Loading...

Table of Content

    15 September 2022 Volume 40 Issue 9
      
    Commentary
    Advances in the diagnosis and treatment of neonatal necrotizing enterocolitis
    ZHU Xueping, QIAN Jihong
    Journal of Clinical Pediatrics. 2022, 40(9):  641-646.  doi:10.12372/jcp.2022.22e1060
    Abstract ( 545 )   HTML ( 70 )   PDF (1168KB) ( 319 )  
    Figures and Tables | References | Related Articles | Metrics

    It is difficult to early identify necrotizing enterocolitis (NEC) and its severity of illness. The Bell staging criteria is widely utilized to diagnose and evaluate the severity of NEC in clinical practice. Thanks to much advancement that have been achieved in molecular biology and neonatology, the preventive and therapeutic strategies for NEC are significantly improved. However, the morbidity and mortality of NEC are still unchanged. In recent years, the combination of omics and clinical data to find relevant biomarkers for early prediction of NEC, the prevention of NEC by breastfeeding and maintenance of gut microbiota homeostasis, and the exploration of stem cell and exosome related treatment have all brought new directions for the diagnosis and treatment of NEC. These means above will bring some new hopes to reduce the morbidity and mortality of NEC and improve its long-term outcomes.

    Expert Review
    Transfusion-associated necrotizing enterocolitis
    LEI Xiaoping, LUO Lijuan
    Journal of Clinical Pediatrics. 2022, 40(9):  647-653.  doi:10.12372/jcp.2022.22e0361
    Abstract ( 513 )   HTML ( 51 )   PDF (1253KB) ( 251 )  
    Figures and Tables | References | Related Articles | Metrics

    Neonatal necrotizing enterocolitis (NEC) is a serious and life-threatening gastrointestinal disease in the neonatal period. The atypical clinical manifestations of NEC, especially in premature infants, are abdominal distension, vomiting, bloody stools and shock. At present, the widely known pathogenesis of NEC includes preterm birth, infection, hypoxia-ischemia and improper feeding, etc. In recent years, the association between red blood cell transfusion (RBCT) and NEC was widely concerned. This article reviewed the relationship between RBCT and NEC, the influence factors, possible pathologic mechanism and the prevention strategies of transfusion-associated necrotizing enterocolitis (TANEC). Based on the available evidences, the author believes that TANEC is a clinical condition. However, anemia is the basis for the onset of TANEC. Prevention of anemia and reasonable blood transfusion are the basic strategies to reduce TANEC.

    Research status and potential application of intestinal microbiota and its metabolites in neonatal necrotizing enterocolitis
    LI Luquan, LIU Xiaochen
    Journal of Clinical Pediatrics. 2022, 40(9):  654-660.  doi:10.12372/jcp.2022.22e0301
    Abstract ( 270 )   HTML ( 15 )   PDF (1199KB) ( 156 )  
    References | Related Articles | Metrics

    The early prediction of necrotizing enterocolitis (NEC) by intestinal microbiota and its metabolites has been a hot research topic in recent years. Recent studies have found that infants with necrotizing enterocolitis (NEC) not only have low biodiversity of the intestinal microbiota, but also the composition proportion of microbiota is significantly different from that of healthy newborns. There are also abnormalities in amino acid, lipid metabolism and related metabolic enzymes in infants with NEC. Intestinal microbiota and its metabolites have certain value in predicting the onset and progression of NEC, but they can only be used as the basis for scientific research. High-quality, multi-center, and large-scale clinical studies are needed for clinical application in the future.

