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Contrast sensitivity before and after refractive error correction among refractive error patients in Hawassa, Sidama, Ethiopia 2023. 2023年埃塞俄比亚希达马阿瓦萨屈光不正患者屈光不正矫正前后的对比敏感度。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-07 DOI: 10.1186/s12886-024-03817-8
Balcha Negese Kebede, Seid Mohammed Seid, Eyerus Gesesse Samuel

Background: Contrast sensitivity is an important measure of vision quality. Risk of falling injury is strongly associated with poor contrast sensitivity compared with poor near- and distance visual acuity. Since good visual acuity is not necessarily associated with good visual performance in the "real world" it is important to consider contrast sensitivity when prescribing corrective lenses. There is limited evidence on how refractive error and its correction affect contrast sensitivity in the study area. Therefore, this study is important to understand how refractive correction affects contrast sensitivity, which is important baseline information for prescribing refractive error correction.

Objective of this study: This study aimed to measure the mean difference in contrast sensitivity with and without corrective lenses in patients with refractive error.

Methods: Objective and subjective refractions were done for each patient, then Pelli- Robson contrast sensitivity was measured for them using computer based Pelli-Robson chart at 1 m. Pelli- Robson contrast sensitivity value (Log CS) with and without corrective lenses were recorded for each study participant. The collected data were checked for completeness and analyzed using SPSS 26. Descriptive analyses, independent sample t-tests, and one-way ANOVA were performed to compare CS means; the findings are presented using tables and pie charts. A P-value of ≤ 0.05 was used to indicate statistical significance.

Results: One hundred sixty-two patients attending refraction clinics participated in this study with response rate 98.19% of which 51.9% were male. The mean age of the participants was 34.28 ± 12.79 (SD). The mean contrast sensitivity increased from 1.29 ± 0.35 (SD) to1.51 ± 0.28 (SD) LogCS units with refractive correction (p = 0.000). There is no significant difference in contrast sensitivity between the types of refractive errors.

Conclusion and recommendation: Uncorrected refractive can affect contrast sensitivity; therefore, proper refractive correction is essential to improve visual acuity and contrast sensitivity.

背景:对比灵敏度是衡量视觉质量的重要指标。与较差的近距离和远距离视力相比,较差的对比敏感度与坠落损伤的风险密切相关。由于良好的视力并不一定与“现实世界”中的良好视觉表现相关,因此在处方矫正镜片时考虑对比灵敏度是很重要的。关于屈光不正及其矫正如何影响研究区域的对比灵敏度的证据有限。因此,这项研究对于了解屈光矫正如何影响对比敏感度具有重要意义,这是处方屈光不正矫正的重要基线信息。本研究目的:本研究旨在测量屈光不正患者配戴和不配戴矫正镜片对比敏感度的平均差异。方法:分别对患者进行客观和主观屈光检查,并在1 m处采用计算机Pelli-Robson对比敏感度测定。记录每位受试者佩戴和不佩戴矫正镜时的Pelli- Robson对比敏感度值(Log CS)。收集的数据进行完整性检查,并使用SPSS 26进行分析。采用描述性分析、独立样本t检验和单因素方差分析比较CS均值;研究结果用表格和饼状图呈现。p值≤0.05表示差异有统计学意义。结果:就诊于屈光诊所的162例患者参与了本研究,有效率为98.19%,其中男性占51.9%。参与者平均年龄为34.28±12.79 (SD)。平均对比敏感度从1.29±0.35 (SD)增加到1.51±0.28 (SD) LogCS单位(p = 0.000)。不同类型屈光不正的对比敏感度无显著差异。结论与建议:未矫正的屈光会影响对比敏感度;因此,适当的屈光矫正对于提高视力和对比敏感度至关重要。
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引用次数: 0
Coats' disease in adulthood with preserved vision after intravitreal aflibercept injection combined with laser photocoagulation : a case report. 玻璃体内注射阿布西普联合激光光凝术后视力保留的成年Coats病1例
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-06 DOI: 10.1186/s12886-024-03829-4
Safaa Abatli, Sameeha Ziad Shweiki

Background: This case report describes a rare case of Coats disease in adult female patient with preserved vision after intravitreal Aflibercept injection and laser photocoagulation.

Case presentation: A female patient of Asian Palestinian descent, aged 20, exhibited a progressive and painless deterioration in the vision of her left eye over a period of two weeks. She exhibited no additional ocular symptoms. Prior to her presentation, she had no notable medical history and her vision was normal in both eyes. Inferotemporal telangiectasia, sausage-like blood vessels with perivascular sheathing in the peripheral fundus, extensive exudate involving the macula, severe macular edema, and localized inferotemporal exudative retinal detachment were observed upon examination of the posterior segment of her left eye. Following this, optical coherence tomography (OCT) identified subretinal exudate, intraretinal and subretinal fluid. After establishing the diagnosis of stage 3 Coats' disease, the patient was treated with intravitreal Aflibercept (Eylea) injections and sectoral laser photocagulation. The third injection resulted in the absence of intraretinal and subretinal fluid by OCT, but the subretinal exudate remained unresolved. One month subsequent to the previous injection, FFA guided sectoral laser photoagulation was applied to the inferiotemporal ischemic area. The patient was subsequently monitored monthly, and her vision improved. Five months after treatment, her vision has improved to 0.7 (6/8.7) and she has remained stable ever since. At present, the patient is undergoing routine outpatient follow-up.

