristian Heldal, Telemark Hospital Trust, Norway Lars Morgan Karlsen, DIPS ASA, Norway Shinji Kobayashi, National Institute of Public Health, Japan Heather Leslie, Atomica Informatics, Australia (openEHR Editor) Hugh Leslie, Ocean Informatics, Australia Ian McNicoll, freshEHR Clinical Informatics, United Kingdom (openEHR Editor) Bjoern Naess, DIPS ASA, Norway Andrej Orel, Marand d.o.o., Slovenia Rune Pedersen, Universitetssykehuset i Nord Norge, Norway Line Sæle, Nasjonal IKT HF, Norway John Tore Valand, Haukeland Universitetssjukehus, Norway (Nasjonal IKT redaktør) in_development This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/. openEHR Foundation Heather Leslie, Ocean Informatics, heather.leslie@oceaninformatics.com org.openehr openEHR Foundation org.openehr 79C98917A26378147AC057229082E613 dbc08042-a412-4211-8631-6f3a67ea3c89 0.0.1-alpha

ISO_639-1 de *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) Bericht Report *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 sv *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) rapport *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 fi *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) *report(en) *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 ko *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) 리포트 *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 pt-br *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) relatório *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 en To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. report Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. © openEHR Foundation

ISO_639-1 ar-sy *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) تقرير *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 it *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) rapporto *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 zh *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) 报告 *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 nb *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) rapport svar svarrapport *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 es-ar *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) informe *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 sl *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) *report(en) *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 nl *To carry information about a clinical investigation, such as the result of an interview or complete investigation into a death or occurrence of an infectious disease. (en) rapportage *Use to carry information about a clinical investigation, such as the record of an interview or investigation into a death or infectious disease notification. The main Sections/Content component has been deliberately left unconstrained. This will allow it to be populated with any SECTION or ENTRY archetypes appropriate for the clinical purpose within a template. (en) *Not to be used to carry information about the initial notification of a death or infectious disease for surveillance purposes. Use COMPOSITION.report-clinical_notification for this purpose. (en) © openEHR Foundation

ISO_639-1 de Ramona Wellmann, Natalia Strauch Medizinische Hochschule Hannover Strauch.Natalia@mh-hannover.de ISO_639-1 fi ISO_639-1 sv Sofia Janstad, Åsa Skagerhult SLL, Region Östergötland sofia.lang-janstad@sll.se, asa.skagerhult@regionostergotland.se ISO_639-1 es-ar Alan March Hospital Universitario Austral - Buenos Aires - Argentina alandmarch@gmail.com physician ISO_639-1 nb John Tore Valand, Liv Laugen, Silje Ljosland Bakke Helse Bergen, ​Oslo University Hospital, Norway, Helse Vest IKT AS liv.laugen@ous-hf.no, silje.ljosland.bakke@helse-vest-ikt.no ISO_639-1 ko Seung-Jong Yu InfoClinic Co.,Ltd. seungjong.yu@gmail.com Certified Board of Family Medicine in South Korea ISO_639-1 pt-br Adriana Kitajima, Débora Farage, Fernanda Maia, Laíse Figueiredo, Marivan Abrahão Core Consulting contato@coreconsulting.com.br Hospital Alemão Oswaldo Cruz (HAOC) ISO_639-1 sl ? ISO_639-1 ar-sy Mona Saleh ISO_639-1 it Francesca Frexia CRS4 - Center for advanced studies, research and development in Sardinia, Pula (Cagliari), Italy francesca.frexia@crs4.it ISO_639-1 nl Pieter Bos, Jelte Zeilstra Nedap Healthcare ISO_639-1 zh Yexuan Cheng 浙江大学 3160100913@zju.edu.cn 4f624d13-588c-493b-ac05-b221b5db4e79 openEHR-EHR-COMPOSITION.report-case_classification.v0 1.4 at0000.1 openEHR-EHR-COMPOSITION.report.v1 COMPOSITION true true false false 1 1 at0000.1 category true true false false 1 1 DV_CODED_TEXT true true false false 1 1 defining_code true true false false 1 1 CODE_PHRASE true true false false 1 1 openehr 433 context true true false false 0 1 EVENT_CONTEXT true true false false 1 1 other_context true true false false 0 1 ITEM_TREE true true false false 1 1 at0001 items true true false false 0 1 ELEMENT true true false false 0 1 at0002 value true true false false 0 1 DV_TEXT true true false false 1 1 ELEMENT true true false false 0 1 at0005 value true true false false 0 1 DV_TEXT true true false false 1 1 CLUSTER true false true 0 at0006 archetype_id/value matches {/.