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Salvetat, M.L.; Pellegrini, F.; Spadea, L.; Salati, C.; Musa, M.; Gagliano, C.; Zeppieri, M. Corticosteroids for the Management of Diabetic Macular Edema. Encyclopedia. Available online: https://encyclopedia.pub/entry/55855 (accessed on 16 April 2024).
Salvetat ML, Pellegrini F, Spadea L, Salati C, Musa M, Gagliano C, et al. Corticosteroids for the Management of Diabetic Macular Edema. Encyclopedia. Available at: https://encyclopedia.pub/entry/55855. Accessed April 16, 2024.
Salvetat, Maria Letizia, Francesco Pellegrini, Leopoldo Spadea, Carlo Salati, Mutali Musa, Caterina Gagliano, Marco Zeppieri. "Corticosteroids for the Management of Diabetic Macular Edema" Encyclopedia, https://encyclopedia.pub/entry/55855 (accessed April 16, 2024).
Salvetat, M.L., Pellegrini, F., Spadea, L., Salati, C., Musa, M., Gagliano, C., & Zeppieri, M. (2024, March 05). Corticosteroids for the Management of Diabetic Macular Edema. In Encyclopedia. https://encyclopedia.pub/entry/55855
Salvetat, Maria Letizia, et al. "Corticosteroids for the Management of Diabetic Macular Edema." Encyclopedia. Web. 05 March, 2024.
Corticosteroids for the Management of Diabetic Macular Edema
Edit

Diabetic macular edema (DME) is a common complication of diabetes mellitus and a leading cause of visual impairment worldwide. It is defined as the diabetes-related accumulation of fluid, proteins, and lipids, with retinal thickening, within the macular area. DME affects a significant proportion of individuals with diabetes, with the prevalence increasing with disease duration and severity. Corticosteroids (CSs) are a group of hormones produced by the adrenal cortex.

diabetic macular edema diabetic retinopathy intravitreal corticosteroids triamcinolone acetonide

