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81.
《Disability and health journal》2022,15(3):101324
BackgroundIn the United States nearly 20% of children ages 12–17 have developmental disorders. Some attain population-based developmental milestones after a delay, or increase functioning through special education, medication, technology, or therapy. Others have severe lasting impairments. An indicator identifying those groups in surveys of adults could help shape policies to improve lives.HypothesesWe hypothesized that survey histories of special education could indicate functional status levels.MethodsData were from the nationally representative Panel Study of Income Dynamics (1997–2017, n = 2745). With measures of diagnoses, behaviors, functional status, service use, and adult outcomes, we tested three special education groups as indicators of: (1) no impairment (no special education), (2) disorders, developmental diagnoses that adversely affect educational performance, but with development after a period of delay or only moderate disability, indicated by transfer from special education; and (3) severe lasting disability, the diagnoses combined with life-long needs for supports or services, with limitations in areas including self-care, mobility, and capacity for independent living, indicated by special education in the individual's final year of school.ResultsAcross the special education groups, from no impairment to severe lasting disability, there were trends of: increasing severe and lasting disability (respectively 4.8%, 35.6%, 76.4%); increasing special services use (13.5%, 43.1%, 83.7%); increasing severe emotional disorders (2.3%, 11.3%, 17.9%); lower percentages attaining at least an associate's degree by age 25 (42.1%, 20.7%, and 8.9%); and more chronic diseases.ConclusionsSpecial education histories provide a useful indicator of developmental disability impairment levels in adults. 相似文献
82.
《Journal of vascular and interventional radiology : JVIR》2022,33(5):518-524.e3
PurposeTo compare the characteristics of polidocanol (POL) and ethanolamine oleate (EO) sclerosing foams produced by a Shirasu porous glass membrane (SPGM) device with those made using a 3-way stopcock (3WSC).Materials and MethodsFoam half-life times were measured in an ex-vivo benchtop study. Computed tomography (CT) images of each foam were obtained over the time course, and a CT texture analysis was conducted. The bubble size in each foam was measured by an optical microscope.ResultsMedian foam half-life times were longer in the SPGM group than in the 3WSC group (POL: 198 vs 166 s, P = .02; EO: 640 vs 391 s, P < .01). In the CT texture analysis, median standard deviation (SD) and entropy (randomness) were lower, and median energy (uniformity) and gray-level cooccurrence matrix (GLCM) homogeneity were higher in the SPGM group than in the 3WSC group (POL SD: at 30 s and 50–300 s; POL entropy: at 0–60 s; EO SD: at 0–600 s; EO entropy: at 0–460 s; POL energy: at 0–40 s; POL GLCM homogeneity: at 0–250 s; EO energy: at 0–360 s; EO GLCM homogeneity: at 0–480 s; all P < .05). Median bubble diameters in the SPGM group and in the 3WSC group were 69 and 83 μm (P < .01), respectively, in the POL foam; and 36 and 36 μm (P = .45), respectively, in the EO foam.ConclusionsPOL and EO foams had greater uniformity and longer foam half-life time when prepared with an SPGM device than with a 3WSC. 相似文献
83.
《Seminars in perinatology》2022,46(7):151635
The Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network (NRN) maintains a database of extremely preterm infants known as the Generic Database (GDB). Begun in 1987, this database now includes more than 91,000 infants, most of whom are extremely preterm (<29 weeks gestation). The GDB has been the backbone of the NRN, providing high quality, prospectively collected data to study the changing epidemiology of extreme prematurity and its outcomes over time. In addition, GDB data have been used to generate hypotheses for prospective studies and to develop new clinical trials by providing information about the numbers and characteristics of available subjects and the expected event rates for conditions and complications to be studied. Since its inception, the GDB has been the basis of more than 200 publications in peer-reviewed journals, many of which have had a significant impact on the field of neonatology. 相似文献
84.
Induction of labour is a common obstetrical procedure and is undertaken when the benefits of delivery are considered to outweigh the risks of continuation of pregnancy. However, more than one-fifth of induction cases fail to result in vaginal births and lead to unplanned caesarean deliveries, which compromise the birth experience and have negative clinical and resource implications. The need for accurate prediction of successful labour induction is increasingly recognised and many researchers have attempted to evaluate the potential predictability of different factors including maternal characteristics, Bishop score, various biochemical markers and ultrasound markers and derive predictive models to address this issue. 相似文献
85.
目的 慢性牙周炎表现的病理性骨吸收非常常见,牙周膜干细胞(PDLSCs)的外泌体(Exo)对骨吸收的作用和影响尚不明确,本研究分析了该Exo蛋白组分对破骨细胞分化的影响。方法 分别从正畸前拔牙患者和慢性牙周炎患者的牙周膜组织中提取PDLSCs,通过流式细胞术检测表面标记物;通过差速离心分别提取2种细胞的Exo,即Exo-WT和Exo-CP,并通过Western blot、透射电子显微镜(TEM)、蛋白浓度检测、纳米粒径追踪检测Exo特征;通过蛋白质谱检测2种Exo的蛋白组分;通过酶联免疫吸附(ELISA)验证了差异表达蛋白肿瘤坏死因子α(TNF-α)、核因子κB受体活化因子配体(RANKL)、白细胞介素(IL)-1α、转化生长因子β(TGF-β)、骨形态发生蛋白2(BMP-2)表达水平;将10、100、1 000 μg·mL-1的Exo-CP或Exo-WT加入RAW264.7培养基中并于5 d时通过实时荧光定量聚合酶链反应(RT-qPCR)、Western blot、抗酒石酸酸性磷酸酶(TRAP)染色检测破骨分化相关指标表达情况;采用SPSS 24.0软件对实验数据进行统计学分析。结果 Exo-CP富集的差异表达蛋白主要与破骨细胞分化的TNF信号通路、核转录因子κB(NF-κB)信号通路相关;ELISA实验证实了Exo-CP中高表达TNF-α、RANKL、IL-1α,低表达TGF-β1、BMP-2(P<0.05);Exo-CP作用于RAW264.7,显著提高了细胞的破骨分化相关基因及蛋白的表达水平,TRAP染色可见分化的破骨细胞,且呈现浓度依赖性,100、1 000 μg·mL-1浓度Exo-CP对破骨细胞分化的促进作用显著高于10 μg·mL-1浓度组(P<0.05)。结论 慢性牙周炎的病理性骨吸收可能由炎性PDLSCs所分泌的Exo通过促进破骨细胞分化引起,Exo中主要的作用蛋白可能为RANKL和TNF-α,本研究为慢性牙周炎骨吸收的发病机制提供了新视角。 相似文献
86.
