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Feasibility of quantitative measurement of fetal trachea and bilateral bronchial angles by ultrasound to diagnose heterotaxy syndrome in middle and late pregnancy 超声定量测量胎儿气管及双侧支气管角诊断妊娠中晚期异位综合征的可行性
Q4 Medicine Pub Date : 2019-12-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.12.003
Peng Tu, Xiao-Mei Gu, Xiaohang Zhang, Hongmei Dong, Xue-mei Zhang, Yun Lin, Yihua He, S. Ran
Objective To analyze the feasibility of prenatal ultrasound quantitative measurement of the angles between trachea and bilateral bronchi as a new diagnostic tool for fetuses with heterotaxy syndrome. Methods The angles between trachea and bilateral bronchi were measured at 18-34+6 gestational weeks for 200 fetuses with normal ultrasound findings (normal group) and 41 fetuses with heterotaxy syndrome [35 right atrial isomerisms (right group) and six left atrial isomerisms (left group)] diagnosed by ultrasound and confirmed after abortion or induction (case group) in Chongqing Health Center for Women and Children from October 2015 to December 2018. Scatter plots of left/right bronchus angle (α/β) ratios were drawn. Differences in bilateral bronchus angles between the three groups were statistically analyzed using one-way analysis of variance and paired t-test. Results In the normal group, scatter plots showed the α/β ratios were relatively constant at 0.8-1.0 with larger β than α (t=-33.14, P 0.05] and presented as bilateral right bronchial angle; in the left group, the β value decreased and was close to the α value [(147.38±3.16)° vs (148.82±5.56)°, t=-1.18, P>0.05] and presented as bilateral left bronchial angle. There were significant differences in the α and β values among the normal group, the right and left groups (all P<0.05), and the bronchial angles of the right group were both greater than those of the left group (all P<0.05). Conclusions Prenatal ultrasound measurement of the angles between trachea and bilateral bronchi can be used as an indirect indicator for the diagnosis of heterotaxy syndrome. Key words: Heterotaxy syndrome; Ultrasonography, prenatal; Trachea; Bronchi
目的分析产前超声定量测量气管与双侧支气管夹角作为胎儿异位综合征新诊断工具的可行性。方法对重庆市卫生院超声检查正常的200例胎儿(正常组)和超声诊断为异位综合征的41例胎儿[35例右心房异构体(右组)和6例左心房异构体[左组)],于18-34+6孕周测量气管与双侧支气管夹角(病例组)2015年10月至2018年12月期间的妇女和儿童。绘制左/右支气管角(α/β)比值的散点图。采用单向方差分析和配对t检验对三组患者双侧支气管角度的差异进行统计学分析。结果散点图显示,正常组α/β比值相对恒定,为0.8-1.0,β大于α(t=-33.14,P>0.05),表现为双侧右支气管角;左侧组β值下降,接近α值[(147.38±3.16)°vs(148.82±5.56)°,t=-1.18,P>0.05],表现为两侧左支气管角。α、β值在正常组、左右两组间有显著性差异(均P<0.05),结论产前超声测量气管与双侧支气管夹角可作为诊断异位综合征的间接指标。关键词:异质性综合征;产前超声检查;气管;支气管
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引用次数: 0
Advances in antenatal corticosteroids for improving perinatal outcomes of extremely preterm infants 产前皮质类固醇改善极早产儿围产期结局的研究进展
Q4 Medicine Pub Date : 2019-12-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.12.012
Siwei Luo
Large population-based cohort studies conducted in the industrialized countries in different eras revealed that the use of antenatal corticosteroids for extremely preterm births (EPT, <28 gestational weeks) reached 60% or higher in the mid-1990s, accompanying by steadily declined perinatal mortality to 13%-22% in EPT with gestational age ≥25 weeks in developed countries. Notably, the survival rate of EPT with 23-24 weeks of gestation was over 50% in Sweden since 2005. There's a link between the increment of antenatal corticosteroids use and steady decline of mortality in EPT in the past three decades. High-quality evidence is needed to demonstrate the impact of antenatal corticosteroids on EPT perinatal outcomes under the current healthcare background in China. This review, focusing on the progression of antenatal corticosteroid treatment for EPT, may facilitate the quality improvement of maternal-fetal and infant healthcare in China. Key words: Glucocorticoids; Infant, extremely premature; Peripartum period; Prognosis
在工业化国家不同时期进行的大规模人群队列研究显示,在20世纪90年代中期,极早产儿(EPT, <28孕周)的产前皮质类固醇使用率达到60%或更高,同时在发达国家,胎龄≥25周的EPT的围产期死亡率稳步下降至13%-22%。值得注意的是,自2005年以来,瑞典妊娠23-24周的EPT存活率超过50%。在过去的三十年中,产前皮质类固醇使用的增加与EPT死亡率的稳步下降之间存在联系。在中国目前的医疗背景下,需要高质量的证据来证明产前皮质类固醇对EPT围产儿结局的影响。本文综述了EPT产前皮质类固醇治疗的进展,以期促进中国母婴保健质量的提高。关键词:糖皮质激素;婴儿,极度早产儿;Peripartum时期;预后
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引用次数: 0
Streptococcal toxic shock syndrome in third trimester: a report of two cases and literature review 妊娠晚期链球菌中毒性休克综合征2例报告及文献复习
