دورية أكاديمية
أعرض في EDS

Risk factors and intervention of caregiver burden in Parkinson's disease: a systematic review and meta-analysis.

التفاصيل البيبلوغرافية
العنوان: Risk factors and intervention of caregiver burden in Parkinson's disease: a systematic review and meta-analysis.
المؤلفون: Zhao Y; Department of Nursing, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China., Wu W; Department of Nursing, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China., Wu J; Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.; National Center for Neurological Disorders, Shanghai, China., Shen B; Department of Nursing, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China., Cao Y; Department of Nursing, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China. caoyanpeihs@yeah.net., Xu Y; Department of Nursing, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, China. yafang_xu@fudan.edu.cn.; National Center for Neurological Disorders, Shanghai, China. yafang_xu@fudan.edu.cn.; Huashan Rare Disease Center, Huashan Hospital, Fudan University, Shanghai, China. yafang_xu@fudan.edu.cn.
المصدر: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation [Qual Life Res] 2024 Jul; Vol. 33 (7), pp. 1753-1766. Date of Electronic Publication: 2024 Apr 04.
نوع المنشور: Journal Article; Systematic Review; Meta-Analysis
اللغة: English
بيانات الدورية: Publisher: Springer Netherlands Country of Publication: Netherlands NLM ID: 9210257 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2649 (Electronic) Linking ISSN: 09629343 NLM ISO Abbreviation: Qual Life Res Subsets: MEDLINE
أسماء مطبوعة: Publication: 2005- : Netherlands : Springer Netherlands
Original Publication: Oxford, UK : Rapid Communications of Oxford, Ltd, c1992-
مواضيع طبية MeSH: Parkinson Disease*/psychology , Parkinson Disease*/therapy , Caregiver Burden*/psychology , Caregivers*/psychology, Humans ; Risk Factors ; Cost of Illness ; Quality of Life ; Adaptation, Psychological
مستخلص: Purpose: This study summarized characteristics and risk factors of caregiver burden in PD patients and used meta-analysis to verify the effectiveness of the intervention on caregiver burden.
Methods: Systematic review and meta-analysis were conducted.
Results: Forty-nine articles that involved 5387 caregivers of patients with PD were included in this study. Results of systematic review indicated that Zarit burden Inventory (ZBI) was the most used scale to measure the caregiver burden. All scales revealed caregivers of PD patients had mild to moderate caregiver burden. For the PD patients with longer disease duration, severer disease severity, more negative emotion and cognition impairment, their caregivers intended to have higher caregiver burden. The caregiver with negative emotion and who spent more time on caregiving indicated higher caregiver burden than the others. The caregiver burden was not improved after deep brain stimulation (DBS). Meta-analysis showed that cognitive behavior therapy and palliative care had no significant effect to reduce caregiver burden in PD patients' caregiver.
Conclusion: Caregivers of PD patients experienced mild to moderate caregiver burden. Demographic factor, diseased-related factor and negative emotional factor were the risk factors of caregiver burden. Health education and care support for long-term management after DBS surgery should be provided for patients and caregivers to decrease caregiver burden.
(© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
References: Analytics, D. o. D. a. (2020). WHO methods and data sources for global burden of disease estimates 2000–2019.
