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DPS
|
Digital Pathology System An image-based computer system that enables the acquisition, management and interpretation of pathology information generated from a digitized glass slide in order to achieve better, faster, and less costly diagnosis, prognosis, and prediction of diseases. https://digitalpathologyassociation.o rg/_data/files/Archival_and_Retriev al_in_Digital_Pathology_Systems.p
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DRG
|
Diagnosis Related Group A system to classify hospital cases into one of 467 groups, with the last group being "Ungroupable", with the intent to identify the "products" that a hospital provides. DRGs, used in the US since 1982, determine how much Medicare reimburses the hospital for each "product", and are also standard practice for establishing payment for other Medicare related reimbursements. http://library.ahima.org/xpedio/grou ps/public/documents/ahima/bok1_0 47260.hcsp?dDocName=bok1_047 260
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eCC
|
Electronic Cancer Checklist An electronic version of the more than 70 CAP Cancer Checklists in XML format, that aid pathologists in management of information and in promotion of interoperability, as it offers a standardized way to report cancer data electronically. The CAP Cancer Committee develops these guidelines in collaboration with cancer experts, such as oncologists, radiologists, surgeons, cancer registrars, and other health care professionals. http://www.cap.org/apps//cap.portal ?_nfpb=true&cntvwrPtlt_actionOver ride=%2Fportlets%2FcontentViewe r%2Fshow&_windowLabel=cntvwrP tlt&cntvwrPtlt%7BactionForm.conte ntReference%7D=reference%2Fec c.html&_state=maximized&_pageL abel=cntvwr
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eDOS
|
Electronic Directory of Service An initiative of ONC Standards and Interoperability (S&I) Framework Laboratory Initiatives Pilots that aims to provide an electronic interchange of a laboratory’s directory of services in an structured format based on HL7 2.5.1. http://wiki.siframework.org/LOI+- +eDOS
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Eligible Hospital
|
Acute Care Hospitals (including Cancer and Critical Access Hospitals) where the Average Length of Stay (ALOS) is 25 days or less. Under the Medicaid EHR Incentive Programs, eligible hospitals can qualify for incentive payments if they adopt, implement, upgrade or demonstrate meaningful use of certified EHR technology during the first participation year or successfully demonstrate meaningful use of certified EHR technology in subsequent participation years. http://www.cms.gov/Regulations-
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EHR
|
Electronic Health Record The aggregate electronic record of health-related information on an individual that is created, gathered and shared cumulatively across multiple facilities or healthcare organizations and is managed and consulted by licensed clinicians and staff involved in the individual's health and care. Sometimes used interchangeably with EMR (Electronic Medical Record). http://www.healthit.gov/providers- professionals/learn-ehr-basics
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ELR
|
Electronic Laboratory Reporting The automated transmission of laboratory-related data from commercial, public health, hospital, and other labs to state and local public health departments through an electronic health records (EHR) system or a Laboratory Information System (LIS). ELR is a requirement of Meaningful Use Stage 2. http://wwwn.cdc.gov/nndss/script/m u_elr.aspx
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EMR
|
Electronic Medical Record A digital version of the traditional paper-based medical record for an individual. The EMR represents a medical record within a single facility, such as a doctor's office, clinic, or hospital, and it is the source of data for the EHR. Sometimes used interchangeably with EHR (Electronic Health Record). http://www.himssanalytics.org/docs/ WP_EMR_EHR.pdf
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EP
|
Eligible Professional (also known as Eligible Provider) An eligible professional is a healthcare provider who has demonstrated their understanding of electronic medical records (EMRs) by implementing criteria based on EMR patient updates and Meaningful Use laws. Eligible professionals include Nurses, Physician assistants, Physicians, and Social workers. http://www.healthit.gov/policy-
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ePUB
|
Electronic Publication A free and open ebook standard by the International Digital Publishing Forum. http://idpf.org/epub
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FHIR
|
Fast Healthcare Interoperability Resources (HL7 group) (pronounced 'FIRE') A next generation standards framework created by HL7 that is suitable for use in a wide variety of contexts. http://www.hl7.org/implement/stand ards/fhir/summary.html
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FISH
|
Fluorescence in situ hybridization Test method that provides researchers with a way to visualize and map the genetic material in an individual's cells, including specifc genes or portions of genes. Because a FISH test can detect genetic abnormalities associated with cancer, it's useful for diagnosing some types of the disease. In some cases when the type of cancer has previously been diagnosed, a FISH test also can provide additional information to help predict a patient's outcome and whether he or she is likely to respond to chemotherapy drugs. http://www.genome.gov/10000206 6 of 14
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FNA
|
