Quote Of The Year

Timeless Quotes - Sadly The Late Paul Shetler - "Its not Your Health Record it's a Government Record Of Your Health Information"

or

H. L. Mencken - "For every complex problem there is an answer that is clear, simple, and wrong."

Wednesday, September 05, 2007

The Australian College of Health Informatics Elects a New President!

At MedInfo2007 last week the Australian College of Health Informatics (ACHI) elected a new president. Following this election Dr Hannan has developed a short position paper describing the direction he wishes to take the, still young, College over the next couple of years.

The following is a slightly edited version of this position paper.

-----

President’s Report September 2007

Dr Terry Hannan MBBS: FRACP; FACHI; FACMI

As the position of President of ACHI is elected by peers I first acknowledge with humility and respect the confidence you have expressed, and I look forward to working creatively and cooperatively in this role for the next two years.

ACHI is a ‘young’ organisation so it is worth reflecting on achievements to date. Since its inception in 2002 our College has seen a gradual growth in the numbers of Fellows and Members to a total of 44. While not a large number this is a solid foundation on which to analyse sources of membership, and further opportunities for recruitment.

It is in the domain of health informatics research, that ACHI has come to prominence. Members are growing in international recognition through research publications which can be seen in a standardised PubMed internet enquiry covering 2006-2007.

At the recent MEDINFO 2007 conference in Brisbane it was pleasing to hear Don Detmer, President of AMIA and Paul Tang, President Elect of AMIA, endorse the quality of research by ACHI members, thus reinforcing our local and international standing in health informatics.

Publications in the Journal of the American Medical Informatics Association (JAMIA) are considered world standard, and it is a pleasure to see that the work of several ACHI Fellows are attaining recognition at this level.

Yet, in spite of this progress we face new challenges as the role of ACHI and its relationships with partners and stakeholders is redefined and evolves over this 3-5 year phase.

From my perspective, our strong focus on the following three issues should serve to broaden our reach and reputation.

  1. Education.
    1. Evelyn Hovenga justifiably deserves acknowledgement for her contribution to the development of health informatics education in Australia. Her presentation with Professor Bill Hersch, Chair of Medical Informatics and Clinical Epidemiology, Oregon State University, the at the AGM, on the outcomes of the University of Central Queensland education program revealed the enormous challenge and at times rethink an organisation like ACHI faces when the intended goals are not achieved.
    2. Bill Hersch outlined his experiences in informatics education that ultimately led to the development of the 10 X 10 program in North America. The AMIA 10x10 Program's goal aims to train 10,000 health care professionals in applied health and medical informatics by the year 2010 (10,000 by 2010 = 10x10). With reference to this experience ACHI can evolve variations to the initial program developed by the University of Central Queensland to roll out a different education model, and set some moderate targets to achieve.
    3. I am of the view that there are several key deficiencies in health informatics education. Key among these is that ACHI does not have enough clinicians (nurses, pharmacists, doctors, physiotherapists, and other allied health professionals) and health administrators in its numbers. I strongly believe that ACHI has the opportunity (and mandate) to influence Royal Colleges (and other relevant training institutions in health care) as well as schools of health administration, to expand the role of health informatics with the ultimate aim of making this discipline an essential component of the undergraduate or immediate post-graduate course curriculum. Over the next 2 years a core focus of my activities will be to investigate how ACHI can take a lead in overcoming this deficiency.

  1. ACHI Development and Promotion.
    1. At MEDINFO some of the ACHI Committee had an opportune discussion with Professor Don Detmer (President of AMIA) and Professor Paul Tang (President-Elect of AMIA) during which they clarified the relationship between AMIA and ACMI. This provides a helpful guide to redefining all aspects the ACHI-HISA relationship particularly for promotion and marketing.
    2. The new promotional brochure for ACHI, launched at MEDINFO 2007, is a sound first step to elevate the profile of this College.
    3. As an organization we need to define and promote the collective expertise of ACHI to hospital administrators, chief information officers and policy makers in health care institutions and to all levels of government. Only then can we begin to influence a change in focus from solely administrative health informatics to the wider domain of clinical informatics both in Primary Care and Hospitals.
    4. To this end I would like to build and maintain on our member talent bank. I will be requesting all ACHI members to provide details of their expertise and domains. While adding to the ACHI Fellowship it will make us more efficient at identifying experts within our organization who can promote our own development as well as acting as key advisors to external sources.

  1. Research.
    1. The core principle of health informatics lies in the tenet, “to improve care you have to be able to measure it” (W. Tierney, Regenstrief, Indiana).
    2. An ability to measure and evaluate health care initiatives depends upon research resources and facilities. ACHI is fortunate to have a number of these recognised facilities in health informatics in Australia such as the University of New South Wales, Sydney University, Central Queensland University and Adelaide University.
    3. These institutions will provide leadership to the wider informatics community and industry by innovative research in health informatics technologies and of equal importance research models in the direct patient care process.
    4. Research in the modern era requires significant funding and Academic-Enterprise cooperation is essential. This will not always be a comfortable relationship as was demonstrated during the MEDINFO workshop on this topic. The issues needing consideration by ACHI must include the:

i. Diversification of sources of research and infrastructure support

ii. Support for career development (student internships, recruitment of graduates, consulting opportunities for faculty members)

iii. Assessment of “Real-world” impact of academic research products with the issues relating to technology transfer, licensing agreements, etc.

iv. Impact of “contracting” often with circuitous legal issues such as intellectual property ownership and ultimate benefits for industrial partners.

v. Avoidance of the elitist perspective sometimes attributed to university based organizations.

On behalf of the ACHI I welcome our new Fellows for 2007, who add a diverse mix of scientific disciplines and national origins which should serve to increase the intellectual capital of ACHI. The flowing three received their certificates from Professor Bill Hersch during the AGM.

1. Joanne Callen

2. Vitali Sintchenko

3. Dougie Boyle

4. Chris Pearce

For the duration of my tenure I hope that my performance sees the enhancement of ACHI’s profile, the expansion of its membership. Also I hope to see ACHIS’ influence on academic curriculum to promote health informatics as a core discipline. Our organisation must continue to push the boundaries of research both in Australia and overseas.

Your input is encouraged at all times to facilitate frank and robust debate. I looking forward to a successful working relationship with you all over the next 2 years.