Q4 Medicine Pub Date : 2019-12-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.12.007
Qiu-lan Yang, Min Song, Qian Sun, Xiang Wang, Aiqin Han
Objective To analyze the clinical characteristics of streptococcal toxic shock syndrome (STSS) caused by Streptococcus pyogenes (S. pyogenes) in the third trimester to improve clinical awareness of this disease. Methods A retrospective study was conducted to analyze the clinical data of two patients with STSS caused by S. pyogenes in Jinan Maternal and Child Health Care Hospital and nine reported cases of healthy pregnant women infected with S. pyogenes at 28-42 gestational weeks with detailed data retrieved from Chinese National Knowledge Infrastructure and PubMed database from January 1997 to December 2018. Results The two cases admitted to our hospital were both multiparas, with onset in winter and no specific symptoms in early stage. Disseminated intravascular coagulation (DIC) was developed in both cases on admission. In one case, the fetal heart rate was reduced and disappeared soon after admission. The other patient was diagnosed as stillbirth on admission. Both patients died and blood culture revealed infection of group A streptococcus. Nine previous cases were reported in one Chinese and five English articles. No high-risk pregnancy or premature rupture of membranes was reported in these 11 cases. Among the 11 cases, ten were positive for S. pyogenes indicated by blood or tissue culture and one was positive for streptococcal toxin. Ten cases had high fever and three presented with respiratory symptoms in early stage. Abdominal pain and watery diarrhea were common symptoms and all patients developed multiple organ dysfunction and DIC. Cases occurred in winter or spring were more common. Nine women died within 36 h after the onset of fulminant symptoms. Only two survived and hospitalized for 90 d and 25 d, respectively, after emergent cesarean section indicated by reduced fetal heart rate. Unfortunately, both neonates died after birth. For the babies, there were seven intrauterine fetal deaths, one stillbirth and three live births, but only one survived (whose mother developed respiratory cardiac arrest 90 min after delivery). Conclusions STSS caused by S. pyogenes in pregnant women exacerbates rapidly with a high mortality. Early identification of clinical manifestations and rapid progress of the disease are crucial for early diagnosis and treatment, which may help improve maternal and fetal outcomes. Key words: Shock, septic; Streptococcal infections; Streptococcus pyogenes; Pregnancy trimester, third
目的分析妊娠晚期化脓性链球菌引起的链球菌中毒性休克综合征(STSS)的临床特点,提高临床对该病的认识。方法回顾性分析1997年1月至12月济南市妇幼保健院2例化脓性链球菌性STSS患者和9例28~42周健康孕妇感染化脓性链球菌的临床资料2018.结果我院收治的2例均为经产,冬季发病,早期无特异性症状。两例患者入院时均出现弥散性血管内凝血(DIC)。在一个病例中,胎儿心率降低,入院后不久就消失了。另一名患者入院时被诊断为死产。两名患者均死亡,血培养显示感染了A组链球菌。在一篇中文和五篇英文文章中报告了9例先前的病例。在这11例病例中,没有高危妊娠或胎膜早破的报告。在11例病例中,10例血液或组织培养显示化脓性链球菌呈阳性,1例链球菌毒素呈阳性。10例早期出现高热,3例早期出现呼吸道症状。腹痛和水样腹泻是常见症状,所有患者都出现了多器官功能障碍和DIC。发生在冬季或春季的病例更为常见。9名妇女在出现暴发性症状后36小时内死亡。在胎儿心率降低的紧急剖宫产术后,只有两人存活下来,分别住院90天和25天。不幸的是,两名新生儿都在出生后死亡。对于这些婴儿,有7例宫内胎儿死亡,1例死产和3例活产,但只有一例存活下来(其母亲在分娩后90分钟出现呼吸性心脏骤停)。结论妊娠化脓性链球菌引起的STSS病情迅速加重,死亡率高。早期发现临床表现和疾病的快速进展对于早期诊断和治疗至关重要,这可能有助于改善孕产妇和胎儿的预后。关键词:休克、败血症;链球菌感染;化脓性链球菌;妊娠三个月,第三个
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引用次数: 0
Variations of coagulation biochemical markers in normal pregnant women in early and late pregnancy 正常孕妇妊娠早期和晚期凝血生化指标的变化
Q4 Medicine Pub Date : 2019-12-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.12.006
Ling-ying Kong, Huixia Yang
Objective To investigate the changes of coagulation indexes in normal pregnant women in early and late pregnancy. Methods The coagulation indexes in early and late pregnancy including activated partial thromboplastin time (APTT), APTT ratio, prothrombin time (PT), PT ratio, prothrombin activity, international normalized ratio, fibrinogen (Fib) and thrombin time (TT) were retrospectively collected from 196 normal pregnant women delivered in Peking University First Hospital from August 2013 to September 2014. Differences in these indexes before and after the seventh gestational week of early pregnancy and in early and late pregnancy were compared. In addition, the normal reference values were calculated. Paired t test and sum-rank test were used for statistical