Armstrong, M. J., & Okun, M. S. (2020). Diagnosis and treatment of Parkinson disease: A review. JAMA, 323(6), 548–560. https://doi.org/10.1001/jama.2019.22360. (PMID: 10.1001/jama.2019.2236032044947)
Bagheri, S., Zare, N., Mazlom, S. R., Mohajer, S., & Soltani, M. (2019). Effect of implementing family-centered empowerment model on burden of care in caregivers of the elderly with Parkinson’s disease. Journal of Evidence-based Care, 9(3), 40–48. https://doi.org/10.22038/EBCJ.2019.14043. (PMID: 10.22038/EBCJ.2019.14043)
Balestrino, R., & Schapira, A. H. V. (2020). Parkinson disease. European Journal of Neurology, 27(1), 27–42. https://doi.org/10.1111/ene.14108. (PMID: 10.1111/ene.1410831631455)
Bloem, B. R., Okun, M. S., & Klein, C. (2021). Parkinson’s disease. Lancet, 397(10291), 2284–2303. https://doi.org/10.1016/S0140-6736(21)00218-X. (PMID: 10.1016/S0140-6736(21)00218-X33848468)
Carod-Artal, F. J., Mesquita, H. M., Ziomkowski, S., & Martinez-Martin, P. (2013). Burden and health-related quality of life among caregivers of Brazilian Parkinson’s disease patients. Parkinsonism & Related Disorders, 19(11), 943–948. https://doi.org/10.1016/j.parkreldis.2013.06.005. (PMID: 10.1016/j.parkreldis.2013.06.005)
Chahine, L. M., Feldman, R., Althouse, A., Torsney, B., Alzyoud, L., Mantri, S., Edison, B., Albert, S., Daeschler, M., Kopil, C., & Marras, C. (2021). Contribution of neuropsychiatric symptoms in Parkinson’s disease to different domains of caregiver burden. Journal of Neurology, 268(8), 2961–2972. https://doi.org/10.1007/s00415-021-10443-7. (PMID: 10.1007/s00415-021-10443-7336291818289810)
Church, F. C. (2021). Treatment options for motor and non-motor symptoms of Parkinson’s disease. Biomolecules, 11(4), 612. https://doi.org/10.3390/biom11040612. (PMID: 10.3390/biom11040612339241038074325)
Delfino, L. L., Komatsu, R. S., Komatsu, C., Neri, A. L., & Cachioni, M. (2021). Neuropsychiatric symptoms associated with family caregiver burden and depression. Dementia e Neuropsychologia, 15(1), 128–135. https://doi.org/10.1590/1980-57642021dn15-010014. (PMID: 10.1590/1980-57642021dn15-010014)
Dissanayaka, N. N. W., Pye, D., Mitchell, L. K., Byrne, G. J., O’Sullivan, J. D., Marsh, R., & Pachana, N. A. (2017). Cognitive behavior therapy for anxiety in Parkinson’s disease: Outcomes for patients and caregivers. Clinical Gerontologist, 40(3), 159–171. https://doi.org/10.1080/07317115.2016.1240131. (PMID: 10.1080/07317115.2016.124013128452666)
Dobkin, R. D., Menza, M., Allen, L. A., Gara, M. A., Mark, M. H., Tiu, J., Bienfait, K. L., & Friedman, J. (2011). Cognitive-behavioral therapy for depression in Parkinson’s disease: A randomized, controlled trial. American Journal of Psychiatry, 168(10), 1066–1074. https://doi.org/10.1176/appi.ajp.2011.10111669. (PMID: 10.1176/appi.ajp.2011.1011166921676990)
Draper, B. M., Poulos, C. J., Cole, A. M., Poulos, R. G., & Ehrlich, F. (1992). A comparison of caregivers for elderly stroke and dementia victims. Journal of the American Geriatrics Society, 40(9), 896–901. https://doi.org/10.1111/j.1532-5415.1992.tb01986.x. (PMID: 10.1111/j.1532-5415.1992.tb01986.x1512385)
Eglit, G. M., Lopez, F., Schiehser, D. M., Pirogovsky-Turk, E., Litvan, I., Lessig, S., & Filoteo, J. V. (2021). Delineation of apathy subgroups in Parkinson’s disease: Differences in clinical presentation, functional ability, health-related quality of life, and caregiver burden. Movement disorders clinical practice, 8(1), 92–99. https://doi.org/10.1002/mdc3.13127. (PMID: 10.1002/mdc3.1312733426163)
