Nörolojik Hastalık ve Evlilik

Evlilik, insanların mutluluğunu ve yaşam süresini etkiler. Araştırmalar, evli insanların daha sağlıklı, daha mutlu ve diğer insanlardan (bekar, boşanmış ve dul) daha uzun ömürlü oldukları fikrini desteklemektedir. Dünyada nörolojik hastalıkların insidansı gün geçtikçe artmaktadır. Bu hastalıklar, hastaları, ailelerini ve toplumlarını etkiler. Bununla birlikte, medeni hal, evlilik ilişkisi ve eş durumu hastanın hastalığa kabulünü ve hastalıkla baş etmesini etkiler. Amyotrofik lateral skleroz (ALS), Multipl Skleroz (MS), Alzheimer Hastalığı (AD), Parkinson Hastalığı (PD) ve inme hastaları gibi nörolojik hastalıklarda, evli hastalar diğer hastalardan daha sağlıklı ve uzun ömürlüdür. Ayrıca, evli hastalarda, MS ve epilepsi gibi hastalıklar boşanma için bir risk faktörü olabilir veya eşlerini veya evlilik ilişkilerini olumsuz etkiler. Çalışmamızda nörolojik hastalıklar ile medeni durum, boşanma, eşlerin durumu ve evlilik ilişkisi arasındaki ilişkiyi incelemeyi amaçladık.

Anahtar Kelimeler:

Nörolojik hastalıklar, evlilik, sağlık, hayat

Neurological Disease and Marriage

Marriage affects people's happiness and lifetime. Researches support the idea that married people are more healthier and happier and they have longevity than other people (single, divorced and widowed). In the world, incidence of neurological diseases increase day by day. They affects patients, their families and societies. However, marital status, marital relationship, and spouses situation affect patient's acceptance to and cope with illness. In neurological diseases such as Amyotrophic lateral sclerosis (ALS), Multiple Sclerosis (MS), Alzheimer Disease (AD), Parkinson's Disease (PD) and stroke patients, married patients are more healthier and have long life span than other patients. Then, in married patients, diseases such as MS and epilepsy can be risk factor to divorce or negatively affects their spouses or marital relationship. In the study, we aimed to examine the relation between neurological diseases and marital status, divorce, spouses' situation and marital relationship.

Keywords:

Neurological diseases, marriage, health, life,

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1. Gough EK. The Nayars and the definition of marriage. The Journal of the Royal Anthropological Institute of Great Britain and Ireland. 1959;89(1):23-34.
2. Spataro R, Volanti P, Lo Coco D, La Bella V. Marital status is a prognostic factor in amyotrophic lateral sclerosis. Acta Neurologica Scandinavica. 2017;136(6):624-30.
3. Meyer JM, Percheski C. Health behaviors and union dissolution among parents of young children: Differences by marital status. PloS one. 2017;12(8).
4. Myers JE, Madathil J, Tingle LR. Marriage satisfaction and wellness in India and the United States: A preliminary comparison of arranged marriages and marriages of choice. Journal of Counseling & Development. 2005;83(2):183-90.
5. Feigin VL, Vos T. Global Burden of Neurological Disorders: From Global Burden of Disease Estimates to Actions. Neuroepidemiology. 2019;52(1-2):1-2.
6. Lindvall O, Kokaia Z. Stem cells for the treatment of neurological disorders. Nature. 2006;441(7097):1094-6.
7. Landfeldt E, Castelo-Branco A, Svedbom A, Löfroth E, Kavaliunas A, Hillert J. The long-term impact of multiple sclerosis on the risk of divorce. Multiple sclerosis and related disorders. 2018;24:145-50.
8. Atkins L, Brown RG, Leigh PN, Goldstein LH. Marital relationships in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 2010;11(4):344-50.
9. Smith LJ, Shaw RL. Learning to live with Parkinson’s disease in the family unit: an interpretative phenomenological analysis of well-being. Medicine, Health Care and Philosophy. 2017;20(1):13-21.
10. Goutman SA, Nowacek DG, Burke JF, Kerber KA, Skolarus LE, Callaghan BC. Minorities, men, and unmarried amyotrophic lateral sclerosis patients are more likely to die in an acute care facility. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 2014;15(5-6):440-3.
11. Del Aguila M, Longstreth W, McGuire V, Koepsell T, Van Belle G. Prognosis in amyotrophic lateral sclerosis: a population-based study. Neurology. 2003;60(5):813-9.
12. Fegg MJ, Kögler M, Brandstätter M, Jox R, Anneser J, Haarmann-Doetkotte S, et al. Meaning in life in patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 2010;11(5):469-74.
13. Imaizumi Y. Mortality rate of amyotrophic lateral sclerosis in Japan: effects of marital status and social class, and geographical variation. Japanese journal of human genetics. 1986;31(2):101-11.
14. Mickens MN, Perrin PB, Aguayo A, Rabago B, Macías-Islas MA, Arango-Lasprilla JC. Mediational model of multiple sclerosis impairments, family needs, and caregiver mental health in Guadalajara, Mexico. Behavioural neurology. 2018;2018.
15. Carletto S, Borghi M, Francone D, Scavelli F, Bertino G, Cavallo M, et al. The efficacy of a Mindfulness Based Intervention for depressive symptoms in patients with Multiple Sclerosis and their caregivers: study protocol for a randomized controlled clinical trial. BMC neurology. 2016;16(1):7.
16. Simpson Jr S, Taylor KL, Jelinek GA, De Livera AM, Brown CR, O'Kearney E, et al. Associations of demographic and clinical factors with depression over 2.5-years in an international prospective cohort of people living with MS. Multiple sclerosis and related disorders. 2019;30:165-75.
17. Taylor KL, Hadgkiss EJ, Jelinek GA, Weiland TJ, Pereira NG, Marck CH, et al. Lifestyle factors, demographics and medications associated with depression risk in an international sample of people with multiple sclerosis. BMC psychiatry. 2014;14(1):327.
18. Greenberg B, Fan Y, Carriere L, Sullivan A. Depression and Age at First Neurology Appointment Associated with Receipt of Behavioral Medicine Services Within 1 Year in a Multiple Sclerosis Population. International journal of MS care. 2017;19(4):199-207.
19. Maryam Abbasi M, Nabavi SM, Seyed-Mohammad Fereshtehnejad M, Nikan Zerafatjou M, Vahid Shayegannejad M, Seyed Ehsan Mohammadianinejad M, et al. Risk factors of Multiple sclerosis and their Relation with Disease Severity: A Cross-sectional Study from Iran. Archives of Iranian medicine. 2016;19(12):852.
20. Baumstarck-Barrau K, Simeoni M-C, Reuter F, Klemina I, Aghababian V, Pelletier J, et al. Cognitive function and quality of life in multiple sclerosis patients: a cross-sectional study. BMC neurology. 2011;11(1):17.
