Open access peer-reviewed chapter

Cataract Surgery in Patients with Uveitis: Preoperative and Surgical Considerations

By Alejandro Rodriguez-Garcia and C. Stephen Foster

Submitted: April 20th 2017Reviewed: September 18th 2017Published: December 20th 2017

DOI: 10.5772/intechopen.71031

Downloaded: 438

Abstract

Cataract is one of the most frequent visual impairment complications of uveitis, accounting for up to 40% of the visual loss seen in these patients. In general, uveitis patients differ from the general cataract population in that they are younger and have a higher rate of comorbidities, however the rates of inflammatory sequelae vary markedly among uveitic entities. Cataract development may be influenced by the cause and duration of uveitis, the degree of inflammation control, and the use of corticosteroid therapy. Cataract surgery in patients with uveitis represents a serious challenge due to pre-existing ocular comorbidities that may limit the visual outcome and difficult the surgical procedure; the need for preoperative control of inflammation; and the efficacy of postoperative management to avoid immediate and late ocular complications. A detailed ophthalmologic exam prior to surgery is essential to know the status of pre-existing pathologic changes, adjust the medical therapy to achieve absolute control of inflammation, establish a surgical plan, and deliver an objective visual prognosis to the patient or the relatives. The key point to surgical success is the absolute control of inflammation, meaning no cells in the anterior chamber for at least 3 months prior to surgery. Today, minimally invasive phacoemulsification with acrylic foldable intraocular lens implantation is the standard of care for most patients with uveitis. It must be taken into consideration that higher rates of intraoperative and postoperative complications may occur. Vision-limiting pathology related to pre-existing uveitis complications are the major contributing factors for limited postoperative visual outcome.

Keywords

  • uveitis
  • cataract
  • phacoemulsification
  • intraocular lens
  • steroids
  • macular edema
  • glaucoma

1. Introduction

Cataract represents a significant burden in the management and visual outcome of uveitis patients. Up to 40% of the visual loss seen in these patients is either solely or largely due to cataract [1]. Lens opacification is caused by repeated episodes or sustained intraocular inflammation characterized by the release of free oxygen radicals, lysosomal enzymes, immune complex deposition on the lens capsule, hypoxia, and altered composition of the aqueous humor [2]. The development of cataract depends on the type of uveitis, the degree and duration of the inflammatory process, and on the prolonged and excessive use of corticosteroids [3, 4, 5].

Cataract surgery in patients with uveitis represents a serious challenge for the anterior segment surgeon [6, 7]. Nowadays, clear cornea phacoemulsification with intraocular lens (IOL) implantation is the standard of care for most patients with uveitis [8, 9]. However, despite remarkable progress on surgical techniques and IOL materials, certain specific considerations should be taken into account regarding patient selection, preoperative preparation, as well as perioperative and postoperative management for successful long-term results [10, 11]. Nearly one-third of all uveitic eyes have small pupils, which represent a surgical technical difficulty [2]. In such cases, higher rates of additional intraoperative maneuvers are required to obtain proper visualization and phacoemulsification of the cataract [4, 12, 13]. And, while surgery is associated with an improvement in best corrected visual acuity (BCVA), higher rates of both, intraoperative and postoperative complications have been reported [14, 15]. Moreover, it has been shown that the final BCVA in uveitic eyes is worse than in non-uveitic ones [14]. Therefore, identifying the cause of uveitis and pre-existing pathologic changes that affect the visual outcome, achieving absolute control of inflammation before surgery, careful surgical planning, and solving intraoperative and postoperative complications are crucial to obtain a successful result (BCVA ≥ 20/40).

2. Epidemiology

Cataract is the most common ocular complication in children with chronic uveitis with an estimated rate from 35 to 52.0% [16]. In juvenile idiopathic arthritis (JIA)-associated uveitis, the prevalence varies from 40 to 60% and the incidence of new-onset cataract formation has been estimated as 0.04/eye-year [17, 18]. On the other hand, in adult patients it is one of the most frequent complications of uveitis with a prevalence rate as high as 50% as seen in Fuchs uveitis [6, 14, 19, 20]. In HLA-B27-associated anterior uveitis, the most common cause of uveitis in adults, cataract formation is the third most frequent complication with an estimated prevalence of 14%, and an incidence rate of 0.091 during follow-up time (Table 1) [21]. Cataract prevalence varies among different causes of uveitis and depends on multiple factors including etiology, localization of the inflammatory process, time elapsed between the onset and diagnosis of uveitis, the degree of inflammation, the clinical course, and the use of corticosteroids [1, 18, 22, 23].

