Western Canada Chronic Disease Management Infostructure Initiative

Western Health Information Collaborative (WHIC) Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Me...
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Western Health Information Collaborative (WHIC)

Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

FINAL 06/29/2005 1:30 PM

Prepared by Western Health Information Collaborative June 29, 2005 - Version 7.1

Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

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TABLE OF CONTENTS 1. Introduction ............................................................................................................................... 1 2. Coding Systems......................................................................................................................... 3 2.1. Brief Description of the Coding Systems ........................................................................ 3 2.1.1. LOINC ............................................................................................................... 3 2.1.2. ICD-10-CA ......................................................................................................... 4 2.1.3. DSM-IV.............................................................................................................. 4 2.1.4. CCI ............................................................................................................... 4 2.1.5. ATC / DDD ........................................................................................................ 5 2.1.6. SNOMED CT ..................................................................................................... 5 2.2. Process for Selection of Coding Systems ........................................................................ 6 2.3. Specific CDM Coding Considerations and Explanations................................................ 7 2.3.1. LOINC Code Selection....................................................................................... 7 2.3.2. Specific Coding Systems .................................................................................... 7 2.3.3. “x LOINC” Codes .............................................................................................. 8 2.3.4. Type Code Sets and Value Code Sets ................................................................ 8 2.3.5. Object Identifiers (OIDs).................................................................................... 8 2.3.6. Symbols in Code Tables ..................................................................................... 9

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

1.

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INTRODUCTION The primary purpose of the Western Canada Chronic Disease Management (CDM) Infostructure Initiative is to develop chronic disease management data standards and information interchange messages, and to support the implementation of this infostructure within the four participating western provinces (British Columbia, Alberta, Saskatchewan, and Manitoba). The CDM Data Standards have been prepared to describe in clinical terms the scope, content and details of the CDM Data Standards developed for the Western Canada CDM Infostructure Initiative. This document is intended primarily for a clinical / business audience1. The CDM Data Standards have been organized as follows: •

CDM Data Standards – Introduction This document provides background information on the Western Canada CDM Infostructure Initiative, provides an overview of the Phase 2 Data Standards and HL7 Messaging project, describes the Chronic Disease Model, and provides an overview of the record and clinical data elements.



Appendix A – Coding Systems Includes an overview of the coding systems considered for the CDM Data Standards, describes the criteria and process for selection, and identifies special considerations and explanations for the selected code systems.



Appendix B – Record Level Data The record level data or structural data elements are generic data elements that are ‘fixed’ and are provided regardless of the type of chronic disease. This appendix provides the data definition, and identifies the data type and valid values for each of the data elements.

1

For more technical documentation on the CDM HL7 Message Specifications, please refer to the CDM HL7 Message Specifications – Implementation Guide.

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems



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Appendix C – Clinical Data Clinical data elements are specific data elements that pertain to chronic diseases. These data elements provide clinical information to assist clinicians in managing individuals with chronic diseases. This appendix provides the data definition, and identifies the data type (type code, type code value, type code name) and code table for each of the data elements.



Appendix D – Detail Data The detailed data attributes give additional specifics on the clinical data elements. The attributes describe the characteristics or details to be captured on person history, physical exams, lab tests, medications, procedures, etc. This appendix provides the data definition, and identifies the data type and valid values for each of the data elements.



Appendix E – Code Tables This appendix provides the details for the defined code sets that will be used for the CDM data elements (e.g. Code table name, source, codes, descriptions, print names, etc.).

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

2.

CODING SYSTEMS

Several coding systems were examined to determine their appropriateness for the CDM Data Standards and subsequently the HL7 Message Specifications. This section provides an overview of the coding systems, and describes the process and rationale used in their selection.

