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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 臨床醫學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/61442
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陳偉勵
dc.contributor.authorJen-Pin Sunen
dc.contributor.author孫仁彬zh_TW
dc.date.accessioned2021-06-16T13:03:07Z-
dc.date.available2013-09-24
dc.date.copyright2013-09-24
dc.date.issued2013
dc.date.submitted2013-08-06
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2. Bonanno JA. Molecular mechanisms underlying the corneal endothelial pump. Exp Eye Res 2012;95(1):2-7.
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4. Caldwell MC, Afshari NA, Decroos FC, Proia AD. The histology of graft adhesion in descemet stripping with endothelial keratoplasty. Am J Ophthalmol 2009;148(2):277-81.
5. Chang PY, Carrel H, Huang JS, et al. Decreased density of corneal basal epithelium and subbasal corneal nerve bundle changes in patients with diabetic retinopathy. Am J Ophthalmol 2006;142(3):488-90.
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7. Chen M, Gong L, Xu J, et al. Ultrastructural and in vivo confocal microscopic evaluation of interface after Descemet's Stripping Endothelial Keratoplasty in rabbits. Acta Ophthalmol 2012;90(1):e43-7.
8. Chen WL, Chang HW, Hu FR. In vivo confocal microscopic evaluation of corneal wound healing after epi-LASIK. Invest Ophthalmol Vis Sci 2008;49(6):2416-23.
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11. Dapena I, Ham L, Melles GR. Endothelial keratoplasty: DSEK/DSAEK or DMEK--the thinner the better? Curr Opin Ophthalmol 2009;20(4):299-307.
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14. Espana EM, Huang B. Confocal microscopy study of donor-recipient interface after Descemet's stripping with endothelial keratoplasty. Br J Ophthalmol 2010;94(7):903-8.
15. Gorovoy MS. Descemet-stripping automated endothelial keratoplasty. Cornea 2006;25(8):886-9.
16. Hatanaka H, Koizumi N, Okumura N, et al. A study of host corneal endothelial cells after non-Descemet stripping automated endothelial keratoplasty. Cornea 2013;32(1):76-80.
17. Hatou S. Hormonal regulation of Na+/K+-dependent ATPase activity and pump function in corneal endothelial cells. Cornea 2011;30 Suppl 1:S60-6.
18. Huang D, Swanson EA, Lin CP, et al. Optical coherence tomography. Science 1991;254(5035):1178-81.
19. Huang HW, Hu FR, Wang IJ, et al. Migration of limbal melanocytes onto the central cornea after ocular surface reconstruction: an in vivo confocal microscopic case report. Cornea 2010;29(2):204-6.
20. Huang YH, Chu HS, Hu FR, et al. Recurrent advancing wavelike epitheliopathy from the opposite side of the initial presentation. Cornea 2008;27(1):111-3.
21. Ide T, Yoo SH, Kymionis GD, et al. Descemet stripping automated endothelial keratoplasty tissue preparation with femtosecond laser and contact lens. Cornea 2010;29(1):93-8.
22. Ivarsen A, Thogersen J, Keiding SR, et al. Plastic particles at the LASIK interface. Ophthalmology 2004;111(1):18-23.
23. Jonas JB, Vossmerbaeumer U. Femtosecond laser penetrating keratoplasty with conical incisions and positional spikes. J Refract Surg 2004;20(4):397.
24. Kaufman SC, Kaufman HE. How has confocal microscopy helped us in refractive surgery? Curr Opin Ophthalmol 2006;17(4):380-8.
25. Khor WB, Mehta JS, Tan DT. Descemet stripping automated endothelial keratoplasty with a graft insertion device: surgical technique and early clinical results. Am J Ophthalmol 2011;151(2):223-32 e2.
26. Kobayashi A, Yokogawa H, Sugiyama K. Non-Descemet stripping automated endothelial keratoplasty for endothelial dysfunction secondary to argon laser iridotomy. Am J Ophthalmol 2008;146(4):543-9.
27. Kobayashi A, Yokogawa H, Sugiyama K. In vivo laser confocal microscopy after non-Descemet's stripping automated endothelial keratoplasty. Ophthalmology 2009;116(7):1306-13.
28. Kobayashi A, Mawatari Y, Yokogawa H, Sugiyama K. In vivo laser confocal microscopy after descemet stripping with automated endothelial keratoplasty. Am J Ophthalmol 2008;145(6):977-85.
29. Kymionis GD, Suh LH, Dubovy SR, Yoo SH. Diagnosis of residual Descemet's membrane after Descemet's stripping endothelial keratoplasty with anterior segment optical coherence tomography. J Cataract Refract Surg 2007;33(7):1322-4.
