Friday 27 November 2015
"Benefits Realisation" or "Impact Analysis"
Far too many projects have no follow-up at all. The job is done and everyone moves on. "Benefits Realisation" is an improvement - but there is a risk that in focusing on benefits the overall impact of the project is missed - and that lessons learned are missed. Any project that is self-aware enough to have committed effort to "Benefits Realisation" should be self-aware enough to realise that "Impact Analysis" would be more useful and clear sighted.
Monday 9 November 2015
SNOMED is good for health records, but why not also for Policy, Regulaton, and Evidence
The NHS has rightly said that having a standard terminology will make a real difference to the ability to analyse electronic health records and really get value out of their contents.
What is weird is that this enthusiasm for SNOMED coding of Electronic Health Records does not extend to NHS Health Policy Documents, Regulations, or Guideline documents.
Why are these not SNOMED coded -- this would:
The rich semantics of SNOMED CT is ideally suited to such documents -- if SNOMED CT will add value to individual health records, how much more value will it add to health service organisations under constant organisational change that much provide care plans for their populations.
What is weird is that this enthusiasm for SNOMED coding of Electronic Health Records does not extend to NHS Health Policy Documents, Regulations, or Guideline documents.
Why are these not SNOMED coded -- this would:
- make it easier to compare different policy documents
- remove ambiguity form the documents (what cancer is being talked about, what is the definition of Diabetes, etc)
- Make it easier to link indicators to the policy - how will we know whether the policy has been enacted, and how will we know if it has worked. What are the intended benefits, and what are the metrics that will be used as evidence for those benefits?
- Make it easier for groups within and beyond the NHS to show that what they are doing (or propose to do) delivers of the Policy.
- Make it easier for commissioners to purchase in line with policy (or to knowingly deviate)
The rich semantics of SNOMED CT is ideally suited to such documents -- if SNOMED CT will add value to individual health records, how much more value will it add to health service organisations under constant organisational change that much provide care plans for their populations.
Monday 7 September 2015
Healthcare is a Complex Adaptive System with different perspectives and ways of seeing
Healthcare can be seen as a complex adaptive system, as can the information that underpins, permeates and radiates from it.
According to the TED talk below, complexity implies that the system cannot be understood from one perspective alone, or using a single language.
Adaptive means that the behaviour of the system cannot be fully anticipated, but that its behaviour is determined by its previous state, and the changing environment that it is in. Of course for healthcare the environment is complex and adaptive too.
Healthcare information provision can be seen, categorised and described from a vast number perspectives.
The following list can be read in two ways. One is as a set of perspectives. How the health service looks to me as a patient and how it looks to me as a programmer are different. How it impinges on the life of a tumour or what the health service looks like from the perspective of a tumour is different again.
The other way of reading the list is as a set of categories - what is being looked for from a particular perspective. As a patient I may be totally unaware of the costs and money flows associated with my treatment - or I may be very sensitive to it. From each perspective there are many different ways of seeing.
The list is not intended to be exhaustive - in two significant ways - the set of categories / perspectives is not complete, and nor is is the only way of categorising the space. Indeed the selection/discovery of categories/perspectives is part of the process of engaging with subject matter, and is an area where good choices can help to make that engagement more fruitful.
- The actual people involved (who does what when and why)
- The job descriptions / roles of the people involved (patient, doctor, parent, friend, guardian, nurse, programmer, venture capitalist, politician, voter, neighbour, manager, ...)
- The products (software, hardware, intellectual property, etc)
- The projects and programs involved
- The money involved (who pays how much for what, the result of a particular payment, etc)
- The activities (treatments, tasks, events, actions, encounters, processes)
- The subjects of care (genes, tumours, organs, patients, families, groups, populations, citizens, etc)
- The organisations involved (providers, suppliers, payers, interest groups etc)
- Purposes and Outcomes (what is the point - comfort, autonomy, health, care, QALY, social cohesion, individual care, public health,...)
- Metrics (what can be measured? what can be compared? what questions can be answered?)
- Information Standards and Specifications, and the organisations that maintain them.
