This wiki has undergone a migration to Confluence found Here
Difference between revisions of "Clinician on FHIR - May 2016 Montreal, Canada"
Jump to navigation
Jump to search
| Line 14: | Line 14: | ||
==Observation== | ==Observation== | ||
Rob to host | Rob to host | ||
| − | Goals for “Observation” | + | * Goals for “Observation” |
| − | + | ** Explore the boundaries of observation (fit for purpose?) | |
| − | + | *** How do we represent microbiology – culture and sensitivity/susceptibility? | |
| − | + | **** Rob – will find examples | |
| − | + | ** Inpatient vs Outpatient – how do you follow observations over time for outpatient visits over different encounters….? (may be synchronous capture or asynchronous capture) | |
| − | + | * Document Vital signs over one encounter (inpatient) – can we trend? | |
| − | + | ** HR | |
| − | + | ** Temp | |
| − | + | ** POx | |
| − | + | * Document Vital signs (Height, Weight, glucose?) over multiple encounters (Outpatient visits) | |
| − | + | ** – can we trend? i.e H and/or W on a growth chart? | |
| − | + | ** How is a panel observation like apgar scores documented? (synchronous capture) | |
| − | + | *** Apgar Score (put values here) | |
| − | + | *** hemodynamic monitoring – Swan Ganz data (BP, HR, RR, Temp, Pox, (BP/MAP), wedge, CVP – Swan ganz – things that are together and stay together?) | |
| − | + | *** How are they captured, how are they managed as a set maintaining their relationship – such as the systolic is always linked to its relative diastolic? | |
| − | + | ** Provide observation use cases to work through during the session – | |
| − | + | *** Perhaps in Aug/Sept - Explore the workflow in OO/FHIR – lab orders and lab results back in observation? | |
| − | |||
=Planning Calendar= | =Planning Calendar= | ||
Revision as of 03:46, 12 May 2016
Back to: Patient Care
Return to: FHIR Clinical Resources - PCWG
Return to: Clinicians on FHIR
Return to: Clinician on FHIR 2016
Introduction
Planning Notes
Observation
Rob to host
- Goals for “Observation”
- Explore the boundaries of observation (fit for purpose?)
- How do we represent microbiology – culture and sensitivity/susceptibility?
- Rob – will find examples
- How do we represent microbiology – culture and sensitivity/susceptibility?
- Inpatient vs Outpatient – how do you follow observations over time for outpatient visits over different encounters….? (may be synchronous capture or asynchronous capture)
- Explore the boundaries of observation (fit for purpose?)
- Document Vital signs over one encounter (inpatient) – can we trend?
- HR
- Temp
- POx
- Document Vital signs (Height, Weight, glucose?) over multiple encounters (Outpatient visits)
- – can we trend? i.e H and/or W on a growth chart?
- How is a panel observation like apgar scores documented? (synchronous capture)
- Apgar Score (put values here)
- hemodynamic monitoring – Swan Ganz data (BP, HR, RR, Temp, Pox, (BP/MAP), wedge, CVP – Swan ganz – things that are together and stay together?)
- How are they captured, how are they managed as a set maintaining their relationship – such as the systolic is always linked to its relative diastolic?
- Provide observation use cases to work through during the session –
- Perhaps in Aug/Sept - Explore the workflow in OO/FHIR – lab orders and lab results back in observation?
Planning Calendar