Eichel, H. V., Heine, J., Wegner, F., Rogozinski, S., Stiel, S., Groh, A., Krey, L., Höglinger, G. U., & Klietz, M. (2022). Neuropsychiatric symptoms in Parkinson’s disease patients are associated with reduced health-related quality of life and increased caregiver burden. Brain Sciences, 12(1), 89. https://doi.org/10.3390/brainsci12010089. (PMID: 10.3390/brainsci1201008935053832)
Gao, W., Wilson, R., Hepgul, N., Yi, D., Evans, C., Bajwah, S., Crosby, V., Wilcock, A., Lindsay, F., Byrne, A., Young, C., Groves, K., Smith, C., Burman, R., Chaudhuri, K. R., Silber, E., Higginson, I. J., & Investigators, O. N. T. (2020). Effect of short-term integrated palliative care on patient-reported outcomes among patients severely affected with long-term neurological conditions: A randomized clinical trial. JAMA Network Open, 3(8), e2015061. https://doi.org/10.1001/jamanetworkopen.2020.15061. (PMID: 10.1001/jamanetworkopen.2020.15061328571517455856)
Genç, F., Yuksel, B., & Tokuc, F. E. U. (2019). Caregiver burden and quality of life in early and late stages of idiopathic Parkinson’s disease. Psychiatry Investigation, 16(4), 285–291. https://doi.org/10.30773/pi.2019.02.20. (PMID: 10.30773/pi.2019.02.20310426906504774)
Gulke, E., & Potter-Nerger, M. (2022). Caregiver burden in partners of parkinsonian patients with deep brain stimulation. Brain Sciences, 12(2), 238. https://doi.org/10.3390/brainsci12020238. (PMID: 10.3390/brainsci12020238352040018870343)
McDowell, F. H. (1992). Rehabilitation in Parkinson’s disease, day care programs for demented patients, and aids for living and home modifications for patients with neurologic physical disability. In Principles and Practice of Restorative Neurology (pp. 152–160). Butterworth-Heinemann.
Hagell, P., Alvariza, A., Westergren, A., & Arestedt, K. (2017). Assessment of burden among family caregivers of people with Parkinson’s disease using the Zarit burden interview. Journal of Pain and Symptom Management, 53(2), 272–278. https://doi.org/10.1016/j.jpainsymman.2016.09.007. (PMID: 10.1016/j.jpainsymman.2016.09.00727810571)
He, H. Y., Zhou, M. Z., Lu, L. X., Wu, J. Y., Gan, J., Chen, W., & Liu, Z. G. (2010). Burden and related factors among care-takers of patients with Parkinson’s disease. Chinese Journal of Epidemiology, 31(6), 692–695. (PMID: 21163106)
Happe, S., & Berger, K. (2002). The association between caregiver burden and sleep disturbances in partners of patients with Parkinson’s disease. Age and ageing, 31(5), 349–354. (PMID: 10.1093/ageing/31.5.34912242196)
Hiseman, J. P., & Fackrell, R. (2017). Caregiver burden and the nonmotor symptoms of Parkinson’s disease. International Review of Neurobiology, 133, 479–497. https://doi.org/10.1016/bs.irn.2017.05.035. (PMID: 10.1016/bs.irn.2017.05.03528802929)
Jackowiak, E., Maher, A. C., Persad, C., Kotagal, V., Wyant, K., Heston, A., Patil, P. G., & Chou, K. L. (2020). Caregiver burden worsens in the second year after subthalamic nucleus deep brain stimulation for Parkinson’s disease. Parkinsonism & Related Disorders, 78, 4–8. https://doi.org/10.1016/j.parkreldis.2020.06.036. (PMID: 10.1016/j.parkreldis.2020.06.036)
James, K., Chin-Bailey, C., Holder-Nevins, D., Thompson, C., Donaldson-Davis, K., & Eldemire-Shearer, D. (2021). Zarit burden interview among caregivers of community-dwelling older adults in a caribbean setting (Jamaica): Reliability and factor structure. Health and Social Care in the Community, 29(5), e79–e88. https://doi.org/10.1111/hsc.13244. (PMID: 10.1111/hsc.1324433252838)
Jones, A. J., Kuijer, R. G., Livingston, L., Myall, D., Horne, K., MacAskill, M., Pitcher, T., Barrett, P. T., Anderson, T. J., & Dalrymple-Alford, J. C. (2017). Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI). Transl Neurodegener, 6, 17. https://doi.org/10.1186/s40035-017-0085-5. (PMID: 10.1186/s40035-017-0085-5286385985474856)
Jose, A., Bhargavan, A., Appireddy, R., Raghunath, S. P., Rajan, R., & Iype, T. (2021). Neuropsychiatric symptoms and caregiver’s burden in Parkinson’s disease patients in a tertiary care Teaching Hospital in South India: A cross-sectional study. Neurology India, 69(6), 1706–1710. https://doi.org/10.4103/0028-3886.333437. (PMID: 10.4103/0028-3886.33343734979673)
Juneja, A., Anand, K., Chandra, M., Deshpande, S., Dhamija, R., Kathuria, P., & Mahajan, R. (2020). Neuropsychiatric symptoms and caregiver burden in Parkinson’s disease. Annals of Indian Academy of Neurology, 23(5), 656–660. https://doi.org/10.4103/aian.AIAN_91_20. (PMID: 10.4103/aian.AIAN_91_20336232677887493)
Karlstedt, M., Fereshtehnejad, S. M., Aarsland, D., & Lökk, J. (2020). Mediating effect of mutuality on caregiver burden in Parkinson’s disease partners. Aging & Mental Health, 24(9), 1421–1428. https://doi.org/10.1080/13607863.2019.1619165. (PMID: 10.1080/13607863.2019.1619165)
Kim, M. J., Chang, K. W., Park, S. H., Chang, W. S., Jung, H. H., & Chang, J. W. (2021). Stimulation-induced side effects of deep brain stimulation in the ventralis intermedius and posterior subthalamic area for essential tremor. Frontiers in Neurology, 12, 678592. https://doi.org/10.3389/fneur.2021.678592. (PMID: 10.3389/fneur.2021.678592341777848220085)
Klietz, M., Drexel, S. C., Schnur, T., Lange, F., Groh, A., Paracka, L., Greten, S., Dressler, D., Höglinger, G. U., & Wegner, F. (2020). Mindfulness and Psychological Flexibility Are Inversely Associated With Caregiver Burden in Parkinson’s disease. Brain Sciences, 10(2), 111. https://doi.org/10.3390/brainsci10020111. (PMID: 10.3390/brainsci10020111320931887071391)
Klietz, M., Schnur, T., Drexel, S., Lange, F., Tulke, A., Rippena, L., Paracka, L., Dressler, D., Höglinger, G. U., & Wegner, F. (2020). Association of motor and cognitive symptoms with health-related quality of life and caregiver burden in a German cohort of advanced Parkinson’s Disease patients. Parkinsons Disease, 2020, 5184084. https://doi.org/10.1155/2020/5184084. (PMID: 10.1155/2020/5184084)
Klietz, M., Schnur, T., Drexel, S. C., Lange, F., Paracka, L., Huber, M. K., Dressler, D., Höglinger, G. U., & Wegner, F. (2020). Alexithymia is associated with reduced quality of life and increased caregiver burden in Parkinson’s disease. Brain Sciencs, 10(6), 401. https://doi.org/10.3390/brainsci10060401. (PMID: 10.3390/brainsci10060401)
Kluger, B. M., Miyasaki, J., Katz, M., Galifianakis, N., Hall, K., Pantilat, S., Khan, R., Friedman, C., Cernik, W., Goto, Y., Long, J., Fairclough, D., Sillau, S., & Kutner, J. S. (2020). Comparison of integrated outpatient palliative care with standard care in patients with parkinson disease and related disorders: A randomized clinical trial. JAMA Neurology, 77(5), 551–560. https://doi.org/10.1001/jamaneurol.2019.4992. (PMID: 10.1001/jamaneurol.2019.499232040141)