21. Sanuade OA, Dodoo FN-A, Koram K, Aikins Ad-G. Prevalence and correlates of stroke among older adults in Ghana: Evidence from the Study on Global AGEing and adult health (SAGE). PloS one. 2019;14(3).
22. Dupre ME, Lopes RD. Marital history and survival after stroke. Journal of the American Heart Association. 2016;5(12):e004647.
23. Liu Q, Wang X, Wang Y, Wang C, Zhao X, Liu L, et al. Association between marriage and outcomes in patients with acute ischemic stroke. Journal of neurology. 2018;265(4):942-8.
24. Andersen K, Olsen T. Stroke case‐fatality and marital status. Acta Neurologica Scandinavica. 2018;138(4):377-83.
25. Saada F, Wang ZS, Bautista RED. In focus: The everyday lives of families of adult individuals with epilepsy. Epilepsy & Behavior. 2015;50:10-3.
26. Tedrus GMAS, Fonseca LC, Pereira RB. Marital status of patients with epilepsy: factors and quality of life. Seizure. 2015;27:66-70.
27. Kinariwalla N, Sen A. The psychosocial impact of epilepsy on marriage: a narrative review. Epilepsy & Behavior. 2016;63:34-41.
28. Elliott JO, Charyton C, Sprangers P, Lu B, Moore JL. The impact of marriage and social support on persons with active epilepsy. Epilepsy & behavior. 2011;20(3):533-8.
29. Ferro MA. A population-based study of the prevalence and sociodemographic risk factors of self-reported epilepsy among adults in the United Kingdom. Seizure. 2011;20(10):784-8.
30. Staniszewska A, Religioni U, Dąbrowska-Bender M. Acceptance of disease and lifestyle modification after diagnosis among young adults with epilepsy. Patient preference and adherence. 2017;11:165.
31. Dobkin RD, Rubino JT, Allen LA, Friedman J, Gara MA, Mark MH, et al. Predictors of treatment response to cognitive-behavioral therapy for depression in Parkinson's disease. Journal of Consulting and Clinical Psychology. 2012;80(4):694.
32. Kadastik-Eerme L, Rosenthal M, Paju T, Muldmaa M, Taba P. Health-related quality of life in Parkinson’s disease: a cross-sectional study focusing on non-motor symptoms. Health and quality of life outcomes. 2015;13(1):83.
33. Cui S-S, Du J-J, Fu R, Lin Y-Q, Huang P, He Y-C, et al. Prevalence and risk factors for depression and anxiety in Chinese patients with Parkinson disease. BMC geriatrics. 2017;17(1):270.
34. Li W, Ng HL, Li W, Piano AN, Karim SA, Tay KY, et al. Treatment Preferences at the End‐of‐Life in P arkinson's Disease Patients. Movement disorders clinical practice. 2016;3(5):483-9.
35. Mancino R, Martucci A, Cesareo M, Giannini C, Corasaniti MT, Bagetta G, et al. Glaucoma and Alzheimer disease: one age-related neurodegenerative disease of the brain. Current neuropharmacology. 2018;16(7):971-7.
36. Dijkstra A, Sipsma DH, Dassen TW. Care dependency and survival among female patients with Alzheimer's disease: a two-year follow-up. Croatian medical journal. 1998;39:365-70.
37. Steenland K, MacNeil J, Vega I, Levey A. Recent trends in Alzheimer's disease mortality in the United States, 1999-2004. Alzheimer disease and associated disorders. 2009;23(2):165.
38. Hernandez S, McClendon MJ, Zhou X-HA, Sachs M, Lerner AJ. Pharmacological treatment of Alzheimer's disease: effect of race and demographic variables. Journal of Alzheimer's Disease. 2010;19(2):665-72.
39. Apostolova LG, Di LJ, Duffy EL, Brook J, Elashoff D, Tseng C-H, et al. Risk factors for behavioral abnormalities in mild cognitive impairment and mild Alzheimer's disease. Dementia and geriatric cognitive disorders. 2014;37(5-6):315-26.
40. McNulty JK, Widman L. Sexual narcissism and infidelity in early marriage. Archives of sexual behavior. 2014;43(7):1315-25.
41. Mapulanga M, Nzala S, Mweemba C. The Socio‑economic Impact of Stroke on Households in Livingstone District, Zambia: A Cross‑sectional Study. Annals of medical and health sciences research. 2014;4(8):123-7.
42. Daniel K, Wolfe CD, Busch MA, McKevitt C. What are the social consequences of stroke for working-aged adults? A systematic review. Stroke. 2009;40(6):e431-e40.
43. Kim M-K, Kwon O-Y, Cho Y-W, Kim Y, Kim S-E, Kim H-W, et al. Marital status of people with epilepsy in Korea. Seizure. 2010;19(9):573-9.
44. Riasi H, Sanati AR, Ghaemi K. The stigma of epilepsy and its effects on marital status. SpringerPlus. 2014;3(1):762.
45. Agarwal P, Mehndiratta M, Antony A, Kumar N, Dwivedi R, Sharma P, et al. Epilepsy in India: nuptiality behaviour and fertility. Seizure. 2006;15(6):409-15.
