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Items: 1 to 20 of 102

1.

Deferred consent in a minimal-risk study involving critically ill subarachnoid hemorrhage patients.

Topolovec-Vranic J, Santos M, Baker AJ, Smith OM, Burns KE.

Can Respir J. 2014 Sep-Oct;21(5):293-6. Epub 2014 Jun 10.

2.

The Experience of Surrogate Decision Makers on Being Approached for Consent for Patient Participation in Research. A Multicenter Study.

Burns KE, Prats CJ, Maione M, Lanceta M, Zubrinich C, Jeffs L, Smith OM; Canadian Critical Care Trials Group.

Ann Am Thorac Soc. 2017 Feb;14(2):238-245. doi: 10.1513/AnnalsATS.201606-425OC.

PMID:
27849142
3.

An Alternative Consent Process for Minimal Risk Research in the ICU.

Terry MA, Freedberg DE, Morris MC.

Crit Care Med. 2017 Sep;45(9):1450-1456. doi: 10.1097/CCM.0000000000002539.

PMID:
28617695
4.

Surrogate and patient discrepancy regarding consent for critical care research.

Newman JT, Smart A, Reese TR, Williams A, Moss M.

Crit Care Med. 2012 Sep;40(9):2590-4. doi: 10.1097/CCM.0b013e318258ff19.

5.

Research recruitment practices and critically ill patients. A multicenter, cross-sectional study (the Consent Study).

Burns KE, Zubrinich C, Tan W, Raptis S, Xiong W, Smith O, McDonald E, Marshall JC, Saginur R, Heslegrave R, Rubenfeld G, Cook DJ; Canadian Critical Care Trials Group.

Am J Respir Crit Care Med. 2013 Jun 1;187(11):1212-8. doi: 10.1164/rccm.201208-1537OC.

PMID:
23525935
6.

A Canadian Critical Care Trials Group project in collaboration with the international forum for acute care trialists - Collaborative H1N1 Adjuvant Treatment pilot trial (CHAT): study protocol and design of a randomized controlled trial.

Burns KE, Chant C, Smith O, Cuthbertson B, Fowler R, Cook DJ, Kruger P, Webb S, Alhashemi J, Dominguez-Cherit G, Zala C, Rubenfeld GD, Marshall JC.

Trials. 2011 Mar 9;12:70. doi: 10.1186/1745-6215-12-70.

7.

Ability of family members to predict patient's consent to critical care research.

Ciroldi M, Cariou A, Adrie C, Annane D, Castelain V, Cohen Y, Delahaye A, Joly LM, Galliot R, Garrouste-Orgeas M, Papazian L, Michel F, Barnes NK, Schlemmer B, Pochard F, Azoulay E.

Intensive Care Med. 2007 May;33(5):807-813. doi: 10.1007/s00134-007-0582-6. Epub 2007 Mar 15.

PMID:
17361388
8.

Informed consent in paediatric critical care research--a South African perspective.

Morrow BM, Argent AC, Kling S.

BMC Med Ethics. 2015 Sep 9;16:62. doi: 10.1186/s12910-015-0052-6.

9.
10.

Key stakeholder perceptions about consent to participate in acute illness research: a rapid, systematic review to inform epi/pandemic research preparedness.

Gobat NH, Gal M, Francis NA, Hood K, Watkins A, Turner J, Moore R, Webb SA, Butler CC, Nichol A.

Trials. 2015 Dec 29;16:591. doi: 10.1186/s13063-015-1110-6. Review.

11.

Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?

Mendyk AM, Labreuche J, Henon H, Girot M, Cordonnier C, Duhamel A, Leys D, Bordet R.

BMC Med Ethics. 2015 Apr 24;16:26. doi: 10.1186/s12910-015-0018-8.

12.

Obtaining surrogate consent for a minimal-risk research study in the intensive care unit setting.

Larkin ME, Beauharnais CC, Magyar K, Macey L, Grennan KB, Boykin EE, Russell SJ.

Clin Trials. 2013 Feb;10(1):93-6. doi: 10.1177/1740774512464727. Epub 2012 Nov 20.

PMID:
23169873
13.

Feasibility of conducting prospective observational research on critically ill, dying patients in the intensive care unit.

van Beinum A, Hornby L, Dhanani S, Ward R, Chambers-Evans J, Menon K.

J Med Ethics. 2017 Jan;43(1):47-51. doi: 10.1136/medethics-2016-103683. Epub 2016 Oct 13.

PMID:
27738255
14.

A computer-based education intervention to enhance surrogates' informed consent for genomics research.

Shelton AK, Freeman BD, Fish AF, Bachman JA, Richardson LI.

Am J Crit Care. 2015 Mar;24(2):148-55. doi: 10.4037/ajcc2015983.

15.

Informed consent in the critically ill: a two-step approach incorporating delirium screening.

Fan E, Shahid S, Kondreddi VP, Bienvenu OJ, Mendez-Tellez PA, Pronovost PJ, Needham DM.

Crit Care Med. 2008 Jan;36(1):94-9.

PMID:
18090168
16.

Improving the process of informed consent in the critically ill.

Davis N, Pohlman A, Gehlbach B, Kress JP, McAtee J, Herlitz J, Hall J.

JAMA. 2003 Apr 16;289(15):1963-8.

PMID:
12697799
17.
18.

Barriers to obtaining consent in dementia research: implications for surrogate decision-making.

Baskin SA, Morris J, Ahronheim JC, Meier DE, Morrison RS.

J Am Geriatr Soc. 1998 Mar;46(3):287-90.

PMID:
9514373
19.

Ethical considerations in consenting critically ill patients for bedside clinical care and research.

Rincon F, Lee K.

J Intensive Care Med. 2015 Mar;30(3):141-50. doi: 10.1177/0885066613503279. Epub 2013 Sep 9. Review.

PMID:
24019298
20.

Prevalence of and Factors Related to Discordance About Prognosis Between Physicians and Surrogate Decision Makers of Critically Ill Patients.

White DB, Ernecoff N, Buddadhumaruk P, Hong S, Weissfeld L, Curtis JR, Luce JM, Lo B.

JAMA. 2016 May 17;315(19):2086-94. doi: 10.1001/jama.2016.5351.

PMID:
27187301

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