Conclusion: Coats disease is an idiopathic, progressive disease that mostly affects male infants, yet adult cases have been documented. Our case and the existing body of literature indicate that adult individuals have a favorable visual prognosis in the small proportion of cases where this occurs. It appeared that the implementation of intravitreal therapies and increased use of lasers led to enhanced visual outcomes. It is recommended to perform lifelong follow-up to monitor for recurrences and complications.

背景:本文报告一例罕见的成年女性科茨病患者,在玻璃体内注射阿非利西普和激光光凝治疗后视力保留。病例介绍:一名20岁的亚裔巴勒斯坦裔女性患者,左眼视力在两周内出现进行性无痛性恶化。她没有出现其他眼部症状。在此之前,她没有明显的病史,双眼视力正常。左眼后段检查发现颞下毛细血管扩张,眼底周围有香肠样血管鞘,大量渗出物累及黄斑,黄斑水肿严重,局部颞下渗出性视网膜脱离。在此之后,光学相干断层扫描(OCT)发现视网膜下渗出液,视网膜内和视网膜下液体。确诊为3期Coats病后,患者接受玻璃体内注射Aflibercept (Eylea)和局部激光光调节治疗。第三次注射导致OCT检查视网膜内和视网膜下没有液体,但视网膜下渗出物仍未解决。在前一次注射后1个月,将FFA引导的扇形激光光调控应用于颞下缺血区。患者随后每月接受监测,视力有所改善。治疗5个月后,她的视力改善到0.7(6/8.7),此后一直保持稳定。目前,患者正在进行常规门诊随访。结论:Coats病是一种特发性、进行性疾病,主要影响男性婴儿,但成人病例已被记录。我们的病例和现有的文献表明,在一小部分发生这种情况的病例中,成人个体有良好的视觉预后。玻璃体内治疗的实施和激光的增加使用似乎可以提高视力。建议终身随访,监测复发和并发症。
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引用次数: 0
Transcanalicular laser-assisted and external dacryocystorhinostomy anatomical and functional success in primary acquired nasolacrimal duct obstruction: systematic review and meta-analysis. 经导管激光辅助和外部泪囊鼻腔造口术治疗原发性获得性鼻泪管阻塞的解剖和功能成功:系统回顾和荟萃分析。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-06 DOI: 10.1186/s12886-024-03818-7
Khalid W Helmi, Ahmed S Abdulhamid, Mohammed S Alomari, Ali S Alsudais, Badran S Alqurashi, Abdullah Alsharif, Abdulrahman H Alzahrani, Abdulrahman M Bahalaq, Mohammed F Qutub, Hashem S Almarzouki

Background: Primary acquired nasolacrimal duct obstruction (PANDO) is a condition in which tear ducts are blocked, leading to epiphora and dacryocystitis. This systematic review and meta-analysis aimed to measure the ability of transcanalicular dacryocystorhinostomy (TC-DCR) as an alternative approach to PANDO compared to traditional external dacryocystorhinostomy (EX-DCR).

Methods: Our search included Embase, Medline, and the Cochrane Central Register of Controlled Trials (CENTRAL). We included only observational studies, randomized controlled trials (RCTs), and quasi-experimental studies that compared TC-DCR and EX-DCR. The outcomes measured were anatomical and functional success rates, intraoperative complications, postoperative complications, and surgical time. Statistically significant results were determined as a p value of less than 0.05; thus, a confidence interval of 95% was used. Dichotomous outcomes were reported via risk ratios (RR), whereas continuous outcomes were reported using standardized mean differences (SMD).

Results: There was a statistically significant difference in anatomical success (RR = 0.84, 95% CI 0.72-0.97; P = 0.02), favoring EX-DCR; functional success (RR = 0.87, 95% CI 0.78-0.97; P = 0.01), favoring EX-DCR; operative (OR) time (SMD = -2.42, 95% CI -2.92 - -1.91; P < 0.00001) favoring TC-DCR; and intraoperative complications (RR = 0.16, 95% CI 0.06-0.43; P = 0.0003), favoring TC-DCR. Moreover, the subgroup analysis comparing single-diode TC-DCR to EX-DCR revealed a statistically significant difference in terms of anatomical success and functional success; however, the comparison of multidiode TC-DCR to EX-DCR revealed no statistically significant difference.

Conclusions: More research should be conducted to compare the anatomical and functional success of muli-diode TC-DCR with EX-DCR because the analysis performed comparing them revealed no statistical significance.

