Square-edge polymethylmethacrylate intraocular lens design for reducing posterior capsule opacification following paediatric cataract surgery: initial experience

Purpose: To compare the incidence and severity of development of posterior capsule opacification (PCO) following implantation of square‐edged polymethylmethacrylate (PMMA) or hydrophobic acrylic intraocular lenses (IOLs) following paediatric cataract surgery. Design: Prospective, consecutive, interventional, comparative, randomized and cross‐sectional study of 40 eyes of 32 children aged between 4 and 12 years who underwent phacoemulsification and posterior chamber IOL implantation. Methods: The patients were randomized into two groups of 20 eyes each. Group 1 eyes received a square‐edge hydrophobic acrylic IOL (Acrysof SA 60 AT, Alcon Surgical, Fort Worth, Texas), and Group 2 eyes received a square‐edge single‐piece PMMA lens (Aurolab SQ 3600 Aurolab IOL Division, Madurai, India) in the capsular bag. No eye underwent a primary posterior capsulotomy. The PCO density was evaluated on slitlamp retroillumination photographs by using POCOman software at 3, 6, 9 and 12 months post surgery. Results: The average percentage PCO on POCOman analysis was 51.23 for Group 1 and 49.49 for Group 2 (P = 0.09), and the average PCO severity grade was 1.34 in Group 1 and 1.12 in Group 2 (P = 0.08). Visual axis remained clear in 14 of 20 eyes with the acrylic lens as compared with 13 of 20 eyes with the PMMA lens. (P = 0.32). Conclusions: Square‐edge PMMA IOLs offer a significant cost advantage over acrylic lenses at similar rates of PCO formation following paediatric cataract surgery, which is of significant value in developing countries.     

Posterior capsule opacification after phacoemulsification: foldable acrylic versus poly(methyl methacrylate) intraocular lenses

PURPOSE: To study the effects of foldable acrylic and poly(methyl methacrylate) (PMMA) intraocular lens (IOL) implantation on posterior capsule opacification (PCO). SETTING: Department of Ophthalmology, Dokuz Eylül University School of Medicine, Izmir, Turkey. METHODS: This consecutive series comprised 157 eyes having phacoemulsification with implantation of a foldable acrylic IOL with rectangular optic edges and a 5.5 mm optic (AcrySof) (n = 80 eyes) or a PMMA IOL with rounded optic edges and 5.5 mm optic (n = 77). Evaluated were incidence, location, and degree of PCO. Mean postoperative follow-up was 17.8 months +/- 1.7 (SD) (range 16 to 22 months). RESULTS: Posterior capsule opacification occurred in 8.7% of eyes in the foldable acrylic IOL group and in 24.7% of eyes in the PMMA IOL group. The difference between the 2 groups was statistically significant (P < .01). Centrally located PCO was significantly lower in the acrylic group (P < .01). There were 3 eyes with severe PCO in the PMMA group and none in the acrylic group. Anterior capsule contraction and fibrosis were present in 4 eyes in the PMMA group but none in the acrylic group. Soemmering's ring cataract formation was detected in 3 eyes, all with the AcrySof IOL. CONCLUSION: In addition to its optic material and rectangular optic edges, the AcrySof IOL provides additional advantages in lowering the incidence of PCO compared with rounded-edge PMMA IOLs.     

Primary IOL implantation in children: a risk analysis of foldable acrylic v PMMA lenses