analysis. The reference values were presented with P2.5-P97.5. Results In early pregnancy, some coagulation indexes after the seventh weeks were shorter than those before, such as APTT [30.3 (26.1-35.5) vs 32.1 (27.9-36.8) s, Z=25.850, P<0.001] and TT [13.8 (12.2-16.0) vs 14.5 (12.3-16.4) s, Z=16.720, P<0.001], but Fib [3.3 (2.5-4.3) vs 2.9 (2.2-3.8) g/L, Z=43.180, P<0.001] became higher. APTT [(27.5±1.6) vs (31.4±2.4) s, t=24.736, P<0.001], PT [(9.7±0.5) vs (11.0±0.8) s, t=18.647, P<0.001] and TT [(13.3±0.8) vs (14.2±1.0) s, t=9.255, P<0.001] were significantly shorter, while Fib [(4.4±0.5) vs (3.1±0.4) g/L, t=-29.152, P<0.001] was higher in late pregnancy than in early pregnancy. The reference values of APTT, PT, Fib and TT in early pregnancy were 26.5-36.0 s, 9.4-12.4 s, 2.4-4.0 g/L and 12.3-16.4 s, and those in late pregnancy were 25.0-31.2 s, 8.8-10.6 s, 3.4-5.4 g/L and 12.0-14.9 s, respectively. Conclusions The coagulation indexes of pregnant women change significantly since the beginning of early pregnancy. APTT, PT and TT are shorter, while Fib is higher in late pregnancy than in early pregnancy. Key words: Partial thromboplastin time; Prothrombin time; Thrombin time; Fibrinogen; Pregnancy trimester, first; Pregnancy trimester, third
目的探讨正常孕妇妊娠早期和晚期凝血指标的变化。方法回顾性收集2013年8月至2014年9月在北京大学第一医院分娩的196例正常孕妇妊娠早期和晚期凝血指标,包括活化部分凝血活素时间(APTT)、APTT比值、凝血酶原时间(PT)、PT比值、凝血酶原活性、国际标准化比值、纤维蛋白原(Fib)、凝血酶时间(TT)。比较妊娠早、晚、早7孕周前后这些指标的差异。此外,还计算了正常参考值。采用配对t检验和和秩检验进行统计分析。参考值用p2.5 ~ p97.5表示。结果妊娠早期,7周后部分凝血指标APTT [30.3 (26.1-35.5) vs 32.1 (27.9-36.8) s, Z=25.850, P<0.001]、TT [13.8 (12.2-16.0) vs 14.5 (12.3-16.4) s, Z=16.720, P<0.001]较妊娠前缩短,Fib [3.3 (2.5-4.3) vs 2.9 (2.2-3.8) g/L, Z=43.180, P<0.001]增高。APTT[(27.5±1.6)vs(31.4±2.4)s, t=24.736, P<0.001]、PT[(9.7±0.5)vs(11.0±0.8)s, t=18.647, P<0.001]、TT[(13.3±0.8)vs(14.2±1.0)s, t=9.255, P<0.001]在妊娠晚期明显低于妊娠早期,Fib[(4.4±0.5)vs(3.1±0.4)g/L, t=-29.152, P<0.001]明显高于妊娠早期。妊娠早期APTT、PT、Fib、TT参考值分别为26.5 ~ 36.0 s、9.4 ~ 12.4 s、2.4 ~ 4.0 g/L、12.3 ~ 16.4 s,妊娠晚期APTT参考值分别为25.0 ~ 31.2 s、8.8 ~ 10.6 s、3.4 ~ 5.4 g/L、12.0 ~ 14.9 s。结论孕妇凝血指标从妊娠早期开始就有明显变化。APTT、PT、TT较短,而Fib在妊娠后期高于妊娠早期。关键词:部分凝血活酶时间;凝血酶原时间;凝血酶时间;纤维蛋白原;妊娠三个月,第一;妊娠三个月,第三
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引用次数: 0
Effect of early essential newborn care on omphalitis in vaginally born preterm infants 早期新生儿基本护理对阴道出生早产儿脐炎的影响
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.007
Xiaoyang Wang, Junge Zhao, Shengling Li, Y. Qiu, Cai-jiang Sun, Qin Liu
Objective To explore the influence of early essential newborn care(EENC) on the development of omphalitis in preterm infants following normal delivery. Methods A total of 184 preterm infants, admitted to General Hospital of Ningxia Medical University from January 2017 to December 2017, were retrospectively collected as EENC group. During the same period, 161 preterm infants who were born in Yinchuan Maternal and Child Health Hospital were included in the control group. Preterm infants in EENC group were managed based on the clinical practice guideline of "Early Essential Newborn Care", while those in the control group underwent routine care after birth. The incidence of omphalitis between the two groups were compared using independent-samples t test and Chi-square test. Influencing factors of omphalitis were analyzed using univariate analysis and multivariate logistic regression analysis. Results The incidence of mild omphalitis was lower [5.4% (10/184) vs 11.8% (19/161), χ2=4.520, P<0.05], and the separation and drying up time of cord stump were both earlier in the EENC group than those in the control group [(5.5±1.5) vs (8.2±1.2) d, t=4.169; (2.6±1.4) vs (3.2±1.4) d, t=4.513; both P<0.05]. Logistic regression analysis showed that gestational age≤34 weeks (OR=1.885, 95%CI: 1.109-6.757, P=0.032), early umbilical cord clamping (OR=3.615, 95%CI: 1.372-9.381, P=0.001) and bandaging of the umbilical stump (OR=1.921, 95%CI: 1.257-11.893, P=0.035) were independent risk factors of omphalitis in preterm infants. Conclusions Umbilical cord treatment based on EENC could reduce the incidence of omphalitis by avoiding its risk factors in preterm infants following normal delivery. Key words: Infant, premature; Umbilicus; Inflammation; Umbilical cord; Constriction; Neonatal nursing
