vitreous body

玻璃体
  • 文章类型: Journal Article
    背景:抗糖尿病治疗是有效的,但可以间接改变眼部微环境中的炎症反应;因此,一项研究旨在评估糖尿病视网膜病变患者在接受抗糖尿病药物治疗时玻璃体液中的炎性细胞因子分布。
    方法:观察性,比较,回顾性,横断面研究。白细胞介素1β,在2型糖尿病患者的玻璃体液中评估了6、8、10和肿瘤坏死因子-α(TNFα),增生性糖尿病视网膜病变,并伴有视网膜脱离或玻璃体出血,并且已经使用胰岛素或二甲双胍+格列本脲进行抗糖尿病治疗。通过细胞计数珠阵列(CBA)技术对每种细胞因子进行定量分析;获得中位数和四分位数范围,并使用Mann-WhitneyU检验在组间比较结果,其中p值<0.05被认为是显著的。
    结果:38个样本;服用胰岛素的患者组中TNFα浓度的定量更高,而白细胞介素-8较低;在二甲双胍+格列本脲联合治疗组中,相反地发生了。在分层分析中,白细胞介素-8和肿瘤坏死因子α的最高浓度发生在玻璃体出血患者中;视网膜脱离患者存在唯一的统计学差异,联合治疗组中的TNFα浓度最低(53.50(33.03-86.66),p=0.03)。白细胞介素1β,6和10没有检测到。
    结论:治疗组之间的白细胞介素-8和TNFα浓度相反;这种变化在增生性糖尿病视网膜病变和玻璃体出血患者中更为明显,这两种细胞因子的浓度最高,虽然只有TNFα有统计学差异。
    BACKGROUND: Antidiabetic therapies are effective, but could indirectly modify the inflammatory response in the ocular microenvironment; therefore, a study was developed to evaluate the inflammatory cytokine profile in the vitreous humor of diabetic patients with retinopathy under treatment with antidiabetic drugs.
    METHODS: Observational, comparative, retrospective, cross-sectional study. Interleukins 1β, 6, 8, 10, and tumor necrosis factor-alpha (TNFα) were evaluated in the vitreous humor obtained from patients with type 2 diabetes mellitus, proliferative diabetic retinopathy, and concomitant retinal detachment or vitreous hemorrhage, and who were already on antidiabetic treatment with insulin or metformin + glibenclamide. The quantification analysis of each cytokine was performed by the cytometric bead array (CBA) technique; medians and interquartile ranges were obtained, and the results were compared between groups using the Mann-Whitney U test, where a p-value < 0.05 was considered significant.
    RESULTS: Thirty-eight samples; quantification of TNFα concentrations was higher in the group of patients administered insulin, while interleukin-8 was lower; in the metformin + glibenclamide combination therapy group, it occurred inversely. In the stratified analysis, the highest concentrations of interleukin-8 and TNFα occurred in patients with vitreous hemorrhage; however, the only statistical difference existed in patients with retinal detachment, whose TNFα concentration in the combined therapy group was the lowest value found (53.50 (33.03-86.66), p = 0.03). Interleukins 1β, 6, and 10 were not detected.
    CONCLUSIONS: Interleukin-8 and TNFα concentrations are opposite between treatment groups; this change is more accentuated in patients with proliferative diabetic retinopathy and vitreous hemorrhage, where the highest concentrations of both cytokines are found, although only TNFα have statistical difference.
