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Supplementary prescribing is defined as a voluntary prescribing partnership between an independent prescriber and a supplementary prescriber to implement an agreed patientspecific CMP with the patients agreement. There are a number of criteria that must be met for supplementary prescribing to occur (www. gov. ukenPublicationandstatistics). For instance, the independent prescriber must be a doctor or dentist; the supplementary prescriber must be from a professional group that is legally allowed to be a supplementary prescriber (such as radiographer, nurse, pharmacist, chiropodist, physiotherapist, optometrist); and there must a written CMP relating to a named patient and their specific condition(s).
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.
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