Intravitreal Corticosteroids Used in DME
The direct injection of corticosteroid into the vitreous allows the administration of a large bolus of drug. The therapeutic level is rapidly achieved and the drug is administered in the vicinity of the target tissue. Moreover, systemic absorption and systemic side effects are minimized. The most common corticosteroids used for intravitreal administration are triamcinolone acetonide, fluocinolone acetonide and dexamethasone.
Triamcinolone acetonide is minimally water soluble and is administered as a suspension. Most frequently the 4 mg dose is used and its duration of action is approximately 3 months [
7]. Compared with triamcinolone, dexamethasone is more potent with a shorter duration of action [
8]. The intravitreal administration of dexamethasone has been studied at 0.4 and 0.8 mg. Due to its short duration of action, a single injection is not sufficient to achieve a sustained therapeutic effect in DME which is a chronic disease [
9].
Repeated intravitreal administration of corticosteroids for maintaining therapeutic effects increases the risk of adverse events, such as endophthalmitis or vitreous haemorrhage [
7,
10]. Sustained-release implants have, therefore, been developed to reduce injection frequency and reduce the risk of such complications [
11]. These implants are either biodegradable or non-biodegradable. With non-biodegradable implants, the release of the corticosteroid is more precise with a longer therapeutic effect [
4].
Retisert
® (Bausch and Lomb, Inc., Rochester, NY, USA) is a non-biodegradable implant that is inserted via the pars plana. It is sutured to the sclera and fluocinolone acetonide is released for 30 months at a controlled rate [
12]. This drug has no license in Europe and will not be discussed in this review.
ILUVIEN
® (Alimera Sciences, Inc, Alpharetta, GA, USA) is a non-biodegradable implant inserted into the vitreous cavity via the pars plana through a 25-gauge needle. Fluocinolone acetonide is released at a rate of 0.2 µg per day for up to 36 months [
13].
Ozurdex
® (Allergan, Inc, Irvine, CA, USA) is a biodegradable sustained-release device that is inserted into the vitreous cavity using a stepped incision through a 23-gauge needle. One dexamethasone implant contains 700 μg of dexamethasone which is released for up to 6 months [
14].
Pharmacokinetics of Intravitreal Corticosteroids
Steroids administered in the vitreous are eliminated via two main pathways. The flow of aqueous humor through the anterior chamber angle is the first pathway and the second is posteriorly through the blood-retinal barrier [
11,
15]. The concentration of the intravitreal corticosteroids, and consequently its duration of action, depends on the clearance rate from the vitreous [
16,
17].
Direct measurements of corticosteroid concentrations in vitreous are difficult and experimental animal models have been developed: triamcinolone acetonide in rabbit [
18,
19], dexamethasone implants (Ozurdex) in monkey [
20], fluocinolone acetonide (ILUVIEN) in rabbit [
21]. Nevertheless, small series have been performed in human for triamcinolone acetonide [
7], fluocinolone acetonide (ILUVIEN) [
22,
23]. No study has been published for dexamethasone implants (Ozurdex) in the human eye.
From these pharmacokinetic studies, the duration of the therapeutic window has been evaluated to be ~1–3 months for triamcinolone acetonide 4 mg, ~2–4 months for Ozurdex (700 µg of dexamethasone) and up to 36 months for ILUVIEN (0.2 µg/day of fluocinolone acetonide) [
24].
Evidence Base for Corticosteroid-Induced Ocular Hypertension
Topical, intravitreal and high-dose and long-term systemic corticosteroid therapy can induce subacute or chronic elevation of IOP and particularly in patients with POAG [
25,
26]. Thus, IOP elevation has been observed in 40% of normal subjects after 4–6 weeks of treatment with topical 0.1% dexamethasone and 100% of patients with POAG [
4].
It has been suggested that POAG and steroid-induced glaucoma share common pathogenic mechanisms; OHT induced by corticosteroids is similar to POAG since, in both cases, the outflow facility is decreased [
27]. The ultrastructural basis of corticosteroid-induced obstruction within the trabecular meshwork remains poorly understood. Some studies suggested that extracellular matrix alterations contribute to decreased outflow facility within the trabecular meshwork or the juxtacanalicular connective tissue [
28]. The upregulation of the gene of myocilin has been evidenced in cultured trabecular meshwork cells [
29]. Moreover, mutations of this gene have been found to be associated with POAG [
30].