- "Evidence-based medicine" is a way of seeing healthcare that has a lot of value, but it is not the only way of seeing. We do not insist on evidence-based marriage, or evidence-based cooking. In both cases there is relevant research but for most of us that is not the best language to use. The research indirectly informs us, but we do not see it as the basis of how we love or feed each other.
- Patient-centric. The patient's is a valuable perspective to consider. However if I need an operation on my knee, I want to know that the place I am going to will do a good job on my knee. I want them to really care about doing great operations, and that the staff want to be working there. As a potential patient, I care less about it being patient focused, and more about it doing a great job.
As we engage with healthcare information we seeing in a particular way from a particular perspective and can strive to achieve particular outcomes. This involves working with others who have different perspectives and ways of seeing. Healthcare Informatics is about helping to build and sustain those bridges, as well as making it easier to deliver outcomes from a particular perspective and way of seeing.
Information standards and specifications fit into this complex adaptive system as tools that can be used, and as points around which collaborative momentum can be built. They emerge as part of the complex adaptive system where and when there are the resources and engagement necessary for their creation and maintenance. Different perspectives and ways of seeing will engender different metrics for evaluating them, and different outcomes to expect from their use.
How this diversity of perspectives and ways of seeing impacts specific information standards or healthcare outcomes are topics for another day.
Written in reaction to:
TEDxRotterdam - Igor Nikolic - Complex adaptive systems
Friday 26 July 2013
trafficlight CDA to manage scope and support document evolution
Managing scope is a key part of delivering a successful project - and this is particularly true when using information standards in healthcare projects. The challenge is that the standards are designed to meet a wide range of requirements, and the project's success will be measured against a specific set of local requirements.
Green CDA was envisaged as a way to take the full CDA specification, and reduce the complexity for implementers by exposing just the information items that matter to the project. These information items could then either be exposed to the developer as an API, with full CDA documents being generated and shared "over the wire", or could be serialised as an XML document that just contains the Green CDA elements.
One of the problems with Green CDA is that it does not do enough - it tells you the information items that matter to the project - but it does not tell you what to do with the rest of the information items.
TrafficLight CDA is a way to specify more.
Adoption of TrafficLight specifications for how CDA documents are handled will make it easier for suppliers and those testing systems to know what they have to do - and more importantly will ensure that users can clearly understand what will happen when they share a document.
This can be done is a very light-weight way -- saying that anything that is not Green is White (open templates) or saying that anything that is not Green is Red (closed templates). In practice using the TrafficLights will help projects retain flexibility in an affordable way - enabling explicit distributed evolution of the document set that is supported within a configuration management framework - but that is for another post...
Green CDA was envisaged as a way to take the full CDA specification, and reduce the complexity for implementers by exposing just the information items that matter to the project. These information items could then either be exposed to the developer as an API, with full CDA documents being generated and shared "over the wire", or could be serialised as an XML document that just contains the Green CDA elements.
One of the problems with Green CDA is that it does not do enough - it tells you the information items that matter to the project - but it does not tell you what to do with the rest of the information items.
TrafficLight CDA is a way to specify more.
- Green for the information items that matter in the project, and that receivers are expected to process or knowingly deal with. The sender can reasonably expect the receiver to have dealt with this data.
- White for information items that may be ignored or processed by the receiver. The Sender cannot assume that the receiver will process these, but nor can the sender or receiver expect that the receiving user will see this information.
- Yellow for information that the receiving system must log as out of scope, but which does not need to be brought to the attention of a user before the document is processed or viewed. The logs must be available for review by the receiving organisation.
- Amber for information that is out of scope, and the inclusion of which should generate a warning which has to be acknowledged by the receiver before the document is processed.
- Red for information items that must result in the document being rejected, and the sender being informed that the document has not been accepted.
Adoption of TrafficLight specifications for how CDA documents are handled will make it easier for suppliers and those testing systems to know what they have to do - and more importantly will ensure that users can clearly understand what will happen when they share a document.
