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综合评论:1970 年至今,提供者在照顾镰状细胞病患者方面的知识、态度、观念和感知障碍的演变。

An Integrative Review: The Evolution of Provider Knowledge, Attitudes, Perceptions and Perceived Barriers to Caring for Patients with Sickle Cell Disease 1970-Now.

机构信息

M. Louise Fitzpatrick College of Nursing, 16196Villanova University, Villanova, PA, USA.

Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Pediatr Hematol Oncol Nurs. 2023 Jan-Feb;40(1):43-64. doi: 10.1177/27527530221090179. Epub 2022 Jul 19.

Abstract

Approximately 100,000 Americans have sickle cell disease (SCD). In the USA, the majority of patients with SCD are of African descent. Due to persistent racial and ethnic disparities in healthcare in the USA, patients with SCD experience disproportionately more health inequities because of providers' implicit biases regarding patient race. Lack of access to health insurance, lack of transportation to healthcare providers, and inadequate provider knowledge contribute to the morbidity and mortality of patients with SCD. The purpose of this integrative review was to analyze and synthesize the literature on providers' knowledge, perceptions, beliefs, and attitudes toward patients with SCD. A modified (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) method was used to conduct a comprehensive review of the literature yielding 31 publications included in this review. Three connected, yet distinct areas of focus were identified: (1) providers' knowledge, attitudes, and perceptions of patients with SCD; (2) providers' perceived or true barriers to caring for patients with SCD; and (3) interventions to improve providers' attitudes, perceptions, and care of patients with SCD. In each area of focus, research has evolved over time. Also included in this integrative review is a synthesis of measurement instruments used to assess provider knowledge, attitudes, perceptions, and perceived and true barriers to caring for patients with SCD. Adolescents with SCD who are transitioning from pediatric to adult care are at a particularly high risk for morbidity and mortality, so this review focused on the many opportunities that exist to advance the healthcare for young adults with SCD to improve patient outcomes later in life. This includes improving providers' knowledge, perceptions, beliefs, and attitudes, and lessening the real or perceived barriers to care for patients with SCD.

摘要

大约有 10 万名美国人患有镰状细胞病(SCD)。在美国,大多数 SCD 患者为非裔。由于美国医疗保健领域持续存在种族和民族差异,SCD 患者由于提供者对患者种族的隐性偏见,经历了不成比例的更多健康不平等。由于缺乏医疗保险、获得医疗保健提供者的交通方式不足以及提供者知识不足,导致 SCD 患者的发病率和死亡率增加。本综合评价的目的是分析和综合关于提供者对 SCD 患者的知识、看法、信念和态度的文献。使用改良(系统评价和荟萃分析的首选报告项目)方法对文献进行全面审查,共纳入 31 篇文献。确定了三个相互关联但又不同的重点领域:(1)提供者对 SCD 患者的知识、态度和看法;(2)提供者认为或真正的护理 SCD 患者的障碍;(3)改善提供者对 SCD 患者的态度、看法和护理的干预措施。在每个重点领域,研究都随着时间的推移而发展。本综合评价还综合了用于评估提供者知识、态度、看法以及护理 SCD 患者的感知和真实障碍的测量工具。从儿科过渡到成人护理的 SCD 青少年处于高发病率和死亡率的特别高风险中,因此,本综述重点关注为改善青少年 SCD 患者的医疗保健以改善其以后生活的患者结局而存在的许多机会。这包括提高提供者的知识、看法、信念和态度,以及减少对 SCD 患者的护理的实际或感知障碍。

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