Electronic ISSN 2287-0237

VOLUME

INTEGRATIVE REVIEW FOR FACTORS RELATED TO FAMILY FUNCTIONING IN THE FAMILY LIVING WITH THE CHILDREN WITH THALASSEMIA

SEPTEMBER 2020 - VOL.16 | REVIEWS ARTICLE
  1. Keshvari M, Ebrahimi A, Abedi H. Relation between children’s well-being and family function in children with thalassemia major in Isfahan in 2013. Global J Health Science 2016; 8(12): 170-7. doi:10.5539/gjhs.v8n12p170

  2. Vaz JC, Milbrth VM, Gbatz RI, et al. Care for families of children with chronic disease: Integrative review. J Nurse UFPE online 2018;12(5):1397-408.

  3. Adanir AS, Taskiran G, Fettahoglu EC, et al. Psychopathology and family functioning in adolescents with beta thalassemia. Adolescent Psychiatry 2017;7(1):4-12.

  4. Wacharasin C, Phaktoop M, Sananreangsak S. A family empowerment program for families having children with thalassemia, Thailand. Nurs Health Sci 2015;17(3):387-94.

  5. Herzer M, Godiwala N, Hommel KA, et al. Family function- ing in the context of pediatric chronic conditions. J Dev Behav Pediatr 2010;31(1):26-34.

  6. Punaglom N, Kongvattananon P, Somprasert C. Experience of parents caring for their children with thalassemia: Challenges and issues for integrative review. BKK Med Jl 2019; 15(1): 100-6.

  7. Thanarattanakorn P, Louthrenoo O, Sittipreechacharn S, et al. Family functioning in children with thalassemia. Clin Pediatr 2003; 42(1): 79-82.

  8. Pouraboli B, Abedi HA, Abbaszadeh A, et al. The burden of care: Experiences of parents of children with thalassemia. J Nurs Care 2017;6(2). doi: 10.4172/2167-1168.1000389

  9. Aziz A, Mohammed S, Aburaghif L. Burden of caregiver care for children with thalassemia at Babylon Child and Mater- nity Teaching Hospital / Babylon Governorate / Iraq. IOSR J Nurs Health Scie 2015;4(6):82–7. 

  10. Shosha GA, Kalaldeh MA. Challenges of having a child with thalassemia major: a phenomenological study. J Res Nurs 2018; 23(1): 9-20.

  11. Moher D, Shamseer L, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Systematic Reviews. (Accessed January 16, 2017 at http://dx.doi.org/10.1186/2046-40-1).

  12. Joanna Briggs Institute. Joanna Briggs Institute reviewers’ manual: 2014 edition. Adelaide: SA, 2014. (Accessed January 16, 2017 at http://joannabriggs.org/assets/docs/sumari/Re- viewersManual-2014.pdf.).

  13. Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA Statement. PLoS Med 2009; (7): e1000097.

  14. Anum J, Dasti R. Caregiver burden, spirituality, and psycho- logical well-being of parents having children with thalassemia. J Relig Health 2016; 55(3): 941-55.

  15. Efe E, Isler A, Sarvan S, et al. Complementary and alternative medicine use in children with thalassemia. J Clin Nurs 2012; 22: 760–69.

  16. Nabors LA, Kichler JC, Brassell A, et al. Factors related to caregiver state anxiety and coping with a child’s chronic illness. Fam Syst Health 2013;31(2):171-80.

  17. Kermansaravi F, Najafi F, Rigi S. Coping behaviors in parents of children with thalassemia major. Med Surg Nurs J 2018;7(1):e81173.

  18. Chusri O, Deoisres W, Riper MV. Influencing of family management in families with thalassemic children on health- related quality of life and family functioning: SEM approach. Walailak J Sci Tech 2019;16(1):27-38.

  19. Maheen H, Malik F, Siddique B, et al. Assessing parental knowledge about thalassemia in a thalassemia center of Ka- rachi, Pakistan. J Genet Counsel 2015;24(6):945–51.

  20. Zaheer Z, Wazir S, Hameed B, et al. Psychological burden in β-thalassemia affected families. J Postgrad Med Inst 2015;29(4):260-3.

  21. Habibzadeh F, Yadollahie M, Roshanipoor M, et al. Reproductive behaviour of mothers of children with beta-thalassaemia major. East Mediterr Health J 2012;18(3): 246-50.

  22. Gold JI, Treadwell M, Weissman L, et al. An expanded transactional stress and coping model for siblings of children with sickle cell disease: family functioning and sibling coping, self-efficacy and perceived social support. Child Care Health Dev 2008;34(4):491–502.

  23. Kostak MA, Avci G. Hopelessness and depression levels of parents of children with cancer. Asian Pac J Cancer Prev 2013;14(11):6833-8.

  24. Chaiyasit Y, Thong-on R, Piboonrungroj P, et al. The role of the spirituality in people living with HIV/AIDS: A qualitative meta-synthesis. BKK Med J 2019;15(1):113-20.

  25. Årestedt L, Benzein E, Persson C. Families living with chronic illness: Beliefs about illness, family, and health care. J Fam Nurs 2015; 21(2): 206–31.

  26. Rosland AM, Heisler M, Piette JD. The impact of family behaviors and communication patterns on chronic illness outcomes: A systematic review. J Behav Med2012;35:221-39.

  27. Ghazanfari Z, Arab M, Forouzi M, et al. Knowledge level and educational needs of thalassemic children’s parents in Kerman. J Crit Care Nurs 2010;3:e7143.

  28. Wahab JA, Naznin M, Nora MZ, et al. Thalassaemia: a study on the perception of patients and family members. Med J Malaysia 2011;6:326-34.

  29. Ishfaq K, Ali AA, Hashmi M. Mothers’ awareness and experiences of having a thalassemic child: A qualitative ap- proach. PJSS 2015:35(1):109-21.

SEARCH VOLUME & NUMBER
GO
RECENT VOLUME & NUMBER