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Consent and information giving in radiotherapy

Published online by Cambridge University Press:  01 December 2007

Gillian Thompson
Gillian Thompson*
Affiliation:
Senior Lecturer, Sheffield Hallam University and Professional Development Facilitator, Northern Centre for Cancer Treatment, Newcastle, UK
*
Correspondence to: Gillian Thompson, E-mail: G.Thompson@shu.ac.uk
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Abstract

This paper explores some of the issues around implementing a consent policy within the radiotherapy department. Consent can be defined as a patient’s agreement for a health care professional to provide care. The NHS Plan1 highlighted the need for quality care centred around the patient and for changes in the way patients are asked to give their consent to treatment. This led to the Department of Health (DoH) publishing a Good Practice in Consent Implementation Guide (2001)2 for use within all NHS Trusts from 1 April 2002, which aimed to provide consistency across the NHS and provides a policy model and generic consent forms.

The policy recommends that the health professional carrying out the procedure is ultimately responsible for ensuring that the patient is genuinely consenting to what is being done, as it is they who would be held responsible in law should a case be made by a patient against a health professional. In radiotherapy, it is the Clinical Oncologist who obtains consent as they are responsible for prescribing courses of treatment; however, it is the Radiographer’s role to deliver this treatment. This paper discusses some of the issues around implementing a consent policy in terms of who can give and confirm consent, and what are the requirements for training if the patient is to receive the appropriate information before making the decision to consent to treatment.

Keywords

consentconsent policypatient informationradiotherapy
Type
Original Article
Information
Journal of Radiotherapy in Practice , Volume 6 , Issue 4 , December 2007 , pp. 217 - 223
Copyright
Copyright © Cambridge University Press 2007

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