背景:原发性获得性鼻泪管阻塞(PANDO)是一种泪管阻塞,导致泪漏和泪囊炎的疾病。本系统综述和荟萃分析旨在衡量经导管泪囊鼻腔造口术(TC-DCR)作为PANDO替代方法的能力,与传统的外泪囊鼻腔造口术(EX-DCR)相比。方法:我们的检索包括Embase、Medline和Cochrane中央对照试验登记处(Central)。我们只纳入了比较TC-DCR和EX-DCR的观察性研究、随机对照试验(rct)和准实验研究。测量的结果包括解剖和功能成功率、术中并发症、术后并发症和手术时间。以p值< 0.05判定结果有统计学意义;因此,采用95%的置信区间。通过风险比(RR)报告二分结果,而使用标准化平均差异(SMD)报告连续结果。结果:两组解剖成功率差异有统计学意义(RR = 0.84, 95% CI 0.72-0.97;P = 0.02),支持EX-DCR;功能成功(RR = 0.87, 95% CI 0.78-0.97;P = 0.01),支持EX-DCR;手术(OR)时间(SMD = -2.42, 95% CI = -2.92 ~ -1.91;P结论:多二极管TC-DCR与EX-DCR在解剖和功能上的成功比较尚需进一步研究,因为两者的比较分析没有统计学意义。
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引用次数: 0
Detection of Mycobacterium tuberculosis DNA in intraocular fluid of 11 suspected tuberculous uveitis patients by multiplex PCR. 多重PCR检测11例疑似结核性葡萄膜炎患者眼内液结核分枝杆菌DNA。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-06 DOI: 10.1186/s12886-025-03843-0
Huirong Xu, Min Xu, Fang Chen, Hong Chen, Wei Du, Jing Yu

Background: This study aims to detect Mycobacterium tuberculosis complex (MTBC) DNA in intraocular fluid from clinically suspected tuberculous uveitis patients using multiplex polymerase chain reaction (PCR) and investigate the diagnostic utility of multiplex PCR for tuberculous uveitis.

Methods: Primers targeting three specific genes (MPB64, CYP141, and IS6110) within the MTBC genome were designed. Multiplex PCR was conducted using DNA from the H37Rv strain as well as DNA extracted from fluids of confirmed tuberculosis patients to assess primer specificity and method feasibility. Intraocular fluid samples were collected during the initial visit for multiplex PCR detection of MTBC DNA. The results of multiplex PCR tests were correlated with intraocular fluid findings and clinical profiles of patients clinically diagnosed with tuberculous uveitis who underwent standard antituberculosis therapy.

Results: Multiplex PCR was employed to detect MTBC DNA in intraocular fluid samples from 15 patients clinically suspected of having tuberculous uveitis, with no amplification bands observed in the DNA lanes for the three target genes. T-cell spot test (T-SPOT) results were positive in 11 patients (100%), while purified protein derivative (PPD) tests were positive in 5 patients (45.5%). Abnormal chest CT findings were noted in 4 patients (36.4%), including one case of active pulmonary tuberculosis and three cases of inactive pulmonary tuberculosis. Retinal vasculitis was observed in 6 eyes (46.2%), panuveitis in 5 eyes (38.5%), and intermediate uveitis in 2 eyes (15.4%). The average duration of antituberculosis therapy administered to the 11 patients was 7.1 months (range: 6-10 months). The medium LogMAR Best Corrected Visual Acuity (BCVA) significantly improved at the last follow-up (Z=-2.371, P = 0.018).

Conclusions: Standard antituberculosis therapy demonstrated effectiveness in treating 11 patients clinically suspected of having tuberculous uveitis despite the absence of detectable MTBC DNA in intraocular fluid via multiplex PCR. Further investigation is warranted to elucidate the role of PCR in diagnosing ocular tuberculosis among Chinese individuals.