Cause of uveitisCataract prevalence range (median)Successful outcome BCVA ≥ 20/40 (Snellen)Frequent complicationsReferences
Fuchs uveitis15–75% (50%)83%Intraoperative AC hemorrhage (3.6–76%)
Hyphema
Ocular hypertension (glaucoma) (3–35%)
PCO (14.6%)
Progressive vitreous opacification
[20, 27, 48, 49]
Herpetic uveitis15–75% (24%)72.2%Viral reactivation
Iris posterior synechiae
Secondary glaucoma
[63, 151, 152, 153]
Juvenile idiopathic arthritis-associated uveitis40–60% (50%)60–70% (67%)Exuberant postoperative inflammation
Iris posterior synechiae
Secondary glaucoma (25%)
CME
Cyclitic membrane
Hypotony (Phthisis bulbi)
[4, 17, 18, 25, 26, 81, 95, 97, 98, 99, 101, 110]
HLA-B27 associated uveitis9.2–20.1%NARecurrent uveitis
CME
Iris synechiae
[21]
Pars planitis36–42% (40%)50–83%Persistent vitritis (haze)
CME (50%)
Glaucoma (10%)
PCO (10%)
IOL Cocooning (29%)
ERM
Optic nerve atrophy
[23, 28, 140, 154]
Adamantiades-Behcet disease21–26% (38.5%)72.5% (42.4%)Exuberant inflammation (12.5%)
Iris posterior synechiae (17.5%)
CME (12.5%)
ERM (7.5%)
Papillitis (optic nerve atrophy) (5%)
PCO (37.5% most common)
[148, 155, 156]
Vogt-Koyanagi-Harada disease10–35%68%Exuberant inflammation
Iris anterior and posterior synechiae
Pupillary membrane
PCO (76%)
Macular scarring
[135, 157]
Sympathetic ophthalmia31.8%67.79% (72.2%)PCO (77.7%)
Glaucoma
[158]
Sarcoidosis21%61%PCO (57.1%)
Recurrent uveitis
CME
Glaucoma
[159]

Table 1.

Prevalence, visual outcome, and complications of cataract surgery in uveitis.

AC = anterior chamber; PCO = posterior capsule opacification; CME = cystoid macular edema; ERM = epiretinal membrane.

3. Clinical characteristics of diverse forms of uveitis

In general, the uveitic population differs from the general population suffering from cataract in that they are younger and have a higher rate of comorbidities [15]. However, the rates of inflammatory sequelae vary markedly among uveitic entities [7, 24]. For this reason, each uveitis syndrome must be analyzed separately with respect to ocular complications and visual outcome [6, 14] (Table 1). While Fuchs uveitis regularly has the best visual prognosis and the least postoperative complications, JIA-associated uveitis has one of the most fear prognosis due to frequent pre-existing pathology, difficulties in reaching absolute control of inflammation, and multiple intraoperative and postoperative complications [4, 25, 26, 27].

4. Preoperative evaluation

A correct classification and etiologic diagnosis of the uveitic entity is very helpful to establish the appropriate surgical strategy and to determine the prognosis [8]. Moreover, a complete preoperative ophthalmologic examination is essential since pre-existing pathology will have significant therapeutic and prognostic visual implications [16, 28]. For instance, corneal opacity, vitreous haze, macular edema, and optic nerve atrophy usually result in a poor visual outcome [6, 19]. Therefore, it is very important that the patient and/or their relatives have an objective report on the status of the eye to be operated in order to have a realistic expectation of the final visual result. Ancillary diagnostic tests are always necessary to detect pre-existing pathologic changes that will allow us to render a more accurate visual prognosis. In most cases, it is helpful to perform a macular function test. Several methods are available for this purpose including the potential acuity meter (PAM), the laser interferometer (LI), and the focal electroretinogram (fERG) [29, 30]. The PAM test has proven an accuracy of 84% in patients with poor visual acuity (<20/40) [30]. On the other hand, LI has shown a lower accuracy (65%) and a tendency for over-predicting vision compared to the PAM in these patients [29, 30]. Focal cone ERG is very sensitive for detecting macular pathology, showing 91% accuracy in eyes with poor visual acuity [30].

Linear A-B ultrasound is necessary to identify vitreous hemorrhage and opacity, as well as posterior segment changes like, retinal detachment, optic nerve swelling, and sclerochoroidal thickness [31]. Another very useful device is high-frequency ultrabiomicroscopy (UBM), which generates high-resolution images at an almost histological level. In vivo image sections may be obtained up to 3–6 mm in depth, permitting visualization of anterior segment structures [32]. Frequent indications for UBM in uveitis include uveitis-glaucoma-hyphema syndrome (UGH), sclerouveitis, herpetic anterior uveitis, pars planitis, pseudophakic uveitis, hypotony, peripheral toxocariasis, and ciliary body pathology [32, 33].

