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Interviews of living kidney donors to assess donation-related concerns and information-gathering practices

BACKGROUND: Efforts are underway to improve living kidney donor (LKD) education, but current LKD concerns and information-gathering preferences have not been ascertained to inform evidence-based resource development. As a result, prior studies have found that donors desire information that is not in...

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Autores principales: Ruck, Jessica M., Van Pilsum Rasmussen, Sarah E., Henderson, Macey L., Massie, Allan B., Segev, Dorry L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994029/
https://www.ncbi.nlm.nih.gov/pubmed/29884126
http://dx.doi.org/10.1186/s12882-018-0935-0
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author Ruck, Jessica M.
Van Pilsum Rasmussen, Sarah E.
Henderson, Macey L.
Massie, Allan B.
Segev, Dorry L.
author_facet Ruck, Jessica M.
Van Pilsum Rasmussen, Sarah E.
Henderson, Macey L.
Massie, Allan B.
Segev, Dorry L.
author_sort Ruck, Jessica M.
collection PubMed
description BACKGROUND: Efforts are underway to improve living kidney donor (LKD) education, but current LKD concerns and information-gathering preferences have not been ascertained to inform evidence-based resource development. As a result, prior studies have found that donors desire information that is not included in current informed consent and/or educational materials. METHODS: We conducted semi-structured interviews with 50 LKDs who donated at our center to assess (1) concerns about donation that they either had personally before or after donation or heard from family members or friends, (2) information that they had desired before donation, and (3) where they sought information about donation. We used thematic analysis of verbatim interview transcriptions to identify donation-related concerns. We compared the demographic characteristics of participants reporting specific concerns using Fisher’s exact test. RESULTS: We identified 19 unique concerns that participants had or heard about living kidney donation. 20% of participants reported having had no pre-donation concerns; 38% reported no post-donation concerns. The most common concern pre-donation was future kidney failure (22%), post-donation was the recovery process (24%), and from family was endangering their family unit (16%). 44% of participants reported being less concerned than family. 26% of participants wished they had had additional information prior to donating, including practical advice for recovery (10%) and information about specific complications (14%). Caucasian participants were more likely to hear at least one concern from family (76% vs. 33%, p = 0.02). The most commonly consulted educational resources were health care providers (100%) and websites (79% of donors since 2000). 26% of participants had had contact with other donors; an additional 20% desired contact with other LKDs. CONCLUSIONS: Potential donors not only have personal donation-related concerns but frequently hear donation-related concerns from family members and friends. Current gaps in donor education include an absence of practical, peer-to-peer advice about donation from other prior donors and materials directed and potential donors’ family members and friends. These findings can inform the development of new educational practices and resources targeted not only at LKDs but at their social networks.
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spelling pubmed-59940292018-07-05 Interviews of living kidney donors to assess donation-related concerns and information-gathering practices Ruck, Jessica M. Van Pilsum Rasmussen, Sarah E. Henderson, Macey L. Massie, Allan B. Segev, Dorry L. BMC Nephrol Research Article BACKGROUND: Efforts are underway to improve living kidney donor (LKD) education, but current LKD concerns and information-gathering preferences have not been ascertained to inform evidence-based resource development. As a result, prior studies have found that donors desire information that is not included in current informed consent and/or educational materials. METHODS: We conducted semi-structured interviews with 50 LKDs who donated at our center to assess (1) concerns about donation that they either had personally before or after donation or heard from family members or friends, (2) information that they had desired before donation, and (3) where they sought information about donation. We used thematic analysis of verbatim interview transcriptions to identify donation-related concerns. We compared the demographic characteristics of participants reporting specific concerns using Fisher’s exact test. RESULTS: We identified 19 unique concerns that participants had or heard about living kidney donation. 20% of participants reported having had no pre-donation concerns; 38% reported no post-donation concerns. The most common concern pre-donation was future kidney failure (22%), post-donation was the recovery process (24%), and from family was endangering their family unit (16%). 44% of participants reported being less concerned than family. 26% of participants wished they had had additional information prior to donating, including practical advice for recovery (10%) and information about specific complications (14%). Caucasian participants were more likely to hear at least one concern from family (76% vs. 33%, p = 0.02). The most commonly consulted educational resources were health care providers (100%) and websites (79% of donors since 2000). 26% of participants had had contact with other donors; an additional 20% desired contact with other LKDs. CONCLUSIONS: Potential donors not only have personal donation-related concerns but frequently hear donation-related concerns from family members and friends. Current gaps in donor education include an absence of practical, peer-to-peer advice about donation from other prior donors and materials directed and potential donors’ family members and friends. These findings can inform the development of new educational practices and resources targeted not only at LKDs but at their social networks. BioMed Central 2018-06-08 /pmc/articles/PMC5994029/ /pubmed/29884126 http://dx.doi.org/10.1186/s12882-018-0935-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ruck, Jessica M.
Van Pilsum Rasmussen, Sarah E.
Henderson, Macey L.
Massie, Allan B.
Segev, Dorry L.
Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title_full Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title_fullStr Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title_full_unstemmed Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title_short Interviews of living kidney donors to assess donation-related concerns and information-gathering practices
title_sort interviews of living kidney donors to assess donation-related concerns and information-gathering practices
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994029/
https://www.ncbi.nlm.nih.gov/pubmed/29884126
http://dx.doi.org/10.1186/s12882-018-0935-0
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