This can be done is a very light-weight way -- saying that anything that is not Green is White (open templates) or saying that anything that is not Green is Red (closed templates). In practice using the TrafficLights will help projects retain flexibility in an affordable way - enabling explicit distributed evolution of the document set that is supported within a configuration management framework - but that is for another post...
Monday 11 February 2013
Self monitoring vs telehealth
Excellent comment my Mary Hawkins on the EHI article. There is a lack of evidence for most specific implementations of telehealth. This could be because, as Mary suggests, self-monitoring already happens without devices being directly linked to the EHR or health services - but with the patient or local carer doing the monitoring and calling the health services when needed.
It may be that the technology is moving on faster than the evidence base can keep up with, so there is little incentive to invest in long-term research projects to evaluate technology and methods that will be out of date when the research results are out.
It could also be that we will not call it "telehealth" when it works. Thousands of people are using online weight monitoring and calorie counting tools - these could be linked up to provide extracts to the NHS. Gym equipment and pedometers provide electronic logs of the exercise that people are doing in a way that could be linked to EHR data - either for routine care, or for better targeting of care.
Maybe the way to get "telehealth" working is not to look at buying and installing new kit -- but looking at the way that existing kit and information is being used, and seeing how services can be adapted to make better use of the existing infromation landscape. Helping patient to become "expert patients" and use the data and data processing tools that they have, and helping healthcare delivery services to be more proactive in finding and reaching out to those who will benefit from their attention, rather than waiting for patients to make appointments. This will accelerate improvements in health outcomes, and will result in a better definition of what useful telecare services might look like.
Monitoring devices and the "Tele" bit: http://www.ehi.co.uk/news/EHI/8375/pathfinders-losing-their-way
It may be that the technology is moving on faster than the evidence base can keep up with, so there is little incentive to invest in long-term research projects to evaluate technology and methods that will be out of date when the research results are out.
It could also be that we will not call it "telehealth" when it works. Thousands of people are using online weight monitoring and calorie counting tools - these could be linked up to provide extracts to the NHS. Gym equipment and pedometers provide electronic logs of the exercise that people are doing in a way that could be linked to EHR data - either for routine care, or for better targeting of care.
Maybe the way to get "telehealth" working is not to look at buying and installing new kit -- but looking at the way that existing kit and information is being used, and seeing how services can be adapted to make better use of the existing infromation landscape. Helping patient to become "expert patients" and use the data and data processing tools that they have, and helping healthcare delivery services to be more proactive in finding and reaching out to those who will benefit from their attention, rather than waiting for patients to make appointments. This will accelerate improvements in health outcomes, and will result in a better definition of what useful telecare services might look like.
Monitoring devices and the "Tele" bit: http://www.ehi.co.uk/news/EHI/8375/pathfinders-losing-their-way
Saturday 11 August 2012
Information Architecture, Archigram, and the Olympics
The Olympics venues in London have been built with reuse in mind, building on the ideas of the Archigram architects, the structures are modular, can be reconfigured, repurposed, or relocated with relative ease (relative being an important word here). There is a delightful BBC piece describing this [1].
Large Health Information System architectures need a similar flexibility and usability. Olympic buildings take upto seven years to plan and build, and have to find a new purpose after only 4 weeks of use. For healthcare information systems the planning and building should be shorter than that, but there is not even an initial four weeks that can be relied on where they will be needed and used in the way that was anticipated when planning and building began.
Like the very successful planners for the London Olympics, Healthcare Informaticians could do worse than reread some of the Archigram literature.
[1] http://www.bbc.co.uk/news/entertainment-arts-18811200
[2] http://en.wikipedia.org/wiki/Archigram
Large Health Information System architectures need a similar flexibility and usability. Olympic buildings take upto seven years to plan and build, and have to find a new purpose after only 4 weeks of use. For healthcare information systems the planning and building should be shorter than that, but there is not even an initial four weeks that can be relied on where they will be needed and used in the way that was anticipated when planning and building began.
Like the very successful planners for the London Olympics, Healthcare Informaticians could do worse than reread some of the Archigram literature.