Retina fluorescein angiography (FA) allows the detection of many different forms of posterior segment inflammatory changes. It is used to evaluate the activity and extent of chorioretinitis and optic nerve involvement; identify macular edema and choroidal neovascularization; diagnose certain posterior uveitic entities with typical features; evaluate retinal vascular involvement and neovascularization; and to monitor the therapeutic response [34]. However, many inflammatory changes occur in the peripheral retina where visualization may be difficult with conventional angiography. Wide field scanning laser ophthalmoscopy performs ultra-wide angle FA allowing clear identification of peripheral lesions and accurate documentation of disease progression [35]. This recently new image technology has replaced conventional angiography for the diagnosis and monitoring of intermediate and many forms of posterior uveitis [35].

Indocyanine green angiography (ICGA) allows the detection of choroidal inflammation. Two patterns of choroidal vasculitis have been described: primary inflammatory choriocapillaropathy and stromal inflammatory vasculopathy [36]. The first pattern is characterized by non-perfusion of the choriocapillaris found in entities like, multiple evanescent white dot syndrome, acute posterior multifocal placoid pigment epitheliopathy, multifocal choroiditis, and serpiginous choroidopathy [36]. The choroidal stromal inflammatory vasculopathy pattern is seen in active Vogt-Koyanagi-Harada disease (VKH), ocular sarcoidosis, tuberculosis, and birdshot chorioretinopathy [37]. In Behcet’s disease, as in other forms of uveitis, both ICGA vascular patterns may be seen at different stages of inflammation [38].

Today, the most frequently used imaging technique to detect and monitor macular inflammatory changes is optical coherence tomography (OCT). With an axial resolution in the 5–7 μm range, it provides close to an in-vivo histologic view of the retina [39]. There are several types of OCT available for clinical purposes. The spectral-domain OCT is the most used method [40]. It allows high-speed, accurate images of the retina, particularly macular pathology like, cystoid and diffuse macular edema, subretinal fluid accumulation, epiretinal membrane formation, macular holes, and choroidal neovascularization [41]. Longer wavelength OCT systems, including the swept-source technology and en-face imaging, enhance the detection of subtle microstructural changes in chorioretinal disorders by improving imaging of the choroid [42, 43, 44]. A technique that produces high-resolution cross-sectional images of the entire choroid called enhanced depth imaging technique (EDI-OCT) has identified increased subfoveal choroidal thickness in patients with active Behcet [45] and VKH disease, as well as loss of focal hyperreflectivity of the inner choroid in the acute and convalescent phases of VKH [46].

Once the preoperative evaluation is completed, a postoperative visual prognosis may be assumed, therapeutic adjustments may be applied, and a surgical plan is prepared based on pre-existing pathologic findings.

5. Preoperative preparation and therapeutic strategies

The key to surgical success in patients with uveitic cataract is the absolute control of inflammation, meaning no cells in the anterior chamber for at least 3 months prior to surgery [7]. This requisite is crucial to obtain an optimal surgical result and to minimize postoperative complications [7, 24]. Active uveitis at the time of cataract surgery has been associated with worse visual outcomes [15, 47]. Moreover, postoperative cystoid macular edema (CME) is more likely to develop in eyes with active inflammation within a 3-month period before surgery (relative risk 6.19) than those under control [41]. However, this general consensus of no cells in the anterior chamber prior to surgery has its exemptions [2]. In Fuchs uveitis, minimal but persistent anterior chamber cells and flare are frequently found despite intensive and sustained treatment with topical corticosteroids [48]. Hence, anti-inflammatory treatment is not indicated for the low-grade anterior chamber reaction seen in Fuchs uveitis and only occasionally, a short-course of corticosteroids is indicated for symptomatic exacerbations [49]. Other exemptions are related to the necessity for prompt surgical intervention in cases like, lens-induced uveitis, cyclitic membrane formation with hypotony, persistent vitreous opacity or hemorrhage, and retinal detachment [50, 51].

Preoperative management depends specifically on the type and etiology of uveitis. For inactive idiopathic anterior non-granulomatous uveitis as for Fuchs uveitis, topical administration of prednisolone acetate 1% four times a day, starting 3–7 days before surgery may be sufficient to avoid an outburst of postoperative inflammation [24]. On the contrary, patients with JIA-associated uveitis, anterior granulomatous uveitis, intermediate, posterior, and panuveitis also require oral prednisone (1.0 mg/kg/day) starting 3 days before surgery and continued for a week after cataract removal and then tapered slowly according to the inflammatory status [52, 53]. Preoperative oral steroids have been shown to be effective in reducing the risk of CME [41]. If patients are on immunosuppressive chemotherapy and/or biologics, they should be continued at current dosage [11]. In case that systemic corticosteroids are contraindicated (e.g., diabetes mellitus, metabolic disease, acid-peptic disease, obesity, or osteoporosis), periocular administration (transseptal or sub-Tenon’s) of triamcinolone acetonide (40 mg/ml) should be considered [54, 55]. Alternative immunosuppressive agents like, cyclosporin-A, tacrolimus, or anti-metabolites may be administered to these patients considering that most of these medications require a longer period of time (usually 4–6 weeks) to reach an optimal therapeutic effect [56].

