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22 Health Service Journal 11 November 2015 hsj.co.uk
ROUNDTABLE
ROUNDTABLEPARTICIPANTS
Adele Waters HSJ executive editor
(roundtable chair)
Dr Ken Fullerton associate medical
director, Belfast Health and Social
Care Trust
Colin Henderson managing director
UK and Ireland, Orion Health
Dr Michael Gregory clinical director
for policy and strategy, NHS Trafford
Marina Lupari RCN professional
lead for primary and community
care
Neal Patel pharmacist and head of
corporate communications, Royal
Pharmaceutical Society
Dr Nigel Millar chief medical officer
Canterbury District Health Board,
New Zealand
Dr Rebecca Rosen GP, Nuffield Trust
senior fellow and member of
Greenwich CCG
Keith Strahan representing the
Association of Directors of Adult
Social Services – programme
manager for the health and social
care information sharing project,
Health and Social Care
Information Centre
DOING
THEIR
SHARE
KeythemesinadebateoverhowtogettheNHSsharing
patientdataatscaleincludedtheimportanceoftakingsmall,
pragmaticstepsandgettingnursesinvolved.ByAlisonMoore
Almost every NHS organisation
is looking at how it can integrate
services better to improve
patient care – either within its
own organisation, with other
NHS partners, or with other
health and social care providers.
Yet the flow of information
about patients sometimes does
not support these approaches –
and can mean they don’t receive
the safe, individually focused
care they want as quickly as they
should. Those involved in their
care can sometimes have to
make decisions without all the
information they would wish for.
Delays in sharing information
can impact on NHS efficiency as
well – leading to duplicate tests
and delays, both in patients
receiving appropriate healthcare
and in transfer out of a hospital
bed.
While some NHS
organisations have effective
electronic systems which allow
for the sharing of information
by all involved with patient care,
many are still sharing
information through faxing and
passing on physical records.
Faxing is particularly common
when a patient needs social care
input as well as healthcare.
An HSJ roundtable,
sponsored by Orion Health,
looked at the myriad questions
around sharing information and
how some of the barriers could
be overcome. HSJ executive
editor Adele Waters, chairing the
debate, said: “It’s not the case
that anyone in any organisation
necessarily has access to the
information they need about
that patient’s care and past
treatment. We need to get better
at that.” She added that any
solutions needed to be capable
of being implemented at scale.
The issues around sharing
information are not limited to
the UK: most healthcare
systems in the developed world
have been wrestling with them.
One of the most remarkable
success stories has come from
the Canterbury area of New
Zealand’s South Island, which
‘The challenges in
getting everyone
to accept such a
change were huge’
us saying it is unsafe for us not
to have access,” he said.
The system adopted by the
district health board is
evolutionary and capable of
being added to – for example, it
is now being extended to
pharmacists. But while there
was no question that shared
information had made things
possible which might not have
happened otherwise, he
conceded that it was difficult to
measure the impact of the
project.
Asked what were the critical
factors in getting a shared
e-health record system up and
running, he said having a long
term vision and then working
out what was needed in terms of
technology to achieve that
has introduced sharing across its
health economy. Dr Nigel Millar,
chief medical officer of the
Canterbury District Health
Board, has been key to this.
He outlined how plans to share
records dated back to 2007 but
had initially concentrated on a
“big solution” that was later
abandoned. Many areas were
happy with their existing
computer systems and did not
want to change them – but they
did want a way to share
information across health and
social care.
Stimulus to change
A surprising turning point was
the 2011 earthquake in
Christchurch, the main city in
the health board’s region,
which caused enormous
disruption to health services
and infrastructure. “It’s not
recommended but it was a
stimulus to change,” he said.
Eleven days after the
earthquake, the decision was
made to push ahead with a
scheme using a shared electronic
space which would eventually
allow all partners in health and
social care to upload and share
records while continuing on
different systems.
While introducing the
technology to drive this was
“quite easy,” the challenges in
getting everyone to accept such a
change were huge, he added. It
was helped by a high level of
trust in the health system which
provided a basis to build on. “We
have started the model, created
the space and are sharing
information,” he said. “We now
have health providers coming to
11 November 2015 Health Service Journal 23hsj.co.uk
WILDEFRY
incrementally was important. A
degree of opportunism was also
needed, along with strong
clinical leadership and a
willingness to challenge each
other.
