This appeared
a little while ago. The document is date 1st Feb, 2019. It seemed
pretty excited.
A MyHealth Record message for anaesthetists
AUSTRALIAN DIGITAL HEALTH AGENCY
In February, a My Health Record (MHR) was
created for every Australian who chose not to opt out of the system. The
Australian Digital Health Agency’s rollout of MHR to healthcare providers was
initially focussed on GPs, pharmacists, pathologists and diagnostic imaging
services.
The Agency is now looking to engage more
specialists – including anaesthetists.
What does this mean for anaesthetists?
MHR is a secure, online health summary where
clinicians involved in a patient’s care can access their health information.
Information available may include a patient’s medical history, medicines view
(incorporating prescription and dispense records), allergies, adverse drug
reactions, immunisations, hospital discharge summaries, pathology results,
diagnostic imaging reports, event summaries, advance care plan and custodian
information.
It is an additional source of information to
support clinical decision making — and does not replace other important
information such as the medical records held in a clinical information system,
or essential clinical conversations with a patient and other healthcare
providers.
Clinicians
decide who would benefit the most by using MHR such as those on multiple
medications, complex and chronic patients or patients who travel or are older.
Therefore, it will not necessarily be used for all patients.
At this early
stage of implementation, a record requires initial activation by its owner or
their clinician and may contain little or no information. As more provider
organisations connect and healthcare interventions occur, the information
gathered in a person’s record will grow.
To date more
than 15,000 healthcare provider organisations, including specialists, GPs, community
pharmacies, pathology and diagnostic imaging services, public and private
hospitals, and residential aged care facilities have connected.
The MHR
system gives clinicians access to their patients’ records, however harsh
penalties apply for inappropriate or unauthorised use. Patient control is at
the core of MHR where they can set access controls to limit who can see their
record and the information it contains.
Additionally,
Australians have a choice whether they want a MHR and can choose to permanently
delete their entire record and any backups at any time in their life.
Parliament recently passed legislation to strengthen the privacy protections in
My Health Records Act 2012 including:
Benefits
for anaesthetists
MHR aims to
support improvements in the safety, quality and efficiency of Australia’s
healthcare system by allowing timely access to information stored in one place
Dr Marie
Bismark, joining two other specialists to discuss My Health record on video,
said in relation to working in private practice:
“I think you
can feel quite isolated from decisions being made by other specialists. You
don’t have that multidisciplinary team environment as you do in a hospital ward
and it almost becomes more important to know what decisions are being made and
what medications are being prescribed by other people involved in the patient’s
care.” MHR makes this information available.
What next?
Anaesthetists
can access MHR as an employee of a health care organisation connected to the
system. To find out more anaesthetists can request a digital health education
session by contacting the ASA office or the ANZCA or the Australian Digital
Health Agency at clinicalpartnerships@digitalhealth.gov.au.
Further
information on MHR and getting connected can be found at
www.myhealthrecord.gov.au or by contacting the Helpline on 1800 723 471. For
more information and assistance.
Here is the
link:
Let me first
make it clear this screed comes intended for practice managers and seems to be
at least partly put together for the ADHA.
The page is
here:
The Aust. Society
of Anaesthetists also has a position
paper which seems to be much later according to the .pdf – dated 14/10/2019.
Here is the
link to the page – it is Item 17 and has been revised.
It paints a
slightly more reticent view – to say the least!
Position statement – ASA PS17
My Health Record (MHR)Preamble
The ASA
supports the notion of an electronic health record that is ‘fit for purpose’,
reliable, accurate, adequately resourced, consumer focussed, equitable,
universally accessible, easy to use, maintains people’s privacy and safeguards
against the misuse of data. The current 2018 My Health Record, (MHR), has attempted
to address some of these concerns. The ASA will continue to collaborate with stakeholders
to resolve the outstanding issues that present a barrier to the successful implementation
of an effective e-health record.
Introduction
The practice of
medicine in Australia has evolved organically from generic practitioners and bush
hospitals to specialised generalists in primary care, specialists, sub-specialists
in secondary and tertiary centres.
Healthcare services
are distributed geographically across rural, regional and metropolitan centres reflecting
Australia’s population mal-distribution and across the public and private sectors.
This healthcare practice is supported and augmented by pharmacists, nurses,
allied health professionals and diagnostic technicians. The net result is often
uncoordinated care occurring in silos that may be duplicative, unnecessary, wasteful
and potentially harmful1.
Having access
to an accurate e-health record could theoretically improve this fragmentation of
care. In 2012 the Personally Controlled Electronic Health Record (PCEHR), was
introduced to improve health outcomes by sharing health information and
increase consumer engagement through an ‘opt-in’ approach2. Low community
uptake prompted further research, education and promotion culminating in the
relaunch of MHR in 2016.
Potential advantages of an ideal e-health medical record
Reducing
fragmented care
Medical
information often exists in silos. This information should follow the patient3,
to allow healthcare professionals to provide timely, safe and appropriate care.
This is particularly relevant for those with special needs, complex multisystem
disease, chronic disease, the elderly and disadvantaged. Multiple medications
may introduce the potential for drug interactions, allergic and adverse drug reactions.
An up-to-date drug reconciliation tool would significantly reduce these potential
errors particularly when patients are transitioning from one setting to another
or changing geographical locations. Having an accurate current medical record assists
with discharge planning and handover of care.
Safer care
in emergencies
Emergency
access to reliable, current medical information may be lifesaving.
Improved
efficiencies
Uncoordinated
care is wasteful. It often results in duplication of investigations and referrals.
This is expensive and may result in increased exposure to risks.
Consumer
centric
Allowing patients
to have input into their medical record, how the data is managed and who has access
to it, empowers them to take an active role in decisions about their care. It increases
awareness, choice and control4.
