中国小儿急救医学最新文献

{"title":"Study on the expression level of zonula occludens 1 and zonula occludens 1 related nucleic acid binding protein in alveolar epithelial cells in hyperoxia induced bronchopulmonary dysplasia newborn rats","authors":"A′na Hou","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.002","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.002","url":null,"abstract":"Objective \u0000Previous studies have found abnormal proliferation and transdifferentiation of alveolar epithelial cells(AECs)in hyperoxic lung injury of neonatal rats.The purpose of this study was to clarify the expression of zonula occludens 1(ZO-1) and ZO-1 related nucleic acid binding protein(ZONAB)in AECs in hyperoxic lung injury model, in order to investigate its effect on the proliferation and transdifferentiation of AECs in the injured lung tissue. \u0000 \u0000 \u0000Methods \u0000Full-term neonatal Wistar rats were randomly divided into two groups within 12 h after birth, model group(inhaled oxygen concentration 85%)and control group(inhaled air). Lung specimens were collected at 7, 14 and 21 days after exposure.The expression of ZONAB in typeⅡalveolar epithelial cells(AECⅡ)was observed by double immunofluorescence staining.At the same time, AEC Ⅱ was isolated from lung tissues of animal models at these time points, and the expression levels of ZO-1, ZONAB protein and mRNA in lung tissues and AECⅡof the two groups were detected by Western blot and Real-Time PCR.In addition, AEC Ⅱ was isolated from lung tissue of normal newborn rats and then divided into model group(85% oxygen concentration)and control group(21% oxygen concentration). After 48 hours of culture in vitro, the expression levels of ZO-1, ZONAB protein and mRNA were detected, and the expression level and location of ZONAB were observed by immunofluorescence staining. \u0000 \u0000 \u0000Results \u0000Double immunofluorescence staining showed that the expression of ZONAB in AECⅡin model group was significantly lower than that in control group.The protein and mRNA expression levels of ZO-1 and ZONAB in AECⅡisolated from lung tissue of model group were both significantly lower than those from control group, starting from 7 d after hyperoxia exposure.AECⅡisolated from lung tissue of normal newborn rats, were then incubated for 48 hours under hyperoxia or normoxia in vitro, the protein and mRNA expression levels of ZO-1 and ZONAB significantly decreased in model group compared with those in control group.The results of immunofluorescence staining showed that the expression of ZONAB was higher in AECⅡof the control group, and ZONAB was mostly located in the junction and nucleus of cells, while the expression of ZONAB in the model group significantly decreased than that in the control group, and the expression sites were clustered in the cytoplasm, with little expression in the junction and nucleus. \u0000 \u0000 \u0000Conclusion \u0000ZO-1, as a tight junction-related protein, is down-regulated in hyperoxic lung injury model.In addition to destroying pulmonary epithelial barrier to mediate pulmonary edema, it also participated in the regulation of proliferation and differentiation of AECs by regulating transcription factor ZONAB, suggesting that this may be another pathway leading to hyperoxic lung injury. \u0000 \u0000 \u0000Key words: \u0000Hyperoxia; Alveolar epithelial cell; Transdifferentiation; Zonula occludens 1; Zonula occludens 1 related nucleic acid bindi","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"806-812"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41354107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reliability evaluation of two non-invasive cardiac function monitoring methods for preterm infants′ early cardiac function monitoring","authors":"Yulan Yang, Guichao Zhong, Lin Yang, Lu Ding, Benqing Wu","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.006","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.006","url":null,"abstract":"Objective \u0000To evaluate the consistency of ultrasonic cardiac output monitor (USCOM) and electric impedance (ICON) in cardiac function monitoring in preterm infants compared with echocardiography (ECHO). \u0000 \u0000 \u0000Methods \u0000All enrolled children were monitored with ECHO, USCOM and ICON on the 2nd and 7th day after birth.Heart rate (HR) and cardiac index (CI) were recorded. \u0000 \u0000 \u0000Results \u0000On the second day after birth, the CI measured by ECHO was (3.26±0.68) L/(min·m2), the CI measured by USCOM was (3.21±0.66) L/(min·m2), and the CI measured by ICON was (3.67 ±0.69) L/(min·m2), with an average percent error of 27.9% and 42.3%, respectively.On the 7th day after birth, the CI measured by ECHO was (3.53±0.57) L/(min·m2), the CI measured by USCOM was (3.47±0.59) L/(min·m2), and the CI measured by ICON was (3.73±0.67)L/(min·m2), with an average percent error of 25.8% and 28.3%, respectively. \u0000 \u0000 \u0000Conclusion \u0000Comparing USCOM with ECHO in cardiac output monitoring of preterm infants, the consistency is good at each time point after birth.Compared with ECHO, ICON has poor consistency in early postnatal cardiac index monitoring, but dynamic monitoring has a certain reference value after one week of birth. \u0000 \u0000 \u0000Key words: \u0000Premature infants; Cardiac function; Echocardiography; Electric impedance; Ultrasonic cardiac output monitoring","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"830-835"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42128320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Study on the variation of visual evoked potential and its diagnostic value in children with optic neuritis","authors":"Jingyong Sun, Xin Wang, Wenmin Yang, Xiaoyue Wang","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.008","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.008","url":null,"abstract":"Objective \u0000To investigate the characteristics and clinical value of visual evoked potentials(VEP) in children with optic neuritis. \u0000 \u0000 \u0000Methods \u0000The VEP of 33 children with optic neuritis were tested by NICOLET evoked potential instrument.The results were compared with those of cranial and/or orbital MRI and fundus examination, and the consistency with visual performance was analyzed.The correlation between visual sensitivity and VEP results was analyzed. \u0000 \u0000 \u0000Results \u0000Among 33 children with optic neuritis, the abnormal rate of VEP in 52 abnormal eyes was 88.5%; the abnormal rate of cranial and/or orbital MRI was 38.5%; the abnormal rate of fundus examination was 62.2%; the abnormal rate of VEP examination was significantly higher than that of cranial and/or orbital MRI and fundus examination (P<0.05); the consistency rate between VEP examination and visual acuity was 84.8%.The consistency rate between pattern reversal visual evoked potential (P-VEP) and visual acuity was 86.8%, and that between flash visual evoked potential (F-VEP) and visual acuity was 82.1%.With the increase of visual impairment, the percentage of P100 wave loss increased gradually.There was no correlation between visual acuity and the prolongation of P100 wave latency. \u0000 \u0000 \u0000Conclusion \u0000There are significant differences between VEP and fundus examination and MRI, the sensitivity of VEP is superior to both.P-VEP is more consistent with visual acuity than F-VEP.VEP has certain value in evaluating the degree of visual impairment in children with optic neuritis.It can not be used to evaluate the level of optic sensitivity when the latency of P100 wave is prolonging. \u0000 \u0000 \u0000Key words: \u0000Optic neuritis; Visual evoked potentials; Visual; Children","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"840-845"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49523719","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Adverse Tracheal Intubation-Associated Events in Pediatric Patients at Nonspecialist Centers: A Multicenter Prospective Observational Study","authors":"方伯梁, 钱素云","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.102","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.102","url":null,"abstract":"目的 \u0000三级医院PICUs中常见不良气管插管相关事件(adverse tracheal intubation associated events，TIAEs)，占20%，严重TIAEs 3%～6.5%。然而患儿常就诊于无专业医师的医院且需当地团队气管插管。此类情况下的TIAEs率并无确切研究。本研究假定无专业医师医院内TIAEs率较高。 \u0000 \u0000 \u0000设计和场所 \u0000本研究设计了一项包含英国北泰晤士和东安格里亚47家地区医院的多中心前瞻性观察性研究。 \u0000 \u0000 \u0000对象 \u00002016年6月至2018年5月间经儿童紧急转运服务(children's acute transport service，CATS)转运的气管插管患儿。 \u0000 \u0000 \u0000干预 \u0000无。 \u0000 \u0000 \u0000测量方法与主要结果 \u00001 051/1 237(85%)例符合纳入标准患儿数据可用。TIAEs总体发生率22.7%，严重TIAEs发生率13.8%。小年龄，体格发育落后及困难气道患儿合并症发生率较高。存在合并症及困难气道患儿严重TIAEs发生率增加。最常见TIAEs为支气管内插管(6.2%)，低血压(5.4%)以及心动过缓(4.2%)。