甘肃医药
甘肅醫藥
감숙의약
Gansu Medical Journal
2014年
11期
816-818
,共3页
程芳%邱煦%陈凤华%闫爱民%李雪
程芳%邱煦%陳鳳華%閆愛民%李雪
정방%구후%진봉화%염애민%리설
缩小切口%超声乳化白内障术%术源性散光
縮小切口%超聲乳化白內障術%術源性散光
축소절구%초성유화백내장술%술원성산광
narrow incision%phacoemulsification%surgery source astigmatism
目的:探讨通过改变灌注套管与超声乳化针头的配套,缩小白内障超声乳化手术切口,减少术源性散光。方法:选取年龄相关性白内障患者98例(120眼),年龄52~80岁,晶状体混浊2-3级,按随机数字表法分为2组,A 组46例(60眼),B组52例(60眼)。A组将(美国Bausch&Lomb公司) Stellaris超声乳化仪的3.2mm超声乳化针头更换为1.8mm的针头,但仍用原3.2mm灌注套管,将手术切口减小到2.2 mm行同轴微切口白内障超声乳化联合人工晶状体植入术,B组行3.2 mm 传统同轴超声乳化联合人工晶状体植入术。术中记录超声乳化时间和能量,术后第1天、第1周和第1个月观察随访,记录术后的裸眼视力、散光改变、超声乳化时间及能量,并对所得数据进行分析。结果:术前与术后相比,角膜散光均有不同程度改变;术后第1天、第1周和第1个月,A组角膜散光均小于B组,差异有统计学意义(P<0.05)。视力变化:术后第1周,A组裸眼视力好于B组,两组之间存在统计学差异(P<0.05),术后第1天和第1个月视力无统计学差异(P>0.05)。平均超声乳化时间、有效超声乳化时间、平均超声乳化能量均无统计学差异(P>0.05)。结论:通过改变灌注套管与超声乳化针头的配套即可将传统3.2mm手术切口缩小至2.2 mm ,既满足人工晶体植入的要求,又有效减少术源性散光,早期视力恢复快,前房密闭稳定,手术安全可靠。
目的:探討通過改變灌註套管與超聲乳化針頭的配套,縮小白內障超聲乳化手術切口,減少術源性散光。方法:選取年齡相關性白內障患者98例(120眼),年齡52~80歲,晶狀體混濁2-3級,按隨機數字錶法分為2組,A 組46例(60眼),B組52例(60眼)。A組將(美國Bausch&Lomb公司) Stellaris超聲乳化儀的3.2mm超聲乳化針頭更換為1.8mm的針頭,但仍用原3.2mm灌註套管,將手術切口減小到2.2 mm行同軸微切口白內障超聲乳化聯閤人工晶狀體植入術,B組行3.2 mm 傳統同軸超聲乳化聯閤人工晶狀體植入術。術中記錄超聲乳化時間和能量,術後第1天、第1週和第1箇月觀察隨訪,記錄術後的裸眼視力、散光改變、超聲乳化時間及能量,併對所得數據進行分析。結果:術前與術後相比,角膜散光均有不同程度改變;術後第1天、第1週和第1箇月,A組角膜散光均小于B組,差異有統計學意義(P<0.05)。視力變化:術後第1週,A組裸眼視力好于B組,兩組之間存在統計學差異(P<0.05),術後第1天和第1箇月視力無統計學差異(P>0.05)。平均超聲乳化時間、有效超聲乳化時間、平均超聲乳化能量均無統計學差異(P>0.05)。結論:通過改變灌註套管與超聲乳化針頭的配套即可將傳統3.2mm手術切口縮小至2.2 mm ,既滿足人工晶體植入的要求,又有效減少術源性散光,早期視力恢複快,前房密閉穩定,手術安全可靠。
목적:탐토통과개변관주투관여초성유화침두적배투,축소백내장초성유화수술절구,감소술원성산광。방법:선취년령상관성백내장환자98례(120안),년령52~80세,정상체혼탁2-3급,안수궤수자표법분위2조,A 조46례(60안),B조52례(60안)。A조장(미국Bausch&Lomb공사) Stellaris초성유화의적3.2mm초성유화침두경환위1.8mm적침두,단잉용원3.2mm관주투관,장수술절구감소도2.2 mm행동축미절구백내장초성유화연합인공정상체식입술,B조행3.2 mm 전통동축초성유화연합인공정상체식입술。술중기록초성유화시간화능량,술후제1천、제1주화제1개월관찰수방,기록술후적라안시력、산광개변、초성유화시간급능량,병대소득수거진행분석。결과:술전여술후상비,각막산광균유불동정도개변;술후제1천、제1주화제1개월,A조각막산광균소우B조,차이유통계학의의(P<0.05)。시력변화:술후제1주,A조라안시력호우B조,량조지간존재통계학차이(P<0.05),술후제1천화제1개월시력무통계학차이(P>0.05)。평균초성유화시간、유효초성유화시간、평균초성유화능량균무통계학차이(P>0.05)。결론:통과개변관주투관여초성유화침두적배투즉가장전통3.2mm수술절구축소지2.2 mm ,기만족인공정체식입적요구,우유효감소술원성산광,조기시력회복쾌,전방밀폐은정,수술안전가고。
Objective:To observe the clinical outcome of phacoemulsification through 1.8 mm coaxial microincision and compare it with that of phacoemulsification through 3.2 mm coaxial incision. Methods: Sixty eyes of 46 patients with age-related cataract (grade Ⅲ lens opacity) at the age of 52 to 80 years were randomly divided into group A (n=60) and group B (n=60). Eyes in group A underwent phacoemulsification through 1.8 mm coaxial microincision and artificial lens implantation while those in group B underwent phacoemulsification through 3.2 mm coaxial incision and artificial lens implantation. Phaco power and time were recorded during operation. The patients were followed up in 1 day,1 week and 1 month after operation,during which corneal astigmatism,visual acuity of naked eyes, corneal endothelial cell count and complications were recorded. Results:No significant difference was found in the average phaco time(APT) ,effective phaco time(EPT) and average phaco power(AVE) between the two groups during operation(P>0.05) . The visual acuity of naked eyes was better in group A than in group B in the first week after operation(P<0.05) with no significant difference between the two groups on 1 day and in the first month after operation (P>0.05) . The surgical astigmatism in group A was less than that of group B in every time point (P<0.05).No statistically significant difference was found in the corneal endothelial cell count between the two groups in every time position after operation (P>0.05). Conclusion:Phacoemulsification through 1.8 mm coaxial microincision can reduce thecorneal astigmatism,rapidly restore the early.