Uterine Fibroid Diagnosis by Race and Ethnicity in an Integrated Health Care System.

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Susanna D Mitro, Wendy Dyer, Catherine Lee, Ameek Bindra, Lana Wang, Miranda Ritterman Weintraub, Monique M Hedderson, Eve Zaritsky
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引用次数: 0

Abstract

Importance: Uterine fibroids are benign tumors that can cause severe symptoms. Fibroid burden among Asian or Pacific Islander individuals, particularly in specific subgroups, remains largely unexamined.

Objective: To describe fibroid diagnosis rates by race and ethnicity.

Design, setting, and participants: This retrospective cohort study (January 2009 to December 2022) used data from electronic health records of the Kaiser Permanente Northern California (KPNC) integrated health care system. Eligible participants included female (sex assigned at birth) KPNC members aged 18 to 54 years with at least 12 months of continuous membership, no prior fibroid diagnosis, and no history of hysterectomy. Data were analyzed January to September 2024.

Exposure: Race and ethnicity was categorized into 9 groups: Black (African American, other Black [ie, any Black race or ethnicity not otherwise specified], and unknown Black race or ethnicity), East Asian (Chinese, Japanese, and Korean), Hispanic (Hispanic or Latino), South Asian (Asian Indian, Bangladeshi, East Indian, Nepali, Sri Lankan, and any South Asian ethnicity not otherwise specified), Southeast Asian (Filipino, Vietnamese, and other Southeast Asian [ie, any Southeast Asian ethnicity not otherwise specified]), White (White or White Middle Eastern), other Asian or Pacific Islander (Native Hawaiian or Pacific Islander, multiethnic Asian, and other or unspecified Asian ethnicity [ie, any Asian ethnicity not otherwise specified]), other races and ethnicities (American Indian or Alaska Native and multiracial), and unknown race or ethnicity.

Main outcomes and measures: Incident fibroid diagnosis was identified using diagnostic codes. Poisson regression models were used to calculate incidence rates of fibroid diagnosis by racial and ethnic group, standardized to the 2022 US female population. Incidence rate ratios (IRRs) and 95% CIs compared incidence within each racial and ethnic group with White participants.

Results: A total of 1 917 794 patients were included (median [IQR] percentage, 7% [6%-7%] Black; 5% [5%-6%] East Asian; 22% [21%-23%] Hispanic; 3% [2%-3%] South Asian; 7% [7%-8%] Southeast Asian; 42% [39%-45%] White; 8% [6%-10%] other Asian or Pacific Islander; 2% [2%-2%] of other races and ethnicities; 4% [4%-5%] unknown or missing race and ethnicity), and 84 206 patients (4.4%) received a first fibroid diagnosis during the study period. Compared with White patients, there was a higher rate of fibroid diagnosis among Southeast Asian (IRR, 1.29; 95% CI, 1.26-1.33), East Asian (IRR, 1.47; 95% CI, 1.43-1.51), and South Asian patients (IRR, 1.71; 95% CI, 1.65-1.78). Black (IRR, 3.11; 95% CI, 3.05-3.17) and Hispanic patients (IRR, 1.37; 95% CI, 1.34-1.39) also had elevated rates of fibroid diagnosis. All Asian patients were less likely than other groups to have ICD-9 or ICD-10 coded symptoms before diagnosis.

Conclusions and relevance: In this cohort study of nearly 2 million KPNC patients, South Asian, East Asian, Southeast Asian, Hispanic, and Black patients had higher fibroid diagnosis rates than White patients. If diagnosis rates reflect true variation in disease prevalence, future research should identify sources of these disparities and strategies to reduce them.

重要性:子宫肌瘤是一种可引起严重症状的良性肿瘤。亚裔或太平洋岛民的子宫肌瘤负担,尤其是在特定亚群体中的负担,在很大程度上仍未得到研究:目的:描述不同种族和族裔的子宫肌瘤诊断率:这项回顾性队列研究(2009 年 1 月至 2022 年 12 月)使用的数据来自北加州凯撒医疗保健公司(KPNC)综合医疗保健系统的电子健康记录。符合条件的参与者包括年龄在 18 至 54 岁之间、连续加入 KPNC 至少 12 个月、既往无子宫肌瘤诊断且无子宫切除史的女性(出生时已分配性别)会员。数据分析时间为 2024 年 1 月至 9 月:种族和民族分为 9 组:暴露:种族和人种分为 9 组:黑人(非裔美国人、其他黑人[即未另作规定的任何黑人种族或人种]以及未知黑人种族或人种)、东亚人(中国人、日本人和韩国人)、西班牙裔(西班牙裔或拉丁裔)、南亚人(亚裔印度人、孟加拉人、东印度人、尼泊尔人、斯里兰卡人以及未另作规定的任何南亚人种)、东南亚人(菲律宾人、越南人以及其他东南亚人[即未另作规定的任何东南亚人种])、白人或中东白人)、其他亚洲人或太平洋岛民(夏威夷原住民或太平洋岛民、多种族亚洲人以及其他或未指定的亚洲人种[即未指定的任何亚洲人种])、其他种族和族裔(美国印第安人或阿拉斯加原住民以及多种族)以及未知种族或族裔。主要结果和测量指标:使用诊断代码确定子宫肌瘤诊断。采用泊松回归模型计算不同种族和族裔群体的子宫肌瘤诊断发病率,并以 2022 年美国女性人口为标准。将每个种族和民族群体的发病率与白人参与者的发病率进行比较,得出发病率比(IRRs)和 95% CIs:共纳入 1 917 794 名患者(百分比中位数[IQR],7% [6%-7%]黑人;5% [5%-6%]东亚人;22% [21%-23%]西班牙裔;3% [2%-3%]南亚人;7% [7%-8%]东南亚人;42%[39%-45%]白人;8%[6%-10%]其他亚洲人或太平洋岛民;2%[2%-2%]其他种族和族裔;4%[4%-5%]未知或种族和族裔缺失),以及 84 206 名患者(4.有 84 206 名患者(4.4%)在研究期间首次确诊为子宫肌瘤。与白人患者相比,东南亚(IRR,1.29;95% CI,1.26-1.33)、东亚(IRR,1.47;95% CI,1.43-1.51)和南亚患者(IRR,1.71;95% CI,1.65-1.78)的子宫肌瘤诊断率较高。黑人(IRR,3.11;95% CI,3.05-3.17)和西班牙裔患者(IRR,1.37;95% CI,1.34-1.39)的子宫肌瘤诊断率也较高。与其他群体相比,所有亚裔患者在诊断前出现 ICD-9 或 ICD-10 编码症状的可能性较低:在这项包含近 200 万名 KPNC 患者的队列研究中,南亚、东亚、东南亚、西班牙裔和黑人患者的子宫肌瘤诊断率高于白人患者。如果诊断率反映了疾病患病率的真实差异,那么未来的研究应找出这些差异的根源并制定减少差异的策略。
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来源期刊
JAMA Network Open
JAMA Network Open Medicine-General Medicine
CiteScore
16.00
自引率
2.90%
发文量
2126
审稿时长
16 weeks
期刊介绍: JAMA Network Open, a member of the esteemed JAMA Network, stands as an international, peer-reviewed, open-access general medical journal.The publication is dedicated to disseminating research across various health disciplines and countries, encompassing clinical care, innovation in health care, health policy, and global health. JAMA Network Open caters to clinicians, investigators, and policymakers, providing a platform for valuable insights and advancements in the medical field. As part of the JAMA Network, a consortium of peer-reviewed general medical and specialty publications, JAMA Network Open contributes to the collective knowledge and understanding within the medical community.
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