超声乳化联合IOL植入术围手术期瞳孔直径和反应的变化

探究晶状体超声乳化联合人工晶状体（IOL）植入术围手术期瞳孔直径、反应的变化。方法：前瞻性临床研究。收集于2016年1-9月上海交通大学医学院附属第九人民医院眼科行超声乳化联合IOL植入术的连续白内障和高度近视透明晶状体置换患者。采用动态瞳孔测量仪（Metro-vision MONCV3）测量术前、术后1周、术后1个月在4种光照度下（0、1、10和100 cd/m2 ）的瞳孔直径,并检测瞳孔反应（如瞳孔初始直径、收缩幅度、收缩潜伏期、收缩持续时间、收缩速度、扩张潜伏期、扩张持续时间和扩张速度等）。采用重复测量方差分析、Pearson相关分析及Spearman相关分析对数据进行分析。结果：共纳入患者53例（53眼）。在4种光照度下,术前瞳孔直径随年龄增加而下降（r0=-0.467,P0<0.001;r1=-0.383,P1=0.005;r10=-0.374,P10=0.006;r100=-0.312,P100=0.023）。 4种光照强度下瞳孔直径手术前后总体差异有统计学意义（F0=206.9,P0<0.001;F1=106.8,P1<0.001; F10=41.7,P10<0.001;F100=36.7,P100<0.001）,与术前相比,4种光照强度下瞳孔直径术后1周、1个月均下降（均P<0.001）。手术前后瞳孔反应的初始直径、收缩幅度、收缩和扩张速度总体差异有统计学意义（F初始直径=99.5,P初始直径<0.001;F收缩幅度=36.2,P收缩幅度<0.001;F收缩速度=51.9,P收缩速度<0.001;F扩张速度=23.8,P扩张速度<0.001）,与术前相比,术后1周、1个月初始直径、收缩幅度、收缩和扩张速度均下降（均P<0.001）。结论：超声乳化联合IOL植入术后1个月内可引起瞳孔缩小,瞳孔反应的收缩、扩张速度变慢,为IOL设计中确定有效光学区范围提供依据。     

非对称区域折射型多焦点人工晶状体植入术后中期临床效果的研究

目的探讨SBL-3新型区域折射型多焦点人工晶状体(MIOL)植入术后的中期临床效果。 方法前瞻性研究。选取2016年6月至2018年1月在成都爱尔眼科医院诊断为年龄相关性白内障,并行超声乳化白内障吸除联合人工晶状体植入的患者59例(87只眼)为研究对象。根据植入人工晶状体类型的不同分为两组。其中,30例(40只眼)植入SBL-3新型区域折射多焦点人工晶状体为多焦组;29例(47只眼)植入Softec HD单焦点人工晶状体为单焦组。术后随访3~12个月,记录术后裸眼远距离(5 m)、中距离(80 cm)、近距离(40 cm)的裸眼视力,矫正远视力及术后等效球镜屈光度;利用VF-14量表行主观问卷调查;对术后眩光的发生率、日常生活老视眼镜依赖与否进行问卷记录;采用双通道视觉质量分析系统测量客观散射指数(OSI)、调制传递函数截止空间频率(MTF cutoff)、斯特尔比值(SR)、对比度视力(包含100%、20%及9%三种)及调节幅度等指标。单焦组和多焦组两组患者各个指标的比较采用独立样本t检验,术前术后的比较采用配对t检验。 结果单焦组与多焦组患者术后裸眼远距离视力均较术前有显著提高,差异有统计学意义(t＝-10.859,-13.382;P<0.05)。多焦组与单焦组术后等效球镜屈光度差异无统计学意义(t＝1.370,P>0.05)。多焦组与单焦组患者术后裸眼远距离视力分别为(0.87±0.17)与(0.82±0.21),差异无统计学意义(t＝-1.129,P>0.05)。多焦组与单焦组患者术后矫正远距离视力分别为(0.91±0.13)与(0.91±0.14),差异无统计学意义(t＝0.081,P>0.05)。多焦组与单焦组患者术后裸眼中距离视力分别为(0.70±0.17)与(0.54±0.22),差异具有统计学意义(t＝-3.888,P<0.05)。多焦组与单焦组患者术后裸眼近距离视力分别为(0.71±0.20)与(0.28±0.10),差异具有统计学意义(t＝-12.340,P<0.05)。单焦组与多焦点组患者采用VF-14表评分分别为(75.39±10.30)与(97.50±4.50),前者低于后者,差异有统计学意义(t＝-9.837,P<0.05)。多焦组与单焦组患者对老视眼镜的依赖程度分别为5%(2/40)与93.6%(44/47),差异有统计学意义(χ²＝68.104,P<0.05)。多焦组与单焦组患者术后眩光的发生率分别为7.5%(3/40)与4.26%(2/47),差异无统计学意义(χ²＝0.035,P>0.05)。多焦组与单焦组患者的MTF cutoff分别为(24.17±7.68)c/deg与(27.00±10.98)c/deg,差异无统计学意义(t＝1.398,P>0.05)。多焦组与单焦组患者的OSI分别为(2.0±0.7)与(1.7±0.8),差异无有统计学意义(t＝-2.139,P>0.05)。多焦组与单焦组患者的SR分别为(0.13±0.03)与(0.15±0.06),差异有统计学意义(t＝2.130,P<0.05)。多焦组与单焦组患者在100%、20%及9%对比度视力比较,差异均无统计学意义(t＝1.545,1.886,1.968;P>0.05)。多焦组与单焦组患者术眼调节幅度分别为(2.30±0.80)D与(1.60±0.70)D,差异有统计学意义(t＝-3.600,P<0.05)。 结论SBL-3新型区域折射多焦点人工晶状体可以提供较好的全程视力和视觉质量,术后患者满意度较高。     

