Difference between revisions of "2012-02-27 PCD Pulse Oximetry Project Meeting"
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(Created page with "=Weekly Conference Call= Date: Monday, February 27th, 2012 Meeting will at 1 pm. ==Attendees== - ''expected'' * [mailto:john.rhoads@philips.comm John Rhoads - PCD TC co-chair...") |
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#''(05 min)'' Roll call and [2012-02-27 PCD Pulse Oximetry Project Meeting | meeting minutes] approval | #''(05 min)'' Roll call and [2012-02-27 PCD Pulse Oximetry Project Meeting | meeting minutes] approval | ||
− | #''( | + | #''(25 min)'' '''Use case discussion''': this will include a discussion of the trigger events that initiate an exchange of pulse oximeter results from a device. We need to reach consensus on the distinction between the probe and the device that intended to exchange information. We will also discuss aspects of the workflow to clarify how and where the device data is validated for each use cases. We need to clarify whether the Anesthesia Record will contain validated results, raw device results, or a combination of the two. |
− | #''( | + | #''(25 min)'' '''Data Requirements Analysis''': The information exchanged along with the results for pulse and oxygen saturation. This may include: device allowable ranges, patient-type (e.g. adult, pediatric) reference ranges (from device, from device manager, or added in the receiving system), verification indicator specifying the clinicians validated a result, operator identity - for verified results. We will also discuss alarm conditions intended to be reported to the clinical information system - primarily for those results that were not validated at the point of care. |
− | #''(5 min)'' '''Action item update | + | #''(5 min)'' '''Action item update''' |
− | |||
==Meeting Notes== | ==Meeting Notes== |
Revision as of 00:41, 21 February 2012
Weekly Conference Call
Date: Monday, February 27th, 2012 Meeting will at 1 pm.
Attendees
- expected
Agenda
- draft
- (05 min) Roll call and [2012-02-27 PCD Pulse Oximetry Project Meeting | meeting minutes] approval
- (25 min) Use case discussion: this will include a discussion of the trigger events that initiate an exchange of pulse oximeter results from a device. We need to reach consensus on the distinction between the probe and the device that intended to exchange information. We will also discuss aspects of the workflow to clarify how and where the device data is validated for each use cases. We need to clarify whether the Anesthesia Record will contain validated results, raw device results, or a combination of the two.
- (25 min) Data Requirements Analysis: The information exchanged along with the results for pulse and oxygen saturation. This may include: device allowable ranges, patient-type (e.g. adult, pediatric) reference ranges (from device, from device manager, or added in the receiving system), verification indicator specifying the clinicians validated a result, operator identity - for verified results. We will also discuss alarm conditions intended to be reported to the clinical information system - primarily for those results that were not validated at the point of care.
- (5 min) Action item update
Meeting Notes
Links
- Link to the final presentation.
Action Items
- Item:
- Item: