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Using a Pocket Card to Improve End-of-life Care on Internal Medicine Clinical Teaching Units: A Cluster-randomized Controlled Trial

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Abstract

Background

End-of-life care is suboptimally taught in undergraduate and postgraduate education in Canada. Previous interventions to improve residents’ knowledge and comfort have involved lengthy comprehensive educational modules or dedicated palliative care rotations.

Objective

To determine the effectiveness of a cheap, portable, and easily implemented pocket reference for improving residents’ knowledge and comfort level in dealing with pain and symptom management on the medical ward.

Design

Cluster-randomized controlled trial conducted from August 2005 to June 2006.

Setting

Medical clinical teaching units (CTUs) in 3 academic hospitals in Toronto, Canada.

Participants

All residents rotating through the medical CTUs who consented to participate in the study.

Intervention

Residents at 1 hospital received a pocket reference including information about pain and symptom control, as well as 1–2 didactic end-of-life teaching sessions per month normally given as part of the rotation. Residents at the other 2 hospitals received only the didactic sessions.

Main Outcome Measures

A 10-question survey assessing knowledge and comfort level providing end-of-life care to medical inpatients, as well as focus group interviews.

Results

One hundred thirty-six residents participated on 3 CTUs for a participation rate of approximately 75%. Comfort levels improved in both control (p < .01) and intervention groups (p < .01), but the increase in comfort level was significantly higher in the intervention group (z = 2.57, p < .01). Knowledge was not significantly improved in the control group (p = .06), but was significantly improved in the intervention group (p = .01). Greater than 90% of residents in the intervention group used the card at least once per week, and feedback from the focus groups was very positive.

Conclusions

Our pocket card is a feasible, economical, and educational intervention that improves resident comfort level and knowledge in delivering end-of-life care on CTUs.

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Acknowledgements

This research was funded by grants provided by Associated Medical Services, Inc. and the University of Toronto Faculty of Medicine Dean’s Excellence Fund in Medical Education. Neither had a role in the design and conduct of the study; the collection, management analysis, or interpretation of the data; or the preparation, review, or approval of the manuscript.

JM contributed to the conception and design, analysis and interpretation of the data, drafting and critical revision of the manuscript, obtaining funding, and general supervision of the study. JM had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. JD contributed to the conception and design, acquisition of data, analysis and interpretation of the data, drafting and critical revision of the manuscript, obtaining funding, providing administrative support, and general supervision of the study. LB contributed to the acquisition, analysis and interpretation of data, the drafting of the manuscript, and the statistical analysis.

Conflict of Interest

None disclosed.

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Authors and Affiliations

Authors

Corresponding author

Correspondence to Joseph Mikhael MD, MEd, FRCPC.

Appendix A

Questionnaire: Pre and Post Intervention Survey (All Sites)

Year of Training CC3 CC4 PGY1 PGY2 PGY3

Program Medicine Surgery Family Other:

Date (months of rotation):

Were you given a copy of the Study Pocket Card? YES NO

Have you ever used the Pocket Card? YES NO

If yes, how many times per week did you use the card? __________

In treating acute pain, the approximate equivalence dose between oral and parenteral (IV) morphine is:

  1. a.

    1:1

  2. b.

    2:1

  3. c.

    4:1

  4. d.

    5:1

  5. e.

    7:1

Which of the following is an appropriate adjuvant medication for treating neuropathic pain?

  1. a.

    Pamidronate (Aredia)

  2. b.

    Carbamazepine (Tegretol)

  3. c.

    Hydromorphone (Dilaudid)

  4. d.

    Haloperidol (Haldol)

All of the following are appropriate first-line drugs for opioid-induced nausea except:

  1. a.

    Metoclopramide (Maxeran)

  2. b.

    Prochlorperazine (Stemetil)

  3. c.

    Ondansetron (Zofran)

  4. d.

    Haloperidol (Haldol)

The composition of a “Tylenol #2” is:

  1. a.

    Acetaminophen 300 mg + Codeine 10 mg + Caffeine 15 mg

  2. b.

    Acetaminophen 300 mg + Codeine 15 mg + Caffeine 15 mg

  3. c.

    Acetaminophen 300 mg + Codeine 20 mg + Caffeine 15 mg

  4. d.

    Acetaminophen 300 mg + Codeine 30 mg + Caffeine 15 mg

When treating pain, breakthrough (PRN) doses of oral opiates should be given with what frequency?

  1. a.

    1 hour

  2. b.

    2 hours

  3. c.

    4 hours

  4. d.

    8 hours

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Mikhael, J., Baker, L. & Downar, J. Using a Pocket Card to Improve End-of-life Care on Internal Medicine Clinical Teaching Units: A Cluster-randomized Controlled Trial. J GEN INTERN MED 23, 1222–1227 (2008). https://doi.org/10.1007/s11606-008-0582-4

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  • DOI: https://doi.org/10.1007/s11606-008-0582-4

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