Dr Terry J. Hannan MBBS;FRACP;FACHI;FACMI

Consultant Physician

President Australian College of Health Informatics

Department of Medicine

Launceston General Hospital

Charles Street

Launceston 7250

Ph. 61 3 6348 7578

Email terry.hannan-at-dhhs.tas.gov.au

-----

I had a number of purposes in publish this short position statement.

The first was to introduce to those blog readers who do not know of ACHI who it is and what it is aiming to achieve.

The second was to suggest that if any of this sounds interesting that a visit to www.achi.org.au would be very worthwhile.

The third was to ensure that those who might be interested in becoming a Member / Fellow of ACHI understand that appropriate senior experience in Health Informatics in Health Services, Government, the Health IT Industry and Academe are all valued. To do its job well it needs to have a broad representative base. ACHI wishes to properly represent the experienced and professional skills that are available in Health Informatics in Australia.

It is important to also recognise for those beginning their careers in Health Informatics, or those who want to explore what Health Informatics is all about the Health Information Society of Australia (www.hisa.org.au) is also a useful and central place to start and learn.

Please consider what you might have to offer and visit the either of the web site(s) depending on your interest and need.

Dr Hannan (Terry) has told me he is happy for e-mail contact to be made if you wish to discuss ACHI further.

HISA contact details are also available at its web site.

David.

Tuesday, September 04, 2007

Vale The Access Card – Dead as a Dodo!

It has been a big few weeks on the Access Card front.

First we had the following from the Federal Privacy Commissioner.

Media release: Access Card Bill makes progress in promoting privacy, says Privacy Commissioner

22/08/2007

The Privacy Commissioner, Karen Curtis, has acknowledged the progress made with the second public exposure draft of the Human Services (Enhanced Service Delivery) Bill 2007, in advancing privacy protections for the Government's proposed Access Card.

"While there are still a number of steps that can be taken to enhance the Access Card's privacy safeguards, the Bill provides protections for confidentiality and information integrity which usefully adds to what was in the first Bill," Ms Curtis said.

In a submission to the Department of Human Services, Ms Curtis recommended additional privacy safeguards to supplement the Bill, including:

  • to advance the object of the Bill that the card should not become an ID card, the photograph on the card surface should be made optional;
  • making the Bill's Administration Rules detailed and clear in how they affect information handling;
  • creating civil remedies to allow individuals to seek redress where Access Card information is mishandled; and
  • having a regular statutory review mechanism for the card.

Ms Curtis welcomed the following aspects of the Bill:

  • the oversight mechanisms it proposes, including review and appeals processes, mandatory consultation with the Privacy Commissioner, Parliamentary scrutiny of Administration Rules, and annual reporting requirements;
  • its listing of the Bill's objects and the intention that the Act should be interpreted to limit impacts on privacy;
  • its provisions on confidentiality, and the combination of offences and infringement notices; and
  • the limits it sets on the disclosure of protected information, such as for law enforcement purposes.

----- End Release

In summary her view was “good try – but really not good enough”.

Then we had:

http://www.australianit.news.com.au/story/0,25197,22297566-15306,00.html

Smartcard on hold till next year

Patricia Karvelas | August 24, 2007

PLANS for a national smartcard have been postponed for at least a year with the Government admitting the deadline for its introduction was unrealistic.

The proposal for one-card access to welfare payments has been dogged by controversy since it was raised in 2003, with opponents claiming it is an underhand method of introducing a national identification system.

Despite government hopes of introducing a bill this year, Human Services Minister Chris Ellison yesterday said public support was essential if the $1.1billion scheme was to succeed, and there was no way he would put forward legislation before 2008.

….. (see full article at URL above)

This is essentially an admission that it was all getting much too hard and that public concern was such that the Access Card needed to be neutralised as a political problem in the light of the looming election.

Then we had:

http://www.theage.com.au/news/national/labor-pledges-to-kill-off-access-card/2007/08/28/1188067111116.html

Labor pledges to kill off Access Card

Annabel Stafford
August 29, 2007

THE $1.1 billion Access Card could soon be dead, with the Labor Party confirming it would kill off the proposal if it won this year's election.

Coming after the Federal Government last week confirmed it would put off introducing legislation for the Access Card until after the election, Labor has confirmed a Rudd government would scrap the idea.

"As far as we're concerned, (the Access Card) is dead," Labor human services spokeswoman Tanya Plibersek said.

….. (see full article at URL above)

Interesting that the small target approach Opposition chooses this issue to make a stand. Tells you the internal polling is suggesting that this is not a winner for the present Government.

Last we have today some accounting for the Access Card so far!

http://www.australianit.news.com.au/story/0,24897,22356770-15306,00.html

Smartcard costs hit $52 million

Karen Dearne | September 04, 2007

SPENDING on the federal Government's mooted welfare smartcard has reached $52 million, despite uncertainty over whether the $1.1 billion program will proceed.

New contracts worth nearly $10 million have been signed by the Department of Human Services since June, with most due for completion well before the end of this year.

This may signal a slowdown of work, pending the outcome of the federal election.

In June, Human Services Minister Chris Ellison effectively put the controversial Access Card on ice, as opponents claimed it would become a national identity card.

The project's lead adviser, Booz Allen Hamilton, collected $30.5 million in fees during the past financial year, including $5 million for the months of May and June, and a slimmer $5.2 million for the current four months to October 26.

….. (see the rest of the breakdown at the Australian IT Site above)

What to do? Really that is quite easy.

Whoever wins the election needs to undertake a Strategic Review of Electronic Identity Management in Australia – reviewing all the rapidly proliferating set of initiatives – from the Access Card to the NEHTA UHI and the Document Verification Service and plan for one decent reliable fit for purpose system.

It would not be an easy task – but it could likely save billions of dollars if done well over the next few years.

David.

Monday, September 03, 2007

Senator Helen Coonan – Applying to be Minister for e-Health?

A few days ago the following article appeared on the MIS Australian web site.

Coonan moots plan to stitch up e-health

Julian Bajkowski

The Australian Financial Review | 31 Aug 2007 | Information

The Howard government's tactic of staging federal interventions in state health matters is primed to escalate after Communications Minister Helen Coonan gave the strongest indication yet that Canberra was ready to create a national electronic health record.

Senator Coonan yesterday confirmed that discussions with Health Minister Tony Abbott on a standardised national electronic health record were well advanced and had included how costs and medical fee structures could be affected.

"This issue has been identified in the Health Department and my understanding is that they are well advanced in getting an announcement [ready]," Senator Coonan said.

Senator Coonan's comments came during the announcement of $29.5 million in federal funding for five new electronic health projects under the $117 million Clever Networks program.