多参数分析显示TIAEs独立预测因子包括尝试插管次数(>4次尝试相比1次尝试 OR 19.1，95%CI 5.9-61.4)及插管者专业(急诊医学相比于麻醉医师 OR 6.9，95%CI 1.1-41.4)。 \u0000 \u0000 \u0000结论 \u0000TIAEs常见于就诊于无专业医师医院的危重患儿。此类医院中严重TIAEs率远高于PICU。需重点关注提高无专业医师医院气管插管安全性。","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"880-880"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43808757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Risk factors for extubation failure after congenital heart surgery","authors":"Linhong He","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.012","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.012","url":null,"abstract":"目的 \u0000探讨儿童先天性心脏病(congenital heart disease，CHD)术后撤机失败的危险因素。 \u0000 \u0000 \u0000方法 \u0000回顾分析2016年1月至2017年1月行心内直视手术CHD患儿的临床资料，以术后撤离呼吸机72 h内需要再次上机为撤机失败，将纳入患儿分为撤机失败组与撤机成功组，比较两组患儿术前、术中和术后相关因素的差异，并采用Logistics回归分析撤机失败的危险因素。 \u0000 \u0000 \u0000结果 \u0000共纳入CHD患儿257例，撤机失败30例(11.7%)。撤机失败组与撤机成功组患儿在年龄、体重、合并气道畸形、合并21-三体综合征、术前机械通气(mechanical ventilation，MV)、先天性心脏病手术风险分级、体外循环时间、撤机前MV时间及撤机前并发呼吸机相关性肺炎的差异有统计学意义(P 7 d是撤机失败的独立危险因素。 \u0000 \u0000 \u0000结论 \u0000撤机失败在CHD术后患儿中并不少见；年龄 7 d的CHD患儿发生术后撤机失败的风险较高。","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"863-866"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48535816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Clinical characteristics and risk factors of coronary artery abnormities in infants with Kawasaki disease","authors":"Ce Wang","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.007","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.007","url":null,"abstract":"Objective \u0000To analyze the clinical characteristics of Kawasaki disease in infants and explore the risk factors of coronary artery abnormities in Kawasaki disease. \u0000 \u0000 \u0000Methods \u0000The clinical data of 300 children with Kawasaki disease from January 1, 2018 to December 31, 2018 were retrospectively analyzed, including laboratory tests and coronary ultrasound results.The clinical characteristics of infants with Kawasaki disease and elderly children with Kawasaki disease were compared.The risk factors of coronary artery injury in infants with Kawasaki disease were analyzed. \u0000 \u0000 \u0000Results \u0000The majority of infants with Kawasaki disease were atypical Kawasaki disease, and the typical changes of conjunctival congestion, perianal changes and plaque were significantly higher than those of elderly children (P<0.01). Leukocyte count and platelet count were higher in the infant group, and the number of children with abnormal liver function was significantly higher than that in the older group (P<0.05). Coronary artery dilatation occurred in 11% of infants with Kawasaki disease, and most of them returned to normal within 3 months.Logistic model design was used to analyze the risk factors of coronary artery injury in infants with Kawasaki disease.It was found that boys and CRP increased significantly were the risk factors of coronary artery injury in infants with Kawasaki disease. \u0000 \u0000 \u0000Conclusion \u0000Infant Kawasaki disease has its own characteristics.The incidence of coronary artery injury is high.Timely diagnosis, differential diagnosis and symptomatic treatment may reduce the incidence of coronary artery injury.At the same time, follow-up should be maintained to monitor the changes of coronary artery by echocardiography. \u0000 \u0000 \u0000Key words: \u0000Infants; Kawasaki disease; Coronary artery abnormities; Risk factors","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"836-839"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46901314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Progress of inhaled nitric oxide on treatment of persistent pulmonary hypertension of new-born","authors":"Chang Liu, Shuqing Zhang, Dongmei Yue","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.011","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.011","url":null,"abstract":"Persistent pulmonary hypertension is a serious disease among new-borns.Despite the variety of causes, similar physiopathologic changes characterize this syndrome: a persistently raised pulmonary vascular resistance after birth, which leads to severe hypoxemia due to extrapulmonary shunting.The fundamental treatment is to reduce pulmonary vascular pressure and improve hemodynamics.Modern treatments such as inhaled nitric oxide, high-frequency oscillation ventilation, extracorporeal membrane