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In the course of prescribing, the supplementary prescriber must enter into a prescribing partnership and agree the CMP with the independent prescriber. They must also arrange for access to prescribing pads and a budget to meet the costs of prescriptions and any other costs. Individuals selected and trained to be supplementary prescribers must have the opportunity to prescribe in partnership with an independent prescriber on completion of training. Approved training programmes are at degree level and consist of at least days provided by an Institution of Higher Education and at least of learning in practice must be under supervision of a designated medical practitioner who will provide the student with support and opportunities to develop competence in prescribing practice. An outline curriculum has been developed and agreed with the HPC who also accredits programmes provided by Higher Education Institutions.
Neither can the use of a PGD be delegated by a radiographer. As a consequence of this, until recently, each adjunct medicine would have been approved by an independent prescriber on a patient-specific basis or the doctor themselves would have administered it. Not surprisingly, this was a time-consuming process and as a result, on the advice of Administration of Radioactive Substances Advisory Committee, new legislation has been passed. The British Nuclear Medicine Society has interpreted this legislation and offered guidance by providing clarification about its possible implementation. BNMS explains that it allows locally written protocols to be used for the administration of adjunct medicines and in essence, these might look similar to PGDs. The only difference is that technicians can work within these new protocols, thereby allowing for a more efficient method of working.
The structure, format and terms of reference of medicines management structures and committees vary between Trusts because they are locally agreed, but the existence of medicines management procedures is mandatory. The Drug and Therapeutics Committee plays a critical role in the evaluation of the evidence surrounding a new medicine that is being considered for use within the Trust. This committee has significant support from senior pharmacy and medical staff and it often has the power to review local processes, documentation and systems. As far as radiography is concerned, this committee can have a direct impact on practice. Of aspects such as efficacy andor cost implications, and could therefore replace one medicine with another. If radiographers are using the old medicine as part of a PGD then that PGD would need urgent updating.
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