These included electronic medical record sharing facilities for the Royal Flying Doctor Service, interoperability funding for remote Western Australian hospitals and funding for new applications in the NSW Hunter-New England region.

….. (go to www.misaustralia.com to read full article)

If this was not enough we also have this announcement:

http://www.minister.dcita.gov.au/media/media_releases/clever_networks_improving_the_quality_of_life_in_australian_communities

Clever Networks: improving the quality of life in Australian communities

…..

“Round Two projects (in the Clever Networks Program), include:

  • $5.2 million for the Loddon Mallee Virtual Trauma Care Unit project to install videoconferencing units connecting Bendigo, Echuca, Swan Hill and Mildura regional hospitals with base hospitals in Melbourne. This will allow metropolitan trauma specialists to provide ‘virtual’ consultations with doctors in emergency rooms across the Loddon Mallee region of Victoria.

  • $9.3 million for the Bush Medivac Western Australia project to implement interoperable data networks to enhance the communications and coordination capabilities of all major health and emergency services in the state. This will make a significant contribution to Western Australia’s ability to respond to emergency incidents and health crisis situations in regional and remote areas. This project builds on a Round 1 proposal and also dovetails with the following proposal.

  • $2.7 million for the eHealth for Remote Australiaproject for an electronic medical record system providing essential patient information. This will allow the Royal Flying Doctor Service to provide better primary health care for up to 750,000 Australians living in remote and isolated areas of New South Wales, South Australia, Queensland and Western Australia.

  • $3.1 million for the Enhancement of Telehealth in Western Australia project to enable improved health service delivery for up to 454,740 residents in regional, rural and remote communities across the state, including more than 44,900 Indigenous Western Australians. This will address problems such as low life-expectancy and retention of health professionals in remote communities of the state.

  • $3 million for the Clinical Outreach – Hunter New England project to provide greater access to advanced clinical applications to an additional 23 health facilities in the New England region. This will promote better health outcomes for residents of the region by improving communication, minimising treatment delays and supporting clinical practice. It also brings the total number of New South Wales hospitals and health facilities that are benefiting from the program to 138.”

….. (go to the URL above for the full release)

And as well as that we have:

http://www.minister.dcita.gov.au/media/speeches/address_to_5th_annual_australian_telecommunications_summit

Strengthening Communities Through Technology

Address to 5th Annual Australian Telecommunications Summit

Sydney Thursday, 30 August 2007

Here we hear about the following (in part)

“For example, many communities in regional, Tasmania will benefit from improved medical care thanks to the VirtualCare@TAS project, which I announced in July at the Launceston General Hospital.

It is worth explaining what this project has done to improve health care services throughout northern Tasmania by linking patients in the region with high-quality expertise via wireless and video conference technology and associated specialist equipment.

The VirtualCare@TAS program is made up of four innovation streams:

  • The Statewide Medical Advice, Referral and Transfer Network;
  • The Chronic Disease Health Coaching Network;
  • The Remember Me Aged Care Network; and
  • The Telehealth Tasmania Outreach Network.

This new service will focus on rural emergency management, diabetes, oncology, aged care and mental health rehabilitation in regional, rural and remote Tasmania.

The Statewide Medical Advice, Referral and Transfer Network will provide a first response remote medical advice, patient triage and assessment capacity, with access to specialist advice for rural hospital staff in an emergency.

During a medical emergency the network will provide access to remote specialist clinical support for patients in small rural hospitals.

Remote specialist advice will likely be invaluable to volunteer ambulance and emergency officers responding to an emergency in a remote location such as Flinders Island.

The Chronic Disease Health Coaching Network will provide remote clinical supervision for diabetes, cancer, mental health and spinal care and it will help people living in rural and remote Tasmanian communities, and there are many.

This means that a cancer patient will be able to undergo chemotherapy treatment locally administered by their local health professionals delivered via satellite clinics and video conferencing units.

These video conference units will enable peer support and specialist advice in the treatment of patients.

This will reduce the risks of severely ill patients in remote areas travelling long distances to receive their treatment in major centres.

When it comes to treating the sense of isolation in these communities, it’s not just the patients who benefit.

The opportunity for health professionals to increase skills and to engage in professional development without travelling vast distances and leaving these communities is an essential part of recruitment and retention.

The VirtualCare@TAS Program will tackle these critical issues head-on and, in this way, will not only keep more Australians healthy, but keep more Australian communities vibrant and viable.”

Suddenly Minister Coonan is all over the country announcing e-health initiatives and pre-empting Minister Abbott (who is meant to be the Minister for e-Health) by letting it be known there is to be a standardised national electronic health record!

What is to be made of all this?

Can I suggest a few things.

First it is hard to escape the conclusion – on the basis of these announcements – which are not even joint announcements with Health – that state agencies and area health services have got sick of asking the Health Department (DoHA) for e-health network infrastructure and have simply gone elsewhere in frustration.

Second it is clear there is no co-ordinated e-Health agenda or plan existing within Government or there would be much better co-ordination than this!

Third having Minister Coonan announce a EHR initiative is really bizarre. No wonder the NEHTA CEO felt the need to offer ‘no comment’ when asked..given this is what NEHTA said it was doing as recently as a few days ago. Were I him I would be feeling a little gazumped!

Fourth it seems clear DoHA has lost control the e-Health strategy and now any agency that feels like it can just announce what they want when they want. One really wonders how sustainable this flourish of little initiatives will be in the long term. One never seems to see much in the way of evaluation if initiatives of this ilk become public.

All this is really bit part nonsense and puts off further the day when common sense and rationality will be applied to the e-Health domain in Australia. It is virtually inevitable, in my view, a good portion of these funds will wind up being wasted – we can just hope not!

The pre-election period we are presently in does really yield much strangeness.

David.

Sunday, September 02, 2007

Useful and Interesting Health IT Links from the Last Week – 2/09/2007

Again, in the last week, I have come across a few reports and news items which are worth passing on.

These include first:

http://www.computerworld.com.au/index.php?id=543270264&eid=-6787

Tassie ambos move to electronic reporting

Rugged computers to replace pen and paper

Rodney Gedda 27/08/2007 11:37:50

The Tasmanian Ambulance Service (TAS) will procure some 70 rugged notebook computers over four years to facilitate the migration off its paper-based patient care reporting process to a new electronic system.

