Patients educating health care providers on Lynch syndrome
Objective<strong>: </strong>Lynch syndrome (LS) patients are at an elevated risk for early-onset cancers, including endometrial and colorectal (CRC). Prior research has shown a deficit in provider knowledge of LS, which may affect patient satisfaction and adherence to recommended screeni...
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The Beryl Institute
2018
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oai:doaj.org-article:37051f47fbf348068e1963e242a534b02021-11-15T04:25:59ZPatients educating health care providers on Lynch syndrome2372-0247https://doaj.org/article/37051f47fbf348068e1963e242a534b02018-11-01T00:00:00Zhttps://pxjournal.org/journal/vol5/iss3/12https://doaj.org/toc/2372-0247Objective<strong>: </strong>Lynch syndrome (LS) patients are at an elevated risk for early-onset cancers, including endometrial and colorectal (CRC). Prior research has shown a deficit in provider knowledge of LS, which may affect patient satisfaction and adherence to recommended screening and surveillance regimens. Studies suggest patients with LS may educate providers perceived as lacking LS knowledge; however, little is known about these interactions. The goal of this study is to assess patient-reported outcomes from clinical interactions where LS patients educate their providers. Methods<strong>: </strong>Participants (n=55) were asked to complete an in-depth telephone interview. <strong></strong> Results<strong>: </strong>Out of 55 participants, approximately two-thirds (n=37) reported engaging in educational interactions. Participants reported feeling satisfied with the provider response in over half of the reported educational interactions (n=24). Participants reported changes in their patient-provider relationship ranging from improvements in their relationship to termination of services.<strong> </strong>Conclusion<strong>: </strong>Patients with LS report educating providers on their diagnosis as well as their screening and surveillance requirements. Patient-reported outcomes of these educational interactions vary based on the provider’s response to the interaction. Providers should be open and receptive to these educational interactions and follow-up on the discussion to improve patient satisfaction. <strong></strong>Kelsey HennigBarry DeCosterRebecca ChuWendy ParkerLisa Campo-EngelsteinAllison Burton-ChaseThe Beryl Institutearticlelynch syndromecolorectal cancerpatient-provider communicationshared decision makingpatient-centered careMedicine (General)R5-920Public aspects of medicineRA1-1270ENPatient Experience Journal (2018) |
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DOAJ |
language |
EN |
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lynch syndrome colorectal cancer patient-provider communication shared decision making patient-centered care Medicine (General) R5-920 Public aspects of medicine RA1-1270 |
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lynch syndrome colorectal cancer patient-provider communication shared decision making patient-centered care Medicine (General) R5-920 Public aspects of medicine RA1-1270 Kelsey Hennig Barry DeCoster Rebecca Chu Wendy Parker Lisa Campo-Engelstein Allison Burton-Chase Patients educating health care providers on Lynch syndrome |
description |
Objective<strong>: </strong>Lynch syndrome (LS) patients are at an elevated risk for early-onset cancers, including endometrial and colorectal (CRC). Prior research has shown a deficit in provider knowledge of LS, which may affect patient satisfaction and adherence to recommended screening and surveillance regimens. Studies suggest patients with LS may educate providers perceived as lacking LS knowledge; however, little is known about these interactions. The goal of this study is to assess patient-reported outcomes from clinical interactions where LS patients educate their providers.
Methods<strong>: </strong>Participants (n=55) were asked to complete an in-depth telephone interview. <strong></strong>
Results<strong>: </strong>Out of 55 participants, approximately two-thirds (n=37) reported engaging in educational interactions. Participants reported feeling satisfied with the provider response in over half of the reported educational interactions (n=24). Participants reported changes in their patient-provider relationship ranging from improvements in their relationship to termination of services.<strong> </strong>Conclusion<strong>: </strong>Patients with LS report educating providers on their diagnosis as well as their screening and surveillance requirements. Patient-reported outcomes of these educational interactions vary based on the provider’s response to the interaction. Providers should be open and receptive to these educational interactions and follow-up on the discussion to improve patient satisfaction. <strong></strong> |
format |
article |
author |
Kelsey Hennig Barry DeCoster Rebecca Chu Wendy Parker Lisa Campo-Engelstein Allison Burton-Chase |
author_facet |
Kelsey Hennig Barry DeCoster Rebecca Chu Wendy Parker Lisa Campo-Engelstein Allison Burton-Chase |
author_sort |
Kelsey Hennig |
title |
Patients educating health care providers on Lynch syndrome |
title_short |
Patients educating health care providers on Lynch syndrome |
title_full |
Patients educating health care providers on Lynch syndrome |
title_fullStr |
Patients educating health care providers on Lynch syndrome |
title_full_unstemmed |
Patients educating health care providers on Lynch syndrome |
title_sort |
patients educating health care providers on lynch syndrome |
publisher |
The Beryl Institute |
publishDate |
2018 |
url |
https://doaj.org/article/37051f47fbf348068e1963e242a534b0 |
work_keys_str_mv |
AT kelseyhennig patientseducatinghealthcareprovidersonlynchsyndrome AT barrydecoster patientseducatinghealthcareprovidersonlynchsyndrome AT rebeccachu patientseducatinghealthcareprovidersonlynchsyndrome AT wendyparker patientseducatinghealthcareprovidersonlynchsyndrome AT lisacampoengelstein patientseducatinghealthcareprovidersonlynchsyndrome AT allisonburtonchase patientseducatinghealthcareprovidersonlynchsyndrome |
_version_ |
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