In contrast, shared
information in the NHS is “a
patchwork quilt. Every area is at
a different place,” suggested Dr
Rebecca Rosen, Greenwich GP
and a senior fellow at the
Nuffield Trust. “I would endorse
what you say about not seeking
perfection and a big bang
solution.”
In her area, a conversation
about sharing information had
been going on for three or four
years before changes to the
structure of local hospital trusts
proved to be the impetus to push
forward with plans. “It was
piggybacked on some work
which was already going on. It
required a certain pragmatism,”
she said.
“Our vision would have been
for a ‘read and write’ solution for
the full medical records. But we
made a pragmatic decision to go
hospitals and have executive
sponsors. Each CCG person is a
link to an executive sponsor in a
trust.”
However, when clinical
engagement is discussed it is
often very focused around
doctors, despite nurses
frequently being the largest
group accessing and adding to
patient records.
Ensuring nurses’ voices were
heard – and giving them a seat
at the top table when IT changes
were being discussed and
decided – could contribute to
smoother implementations and
greater take up, argued Marina
Lupari, Royal College of Nursing
professional adviser for primary
and community care. She said
there were only a handful of
nurse leaders in this area.
In a lot of cases nurses could
manage patients in their own
homes if they had the right
information available, she said,
but they did not always have
access to IT to get this
information when it was needed.
There was an issue of whether
for something that was already
being worked up. Now we are in
the process of rollout. We have
some GP practices who are
using it and some who are
probably unaware of it.”
Impetus for change
Practices who had piloted the
system now spoke at meetings
about how it was working for
them, she said. The “word on the
street” was getting out slowly,
she said.
One barrier to implementing
a new system was getting people
to change the way they acted,
said Dr Rosen. “Getting people
to change their professional
behaviour so that the whole
In association with
system works better is hard,” she
said, citing care plans as an
example. Currently, GPs did not
write care plans with the
intention that other healthcare
professionals would add to
them. “It will give us some
developmental changes to
make,” she said – but it did offer
an opportunity to get people
working better, enabled by
technology.
The need for clinical
engagement if changes are to be
successfully implemented was
echoed by many round the table
who had experience of trying to
introduce both IT and changes
to working practices.
“I think an IT solution is a
wonderful thing but we do need
the clinical buy in and
relationships,” said Dr Michael
Gregory, clinical director for
policy and strategy at NHS
Trafford, which has brought in a
shared information system.
“One of the challenges we
have is that the consultants love
the ideas but we also have to
manage the relationships with
Clockwise from top
left: Dr Ken
Fullerton; Neal
Patel; Marina
Lupari; Adele
Waters; Colin
Henderson; Keith
Strahan; Dr Rebecca
Rosen (top) and
Dr Michael Gregory;
Dr Nigel Millar
‘There is a need
for clinical
engagement if
changes are to be
implemented’
24 Health Service Journal 11 November 2015
ROUNDTABLE
they should use their own
devices to access this, something
the RCN advised against.
More generally, nurse
engagement did not seem to be
high up the IT agenda, even
though they were important
users. “I think nurses will be
given priority when they become
the block to progress [ie at
rollout stage]. But at the
moment it is happening around
us,” Ms Lupari added.
Another professional group
which is beginning to benefit
from access to electronic records
is pharmacists.
Neal Patel, head of corporate
communications at the Royal
Pharmaceutical Society, said
they had a professional vision of
moving from supplying a
product to being more involved
in healthcare advice. There was
an opportunity to develop new
roles for them as there is
currently a surplus of
pharmacists.
A lot of the extended roles for
pharmacists either in place or
being talked about would
require access to patient
information. There had been a
and a patient portal. That will be
as live as it can be,” he said.
This should enable more
efficient progress through the
system – for example, spotting
where necessary tests had not
been carried out, or ensuring
that community staff did not try
to visit patients when they were
at a hospital appointment.
Thirty three community
elective pathways were being
looked at. There was also the
capacity to identify patients at
risk of admission through risk
stratification and information
coming in through live feeds.
Nurses would manage this
caseload: “They will know the
patients and make sure that they
are getting all the services they
need,” he said.