Fine Needle Aspiration A diagnostic, minor surgical procedure used to investigate superficial lumps or masses, utilizing a thin, hollow needle inserted into the mass for sampling of cells that, after being stained, are examined microscopically. http://www.ncbi.nlm.nih.gov/pmc/art icles/PMC498011/
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FTP
|
File transfer protocol A standard network protocol used to transfer files from one host to another host over a Transmission Controlled Protocol (TCP)-based network, such as the Internet. FTPs promote sharing of files (computer programs and/or data) and transfer data reliably and efficiently. http://tools.ietf.org/html/rfc959
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Information Set
|
A widely used tool consisting of 81 measures across 5 domains of care in the managed care industry for measuring performance of care and service, developed and maintained by the National Committee for Quality Assurance (NCQA). http://www.ncqa.org/HEDISQuality Measurement/WhatisHEDIS.aspx
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HHS
|
Health and Human Services (Department of) The U.S. governments main agency for protecting the health and providing essential human services of all Americans. http://www.hhs.gov/
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HIE
|
Health Information Exchange Created when health care information is electronically collected across organizations within a region, community or health system. Grants to support some of these exchanges were legislated into the HITECH part of ARRA. Sometimes called Regional Health Information Organizations (RHIOs). http://healthit.hhs.gov/portal/server. pt?open=512&objID=1488&parentn ame=CommunityPage&parentid=5 8&mode=2&in_hi_userid=11113&c ached=true
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Systems Society
|
A not-for-profit global organization, founded in 1961, dedicated to imporving healthcare through the optimal use of information technology and management systems. http://www.himss.org/
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Accountability Act
|
A U.S. federal act aimed to improve portability and continuity of health insurance coverage, to combat waste, fraud, and abuse in health insurance and health care delivery, to promote the use of medical savings accounts, to improve access and coverage to long-term care services, to simplify the administration of health insurance, and to ensure an individuals right to medical privacy. http://www.hhs.gov/ocr/privacy/
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HIT
|
Health Information Technology The comprehensive management and exchange of health information across computerized systems. http://en.wikipedia.org/wiki/Health_i nformation_technology
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HITECH
|
Health Information Technology for Economic and Clinical Health Act Enacted as part of the American Recovery and Reinvestment Act of 2009, signed into law on February 17, 2009, promotes the adoption and meaningful use of health information technology. http://www.hhs.gov/ocr/privacy/hipa a/administrative/enforcementrule/hit echenforcementifr.html
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HITPC
|
Health Information Technology (HIT)Policy Committee The American Recovery and Reinvestment Act of 2009 (ARRA) provideed that the HIT Policy Committee be created under the Federal Advisory Committee Act (FACA) and charged with making recommendations to the National Coordinator for Health IT on a policy framework for the development and adoption of a nationwide health information infrastructure, including standards, implementation specifications, and certification criteria, for the exchange of patient medical information http://www.healthit.gov/policy- researchers-implementers/health-it-
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Standards Committee
|
A federal committee created by the American Recovery and Reinvestment Act of 2009 (ARRA) that advises the Office of the National Coordinator for Health IT (ONC) on matters of standards, certification criteria and other issues surrounding electronic health records (EHRs) and meaningful use. This committee focuses mainly on the policies developed by the health information technology (HIT) policy committee, and also provides for testing of the same by the National Institute for Standards and Technology (NIST). http://www.healthit.gov/facas/health- it-standards-committee
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Standards Panel
|
An organization comprised of healthcare experts from both public and private sectors, created to promote standardization and broad scale interoperability among healthcare applications and information systems. HITSP sponsors numerous specifications that define standards for interoperability and information sharing. http://www.hitsp.org/
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HL7
|
Health Level Seven, Inc. An international standards organization that develops and publishes voluntary consensus technical standards for interoperability of health information technology. http://www.hl7.org/ 7 of 14
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ICE
|
Informatics Committee (formerly DIHIT) A CAP committee whose mission is to establish the role of pathologists on the health care team as recognized stewards of clinical and diagnostic data integration and utilization, and reports to the Clinical Informatics Steering Committee (CISC). www.cap.org
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IDR
|
