The following is a list of current standards and technical reports from the ADA Standards Committee on Dental Informatics (SCDI). To purchase any document below, please visit the ADA Store.
ADA members receive technical reports at no charge and standards are available at a discounted rate. Additionally, ADA members have access to executive summaries of all documents below as a member benefit.
The purpose of this standard is to present a standard logical data model and documentation for a clinical data architecture capable of supporting healthcare information systems and the interoperability of health information. This standard is independent of the constraints of healthcare profession and specialty, the modality of healthcare processes, and the location and environment in which care is delivered. This standard is also independent of data management approach, and the data structures presented in the data model are culture and language neutral.
This document describes the modeling method and conventions employed, and presents the logical data model by subject area for the standard, along with its design rationale and explanatory scenarios.
The scope of this document identifies and describes those data structures needed to support the delivery of healthcare services to individuals and populations, for human and other living beings, and the management of those resources needed to enable these care delivery processes, along with the relationships among those data structures.
This standard continues to be a dynamic, living document that is maintained current with advances in the arts and sciences of the health professions and the changing environment of health care delivery.
This Technical Report is intended as a working document to assist in developing standards for infection control guidelines for dental informatics devices and equipment. Dental informatics equipment and devices consist of the computerized clinical information systems used in dentistry. Devices are those items intended for intraoral use and include digital radiographic equipment, intraoral camera and microscope systems, periodontal probing devices, occlusal force analysis systems, pulp testers, apex locators, and intraoral printers. Equipment is used to support these devices and includes foot controls, headsets, keyboards, pointing devices, and computers and other peripheral hardware such as printers, scanners, CD players, and monitors. This report addresses infection control issues related to the devices and equipment used in dental informatics and is based on the existing infection control protocols related to dental patient care. Devices and equipment used in patient treatment areas should be designed or be able to be adapted to allow appropriate infection control protocols which prevent patient cross-contamination as well as the introduction of environmental infectious agents into the operative site.
Practitioners need to understand exactly the specific requirements that may be indicated to provide security and how to address each requirement. While security refers to “ensuring” protection of electronic protected health information (ePHI), providers are not expected to implement security protection regardless of the cost. One needs to balance the risks of inappropriate use or disclosure of ePHI against the cost of various protective measures. The size and capabilities of the provider also may be taken into account. Smaller practices will not be expected to implement the levels of security in the same manner and at the same cost as a large entity, since risk and vulnerability increase with size and complexity of practice. Small practices tend to be less complex entities, have less sophisticated technology, have fewer resources to expend on security, and may have a lower risk of inappropriate use and disclosure of ePHI as a result of having a smaller staff. This report discusses requirements for practices to ensure transmission security to protect the integrity of data sent over the Internet and to authenticate the data received.
This report presents options available to prevent data loss and corruption, maintain data integrity and maintain and restore access to data. It also discusses appropriate contingency plans in emergency situations for recovery and authentication of the data as well as accessing the information.
This report provides a technical standard based on the DICOM version 3 Standard as it applies to dentistry with the goal of increasing interoperability between digital radiographic systems. It lists the components required for intraoral and extra-oral digital radiography.
With this implementation guide vendors, developers and other users can efficiently and economically build clinical databases and data systems from the ANSI/ADA 1000 Standard. This implementation guide shows how to migrate the data model components in the standard to a functioning data system, including how to optimize these models.
The focus of this Technical Report is to provide basic information on the use of digital photography in dentistry and to help facilitate: 1). The appropriate selection of the necessary equipment; 2). Consistent communication between concerned parties with and interoperability of digital images and the information the contained therein. The information provided will address the digital imaging needs of the various dental specialties, the general dental practitioner, other health care providers, the patient and any interested third parties such as insurance carriers, prosthetic and pathology laboratories. These discussions take into consideration the interoperability requirements to insure proper identification, exporting and importing of the image and database management of the image. To capture a quality digital image is not enough- the image has to have proper and standardized labeling of what it contains (the structures that are visible in the image) and the necessary DICOM descriptors of what, how and when it was captured.
This technical report is intended to increase the awareness and knowledge of dentists and dental healthcare providers about key concepts of the Electronic Dental Record (EDR) and the standards development process. The document can serve as a primer on the subject and as a tool to help dental offices implement an EDR. This report is useful because the application of computer-based systems in the management of dental practices, both private and institutional, have proven to be a significant and necessary resource.
The purpose of this document is to develop and present a shared understanding of the structure and content of data needed to support healthcare processes. This conceptual model forms the foundation for more detailed data representations in clinical information and the structure and content of data presented in the various types of electronic health and patient records.
The scope of this technical report is to present the types of data and electronic format necessary to create an electronic dental laboratory prescription. Another goal of this report is to create security awareness and education for the dental practitioner associated with electronic dissemination of patient information offsite to the outsourced dental laboratory.