“We have found that we can
have systems in place but
sometimes they are not followed.
You have to design something
which makes our lives easier.”
The Trafford scheme hoped to
reach this point by year three of
a five year programme. Booking
systems went live in July and the
aim was to have at least one
hospital and 60 per cent of GP
practices set up online later this
year, he said.
In Northern Ireland, work
started in 2007 with a clinically
led group which was
commissioned to carry out a
“proof of concept” project. This
looked at feasibility, clinical
impact and efficiency, involving
one hospital in Belfast and
another outside it, and two large
GP practices.
“We never really had to sell
the concept of an electronic
health record,” said Dr Ken
Fullerton, associate medical
director at the Belfast Health
and Social Care Trust, who has
been closely involved in the
project since its inception. Staff
interest was high: in the early
stages of the project, if he logged
Clockwise from top left: Keith Strahan; Adele
Waters; Marina Lupari; Dr Nigel Millar; Dr Ken
Fullerton; Dr Michael Gregory; Colin Henderson
programme to ensure
connectivity between
pharmacies and the wider NHS
– for example, the ability to
connect to the “spine” has been
established and community
pharmacies are being given
access to the summary care
record. “I think that will help
enormously, especially out of
hours,” he added. However,
ideally pharmacists would like to
be able to write into the record
rather than just read it.
Some areas in the UK are
more advanced than others, with
information already shared
across key players in their local
health economies. Dr Gregory
said local commissioners had
developed a care coordination
system which he described as
being like an “air traffic control”
system enabling an overview of
where people were in the system.
Implementation began with
the booking and ambulance
systems, and then extended into
unscheduled care. “Feeds come
in from primary care, acute
hospitals, mental health, social
care and community providers.
There will be a clinical portal
‘We never really
had to sell the
concept of an
electronic
health record’
11 November 2015 Health Service Journal 25
WILDEFRY
into the system from any
terminal in his hospital he would
find a number of staff gathered
to watch.
The report from the project
group showed not only clinical
effectiveness but also savings
due to, for example, fewer
unnecessary outpatient
appointments. The decision was
made in July 2013 to roll out the
solution more widely.
“We set seven year targets in
terms of users and access. We
have already passed these,” Dr
Fullerton said. Since then
775,000 patient records had
been accessed, and there had
been five million unique logins.
Ninety per cent of doctors were
already using the system but the
biggest single group of users
was nurses. Specialist nurses
working between hospitals and
community had been
particularly enthusiastic users in
the pilot stage but some groups
had been harder to engage.
“Pharmacy is about 2 per cent.
We have work to do there but
there is progress,” he added.
Change had been made
incrementally and was still
going on. “We now have a road
map. We are no longer read only.
Various aspects had been taken
forward by largely clinical
groups,” he said. This included
“e triage” and virtual
multidisciplinary team meetings.
Any new IT systems adopted
now had to be compatible with
the electronic care record, and
there was increasing
involvement from other parts of
the health system. Ambulance
services could access
information but not yet from
ambulances themselves, the
local hospice had signed up and
independent sector providers
were interested as well.
Patient reluctance for their
records to be shared is often
seen as an obstacle but in
Northern Ireland this had not
turned out to be the case.
at the helm of the project and
having the right clinical
advocate to take that out to their
peers is vital.”
As well as clinical
engagement, there was a need
for executive sponsorship.
Sometimes there was a need for
difficult conversations to take
place: during discussions about
the Canterbury system there had
been an agreement that people
could walk away from the table
as long as they came back, he
said. It was early days to see the
evidence that better access to,
and sharing of, information
improved patient care.
Mr Henderson said that
organisations did start to see the
benefits, which might be as
simple as fewer duplicate tests
or not duplicating visits to
people, as well as time saved by
not having to search for
information.
Dr Millar added some other
benefits: with shared
information, pharmacists no
longer had to guess the patient’s
diagnosis from what they knew
about their medications.
And ultimately IT made
business improvement and
system transformation possible.
It could also create opportunities
to improve patient safety if it
was recognised that patients
could fall through the gaps, said
Dr Fullerton.
He stressed that electronic
interventions did not solve the
problems of healthcare: they
were enablers and raised
questions such as who had the
responsibility for reviewing and
signing off test results which
might have been ordered by one
doctor but then seen by others as
patient care was transferred.