*/} Boolean 2007 false String archetype_id/value attribute C_STRING .* constraint ELEMENT true true false false 0 1 at0.1 value true true false false 0 1 DV_TEXT true true false false 1 1 name true true false false 1 1 DV_CODED_TEXT true true false false 1 1 defining_code true true false false 1 1 CODE_PHRASE true true false false 1 1 local at0.10 at0.11 ELEMENT true true false false 0 1 at0.2 value true true false false 0 1 DV_TEXT true true false false 1 1 ELEMENT true true false false 0 1 at0.23 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 CLUSTER true false true 0 at0.25 archetype_id/value matches {/openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1/} Boolean 2007 false String archetype_id/value attribute C_STRING openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1 constraint ELEMENT true true false false 0 1 at0.4 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 CLUSTER true false true 0 at0.5 archetype_id/value matches {/openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1/} Boolean 2007 false String archetype_id/value attribute C_STRING openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1 constraint ELEMENT true true false false 0 1 at0.18 value true true false false 0 1 DV_TEXT true true false false 1 1 ELEMENT true true false false 0 1 at0.7 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 CLUSTER true false true 0 at0.12 items true true false false 1 1 ELEMENT true true false false 0 1 at0.27 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 ELEMENT true false true 0 at0.8 value true true false false 0 1 DV_TEXT true true false false 1 1 CLUSTER true false true 0 at0.14 archetype_id/value matches {/openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1/} Boolean 2007 false String archetype_id/value attribute C_STRING openEHR-EHR-CLUSTER\.person(-[a-zA-Z0-9_]+)*\.v1|openEHR-EHR-CLUSTER\.organisation(-[a-zA-Z0-9_]+)*\.v1 constraint ELEMENT true true false false 0 1 at0.13 value true true false false 0 1 DV_TEXT true true false false 1 1 ELEMENT true true false false 0 1 at0.15 value true true false false 0 1 DV_TEXT true true false false 1 1 ELEMENT true true false false 0 1 at0.16 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 ELEMENT true true false false 0 1 at0.20 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 false false true false true 1 ELEMENT true true false false 0 1 at0.9 value true true false false 0 1 DV_DATE_TIME true true false false 1 1 false false true false true 0 *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) تقرير وثيقة لتوصيل المعلومات للآخرين, عادة كاستجابة لطلب من طرف آخر. *Tree(en) *@ internal @(en) العنصر التعريفي الفريد للتقرير معلومات التعريف حول التقرير الحالة حالة التقرير بشكل كلي. و لا تمثل هذه الحالة جزءا من التقرير و إنما جميعه ككل. *Extension(en) *Additional information required to capture local context or to align with other reference models/formalisms.(en) * e.g. Local hospital departmental infomation or additional metadata to align with FHIR or CIMI equivalents.(en) *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Poročilo *Document to communicate information to others, commonly in response to a request from another party.(en) Tree *@ internal @(en) ID Poročila *Identification information about the report.(en) Status *The status of the entire report. Note: This is not the status of any of the report components.(en) *Extension(en) *Additional information required to capture local context or to align with other reference models/formalisms.(en) * e.g. Local hospital departmental infomation or additional metadata to align with FHIR or CIMI equivalents.