Kudlicka, A., Clare, L., & Hindle, J. V. (2014). Quality of life, health status and caregiver burden in Parkinson’s disease: Relationship to executive functioning. International Journal of Geriatric Psychiatry, 29(1), 68–76. https://doi.org/10.1002/gps.3970. (PMID: 10.1002/gps.397023625583)
Lennaerts-Kats, H., Ebenau, A., van der Steen, J. T., Munneke, M., Bloem, B. R., Vissers, K. C. P., Meinders, M. J., & Groot, M. M. (2022). “No one can tell me how Parkinson’s disease will unfold”: A mixed methods case study on palliative care for people with Parkinson’s disease and Their Family Caregivers. Journal of Parkinson’s Disease, 12(1), 207–219. https://doi.org/10.3233/jpd-212742. (PMID: 10.3233/jpd-212742345420318842750)
Leroi, I., McDonald, K., Pantula, H., & Harbishettar, V. (2012). Cognitive impairment in Parkinson disease: Impact on quality of life, disability, and caregiver burden. Journal of Geriatric Psychiatry and Neurology, 25(4), 208–214. https://doi.org/10.1177/0891988712464823. (PMID: 10.1177/089198871246482323172765)
Lubomski, M., Davis, R. L., & Sue, C. M. (2021). Health-related quality of life for Parkinson’s disease patients and their caregivers. Journal of Movement Disorders, 14(1), 42. https://doi.org/10.14802/jmd.20079. (PMID: 10.14802/jmd.20079334234357840244)
Macchi, Z. A., Koljack, C. E., Miyasaki, J. M., Katz, M., Galifianakis, N., Prizer, L. P., Sillau, S. H., & Kluger, B. M. (2020). Patient and caregiver characteristics associated with caregiver burden in Parkinson’s disease: A palliative care approach. Annals of Palliative Medicine, 9, S24–S33. https://doi.org/10.21037/apm.2019.10.01. (PMID: 10.21037/apm.2019.10.0131735048)
Martinez-Martin, P., Arroyo, S., Manuel Rojo-Abuin, J., Rodriguez-Blazquez, C., Frades, B., de Pedro Cuesta, J., & Longitudinal Parkinsons Dis, P. (2008). Burden, perceived health status, and mood among caregivers of Parkinson’s disease patients. Movement Disorders, 23(12), 1673–1680. https://doi.org/10.1002/mds.22106. (PMID: 10.1002/mds.2210618709684)
Martínez-Martín, P., Forjaz, M. J., Frades-Payo, B., Rusinol, A. B., Fernández-García, J. M., Benito-León, J., Arillo, V. C., Barberá, M. A., Sordo, M. P., & Catalán, M. J. (2007). Caregiver burden in Parkinson’s disease. Movement Disorders, 22(7), 924–931. https://doi.org/10.1002/mds.21355. (PMID: 10.1002/mds.2135517238193)
Martinez-Martin, P., Rodriguez-Blazquez, C., Forjaz, M. J., Frades-Payo, B., Agueera-Ortiz, L., Weintraub, D., Riesco, A., Kurtis, M. M., & Chaudhuri, K. R. (2015). Neuropsychiatric symptoms and caregiver’s burden in Parkinson’s disease. Parkinsonism & Related Disorders, 21(6), 629–634. https://doi.org/10.1016/j.parkreldis.2015.03.024. (PMID: 10.1016/j.parkreldis.2015.03.024)
Martinez-Martin, P., Rodriguez-Blazquez, C., & Forjaz, M. J. (2012). Quality of life and burden in caregivers for patients with Parkinson’s disease: Concepts, assessment and related factors. Expert Review of Pharmacoeconomics & Outcomes Research, 12(2), 221–230. (PMID: 10.1586/erp.11.106)
Mendorf, S., Witte, O. W., Zipprich, H., & Prell, T. (2020). Association between nonmotor symptoms and nonadherence to medication in Parkinson’s disease. Frontiers in Neurology, 11, 551696. https://doi.org/10.3389/fneur.2020.551696. (PMID: 10.3389/fneur.2020.551696331929837604271)
Okun, M. S., Tagliati, M., Pourfar, M., Fernandez, H. H., Rodriguez, R. L., Alterman, R. L., & Foote, K. D. (2005). Management of referred deep brain stimulation failures. American Medical Association, 62, 1250–1255.
