Das Priya Mehta-Gupta, Madewell Zachary J, Blau Dianna M, Whitney Cynthia G, Ramakrishnan Usha, Stein Aryeh D, Young Melissa F, Suchdev Parminder S
Rollins School of Public Health, Emory University, Atlanta, Georgia, USA
Global Health Center, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
BMJ Open. 2025 Feb 17;15(2):e089874. doi: 10.1136/bmjopen-2024-089874.
To evaluate how postmortem anthropometric malnutrition (PAM) measures align with expert panel attribution of malnutrition as a causal or significant condition in under-5 mortality (U5M).
Cohort study using data from the Child Health and Mortality Prevention Surveillance network, incorporating clinical records, postmortem anthropometrics, minimally invasive tissue sampling, clinical abstraction and verbal autopsy to determine multiple causes of death.
SETTING/PARTICIPANTS: 1405 deaths of children aged 1-59 months from six African countries between 2016 and 2023.
PAM was determined using z-scores from the WHO Child Growth Standards: underweight (weight-for-age<(-2)), wasting (arm circumference-for-age or weight-for-length<(-2)) and stunting (length-for-age <(-2)). Performance metrics (sensitivity (SE), specificity (SP) and positive predictive values (PPV)) were calculated to determine the alignment between PAM and expert panel attribution of malnutrition as a causal or significant condition to death.
Nearly 75% of cases demonstrated moderate-to-severe malnutrition by PAM, while expert panels attributed malnutrition in 41% of cases. Performance metrics varied across anthropometric indices: underweight exhibited the highest SE (89.7%), while wasting based on arm circumference had the highest SP (81.9%) and PPV (76.8%). Discrepancies between PAM classification and expert panel attribution differed significantly by site, age, location of death and preventability of death (p<0.05). Adjusted multivariate regression showed that expert panel attribution was more likely with increasing severity of PAM.
The proportion of U5M attributable to malnutrition ranged between 41% (expert panel attribution) and 74% (PAM). Variability in classification underscores the need for monitoring and quality improvement measures to address discrepancies. Improved alignment between PAM and panel assessments is essential for accurately identifying malnutrition-related deaths and designing effective interventions to reduce U5M.
评估死后人体测量营养不良(PAM)指标与专家小组将营养不良认定为5岁以下儿童死亡(U5M)的因果或重要病因的一致性。
队列研究,使用儿童健康与死亡率预防监测网络的数据,纳入临床记录、死后人体测量、微创组织采样、临床摘要和口头尸检以确定多种死因。
设置/参与者:2016年至2023年间来自六个非洲国家的1405例1至59个月儿童的死亡病例。
使用世界卫生组织儿童生长标准的z评分确定PAM:体重不足(年龄别体重<(-2))、消瘦(年龄别上臂围或身长别体重<(-2))和发育迟缓(年龄别身长<(-2))。计算性能指标(敏感性(SE)、特异性(SP)和阳性预测值(PPV))以确定PAM与专家小组将营养不良认定为死亡的因果或重要病因之间的一致性。
近75%的病例通过PAM显示为中度至重度营养不良,而专家小组认定41%的病例存在营养不良。性能指标因人体测量指标而异:体重不足的SE最高(89.7%),而上臂围消瘦的SP最高(81.9%)和PPV最高(76.8%)。PAM分类与专家小组认定之间的差异在不同地点、年龄、死亡地点和死亡可预防性方面有显著差异(p<0.05)。调整后的多变量回归显示,随着PAM严重程度的增加,专家小组认定的可能性更大。
U5M中归因于营养不良的比例在41%(专家小组认定)至74%(PAM)之间。分类的变异性凸显了监测和质量改进措施以解决差异的必要性。PAM与小组评估之间更好的一致性对于准确识别与营养不良相关的死亡以及设计有效的干预措施以降低U5M至关重要。