Study for Pathophysiology in Vitreo-retinal surgery

玻璃体视网膜手术的病理生理学研究

基本信息

  • 批准号:
    12470361
  • 负责人:
  • 金额:
    $ 7.81万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    2000
  • 资助国家:
    日本
  • 起止时间:
    2000 至 2001
  • 项目状态:
    已结题

项目摘要

We studied the effects of vitreoretinal surgery on retinal function and morphology. Vitrectomy is one of the effective treatments for improvements of retinal pathological conditions by removing the diseased vitreous and proliferative tissues. Conversely, however, the procedure itself may give adverse effects on the retinal function and/or retinal circulation. We evaluated the effects of removal of internal limiting membrane on macular retinal function in idiopathic macular hole surgery by focal macular ERG (FMERG) and concluded that this procedure had no adverse effect on visual acuity. However, the selective delay of recovery of the FMERG b-wave after surgery suggests an alteration of retinal physiology in the macular region(IOVS200 1). We further evaluated the macular morphology using optical coherent tomography in diabetic macular edema with visible vitreous traction and concluded that the structure recovered well after surgery, although the recovery of visual acuity was limited because of their preoperative retinal pahological conditions(AJO2001). We further studied the local macular and full-field retinal functions of age related macular degeneration (AMD) after removal of choroidal neovascularization and macular translocation surgery, respectively(IOVS2002) (IOVS2002). These study demonstrated the recovery of macular function was contributed by the decreased retinal thickness. Macular translocation surgery may be well feasible technique, however, the total function of the retina was decreased after surgery. In our additional study, the histopathology of polypoidal choroidal vasculopathy obtained during macular translocation surgery demonstrated the similarity to those of the AMD(BJO2002).
我们研究了玻璃体视网膜手术对视网膜功能和形态的影响。玻璃体切除术是通过切除病变玻璃体和增生组织来改善视网膜病变的有效治疗方法之一。然而,相反,手术本身可能对视网膜功能和/或视网膜循环产生不利影响。我们通过焦点黄斑ERG(FMERG)评价了特发性黄斑裂孔手术中内界膜去除对黄斑视网膜功能的影响,并得出结论,该手术对视力无不良影响。然而,术后FMERG b波恢复的选择性延迟表明黄斑区视网膜生理学的改变(IOVS 200 1)。我们使用光学相干断层扫描进一步评价了糖尿病性黄斑水肿伴可见玻璃体牵引的黄斑形态,并得出结论,该结构在手术后恢复良好,尽管由于术前视网膜病理学状况,视力恢复有限(AJO 2001)。我们进一步研究了年龄相关性黄斑变性(AMD)在脉络膜新生血管切除术和黄斑移位手术后的局部黄斑和全视野视网膜功能(IOVS 2002)(IOVS 2002)。这些研究表明,黄斑功能的恢复与视网膜厚度的减少有关。黄斑移位术是一种可行的手术方法,但术后视网膜的整体功能下降。在我们的附加研究中,在黄斑移位手术期间获得的息肉状脉络膜血管病变的组织病理学证明了与AMD的相似性(BJO 2002)。

项目成果

期刊论文数量(218)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Bach M, Hawlina M, Holder GE, Marmor MF, Meigen T, Vaegan, Miyake Y: "Standard for pattern electroretinography"Doc Ophthalmol. 100. 11-18 (2000)
Bach M、Hawlina M、Holder GE、Marmor MF、Meigen T、Vaegan、Miyake Y:“图形视网膜电图检查标准”Doc Ophamol。
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    0
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Horio N, Horiguchi M, Murakami K, Yamamoto E, Miyake Y: "Stenotrophomonas maltophilia endophthalmitis after intraocular lens implantation"Graefe's Arch Clin Exp Ophthalmol. 238. 299-301 (2000)
Horio N、Horiguchi M、Murakami K、Yamamoto E、Miyake Y:“人工晶状体植入后嗜麦芽寡养单胞菌眼内炎”Graefes Arch Clin Exp Ophthalmol。
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RadnerW, Sadda SR, Humayuu MS, Suzuki S, et al.: "Light-Driven Retinal Ganglion Cell Responses in Blind rd Mice after Neural Retinal Transplantation"Invest Ophthalmol Vis Sci. 42. 1057-1065 (2001)
RadnerW、Sadda SR、Humayuu MS、Suzuki S 等人:“神经视网膜移植后盲人小鼠的光驱动视网膜神经节细胞反应”Invest Ophamol Vis Sci。
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    0
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Horio N, Kachi S.Hori K, Okamoto Y, Yamamoto E, Terasaki H, Miyake Y: "Progressive change of optical coherence tomography scans in retinaldegeneration slow (rds) mice"Arch Ophthalmol. 119. 1329-1332 (2001)
Horio N、Kachi S.Hori K、Okamoto Y、Yamamoto E、Terasaki H、Miyake Y:“视网膜变性慢 (rds) 小鼠光学相干断层扫描的渐进变化”Arch Ophasemol。
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    0
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Miyagawa A, Kobayashi M, Fujita Y, Nakamura M, Hirano K, Kobayashi K,Miyake Y: "Surface topology of collagen fibrils associated with proteoglycans in mouse cornea and sclera"Jpn J Ophthalmol. 44. 591-595 (2000)
Miyakawa A、Kobayashi M、Fujita Y、Nakamura M、Hirano K、Kobayashi K、Miyake Y:“与小鼠角膜和巩膜中的蛋白多糖相关的胶原原纤维的表面拓扑”Jpn J Ophthalmol。
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TERASAKI Hiroko其他文献

TERASAKI Hiroko的其他文献

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{{ truncateString('TERASAKI Hiroko', 18)}}的其他基金

Elucidating the molecular pathology and development of treatment modalities for ischemic retinopathies
阐明缺血性视网膜病的分子病理学和治疗方式的发展
  • 批准号:
    20390448
  • 财政年份:
    2008
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Investigation of pathogenegs and new treatment for developmental, age-related and inherited chorioretinal diaasse
发育性、年龄相关性和遗传性脉络膜视网膜疾病的病因研究和新疗法
  • 批准号:
    18390466
  • 财政年份:
    2006
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
New treatment and functional analysis of age related macular diseases
年龄相关性黄斑疾病的新治疗方法及功能分析
  • 批准号:
    16390497
  • 财政年份:
    2004
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Pathophysiology of vitreous and new therapeutic modality
玻璃体的病理生理学和新的治疗方式
  • 批准号:
    14370557
  • 财政年份:
    2002
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Study on endoscopic fluorescein angiography of extreme peripheral retina
内镜下视网膜末梢荧光血管造影研究
  • 批准号:
    09671791
  • 财政年份:
    1997
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Study on visual function in dominantly inherited juvenile optic atrophy.
显性遗传性青少年视神经萎缩的视功能研究。
  • 批准号:
    07671911
  • 财政年份:
    1995
  • 资助金额:
    $ 7.81万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
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