The rationale for ophthalmic vigilance during the 2026 Hantavirus outbreak.
Zhao Aaron T AT, Deaner Jordan D JD
CSL Vifor · ADRB1 · 小分子
carteolol 是一种小分子,由CSL Vifor研发。该药已获批,用于治疗相关适应症,给药途径:Others、Topical。
| 商品名 | OPC1085, Ocupress, Mikelan, ophthalmic |
| 公司 | CSL Vifor |
| 药物类别 | 小分子 |
| 分子靶点 | ADRB1, ADRB2 |
| 给药途径 | Others, Topical |
| 状态 | Approved |
carteolol 作用于 2 个分子靶点:
| ADRB1 | adrenoceptor beta 1 (B1AR, RHR) |
| ADRB2 | adrenoceptor beta 2 (B2AR, ADRBR) |
carteolol 针对 1 个适应症,涉及 1 个治疗领域。
| 治疗领域 | 疾病/病症 | 分期 |
|---|---|---|
| Eye disorders | Glaucoma | ✓ Approved |
Zhao Aaron T AT, Deaner Jordan D JD
Shimoi Akihiro A, Yoshida Keisuke K, Akaji Kazunori K, Terada Tomoaki T
Anterior cranial fossa dural arteriovenous fistulas (ACF DAVFs) are high-risk lesions because of cortical venous drainage and are generally treated by surgical interruption of the draining vein or transarterial embolization (TAE). Transvenous embolization (TVE) has recently emerged as an alternative treatment in selected cases. A 67-year-old man with a residual ACF DAVF after previous bilateral ophthalmic artery Onyx (Medtronic, Irvine, CA, USA) embolization was referred for additional treatment. Repeat TAE was considered anatomically difficult because of distal ophthalmic artery occlusion after prior treatment. Craniotomy was presented as the standard treatment but was declined by the patient. Preoperative imaging demonstrated focal shunt localization and feasible venous access to the foot of the draining vein. TVE was therefore performed using selective venous catheterization and Onyx embolization. Complete angiographic obliteration was achieved without neurological deficit, hemorrhagic complication, or postoperative olfactory disturbance. Because of strong resistance during catheter retrieval, the microcatheter was intentionally retained to avoid venous injury. TVE may represent a feasible alternative for selected residual ACF DAVFs after prior embolization when additional arterial access is limited and the venous anatomy is favorable. Careful patient selection and meticulous procedural planning remain essential.
Kumar Annuj A, Shruthi Munjam M, Sujeeth Thiruppathy T, Mohideen Abubacker Kaja AK et al.
Early and accurate detection of diabetic retinopathy (DR) is essential to prevent irreversible vision loss; however, manual screening is labor-intensive and subject to inter-observer variability. To address these limitations, we propose ARTNet, an Adaptive channel-wise and Region-aware Transformer Network for automated DR classification and segmentation from retinal fundus images. ARTNet integrates three sub-network mechanisms. The Adaptive Channel-wise Feature Network (ACFNet) performs channel recalibration using dual pooling and shared multilayer perceptrons to enhance discriminative retinal representations while suppressing irrelevant responses. The Ophthalmic Region-Aware Attention Network (ORAANet) applies spatial attention to highlight clinically significant regions, including lesions and abnormal vasculature. The Retinal Patch Aggregation Encoder Network (RPAENet), built on multi-head self-attention, captures long-range dependencies and global retinal context for hierarchical feature modeling. Convolutional refinement and global average pooling enable robust five-class DR classification, while a class-balanced focal loss mitigates data imbalance and improves minority-class sensitivity. Extensive experiments on benchmark datasets demonstrate the superiority of ARTNet over intermediate and state-of-the-art models. On the Diabetic Retinopathy Detection dataset, ARTNet achieves 96.45% accuracy, 96.85% precision, 96.34% recall, and 96.60% F1-score. The model is further validated on the APTOS-2019 Blindness Detection and IDRiD datasets. Classification performance is evaluated using image-level DR grading metrics, whereas lesion segmentation performance is evaluated using the pixel-level lesion annotations available only in the IDRiD dataset. Results show that dual attention with transformer-based global reasoning improves feature representation and classification reliability. Its efficiency and stability support real-time ophthalmic screening and a clinical decision system.
Saeed Amber A, Naheed Farah F, Ullah Saif S, Ullah Asad A et al.