    Neonatal Disease
    Risk factors of necrotizing enterocolitis in small for gestational age neonates
    HUANG Dan, JIANG Yajun, ZHANG Zhongyao, LI Luquan
    Journal of Clinical Pediatrics. 2022, 40(9):  661-665.  doi:10.12372/jcp.2022.22e0213
    Abstract ( 268 )   HTML ( 16 )   PDF (1188KB) ( 144 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To explore the risk factors of necrotizing enterocolitis (NEC) in small for gestational age (SGA) neonates. Methods The SGA patients suffering from NEC from January 2008 to December 2021 were selected as the research subjects. The SGA patients without NEC in the same period were selected as the control group, and 1∶2 matching was performed according to gestational age difference <3 d, birth weight difference <200 g, and date of admission difference <3 months. The influencing factors of NEC occurrence in SGA neonates were analyzed by conditional logistic regression. Results A total of 5 365 SGA neonates were admitted during the study period, among whom 147 SGA neonates met the diagnostic criteria of NEC stage Ⅱ or above, and the incidence rate was 2.70%. After screening and exclusion, 140 patients were finally included. A total of 280 SGA neonates were involved in the control group by 1∶2 matching. Compared with the control group, the NEC group had higher rates of anemia, neonatal sepsis, death or treatment abandonment, longer hospital stay, and lower rates of prenatal exposure to glucocorticoids and oral probiotics, and the differences were statistically significant (P<0.05). Conditional logistic regression analysis showed that sepsis and anemia were independent risk factors for NEC in SGA (P<0.05), while prenatal glucocorticoids exposure and oral probiotics were independent protective factors (P<0.05). Conclusions The SGA neonates with anemia and sepsis are more likely to develop NEC, while oral probiotics and prenatal exposure to glucocorticoids can reduce the risk of NEC..

    Risk factors of transfusion-associated necrotizing enterocolitis in very preterm infants
    WEI Lele, SONG Juan, DONG Huimin, JUE Zhenzhen, LI Wendong, XU Falin, WANG Jun
    Journal of Clinical Pediatrics. 2022, 40(9):  666-671.  doi:10.12372/jcp.2022.21e1387
    Abstract ( 270 )   HTML ( 13 )   PDF (1176KB) ( 294 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To identify the risk factors of transfusion-associated necrotizing enterocolitis (TA-NEC) in very preterm infants. Methods The very premature infants admitted to the neonatal intensive care unit between April 2013 and April 2021 who received red blood cell transfusion were selected as the study subjects. The very premature infants meeting the inclusion criteria of the TA-NEC group were included in the TA-NEC group. Non-NEC very premature infants of the same gender, gestational age (±3 d), birth weight (±200 g) and transfusion age (±3 d) at the same time were matched as the control group at a ratio of 1∶2. The clinical characteristics between the two groups were compared to explore the risk factors of TA-NEC. Results A total of 204 very premature infants (138 boys and 66 girls) were included. The mean gestational age was (29.0±1.5) weeks, and the median birth weight was 1100.0 (951.0-1200.0) g. Sixty-eight patients were in the TA-NEC group and 136 in the control group. The multivariate conditional logistic regression analysis showed that fetal distress, chorioamnionitis and late-onset sepsis were independent risk factors of TA-NEC (P<0.05), and full oral feeding was an independent protective factor against TA-NEC (P<0.05) in very premature infants. Conclusions The very premature infants with fetal distress, chorioamnionitis and/or late-onset sepsis are more likely to develop NEC within 48hours after a transfusion of red blood cells. The prevention of perinatal hypoxia and sepsis and the completion of the transition to full oral feeding safely have a positive role in reducing the incidence of TA-NEC in very preterm infants.

