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1.
目的联合使用国际子宫内膜肿瘤分析(IETA)经阴道常规超声与超声造影评估子宫内膜癌(EC)患者肌层浸润深度及宫颈有无侵犯,预测EC的病理分期;比较此2种方法的诊断价值。 方法将南方医科大学深圳医院及中山大学附属第七医院2017年1月至2020年12月间83例已手术的EC患者纳入研究,所有患者术前1个月内均行经阴道常规超声及超声造影检查,由2名具有10年以上妇产超声工作经验的超声医师,掌握IETA专家小组拟定的子宫内膜病变共识的具体内容,对所有入组病例的常规超声及超声造影图像进行盲法分析,以病理结果为参考,比较分析常规超声主、客观测量法及超声造影主、客观测量法对EC病理分期的诊断符合率,采用Kappa检验分析超声与病理结果的一致性。同时采用受试者操作特征(ROC)曲线分析超声客观测量方法对EC深肌层浸润及宫颈有无侵犯的诊断效能。 结果本研究发现IETA专家共识总结的子宫内膜厚度、病灶回声、宫腔线的形状、子宫内膜-肌层交界处(结合带)情况、无“亮边”征及子宫内膜病灶血管模式在不同病理分期的EC中,均有较高的特异度及一致性,是预测EC较好的超声指标。超声造影主观评估法(Kappa=0.873,P<0.001)、超声造影客观测量法(Kappa=0.842,P<0.001)、IETA常规超声主观评估法(Kappa=0.811,P<0.001)、IETA常规超声客观测量法(Kappa=0.764,P<0.001)此4种诊断方法与病理结果一致性均良好,超声造影较常规超声对EC病理分期的诊断符合率有一定程度的提高[主观评估法、客观评估法:(90.36%、87.95%) vs(85.54%、81.93%)]。常规超声或超声造影显示病灶前后径、病灶的体积、病灶与子宫前后径的比值对预测EC深肌层浸润(浸润深度≥1/2)均有较好的诊断效能,ROC曲线下面积(AUC)均≥0.945,常规超声或超声造影显示病灶外缘与浆膜层的最小距离评估法诊断效能较差,AUC仅为0.414、0.462。常规超声或超声造影显示病灶下缘与宫颈外口距离评估法对预测EC有无宫颈侵犯的诊断效能一般,AUC为0.521、0.559。 结论IETA经阴道常规超声声像特征与超声造影对EC的诊断及预测病理分期均具有较好的效果,且对超声术语进行规范化描述,临床上值得推荐使用。超声造影较经阴道常规超声的诊断效能有一定程度提高,能更好地显示病变对周围肌层及宫颈的浸润深度、侵犯范围;超声造影联合经阴道常规超声,可能达到EC早期发现、准确分期、早期治疗的目的。  相似文献   
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目的 探讨肥胖患者腹腔镜下袖状胃切除术(LSG)前后肠道菌群的变化,及对非酒精性脂肪肝(NALFD)的影响。方法 收集2020年7月至2021年1月在安徽医科大学第二附属医院胃肠减重代谢外科就诊并接受LSG治疗的30例肥胖合并NAFLD患者的临床资料,观察并记录LSG术前和术后3个月的体质量参数、血清检验结果和粪便菌群测序等指标。计算LSG治疗前后患者肝脏脂肪(FLI)指数和FIB-4评分,评估手术后患者肝脂肪变性和纤维化的改善情况。结果 LSG术后患者身体质量参数、FLI及FIB-4评分较术前降低,差异有统计学意义(P<0.05)。Wilcoxon秩和检验显示术后肠道菌群的丰度和多样性较术前增加,其中梭杆菌的比例增加,厚壁菌比例减少,差异有统计学意义(P<0.05)。白介素-1β(IL-1β)、肿瘤坏死因子-a (TNF-a)水平较术前降低,白介素-4(IL-4)水平较术前升高,差异均有统计学意义(P<0.05)。细胞因子与菌群的Spearman相关性分析显示,梭杆菌与TNF-a,IL-1β呈负相关(r=-0.203、-0.329,P<0.05),厚壁菌与TNF-a,IL-1β呈正相关(r=0.315、0.459,P<0.05)。术前Pearson相关性分析显示TNF-a、IL-1β分别与FLI、FIB-4评分呈正相关(r=0.391、0.435、0.402、0.373,P<0.05),IL-4与FLI、FIB-4评分呈负相关(r=-0.523、-0.410,P<0.05)。术后相关性分析提示同样结果。结论 LSG可改善肠道菌群的丰度及分布,降低FLI和FIB-4评分进而缓解了肥胖患者肝脂肪变性和纤维化,IL-1β、IL-4和TNF-a可能在肠-肝轴中起到调节作用。  相似文献   
3.
BackgroundRecent advances in respiratory management have improved survival for patients with Fukuyama congenital muscular dystrophy (FCMD), characterized by congenital muscular dystrophy and brain malformation. Previous studies reported that more than half of patients exhibit seizures in childhood. However, little is known about epilepsy after childhood.MethodsTo elucidate the long-term clinical course of epilepsy, we retrospectively reviewed all medical records in nine patients (6 males, mean age 20.7 years) with FCMD diagnosed between 1981 and 2019.ResultsThe follow-up periods ranged from 6 to 30 years (mean 18.4 years). A total of 75 EEG recordings were available from nine patients. In some patients, EEGs were normal during early childhood but tended to show paroxysmal discharges with age. Overall, epileptic seizures were observed in six patients. Except for one presenting with afebrile seizure at one year of age, the remaining five patients developed epilepsy between 13 and 22 years of age. The most common seizure type was focal impaired awareness seizure. After adolescence, four patients exhibited status epilepticus. Their convulsive movements of the seizures became less prominent with progression of the disease. At the last evaluation, most patients (5/6) had uncontrolled seizures.ConclusionsDespite presence of distinct brain malformation, epileptic seizures may develop after childhood in FCMD patients. Our experience suggests that clinicians should be careful not to overlook epileptic seizures, especially in advanced-stage patients who had profound muscle weakness.  相似文献   
4.