目的探讨新生儿早期基本护理(EENC)对正常分娩后早产儿脐炎发生的影响。方法回顾性收集2017年1月至2017年12月宁夏医科大学总医院收治的184例早产儿为EENC组。同期,在银川市妇幼保健院出生的161名早产儿被纳入对照组。EENC组的早产儿根据“新生儿早期基本护理”的临床实践指南进行管理,而对照组的早产儿在出生后接受常规护理。采用独立样本t检验和卡方检验比较两组患者的脐炎发生率。采用单因素分析法和多因素logistic回归分析法对脐炎的影响因素进行分析。结果轻度脐炎的发生率较低[5.4%(10/184)vs 11.8%(19/161),χ2=4.520,P<0.05,EENC组脐带残端分离和干燥时间均早于对照组[(5.5±1.5)vs(8.2±1.2)d,t=4.169;(2.6±1.4)vs(3.2±1.4)d,t=4.513;均P<0.05],早期脐带夹闭(OR=3.615,95%CI:1.372-9.381,P=0.001)和脐带残端包扎(OR=1.921,95%CI:1.257-11.893,P=0.035)是早产儿脐炎的独立危险因素。结论基于EENC的脐带治疗可以避免早产后脐炎的危险因素,从而降低脐炎的发生率。关键词:婴儿、早产;脐;炎症;脐带;缩窄;新生儿护理
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引用次数: 0
Multiplex polymerase chain reaction-based reverse line blot hybridization to detect pathogens causing neonatal bacterial meningitis and relevant drug resistance genes 基于多重聚合酶链式反应的反向线杂交检测新生儿细菌性脑膜炎病原体及相关耐药基因
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.003
Jinjing Zhang, Yajuan Wang
Objective To evaluate the performance of multiplex polymerase chain reaction-based reverse line blot hybridization (mPCR/RLB) in the detection of pathogens causing neonatal bacterial meningitis and associated drug resistance genes. Methods Clinical data and cerebrospinal fluid (CSF) samples were collected retrospectively from 80 cases diagnosed with neonatal bacterial meningitis in Beijing Children's Hospital from January 1, 2012 to December 31, 2018. A total of 100 CSF samples were obtained including 80 samples collected after admission (12 before and 68 after antibiotic treatment) and 20 recollected at follow-up. All CSF samples were analyzed by conventional culture, susceptibility test and mPCR/RLB. Differences in the detection of pathogens and drug resistance genes were analyzed by Chi-square test. Results (1) Among the 80 first-collected CSF samples, mPCR/RLB revealed significantly higher positive rate than conventional culture [26.3% (21/80) vs 7.5% (6/80), χ2=10.025, P=0.002]. No significant difference was showed between the two methods in analyzing the 12 samples collected before antibiotic therapy (9/12 vs 5/12, χ2=1.543, P=0.214), while the positive rate in 68 samples collected after antibiotic intervention detected by mPCR/RLB was obviously higher than that by conventional culture [17.6% (12/68) vs 1.5% (1/68), χ2=13.176, P<0.001]. (2) Conventional culture results of the 20 samples collected during follow-up were all negative, but four were positive using mPCR/RLB, which were also positive previously. Furthermore, the results of both methods in previous detections were identical. (3) According to the conventional culture results, the pathogens were Escherichia coli (three cases), Group B Streptococcus (two cases) and Listeria monocytogenes (one case), while mPCR/RLB detected Escherichia coli (four cases), Group B Streptococcus (five cases), Listeria monocytogenes (four cases), Neisseria meningitidis (four cases), Haemophilus influenzae b (one case), Gram-negative bacteria (one case), Gram-positive bacteria (one case), and Listeria monocytogenes and Haemophilus influenzae b coinfection (one case) in 80 first-collected CSF samples. (4) Antibiotic susceptibility test showed that one Escherichia coli strain produced extended spectrum beta-lactamases. Drug resistance gene detection by mPCR/RLB showed that acrA, acrB, CTX-M (consistent with antibiotic susseptibility test) and TetM genes were positive in three, two, one and one case, respectively. Conclusions mPCR/RLB is of great clinical value due to its higher detection rate and better accuracy compared with bacterial culture and can also detect drug resistance genes. Key words: Meningitis, bacterial; beta-Lactamases; Multiplex polymerase chain reaction; Nucleic acid hybridization; Drug resistance, bacterial; Infant, newborn
目的评价基于多重聚合酶链反应的逆行杂交技术(mPCR/RLB)在新生儿细菌性脑膜炎病原菌及相关耐药基因检测中的应用价值。方法回顾性收集2012年1月1日至2018年12月31日北京儿童医院诊断为新生儿细菌性脑膜炎的80例患儿的临床资料和脑脊液样本。共采集脑脊液样本100份,其中入院后采集80份(抗生素治疗前12份,抗生素治疗后68份),随访时收集20份。所有脑脊液标本经常规培养、药敏试验和mPCR/RLB分析。采用卡方检验分析病原菌和耐药基因检测的差异。结果(1)首次采集的80份脑脊液标本中,mPCR/RLB阳性率显著高于常规培养[26.3% (21/80)vs 7.5% (6/80), χ2=10.025, P=0.002]。在抗生素治疗前采集的12份样本中,两种方法的检出率差异无统计学意义(9/12 vs 5/12, χ2=1.543, P=0.214),而抗生素干预后采集的68份样本中,mPCR/RLB检出率明显高于常规培养[17.6% (12/68)vs 1.5% (1/68), χ2=13.176, P<0.001]。(2)随访中采集的20份样本,常规培养结果均为阴性,但mPCR/RLB培养结果为阳性的4份样本,此前均为阳性。此外,两种方法在以往的检测结果是相同的。(3)常规培养结果检出病原菌为大肠埃希菌(3例)、B群链球菌(2例)、单核增生李斯特菌(1例),而mPCR/RLB检出大肠埃希菌(4例)、B群链球菌(5例)、单核增生李斯特菌(4例)、脑膜炎奈瑟菌(4例)、流感嗜血杆菌B(1例)、革兰氏阴性菌(1例)、革兰氏阳性菌(1例)、革兰氏阴性菌(1例)、革兰氏阳性菌(1例)。80份首次采集的脑脊液样本中单核细胞增生李斯特菌和流感嗜血杆菌b型共感染(1例)。(4)药敏试验表明,1株大肠杆菌产生广谱β -内酰胺酶。mPCR/RLB耐药基因检测结果显示,acrA、acrB、CTX-M(与药敏试验一致)和TetM基因分别阳性3例、2例、1例和1例。结论与细菌培养相比,mPCR/RLB具有较高的检出率和较好的准确性,并可检测耐药基因,具有重要的临床应用价值。关键词:脑膜炎;细菌性脑膜炎;beta-Lactamases;多重聚合酶链反应;核酸杂交;耐药,细菌;婴儿,新生
