caregiver quality
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2021 ◽  
Vol 5 (2) ◽  
pp. 347
Author(s):  
Medina Hayati ◽  
Rin Widya Agustin ◽  
Rahmah Saniatuzzulfa

<p><strong>Abstract. </strong><em>Relapse is a state of recurrence and worsening symptom experienced by patient. Acceptance and quality of life of caregivers can affect their attitude toward patient and might be affecting the possibility of schizophrenia relapse</em>. <em>This study intended to seek the correlation between caregiver’s acceptance and quality of life with relapse of schizophrenia outpatient in Surakarta Regional Psychiatric Hospital that involved 35 caregivers with incidental sampling technique. The measurement used on this study are BPRS for assessing schizophrenia relapse (α = 0,908), Caregiver Acceptance Scale (α = 0,934), and Caregiver Quality of Life Scale (α = 0,960). This study used multiple linear regression analysis to analyze the output.</em> <em>Based on the data showed that the level of acceptance and quality of life perceived by caregivers didn’t affect the likelihood of relapse of schizophrenia outpatient in Surakarta Regional Psychiatric Hospital.</em></p><p><strong><em>Keywords: </em></strong><em>Acceptance, Caregiver, Schizophrenia Relapse, Quality of Life</em><strong></strong></p><p><strong>Abstrak.</strong><em> </em><em>Relapse </em>merupakan keadaan muncul kembali dan bertambah parah simptom yang dialami oleh pasien skizofrenia. Penerimaan dan kualitas hidup dari <em>caregiver </em>dapat mempengaruhi sikapnya dalam merawat pasien sehingga mungkin mempengaruhi kemungkinan terjadinya <em>relapse</em>. Penelitian ini bertujuan untuk mengetahui hubungan antara penerimaan dan kualitas hidup <em>caregiver</em> dengan <em>relapse </em>pada pasien rawat jalan skizofrenia di RSJ Daerah Surakarta yang melibatkan 35 <em>caregiver</em> dengan teknik <em>incidental sampling</em>. Instrumen yang digunakan adalah Skala <em>Relapse </em>Skizofrenia (α = 0,908), Skala Penerimaan <em>Caregiver </em>(α = 0,934), dan Skala Kualitas Hidup <em>Caregiver </em>(α = 0,960). Analisis data dalam penelitian ini menggunakan uji regresi linear berganda. Berdasarkan hasil data penelitian menunjukkan bahwa tingkatan penerimaan dan kualitas hidup dari <em>caregiver </em>tidak memiliki pengaruh terhadap munculnya <em>relapse </em>pada pasien rawat jalan skizofrenia di RSJ Daerah Surakarta.</p><strong>Kata Kunci: </strong><em>Caregiver</em>, Kualitas Hidup, Penerimaan,<em> Relapse </em>Skizofrenia


2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Alana Aylward ◽  
Steven A. Gordon ◽  
Morganne Murphy-Meyers ◽  
Chelsea McCarty Allen ◽  
Neil Patel ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Michal Lubomski ◽  
Ryan L. Davis ◽  
Carolyn M. Sue

Objectives: Cognitive impairment impacts negatively on Parkinson's disease (PD) patient and caregiver quality of life (QoL). We examined cognitive impairment in PD patients and their caregivers to determine if caregiver cognition affected their PD relative.Methods: Validated cognition and clinical outcome measures were assessed in 103 PD patients and 81 caregivers.Results: PD patients showed more cognitive impairment than their carers, with 48.6% having possible Mild Cognitive Impairment (MCI) and 16.5% having PD dementia. Increasing age, male gender, lower education level, various non-motor symptoms and certain therapies, associated with poorer cognition in PD. Eighteen and a half percent of caregivers were found to have MCI, in association with a lower physical and mental QoL. This reflected in lower QoL and mood for the respective PD patients.Conclusion: Impaired cognition and QoL in caregivers was associated with decreased QoL and mood for respective PD patients, suggesting MCI in caregivers is an important consideration for the management of PD.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Seyedeh Azam Sajadi ◽  
Zahra Farsi ◽  
Roghayeh Akbari ◽  
Atefeh Sadeghi ◽  
Abazar Akbarzadeh Pasha

Abstract Background Family caregivers of hemodialysis patients are the first and most crucial source of care at home. They experience many problems in the care of hemodialysis patients, which can affect their quality of life and hope, affecting the quality of care provided to patients. This study aimed to determine the relationship between quality of life and hope in family caregivers of hemodialysis patients. Methods A cross-sectional (descriptive-analytical) study performed on 300 family caregivers in the east of Mazandaran province in Iran. Data were collected using the Family Caregiver Quality of Life (FQOL), SF8 and adult hope scale. Data analysis was performed in SPSS version 16, and a P-value of below 0.05 was considered statistically significant. Results The results showed that, there was a direct and significant relationship between hope and quality of life. However, the quality of life was significantly lower in suburban residents, the unemployed, spouses, people with lower education and income levels, caregivers who cannot leave their patients alone, those living with their patients in the same house, and those taking care of male patients, compared to other participants (P < 0.05). Suburban residents, the unemployed, people with an insufficient level of income, and those living with their patients in the same house had significantly lower hope, compared to other subjects. Conclusion Since an increase of hope and quality of life of caregivers can cause improved quality of patient care, it is recommended that hope-based educational programs and interventions be implemented for caregivers.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 3055-3055
Author(s):  
Anca Prica ◽  
Vinita Dhir ◽  
Rachel Aitken ◽  
Harminder K Paul ◽  
Osvaldo Espin-Garcia ◽  
...  

