Literature DB >> 7792634

The psychosocial problems of sickle cell disease sufferers and their methods of coping.

J U Ohaeri1, W A Shokunbi, K S Akinlade, L O Dare.   

Abstract

We interviewed 170 sickle cell disease (SCD) patients (mean age 25 years) with a modified version of the Frankfurter Befindlichkeitskala (FBS, 33-item) and the 12-item General Health Questionnaire (GHQ-12), with a view to highlighting the psychosocial issues which worry them, the way they cope with these problems, and the factors associated with these issues. The mean FBS score of SCD patients was comparable with those of insulin dependent diabetics, but significantly higher than that of non-insulin dependent diabetics. The FBS scores were significantly correlated with GHQ-12 scores. Feelings of inadequacy of social contact were significantly associated with high FBS and GHQ scores. Some common complaints were: the limitations illness placed on social life; depressive feelings; abnormal habitus; suicidal ideation during crises; and the burden of illness on the family. They frequently resorted to prayers as a method of coping, as most had no clear ideas on how to deal with these issues. Worries over psychosocial consequences of SCD, seem to add considerably to the burden of illness, and clinicians will offer better care to patients if they routinely enquire into some of these issues and offer health education and counselling in a group setting.

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Year:  1995        PMID: 7792634     DOI: 10.1016/0277-9536(94)00154-l

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  18 in total

1.  Relation Between Religious Perspectives and Views on Sickle Cell Disease Research and Associated Public Health Interventions in Ghana.

Authors:  Jemima A Dennis-Antwi; Kwaku Ohene-Frempong; Kofi A Anie; Helen Dzikunu; Veronica A Agyare; Richard Okyere Boadu; Joseph Sarfo Antwi; Mabel K Asafo; Oboshie Anim-Boamah; Augustine K Asubonteng; Solomon Agyei; Ambroise Wonkam; Marsha J Treadwell
Journal:  J Genet Couns       Date:  2018-09-01       Impact factor: 2.537

2.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

3.  Psychosocial stressors of sickle cell disease on adult patients in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2014-02-21       Impact factor: 2.537

4.  Utility of WHOQOL-BREF in measuring quality of life in sickle cell disease.

Authors:  Monika R Asnani; Garth E Lipps; Marvin E Reid
Journal:  Health Qual Life Outcomes       Date:  2009-08-10       Impact factor: 3.186

5.  Depression and loneliness in Jamaicans with sickle cell disease.

Authors:  Monika R Asnani; Raphael Fraser; Norma A Lewis; Marvin E Reid
Journal:  BMC Psychiatry       Date:  2010-06-07       Impact factor: 3.630

6.  Tackling Africa's chronic disease burden: from the local to the global.

Authors:  Ama de-Graft Aikins; Nigel Unwin; Charles Agyemang; Pascale Allotey; Catherine Campbell; Daniel Arhinful
Journal:  Global Health       Date:  2010-04-19       Impact factor: 4.185

7.  Psychosocial impact of sickle cell disorder: perspectives from a Nigerian setting.

Authors:  Kofi A Anie; Feyijimi E Egunjobi; Olu O Akinyanju
Journal:  Global Health       Date:  2010-02-20       Impact factor: 4.185

8.  The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study.

Authors:  Shawn M Bediako; Sophie Lanzkron; Marie Diener-West; Gladys Onojobi; Mary C Beach; Carlton Haywood
Journal:  J Health Psychol       Date:  2014-07-04

9.  Psychosocial burden of sickle cell disease on caregivers in a Nigerian setting.

Authors:  Jude U Ohaeri; Wuraola A Shokunbi
Journal:  J Natl Med Assoc       Date:  2002-12       Impact factor: 1.798

10.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

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