The Business and Risk Strategy Branch of the Department of Health and Human Services (DHHS), on behalf of TAS, is seeking offers from a business capable of supplying Panasonic CF19 Toughbook computers to be used in the new Electronic Patient Care Record (ePCR) project.

"TAS is in the process of implementing a major improvement to its management of patient care reporting by changing from a complex paper-based patient care report system to an electronic tablet system," according to the department. "In parallel with this new initiative are a number of associated business improvement activities based on adoption of the ePCR and supported, where appropriate, by a range of modern DHHS ICT capabilities."

The new business improvement initiatives are being coordinated through DHHS information systems, the state's HealthConnect program, and TAS.

…..( see the URL above for full article)

This is a really sad article. Why? First that the purchase of a few laptops to capture ambulance transport and presentation details would be seen as an e-Health initiative and second that there is continued mention of the now totally dead HealthConnect initiative with which this purchase has absolutely no relationship. More political pork I reckon.

Second we have:

http://www.australianit.news.com.au/story/0,24897,22317999-15306,00.html

Tax office gets tough on file privacy

Ben Woodhead | August 28, 2007

FRAUD detection systems have uncovered a rash of privacy breaches at the Australian Taxation Office as employees flout tough data protection rules despite ongoing monitoring and training.

The sweeps of data access logs led to three sackings during the 2007 financial year and another nine staff resigned after the ATO detected unauthorised access to taxpayer records.

The breaches came despite extensive privacy education programs at the agency and closely matched the 24 instances of tax officers inappropriately accessing client information that were uncovered in the 2006 financial year.

"While no level of unauthorised access is acceptable, in an organisation of about 22,000 people it is inevitable that a very small number of people will be tempted to do the wrong thing," an ATO spokeswoman said.

…..( see the URL above for full article)

This is an important report as it adds the Tax Office to Centerlink, Hospitals and Motor Registry Offices around the country that have had private information leaked or snooped upon. It seems to me this sort of abuse is inevitable and that what is needed is to ensure the monitoring of and punishment of offenders needs to be sufficiently draconian to make people very hesitant to mis-behave.

With patient records it is vital that the public is assured that snoops will be reliably identified and punished.

Third we have:

http://www.theage.com.au/news/national/labor-pledges-to-kill-off-access-card/2007/08/28/1188067111116.html

Labor pledges to kill off Access Card

Annabel Stafford
August 29, 2007

THE $1.1 billion Access Card could soon be dead, with the Labor Party confirming it would kill off the proposal if it won this year's election.

Coming after the Federal Government last week confirmed it would put off introducing legislation for the Access Card until after the election, Labor has confirmed a Rudd government would scrap the idea.

"As far as we're concerned, (the Access Card) is dead," Labor human services spokeswoman Tanya Plibersek said.

Voters worried about the card now had a clear choice between a Coalition government that would introduce the smartcard — which would replace up to 17 social services cards and be required by anyone wanting to access government payments — and one that would not, Ms Plibersek said.

…..( see the URL above for full article)

This is an interesting announcement by Labor – as, while in most policy areas they are seeking to only identify difference in those areas there is strong reasons to do so, it has been selected as an area of differentiation.

This decision also suggests – given the stated position of opposition of the other political parties – that this project may indeed face permanent cancellation.

This outcome would seem to be likely to bring some additional focus brought to bear on the NEHTA UHI service – which I note is increasingly being mentioned in submissions regarding the Access Card. The tenor of these submissions has been to ask how these initiatives are linked, and why are citizens being given multiple identifying numbers without any apparent co-ordination.

Fourth we have:

http://www.modernhealthcare.com/apps/pbcs.dll/article?AID=/20070830/FREE/308290018/1029/FREE

RHIO experts talk problems, future of movement

By: Joseph Conn / HITS staff writer

Story posted: August 30, 2007 - 5:59 am EDT

The recent faltering of a regional health information organization in Portland, Ore., and the outright folding of a RHIO in Scranton, Pa., may be indicative of a scaling back of some of the more ambitious goals of the RHIO movement, according to industry observers.

Are RHIOs like those proposed in Oregon and Pennsylvania between competing entities and multiple information technology systems dead?

"I'm definitely in the category of I don't know," said David Lansky, senior director of the health program at the Markle Foundation, who admits not having spent a lot of time tracking individual regional activities, but works primarily "one level up" on how regional networks communicate with each other. Markle was a participant in one of three consortia to present a prototype to HHS of a national health information network. The Markle collaborators moved electronic messages between RHIOs in Boston, Indianapolis and Mendocino County, Calif.

"It's not yet clear if the incentives exist for healthcare organizations to share information," he said. "So, I think it's become time to have more discussions about getting the incentives right. How? That's a deep question. Ultimately, it will be how we pay for healthcare."

…..( see the URL above for full article)

http://www.modernhealthcare.com/apps/pbcs.dll/article?AID=/20070831/FREE/308310001/1029/FREE

Pact would coordinate key IT panels' activities

By: Joseph Conn / HITS staff writer

Story posted: August 31, 2007 - 5:59 am EDT

The leaders of two federally supported organizations—one tasked with anointing health information technology communications standards and the other with testing and certifying clinical IT systems—have proposed a formal agreement on how to coordinate their activities.

The proposed five-point memorandum of understanding would guide the relationship between the Certification Commission for Healthcare Information Technology and the Healthcare Information Technology Standards Panel. The proposal was worked out between the physician chairmen of the two organizations, Mark Leavitt of CCHIT and John Halamka of the HITSP. It is subject to review and possible amendment by the controlling bodies of the two organizations as well as their approval before it becomes effective, those leaders said. The proposal will be presented to the controlling bodies this month, they said.

The Certification Commission for Healthcare Information Technology was formed in 2004 by the American Health Information Management Association, Healthcare Information and Management Systems Society and the National Alliance for Health Information Technology as a private-sector organization to promote the adoption, particularly by office-based physicians of electronic health-record systems and other IT. In 2005, HHS awarded CCHIT a three-year contract totaling $7.5 million to develop a process to certify health IT products.

....( see the URL above for full article)

The Certification Commission for Healthcare Information Technology (CCHIT) and the Healthcare Information Technology Standards Panel (HITSP) are core players in determining the forward Standards directions in the US. This announcement seems to me to be unequivocally good news.

http://www.e-health-insider.com/news/2988/call_for_electronic_consent_for_secondary_uses

Call for electronic consent for secondary uses

30 Aug 2007

Consent to use patient records for secondary uses should be recorded using electronic mechanisms integrated with core NHS systems, the Working Group on the Secondary Uses of Patient Information has recommended.

