scholarly journals Family Caregiving Subtypes in the Caregiving Transitions Study: A Latent Class Analysis

2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 798-798
Author(s):  
John Bentley ◽  
Carly Lupton-Smith ◽  
David Roth

Abstract Family caregiving requires activities and experiences that have negative and positive features, producing stress but also providing benefits. The Caregiving Transitions Study (CTS) enrolled 283 caregivers from a national epidemiologic study, of which 32 were caregivers prior to enrollment in the parent study, and 251 became caregivers while participating in the parent study. Telephone interviewers were conducted after caregivers provided care for a minimum of 1.6 years (mean=7.7 years). Latent class analysis (LCA) was used to detect unobserved groups of caregivers. Number of problems (i.e., ADL, IADL, communication, emotional, disruptive behavior), average burden per problem, depressive symptoms, perceived stress, purpose in life, positive aspects of caregiving, hours of care, and duration providing care were used as indicators. Classes were subsequently compared on several external variables, including demographics, quality of life, leisure activities, and caregiving strain. The best-fitting model consisted of three classes (4.6% long-term, 27.6% high-distress, and 67.8% moderate-distress). Classes were similar with respect to sex, age, race, and primary caregiving status of the caregiver. Long-term caregivers had much longer caregiving durations and commonly provided care to a child. The high-distress class was noteworthy in terms of greater number of experienced patient problems; greater likelihood of caring for a person with dementia; higher levels of caregiving strain, depressive symptoms, perceived stress, and perceived burden; and lower levels of quality of life, purpose in life, positive aspects of caregiving, and leisure activities. These findings suggest that caregivers can be classified into distinct subtypes, with one subtype characterized as experiencing high distress.

Author(s):  
Andrew J. MacGregor ◽  
Amber L. Dougherty ◽  
Edwin W. D’Souza ◽  
Cameron T. McCabe ◽  
Daniel J. Crouch ◽  
...  

2020 ◽  
Vol 32 (7) ◽  
pp. 849-861
Author(s):  
Darina V. Petrovsky ◽  
Karen B. Hirschman ◽  
Miranda Varrasse McPhillips ◽  
Justine S. Sefcik ◽  
Alexandra L. Hanlon ◽  
...  

ABSTRACTObjectives:Daytime sleepiness is associated with multiple negative outcomes in older adults receiving long-term services and supports (LTSS) including reduced cognitive performance, need for greater assistance with activities of daily living and decreased social engagement. The purpose of this study was to identify predictors of change in subjective daytime sleepiness among older adults during their first 2 years of receiving LTSS.Design and Setting:Secondary analysis of data from a prospective longitudinal study of older adults who received LTSS in their homes, assisted living communities or nursing homes interviewed at baseline and every 3 months for 24 months.Participants:470 older adults (60 years and older) newly enrolled in LTSS (mean = 81, SD = 8.7; range 60–98; 71% women).Measurements:Subjective daytime sleepiness was assessed every 3 months through 2 years using the Epworth Sleepiness Scale. Multiple validated measures were used to capture health-related quality of life characteristics of enrollees and their environment, including symptom status (Symptom Bother Scale), cognition (Mini Mental Status Exam), physical function (Basic Activities of Daily Living), physical and mental general health, quality of life (Dementia Quality of Life, D-QoL), depressive symptoms (Geriatric Depression Scale) and social support (Medical Outcomes Survey-Social Support).Results:Longitudinal mixed effects modeling was used to examine the relationship between independent variables and continuous measure of daytime sleepiness. Increased feelings of belonging, subscale of the D-QoL (effect size = −0.006, 95% CI: −0.013 to −0.0001, p = 0.045) and higher number of depressive symptoms (effect size = −0.002, 95% CI: −0.004 to −0.001, p = 0.001) at baseline were associated with slower rates of increase in daytime sleepiness over time.Conclusions:Comprehensive baseline and longitudinal screening for changes in daytime sleepiness along with depression and perceived quality of life should be used to inform interventions aimed at reducing daytime sleepiness among older adults receiving LTSS.


2006 ◽  
Vol 247 (2) ◽  
pp. 149-156 ◽  
Author(s):  
G.M.S Nys ◽  
M.J.E van Zandvoort ◽  
H.B van der Worp ◽  
E.H.F de Haan ◽  
P.L.M de Kort ◽  
...  