1. The Corticosteroids

a
Definition
Corticosteroids (CSs) are a group of hormones produced by the adrenal cortex; they are classified into glucocorticoids, including cortisol and cortisone, that regulate the metabolism of carbohydrates, proteins, and lipids and mineralocorticoids, such as aldosterone, that control salt and water balance in the body [1][2].
b
History of the CSs’ pharmacological use
The idea to use glucocorticoids to treat inflammatory diseases dates back to 1948 and was related to the observation that rheumatoid arthritis had a tendency to improve during pregnancy and in patients affected by jaundice, with both conditions being characterized by high glucocorticoid levels [1][2]. After that, CSs were used to treat several different inflammatory diseases, and ophthalmologists introduced their use to treat uveitis in the early 1950s [1][2]. During the last 70 years, several new steroids have been synthesized and released for therapeutic use. The first treatment of DME with CSs was published in 2001 [3].
c
Biological effects
CSs have extremely complex biological effects that involve the regulation of multiple genes. Both endogenous and synthetic steroids bind specific glucocorticoid receptors and regulate the expression of approximately 10–20% of the human genome in almost all cell types, resulting in glucose metabolism, growth, development, survival, and inflammation control [1][2]. Different steroid molecules differ in molecular weight and structure, receptor binding affinity, and gene modulation pattern profile. Their biological properties and side effects vary in different cells and different subjects depending on many variables that may explain the resistance or hypersensitivity to steroids, including receptor expression, receptor polymorphisms, sex, and disease variables, such as the glycemic status, and therapy duration [1][2].
d
Therapeutic effects
Corticosteroids are commonly prescribed with a variety of indications due to their wide range of effects on the human body [1][2]. Because of their anti-inflammatory and immune-suppressive effects, CSs are used to treat many inflammatory, allergic, and autoimmune diseases, including asthma, allergic rhinitis, hay fever, urticaria, atopic eczema, chronic obstructive pulmonary disease, rheumatoid arthritis, lupus, Crohn’s disease, ulcerative colitis, giant cell arteritis, polymyalgia rheumatic, multiple sclerosis, inflamed joints, muscles and tendons, non-infective uveitis, etc. [1][2].
e
Side effects
Steroids have many side effects targeting different tissues and organs, including hypertension, dyslipidemia, glucose intolerance and diabetes mellitus, obesity, hirsutism, gastrointestinal irritation, peptic ulcer, osteoporosis, delayed wound healing, increased risk of infections, virus reactivation, fluid retention, growth retardation, hypothalamic-pituitary axis suppression, mood disturbance, depression, insomnia, psychosis, etc. [1][2]. The CSs’ side effects on the eye include mainly ocular hypertension (OHT), glaucoma and cataract development, and, less frequently, central serous chorioretinopathy (CSCR) and infections reactivation [4][5][6][7][8][9].
-
Steroid-induced OHT and steroid-induced glaucoma (SIG) are the most frequent and dangerous side effects of the systemic and, most frequently, local use of CSs [8]. Subjects who respond to treatment with glucocorticoids with an IOP rise are referred to as “steroid-responders”, whose definition is not univocal and may include the following cases: IOP increase of >5 mmHg or >10 mmHg from baseline or IOP > 21 o 24 mmHg [8]. SIG can be considered to be a dangerous form of secondary open-angle glaucoma because it is frequently diagnosed late and is characterized by IOP levels that can be particularly high and lead to significant optic disc and perimetric damages within a short time [8].
The pathogenesis of the steroid-induced OHT and SIG is still unclear. It has been demonstrated that steroids regulate the expression of several genes at the level of the trabecular meshwork and can cause an increased aqueous humor outflow resistance by both increasing deposition of extracellular matrix proteins as well as inducing trabecular meshwork cell dysfunction [8].
The prevalence of the steroid-induced OHT and SIG is variable. Considering a normal population, approximately 61–63% can be classified as non-responders, showing an IOP rise of <5 mmHg; 33% are low-moderate responders, with an IOP elevation ranging from 6 to 15 mmHg; and 4–6% are high responders, with an IOP increase of >15 mmHg [10]. On the other hand, amongst glaucomatous patients, 46–92% show a significant IOP rise after topical steroid administration [10].
Risk factors for the development of steroid-induced OHT and SIG are as follows: individual susceptibility, likely related to different isoforms of the glucocorticoids receptors; older and younger age, especially children younger than 6 years; glaucomatous patients and first-degree relatives of glaucomatous patients; connective tissue diseases; and high myopia, DM type I [8].
Steroid-induced OHT is usually reversible by the interruption of CS therapy, with IOP usually returning to normal levels in 2–4 weeks after discontinuing the steroids [8].
-
Steroid-induced cataract: Prolonged use of high doses of CSs, especially if systemically administered, is a significant risk factor for the development of bilateral posterior subcapsular cataracts, with a higher incidence in children and susceptible subjects [7]. CSs are the fourth leading risk factor for cataract development, following diabetes, myopia, and glaucoma, and it has been calculated that approximately 4.7% of all cataracts are steroid-induced [7].
The mechanisms underlying lens opacification, also when associated with CS-therapy, are still unknown. It is supposed that the steroid-induced reduction of the VEGF and other growth factors in the aqueous humor may prevent the normal differentiation of the lens epithelial cells into fiber cells. The undifferentiated lens epithelial cells migrate along the capsule until reaching the posterior pole, where they form an irregular aggregate of cells that scatter light [7]:
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Because of their immunosuppressive effect, steroids may favor opportunistic bacterial, viral, and fungal ocular infections that are most often associated with the topical use of CSs [4][9].
-
Central serous chorioretinopathy (CSCR) development or recurrence: CSCR is an idiopathic retinal disease characterized by leakage of fluid through the RPE into the subretinal space, with serous detachments of the neurosensory retina and RPE, leading to central vision loss and metamorphopsia. Although still debated, the association between CRSC and CSs has been widely reported [5][6]. The proposed pathogenic mechanisms are a steroid-induced RPE active fluid pump impairment and an increase in the choroidal vessel permeability [5][6].
f
The rationale of the use of steroids in the pharmacological approach to DME
CSs have gained great interest in DME management over the last years, and the rationale for their use is clear evidence that inflammation plays a fundamental role in DME pathogenesis and that several inflammatory pathways beyond VEGF are involved in this process [11][12][13].
CSs represent an alternative therapeutic strategy in DME because of their multiple anti-inflammatory and anti-angiogenic effects [14][15] (Table 2), and their use in DME may be theoretically more rationale and comprehensive [14] than that of anti-VEGF agents that target only a part of the inflammatory cascade [16].
Table 2. Anti-inflammatory and anti-angiogenic properties of intra-vitreal corticosteroids.
Animal experiments and clinical studies on DME patients have shown that IV injections of CSs are able to reduce the aqueous and vitreal levels of several pro-inflammatory chemokines and cytokines, including VEGF, whereas anti-VEGF agents decrease the VEGF concentration but do not alter the levels of other inflammatory molecules [17]. These findings can explain the persistence of DME despite repeated anti-VEGF IV injections [18][19][20][21].