This report provides a technical standard based on the DICOM (Digital Imaging and Communications in Medicine) version 3 Standard as it applies to dentistry with the goal of increasing interoperability between practitioners. In particular, this report highlights the benefits of the ZIP File over Email Interchange Profiles of the DICOM Standard for dentists or specialists who don't share the same image data repository, but need to exchange patient data in a fast and secure manner.
This report provides a technical standard based on the DICOM Standard as it applies to dentistry with the goal of increasing interoperability within and between institutional digital radiographic systems. This report will illustrate through high-level interaction use cases how to achieve interoperability for typical dental imaging tasks. They are: (1) view images on removable media; (2) create interoperable removable media images; (3) share images among various networked multi-vendor storage and acquisition systems; (4) ability to exchange visible light photographic and endoscopic images within a dental image acquisition context; (5) create and exchange DICOM structured display objects; (6) perform scheduled workflow to integrate digital images with an electronic dental records system; (7) import and reconcile Images from outside the institution into the electronic dental records system; (8) securely transfer DICOM images via email, and; (9) access DICOM images via the Internet. These use cases show the DICOM requirements in context, describing them in clear relationship to the clinical tasks of the dental provider.
This technical report presents the types of data and electronic format necessary to be included on an electronic dental laboratory prescription. The goal of this report is to address the need for electronic transmission of patient information from the dental practitioner to the outsourced dental laboratory with the necessary security and interoperability.
This report discusses the issues involving interoperability that arise when digital radiography and photography are integrated into a dental practice. The report describes the features of DICOM that facilitate resolution of these issues and allows a dental practice to achieve interoperability within their imaging and practice management systems and with outside healthcare data systems and networks. Descriptions of the components of a digital radiography system and guidelines on what to look for when choosing digital radiography components also are included.
The purpose of this standard is to develop uniform nomenclature for the description of forensic dental data and define a standardized set of uniform terms to convey this information. The goal of the standard is not to define the extent of information collected, only to be certain that common terms are used in order to aid in an identifying human remains or a living amnesiac.
In the current DICOM documentation, cephalograms are not addressed directly. This technical report (TR) was developed to fill the gap in such a way as to provide imaging equipment vendors an approved way of storing cephalograms, along with their clinically relevant data, in an interoperable way.
In addition, this TR shall serve as a part of the foundation for the definition of ADA SCDI approved guidelines for the storage and transfer of orthodontic electronic patient records through the utilization of existing popular informatics standards. This TR shall be included in the definition of an ADA SCDI document to specify the integration of DICOM and HL7 standards for orthodontic data.
This document was initially designed for scanned film-based cephalograms, but is intended to be used for digitally created cephalograms as well.
The purpose of this document is to identify the minimum functionality required of an electronic dental system to perform effectively in an interoperable and coordinated care environment.
The scope of this white paper is to present and establish the guidelines for standard electronic prescriptions in dentistry. The NCPDP/SCRIPT standard addresses prescription transactions between provider/office practice and retail pharmacy and currently has the broadest acceptance in the ambulatory setting.
The scope of this technical report is to present the types of data and electronic format necessary to be included on an electronic orthodontic dental laboratory prescription. The goal of this report is to address the need for electronic transmission of patient information from the orthodontic provider to the outsourced dental laboratory with the necessary security and interoperability. This technical report provides additional guidelines for the format, content and security of patient data disseminated offsite to the outsourced dental laboratory. The recommendations provided herein are designed to be technology-neutral and to be scalable to address the needs of both large and small facilities.
Forensic dental age assessment produces an estimate of chronologic age through dental analysis. The intent of this technical report is to describe current best practices for the process of human dental age assessment; however, it is not intended to supersede local, state, or federal regulations. As a resource, this document could assist in the development of regulations for those agencies. This document describes the methodologies and best practices for estimating the chronologic age of a living or deceased individual by analysis of the human dentition and associated maxillofacial structures.
Third-party payers may require submission of supporting documentation (e.g., radiographs, narratives, measurements, periodontal charts) before claims can be adjudicated. Increased application of information technology standards and electronic transactions reduces the time required for claims processing and the costs associated with it by providing a seamless information exchange. A great deal of information is gathered during a comprehensive evaluation of the patient so that the dentist can formulate a diagnosis and treatment plan. Much of the information sent by dentists to third-party payers may not aid in claims adjudication. This standard describes content for electronic claims attachments submitted to third-party payers.
The Food and Drug Administration (FDA) has issued a rule to establish a system to adequately identify devices through distribution. This rule requires the label of medical devices to include a unique device identifier (UDI), except where the rule provides for an exception or alternative placement. The labeler must submit product information to the FDA's Global Unique Device Identification Database (GUDID), unless subject to an exception or alternative. The rule further requires the label and package of each medical device to include a UDI and requires the UDI to be directly marked on the device itself if the device is intended to be used more than once. Practitioners need to have an understanding of this rule and what it will entail as it is required to go into practice, from a clinician side. The manufacture chain and responsibilities have been clearly identified by the FDA, but the clinical use has not; and thus that was determined to be the main focus of this paper.
