west china medical publishers
Keyword
  • Title
  • Author
  • Keyword
  • Abstract
Advance search
Advance search

Search

find Keyword "婴儿" 83 results
  • Interpretation of European Respiratory Society statement on obstructive sleep disordered breathing in 1 to 23-month-old children

    In order to guide diagnosis and treatment in children with sleep disordered breathing aged 1 to 23 months, the European Respiratory Society(ERS) summarized the evidence and released the European Respiratory Society statement based on clinical experience in 2016. This article aims to interpret the ERS statement. Children with apparent upper airway obstruction during wakefulness and those with SDB symptoms and complex conditions requires treatment. Adenotonsillectomy and continuous positive airway pressure are the most frequently used treatment measures along with interventions targeting specific conditions. Obstructive SDB in children aged 1 to 23 months is a multifactorial disorder that requires objective assessment and treatment of all underlying abnormalities.

    Release date:2019-04-19 09:26 Export PDF Favorites Scan
  • 婴儿期癫痫性痉挛的检查诊断干预原则及预后

    癫痫为神经科常见疾病, 而婴儿期为癫痫发作的高峰年龄。婴儿期癫痫中痉挛发作最为常见, 且病因复杂多样。随着遗传学研究的深入, 很多以往未明确病因的婴儿期癫痫性痉挛可能为遗传因素所致, 且可能为皮层起源, 不同的遗传背景提示不同的治疗方案和预后。结合《2015年国际抗癫痫联盟关于婴儿期癫痫管理推荐共识——ILAE儿科委员会协作组报告》及我国的实际情况, 通过回顾文献提出婴儿期癫痫性痉挛的检查诊断、干预原则及预后, 希望对临床医生的工作提供帮助, 从而提高婴儿期癫痫的诊治水平, 更好地改善预后。促肾上腺皮质激素(Adreno cortico tropic hormone, ACTH)大剂量与小剂量应用均有比较良好的治疗效果。ACTH治疗后短时间内的发作控制对于患儿的精神运动发育有利。结节性硬化症患儿的癫痫性痉挛, 氨己烯酸表现出较好的治疗效果。托吡酯对于癫痫控制有一定的效果, 而其他抗癫痫药物、生酮饮食、手术治疗的效果仍不明确。对于代谢性病因所致的癫痫性痉挛, 明确病因非常重要; 结合具体病因采取相应治疗方案即可。不同因素所致婴儿期癫痫性痉挛提示不同的治疗方案。早期全面的筛查明确病因对于指导治疗具有非常重要的意义。在药物选择上, 临床医生一方面应考虑到病因的个体化差异; 另一方面应关注治疗的及时有效性, 从而保证患儿发作的控制及精神运动的发育

    Release date: Export PDF Favorites Scan
  • 西安地区192例婴幼儿眼内疾病构成分析

    Release date:2016-09-02 05:41 Export PDF Favorites Scan
  • 维生素B6反应性癫痫

    维生素B6(VitaminB6, VB6) 相关性癫痫或发作主要包括VB6缺乏性惊厥、VB6依赖性癫痫和VB6反应性癫痫,前二者由于社会和科学的进步可以被预防逐渐被人们认识并得到有效治疗,但VB6反应性癫痫尚未得到广泛重视。VB6反应性癫痫是指发作可被VB6单药控制,或在已有抗癫痫药物不能控制的基础上加用VB6后发作控制达1个月以上,治疗一定时间后可停用而不会复发。其临床特点包括:① 发作起始年龄在3个月~5岁,大多数在1岁以内;② 癫痫多为婴儿痉挛,少数为Lennox-Gastaut综合征、强直-阵挛发作或局灶运动性发作;③ 病因不仅为特发性或隐源性,也可为有器质性脑损伤的症状性;④ 色氨酸负荷试验通常为阴性;⑤ 口服大剂量VB6可使发作减少或消失;⑥ 排除VB6缺乏性惊厥和VB6依赖性癫痫。VB6反应性癫痫的发病机制尚不清楚,可能与年龄依赖的酶功能异常,或与VB6依赖性神经递质的功能成熟关键阶段有关,预后良好。

    Release date:2017-05-24 05:46 Export PDF Favorites Scan
  • Surgical Treatment for Infants Under Six Months with Tetralogy of Fallot

    Objective To investigate the optimal timing for surgical treatment of infants less than six months of age with tetralogy of Fallot (TOF), and to improve surgical results and reduce early mortality. Methods Clinical material of 108 consecutive patients with TOF who were less than six months of age undergoing early surgery from Oct.1996 to Dec. 2006 were retrospectively reviewed. There were 70 males and females with mean age of 4.70 months (9 d-6 months). 104 patients underwent complete repair and four patients underwent BlalockTaussig (B T) shunt. Emergency procedures have been performed in 5 patients. Results Five patients (4.63%) died of low cardiac output syndrome (3 patients), pulmonary infection and acute respiratory distress syndrome (1 patient), and acute necrotizing enteritis (1 patient).82 patients were followed up, followup period was 31.17±40.00 months.21 patients lost to followup. One patient(0.92%) required additional intervention for pulmonary valve stenosis 6 months after operation. Heart functional class(New York Heart Association) recovered toⅠ-Ⅱgrading in other patients. Echocardiography shows: no residual ventricular shunt, no stenosis in right ventricular outflow tract and pulmonary valve, pressure difference≤50 mm Hg. No late deaths. Conclusion Early definitive repair of TOF can be performed safely on infants less than six months of age, the results of low mortality is acceptable.