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  • 文章类型: Journal Article
    背景:已经在脑脊液和血液中广泛研究了蛋白质生物标志物,用于检测神经退行性疾病,然而,临床上有用的诊断测试,以早期发现,症状前的阿尔茨海默病(AD)仍然难以捉摸。我们进行了这项研究来量化Aβ40,Aβ42,总Tau(t-Tau),高磷酸化Tau(ptau181),相对于血液,眼液中的神经胶质纤维酸性蛋白(GFAP)和神经丝轻链(NfL)。
    方法:在这项横断面研究中,我们收集了玻璃体液,房水,眼病手术患者的泪液和血浆。通过数字免疫测定对所有6种生物标志物进行定量测量。进行Spearman和Bland-Altman相关性分析以评估眼液和血浆之间的水平一致性。
    结果:79名成年人至少有一只眼睛接受了玻璃体切割术。79人中有77个玻璃体,67血,56泪液,和51个含水样品。在每个生物样本中对所有六个生物标志物进行了定量,除了泪液中的GFAP和NfL,由于样品体积较低。与血浆样品相比,所有六种生物标志物在玻璃体液中升高。T-Tau,水溶液中的ptau181,GFAP和NfL高于血浆中,泪液中t-Tau和ptau181的浓度高于血浆。血浆中Aβ40与泪液存在显著相关性(r=0.5;p=0.019),血浆和玻璃体中的t-Tau(r=0.4;p=0.004),血浆和玻璃体中的NfL(r=0.3;p=0.006)以及血浆和水溶液中的NfL(r=0.5;p=0.004)。相对于血浆,眼液中的Aβ42,ptau181和GFAP未发现显着关联。Bland-Altman分析显示房水在所有生物标志物中与血浆最接近。眼液中的生物标志物水平显示,t-Tau的玻璃体和房水之间存在统计学上的显着关联(r=0.5;p=0.001),GFAP(r=0.6;p<0.001)和NfL(r=0.7;p<0.001)。
    结论:AD生物标志物在眼液中的检测量大于血浆中的检测量,并显示与血浆水平的相关性。未来的研究需要评估眼液生物标志物作为AD诊断和预后标志物的实用性。尤其是那些有眼病风险的人。
    BACKGROUND: Protein biomarkers have been broadly investigated in cerebrospinal fluid and blood for the detection of neurodegenerative diseases, yet a clinically useful diagnostic test to detect early, pre-symptomatic Alzheimer\'s disease (AD) remains elusive. We conducted this study to quantify Aβ40, Aβ42, total Tau (t-Tau), hyperphosphorylated Tau (ptau181), glial fibrillary acidic protein (GFAP) and neurofilament light chain (NfL) in eye fluids relative to blood.
    METHODS: In this cross-sectional study we collected vitreous humor, aqueous humor, tear fluid and plasma in patients undergoing surgery for eye disease. All six biomarkers were quantitatively measured by digital immunoassay. Spearman and Bland-Altman correlation analyses were performed to assess the agreement of levels between ocular fluids and plasma.
    RESULTS: Seventy-nine adults underwent pars-plana vitrectomy in at least one eye. Of the 79, there were 77 vitreous, 67 blood, 56 tear fluid, and 51 aqueous samples. All six biomarkers were quantified in each bio-sample, except GFAP and NfL in tear fluid due to low sample volume. All six biomarkers were elevated in vitreous humor compared to plasma samples. T-Tau, ptau181, GFAP and NfL were higher in aqueous than in plasma, and t-Tau and ptau181 concentrations were higher in tear fluid than in plasma. Significant correlations were found between Aβ40 in plasma and tears (r = 0.5; p = 0.019), t-Tau in plasma and vitreous (r = 0.4; p = 0.004), NfL in plasma and vitreous (r = 0.3; p = 0.006) and plasma and aqueous (r = 0.5; p = 0.004). No significant associations were found for Aβ42, ptau181 and GFAP among ocular fluids relative to plasma. Bland-Altman analysis showed aqueous humor had the closest agreement to plasma across all biomarkers. Biomarker levels in ocular fluids revealed statistically significant associations between vitreous and aqueous for t-Tau (r = 0.5; p = 0.001), GFAP (r = 0.6; p < 0.001) and NfL (r = 0.7; p < 0.001).
    CONCLUSIONS: AD biomarkers are detectable in greater quantities in eye fluids than in plasma and show correlations with levels in plasma. Future studies are needed to assess the utility of ocular fluid biomarkers as diagnostic and prognostic markers for AD, especially in those at risk with eye disease.
