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在联邦合格健康中心开展集中结直肠癌筛查外展活动:一项随机临床试验。

Centralized Colorectal Cancer Screening Outreach in Federally Qualified Health Centers: A Randomized Clinical Trial.

机构信息

Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill.

Department of Medicine, Division of General Medicine and Clinical Epidemiology, University of North Carolina School of Medicine, Chapel Hill.

出版信息

JAMA Netw Open. 2024 Nov 4;7(11):e2446693. doi: 10.1001/jamanetworkopen.2024.46693.

Abstract

IMPORTANCE

Colorectal cancer (CRC) screening is effective but remains underused in federally qualified health centers (FQHCs).

OBJECTIVE

To assess the effectiveness of a centralized CRC screening outreach intervention involving mailed fecal immunochemical testing (FIT) outreach and patient navigation to colonoscopy after abnormal results of FIT.

DESIGN, SETTING, AND PARTICIPANTS: A pragmatic randomized clinical trial was conducted, using intention-to-treat analysis. Participants were enrolled from July 6, 2020, to September 17, 2021, and analyses were performed from July 6, 2023, to January 31, 2024. The study was conducted at independent FQHCs comprising 12 clinical delivery sites in North Carolina. The outreach intervention was centralized at an academic cancer center. Active individuals aged 50 to 75 years at average risk for CRC and not current with screening per US Preventive Services Task Force recommendations were included.

INTERVENTION

In addition to usual care, intervention participants received mailed screening outreach materials including an introductory letter, FIT kit packet with instructions and return postage, and 2 reminder letters if needed. Intervention participants with positive results of mailed FIT were offered navigation to facilitate follow-up colonoscopy completion. Control participants received usual care alone.

MAIN OUTCOMES AND MEASURES

The primary outcome was completion of a US Preventive Services Task Force-recommended CRC screening test within 6 months determined by electronic health record review. Secondary outcomes were colonoscopy completion within 6 months after positive FIT results and detection of advanced colorectal neoplasia, defined as advanced adenoma or CRC.

RESULTS

A total of 4002 participants were included (mean [SD] age, 59.6 [6.8] years; 2256 [56.4%] female; 364 (9.1%) Hispanic; 1082 [27.0%] non-Hispanic Black; 2288 [57.2%] non-Hispanic White; 1198 [29.9%] commercially insured; 617 [15.4%] Medicaid; 1227 [30.7%] Medicare; and 960 [24.0%] uninsured), with 2001 randomized to each group. Compared with controls, intervention participants were more likely to complete screening within 6 months of randomization (30.0% vs 9.7%; difference, 20.29 percentage points; 95% CI, 17.85-22.73 percentage points). The intervention was effective in all insurance types. In the intervention arm, 33 of 48 participants with positive FIT results (68.8%) completed follow-up colonoscopy within 6 months compared with 8 of 18 participants (44.4%) in the control arm (difference, 24.3 percentage points; 95% CI, -2.13 to 50.74 percentage points). Advanced colorectal neoplasia was detected in 29 intervention participants (1.4%) and 15 control participants (0.7%) (difference, 0.68 percentage points; 95% CI, 0.05-1.35 percentage points).

CONCLUSIONS AND RELEVANCE

In this randomized clinical trial of centralized screening outreach intervention in diverse patients served by independent FQHCs, CRC screening completion and advanced colorectal neoplasia detection were substantially increased. Future studies should examine the cost and scalability of this intervention in this context.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT04406714.

摘要

重要性

结直肠癌(CRC)筛查是有效的,但在合格的联邦健康中心(FQHC)中仍未得到充分利用。

目的

评估涉及邮寄粪便免疫化学检测(FIT)外展和 FIT 结果异常后对结肠镜检查的患者导航的集中 CRC 筛查外展干预的有效性。

设计、设置和参与者:进行了一项实用随机临床试验,采用意向治疗分析。参与者于 2020 年 7 月 6 日至 2021 年 9 月 17 日入组,分析于 2023 年 7 月 6 日至 2024 年 1 月 31 日进行。该研究在北卡罗来纳州的 12 个临床服务站点组成的独立 FQHC 中进行。外展干预集中在一家学术癌症中心。纳入年龄在 50 至 75 岁之间、平均 CRC 风险且不符合美国预防服务工作组建议的常规筛查的活跃个体。

干预措施

除常规护理外,干预组参与者还接受了邮寄筛查外展材料,包括介绍信、带有说明和回邮邮资的 FIT 试剂盒包以及如果需要的 2 封提醒信。邮寄 FIT 阳性结果的干预组参与者获得了导航服务,以促进后续结肠镜检查的完成。对照组仅接受常规护理。

主要结果和措施

主要结局是通过电子健康记录审查确定的在 6 个月内完成美国预防服务工作组推荐的 CRC 筛查测试。次要结局是在阳性 FIT 结果后 6 个月内完成结肠镜检查和检测高级结直肠肿瘤,定义为高级腺瘤或 CRC。

结果

共纳入 4002 名参与者(平均[标准差]年龄 59.6[6.8]岁;2256[56.4%]名女性;364[9.1%]名西班牙裔;1082[27.0%]名非西班牙裔黑人;2288[57.2%]名非西班牙裔白人;1198[29.9%]名商业保险;617[15.4%]名医疗补助;1227[30.7%]名医疗保险;960[24.0%]名无保险),随机分为两组,每组 2001 名。与对照组相比,干预组在随机分组后 6 个月内完成筛查的可能性更高(30.0% vs 9.7%;差异,20.29 个百分点;95%CI,17.85-22.73 个百分点)。该干预措施在所有保险类型中均有效。在干预组中,48 名阳性 FIT 结果患者中有 33 名(68.8%)在 6 个月内完成了后续结肠镜检查,而对照组中有 18 名患者中的 8 名(44.4%)(差异,24.3 个百分点;95%CI,-2.13 至 50.74 个百分点)。在 29 名干预参与者(1.4%)和 15 名对照组参与者(0.7%)中检测到高级结直肠肿瘤(差异,0.68 个百分点;95%CI,0.05-1.35 个百分点)。

结论和相关性

在这项针对由独立 FQHC 服务的不同患者的集中筛查外展干预的随机临床试验中,CRC 筛查完成率和高级结直肠肿瘤检出率均有显著提高。未来的研究应在该背景下评估该干预措施的成本和可扩展性。

试验注册

ClinicalTrials.gov 标识符:NCT04406714。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee1/11589799/325d3a6947c5/jamanetwopen-e2446693-g001.jpg

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