    Investigation of the relationship between gene polymorphisms and neonatal hyperbilirubinemia in southwest China
    LIU Ling, JIANG Yuhui, NIE Panrong, ZENG Limei, DUAN Gaiyuan, LI Yuchen
    Journal of Clinical Pediatrics. 2022, 40(9):  672-678.  doi:10.12372/jcp.2022.21e1598
    Abstract ( 282 )   HTML ( 7 )   PDF (2499KB) ( 134 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To investigate the relationship between uridine diphosphate-glucuronosyl transferase 1A1 (UGT1A1), organic anion transporter family member 1B1 (SLCO1B1) and glucose-6-phosphate dehydrogenase (G6PD) gene polymorphisms and neonatal hyperbilirubinemia in southwest China. Methods A total of 190 neonates with neonatal hyperbilirubinemia from September 2016 to December 2019 in Yunnan, Guizhou and Sichuan provinces were selected as the study group, and 200 neonates without jaundice who were hospitalized during the same period were randomly selected as the control group. Genomic DNA was extracted from venous blood and 17 SNPs sites were genotyped by Sequenom-specific SNP detection. Genotype and allele frequency were compared between the study and control groups. Results There were 190 patients (98 boys and 92 girls) in the study group, and the average gestational age was (38.7±1.2) weeks. In the control group, there were 200 neonates (116 boys and 84 girls), and the average gestational age was (38.9±1.3) weeks. The allele frequencies of UGT1A1 rs873478, rs34946978 and rs4148323 were higher in the study group than those in the control group, while the allele frequency of SLCO1B1 rs72559748 was lower in the study group than that in the control group, and the differences were statistically significant (P<0.05). The G6PD rs72554664 variant was detected in two boys with hyperbilirubinemia, and the detection rate was 1.05%. There was significant difference in the distribution of risk alleles between the study group and the control group (P<0.05), and the proportion of risk alleles ≥2 was higher in the study group. Conclusions The UGT1A1 rs873478, rs34946978 and rs4148323 polymorphisms were associated with higher risk of neonatal hyperbilirubinemia in southwest China. The SLCO1B1 polymorphism was not significantly associated with the incidence of neonatal hyperbilirubinemia and lack of G6PD enzyme activity may not be a major risk factor for neonatal hyperbilirubinemia in this region.

    Correlation analysis of amplitude-integrated electroencephalogram follow-up indicators and neurological prognosis of very low birth weight infants
    ZENG Xiaoliang, MIN Qing, WU Shuyuan
    Journal of Clinical Pediatrics. 2022, 40(9):  679-684.  doi:10.12372/jcp.2022.21e1476
    Abstract ( 202 )   HTML ( 5 )   PDF (1231KB) ( 99 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To analyze the correlation between amplitude-integrated electroencephalogram (aEEG) follow-up indicators and the neurological prognosis in very low birth weight infants. Methods A total of 224 very low birth weight infants delivered from January 2016 to January 2019 were selected for aEEG monitoring within one week after birth and at 3, 6 and 12 months of corrected gestational age. According to the neurological development outcome at 12 months of corrected gestational age, the infants were divided into normal group and abnormal group, and the difference of aEEG monitoring score between the two groups was compared. Results A total of 224 very low birth weight infants (125 boys and 99 girls) were included, the gestational age was (30.01±1.49) weeks and the birth weight was (1366.64±119.43) g. At 12 months of corrected gestational age, the nervous system development outcome was normal in 153 cases and abnormal in 71 cases. Within one week of birth, there was a statistically significant difference in sleep cycle (Cy) and total (T) scores between normal and abnormal groups (P<0.05). There were significant differences in graph continuity (Co), Cy and T scores between the two groups at 3 and 6 months of corrected gestational age (P<0.05). At 12 months of corrected gestational age, there were significant differences in Co, lower bound amplitude (LB), Cy, bandwidth (B) and T scores between the two groups (P<0.05). Binary logistic regression analysis showed that Co, Cy and T scores in aEEG monitoring indexes at 12 months of corrected gestational age were significantly correlated with the nervous system development outcome of very low birth weight infants (P<0.01), and the lower the score, the greater the risk of abnormal neurodevelopmental outcome. By drawing ROC curve, Co and T scores of aEEG at 12 months of gestational age were found to have moderate predictive value for the neurological outcome of very low birth weight infants (AUC 0.71 and 0.82). Conclusions The aEEG follow-up indicators are correlated with the neurological prognosis in very low birth weight infants and have certain predictive value.