背景:本研究旨在应用多重聚合酶链反应(PCR)检测临床疑似结核性葡萄膜炎患者眼内液中结核分枝杆菌复体(MTBC) DNA,探讨多重聚合酶链反应(PCR)对结核性葡萄膜炎的诊断价值。方法:设计针对MTBC基因组中三个特定基因(MPB64、CYP141和IS6110)的引物。采用H37Rv菌株DNA和结核确诊患者体液提取的DNA进行多重PCR,评估引物特异性和方法可行性。初次就诊时采集眼内液标本,进行多重PCR检测MTBC DNA。多重PCR检测结果与临床诊断为结核性葡萄膜炎并接受标准抗结核治疗的患者的眼内液表现和临床特征相关。结果:应用多重PCR检测15例临床疑似结核性葡萄膜炎患者眼内液MTBC DNA, 3个靶基因的DNA条带均未见扩增。t细胞斑点试验(T-SPOT)阳性11例(100%),纯化蛋白衍生物(PPD)试验阳性5例(45.5%)。胸部CT异常4例(36.4%),其中活动性肺结核1例,非活动性肺结核3例。视网膜血管炎6眼(46.2%),全葡萄膜炎5眼(38.5%),中度葡萄膜炎2眼(15.4%)。11例患者接受抗结核治疗的平均时间为7.1个月(范围:6-10个月)。中LogMAR最佳矫正视力(BCVA)在末次随访时显著提高(Z=-2.371, P = 0.018)。结论:标准抗结核治疗在治疗11例临床怀疑患有结核性葡萄膜炎的患者中显示出有效性,尽管通过多重PCR在眼内液中检测不到MTBC DNA。PCR在中国人眼结核诊断中的作用有待进一步研究。
{"title":"Detection of Mycobacterium tuberculosis DNA in intraocular fluid of 11 suspected tuberculous uveitis patients by multiplex PCR.","authors":"Huirong Xu, Min Xu, Fang Chen, Hong Chen, Wei Du, Jing Yu","doi":"10.1186/s12886-025-03843-0","DOIUrl":"https://doi.org/10.1186/s12886-025-03843-0","url":null,"abstract":"<p><strong>Background: </strong>This study aims to detect Mycobacterium tuberculosis complex (MTBC) DNA in intraocular fluid from clinically suspected tuberculous uveitis patients using multiplex polymerase chain reaction (PCR) and investigate the diagnostic utility of multiplex PCR for tuberculous uveitis.</p><p><strong>Methods: </strong>Primers targeting three specific genes (MPB64, CYP141, and IS6110) within the MTBC genome were designed. Multiplex PCR was conducted using DNA from the H37Rv strain as well as DNA extracted from fluids of confirmed tuberculosis patients to assess primer specificity and method feasibility. Intraocular fluid samples were collected during the initial visit for multiplex PCR detection of MTBC DNA. The results of multiplex PCR tests were correlated with intraocular fluid findings and clinical profiles of patients clinically diagnosed with tuberculous uveitis who underwent standard antituberculosis therapy.</p><p><strong>Results: </strong>Multiplex PCR was employed to detect MTBC DNA in intraocular fluid samples from 15 patients clinically suspected of having tuberculous uveitis, with no amplification bands observed in the DNA lanes for the three target genes. T-cell spot test (T-SPOT) results were positive in 11 patients (100%), while purified protein derivative (PPD) tests were positive in 5 patients (45.5%). Abnormal chest CT findings were noted in 4 patients (36.4%), including one case of active pulmonary tuberculosis and three cases of inactive pulmonary tuberculosis. Retinal vasculitis was observed in 6 eyes (46.2%), panuveitis in 5 eyes (38.5%), and intermediate uveitis in 2 eyes (15.4%). The average duration of antituberculosis therapy administered to the 11 patients was 7.1 months (range: 6-10 months). The medium LogMAR Best Corrected Visual Acuity (BCVA) significantly improved at the last follow-up (Z=-2.371, P = 0.018).</p><p><strong>Conclusions: </strong>Standard antituberculosis therapy demonstrated effectiveness in treating 11 patients clinically suspected of having tuberculous uveitis despite the absence of detectable MTBC DNA in intraocular fluid via multiplex PCR. Further investigation is warranted to elucidate the role of PCR in diagnosing ocular tuberculosis among Chinese individuals.</p>","PeriodicalId":9058,"journal":{"name":"BMC Ophthalmology","volume":"25 1","pages":"7"},"PeriodicalIF":1.7,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11702118/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142944257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prophylactic barrage laser in patients with previous vitreous loss during cataract surgery: a randomized clinical trial. 预防性弹幕激光在白内障手术中玻璃体丢失患者中的应用:一项随机临床试验。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-06 DOI: 10.1186/s12886-024-03833-8
Ehsan Namvar, Mostafa Abuali, Mohammad Amin Setoodehmanesh, Mehdi Moalem

Background: One of the significant challenges that can arise during cataract surgery is the occurrence of posterior capsule rupture (PCR) and vitreous loss. It may result in different complications including cystoid macular edema, endophthalmitis, glaucoma, and considerably retinal detachment which consequently contributes to poor functional outcomes.

Methods: This study was a prospective double blinded randomized clinical trial including 42 patients with previous complicated cataract surgery including posterior capsular rupture and consequently vitreous loss that anterior vitrectomy was done for them. The patients were randomly categorized in to two groups by simple randomization. One group (25 patients) received sham laser and the other group (17 patients) received prophylactic 360° barrage laser 4 weeks after cataract surgery. After eighteen months, rate of retinal detachment was compared between two groups.

Results: In terms of gender, age, axial length, maturity, pseudophakia v/s aphakia, type of IOL and type of cataract surgery, there was no statistically significant difference between intervention and control groups. Distribution of RRD was clinically different between 2 groups (intervention and control group). In addition, there was a statistically significant difference between the rate of RRD in control group (non-laser patients) and normal population (0.08 vs. 0.0001). (P-value < 0.001).

Conclusion: Prophylactic barrage laser might be a useful intervention in eyes with posterior capsule rupture and vitreous loss during cataract surgery to prevent rhegmatogenous retinal detachment. However, further studies with larger sample sizes are indicated.

Trial registration: Iranian Clinical Trial Registry: IRCT20201120049450N2, Registered 13 Jul 2023, https://irct.behdasht.gov.ir .