Integrated Disease Reporting A CAP DIHIT project formed with the intent to develop use cases for next generation reports and the benefits for primary care and mid-level providers. The project will also define "structured data" and "what is a report" as well as the pathologist role and liability when changing the structure and user interface to meet customer expectations. The output of the efforts will be a White Paper with detailed definitions and requirements for next generation reporting that support interoperability, Meaningful Use, and reuse of data. http://www.pathologyinformatics.org /content/api-webinar-integrated- disease-reporting-order-almost-
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IHE
|
Integrating the Healthcare Enterprise An initiative by healthcare professionals and industry to improve the way computer systems in healthcare share information to achieve optimal patient care. There are 12 domains within IHE, including laboratory and anatomic pathology. http://www.ihe.net/
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Anatomic Pathology
|
IHE Anatomic Pathology Domain addresses information sharing, workflow and patient care in anatomic pathology, including surgical pathology, cytopathology, autopsy, electron microscopy, and molecular pathology. http://wiki.ihe.net/index.php?title=A natomic_Pathology
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Laboratory
|
IHE Laboratory Domain addresses information sharing and workflow related to in vitro diagnostic testing in both clinical laboratories as well as point of care testing. The IHE Laboratory Domain, established in 2003, manages the Laboratory Profiles and the Laboratory Technical Framework. http://wiki.ihe.net/index.php?title=La
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boratory
|
IHTSDO® International Health Terminology Standards Development Organisation® An international non-profit standards development organisation whose mission is to develop, maintain, promote and deliver medical terminology products in order to improve health in a global scale through the development and application of appropriately standardized clinical terminologies. IHTSDO owns, maintains, and administers the rights to SNOMED CT and related terminology standards. http://www.ihtsdo.org/
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IICC
|
IVD Industry Connectivity Consortium A global nonprofit organization dedicated to creating and encouraging adoption of a unified connectivity standard to reduce the cost and variability of data exchange between IVD devices and healthcare informatics with the goal to improve healthcare efficiency and patient care. http://ivdconnectivity.org/cms/
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ILW
|
Inter Laboratory Workflow An IHE profile that covers the workflow of orders and results beween a requesting lab (providing the specimens and the orders) and a subcontracting lab (performing the tests and reporting the results to the former one). This workflow is able to carry the payors information along with the order. http://wiki.ihe.net/index.php?title=Int er_Laboratory_Workflow
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Informatics
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The study and application of information management. http://en.wikipedia.org/wiki/Informati
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Interface engines
|
An HL7 interface engine is an interface or integration engine built specifically for the healthcare industry. It connects legacy systems by using a standard messaging protocol. http://www.hl7.com/interface- engine.html
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Standardization
|
An international standard-setting body composed of representatives from various national standards organizations that promotes worldwide proprietary, industrial and commercial standards. http://www.iso.org/iso/home.html
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In Vitro Diagnostics
|
Tests that can detect diseases, conditions, or infections and may be used in a laboratory or other health professional settings or by consumers' use at home. http://www.edma- ivd.be/index.php?page=About-In-
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JAHIS
|
Japanese Association of Healthcare Information Systems Industry One of three sponsors of IHE Lab, JAHIS is a Japanese organization that strives to improve healthcare information systems, ensuring quality and safety, and promoting standardization in order to contribute to the sound development of the healthcare information systems industry, as well as the improvement of public health, medical and welfare services. http://www.jahis.jp/english/greeting/
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LAW
|
Laboratory Analytical Workflow Profile An IHE Lab profile that addresses the exchange of information related to both patient and QC test orders and results between IVD testing systems and health informatics systems to improve interoperability. http://wiki.ihe.net/index.php?title=La boratory_Analytical_Workflow_Profi
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LBL
|
Laboratory Barcode Labeling An IHE Lab profile that supports the robotization of specimen container identification and delivery at blood sample collection time, in the context of laboratory test requests. http://wiki.ihe.net/index.php?title=La boratory_Barcode_Labeling
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LCC
|
Laboratory Clinical Communications An IHE Lab profile that will enable rapid, standardized, and automated capture of electronic communication between the clinician and the laboratory related to orders and questions regarding results. This could be utilized when the laboratory wishes to propose a more appropriate test order to the clinician or the clinician wishes to obtain a pathologist's interpretation of patient results. This information will then be logged, tracked, and included in QA studies and process improvement projects. http://wiki.ihe.net/index.php?title=L CC_Long_Proposal_-_wiki