Moriarty, H., Bunting-Perry, L., Robinson, J. P., & Bradway, C. W. (2016). The experience of women who care for spouses with Parkinson’s disease and lower urinary tract symptoms. Journal of Obstetric, Gynecologic, and Neonatal Nursing, 45(5), 737–748. https://doi.org/10.1016/j.jogn.2016.04.008. (PMID: 10.1016/j.jogn.2016.04.00827444841)
Mosley, P. E., Breakspear, M., Coyne, T., Silburn, P., & Smith, D. (2018). Caregiver burden and caregiver appraisal of psychiatric symptoms are not modulated by subthalamic deep brain stimulation for Parkinson’s disease. NPJ Parkinson’s Disease, 4(1), 12. https://doi.org/10.1038/s41531-018-0048-2. (PMID: 10.1038/s41531-018-0048-2296754635904120)
Novak, M., & Guest, C. (1989). Application of a multidimensional caregiver burden inventory. The Gerontologist, 29(6), 798–803. (PMID: 10.1093/geront/29.6.7982516000)
Nurjono, M., Shrestha, P., Ang, I. Y. H., Shiraz, F., Eh, K. X., Toh, S. E. S., & Vrijhoef, H. J. M. (2020). Shifting care from hospital to community, a strategy to integrate care in Singapore: Process evaluation of implementation fidelity. BMC Health Services Research, 20(1), 452. https://doi.org/10.1186/s12913-020-05263-w. (PMID: 10.1186/s12913-020-05263-w324482837245814)
Oh, Y. S., Lee, J. E., Lee, P. H., & Kim, J. S. (2015). Neuropsychiatric symptoms in Parkinson’s disease dementia are associated with increased caregiver burden. Journal of Movement Disorders, 8(1), 26–32. https://doi.org/10.14802/jmd.14019. (PMID: 10.14802/jmd.14019256147834298716)
Okai, D., Askey-Jones, S., Samuel, M., O’Sullivan, S. S., Chaudhuri, K. R., Martin, A., Mack, J., Brown, R. G., & David, A. S. (2013). Trial of CBT for impulse control behaviors affecting Parkinson patients and their caregivers. Neurology, 80(9), 792–799. (PMID: 10.1212/WNL.0b013e3182840678233259113598451)
Ozdilek, B., & Gunal, D. I. (2012). Motor and non-motor symptoms in turkish patients with Parkinson’s disease affecting family caregiver burden and quality of life. The Journal of Neuropsychiatry and Clinical Neurosciences, 24(4), 478–483. (PMID: 10.1176/appi.neuropsych.1110031523224455)
Rajiah, K., Maharajan, M. K., Yeen, S. J., & Lew, S. (2017). Quality of life and caregivers’ burden of Parkinson’s disease. Neuroepidemiology, 48(3–4), 131–137. https://doi.org/10.1159/000479031. (PMID: 10.1159/00047903128728161)
Razali, R., Ahmad, F., Abd Rahman, F. N., Midin, M., & Sidi, H. (2011). Burden of care among caregivers of patients with Parkinson disease: A cross-sectional study. Clinical Neurology and Neurosurgery, 113(8), 639–643. https://doi.org/10.1016/j.clineuro.2011.05.008. (PMID: 10.1016/j.clineuro.2011.05.00821684679)
Rui, Z., Yuqin, W., Huanyun, L., Jinfeng, H., Caili, D., & Chao, L. (2019). The application of psychological nursing combined with health education in deep brain stimulation for Parkinson′s disease. Journal of Qilu Nursing, 25(4), 41–43.
