Bansal Pallavi, Shah Dheeraj, Meena Rajesh Kumar, Rai Gargi, Das Shukla, Narang Manish, Gupta Piyush
Pediatrics, University College of Medical Sciences, Delhi, IND.
Microbiology, University College of Medical Sciences, Delhi, IND.
Cureus. 2023 Dec 14;15(12):e50546. doi: 10.7759/cureus.50546. eCollection 2023 Dec.
is an important cause of diarrhea in children under five, often missed by conventional laboratory methods. Blood in stools has always been a syndromic indicator for diarrhea, but most cases present with watery diarrhea without blood. This study aimed to determine the frequency of detected by molecular and conventional methods in children under five. Additionally, we aimed to study the clinical profile and outcome of children with diarrhea managed as per current diarrhea treatment guidelines.
In this hospital-based prospective observational study, stool samples from 150 children (age range: one month to five years) with acute diarrhea (duration < seven days) were subjected to routine microscopic examination, stool culture, and DNA extraction. The extracted DNA from stored stool samples was subjected to polymerase chain reaction (PCR) amplification using a specific primer for the invasion plasmid antigen H gene sequence (ipaH) gene at 424 bp. Results were interpreted in the context of the percentage of isolation of by molecular (PCR) and conventional methods (stool microscopy and culture) and the follow-up outcome in terms of recurrence of diarrhea or dysentery and growth faltering over three months after discharge.
infection was diagnosed in stool samples by PCR from 13 (8.7%) children, whereas it was isolated by conventional stool culture in only one (0.7%) child. The sensitivity of culture was only 7.7% against PCR for the diagnosis of infection, whereas blood in stools had a sensitivity of 15.4%. The majority of PCR-positive cases (11 out of 13) presented with non-bloody diarrhea. None of the evaluated clinical predictors had a significant association with the infection. No statistically significant difference was found between PCR-positive and PCR-negative children at the end of follow-up (P>0.05).
The majority of children with infection present with watery diarrhea rather than bloody diarrhea, and a history of blood in stools is a poor marker for the diagnosis of shigellosis. The diagnostic performance of stool culture is also very low compared to stool PCR for the diagnosis of diarrhea.
是五岁以下儿童腹泻的重要病因,常被传统实验室方法漏诊。便血一直是腹泻的综合征指标,但大多数病例表现为无血的水样腹泻。本研究旨在确定五岁以下儿童中通过分子方法和传统方法检测到的频率。此外,我们旨在研究按照当前腹泻治疗指南管理的腹泻儿童的临床特征和结局。
在这项基于医院的前瞻性观察研究中,对150名年龄在1个月至5岁之间的急性腹泻(病程<7天)儿童的粪便样本进行常规显微镜检查、粪便培养和DNA提取。从储存的粪便样本中提取的DNA使用针对侵袭质粒抗原H基因序列(ipaH)基因424bp的特异性引物进行聚合酶链反应(PCR)扩增。根据分子(PCR)和传统方法(粪便显微镜检查和培养)分离的百分比以及出院后三个月内腹泻或痢疾复发和生长发育迟缓方面的随访结果来解释结果。
通过PCR在13名(8.7%)儿童的粪便样本中诊断出感染,而通过传统粪便培养仅在1名(0.7%)儿童中分离出该病原体。培养对于诊断感染的敏感性仅为7.7%,而便血的敏感性为15.4%。大多数PCR阳性病例(13例中的11例)表现为非血性腹泻。所评估的临床预测指标均与感染无显著关联。随访结束时,PCR阳性和PCR阴性儿童之间未发现统计学显著差异(P>0.05)。
大多数感染儿童表现为水样腹泻而非血性腹泻,便血病史对志贺菌病的诊断价值不大。与粪便PCR相比,粪便培养对腹泻的诊断性能也非常低。