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Vol 274 No 7337 p213-214
19 February 2005

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Supplementary prescribing in action — an example from primary care

In this article, Lorna Smalley describes how supplementary prescribing can work in primary care, in a pharmacist-led hypertension clinic


Lorna Smalley is medicines management pharmacist at Greater Derby Primary care Trust and practice pharmacist at Derwent Valley Medical Practice, Derby
(e-mail lorna.smalley@nhs.net)

Lorna Smalley

The author at work in her medical practice’s pharmacist-led hypertension clinic

In March 2004, I qualified as one of the first cohort of supplementary prescribing pharmacists from Keele University. I then began working at Derwent Valley Medical Practice in Derby. However I found myself in a position where I was qualified to provide a service, but with no framework of how the service should run. Which patients would be suitable? How would their agreement be recorded? How should care management plans be recorded in the patient records? How should repeat prescriptions be managed?

Eight months on, we in the practice have found the answers to many of our questions. Our pharmacist-led hypertension clinic has evolved into a successful service that provides evidence-based clinical care within the legal framework of supplementary prescribing. In this article, I offer our service as a practical example of how supplementary prescribing can work successfully in primary care setting.

Preparation

A month before I qualified we started to plan our service. We decided that we would run a two-hour clinic with 20-minute appointments each week, initially at our main surgery, and then expanding to a second clinic to cover our branch surgery. We also developed our care management plan (CMP) template, which would be adapted for individual patients, and considered how this document should be attached to patients’ records. Options included scanning, including a paper copy in the notes and attaching an electronic copy to the computer record. We chose the third option.

CMPs must refer to a local or national clinical guideline that the supplementary prescriber will follow. However, in early 2004, the British Hypertension Society updated its guidance, and the National Institute for Clinical Excellence was about to launch its guidance. With our service due to go live in early May, which guidance should we include in the CMP? The answer for us was to write a practice hypertension protocol that would be based on the current evidence-based national guidance, and updated upon the publication of new local or national guidance. When further guidance is issued I simply update our practice protocol accordingly, rather than amend each patient’s CMP to refer to the new guidance.

Supplementary prescribing is a voluntary agreement between a patient, a supplementary prescriber and an independent prescriber. We wanted to provide patients with a written explanation of supplementary prescribing, ideally before they agreed to participate, to facilitate informed consent. We chose to adapt the leaflet designed by the College of Pharmacy Practice Faculty of Prescribing and Medicines Management because it provides a concise, patient friendly summary of supplementary prescribing.

We also spent time making sure that the entire practice team were aware of the new clinic, and how we envisaged its operation. We placed posters in the consulting rooms to inform and remind infrequent prescribers that supplementary prescribing was operating in our practice. In addition, we wrote an article for the practice newsletter, shared our start date with the local non-medical prescribing forum, and contacted local community pharmacists, detailing the start date, and the area in which I would be prescribing.

Other preparations including writing my job description, obtaining adequate indemnity insurance and confirming our understanding of the stepping stones between qualification and receiving prescription pads.

Patient selection

Patients access our clinic via two pathways: computer search or referral from a member of the clinical team.

We use an EMIS search to identify potential patients. We search for hypertensive patients and exclude those with other chronic diseases, since these patients are already being managed in disease-specific clinics. We also think it would be inappropriate to ask them to attend multiple clinics within the practice. We also exclude the elderly, the housebound and those in residential or nursing home care.

Although this could be considered as making the service inaccessible to those who may need it most, we thought that it was important to establish our service and for me to develop my skills as a prescriber in the practice setting before extending to the wider community. We also believe that gaining informed consent from some patients within these groups may be difficult, although we hope to overcome these issues in the future.

We review our list of potential patients and highlight poor attenders, newly diagnosed hypertensive patients, those with potential compliance problems and those with uncomplicated hypertension. I then contact my independent prescriber via an electronic practice note to confirm that she is happy for me to approach the patient. Practice notes become permanently linked to a patient’s EMIS record, which provides a clear audit trail. We have also found them particularly useful because they reduce the need for contact time with my independent prescriber, which can be difficult to arrange in a busy practice.

Patients are also referred to me following routine appointments with GPs or the nursing team. I check the patient’s record and, if I think that it is appropriate for me to manage their care and I am competent to do so, I contact my independent prescriber by practice note as above. More recently, a third pathway has been identified, whereby spouses of two of our clinic patients have requested that they come along, too.

Patient contact and adapting the CMP

Once I have received a practice note confirming that my independent prescriber is happy for me to proceed, I write to the patient and invite him or her to the clinic, usually about two weeks later. The letter is electronically attached to the EMIS record, again to assist in the audit trail. We also send a copy of our “Patients’ guide to supplementary prescribing” to allow the patient to decide whether they want to participate in the clinic.

We invite three to five new patients each week, depending on clinic availability. We always leave one or two appointments open for existing patients requiring follow up. We have also found that booking new patients into every other slot helps my time management because, if I overrun, the excess is usually absorbed by the generally shorter follow-up appointments.