The use of topical non-steroidal anti-inflammatory drugs (NSAIDs) like, ketorolac 0.4%, nepafenac 0.15%, or bromfenac 0.09%, have become a standard of care practice for the perioperative management of inflammation, pain, surgical-induced miosis, and cystoid macular edema in uneventful and also in uveitic cataract surgery [57, 58, 59]. A systematic review found high-quality evidence that topical NSAIDs are more effective than topical steroids in preventing the short-term pseudophakic CME in non-uveitic cataract surgery [60]. On the other hand, a recent evidence-based review conducted by the American Academy of Ophthalmology found that the claimed made about the synergistic effect of combined topical steroids and NSAIDs remains unproven [61]. In addition, NSAIDs have only a short-term therapeutic effect on prompt visual recovery and reduction of established CME, but no effect on the long-term visual outcome [57, 58, 61]. There is good collective clinical evidence and rationale that the application of a topical NSAID 3 days before surgery reduces CME and improves vision in the short-term [61]. Because the COX-2 enzyme is inducible and mostly responsible for the inflammatory process, the selective inhibitory effect of nepafenac and bromfenac makes them more suitable for this purpose [62]. Nepafenac has shown the shortest time to reach maximal concentration and the greatest aqueous humor peak concentration compared to ketorolac and bromfenac in eyes having cataract surgery [62]. After the surgical procedure, topical NSAIDs use is usually extended for 4–6 weeks [1, 10].

There are other special conditions in uveitis in which certain specific actions should be taken before cataract extraction is performed. Such is the case of herpetic uveitis in which prophylactic anti-viral therapy with acyclovir or valacyclovir should be administered at least 1 week before surgery in order to avoid recurrent viral infection [63, 64]. Other special consideration is the preoperative management of prominent band keratopathy interfering with cataract visualization which may be treated with EDTA 1–2% calcium chelation, or Excimer laser PTK before cataract surgery [65, 66].

Cataract and glaucoma frequently coexist as uveitis complications, and a combined surgical procedure may be associated with an increased risk of glaucoma surgery failure [67, 68]. In such cases, it may result better to perform a clear cornea small-incision cataract extraction first, followed later on by filtration surgery or a valve implantation with anti-metabolites [69, 70]. One must consider that uveitic glaucoma eyes operated for trabeculectomy with mitomycin-C which had previous cataract surgery or granulomatous uveitis, have a higher risk of surgical failure (RR = 2.957, P = 0.0344, and RR = 3.805, P = 0.0106, respectively) [71]. A higher risk of glaucoma surgical failure has also been associated with idiopathic, intermediate, and Fuchs uveitis; active intraocular inflammation at the time of surgery; and relapse of uveitis [72]. Moreover, the success rate of filtration surgery in uveitic eyes is significantly lower than that of non-uveitic, and many patients with successful intraocular pressure (IOP) control still require anti-glaucoma therapy to maintain adequate IOP levels in the postoperative period [72].

Posterior vitrectomy and cataract extraction may be an alternative for patients with prominent posterior segment pathology including vitreous opacity, hemorrhage, cystoid macular edema, and tractional retinal detachment [73]. There is reasonable evidence that cataract phacoemulsification combined with posterior vitrectomy has a favorable visual outcome for some patients with refractory inflammation, particularly those with significant vitreous opacity and chronic macular edema [13, 74]. In children, this combined surgical approach has been used for JIA-associated uveitis, pars planitis, and other forms of posterior uveitis [75]. However, this technique is not exempt of serious postoperative complications like, glaucoma, macular edema, and exuberant inflammation [75, 76]. For specific cases with various ocular complications, multiple combined surgical strategies have been postulated including phacoemulsification with IOL implantation, posterior vitrectomy, intravitreal sustained-release corticosteroid injection, and glaucoma tube implantation with promising results [77].

6. Surgical technique and intraoperative maneuvers

Nowadays, small clear corneal incision phacoemulsification surgery is preferred over extracapsular cataract extraction (ECCE) and lensectomy for most patients with uveitis [78, 79]. Since cataract surgery in these patients is frequently complicated by corneal opacification, iris synechiae, pupillary and cyclitic membranes, among others, the surgical technique should be minimally invasive with precise and delicate maneuvers [10, 24] (Figure 1). Most studies report a higher rate of additional maneuvers, notably iris and pupillary manipulation within a range between 19 and 67% of eyes [4, 5, 6, 25].

