Global Program in Pediatric Respiratory Sciences, Eudowood Division of Pediatric Respiratory Sciences, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD, USA; Department of International Health, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Projahnmo Research Foundation, Dhaka, Bangladesh.
Lancet Respir Med. 2023 Sep;11(9):769-781. doi: 10.1016/S2213-2600(23)00098-X. Epub 2023 Apr 7.
Hypoxaemic pneumonia mortality risk in low-income and middle-income countries is high in children who have been hospitalised, but unknown among outpatient children. We sought to establish the outpatient burden, mortality risk, and prognostic accuracy of death from hypoxaemia in children with suspected pneumonia in Bangladesh.
We conducted a prospective community-based cohort study encompassing three upazila (subdistrict) health complex catchment areas in Sylhet, Bangladesh. Children aged 3-35 months participating in a community surveillance programme and presenting to one of three upazila health complex Integrated Management of Childhood Illness (IMCI) outpatient clinics with an acute illness and signs of difficult breathing (defined as suspected pneumonia) were enrolled in the study; because lower respiratory tract infection mortality mainly occurs in children younger than 1 year, the primary study population comprised children aged 3-11 months. Study physicians recorded WHO IMCI pneumonia guideline clinical signs and peripheral arterial oxyhaemoglobin saturations (SpO) in room air. They treated children with pneumonia with antibiotics (oral amoxicillin [40 mg/kg per dose twice per day for 5-7 days, as per local practice]), and recommended oxygen, parenteral antibiotics, and hospitalisation for those with an SpO of less than 90%, WHO IMCI danger signs, or severe malnutrition. Community health workers documented the children's vital status and the date of any vital status changes during routine household surveillance (one visit to each household every 2 months). The primary outcome was death at 2 weeks after enrolment in children aged 3-11 months (primary study population) and 12-35 months (secondary study population). Primary analyses included estimating the outpatient prevalence, mortality risk, and prognostic accuracy of hypoxaemia for death in children aged 3-11 months with suspected pneumonia. Risk ratios were produced by fitting a multivariable model that regressed predefined SpO ranges (<90%, 90-93%, and 94-100%) on the primary 2-week mortality outcome (binary outcome) using Poisson models with robust variance estimation. We established the prognostic accuracy of WHO IMCI guidelines for death with and without varying SpO thresholds.
Participants were recruited between Sept 1, 2015, to Aug 31, 2017. During the study period, a total of 7440 children aged 3-35 months with the first suspected pneumonia episode were enrolled, of whom 3848 (54·3%) with an attempted pulse oximeter measurement and 2-week outcome were included in our primary study population of children aged 3-11-months. Among children aged 3-11 months, an SpO of less than 90% occurred in 102 (2·7%) of 3848 children, an SpO of 90-93% occurred in 306 (8·0%) children, a failed SpO measurement occurred in 67 (1·7%) children, and 24 (0·6%) children with suspected pneumonia died. Compared with an SpO of 94-100% (3373 [87·7%] of 3848), the adjusted risk ratio for death was 10·3 (95% CI 3·2-32·3; p<0·001) for an SpO of less than 90%, 4·3 (1·5-11·8; p=0·005) for an SpO of 90-93%, and 11·4 (3·1-41·4; p<0·001) for a failed measurement. When not considering pulse oximetry, of the children who died, WHO IMCI guidelines identified only 25·0% (95% CI 9·7-46·7; six of 24 children) as eligible for referral to hospital. For identifying deaths, in children with an SpO of less than 90% WHO IMCI guidelines had a 41·7% sensitivity (95% CI 22·1-63·4) and 89·7% specificity (88·7-90·7); for children with an SpO of less than 90% or measurement failure the guidelines had a 54·2% sensitivity (32·8-74·4) and 88·3% specificity (87·2-89·3); and for children with an SpO of less than 94% or measurement failure the guidelines had a 62·5% sensitivity (40·6-81·2) and 81·3% specificity (80·0-82·5).
These findings support pulse oximeter use during the outpatient care of young children with suspected pneumonia in Bangladesh as well as the re-evaluation of the WHO IMCI currently recommended threshold of an SpO less than 90% for hospital referral.