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  • 文章类型: Journal Article
    我们研究了磁共振成像是否可以通过滴眼液的眼药水可视化玻璃体腔中的分布,钆造影剂,和17O-水,并阐明超重T2加权序列在眼内分布研究中的有用性。五种不同的解决方案(V-ROHTO,Travatanz,gadobutrol,H217O,和盐水)给予切除的猪眼标本。使用T1作图扫描样品,T2映射,3DT2加权(回波时间(TE):500、3200和4500ms),半傅立叶单发涡轮自旋回波序列(HASTE;TE:440和3000ms),和滴眼液给药前的3D真实反转恢复。随后,我们用塑料滴管滴0.5毫升的溶液,并在26小时后获得图像。比较前房和玻璃体腔的T1和T2值的时间变化。通过将时间信号变化确定为与“无下降”相比的信号强度比(SIR)来评估其他序列。“用gadobutrow和H217O处理的样品的T1和T2值随着时间的推移而降低。用gadobutrol和H217O处理的样品的SIR在3DT2加权图像中显示出显着的变化,而在其他解决方案中没有观察到显着的时间变化。更长的TE导致了显着的变化。我们证明了通过滴眼液可以通过使用gadobutrol和H217O切除猪眼睛来实现玻璃体腔内分布的可视化,但不是眼用溶液。超重T2加权序列对于滴眼液的眼内分布的早期和高度敏感的可视化可能是有希望的。
    We investigated whether magnetic resonance imaging can visualize the distribution in the vitreous cavity via eye drops of ophthalmic solutions, gadolinium-based contrast agent, and 17O-water, and to clarify the usefulness of ultra-heavily T2-weighted sequences in the research of intraocular distribution. Five different solutions (V-ROHTO, TRAVATANZ, gadobutrol, H217O, and saline) were administered to excised pig eye specimens. The samples were scanned using T1 mapping, T2 mapping, 3D T2-weighted (echo times (TE): 500, 3200, and 4500 ms), a half-Fourier single-shot turbo-spin echo sequence (HASTE; TE: 440 and 3000 ms), and 3D-real inversion-recovery before eye drops administration. Subsequently, we used a plastic dropper to drop a 0.5 mL solution each, and images were obtained up to 26 h later. Temporal changes in the T1 and T2 values of the anterior chamber and vitreous cavity were compared. The other sequences were evaluated by determining temporal signal changes as signal intensity ratio (SIR) compared to \"No drop.\" The T1 and T2 values of samples treated with gadobutrol and H217O decreased over time. The SIR of samples treated with gadobutrol and H217O showed remarkable changes in the 3D T2-weighted images, whereas no remarkable temporal changes were observed in the other solutions. Longer TEs resulted in remarkable changes. We demonstrated that visualization of distribution in the vitreous cavity via eye drops could be achieved with excised pig eyes using gadobutrol and H217O, but not with ophthalmic solutions. Ultra-heavily T2-weighted sequences may be promising for the early and highly sensitive visualization of the intraocular distribution of eye drops.
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  • 文章类型: Journal Article
    背景:本研究旨在探讨有无糖尿病性视网膜病变(DR)患者玻璃体液代谢物和代谢途径的差异,并确定潜在的代谢物生物标志物。
    方法:从125例患者(40例无糖尿病,85与DR)。使用超高效液相色谱法分析了玻璃体液样品的代谢物谱,Q-活性质谱,和多元统计分析。基于最小绝对收缩率和选择算子正则化逻辑回归的机器学习模型用于基于选定的代谢物水平构建风险评分模型。通过逻辑回归模型将候选代谢物回归到糖化血红蛋白水平。
    结果:在DR组和对照组之间鉴定出20种差异代谢物,并且在五种京都基因和基因组途径(精氨酸生物合成;三羧酸循环;丙氨酸,天冬氨酸,和谷氨酸代谢;酪氨酸代谢;和D-谷氨酸代谢)。抗坏血酸亚铁显著有助于较差的血糖控制结果,提供对DR潜在新致病途径的见解。
    结论:精氨酸生物合成代谢途径紊乱,三羧酸循环,丙氨酸,天冬氨酸,谷氨酸代谢,酪氨酸代谢,D-谷氨酸代谢与DR相关。基于玻璃体液代谢物的风险评分可用于DR的诊断和管理。抗坏血酸亚铁可以为DR的潜在新致病途径提供见解。
    BACKGROUND: This study aimed to explore differences in vitreous humour metabolites and metabolic pathways between patients with and without diabetic retinopathy (DR) and identify potential metabolite biomarkers.
    METHODS: Clinical data and vitreous fluid samples were collected from 125 patients (40 without diabetes, 85 with DR). The metabolite profiles of the vitreous fluid samples were analysed using ultra-high performance liquid chromatography, Q-Exactive mass spectrometry, and multivariate statistical analysis. A machine learning model based on Least Absolute Shrinkage and Selection Operator Regularized logistic regression was used to build a risk scoring model based on selected metabolite levels. Candidate metabolites were regressed to glycated haemoglobin levels by a logistic regression model.
