首诊于基层医疗机构的婴幼儿可能严重感染的临床特征及其相关死亡率。
Clinical signs of possible serious infection and associated mortality among young infants presenting at first-level health facilities.
机构信息
Department of Maternal, Neonatal, Child and Adolescent Health and Ageing, World Health Organization, Geneva, Switzerland.
Department of Community Health, Kinshasa School of Public Health, Kinshasa, DR Congo.
出版信息
PLoS One. 2021 Jun 30;16(6):e0253110. doi: 10.1371/journal.pone.0253110. eCollection 2021.
BACKGROUND
The World Health Organization recommends inpatient hospital treatment of young infants up to two months old with any sign of possible serious infection. However, each sign may have a different risk of death. The current study aims to calculate the case fatality ratio for infants with individual or combined signs of possible serious infection, stratified by inpatient or outpatient treatment.
METHODS
We analysed data from the African Neonatal Sepsis Trial conducted in five sites in the Democratic Republic of the Congo, Kenya and Nigeria. Trained study nurses classified sick infants as pneumonia (fast breathing in 7-59 days old), severe pneumonia (fast breathing in 0-6 days old), clinical severe infection [severe chest indrawing, high (> = 38°C) or low body temperature (<35.5°C), stopped feeding well, or movement only when stimulated] or critical illness (convulsions, not able to feed at all, or no movement at all), and referred them to a hospital for inpatient treatment. Infants whose caregivers refused referral received outpatient treatment. The case fatality ratio by day 15 was calculated for individual and combined clinical signs and stratified by place of treatment. An infant with signs of clinical severe infection or severe pneumonia was recategorised as having low- (case fatality ratio ≤2%) or moderate- (case fatality ratio >2%) mortality risk.
RESULTS
Of 7129 young infants with a possible serious infection, fast breathing (in 7-59 days old) was the most prevalent sign (26%), followed by high body temperature (20%) and severe chest indrawing (19%). Infants with pneumonia had the lowest case fatality ratio (0.2%), followed by severe pneumonia (2.0%), clinical severe infection (2.3%) and critical illness (16.9%). Infants with clinical severe infection had a wide range of case fatality ratios for individual signs (from 0.8% to 11.0%). Infants with pneumonia had similar case fatality ratio for outpatient and inpatient treatment (0.2% vs. 0.3%, p = 0.74). Infants with clinical severe infection or severe pneumonia had a lower case fatality ratio among those who received outpatient treatment compared to inpatient treatment (1.9% vs. 6.5%, p<0.0001). We recategorised infants into low-mortality risk signs (case fatality ratio ≤2%) of clinical severe infection (high body temperature, or severe chest indrawing) or severe pneumonia and moderate-mortality risk signs (case fatality ratio >2%) (stopped feeding well, movement only when stimulated, low body temperature or multiple signs of clinical severe infection). We found that both categories had four times lower case fatality ratio when treated as outpatient than inpatient treatment, i.e., 1.0% vs. 4.0% (p<0.0001) and 5.3% vs. 22.4% (p<0.0001), respectively. In contrast, infants with signs of critical illness had nearly two times higher case fatality ratio when treated as outpatient versus inpatient treatment (21.7% vs. 12.1%, p = 0.097).
CONCLUSIONS
The mortality risk differs with clinical signs. Young infants with a possible serious infection can be grouped into those with low-mortality risk signs (high body temperature, or severe chest indrawing or severe pneumonia); moderate-mortality risk signs (stopped feeding well, movement only when stimulated, low body temperature or multiple signs of clinical severe infection), or high-mortality risk signs (signs of critical illness). New treatment strategies that consider differential mortality risks for the place of treatment and duration of inpatient treatment could be developed and evaluated based on these findings.
CLINICAL TRIAL REGISTRATION
This trial was registered with the Australian New Zealand Clinical Trials Registry under ID ACTRN 12610000286044.
背景
世界卫生组织建议对两个月龄以内、有任何可能严重感染迹象的婴幼儿进行住院治疗。然而,每种症状的死亡风险可能不同。本研究旨在计算按门诊或住院治疗分层的、有个体或合并可能严重感染迹象的婴儿的病死率。
方法
我们分析了在刚果民主共和国、肯尼亚和尼日利亚的五个地点进行的非洲新生儿败血症试验的数据。经过培训的研究护士将患病婴儿分为肺炎(7-59 天龄时呼吸急促)、严重肺炎(0-6 天龄时呼吸急促)、临床严重感染[严重胸部凹陷、体温高(≥38°C)或低(<35.5°C)、停止良好喂养、或仅在刺激时活动]或危重病(抽搐、完全无法喂养、或完全无活动),并将其转诊至医院进行住院治疗。拒绝转诊的婴儿接受门诊治疗。计算了第 15 天的病死率,并按个体和合并临床体征分层,按治疗地点进行分层。有临床严重感染或严重肺炎症状的婴儿被重新归类为低死亡率风险(病死率≤2%)或中死亡率风险(病死率>2%)。
结果
在 7129 例可能有严重感染的婴幼儿中,呼吸急促(7-59 天龄)最为常见(26%),其次是体温高(20%)和严重胸部凹陷(19%)。患有肺炎的婴儿病死率最低(0.2%),其次是严重肺炎(2.0%)、临床严重感染(2.3%)和危重病(16.9%)。患有临床严重感染的婴儿,其个体症状的病死率范围很广(0.8%至 11.0%)。门诊和住院治疗的肺炎婴儿病死率相似(0.2%比 0.3%,p = 0.74)。接受门诊治疗的临床严重感染或严重肺炎婴儿病死率低于住院治疗(1.9%比 6.5%,p<0.0001)。我们将婴儿分为低死亡率风险(病死率≤2%)的临床严重感染(高热或严重胸部凹陷)或严重肺炎,以及中死亡率风险(病死率>2%)(停止良好喂养、仅在刺激时活动、低体温或多个临床严重感染症状)。我们发现,无论哪种类别,门诊治疗的病死率都比住院治疗低四倍,即 1.0%比 4.0%(p<0.0001)和 5.3%比 22.4%(p<0.0001)。相比之下,有危重病症状的婴儿门诊治疗的病死率比住院治疗高近两倍(21.7%比 12.1%,p = 0.097)。
结论
死亡风险因临床症状而异。可能有严重感染的婴幼儿可分为低死亡率风险(高热、严重胸部凹陷或严重肺炎)、中死亡率风险(停止良好喂养、仅在刺激时活动、低体温或多个临床严重感染症状)或高死亡率风险(危重病症状)。可根据这些发现,制定和评估考虑治疗地点和住院治疗时间的差异死亡率风险的新治疗策略。
临床试验注册
本试验在澳大利亚和新西兰临床试验注册中心注册,注册号为 ACTRN 12610000286044。
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