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LCSD
|
Laboratory Code Sets Distribution An IHE Lab profile that electronically establishes and maintains a common vocabulary between systems involved in laboratories workflows. http://wiki.ihe.net/index.php?title=La boratory_Code_Sets_Distribution
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LDA
|
Laboratory Device Automation IHE Lab profile that covers the exchanges between an Automation Manager (Actor played by a Laboratory Information System or by a Laboratory Automation System) and a set of automated Laboratory Devices to process a Work Order, perform the tests on the related specimens and retrieve their results. This processing includes the pre-analytical process of the specimen (sorting, centrifugation, aliquoting, transportation, decapping) the analytical process itself (run of the ordered tests on the specimen) and the post-analytical process (recapping, transportation, rerun, storage and retrieval). This profile is restricted to operations performed in a clinical laboratory setting and does not include point of care testing. http://wiki.ihe.net/index.php?title=La boratory_Device_Automation
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LDT
|
Laboratory Developed Tests An vitro diagnostic test that is manufactured by and used within a single laboratory (i.e. a laboratory with a single CLIA certificate). LDTs are also sometimes called in-house developed tests, or “home brew” tests. LDTs are considered “devices,” as defined by the FFDCA, and are therefore subject to regulatory oversight by FDA. When a laboratory develops an LDT in-house without receiving FDA clearance or approval, CLIA prohibits the release of any test results prior to the laboratory establishing certain performance characteristics relating to analytical validity for the use of that test system in the laboratory’s own environment. https://www.cms.gov/Regulations-
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LOI
|
Laboratory Orders Interface An S&I Framework iniative that is focused on the development of a Laboratory Orders IG for ambulatory settings that aligns with the LRI IG and ELINCS Laboratory Orders IG, will incorporate support for the adoption and use of the Test Compendium Framework, i.e., eDOS, and develop validation tools to facilitate the evaluation and adoption of the LOI IG. http://wiki.siframework.org/Laborato ry+Orders+Interface+Charter+Page
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Implementation Guide
|
U.S. based Laboratory Results Interface Implementation Guide developed by the S&I Framework LRI Iniative, that provides guidance for ambulatory laboratory to ambulatory provider interfaces for laboratory results. http://www.hl7.org/implement/stand ards/product_brief.cfm?product_id= 279
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and Codes
|
A database hosted by Regenstrief Institute that provides a universal code system for reporting laboratory and other clinical observations which is available in multiple languages. In addition to laboratory tests, LOINC also includes clinical measures, imaging tests, and document architecture. http://www.regenstrief.org/loinc/
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LRI
|
Laboratory Results Interface An S&I Framework iniative whose ultimate goal is to develop an Implementation Guide that will define the core data elements required for ambulatory care clinical laboratory test results in the U.S. Realm. The clinical laboratory test results will use standardized structured data so that they can be incorporated into a certified EHR. http://wiki.siframework.org/Laborato ry+Results+Interface+Quickstart+P
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LTW
|
Laboratory Testing Workflow An IHE Lab profile that integrates the ordering, scheduling, processing, and result reporting activities associated with in vitro diagnostic tests performed by clinical laboratories in healthcare institutions, and supports all laboratory specialties with the exception of anatomic pathology. http://wiki.ihe.net/index.php?title=La boratory_Testing_Workflow
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Middleware
|
Software that mediates between an application program and a network. It manages the interaction between disparate applications across the heterogeneous computing platforms. http://foldoc.org/middleware
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Meaningful Use
|
The American Recovery and Reinvestment Act of 2009 specifies three main components of Meaningful Use: 1. The use of a certified EHR in a meaningful manner, such as e-prescribing. 2. The use of certified EHR technology for electronic exchange of health information to improve quality of health care. 3. The use of certified EHR technology to submit clinical quality and other measures. Simply put, “meaningful use” means providers need to show they're using certified EHR technology in ways that can be measured significantly in quality and in quantity. http://www.cms.gov/Regulations-
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NAACLS
|
National Accrediting Agency for Clinical
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Laboratory Sciences
|
An agency that accredits and approves education programs in the clinical laboratory sciences and related health care professions. NAACLS provides services including program accreditation, program approval, consultation, and continuing education, for educational programs, students, employers, and health care consumers. http://www.naacls.org/
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Biochemistry
|