    Release date:2016-08-30 06:06 Export PDF Favorites Scan
  • 母源KCNQ3基因突变致自限性家族性新生儿癫痫一例

    Release date:2024-07-03 08:46 Export PDF Favorites Scan
  • Power spectral density characteristics in EEG of infantile epileptic spasms syndrome

    ObjectiveTo compare and analyze the electroencephalographic (EEG) characteristics of infants with infantile epileptic spasms syndrome (IESS) and healthy infants during sleep using power spectral density (PSD) analysis. MethodsInfants aged 5 to 9 months with IESS were included, along with an equal number of age-matched healthy controls. EEG signals during sleep were recorded using the Nihon Kohden EEG-1200C system. The energy distribution in the theta (θ), alpha (α), sigma (σ), and beta (β) frequency bands, as well as the morphology and values of PSD within the 4 ~ 30 Hz range, were analyzed. Additionally, spectral entropy (SpEn) was calculated to evaluate signal complexity. Results A total of 10 IESS patients and 10 healthy infants were included. There were no significant differences in gender or age between the two groups (P=0.64, P=0.88). In both groups, PSD values showed a linear decreasing trend with increasing frequency. However, the IESS group showed notable differences in PSD morphology, amplitude, and energy distribution compared to controls. These included the absence of a σ-band peak, greater PSD dispersion across electrodes, significant alterations in energy distribution across θ, α, σ, and β bands, and significantly higher PSD values in the 4 ~ 30 Hz range (P<0.000 1). SpEn analysis revealed significantly elevated spectral entropy across the sigma band in the IESS group, indicating a lack of dominant frequencies, increased complexity, reduced rhythmicity, and enhanced disorder. In contrast, healthy controls exhibited elevated SpEn in the alpha band, reflecting the physiological reduction or disappearance of dominant alpha rhythms during sleep. Conclusion Infants with IESS demonstrate distinct EEG characteristics in both PSD and SpEn analyses compared to healthy infants. These quantitative spectral features reflect the underlying abnormalities of EEG in IESS and provide objective insights that complement conventional visual assessment, offering a novel perspective for early diagnosis and therapeutic monitoring.

    Release date:2025-07-22 10:02 Export PDF Favorites Scan
  • Human retinal proteomics study of adults and two-month old infants

      Objective  To identify proteins that have expressed in human eyes from adults and two-month old infants by proteomics approach, so as to build a two-dimensional gel electrophoresis (two-DE) reference map for human retina. The difference of proteomics between the retinas of adults and two-month old infants are also studied. Methods  Human retina tissues were collected from donor eyes (nine adults and two infants). Proteins were separated by two-DE. The gels were analyzed by image software. Protein spots were excised from the gels and detected by matrix assisted laser desorption ionization time off light mass spectrometry (MALDI-TOF-MS). Results  A total of 1179 spots and 1295 spots were detected respectively on two-DE gels of Coomassie-stained adults and two-month old infants retina, of which 1039 spots were matched in the position. Five spots up-regulated were successfully identified. Human serum albumin and 4 guanylate kinase 1 (GUK1) were identified in adult retina. beta;2-tubulin, transaldolase1 and alpha A-crystallin were identified in infant retina. Conclusion  The two-DE reference map for retina proteomics is successfully established. This study provides an evidence of changes in retinal protein levels between adults and infants and biochemical pathways for future studies of human retina development.

    Release date:2016-09-02 05:41 Export PDF Favorites Scan
  • 婴儿先天性视神经缺损合并脉络膜缺损光相干断层扫描检查一例

    Release date:2017-09-19 03:09 Export PDF Favorites Scan
  • 婴儿特发性血小板减少性紫癜的临床分析

    目的 分析婴儿期特发性血小板减少性紫癜(ITP)的诱因、临床特点、实验室资料、治疗反应和转归,为临床治疗和预后评估提供依据。 方法 2007年1月-2008年6月共收治32例ITP住院婴儿,男20例,女12例,中位年龄5个月,对其临床特征、治疗、转归进行回顾性分析。 结果 32例中14例有前驱感染,5例发病前2周~3个月内有过疫苗预防接种史。病程<3 d者25例,3~7 d者5例,>7 d者2例。主要表现为不同程度的皮肤、黏膜出血(包括消化道出血)。治疗以地塞米松单独或联合静脉用人血丙种球蛋白冲击,并以适量泼尼松短期维持。出血停止并且血小板计数恢复正常<3 d者16例,3~7 d者14例,>7 d者2例。经地塞米松冲击治疗的21例中,3例停药后又复发,再次给予联合冲击治疗,均在1周内恢复。中位随访时间12个月,无1例转为慢性或难治性病例。 结论 婴儿ITP是一组预后良好的疾病,地塞米松单独或联合静脉用人血丙种球蛋白冲击是有效治疗。免疫接种引起的ITP预后亦佳。

    Release date:2016-09-08 09:16 Export PDF Favorites Scan
9 pages Previous 1 2 3 ... 9 Next

Format

Content