瞳孔成形联合虹膜夹人工晶状体植入术治疗外伤性无晶状体眼疗效观察

目的 观察瞳孔成形联合虹膜夹人工晶状体植入术治疗外伤性无晶状体眼的疗效.方法 回顾性分析在我院采用瞳孔成形联合虹膜夹人工晶状体植入术治疗的外伤后无晶状体眼患者17例17眼的临床资料.观察术后视力、角膜内皮细胞计数、眼压、人工晶状体位置、瞳孔情况及术后并发症.结果 17例患者均顺利修补损伤虹膜,瞳孔成形后成功植入虹膜夹人工晶状体,未发生严重手术并发症,人工晶状体位置稳定.术后6个月裸眼视力(0.52 +0.17),较术前视力(0.04±0.02)及术前最佳矫正视力(0.44±0.13)提高.术后6个月角膜内皮细胞计数为(1993.88±127.24)个·mm-1,较术前(2178.88±132.61)个·mm-2减少(P＜0.05),但术后未发现角膜失代偿.术前眼压(15.91 ±2.73)mmHg(1 kPa=7.5 mmHg)与术后眼压(16.69±2.61) mmHg无明显差异(P＞0.05).术后瞳孔大小(4.4±0.2)mm较术前(5.5 +0.3)mm缩小(P＜0.05),患者术后无明显畏光、眩光、复视等不适症状.结论 瞳孔成形联合虹膜夹人工晶状体植入术是治疗外伤虹膜损伤并无有效晶状体囊膜支持的无晶状体眼的安全有效方法.     

四环单结瞳孔成形术在青光眼白内障联合手术中的应用

目的：观察四环单结瞳孔成形术在青光眼白内障联合手术中的应用效果。

方法：收集2015-08/2018-03我院青光眼急性发作后大瞳孔且合并有白内障的患者28例30眼。所有患者均行白内障超声乳化吸除与人工晶状体植入,联合房角分离或小梁切除术及四环单结瞳孔成形术治疗。观察术前及术后7d的矫正视力、瞳孔直径、术中及术后并发症,并进行术前和术后3mo的视觉质量调查。

结果：术后7d矫正视力较术前有明显提高,且术后无复视、眩光等视觉不良反应。术前瞳孔直径5.9±0.25mm,术后7d为4.1±0.13mm(P<0.05)。术后3mo视觉质量较术前有较大提高(P<0.05)。术中并发症：有5例5眼缝合出现虹膜分层撕脱,1例1眼成形瞳孔旁出现小裂孔,3例3眼虹膜根部少量渗血,经相应处理后均恢复良好。术后早期并发症以前房炎症反应常见,抗炎治疗后炎症吸收。长期观察未见瞳孔区线结松动、脱落。

结论：四环单结瞳孔成形术操作简单、安全、有效,能明显消除因青光眼急性发作后由大瞳孔引起的复视、眩光等视觉障碍。     

Surgical management of iris defects with prosthetic iris devices

PURPOSE: To evaluate the safety and efficacy of surgical implantation of prosthetic iris devices in patients with iris deficiency. METHODS: Nine patients with traumatic iris defects, congenital aniridia or iris coloboma, and surgical or optical iridectomies were included in a noncomparative case series. Cataract surgery with intraocular lens and prosthetic iris implantation was performed in 10 eyes. The visual acuity, subjective degree of glare disability, postoperative anatomic results, and intraoperative and postoperative complications were evaluated. RESULTS: The mean follow-up was 17.75 months (range 4-48 months). Best-corrected visual acuity improved in nine of 10 eyes (90%) and remained unchanged in one eye. Glare subjectively improved in four of five eyes (80%) of patients complaining of glare preoperatively. All eyes achieved the desired anatomic result. Intraoperative complications included one anterior capsular tear. Postoperative complications included a short period of mild postoperative anterior uveitis in four eyes. Secondary glaucoma was absent. CONCLUSION: In patients with iris deficiency, implantation of prosthetic iris device, and intraocular lens implant following cataract surgery appears to be safe and effective in reducing glare disability and improving visual outcomes.     

