J Y Cai, C Y Yan, X Q Wang, Z X Luo, J Luo, Q B Li, E M Liu, Y Deng
{"title":"[Clinical characteristics and risk factors for bronchoscopic airway mucus hypersecretion in childhood pneumonia infected by different pathogens].","authors":"J Y Cai, C Y Yan, X Q Wang, Z X Luo, J Luo, Q B Li, E M Liu, Y Deng","doi":"10.3760/cma.j.cn112140-20230315-00184","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230315-00184","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the risk factors for airway mucus hypersecretion in childhood pneumonia infected by different pathogens. <b>Method:</b> A retrospective cohort included 968 children who were hospitalized for <i>Mycoplasma pneumoniae</i> pneumonia (MPP), respiratory syncytial virus (RSV) pneumonia, adenovirus pneumonia and underwent bronchoscopy in Respiratory Department of Children's Hospital of Chongqing Medical University from January 2019 to December 2021 was conducted. The children were divided into two groups distinguished by airway mucus secretion according to the airway mucus hypersecretion score which were scored according to the mucus secretion under the bronchoscope. The demographic characteristics, clinical characteristics, laboratory tests and disease severity of the two groups were compared. And the risk factors for the development of airway mucus hypersecretion in two groups were analyzed. Chi square test, Mann-Whithey <i>U</i> test and Fisher exact test were used to analyze the differences between the two groups, and multivariate Logistic regression was used to analyze the influencing factors. <b>Result:</b> There were 559 males and 409 females in the 968 children, with an age of 4.0 (1.4, 6.0) years. Among the 642 children with MPP, 185 cases were in the hypersecretion group and 457 cases were in the non-hypersecretion group. There were 41 cases in the hypersecretion group and 160 cases in the non-hypersecretion group of 201 children with RSV pneumonia. In the 125 children with adenovirus pneumonia, there were 39 cases in the hypersecretion group and 86 cases in the non-hypersecretion group. In these children, the age of children in the hypersecretion group was older than that in the non-hypersecretion group (6.0 (4.0, 7.0) <i>vs.</i> 5.0 (3.0, 7.0) years old, 1.5 (0.5, 3.6) <i>vs</i>. 0.8 (0.4, 1.6) years old, 2.0 (1.2, 4.5) <i>vs.</i> 1.3 (0.8, 2.0) years old, <i>U</i>=35 295.00, 2 492.00, 1 101.00, all <i>P</i><0.05). Through multivariate Logistic regression analysis it found that increased risk of airway mucus hypersecretion was present in childhood MPP with increase in peripheral blood white blood cell count (<i>OR</i>=3.30, 95%<i>CI</i> 1.51-7.93, <i>P</i>=0.004) or increase in neutrophil ratio (<i>OR</i>=2.24, 95%<i>CI</i> 1.16-4.33, <i>P</i>=0.016) or decrease in lymphocyte count (<i>OR</i>=3.22, 95%<i>CI</i> 1.66-6.31, <i>P</i><0.001) or decrease in serum albumin (<i>OR</i>=2.00, 95%<i>CI</i> 1.01-3.98, <i>P</i>=0.047). The risk of airway mucus hypersecretion was increased in children with RSV pneumonia combined with elevated peripheral blood eosinophils (<i>OR</i>=3.04, 95%<i>CI</i> 1.02-8.93, <i>P</i>=0.043). Meanwhile, airway mucus hypersecretion was associated with severe pneumonia (<i>OR</i>=2.46, 95%<i>CI</i> 1.03-6.15, <i>P</i>=0.047) in children with RSV pneumonia. Older age was associated with increased risk of airway mucus hypersecretion in children with adenovirus pneumonia (<i>OR</i>=1.02","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"719-725"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9925462","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}
L Chen, X D Yu, F Yang, M Mao, Z Y Zhao, T Y Li, F Jiang
{"title":"[Summary to the Sixth Special Summit on Child Health and Early Prevention of Adult Diseases].","authors":"L Chen, X D Yu, F Yang, M Mao, Z Y Zhao, T Y Li, F Jiang","doi":"10.3760/cma.j.cn112140-20230605-00378","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230605-00378","url":null,"abstract":"","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"764-765"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9925461","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":"[Expert consensus for the management of congenital micropenis].","authors":"","doi":"10.3760/cma.j.cn112140-20230111-00025","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230111-00025","url":null,"abstract":"先天性小阴茎是一种临床症状体征,可反映机体存在内分泌或遗传性疾病,也是患儿和家长担心的心理社会问题。其病因复杂,诊疗管理争议大,国内外尚无针对此类疾病的管理共识、指南或规范。为规范小阴茎的临床管理,尽量减少不当诊疗带来的一系列问题,经多个学组多学科专家共同讨论,并参考国内外的最新研究进展,制定了先天性小阴茎临床管理中国专家共识。.","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"679-684"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9925463","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}