NACB is the Academy of the AACC comprised of doctoral level clinical scientists and whose mission is to further the practice of clinical biochemistry for the benefit of all. http://www.aacc.org/members/nacb /pages/default.aspx#
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NCCLS
|
National Committee for Clinical Laboratory Standards (Now CLSI) A volunteer-driven, membership-supported, not-for-profit, standards development organizationthat promotes the development and use of voluntary laboratory consensus standards and guidelines within the health care community. (see CLSI) http://clsi.org/
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NCI
|
National Cancer Institute Part of the National Institutes of Health (NIH), which coordinates the U.S. National Cancer Program and conducts and supports research, training, health information dissemination, and other activities related to the causes, prevention, diagnosis, and treatment of cancer; the supportive care of cancer patients and families; and cancer survivorship. http://www.cancer.gov/
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Assurance
|
A private, not-for-profit organization founded in 1990, dedicated to improving health care quality, through the administration and utilization of evidence-based standards, measures, programs, and accreditation. http://www.ncqa.org/
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NCRA
|
National Cancer Registrars Association Established in 1974, the National Cancer Registrars Association is a non-profit organization that represents more than 5,000 cancer registry professionals and Certified Tumor Registrars (CTR®). Its mission is to serve as an education, credentialing, and advocacy resource for cancer data professionals. Cancer Registrars capture a complete summary of the history, diagnosis, treatment & disease status for every cancer patient, which leads to better information used in the management of cancer, and ultimately, cures. http://www.ncra- usa.org/i4a/pages/index.cfm?pagei d=1
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NIH
|
National Institutes of Health The NIH, part of the U.S. Department of Health and Human Services, is the nation’s medical research agency—making important discoveries that improve health and save lives. It is the largest source of funding for medical research in the world. The NIH both conducts its own scientific research through its Intramural Research Program (IRP) and provides major biomedical research funding to non-NIH research facilities through its Extramural Research Program. http://www.nih.gov/ 10 of 14
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NIST
|
National Institute of Standards and
|
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NLM
|
National Library of Medicine The NLM is operated by the U.S. federal government, and is the world's largest medical library, with over 7 million scientific and medical works. The NLM freely distributes SNOMED CT within the U.S., and also hosts PubMed, which contains over 23 million citations for biomedical literature. http://www.nlm.nih.gov/
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ONC
|
Office of the National Coordinator for Health Information Technology (under HHS) A position within the US Department of Health & Human Services (HHS) created by Executive Order in 2004 and written into legislation by the HITECH Act. Its purpose is to promote a national health Information Technology infrastructure and oversee its development. http://healthit.hhs.gov/portal/server. pt?open=512&objID=1200&mode= 2 O&O Orders and Observations An HL7 special committee whose intent is to define information exchange capabilities to support the order/scheduling and clinical event management/reporting requirements between the stakeholders in the healthcare organization regarding patients, non-patients, other species, or inanimate objects. These information exchanges may cross organizational boundaries, and may involve messages, documents, services, and other HL7 constructs. O&O supports the ongoing development of HL7 Version 2.x and ensures that equivalent functionality is present in HL7 Version 3.0 and FHIR. http://www.hl7.org/Special/committ ees/orders/index.cfm
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PathLex
|
Anatomic Pathology Lexicon The PathLex project is an interface terminology launched by IHE and HL7 Anatomic Pathology, with the collaboration of other Anatomic Pathology organizations. The Pathlex project has been “designed to satisfy the needs of Anatomic Pathology information system vendors and users by adopting the best features of existing terminology systems, while producing new terms to fill critical gaps". PathLex unifies and supplements other terminology systems, such as SNOMED-CT, CIM-O or various vocablary tables defined by DICOM and HL7. http://www.google.com/url?url=http: //www.hl7.org/documentcenter/publi c/wg/anatomicpath/20100831_Path Lex.docx&rct=j&frm=1&q=&esrc=s &sa=U&ei=R7y1U_z2AYidyASX2Y CABA&ved=0CCEQFjAC&usg=AF QjCNFRKyevb740dn5uW98hXpraL
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PDF
|
Portable Document Format A file format used to represent documents in a manner independent of application software, hardware, and operating systems. http://en.wikipedia.org/wiki/Portable _Document_Format
|
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Committee
|
The Pathology Electronic Reporting Committee of the CAP was formed in 2007 to help guide the development and maintenance of the electronic Cancer Checklists (eCC). PERT serves to both oversee eCC informatics issue reconciliation as well as to interact with the CAP Cancer Committee regarding eCC content issues and paper/ electronic checklist release coordination, and reports to the Clinical Informatics Steering Committee (CISC). www.cap.org