Outcomes of prosthetic iris implantation in patients with albinism

PURPOSE: To assess the safety and efficacy of implantation of prosthetic iris devices in patients with albinism. SETTING: Private practice, Cincinnati, Ohio, USA. METHODS: This retrospective noncomparative case series comprised 13 eyes of 8 patients with diminished pigment epithelium of the iris secondary to albinism. All eyes had anterior segment surgery with intraocular lens (IOL) and prosthetic iris device implantation. Eleven eyes received an endocapsular-type iris reconstruction implant (Morcher aniridia interdigitating rings), and 2 eyes (1 patient) received a combined iris-IOL device (Ophtec model 311). The visual acuity, subjective glare reduction, postoperative anatomical outcomes, and intraoperative or postoperative complications were reviewed. RESULTS: All eyes achieved the desired anatomic result. The best corrected visual acuity improved in 8 of 13 eyes, remained stable in 3 eyes, and decreased in 2 eyes. Glare and photophobia improved subjectively in 6 of 8 patients, remained unchanged in 1 patient, and increased in 1 patient after implantation of an artificial iris diaphragm. There were no intraoperative or postoperative complications. CONCLUSIONS: Implantation of prosthetic iris devices appears to be useful in the management of patients with iris deficiency secondary to albinism. The procedure was safe and particularly effective in reducing glare and photophobia in most patients.     

Endocapsular iris reconstruction implants for acquired iris defects: a clinical study

PURPOSE: To report the clinical efficacy, safety, and long-term follow-up data on the use of endocapsular iris reconstruction implants (IRIs) during cataract surgery in patients with acquired iris defects. METHODS: Single centre, retrospective, noncomparative, interventional case series. Five eyes of four patients with acquired iris defects and visually significant cataracts underwent clear cornea phacoemulsification and intraocular lens (IOL) implantation combined with insertion of endocapsular IRI. Data on the best-corrected visual acuity (BCVA), degree of preoperative and postoperative glare, photophobia, surgical complications, and long-term implant stability were analysed. Results: In all patients, IRI were successfully placed within the capsular bag during cataract surgery. There were no intraoperative or postoperative complications. Mean follow-up period was 29 months (range, 16-42). BCVA, subjective glare, and photophobia improved in all five eyes. Desired anatomic results were achieved in all of them. CONCLUSIONS: In patients with acquired iris defects, implantation of endocapsular IRI during cataract surgery appears to be a safe and effective procedure. At a mean time gate of 29 months, both IOLs and IRI appeared to remain stable within the capsular bag.     

Coreoplasty and Artisan Intraocular Lens Implantation for Mydriasis and Aphakic Correction in Post-traumatic Vitrectomized Eyes

 PURPOSE: To evaluate the efficacy and safety of using coreoplasty, and an iris-supported Artisan intraocular lens (IOL), for mydriasis and aphakic correction in post-traumatic vitrectomized eyes. METHODS: A total of 17 aphakic patients were admitted between April 2009 and April 2010 to the ophthalmologic department of Xiamen Eye Center. All eyes had previously received lens removal and vitrectomy. After the retina stabilized and corrected visual acuity improved, the iris was sutured. The Artisan IOL was fixated onto the iris surface. Patients were followed-up at one day, one week, one month and three months postoperatively. The following outcomes were assessed: symptoms of photophobia and glare, uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), intraocular pressure (IOP), endothelial cell density (ECD). The diameter of pupil and the anterior chamber depth (ACD) were measured by the anterior segment optical coherence tomography (OCT). RESULTS: Artisan IOLs were successfully implanted in all aphakic eyes. Postoperatively, improvement was observed in photophobia and glare symptoms. UCVA was enhanced in all patients (six eyes had better UCVA postoperatively than BCVA preoperatively). However, there were no significant changes in IOP. Mean loss of ECD was 336.06/mm2. Mean postoperative pupil diameter was 3.67±0.41mm, compared with 5.67±0.57mm preoperatively (P<0.05). Mean ACD was reduced by 0.88mm (3.38±0.33mm preoperatively vs 2.50±0.35mm postoperatively, P<0.05). CONCLUSION: Surgery that combined coreoplasty and Artisan IOL implantation was a safe and effective treatment for correcting aphakia and mydriasis in post-traumatic vitrectomized eyes.     