L J Luo, J Wang, W J Chen, Y J Zhou, Y J Zhou, Y H Song, N Shen, Q Cao
{"title":"[Clinical features of post-neurosurgical bacterial meningitis in children].","authors":"L J Luo, J Wang, W J Chen, Y J Zhou, Y J Zhou, Y H Song, N Shen, Q Cao","doi":"10.3760/cma.j.cn112140-20230424-00295","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230424-00295","url":null,"abstract":"<p><p><b>Objective:</b> To understand the characteristics of bacterial meningitis after pediatric neurosurgical procedures. <b>Methods:</b> This was a retrospective observational study. From January 2016 to December 2022, 64 children diagnosed with post-neurosurgical bacterial meningitis based on positive cerebrospinal fluid (CSF) culture in Department of Neurosurgery of Shanghai Children's Medical Center were selected as the study population. The clinical characteristics, onset time, routine biochemical indexes of cerebrospinal fluid before anti infection treatment, bacteriology characteristics and sensitivity to antibiotics of bacteria cultured from cerebrospinal fluid were analyzed. Based on the CSF culture results, the patients were divided into the Gram-positive bacteria infection group and the Gram-negative bacteria infection group. The clinical characteristics of the two groups were compared using <i>t</i>-tests or Wilcoxon rank-sum tests, and chi-square tests. <b>Results:</b> There were 64 children,42 boys and 22 girls, with onset age of 0.83 (0.50, 1.75) years. Seventy cases of post-neurosurgical bacterial meningitis occurred in the 64 children, of which 15 cases (21%) in spring, 23 cases (33%) in summer, 19 cases (27%) in autumn, and 13 cases (19%) in winter. The time of onset was 3.5 (1.0, 10.0) months after surgery; 15 cases (21%) occurred within the first month after the surgery, and 55 cases (79%) occurred after the first month. There were 38 cases (59%) showing obvious abnormal clinical manifestations, fever 36 cases (56%), vomiting 11 cases (17%). Forty-eight cases (69%) were caused by Gram-positive bacteria, with Staphylococcus epidermidis 24 cases; 22 cases (31%) were caused by Gram-negative bacteria, with Acinetobacter baumannii the prominent pathogen 7 cases. The Gram-positive bacterial infection was more common in summer than the Gram-negative bacterial infection (20 cases (42%) <i>vs.</i> 3 cases (14%), <i>χ</i><sup>2</sup>=5.37, <i>P=</i>0.020), while the Gram-negative bacterial infection was more in autumn and within the first month after surgery than the Gram-positive bacterial infection (11 cases (50%) <i>vs</i>. 8 cases (17%), 15 cases (67%) <i>vs.</i> 5 cases (33%), <i>χ</i><sup>2</sup><i>=</i>8.48, 9.02; <i>P=</i>0.004, 0.003). Gram-positive bacteria resistant to vancomycin and <i>Acinetobacter baumannii</i> resistant to polymyxin were not found. However, <i>Acinetobacter baumannii</i> showed only 45% (10/22) susceptibility to carbapenem antibiotics. <b>Conclusions:</b> The clinical presentation of post-neurosurgical bacterial meningitis in children is atypical. Gram-positive bacteria are the main pathogens causing post-neurosurgical bacterial meningitis; Gram-negative bacterial meningitis are more likely to occur in autumn and within the first month after surgery. <i>Acinetobacter baumannii</i> has a high resistance rate to carbapenem antibiotics, which should be taken seriously.</p>","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"690-694"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10282727","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}
F Wu, X N Ji, M X Shen, Y Y Gao, P P Zhang, S P Li, Q Chen