    Clinical analysis of 8 neonates with cerebral white matter venous infarction
    LIN Yayin, ZHENG Zhi, ZHAO Feng
    Journal of Clinical Pediatrics. 2022, 40(9):  685-689.  doi:10.12372/jcp.2022.21e1338
    Abstract ( 259 )   HTML ( 7 )   PDF (1866KB) ( 197 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To investigate the risk factors, clinical manifestations and imaging characteristics of cerebral deep white matter venous infarction in neonates. Methods The clinical data of 8 neonates with cerebral deep white matter venous infarction confirmed by cranial imaging during January 1, 2017 to December 31, 2019 were retrospectively analyzed, and the etiological factors, clinical manifestations and imaging characteristics of the neonates were analyzed and summarized. Results Among the 8 neonates with deep white matter venous infarction, 6 were premature and 2 were full term. The mean gestational age was (32.2±3.9) weeks and the mean birth weight was (1932.0±794.0) g. The age of onset ranged from 1 day to 30 days. Five neonates underwent pathological examination of placenta, including 4 cases of chorioamnionitis and 1 case of intervillous thrombus. Four cases were complicated with purulent meningitis, 3 cases had a history of perinatal hypoxia, and 1 case had intrauterine rubella virus infection with polycythemia. Among the 8 neonates, 4 had fever, 3 had transient seizures, and 2 were asymptomatic. One patient underwent puncture at the site of craniocerebral infarction, and 60mL of bleeding like fluid was aspirated, and bacterial culture was negative. Cranial MRI was performed between 2 and 54 days after onset. MRI showed that white matter venous infarction mostly occurred in the frontal parietal white matter (6/8), with enhanced signals surrounding the lesions. Cerebral infarction site could be accompanied by liquefaction and cavity, which is easily confused with cerebral abscess. Conclusions Chorioamnionitis, purulent meningitis and perinatal hypoxia are the main inducing factors of neonatal deep white matter venous infarction. The clinical manifestations of cerebral venous infarction are easy to be ignored. Their MRI findings are often confused with cerebral abscesses, and attention should be paid tothe identification.

    General Report
    Analysis of echocardiographic assessment of coronary artery abnormalities in children with Kawasaki disease
    SUN Rui, CAO Aimei, LI Xiaohui, YUAN Yue, ZHANG Mingming, LI Dan, SHI Lin
    Journal of Clinical Pediatrics. 2022, 40(9):  690-695.  doi:10.12372/jcp.2022.21e1282
    Abstract ( 257 )   HTML ( 4 )   PDF (1232KB) ( 104 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Four echocardiographic methods for assessing Kawasaki disease (KD) complicated with coronary artery abnormalities were analyzed to provide a basis for early accurate clinical assessment. Methods The KD children combined with coronary artery lesions who were hospitalized in the Department of Cardiology from December 2017 to July 2020 were selected as the study subjects. Three Z-value formulas (Kobayashi, Dallaire and Olivieri) and 1988 domestic standard were used to evaluate the coronary artery abnormalities caused by KD. Results A total of 94 patients (59 boys and 35 girls) were enrolled with a median age of 18.1 (7.3-31.7) months. There were statistically significant differences in the lesions degree evaluation of proximal right coronary artery (pRCA), left main coronary artery (LMCA) and left anterior descending artery (LAD) among the four coronary artery lesions assessment methods (P<0.01). The detection rate of large coronary aneurysms in pRCA by Olivieri method was significantly lower than that by Dallaire method (P<0.05). The detection rate of Olivier method was significantly higher than the other three methods in the evaluation of normal and only dilated LMCA (P<0.05). For small coronary aneurysms, the detection rate of Olivier method was significantly lower than Kobayashi method and domestic standard in 1988 (P<0.05). Dallaire's detection rate was significantly higher than Kobayashi's and Olivieri's for large coronary aneurysms of LAD (P<0.05). When evaluating the right coronary artery (RCA) using the Dallaire method, it was found that if the pRCA was measured alone, the extent of RCA lesion expansion in 11.7% of patients would be underestimate, as well as 52.1% of middle RCA lesions and 27.7% of distant RCA lesions would be missed. Among the children who measured the middle of LAD, 30% of the children with abnormal middle of LAD were missed by Z-value evaluation of the proximal LAD alone. Conclusions In order to reduce the misdiagnosis of coronary artery lesions at the early stage of KD, all the different segments of the 4 coronary arteries should be measured as much as possible by echocardiography. The proximal and distal segments of RCA should be evaluated by Dallaire method. The criterion of a dimension >1.5 times should be used for the middle of LAD. For the middle of LAD, a ratio greater than 1.5 times the diameter of the surrounding segments is recommended.