Whichever corticosteroid drug is administered into the vitreous, the incidence of OHT increases with the dose: 32.1% and 45.9% for triamcinolone 4 and 25 mg [
4], 37.1% and 45% for ILUVIEN 0.2 and 0.5 µg/day [
31], 27% and 32% for Ozurdex 0.35 and 0.7 mg [
32], respectively. There is a correlation between the steroid concentration in aqueous humor and the increased risk of OHT in DME patients after intravitreal administration of fluocinolone acetonide [
23]. The authors concluded that, in susceptible patients, prolonged aqueous levels of fluocinolone acetonide >1 ng/ml moderately increases the risk of IOP rise and levels >6 ng/mL are associated with a markedly increased risk. Compared to the control arm, significant anatomical signs of development of glaucoma were not detected in the ILUVIEN studies [
33].
The time course of OHT after intravitreal administration of corticosteroids varies according to the molecule and dose. Moreover, comparisons between studies are limited by the various definitions used for the steroid induced rise of IOP. In the systematic review of Kiddee et al. the onset of OHT defined as IOP ≥21 or ≥10 mmHg from baseline was 2–4 weeks in randomized controlled trials and 1–8 weeks in non-randomized studies after administration of triamcinolone 4 mg [
4]. However, in some studies onset could be observed as early as 1 week or on the contrary 20–24 weeks after administration. With the ILUVIEN 0.2 µg/day implants, the onset of OHT began within 2–4 weeks with a maximum at 24–48 weeks and a return to basal values 9–12 months after implantation [
22,
34,
35]. The time course of OHT has not been reported with the dexamethasone implant. Nevertheless, the peak IOP occurred 60 days after implantation and returned to basal values within 6 months [
36‐
39].
Although diabetes has been reported as a risk factor of development of POAG after intravitreal triamcinolone administration in a small retrospective study (
p = 0.050) [
40], diabetes was not considered a predictor of development of POAG in both independent Ocular Hypertension Treatment Study (OHTS) (ClinicalTrials.gov identifier, NCT00000125) and European Glaucoma Prevention Study [
6,
7]. Elevated IOP >21 mmHg after administration of 20 or 25 mg of triamcinolone was statistically independent of diabetes (
p = 0.74 and
p = 0.37, respectively) [
41,
42]. Another study with triamcinolone 4 or 8 mg did not find a relationship between an IOP rise and diabetes [hazard ratio, 0.91; 95% confidence interval (CI), 0.47–1.61,
p = 0.760] [
43]. There is an increased risk of glaucoma in patients with diabetes regardless of IOP level [
44], possibly explained by vascular mechanisms, as diabetes causes microvascular damage and may affect vascular autoregulation of the retina and optic nerve.
Some authors hypothesized that side effects related to corticosteroids may be explained in part by the differences in drug lipophilicity and partitioning into trabecular meshwork and lens [
45]. However, these results have been recently rejected in the scientific literature [
46].
Evidence Base for Elevated IOP After Corticosteroids in DME
The effects on IOP of intravitreal administration of corticosteroids during large trials for the treatment of DME are summarized in Table
1. The results of IOP elevation are, however, difficult to compare since IOP was not a primary endpoint and only reported as an adverse event. Moreover, definitions of IOP were not standardized with different cut-offs for IOP elevation or OHT. Overall, the safety results regarding elevated IOP in patients with DME are similar to those reported in the systematic review of Kiddee et al. which included patients regardless of diabetes status [
4]. Nevertheless, a large proportion of patients with DME received IOP-lowering medical treatments and were largely well controlled (Table
1). Some patients underwent laser trabeculoplasty or incisional glaucoma surgery, but the proportion was low, except for one study of triamcinolone in which 9% underwent glaucoma surgery [
47].