《Clinical neurophysiology》2021,132(9):2003-2011
ObjectiveA large N20 and P25 of the median nerve somatosensory evoked potential (SEP) predicts short survival in amyotrophic lateral sclerosis (ALS). We investigated whether high frequency oscillations (HFOs) over N20 are enlarged and associated with survival in ALS.MethodsA total of 145 patients with ALS and 57 healthy subjects were studied. We recorded the median nerve SEP and measured the onset-to-peak amplitude of N20 (N20o-p), and peak-to-peak amplitude between N20 and P25 (N20p-P25p). We obtained early and late HFO potentials by filtering SEP between 500 and 1 kHz, and measured the peak-to-peak amplitude. We followed up patients until endpoints (death or tracheostomy) and analyzed the relationship between SEP or HFO amplitudes and survival using a Cox analysis.ResultsPatients showed larger N20o-p, N20p-P25p, and early and late HFO amplitudes than the control values. N20p-P25p was associated with survival periods (p = 0.0004), while early and late HFO amplitudes showed no significant association with survival (p = 0.4307, and p = 0.6858, respectively).ConclusionsThe HFO amplitude in ALS is increased, but does not predict survival.SignificanceThe enlarged HFOs in ALS might be a compensatory phenomenon to the hyperexcitability of the sensory cortex pyramidal neurons.  相似文献   
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《Clinical therapeutics》2019,41(5):943-960.e4
PurposePatients’ perceptions of benefit–risk are essential to informing the regulatory process and the context in which potential therapies are evaluated. To bring this critical information to regulators, Cure SMA launched a first-ever Benefit-Risk Survey for spinal muscular atrophy (SMA) to characterize decision-making and benefit–risk trade-offs in SMA associated with a potential therapy. We hypothesized that risk tolerance would be correlated with SMA type/severity and disease progression. This article presents the results of a benefit–risk survey to enhance understanding of how patients with SMA and caregivers evaluate specific benefits and risks associated with potential therapies.MethodsAffected adults, representing all SMA types (I–IV) within the Cure SMA database, and caregivers of affected individuals of all ages/types were invited via e-mail to participate. Best–worst scaling (BWS) was used to assess participants’ priorities on benefit–risk trade-offs, as it provides higher discrimination and importance scaling among tested attributes. Twelve potentially clinically meaningful treatment benefits and 11 potential risks (ranging in severity and immediacy) were tested. Multiple factors were correlated with individual responses, including: SMA type/disease severity, stage of disease, respondent type, sex, and quality of life/level of independence (current and expected). Survey respondents were also evaluated for "risk-taking attitudes."FindingsA total of 298 responses were evaluated (28% affected adults and 72% caregivers, mostly parents). Most respondents were diagnosed >5 years ago (67.3%), with 22.1% SMA type I, 45.6% SMA type II, and 27.9% SMA type III. No strong correlation was found between risk tolerance and SMA type, stage of disease progression, respondent type, sex, quality of life assessment, or rated levels of independence. Irrespective of SMA type, respondents consistently rated the following risks, associated with a potential treatment, as "least tolerable": life-threatening allergic reactions; 1 in 1000 risk of life-threatening side effects leading to possible organ failure; or worsening quality of life. Furthermore, all SMA type respondents rated these risks as "most tolerable": invasive mode of treatment administration (including need for general anesthesia); side effect of dizziness; and other common side effects such as nausea, vomiting, loss of appetite, headaches, back pain, or fatigue.ImplicationsWith the approval of the first SMA treatment, these findings offer a unique opportunity to assess and characterize baseline risk-tolerance in SMA against which to evaluate future SMA treatment options. Although differences had been expected in risk tolerance among respondents based on disease baseline and certain patient attributes, this was not observed. Survey results should inform future SMA drug development and benefit–risk assessments.  相似文献   
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Introduction: No etiologic therapy is available for Duchenne muscular dystrophy (DMD), but mesenchymal stem cells were shown to be effective in preclinical models of DMD. The objective of this study is to investigate the effect of microfragmented fat extracted on a murine model of DMD. Methods: Fat tissue was extracted from healthy human participants and injected IM into DMD mice. Histological analysis, cytokines, and force measurement were performed up to 4 weeks after injection. Results: Duchenne muscular dystrophy mice injected with microfragmented fat exhibited an improved muscle phenotype (decreased necrosis and fibrosis), a decrease of inflammatory cytokines, and increased strength. Discussion: Administration of microfragmented fat in key muscles may improve muscular phenotype in patients with DMD. Muscle Nerve, 2019  相似文献   
10.
Patients with neuromuscular conditions are frequently seen in final professional clinical examinations as they have good clinical signs, which often point towards the underlying diagnosis. This paper outlines some of the most common neuromuscular disorders that you are likely to come across in orthopaedic practise.  相似文献   
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