Department of Family and Community Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Center for Public Health Initiatives, University of Pennsylvania, Philadelphia.
JAMA Netw Open. 2022 Sep 1;5(9):e2232110. doi: 10.1001/jamanetworkopen.2022.32110.
The COVID-19 pandemic has claimed nearly 6 million lives globally as of February 2022. While pandemic control efforts, including contact tracing, have traditionally been the purview of state and local health departments, the COVID-19 pandemic outpaced health department capacity, necessitating actions by private health systems to investigate and control outbreaks, mitigate transmission, and support patients and communities.
To investigate the process of designing and implementing a volunteer-staffed contact tracing program at a large academic health system from April 2020 to May 2021, including program structure, lessons learned through implementation, results of case investigation and contact tracing efforts, and reflections on how constrained resources may be best allocated in the current pandemic or future public health emergencies.
DESIGN, SETTING, AND PARTICIPANTS: This case series study was conducted among patients at the University of Pennsylvania Health System and in partnership with the Philadelphia Department of Public Health. Patients who tested positive for COVID-19 were contacted to counsel them regarding safe isolation practices, identify and support quarantine of their close contacts, and provide resources, such as food and medicine, needed during isolation or quarantine.
Of 5470 individuals who tested positive for COVID-19 and received calls from a volunteer, 2982 individuals (54.5%; median [range] age, 42 [18-97] years; 1628 [59.4%] women among 2741 cases with sex data) were interviewed; among 2683 cases with race data, there were 110 Asian individuals (3.9%), 1476 Black individuals (52.7%), and 817 White individuals (29.2%), and among 2667 cases with ethnicity data, there were 366 Hispanic individuals (13.1%) and 2301 individuals who were not Hispanic (82.6%). Most individuals lived in a household with 2 to 5 people (2125 of 2904 individuals with household data [71.6%]). Of 3222 unique contacts, 1780 close contacts (55.2%; median [range] age, 40 [18-97] years; 866 [55.3%] women among 1565 contacts with sex data) were interviewed; among 1523 contacts with race data, there were 69 Asian individuals (4.2%), 705 Black individuals (43.2%), and 573 White individuals (35.1%), and among 1514 contacts with ethnicity data, there were 202 Hispanic individuals (12.8%) and 1312 individuals (83.4%) who were not Hispanic. Most contacts lived in a household with 2 to 5 people (1123 of 1418 individuals with household data [79.2%]). Of 3324 cases and contacts who completed a questionnaire on unmet social needs, 907 (27.3%) experienced material hardships that would make it difficult for them to isolate or quarantine safely. Such hardship was significantly less common among White compared with Black participants (odds ratio, 0.20; 95% CI, 0.16-0.25).
These findings demonstrate the feasibility and challenges of implementing a case investigation and contact tracing program at an academic health system. In addition to successfully engaging most assigned COVID-19 cases and close contacts, contact tracers shared health information and material resources to support isolation and quarantine, thus filling local public health system gaps and supporting local pandemic control.
截至 2022 年 2 月,全球已有近 600 万人死于 COVID-19 大流行。虽然包括接触者追踪在内的大流行控制工作一直是州和地方卫生部门的职责范围,但 COVID-19 大流行的速度超过了卫生部门的能力,需要私立卫生系统采取行动调查和控制疫情爆发,减轻传播风险,并支持患者和社区。
调查 2020 年 4 月至 2021 年 5 月期间在一家大型学术卫生系统中设计和实施志愿人员联络追踪计划的过程,包括计划结构、实施过程中的经验教训、病例调查和接触者追踪工作的结果,以及对如何在当前大流行或未来的公共卫生紧急情况下最好分配有限资源的思考。
设计、地点和参与者:本病例系列研究在宾夕法尼亚大学卫生系统的患者中进行,并与费城公共卫生部合作。对 COVID-19 检测呈阳性的患者进行联系,以指导他们安全隔离的做法,确定并支持其密切接触者的隔离,并提供隔离或隔离期间所需的资源,如食物和药品。
在接受志愿者电话联系的 5470 名 COVID-19 检测呈阳性的患者中,有 2982 名(54.5%;中位数[范围]年龄为 42[18-97]岁;2741 例有性别数据的患者中有 1628 例[59.4%]为女性)接受了访谈;在 2683 例有种族数据的患者中,有 110 例为亚洲人(3.9%),1476 例为黑人(52.7%),817 例为白人(29.2%),在 2667 例有族裔数据的患者中,有 366 例为西班牙裔(13.1%),2301 例为非西班牙裔(82.6%)。大多数患者居住在有 2 至 5 人的家庭中(2904 名有家庭数据的患者中有 2125 名[71.6%])。在 3222 名独特的联系人中,有 1780 名密切联系人(55.2%;中位数[范围]年龄为 40[18-97]岁;1565 名有性别数据的联系人中有 866 名[55.3%]为女性)接受了访谈;在 1523 名有种族数据的联系人中,有 69 名亚洲人(4.2%),705 名黑人(43.2%),573 名白人(35.1%),在 1514 名有族裔数据的联系人中,有 202 名西班牙裔(12.8%)和 1312 名非西班牙裔(83.4%)。大多数联系人居住在有 2 至 5 人的家庭中(1418 名有家庭数据的个人中有 1123 名[79.2%])。在完成关于未满足的社会需求调查问卷的 3324 例病例和联系人中,有 907 例(27.3%)经历了严重的物质困难,这使得他们难以安全隔离或隔离。与黑人参与者相比,这种困难在白人参与者中明显较少(优势比,0.20;95%CI,0.16-0.25)。
这些发现证明了在学术卫生系统中实施病例调查和接触者追踪计划的可行性和挑战。除了成功接触到大多数指定的 COVID-19 病例和密切接触者外,接触者追踪者还分享了健康信息和物质资源,以支持隔离和检疫,从而填补了当地公共卫生系统的空白,并支持了当地的大流行控制。