Figure 1.

Anterior segment appearance of a patient with Vogt-Koyanagi-Harada disease showing extensive peripheral anterior and posterior synechiae, shallow anterior chamber and a pupillary membrane in front of a secondary cataract.

Dealing with unexpected intraoperative complications like, corneal stromal edema; anterior chamber hemorrhage; pigment dispersion; posterior capsule rupture with vitreous exposure is key to achieve the best surgical outcome possible [6, 19, 75]. The first challenge that the surgeon faces is an adequate exposure and visualization of the cataract. Iris synechiolysis, pupillary membrane removal, and pupil distension with iris hooks or iris stretch devices are frequently required for proper cataract visualization [80, 81]. There is no general consensus on what is the best way to deal with the pathologic changes of the anterior segment encountered in uveitic eyes. However, it is generally agreed that attempts should be made to minimize surgical maneuvers in order to lessen tissue manipulation and trauma as possible [6, 24, 26].

The capsulorhexis should measure between 5 and 6 mm in diameter because smaller apertures are frequently associated with capsular phimosis and posterior iris synechiae to the anterior capsule remnant [82, 83, 84] (Figure 2). On the other hand, larger diameter capsulorhexis may affect the IOL centration and stability [83]. The phacoemulsification technique may vary depending on the density and zonular status of the cataract, but an effort should be made to use the less ultrasound power and time possible, to perform vigorous cortical and posterior capsule cleaning, and to avoid posterior capsule rupture [11, 19]. Avoiding the latter is crucial to obtain a good postoperative result, especially in chronic and recurrent uveitis like, herpetic uveitis, pars planitis, VKH disease, toxoplasmosis, among others [6, 24, 85]. In these cases, posterior capsule rupture with vitreous exposure may be a contraindication for IOL implantation due to a high probability of postoperative excessive and persistent inflammation [12, 86]. In uveitic eyes with encapsulated and subluxated IOLs with extensive fibrosis, IOL removal may be necessary at some point of the postoperative period to control severe inflammation and reduce its consequences [87, 88, 89]. For eyes with extensive membrane formation in the anterior vitreous, vitrectomy after performing a posterior central capsulorhexis must be considered [90].

Figure 2.

Patient with ankylosing spondylitis and HLA-B27-associated uveitis after cataract surgery showing capsular phimosis and partial adherence of the pigmentary epithelium of the iris to the anterior capsule remnant.

Decision making regarding the type of IOL to be used; anterior or posterior chamber IOL implantation; possible IOL sulcus fixation; combined filtration surgery, MIGS, or valve implantation; central posterior capsulorhexis after PC-IOL implantation with anterior vitrectomy; lensectomy, as well as posterior vitrectomy with or without retinal surgery are frequently met during uveitic cataract surgery, and the surgeon must be prepared to make the best decision for the particular case [91, 92, 93, 94]. The implantation of a foldable IOL “in the bag” is ideal for most cases of uveitis with certain exceptions [4, 95]. Until now, it is not clear how to proceed in children with uveitic cataract, and randomized controlled trials (RCT) are necessary to elucidate this matter [4, 25, 26, 81]. Historically, uveitic cataract surgery during childhood has been associated with a higher rate of surgical complications, particularly excessive postoperative inflammation [6, 10]. In the past, this situation made that the preferred surgical techniques for cataract extraction in this group including ECCE with posterior pars plana vitrectomy or lensectomy [4, 95]. However, recent evidence favors the implantation of foldable PC-IOLs in children with uveitis, including patients with JIA-associated iridocyclitis [25, 26, 96, 97, 98, 99, 100, 101].

Intraocular corticosteroids can be administered during surgery. Intracameral dexamethasone phosphate (400 μg/0.1 ml) or intravitreal triamcinolone (4 mg/0.1 ml) injection (IVTA) may be administered intraoperatively, except in advanced secondary glaucoma or known steroid-responsive patients [4, 102]. A prospective and comparative RCT between oral corticosteroids and preservative-free IVTA injection showed no differences in postoperative anterior chamber reaction, IOP levels, and central macular thickness (CMT) [103]. Another study found a better effect of IVTA versus orbital floor TA on macular edema and postoperative inflammation after cataract surgery in patients with uveitis [55]. However, IVTA injections have a temporary effect therefore, may require repeated injections which are not exempt of serious ocular complications like, elevated IOP (30–43% eyes), bacterial endophthalmitis, vitreous hemorrhage, and retinal detachment [104]. For those eyes at higher risk for intravitreal injection, sub-Tenon’s or transseptal TA can be administered at the end of surgery [19].