2015 ◽  
Vol 33 (29_suppl) ◽  
pp. 93-93 ◽  
Author(s):  
Kristine A. Donovan ◽  
Alexandra Albizu-Rivera ◽  
Hye Sook Chon ◽  
Robert Michael Wenham

93 Background: Pelvic exenteration (PE) has been performed historically in women with gynecologic cancer for palliation of recurrent disease. With advances in operative methods, PE in the well-selected patient can produce 5-year survival rates as high as 60%. Despite a recent increase in rate of PE performed with curative intent, there is a paucity of data on its long-term physical and emotional effects. We sought to characterize women’s long-term quality of life (QOL) and its correlates after PE for recurrent gynecologic cancer. Methods: We conducted a mixed methods study combining quantitative measurement of QOL and its demographic, clinical and psychological correlates with concurrent qualitative assessment to probe women’s cognitive and behavioral responses to PE. Results: From 2005 to 2014, 85 women underwent PE at our institution; 44% were still alive at study initiation. Among eligible women, 72% completed their participation. Mean age of the sample at time of study participation was 57.3 (SD = 9.5) years (range = 43 to 75) and median time since surgery was 3.0 years (range = .9 to 8). Women’s self-reported global QOL score was average (54.4 (23); range = 33.3 to 100) and the relationship between QOL and current age or time since surgery was not significant (p > .05). Women reported mild sleep disturbance, mild to moderate pain, moderate fatigue and anxiety and severe depressive symptoms. All of the women exceeded the cut-off for clinically significant depressive symptoms. Qualitatively, women described profound negative changes in their physical and emotional well-being after PE. In nearly all of the women, the extended survival after PE helped to buffer the effects of these changes. Conclusions: Results suggest women’s health-related QOL may return to, or near, pre-surgical levels in long-term survivorship but that symptom control is suboptimal. Findings should facilitate more informed decision making prior to PE and suggest targets for clinical intervention to enhance QOL and improve symptom control after PE. This study highlights the need for more comprehensive assessments pre- and post-PE to examine the effects of disease- and PE-related variables, cultural norms and social support on patient-reported outcomes.


2012 ◽  
Vol 78 (08) ◽  
pp. 122-128 ◽  
Author(s):  
Tiziana Ciarambino ◽  
Pietro Castellino ◽  
Giuseppe Paolisso ◽  
Ludovico Coppola ◽  
Nicola Ferrara ◽  
...  

2020 ◽  
Author(s):  
Felix J. Clouth ◽  
Arturo Moncada‐Torres ◽  
Gijs Geleijnse ◽  
Floortje Mols ◽  
Felice N. Erning ◽  
...  

2018 ◽  
Vol 28 (1) ◽  
pp. 55 ◽  
Author(s):  
Jessica Tobin ◽  
Kimberly A. Miller ◽  
Lourdes Baezconde-Garbanati ◽  
Jennifer B. Unger ◽  
Ann S. Hamilton ◽  
...  

<p class="Pa7"><strong>Objective: </strong>Acculturation appears to be an important aspect of the association between ethnicity and disease, but it has not been explored in depth among childhood cancer survivors (CCS). The purpose of our study was to identify distinct acculturative profiles among Hispanic CCS and to assess dif­ferences in quality of life and depressive symptoms.</p><p class="Pa7"><strong>Design: </strong>Latent class analysis was used to identify distinct acculturative profiles using 9 indicator items reflecting Hispanic and An­glo cultural orientation. Multinomial logistic regression was performed to explore differ­ences in depressive symptoms and quality of life between acculturation classes.</p><p class="Pa7"><strong>Setting and Participants: </strong>Participants were diagnosed in Los Angeles County, Califor­nia, USA between 2000-2007 and were recruited for the study in 2009.</p><p class="Pa7"><strong>Main Outcome Measures: </strong>Center for Epi­demiologic Studies depression scale and the PedsQL 4.0 quality of life scale.</p><p class="Pa7"><strong>Results: </strong>Three distinct acculturation classes emerged. All classes displayed a high prob­ability of endorsing all Anglo orientation items. One class additionally demonstrated a high probability of endorsing all Hispanic orientation items and was labeled bicultural (40%); another demonstrated low probabil­ity of endorsing the Hispanic items so was labeled assimilated (32%); and the last dem­onstrated a high probability of endorsing only the Hispanic items related to language use and was labeled linguistically Hispanic/ culturally Anglo (LH) (28%).</p><p class="Pa8"><strong>Conclusions: </strong>The assimilated group had significantly more depressive symptoms and lower quality of life than the other two groups. This may indicate that loss of the Hispanic culture may be associated with poorer psychosocial health among CCS.</p><p class="Pa8"><em>Ethn Dis. </em>2018;28(1):55-60; doi:10.18865/ ed.28.1.55.</p>


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