Revealing a Cleft in the Community: A Systematic Review of Sociodemographic Disparities Affecting the Care of Patients With Cleft Lip

FACE Pub Date : 2024-01-30 DOI:10.1177/27325016241227614
Chioma G. Obinero, Alexandra Boyd, Jose E Barrera, Alyssa Valenti, Naikhoba C. O. Munabi, Thomas A. Imahiyerobo, M. Greives
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Abstract

Comprehensive management of cleft lip with or without cleft palate (CL/P) often begins prenatally, continues into adulthood, and involves multidisciplinary collaboration. This study aims to review the current literature and summarize sociodemographic disparities that impact access to care, management, and postoperative outcomes in patients with CL/P. A systematic review was conducted using Pubmed, Embase, and Medline databases. Studies discussing sociodemographic disparities regarding access to care, management, and treatment outcomes for patients with CL/P were included. Studies performed outside the US and published before the year 2000 were excluded. Of 3782 studies initially identified, 26 met the inclusion criteria. Disparities discussed included access to care (n = 11), missed appointments (n = 2), use of nasoalveolar molding [NAM] (n = 3), surgical timing (n = 8), and surgical outcomes (n = 8). Minority race or ethnicity, particularly black, Hispanic, Asian, and Native-American, as well as public insurance were associated with impaired access to care. Other factors causing impaired access to care were non-English primary language and high cost. Predictors for missed appointments were black race and Medicaid insurance. Decreased use of or success with NAM was associated with Asian race, public insurance, and long travel distance to a cleft care center. Factors associated with delayed CL surgery were Asian or black race, Hispanic ethnicity, public insurance, and non-English primary language. Surgical outcomes were assessed using various esthetic, speech, and quality of life measures; factors linked to worse outcomes included black or latin race and public insurance. Patients with CL/P from minority racial or ethnic groups, particularly black, Asian, and Hispanic, as well as those with public insurance are disproportionately impacted by health disparities. Disparities related to age, geographic location, and primary language have also been reported, among others. Statewide or institutional social programs may help address these disparities.
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在社区发现唇裂:影响唇裂患者护理的社会人口差异系统回顾
唇裂伴或不伴腭裂(CL/P)的综合治疗通常从产前开始,一直持续到成年,并涉及多学科协作。本研究旨在回顾现有文献,总结影响 CL/P 患者获得护理、管理和术后效果的社会人口差异。我们使用 Pubmed、Embase 和 Medline 数据库进行了系统性综述。纳入的研究讨论了 CL/P 患者在获得护理、管理和治疗效果方面的社会人口差异。排除了在美国以外进行的研究和 2000 年以前发表的研究。在最初确定的 3782 项研究中,有 26 项符合纳入标准。讨论的差异包括获得治疗的机会(11 例)、错过预约(2 例)、鼻齿槽成型[NAM]的使用(3 例)、手术时机(8 例)和手术结果(8 例)。少数种族或民族(尤其是黑人、西班牙裔、亚裔和美国本土人)以及公共保险与就医障碍有关。其他导致就医障碍的因素包括非英语母语和高额费用。错过预约的预测因素是黑人和医疗补助保险。使用 NAM 的减少或成功率的降低与亚裔、公共保险和前往唇裂护理中心的路途遥远有关。延迟 CL 手术的相关因素包括亚裔或黑人、西班牙裔、公共保险和非英语母语。手术效果通过各种美学、语言和生活质量指标进行评估;与较差的手术效果相关的因素包括黑人或拉丁种族以及公共保险。来自少数种族或民族群体(尤其是黑人、亚裔和西班牙裔)以及有公共保险的 CL/P 患者受到健康差异的影响尤为严重。与年龄、地理位置和主要语言等有关的差异也有报道。全州或机构的社会计划可能有助于解决这些差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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