Summing up the debate, Ms
Waters said the key elements to
deliver shared information were
to have a vision; clinical
leadership – including from
nurses – together with executive
sponsorship; and to
acknowledge that technology is
an enabler but won’t solve all
problems.
There was emerging evidence
that shared information could
deliver improvements and
efficiencies, she concluded. l
In association with
Patients had been able to choose
to opt out of their information
being shared – but less than 200
out of 1.7 million had done so,
said Dr Fullerton. There was
additional protection around
some records, such as those
covering mental health. But he
added, even as a geriatrician, he
found the common response to
shared records from his patients
was “but why were you not
doing that already, doctor?”
Northern Ireland has a
combined health and social care
system – but other parts of the
UK often struggle to get
coordination between the two
sides. Keith Strahan, programme
manager for the health and
social care information sharing
project at the Health and Social
Care Information Centre,
pointed out some of the
challenges in dealing with a
sector which employs 1.6 million
people but with only 9 per cent
working within local authorities.
When it came to technology,
there were some wonderful good
practice examples but the main
way of sharing information with
the NHS was probably still by
fax, he said. He was working in
Shropshire to get secure email
into care homes “but 95 per cent
of the information that goes in
now is faxed. If you come out of
any hospital and move into a
care home, shared information is
likely to be faxed.”
There were changes coming
as CCGs had to produce digital
roadmaps by April 2016, he
added. He questioned whether
in some cases what needed to be
shared was a summary rather
than the whole document or
plan. If everything was shared,
the volume of information could
be overwhelming: he cited GPs
having to search through reams
of reports to find the ones which
were really urgent and required
them to take action. “There are
crucial bits of information which
I want to follow me around. For
example if I go into hospital and
have a home care plan, will the
provider know about it or will
they break down the door
because they think the patient is
lying there unwell?” he said.
Small measures
Small steps could change
behaviour and drive engagement
with electronic records: one
thing which had been tried in
London was replacing a generic
fax number for an organisation
with a generic secure email
address, he added. This had
revealed that faxes were being
used within hospitals to transfer
information internally as well as
between hospitals and other
organisations.
Colin Henderson, Orion
Health’s managing director for
UK and Ireland, said that
implementing technical
solutions took organisations on
a journey.
Taking pragmatic steps to
making information available
could start to drive interest and
lead to further progress. “That’s
when you start to move from the
viewing to the doing. But you
have to do the viewing first and
that has to be enough useful
information to be interesting,”
he said.
“The clinical leadership is
absolutely essential. When you
walk into a room, you can spot
the ones... [where
implementation] will be
successful based on the
individuals in the room.
“I think there are natural
leaders out there. Having them
‘Small steps could
change behaviour
and drive
engagement with
electronic records’
Dr Rebecca RosenNeal Patel

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Orion-Roundtable-11th-Nov-2015

  • 1. 22 Health Service Journal 11 November 2015 hsj.co.uk ROUNDTABLE ROUNDTABLEPARTICIPANTS Adele Waters HSJ executive editor (roundtable chair) Dr Ken Fullerton associate medical director, Belfast Health and Social Care Trust Colin Henderson managing director UK and Ireland, Orion Health Dr Michael Gregory clinical director for policy and strategy, NHS Trafford Marina Lupari RCN professional lead for primary and community care Neal Patel pharmacist and head of corporate communications, Royal Pharmaceutical Society Dr Nigel Millar chief medical officer Canterbury District Health Board, New Zealand Dr Rebecca Rosen GP, Nuffield Trust senior fellow and member of Greenwich CCG Keith Strahan representing the Association of Directors of Adult Social Services – programme manager for the health and social care information sharing project, Health and Social Care Information Centre DOING THEIR SHARE KeythemesinadebateoverhowtogettheNHSsharing patientdataatscaleincludedtheimportanceoftakingsmall, pragmaticstepsandgettingnursesinvolved.ByAlisonMoore Almost every NHS organisation is looking at how it can integrate services better to improve patient care – either within its own organisation, with other NHS partners, or with other health and social care providers. Yet the flow of information about patients sometimes does not support these approaches – and can mean they don’t receive the safe, individually focused care they want as quickly as they should. Those involved in their care can sometimes have to make decisions without all the information they would wish for. Delays in sharing information can impact on NHS efficiency as well – leading to duplicate tests and delays, both in patients receiving appropriate healthcare and in transfer out of a hospital bed. While some NHS organisations have effective electronic systems which allow for the sharing of information by all involved with patient care, many are still sharing information through faxing and passing on physical records. Faxing