Abrupt visual loss during anti-vascular endothelial growth factor treatment for type 3 neovascularization

AIM: To investigate the incidence of abrupt visual loss and its associated factors, during anti-vascular endothelial growth factor (VEGF) treatment for type 3 neovascularization. METHODS: This retrospective study included 137 eyes that were newly diagnosed with type 3 neovascularization. All eyes were treated with anti-VEGF therapy. Abrupt visual loss was defined as loss of 5 or more lines in best-corrected visual acuity (BCVA) in comparison to the previous visit. The incidence and timing of abrupt visual loss as well as the factors associated with it, were determined. In addition, the BCVA at the final follow-up was compared between the eyes with and those without abrupt visual loss. RESULTS: The mean follow-up period was 42.4±18.9mo after diagnosis, and abrupt visual loss was noted in 22 eyes (16.1%) at a mean of 19.6±13.9mo. Abrupt visual loss was found to be associated with subretinal hemorrhage in 11 eyes (50.0%), development of or increase in the height of pigment epithelial detachment with fluid in 8 eyes (36.4%), and tears in the retinal pigment epithelium in 3 eyes (13.6%). The logarithm of minimum angle of resolution (logMAR) mean BCVA at the final follow-up was 2.07±0.67 (Snellen equivalents: 20/2349) and 1.00±0.55 (20/200) in eyes with and without abrupt visual loss, respectively. BCVA was significantly worse in the eyes with abrupt visual loss (P<0.001). CONCLUSION: Abrupt visual loss is noted in 16.1% of patients with type 3 neovascularization and is associated with poor visual outcome. Additional studies are needed to determine how abrupt visual loss can be prevented.     

Expression and Role of Voltage-Gated Sodium Channels in Human Dorsal Root Ganglion Neurons with Special Focus on Nav1.7, Species Differences,and Regulation by Paclitaxel

Voltage-gated sodium channels(Navs) play an important role in human pain sensation. However, the expression and role of Nav subtypes in native human sensory neurons are unclear. To address this issue, we obtained human dorsal root ganglion(hDRG) tissues from healthy donors. PCR analysis of seven DRG-expressed Nav subtypes revealed that the hDRG has higher expression of Nav1.7(~50% of total Nav expression) and lower expression of Nav1.8(~12%), whereas the mouse DRG has higher expression of Nav1.8(~45%) and lower expression of Nav1.7(~18%). To mimic Nav regulation in chronic pain, we treated hDRG neurons in primary cultures with paclitaxel(0.1-1 μmol/L) for 24 h. Paclitaxel increased the Nav 1.7 but not Nav1.8 expression and also increased the transient Na~+ currents and action potential firing frequency in small-diameter(50 μm) hDRG neurons. Thus, the hDRG provides a translational model in which to study"human pain in a dish" and test new pain therapeutics.     

Stromal‐derived factor‐1 gene variations in pediatric patients with primary immune thrombocytopenia

Primary immune thrombocytopenia (ITP) of childhood is an autoimmune disease characterized by abnormally increased destruction of platelets and decreased megakaryopoiesis. Stromal‐derived factor‐1 (SDF‐1) plays a role in megakaryopoiesis and may be involved in the pathogenesis of ITP. Five single nucleotide polymorphisms (SNPs) of the SDF‐1 gene, including rs1801157, rs2839693, rs2297630, rs1065297, and rs266085, were assessed in 100 children with ITP and 126 healthy controls. The genotypes were analyzed by tetra ARMS polymerase chain reaction and confirmed by direct sequencing. Compared with controls, the rs2839693 A/A and rs266085 C/T genotypes were decreased in ITP patients (P = 0.004 and 0.007, respectively). The odds ratios of the latter genotypes were 0.48, 95% CI 0.28–0.82. Further analysis of the relationship between SDF‐1 polymorphisms and clinical features showed that rs2297630 A/G was associated with protection from chronicity (P = 0.002; OR, 0.07; 95% CI, 0.01–0.61) and steroid dependence (P = 0.007; OR, 0.10; 95% CI, 0.01–0.84) in ITP patients. However, rs266085 genotype C/C was associated with risk of steroid dependence (P = 0.012, OR 3.87, 95% CI 1.27–11.77). The findings of this study suggest that SDF‐1 gene variations may be associated with the occurrence and prognosis of childhood ITP.