Prosthetic iris implantation for congenital, traumatic, or functional iris deficiencies.

PURPOSE: To determine the efficacy and safety of surgical implantation of prosthetic iris devices in patients with anatomic or functional iris deficiencies. SETTING: Cincinnati Eye Institute, Cincinnati, Ohio, USA. METHODS: Twenty-five patients were enrolled in an interventional prospective noncomparative case series. Twenty-eight eyes had prosthetic iris diaphragm implantation for traumatic iris defects, congenital aniridia or iris coloboma, herpetic iris atrophy, surgical iris loss, or ocular albinism. Prosthetic iris implantation was performed with phacoemulsification and intraocular lens (IOL) implantation in 20 eyes, secondary IOL implantation in 6 eyes, and IOL exchange in 1 eye. A single pseudophakic eye with disabling glare secondary to traumatic aniridia had secondary prosthetic iris implantation alone. The surgical ease of insertion, intraoperative and postoperative complications, postoperative anatomic results, visual acuity, and subjective glare reduction were evaluated. RESULTS: Patients were followed postoperatively for a mean of 10.2 months (range 1.4 to 25.7 months). All eyes achieved the desired anatomic result. Visual acuity was improved in 22 of 28 eyes (79%), unchanged in 5 eyes, and worsened by a single line in 1 eye. Patients were surveyed postoperatively to determine the change in glare disability. The severity of glare disability was subjectively improved in 23 of 24 patients (96%) who responded to the survey. Intraoperative complications included 3 fractured implants as well as an incomplete or torn capsulorhexis in 3 eyes. Postoperative complications included transient hypotony in 2 eyes, mild persistent inflammation in 1 eye, and macular edema followed by a retinal detachment in 1 eye with recent severe trauma. CONCLUSIONS: Implantation of prosthetic iris devices improved postoperative outcomes by reducing glare disability and, in selected cases, by correcting aphakia. Although operating on traumatized, congenitally aniridic, or uveitic eyes presents special challenges, implantation of prosthetic iris devices appears to be a safe and effective method for reducing the ubiquitous glare in patients with iris deficiency.     

Black diaphragm aniridia intraocular lens for aniridia and albinism

Background Our aim was to assess the safety and efficacy of primary and secondary implantation of a black diaphragm aniridia intraocular lens (IOL) in patients that lacked a complete iris diaphragm.Methods This was a retrospective non-comparative study of six eyes in five patients with iris defects. The causes of such defects included congenital aniridia, traumatic aniridia, and oculocutaneous albinism. Three eyes underwent primary implantations of a black diaphragm IOL, and three eyes were given secondary implantations. The visual acuity, subjective severity of glare, postoperative anatomical outcome and any intraoperative or postoperative complications were reviewed.Results The mean follow-up period was 20.6 months (range 3–29 months). All patients showed stable or improvement in best-corrected visual acuity postoperatively. Glare and photophobia had improved subjectively in all patients after implantation of the black diaphragm IOL. Intraoperative complication included one case of hyphaema and iris damage during insertion of the IOL. Postoperative complications included intraocular inflammation with choroidal detachment, secondary glaucoma, and persistent epithelial defect after surgery. None of the patients developed decentration of IOL after surgery.Conclusion The black diaphragm aniridia IOL is useful in the management of the condition in patients with iris deficiency including oculocutaneous albinism. Intraoperative and postoperative complications are not uncommon, and patients should be monitored carefully in the perioperative period.     