2.1. Brief Description of the Coding Systems Six coding systems were identified, with five being selected for the project. These were: •

LOINC (Logical Observation Identifiers, Names and Codes)



ICD-10-CA (International Classification of Diseases, Canadian)



DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition)



CCI (Canadian Classification of Interventions)



ATC / DDD (Anatomical Therapeutic Chemical Classification System with Defined Daily Doses)



SNOMED CT (SNOMED Clinical Terms)

A brief description of each coding system follows. 2.1.1. LOINC2

The purpose of the LOINC database is to facilitate the exchange and pooling of results, such as blood hemoglobin, serum potassium, or vital signs, for clinical care, outcomes management, and research. Currently, most laboratories and other diagnostic services use HL7 to send their results electronically from their reporting systems to their care systems. However, most laboratories and other diagnostic care services identify tests in these messages by means of their internal and idiosyncratic code values. Thus, the care system cannot fully "understand" and properly file the results they receive unless they either adopt the producer's laboratory codes (which is impossible if they receive results from multiple sources), or invest in the work to map each result producer's code system to their internal code system. LOINC codes are universal identifiers for laboratory and other clinical observations. Therefore, the adoption of LOINC codes facilitates correctly identifying, reporting, exchanging and storing lab results and clinical observations.

2

http://www.regenstrief.org/loinc/. Accessed 18 May 2005

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

The laboratory portion of the LOINC database contains the usual categories of chemistry, hematology, serology, microbiology (including parasitology and virology), and toxicology; as well as categories for drugs and the cell counts reported on a complete blood count or a cerebrospinal fluid cell count. Antibiotic susceptibilities are a separate category. The clinical portion of the LOINC database includes entries for vital signs, hemodynamics, intake / output, EKG, obstetric ultrasound, cardiac echo, urologic imaging, gastroendoscopic procedures, pulmonary ventilator management, selected survey instruments, and other clinical observations. 2.1.2. ICD-10-CA3

The International Statistical Classification of Diseases and Related Health Problems, 10th Revision (ICD-10) is an international standard for reporting clinical diagnoses developed by the World Health Organization. ICD-10-CA is an enhanced version of ICD-10 developed by the Canadian Institute for Health Information (CIHI) for morbidity classification in Canada. ICD-10-CA classifies diseases, injuries and causes of death, as well as external causes of injury and poisoning. The classification has 23 chapters with alpha-numeric categories and subcategories. Unlike ICD-9, ICD-10-CA applies beyond acute hospital care. ICD-10-CA also includes conditions and situations that are not diseases but represent risk factors to health, such as occupational and environmental factors, lifestyle and psycho-social circumstances. 2.1.3. DSM-IV4

Psychiatric diagnoses are categorized by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition. This manual is published by the American Psychiatric Association and covers all mental health disorders for both children and adults. It also lists known causes of these disorders, statistics in terms of gender, age at onset, and prognosis as well as some research concerning the optimal treatment approaches. 2.1.4. CCI5

The Canadian Classification of Health Interventions (CCI) is the new national standard for classifying health care procedures. CCI is the companion classification system to ICD-10-CA. CCI replaces the Canadian Classification of Diagnostic, Therapeutic and Surgical Procedures

3

http://secure.cihi.ca/cihiweb/dispPage.jsp?cw_page=codingclass_icd10_e. Accessed 17 May 2005.

4

http://allpsych.com/disorders/dsm.html. Accessed 08 June 2005.

5

http://secure.cihi.ca/cihiweb/dispPage.jsp?cw_page=codingclass_cci_e. Accessed 17 May 2005

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

(CCP) and the intervention portion of ICD-9-CM in Canada. CCI classifies a broad range of interventions, such as: •

Therapeutic interventions including inpatient and day surgeries, surgical and nonsurgical;



Diagnostic interventions including diagnostic imaging, tests, measurements, biopsies and explorations;



Cognitive, psychosocial and sensory therapeutic interventions;



Other health care interventions such as assistance with activities of daily living, environmental assessments, and counseling; and



Therapeutic interventions strengthening the immune system.

