Literature DB >> 28766464

Stigma and illness uncertainty: adding to the burden of sickle cell disease.

Alphanso Blake1, Vikram Asnani2, Robin R Leger3, June Harris1, Victoria Odesina4, Daileann L Hemmings5, Denise A Morris6, Jennifer Knight-Madden1, Linda Wagner7, Monika Rani Asnani1.   

Abstract

BACKGROUND: Persons with sickle cell disease (SCD) experience multiple medical and physical complications; the disease also has numerous effects on their social and emotional well-being. We hypothesized that adults with SCD in Jamaica experience moderate levels of stigma and illness uncertainty and that these experiences may be associated with socio-demographic factors, such as gender, educational status and economic status.
METHODS: We surveyed 101 adults with SCD (54.5% female; mean age 31.6 ± 10.4 years; 72.2% homozygous SCD) using the Stigma in Sickle Cell Disease Scale (Adult), Mishel Uncertainty in Illness Scale (Adult) and a Socio-Demographic questionnaire.
RESULTS: The mean stigma score was 33.6 ± 21.6 (range: 2-91) with no significant difference between males and females (32.3 ± 21.3 vs. 34.7 ± 21.9; p-value = 0.58). Illness uncertainty was greater in females than in males, though not statistically significant, (88.7 ± 13.5 vs. 82.6 ± 19.2; p-value: 0.07). Stigma and uncertainty had a significant positive correlation (r: 0.31; p-value: 0.01). In an age and sex controlled model, stigma scores were lower with higher numbers of household items (coef: -2.26; p-value: 0.001) and higher in those living in greater crowding (coef: 7.89; p-value: 0.002). Illness uncertainty was higher in females (coef: 6.94; p-value: 0.02) and lower with tertiary as compared with primary education (coef: -16.68; p-value: 0.03).
CONCLUSION: The study highlights socioeconomic factors to be significant to the stigma and illness uncertainty experiences in SCD. Efforts by healthcare workers to reduce patient illness uncertainty may have additional impact, reducing their stigma.

Entities:  

Keywords:  Jamaica; Stigma; illness uncertainty; sickle cell disease; socioeconomic status

Mesh:

Year:  2017        PMID: 28766464     DOI: 10.1080/10245332.2017.1359898

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  5 in total

1.  Stigma of Sickle Cell Disease: A Systematic Review.

Authors:  Dominique Bulgin; Paula Tanabe; Coretta Jenerette
Journal:  Issues Ment Health Nurs       Date:  2018-04-13       Impact factor: 1.835

2.  Exploring self-management in adult sickle cell disease patients' at a Teaching Hospital in Ghana.

Authors:  Ninon P Amertil; Elikem Keli Ayitey; Doris Grace Kpongboe; Priscilla Y A Attafuah
Journal:  Nurs Open       Date:  2020-12-27

3.  To Explore the Application Effect and Value of Evidence-Based Nursing in Patients with Pregnancy-Induced Hypertension Syndrome.

Authors:  Xueying Han; Paul Froilan U Garma; Hongmei Quan; Yuqing Zhang
Journal:  Contrast Media Mol Imaging       Date:  2022-08-26       Impact factor: 3.009

4.  Implementation of Individualized Pain Care Plans Decreases Length of Stay and Hospital Admission Rates for High Utilizing Adults with Sickle Cell Disease.

Authors:  Jena L Welch-Coltrane; Anthony A Wachnik; Meredith C B Adams; Cherie R Avants; Howard A Blumstein; Amber K Brooks; Andrew M Farland; Joshua B Johnson; Manoj Pariyadath; Erik C Summers; Robert W Hurley
Journal:  Pain Med       Date:  2021-08-06       Impact factor: 3.750

5.  Not being heard: barriers to high quality unplanned hospital care during young people's transition to adult services - evidence from 'this sickle cell life' research.

Authors:  Alicia Renedo; Sam Miles; Subarna Chakravorty; Andrea Leigh; Paul Telfer; John O Warner; Cicely Marston
Journal:  BMC Health Serv Res       Date:  2019-11-21       Impact factor: 2.655

  5 in total

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