{"title":"Multiplex polymerase chain reaction-based reverse line blot hybridization to detect pathogens causing neonatal bacterial meningitis and relevant drug resistance genes","authors":"Jinjing Zhang, Yajuan Wang","doi":"10.3760/CMA.J.ISSN.1007-9408.2019.11.003","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1007-9408.2019.11.003","url":null,"abstract":"Objective \u0000To evaluate the performance of multiplex polymerase chain reaction-based reverse line blot hybridization (mPCR/RLB) in the detection of pathogens causing neonatal bacterial meningitis and associated drug resistance genes. \u0000 \u0000 \u0000Methods \u0000Clinical data and cerebrospinal fluid (CSF) samples were collected retrospectively from 80 cases diagnosed with neonatal bacterial meningitis in Beijing Children's Hospital from January 1, 2012 to December 31, 2018. A total of 100 CSF samples were obtained including 80 samples collected after admission (12 before and 68 after antibiotic treatment) and 20 recollected at follow-up. All CSF samples were analyzed by conventional culture, susceptibility test and mPCR/RLB. Differences in the detection of pathogens and drug resistance genes were analyzed by Chi-square test. \u0000 \u0000 \u0000Results \u0000(1) Among the 80 first-collected CSF samples, mPCR/RLB revealed significantly higher positive rate than conventional culture [26.3% (21/80) vs 7.5% (6/80), χ2=10.025, P=0.002]. No significant difference was showed between the two methods in analyzing the 12 samples collected before antibiotic therapy (9/12 vs 5/12, χ2=1.543, P=0.214), while the positive rate in 68 samples collected after antibiotic intervention detected by mPCR/RLB was obviously higher than that by conventional culture [17.6% (12/68) vs 1.5% (1/68), χ2=13.176, P<0.001]. (2) Conventional culture results of the 20 samples collected during follow-up were all negative, but four were positive using mPCR/RLB, which were also positive previously. Furthermore, the results of both methods in previous detections were identical. (3) According to the conventional culture results, the pathogens were Escherichia coli (three cases), Group B Streptococcus (two cases) and Listeria monocytogenes (one case), while mPCR/RLB detected Escherichia coli (four cases), Group B Streptococcus (five cases), Listeria monocytogenes (four cases), Neisseria meningitidis (four cases), Haemophilus influenzae b (one case), Gram-negative bacteria (one case), Gram-positive bacteria (one case), and Listeria monocytogenes and Haemophilus influenzae b coinfection (one case) in 80 first-collected CSF samples. (4) Antibiotic susceptibility test showed that one Escherichia coli strain produced extended spectrum beta-lactamases. Drug resistance gene detection by mPCR/RLB showed that acrA, acrB, CTX-M (consistent with antibiotic susseptibility test) and TetM genes were positive in three, two, one and one case, respectively. \u0000 \u0000 \u0000Conclusions \u0000mPCR/RLB is of great clinical value due to its higher detection rate and better accuracy compared with bacterial culture and can also detect drug resistance genes. \u0000 \u0000 \u0000Key words: \u0000Meningitis, bacterial; beta-Lactamases; Multiplex polymerase chain reaction; Nucleic acid hybridization; Drug resistance, bacterial; Infant, newborn","PeriodicalId":52320,"journal":{"name":"Chinese Journal of Perinatal Medicine","volume":"22 1","pages":"774-780"},"PeriodicalIF":0.0,"publicationDate":"2019-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43830408","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}
引用次数: 0
Prenatal diagnosis of fetal 1p32p31 microdeletion syndrome: a case report 胎儿1p32p31微缺失综合征的产前诊断1例
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.008
Qu Xiaoxing, Y. Meizhen, Zhang Yun, Z. Jia, X. Ya, Zhou Fenhe, Sun Luming
