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Consent in the time of COVID-19
  1. Helen Lynne Turnham1,
  2. Michael Dunn2,
  3. Elaine Hill3,
  4. Guy T Thornburn4,
  5. Dominic Wilkinson5
  1. 1 Paediatric Critical Care, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
  2. 2 The Ethox Centre, University of Oxford, Oxford, UK
  3. 3 Cardiothoracic Critical Care and Anaesthesia, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
  4. 4 Consultant Cleft and Plastic Surgeon (Spires Cleft Centre), Oxford University Hospitals NHS Foundation Trust, Oxford, UK
  5. 5 Oxford Uehiro Centre for Practical Ethics, University of Oxford, Oxford, UK
  1. Correspondence to Dr Helen Lynne Turnham, Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, UK; helen.turnham{at}ouh.nhs.uk

Abstract

The COVID-19 pandemic crisis has necessitated widespread adaptation of revised treatment regimens for both urgent and routine medical problems in patients with and without COVID-19. Some of these alternative treatments maybe second-best. Treatments that are known to be superior might not be appropriate to deliver during a pandemic when consideration must be given to distributive justice and protection of patients and their medical teams as well the importance given to individual benefit and autonomy. What is required of the doctor discussing these alternative, potentially inferior treatments and seeking consent to proceed? Should doctors share information about unavailable but standard treatment alternatives when seeking consent? There are arguments in defence of non-disclosure; information about unavailable treatments may not aid a patient to weigh up options that are available to them. There might be justified concern about distress for patients who are informed that they are receiving second-best therapies. However, we argue that doctors should tailor information according to the needs of the individual patient. For most patients that will include a nuanced discussion about treatments that would be considered in other times but currently unavailable. That will sometimes be a difficult conversation, and require clinicians to be frank about limited resources and necessary rationing. However, transparency and honesty will usually be the best policy.

  • informed consent
  • allocation of health care resources
  • autonomy
  • decision-making
  • Distributive justice
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This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.

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Footnotes

  • Twitter @HelenTurnham, @Neonatalethics

  • Contributors The concept for the piece was formulated by all authors. HLT led the development of the manuscript, HLT, DW, MD, EH, GTT contributed to, edited and approved the final document.

  • Funding DW was supported for this work by a grant from the Wellcome trust WT106587/Z/14/Z.

  • Competing interests DW was supported for this work by a grant from the Wellcome trust WT106587/Z/14/Z.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; internally peer reviewed.

  • Data availability statement There are no data in this work.

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