综合回顾:1970年至今护理镰状细胞病患者的提供者知识、态度、观念和感知障碍的演变

IF 1 4区 医学 Q3 NURSING
Jessie Reich, Mary Ann Cantrell, Suzanne C Smeltzer
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引用次数: 6

摘要

大约100,000美国人患有镰状细胞病(SCD)。在美国,大多数SCD患者是非洲裔。由于美国医疗保健中持续存在种族和民族差异,由于提供者对患者种族的隐性偏见,SCD患者经历了不成比例的更多健康不平等。缺乏获得医疗保险的机会,缺乏前往医疗保健提供者的交通工具,以及提供者知识不足导致SCD患者的发病率和死亡率。本综合综述的目的是分析和综合有关提供者对SCD患者的知识、观念、信念和态度的文献。采用改良的(系统评价和荟萃分析的首选报告项目)方法对纳入本综述的31篇出版物的文献进行综合评价。确定了三个相互关联但又截然不同的重点领域:(1)提供者对SCD患者的知识、态度和看法;(2)提供者对SCD患者护理的感知或真实障碍;(3)改善提供者对SCD患者的态度、认知和护理的干预措施。在每个重点领域,研究都随着时间的推移而发展。该综合综述还包括用于评估提供者知识、态度、观念以及护理SCD患者的感知和真实障碍的测量工具的综合。从儿科过渡到成人护理的青少年SCD发病率和死亡率特别高,因此本综述关注许多存在的机会,以推进年轻SCD患者的医疗保健,以改善患者以后的生活结果。这包括改善提供者的知识、观念、信念和态度,并减少对SCD患者护理的实际或感知障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Integrative Review: The Evolution of Provider Knowledge, Attitudes, Perceptions and Perceived Barriers to Caring for Patients with Sickle Cell Disease 1970-Now.

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.

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CiteScore
3.30
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