British Oncology Pharmacy Association
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Tom Moberly (on the staff of The Journal) reports
on a meeting that heard how medication errors can be drastically
reduced
and
which
looked
ahead
to new treatments and the future of patient choice and internet
information use
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The 7th annual symposium of the British Oncology Pharmacy Association took place in Birmingham from 8 to 10 October.
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Focus on errors in systems, not people, to improve chemotherapy safety

Winson Soo-Hoo: root cause analysis identified weak spots in the
system |
Adverse drug events can be massively reduced by focusing on the systems
that lead to errors, rather than the people who make them, Winson Soo-Hoo
said. He and his team at the Children’s Hospital of Philadelphia
achieved an 84 per cent decrease in chemotherapy medication errors by
implementing such a “systems” approach to chemotherapy safety.
Mr Soo-Hoo argued that it is a mistake to focus on people as the cause
of errors and to expect regulation, litigation and punishment to reduce
errors.
A “systems” approach that recognises that people do make
mistakes, and reflects that fact in the development of systems which
make errors less likely to occur, is much more effective at preventing
medication errors.
In examining its chemotherapy delivery system, the Children’s Hospital
of Philadelphia drew up a 20-page flow sheet of the chemotherapy ordering
and delivery process, which, Mr Soo-Hoo explained, was shown to everyone
involved in medication errors: “All individuals who made errors
were asked to look at the flow chart and, focusing on the system rather
than the individual, we performed root cause analysis to identify weak
spots in the system.”
The Children’s Hospital of Philadelphia then implemented a “rapid
action change” process, in which minimal data were collected, small
changes to the process were made, the changes were piloted, results analysed
and, if appropriate, the change was implemented across the hospital.
Since many of the errors occurred in administration, a principal goal
of the system was to make it so that orders were clear to the nurse. “Even
though our project improved the medication system for the whole process,
it had its greatest impact at the nursing end, because they were the
ones with a lot of the actual errors,” Mr Soo-Hoo explained.
Mr Soo-Hoo and his team also found that non-standard orders led to many
of the medication errors: 13 per cent of all chemotherapy orders were
non-standard orders, but they accounted for 33 per cent of errors. So
they increased the use of standard orders from 60 per cent to 90 per
cent and reduced the number of errors as a result.
Give patients internet information
Although the internet is the second most widely used source of information
for newly referred cancer patients and 65 per cent of them would like their
doctor to choose information for them, only 1 per cent of patients have
internet information provided to them by doctors. So said Nicholas James,
of the Institute of Cancer Studies at the University of Birmingham, describing
the findings of a survey of cancer patients and their carers.
In fact, information from the internet was most often provided by family
or friends: “This is the second most prevalent form of information
used by patients and it’s coming from someone who knows nothing about
their cancer. They might not even know which cancer they have.”
Face-to-face interviews with 800 newly referred patients and 200 carers
were
conducted for the ACCIS (acceptability and usefulness of the internet as
a source of
information for cancer patients) study. Professor James said that the findings
question how pharmacists and other health professionals give information
to patients.
He called on health professionals to reject their negative view of patients
bringing internet printouts to consultations: “There’s a feeling
that it’s something that is actually a bit of a pain, patients coming
in with reams of internet printouts and doctors having to sort out the
consequences of it. Actually I’d like to turn that perception around
and say you need to be pre-empting that by giving patients material from
the internet that is relevant to them, rather than the other way round.”
“One of the biggest problems patients have is figuring out what is the
relevant stuff and what is the irrelevant stuff,” Professor James said.
It is here that health professionals can be an enormous help and this can be
done easily, he said: “There are some simple strategies, for example, directed
web use, which we found worked extraordinarily well and had a big educational
impact. One of the things I do now with patients that I see is I write out a
list of topics as we discuss them. I give them this ‘information prescription’ to
take to our patient information room and then for each of those topics they get
a printout. So they get veryfocused information and it feels like a personalised
service to them.”
