Pengaruh Terapi Kelompok terhadap Peningkatan Kualitas Hidup Penderita Kusta: Literature Review

Ernawati Hatuwe, Arlina Dewi

Abstract


Leprosy is an infectious disease that causes very complex problems. The quality of life of people affected by leprosy is a matter that needs to be considered, Quality of life (QOL) includes physical health, psychological health, level of independence, social occupancy, personal trust, and relationships with the environment. How to improve the quality of life for lepers. Method: Search from 3 databases namely Pubmed, ProQuest and Google Cindekia using keywords of quality of life or Qol or hqrl and leprosy or morbus hansen or leprae or leprosy and self help groups or mutual-help groups or support group or therapy group or self concept This review identified 10 articles that fit the inclusion criteria. Most articles use quantitative, namely cross-sectional design, 6 articles and 1 article using quasi-experiment, 2 qualitative articles and 1 review literature article. Of the 10 articles selected, 4 articles focused on the quality of life for people affected by leprosy and 6 articles that discussed improving the quality of life for people affected by leprosy. Group therapy can improve the quality of life of people affected by leprosy and make leprosy sufferers have a deeper confidence in facing the community or the environment around


Keywords


Quality of life, leprosy, self help group

Full Text:

PDF

References


Dary, D., & Batubara, S. O. (2017). Penderita Lepra Dan Peran Perawat Terkait Stigma Pada Penderita Lepra: Studi Fenomenologi. Media Kesehatan Masyarakat Indonesia. https://doi.org/10.1002/asna.18871160307

de Vries, H. J. C., de Groot, R., & van Brakel, W. H. (2014). Social Participation of Diabetes and Ex-Leprosy Patients in the Netherlands and Patient Preference for Combined Self-Care Groups. Frontiers in Medicine, 1(August), 1–6. https://doi.org/10.3389/fmed.2014.00021

Fajar Rinawati & Moh Alimansur. (2016), (23), 83–88.

Hane, L. O., & Arsin, A. A. (2017). Faktor Yang Mempengaruhi Kualitas Hidup Penderita Kusta Factors Affecting Life Quality Of Leprosy Patients In Central Maluku Regency In 2017 Departemen Epidemiologi , Fakultbas Kesehatan Masyarakat Universitas Hasanuddin Departemen Epidemiologi , Fakultba, 1.

Kemenkes RI. (2018). Jumlah kasus penyakit hipertensi terbanyak di Pekanbaru tahun 2016. https://doi.org/10.1111/evo.12990

Lusli, M., Peters, R., Bunders, J., Irwanto, I., & Zweekhorst, M. (2017). Development of a rights-based counselling practice and module to reduce leprosy-related stigma and empower people affected by leprosy in Cirebon District, Indonesia. Leprosy Review, 88(3), 318–333.

Maziyya, N., Nursalam, & Mariyanti, H. (2016). Kualitas Hidup Penderita Kusta Berbasis Teori Health Belief Models (HBM). Jurnal INJEC, 1(1), 96–102.

Nugraheni, R. (2016). Analisis Konsep Diri Terhadap Kualitas Hidup Penderita Kusta Yang Mengalami Kecacatan Di Rumah Sakit Kusta Kediri. Jurnal Preventia, 1. Retrieved from journal.um.ac.id/index.php/preventia/article/download/8846/4252

Pryce, J., Mableson, H. E., Choudhary, R., Pandey, B. D., Aley, D., Betts, H., … Cross, H. (2018). Assessing the feasibility of integration of self-care for filarial lymphoedema into existing community leprosy self-help groups in Nepal. BMC Public Health, 18(1), 1–13. https://doi.org/10.1186/s12889-018-5099-0

Pusat Data dan Informasi Kementerian Kesehatan RI. (2015). Info, Data, dan Informasi Kusta.

Santos, et al. (2015). Functional Activity Limitation and Quality of Life of Leprosy Cases in an Endemic Area in Northeastern Brazil, 1–8. https://doi.org/10.1371/journal.pntd.0003900

Savassi, L. C. M., Bogutchi, T. R. S., Lima, A. C. L., & Modena, C. M. (2014). Quality of life of leprosy sequelae patients living in a former leprosarium under home care: univariate analysis. Quality of Life Research : An International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation, 23(4), 1345–1351. https://doi.org/10.1007/s11136-013-0590-7

Sermrittirong, S., & van Brakel, W. H. (2014). How to reduce stigma in leprosy – a systematic literature review. Leprosy Review, 85(3), 149–157. Retrieved from http://www.lepra.org.uk/platforms/lepra/files/lr/Sept14/1889.pdf

Susanto, et al. (2017). The experiences of people affected by leprosy who participated in self-care groups in the community : A qualitative study in Indonesia, 543–553.




DOI: http://dx.doi.org/10.33087/jiubj.v19i2.605

Refbacks

  • There are currently no refbacks.


Creative Commons License
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

JIUBJ: Jurnal Ilmiah Universitas Batanghari Jambi
ISSN: 1411-8939 (print), ISSN: 2549-4236 (online)
Telpon: 0741670700
e-mail: jiubj.unbari@gmail.com | lppm@unbari.ac.id

Lisensi Creative Commons
Ciptaan disebarluaskan di bawah Lisensi Creative Commons Atribusi-BerbagiSerupa 4.0 Internasional.