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The Bone & Joint Journal
Vol. 102-B, Issue 11 | Pages 1431 - 1434
1 Nov 2020
Trompeter AJ Furness H Kanakaris NK Costa ML


The Bone & Joint Journal
Vol. 105-B, Issue 8 | Pages 833 - 836
1 Aug 2023
Mancino F Gant V Meek DRM Haddad FS



Bone & Joint Research
Vol. 9, Issue 12 | Pages 870 - 872
21 Dec 2020
Tsang SJ Simpson AHRW


The Bone & Joint Journal
Vol. 100-B, Issue 1 | Pages 1 - 3
1 Jan 2018
Skinner JA Haddad FS


The Bone & Joint Journal
Vol. 98-B, Issue 8 | Pages 1011 - 1013
1 Aug 2016
Masters JPM Nanchahal J Costa ML


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.


Bone & Joint 360
Vol. 3, Issue 5 | Pages 1 - 1
1 Oct 2014
Ollivere B


The Bone & Joint Journal
Vol. 95-B, Issue 1 | Pages 1 - 1
1 Jan 2013
Villar RN