oxygenation, and/or other pulmonary vasodilators could reduce mortality in neonatal persisitent pulmonary hypertension(PPHN). Inhaled nitric oxide is the main method for the treatment of PPHN, which can effectively improve oxygenation and reduce the need for extracorporeal membrane oxygenation(ECMO). The effect of inhaled nitric oxide is different with the gestational age changed.This article aims to summarize the clinical research progress of inhaled nitric oxide in the treatment of PPHN. \u0000 \u0000 \u0000Key words: \u0000Persistent pulmonary hypertensionof the newborn; Inhaled nitric oxide; Pulmonary vasodilator substance","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"858-862"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46632430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Changes and significance of serum midkine in children with allergic purpura and purpura nephritis","authors":"Peng Zhou, Yongchang Yang","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.004","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.004","url":null,"abstract":"Objective \u0000To investigate the role of midkine(MK)in the pathogenesis of Henoch-Schonlein purpura(HSP) and Henoch-Schonlein purpura nephritis(HSPN). \u0000 \u0000 \u0000Methods \u0000In the case group, 35 cases were hospitalized in the pediatric kidney rheumatism immunology ward of Shengjing hospital affiliated to China Medical University from December 2016 to January 2018.Among them, 10 cases were HSP, 25 were HSPN.According to quantitative level of 24-hour urine protein, HSPN group was divided into HSPN(nephrotic level of proteinuria)group of 15 cases and HSPN(non-nephrotic level of proteinuria)group of 10 cases.The control group consisted of 12 healthy cases who underwent physical examination at outpatient department in the same period in the developmental pediatric clinic of our hospital.Blood samples were collected to detect MK.The other clinical datas including renal function, 24-hour urine protein quantitative, immunoglobulin, etc were collected.The serum MK and renal function indexes were compared among groups.The correlation between MK and various clinical indicators was analyzed, and the receiver operating characteristic(ROC) curve was used to analyze the diagnostic significance of MK for HSP and HSPN. \u0000 \u0000 \u0000Results \u0000MK level of case group was higher than that of healthy control group[(289.34±160.70)pg/ml vs.(100.03±56.75)pg/ml, P<0.05]. Moreover, the difference of MK concentration among the HSPN(nephrotic proteinuria)group, the HSPN(non-nephrotic proteinuria)group and the HSP group was still statistically significant[(449.91±141.91)pg/ml vs.(244.04±89.15)pg/ml vs.(175.94±46.30)pg/ml, P<0.05]. MK was positively correlated with urine microalbumin(r=0.54), IgA(r=0.132), IgE(r=0.304), urine β2 microglobulin(r=0.483), 24-hour urine protein /body weight(r=0.503), and urine transferrin level(r=0.509)in the case group(P<0.05). According to the ROC curve, the area under ROC of MK for predicting the diagnosis of HSP was 0.908(95%CI 0.828-0.988). The optimal value in predicting the diagnosis of HSP was 182.762 pg/ml, with sensitivity and specificity of 81.4% and 91.7%.The area under ROC of MK in predicting HSPN was 0.947(95%CI 0.888-1.000), and the optimal value of predicting HSPN was 218.186 pg/ml, with sensitivity and specificity of 84.0% and 95.5%. \u0000 \u0000 \u0000Conclusion \u0000MK may be involved in the pathogenesis of HSP and HSPN.It can provide the basis for clinical diagnosis of HSP and HSPN, and has significance in evaluating the degree of renal damage of HSPN. \u0000 \u0000 \u0000Key words: \u0000Henoch-Schonlein purpura; Henoch-Schonlein purpura nephritis; Midkine; Children","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"820-824"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49526236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Molecular characteristics of Staphylococcus aureus isolated from neonates","authors":"Chen Sun, Yajuan Wang, Xin Yang, Lijuan Wang, Y. Qi, F. Dong, Wenqi Song, Ying-chao Liu, K. Yao, S. Qian","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.003","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.003","url":null,"abstract":"Objective \u0000To study the clinical and molecular characteristics of Staphylococcus aureus(S.aureus ) isolated from neonates of Beijng Children′s