Abstract Introduction Outpatient autologous stem cell transplantation (ASCT) has become standard of care in many centres due to limited inpatient resources and rising financial constraints. Outpatient ASCT involves family members/friends assuming patient care responsibilities during the acute transplant period. Although this may be associated with reduced direct medical costs, less is known about the "out of pocket costs" and "lost opportunity costs" to patients and their caregivers, as well as impact on caregiver quality of life (QOL). Outpatient transplantation is perceived to provide superior QOL for patients, but there is little evidence to support this. Thus, our objectives were to compare the QOL of patients and their caregivers undergoing outpatient and inpatient ASCT, and to quantify indirect costs to them. Methods This is a single centre cohort study of patients with lymphoma and multiple myeloma undergoing ASCT at Princess Margaret Cancer Centre from April 2016 - February 2021. Patients without a primary caregiver were still eligible to complete the QOL portion of the study. Patients completed several questionnaires including FACT-BMT, FACT-F, and EQ-5D. Caregiver questionnaires included: Caregiver Quality of Life Index-Care (C-QOLC), and a caregiver self-administered financial expenditure survey (C-SAFE). Total indirect costs were defined as lost opportunity costs (i.e., wages) plus out-of-pocket costs (e.g., parking, accommodations). Questionnaires were completed at 5 time points: D0 (prior to ASCT), D+7, D+14 (discharge from daily visits), D+28 (discharge from ASCT) and D+100 (follow-up). Demographic and clinical characteristics were assessed using descriptive statistics. Pairwise changes in QOL from baseline were assessed using linear mixed models to account for repeated measures with group, age and sex included as fixed effects. Alpha was defined as p&lt;0.05. Results A total of 97 patients (49 outpatients and 45 inpatients) and 66 caregivers (43 outpatients and 22 inpatients) were enrolled. Patients had a median age of 59 years (range 18-71) and were predominantly male (60%) with 66% diagnosed with multiple myeloma and 34% with lymphoma. Majority of caregivers were spouses (76%). Inpatients were more likely to be employed and have lymphoma. The overall cohort demonstrated a clinically meaningful decrease (≥4 points) from baseline in mean FACT-F scores (fatigue) at D+7, D+14, and D+28 with slight improvements at D+100 (Table 1). Compared to inpatients, outpatients overall exhibited significantly (p=0.011) greater changes in fatigue from baseline at D+7 and D+14, with comparable change scores at D+28 and D+100 between groups (Figure 1a). Moreover, for all patients, there was a clinically meaningful decrease from baseline in mean QOL scores by FACT-BMT (≥4 points) at D+7 and D+14, and a meaningful improvement at D+100, with no differences between groups (Table 1). On the FACT-BMT subscales, outpatients had overall worsening scores compared to inpatients on the Physical (p=0.029), and Functional Well-Being Subscales (p=0.043) (Figure 1c), while no differences were detected on the Emotional and Social Well-being scales. Health utility scores were also calculated from the EQ-5D-3L, with a significant downward trend in the overall sample at D+7; however, no clinically relevant changes (≥ 0.08) were noted, and results were comparable between groups (Figure 1d). With respect to caregiver QOL, there were no differences in mean change scores between the two groups; however overall, caregivers had a significant improvement at D+100 compared to baseline (p&lt;.05; Figure 1e). Outpatient caregivers experienced higher mean out-of-pocket costs ($1360 vs. $789, p=0.03) with the primary caregiver facing significantly greater total indirect costs ($1960 vs. $1068, p=0.025) (Table 2). For fully employed primary caregivers, the mean lost wages were $1231 for inpatients vs. $2150 for outpatients over the 3 month acute ASCT period. Conclusions There was significant deterioration of various measures of QOL in all patients, irrespective of outpatient or inpatient status. Outpatients, however, reported significantly greater changes in fatigue from baseline at D+7, D+14 and D+28. Caregiver QOL appears comparable between the two modalities. The financial burden on caregivers is high, with significantly higher total indirect costs in outpatient caregivers in the acute post-ASCT period. Figure 1 Figure 1. Disclosures Prica: Kite Gilead: Honoraria; Astra-Zeneca: Honoraria. Chen: Astrazeneca: Membership on an entity's Board of Directors or advisory committees; Beigene: Membership on an entity's Board of Directors or advisory committees; BMS: Consultancy, Membership on an entity's Board of Directors or advisory committees; Novartis: Consultancy, Membership on an entity's Board of Directors or advisory committees; Gilead: Consultancy, Membership on an entity's Board of Directors or advisory committees; Janssen: Consultancy. Crump: Novartis: Membership on an entity's Board of Directors or advisory committees; Kyte/Gilead: Membership on an entity's Board of Directors or advisory committees; Epizyme: Research Funding; Roche: Research Funding. Kridel: Gilead Sciences: Research Funding. Kuruvilla: AbbVie: Honoraria; Incyte: Honoraria; Medison Ventures: Honoraria; Merck: Honoraria; Novartis: Honoraria; Gilead: Honoraria; Seattle Genetics: Honoraria; Karyopharm: Honoraria, Other: Data and Safety Monitoring Board; Roche: Honoraria, Research Funding; Janssen: Honoraria, Research Funding; AstraZeneca: Honoraria, Research Funding; TG Therapeutics: Honoraria; Amgen: Honoraria; Pfizer: Honoraria; BMS: Honoraria; Antengene: Honoraria. Reece: Celgene: Consultancy, Honoraria, Research Funding; Takeda: Consultancy, Honoraria, Research Funding; BMS: Honoraria, Research Funding; Janssen: Consultancy, Honoraria, Research Funding; Sanofi: Honoraria; Millennium: Research Funding; Karyopharm: Consultancy, Research Funding; Amgen: Consultancy, Honoraria; GSK: Honoraria.