{"title":"[A case of intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures caused by PHF21A gene variation and review of literature].","authors":"F Wu, X N Ji, M X Shen, Y Y Gao, P P Zhang, S P Li, Q Chen","doi":"10.3760/cma.j.cn112140-20230221-00118","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230221-00118","url":null,"abstract":"<p><p><b>Objective:</b> To discuss the clinical and genetic features of intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures (IDDBCS). <b>Methods:</b> The clinical and genetic records of a patient who was diagnosed with IDDBCS caused by PHF21A gene variation at Children's Hospital Capital Institute of Pediatrics in 2021 were collected retrospectively. Using \" PHF21A gene\" as the keyword, relevant articles were searched at CNKI, Wanfang Data and PubMed from establishment of databases to February 2023. Clinical and genetic features of IDDBCS were summarized in the combination of this case. <b>Results:</b> An 8 months of age boy showed overgrowth (height, weight and head circumference were all higher than the 97<sup>th</sup> percentile of children of the same age and sex) and language and motor developmental delay after birth, and gradually showed autism-like symptoms like stereotyped behavior and poor eye contact. At 8 months of age, he began to show epileptic seizures, which were in the form of a series of spastic seizures with no reaction to adrenocorticotropic hormone but a good response to vigabatrin. Physical examination showed special craniofacial appearances including a prominent high forehead, sparse eyebrows, broad nasal bridge, and downturned mouth with a tent-shaped upper lip. The patient also manifested hypotonia. Whole exome sequencing showed a de novo heterogeneous variant, PHF21A (NM_001101802.1): c.54+1G>A, and IDDBCS was diagnosed. A total of 6 articles (all English articles) were collected, involving this case and other 14 patients of IDDBCS caused by PHF21A gene variation. Clinical manifestations were intellectual disability or developmental delay (15 patients), craniofacial anomalies (15 patients), behavioral abnormalities (12 patients), seizures (9 patients), and overgrowth (8 patients). The main pathogenic variations were frameshift variations (8 patients). <b>Conclusions:</b> IDDBCS should be considered when patients show nervous developmental abnormalities, craniofacial anomalies, seizures and overgrowth. PHF21A gene variation detection helps to make a definite diagnosis.</p>","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"726-730"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10300846","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":"[A case of infectious encephalomyelitis caused by CARD9 gene-associated candida albicans infection].","authors":"J Wang, Y An, G Zhang","doi":"10.3760/cma.j.cn112140-20230104-00005","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230104-00005","url":null,"abstract":"患儿 男,12岁8月龄,因“间断头痛2个月,呕吐10 d”于2021年1月6日入住西安市儿童医院神经外科。结合病史、体格检查、实验室检查、宏基因组二代测序、影像学检查,诊断为白色念珠菌致感染性脑脊髓炎,基因检测结果发现患儿携带CARD9基因NM—052813.5:c.1118G>C(p.R373P)和c.951G>A(p.R317R)复合杂合变异,其中p.R373P可致常染色体隐性遗传的家族性念珠菌2型感染。经两性霉素B静脉点滴及鞘内注射,联合伏立康唑、氟胞嘧啶口服,共治疗4.3个月,好转出院。.","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"737-739"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9925455","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":"[Research progresses of tumor associated macrophages in neuroblastoma].","authors":"S D He, Y Su","doi":"10.3760/cma.j.cn112140-20221117-00980","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20221117-00980","url":null,"abstract":"神经母细胞瘤(NB)是儿童常见的颅外实体肿瘤。NB的发生与各种类型的免疫细胞浸润有关,特别是肿瘤相关巨噬细胞(TAM),TAM具有促进肿瘤生长并抑制免疫的功能。TAM的靶向治疗为NB患儿提供了新的治疗选择。本文对近年来NB与TAM研究领域的相关进展进行综述。.","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"760-763"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10300843","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 presentation and prognosis in children over 10-year-old with primary nephrotic syndrome].","authors":"J Tu, C Y Chen, H X Yang, Y Jia, H Y Geng, H R Li","doi":"10.3760/cma.j.cn112140-20230104-00007","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230104-00007","url":null,"abstract":"<p><p><b>Objective:</b> To summary the clinical presentation and prognosis of primary nephrotic syndrome (PNS) in teenagers. <b>Methods:</b> The clinical data, renal pathological types and prognosis of 118 children over 10-year-old with PNS treated in the Department of Nephrology of the Children's Hospital Affiliated to Capital Institute of Pediatrics from January 2010 to December 2020 were retrospectively analyzed, with 408 children ≤10-year-old as control group synchronously. Chi-square test was used to compare the difference