The group, established to consider the issues around uses of patient-identifiable data for purposes other than direct patient care, said: “Consideration should be given to record consent, and ensure that the consent choices of an individual are automatically adhered to when providing data from their record.”

They argue that the opt-out approach currently suggested is inappropriate for keeping track of a patient’s wishes regarding their personal data where their identity is known to the researcher.

…..( see the URL above for full article )

The report can be found here:

The Report of the CRDB Working Group on the Secondary Use of Patient Information

More next week.

David.

Thursday, August 30, 2007

Privacy and e-Health – The Privacy Commissioner Provides a Very Useful Survey.

A day or so ago the Commonwealth Privacy Commissioner (Ms Karen Curtis) published an invaluable document for all those interested in privacy and health information sharing.

The full document can be downloaded from the this page in either .pdf or MS-Word Format.

The survey questions 1500+ adults about their attitudes on a range of privacy issues and appears to have been conducted in a robust and reliable fashion statistically.

I think the most important findings from the perspective of e-Health implementation and planning are:

1. By and large most Australians trust Health Service Providers to treat their private information in a trustworthy fashion. The more educated are slightly more sceptical than the less educated.

2. Most are happy to share private health information if they see the relevance in doing so.

3. There was a very strong dislike of being required to disclose any form information that is not relevant to the transaction at hand.

4. There was a strong rejection of the use of any information (especially by business and government) for purposes other than that for which it was collected. (This bears directly on what NEHTA is planning to do with Medicare Australia's personal records)

5. “The majority (76%) of Australians believe that inclusion in the National Health Information Network should be voluntary. At 21%, the minority believes all medical records should be entered. A greater proportion (76%) believe inclusion should be voluntary (cf. 64% in 2004 and 66% in 2001). As in 2004, females (80%) were more likely than males (72%) to say this. Unlike 2004 however, there were no significant differences in attitudes between age groups.”

This seems pretty clear cut that the public rejects compulsion in the sharing of their private health information and that the view on this is strengthening over time.

6. “Respondents were then asked whether, if such a database national health information network existed, permission should be sought before releasing their de-identified information. Females (53%) were more likely than males (43%) to say that permission should be sought. “

Again – even when not identified – close to half the population do not want to share without consent.

7. Interestingly, “While opinions varied, 52% thought that health professionals should share health information, but only if relevant to the condition being treated (35%) or if the condition was serious or life threatening (17%). A third (32%) believed health professionals should share health information only with the patient’s consent. The proportion believing anything to do with a patient’s health care could be discussed between health professionals stands at 25%.”

This says to me that people are wanting more control of information sharing, even the sharing of information between relevant professionals.

8.There is a low threshold for individuals to provide false identity information when conducting internet transactions. This has the implication that if access is provided for citizens to access major identity data-bases there will be at least a significant proportion who will provide false information.

It seems to me this survey makes it clear there is an emerging sensitivity in the populace to having their personal information leave their control without their specific consent and approval. All those implementing – or planning to implement – e-Health systems should take careful note of both the absolute values of the views as well as the trends.

NEHTA especially needs to take careful note of the results of this survey. The clear preference of the community is for all interactions with e-Health systems to be on the basis in individual specific consent. Just because it is inconvenient or more expensive to grant the public what they want is no excuse. Ignoring clearly stated public opinion has a habit of rebounding on those who move in these sort of directions. NEHTA you have been warned!

David.

BTW. Page 8 of the NEHTA Approach to Privacy document says:

“As further work on privacy and consent is conducted or finalised, additional information will be made available on the NEHTA website. The next privacy document to be published will be NEHTA’s Privacy Blueprint for the HPI and IHI (planned publication date August 2006). A Privacy Blueprint for the Shared EHR will be released in late 2006. “

It is fair to say these timelines were not met – we saw the UPI privacy draft in December 2006 (followed months later by a risible summary of the comments received – without the actual submissions) and the Privacy Blueprint for the Shared EHR is yet to see the light of day.

D.

Wednesday, August 29, 2007

e-Health in Australia – A Governance Farce that Will Hurt us All.

e-Health in Australia is a ‘rudderless ship’ in a very large storm and is way too close to the rocks!

Just a few short years ago everyone knew who was at least meant to be doing what in the e-Health Space.

We had the Australian Health Ministers Advisory Council (AHMAC) and the Council of Australian Government (COAG) who sorted out major policy directions and provided funds.

The Australian Health Information Council (AHIC) provided e-Health Strategy and Direction.

The Commonwealth Department of Health and Ageing (DoHA) set policy detail, sponsored national initiatives (such as HealthConnect) and tried to foster State co-operation and co-ordination.

Essentially, following the 2004 Boston Consulting Group (BCG) Review the HealthConnect Program was cancelled. It became a ‘change management strategy’ and a few annoying money-wasting remnant projects rolled on to use up the funds that had been committed.

By 2005 AHIC had been canned and the National E-Health Transition Authority (NEHTA) had begun operations. Virtually simultaneously most of the e-Health skills in DoHA left the public service and the place of e-Health was downgraded in the Commonwealth bureaucracy.

Come to 2007 and where are we?

First we have the BCG undertaking a review of the now 2.5 year old NEHTA. This review is a governance nightmare as we have senior health bureaucrats commissioning a report on their performance in managing NEHTA. Ever hear of a senior health bureaucrat criticising their own performance? Clearly the outcome will not say you have all done a poor job managing NEHTA as everyone knows they have. Talk about a conflict of interest!

Second we have the now resuscitated AHIC. It seemed to make some hopeful noises for a little while. The silence is now deafening and with an election due in a month or two we can be sure nothing will ever come of their work.

Last we now have a brand new E-Health Ministerial Advisory Council – established as an effort to blame shift away from the Minister and DoHA who have been negligent in their inactivity. Again we have a secret, non-communicating entity working away in a bureaucratic non-transparent vacuum.

Let’s not even consider the managerial qualities of the State Health IT bureaucrats. Most of them are still tied up in overly slow procurements (WA, SA etc) or are doing rigid state-wide system implementations that have the users more than a little grumpy.

IBA (our largest indigenous e-Health Company in which I have a few not so profitable shares) makes the point in its annual results, just released, that it has been forced overseas to survive as virtually no serious sales are likely until 2008/9 in Australia.

If ever there was a situation where an election offered hope for a re-start and a new plan this is it. What a humongous mess.