Advanced
care plans and advanced care directives
These may be
reliably located in the e-health record.
Increased
engagement
Centralizing the
consumer’s information may stimulate healthcare providers to offer more acceptable,
appropriate and useful products and services.
Area for
research
De-identified
data may be used by legitimate authorised entities to conduct quality improvement
research, planning and policy development
Potential disadvantages of the My Health Record 2018
Incomplete,
inaccurate record
Allowing
consumers to alter their record potentially devalues the clinical integrity. Health
professionals may not be able to reliably provide the best care for their patients
if it is based on inaccurate information. Consumers may have an asymmetry of medical
information that may compromise their ability to make the best decision regarding
what to exclude4. When the MHR has been modified by a patient this is not visible.
It should be made clear if a record has been altered by a patient even if the content
of that change is not.
Access
Many health
professionals, including many specialists, do not have access to the software
required to engage with MHR5. Combined with ‘on going’ compliance obligations
this presents a significant barrier to specialist participation. Incomplete healthcare
provider participation below a critical mass, reduces the universality and overall
value of the MHR. Adequate resources must be invested in the platforms that support
and maintain the integrity and access at the bedside (ideally on a mobile
device) of the MHR data.
Privacy
and security
The potential
for centralised personal data to be corrupted, stolen, used and stored
inappropriately remains a valid concern for all stakeholders. Proposed
government measures go some way to protect patient privacy. No IT system will ever
be totally reliable yet this has not prevented the developments in e-banking or
e-travel. There needs to be assurance that should such a data breach occur, the
FederalGovernment assumes full responsibility. There needs to be consultation with
the medical indemnity industry and some assurance on the limited liability of doctors
utilizing MHR.
‘Opt-out’ may not be fully informed consent
PCEHR went from
‘opt-in’ to ‘opt-out’ in MHR to achieve a greater critical mass of consumer participation
with benefits of scale, greater interconnected participation and the potential for
transformational change6. However, consumers must be fully informed and have a degree
of e-health literacy that permits them to make an informed choice about how to engage,
and to what degree, with MHR.
Implementation barriers
There needs
to be more effective targeted education and promotion to ensure MHR is
acceptable and useful to healthcare providers and patients7. Evaluations of MHR
have demonstrated low levels of usability amongst those with reduced e-health literacy8.
Low levels of awareness and how to utilise the full capabilities of the MHR, may
discriminate against the ‘digitally naïve’. This may include the most vulnerable
people with chronic, multisystem disease, the elderly, those with mental illness,
non-English speaking and from lower socioeconomic backgrounds.
Conclusion
The ASA supports
an e-health record that meets the clinical and consumer expectations. This includes
respecting and protecting patient’s privacy while maintaining the integrity of
the clinical data. The implementation of MHR will require more resources to address
and support these concerns.
References
1.
Hambleton S, Primary Health Care
Advisory Group (2015), ‘Better outcomes for people with chronic and complex
health conditions’, Commonwealth of Australia Department of Health, accessed January
28th, 2019. http://www.health.gov.au/internet/ main/publishing.nsf/content/76B2BDC12AE54540CA257F72001102B9/$File/Primary-Health-Care-Advisory-Group_Final-Report. pdf
2.
Commonwealth of Australia, My Health
Records Act 2012, accessed January 20th,
2019. https://www.legislation.gov.au/Details/
C2012A00063
3.
Bartone T (2018), ‘My Health Record
could save your life one day’, The Sydney
Morning Herald, published July 23rd, 2018.
4.
Wells L (2018), ‘An important overview
of the pros, cons and questions about My Health Record’, Croakey, published June 6th, 2018,
accessed January 20th, 2019.
https://croakey.org/an-important-overview-of-the-pros-cons-and-questions-about-my-
health-record/
5.
Miller AC, ‘My Health
Record important, but let’s fix the problems’, AMA, published October 9th 2018,
accessed January 20th, 2019. https://ama.com.au/ausmed/my-health-record-important-let%E2%80%99s-fix-problems
6.
Van Kasteren Y, Maeser
A, Williams PA, Damarell
R (2017), ‘Consumer perspectives on My Health Record:
A review’, Flinders University, South
Australia, accessed January
28th, 2019. https://www.hisa.org.au/slides/hic17/sci/vanKasteren.pdf
7.
Bartone T (2018), ‘Advocating for the best My Health
record’, Australian Medicine, published
August 9th, 2018,
accessed January 20th, 2019. https://ama.com.au/ausmed/advocating-best-possible-my-health-record
8. Walsh L, Hemsley B, Allan M, Adams N, Balandin S, Georgiou A, Higgins I, McCarthy S, Hill S (2017), ‘The E-health literacy demands of Australia’s My Health record:
A heuristic evaluation of usability’, Perspectives in Health Management, 14 (Fall), accessed January
28th, 2019. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653954/
This seems to
me to say if the #myHR did and was as described on the tin it could be a good
thing, but at the present there are too many holes that need remedy and
investment. The paper for Practice Managers is pure propaganda whereas the position paper is a sensible considered document which sees the spin.
Thus, again we see
the clinicians pretty careful, not that oversold on a solution that isn’t!
David.
2 comments:
The ASA-PS17 Position Statement My Health Record (MHR) Latest Revision 29/01/2019 is a carefully constructed balanced document worthy of this august body of specialist clinicians (anesthetists).
The PS-17 is many light years removed from the rubbish that has been promulgated by the ADHA. The PS-17 contains a wealth of sound reasoning and deep concerns. It is a valuable document.
That the ADHA can still get away with misrepresenting MyHR over seven years after it went live is a disgrace.
A pig in lipstick is more attractive than this so called health record. The best thing about MyHR is it that nobody cares.
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