Santos-Garcia, D., & de la Fuente-Fernandez, R. (2015). Factors contributing to caregivers’ stress and burden in Parkinson’s disease. Acta Neurologica Scandinavica, 131(4), 203–210. https://doi.org/10.1111/ane.12305. (PMID: 10.1111/ane.1230525212106)
Schrag, A., Hovris, A., Morley, D., Quinn, N., & Jahanshahi, M. (2006). Caregiver-burden in Parkinson’s disease is closely associated with psychiatric symptoms, falls, and disability. Parkinsonism & Related Disorders, 12(1), 35–41. https://doi.org/10.1016/j.parkreldis.2005.06.011. (PMID: 10.1016/j.parkreldis.2005.06.011)
Secker, D. L., & Brown, R. G. (2005). Cognitive behavioural therapy (CBT) for carers of patients with Parkinson’s disease: A preliminary randomised controlled trial. Journal of Neurology, Neurosurgery and Psychiatry, 76(4), 491–497. https://doi.org/10.1136/jnnp.2004.042291. (PMID: 10.1136/jnnp.2004.042291157744331739584)
Seritan, A. L., Iosif, A. M., Prakash, P., Wang, S. S., & Eisendrath, S. (2022). Online mindfulness-based cognitive therapy for people with Parkinson’s disease and their caregivers: A pilot study. Journal of Technology in Behavioral Science, 7(3), 381–395. https://doi.org/10.1007/s41347-022-00261-7. (PMID: 10.1007/s41347-022-00261-7355277989059916)
Shah-Zamora, D., Allen, A. M., Rardin, L., Ivancic, M., Durham, K., Hickey, P., Cooney, J. W., Scott, B. L., & Mantri, S. (2021). Mindfulness based stress reduction in people with Parkinson’s disease and their care partners. Complementary Therapies in Clinical Practice, 43, 101377. https://doi.org/10.1016/j.ctcp.2021.101377. (PMID: 10.1016/j.ctcp.2021.10137733831804)
Shin, H., Lee, J. Y., Youn, J., Kim, J. S., & Cho, J. W. (2012). Factors contributing to spousal and offspring caregiver burden in Parkinson’s disease. European Neurology, 67(5), 292–296. https://doi.org/10.1159/000335577. (PMID: 10.1159/00033557722517329)
Shin, H., Youn, J., Kim, J. S., Lee, J.-Y., & Cho, J. W. (2012). Caregiver burden in Parkinson disease with dementia compared to Alzheimer disease in Korea. Journal of Geriatric Psychiatry and Neurology, 25(4), 222–226. https://doi.org/10.1177/0891988712464819. (PMID: 10.1177/089198871246481923172764)
Soileau, M. J., Persad, C., Taylor, J., Patil, P. G., & Chou, K. L. (2014). Caregiver burden in patients with Parkinson disease undergoing deep brain stimulation: An exploratory analysis. Journal of Parkinsons Disease, 4(3), 517–521. https://doi.org/10.3233/jpd-140380. (PMID: 10.3233/jpd-140380)
Tan, M. M. J., Lim, E. C., Nadkarni, N. V., Lye, W. K., Tan, E. K., & Prakash, K. M. (2019). The characteristics of patients associated with high caregiver burden in Parkinson’s disease in Singapore. Frontiers in Neurology, 10, 561. https://doi.org/10.3389/fneur.2019.00561. (PMID: 10.3389/fneur.2019.00561311914446546916)
Tan, Q. Y., Cox, N. J., Lim, S. E. R., Coutts, L., Fraser, S. D. S., Roberts, H. C., & Ibrahim, K. (2021). The experiences of treatment burden in people with Parkinson’s disease and their caregivers: A systematic review of qualitative studies. Journal of Parkinsons Disease, 11(4), 1597–1617. https://doi.org/10.3233/jpd-212612. (PMID: 10.3233/jpd-212612)
Tessitore, A., Marano, P., Modugno, N., Pontieri, F. E., Tambasco, N., Canesi, M., Latorre, A., Lopiano, L., Sensi, M., Quatrale, R., Solla, P., Defazio, G., Melzi, G., Costanzo, A. M., Gualberti, G., di Luzio Paparatti, U., & Antonini, A. (2018). Caregiver burden and its related factors in advanced Parkinson’s disease: Data from the PREDICT study. Journal of Neurology, 265(5), 1124–1137. https://doi.org/10.1007/s00415-018-8816-9. (PMID: 10.1007/s00415-018-8816-9295161695937896)