Beta-thalassemia is associated with systemic complications from chronic anemia, iron overload, and long-term transfusion therapy, which may also affect ocular structures. This study aimed to compare the frequency and patterns of ocular complications between patients with β-thalassemia major and β-thalassemia intermedia. This comparative cross-sectional study included 30 patients (60 eyes) with β-thalassemia major or β-thalassemia intermedia, recruited via convenience nonprobability sampling. All participants underwent comprehensive optometric and ophthalmic evaluation, including assessments of visual acuity, intraocular pressure, stereopsis, tear break-up time, visual field testing, and slit-lamp examination of the anterior and posterior segments. Serum ferritin levels were also recorded, and statistical analysis was performed using SPSS version 21. The mean age of participants was 20. 20.67 ± 7. 44 years, and 60% were female. Serum ferritin levels were significantly higher in patients with β-thalassemia major than in those with β-thalassemia intermedia (4056. 47 ± 2415. 28; p < 0. 001). Uncorrected visual acuity and superior visual field extent were significantly better in the intermedia group (0. 913 ± 0. 196 decimal and 52. 67 ± 7. 74 degrees, respectively; p < 0. 05). Tear break- up time was significantly longer in the major group (9. 87 ± 4. 25 seconds) than in the intermedia group (6. 27 ± 3. 91 seconds; p < 0. 005). Patients receiving chelation therapy for more than 5 years had significantly lower tear break-up time values (p = 0. 04). Lenticular abnormalities were observed in 10% of eyes in both groups, whereas vitreous condensations and peripheral fundus atrophic changes were more frequent in β-thalassemia intermedia. In conclusion, patients with β-thalassemia major have higher serum ferritin levels and poorer visual function, whereas certain posterior segment changes appear more prevalent in β-thalassemia intermedia. These findings highlight the importance of regular ophthalmic screening in patients with thalassemia.
Corda Claudia C, Lixi Filippo F, Budroni Antonio A, Tomi Mara-Ioana MI et al.
To report a case of refractory herpes simplex virus keratitis (HSVK) complicated by keratolysis and severe stromal thinning in a patient with rheumatoid arthritis (RA) under treatment with methotrexate (MTX). A 79‑year‑old patient with a history of HSVK and RA, treated with weekly MTX, presented with pain and photophobia in the right eye. Best‑corrected visual acuity (BCVA) was limited to counting fingers. Slit‑lamp examination revealed a supero-nasal corneal ulcer (area of 2.98 mm2) with deep stromal involvement and keratolysis. A recurrent episode of HSVK was diagnosed, and treatment with 3 times daily oral acyclovir, 4 times daily 0.15% ganciclovir ophthalmic gel, and 3 times daily 0.15% topical dexamethasone was started. After one week, the picture worsened with corneal thinning (corneal thinnest point [CTP] 82 µm) and anterior chamber fibrin. Cycloplegic therapy 3 times daily was added. Considering the refractory course, the history of recurrent HSVK, and the concomitant systemic immunomodulation, the MTX injection scheduled for the subsequent weeks was interrupted. After 2 weeks, conjunctival hyperemia improved (Efron grade II) and a progressive increase of corneal thickness (CTP 199 µm) was documented. Two months later, complete healing was achieved with no signs of active inflammation or recurrence; BCVA improved to 0.4 LogMAR, with mild residual stromal thinning and opacity (CTP 231 µm). This case underscores how systemic immunomodulatory treatment may play a clinically relevant role in patients with recurrent HSVK. In selected cases, a conservative, surgery‑sparing approach through the optimization of systemic therapy can help promoting viral load control and corneal healing.
Chen Jing J, Zhang Ling L
This report describes an 11-year-old girl who presented with a 6-month history of decreased visual acuity in the left eye without ocular pain or redness. She had a history of exposure to cats and dogs. Initial ophthalmic examination showed dense vitreous inflammatory opacities and diffuse fibroproliferative traction involving the posterior pole, but no typical granulomatous lesion was visible before surgery. The patient underwent 25-gauge pars plana vitrectomy with membrane peeling, and periocular triamcinolone acetonide (40 mg) was administered at the end of surgery for residual intraocular inflammation. During surgery, a peripheral grayish-white granulomatous lesion with associated retinal traction was identified. Paired serum and undiluted vitreous fluid testing showed elevated anti-Toxocara IgG levels, and the Goldmann-Witmer coefficient was markedly increased to 63.67, supporting local intraocular anti-Toxocara antibody production. Together with the intraoperative identification of a peripheral granulomatous lesion, these findings strongly supported the diagnosis of ocular toxocariasis. The postoperative course was uneventful, with no recurrent vitritis, new retinal lesion, retinal detachment, clinically evident macular edema, or progression of the peripheral granuloma during 12 months of follow-up. Anatomical stabilization was achieved, although visual recovery remained limited, likely because of long-standing tractional macular distortion and chronic structural damage. This case highlights that ocular toxocariasis should be considered in children with unilateral chronic vitritis and tractional vitreoretinal changes, even when a typical granuloma is not visible before surgery. Paired serum and undiluted vitreous antibody testing, together with calculation of the Goldmann-Witmer coefficient, can provide important diagnostic evidence, while vitrectomy may have both diagnostic and therapeutic value in advanced tractional cases.
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