*West Oxfordshire Community Mental Health Team for Older Adults, Welch Way, Witney, Oxfordshire OX28 6JQ, email: jdtmason{at}msn.com
Newbury Community Mental Health Team for Older Adults, Beechcroft, Berkshire
|
|
|---|
To gauge the acceptability of copying a business-like clinic letter for general practitioners, written by a doctor working in the Newbury Community Mental Health Team for Older Adults. Between August 2004 and March 2006 every letter written by each doctor was stored electronically. The letters contained a clear statement of the diagnosis, the active problems and a bullet-point care plan. Any concerns or reactions to the letters were documented as they were received. Between September and October 2006, 50 service user or carer recipients of the letters were sent a questionnaire, checking whether the letter met standards of clarity, helpfulness and content.
RESULTS
Over 20 months 427 service users and carers received a total of 731 letters. One carer asked for the letter not to be sent in future; four carers asked for details of the letter to be modified; in only one was the content of the letter to the general practitioner modified before it was sent to the service user. The questionnaire about the suitability of the clinic letter had a 90% reply rate and all respondents said the letters were clear, understandable and that their content was of no surprise to them.
CLINICAL IMPLICATIONS
This report of a successful use of a frank business-like letter copied to service users or carers should be understood in the context of the following factors: the doctor who wrote them was familiar with and confident about the clinical work and comfortable with the style of the letter; he had a good rapport with a generally well-educated population and positive support from his colleagues. With these factors in place, the direct style of the letter was well received by patients and carers.
|
|
|---|
There are certain requirements that all such letters need to meet (Royal College of Psychiatrists, 2004): information should be accurate and understandable; the letter should not be unnecessarily distressing to the recipient, nor should it contain surprising information of which they were previously unaware; the service user or an appropriate carer should give consent to the receipt of the letter.
In Berkshire Health Care Trust there is organisational momentum behind information sharing including the copying of letters to service users. The success of copying letters relies on an open and clear clinical engagement, so that the letter is no more than a reminder of everything that has been discussed during clinical contact. The workload of the author would be reduced by drafting only one letter, suitable both for the general practitioner and service user (Spiessl et al, 2006).
In our study, we had three main goals. We wanted to keep prospective information about all letters sent to general practitioners and check how many of them were copied to patients. We also wanted to record any difficulties encountered as a result of copying the letters to service users or their carers and check the acceptability of the letters to their recipients.
|
|
|---|
If the letter was to be copied to anyone else, such as social services, then permission from the service user was also sought. If the plan for further action made reference to nursing colleagues or other professionals, the importance of everyone involved in the case receiving the letter was emphasised. Finally, verbal consent for receipt of the letter by service user or carer was taken.
The decision to send the letter to either the service user or the carer was based on discussion with the doctor and common sense. There were four common scenarios. First, competence was assumed for all patients and, unless there was evidence to the contrary, the doctor suggested that they should receive a copy of their clinical letter. Second, in those cases where there was established significant cognitive impairment that would prevent the user understanding and benefiting from the letter, they were asked if they were happy for the correspondence to be sent to an appropriate carer. Third, in individuals with advanced cognitive decline who lacked capacity to consent to the letter being presented to someone else, it was offered to a carer without consulting the user. Finally, there was a small minority of clients who did not fit into the first three categories, and in these cases the destination of the letter was discussed with the client and their carers.
If a service user wanted to have the letter sent to other people than their carers, it was explained that they were free to do so, but that they were responsible for the confidentiality of its contents and the cost of copying and posting additional letters.
A great effort was made to inform colleagues that the service user/carer was also receiving the clinical correspondence. When areas of contention surfaced during the interview, such as the effect of alcohol misuse or the diagnosis of dementia, the doctor discussed this as fully as possible with the user/carer and explained that the recipient may disagree with this particular point in the letter. The letter always concluded with a clear statement inviting the reader to contact the CMHT to discuss its content (Treloar & Adamis, 2005).