Table 1
Intravitreal corticosteroid in randomized controlled trials for the treatment of DME
| Triamcinolone acetonide | 69 | Triamcinolone (4 mg) vs laser + placebo | 5 years | ΔIOP ≥+5 mmHg: 79% | IOP-lowering medication: 56% Glaucoma surgery: 9% |
| Triamcinolone acetonide | 840 | Triamcinolone (1 or 4 mg) vs laser | 3 years | IOP ≥21 mmHg: 15% and 10% | IOP-lowering medications: 2% and 12% Laser trabeculoplasty (n = 1) and glaucoma surgery (n = 3) with 4 mg |
| Triamcinolone acetonide | 854 | Bevacizumab with deferred or prompt laser vs triamcinolone (4 mg) with deferred or prompt laser | 1 year | Up to 14 weeks and from 14 to 56 weeks for events and management: ΔIOP ≥+10 mmHg: 17% and 10% IOP-lowering medication: 2% and 9% IOP ≥30 mmHg: 4% and 4% Glaucoma surgery: 0% and 1% |
| Dexamethasone (Ozurdex) | 253 | Dexamethasone implant 6 M fixed dosing + laser at M1 vs sham + laser at M1 | 1 year | ΔIOP ≥+10 mmHg: 15.2% IOP ≥25 mmHg: 16.8% IOP ≥35 mmHg: 4.0% | IOP-lowering medication: 15.9% Glaucoma surgery: 0% |
| Dexamethasone (Ozurdex) | 100 | Dexamethasone implant 5 M fixed vs prn dosing | 1 year | IOP >30 mmHg: 20% and 34% | IOP lowering medication: 28 pts Glaucoma surgery: 0% |
| Dexamethasone (Ozurdex) | 80 | Dexamethasone implant prn + laser vs laser alone | 1 year | Not reported | IOP lowering medication: 20% Glaucoma surgery: 0% |
| Dexamethasone (Ozurdex) | 1048 | Dexamethasone implant 6 M fixed dosing (350 or 700 µg) vs sham | 3 years | ΔIOP ≥+10 mmHg: 27.7% IOP ≥25 mmHg: 32.0% IOP ≥35 mmHg: 6.6% | IOP-lowering therapy: 41.5% Laser trabeculoplasty: 0% Glaucoma surgery: 0.9% |
| Dexamethasone (Ozurdex) | 88 | Dexamethasone implant prn (700 µg) vs bevacizumab | 1 year | ΔIOP ≥+5 mmHg: 46% ΔIOP ≥+10 mmHg: 20% | Laser trabeculoplasty: 1 patient |
| Fluocinolone acetonide (ILUVIEN) | 953 | ILUVIEN insert (0.2 or 0.5 μg/day) vs sham/laser | 3 years | Increased IOP: 37.1% | IOP-lowering therapy: 38.4% Laser trabeculoplasty: 1.3% Glaucoma surgery: 4.8% |
Outcomes comparable to those seen in controlled trials were obtained in recent real-world studies [
48‐
51]. The study of Lam et al. assessed the intravitreal dexamethasone implant (Ozurdex) in 120 study eyes (including 34 eyes with diagnosis of DME) in patients with ≥3 months of follow-up after the initial dexamethasone implant [
48]. An IOP rise ≥+10 mmHg from baseline, ≥25 and ≥35 mmHg were reported for 20.6%, 26.5% and 2.9% of patients with DME. Glaucoma surgery was performed for 1.7% of all patients (no patient with DME had surgery). IOP elevation in DME patients or patients with retinal vein occlusion were comparable and IOP-lowering medical treatment was administered to 29.4% of patients with DME and 16.7% of patients with retinal vein occlusion.
The recent 1-year retrospective study of Mazzarella et al. evaluated the effect of intravitreal injection of dexamethasone (Ozurdex) on IOP in 92 patients with macular edema (including 36.5% with diabetic retinopathy) either without OHT (group 1;
n = 65) or associated with glaucoma or OHT (group 2;
n = 27) [
49]. After injection, OHT (>21 mmHg) was observed in 21.5% of eyes of group 1 and 59.3% in group 2. In group 2, all eyes required IOP-reducing treatment vs. 12.3% in group 1. In general the rise of IOP was transitory and only one patient required filtration surgery. These results underscore the need to monitor patients during corticosteroid treatment, especially patients with a previous history of OHT or glaucoma.