30. Lee WB, Jacobs DS, Musch DC, et al. Descemet's stripping endothelial keratoplasty: safety and outcomes: a report by the American Academy of Ophthalmology. Ophthalmology 2009;116(9):1818-30.
31. Li L, Ellis KR, Behrens A, et al. A laboratory model for microkeratome-assisted posterior lamellar keratoplasty utilizing a running graft suture and a sutureless hinged flap. Cornea 2002;21(2):192-5.
32. Maeda N. Optical coherence tomography for corneal diseases. Eye Contact Lens 2010;36(5):254-9.
33. Masaki T, Kobayashi A, Yokogawa H, et al. Clinical evaluation of non-Descemet stripping automated endothelial keratoplasty (nDSAEK). Jpn J Ophthalmol 2012;56(3):203-7.
34. McCartney MD, Wood TO, McLaughlin BJ. Moderate Fuchs' endothelial dystrophy ATPase pump site density. Invest Ophthalmol Vis Sci 1989;30(7):1560-4.
35. Melles GR, Eggink FA, Lander F, et al. A surgical technique for posterior lamellar keratoplasty. Cornea 1998;17(6):618-26.
36. Melles GR, Lander F, Beekhuis WH, et al. Posterior lamellar keratoplasty for a case of pseudophakic bullous keratopathy. Am J Ophthalmol 1999;127(3):340-1.
37. Mondloch MC, Giegengack M, Terry MA, Wilson DJ. Histologic evidence of retained fetal layer of the descemet membrane after presumed total removal for endothelial keratoplasty: a possible cause for graft failure. Cornea 2007;26(10):1263-6.
38. Price FW, Jr., Price MO. Descemet's stripping with endothelial keratoplasty in 50 eyes: a refractive neutral corneal transplant. J Refract Surg 2005;21(4):339-45.
39. Price FW, Jr., Price MO. Descemet's stripping with endothelial keratoplasty in 200 eyes: Early challenges and techniques to enhance donor adherence. J Cataract Refract Surg 2006;32(3):411-8.
40. Price FW, Jr., Price MO. Endothelial keratoplasty to restore clarity to a failed penetrating graft. Cornea 2006;25(8):895-9.
41. Price MO, Price FW, Jr. Descemet's stripping with endothelial keratoplasty: comparative outcomes with microkeratome-dissected and manually dissected donor tissue. Ophthalmology 2006;113(11):1936-42.
42. Price MO, Price FW, Jr., Trespalacios R. Endothelial keratoplasty technique for aniridic aphakic eyes. J Cataract Refract Surg 2007;33(3):376-9.
43. Savastano A, Sbordone S, Piccirillo V, et al. Confocal microscopy after descemet stripping endothelial keratoplasty: a case report. Cornea 2009;28(5):570-4.
44. Sonigo B, Iordanidou V, Chong-Sit D, et al. In vivo corneal confocal microscopy comparison of intralase femtosecond laser and mechanical microkeratome for laser in situ keratomileusis. Invest Ophthalmol Vis Sci 2006;47(7):2803-11.
45. Su PY, Hu FR, Chen YM, et al. Dendritiform cells found in central cornea by in-vivo confocal microscopy in a patient with mixed bacterial keratitis. Ocul Immunol Inflamm 2006;14(4):241-4.
46. Terry MA, Shamie N, Chen ES, et al. Precut tissue for Descemet's stripping automated endothelial keratoplasty: vision, astigmatism, and endothelial survival. Ophthalmology 2009;116(2):248-56.
47. Terry MA, Shamie N, Chen ES, et al. Endothelial keratoplasty: the influence of preoperative donor endothelial cell densities on dislocation, primary graft failure, and 1-year cell counts. Cornea 2008;27(10):1131-7.
