Difference between revisions of "IDCO"

Latest revision as of 13:18, 10 December 2009

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PCD Implantable Device Cardiac Observation

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-'''Implantable Device - Cardiac - Observations (IDCO)''' communicates implantable cardiac device data to EMRs and device management systems.
+#REDIRECT [[PCD Implantable Device Cardiac Observation]]
-__TOC__
-[[Category: PCD Pages Needing Work]]
-==Summary==
-This Supplement adds a new profile to the IHE Patient Care Device Technical Framework
-describing a means to transfer information from an interrogated implantable cardiac device to
-information management systems. This profile is named Implantable Device – Cardiac –
-Observation or IDCO for short.
-==Benefits==
-Cardiac physicians follow patients with implantable cardiac devices from multiple vendors.
-These devices are categorized as pacemakers, implantable cardioverter defibrillators, cardiac
-resynchronization therapy devices, and cardiac monitor devices. As part of patient follow-up an
-interrogation of a cardiac device is performed (either in-clinic or from a remote location).
-Information is collected about the device such as device identification, therapy settings, device
-diagnostics, and device testing. These interrogations are performed by vendor proprietary
-equipment.
-To improve workflow efficiencies Cardiology and Electrophysiology practices require the
-management of “key” summary implantable rhythm control device interrogation information in a
-central system such as an electronic health record system (EHR) or a device clinic management
-system.
-To address this requirement, the Implantable Device – Cardiac – Observation (IDCO) Profile
-defines a standards based translation and transfer of summary device interrogation information
-from the interrogation system to the information management system.
-With the increased use of EHR systems, the networking of in-clinic and remote follow-up
-systems for implanted cardiac devices, and the continued growth of the implantable cardiac
-device market, the importance of this profile to clinicians has become more acute. Strong device
-and EHR vendor participation in the IDCO profile development is an acknowledgement of this
-importance. As the IDCO Profile and associated standards continue to evolve there is little doubt
-that the use of this profile will be a critical component of comprehensive cardiac care.
-==Details==
-''<A few paragraphs, if appropriate, providing more details (mostly in user-speak, not tech-speak) on what the profile does and how it works.>''
-''<If the user might be familiar with the mechanisms used by the profile, you can mention them here.  E.g. Evidence Documents is based on DICOM Structured Report (SR) Templates.>''
-''<If the user might have an appreciation for the problems addressed in the profile, you can mention them here, but keep it short.  E.g. Mapping HL7 Order fields to DICOM Modality Worklist attributes can be inconsistent in the marketplace, so Scheduled Workflow provides vendors with more detailed instructions.>''
-==Systems Affected==
-* ''EHR systems may store, manage, and/or display IDCO reports.''
-'''Actors & Transactions:'''
-[[Image:IDCOActors.pdf]]
-==Specification==
-'''Profile Status:''' [[Comments| Trial Implementation]]
-'''Documents:'''
-:* [[Media:IHE_PCD_TF_Supplement_IDCO_2009.pdf | IDCO Technical Framework Supplement]]
-'''Underlying Standards:'''
-:* [http://www.hl7.org HL7]
-This page is based on the [[Profile Overview Template]]
-[[Category:PCD]]

Difference between revisions of "IDCO"

Latest revision as of 13:18, 10 December 2009

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