We hereby reported a fetus with abnormal head shape, ventricular septal defect, gallbladder enlargement, low-set ears and local umbilical cord glial edema at 22 and 25 weeks of gestation ultrasound scan. A 15.318 Mb heterozygous microdeletion on chromosome 1p32.1p31.1, arr[GRCh37]1p32.1p31.1(61,279,239-76,597,189)×1, was indentified by chromosomal microarray analysis. The chromosome karyotype of the fetus was 46,XY,del(1)(p32.1p31.1). Therefore, this case was diagnosed as 1p32p31 microdeletion syndrome and proved to be a de novo variation based on routine G-banding analysis and chromosomal microarray analysis of the normal parents. This syndrome might present with abnormalities in the head shape, kidney, bladder and central nervous system. The couple decided to terminate the pregnancy after genetic counseling concerning the possible poor outcomes of the fetus. Key words: Chromosome deletion; Chromosomes, human, pair 1; Prenatal diagnosis
我们在此报告一例胎儿在妊娠22周和25周的超声扫描中出现头形异常、室间隔缺损、胆囊肿大、低耳和局部脐带胶质水肿。通过染色体微阵列分析,在染色体1p32.1p31.1上发现一个15.318 Mb的杂合微缺失,arr[GRCh37]1p32.1p31.1(61,279,239-76,597,189)×1。胎儿染色体核型为46、XY、del(1)(p32.1p31.1)。因此,根据正常父母的常规g带分析和染色体微阵列分析,本病例诊断为1p32p31微缺失综合征,证实为新生变异。这种综合征可能表现为头部形状、肾脏、膀胱和中枢神经系统的异常。考虑到胎儿可能出现的不良后果,这对夫妇在进行遗传咨询后决定终止妊娠。关键词:染色体缺失;染色体,人类,1对;产前诊断
{"title":"Prenatal diagnosis of fetal 1p32p31 microdeletion syndrome: a case report","authors":"Qu Xiaoxing, Y. Meizhen, Zhang Yun, Z. Jia, X. Ya, Zhou Fenhe, Sun Luming","doi":"10.3760/CMA.J.ISSN.1007-9408.2019.11.008","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1007-9408.2019.11.008","url":null,"abstract":"We hereby reported a fetus with abnormal head shape, ventricular septal defect, gallbladder enlargement, low-set ears and local umbilical cord glial edema at 22 and 25 weeks of gestation ultrasound scan. A 15.318 Mb heterozygous microdeletion on chromosome 1p32.1p31.1, arr[GRCh37]1p32.1p31.1(61,279,239-76,597,189)×1, was indentified by chromosomal microarray analysis. The chromosome karyotype of the fetus was 46,XY,del(1)(p32.1p31.1). Therefore, this case was diagnosed as 1p32p31 microdeletion syndrome and proved to be a de novo variation based on routine G-banding analysis and chromosomal microarray analysis of the normal parents. This syndrome might present with abnormalities in the head shape, kidney, bladder and central nervous system. The couple decided to terminate the pregnancy after genetic counseling concerning the possible poor outcomes of the fetus. \u0000 \u0000 \u0000Key words: \u0000Chromosome deletion; Chromosomes, human, pair 1; Prenatal diagnosis","PeriodicalId":52320,"journal":{"name":"Chinese Journal of Perinatal Medicine","volume":"22 1","pages":"802-807"},"PeriodicalIF":0.0,"publicationDate":"2019-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45003455","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}
引用次数: 0
Cellular and molecular genetic analysis of sex chromosome chimerism and dicentric isochromosome structural abnormalities: a report of two cases 性染色体嵌合和双心同工染色体结构异常的细胞和分子遗传学分析:附2例报告
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.005
Jian Zhang, Yunrong Ma, Xian-ying Lei, Shuang-Yang Zhang, Yuanyuan Liu, Lulu Guo, Shiyu Zheng, Jingjing Pan
Objective To investigate the value of karyotype analysis, bacterial artificial chromosomes-on-beads (BoBs), chromosome microarray analysis (CMA) and fluorescence in situ hybridization (FISH) in the diagnosis of sex chromosome numerical and structural abnormalities. Methods Conventional G-banding staining technique was used to analyze the karyotypes of amniotic fluid cells and parental peripheral blood cells in two pregnancies with prenatal diagnosis indications. Sex chromosome numerical and structural abnormalities were analyzed based on the results of G-banding, BoBs, CMA and FISH. Results The results of G-banding karyotype analysis showed that there were mosaics in amniotic fluid cells collected from both cases. Karyotype of Case A was 45,X[25]/46,X,idic(Y)(q11.2?)[6], and Case B was 45,X[39]/46,X,psu idic(X)(q21.32?)[44]. Parental peripheral blood karyotypes of both families were normal. Prenatal BoBs indicated copy number abnormalities in sex chromosomes (Y chromosome in Case A and X chromosome in Case B). CMA results suggested a 20.1 Mb duplication in Yp11.32q11.222, and a 7.7 Mb deletion in Yq11.222q11.23 in fetus A with possible karyotype of 46,X,idic(Y)(q11.222); for fetus B, a 92.0 Mb duplication in Xp22.33q21.32, and a 63.0 Mb deletion in Xq21.32q28 were detected, and the karyotype might be 46,X,psu idic(X)(q21.32). The mid-term FISH test of amniotic fluid cells showed that 90% of the amniotic cells from Case A were 45,X, and 10% were 46,X,idic(Y)(q11.2); about 38% were 45,X, and 62% were 46,X,psu dic(X)(q21.3) from Case B. Conclusions Numerical and structural abnormalities of sex chromosomes could be accurately diagnosed by combination of several methods including G-banding karyotype analysis, prenatal BoBs, CMA and FISH, which would help to effectively reduce birth defects. Key words: Sex chromosomes; Chimerism; Sex chromosome aberrations; Karyotyping; Chromosomes, artificial, bacterial; Microarray analysis; In situ hybridization, fluorescence