    RESULTS: Twenty differential metabolites were identified between the DR and control groups and were significantly enriched in five Kyoto Encyclopedia of Genes and Genomes pathways (arginine biosynthesis; tricarboxylic acid cycle; alanine, aspartate, and glutamate metabolism; tyrosine metabolism; and D-glutamate metabolism). Ferrous ascorbate significantly contributes to poorer glycaemic control outcomes, offering insights into potential new pathogenic pathways in DR.
    CONCLUSIONS: Disorders in the metabolic pathways of arginine biosynthesis, tricarboxylic acid cycle, alanine, aspartate, glutamate metabolism, tyrosine metabolism, and D-glutamate metabolism were associated with DR. Risk scores based on vitreous fluid metabolites can be used for the diagnosis and management of DR. Ferrous ascorbate can provide insights into potential new pathogenic pathways for DR.
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  • 文章类型: Journal Article
    自2017年以来,故意摄入亚硝酸盐自杀的发生率有所增加。对于亚硝酸盐/硝酸盐的商业实验室分析存在有限的选择。这项研究调查了在尸检中使用尿液试纸筛查亚硝酸钠的潜在毒性,不太常见,亚硝酸烷基酯。存档的血液样本,尿液,玻璃体液,和来自4例亚硝酸钠/硝酸钠的胃内容物,亚硝酸烷基酯3例,和4个对照病例使用试纸进行了测试。一个快速的,所有4-亚硝酸钠/硝酸盐病例的玻璃体液中都有亚硝酸盐的强烈阳性结果,伴随着2个尿液阳性和1个胃阳性。2烷基亚硝酸根吸入毒性病例均无阳性结果。一个亚硝酸烷基酯摄入病例的尿液呈阳性。4个对照组的尿液阴性:2个玻璃体的结果模棱两可,和1个胃阳性。尿液试纸是亚硝酸盐毒性实验室测试的有用辅助手段,具有成本效益的桌面结果,可以指导进一步测试的需要。玻璃体和尿液似乎是最可靠的标本,尽管胃液测试可能有助于证实口服摄入。试纸可能不是通过吸入途径测试亚硝酸烷基酯毒性的可靠辅助手段。可能是由于与亚硝酸盐摄入情况相比亚硝酸盐浓度低得多。
    UNASSIGNED: The incidence of suicide by intentional nitrite ingestion has increased since 2017. Limited options exist for commercial laboratory analysis for nitrite/nitrate. This study investigates the use of urine dipsticks for screening at autopsy for potential toxicity with sodium nitrite and, less commonly, alkyl nitrite. Archived samples of blood, urine, vitreous fluid, and gastric contents from 4 sodium nitrite/nitrate cases, 3 alkyl nitrite cases, and 4 control cases were tested using dipsticks. A rapid, strong positive result for nitrite was in the vitreous fluid of all 4-sodium nitrite/nitrate cases, along with 2 positive urine and 1 positive gastric. The 2 alkyl nitrite inhalation toxicity cases had no positive results. One alkyl nitrite ingestion case had a positive urine. The 4 controls had negative urine: equivocal results in 2 vitreous, and 1 positive gastric. Urine dipsticks are a useful adjunct to laboratory testing for nitrite toxicity and provide a rapid, cost-effective tableside result that may guide the need for further testing. Vitreous fluid and urine appear to be the most reliable specimens, although testing of gastric liquid may be useful to corroborate oral ingestion. Dipsticks may not be a reliable adjunct for testing for alkyl nitrite toxicity via inhalation route, likely due to the much lower nitrite concentration compared to nitrite ingestion cases.
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  • 文章类型: Journal Article
    背景:我们旨在研究光学相干断层扫描(OCT)的解剖学特征和玻璃体细胞因子水平作为特发性视网膜前膜(iERM)治疗的玻璃体玻璃体切除术联合玻璃体内地塞米松(DEX)植入物的预后预测因子。
    方法:前瞻性,单面具,随机化,对照临床试验包括48只眼。他们以1:1的比例随机分配到DEX组(联合晶状体玻璃体切除术与ERM剥离和Ozurdex植入)和对照组(仅晶状体玻璃体切除术)。在1d时评估最佳矫正视力(BCVA)和中央黄斑厚度(CMT)。1周,1个月,和3个月。对术前OCT的结构特征进行分层分析。使用ELISA测量玻璃体液中的基线可溶性CD14(sCD14)和sCD163水平。
    结果:BCVA和CMT在DEX组和对照组中没有显着差异。基线时具有高反射焦点(HRF)的眼睛在随访期间获得了较好的BCVA(Ptime*组=0.746;P组=0.043,Waldχ²=7.869)和较低的CMT(Ptime*组=0.079;P组=0.001,Waldχ²=6.774)对DEX的反应。在所有患者中,基线时HRF眼sCD163的平均玻璃体水平显著高于无HRF眼(P=0.036,Z=-2.093)。在DEX组中,较高的sCD163预测CMT从基线至1个月的下降幅度更大(r=0.470,P=0.049).
