Wheelock Alyse, Chasaya Mwelwa, Namuziya Natasha, Jumbe Marsden Emilia, Kapasa Monica, Mumba Chibamba, Mulenga Bwalya, Nkole Lisa, Pieciak Rachel, Mudenda Victor, Chikoti Chilufya, Ngoma Benard, Chimoga Charles, Chirwa Sarah, Pemba Lilian, Nzara Diana, Lungu James, Forman Leah, MacLeod William, Moyo Crispin, Wa Somwe Somwe, Gill Christopher
Section of Preventive Medicine and Epidemiology, Chobanian & Avedisian School of Medicine, Boston University, Boston, Massachusetts, USA.
Avencion Limited, Lusaka, Zambia.
J Pediatric Infect Dis Soc. 2025 Jan 20;14(1). doi: 10.1093/jpids/piae129.
In low-to-middle-income countries, acute lower respiratory infection (ALRI) remains the leading infectious cause of death among infants and children under 5 years old. Case-control studies based on upper respiratory sampling have informed current understandings of ALRI etiologies; in contrast, minimally invasive tissue sampling (MITS) offers a method of directly interrogating lower respiratory tract pathogens to establish etiologic distributions. This study performed in the postmortem setting used MITS and a Determination of Cause of Death (DeCoDe) panel to elucidate the causes of fatal pneumonia in the community in Lusaka, Zambia. For deceased infants and children under age 5 years whose next-of-kin provided consent, a verbal autopsy was obtained and 6 lung tissue biopsies from each case were sent for histopathology and multiplex polymerase chain reaction testing. Subsequently, a multi-disciplinary DeCoDe panel met to review each case, determine if the child died of respiratory causes, construct a causal chain of diagnoses directly leading to the death, and determine if the death was preventable (i.e., if an identifiable intervention would have averted the death). Among 106 deaths, 49 were adjudicated as respiratory deaths, with etiologic causes including Klebsiella pneumoniae (13), Streptococcus pneumoniae (5), and Pneumocystis jirovecii (4), among others. Of note, for 21 respiratory deaths, a causative pathogen could not be identified despite clinical and histopathologic evidence of ALRI. A large majority of all deaths were considered preventable (90/106 or 85%). This study demonstrates the impact of certain respiratory pathogens through direct in situ tissue sampling with supportive pathologic data and presents a useful method of studying the etiologic distribution of fatal ALRIs in settings where many deaths occur in the community.
在低收入和中等收入国家,急性下呼吸道感染(ALRI)仍是5岁以下婴幼儿死亡的主要感染性病因。基于上呼吸道采样的病例对照研究为目前对ALRI病因的认识提供了依据;相比之下,微创组织采样(MITS)提供了一种直接检测下呼吸道病原体以确定病因分布的方法。这项在尸检环境中开展的研究使用MITS和死因判定(DeCoDe)小组来阐明赞比亚卢萨卡社区致命性肺炎的病因。对于近亲同意的5岁以下死亡婴幼儿,进行了口头尸检,并将每个病例的6份肺组织活检样本送去做组织病理学检查和多重聚合酶链反应检测。随后,一个多学科的DeCoDe小组开会审查每个病例,确定儿童是否死于呼吸道疾病,构建直接导致死亡的诊断因果链,并确定死亡是否可预防(即是否有可识别的干预措施能够避免死亡)。在106例死亡病例中,49例被判定为呼吸道死亡,病因包括肺炎克雷伯菌(13例)、肺炎链球菌(5例)和耶氏肺孢子菌(4例)等。值得注意的是,在21例呼吸道死亡病例中,尽管有ALRI的临床和组织病理学证据,但仍无法确定致病病原体。所有死亡病例中的绝大多数被认为是可预防的(90/106,即85%)。这项研究通过直接的原位组织采样及支持性病理数据证明了某些呼吸道病原体的影响,并提出了一种在社区发生大量死亡的环境中研究致命性ALRI病因分布的有用方法。