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Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol

INTRODUCTION: In the USA, African American men bear a disproportionate burden of prostate cancer (PCa) compared with all other groups, having a higher incidence and mortality, poorer quality of life and higher dissatisfaction with care. They are also less likely to receive guideline-concordant treat...

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Autores principales: Palmer, Nynikka R, Shim, Janet K, Kaplan, Celia P, Schillinger, Dean, Blaschko, Sarah D, Breyer, Benjamin N, Pasick, Rena J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409964/
https://www.ncbi.nlm.nih.gov/pubmed/32759241
http://dx.doi.org/10.1136/bmjopen-2019-035032
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author Palmer, Nynikka R
Shim, Janet K
Kaplan, Celia P
Schillinger, Dean
Blaschko, Sarah D
Breyer, Benjamin N
Pasick, Rena J
author_facet Palmer, Nynikka R
Shim, Janet K
Kaplan, Celia P
Schillinger, Dean
Blaschko, Sarah D
Breyer, Benjamin N
Pasick, Rena J
author_sort Palmer, Nynikka R
collection PubMed
description INTRODUCTION: In the USA, African American men bear a disproportionate burden of prostate cancer (PCa) compared with all other groups, having a higher incidence and mortality, poorer quality of life and higher dissatisfaction with care. They are also less likely to receive guideline-concordant treatment (eg, undertreatment of aggressive disease). Inadequate patient–provider communication contributes to suboptimal care, which can be exacerbated by patients’ limited health literacy, providers’ lack of communication skills and time constraints in low-resource, safety net settings. This study is designed to examine the communication experiences of African American patients with PCa as they undertake treatment decision-making. METHODS AND ANALYSIS: Using an ethnographic approach, we will follow 25 African American men newly diagnosed with PCa at two public hospitals, from diagnosis through treatment decision. Data sources include: (1) audio-recorded clinic observations during urology, radiation oncology, medical oncology and primary care visits, (2) field notes from clinic observations, (3) patient surveys after clinic visits, (4) two in-depth patient interviews, (5) a provider survey, and (6) in-depth interviews with providers. We will explore patients’ understanding of their diagnoses and treatment options, sources of support in decision-making, patient–provider communication and treatment decision-making processes. Audio-recorded observations and interviews will be transcribed verbatim. An iterative process of coding and team discussions will be used to thematically analyse patients’ experiences and providers’ perspectives, and to refine codes and identify key themes. Descriptive statistics will summarise survey data. ETHICS AND DISSEMINATION: To our knowledge, this is the first study to examine in-depth patient–provider communication among African American patients with PCa. For a population as marginalised as African American men, an ethnographic approach allows for explication of complex sociocultural and contextual influences on healthcare processes and outcomes. Study findings will inform the development of interventions and initiatives that promote patient-centred communication, shared decision-making and guideline-concordant care. This study was approved by the University of California San Francisco and the Alameda Health System Institutional Review Boards.
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spelling pubmed-74099642020-08-17 Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol Palmer, Nynikka R Shim, Janet K Kaplan, Celia P Schillinger, Dean Blaschko, Sarah D Breyer, Benjamin N Pasick, Rena J BMJ Open Qualitative Research INTRODUCTION: In the USA, African American men bear a disproportionate burden of prostate cancer (PCa) compared with all other groups, having a higher incidence and mortality, poorer quality of life and higher dissatisfaction with care. They are also less likely to receive guideline-concordant treatment (eg, undertreatment of aggressive disease). Inadequate patient–provider communication contributes to suboptimal care, which can be exacerbated by patients’ limited health literacy, providers’ lack of communication skills and time constraints in low-resource, safety net settings. This study is designed to examine the communication experiences of African American patients with PCa as they undertake treatment decision-making. METHODS AND ANALYSIS: Using an ethnographic approach, we will follow 25 African American men newly diagnosed with PCa at two public hospitals, from diagnosis through treatment decision. Data sources include: (1) audio-recorded clinic observations during urology, radiation oncology, medical oncology and primary care visits, (2) field notes from clinic observations, (3) patient surveys after clinic visits, (4) two in-depth patient interviews, (5) a provider survey, and (6) in-depth interviews with providers. We will explore patients’ understanding of their diagnoses and treatment options, sources of support in decision-making, patient–provider communication and treatment decision-making processes. Audio-recorded observations and interviews will be transcribed verbatim. An iterative process of coding and team discussions will be used to thematically analyse patients’ experiences and providers’ perspectives, and to refine codes and identify key themes. Descriptive statistics will summarise survey data. ETHICS AND DISSEMINATION: To our knowledge, this is the first study to examine in-depth patient–provider communication among African American patients with PCa. For a population as marginalised as African American men, an ethnographic approach allows for explication of complex sociocultural and contextual influences on healthcare processes and outcomes. Study findings will inform the development of interventions and initiatives that promote patient-centred communication, shared decision-making and guideline-concordant care. This study was approved by the University of California San Francisco and the Alameda Health System Institutional Review Boards. BMJ Publishing Group 2020-08-05 /pmc/articles/PMC7409964/ /pubmed/32759241 http://dx.doi.org/10.1136/bmjopen-2019-035032 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Qualitative Research
Palmer, Nynikka R
Shim, Janet K
Kaplan, Celia P
Schillinger, Dean
Blaschko, Sarah D
Breyer, Benjamin N
Pasick, Rena J
Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title_full Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title_fullStr Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title_full_unstemmed Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title_short Ethnographic investigation of patient–provider communication among African American men newly diagnosed with prostate cancer: a study protocol
title_sort ethnographic investigation of patient–provider communication among african american men newly diagnosed with prostate cancer: a study protocol
topic Qualitative Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409964/
https://www.ncbi.nlm.nih.gov/pubmed/32759241
http://dx.doi.org/10.1136/bmjopen-2019-035032
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