CCI specifies more precisely than ever before what interventions and services health professionals provide. It has been designed to be service provider and service-setting neutral and can be used comprehensively throughout the health system. 2.1.5. ATC / DDD6

The ATC / DDD system classifies therapeutic drugs. The purpose of the ATC / DDD system is to serve as a tool for drug utilization research in order to improve quality of drug use. In the ATC classification system, the drugs are divided into different groups according to the organ or system on which they act and their chemical, pharmacological and therapeutic properties. Drugs are classified into five different levels. Drug consumption statistics (international and other levels) can be presented for each of these five levels. 2.1.6. SNOMED CT7

SNOMED Clinical Terms (SNOMED CT) is a dynamic, scientifically validated clinical health care terminology and infrastructure that makes health care knowledge more usable and accessible. The SNOMED CT Core terminology provides a common language that enables a consistent way of capturing, sharing and aggregating health data across specialties and sites of care. Among the applications for SNOMED CT are electronic medical records, ICU monitoring, clinical decision support, medical research studies, clinical trials, computerized physician order entry, disease surveillance, image indexing and consumer health information services.

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http://www.who.int/classifications/atcddd/en/. Accessed 17 May 2005 http://www.snomed.org/snomedct/. Accessed 17 May 2005

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The SNOMED CT Core terminology contains over 364,400 health care concepts with unique meanings and formal logic-based definitions organized into hierarchies. As of January 2005, the fully populated table with unique descriptions for each concept contains more than 984,000 descriptions. Approximately 1.45 million semantic relationships exist to enable reliability and consistency of data retrieval.

2.2. Process for Selection of Coding Systems The CDM Project Team reviewed the applicable coding systems and considered several criteria in selecting the systems most appropriate for the CDM data standards and HL7 message specifications. The selection criteria included: 1. Canadian health system context: appropriateness of the coding system for use in the Canadian health care system, with a specific focus on chronic disease management (CDM). 2. Availability of coding system: availability and use of the coding system in the Canadian health care system, with a specific focus on chronic disease management. 3. Affordability: costs to obtain licenses for the coding system with an emphasis on minimizing the costs to CDM providers in the health care system. 4. Ease of implementation: relatively easy to implement the coding system within the CDM project timelines. 5. Fit with HL7 model: alignment of the coding system with the HL7 model developed for CDM. 6. Appropriate granularity: the level of detail available in the coding system and its appropriateness in meeting the CDM data requirements. 7. Comprehensiveness: the completeness of the coding system in capturing the CDM data requirements. Using the above criteria, the following table shows the CDM data grouping, the HL7 data groupings, the selected coding system and the key criteria for the coding system selection. In general the criteria were met by all the pertinent coding systems with the exception of SNOMED CT. The major concerns identified with SNOMED CT were the cost of licenses and the current lack of implementations within Canada. The CDM project is aware that SNOMED is currently under review by Canada Health Infoway (CHI) and is seriously being considered as its’ coding standard. If / when SNOMED becomes officially endorsed by Infoway, the CDM data

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Western Canada Chronic Disease Management Infostructure Initiative Phase 2: Data Standards and HL7 Messaging CDM Data Standards – Appendix A Coding Systems

standards may need to be revised to allow for the adoption of SNOMED as an additional code set. CDM Data Groupings Person Demographics Alert Indicators Characteristics Relevant to the Condition Co-morbidities / Complications

HL7 Data Groupings • • •

Record Level Data Exam / Observations Exam / Observations

Coding System • • • •



Other Medical Problems

ICD-10-CA LOINC

All All



ICD-10-CA DSM-IV LOINC

All All All



LOINC

All

• •

CCI LOINC

All All



ATC / DDD

All



LOINC

All

• • •

Markers of Disease Progression

• •

Interventions - Procedures



Interventions - Medications



Screening for Further Complications

2.3.

Lab Results / Plans / Goals Diagnostic Images Procedure

Medications and Immunizations



Lab Results / Plans / Goals



Exam / Observations

HL7 LOINC LOINC

Supporting Criteria All All All

Specific CDM Coding Considerations and Explanations

2.3.1. LOINC Code Selection

The Regenstrief Institute provides a Windows-based mapping utility called the Regenstrief LOINC Mapping Assistant (RELMA®) to facilitate searches through the LOINC database and to assist in mapping local LOINC codes. For this project, clinical terminology identified by the stakeholders, was mapped to the most appropriate LOINC code using specific key words and RELMA. A common problem with LOINC codes is that two distinct codes may apply to very similar concepts, especially for clinical observations. In these situations, the “best matched” LOINC code has been selected and alternate LOINC codes documented where deemed appropriate. 2.3.2. Specific Coding Systems