BACKGROUND:/aims: To compare the relative risks of poly (methylmethacrylate) (PMMA) and soft acrylic (AcrySof) primary intraocular lens (IOL) implantation in paediatric cataract surgery. METHODS: A retrospective analysis of clinical data was performed on eyes of 61 infants and children who underwent cataract surgery with primary IOL implantation. Age at operation ranged from 3 weeks to 15 years. Mean follow up duration was 24.5 months (range 0.5-68 months). Factors examined included type of IOL (PMMA, acrylic), performance of a primary posterior continuous curvilinear capsulorhexis (PCCC) or capsulotomy with limited anterior vitrectomy, perioperative complications, and subsequent intervention for posterior capsule opacification (PCO). Risk factors for perioperative complications were examined with 2x2 tables to give odds ratios (OR) as measures of association. A survival analysis was performed to assess risk of subsequent intervention for PCO with different IOL types. Relative risks (hazards) and confidence intervals (CI) were calculated with Cox regression to adjust for potential confounding. RESULTS: Compared to acrylic, PMMA IOLs were significantly associated with perioperative complications (OR 5.2, 95% CI 1.4 to 19, p = 0.01). However, IOL and type of section were highly correlated factors, and this finding may reflect risks associated with larger scleral wounds used for PMMA IOLs. No statistically significant difference in risk of subsequent intervention for PCO was found between different IOL types. Mean times till intervention for PMMA and acrylic IOLs were 30.1 months (95% CI 22 to 38) and 19.8 months (95% CI 12 to 27) respectively (log rank test statistic 1.53, one degree of freedom, p = 0.22). At 12 months post-implant surgery, 76% (95% CI 59 to 93) of PMMA cases and 54% (95% CI 35 to 72) of acrylic cases had not required intervention for PCO; these proportions fell to 55% (95% CI 35 to 75) and 38% (95% CI 14 to 61) for PMMA and acrylic cases respectively at 2 years post-surgery. After adjustment for age at surgery, primary posterior capsulorhexis, and perioperative complications relative risk of intervention after acrylic IOL implantation was 1.6 (95% CI 0.66 to 3.9, p = 0.29). CONCLUSION: Primary implantation of foldable soft acrylic IOLs in paediatric eyes may allow fewer perioperative complications than rigid PMMA IOLs. Short term safety profiles of primary implantation in paediatric cataract surgery are otherwise comparable for PMMA and soft acrylic IOLs.     

不同设计人工晶状体植入术后3年后囊膜混浊的研究

目的研究不同材料和不同设计的人工晶状体植入术后3年的后囊膜混浊(posterior capsular opacification,PCO)发生率及PCO形态。方法回顾性研究132眼老年性白内障患者,由同一医生进行超声乳化联合人工晶状体(in-traocular lens,IOL)植入术,根据IOL的不同分为4组:Storz Hydroview H60M组(33眼),Silicone折叠式硅胶IOL组(29眼),AcrySof三片式IOL组(36眼)和聚甲基丙稀酸甲酯(poly-methyl methacrylate,PMMA)组(34眼)。术后3年随访患眼的最佳矫正视力(best corrected visual acuity,BCVA),扩瞳后采集PCO数码图像,分析不同IOL组PCO的形态及PCO发生率。结果各种IOL的PCO形态各异,H60M组和AcrySof组分别有10眼和15眼后囊形成皱折,而Silicone和PMMA组为片状混浊。虽然各组BCVA和BCVA下降率差异没有显著性(P>0.05),但PCO发生率差异有非常显著性,分别是AcySof组5.6%,Silicone组30.3%,H60M组31%和PMMA组55.9%。结论AcrySof疏水丙烯酸酯三片式折叠IOL,有直角边缘设计,术后3年能明显降低PCO的发生。     

Nd:YAG capsulotomy rates after use of the AcrySof acrylic three piece and one piece intraocular lenses

BACKGROUND/AIM: Acrylic lens size and shape may influence the rate of posterior capsule opacification (PCO) and need for Nd:YAG capsulotomy. The aim of this study is to compare the Nd:YAG capsulotomy rate of the three piece acrylic/PMMA AcrySof MA series lens with the one piece acrylic AcrySof SA series lens. METHODS: 434 eyes of 329 patients who had cataract extraction and implantation of one of four types of intraocular lenses (IOLs) were evaluated for rate of Nd:YAG capsulotomy. 176 eyes received the acrylic AcrySof MA30AC IOL, 71 eyes the acrylic AcrySof MA60AC IOL, 45 eyes the acrylic AcrySof SA30AL IOL, and 142 eyes the acrylic AcrySof SA60AT IOL. RESULTS: The rates of Nd:YAG capsulotomy with the three piece IOL (MA30AC/MA60AC) and the one piece IOL (SA30AL/SA60AT) were 1.2% and 2.1% at 6 months, 2.8% and 5.9% at 12 months, and 3.6% and 7.5% at 24 months, respectively. The incidence of Nd:YAG capsulotomy was higher in patients who received the one piece IOL (p=0.01, log rank test). There was no difference in Nd:YAG capsulotomy rates when comparing lens optic size, age, sex, history of pars plana vitrectomy, and diabetes mellitus. CONCLUSIONS: This study shows a greater incidence of Nd:YAG capsulotomy in patients who receive one piece acrylic AcrySof lenses when compared to those who receive three piece acrylic AcrySof lenses.     