48. Tillett CW. Posterior lamellar keratoplasty. Am J Ophthalmol 1956;41(3):530-3.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/61442-
dc.description.abstract【研究背景及目的】
傳統的全層角膜移植手術(penetrating keratoplasty)雖然在治療許多角膜病變上有很好的療效,但近幾年來對於治療內皮細胞失能的情形已漸漸被”戴氏膜撕除角膜內皮層移植手術” (DSAEK = Descemet's Stripping Automated Endothelial Keratoplasty)所取代。DSAEK手術的好處是開刀的傷口小、造成的散光少、術中不容易有猛爆性脈絡膜出血的合併症、術後的視力和傷口復原等等也有顯著的優勢。然而因為DSAEK手術目前仍相當新穎,有許多術中的條件設定仍未被充分了解;因此亟需客觀的研究來探討適當的手術方式。ㄧ般來說,DSAEK的手術過程中必須把受贈者本身角膜的戴氏膜(Descemet's membrane)和內皮細胞層(endothelial cell layer)移除,之後貼附上捐贈者之角膜內層瓣(posterior lamellar graft)。然而另一方理論認為在某些情況下角膜內皮細胞層和戴氏膜不需要移除(n-DSAEK, non-Descemet's Stripping Automated Endothelial Keratoplasty),單純地把捐贈者之角膜內層瓣貼上即可,而壓縮在兩層之間的「戴氏膜/角膜內皮細胞層」不至於造成混濁甚至影響視力。到底何種理論正確,目前並無研究佐證。本研究乃針對以上臨床未解的問題,試圖用紐西蘭白兔的動物手術模式加以探討。
【研究方法與設計】
研究中將使用飛秒雷射切割製備角膜內層瓣,之後進行手術移植到兔眼上。被移植的兔眼又分為保留和去除「戴氏膜/角膜內皮細胞層」兩組。術後前三個月、每兩週一次利用「體內共軛焦顯微鏡」觀測夾在兩層之間的「戴氏膜/角膜內皮細胞層」隨時間所產生的變化,並測量其產生之角膜混濁現象。術後三個月取下兔眼,利用「前房光干渉斷層儀」(anterior segment OCT)輔助判斷角膜瓣的癒合和附著狀況,之後切片觀察顯微變化(H&E染色、免疫化學組織染色、穿透式電子顯微鏡)。
【結果】
在無戴氏膜撕除角膜內皮層移植手術(nDSAEK)中保留的受贈者內皮細胞層的細胞密度會隨著時間而逐漸下降。兩種手術方式所產生的交界面模糊程度(interface hazziness)都會隨著時間而下降,但”無戴氏膜撕除角膜內皮層移植手術”所產生的交界面模糊程度在所有的術後時間測量點均比”戴氏膜撕除角膜內皮層移植手術”來的大。
兩種手術方式術後的角膜厚度並沒有顯著的差異。利用H&E染色觀察”無戴氏膜撕除角膜內皮層移植手術”術後三個月之組織切片可以看見受贈者的戴氏膜層與細胞密度降低的內皮細胞層;利用穿透式電子顯微鏡則可以發現上述內皮細胞的型態因為擠壓而產生改變並且在內皮細胞內部可以觀察到和捐贈者基質層相同的纖維。免疫組織化學染色結果顯示這些受贈者內皮細胞原本的幫浦功能在術後三個月已經消失,但並沒有表現出上皮細胞的標誌,而部分受贈者內皮細胞表現出細胞凋亡現象。
【結論】
”無戴氏膜撕除角膜內皮層移植手術”在術後結果與”戴氏膜撕除角膜內皮層移植手術”類似但有較明顯的交界面模糊程度。保留的受贈者內皮細胞會有型態上的改變並表現出吞噬能力,細胞密度可能因產生細胞凋亡而下降。
zh_TW
dc.description.abstract【Background and Study Purpose】
Although traditional penetrating keratoplasty (PK) was a widely accepted procedure, descemet's stripping automated endothelial keratoplasty (DSAEK) becomes popular and has replaced PK in the treatment of endothelial disorders. DSAEK is unique for the smaller wound size, lesser astigmatism, lesser chance of intraoperative expulsive hemorrhage, faster/better visual outcome and faster wound healing. However, there still exist many unknown factors for a better surgery. Most surgeons removed Descemet’s membrane and endothelial layer during DSAEK surgery follower by insertion of posterior corneal lamella. However, still some surgeons keep Descemet’s membrane and endothelial layer before the attachment of the posterior corneal lamella (n-DSAEK). They claim that the remained Descemet’s membrane/ endothelial layer between donor and recipient corneas will not inference corneal clarity and visual prognosis. The purpose of this project is to use New Zealand White Rabbit as the experimental model to find out the best surgical condition for DSAEK.
【Material and Method】
We will use femtosecond laser machine to create donor corneal posterior lamellas. The posterior corneal lamellas will be transplanted to rabbit corneas with or without stripping of Descemet’s membrane/corneal endothelial layer. After operation, the rabbit eyes will receive in vivo confocal microscopic examination every two weeks for totally 3 months. The Descemet’s membrane/corneal endothelial layer between donor and recipient corneas will be examined by morphology and Z-profile. At post-operative 3 months, the rabbit eyes will be obtained, and examined by anterior segment OCT to evaluate the attachment and healing of the transplanted grafts. In addition, the tissue section will be examined by H&E staining, immunohistochemical staining and transmission electron microscopy.