Intravitreal steroid sustained-release devices containing fluocinolone acetonide 0.59 mg or dexamethasone phosphate 0.7 mg have proven to be beneficial for the control of inflammation, prevention of CME, or reduction of CMT if applied a few days to weeks before or during cataract surgery [105]. Although no general consensus exists on the appropriate surgical time, it seems reasonable to perform the cataract surgery within 4–6 weeks from the last steroid implantation [105, 106, 107]. The most fear complication of sustained-release steroid devices is ocular hypertension (OHT). A meta-analysis found that 66% of eyes develop OHT after the implantation of the 0.59 mg fluocinolone acetonide device, compared to 32% following 4 mg IVTA, and only 15% with the 0.7 mg dexamethasone implant [108]. Risk factors for developing OHT include, pre-existing glaucoma, higher baseline IOP, younger age, OHT following previous injection, uveitis, higher steroid dosage, and fluocinolone implant [108]. A new sustained-release implant containing 0.19 mg fluocinolone acetonide has shown promising results improving visual acuity and reducing CMT with a significant reduction of IOP compared to the dexamethasone implant and IVTA [109].

7. Considerations for intraocular lenses

The general consensus regarding cataract surgery in patients with uveitis is that implantation of IOLs may be safely performed when ocular inflammation is completely abolished for a minimum period of 3 months [4, 7]. However, a debate still exists if an IOL should be implanted in specific circumstances like, lens-induced uveitis, JIA-associated iridocyclitis, young children with posterior or panuveitis, and intraoperative rupture of the posterior capsule with vitreous exposure [25, 26, 91, 110]. The implantation of an IOL triggers different intraocular responses including inflammation and foreign body reaction, as well as activation of the complement and coagulation cascades [83, 111, 112, 113]. These reactions along with the breakdown of the blood-aqueous barrier induced by surgery may increase cellular adhesion and lens epithelial cell (LEC) proliferation on the anterior surface of the IOL, resulting in anterior capsule phimosis, fibrosis, and posterior capsule opacification (PCO) [114]. With the advent of technologic development, many advances have been made to reduce IOL-induced reactions and to improve their biocompatibility [115]. The inflammatory response induced by IOLs is inversely related to its biocompatibility, so the higher the biocompatibility, the lower the inflammatory response [15, 83, 115]. Even though they were considered biologically inert, the first IOLs made of polymethyl-methacrylate (PMMA) were capable of producing foreign body reaction, as well as activate the complement and coagulation cascades [113, 116].

Different strategies have been used to reduce the host response, including the modification of the IOL surface by making it hydrophilic, like in heparin-coated PMMA IOLs, or hydrophobic such as surface passivated [83]. Heparin surface-modified IOLs have improved biocompatibility compared with unmodified PMMA IOLs in eyes at risk for severe postoperative inflammation, including those with uveitis [117, 118].

Foldable IOLs may be hydrophobic, including silicone IOLs or hydrophilic, and both surfaces have demonstrated to be relatively inert [114, 119]. Hydrophobic surfaces resist cell adhesion while hydrophilic ones reduce electrostatic forces and cellular adhesion, preventing the attraction of inflammatory cells and their activation, as well as adherence of fibroblasts to the IOL surface [120, 121].

Anterior capsule phimosis has been related to the degree of fibrotic reaction produced by pro-inflammatory cytokines released by residual LEC [122, 123]. Careful vacuuming the undersurface of the anterior capsule helps to reduce the number of LEC [82, 124]. Capsular phimosis has been reported more frequently with hydrogel (poly-HEMA) than acrylic, and silicone IOLs [83, 125]. Foreign body giant cell precipitates are less frequently seen in hydrophilic than on hydrophobic IOL surfaces and heparin-coated PMMA IOLs [115, 126]. The frequency of posterior capsule opacification (PCO) is highest with PMMA IOLs, less with silicone and minimal with acrylic IOLs [124, 127].

Few studies have evaluated the visual outcome following cataract surgery in uveitis with silicone IOL implantation. Overall, only 30% of eyes have achieved 20/40 of better vision with silicone IOLs, fewer than any other type of IOL [15]. Silicone was the first material available for foldable IOLs, but its use has declined particularly because it cannot be used for a monobloc open-loop designed, the preferred choice for preloaded injectors that allow implantation through small corneal incisions [128].