46. Ahmadi Forooshany SH, Yazdkhasti F, Safari Hajataghaie S, Nasr Esfahani MH. Infertile individuals' marital relationship status, happiness, and mental health: a causal model. Int J Fertil Steril. 2014;8(3):315-24.
47. Tompkins SA, Roeder JA, Thomas JJ, Koch KK. Effectiveness of a relationship enrichment program for couples living with multiple sclerosis. International journal of MS care. 2013;15(1):27-34.
48. Amudhan S, Gururaj G, Satishchandra P. Epilepsy in India II: Impact, burden, and need for a multisectoral public health response. Annals of Indian Academy of Neurology. 2015;18(4):369.
49. Moschetta S, Valente KD. Impulsivity and seizure frequency, but not cognitive deficits, impact social adjustment in patients with juvenile myoclonic epilepsy. Epilepsia. 2013;54(5):866-70.
50. Schrag A, Hovris A, Morley D, Quinn N, Jahanshahi M. Caregiver-burden in Parkinson's disease is closely associated with psychiatric symptoms, falls, and disability. Parkinsonism & related disorders. 2006;12(1):35-41.
51. Schrag A, Hovris A, Morley D, Quinn N, Jahanshahi M. Young‐versus older‐onset Parkinson's disease: impact of disease and psychosocial consequences. Movement disorders: official journal of the Movement Disorder Society. 2003;18(11):1250-6.
52. Simonelli C, Tripodi F, Rossi R, Fabrizi A, Lembo D, Cosmi V, et al. The influence of caregiver burden on sexual intimacy and marital satisfaction in couples with an Alzheimer spouse. International Journal of Clinical Practice. 2008;62(1):47-52.
53. Ascher EA, Sturm VE, Seider BH, Holley SR, Miller BL, Levenson RW. Relationship satisfaction and emotional language in frontotemporal dementia and Alzheimer’s disease patients and spousal caregivers. Alzheimer disease and associated disorders. 2010;24(1):49.
54. Grabler MR, Weyen U, Juckel G, Tegenthoff M, Mavrogiorgou-Juckel P. Death anxiety and depression in amyotrophic lateral sclerosis patients and their primary caregivers. Frontiers in neurology. 2018;9:1035.
55. Galvin M, Corr B, Madden C, Mays I, McQuillan R, Timonen V, et al. Caregiving in ALS–a mixed methods approach to the study of burden. BMC palliative care. 2016;15(1):81.
56. Rakhshan M, Ganjalivand S, Zarshenas L, Majdinasab N. The Effect of Collaborative Care Model-Based Intervention on Hope in Caregivers and Patients with Multiple Sclerosis: A Randomized Controlled Clinical Trial. International journal of community based nursing and midwifery. 2018;6(3):218.
57. McKenzie T, Quig ME, Tyry T, Marrie RA, Cutter G, Shearin E, et al. Care partners and multiple sclerosis: differential effect on men and women. International journal of MS care. 2015;17(6):253-60.
58. Costa TFd, Gomes TM, Viana LRdC, Martins KP, Costa KNdFM. Acidente vascular encefálico: características do paciente e qualidade de vida de cuidadores. Revista Brasileira de Enfermagem. 2016;69(5):933-9.
59. Lutz BJ, Young ME, Creasy KR, Martz C, Eisenbrandt L, Brunny JN, et al. Improving stroke caregiver readiness for transition from inpatient rehabilitation to home. The Gerontologist. 2017;57(5):880-9.
60. Penovich PE, Buelow J, Steinberg K, Sirven J, Wheless J. Burden of Seizure Clusters on Patients With Epilepsy and Caregivers. The neurologist. 2017;22(6):207-14.
61. Karakis I, Cole AJ, Montouris GD, San Luciano M, Meador KJ, Piperidou C. Caregiver burden in epilepsy: determinants and impact. Epilepsy research and treatment. 2014;2014.
62. Baik JS, Kim J-S, Koh S-B, Cho JW, Lee PH, Ma H-I, et al. Patients and their caregivers’ burdens for Parkinson’s disease in Korea. Journal of movement disorders. 2017;10(3):109.
63. Tessitore A, Marano P, Modugno N, Pontieri FE, Tambasco N, Canesi M, et al. Caregiver burden and its related factors in advanced Parkinson’s disease: data from the PREDICT study. Journal of neurology. 2018;265(5):1124-37.
64. Alqahtani MS, Alshbriqe AA, Awwadh AA, Alyami TA, Alshomrani MS, Alhazzani A. Prevalence and Risk Factors for Depression among Caregivers of Alzheimer’s Disease Patients in Saudi Arabia. Neurology research international. 2018;2018.
65. Goren A, Montgomery W, Kahle-Wrobleski K, Nakamura T, Ueda K. Impact of caring for persons with Alzheimer’s disease or dementia on caregivers’ health outcomes: findings from a community based survey in Japan. BMC geriatrics. 2016;16(1):122.