背景:白内障手术中可能出现的重大挑战之一是后囊膜破裂(PCR)和玻璃体丢失的发生。它可能导致不同的并发症,包括囊样黄斑水肿、眼内炎、青光眼和相当程度的视网膜脱离,从而导致不良的功能预后。方法:本研究是一项前瞻性双盲随机临床试验,纳入42例既往白内障术后并发后囊膜破裂导致玻璃体丢失并行前玻璃体切除术的患者。采用简单随机法将患者随机分为两组。其中一组(25例)接受假激光治疗,另一组(17例)在白内障术后4周接受预防性360°弹幕激光治疗。18个月后,比较两组的视网膜脱离率。结果:干预组与对照组在性别、年龄、眼轴长度、成熟度、假性晶状体v/s、人工晶状体类型、白内障手术类型等方面差异均无统计学意义。两组(干预组和对照组)RRD分布有临床差异。对照组(非激光患者)与正常人群RRD发生率比较,差异有统计学意义(0.08 vs. 0.0001)。结论:预防性弹幕激光治疗对白内障术后后囊膜破裂、玻璃体丢失的患者可有效预防孔源性视网膜脱离。然而,需要更大样本量的进一步研究。试验注册:伊朗临床试验注册:IRCT20201120049450N2, 2023年7月13日注册,https://irct.behdasht.gov.ir。
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引用次数: 0
Screening for retinopathy of prematurity in China: a five-year cohort study in seven screening centers. 中国早产儿视网膜病变筛查:7个筛查中心的5年队列研究
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-03 DOI: 10.1186/s12886-024-03836-5
Yusheng Zhong, Xiacheng Lin, Yating Yang, Liying He, Na Li, Jun Lu, Yu Zhou, Rong Zhang, Yacong Wang, Zhongyu Zhang, Mochi Yang, Hong Yin, Mingwei Zhao, Xiaoxin Li, Jianhong Liang, Yong Cheng

Background: To analyze the demographic characteristics of retinopathy of prematurity (ROP) in China, attempting to propose optimized screening criteria and hopefully providing valuable information for future updates to the ROP guideline.

Methods: A multicenter, retrospective-cohort study was conducted. The study included infants born between January 1, 2018, and July 31, 2023, who underwent ROP screening and were diagnosed with ROP at seven screening centers in China. Examinations were carried out in accordance with the ROP guidelines in 2014: infants with a gestational age (GA)<32 weeks and/or birth weight (BW)<2000 g, or infants who were suspected to be at risk of ROP. ROP treatment followed the recommendations of the Early Treatment for Retinopathy of Prematurity Cooperative Group. We utilized receiver operating characteristic (ROC) curves to determine the optimal predictive model, and conducted internal validation as well as compared the model to current standards.

Results: Among the 4770 infants diagnosed with ROP after fundus screening, 1330 (27.9%) infants received treatment. The mean GA at birth for all enrolled infants was 29.67 ± 2.45 weeks, with a mean BW of 1295.89 ± 403.64 g. This study proposed the optimization of guidelines to be ≤ 30 weeks of GA and ≤ 1600 g of BW, achieving a sensitivity of 99.4%, as high as the current standard, with an 18.0% reduction in screening requirements.

Conclusion: Considering the decrease in both GA and BW among the population requiring ROP treatment in China, it is imperative to contemplate updating the ROP screening guideline.

背景:分析中国早产儿视网膜病变(ROP)的人口学特征,试图提出优化的筛查标准,并希望为未来ROP指南的更新提供有价值的信息。方法:采用多中心、回顾性队列研究。该研究包括2018年1月1日至2023年7月31日出生的婴儿,他们在中国的七个筛查中心接受了ROP筛查并被诊断为ROP。根据2014年ROP指南进行检查:胎龄(GA)的婴儿。结果:在眼底筛查后诊断为ROP的4770名婴儿中,1330名(27.9%)婴儿接受了治疗。所有入组婴儿出生时平均出生总年龄为29.67±2.45周,平均体重为1295.89±403.64 g。本研究提出的指南优化为GA≤30周,BW≤1600 g,灵敏度达到99.4%,与现行标准相同,筛查要求降低18.0%。结论:考虑到在中国需要ROP治疗的人群中GA和BW的下降,有必要考虑更新ROP筛查指南。
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引用次数: 0
Multifaceted approach to evacuating multi-level premacular hemorrhage in a case of suspected Valsalva retinopathy - a case report. 在一例疑似Valsalva视网膜病变的病例中,采用多方面的方法疏散多层次黄斑前出血-一例报告。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-03 DOI: 10.1186/s12886-024-03842-7
B R Smitha, Naman Sahni, Priyanka Gandhi, Rupal Kathare, Vishma Prabhu, Prathiba Hande, Jay Chhablani, Ramesh Venkatesh

Background: Accurate localization of premacular hemorrhages (PMHs) is crucial as treatment strategies vary significantly based on whether the hemorrhage resides within the vitreous gel, subhyaloid space, or beneath the internal limiting membrane (ILM). This report outlines the clinical features, diagnostic findings, and treatment outcomes in a patient diagnosed with a PMH secondary to suspected Valsalva retinopathy.

Methods: This is a retrospective interventional case report.