Fogarty International Center of the National Institutes of Health (K01TW009988), The Bill & Melinda Gates Foundation (OPP1084286 and OPP1117483), and GlaxoSmithKline (90063241).
在中低收入国家,住院的低氧血症性肺炎患儿死亡率较高,但门诊患儿的死亡率尚不清楚。我们旨在确定孟加拉国疑似肺炎门诊患儿的门诊负担、死亡率和低氧血症死亡的预后准确性。
我们开展了一项前瞻性社区为基础的队列研究,涵盖了孟加拉国锡尔赫特的三个乌扎拉(次级行政区)卫生综合体集水区。参与社区监测计划并因急性疾病和呼吸困难体征(定义为疑似肺炎)到三个乌扎拉卫生综合体综合儿童疾病管理(IMCI)门诊就诊的 3-35 月龄儿童被纳入研究;因为下呼吸道感染的死亡率主要发生在 1 岁以下的儿童中,因此主要研究人群包括 3-11 月龄的儿童。研究医生记录了世卫组织 IMCI 肺炎指南的临床体征和外周动脉血氧饱和度(SpO)在室内空气。他们用抗生素(口服阿莫西林[40mg/kg 剂量,每日两次,共 5-7 天,按当地惯例])治疗肺炎患儿,并建议 SpO<90%、世卫组织 IMCI 危险征象或严重营养不良的患儿吸氧、使用静脉抗生素和住院治疗。社区卫生工作者在常规家庭监测(每两个月对每个家庭进行一次访问)期间记录儿童的生命状态和任何生命状态变化的日期。主要结局是 3-11 月龄(主要研究人群)和 12-35 月龄(次要研究人群)儿童入组后 2 周的死亡。主要分析包括估计疑似肺炎门诊患儿 3-11 月龄儿童的门诊患病率、死亡率和低氧血症对死亡的预后准确性。通过拟合多变量模型,使用具有稳健方差估计的泊松模型,将不同的 SpO 范围(<90%、90-93%和 94-100%)回归到主要的 2 周死亡率(二分类结局),来计算风险比。我们评估了世卫组织 IMCI 指南在不同 SpO 阈值下对死亡的预后准确性。
参与者于 2015 年 9 月 1 日至 2017 年 8 月 31 日期间入组。在研究期间,共纳入了 7440 名 3-35 月龄首次疑似肺炎的儿童,其中 3848 名(54.3%)尝试了脉搏血氧仪测量,并有 2 周结局,纳入了 3-11 月龄儿童的主要研究人群。在 3-11 月龄的儿童中,有 102 名(2.7%)的 SpO<90%,306 名(8.0%)的 SpO 在 90-93%之间,67 名(1.7%)的 SpO 测量失败,24 名(0.6%)的疑似肺炎患儿死亡。与 SpO 为 94-100%(3373 名,占 3848 名)相比,SpO<90%的调整风险比为 10.3(95%CI 3.2-32.3;p<0.001),SpO 在 90-93%的为 4.3(1.5-11.8;p=0.005),SpO 测量失败的为 11.4(3.1-41.4;p<0.001)。如果不考虑脉搏血氧仪,在死亡的儿童中,世卫组织 IMCI 指南仅确定了 25.0%(95%CI 9.7-46.7;24 名死亡儿童中的 9 名)有资格转诊到医院。对于识别死亡,SpO<90%的儿童中,世卫组织 IMCI 指南的敏感性为 41.7%(95%CI 22.1-63.4),特异性为 89.7%(88.7-90.7);对于 SpO<90%或测量失败的儿童,指南的敏感性为 54.2%(32.8-74.4),特异性为 88.3%(87.2-89.3);对于 SpO<94%或测量失败的儿童,指南的敏感性为 62.5%(40.6-81.2),特异性为 81.3%(80.0-82.5)。
这些发现支持在孟加拉国为疑似肺炎的门诊患儿使用脉搏血氧仪,并重新评估目前推荐的世卫组织 IMCI 指南将 SpO<90%作为转诊至医院的阈值。
美国国立卫生研究院福格蒂国际中心(K01TW009988)、比尔和梅琳达·盖茨基金会(OPP1084286 和 OPP1117483)和葛兰素史克(90063241)。