David.

Tuesday, August 28, 2007

Medicare, NEHTA and Your Privacy.

A week or so ago a quiet bit of regulation making occurred in the Federal Parliament. The following regulation was tabled under the Ministerial Authority of Senator Chris Ellison.

Here is the title of the Direction.

Medicare Australia (Functions of Chief Executive Officer) Amendment Direction 2007 (No. 2)

Medicare Australia Act 1973

I, CHRISTOPHER MARTIN ELLISON, Minister for Human Services, make this Direction under paragraph 5 (1) (d) of the Medicare Australia Act 1973.

Dated 8 August 2007

CHRISTOPHER MARTIN ELLISON


The full text is downloadable from here. (It is only a page or two in .pdf format and well worth a read)

In plain language what this does is, without any contestability or assessment of value for money, have Medicare Australia scope, develop, build and test the NEHTA UHI (as defined in the regulation).

It also authorises them to make a copy of the two key identity databases supported by Medicare Australia (as defined in the .pdf file - essentially the client and the provider databases) and use them to provide an identity service.

This is really an amazing thing to be authorised. What seems to have happened is the despite the prohibition in the Commonwealth Privacy Act (2000) of personal information being used for purposes other than for which it was collected by Government Agencies it has been decided that information that was collected to enable Medicare benefits to be paid is to be used to operate the NEHTA UHI.

The implications this has for the trust the population will have in Medicare Australia to keep their private information private must be profound.

There are all sorts of questions this authorisation raises – such as:

1. Are the Consumer Directory Maintenance System and the Provider Directory System operated by Medicare Australia ‘fit for purpose’ in the role of electronic health record identification and linkage? (I think not).

2. How are those whose information is on this copy of the register able to see what is held and how accurate it is?

3. How will this information be protected from un-authorised or unwanted disclosure or look up. It seems every healthcare provider in the country will be able to search the customer data-base to find an associated UHI – this is a really terrible idea and will have victims of domestic violence and the like just terrified?

4. How are the Medicare and UHI data-bases going to be kept in synch as one or the other is updated? If a ‘snapshot’ of the databases is taken – how will the data’s currency be maintained into the future?

5. Where is the Privacy Impact Assessment that validates this approach?

6. Who is going to be responsible if there is a security breach or someone’s details are released and an individual is damaged or harmed. Is it the private company NEHTA or the Government through Medicare Australia?

7. Who is actually going to run the proposed service – NEHTA, Medicare Australia or someone else? Does anyone else notice a certain irony in a private company contracting a Government Agency for the delivery of services – as seems to be the case?

8. Why is such a potentially privacy destructive regulation just slipped through the House of Reps and the Senate with no public announcement etc?

It seems clear to me this proposal represents the health identifier you have when you are not prepared to pay for an identifier that one can be sure is fit for purpose in terms of safety and integrity.

Frankly this is a disaster in my view and should be aborted before it even gets started. If we are to have a UHI service (and I think it is vital) it should be based on privacy and security protections that are appropriate for clinical record linkage.

David.

Note: Comprehensive coverage on the basics of this issue is found in an article by Karen Dearne in the Tuesday Australian IT section of 28th August, 2007. This can be seen on line at the following URL.

http://www.australianit.news.com.au/story/0,24897,22318001-5013040,00.html

Ellison unlocks Medicare databases

Karen Dearne | August 28, 2007

MEDICARE patient and provider databases will be the key sources of a healthcare identifier regime being introduced to support a shift to e-health programs.

Records belonging to 99 per cent of Australians are contained in Medicare's Consumer Directory Maintenance System, considered to be the most up-to-date and accurate government repository of personal information.

Although the law prevents the use of Medicare data for other purposes, Human Services Minister Chris Ellison has unlocked access via a legislative amendment tabled in Parliament on August 16.

Senator Ellison has authorised Medicare's chief executive to enter into a contract with the National E-Health Transition Authority and provide resources in support of the Unique Healthcare Identifier program.

Progress on the individual, healthcare provider and health organisation directories was flagged by NEHTA chief executive Ian Reinecke at MedInfo 2007 in Brisbane last week.

Dr Reinecke said NEHTA had established an operational governance model for contracting a universal identifier services operator, expected to be Medicare Australia.

….. (see URL above for full article)

D.

Monday, August 27, 2007

Minister Abbott’s E-Health Report Card – Hunt the Spin!

The following are the prepared notes for a speech the Health Minister gave last Monday – reviewing the progress that has been made in e-Health in the four years since the Minister took up the reins.

My comments are inserted in the text in italics.

http://www.health.gov.au/internet/ministers/publishing.nsf/Content/sp-yr07-ta-abbsp200807.htm?OpenDocument&yr=2007&mth=8

An E-Health Report Card - Speech Notes for the Australian Health Summit, Sydney

20 August 2007

In November 2003, my first scripted speech as Health Minister concerned e-health. I stated that an electronic health record, communicated electronically among health care providers, would mean safer, better, more convenient and more efficient health care. For doctors and other professionals, it meant less repetitive taking of histories; for governments and other funders, it meant less duplication of diagnostic tests; for patients, it meant more access to their health records and more capacity to manage their own health; for everyone, it meant fewer potentially disastrous mistakes because of avoidable ignorance.

Failure to establish an electronic patient record within five years, I said, would be an indictment against everyone in the system, including the Government. I hope to be judged against that somewhat rashly declared standard; not because it is likely to be fully met but because it would mean that, come next year, I remain the Health Minister!

Clearly the Minister has a high level understanding of the benefits of e-Health – sadly he really has not made substantial progress in reaching his desired end state for e-Health

Back then, my thinking was that people in the health system were at least as capable as those in the finance system. If EFTPOS could link billions of bank accounts and financial institutions around the world, it should surely be possible for every Australian patient’s file to be copied, indexed, stored and securely made available to the patient and authorised treating professionals via the internet. In retrospect, I had underestimated the difficulty of shepherding independent professionals and insular institutions through the thickets of patient privacy and sheer force of habit. Still, although not yet very obvious to patients, much has been achieved in the past four years.

It is a worry that the Minister takes just three paragraphs to start blaming clinicians, rather than understanding that all successful change needs to deliver benefits to those who are asked to change, or the change will be resisted. In a fee-for-service professional payment environment the incentive to use technology, which typically slows a practitioners productivity – at least initially – is very low. Given it is patients and the Government who stand to benefit from more Health IT use, the payment and incentives need to come from those who will benefit.