目的探讨核型分析、细菌人工染色体珠上分析(BoBs)、染色体微阵列分析(CMA)和荧光原位杂交(FISH)对性染色体数量和结构异常的诊断价值。方法采用常规g带染色技术对2例有产前诊断指征的孕妇的羊水细胞和亲代外周血细胞进行核型分析。根据g带、BoBs、CMA和FISH结果分析性染色体数量和结构异常。结果g带核型分析显示,两例羊水细胞均存在嵌合。病例A的核型为45,X[39]/46,X, idic(Y)(q11.2?)[6],病例B的核型为45,X[39]/46,X,psu idic(X)(q21.32?)[44]。两家系外周血核型均正常。产前BoBs提示胎儿A性染色体拷贝数异常(病例A为Y染色体,病例B为X染色体),CMA结果提示胎儿A的Yp11.32q11.222有20.1 Mb的重复,Yq11.222q11.23有7.7 Mb的缺失,核型可能为46,X,idic(Y)(q11.222);胎儿B在Xp22.33q21.32染色体上发现92.0 Mb的重复,在Xq21.32q28染色体上发现63.0 Mb的缺失,核型可能为46,X,psu - idic(X)(q21.32)。羊水细胞中期FISH检测显示,病例A中90%的羊水细胞为45、X, 10%为46、X、idic(Y)(q11.2);病例b中45、X占38%,46、X、psu (X)(q21.3)占62%。结论结合g带核型分析、产前bob、CMA和FISH等多种方法,可以准确诊断性染色体数量和结构异常,有助于有效减少出生缺陷。关键词:性染色体;嵌合现象;性染色体畸变;核型分析;染色体,人工的,细菌的;微阵列分析;原位杂交,荧光
{"title":"Cellular and molecular genetic analysis of sex chromosome chimerism and dicentric isochromosome structural abnormalities: a report of two cases","authors":"Jian Zhang, Yunrong Ma, Xian-ying Lei, Shuang-Yang Zhang, Yuanyuan Liu, Lulu Guo, Shiyu Zheng, Jingjing Pan","doi":"10.3760/CMA.J.ISSN.1007-9408.2019.11.005","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1007-9408.2019.11.005","url":null,"abstract":"Objective \u0000To investigate the value of karyotype analysis, bacterial artificial chromosomes-on-beads (BoBs), chromosome microarray analysis (CMA) and fluorescence in situ hybridization (FISH) in the diagnosis of sex chromosome numerical and structural abnormalities. \u0000 \u0000 \u0000Methods \u0000Conventional G-banding staining technique was used to analyze the karyotypes of amniotic fluid cells and parental peripheral blood cells in two pregnancies with prenatal diagnosis indications. Sex chromosome numerical and structural abnormalities were analyzed based on the results of G-banding, BoBs, CMA and FISH. \u0000 \u0000 \u0000Results \u0000The results of G-banding karyotype analysis showed that there were mosaics in amniotic fluid cells collected from both cases. Karyotype of Case A was 45,X[25]/46,X,idic(Y)(q11.2?)[6], and Case B was 45,X[39]/46,X,psu idic(X)(q21.32?)[44]. Parental peripheral blood karyotypes of both families were normal. Prenatal BoBs indicated copy number abnormalities in sex chromosomes (Y chromosome in Case A and X chromosome in Case B). CMA results suggested a 20.1 Mb duplication in Yp11.32q11.222, and a 7.7 Mb deletion in Yq11.222q11.23 in fetus A with possible karyotype of 46,X,idic(Y)(q11.222); for fetus B, a 92.0 Mb duplication in Xp22.33q21.32, and a 63.0 Mb deletion in Xq21.32q28 were detected, and the karyotype might be 46,X,psu idic(X)(q21.32). The mid-term FISH test of amniotic fluid cells showed that 90% of the amniotic cells from Case A were 45,X, and 10% were 46,X,idic(Y)(q11.2); about 38% were 45,X, and 62% were 46,X,psu dic(X)(q21.3) from Case B. \u0000 \u0000 \u0000Conclusions \u0000Numerical and structural abnormalities of sex chromosomes could be accurately diagnosed by combination of several methods including G-banding karyotype analysis, prenatal BoBs, CMA and FISH, which would help to effectively reduce birth defects. \u0000 \u0000 \u0000Key words: \u0000Sex chromosomes; Chimerism; Sex chromosome aberrations; Karyotyping; Chromosomes, artificial, bacterial; Microarray analysis; In situ hybridization, fluorescence","PeriodicalId":52320,"journal":{"name":"Chinese Journal of Perinatal Medicine","volume":"22 1","pages":"787-792"},"PeriodicalIF":0.0,"publicationDate":"2019-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48781722","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}
引用次数: 0
Effects of rapid growth on weight and blood pressure in small and appropriate for gestational age infants during preschool period 快速生长对学龄前小适龄儿体重和血压的影响
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.002
Nan Li, Tao Zhang, Y. Qiao, Enqing Liu, Ying Liang, Yue Wang, Hongyan Liu, R. Zheng