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PHI
|
Protected Health Information Any information about health status, provision of health care, or payment for health care that can be linked to a specific individual. This may include any part of a patient's medical record or payment history. http://www.hipaa.com/2009/09/hipa a-protected-health-information-what- does-phi-include/
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| null | null |
PHIN VADS
|
Public Health Information Network Vocabulary Access and Distribution
|
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System
|
A web-based enterprise vocabulary system for accessing, searching, and distributing vocabularies used
|
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PHR
|
Personal Health Record A health-related documentation maintained by the individual. http://www.ncbi.nlm.nih.gov/pmc/art icles/PMC1447551/
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PHSA
|
Public Health Service Act A U.S. federal law enacted in 1944 to consolidate and revise the laws relating to the Public Health Service. http://www.fda.gov/regulatoryinform ation/legislation/ucm148717.htm
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PPO
|
Preferred Provider Organization A type of health plan that contracts with medical providers, such as hospitals and doctors, to create a network of participating providers. The insured pay a discounted rate when using providers that belong to the plan’s network and a higher rate for providers outside the network. http://www.ehealthinsurance.com/h ealth-plans/ppo/ 11 of 14
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RCMT
|
Reportable Condition Mapping Table Mapping tool available through the CDC to provide mappings between reportable conditions and their associated LOINC laboratory tests and SNOMED CT results https://phinvads.cdc.gov/vads/Sear chVocab.action Regenstrief Institute Regenstrief Institute An internationally respected non-profit medical research organization, which developed and now maintains
|
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RELMA
|
Regenstrief LOINC Mapping Assistant A mapping program to assist the mapping of local test codes to LOINC codes and to facilitate browsing of the LOINC results. http://www.regenstrief.org/loinc/
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Research Use Only
|
RUOs are products that have not cleared by the FDA for diagnostic use and should only be used in the research environment. According to the FDA, RUO products are described as products “in the laboratory research phase of development and not represented as an effective in vitro diagnostic product.” http://www.fda.gov/medicaldevices/ deviceregulationandguidance/guida ncedocuments/ucm253307.htm
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SAFER Guides
|
Safety Assurance Factors for EHR
|
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Resilience Guides
|
Nine self-assessment guides for healthcare organizations to use to optimize the safety and safe use of EHR systems. http://www.healthit.gov/safer/
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SAFMLS
|
Society of Armed Forces Medical
|
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|
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Laboratory Scientists
|
A non-profit organization, officially established in 1971, dedicated exclusively for charitable, educational and scientific purposes in relationship to the laboratory sciences. The primary objective is to maintain and enhanc high professional standards through improved laboratory policies and technology in support of the health care delivery systems of the Armed Forces, Public Health Services and Veterans Administration. http://www.safmls.org/ S & I Framework Standards and Interoperability
|
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Framework
|
The S&I Framework, adopted by ONC's Office of Standards & Interoperability, is a collaborative community of participants from the public and private sectors who are focused on providing the tools, services and guidance to facilitate the functional exchange of health information. The S&I Framework has many different areas of involvement, such as aLOINC Order Code Initiative, Laboratory Results Interface Initiative (LRI), Structured Data Capture (SDC), and many others. http://www.siframework.org/
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SGR
|
Sustainable Growth Rate A formula currently used by the Centers for Medicare and Medicaid Services to control spending by Medicare on physician services. Generally, this is a method to ensure that the yearly increase in the expense per Medicare beneficiary does not exceed the growth in GDP (gross domestic product). The formula limits growth in spending for physicians’ services by linking updates to target rates of spending growth. https://www.cms.gov/Medicare/Med icare-Fee-for-Service- Payment/SustainableGRatesConFa ct/Downloads/sgr2015p.pdf
|
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SIG
|
Special Interest Group A community within a larger organization that has a shared interest in advancing a specific area of knowledge, learning or technology. SIG members cooperate to affect or to produce solutions within their particular field. http://en.wikipedia.org/wiki/Special_ Interest_Group
|
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SNOMED
|