Hospital. \u0000 \u0000 \u0000Methods \u0000The clinical information of S. aureus infection in newborns of Beijing Children′s Hospital from February 2016 to January 2017 was collected.The molecular biological characteristics of S. aureus isolates were detected.Methicillin-resistant S. aureus (MRSA) and methicillin-susceptible S. aureus(MSSA)were identified, using the cefoxitin disc method and the detection of the mecA gene.Multilocus sequence typing(MLST)and spa typing were analyzed using the PCR, and the staphylococcal chromosomal cassette mec(SCCmec) type was analyzed for the MRSA isolates.Eleven adhesion gene and three virulence genes(pvl, psma, hlα )were also detected by PCR.Antimicrobial susceptibility testing was performed by agra dilution method or E-test method. \u0000 \u0000 \u0000Results \u0000The total of 57 cases of neonatal S. aureus infection were collected during the study.The most common clinical diagnosis was 38 cases (66.7%) of pneumonia and 28 cases (49.1%) of skin infection syndrome (SSTI). There were 31 cases (54.4%) with MRSA infection and 26 cases (45.6%) with MSSA infection.The proportion of SSTI in the MRSA group (64.5%) and the infection of more than 2 sites (61.3%, 19/31) were significantly higher than those in the MSSA group (30.8%, 8/26 and 23.1%, 6/31). There were 16 MLST types and 29 spa types, the most common ones were ST59 (40.4%) and t437 (33.33%), respectively.The most common popular clones of MRSA and MSSA were ST59-SCCmecIVa-t437 (54.8%) and ST22-t309, respectively(11.5%). The sdrE carrying rate of MRSA was higher than that of MSSA, while the sdrD and cna carrying rates were lower than those of MSSA (P<0.05). The other adhesion and virulence gene carrying rates were not significantly different between the two strains.The multi-drug resistance rate of all strains was 61.4%(35/57). Except for lactam antibiotics, the most common resistant phenotypes of MRSA and MSSA were ERY-CLI, accounting for 74.2% and 26.9%, respectively. \u0000 \u0000 \u0000Conclusion \u0000The main types of neonatal S. aureus infection in our hospital were pneumonia and SSTI.SSTI and multi-site infections of MRSA infection are more common.MRSA and MSSA isolates have clonal dissemination characteristics.The most common clones are ST59-SCCmecIVa-t43 and ST22-t309, which show no significant differences in the status of carrying virulence factors between them.The multi-drug resistance rate of neonatal S. aureus isolates is higher. \u0000 \u0000 \u0000Key words: \u0000Staphylococcus aureus; Neonate; Molecular characteristics; Virulence; Antibiotic resistance","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"813-819"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47558767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The clinical manifestations and treatment of hand, foot and mouth disease caused by Coxsackievirus A6","authors":"L. Liang, J. Qiu, Zhenghui Xiao","doi":"10.3760/CMA.J.ISSN.1673-4912.2019.11.010","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1673-4912.2019.11.010","url":null,"abstract":"Hand-foot-and-mouth disease (HFMD) is a common infectious disease caused by human enterovirus (EVs). It is more common in children under 5 years of age.The clinical symptoms are mainly rash and herpes in the hands, feet, mouth and other parts.Some serious cases may suffer from serious complications in nervous system, respiratory system or circulatory system.Since 1998, HFMD has been mainly caused by enterovirus 71 and coxsackievirus A16 (CV-A16). In the past 10 years, coxsackievirus A6(CV-A6) has gradually replaced EV-71 and CV-A16, and become a main pathogen of HFMD.Many literatures have shown that CV-A6 often causes atypical HFMD, which is mainly characterized by a wider and more serious rash and desquamation, and even onychomadesis.At present, there are some reports on the prevalence and detection methods of HFMD caused by CV-A6.The paper reviewed on CV-A6 related etiology, epidemiology, clinical manifestations and treatment of HFMD. \u0000 \u0000 \u0000Key words: \u0000Hand, foot and mouth disease; Coxsackie A6; Pathogen; Epidemiology; Clinical manifestations; Treatment","PeriodicalId":68901,"journal":{"name":"中国小儿急救医学","volume":"26 1","pages":"852-857"},"PeriodicalIF":0.0,"publicationDate":"2019-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48227594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}