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Results: 1 to 20 of 33

Cited In for PubMed (Select 14552854)

1.

A survey of nursing home physicians to determine laboratory monitoring adverse drug event alert preferences.

Boyce RD, Perera S, Nace DA, Culley CM, Handler SM.

Appl Clin Inform. 2014 Oct 29;5(4):895-906. doi: 10.4338/ACI-2014-06-RA-0053. eCollection 2014.

PMID:
25589905
2.

Accuracy of using automated methods for detecting adverse events from electronic health record data: a research protocol.

Rochefort CM, Buckeridge DL, Forster AJ.

Implement Sci. 2015 Jan 8;10(1):5. doi: 10.1186/s13012-014-0197-6.

3.

Epidemiology and potential risk factors of drug-related problems in Hong Kong paediatric wards.

Rashed AN, Wilton L, Lo CC, Kwong BY, Leung S, Wong IC.

Br J Clin Pharmacol. 2014 May;77(5):873-9.

4.

[Magnitude and impact of serious adverse events related to treatment: study of incidence in a hospital in East Central Tunisia].

Bouafia N, Bougmiza I, Bahri F, Letaief M, Astagneau P, Njah M.

Pan Afr Med J. 2013 Oct 25;16:68. doi: 10.11604/pamj.2013.16.68.1161. eCollection 2013. French. No abstract available.

5.

Using structured telephone follow-up assessments to improve suicide-related adverse event detection.

Arias SA, Zhang Z, Hillerns C, Sullivan AF, Boudreaux ED, Miller I, Camargo CA.

Suicide Life Threat Behav. 2014 Oct;44(5):537-47. doi: 10.1111/sltb.12088. Epub 2014 Mar 3.

PMID:
24588679
6.

Problem-based training improves recognition of patient hazards by advanced medical students during chart review: a randomized controlled crossover study.

Holderried F, Heine D, Wagner R, Mahling M, Fenik Y, Herrmann-Werner A, Riessen R, Weyrich P, Zipfel S, Celebi N.

PLoS One. 2014 Feb 20;9(2):e89198. doi: 10.1371/journal.pone.0089198. eCollection 2014.

7.

Whose Voices are Heard in Patient Safety Incident Reports?

Saranto K, Bates DW, Mykkänen M, Härkönen M, Miettinen M.

Nurs Inform. 2012 Jun 23;2012:356. eCollection 2012.

8.

Advancing the research agenda for diagnostic error reduction.

Zwaan L, Schiff GD, Singh H.

BMJ Qual Saf. 2013 Oct;22 Suppl 2:ii52-ii57. doi: 10.1136/bmjqs-2012-001624. Epub 2013 Aug 13.

9.

Adverse drug events in older hospitalized patients: results and reliability of a comprehensive and structured identification strategy.

Klopotowska JE, Wierenga PC, Stuijt CC, Arisz L, Dijkgraaf MG, Kuks PF, Asscheman H, de Rooij SE, Lie-A-Huen L, Smorenburg SM; WINGS Study Group.

PLoS One. 2013 Aug 5;8(8):e71045. doi: 10.1371/journal.pone.0071045. Print 2013.

10.

Exploring the frontier of electronic health record surveillance: the case of postoperative complications.

FitzHenry F, Murff HJ, Matheny ME, Gentry N, Fielstein EM, Brown SH, Reeves RM, Aronsky D, Elkin PL, Messina VP, Speroff T.

Med Care. 2013 Jun;51(6):509-16. doi: 10.1097/MLR.0b013e31828d1210.

11.

E-pharmacovigilance: development and implementation of a computable knowledge base to identify adverse drug reactions.

Neubert A, Dormann H, Prokosch HU, Bürkle T, Rascher W, Sojer R, Brune K, Criegee-Rieck M.

Br J Clin Pharmacol. 2013 Sep;76 Suppl 1:69-77. doi: 10.1111/bcp.12127.

12.

Improving patient safety through the systematic evaluation of patient outcomes.

Forster AJ, Dervin G, Martin C, Papp S.

Can J Surg. 2012 Dec;55(6):418-25. doi: 10.1503/cjs.007811. Review.

13.

Understanding and preventing wrong-patient electronic orders: a randomized controlled trial.

Adelman JS, Kalkut GE, Schechter CB, Weiss JM, Berger MA, Reissman SH, Cohen HW, Lorenzen SJ, Burack DA, Southern WN.

J Am Med Inform Assoc. 2013 Mar-Apr;20(2):305-10. doi: 10.1136/amiajnl-2012-001055. Epub 2012 Jun 29.

14.

Towards the creation of a flexible classification scheme for voluntarily reported transfusion and laboratory safety events.

Whitehurst JM, Schroder J, Leonard D, Horvath MM, Cozart H, Ferranti J.

J Biomed Semantics. 2012 May 18;3:4. doi: 10.1186/2041-1480-3-4.

15.

A systematic review to evaluate the accuracy of electronic adverse drug event detection.

Forster AJ, Jennings A, Chow C, Leeder C, van Walraven C.

J Am Med Inform Assoc. 2012 Jan-Feb;19(1):31-8. doi: 10.1136/amiajnl-2011-000454. Review.

16.

Improving patient safety via automated laboratory-based adverse event grading.

Niland JC, Stiller T, Neat J, Londrc A, Johnson D, Pannoni S.

J Am Med Inform Assoc. 2012 Jan-Feb;19(1):111-5. doi: 10.1136/amiajnl-2011-000513. Epub 2011 Nov 14.

17.

Computerized detection of adverse drug reactions in the medical intensive care unit.

Kane-Gill SL, Visweswaran S, Saul MI, Wong AK, Penrod LE, Handler SM.

Int J Med Inform. 2011 Aug;80(8):570-8. doi: 10.1016/j.ijmedinf.2011.04.005. Epub 2011 May 31.

18.

The effect of an active on-ward participation of hospital pharmacists in Internal Medicine teams on preventable Adverse Drug Events in elderly inpatients: protocol of the WINGS study (Ward-oriented pharmacy in newly admitted geriatric seniors).

Klopotowska JE, Wierenga PC, de Rooij SE, Stuijt CC, Arisz L, Kuks PF, Dijkgraaf MG, Lie-A-Huen L, Smorenburg SM; WINGS study group.

BMC Health Serv Res. 2011 May 25;11:124. doi: 10.1186/1472-6963-11-124.

19.

Using prospective clinical surveillance to identify adverse events in hospital.

Forster AJ, Worthington JR, Hawken S, Bourke M, Rubens F, Shojania K, van Walraven C.

BMJ Qual Saf. 2011 Sep;20(9):756-63. doi: 10.1136/bmjqs.2010.048694. Epub 2011 Mar 1.

20.

Constructing Clinical Decision Support Systems for Adverse Drug Event Prevention: A Knowledge-based Approach.

Koutkias V, Kilintzis V, Stalidis G, Lazou K, Collyda C, Chazard E, McNair P, Beuscart R, Maglaveras N.

AMIA Annu Symp Proc. 2010 Nov 13;2010:402-6.

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