中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
39期
6386-6391
,共6页
吕全%袁均%蔡奕琪%刘轶
呂全%袁均%蔡奕琪%劉軼
려전%원균%채혁기%류질
生物材料%材料相容性%高度近视%屈光手术%后房型人工晶体%植入手术%对比敏感度%术后不良反应%视力稳定性
生物材料%材料相容性%高度近視%屈光手術%後房型人工晶體%植入手術%對比敏感度%術後不良反應%視力穩定性
생물재료%재료상용성%고도근시%굴광수술%후방형인공정체%식입수술%대비민감도%술후불량반응%시력은정성
lenses,intraocular%myopia%contrast sensitivity
背景:眼内屈光手术中有晶状体眼人工晶体植入已被用于屈光度过高及角膜厚度较薄的中高度屈光不正者,其具有可逆性和保留眼部调节力等优点。目的:通过与行准分子激光原位角膜磨镶手术矫正高度近视效果的对比,评价后房型有晶体眼人工晶体植入的安全性与稳定性。方法:纳入126例高度近视在校大学生,其中男女各63例,年龄(21.87±1.18)岁。将126例高度近视志愿者随机均分为试验组与对照组,试验组采用后房型有晶体眼人工晶体植入进行高度近视矫正,对照组采用准分子激光原位角膜磨镶手术进行高度近视矫正,随访1年观察两组裸眼视力、矫正视力、对比敏感度及不良反应,计算两组有效性指数与安全性指数。结果与结论:试验组有效性指数与安全性指数均优于对照组(P<0.05)。试验组随访1年明暗环境下的对比敏感度均高于术前,并且明暗环境下的对比敏感度均高于对照组。随访1年,对照组5例出现夜间视力下降及眩光,试验组1例出现夜间视力下降及眩光。表明后房型有晶体眼人工晶体植入在临床中是安全与稳定的,提高了视觉质量。
揹景:眼內屈光手術中有晶狀體眼人工晶體植入已被用于屈光度過高及角膜厚度較薄的中高度屈光不正者,其具有可逆性和保留眼部調節力等優點。目的:通過與行準分子激光原位角膜磨鑲手術矯正高度近視效果的對比,評價後房型有晶體眼人工晶體植入的安全性與穩定性。方法:納入126例高度近視在校大學生,其中男女各63例,年齡(21.87±1.18)歲。將126例高度近視誌願者隨機均分為試驗組與對照組,試驗組採用後房型有晶體眼人工晶體植入進行高度近視矯正,對照組採用準分子激光原位角膜磨鑲手術進行高度近視矯正,隨訪1年觀察兩組裸眼視力、矯正視力、對比敏感度及不良反應,計算兩組有效性指數與安全性指數。結果與結論:試驗組有效性指數與安全性指數均優于對照組(P<0.05)。試驗組隨訪1年明暗環境下的對比敏感度均高于術前,併且明暗環境下的對比敏感度均高于對照組。隨訪1年,對照組5例齣現夜間視力下降及眩光,試驗組1例齣現夜間視力下降及眩光。錶明後房型有晶體眼人工晶體植入在臨床中是安全與穩定的,提高瞭視覺質量。
배경:안내굴광수술중유정상체안인공정체식입이피용우굴광도과고급각막후도교박적중고도굴광불정자,기구유가역성화보류안부조절력등우점。목적:통과여행준분자격광원위각막마양수술교정고도근시효과적대비,평개후방형유정체안인공정체식입적안전성여은정성。방법:납입126례고도근시재교대학생,기중남녀각63례,년령(21.87±1.18)세。장126례고도근시지원자수궤균분위시험조여대조조,시험조채용후방형유정체안인공정체식입진행고도근시교정,대조조채용준분자격광원위각막마양수술진행고도근시교정,수방1년관찰량조라안시력、교정시력、대비민감도급불량반응,계산량조유효성지수여안전성지수。결과여결론:시험조유효성지수여안전성지수균우우대조조(P<0.05)。시험조수방1년명암배경하적대비민감도균고우술전,병차명암배경하적대비민감도균고우대조조。수방1년,대조조5례출현야간시력하강급현광,시험조1례출현야간시력하강급현광。표명후방형유정체안인공정체식입재림상중시안전여은정적,제고료시각질량。
BACKGROUND:Intraocular refractive operation with phakic intraocular lens implantation has been used in highly refractive errors patients with over-high diopter and thinner corneal thickness, which has the advantages of reversibility and retain the eye's accommodation. OBJECTIVE:To evaluate the safety and stability of posterior chamber phakic intraocular lens implantation in comparison with Lasik correction for high myopia. METHODS:Total y 126 col ege students with high myopia, 63 males and 63 females, aged (21.87±1.18) years, were randomly divided into test and control groups. In the test group, col ege students received posterior chamber phakic intraocular lens implantation, while those in the control group were subject to Lasik correction. During 1-year fol ow-up, naked vision, corrected visual acuity, contrast sensitivity, and postoperative untoward reaction were observed, and the effectiveness and safety indexes were calculated in the two groups. RESULTS AND CONCLUSION:The effectiveness and safety indexes in the test group were both superior to those in the control group (P<0.05). After 1 year of fol ow-up, the contrast sensitivity light and dark environment in the test group was significantly improved, which was also higher than that in the control group. Decreased night vision and glare was found in five cases of the control group and one case of the test group. These findings indicate that posterior chamber phakic intraocular lens implantation is safe and effective that can improve the visual quality in clinic.