Results: A 43-year-old healthy male presented with sudden vision loss in his left eye, reporting a visual acuity of 6/120 since the previous evening. Fundus examination revealed a PMH characterized by a "double-ring sign" accompanied by diffuse retinal hemorrhages. Optical coherence tomography confirmed that the hemorrhage was located in the sub-ILM space. The patient underwent two sessions of YAG laser membranotomy, utilizing energies of 2.5 mJ and 5 mJ, which successfully facilitated drainage of fresh hemorrhage from the sub-ILM space to the subhyaloid space and vitreous cavity. However, the presence of residual coagulated blood over the fovea resulted in persistent visual impairment, necessitating a subsequent pars plana vitrectomy (PPV). The PPV, in conjunction with internal limiting membrane peeling, effectively removed the remaining blood in front of the fovea and restored the visual acuity. By postoperative day 3, the patient experienced a significant improvement in visual acuity, measuring 6/8.

Conclusion: This case underscores the importance of thorough clinical examination and precise diagnostic techniques in the individualized management of PMHs, which is essential for achieving optimal visual outcomes.

背景:准确定位黄斑前出血(PMHs)是至关重要的,因为治疗策略根据出血是在玻璃体凝胶内、玻璃体下间隙内还是在内限制膜(ILM)下而有很大的不同。本报告概述了一名疑似Valsalva视网膜病变继发于PMH的患者的临床特征、诊断结果和治疗结果。方法:回顾性分析介入治疗病例。结果:43岁健康男性,左眼突发性视力丧失,前一晚视力为6/120。眼底检查发现一个以“双环征”为特征的PMH,并伴有弥漫性视网膜出血。光学相干断层扫描证实出血位于ilm下间隙。患者接受了两次YAG激光膜切开术,利用2.5 mJ和5 mJ的能量,成功地将新鲜出血从ilm下腔引流到玻璃体下腔和玻璃体腔。然而,中央窝上残留的凝血导致持续的视力损害,需要后续的玻璃体切割手术。PPV结合内限制膜剥离,有效地清除了中央窝前残留的血液,恢复了视力。术后第3天,患者的视力明显改善,6/8。结论:本病例强调了全面的临床检查和精确的诊断技术在PMHs个性化管理中的重要性,这对于获得最佳的视力结果至关重要。
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引用次数: 0
Comparison of glaucoma progression rate in glaucoma patients at different stages using guided progression analysis with optical coherence tomography. 光学相干断层扫描引导进展分析青光眼不同分期患者青光眼进展率的比较。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1186/s12886-024-03837-4
Okan Akmaz, Murat Gokhan Tokac, Murat Garli, Tuncay Kusbeci

Background: The aim of the present study was to compare the rates of change in Ganglion Cell- Inner Plexiform Layer (GCIPL) and Retinal Nerve Fiber Layer (RNFL) thickness, as measured by Optical Coherence Tomography (OCT) Guided Progression Analysis (GPA) program in control group, Primary Open Angle Glaucoma (POAG) and Pseudoexfoliation Glaucoma (PXG) eyes.

Methods: 60 POAG and 60 PXG patients and 30 control group patients were included in the study. Patients diagnosed with glaucoma were divided into two groups as mild (Mean deviation (MD) > -6.00) and moderate-severe (MD < -6.00). The average, superior and inferior quadrant thinning rates (expressed in micrometers per year) of GCIPL and RNFL in the OCT GPA program were compared between groups.

Results: Average GCIPL thinning rates were -0.23 ± 0.21 μm/year in the control group, -0.64 ± 0.54 μm/year in POAG patients, and -1.06 ± 1.16 μm/year in PXG patients (ANOVA, p < 0.001). Average RNFL thinning rates were -0.33 ± 0.44 μm/year in the control group, -0.86 ± 0.73 μm/year in POAG patients, and -1.33 ± 1.4 μm/year in PXG patients (ANOVA, p < 0.001).

Conclusions: The rates of GCIPL and RNFL thinning were highest in patients with PXG. We found that the glaucoma stage did not affect the rate of RNFL and GCIPL thinning.

