Reed Jennifer L, Palmer Chella A, Casper T Charles, Augustine Erin M, Cruz Andrea T, Elsholz Cara L, Mollen Cynthia J, Pickett Michelle L, Schmidt Sarah K, Stukus Kristin S, Goyal Monika K
Division of Emergency Medicine, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
University of Utah School of Medicine, Salt Lake City.
JAMA Pediatr. 2025 Sep 8. doi: 10.1001/jamapediatrics.2025.2139.
Adolescents account for almost half of the 2.5 million diagnosed sexually transmitted infections in the US annually, and the emergency department functions as the primary source of health care for many adolescents. No recommendations exist for emergency department gonorrhea and chlamydia screening.
To compare usual care against targeted and universally offered gonorrhea and chlamydia screening approaches.
DESIGN, SETTING, AND PARTICIPANTS: This was a comparative effectiveness, multicenter, pragmatic trial with a type 3 hybrid stepped-wedge crossover design implemented over approximately 20 months at 6 pediatric emergency departments in the US. Patients aged 15 to 21 years presenting to the emergency department between January 2021 and September 2022 were included, excluding those who were unable to understand English, were critically ill, were with concern for sexual assault or abuse, had cognitive impairment or altered mental status, or were otherwise unable to provide consent. Of 98 413 emergency department presentations during the study period, 7503 adolescents underwent testing.
Patients completed a computerized sexual health survey. During the universally offered screening intervention, gonorrhea and chlamydia screening was offered to all participants, and clinical decision support for testing was based solely on the patient's decision to undergo testing (survey results were not available to clinicians). During the targeted screening intervention, a validated risk score derived from the survey based on patient-reported behavioral data was integrated into the electronic health record to provide clinical decision support for gonorrhea and chlamydia testing. The usual care phase represented the period before the survey was integrated into emergency department care.
Gonorrhea and chlamydia detection rates per 1000 eligible patients per 2-week intervals among usual care, targeted, and universally offered screening strategies.
Of the 98 413 patient visits, 18 633 (19%) took place during the usual care phase, 41 082 (42%) during the targeted screening phase, and 38 698 (39%) during the universally offered screening phase. The study population was predominantly aged 16 to 18 years (n = 50 927 [51.7%]), with a mean (SD) age of 17.03 (1.42) years. A total of 57 013 participants (57.9%) were female. In the usual care phase, 1432 patients had testing ordered vs 3216 in the targeting screening phase and 2855 in the universal screening phase. Compared to usual care, population-level gonorrhea and chlamydia detection rates were higher during the targeted strategy phase (adjusted difference in infections detected per 1000 patient visits, 2.59; 95% CI, 2.46-2.73) and universally offered strategy phase (adjusted difference, 1.81; 95% CI, 1.67-1.94).
In this comparative effectiveness trial, a targeted or universally offered screening tool in pediatric emergency departments was associated with higher detection rates than usual care, with targeted screening identifying higher rates of infections at the population level. The findings indicate that developing processes to integrate broad-scale gonorrhea and chlamydia screening in emergency departments may be warranted.
ClinicalTrials.gov Identifier: NCT03715335.
在美国,每年250万例确诊的性传播感染病例中,青少年占了近一半,而急诊科是许多青少年的主要医疗保健来源。目前尚无针对急诊科淋病和衣原体筛查的建议。
比较常规护理与针对性和普遍提供的淋病和衣原体筛查方法。
设计、地点和参与者:这是一项比较效果、多中心、实用性试验,采用3型混合阶梯楔形交叉设计,在美国6家儿科急诊科进行了约20个月。纳入了2021年1月至2022年9月期间到急诊科就诊的15至21岁患者,排除那些无法理解英语、病情危急、涉嫌性侵犯或虐待、有认知障碍或精神状态改变或其他无法提供同意的患者。在研究期间的98413次急诊科就诊中,7503名青少年接受了检测。
患者完成了一项计算机化的性健康调查。在普遍提供筛查干预期间,向所有参与者提供淋病和衣原体筛查,检测的临床决策支持仅基于患者接受检测的决定(临床医生无法获得调查结果)。在针对性筛查干预期间,基于患者报告的行为数据从调查中得出的经过验证的风险评分被整合到电子健康记录中,以提供淋病和衣原体检测的临床决策支持。常规护理阶段代表调查纳入急诊科护理之前的时期。
常规护理、针对性和普遍提供筛查策略中每2周间隔每1000名符合条件患者的淋病和衣原体检测率。
在98413次患者就诊中,18633次(19%)发生在常规护理阶段,41082次(42%)发生在针对性筛查阶段,38698次(39%)发生在普遍提供筛查阶段。研究人群主要为16至18岁(n = 50927 [51.7%]),平均(标准差)年龄为17.03(1.42)岁。共有57013名参与者(57.9%)为女性。在常规护理阶段,有1432名患者接受检测,而在针对性筛查阶段为3216名,在普遍筛查阶段为2855名。与常规护理相比,在针对性策略阶段(每1000次患者就诊中检测到的感染调整差异为2.59;95%可信区间,2.46 - 2.73)和普遍提供策略阶段(调整差异为1.81;95%可信区间,1.67 - 1.94),人群水平的淋病和衣原体检测率更高。
在这项比较效果试验中,儿科急诊科的针对性或普遍提供的筛查工具与比常规护理更高的检测率相关,针对性筛查在人群水平上识别出更高的感染率。研究结果表明,可能有必要制定在急诊科整合广泛的淋病和衣原体筛查的流程。
ClinicalTrials.gov标识符:NCT03715335。