    结论:我们发现,在所有iERM患者中,术中DEX植入在3个月内对BCVA和CMT均无有益影响,暗示不建议对所有iERM使用DEX。相比之下,对于在OCT上有HRF的患者,在3个月随访时对DEX植入物的反应更好,而在基线时,其玻璃体液中sCD163的表达水平更高.这些数据支持以下假设:DEX植入物在治疗ERM继发于炎症的病例中可能特别有效。
    背景:该试验已在中国临床试验注册中心注册(https://www.chictr.org.cn)2021/03/12(ChiCTR2100044228)。文章中的所有患者均在注册后入组。
    BACKGROUND: We aimed to investigate the anatomical features of optical coherence tomography (OCT) and vitreous cytokine levels as predictors of outcomes of combined phacovitrectomy with intravitreal dexamethasone (DEX) implants for idiopathic epiretinal membrane (iERM) treatment.
    METHODS: A prospective, single-masked, randomized, controlled clinical trial included 48 eyes. They were randomly assigned in a 1:1 ratio to undergo the DEX group (combined phacovitrectomy with ERM peeling and Ozurdex implantation) and control group (phacovitrectomy only). Best-corrected visual acuity (BCVA) and central macular thickness (CMT) were assessed at 1 d, 1 week, 1 month, and 3 months. The structural features of OCT before surgery were analysed for stratified analysis. Baseline soluble CD14 (sCD14) and sCD163 levels in the vitreous fluid were measured using ELISA.
    RESULTS: BCVA and CMT were not significantly different in the DEX and control groups. Eyes with hyperreflective foci (HRF) at baseline achieved better BCVA (Ptime*group=0.746; Pgroup=0.043, Wald χ²=7.869) and lower CMT (Ptime*group = 0.079; Pgroup = 0.001, Wald χ²=6.774) responses to DEX during follow-up. In all patients, the mean vitreous level of sCD163 in eyes with HRF was significantly higher than that in eyes without HRF (P = 0.036, Z=-2.093) at baseline. In the DEX group, higher sCD163 predicted greater reduction in CMT from baseline to 1 month (r = 0.470, P = 0.049).
    CONCLUSIONS: We found that intraoperative DEX implantation did not have beneficial effects on BCVA and CMT over a 3-month period in all patients with iERM, implying that the use of DEX for all iERM is not recommended. In contrast, for those with HRF on OCT responded better to DEX implants at the 3-month follow-up and thier vitreous fluid expressed higher levels of sCD163 at baseline. These data support the hypothesis that DEX implants may be particularly effective in treating cases where ERM is secondary to inflammation.
    BACKGROUND: The trail has been registered at Chinese Clinical Trail Registry( https://www.chictr.org.cn ) on 2021/03/12 (ChiCTR2100044228). And all patients in the article were enrolled after registration.
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  • 文章类型: Journal Article
    目的:分析眼内炎管理研究(EMS)中的抗生素敏感性,并将其与印度玻璃体视网膜协会(VRSI)成员在印度的玻璃体内抗生素使用趋势进行比较。
    方法:未稀释玻璃体的微生物学检查包括显微镜检查,文化易感性,聚合酶链反应(PCR),和下一代测序(NGS)。VRSI成员被邀请参加调查。EMS常规培养-敏感性(PCR和NGS除外)结果与革兰氏阳性球菌(GPC)相比,革兰氏阴性杆菌(GNB),和较少使用的抗生素与目前推荐的玻璃体内抗生素。p<0.05被认为是显著的。
    结果:培养阳性(培养+PCR/NGS)分别为28.8%和56.1%,分别。GPC对头孢唑啉最敏感,利奈唑胺,和万古霉素;GNB对阿米卡星最敏感,头孢他啶,粘菌素,还有亚胺培南.头孢唑啉与万古霉素(p=0.999)、头孢他啶与亚胺培南(p=1.0)药敏无差异。对GNB,粘菌素优于头孢他啶(p=0.047)。对阿米卡星耐药的GNB(n=14)对头孢他啶和粘菌素同样敏感;对头孢他啶耐药的GNB(n=16)对粘菌素敏感;对粘菌素耐药的GNB(n=7)对头孢他啶敏感。在印度执业的VRSI成员(n=231)的偏好是万古霉素-头孢他啶组合(82%),万古霉素用于GPC(94%),头孢他啶用于GNB(61%),和伏立康唑对真菌(74%)。
    结论:在EMS中,GPC对万古霉素具有良好的敏感性;GNB对头孢他啶和粘菌素具有良好的敏感性。鉴于粘菌素的电阻较低,万古霉素-粘菌素联合治疗可能是印度白内障后眼内炎的替代经验性治疗方法.
