Take one Palliative Care Data Standard, a course of NZ Universal List of Medicines, the New Zealand Formulary and the NZePS. Avoid allergies: Integrate well!
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Take one Palliative Care Data Standard, a course of NZ Universal List of Medicines, the New Zealand Formulary and the NZePS. Avoid allergies: Integrate well!
1. Take one Palliative Care Data Standard, a
course of NZ Universal List of Medicines, the
New Zealand Formulary and the NZePS.
Avoid allergies: Integrate well!
Corinne Gower
Victoria University of Wellington and Houston Medical
Megan Peterson
Arohanui Hospice, Palmerston North
HINZ Presentation, Thursday 28th November 2013
2. Overview of presentation
• Introduction
• End Users Overview (Megan)
– Palliative Care Dataset
– Prescribing Solution
• Implementers Overview (Corinne)
– Palliative Care Dataset
– Prescribing Solution
• Lessons Learned
• Questions
3. Introduction
• Common themes
– Output requirements were specified
– Input and workflow had to be determined
collaboratively.
• Points of difference
– Palliative Care DS: Design and development phase
was the major phase. No third party product
integration.
– Prescribing: UAT phase was the major phase.
Extensive third party product integration.
6. Palliative Care Data Definitions
Standard
HISO 10039.1 and HISO 10039.2
•Provides a basis of a common language for
recording information about service contacts
that can be shared and compared between
stakeholders, and for understanding palliative
care in NZ.
7. Data Issues
Pre Implementation
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Multiple data entry screens
No definitions for fields
Non compulsory data entry
Lack of user understanding
Incomplete and inconsistent data output
Data could not be relied upon
9. End User Recommendations
• Scope the project well.
• Strong working relationship with vendor and
external stakeholders.
• Determine impact on end to end business
processes (eg. referral management).
• Education sessions should including context
and constant reviewing of the data.
(Take with wine, repeat as required!)
10. Prescribing information workflow and
objectives
Workflow
• Prescription Creation
– Medication selection
– Interaction checking – allergies and drug-drug interaction
– Regular Medication recording
• Output – paper and electronic
– Correspondence – information sharing
• Incoming dispensing messages.
Objectives
• Reduce preventable medication errors
• Facilitate greater use of generic (non-trade/brand) drugs.
12. Clinician Requirements
• Doses: A list of doses associated with each medicine. Doses should
be easy to maintain.
• Medication readability:
– ‘paracetamol 500mg tablet’
– ‘paracet 500mg+pseudoeph HCl 30mg (&) chlorpheniramine mal
2mg+paracetamol 500mg+pseudoeph 30mg tabs’,
• Secondary use of prescribing information in correspondence
• Drug Allergy alerts: Recognition of existing drug allergy alerts
• Form/Strength: Option to prescribe either by form (1 tablets, 5 ml)
or by strength (10 mg).
– A pick list of administrative units is confined to units associated with
the medication in the NZULM.
• Supply: Need to request pharmacist to determine supply quantity.
– Administration Unit of ‘QS’
13. Prescribing Functionality Evaluation
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•
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NZF interaction checking is working well
Improved prescription generation
Prescribing data now makes greater clinical sense
Fewer scripts returned or queried by the pharmacy
because supply details have been overlooked
• Some optional fields, such as medication route, are being
omitted because they do not read well on the prescription.
• Increased generic prescribing
– System default and generic/trade cross matching
• No improvements in dose consistency
– Latin/non-Latin frequency and timing instructions.
14. Implementer Challenges
• Relationship Management: Huge overhead when piloting
• Challenge of justifying benefits: Having to sell government
strategy, Connected Health licenses. Documents and
implementation specifications have limited value in
communicating change drivers and benefits directly to
information system end users.
• Technical Complexity: Huge. With integration to third party
products you have to know where the boundaries are.
Medicines are included in the NZULM that are not yet
available.
• Collaboration: Need for regular site visits
• Expectations: Structured data entry is extremely difficult.
15. Community ePrescribing
Recommendations
• More work is needed to understand the
potential impact to clinician’s workflow when
a standard or specifications are developed.
• Need to ensure there is a clear path to convert
data (such as allergies) from old to new
system.
• Useful to have supporting documentation or
web based information, such as case studies,
to support implementation.
16. Lessons Learned
• Scope everything thoroughly
• Set realistic timeframes and adequately
resource the project
• Understand clinician workflow
• Engage clinicians, nurses and allied staff
• The perfect system does not exist
17. The importance of recognition –
What an achievement!
Thanks to:
Arohanui Clinicians
Houston Medical
Developers
Patients First Team
(Peter Jordan)
NZULM (Craig
Mabon)
NZF (Chris Hilder)