虹膜修补瞳孔成形术的临床应用

目的探讨眼外伤或手术致虹膜损伤者进行显微虹膜修补瞳孔成形术的临床手术技巧。方法回顾性分析2010年9月至2013年10月,眼部外伤或手术致虹膜根部断离,虹膜缺损,导致瞳孔异常者施行显微虹膜修补瞳孔成形术12例（12眼）,记录患者术前、术后的视力,瞳孔形状和位置,手术并发症的发生情况。结果随访6～12个月,术后视力有不同程度提高,术后畏光和眩目等症状明显减轻,瞳孔正常生理功能恢复,未发生严重并发症。结论虹膜修补瞳孔成形术是一种比较复杂的手术,在提高患者视力的同时,能够消除畏光、眩目的症状,能最大程度地适应自然光线,提高视觉质量,改善患者外观。     

Surgical management of acute angle-closure glaucoma after toric implantable contact lens implantation

A case of pupillary block after implantation of an implantable contact lens (ICL) is reported, and surgical management and prevention are discussed. In a myopic patient, the best corrected visual acuity in the right eye was 20/50 with -15.50 -3.00 x 175. After uneventful implantation of an ICL, painful acute glaucoma developed with an intraocular pressure beyond measurable values. Apparent anterior vaulting of the ICL suggested a sizing problem. In a situation of a mid-wide dilated pupil, immediate explantation of the ICL was performed. Then, using a preoperative iris photography as guidance, an anterior chamber iris-claw toric phakic intraocular lens was implanted. On postoperative examination, the anterior chamber was deep, the angle open, the natural lens clear, and uncorrected visual acuity was 20/40.     

Open-sky pupilloplasty during phakic penetrating keratoplasty to treat a fixed, dilated pupil

We report a technique in which penetrating keratoplasty is performed in conjunction with open-sky pupilloplasty in a phakic patient. The technique was used in a 27-year-old man with poor vision and severe light sensitivity in the left eye dating back to an episode of presumed herpes simplex keratouveitis 13 years previously. Examination showed a best corrected visual acuity of 20/40, a paracentral midstromal corneal scar, a fixed dilated pupil, and a clear lens. Postoperatively, the pupil was relatively round with a diameter of approximately 4.0 mm, the cosmetic result was favorable, the photophobia had resolved, and the lens and corneal transplant were clear.     

透明角膜切口有晶状体眼虹膜夹型人工晶状体植入治疗高度近视

目的：研究透明角膜切口有晶状体眼虹膜夹型人工晶状体植入治疗高度近视的临床疗效和安全性。

方法：对20例28眼高度近视患者表面麻醉下行透明角膜切口虹膜夹型人工晶状体植入术,观察术中和术后并发症、术后视力、眼压、屈光度数、角膜内皮计数、人工晶状体稳定性及晶状体混浊情况。

结果：高度近视患者28眼均顺利植入了虹膜夹型人工晶状体,术中无并发症发生,术后裸眼视力均达到或超过术前最佳矫正视力。术后随访6mo,所有植入的人工晶状体均基本位于正位,无明显倾斜、偏位。未发现白内障、葡萄膜炎、黄斑囊样水肿及视网膜脱离等并发症。

结论：在具备熟练的眼科显微手术技巧的前提下,有晶状体眼虹膜夹型人工晶状体植入,有较好的预测性及稳定性,可获得满意的术后视力,术后并发症较少,是治疗高度近视患者安全、有效的方法。     

Safety of an artificial iris in a phakic eye

This case report describes the one-year results of the implantation of a sectorial and foldable artificial iris in a phakic eye. To our knowledge, this is the first such report with a follow-up of 1 year. No perioperative or postoperative complications were seen. Corrected distance visual acuity remained unchanged (left eye, 1.5/10), the subjective complaints of glare and photophobia improved considerably, and the patient was very satisfied with the aesthetic result.     

