Harvard Medical School, Boston, Massachusetts, USA.
Division of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Neurogastroenterol Motil. 2024 Mar;36(3):e14742. doi: 10.1111/nmo.14742. Epub 2024 Jan 23.
BACKGROUND: Health disparities and barriers to equitable care for patients from racial and ethnic minority backgrounds are common. We sought to evaluate disparities in management recommendations among Black/African American (AA) patients seeking care for IBS. METHODS: We assembled a retrospective cohort of patients at two tertiary care centers who were self-identifying as Black/AA and attended a first gastroenterology consult for IBS. These patients were age- and sex-matched to White controls with IBS also attending an initial gastroenterology consult. Retrospective chart review determined patient demographics, income, comorbidities, as well as provider management recommendations including pharmacologic therapies and non-pharmacologic interventions. KEY RESULTS: Among 602 IBS patients ages 14-88 (M ± SD = 43.6 ± 18.6 years) with IBS, those who identified as Black/AA (n = 301) had a lower estimated mean income and were significantly more likely to have a number of specific chronic medical conditions. Black/AA patients were significantly less likely to have implemented dietary changes for symptoms prior to receiving a diagnosis of IBS from a gastroenterologist. Black/AA patients were also less likely to receive a referral to a dietician within 1 year following their diagnosis of IBS (p = 0.01). Black/AA patients were prescribed pharmacologic therapy more often for constipation (41.9% vs. 34.6%, p = 0.01). It was more common for White patients to present at the initial encounter having already initiated a neuromodulator (41.9% vs. 27.9%, p < 0.001). CONCLUSION & INFERENCES: Management recommendations for IBS appear to vary by race, specifically for dietary advice and referrals.
背景:在寻求医疗服务的患者中,存在着不同种族和族裔背景的人群之间健康差距和公平护理障碍等普遍问题。我们旨在评估非裔美国人(AA)患者在肠易激综合征(IBS)就诊时的管理建议差异。
方法:我们组建了一个回顾性队列,纳入了在两个三级医疗中心就诊且自我认同为非裔美国人的 IBS 初诊患者。这些患者与白人对照者按照年龄和性别匹配,他们也因 IBS 而首次就诊于胃肠病学门诊。通过回顾性病历审查,确定患者的人口统计学、收入、合并症以及提供者的管理建议,包括药物治疗和非药物干预。
主要结果:在 602 名年龄在 14-88 岁(M ± SD = 43.6 ± 18.6 岁)的 IBS 患者中,那些自我认同为非裔美国人的患者(n = 301)的估计平均收入较低,并且更有可能患有多种特定的慢性疾病。在接受胃肠病学家诊断为 IBS 之前,非裔美国人患者更不可能因症状而改变饮食。在诊断为 IBS 后 1 年内,非裔美国人患者也不太可能被转介给营养师(p = 0.01)。非裔美国人患者更常因便秘而开具药物治疗(41.9% vs. 34.6%,p = 0.01)。在初次就诊时,白人患者更常见的是已经开始使用神经调节剂(41.9% vs. 27.9%,p < 0.001)。
结论与推断:IBS 的管理建议似乎因种族而异,特别是在饮食建议和转诊方面。
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