The Reference Core Data Set (RCDS) provides for the structured electronic data elements to support key information exchange among and between dental and other health care settings. This includes the electronic sharing of essential patients’ demographic and dental encounter/clinical data in a structured, computable format between dental or other health care venues. The standard provides a technical specification to extract, format and transmit essential patients’ demographic and dental and medical encounter and clinical data between one dental information system to another dental or medical health information system to support key syntactic and semantic information exchange.
This Technical Report will describe the essential characteristics of digital tools that collect clinician- or patient-entered information including consideration of systemic co-morbidities for the purposes of creating individual or population estimates of risk for specific oral diseases and associated medical co-morbidities. These characteristics include the input and output elements, usability, security and privacy features, and interoperability. Various potential use-cases for risk assessment software are described.
The goal of this technical report is to provide the best available current information to forensic odontologists, forensic pathologists, medical examiners and coroners, law enforcement personnel, dental schools, emergency planners and others on the best practices recommended by the forensic odontology community. It includes guidelines on how to obtain comparative forensic dental data as well as the recommended methodologies to reconcile that data in order to establish an identification by comparative dental analysis.
This technical report defines inventory management requirements in dental practices for HCT/Ps to ensure traceability from the donor to the recipient and the recipient to the donor. Its intent is also to facilitate reporting of potential adverse reactions, including disease transmission, to all parties involved in processing the HCT/P.
The purpose of this document is to describe the adoption of two Quality Matters Rubrics (Higher Education and Continuing & Professional Education) as an updated standard for online and blended dental education courses for students and professionals.
The purpose of this document is to describe cloud computing and data storage, its use in dental practice, its benefits and risks, and recommendations for use by dental practitioners. The document covers four areas of cloud computing applied to dentistry: What cloud computing entails, how it benefits the dental practice, the risks and issues associated with cloud computing and cloud storage; and business aspects of cloud computing and data storage.
This technical report is a primer for dental providers to facilitate adoption and use of dental diagnostic codes. The report includes information on current diagnostic code sets pertinent to the practice of dentistry and mechanisms to incorporate them in dental records, with real world examples and recommendations for risk management.
Quality assurance can be defined as the planned and systematic activities necessary to provide adequate confidence that a product or service will meet the given requirements. As this relates to digital intra-oral radiography, quality assurance entails the consistent production of x-ray images of high quality in order to provide the maximum amount of diagnostic information with minimal radiation exposure to the patient. Image optimization creates an optimal balance between these two factors: image quality and radiation dose. There are essentially three components involved with any digital intraoral imaging system: the image display device (computer, monitor, and display-software), the x-ray source, the digital image acquisition device (solid-state sensor or PSP imaging plate and scanner, and associated acquisition-software). Each of these components is addressed in this standard to improve their functions for image optimization.
The purpose of this document is to assist covered practitioners in fulfilling their legally mandated obligation to conduct a security risk analysis, develop a plan to protect patient data privacy and security and to train the dental team. In doing so, the document will help covered entities to understand and analyze the risk, and assist in choosing the appropriate partners in the fields (in terms of vendors of software and/or services) in order to help train and protect all the parties involved.
The purpose of this document is to provide requirements for the essential characteristics for digital caries risk assessment resources, including: standardized definitions; clinical input elements; assessment methods for data collection; scoring methodology considerations; and reporting formats. Uses of digital caries risk assessment resources are: To provide clinical decision support for healthcare providers; provide anticipatory guidance for caregivers and patients; and to facilitate the interchange of caries risk assessment data among stakeholders, including individual healthcare providers, healthcare organizations, academic institutions, researchers, third-party payers and public health policy makers.
This white paper presents guidelines for improving the interoperability and transmissibility of visible light intraoral and extraoral images. The codes and enumerated terms presented in this paper permit construction of custom templates (view sets) for sorting images, reorienting intraoral images so that those taken with a mirror appear to be taken directly and sharing of images with minimal human intervention. This paper also demonstrates the view set, VS – 01, introduced in DICOM correction package CP1571, as well as three other custom view sets. Guidelines are shown for creation and transmission of images into templates using a variety of means via a server.
This document describes the essential characteristics for digital periodontitis risk assessment resources including standardized definitions, description of input elements, and components and characteristics of a periodontitis risk assessment report. Use cases for digital periodontitis risk assessment resources include clinical decision support for healthcare providers, care guidance for healthcare providers and patients, and interchange of periodontitis risk assessment data among stakeholders.
This document introduces the use of Artificial Intelligence (AI) and Augmented Intelligence (AuI) in clinical disciplines including prevention, caries and periodontal disease, implants, oral and maxillofacial surgery, endodontics, prosthetics, dentomaxillofacial imaging, orthodontics, temporomandibular joint disorder and sleep disorders. Promising developments in teledentistry, electronic dental records, dental laboratory uses and scanning also are included. This paper further provides information on non-clinical areas, with a focus on payor topics, such as claims processing, payment integrity and quality assurance, and on dental practice administrative issues involving claims preparation, including attachments. The document also provides information on the current regulatory environment, including the U.S. Food and Drug Administration (FDA) and the global framework.