    OBJECTIVE: Analyze antibiotic susceptibility in the Endophthalmitis Management Study (EMS) and compare it with the current intravitreal antibiotic practice trend of members of the Vitreoretinal Society of India (VRSI) practicing in India.
    METHODS: The microbiology work-up of undiluted vitreous included microscopy, culture-susceptibility, polymerase chain reaction (PCR), and next-generation sequencing (NGS). VRSI members were invited to the survey. The EMS conventional culture-susceptibility (PCR and NGS excluded) results were compared vis-a-vis gram-positive cocci (GPC), gram-negative bacilli (GNB), and less commonly used antibiotics with the current recommended intravitreal antibiotics. p < 0.05 was considered significant.
    RESULTS: Culture and positivity (culture + PCR/NGS) positivity was 28.8% and 56.1%, respectively. GPC was most susceptible to cefazolin, linezolid, and vancomycin; GNB was most susceptible to amikacin, ceftazidime, colistin, and imipenem. There was no susceptibility difference between cefazolin and vancomycin (p = 0.999) and between ceftazidime and imipenem (p = 1.0). Colistin was superior to ceftazidime (p = 0.047) against GNB. The GNB resistant to amikacin (n = 14) were equally susceptible to ceftazidime and colistin; resistant to ceftazidime (n = 16) were susceptible to colistin; and resistant to colistin (n = 7) were susceptible to ceftazidime. The preference of VRSI members (n = 231) practicing in India was a vancomycin-ceftazidime combination (82%), vancomycin for GPC (94%), ceftazidime for GNB (61%), and voriconazole for fungi (74%).
    CONCLUSIONS: In EMS, GPC had good susceptibility to vancomycin; GNB had good susceptibility to ceftazidime and colistin. Given the lower resistance of colistin, a vancomycin-colistin combination could be an alternative empiric treatment in post-cataract endophthalmitis in India.
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  • 文章类型: Clinical Trial Protocol
    背景:玻璃体漂浮物是一种常见的眼部疾病,会影响所有年龄段的个体。虽然玻璃体漂浮物通常是良性的,它们会显著损害视力和生活质量。激光玻璃分解,使用Nd:YAG激光蒸发胶原玻璃体混浊,越来越多地被用作治疗选择。然而,目前缺乏关于其疗效和适当应用时机的证据.本研究旨在评估YAG激光玻璃体溶解术早期干预治疗有症状的玻璃体漂浮物的疗效和安全性。
    方法:本研究是一项随机研究,控制,双盲临床试验。前瞻性招募了70名患有症状性漂浮物1个月的参与者。这些参与者将被随机分配到两组,每组35例:早期治疗组和延迟治疗组。分配到早期治疗组的参与者将立即进行YAG激光玻璃体溶解,3个月后进行假激光治疗。另一方面,延迟治疗组的参与者将接受假激光治疗,3个月后接受YAG激光玻璃体溶解术.随访时间点将是从随机化开始的1、3、6和12个月。主要结果是参与者自我报告的视力障碍改善程度为1至10,以及他们在国家眼科研究所视觉功能问卷25(NEIVFQ-25)上的得分。次要结果将是通过OCT和眼底照相以及跟踪与眼睛或整体健康相关的任何不良事件来客观评估治疗在减少玻璃体漂浮物方面的有效性。
    结论:本临床试验旨在评估YAG激光玻璃体溶解术治疗有症状的玻璃体漂浮物的有效性,并评估YAG激光玻璃体溶解术早期干预的安全性。
    背景:ClinicalTrials.govNCT05800353。2023年3月10日注册。
    BACKGROUND: Vitreous floaters are a common ocular condition that affects individuals of all ages. Although vitreous floaters are typically benign, they can significantly impair visual acuity and quality of life. Laser vitreolysis, which uses an Nd: YAG laser to vaporize collagenous vitreous opacities, is increasingly being used as a treatment option. However, there is currently a lack of evidence regarding its efficacy and the appropriate timing of its application. This study aims to evaluate the efficacy and safety of early intervention with YAG laser vitreolysis in treating symptomatic vitreous floaters.
