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"I Won't Put Myself or My Family Through That": Decision Preferences, Family Experiences, and Kidney Disease Decision Making.

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Title: "I Won't Put Myself or My Family Through That": Decision Preferences, Family Experiences, and Kidney Disease Decision Making.
Authors: Hamler, Tyrone C1, Cutforth, Asia1, O'Donnell, Kari2, Miller, Emily K3
Source: Gerontologist. May2025, Vol. 65 Issue 5, p1-11. 11p.
Subject Terms: *Content analysis, *Decision making, *Experience, Families & psychology, Treatment of chronic kidney failure, Medical quality control, Research funding, Continuum of care, Chronic kidney failure, Thematic analysis, Phenomenology
Abstract: Background and Objectives Chronic kidney disease (CKD) is a major public health concern that uniquely affects older Black Americans, a population also likely to have family members also diagnosed with CKD. This study aimed to (1) describe how participants viewed their decision preferences considering the experiences of family, and friends previously diagnosed with CKD, and (2) to understand how these social complexities informed their own decisions for future CKD care. Research Design and Methods Utilizing a phenomenologically informed approach, this study explored participants' perceptions of how patients and their family members' experiences with CKD influenced treatment-related decision making. A reflexive, thematic content analysis was conducted to identify patterns across participant responses (N  = 52). Participants were predialysis, diagnosed with stage 4 or 5 CKD, and were receiving outpatient nephrology care at a large, urban midwestern hospital. Results Three primary themes emerged: (1) uncertainty regarding decision making, (2) lived experience of racism, and (3) impact of quality of care, information, and education on decision making. These 3 interconnected themes centered on factors that influenced why and how decisions related to CKD were made and how racial identity and prior family experiences with CKD influenced these decisions. Discussion and Implications Over the next 40 years, the population of Black Americans aged ≥65 years will nearly triple. Because of the complex support requirements and burden(s) of care for CKD patients, there are implications for reshaping the negative and disorienting narratives that influence decision-making conflicts. [ABSTRACT FROM AUTHOR]
Copyright of Gerontologist is the property of Oxford University Press / USA and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Education Research Complete
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: "I Won't Put Myself or My Family Through That": Decision Preferences, Family Experiences, and Kidney Disease Decision Making.
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– Name: Abstract
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  Data: Background and Objectives Chronic kidney disease (CKD) is a major public health concern that uniquely affects older Black Americans, a population also likely to have family members also diagnosed with CKD. This study aimed to (1) describe how participants viewed their decision preferences considering the experiences of family, and friends previously diagnosed with CKD, and (2) to understand how these social complexities informed their own decisions for future CKD care. Research Design and Methods Utilizing a phenomenologically informed approach, this study explored participants' perceptions of how patients and their family members' experiences with CKD influenced treatment-related decision making. A reflexive, thematic content analysis was conducted to identify patterns across participant responses (N  = 52). Participants were predialysis, diagnosed with stage 4 or 5 CKD, and were receiving outpatient nephrology care at a large, urban midwestern hospital. Results Three primary themes emerged: (1) uncertainty regarding decision making, (2) lived experience of racism, and (3) impact of quality of care, information, and education on decision making. These 3 interconnected themes centered on factors that influenced why and how decisions related to CKD were made and how racial identity and prior family experiences with CKD influenced these decisions. Discussion and Implications Over the next 40 years, the population of Black Americans aged ≥65 years will nearly triple. Because of the complex support requirements and burden(s) of care for CKD patients, there are implications for reshaping the negative and disorienting narratives that influence decision-making conflicts. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
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  Data: <i>Copyright of Gerontologist is the property of Oxford University Press / USA and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=ehh&AN=185104898
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1093/geront/gnaf019
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      – Code: eng
        Text: English
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        PageCount: 11
        StartPage: 1
    Subjects:
      – SubjectFull: Content analysis
        Type: general
      – SubjectFull: Decision making
        Type: general
      – SubjectFull: Experience
        Type: general
      – SubjectFull: Families & psychology
        Type: general
      – SubjectFull: Treatment of chronic kidney failure
        Type: general
      – SubjectFull: Medical quality control
        Type: general
      – SubjectFull: Research funding
        Type: general
      – SubjectFull: Continuum of care
        Type: general
      – SubjectFull: Chronic kidney failure
        Type: general
      – SubjectFull: Thematic analysis
        Type: general
      – SubjectFull: Phenomenology
        Type: general
    Titles:
      – TitleFull: "I Won't Put Myself or My Family Through That": Decision Preferences, Family Experiences, and Kidney Disease Decision Making.
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            NameFull: Hamler, Tyrone C
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            NameFull: Cutforth, Asia
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            NameFull: O'Donnell, Kari
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            NameFull: Miller, Emily K
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            – D: 01
              M: 05
              Text: May2025
              Type: published
              Y: 2025
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              Value: 65
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