(en) Case classification report Container archetype to carry information about a clinical investigation. Index item The name or type of the health item under investigation. Report type The type of report. For example: hospital investigation; or community investigation. Date investigation initiated The date when the investigation was assigned to an investigator. Classifier Details about the individual(s) assigned to investigate the disease notification. Date of classification The date when the investigation report was completed. Index infectious disease Name of the infectious disease under investigation. Index health event Type of health event under investigation. Review type Identification of the category or level of review. For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. Date report submitted Date when the final report was submitted to the final health authority. Reviewed by Details about the review process and reviewers of the report. Reviewer role The formal role or position of the reviewer. For example: regional epidemiologist; or Ministry of Health. Reviewer Structured details about the individual or organisation who reviewed the report. Report comment Narrative response to the content of the report by the reviewer. Date review completed Date when the review of the report was completed. Health region Identification of the local health region where the index case was identified or the index event happened. This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. Date review submitted Date when the review was submitted to the next level of review. Date of notification Date when the disease or event notification was submitted. Notifier Identification of the facility or individual notifying about the disease or event. Date received for review Report Document to communicate information to others, commonly in response to a request from another party. Tree @ internal @ Report ID Identification information about the report. Status The status of the entire report. Note: This is not the status of any of the report components. Extension Additional information required to capture local context or to align with other reference models/formalisms. For example: local information requirements or additional metadata to align with FHIR or CIMI equivalents. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Informe Documento para comunicar información a otros, comunmente en respuesta a la solicitud de un tercero. Tree @ internal @ ID del informe Información para la identificación del informe. Estado El estado del informe como un todo. Nota: no se refiere al estado de alguno de los componentes del informe. *Extension(en) *Additional information required to capture local context or to align with other reference models/formalisms.(en) * e.g. Local hospital departmental infomation or additional metadata to align with FHIR or CIMI equivalents.(en) *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Relatório Documento para comunicar informações a outros, comumente em resposta a uma solicitação de terceiros. Tree @ internal @ Identificador do relatório Informação de identificação sobre o relatório. Estado O estado de todo o relatório. Nota: este não é o estado de qualquer dos componentes do relatório. Extensão Informação adicional requerida para capturar o contexto local ou para alinhar a outros modelos de referência/formalismos. Por exemplo: requisitos de informações locais ou metadados para alinhar com equivalentes do FHIR or CIMI. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Rapport Dokument som brukes for å kommunisere informasjon til andre, ofte som svar på en forespørsel. Tree @ internal @ Rapport ID Informasjon som identifiserer rapporten. Status Status for hele rapporten. Merk: Dette er ikke statusen for noen av enkeltkomponentene i rapporten. Tilleggsinformasjon Ytterligere informasjon som trengs for å kunne registrere lokalt definert innhold eller for å tilpasse til andre referansemodeller/formalismer. For eksempel lokale informasjonsbehov eller ytterligere metadata for å kunne tilpasse til tilsvarende konsepter i FHIR eller CIMI. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Bericht Ein Dokument zur Übermittlung von Informationen an andere, meist als Antwort auf eine Anfrage. Tree @ internal @ Bericht ID Identifizierungsmerkmal des Berichts. Status Der Status des gesamten Berichts. Hinweis: Dies ist nicht der Status einer Berichtskomponente. Erweiterung Zusätzliche Informationen zur Erfassung lokaler Inhalte oder Anpassung an andere Referenzmodelle/Formalismen. Zum Beispiel: lokaler Informationsbedarf oder zusätzliche Metadaten zur Anpassung an FHIR-Ressourcen oder CIMI-Modelle. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) *Report(en) 일반적으로 다른 상대의 요청에 대한 응답으로, 다른 사람들과 정보를 통신하는 문서. Tree @ internal @ *Report ID(en) 리포트에 대한 식별 정보. *Status(en) 전체 리포트의 상태. 