Neodymium:YAG capsulotomy rates following phacoemulsification with implantation of PMMA, silicone, and acrylic intraocular lenses

BACKGROUND AND OBJECTIVE: Posterior capsular opacification (PCO) is the most common visually disabling sequela of modern cataract surgery. Methods of reducing its incidence include the development of newer surgical techniques and intraocular lens (IOL) materials and designs. The aim of this study was to compare the incidence and time interval of development of PCO, and the requirement of laser capsulotomy in patients implanted with a polymethylmethacrylate (PMMA), silicone, or acrylic IOL. PATIENTS AND METHODS: The data of 340 consecutive patients who underwent phacoemulsification and implantation ofa PMMA, silicone, or acrylic intraocular lens were analyzed. The aim of this study was to compare the incidence and time interval of development of PCO, and the requirement of laser capsulotomy in patients implanted with a PMMA, silicone, or acrylic IOL. RESULTS: The incidence of PCO was found to be significantly less in the acrylic group (6.5% as compared to 21.74% and 26.6% in the PMMA and silicone groups, respectively; P = 0.01297 and 0.0039). Most patients (65%) exhibiting PCO in the PMMA group developed it within the first six months. In the silicone group, development of PCO was delayed. In 60% of patients, it appeared 18 months after surgery. Neodymium:YAG capsulotomy was required in 45% and 60% of patients developing PCO in the PMMA and silicone groups, respectively, while it was required in only 1 of the 4 patients developing PCO in the acrylic group. CONCLUSION: This study indicates that implantation of an acrylic IOL helps reduce the incidence of PCO as well as the need for Nd:YAG capsulotomy. PMMA IOLs require Nd:YAG capsulotomy earlier in the postoperative period as compared to silicone IOLs.     

Role of posterior capsulotomy with vitrectomy and intraocular lens design and material in reducing posterior capsule opacification after pediatric cataract surgery

PURPOSE: To study the effect of primary posterior capsulotomy with anterior vitrectomy (PPC + AV) and intraocular lens (IOL) design and material on the development of posterior capsule opacification (PCO) after pediatric cataract surgery. SETTING: Tertiary care institution in India. PATIENTS: Sixty-four eyes of 52 children ranging in age from 3 months to 12 years who had cataract extraction with IOL implantation were prospectively evaluated for a minimum postoperative period of 2 years. METHODS: Thirty-two eyes received a hydrophobic acrylic lens with a truncated, square edge and 32, a single-piece poly(methyl methacrylate) (PMMA) lens that was not heparin surface modified. Sixteen eyes in each IOL group had PPC + AV; in the remaining 16 eyes in each group, the posterior capsule was left intact. RESULTS: Postoperatively, 25 eyes in the intact capsule group and 5 in the PPC + AV group developed PCO; the difference between groups was significant (P<.05). Of eyes with an intact capsule, 12 with an acrylic IOL and 13 with a PMMA IOL developed PCO (P>.05). In the PPC + AV group, 2 eyes with an acrylic IOL and 3 with a PMMA IOL developed PCO (P>.05). Overall, 14 eyes with an acrylic lens and 16 eyes with a PMMA lens developed PCO (P>.05). After surgery, there was a significant short-term delay in the development of PCO in the acrylic group (14 eyes; mean 6.66 months +/- 1.57 [SD]) compared to the PMMA group (16 eyes; mean 3.16 +/- 0.83 months) (P<.05). CONCLUSIONS: It is the management of the posterior capsule rather than IOL design and material that influences the incidence of PCO after cataract surgery in children. Development of PCO in the postoperative period was delayed with a hydrophobic acrylic IOL with square edges compared with a PMMA lens without square edges.     