87.
目的分析超长住院患者分布及影响因素,探讨减少超长住院日的措施。方法从江苏省某三甲医院病案管理系统中调取2020年1月1日-2020年12月31日134016例出院患者的住院病案首页资料,对住院时间≥30天的1401例超长住院患者的分布特征进行统计描述,采用Logistic回归模型分析超长住院日的影响因素。结果2020年全院平均住院日为7.13天,其中超长住院患者平均住院日为41.85天。超长住院患者以60岁以上年龄组最多(39.61%);出院科室主要分布在血液科(42.18%)、普通外科(11.85%)、骨科(7.49%)等;疾病类别主要为肿瘤(47.32%)、影响健康状态和与保健机构接触的因素(10.56%)、循环系统疾病(7.07%)等;多因素Logistic回归结果显示,男性(OR=1.188)、离院方式为非医嘱离院或其他(OR=2.046)和死亡病例(OR=3.362)是超长住院的危险因素。结论控制超长住院日对平均住院日影响显著,医院应加强重点人群、重点科室和重点病种管理提高诊疗管理水平,缩短平均住院日。 相似文献
88.
目的 基于网络药理学研究香菇多糖抑制三阴乳腺癌(TNBC)的作用机制并采用细胞和动物实验进行验证。方法 通过GeneCards数据库和DisGeNET数据库筛选与TNBC相关基因靶点,利用TCMID、PubChem、SwissTargetPrediction和GeneCards数据库查询香菇多糖相关基因靶点。使用Sangerbox软件进行基因本体论(GO)富集和京都基因与基因组百科全书(KEGG)通路富集分析。结合STRING数据库与Cytoscape 3.7.0软件将共同靶点进行可视化处理,筛选核心靶点,构建"化合物-靶点-通路"网络。利用Metascape软件进行转录因子及相关调控基因特异富集。体外培养小鼠TNBC细胞4T1和人TNBC细胞MDA-MB-231,磺酰罗丹明B染色法观察香菇多糖(31.25、62.5、125、250、500、1 000μg·mL-1)对细胞存活率的影响;健康雌性BABLC小鼠sc接种1×106个4T1-Luc细胞构建TNBC模型,通过小动物活体成像系统观察香菇多糖(100、200 mg·kg-1)对肿瘤生长的影响,实时荧光定量PCR (qRT-PCR)技术检测肿瘤组织信号转导和转录活化因子3(STAT3)和血管内皮生长因子A (VEGFA) mRNA表达。结果 数据库及软件分析得到香菇多糖治疗TNBC关键靶点52个,靶点主要涉及PI3K-Akt、AGE-RAGE、HIF-1、MAPK信号通路和肿瘤蛋白多糖相关通路,PPI分析得到VEGFA、STAT3、MAPK1、IL2、TNF、RELA、AKT1、MAPK3、BCL2L1和HSP90AA1 10个hub基因。与对照组比较,香菇多糖对4T1和MDA-MB-231细胞存活率均有显著抑制作用(P<0.05、0.01),且作用呈浓度相关性;在给药14、21d后,与模型组比较,香菇多糖能够剂量相关性地抑制小鼠TNBC肿瘤的生长,高剂量组差异显著(P<0.05、0.01),21 d抑制率达到(91.9±4.7)%;与对照组比较,香菇多糖给药后能够剂量相关性抑制STAT3和VEGFA的mRNA表达,高剂量组差异显著(P<0.05、0.01)。结论 香菇多糖可通过多靶点、多途径协同作用抑制TNBC的生长。 相似文献
89.
《Journal of cystic fibrosis》2022,21(6):908-921
This paper is the first in a series providing updated guidance on the definition, evaluation and management of people with a Cystic Fibrosis Transmembrane conductance Regulator (CFTR)-Related Disorder (CFTR-RD). The need for this update relates to more precise characterisation of CFTR gene variants and improved assessment of CFTR protein dysfunction. The exercise is co-ordinated by the European CF Society Standards of Care Committee and Diagnostic Network Working Group and involves stakeholder engagement. This first paper was produced by a core group using an extensive literature review and papers graded for their quality. Subsequent wider stakeholder agreement was achieved.The definition of a CFTR-RD remains “a clinical condition with evidence of CFTR protein dysfunction that does not fulfil the diagnostic criteria for CF”. Clearer guidance on CFTR dysfunction and relevant CFTR variants will be provided. Thresholds for clinical presentations are presented and the paradigm that pathobiological processes may be evident in more than one organ is agreed. In this paper we reflect on the early patient journey, highlighting that CF specialists as well as other relevant specialists should be involved in the care of people with a CFTR-RD. 相似文献