With the advent of acrylic foldable IOLs, the biocompatibility issue has become a minor concern, but controversy still exists of which material, hydrophilic or hydrophobic is best suitable for patients with uveitis [120, 126, 129]. Since the lens is surrounded by aqueous humor, it was thought that hydrophilic materials were more biocompatible than hydrophobic for patients with uveitis [89, 92]. However, there is insufficient evidence to determine the effects of different types of IOL materials, including hydrophobic and hydrophilic acrylic IOLs in patients with uveitis [129]. Results from the largest RCT provide only preliminary evidence that acrylic IOLs may perform better than silicone IOLs in terms of improving vision and reducing the chances of postoperative inflammation and complications [129, 130]. A large multicenter RCT with standardized outcome measurements is necessary to properly address the surgical outcome of patients with uveitic cataract.

8. Immediate postoperative management

The postoperative management is as important as the preoperative preparation and the surgical procedure itself. Since the first postoperative moments, intense topical corticosteroids (1% prednisolone acetate hourly), topical NSAIDs (anti-COX-2 selective), topical wide spectrum antibiotics (fourth generation fluoroquinolones), overnight steroid ointment, as well as mydriatic-cycloplegic combinations (e.g., 1% tropicamide + 5% phenylephrine every 6-hours × 5–7 days) should be administered [11, 24, 131]. Topical corticosteroids are wined down according to the grade of anterior chamber inflammatory reaction, the presence of glaucoma, or OHT in steroid-responders [54]. In case the patient was given systemic corticosteroids, they should be maintained at immunosuppressive levels (1 mg/kg/day) for 7–10 days before reducing them slowly to a minimum dose of 7.5 mg/day [56]. In case the patient is on immunosuppressive chemotherapy or biologic therapy, it should be continued at maintenance dose [19, 131]. Systemic anti-virals used for herpetic uveitis should be kept at therapeutic dose for 7–14 days postoperative, and then reduced to prophylactic levels (acyclovir, 600–800 mg/day and valacyclovir 500–1000 mg/day) for several weeks to months before stopping them [63, 64, 132].

9. Postoperative complications and their management

Postoperative complications after cataract surgery in patients with uveitis are relatively frequent [8]. The reported prevalence of complications is higher in ECCE than in phacoemulsification [78, 79, 133]. The risk for postoperative complications also depends on the type of uveitis and the degree of ocular involvement [8, 12, 85] (Table 1). Despite all preventive measurements taken before and during surgery, the most frequent and fear postoperative complication is the outburst of inflammation out of expected proportions [5]. Significant inflammation characterized by >2+ anterior chamber cells, extensive protein exudation with fibrin and plasmoid bodies formation, as well as fibrinoid membranes covering the pupil, and hypopyon may be seen [7, 19, 24, 134]. This aggressive inflammatory response is commonly associated with early postoperative iris synechiae formation and pupillary inflammatory membranes, particularly in disorders like JIA-associated uveitis, and VKH, among others [4, 6, 131, 135]. The best way to deal with this unexpected postoperative inflammatory response consists on avoiding it by previous absolute control of inflammation and the implementation of perioperative measurements discussed before. Nevertheless, in those cases in which a significant inflammatory reaction occurs, an adjustment to the systemic prednisone dose and the administration of atropine 1% will help to control the inflammation [52, 53, 54].

Other immediate postoperative complications that may be seen are hyphema and significant pigment dispersion throughout the anterior segment [19, 24]. Pigment dispersion is related to a variety of factors including, surgical trauma, small pupil, and age [24, 83, 91]. In both cases, regular tonometry is mandatory for opportune detection of severe OHT related to clogging of the trabecular meshwork by ghost cells or pigment, respectively [6]. If anti-glaucoma therapy is required, prostaglandin analogs as well as alpha-adrenergic drugs should be avoided as possible because they may exacerbate the inflammatory process [69]. In some patients with corneal stromal edema and Descemet folds due to high IOP, oral carbonic anhydrase inhibitors (e.g., acetazolamide 250 mg, 3–4 times a day) may be administered [69]. If the IOP becomes uncontrollable with medical therapy, filtration surgery or valve implantation should be considered to avoid further optic nerve damage [69, 136]. Finally, an excessive postoperative inflammatory process may produce significant vitreous opacity and membrane formation [5]. Once acute infectious endophthalmitis has been ruled out in such cases, aggressive anti-inflammatory therapy with systemic, periocular, and even intravitreal corticosteroids should be administered [52, 54, 55, 106]. If vitreous condensation and organization persist, a pars plana vitrectomy with or without intravitreal corticosteroid injection should be performed [13, 73, 75, 137].

In the late postoperative period, ocular complications are usually related with recurrent intraocular inflammation occurring from 8.3 to 53% of cases [8, 12, 85, 133]. Recurrent postoperative uveitis may produce anterior and/or posterior iris synechiae which may cause an angle or pupillary block glaucoma, respectively [69].