The 1-year prospective study of Massin et al. evaluated the fluocinolone acetonide intravitreal implant (ILUVIEN) in 16 patients (17 eyes) with DME insufficiently responsive to laser and anti-VEGF therapy. Patients with a history of an IOP rise after intravitreal corticosteroids were excluded. Elevation of IOP was reported in three patients who were well controlled by IOP-lowering eyedrops [
50].
Overall, these studies indicate that diabetic patients with intravitreal steroids have an incidence of IOP increase and OHT comparable with those of non-diabetic patients. When necessary, IOP-lowering medical treatment or laser trabeculoplasty is sufficient for a large majority of patients and glaucoma surgery is needed for only a small proportion of patients.
Evidence Base for Onset of Glaucoma Related to Ocular Hypertension
The OHTS was a multicenter, randomized, prospective clinical trial designed to assess the relationship between primary OHT and onset of glaucoma. For this purpose, 1636 patients aged from 40 to 80 years with high IOP were randomized between IOP-lowering treatment and no treatment [
52]. The goal was to achieve IOP <24 mmHg and an IOP decrease of at least 20% from baseline. The primary outcome was the development of open-angle glaucoma (visual field defects or optic disc deterioration). The IOP was reduced by 22.5% in the treated group and 4.4% in the no treatment group [
53]. The main results indicated that around 90% of patients with OHT (baseline IOP between 24 and 32 mmHg) who are not treated had no glaucoma after 5 years. IOP reduction by at least 20% was found to decrease the risk of conversion from OHT to glaucoma by 50%. This large randomized controlled study confirmed that IOP reduction decreases the incidence of glaucoma in patients with OHT [
5]. The risk of developing glaucoma as a result of a corticosteroid-induced IOP rise may not be the same as that for the development of primary open-angle glaucoma in patients with OHT. Hence, new studies are still needed to identify the risk of developing glaucoma after treatment with a steroid.
Is A ‘Steroid Provocative Test’ Useful?
Few studies have directly addressed this point i.e. initiating a short-acting steroid treatment to assess a ‘steroid response’ on IOP before initiating a sustained steroid release treatment. However, previous studies on the effect of topical corticosteroids on IOP are available. Thus, pioneering studies in the 1960s showed that topical corticosteroids caused elevated IOP in a large proportion of patients [
27,
54,
55]. These early studies showed that increased IOP is observed in approximately one-third of people after administration of topical corticosteroids for several days (more than 90% in patients with chronic glaucoma). Among ‘responders’, the majority were low responders (IOP rise <6 mmHg) and one-third were intermediate responders (IOP rise from 6 to 15 mmHg) and 4–6% were high responders (IOP rise >15 mmHg) [
27,
54‐
56]. This IOP elevation was usually transient, with a return to normal within 2 weeks after discontinuation, provided the treatment duration was short. Persistent IOP elevations refractory to IOP-lowering treatment were observed in 1–5% of cases [
56].
More recently, Breusegem et al. investigated the diagnostic value for a steroid response of a topical dexamethasone provocative test before intravitreal triamcinolone acetonide injection [
57]. The dexamethasone test had a sensitivity of 25% (CI 95%, 0.07–0.52), a specificity of 100% (95% CI, 0.83–1.00), a positive predictive value of 100% (95% CI, 0.40–1.00) and a negative predictive value of 62% (95% CI, 0.44–0.79). It was thus concluded that a positive response to topical dexamethasone is a strong predictor of the response to intravitreal triamcinolone acetonide; however, a negative response does not guarantee there will be no response to intravitreal triamcinolone acetonide.
In the panel’s opinion, the benefit of a corticosteroid provocation test is equivocal. Since the great majority of steroid-induced OHT can be managed with medical or laser therapy, a positive steroid challenge does not necessarily imply that a patient would not benefit from intravitreal steroids; the clinician and patient should consider the benefit-risk balance before deciding on the best course of action.