Transparency is key to champion choice
“We want people with cancer to be able to exercise choice in treatment
and care,” said Joanne Rule, chief executive of CancerBACUP, adding
that transparency is essential to this patient-centred agenda. “I
firmly believe that you can’t have choice without transparency and
that transparency will create a strong driver towards equity.”
Transparency will also, she argued, help to ease tensions between the level
of choice patients have been led to expect and what they will receive.
It will not, for instance, be possible for all cancer patients to be
offered a choice of four or five treatment
locations, particularly if the capacity does not exist in their area.
One of the challenges the choice agenda poses for all health professionals
is, Ms Rule argued, providing patients with a meaningful understanding
of the risks and benefits of different treatments: “Most health professionals
are much better at communicating risk than they are at providing any really
good communication of benefit in which to frame it.”
She added that oncology pharmacists will champion patient choice by extending
their roles.
Look ahead to ensure equity of access to new treatments
Horizon scanning helps to ensure equity of access to appropriate treatments,
Joanne Andrew, oncology horizon scanning pharmacist at Glasgow Royal Infirmary,
argued.
The likely impact of drugs coming to market in the next year or two, in
terms of number of patients treated for a given cost, can be
determined, she said, from the size and nature of the patient population,
the results of any clinical trials, the time to launch, and clinical need.
Aspects such as patient eligibility testing are likely to become more important
in the future, given the number of new drugs targeted to specific tumour
characteristics.
Mrs Andrew highlighted a wide range of exciting new treatments for which
an assessment of likely impact would be important, including: encapsulated
paclitaxel (Taxol) for the treatment of breast cancer; bevacizumab (Avastin),
an anti-angiogenesis drug for colorectal cancer; cisplatin, vinorelbine
(Navelbine), pemetrexed (Alimta), gefitinib (Iressa) and erlotinib (Tarceva)
for lung cancer; and cetuximab (Erbitux), gefitinib, and tirapazamine for
head and neck cancer.
In addition to scanning for new drugs, Mrs Andrew argued that it is also
important to review new and extended uses for existing medicines. For instance,
the roles of aromatase inhibitors, including letrozole (Femara), anastrozole
(Arimidex) and exemestane (Aromasin) in the adjuvant and neoadjuvant treatment
of breast cancer are expanding, and possible new indications for docetaxel
(Taxotere) in prostate and breast cancer are likely to have a significant
impact in 2005. Extended indications for colorectal cancer for oxaliplatin
and capecitabine, and new indications for rituximab (MabThera) in the treatment
of
lymphoma are also expected to have a significant impact on clinical practice
next year.
Fitting new drugs into multiple myeloma treatment regimens
The field of multiple myeloma treatment has been through interesting times,
but the challenge over the next few years will be to define precisely where
new drugs, such as thalidomide, bortezomib, Revimid, Actimid and arsenic
trioxide, fit into the treatment algorithm for patients with myeloma, Prem
Mahendra, consultant haemato-oncologist, University Hospital Birmingham,
said.
Future treatments may, she said, involve incorporating bortezomib (Velcade)
up front: “VAD [vincristine, adriamycin and dexamethasone] has been
around for about 25 years and there has been nothing found that is better
than VAD, but whether Velcade and chemotherapy might be more effective
than VAD remains to be seen.”
The immunomodulatory agents Revimid (CC-5013) and Actimid (CC-4047) may
also prove useful in future. These have been termed the “sons of
thalidomide”, because they appear to retain the immunomodulatory
effects of thalidomide, but do not cause phocomelia. It may also be possible
to use Revimid and Actimid in patients to whom it would be difficult to
give thalidomide and Revimid may be useful during maintenance or after
an autograft.
Dr Mahendra added that use of bone-targeting methods is
another possible avenue for treatment of multiple myeloma. This could work
by inhibiting part of the tumour-necrosing factor ligand responsible for
osteoclast activity. Disrupting these feedback loops may be an important
treatment for bone disease and may also help with treatment of the disease
as a whole.
Other agents that may be used in the future and which are currently involved
in trials include arsenic trioxide and neovastat,
a compound found in shark cartilage, which has multiple anti-angiogenic
properties.
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