    Therapeutic effect of chemotherapy on lung metastases of nephroblastoma
    SHI Yan, YANG Meng, HUANG Yitian, XU Junjie, WEN Sheng, HE Dawei, WEI Guanghui, HUA Yi
    Journal of Clinical Pediatrics. 2022, 40(9):  696-700.  doi:10.12372/jcp.2022.21e1243
    Abstract ( 243 )   HTML ( 7 )   PDF (1251KB) ( 104 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To observe the outcome of lung metastases in Wilms’ tumor (WT) and to explore the efficacy of different chemotherapy regimens. Methods The clinical data of WT children with lung metastases who were treated and followed up regularly from 2012 to 2020 were retrospectively analyzed to explore the difference in response to different chemotherapy regimens. Results There were 20 WT children (11 boys and 9 girls) with lung metastases, and the median age was 38.0(5.8~20.0) months. There were 17 cases of favorable histology (FH) type and 3 cases of unfavorable histology (UFH) type. Single lung metastasis was found in 13 cases and bilateral lung metastases were in 7 cases. At the initial diagnosis, 1 case was diagnosed as stageⅠ, 5 cases as stageⅡ, 3 cases as stage Ⅲ and 9 cases as stage Ⅳ. Two cases were first diagnosed in other hospitals with unknown stage. Lung metastases were found preoperatively in 12 cases and postoperatively in 8 cases. Eight cases were complicated with other distant metastases. After chemotherapy, the metastatic response was complete remission in 8 cases, partial remission in 4 cases, stable in 4 cases and progressive in 4 cases. Ordered logistic regression analysis was used for multivariate analysis. The results showed that the partial regression coefficient of CCCG-WT-2016 chemotherapy regimen was -2.05, presenting significance at the test level of 0.05 (Z=-2.03, P=0.043). It was suggested that CCCG-WT-2016 regimen was superior to NWTS-5 regimen in lung metastasis response. Conclusions The objective response in children treated with CCCG-WT-2016 regimen was significantly better than that of children treated with NWTS-5 regimen.

    Genotype-phenotype correlation of four cases of SHANK2-associated neurodevelopmental disorders in a family with different severity
    TIAN Maoqiang, SHU Xiaomei, LI Juan, LEI Wenting, CHEN Jing, YU Xiaohua, PENG Longying
    Journal of Clinical Pediatrics. 2022, 40(9):  701-704.  doi:10.12372/jcp.2022.21e1195
    Abstract ( 288 )   HTML ( 8 )   PDF (1485KB) ( 98 )  
    Figures and Tables | References | Related Articles | Metrics

    Neurodevelopmental disorders (NDDs) have strong clinical heterogeneity and complex genotype-phenotype correlation. To improve clinicians' understanding of the genotype-phenotype correlation of SHANK2, this study reported the patients presenting with different degrees of NDDs and carrying three combinations of SHANK2 variations from the same family. A total of 4 patients in the 2 generations of this family showed mild to severe mental retardation. Genetic testing found SHANK2 gene variations, including monoallelic variation c.2309-2A>C (mother) and monoallelic exon 11-16 deletion (father), and two children (the proband and his second sister) who carried the biallelic variations. The father with the monoallelic deletion variation showed mild intellectual disability, the mother with the monoallelic c.2309-2A>C variation showed moderate intellectual disability, and the two patients with the biallelic variations manifested severe intellectual disability. The severity of SHANK2-related NDDs may be associated with SHANK2 quantity dependence, and this quantity dependence provides help for understanding the genotype-phenotype correlation of SHANK2-related NDDs.