Since the late 1990s, the federal Government has provided more than $700 million – or about $40,000 per full-time doctor – to support the use of information technology in general practice. There are still doctors taking case notes on cards, hand-writing prescriptions and relying on receptionists to find files in cabinets in the time-honoured way. There are also hospitals such as the Epworth East where each bed is equipped with a computer screen and keyboard so doctors’ and nurses’ notes instantly integrate into patients’ records. Some health funds are beginning to offer their members personal health records that will enable the storage of diagnostic test results as well as treatment records and general health information. Doctors especially still tend to be much more enthusiastic about clinical than administrative technology, even though both are equally necessary for effective clinical practice. Even so, a rightly conservative but highly perceptive profession is adapting to change because it’s in doctors’ own and their patients’ best interests.

Last year, according to data published in the Medical Journal of Australia, 94 per cent of general practices had a computer (up from 15 per cent in 1997 and 70 per cent in 2000). Of GPs with a computer, 94 per cent used it for prescribing, 82 per cent to write referral letters, 70 per cent for some medical records functions, and 68 per cent to create management plans. Of GPs with a computer, 33 per cent had fully computerised their patients’ medical records while 78 per cent of GPs worked in practices that used computers for scheduling appointments or recalling patients.

This is good news – but clearly there is more to do!

Cultural shifts take time but over a decade the computer on doctors’ desks has gone from expensive paperweight to an all-but-essential part of medical practice. Of course, it’s one thing to use a computer for internal practice purposes; another to make use of IT for ordering tests or sharing information. Last year, only 53 per cent of GPs with a computer used it for email. Still, progress in this area makes e-health possible if not inevitable.

As well, the Government’s $100 million investment in HealthConnect has helped to facilitate the electronic transfer of admission and discharge information between some GPs and public hospitals in Tasmania, South Australia and Western Australia. In Sydney’s west, up to 50,000 patients at Westmead Hospital are being offered a Shared Electronic Health Record accessible to their specialists and GPs. In Bendigo, a link between GPs, specialists, allied health professionals and community care providers is improving the management of chronic disease. These trial projects, among others, are exploring potential best practice for what should become standard arrangements in the future.

Neither Healthelink (the NSW Site) or the Bendigo site have been evaluated as yet. The earlier $100 Million investment was essentially totally wasted – and given all that has been published is a summary report that essentially said it looked promising but did not work as yet.

The federal Government has also invested in initiatives to support clinical practice such as electronic publishing of the Pharmaceutical Benefits Schedule and the Medicare Benefits Schedule. The Government has worked with the states and territories to remove legislative barriers to electronic prescribing and referring. It has negotiated a subscription to the online Cochrane Library to provide Australians with free access to evidence-based information on best practice.

The federal Government has committed $69 million to providing broadband access for GPs and pharmacists. More than 90 per cent of pharmacies have broadband and 78 per cent of doctors work in General Practices with broadband access. The most recent Pharmacy Agreement gave pharmacists 40 cents a prescription for using PBS Online, a real time record keeping and eligibility checking system.

The federal Government has committed $98 million to Medicare Australia for services such as EasyClaim. At participating practices, a card swipe can provide patients with their Medicare rebate on line from their doctor’s surgery. The Government is now talking to the AMA about incentives, similar to those offered to pharmacists, to encourage privately-billing doctors to give this convenience to their patients.

These are really just general investments in the provision of basic infrastructure. The EasyClaim project is, of course, stalled as the AMA has realised that use of the system will increase practice workloads and costs, for no financial reward. Increasing practice costs – without re-imbursement – was never going to be a winner!

Finally, the federal Government has committed $79 million towards the National E-Health Transition Authority (NEHTA) which is developing unique IDs for patients and providers and developing a common language so that particular terms have the same clinical meaning across different record systems.

These comments are interesting. It would have been difficult for the Minister to say less about NEHTA – especially given it is spending $79 million on it over the next three years. Hardly an enthusiastic endorsement of what NEHTA is doing.

It would be fair to say that policy-makers have been impatient to see an operational return on these investments rather than a proliferation of trial projects and pilot schemes. A particularly successful one has been the Shared Electronic Health Record trial in the Katherine region of the Northern Territory involving nearly 12,000 patients. This has been an important means of delivering better health care to a mobile population subject to high levels of chronic disease. This Shared Electronic Health Record currently includes a health profile (with blood type, chronic conditions and allergies), an individual event summary (visits to the GP, emergency department presentations and hospitalisations) and pathology results.

This is very interesting – as when the project was evaluated a year or so back the level of usage and clinical content was not as is indicated here. It would be good to get a new public evaluation of progress to date here – so we can assess how sensible further investment is. It could be that great success has been achieved – and if so it would be good if this information was shared. Without such sharing I remain just a trifle skeptical.

Today, I can announce that the federal Government will fast-track the roll-out of a Shared Electronic Health Record throughout the remote parts of the Northern Territory. This should help to ensure that the health issues identified through child health checks are properly followed-up. A comprehensive health record is absolutely necessary if the goodwill and hard work of visiting and resident professionals is to resolve identified health problems and prevent their recurrence.

With consent, the Shared Record will be accessible to any authorised health professional in the NT. This means that after the initial health check, a patient’s health information will be available to professionals in general practices, community health centres or hospitals, so that effective follow-up care can be delivered. The Shared Record will support ongoing care by triggering recalls and reminders as children advance through life.

A child with a Shared Record will have his or her health information updated, if the infrastructure is available, at the point of the health check. A child without a Shared Record will have one created, if the infrastructure is available, at the health check. If the infrastructure is not available, a paper record will be created at the health check and the information will be used to update or to create a Shared Record. One way or another, all remote area indigenous children will have the opportunity to gain a Shared Health Record.

A good idea – and suggested on this blog within days of the ‘Emergency Intervention’ being announced.

As the British Government has discovered, it’s much easier to spend money on health IT than to produce a functioning e-health system. So far, despite its 15 billion pound budget, the NHS HealthSpace is far from fully operational. On line access to a full electronic primary health care record is still only being trialled in a limited number of practices. Few practices offer their patients on-line booking or prescription re-ordering. Only some patients have some access to a limited range of specialist records.

I think this is more dismissive than current progress suggests – and I suspect this is because of concern as to how much it might cost to do things properly!

In Australia, the Government eventually decided against creating a single, national comprehensive electronic health record designed and managed by officials. The ordinary difficulties associated with government projects are magnified, it seems, in such a protean field. The Eclipse experience shows how hard it is for governments to design systems for a myriad of users rather than to encourage people to devise systems which work for them.