At this stage I merge the CMP template, which is stored on the network as a word document, with the patient’s EMIS record. This provides the basis of the patient’s individualised CMP, which I then modify further, for example, by adding drugs, conditions and guidelines that I am competent to manage, before dating the CMP to show my agreement and saving it in the patient’s computer record. I link the entry to the Read code “hypertension CMP” (8CR4), again for audit purposes, and send a practice note to my independent prescriber to agree the CMP, including the date that the patient is due in clinic. My independent prescriber then dates the CMP, and makes a consultation entry of the Read code “CMP agreed” (661M) and the condition(s) that I will be treating. My independent prescriber then returns the practice note confirming that the agreement is complete. This method of agreeing CMPs exploits the fact that CMPs require agreement, not signatures, and is permanently linked to the computer record.

Producing and agreeing the CMP before the patient has agreed could result in wasted time if the patient did not attend this clinic. However, we have found that this happens extremely rarely. In addition, having the CMP prepared and agreed means that I can prescribe during the initial consultation if necessary.

Initial consultation

During the initial consultation I introduce myself to the patient and explain our reasons for running the clinic. I explain that participation is voluntary, and can be stopped at any stage if the patient would prefer. I explain the CMP and that, once a year, we will need to meet the independent prescriber if my prescribing is to continue. I explain the frequency of clinics, from weekly to six-monthly. I also explain that, although patients can see their GP at any time, where possible they should attend the pharmacist-led hypertension clinic regarding their blood pressure. I then answer any questions the patient may have, but I frequently find that by this stage they already have their sleeves rolled up.

If patients confirm that they are happy to participate, I date the CMP and record their agreement in the computer record, because there is not currently a Read code for patient agreement. In addition, I add a diary entry to the computer record using the Read code “CMP review” (661N) to prompt annual review, and add an EMIS major alert stating that the patient attends my clinic. This alert is displayed when the patient record is opened, and acts as a reminder to other prescribers of their involvement in supplementary prescribing. This complete, I then proceed with the clinical review, write prescriptions, if required, and agree the next appointment interval.

Repeat prescribing

The practice decided that I should manage my own repeat prescribing. Although this is not made easy by the fact that I am not yet able to generate my prescriptions electronically, we believed that it might not be entirely appropriate for GPs to sign repeat prescriptions for patients that they may not have seen for several months. If a patient requires a repeat prescription, I print a repeat slip and write “For Lorna” underneath the name of the medicine. When this is presented at reception, it is directed to me and I write the repeat and update the computer record. This system also allows me to prompt patients when their review is coming up, by adding a note to their repeat prescription. If a patient’s repeat prescription contains a medicine that I am unable to prescribe, I produce an FP10 for those items and attach my handwritten prescription to it. This method ensures that the patient is able to collect all their medicines together.

Suspending CMPs

Following routine investigations, our clinic has identified one patient with atrial fibrillation, three with undiagnosed type 2 diabetes, and two patients who require referral to the urology team. Since these conditions are outside the terms of the CMP and my competence, we suspended the CMPs. We removed the major alert and diary entry and add a note stating “CMP suspended”, having spoken to the patients to ensure they understand the decision to remove them from the clinic. Although it is disappointing to lose patients from the clinic, knowing that I have improved their long-term prognoses gives me a great deal of professional satisfaction.

Clinic statistics

Since starting clinics in May 2004, we have invited 67 patients to attend, of whom 62 (93 per cent) have attended their first appointment. Only two patients (3 per cent) decided not to participate after attending the clinic, one who found the clinic times difficult, and one who preferred to see his regular GP. We think that this demonstrates the acceptability of our service to patients.

We currently do not routinely chase those who fail to attend the first consultation, but we write to those patients who have not attended a clinic beyond the agreed date. The letter acts as a reminder to those who have generally forgotten, and also asks those who have intentionally failed to attend to inform the practice. To date, we have sent six reminder letters. Two patients have not responded to reminder letters and have been removed from our clinic list.

Summary

Supplementary prescribing is not about replacing doctors with less expensive prescribers. Nor is it a quick fix to maximise achievement of new general medical services quality indicators. It is about enhancing the quality of care for patients with chronic diseases. It is time consuming, especially in the early days as we learn how to manage time and how to target those patients who would benefit the most. We have experienced problems with room availability, conflicting guidelines and the developing PCT infrastructure. However, supplementary prescribing is a long-term investment in the future of our patients in the hope that we can prevent complications of chronic diseases.

My experience of supplementary prescribing is that it is a varied and challenging role that provides a natural extension to the role of the pharmacist within the health care team.

We have shown that supplementary prescribing is acceptable to patients and beneficial to the practice. It does not suit all patients or all diseases, but it does provide another option for forward-thinking practices and patients to make full use of the pharmacist’s broad skill base.

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