is particularly common when a patient needs social care input as well as healthcare. An HSJ roundtable, sponsored by Orion Health, looked at the myriad questions around sharing information and how some of the barriers could be overcome. HSJ executive editor Adele Waters, chairing the debate, said: “It’s not the case that anyone in any organisation necessarily has access to the information they need about that patient’s care and past treatment. We need to get better at that.” She added that any solutions needed to be capable of being implemented at scale. The issues around sharing information are not limited to the UK: most healthcare systems in the developed world have been wrestling with them. One of the most remarkable success stories has come from the Canterbury area of New Zealand’s South Island, which ‘The challenges in getting everyone to accept such a change were huge’ us saying it is unsafe for us not to have access,” he said. The system adopted by the district health board is evolutionary and capable of being added to – for example, it is now being extended to pharmacists. But while there was no question that shared information had made things possible which might not have happened otherwise, he conceded that it was difficult to measure the impact of the project. Asked what were the critical factors in getting a shared e-health record system up and running, he said having a long term vision and then working out what was needed in terms of technology to achieve that has introduced sharing across its health economy. Dr Nigel Millar, chief medical officer of the Canterbury District Health Board, has been key to this. He outlined how plans to share records dated back to 2007 but had initially concentrated on a “big solution” that was later abandoned. Many areas were happy with their existing computer systems and did not want to change them – but they did want a way to share information across health and social care. Stimulus to change A surprising turning point was the 2011 earthquake in Christchurch, the main city in the health board’s region, which caused enormous disruption to health services and infrastructure. “It’s not recommended but it was a stimulus to change,” he said. Eleven days after the earthquake, the decision was made to push ahead with a scheme using a shared electronic space which would eventually allow all partners in health and social care to upload and share records while continuing on different systems. While introducing the technology to drive this was “quite easy,” the challenges in getting everyone to accept such a change were huge, he added. It was helped by a high level of trust in the health system which provided a basis to build on. “We have started the model, created the space and are sharing information,” he said. “We now have health providers coming to
  • 2. 11 November 2015 Health Service Journal 23hsj.co.uk WILDEFRY incrementally was important. A degree of opportunism was also needed, along with strong clinical leadership and a willingness to challenge each other. In contrast, shared information in the NHS is “a patchwork quilt. Every area is at a different place,” suggested Dr Rebecca Rosen, Greenwich GP and a senior fellow at the Nuffield Trust. “I would endorse what you say about not seeking perfection and a big bang solution.” In her area, a conversation about sharing information had been going on for three or four years before changes to the structure of local hospital trusts proved to be the impetus to push forward with plans. “It was piggybacked on some work which was already going on. It required a certain pragmatism,” she said. “Our vision would have been for a ‘read and write’ solution for the full medical records. But we made a pragmatic decision to go hospitals and have executive sponsors. Each CCG person is a link to an executive sponsor in a trust.” However, when clinical engagement is discussed it is often very focused around doctors, despite nurses frequently being the largest group accessing and adding to patient records. Ensuring nurses’ voices were heard – and giving them a seat at the top table when IT changes were being discussed and decided – could contribute to smoother implementations and greater take up, argued Marina Lupari, Royal College of Nursing professional adviser for primary and community care. She said there were only a handful of nurse leaders in this area. In a lot of cases nurses could manage patients in their own homes if they had the right information available, she said, but they did not always have access to IT to get this information when it was needed. There was an issue of whether for something that was already being worked up. Now we are in the process of rollout. We have some GP practices who are using it and some who are probably unaware of it.” Impetus for change Practices who had piloted the system now spoke at meetings about how it was working for them, she said. The “word on the street” was getting out slowly, she said. One barrier to implementing a new system was getting people to change the way they acted, said Dr Rosen. “Getting people to change their professional behaviour so that the whole In association with system works better is hard,” she said, citing care plans as an example. Currently, GPs did not write care plans with the intention that other healthcare professionals would add to them. “It will give us some developmental changes to make,” she said – but it did offer an opportunity to get people working better, enabled by technology. The need for clinical engagement if changes are to be successfully implemented was echoed by many round the table who had experience of trying to introduce both IT and changes to working practices. “I think an IT solution is a wonderful thing but we do need the clinical buy in and relationships,” said Dr Michael Gregory, clinical director for policy and strategy at NHS Trafford, which has brought in a shared information system. “One of the challenges we have is that the consultants love the ideas but we also have to manage the relationships with Clockwise from top left: Dr Ken Fullerton; Neal Patel; Marina Lupari; Adele Waters; Colin Henderson; Keith Strahan; Dr Rebecca Rosen (top) and Dr Michael Gregory; Dr Nigel Millar ‘There is a need for clinical engagement if changes are to be implemented’