Has anyone told NEHTA that the National Shared EHR has been cancelled? I note how long it has taken for this decision to become public. Pity there is no clarity regarding what is now planned in the area of clinical information sharing.

In health IT, the Government’s role is to remove regulatory barriers, provide incentives for change, promote “inter-operability” of systems and explain to the public how and why e-health can improve their health care experience. Its job is not to build complete systems from scratch or to impose uniform infrastructure on health providers but to make it more realistic and affordable for healthcare providers to move into the IT age.

In the short term, the Government will introduce more Medicare items to support telehealth services. There’s already a rebate for psychiatry consultations over the phone. The Government is considering a rebate for dermatologists consulting remotely with patients in GPs surgeries via a diagnostic camera. The Government will foster the development of one or more secure repositories for personal Electronic Health Records. It will begin to link the various existing illness or health registers so that information on significant diseases, screening and immunisation can be incorporated into a patient record. Eventually, this work will provide a foundation for much more effective monitoring of the performance of drugs and health devices.

It’s likely that, in the next two to five years, the Government will make access to Practice Incentive Payments or even the MBS itself subject to best practice in health record-keeping. For instance, team care plans should be a standard feature of primary health care for people with chronic disease and complex care needs. It would be almost impossible to create and monitor these care plans effectively without the use of IT. In the years to come, effective use of IT should be as much a part of professional practice as the provision of suitable premises. It could be expected, even mandatory, in much the same way as continuing professional education.

This is the sort of approach – the so called “pay for performance” approach with an Australian flavour – which might work. Of course there are all sorts of hurdles to be addressed and all sorts of issues about the sort of information collection infrastructure that may be required.

In the near future, routine follow-up after an initial consultation, subsequent consultation as part of a broader care plan, and lifestyle modification advice for people with chronic illness could readily be delivered by phone or over the net. Of course, some issues would have to be resolved first, such as whether these items could only be provided by the patient’s usual doctor or whether a face to face consultation would be required prior to tele-consultations or e-consultations. Clearly, this would be more feasible for some specialities than others and there are complex billing arrangements that would need to be sorted through. Still, it’s hard to imagine that health care delivery in the years ahead won’t make much better use of convenience technology.

To help meet these challenges, the Government has established an e-health Ministerial Advisory Council. It’s chaired by Roger Allen, a former Deputy Chairman of Austrade and IT entrepreneur. It comprises leading representatives of medical and health organisations and is meant to ensure that government e-health initiatives are actually making a difference to health practice not just providing business openings for the IT industry. If e-health doesn’t help practitioners and patients, it’s hardly worth doing.

Oh dear – another committee. I wonder where this E-Health Ministerial Advisory Council fits in between AHMAC, ACHI, NEHTA etc. I wonder is this Council have a go at developing a plan – some-one sure needs to!

A pre-requisite for a functioning e-health system is secure messaging. From next month, the Government will be working with Divisions of General Practice to offer GPs public key infrastructure. This will provide them with the ability to transfer information and images safely and securely between computers. Participating practices will receive a CD to download the necessary software and individual GPs will receive a PIN plus a personal data stick for their computer to verify identity. This offer will also be made to allied health professionals registered with Medicare. The system will provide users with the assurance that information comes from a trusted source and has not been tampered with. It will enable GPs to order laboratory tests, X-rays and other diagnostic procedures, prescribe drugs and other remedial treatments, and issue recalls, reminders and referrals confident that the information will not go astray or be misused.

As long as this is highly usable and works well this is a great idea.

The Government will also provide expanded access to on-line health information through the purchase of additional access licenses for recognized health learning resources. This will give health professionals throughout Australia accessible, authoritative and up-to-date information and should help to promote best practice health care. The Government will work with the professions to identify the clinical guidelines, on-line journals and on-line reviews that can best help.

Excellent idea – just spread the NSW Health Clinical Information Access Program nationally would be a good start!

The Government will soon to go tender for organisations to facilitate, in a particular region or community, a comprehensive e-health environment. Successful organisations will be expected to work with local GPs, aged care facilities, hospitals, diagnostic providers and other health professionals to ensure that they can electronically share information. Importantly, payment to these organisations will depend upon the volume of clinical information electronically transmitted.

This adopts a key suggestion this blog has been on about for a good while. Start locally and simply and progress at a pace those involved can accept and utilise.

Finally, I can announce today that by early next year, every Australian will be able to access his or her comprehensive Medicare claims history on-line. Patients will have secure access via the Internet to a full record of their Medicare rebates. There will also be a layman’s guide to item descriptors so that patients can readily appreciate the services they have received. Within 12 months, there will be similar arrangements to allow patients on-line access to their PBS claims history.

The first step towards a Personal EHR for Australians. Good idea and, strategically , possibly the core of a Shared EHR that might work.

The new measures announced today will cost about $25 million in total over the next three years.

Note this is an investment of a little over $8 Million a year. Given the Australian Health Budget is about $80 Billion a year – pretty trivial I must say.

These measures will not, of themselves, mean that every Australian has a personal, securely accessible comprehensive electronic health record by the 2008 deadline I once set. Nevertheless, it is substantial progress and is starting to be noticeable to patients. I am reluctant to set a new deadline but am confident that, within a few years, most Australians will be able to access a comprehensive electronic health file that is kept automatically updated by health service providers.

Since 2003, the Government has learned that the best can easily be the enemy of the good, at least in this area. As a funder and organizer, the Government looks likely to achieve far more than it could as an e-health builder and director. As is so often the case in Australia’s health system, the Government has turned out to be much better at funding services that other people deliver than at delivering services itself.

ENDS

Thus far the Commonwealth has hardly funded or organised anything in e-Health to any significant degree. I wonder will that change as the election approaches?

Final comment – the quote “best can easily be the enemy of the good, at least in this area” is very true – sad that NEHTA does not realise this and get on with providing some practical easily implemented solutions to major the problems we all understand. I would not want to be accused of “reading between the lines” but I have the distinct feeling NEHTA is not much in favour with the Minister. If they were would there be a new Advisory Council now commissioned?

All in all this really is a very sad report card – and has hardly moved much from my earlier report card which is found here.

As ever the issue is that the Minister is articulating a dis-coordinated set of little initiatives which will make little difference in the absence of a coherent National Plan. Another missed opportunity!

David.