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格林纳达的镰状细胞病:生活质量和医疗障碍。

Sickle cell disease in Grenada: Quality of life and barriers to care.

机构信息

School of Allied Health, Baylor College of Medicine, Houston, TX, USA.

Department of Biochemistry, St. George's University School of Medicine, St. George's, Grenada.

出版信息

Mol Genet Genomic Med. 2021 Jan;9(1):e1567. doi: 10.1002/mgg3.1567. Epub 2020 Dec 17.

Abstract

BACKGROUND

Grenada is a small, resource-limited Caribbean country with a high incidence of sickle cell disease (SCD). Since little is known about the challenges facing individuals living with SCD in the West Indies, we sought to assess barriers to healthcare and the impact of SCD on quality of life in Grenada.

METHODS

Both adults aged 18+ (n = 19) and caregivers of children aged 2-17 (n = 26) completed validated survey measures regarding barriers to care and quality of life, along with a genetics knowledge questionnaire. Caregivers also completed a caregiver burden scale. Survey scores were calculated, and responses were analyzed for an association between demographic variables.

RESULTS

The Barriers to Care Questionnaire, in which lower scores indicate more barriers, revealed that both adults (mean = 69.9) and children (mean = 75.5) with SCD experienced reduced access to care. The Adult Sickle Cell Quality of Life Measurement Information System indicated increased depression and loneliness in adults, with the lowest scores in the Emotional subscale. However, the Pediatric Quality of Life Inventory answered by caregivers of children with SCD showed the lowest scores in the Physical Functioning subscale. Further analysis using the Caregiver Burden Scale-Zarit Burden Interview revealed that 53.8% of caregivers of children with SCD indicated "little to no burden," which may reflect a difference in cultural expectations of a caregiver between high-income countries and Grenada. Finally, ~80% of respondents knew that SCD was a genetic condition; however, 61%-84% could not correctly indicate recurrence risks, demonstrating a need for additional education.

CONCLUSION

These data provide new insights regarding the experience of living with SCD in Grenada and support the need for further investigations into specific barriers to healthcare delivery, which could also improve education and well-being for those affected by SCD in Grenada and in the broader Caribbean community.

摘要

背景

格林纳达是一个资源有限的加勒比小国,镰状细胞病(SCD)发病率很高。由于人们对西印度群岛中患有 SCD 的个体所面临的挑战知之甚少,因此我们试图评估格林纳达医疗保健的障碍以及 SCD 对生活质量的影响。

方法

年龄在 18 岁及以上的成年人(n=19)和年龄在 2-17 岁的儿童的照顾者(n=26)都完成了有关障碍和生活质量的验证性调查措施,以及一个遗传知识问卷。照顾者还完成了照顾者负担量表。计算了调查评分,并分析了人口统计学变量之间的关联。

结果

障碍量表(Barriers to Care Questionnaire)的得分越低表明障碍越大,结果表明患有 SCD 的成年人(平均得分=69.9)和儿童(平均得分=75.5)都面临着医疗服务减少的问题。成人 Sickle Cell Quality of Life Measurement Information System 表明成年人的抑郁和孤独感增加,其中情绪子量表的得分最低。但是,由患有 SCD 的儿童的照顾者回答的儿科生活质量清单(Pediatric Quality of Life Inventory)显示,生理功能子量表的得分最低。进一步使用照顾者负担量表-Zarit 负担访谈进行分析发现,61%-84%的照顾者不能正确指出复发风险,这表明需要进一步的教育。

结论

这些数据提供了关于格林纳达 SCD 患者生活体验的新见解,并支持对医疗保健提供的具体障碍进行进一步研究,这也可以改善格林纳达和更广泛的加勒比社区中受 SCD 影响的人的教育和福祉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f85d/7963427/454cbd3ad399/MGG3-9-e1567-g001.jpg

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