Warren Alpert Medical School of Brown University, Providence, RI.
J Pediatr Orthop. 2022 Oct 1;42(9):e954-e959. doi: 10.1097/BPO.0000000000002224. Epub 2022 Aug 11.
Health care disparities are prevalent within pediatric orthopaedics in the United States. Social determinants of health, such as income, race, social deprivation, place of residence, and parental involvement, all play a role in unequal access to care and disparate outcomes. Although there has been some effort to promote health equity both within pediatric orthopaedics and the US health care system altogether, disparities persist. In this review, we aim to identify major sources of inequality and propose solutions to achieve equitable care in the future.
We searched the PubMed database for papers addressing disparities in pediatric orthopaedics published between 2016 and 2021, yielding 283 papers.
A total of 36 papers were selected for review based upon new findings. Insurance status, race, and social deprivation are directly linked to poorer access to care, often resulting in a delay in presentation, time to diagnostic imaging, and surgery. Although these disparities pervade various conditions within pediatric orthopaedics, they have most frequently been described in anterior cruciate ligament/meniscal repairs, tibial spine fractures, adolescent idiopathic scoliosis, and upper extremity conditions. Treatment outcomes also differ based on insurance status and socioeconomic status. Several studies demonstrated longer hospital stays and higher complication rates in Black patients versus White patients. Patients with public insurance were also found to have worse pain and function scores, longer recoveries, and lower post-treatment follow-up rates. These disparate outcomes are, in part, a response to delayed access to care.
Greater attention paid to health care disparities over the past several years has enabled progress toward achieving equitable pediatric orthopaedic care. However, delays in access to pediatric orthopaedic care among uninsured/publicly insured, and/or socially deprived individuals remain and consequently, so do differences in post-treatment outcomes. Reducing barriers to care, such as insurance status, transportation and health literacy, and promoting education among patients and parents, could help health care access become more equitable.
Level IV-narrative review.
在美国儿科骨科领域,医疗保健差异普遍存在。健康的社会决定因素,如收入、种族、社会贫困、居住地和父母参与度,都对获得医疗保健的不平等和不同的结果产生影响。尽管在儿科骨科和整个美国医疗保健系统内都有一些促进健康公平的努力,但差异仍然存在。在这篇综述中,我们旨在确定不平等的主要来源,并提出未来实现公平医疗的解决方案。
我们在 PubMed 数据库中搜索了 2016 年至 2021 年期间发表的关于儿科骨科领域差异的论文,共得到 283 篇论文。
根据新发现,共选择了 36 篇论文进行综述。保险状况、种族和社会贫困与较差的医疗保健获取直接相关,这往往导致就诊延迟、影像学诊断和手术时间延迟。尽管这些差异普遍存在于儿科骨科的各种疾病中,但在前交叉韧带/半月板修复、胫骨棘突骨折、青少年特发性脊柱侧凸和上肢疾病中最为常见。治疗结果也因保险状况和社会经济地位而异。几项研究表明,黑人患者比白人患者的住院时间更长,并发症发生率更高。还发现,有公共保险的患者疼痛和功能评分更差、恢复时间更长、治疗后随访率更低。这些不同的结果部分是由于获得医疗保健的延迟。
过去几年,人们更加关注医疗保健差异,这使得在实现公平的儿科骨科护理方面取得了进展。然而,无保险/公共保险和/或社会贫困人群获得儿科骨科护理的延迟仍然存在,因此,治疗后结局的差异仍然存在。减少医疗保健障碍,如保险状况、交通和健康素养,以及促进患者和家长的教育,可能有助于使医疗保健获得更加公平。
四级-叙述性综述。