背景:本研究的目的是比较用光学相干断层扫描(OCT)引导进展分析(GPA)程序测量的对照组、原发性开角型青光眼(POAG)和假性脱落型青光眼(PXG)的神经节细胞-内丛状层(GCIPL)和视网膜神经纤维层(RNFL)厚度的变化率。方法:选取60例POAG、60例PXG患者及30例对照组患者作为研究对象。结果:对照组GCIPL平均变薄率为-0.23±0.21 μm/年,POAG患者为-0.64±0.54 μm/年,PXG患者为-1.06±1.16 μm/年(方差分析,p)。结论:PXG患者GCIPL和RNFL变薄率最高。我们发现青光眼分期不影响RNFL和GCIPL变薄的速率。
{"title":"Comparison of glaucoma progression rate in glaucoma patients at different stages using guided progression analysis with optical coherence tomography.","authors":"Okan Akmaz, Murat Gokhan Tokac, Murat Garli, Tuncay Kusbeci","doi":"10.1186/s12886-024-03837-4","DOIUrl":"10.1186/s12886-024-03837-4","url":null,"abstract":"<p><strong>Background: </strong>The aim of the present study was to compare the rates of change in Ganglion Cell- Inner Plexiform Layer (GCIPL) and Retinal Nerve Fiber Layer (RNFL) thickness, as measured by Optical Coherence Tomography (OCT) Guided Progression Analysis (GPA) program in control group, Primary Open Angle Glaucoma (POAG) and Pseudoexfoliation Glaucoma (PXG) eyes.</p><p><strong>Methods: </strong>60 POAG and 60 PXG patients and 30 control group patients were included in the study. Patients diagnosed with glaucoma were divided into two groups as mild (Mean deviation (MD) > -6.00) and moderate-severe (MD < -6.00). The average, superior and inferior quadrant thinning rates (expressed in micrometers per year) of GCIPL and RNFL in the OCT GPA program were compared between groups.</p><p><strong>Results: </strong>Average GCIPL thinning rates were -0.23 ± 0.21 μm/year in the control group, -0.64 ± 0.54 μm/year in POAG patients, and -1.06 ± 1.16 μm/year in PXG patients (ANOVA, p < 0.001). Average RNFL thinning rates were -0.33 ± 0.44 μm/year in the control group, -0.86 ± 0.73 μm/year in POAG patients, and -1.33 ± 1.4 μm/year in PXG patients (ANOVA, p < 0.001).</p><p><strong>Conclusions: </strong>The rates of GCIPL and RNFL thinning were highest in patients with PXG. We found that the glaucoma stage did not affect the rate of RNFL and GCIPL thinning.</p>","PeriodicalId":9058,"journal":{"name":"BMC Ophthalmology","volume":"25 1","pages":"1"},"PeriodicalIF":1.7,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11694462/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142920466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association of obesity with orbital fat expansion in thyroid eye disease. 甲状腺眼病中肥胖与眶脂肪扩张的关系
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1186/s12886-024-03824-9
Po-Chin Kuo, Shu-Chun Kuo, Yi-Shan Teng, Chun-Chieh Lai

Background: To investigate the association between obesity and orbital fat expansion in proptosis of thyroid eye disease.

Methods: This observational study retrospectively enrolled 87 participants who received orbital fat decompression surgery for thyroid eye disease. Primary outcome measures included average body mass index (BMI) and the proportion of the study sample with overweight and obesity, compared with the general Taiwanese population. Secondary outcome measures included the association of obesity with proptosis severity, removed fat volume, and thyroid status.

Results: The average BMI (25.59 ± 4.36 kg/m2) of the study sample was significantly higher than that in the general population of Taiwan (24.5 kg/m2; P = 0.012). Participants with overweight (19.52 ± 3.52 mm) and obesity (21.25 ± 3.76 mm) exhibited significantly more severe proptosis than participants without overweight (18.05 ± 3.37 mm) and without obesity (18.09 ± 3.02 mm; P = 0.029 and P < 0.001, respectively). In addition, a significantly greater orbital fat volume was removed from the group with obesity (4.61 ± 1.17 ml) versus that without obesity (3.57 ± 1.12 ml; P = 0.021). A positive correlation between BMI and removed fat volume was noted (correlation coefficient = 0.291, P = 0.005). BMI was an independent factor predicting both proptosis severity (P < 0.001) and removed orbital fat volume (P = 0.02).

Conclusions: Obesity is associated with orbital fat expansion and consequently more severe proptosis in thyroid eye disease. Weight control may be a potential strategy to prevent thyroid-associated exophthalmos.

背景:探讨甲状腺眼病前病变中肥胖与眼眶脂肪扩张的关系。方法:本观察性研究回顾性纳入87例接受眼窝脂肪减压手术治疗甲状腺眼病的患者。主要结果测量包括平均身体质量指数(BMI)和研究样本中超重和肥胖的比例,并与台湾一般人群进行比较。次要结局指标包括肥胖与预后严重程度、去除脂肪量和甲状腺状态的关系。结果:研究样本的平均BMI(25.59±4.36 kg/m2)显著高于台湾普通人群(24.5 kg/m2;p = 0.012)。超重(19.52±3.52 mm)和肥胖(21.25±3.76 mm)的参与者比非超重(18.05±3.37 mm)和非肥胖(18.09±3.02 mm)的参与者表现出更严重的突出;结论:肥胖与眼窝脂肪扩张相关,从而导致甲状腺眼病更严重的眼球突出。控制体重可能是预防甲状腺相关性突出症的一种潜在策略。
{"title":"Association of obesity with orbital fat expansion in thyroid eye disease.","authors":"Po-Chin Kuo, Shu-Chun Kuo, Yi-Shan Teng, Chun-Chieh Lai","doi":"10.1186/s12886-024-03824-9","DOIUrl":"10.1186/s12886-024-03824-9","url":null,"abstract":"<p><strong>Background: </strong>To investigate the association between obesity and orbital fat expansion in proptosis of thyroid eye disease.</p><p><strong>Methods: </strong>This observational study retrospectively enrolled 87 participants who received orbital fat decompression surgery for thyroid eye disease. Primary outcome measures included average body mass index (BMI) and the proportion of the study sample with overweight and obesity, compared with the general Taiwanese population. Secondary outcome measures included the association of obesity with proptosis severity, removed fat volume, and thyroid status.</p><p><strong>Results: </strong>The average BMI (25.59 ± 4.36 kg/m<sup>2</sup>) of the study sample was significantly higher than that in the general population of Taiwan (24.5 kg/m<sup>2</sup>; P = 0.012). Participants with overweight (19.52 ± 3.52 mm) and obesity (21.25 ± 3.76 mm) exhibited significantly more severe proptosis than participants without overweight (18.05 ± 3.37 mm) and without obesity (18.09 ± 3.02 mm; P = 0.029 and P < 0.001, respectively). In addition, a significantly greater orbital fat volume was removed from the group with obesity (4.61 ± 1.17 ml) versus that without obesity (3.57 ± 1.12 ml; P = 0.021). A positive correlation between BMI and removed fat volume was noted (correlation coefficient = 0.291, P = 0.005). BMI was an independent factor predicting both proptosis severity (P < 0.001) and removed orbital fat volume (P = 0.02).</p><p><strong>Conclusions: </strong>Obesity is associated with orbital fat expansion and consequently more severe proptosis in thyroid eye disease. Weight control may be a potential strategy to prevent thyroid-associated exophthalmos.</p>","PeriodicalId":9058,"journal":{"name":"BMC Ophthalmology","volume":"25 1","pages":"2"},"PeriodicalIF":1.7,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11694364/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142920537","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Systemic adverse drug events to topical prostaglandin analogs for treating glaucoma: a retrospective focused pharmacovigilance study. 局部前列腺素类似物治疗青光眼的系统性药物不良事件:一项回顾性重点药物警戒研究。
IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2024-12-31 DOI: 10.1186/s12886-024-03823-w
Kannan Sridharan