For 50 consecutive letters sent out during September and October 2005 a questionnaire (Box 2) was enclosed to obtain the recipients views of the letter.
|
|
|---|
| Box 1. Letter structure
|
Those who accepted the letter
In total, over the 20 months of the duration of the study, 731 letters
about 427 service users were sent out; 199 were sent to service users and 532
to carers. Of those sent to carers, 474 were sent to family members and 58 to
friends of the service user. The diagnosis given to service users and clearly
stated in the letter, as well as the list of the recipients, is set out in the
online Tables DS1 and DS2.
| Box 2. Questionnaire on the quality of the letter QUALITY OF CLINICAL LETTER YOU HAVE RECEIVED Thank you for taking time to fill in this questionnaire about the letter you have received. To help us maintain and improve the standard of the letters sent to service users or their carers could you please circle a response to each question.
|
Questionnaire
In September and October 2006, 50 questionnaires were sent out to service
users/carers; 45 were returned without prompting or sending the questionnaire
again. This very high response rate was probably due to appreciation of the
letter and its novelty - the recipients were both pleased and surprised to
receive it and they responded in kind. One letter contained inaccurate
biographical details, but on the whole the letters were accurate. All
respondents said the letter was clear. They knew from the specialist they
consulted that they would receive it; no information was was missed
(Box 1, question 6); recipients
knew who to contact if they were concerned about it; and there was no
unexpected or upsetting material in the letter. For 32 respondents the letter
was very useful and for 13 it was quite useful.
Other comments were general thanks for the letter, statements that it
reassured recipients that they had been listened to and, paradoxically, that
its value was undermined by having known its contents before receiving it.
Though the questionnaire was anonymous, responders may have felt constrained
from adding additional information for fear of being readily identifiable.
This may have prevented a full and honest response to the letters and this
should be taken into consideration when interpreting the findings.
Corrections
There were four letters where the recipients asked for changes to be made.
In response to two letters, carers challenged the account of cognitive decline
believing that the letter exaggerated the symptoms. In neither case were the
diagnoses challenged and there was no breakdown in the therapeutic
relationship, with clinical contact carrying on as normal. In reply, the
doctor wrote a new letter highlighting the concern raised and at subsequent
visits time was spent agreeing the severity of the symptoms of cognitive
impairment that were to be recorded in the case notes and the letter.
One carer and one service user asked to correct biographical details. For one it related to the professional grade that the patients father had reached during his working life and for the second it was the length of time that the service user had lived in their current accommodation. In both cases apologies were expressed and corrected correspondence was sent out to the general practitioner and the user.
Modification of content
Only one letter had the content modified in comparison to the one sent to
the general practitioner. At the request of a family carer, third-party
information was removed from a letter that a service user received.
Reaction to the letter
The reaction to the letters was generally positive and only one carer, of a
person with Alzheimers disease, asked that the letter not be sent in
future, as it upset the service user. The only terms that needed clarification
in the letter were the acronyms: MMSE (Mini Mental State Examination); BADLS
(Bristol Activities of Daily Living Scale) and DemTect (a screening tool for
cognitive impairment; Kalbe et al,
2004), but these were explained to recipients by the professionals
who administered these instruments before sending out the letter.
Authors impression
The clear sustained response to the letters was that of appreciation.
Service users and their carers, when motivated, readily understood
correspondence that was primarily written for general practitioners. Ensuring
all aspects of the care plan progressed as planned was easier because, once
armed with the correspondence, the service user/carer would contact the CMHT
to ask why they had not received a radiology appointment or a visit from
social services. Though this was embarrassing if it turned out that the
request for the service had not been sent off, it was infinitely better than
appearing at the next clinical appointment without the intended report.
The letters also reduced splitting within families and between team members (Cape et al, 2005). The clear statements of the diagnosis, problems and care plan prevented users/carers having false expectations. Though the diagnosis can often be upsetting, the recipients appreciated that a clear statement of the diagnosis from a doctor gained them access to support services.
|
|
|---|
To improve the practice of copying clinical correspondence to all service users, reports from the full array of clinical and social contexts are required. Different subspecialties and different social groups, such as non-English speakers, ethnic minorities and those with limited educational attainment, potentially present different challenges not met in the population who received the letters in this report. Novel and successful approaches to dealing with copying clinical correspondence to patients should be reported so that clinical teams can adopt proven, suitable strategies. This should include methods of training and supervising inexperienced clinicians in what is expected of letters sent to service users and their carers.
|
|
|---|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||