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The Bone & Joint Journal
Vol. 101-B, Issue 7 | Pages 755 - 756
1 Jul 2019
Kakar S Haddad FS


The Bone & Joint Journal
Vol. 101-B, Issue 11 | Pages 1321 - 1324
1 Nov 2019
Kerr S Warwick D Haddad FS


The Bone & Joint Journal
Vol. 99-B, Issue 5 | Pages 563 - 565
1 May 2017
Perry DC Griffin XL Dritsaki M Costa ML Parsons N



The Bone & Joint Journal
Vol. 99-B, Issue 2 | Pages 147 - 150
1 Feb 2017
Costa ML Tutton E Achten J Grant R Slowther AM

Traditionally, informed consent for clinical research involves the patient reading an approved Participant Information Sheet, considering the information presented and having as much time as they need to discuss the study information with their friends and relatives, their clinical care and the research teams. This system works well in the ‘planned’ or ‘elective’ setting. But what happens if the patient requires urgent treatment for an injury or emergency?

This article reviews the legal framework which governs informed consent in the emergency setting, discusses how the approach taken may vary according to the details of the emergency and the treatment required, and reports on the patients’ view of providing consent following a serious injury. We then provide some practical tips for managing the process of informed consent in the context of injuries and emergencies.

Cite this article: Bone Joint J 2017;99-B:147–150.


The Bone & Joint Journal
Vol. 98-B, Issue 7 | Pages 865 - 866
1 Jul 2016
Haddad FS


The Bone & Joint Journal
Vol. 97-B, Issue 12 | Pages 1589 - 1590
1 Dec 2015
Haddad FS