Systematized Nomenclature of Medicine older version of SNOMED CT. a systematic, computer-processable collection of medical terms, both human and veterinary, to provide codes, terms, synonyms and definitions which cover anatomy, diseases, findings, procedures, microorganisms, substances, etc. SNOMED was started in the U.S. by the College of American Pathologists in 1973 and revised into the 1990s. In 2002, SNOMED was merged and expanded with the UK National Health Service to become SNOMED CT. http://www.nlm.nih.gov/research/um ls/sourcereleasedocs/current/SNM/ SNOMED CT® SNOMED Clinical Terms® A systematically organized computer processable collection of medical terms (over 311,000 concepts) providing codes, terms, synonyms and definitions used in clinical documentation and reporting, originally creatred by the College of American Pathologists. SNOMED CT provides the core general terminology for electronic health records, and is used to encode qualitative laboratory results and microorganism identifications, as well as many other medical terms. SNOMED CT is one of two current terminologies required for Meaningful Use, along with LOINC, for the encoding of laboratory results. http://www.ihtsdo.org/snomed- ct/snomed-ct0/ 12 of 14
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Protocol
|
The networking model and group of communications protocols used for the Internet and similar networks utilizing the Transmission Control Protocol (TCP) and the Internet Protocol (IP), which were the first networking protocols defined in this standard. TCP/IP provides end-to-end connectivity specifying how data should be formatted, addressed, transmitted, routed and received at the destination. http://www.protocols.com/pbook/tcp ip1.htm
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Telemedicine
|
The use of medical information exchanged from one site to another via electronic communications to improve a patient’s clinical health status. Telemedicine includes a growing variety of applications and services using two-way video, email, smart phones, wireless tools and other forms of telecommunications technology. http://www.medicaid.gov/Medicaid- CHIP-Program-Information/By- Topics/Delivery- Systems/Telemedicine.html
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Telepathology
|
A form of communication between medical professionals that includes the transmission of pathology images and associated clinical information for the purpose of various clinical applications including, but not limited to, primary diagnoses, rapid cytology interpretation, intraoperative and second opinion consultations, ancillary study review, archiving, and quality activities. http://www.medterms.com/script/m ain/art.asp?articlekey=33621
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| null | null |
UCUM
|
Unified Codes for Units of Measure A code system of standardized codes for measurement units used in medicine and pharmacy, based on 7 standard units. This industry standard, in international use since 1999, is published in English by the Regenstrief Institute. Medical documentation IT applications use UCUM for the unambiguous communication of measurements based on standard SI units. Application areas include the representation of laboratory tests, clinical examinations, and pharmaceutical data. http://unitsofmeasure.org/trac/
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| null | null |
UICC
|
Union for International Cancer Control (Union Internationale Contre le Cancer) Previously known as the International Union Against Cancer, the UICC is a membership organisation that exists to help the global health community accelerate the fight against cancer. UICC was founded in 1933 and is based in Geneva, Switzerland, with a membership of over 800 organisations across 155 countries. http://www.uicc.org/
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| null | null |
USCAP
|
United States and Canadian Academy of
|
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Pathology
|
An organization with more than 10,000 members whose mission is to provide pathologists with high quality information at the investigative and applied practice level to reinforce and update their knowledge of pathology in their unique area(s) of interest, from anatomic to molecular pathology. http://www.uscap.org/
|
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| null | null |
VA
|
U.S. Department of Veterans Affairs A U.S. government-run military veteran benefit system that provides patient care and federal benefits to veterans and their dependents. The Department has three main subdivisions, known as Administrations: Veterans Health Administration (VHA), Veterans Benefits Administration (VBA), and National Cemetery Administration. http://www.va.gov/
|
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| null | null |
VPN
|
Virtual Private Network A private network that interconnects remote (and often geographically separate) networks through primarily public communication infrastructures such as the Internet. VPNs provide security through tunneling protocols and security procedures [1] such as encryption. For example, a VPN could be used to securely connect the branch offices of an organization to a head office network through the public Internet. http://en.wikipedia.org/wiki/Virtual_p rivate_network
|
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| null | null |
WASPaLM
|
World Association of Societies of Pathology and Laboratory Medicine An international organization to improve health throughout the world by promoting the teaching and practice of all aspects of Pathology and Laboratory Medicine, by promoting education, research, and international quality standards, through the Committees and Secretariats of WASPaLM and the World Pathology Foundation. http://www.waspalm.org/
|
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| null | null |
WHO
|