Ting, W., & Hongmei, Y. (2019). Influencing factors of the burden among caregivers of patients with Parkinson’s disease. Chinese Nursing Research, 33(11), 1930–1933. https://doi.org/10.12102/j.issn.1009-6493.2019.11.025. (PMID: 10.12102/j.issn.1009-6493.2019.11.025)
Trapp, S., MacKenzie, J., Gonzalez-Arredondo, S., Rodriguez-Agudelo, Y., & Arango-Lasprilla, J. C. (2019). Mediating role of caregiver burden among family caregivers of patients with Parkinson’s disease in Mexico. International Journal of Psychiatry in Medicine, 54(3), 203–216. https://doi.org/10.1177/0091217418791460. (PMID: 10.1177/009121741879146030278803)
Viwattanakulvanid, P., Kaewwilai, L., Jitkritsadakul, O., Brenden, N. R., Setthawatcharawanich, S., Boonrod, N., Mekawichai, P., & Bhidayasiri, R. (2014). The impact of the nocturnal disabilities of Parkinson’s disease on caregivers’ burden: Implications for interventions. Journal of Neural Transmission, 121, S15–S24. https://doi.org/10.1007/s00702-014-1200-8. (PMID: 10.1007/s00702-014-1200-824682360)
Wagner, K. C., & Byrd, G. D. (2004). Evaluating the effectiveness of clinical medical librarian programs: A systematic review of the literature. Journal of the Medical Library Association, 92(1), 14. (PMID: 14762460314100)
Jue, W., Ranran, H., Dianyou, L., Congcong, Y., Linbin, W., Bomin, S., & Xian, Q. (2019). A study on the health-education needs of primary caregivers of Parkinson’s disease patients after deep brain stimulation. Journal of Nurses Training, 34(19), 1814–1817.
Wuthrich, V. M., & Rapee, R. M. (2019). Telephone-delivered cognitive behavioural therapy for treating symptoms of anxiety and depression in Parkinson’s disease: A pilot trial. Clinical Gerontologist, 42(4), 444–453. https://doi.org/10.1080/07317115.2019.1580811. (PMID: 10.1080/07317115.2019.158081130821649)
Xihong, G., Yin, Y., Guoping, Y., Yonghai, D., & Jianyun, L. (2017). Effect of reminiscence therapy on caregiver burden and positive experience of spouses of patients with Parkinson’s disease. China Journal of Health Psychology, 25(7), 1073–1075.
Yan, H., & Yufang, H. (2018). Evidence-based nursing. People’s Sanitary Publishing Press.
Yang, Z., Tian, Y., Fan, Y., Liu, L., Luo, Y., Zhou, L., & Yu, H. (2019). The mediating roles of caregiver social support and self-efficacy on caregiver burden in Parkinson’s disease. Journal of Affective Disorders, 256, 302–308. https://doi.org/10.1016/j.jad.2019.05.064. (PMID: 10.1016/j.jad.2019.05.06431200168)
Yinghua, X., Yi, L., & Qiuping, L. (2015). Research status on family caregiver burden scale for cancer patients. Chinese Nursing Management, 15(2), 246–249. https://doi.org/10.3969/j.issn.1672-1756.2015.02.038. (PMID: 10.3969/j.issn.1672-1756.2015.02.038)
Zhang, Q., Miao, L., He, L., & Wang, H. (2022). The relationship between self-concept and negative emotion: A moderated mediation model. International Journal of Environmental Research and Public Health, 19(16), 10377. https://doi.org/10.3390/ijerph191610377. (PMID: 10.3390/ijerph191610377360120219407814)
Zhong, M., Evans, A., Peppard, R., & Velakoulis, D. (2013). Validity and reliability of the PDCB: A tool for the assessment of caregiver burden in Parkinson’s disease. International Psychogeriatrics, 25(9), 1437–1441. https://doi.org/10.1017/s1041610213000586. (PMID: 10.1017/s104161021300058623635603)
معلومات مُعتمدة: FNF202324 Fu Xing Nursing Scientific Research Fund of Fudan University
فهرسة مساهمة: Keywords: Caregiver burden; DBS; Deep brain stimulation; Meta-analysis; Parkinson disease; Systematic review
تواريخ الأحداث: Date Created: 20240404 Date Completed: 20240613 Latest Revision: 20240617
رمز التحديث: 20240617
DOI: 10.1007/s11136-024-03616-0
PMID: 38573387
قاعدة البيانات: MEDLINE
الوصف
تدمد:1573-2649
DOI:10.1007/s11136-024-03616-0