    METHODS: The present study is a randomized, controlled, double-blind clinical trial. A total of 70 participants with symptomatic floaters for 1 month were prospectively recruited. These participants will be randomly assigned to two groups, with 35 individuals in each group: the early treatment group and the delayed treatment group. Participants assigned to the early treatment group will undergo YAG laser vitreolysis immediately, followed by a sham laser treatment 3 months later. On the other hand, participants assigned to the delayed treatment group will receive a sham laser treatment and then undergo YAG laser vitreolysis 3 months later. The follow-up time points will be 1, 3, 6, and 12 months from randomization. Primary outcomes will be participants\' self-reported improvement in visual disturbance on a scale of 1 to 10 and their scores on the National Eye Institute Visual Functioning Questionnaire 25 (NEI VFQ-25). Secondary outcomes will be an objective evaluation of the effectiveness of the treatment in reducing vitreous floaters through OCT and fundus photography and tracking any adverse events related to the eyes or overall health.
    CONCLUSIONS: This clinical trial aims to evaluate the effectiveness of YAG laser vitreolysis in treating symptomatic vitreous floaters and assess the safety of performing early intervention with YAG laser vitreolysis.
    BACKGROUND: ClinicalTrials.gov NCT05800353 . Registered on 10 March 2023.
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  • 文章类型: Comparative Study
    目的:研究炎症评分(IS)从角膜计算,前房,虹膜,和玻璃体,表示眼内炎的严重程度。
    方法:在一项前瞻性研究中,我们招募了在手术后6周内临床诊断为白内障后眼内炎的连续成人.患者被分配到基于IS的主要治疗(IS<10:玻璃体内注射和IS≥10:玻璃体切除术),并随机分配到两种玻璃体内抗生素组合(万古霉素+头孢他啶和万古霉素+亚胺培南)。未稀释的玻璃体微生物学检查包括培养物易感性,聚合酶链反应,桑格测序,和靶向下一代测序。
    结果:175人平均年龄为63.4±10.7岁,包括52.6%的小切口白内障手术和47.4%的超声乳化手术。严重眼内炎(IS≥20),诊断为27.4%的人,出现症状的时间较短(平均5.4天vs8.7天;P=0.018),视力较差(均≤手部运动),较高的培养阳性率(50%vs30.7%;P=0.032),革兰阴性菌感染率较高(70.8%vs46.2%;P=0.042)。对于IS≥20判别和革兰氏阴性感染,斯皮尔曼系数为0.7[P<0.0001,95%置信区间(CI)0.59-0.82],受试者工作特性曲线下面积为0.9(95%CI0.85-0.94,P<0.0001),尤登指数J为0.74,灵敏度为87.2%,特异性为87.5%。50.2%和29.1%的人恢复了>20/400和>20/100的最终视力,分别。常见革兰阳性球菌和革兰阴性杆菌的敏感性最高的是万古霉素(95.0%)和粘菌素(88.6%),分别。NGS在88.5%的培养阴性眼内炎中检测到多微生物感染。
    结论:较高的炎症评分表明白内障后眼内炎有严重的疾病和革兰氏阴性感染。
    OBJECTIVE: To investigate if inflammation score (IS), calculated from the cornea, anterior chamber, iris, and vitreous, indicates endophthalmitis severity.
    METHODS: In a prospective study, consecutive adults with a clinical diagnosis of post-cataract endophthalmitis within 6 weeks of surgery were recruited. Patients were allocated to IS-based primary treatment (IS < 10: intravitreal injection and IS ≥ 10: vitrectomy) and randomized to two intravitreal antibiotics combinations (vancomycin + ceftazidime and vancomycin + imipenem). Undiluted vitreous microbiology work-up included culture susceptibility, polymerase chain reaction, Sanger sequencing, and targeted next-generation sequencing.