【Results】
The interface recipient endothelial cell density in nDSAEK gradually decreased in the follow-up period. The interface haziness of DSAEK and nDSAEK diminished gradually, and nDSAEK has greater interface opacity than DSAEK at all time points examined.
There was no significant difference of total corneal thickness between DSAEK and nDSAEK at all time points. Tissue section using H&E staining showed preserved interface recipient Descemet’s membrane and decreased endothelial cell density three months after nDSAEK. Transmission electron microscopy revealed morphologically changed interface recipient endothelial cell and some collagen fibers similar as in graft stroma in recipient endothelial cell in nDSAEK three months after operation. The recipient endothelial cell didn’t express markers of pump function and epithelial cell by immunohistochemical staining. However some recipient endothelial cell went apoptotic pathway.
【Conclusion】
NDSAEK has similar surgical results as DSAEK in all parameters measured in this study. However, the interface haziness was greater than DSAEK, and recipient endothelial cell at the interface underwent morphological change and showed some phagocytic activity during the whole observational process. The endothelial cell density decreased due to cell apoptosis
en
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Previous issue date: 2013
en
dc.description.tableofcontents誌謝…………………………………………………………………………………... 1
中文摘要…………………………………………………………………. ……….. 2-3
英文摘要…………………………………………………………………..……….. 4-6
目錄………………………………………………………………………..……….. 7-8
圖目錄……………………………………………………………………….……... ...9
碩士論文內容
第一章 緒論………………………………………………………… …………10-15
1.1 研究背景概論…………………………………………………………. 10-11
1.2 DSEK, DSAEK, nDSAEK 術式簡介………………………………… 11-12
1.3 共軛焦顯微鏡在DSAEK/ nDSAEK的應用………………………….12-13
1.4 飛秒雷射與角膜移植…………………………………………………….. 13
1.5 前房光干涉斷層儀…………………………………………………..…13-14
1.6 DSAEK的未解疑問………………………………………………………14
1.7 研究目的……………………………………………………………….14-15
第二章 研究方法與材料………………………………………………………..16-20
2. 1 藉由飛秒雷射完成角膜內層移植瓣……………………………………...16
2.2 DSAEK手術……………………………………………………… .....16-17
2.3 前房光干涉斷層儀………………………………………………….….…17
2.4 體內共軛焦顯微鏡………………………………………………….…17-18
2.5 組織切片檢查……………………………………………………………18
2.6 免疫組織化學染色……………………………………………………18-19
2.7 穿透式電子顯微鏡……………………………………………………… 19
2.8 實驗設計流程…………………………………………………………….20
第三章 研究結果…..…………………………………………………………...21-22
3.1 移植瓣厚度與總角膜厚度……………………………………………… 21
3.2 體內共軛焦顯微鏡……………………………………………………….21
3.3 Hematoxylin and eosin染色……………………………………………...22
3.4 免疫組織化學染色……………………………………………………….22
3.5 穿透式電子顯微鏡……………………………………………………….22
第四章 討論…..…………………………………………………………….... ..23-27
4.1 nDSAEK手術………………………………………………………...23-24
4.2 受贈者內皮細胞術後變化……………………………………………24-25
4.3 交界面模糊程度……………………………………………………... 25-26
4.4 實驗動物的選擇………………………………………………………… 26
4.5 本實驗的優勢與限制…………………………………………………26-27
4.6 未來實驗研究方向修正與延伸………………………………………… 27
第五章 結論…..……………………………………………………………........... 28
圖………………………………………………………………………………… 29-44
參考文獻…………………………………………………………………………. 45-51
dc.language.isozh-TW
dc.title利用體內共軛焦顯微鏡探討角膜內皮層移植術後之傷口癒合狀況zh_TW
dc.titleUsing In Vivo Confocal Microscopy to Detect the Wound Healing Process after DSAEK and NDSAEKen
dc.typeThesis
dc.date.schoolyear101-2
dc.description.degree碩士
dc.contributor.oralexamcommittee胡芳蓉,楊偉勛
dc.subject.keyword戴氏膜撕除角膜內皮層移植手術,無戴氏膜撕除角膜內皮層移植手術,共軛焦顯微鏡,交界面模糊程度,角膜內皮細胞,細胞凋亡,zh_TW
dc.subject.keywordDSAEK,nDSAEK,confocal microscopy,interface haziness,corneal endothelial cell,apoptosis,en
dc.relation.page51
dc.rights.note有償授權
dc.date.accepted2013-08-06
dc.contributor.author-college醫學院zh_TW
dc.contributor.author-dept臨床醫學研究所zh_TW
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