2021 ◽  
Vol 20 ◽  
pp. S133
Author(s):  
W. Nesser ◽  
S. Snyder ◽  
K. Driscoll ◽  
A. Modi

2021 ◽  
Vol 35 (7) ◽  
pp. 1042-1045
Author(s):  
Matthew P. Martin ◽  
Mindy L. McEntee ◽  
Yash Suri

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Chun Fan Lee ◽  
Dennis C. C. Seow ◽  
Irene Teo ◽  
Shirlyn H. S. Neo ◽  
Grace M. Yang ◽  
...  

Abstract Purpose The Singapore Caregiver Quality of Life Scale – Dementia (SCQOLS-D), developed based on the Singapore Caregiver Quality of Life Scale (SCQOLS), comprises 5 domains and 63 items. It has been shown to be a valid and reliable measurement scale. This study aimed to develop and evaluate a short form of the SCQOLS-D. Methods Data were collected from 102 family caregivers of person with dementia in Singapore. Candidate items were shortlisted by factor analysis, correlation and best subset regression. Shortlisted items with the best measurement properties including correlations with the long form and other established measures, internal consistency and test-retest reliability were identified. Their properties were compared with the corresponding domain scores in the long form of SCQOLS-D and a short form of the SCQOLS. A total score based on the average of the domain scores was also evaluated. Results A total of fifteen items, two to four items per domain, were selected. The total and domain scores generated from these items strongly correlated with the corresponding score of the long form (correlation coefficients: 0.83–0.97). The short and long forms had comparable correlation coefficients with Negative Personal Impact and Positive Personal Impact measures. The short form showed good internal consistency (Cronbach’s alpha: 0.84–0.92) and test-retest reliability (intra-class correlation coefficient: 0.72–0.93). These 15 items form the SCQOLS-D-15, an abbreviated version of the SCQOLS-D. Conclusion The SCQOLS-D-15 showed acceptable measurement properties. This serves as an alternative to the SCQOLS-D to provide rapid assessment of the overall and domain-specific quality of life of caregivers of persons with dementia.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anna Markella Antoniadi ◽  
Miriam Galvin ◽  
Mark Heverin ◽  
Orla Hardiman ◽  
Catherine Mooney

AbstractAmyotrophic Lateral Sclerosis (ALS) is a rare neurodegenerative, fatal and currently incurable disease. People with ALS need support from informal caregivers due to the motor and cognitive decline caused by the disease. This study aims to identify caregivers whose quality of life (QoL) may be impacted as a result of caring for a person with ALS. In this study, we worked towards the identification of the predictors of a caregiver’s QoL in addition to the development of a model for clinical use to alert clinicians when a caregiver is at risk of experiencing low QoL. The data were collected through the Irish ALS Registry and via interviews on several topics with 90 patient and caregiver pairs at three time-points. The McGill QoL questionnaire was used to assess caregiver QoL—the MQoL Single Item Score measures the overall QoL and was selected as the outcome of interest in this work. The caregiver’s existential QoL and burden, as well as the patient’s depression and employment before the onset of symptoms were the features that had the highest impact in predicting caregiver quality of life. A small subset of features that could be easy to collect was used to develop a second model to use it in a clinical setting. The most predictive features for that model were the weekly caregiving duties, age and health of the caregiver, as well as the patient’s physical functioning and age of onset.


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