Secondary membrane formation after cataract surgery with primary intraocular lens implantation in children

To evaluate the risk factors for secondary membrane (SM) formation after congenital cataract surgery with intraocular lens (IOL) implantation. A retrospective non-interventional comparative study. Thirty-nine patients (63 eyes) aged 1–135 months. The study included patients who underwent cataract extraction and primary IOL implantation between 1994 and 2001 at the University Hospital. The postoperative follow-up was 6–24 months. Thirty-three eyes received a poly(methyl methacrylate) (PMMA) IOL without square edges, 29 eyes received a hydrophobic acrylic IOL with truncated square edges (AcrySof), and there was no data for IOL type in one eye. Thirty-nine eyes had primary posterior capsulotomy (PPC) and anterior vitrectomy (AV) and in 24 eyes the posterior capsule was left intact. Cox proportional hazard regression analysis was performed to identify significant risk factors for SM formation, and Wilcoxon test to evaluate the difference in time from surgery to SM formation. SM developed in 24 eyes (38 %)—58 % of eyes with an intact posterior capsule and 26 % of eyes having PPC and AV, 42 % of eyes with a PMMA IOL, and 34 % of eyes with an AcrySof lens. In multivariate Cox regression analysis intraoperative PPC and AV (P = 0.02) and AcrySof lens implantation (P = 0.097) were associated with decreased postoperative incidence of SM formation. Median time until SM development was 2.9 months with PMMA IOLs (range 1–17 months) and 6 months with AcrySof lenses (range 1–21.8 months) (P = 0.037). Posterior capsule management as well as IOL design and material influence the incidence and the timing of SM formation after primary IOL implantation in children.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

青光眼白内障联合术植入不同材料人工晶状体效果评价

目的比较青光眼白内障联合术中植入不同材料人工晶状体（IOL）的临床效果。方法回顾性分析行青光眼白内障联合术70例（76眼），其中植入PMMA IOL30例（36眼），硅胶IOL23例（23眼），丙烯酸酯折叠IOL17例（17眼）。对治疗效果进行评价，平均随访期限为10．5月。结果3组间术后眼压和最佳矫正视力差异无统计学意义。前房纤维素样渗出物和IOL表面沉积物发生率，硅胶组高于PMMA组和丙烯酸酯组，但差异无统计学意义。后发障发生率，丙烯酸酯组和硅胶组显著低于PMMA组，差异有统计学意义。结论行青光眼白内障联合术植入PMMA，硅胶与丙烯酸酯IOL在降眼压和提高视力方面具有相似的效果。但硅胶IOL的前房纤维素样渗出物及IOL表面沉积物发生率高于PMMA和丙烯酸酯IOL。丙烯酸酯和硅胶IOL的后发障发生率低于PMMA IOL。     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.     

不同丙烯酸材料的人工晶状体对后发性白内障的影响

目的 探讨三种不同的丙烯酸材料的人工晶状体应用于白内障超声乳化吸除联合人工晶状体植入术后对后发性白内障的影响作用.方法 超声乳化白内障吸除联合人工晶状体植入术的960例白内障患者(964只眼),Sensar组310只眼,Acrysof三片组332只眼,Acrysof一片组322只眼,术后定期随访18～28个月,观察视力、后发性白障的发生情况.结果 术后随访24月时,发生1级以上后囊膜混浊SensarIOL组的发生率(13.5%),明显高于Acrysof一片式IOL组及Acrysof三片式IOL组的发生率(7.5%,3.7%).经卡方检验,P值均<0.05,有显著性差异,而Acrysof三片式IOL组后囊膜混浊的发生率较Aerysof 一片式IOL组高,P<0.05.结论 AcrySof丙烯酸式一片式人工晶状体植入后出现后发性白内障的发生率在三组中最低.可以减少后发性白内障的发生降低Nd:YAG激光的使用率,提高手术效果,是现代白内障手术可选择的理想的人工晶状体.