Background: Prostaglandin analogs are first-line treatments for open-angle glaucoma due to their proven efficacy in reducing intraocular pressure. Despite their topical administration, systemic adverse drug Events (ADEs) have been reported. This study investigates the systemic ADEs associated with topical prostaglandin analogs using the United States Food and Drug Administration (USFDA) Adverse Drug Event Reporting System (AERS) database.

Methods: The USFDA AERS database was queried for reports on prostaglandin analogs from March 2004 to March 2024 in this retrospective pharmacovigilance study. Data were deduplicated and analyzed using disproportionality analysis with both frequentist and Bayesian approaches. Reports on systemic ADEs where topical prostaglandin analogs were the primary suspect were included. Statistical analysis was performed using descriptive statistics and the chi-square test for categorical variables.

Results: A total of 30,853 reports were analyzed, predominantly involving latanoprost and bimatoprost, with most patients being elderly and female. In general, hypersensitivity reactions were the most common systemic adverse events reported with prostaglandin analogs. Varied systemic adverse events were observed within the class as latanoprost was linked to conditions like angina pectoris, atrial tachycardia and Meniere's disease, bimatoprost to lentigo maligna melanoma, and tafluprost to labyrinthitis and skin discoloration. Notably, tafluprost had a significantly higher occurrence of death compared to other prostaglandin analogs, yet the causal relationship has not been established for this association due to unavailability of critical data on temporality and potential confounders including concomitant diseases/drugs and severity of the disease.

Conclusion: Prostaglandin analogs are associated with systemic ADEs, particularly in elderly and female patients. The most reported systemic adverse event was hypersensitivity reactions for the class and cardiac events for latanoprost. Tafluprost was observed with higher mortality statistically, yet causal relationship could not be established in the absence of details on the potential confounders. The findings emphasize the need for continuous monitoring of adverse reactions, and consideration of patient-specific factors when prescribing these medications.

背景:前列腺素类似物是开角型青光眼的一线治疗方法,因为它们具有降低眼压的疗效。尽管局部用药,系统性药物不良事件(ADEs)已被报道。本研究使用美国食品和药物管理局(USFDA)不良药物事件报告系统(AERS)数据库调查与局部前列腺素类似物相关的系统性ade。方法:在2004年3月至2024年3月的回顾性药物警戒研究中,查询USFDA AERS数据库中前列腺素类似物的报告。数据删除和分析使用歧化分析与频率和贝叶斯方法。报道了局部前列腺素类似物为主要怀疑的系统性ade。对分类变量采用描述性统计和卡方检验进行统计分析。结果:共分析30,853份报告,主要涉及拉坦前列素和比马前列素,大多数患者为老年人和女性。一般来说,超敏反应是前列腺素类似物最常见的系统性不良事件。在这类药物中观察到不同的系统性不良事件,如拉坦前列素与心绞痛、房性心动过速和梅尼埃病有关,比马托前列素与慢性恶性黑色素瘤有关,他氟前列素与迷宫炎和皮肤变色有关。值得注意的是,与其他前列腺素类似物相比,他氟前列素的死亡发生率明显更高,但由于缺乏关于暂时性和潜在混杂因素(包括伴随疾病/药物和疾病严重程度)的关键数据,因此尚未确定这种关联的因果关系。结论:前列腺素类似物与系统性ade有关,特别是在老年和女性患者中。报告最多的系统性不良事件是类药物的过敏反应和拉坦前列素的心脏事件。统计上观察到他氟前列素与较高的死亡率,但由于缺乏潜在混杂因素的详细信息,无法建立因果关系。研究结果强调需要持续监测不良反应,并在处方这些药物时考虑到患者的具体因素。
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引用次数: 0
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BMC Ophthalmology
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