Objective To investigate whether rapid weight gain in the first year of life was associated with incidence of overweight and higher blood pressure in small for gestational age (SGA) and appropriate for gestational age (AGA) infants at preschool age. Methods From March 1, 2017 to June 30, 2018, a total of 12 150 children aged six years from 50 municipal kindergartens in Tianjin were enrolled in a cross-sectional survey. Their body weight, height and blood pressure were measured. Body length and weight at birth and one year of age were retrospectively collected. Rapid catch-up growth was defined as the difference of weight-for-height Z-score between one year old and at birth >0.67. The relationship between rapid growth with overweight and blood pressure in SGA and AGA infants at preschool age were analyzed using t test, analysis of variance and Chi-square test. Results At the age of six, children with rapid growth had a higher rate of overweight [28.6% (2 095/7 328) vs 17.5% (842/4 822), t=196.457, P<0.001], and higher systolic blood pressure [(99.4±10.0) vs (98.4±10.1) mmHg (1 mmHg=0.133 kPa), t=29.260, P<0.001] and diastolic blood pressure [(60.0±7.7) vs (59.4±7.8) mmHg, t=16.079, P<0.001] compared with children without rapid growth. SGA children with rapid growth had higher body weight [(21.5±4.4) vs (19.2±3.7) kg, t=3.747, P<0.001], height [(117.4±5.5) vs (114.8±5.4) cm, t=3.557, P<0.001] and systolic blood pressure [(98.4±9.9) vs (95.6±11.2) mmHg, t=2.080, P=0.038] compared with those without. Comparing to AGA children, SGA children had lower overweight rate [17.5% (144/824) vs 24.7% (2 793/11 326), t=21.630, P<0.001] and systolic blood pressure [(98.2±10.0) vs (99.0±10.1) mmHg, t=2.431, P=0.015]. Among the AGA children with rapid growth, 29.8% (1 958/6 564) were overweight. Conclusions Rapid growth in infancy is associated with overweight and higher systolic blood pressure at preschool age. A proper weight gain should be emphasized for both SGA and AGA infants. Key words: Overweight; Blood pressure; Growth; Infant, small for gestational age; Child, preschool
目的探讨出生后第一年体重快速增加是否与学龄前小于胎龄和适合胎龄婴儿超重和高血压的发生率有关。方法自2017年3月1日至2018年6月30日,对天津市50所市属幼儿园的12150名6岁幼儿进行横断面调查。测量了他们的体重、身高和血压。对出生时和一岁时的体长和体重进行回顾性收集。快速追赶生长被定义为一岁和出生时体重与身高Z评分的差异>0.67。采用t检验、方差分析和卡方检验对学龄前SGA和AGA婴儿的快速生长与超重与血压的关系进行了分析。结果与未快速生长的儿童相比,6岁时快速生长儿童的超重率较高[28.6%(2095/7328)vs 17.5%(842/4822),t=196.457,P<0.001],收缩压较高[(99.4±10.0)vs(98.4±10.1)mmHg(1mmHg=0.133kPa),t=29.260,P<0.001]和舒张压较高[[(60.0±7.7)vs(59.4±7.8)mmHg,t=16.079,P<0.001]。生长迅速的SGA儿童的体重[(21.5±4.4)vs(19.2±3.7)kg,t=3.747,P<0.001]、身高[(117.4±5.5)vs(114.8±5.4)cm,t=3.557,P<0.001]和收缩压[(98.4±9.9)vs(95.6±11.2)mmHg,t=2.080,P=0.038]均高于未生长的儿童。与AGA儿童相比,SGA儿童的超重率较低[17.5%(144/824)vs 24.7%(2793/11 326),t=21.630,P=0.001],收缩压较低[(98.2±10.0)vs(99.0±10.1)mmHg,t=2.431,P=0.015]。在生长迅速的AGA儿童中,29.8%(1958/6 564)超重。结论婴儿期的快速生长与超重和学龄前收缩压升高有关。SGA和AGA婴儿都应强调适当的体重增加。关键词:超重;血压;增长;婴儿,小于胎龄;儿童,学前班
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引用次数: 0
Transnational preconception cohort studies: a review 跨国先入为主队列研究综述
Q4 Medicine Pub Date : 2019-11-16 DOI: 10.3760/CMA.J.ISSN.1007-9408.2019.11.012
Changqian Wu, Hong Jiang, Yu Zhang, Xiaoying Ma, X. La, X. Qian
Preconception cohort studies allow us to conduct in-depth investigations on exposures and heath related factors of couples before pregnancy, and to explore the impact on reproductive health of the couples and on short- and long-term health of the offspring. As a critical window into early life, this area has been gradually gaining much attention worldwide. This paper summarized the characteristics of 21 transnational preconception cohort studies with large samples size, to provide information for relevant researchers in China. Emphasis on international cooperation, application of highly efficient data systems or research tools, and long-term longitudinal survey on parents and their offspring are the direction of further preconception cohort researches. Key words: Preconception care; Cohort studies; Prospective studies
孕前队列研究使我们能够深入调查夫妇在怀孕前的暴露和健康相关因素,探索对夫妇生殖健康和后代短期和长期健康的影响。作为研究早期生活的一个关键窗口,这一领域逐渐受到全世界的关注。本文总结了21项跨国大样本量孕前队列研究的特点,以期为国内相关研究人员提供参考。重视国际合作,应用高效的数据系统或研究工具,对父母及其后代进行长期的纵向调查,是进一步孕前队列研究的方向。关键词:孕前护理;队列研究;前瞻性研究
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引用次数: 0
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中华围产医学杂志
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