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Informed consent in refractive surgery: in-person vs telemedicine approach
PURPOSE: The aim of this study was to compare the quality of consent process in refractive surgery between patients who had a preoperative consent discussion with the surgeon using a telemedicine approach and those who had a face-to-face discussion. METHODS: Patients treated between January and Dece...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278698/ https://www.ncbi.nlm.nih.gov/pubmed/30568424 http://dx.doi.org/10.2147/OPTH.S183249 |
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author | Schallhorn, Steven C Hannan, Stephen J Teenan, David Pelouskova, Martina Schallhorn, Julie M |
author_facet | Schallhorn, Steven C Hannan, Stephen J Teenan, David Pelouskova, Martina Schallhorn, Julie M |
author_sort | Schallhorn, Steven C |
collection | PubMed |
description | PURPOSE: The aim of this study was to compare the quality of consent process in refractive surgery between patients who had a preoperative consent discussion with the surgeon using a telemedicine approach and those who had a face-to-face discussion. METHODS: Patients treated between January and December 2017 (8,184 laser vision correction [LVC] and 3,754 refractive lens exchange [RLE] patients) that attended day 1 and 1-month postoperative visit were retrospectively reviewed. Preoperative consent preparation included a consultation with an optometrist, observation of an educational video, and written information. Patients then selected either a face-to-face appointment with their surgeon (in-clinic group) or a telemedicine appointment (remote group) for their consent discussion, according to their preference. Patient experience questionnaire and clinical data were included in a multivariate model to explore factors associated with consent quality. RESULTS: Prior to surgery, 80.1% of LVC and 47.9% of RLE patients selected remote consent. Of all LVC patients, 97.5% of in-clinic and 98.3% of remote patients responded that they were adequately consented for surgery (P=0.04). Similar percentages in the RLE group were 97.6% for in-clinic and 97.9% for remote patients (P=0.47). In a multivariate model, the major predictor of patient’s satisfaction with the consent process was postoperative satisfaction with visual acuity, responsible for 80.4% of variance explained by the model. Other significant contributors were postoperative visual phenomena and dry eyes, difficulty with night driving, close-up and distance vision, postoperative uncorrected distance visual acuity, change in corrected distance visual acuity, and satisfaction with the surgeon’s approach. The type of consent (remote or in-clinic) had no impact on patient’s perception of consent quality in the regression model. CONCLUSION: The majority of patients opted for telemedicine-assisted consent. Those who chose it were equally satisfied as those who had a face-to-face meeting with their surgeon. Dissatisfaction with surgical outcome was the major factor affecting patient’s perception of consent quality, regardless of the method of their consent. |
format | Online Article Text |
id | pubmed-6278698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62786982018-12-19 Informed consent in refractive surgery: in-person vs telemedicine approach Schallhorn, Steven C Hannan, Stephen J Teenan, David Pelouskova, Martina Schallhorn, Julie M Clin Ophthalmol Original Research PURPOSE: The aim of this study was to compare the quality of consent process in refractive surgery between patients who had a preoperative consent discussion with the surgeon using a telemedicine approach and those who had a face-to-face discussion. METHODS: Patients treated between January and December 2017 (8,184 laser vision correction [LVC] and 3,754 refractive lens exchange [RLE] patients) that attended day 1 and 1-month postoperative visit were retrospectively reviewed. Preoperative consent preparation included a consultation with an optometrist, observation of an educational video, and written information. Patients then selected either a face-to-face appointment with their surgeon (in-clinic group) or a telemedicine appointment (remote group) for their consent discussion, according to their preference. Patient experience questionnaire and clinical data were included in a multivariate model to explore factors associated with consent quality. RESULTS: Prior to surgery, 80.1% of LVC and 47.9% of RLE patients selected remote consent. Of all LVC patients, 97.5% of in-clinic and 98.3% of remote patients responded that they were adequately consented for surgery (P=0.04). Similar percentages in the RLE group were 97.6% for in-clinic and 97.9% for remote patients (P=0.47). In a multivariate model, the major predictor of patient’s satisfaction with the consent process was postoperative satisfaction with visual acuity, responsible for 80.4% of variance explained by the model. Other significant contributors were postoperative visual phenomena and dry eyes, difficulty with night driving, close-up and distance vision, postoperative uncorrected distance visual acuity, change in corrected distance visual acuity, and satisfaction with the surgeon’s approach. The type of consent (remote or in-clinic) had no impact on patient’s perception of consent quality in the regression model. CONCLUSION: The majority of patients opted for telemedicine-assisted consent. Those who chose it were equally satisfied as those who had a face-to-face meeting with their surgeon. Dissatisfaction with surgical outcome was the major factor affecting patient’s perception of consent quality, regardless of the method of their consent. Dove Medical Press 2018-11-29 /pmc/articles/PMC6278698/ /pubmed/30568424 http://dx.doi.org/10.2147/OPTH.S183249 Text en © 2018 Schallhorn et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Schallhorn, Steven C Hannan, Stephen J Teenan, David Pelouskova, Martina Schallhorn, Julie M Informed consent in refractive surgery: in-person vs telemedicine approach |
title | Informed consent in refractive surgery: in-person vs telemedicine approach |
title_full | Informed consent in refractive surgery: in-person vs telemedicine approach |
title_fullStr | Informed consent in refractive surgery: in-person vs telemedicine approach |
title_full_unstemmed | Informed consent in refractive surgery: in-person vs telemedicine approach |
title_short | Informed consent in refractive surgery: in-person vs telemedicine approach |
title_sort | informed consent in refractive surgery: in-person vs telemedicine approach |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278698/ https://www.ncbi.nlm.nih.gov/pubmed/30568424 http://dx.doi.org/10.2147/OPTH.S183249 |
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