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Intensity of care and perceived burden among informal caregivers to persons with chronic medical conditions: a systematic review and meta-analysis
被引:4
|作者:
Carboni-Jimenez, Andrea
[1
,2
]
Rice, Danielle B.
[1
,3
]
Levis, Brooke
[4
]
Canedo-Ayala, Mara
[1
]
Imran, Mahrukh
[1
]
Chiovitti, Matthew
[1
]
Benedetti, Andrea
[5
,6
,7
]
Thombs, Brett D.
[1
,2
,3
,5
,7
,8
,9
]
机构:
[1] Jewish Gen Hosp, Lady Davis Inst Med Res, 4333 Cote St Catherine Rd, Montreal, PQ H3T 1E4, Canada
[2] McGill Univ, Dept Psychiat, Montreal, PQ, Canada
[3] McGill Univ, Dept Psychol, Montreal, PQ, Canada
[4] Keele Univ, Ctr Prognosis Res, Sch Med, Keele, Staffs, England
[5] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
[6] McGill Univ Hlth Ctr, Resp Epidemiol & Clin Res Unit, Montreal, PQ, Canada
[7] McGill Univ, Dept Med, Montreal, PQ, Canada
[8] McGill Univ, Dept Educ & Counselling Psychol, Montreal, PQ, Canada
[9] McGill Univ, Biomed Eth Unit, Montreal, PQ, Canada
基金:
加拿大健康研究院;
关键词:
Systematic review;
meta-analysis;
chronic disease;
informal caregivers;
perceived burden;
QUALITY-OF-LIFE;
AMYOTROPHIC-LATERAL-SCLEROSIS;
SPINAL-CORD-INJURY;
PARKINSONS-DISEASE;
FAMILY CAREGIVERS;
PERITONEAL-DIALYSIS;
HEART-FAILURE;
CHAINED EQUATIONS;
PHYSICAL HEALTH;
PARTNER BURDEN;
D O I:
10.1080/09638288.2021.1966675
中图分类号:
R49 [康复医学];
学科分类号:
100215 ;
摘要:
Purpose Informal caregivers provide ongoing assistance to a loved one with a health condition. No studies have compared caregiving intensity and perception of burden across chronic medical conditions. Materials and methods Databases were searched from inception through 11 September 2020 to identify studies that included the Level of Care Index or the Zarit Burden Inventory (ZBI) among caregivers for people with chronic diseases. Pooled mean ZBI scores and 95% confidence intervals by medical condition were calculated using a random effects model and heterogeneity with I-2. Results Ninety-seven included articles reported on 98 unique samples across 21 chronic diseases. No study used the Level of Care Index. Among 12 disease groups with more than one study, heterogeneity was too high (I-2 range: 0-99.6%, >= 76.5% in 11 groups) to confidently estimate burden. The percent of studies rated high risk of bias ranged from 0% to 98%, but all external validity items were rated as high-risk in >50% of studies. Conclusions Findings highlight the need for studies on caregiver burden to improve sampling techniques; better report sampling procedures and caregiver and care recipient characteristics; and develop a standard set of outcomes, including a measure of caregiving intensity. Systematic Review Registration: CRD42017080962
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页码:6230 / 6246
页数:17
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