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In response to Ballantyne and Schaefer’s ‘Consent and the ethical duty to participate in health data research’

Authors

  • Nilay Hepgul Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King’s College London, London, UK PubMed articlesGoogle scholar articles
  • Katherine E Sleeman Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King’s College London, London, UK PubMed articlesGoogle scholar articles
  • Alice M Firth Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King’s College London, London, UK PubMed articlesGoogle scholar articles
  • Anna Johnston Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King’s College London, London, UK PubMed articlesGoogle scholar articles
  • James T H Teo King’s College Hospital NHS Foundation Trust, London, UK PubMed articlesGoogle scholar articles
  • William Bernal King’s College Hospital NHS Foundation Trust, London, UK PubMed articlesGoogle scholar articles
  • Richard J B Dobson Department of Biostatistics and Health Informatics, Institute of Psychiatry Psychology and Neuroscience, King’s College London, London, UK PubMed articlesGoogle scholar articles
  • Irene J Higginson Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King’s College London, London, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Nilay Hepgul, Cicely Saunders Institute of Palliative Care, Policy & Rehabilitation, Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King’s College London, London SE5 9PJ, UK; nilay.hepgul{at}kcl.ac.uk
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Citation

Hepgul N, Sleeman KE, Firth AM, et al
In response to Ballantyne and Schaefer’s ‘Consent and the ethical duty to participate in health data research’

Publication history

  • Received November 23, 2018
  • Revised December 4, 2018
  • Accepted December 12, 2018
  • First published January 7, 2019.

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