PD CEN ISO/TS 22756:2020 Health Informatics

Standard Number: PD CEN ISO/TS 22756:2020

Pages: 42

Released: 2020-10-05

ISBN: 978 0 539 00616 2

Status: Standard

Overview

In the rapidly evolving field of healthcare, the integration of technology and informatics is crucial for enhancing patient care and optimizing clinical outcomes. The PD CEN ISO/TS 22756:2020 Health Informatics standard is a pivotal document that outlines the requirements for a knowledge base designed to support clinical decision-making systems, specifically in medication-related processes. This standard is essential for healthcare professionals, IT specialists, and organizations aiming to implement or enhance clinical decision support systems (CDSS) within their medication management workflows.

Purpose and Importance

The primary purpose of this standard is to provide a comprehensive framework that ensures the development and implementation of effective knowledge bases for CDSS. These systems are integral in assisting healthcare providers with making informed decisions regarding medication prescriptions, administration, and monitoring. By adhering to the guidelines set forth in this standard, healthcare institutions can significantly reduce medication errors, improve patient safety, and enhance the overall quality of care.

Key Features

• Comprehensive Guidelines: The standard offers detailed instructions on creating and maintaining a robust knowledge base that supports clinical decision-making in medication-related processes.
• Interoperability: It emphasizes the importance of interoperability between different healthcare systems, ensuring seamless integration and communication across various platforms and devices.
• Evidence-Based Recommendations: The standard encourages the use of evidence-based data to inform decision-making, ensuring that healthcare providers have access to the most current and reliable information.
• Patient Safety: By focusing on reducing medication errors, the standard plays a crucial role in enhancing patient safety and improving clinical outcomes.
• Scalability: The guidelines are designed to be scalable, making them applicable to healthcare institutions of all sizes, from small clinics to large hospital networks.

Who Should Use This Standard?

This standard is invaluable for a wide range of stakeholders in the healthcare industry, including:

• Healthcare Providers: Physicians, pharmacists, and nurses can utilize the standard to enhance their clinical decision-making processes, particularly in medication management.
• Healthcare IT Professionals: IT specialists responsible for developing and maintaining CDSS can leverage the standard to ensure their systems are effective and compliant with industry best practices.
• Healthcare Administrators: Administrators and decision-makers can use the standard to guide the implementation of CDSS within their organizations, ensuring alignment with strategic goals and regulatory requirements.
• Regulatory Bodies: Organizations responsible for setting healthcare standards and regulations can reference this document to inform policy development and compliance monitoring.

Benefits of Implementing the Standard

Implementing the PD CEN ISO/TS 22756:2020 standard offers numerous benefits, including:

• Enhanced Clinical Decision-Making: By providing healthcare professionals with access to a reliable and comprehensive knowledge base, the standard supports more informed and accurate clinical decisions.
• Improved Patient Outcomes: With a focus on reducing medication errors and optimizing treatment plans, the standard contributes to better patient outcomes and higher satisfaction rates.
• Increased Efficiency: Streamlining medication-related processes through effective CDSS can lead to increased operational efficiency and reduced costs for healthcare organizations.
• Regulatory Compliance: Adhering to the standard ensures compliance with industry regulations and best practices, reducing the risk of legal and financial penalties.

Conclusion

The PD CEN ISO/TS 22756:2020 Health Informatics standard is an essential resource for any healthcare organization looking to enhance its clinical decision support systems, particularly in the realm of medication management. By providing a clear and comprehensive framework, this standard helps ensure that healthcare providers have the tools and information they need to deliver safe, effective, and high-quality care to their patients. Whether you are a healthcare provider, IT professional, or administrator, this standard is a valuable asset in your efforts to improve patient care and optimize clinical outcomes.

PD CEN ISO/TS 22756:2020

This standard PD CEN ISO/TS 22756:2020 Health Informatics. Requirements for a knowledge base for clinical decision support systems to be used in medication-related processes is classified in these ICS categories:

• 35.240.80 IT applications in health care technology

This document specifies the requirements for developing a knowledge base for drug-related problems that cohere with the intended drug use, to be used in rule-based clinical decision support systems (CDSS), such as the criteria for selecting a raw data source and the quality criteria for the development and maintenance for the rules or clinical rules for drug safety. It also describes the process of how to develop a knowledge base, the topics to be considered by the developers of a knowledge base, and it gives guidance on how to do this.

This document gives guidelines for the development of a knowledge base:

• with rules to enhance decisions and actions in drug-related problems that cohere with the intended drug use;

• which can be used by all kinds of healthcare professionals, such as those who prescribe, dispense, administer or monitor medicines;

• which can be used in every care setting, including chronic and acute care, primary and specialized care;

• which is a repository of evidence/practice bases rules, assessed by experts;

• which is meant to be used in conjunction with a medicinal product dictionary;

• whose knowledge is structured in rules and therefore to be used in the type of rule-based CDSS.

This document does not:

• describe the exact content of a knowledge base i.e. the outcome of the process of developing rules.

• provide the requirements for a clinical decision support system, the software that uses the knowledge base combined with the patient’s data, and presents the outcome of the rules to the healthcare professional. These requirements are described in ISO /DTS  22703 ¹

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  Under preparation. Stage at the time of publication: ISO /DTS  22703 .

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• give the requirements for non-medication knowledge bases. Some aspects of the requirements in this document are general in nature and applicable to other kinds of knowledge bases, but this document does not address all of the requirements of non-medication knowledge bases.