///2012 Abstract Details
2012 Abstract Details2018-05-01T17:55:36+00:00

Educating Anesthesia Residents to Obtain and Document Informed Consent for Epidural Labor Analgesia: Does Simulation Play a Role?

Abstract Number: S-43
Abstract Type: Original Research

Andreas V Antoniou MD, MSc, FRCPC1 ; Kristine Marmai MD, FRCPC2; Richard Cherry MD, FRCPC3; Sudha Singh MD, FRCPC4; Philip Jones MD, FRCPC5

PURPOSE

This study aims to assess the ability of anesthesia residents to acquire and retain knowledge regarding informed consent documentation for epidural labor analgesia, in the setting of didactic teaching versus simulation. It also assesses how well this knowledge is translated to practical clinical ability by assessing the verbal informed consent process during an interaction with a standardized patient.

METHODS

Twenty anesthesia residents in various years of training were randomized to a ‘didactic group’ or ‘simulation group’. Each resident was presented with a written scenario and asked to document the informed consent process as they normally would in clinical practice (pre-test). The didactic group then had a presentation about informed consent, while the residents in the simulation group each interviewed a simulated patient (high fidelity simulation mannequin) where scenarios focused on different aspects of informed consent. All residents were then again asked to read a scenario and document the informed consent process (post-test). Six weeks later all residents interviewed a standardized patient in labor and documented the informed consent from this interaction (6 week test).

The documentation and the verbal interaction with the standardized patient were scored independently by two investigators using a points system based on Canadian Medical Protective Association guidelines as well as current literature and expert opinion from several experienced obstetrical anaesthesiologists.

RESULTS

There was no significant difference in the baseline performance between the two groups. The didactic group performed better than the simulation group at both the immediate time point and six week time point. Both groups had a significant improvement in their written consent documentation at the immediate time point compared to baseline, but the improvement in the didactic group was greater. The didactic group retained their acquired knowledge at the six week time point better than the simulation group. Clinical test scores (acquisition of oral informed consent from a standardized patient) did not differ statistically between groups.

DISCUSSION

A didactic teaching method was better than simulation for residents to acquire and retain knowledge regarding informed consent. The difference between the two groups at the immediate time point could be either due to a real effect, to the method of teaching between the two groups or to unrecognized differences in the content delivered. However the absence of a difference in the clinical test scores indicates that didactic teaching is not superior to simulation training during a conversation observed between a resident and a standardized patient to obtain informed consent.

REFERENCES

1. Canadian Medical Protective Association. Consent: A guide for Canadian physicians, 2006.

2. Middle JV, Wee MYK. Informed consent for epidural analgesia in labour: a survey of UK practice. Anaesthesia 2009; 64:161-164.

SOAP 2012