주의: 이것은 리포트 컴포넌트들 중 어떤 부분의 상태가 아님. *Extension(en) 로컬 컨텍스트를 획득하는데 필요하거나 다른 참조 모델/표현과 조정에 필요한 추가 정보 예: 로컬 정보 요구사항 또는 FHIR나 CIMI의 동등한 것들과 조정하는 추가 메타데이터 *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Raportti Asiakirja tiedon välittämiseksi muille, vastauksena yleensä toisen osapuolen pyyntöön. Tree @ internal @ Raportti ID Raportin tunnistetiedot Status Koko raportin tila. Huomaa: Tämä ei ole minkään raporttiosien tila. Laajennus Tarvitaan lisätietoja paikallisen tilanteen mallintamiseksi tai yhdenmukaistamiseksi muiden vertailumallien / muodollisuuksien kanssa. Esimerkiksi: paikalliset tietovaatimukset tai ylimääräiset metatiedot FHIR- tai CIMI-vastaavien mukaisiksi. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Rapporto Documento per comunicare informazioni ad altri, comunemente in risposta ad una richiesta di un altro soggetto. Tree @ internal @ ID del rapporto Informazioni di identificazione del rapporto Stato Lo stato dell'intero rapporto. Nota: Questo non è lo stato di alcuna delle componenti del rapporto. Estensione Informazioni aggiuntive necessarie per catturare il contesto locale o per allinearsi con altri modelli/formalismi di riferimento. Per esempio: requisiti informativi locali o metadati aggiuntivi per allinearsi con gli equivalenti FHIR o CIMI. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Rapportage Document om informatie met anderen te communiceren, vaak op verzoek van een andere partij. Tree @ internal @ Rapportage ID Identificerende informatie over deze rapportage. Status De status van de rapportage. Let op, dit is niet de status van een van de onderdelen van de rapportage. Uitbreiding Extra informatie nodig om de context te beschrijven of te voldoen aan andere modellen of formalismen. Bijvoorbeeld: lokale informatievereisten of aanvullende metadata om overeen te komen met FHIR- of CIMI-equivalenten. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) Rapport Dokument för att förmedla information till andra, vanligen som svar på en begäran från en annan part. Tree @ internal @ Rapport-id Information som identifierar rapporten. Status Status för hela rapporten. Observera att detta inte är status för någon av rapportkomponenterna. Tilläggsinformation Plats för tilläggsinformation som krävs för lokala anpassningar eller anpassning till andra referensmodeller eller formella krav. Exempelvis lokala informationskrav eller metadata för anpassning till FHIR- eller CIMI-motsvarigheter. *Case classification report (en) *Container archetype to carry information about a clinical investigation. (en) *Index item (en) *The name or type of the health item under investigation. (en) *Report type (en) *The type of report. (en) *For example: hospital investigation; or community investigation. (en) *Date investigation initiated (en) *The date when the investigation was assigned to an investigator. (en) *Classifier (en) *Details about the individual(s) assigned to investigate the disease notification. (en) *Date of classification (en) *The date when the investigation report was completed. (en) *Index infectious disease (en) *Name of the infectious disease under investigation. (en) *Index health event (en) *Type of health event under investigation. (en) *Review type (en) *Identification of the category or level of review. (en) *For example: review by the facility or institution where the investigation was carried out; the local regional authority; or the national authority. (en) *Date report submitted (en) *Date when the final report was submitted to the final health authority. (en) *Reviewed by (en) *Details about the review process and reviewers of the report. (en) *Reviewer role (en) *The formal role or position of the reviewer. (en) *For example: regional epidemiologist; or Ministry of Health. (en) *Reviewer (en) *Structured details about the individual or organisation who reviewed the report. (en) *Report comment (en) *Narrative response to the content of the report by the reviewer. (en) *Date review completed (en) *Date when the review of the report was completed. (en) *Health region (en) *Identification of the local health region where the index case was identified or the index event happened. (en) *This data element supports reporting by a jurisdictional grouping rather than a specific facility or institution, place or physical address. This data element may be able to be derived from the precise recording of 'Investigation site'. (en) *Date review submitted (en) *Date when the review was submitted to the next level of review. (en) *Date of notification (en) *Date when the disease or event notification was submitted. (en) *Notifier (en) *Identification of the facility or individual notifying about the disease or event. (en) *Date received for review (en) 报告 用于交流信息的文件，通常是为了响应某一方的请求 Tree @ internal @ 报告ID 关于这份报告的标识信息。 状态 整份报告的状态。注意：这不是指报告的任何一个组成部分的状态 扩展 用于捕获本地的上下文或与其他参考模型/形式保持一致所需的其他信息。 比如：本地的信息需求或是为了与FHIR或CIMI保持一致的其他元数据。