Functional and cosmetic outcomes of combined penetrating keratoplasty and iris reconstruction lens implantation in eyes with a history of trauma

PURPOSE: To determine the functional and cosmetic outcomes of combined iris reconstruction lens (Ophtec) implantation and penetrating keratoplasty (PK) in eyes with acquired partial or complete aniridia. SETTING: Jules Stein Eye Institute and the Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA. METHODS: In a prospective nonrandomized single-center interventional case series, efficacy measures included improvement in cosmesis and reduction in glare, star bursts, and photophobia. Safety measures included changes in best corrected visual acuity (BCVA), reports of adverse events, and surgical complications. RESULTS: The 9 eyes in the study had a history of penetrating or blunt trauma and were aphakic or in need of cataract surgery. Corneal pathologies necessitating transplantation included scarring, decompensation, or failure of a previous graft. Postoperatively, all patients were pleased with the cosmetic improvement of the study eye and all reported a reduction in visual disturbances. By the final follow-up examination, the BCVA improved in 4 patients but worsened in 5. Three adverse events were reported. There were no intraoperative surgical complications. The most serious postoperative complications were a pressure spike leading to loss of light perception, corneal graft rejection, and graft failure. The most common postoperative problem was surgically induced irregular corneal astigmatism. CONCLUSIONS: Ophtec iris reconstruction lens implantation and simultaneous PK reduced visual disturbances and improved the aesthetic appearance of the eyes. The long-term safety of the procedure, judged by BCVA and postoperative complications, was mixed, with both good and bad outcomes.     

Artificial iris-lens diaphragm in reconstructive surgery for aniridia and aphakia

PURPOSE: To determine the efficacy and safety of surgical implantation of artificial iris-lens diaphragm in patients with anatomic or functional iris deficiencies, aphakia or cataract. SETTING: Svyatoslav Fyodorov MNTK Eye Microsurgery, Cheboksary, Russia. METHODS: Twenty eyes of 19 consecutive patients with combined iris and lens pathology of traumatic or congenital etiology were identified for an interventional noncomparative case series. The newly proposed model of an elastic iris-lens diaphragm with a colored haptic and additional support elements was implanted using various fixation approaches. RESULTS: Fifteen eyes (75%) experienced improvement in corrected visual acuities. The best spectacle-corrected visual acuity (BSCVA) in 2 eyes did not change, while the uncorrected visual acuity (UCVA) in these eyes increased. There were 3 eyes in which BSCVA deteriorated with no change or even slight improvement in UCVA. All patients were satisfied with the cosmetic results of the surgery and reported a decrease in glare and photophobia. There was 1 intraoperative complication of vitreous hemorrhage. Postoperatively, 2 cases of hyphema, 1 case of ciliochoroidal detachment, 4 eyes with exaggerated immediate postoperative reaction, and 1 eye with persistent low-grade cyclitis were observed. In 1 eye, there was persistent intraocular pressure rise. One eye showed signs of cystoid macular edema. No iris-lens diaphragm decentrations and no new or extensions of old retinal detachments were seen during the follow-up period. CONCLUSIONS: Artificial iris-lens diaphragm implantation effectively improved postoperative outcomes by correcting aphakia, reducing glare disability, and addressing cosmetic issues faced by iris-deficient, and aphakic or cataract patients. Although the iris-lens diaphragm appears to be safe, long-term results must be clarified in studies with longer follow-up and a larger patient population.     

Iris reconstruction combined with iris-claw intraocular lens implantation for the management of iris-lens injured patients

Aim:To study the efficiency and safety of iris reconstruction combined with iris-claw intraocular lens (IOL) implantation in the patients with iris-lens injuries.Results:Uncorrected VA (UCVA) in all injured eyes before combined surgery was equal to or <20/1000. Within a 1.1–4.2-year follow-up period, a significant increase, equal to or better than 20/66, in UCVA was observed in six (55%) cases, and in best-corrected VA (BCVA) was observed in nine (82%) cases. Postoperative BCVA was 20/40 or better in seven cases (64%). After combined surgery, the iris returned to its natural round shape or smaller pupil, and the iris-claw IOLs in the 11 eyes were well-positioned on the anterior surface of reconstructed iris. No complications occurred in those patients.Conclusions:Iris reconstruction combined with iris-claw IOL implantation is a safe and efficient procedure for an eye with iris-lens injury in the absence of capsular support.     