of clinical types, pathologic types, response to steroids and tubulointerstitial changes between the groups. The teenagers with steroid resistant nephrotic syndrome (SRNS) were divided into initial non-responder group and late non-responder group. Kaplan-Meier method was used to compare the difference of persistent proteinuria, and Fisher's exact test for the histological types. <b>Results:</b> There were 118 children >10-year-old, including 74 males and 44 females, with the onset age of 12.1 (10.8, 13.4) years; and 408 children ≤10-year-old with the onset age of 4.5 (3.2, 6.8) years. The proportion of SRNS was significantly higher in patients >10-year-old than those ≤10-year-old (24.6% (29/118) <i>vs.</i> 15.9% (65/408), <i>χ</i><sup>2</sup>=4.66, <i>P=</i>0.031). There was no statistical difference in the pathological types between >10-year-old and ≤10-year-old (<i>P</i>>0.05), with minimal change disease the most common type (56.0% (14/25) <i>vs.</i> 60.5% (26/43)). The percentage of cases with renal tubulointerstitial lesions was significantly higher in children >10-year-old compared to those ≤10-year-old (60.0% (15/25) <i>vs.</i> 23.3% (10/43), <i>χ</i><sup>2</sup>=9.18, <i>P=</i>0.002). There were 29 cases presented with SRNS in PNS over 10-year-old, including 19 initial non-responders and 10 late non-responders. Analyzed by Kaplan-Meier curve, it was shown that the percentage of persistent proteinuria after 6 months of immunosuppressive treatments was significantly higher in initial non-responders than those of the late non-responders ((22±10)% <i>vs.</i> 0, <i>χ</i><sup>2</sup>=14.68, <i>P<</i>0.001); the percentage of minimal change disease was significantly higher in patients of late non-responders than those of the initial non-responders (5/6 <i>vs.</i> 3/13, <i>P=</i>0.041). Of the 63 >10-year-old with steroid-sensitive nephrotic syndrome followed up more than one year, 38 cases (60.3%) had relapse, and 14 cases (22.2%) were frequent relapse nephrotic syndrome and steroid dependent nephrotic syndrome. Among the 45 patients followed up over 18-year-old, 22 cases (48.9%) had recurrent proteinuria continued to adulthood, 3 cases of SRNS progressed to kidney insufficiency, and one of them developed into end stage kidney disease and was administrated with hemodialysis. <b>Conclusions:</b> Cases over 10-year-old with PNS tend to present with SRNS and renal tubulointerstitial lesions. They have a favorable prognosis, ","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"708-713"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9916575","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}
S Wang, Y Mei, Z Y Yang, Q Zhang, R L Li, Y Y Wang, W H Zhao, T Xu
{"title":"[Comparison of two child growth standards in assessing the nutritional status of children under 6 years of age].","authors":"S Wang, Y Mei, Z Y Yang, Q Zhang, R L Li, Y Y Wang, W H Zhao, T Xu","doi":"10.3760/cma.j.cn112140-20230505-00314","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20230505-00314","url":null,"abstract":"<p><p><b>Objective:</b> To compare the application of China growth standard for children under 7 years of age (China standards) and World Health Organization child growth standards (WHO standards) in evaluating the prevalence of malnutrition in children aged 0-<6 years in China. <b>Methods:</b> The research data came from the national special program for science & technology basic resources investigation of China, named \"2019-2021 survey and application of China's nutrition and health system for children aged 0-18 years\". Multi-stage stratified random sampling was used to recruit 28 districts (regions) in 14 provinces, autonomous regions or municipalities across the country. Children (<i>n</i>=38 848) were physically measured and questionnaires were conducted in the guardians of the children. The indicators of stunting, underweight, wasting, overweight and obesity were evaluated by China standards and WHO standards respectively. Chi-square test was used to comparing the prevalence of each nutritional status between the two standards, as well as the comparison between the two standards by gender and age. <b>Results:</b> Among the 38 848 children, 19 650 were boys (50.6%) and 19 198 were girls (49.4%), 19 480 urban children (50.1%) and 19 368 rural children (49.9%). The