    Progressive myoclonic epilepsy caused by SEMA6B gene variations: a case report
    ZHAO Jinhua, TANG Jihong, HUANG Jing, XIAO Xiao, ZHANG Bingbing, XING Yujiao, SHI Xiaoyan
    Journal of Clinical Pediatrics. 2022, 40(9):  705-709.  doi:10.12372/jcp.2022.21e1029
    Abstract ( 303 )   HTML ( 20 )   PDF (2440KB) ( 161 )  
    Figures and Tables | References | Related Articles | Metrics

    A 15-year-old female patient was admitted to the hospital due to developmental retardation for 14 years and significant motor and cognitive regression for more than 1 year. The clinical features of this patient were myoclonus, intention tremor, ataxia, tendon hyperreflexia, hypertonia, dysarthria, speech regression, intellectual disability and multifocal seizures. Electroencephalogram showed typical epileptic discharge and the epilepsy was refractory. The patient had developmental retardation since childhood. Walking gait instability gradually aggravated, and eventually developed into walking difficulties with tremor of limbs. In addition of seizures, language and cognitive regression of the patient was evident. Genetic testing found a variation of SEMA6B gene in the child, which was determined as a pathogenic variation combined with genetic characteristics and clinical phenotype, and the child was diagnosed as progressive myoclonic epilepsy (PME). Treatment of PME is generally anti-seizure, as well as palliative support and rehabilitation measures. Most patients have poor prognosis. Genetic testing contributes to the diagnosis and treatment of patients with refractory epilepsy. SEMA6B gene variation can lead to PME phenotype. The gene variation C.2149 (exon17) C>T has not been reported before, which expands the gene variation spectrum of PME.

    Literature Review
    Research progress of extracorporeal membrane oxygenation combined with renal replacement therapy in children
    Reviewer: YANG Baowang, Reviser: HONG Xiaoyang, FENG Zhichun
    Journal of Clinical Pediatrics. 2022, 40(9):  710-714.  doi:10.12372/jcp.2022.21e1326
    Abstract ( 226 )   HTML ( 8 )   PDF (1097KB) ( 105 )  
    References | Related Articles | Metrics

    Extracorporeal membrane oxygenation (ECMO), as a salvage treatment for severe cardiopulmonary failure, has been widely applied in pediatric patients with severe diseases. Although the survival rate of children is gradually improved after the use of this technique, there are still some complications, such as acute kidney injury, systemic infection, hemorrhage and thrombosis. Studies have shown that acute kidney injury and fluid overload can significantly increase the mortality and prolong the running time of ECMO in children. Therefore, renal replacement therapy is increasingly used for the management of fluid overload and acute kidney injury in patients with ECMO. This article reviewed the strategies of ECMO combined with renal replacement therapy in children, and discussed the incidence and risk factors of acute kidney injury, timing of renal replacement therapy, management strategy of renal replacement therapy, prognosis, and advantages and disadvantages of different renal replacement therapy strategies.

    Continuing Medical Education
    Advances in Bifidobacterium longum and intestinal health during infancy
    WU Shiyin, CAI Meiqin
    Journal of Clinical Pediatrics. 2022, 40(9):  715-720.  doi:10.12372/jcp.2022.21e0107
    Abstract ( 235 )   HTML ( 12 )   PDF (1259KB) ( 237 )  
    Figures and Tables | References | Related Articles | Metrics

    Bifidobacterium longum is a commensal microbiota beneficial to the intestine, which is closely related to gut health during infancy. This paper reviews the physiological characteristics and the biological characteristics of genomics, metabolomics and proteomics, the prebiotic function in treating or alleviating gastrointestinal diseases in infants, and the research progress and application development prospect at home and abroad of Bifidobacterium longum. This review also analyzes the efficacy and possible mechanism of different strains of Bifidobacterium longum in the treatment of infantile functional constipation, irritable bowel syndrome and inflammatory bowel disease in order to provide scientific basis for the application of Bifidobacterium longum in clinical treatment or alleviation of gastrointestinal diseases in infants, and provide ideas for the development of Bifidobacterium longum functional strains and their in-depth research on promoting intestinal health.