前房型虹膜夹人工晶状体植入术治疗无足够囊膜支撑的无晶状体眼的疗效和安全性

目的 探讨前房型虹膜夹人工晶状体植入术治疗无足够囊膜支撑的无晶状体眼的疗效和安全性。方法 选择河北省眼科医院白内障科2013年1月至2020年12月行晶状体摘出一期或二期植入前房型虹膜夹人工晶状体的患者53例62眼作为研究对象,62眼患者均为无足够囊膜支撑的无晶状体眼。术后随访3～9(5.68±1.29)年,收集患者手术前和末次随访裸眼视力(UCVA)、等效球镜度、眼压、前房深度、人工晶状体眼内固定位置及稳定性、角膜内皮细胞密度(ECD)、术后并发症等指标和临床信息。评价前房型虹膜夹人工晶状体植入术治疗无足够囊膜支撑的无晶状体眼的疗效和安全性。结果 术前62眼UCVA(logMAR)为1.55±0.56,术后为0.23±0.15,术后UCVA较术前显著提高(t=18.64,P=0.00)。术后和末次随访UCVA (logMAR)(0.22±0.14)比较,差异无统计学意义(t=1.43,P=0.16),患者术后视力保持稳定。术后末次随访1眼等效球镜度为-1.25 D(为根据另一眼预留),等效球镜度-1.00～<-0.50 D者10眼,-0.50～+0.50 D者51眼。62眼术前...     

粘连性小瞳孔白内障超声乳化吸除及人工晶状体植入术

目的探讨粘连性小瞳孔白内障超声乳化吸除手术方法及技巧。方法对36例(42眼)粘连性小瞳孔白内障行超声乳化吸除及人工晶状体植入术,术中不分离虹膜后粘连,利用拦截劈裂法乳化晶状体核,通过4mm大小瞳孔完成手术。结果所有病例视力有不同程度提高,获得生理性圆或近圆瞳孔,主要并发症包括角膜内皮水肿,前房纤维素渗出。结论采用本方法治疗粘连性小瞳孔白内障操作相对简单,术后反应轻,并发症少。     

瞳孔整复术在人工晶体植入中的应用

目的：对临床上遇到的合并有虹膜缺损、瞳孔散大、瞳孔移位的无晶体眼或白内障病例,植入人工晶体的内时行瞳孔整复术,以恢复瞳孔的圆形及居中,提高术后视力并预防单眼复视、眩光等。方法：9点至3点方位的虹膜缺损及瞳孔上移者用10－0聚丙烯缝线直接在上方切口处行虹膜缝合（开放式）;3点至9点方位的虹膜缺损则采用前房外缝合虹膜（闭合式）。结果：22例中术后视力0．5以上者占65％,瞳孔接近圆型占67％,瞳孔直径小于等于3mm占73％,瞳孔基本居中占67％。结论：人工晶体植入的同时进行瞳孔整复术,可以使各种原因引起的瞳孔变形恢复接近正常的形态、大小有位置;聚丙烯缝线应用于虹膜缝合,反应轻,效果好。     

小切口非超声乳化白内障摘出术中后囊破裂人工晶状体一期植入临床观察

【摘目的探讨小切口非超声乳化白内障摘出术中发生后囊破裂人工晶状体一期植入的安全性和有效性。方法对346例（381眼）行小切口非超声乳化白内障摘出术,术中发生晶状体后囊破裂2l眼,其中18眼一期植入后房人工晶状体,3眼未植入人工晶状体,观察后囊破裂人工晶状体一期植人病例的并发症及术后3月视力。结果一过性眼压升高3眼（16．67％）,角膜水肿16眼（88．89％）,人工晶状体轻度偏位2眼（11．11％）,瞳孔欠圆、轻度移位5眼（27．78％）,术后3月最佳矫正视力≥O．5者13眼（72．22％）,无严重并发症发生。结论小切口非超声乳化白内障摘出术中后囊破裂时,视具体情况后房型人工晶状体一期植入是安全的,并可取得较好的视力。