stunting, underweight and wasting cases in the study population were 2 090 children (5.4%), 1 354 children (3.5%) and 1 276 children (3.3%) according to the China standards, and 1 474 children (3.8%), 701 children (1.8%) and 824 children (2.1%) according to the WHO standards, respectively; the above rates according to the China standards were slightly higher than those to the WHO standards (<i>χ</i><sup>2</sup>=111.59, 213.14, and 99.99, all <i>P<</i>0.001). The overweight and obesity cases in the study population were 2 186 children (5.6%) and 1 153 children (3.0%) according to the China standards, and 2 210 children (5.7%) and 1 186 children (3.1%) according to the WHO standards, with no statistically significant differences (<i>χ</i><sup>2</sup>=0.14 and 0.48, <i>P=</i>0.709 and 0.488, respectively). Compared to the results based on WHO standards, the China standards showed a lower prevalence of overweight and obesity in boys (<i>χ</i><sup>2</sup>=14.95 and 5.85, <i>P</i><0.001 and =0.016, respectively), and higher prevalence of overweight in girls (<i>χ</i><sup>2</sup>=12.60, <i>P<</i>0.001); but there was no statistically significant differences in girls' obesity prevalence between the two standards (<i>χ</i><sup>2</sup>=2.62, <i>P</i>=0.106). <b>Conclusions:</b> In general, the prevalence of malnutrition among children aged 0-<6 years based on China standards is slightly higher than that on WHO standards. To evaluate the nutritional status of children, it is advisable to select appropriate child growth standards based on work requirements, norms or research objectives.</p>","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"700-707"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9916579","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}
Y Zhang, X M Li, H Jiang, Y Q Jin, M T Li, Y L Gu, H M Zhou
{"title":"[Clinical characteristics of 42 children with focal atrial tachycardia originated from the right atrial appendage].","authors":"Y Zhang, X M Li, H Jiang, Y Q Jin, M T Li, Y L Gu, H M Zhou","doi":"10.3760/cma.j.cn112140-20221227-01067","DOIUrl":"https://doi.org/10.3760/cma.j.cn112140-20221227-01067","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the feature and treatment of atrial tachycardia (AT) originated from right atrial appendage (RAA) in children. <b>Methods:</b> The data of 42 children with AT originated from RAA, who were admitted the First Hospital of Tsinghua University from January 2010 to September 2022 were analyzed retrospectively.The clinical characteristics, treatment and efficacy were analyzed. The children were divided into tachycardia cardiomyopathy group and normal cardiac function group. The differences in the ablation age and the heart rate during AT between two groups were compared by independent sample <i>t</i>-test. <b>Results:</b> Among 42 children, there were 20 males and 22 females. The age of onset was 2.7 (0.6, 5.1) years. Their age at radiofrequency ablation was (6.5±3.6) years, and the weight was (23.4±10.0) kg. Thirty-two children (76%) had sustained AT. The incidence of tachycardia cardiomyopathy was 43% (18/42). Compared to that of the normal cardiac function group, the ablation age and the heart rate at atrial tachycardia of the tachycardia cardiomyopathy group were higher ((8.1±3.8) <i>vs.</i> (5.3±3.1) years, <i>t</i>=-2.63, <i>P</i>=0.012; (173±41) <i>vs.</i> (150±30) beats per minute, <i>t</i>=-2.05, <i>P</i>=0.047. Thirty-eight children (90%) responded poorly to two or more antiarrhythmic drugs. The immediate success rate of radiofrequency ablation (RFCA) was 57% (24/42), and the AT recurrence rate was 17% (4/24). Twenty-two children underwent RAA resection, and their AT were all converted to sinus rhythm after the surgery. During the RAA resection, 10 cases of right atrial appendage aneurysm were found, 9/18 of which failed the RFCA. <b>Conclusions:</b> The AT originated from the RAA in children tend to present with sustained AT, respond poorly to antiarrhythmic drugs, and has a low success rate of RFCA as well as high recurrence rate. Resection of the RAA is a safe and effective complementary treatment.</p>","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 8","pages":"714-718"},"PeriodicalIF":0.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9922399","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}