  • 3. 24 Health Service Journal 11 November 2015 ROUNDTABLE they should use their own devices to access this, something the RCN advised against. More generally, nurse engagement did not seem to be high up the IT agenda, even though they were important users. “I think nurses will be given priority when they become the block to progress [ie at rollout stage]. But at the moment it is happening around us,” Ms Lupari added. Another professional group which is beginning to benefit from access to electronic records is pharmacists. Neal Patel, head of corporate communications at the Royal Pharmaceutical Society, said they had a professional vision of moving from supplying a product to being more involved in healthcare advice. There was an opportunity to develop new roles for them as there is currently a surplus of pharmacists. A lot of the extended roles for pharmacists either in place or being talked about would require access to patient information. There had been a and a patient portal. That will be as live as it can be,” he said. This should enable more efficient progress through the system – for example, spotting where necessary tests had not been carried out, or ensuring that community staff did not try to visit patients when they were at a hospital appointment. Thirty three community elective pathways were being looked at. There was also the capacity to identify patients at risk of admission through risk stratification and information coming in through live feeds. Nurses would manage this caseload: “They will know the patients and make sure that they are getting all the services they need,” he said. “We have found that we can have systems in place but sometimes they are not followed. You have to design something which makes our lives easier.” The Trafford scheme hoped to reach this point by year three of a five year programme. Booking systems went live in July and the aim was to have at least one hospital and 60 per cent of GP practices set up online later this year, he said. In Northern Ireland, work started in 2007 with a clinically led group which was commissioned to carry out a “proof of concept” project. This looked at feasibility, clinical impact and efficiency, involving one hospital in Belfast and another outside it, and two large GP practices. “We never really had to sell the concept of an electronic health record,” said Dr Ken Fullerton, associate medical director at the Belfast Health and Social Care Trust, who has been closely involved in the project since its inception. Staff interest was high: in the early stages of the project, if he logged Clockwise from top left: Keith Strahan; Adele Waters; Marina Lupari; Dr Nigel Millar; Dr Ken Fullerton; Dr Michael Gregory; Colin Henderson programme to ensure connectivity between pharmacies and the wider NHS – for example, the ability to connect to the “spine” has been established and community pharmacies are being given access to the summary care record. “I think that will help enormously, especially out of hours,” he added. However, ideally pharmacists would like to be able to write into the record rather than just read it. Some areas in the UK are more advanced than others, with information already shared across key players in their local health economies. Dr Gregory said local commissioners had developed a care coordination system which he described as being like an “air traffic control” system enabling an overview of where people were in the system. Implementation began with the booking and ambulance systems, and then extended into unscheduled care. “Feeds come in from primary care, acute hospitals, mental health, social care and community providers. There will be a clinical portal ‘We never really had to sell the concept of an electronic health record’
  • 4. 11 November 2015 Health Service Journal 25 WILDEFRY into the system from any terminal in his hospital he would find a number of staff gathered to watch. The report from the project group showed not only clinical effectiveness but also savings due to, for example, fewer unnecessary outpatient appointments. The decision was made in July 2013 to roll out the solution more widely. “We set seven year targets in terms of users and access. We have already passed these,” Dr Fullerton said. Since then 775,000 patient records had been accessed, and there had been five million unique logins. Ninety per cent of doctors were already using the system but the biggest single group of users was nurses. Specialist nurses working between hospitals and community had been particularly enthusiastic users in the pilot stage but some groups had been harder to engage. “Pharmacy is about 2 per cent. We have work to do there but there is progress,” he added. Change had been made incrementally and was still going on. “We now have a