Certainly one of the most frequent ocular complications observed in this late period is posterior capsule opacification seen in up to 58% of cases [82, 83, 85, 124, 133]. Nd-Yag laser capsulotomy usually resolves this problem, but in some cases retrolental hyaloid-vitreous opacification or significant deposition of pigment and inflammatory debris on the IOL surface may occur therefore, recurrent low-energy Nd-Yag laser and other operative procedures may be needed for polishing the IOL [82, 138]. It must be considered that Nd-Yag laser capsulotomy in patients with uveitis is associated with a higher risk for vision-threatening complications, including OHT, CME, IOL damage or luxation, as well as retinal detachment [40, 139].

Another very important visual-threatening postoperative complication is macular edema occurring from 33 to 56% after ECCE and from 12 to 59% after phacoemulsification [12, 85, 133, 140]. The appearance of CME depends on multiple factors including the cause of uveitis and the type of surgical procedure performed [41]. Treatment of uveitic macular edema (UME) includes the administration of periocular injections of depot corticosteroids [54, 141]. However, as stated before, IVTA has shown to be superior to orbital floor injection for the treatment of UME [55, 142]. OHT is a potential complication of both types of steroid administration and should always be considered, particularly after repeated intravitreal injections [55, 108, 143]. Sustained-delivery corticosteroid devices may also be administered for this purpose [105, 106, 144]. In patients with bilateral UME, steroid-responders or those who do not accept periocular or intravitreal corticosteroid injections, oral prednisone along with oral carbonic anhydrase inhibitor (e.g., acetazolamide 250 mg every 12 hours) may be administered [54]. Epiretinal membrane formation is more commonly seen in patients with chronic UME with a prevalence ranging from 15 to 56% [12, 145, 146]. Treatment consists of pars plana vitrectomy and internal limiting membrane delamination [73, 146, 147].

Other less common, but serious complications is retinal detachment and hypotony [5, 26]. Hypotony may be related to the retinal detachment per se, or to a low aqueous humor production due to inflammation of the ciliary process, or tractional detachment of the ciliary body due to cyclitic membrane formation [26]. Postoperative hypotony may evolve to pthisis bulbi [10, 88]. Both complications should be attended immediately by retinopexy, and/or posterior vitrectomy with cyclitic membrane and sometimes intraocular lens removal, as well as peri- or intraocular corticosteroid administration [87, 88].

10. Prognosis and visual outcome

The outcome of cataract surgery in patients with uveitis is less predictable than in other causes of cataract. Many factors may contribute to this uncertainty including, pre-existing pathologic changes, intraoperative technical challenges, the impact of postoperative exuberant inflammation, and the reversibility of postoperative complications derived from it [14]. Vision-limiting pathology related to pre-existing uveitis complications, especially macular edema and optic neuropathy are probably the major contributing factors for limited postoperative visual outcome [8, 15, 85].

Different studies suggest that visual prognosis varies according to uveitis subtypes [5, 15, 26]. For instance, the proportion of eyes achieving 20/40 or better vision is better in Fuchs uveitis and worse in Behcet’s disease, VKH disease, or sympathetic ophthalmia [20, 27, 47, 148]. In general, diseases that spare the posterior segment have a better prognosis than those affecting it, particularly macular and optic nerve involvement [5, 6, 8, 85]. In addition, acute uveitic entities tend to be associated with better outcome than chronic ones [12].

Uveitic cataract surgery has been associated with worse postoperative visual acuity, higher IOP, and more than double prevalence of UME when compared with non-uveitic cataract surgery [14]. Moreover, the visual outcome following uveitic cataract extraction is not as good as that of age-related cataract surgery with the exception of Fuchs uveitis [27, 149]. Systematic reviews found a successful visual outcome (20/40 or better) in 96% of eyes with age-related cataract surgery compared to 70% in uveitic eyes undergoing either phacoemulsification or ECCE [15, 149]. ECCE and phacoemulsification seem to have similar visual outcomes compared to half less successful rate after pars plana lensectomy [15]. With respect to the comparable visual results reported between ECCE and phacoemulsification, it must be taken into account that most ECCE trials have more exclusion criteria than phacoemulsification studies, favoring better visual outcomes [15, 85, 150].

Finally, regarding IOL implantation, more eyes (71%) undergoing cataract surgery with IOL implantation than eyes left aphakic (52%) achieved a BCVA ≥ 20/40 vision postoperatively [14]. Eyes receiving acrylic IOLs or heparin surface-modified PMMA had better visual outcomes than those receiving non-heparin-PMMA or silicone IOLs [14, 15, 83, 94].

© 2017 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Alejandro Rodriguez-Garcia and C. Stephen Foster (December 20th 2017). Cataract Surgery in Patients with Uveitis: Preoperative and Surgical Considerations, Difficulties in Cataract Surgery, Artashes Zilfyan, IntechOpen, DOI: 10.5772/intechopen.71031. Available from:

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