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The final chapter Prescribing in Practice consists of contributions from podiatry, radiography and physiotherapy colleagues. They have described the use of xvi PREFACE various forms of access, supply, administration and prescription of medicines in their professions today and considered future developments in the light of the recent legislation allowing pharmacists and nurses to train as independent prescribers.
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A supplementary prescriber should not agree to prescribe any medicine unless they are confident that it falls within their knowledge and competence. prescriber A professional relationship between the independent prescriber and the supplementary prescriber is paramount to safe and effective supplementary prescribing. The two should be able to communicate easily, share access to the same common patient record and any guidelines used in the CMP, agree common understanding of and access to the written CMP and ideally review the patients progress together at agreed intervals. The responsibilities of the independent prescriber are given below: Initial clinical assessment and diagnosis of the patient Agreement with the supplementary prescriber about the limits of their responsibility Provision of advice and support to the supplementary prescriber Review of patients progress at appropriate intervals with the supplementary prescriber if possible Sharing patients records with supplementary prescriber Reporting of adverse drug reactions. The responsibilities of the supplementary prescriber are: Contributing to development of the CMP Prescribing for the patient according to the CMP Altering medicines andor dosages within limits agreed in the CMP if appropriate Monitoring and assessing patients progress Working at all times within clinical competence and professional code of conduct Recognizing when not competent to act Consulting the independent prescriber when necessary Accepting professional accountability and clinical responsibility for prescribing Passing prescribing responsibility back to independent prescriber as appropriate Reporting adverse reactions and inform independent prescriber of them Informing independent prescriber of any clinically significant events Recording prescribing and monitoring activity in the CMP In addition to the responsibilities shown above, the supplementary prescriber must be a registered professional with the HPC and have a minimum of three years professional experience. It is up to individuals to negotiate with their employer that supplementary prescribing should form part of their job.
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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.