    RESULTS: The average age of 175 people was 63.4 ± 10.7 years and included 52.6% small incision cataract surgery and 47.4% phacoemulsification surgery. Severe endophthalmitis (IS ≥ 20), diagnosed in 27.4% of people, had a shorter time to symptoms (average 5.4 vs 8.7 days; P = 0.018), poorer presenting vision (all ≤ hand motion), higher culture positivity (50% vs 30.7%; P = 0.032), and higher Gram-negative bacterial infection (70.8% vs 46.2%; P = 0.042). For IS ≥ 20 discriminant and Gram-negative infection, Spearman\'s coefficient was 0.7 [P < 0.0001, 95% confidence interval (CI) 0.59-0.82], with an area under the receiver operating characteristic curve of 0.9 (95% CI 0.85-0.94, P < 0.0001), a Youden index J of 0.74, a sensitivity of 87.2%, and a specificity of 87.5%. The final vision of >20/400 and >20/100 was regained in 50.2% and 29.1% of people, respectively. The susceptibility of common Gram-positive cocci and Gram-negative bacilli was the highest for vancomycin (95.0%) and colistin (88.6%), respectively. NGS detected polymicrobial infection in 88.5% of culture-negative endophthalmitis.
    CONCLUSIONS: Higher inflammation scores indicated severe disease and Gram-negative infection in post-cataract endophthalmitis.
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  • 文章类型: Journal Article
    目的:探讨使用可折叠的囊状玻璃体(FCVB)处理严重眼外伤和硅油依赖性眼睛的可行性和安全性。
    方法:这是一项对61例眼外伤患者(61只眼)的回顾性研究,河北省眼科医院2018年5月1日至2019年5月31日,其中男性患者51例(51眼),女性患者10例(10眼),平均年龄44.98±14.60岁。最大的病人是75岁,最小的是8岁。这些病例代表51眼严重眼球破裂和10眼严重,复杂的眼外伤,手术后变得依赖硅油。这些患者接受了FCVB植入物,以及关于他们视力的数据,眼内压,眼轴的变化,角膜,视网膜,术后记录FCVB状态。
    结果:在所有患者中,FCVB定位正确,并得到视网膜的良好支持.所有61例患者均清除了1-36个月的随访窗口,没有视力发生重要变化的报告。在患者中,91.8%报告眼压正常,视网膜复位率达到100%,眼球萎缩控制率达到100%。没有FCVB破裂的报告,对硅胶过敏,眼内感染,眼内出血,硅油乳化,或者交感性眼炎.
    结论:设计用于模拟天然玻璃体的可折叠的囊状玻璃体(FCVB)适合作为长期的眼部植入物,可以为视网膜提供持续的支持,而不需要任何特殊的术后姿势。它们的屏障功能可以有效地延长填塞物的保留时间,并防止由于眼组织与填塞物直接接触而引起的各种并发症。
    OBJECTIVE: To explore the feasibility and safety of using a foldable capsular vitreous body (FCVB) in managing severe ocular trauma and silicone oil-dependent eyes.
    METHODS: This is a retrospective study of 61 ocular trauma patients (61 eyes) who presented to the Department of Eye Emergency, Hebei Eye Hospital from May 1, 2018, to May 31, 2019, including 51 male patients (51 eyes) and 10 female patients (10 eyes) with an average age of 44.98 ± 14.60 years old. The oldest patient was 75 years old, and the youngest was 8 years old. These cases represented 51 eyes with severe eyeball rupture and 10 eyes with severe, complicated ocular trauma, which became silicone oil-dependent after the operation. These patients received FCVB implants, and data regarding their visual acuity, intraocular pressure, changes in eye axis, cornea, retina, and FCVB state were recorded after the operation.
    RESULTS: In all patients, the FCVB was properly positioned and well supported with the retina. All 61 patients cleared a follow-up window of 1-36 months with no reports of important changes in their visual acuity. Among the patients, 91.8% reported normal intraocular pressure, the retinal reattachment rate reached 100%, and the eyeball atrophy control rate reached 100%. There was no report of rupture of the FCVB, allergies to silicone, intraocular infection, intraocular hemorrhage, silicone oil emulsification, or sympathetic ophthalmia.
    CONCLUSIONS: Foldable capsular vitreous bodies (FCVBs) designed to mimic natural vitreous bodies are suitable as long-term ocular implants that can provide sustained support for the retina without the need for any special postoperative postures. Their barrier function may effectively prolong the retention time of the tamponade and prevent various complications caused by direct contact of the eye tissues with the tamponade.
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