While specific coding systems are being used for the CDM data standards and HL7 message specifications, it is not necessary for the source system to use these coding systems in their

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applications. For example, ICD-10-CA is used in the CDM data and HL7 message specifications. However, a jurisdiction is not required to use ICD-10-CA in its application and could use ICD-9 CM to store data, and translate to ICD-10-CA codes when exchanging information with other applications via the HL7 message specifications. 2.3.3. “x LOINC” Codes

For some CDM data elements, specific LOINC codes do not exist. In these cases the CDM project team developed “x LOINC” codes which will be submitted as proposed codes to the Regenstrief Institute, the organization responsible for maintaining the LOINC database and the supporting documentation. 2.3.4. Type Code Sets and Value Code Sets

Two types of code sets are used. To classify a specific type of data element, LOINC codes are used as they are universal identifiers for laboratory and other clinical observations. As well LOINC codes directly relate to terminology used in HL7 data models. HL7 groups data as observations, examinations, diagnoses, results, referrals and imaging. In the CDM Infostructure Initiative the HL7 data groupings are shown on the data element spreadsheet as part of the row headings; e.g., Exam / Observations. To classify a specific data element within a type of data, a further classification using a value code is given. For example, LOINC has a type code for diagnosis—primary. All primary diagnoses are coded using this type code. However, to give information on the specific kind of diagnosis requires another classification system. In the Western Canada CDM Infostructure Initiative, the classification system used for diagnosis is either ICD-10-CA or in the case of psychiatric diagnoses, DSM-IV. 2.3.5. Object Identifiers (OIDs)

OIDs refer to an ISO Standard for uniquely qualifying all identifiers globally. In HL7 v3, all identifiers are defined by the II (Instance Identifier) datatype. This includes all identifiers for each CDM data element such as lab result identifiers, care plan identifiers, prescriptions identifiers, dispense record identifiers, etc. These identifiers use a combination of a mandatory OID root with an optional alpha-numeric extension to convey globally unique identifiers. The OID provides the namespace for the identifier, corresponding with who issued the identifier and what type of identifier it is.

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The CDM HL7 message specifications require the following types of identifiers: • Common identifiers: common identifiers are used across all applications such as the person identifier (e.g., provincial health number) and provider identifier (e.g., provider identifier given by professional affiliation). •

Application-specific identifiers: application-specific identifiers are created for records produced by clinical applications; e.g., procedure, observation, and care plan identifiers.

Common identifiers must be registered with HL7. All applications use the same OID for the same concept. For example, there will be one and only one OID used for the BC provincial health number. This would be used for all v3 specifications across all v3 standards. Application-specific identifiers need to be issued by the application that creates the item. This means that every application has to register for its own OID. Within its own OID structure, the application will need to create a sub-id for each type of identifier it produces. The set of application-specific identifiers in the CDM HL7 message specifications include procedure identifier, medication / vaccine prescription or dispense identifier, observation identifier, diagnostic image identifier, referral identifier, and care plan identifier. In addition to identifiers, OIDs are used to identify coding systems for code sets (e.g., ICD-10CA, CCI, gender codes) and HL7 artifacts (e.g., interaction ids, message ids, etc.). A full explanation of OIDS is included in the CDM HL7 Message Specifications – Implementation Guide. 2.3.6. Symbols in Code Tables



Use of **. The valid codes for a field that contain ** indicate that all applicable values or valid codes within that code set would be accepted. For example, “E10**” for diabetes means that all codes within that range for diabetes would be accepted.



Use of ^^. The CCI Code Structure is hierarchical. Each distinct code has up to nine different elements, with the first five being mandatory [CCI Base (Mandatory)] as follows: CCI Base (Mandatory) Position 1 – Section Position 2-3 – Group Position 4-5 – Intervention

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Where the concept is defined only to a certain position (i.e., up to position 5), all subsequent details [i.e., positions beyond position 5; referred to as CCI Qualifiers (Optional)] that are not being indicated are displayed as ^^. The CCI Qualifiers (Optional) follow: CCI Qualifiers (Optional) Position 6-7 – Technique or Reason Position 8-9 – Device or Method

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