[1] http://www.bbc.co.uk/news/entertainment-arts-18811200
[2] http://en.wikipedia.org/wiki/Archigram
Wednesday 1 August 2012
Steps to open healthcare data - lets get open specifciations and examples first
Open access to interface specifications and example data for all healthcare IT systems funded by the NHS would enable innovation and quality improvement in the health service. It is a cheap and effective policy option, aligned with current politics.
It is understandable that healthcare data such as prescriptions and extracts of medical records are not routinely published for anyone to see. We all know that this information is private, and belongs to the patient, with the clinicians that recorded it, and the organisations that they work for having some rights and responsibilities to use, take care of, and make available the data the data when appropriate.
It is understandable that "cleaning" real data so that the patients cannot be identified is hard, and that to do so reliably enough to be comfortable publishing the clean data openly on the internet would be expensive.
What is less understandable is that the specifications for the formats that data may be made available, and invented examples for fictional patients are not available. The specifications exist but are often only shared once a contract between suppliers and a provider organisation is signed. They may be based on standards from one of the many SDOs (for which there are rarely examples available), but that is not well published.
Access to specifications and example data would allow new suppliers to show what they could do, and would allow standards organisations (including those setting standards within the NHS) to identify and promote common approaches where there is evident need. It will allow new entrants to show innovative solutions without requiring "rip-and-replace" for existing systems that deliver value.
It is reasonable that access to healthcare data should be controlled on behalf of the patient -- but open access to the specifications and example data will help to create a vibrant marketplace in healthcare IT systems - which is in the interests of patients, clinicians, the NHS and that UK economy.
The Following advice to DHID from an Ehealth Insider editorial in May 2012 puts it very well:
"First, it [DHID] should re-procure the spine as a platform, or series of core re-usable national services, these should be as easy to access and connect to with clear certification criteria. Currently it can take a ludicrous 18 months to go through a Byzantine assurance process. Apple publishes its criteria and manages a rigorous approvals process in less than a month.
The next step would be to
establish open statements saying what has to be done to connect to these
interfaces - including the certification criteria and costs. But getting from where we are to a vibrant market will not be done in one step, so get the APIs published first so that people can create viable and valuable products, then simplify the environment for buying and selling them.
It is understandable that healthcare data such as prescriptions and extracts of medical records are not routinely published for anyone to see. We all know that this information is private, and belongs to the patient, with the clinicians that recorded it, and the organisations that they work for having some rights and responsibilities to use, take care of, and make available the data the data when appropriate.
It is understandable that "cleaning" real data so that the patients cannot be identified is hard, and that to do so reliably enough to be comfortable publishing the clean data openly on the internet would be expensive.
What is less understandable is that the specifications for the formats that data may be made available, and invented examples for fictional patients are not available. The specifications exist but are often only shared once a contract between suppliers and a provider organisation is signed. They may be based on standards from one of the many SDOs (for which there are rarely examples available), but that is not well published.
Access to specifications and example data would allow new suppliers to show what they could do, and would allow standards organisations (including those setting standards within the NHS) to identify and promote common approaches where there is evident need. It will allow new entrants to show innovative solutions without requiring "rip-and-replace" for existing systems that deliver value.
It is reasonable that access to healthcare data should be controlled on behalf of the patient -- but open access to the specifications and example data will help to create a vibrant marketplace in healthcare IT systems - which is in the interests of patients, clinicians, the NHS and that UK economy.
The Following advice to DHID from an Ehealth Insider editorial in May 2012 puts it very well:
"First, it [DHID] should re-procure the spine as a platform, or series of core re-usable national services, these should be as easy to access and connect to with clear certification criteria. Currently it can take a ludicrous 18 months to go through a Byzantine assurance process. Apple publishes its criteria and manages a rigorous approvals process in less than a month.
The second step would be to insist that all vendors who want to be
funded by the NHS meet very basic minimum data standards. Yes, the NHS
Commissioning Board is to look at standards, but giving a clear
recommendation would avoid re-inventing the wheel. The third step would
be to insist that all vendors publish clear, usable Application
Programming Interfaces. No API, no funds."
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