World Health Organization A specialized agency of the United Nations (UN) established in 1948 that is concerned with international public health. It is responsible for providing leadership on global health matters, shaping the health research agenda, setting norms and standards, articulating evidence-based policy options, providing technical support to countries, and monitoring and assessing health trends. http://www.who.int/en/ 13 of 14
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Whole Slide Imaging
|
Whole slide digital imaging uses computerized technology to scan and convert pathology specimen glass slides into digital images which are then accessible for viewing using a computer monitor and viewing software. This is known as virtual microscopy because the images are viewed without the use of a microscope or slides. http://www.jpathinformatics.org/artic le.asp?issn=2153- 3539;year=2011;volume=2;issue=1 ;spage=36;epage=36;aulast=Panta
|
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| null | null |
XML
|
Extensible Markup Language A markup language that defines a set of rules for encoding documents in a format that is both human- readable and machine-readable http://en.wikipedia.org/wiki/Xml 14 of 14
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Siebel
|
Clinical Trial Management System Guide
|
[
"clinical-trial-management-system-guide.pdf"
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|
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|
glossary.json
| null | null |
Integration
|
This task describes how to configure the Web services that are required for clinical data management system integration. For more information about configuring Web services, see Integration Platform Technologies: Siebel Enterprise Application Integration . Note: It is recommended that you use HTTPS authentication. For information about configuring Secure Sockets Layer (SSL) for HTTPS authentication, see Siebel Security Guide . This task is a step in Process of Setting Up Clinical Data Management System Integration. To configure Web services for clinical data management system integration 1. Navigate to the Administration - Web Services screen, then the Inbound Web Services view. 2. Query for each of the following Web services, and update the language and address variables: ◦ ClinicalSubject Inbound Web service. ◦ LS Clinical Protocol Site Interface Service 3. Click Clear Cache on the Inbound Web Services applet. Integrating Data for Subject Visits with Data for Activities Subject visit templates allow you to set up a template schedule. The template schedule is based on the protocol document. You use the template schedule to generate screening, rescreening, and enrollment schedules for each subject, according to the subject’s screening, rescreening, and enrollment dates. The Clinical Item Integration field in the subject visit template is used for integrating visit data with activity data between Siebel Clinical and Oracle Health Sciences InForm. To integrate data for subject visits with data for activities 1. Navigate to the Administration - Clinical screen, then the Visit Templates view. 2. In the Subject Visit Templates list, create a new record and complete the necessary fields. The Clinical Item fields in the Visits and Activities applets are automatically populated. 223
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| null | null |
Siebel Clinical
|
The tasks that a user of the Siebel Mobile application for Siebel Clinical can execute in online and offline mode include the following: • Getting Started with Siebel Mobile Disconnected Applications (general tasks) • Switching to Offline Mode and Synchronizing Data • Managing My Site Visits for Siebel Clinical • Managing My Sites for Siebel Clinical Note: You must complete the relevant setup tasks detailed in this guide before using the Siebel Mobile disconnected application for Siebel Clinical. Getting Started with Siebel Mobile Disconnected Applications For information about how to get started with Siebel Mobile disconnected applications and about the common procedures that you can execute in online (connected) and offline (disconnected) mode in all applications, see the Getting Started chapter in Siebel Mobile Guide: Disconnected which includes information about the following: • Logging in to and out of Siebel Mobile • Navigating the Siebel Mobile user interface • Managing records in Siebel Mobile • Reviewing notification messages in Siebel Mobile • Configuring application settings for Siebel Mobile • Displaying location details in Siebel Mobile • Running predefined queries in Siebel Mobile • Using Attachments in Siebel Mobile • Printing from Siebel Mobile • Process of using Siebel Mobile disconnected applications in offline mode 231
|
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|
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| null | null |
Preface
|
This preface introduces information sources that can help you use the application and this guide. Using Oracle Applications To find guides for Oracle Applications, go to the Oracle Help Center at https://docs.oracle.com/. Documentation Accessibility For information about Oracle's commitment to accessibility, visit the Oracle Accessibility Program website.
|
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| null | null |
Contacting Oracle
|
Access to Oracle Support Oracle customers that have purchased support have access to electronic support through My Oracle Support. For information, visit My Oracle Support or visit Accessible Oracle Support if you are hearing impaired. Comments and Suggestions Please give us feedback about Oracle Applications Help and guides! You can send an email to: oracle_fusion_applications_help_ww_grp@oracle.com.
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| null | null |
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