road map. We are no longer read only. Various aspects had been taken forward by largely clinical groups,” he said. This included “e triage” and virtual multidisciplinary team meetings. Any new IT systems adopted now had to be compatible with the electronic care record, and there was increasing involvement from other parts of the health system. Ambulance services could access information but not yet from ambulances themselves, the local hospice had signed up and independent sector providers were interested as well. Patient reluctance for their records to be shared is often seen as an obstacle but in Northern Ireland this had not turned out to be the case. at the helm of the project and having the right clinical advocate to take that out to their peers is vital.” As well as clinical engagement, there was a need for executive sponsorship. Sometimes there was a need for difficult conversations to take place: during discussions about the Canterbury system there had been an agreement that people could walk away from the table as long as they came back, he said. It was early days to see the evidence that better access to, and sharing of, information improved patient care. Mr Henderson said that organisations did start to see the benefits, which might be as simple as fewer duplicate tests or not duplicating visits to people, as well as time saved by not having to search for information. Dr Millar added some other benefits: with shared information, pharmacists no longer had to guess the patient’s diagnosis from what they knew about their medications. And ultimately IT made business improvement and system transformation possible. It could also create opportunities to improve patient safety if it was recognised that patients could fall through the gaps, said Dr Fullerton. He stressed that electronic interventions did not solve the problems of healthcare: they were enablers and raised questions such as who had the responsibility for reviewing and signing off test results which might have been ordered by one doctor but then seen by others as patient care was transferred. Summing up the debate, Ms Waters said the key elements to deliver shared information were to have a vision; clinical leadership – including from nurses – together with executive sponsorship; and to acknowledge that technology is an enabler but won’t solve all problems. There was emerging evidence that shared information could deliver improvements and efficiencies, she concluded. l In association with Patients had been able to choose to opt out of their information being shared – but less than 200 out of 1.7 million had done so, said Dr Fullerton. There was additional protection around some records, such as those covering mental health. But he added, even as a geriatrician, he found the common response to shared records from his patients was “but why were you not doing that already, doctor?” Northern Ireland has a combined health and social care system – but other parts of the UK often struggle to get coordination between the two sides. Keith Strahan, programme manager for the health and social care information sharing project at the Health and Social Care Information Centre, pointed out some of the challenges in dealing with a sector which employs 1.6 million people but with only 9 per cent working within local authorities. When it came to technology, there were some wonderful good practice examples but the main way of sharing information with the NHS was probably still by fax, he said. He was working in Shropshire to get secure email into care homes “but 95 per cent of the information that goes in now is faxed. If you come out of any hospital and move into a care home, shared information is likely to be faxed.” There were changes coming as CCGs had to produce digital roadmaps by April 2016, he added. He questioned whether in some cases what needed to be shared was a summary rather than the whole document or plan. If everything was shared, the volume of information could be overwhelming: he cited GPs having to search through reams of reports to find the ones which were really urgent and required them to take action. “There are crucial bits of information which I want to follow me around. For example if I go into hospital and have a home care plan, will the provider know about it or will they break down the door because they think the patient is lying there unwell?” he said. Small measures Small steps could change behaviour and drive engagement with electronic records: one thing which had been tried in London was replacing a generic fax number for an organisation with a generic secure email address, he added. This had revealed that faxes were being used within hospitals to transfer information internally as well as between hospitals and other organisations. Colin Henderson, Orion Health’s managing director for UK and Ireland, said that implementing technical solutions took organisations on a journey. Taking pragmatic steps to making information available could start to drive interest and lead to further progress. “That’s when you start to move from the viewing to the doing. But you have to do the viewing first and that has to be enough useful information to be interesting,” he said. “The clinical leadership is absolutely essential. When you walk into a room, you can spot the ones... [where implementation] will be successful based on the individuals in the room. “I think there are natural leaders out there. Having them ‘Small steps could change behaviour and drive engagement with electronic records’ Dr Rebecca RosenNeal Patel