2. Intravitreal Corticosteroids Used for the Treatment of DME

Intravitreal injection represents the most common route for the CSs’ ophthalmic administration in DME management, allowing rapid delivery of a large volume of drugs immediately available to the target site and limiting possible systemic side effects. Sustained-release CS implants have been developed in order to reduce the need for frequent IV injections [14][15].
Intravitreal CSs used to treat DME include triamcinolone acetonide (TA), dexamethasone (DEX), and fluocinolone acetonide (FAc) [14][15]. These three molecules have different receptor affinity, solubility, pharmacokinetic, and different gene regulation patterns, with consequently different clinical effects and safety characteristics [14][15].
a
Tiamcinolone acetonide (TA) [22]: This is commercially available as Kenalog-40 (Bristol-Myers Squibb, New York, NY, USA) or Tajoftal (Sooft Italia s.p.a. Montegiorgio, Udine, Italy), which is a crystalline powder available as an injectable suspension containing 40 mg/mL TA in isotonic saline solution and is delivered using a 30-gauge needle. TA is not approved for intraocular use, but it is used off-label to treat vitreoretinal diseases in a dose ranging between 1 and 4 mg [23], with functional and anatomical efficacy within 3–6 months post-injection [24]. Two other administration routes of TA tested in DME eyes, the posterior sub-tenon injection of 20 or 40 mg of TA [25] and the suprachoroidal injection of 2 or 4 mg of TA [26], have shown results comparable to those obtained with the IV TA injections, with less side effects. There is a preservative-free TA approved for intraocular use, though it is not for DME per se and not easily available, Triesence (Alcon Pharmaceuticals, Ft. Worth, TX, USA).
b
Dexamethasone (DEX) [27]: This is commercially available as a sustained-release biodegradable insert, the Ozurdex intravitreal implant (Allergan, Dublin, Ireland), which is a cylindrical tube (6 mm × 0.46 mm) composed of polylactic-co-glycolic acid polymers containing 0.7 mg of DEX, degrading into carbon dioxide and water as DEX is released into the vitreous body [28]. Ozurdex is delivered into the vitreous cavity using a single-use applicator with a 22-gauge needle for IV injection, and it was projected to endure a continuous IV release of micronized DEX over a period of ≤6 months. The peak of the functional and anatomical efficacy of the Ozurdex insert is typically reached at 2 months post-injection and has a duration of action of approximately 6 months [28].
The 3-year, randomized, multicenter, masked, sham-controlled clinical trial MEAD study led to the approval of the DEX 0.7 mg implant (Ozurdex) [27]. The FDA approved the Ozurdex IV implant for the treatment of adult patients with DME in 2014; the EMA approved Ozurdex in 2014 for the treatment of adult patients with visual impairment due to DME, retina vein occlusion, and noninfectious posterior segment uveitis, who are pseudophakic or who are considered insufficiently responsive or unsuitable for non-corticosteroid therapy [29]. The official product label in Europe recommends re-treatment of Ozurdex after approximately 6 months, and it does not recommend simultaneous administration in both eyes.
c
Fluocinolone acetonide (FAc) [30]: This is commercially available as an IluvienTM IV implant (Alimera Sciences Inc., Alpharetta, GA, USA), which is a sustained-release non-biodegradable IV insert containing 0.19 mg of FAc. Iluvien is a cylindrical tube (3.5 mm × 0.37 mm) of polymer loaded with FAc that is inserted into the vitreous cavity through a 25-gauge needle and releases 0.2 µg/day of FAc. The FAMOUS study has demonstrated that the Iluvien IV implant is able to maintain a therapeutic concentration of FAc over a period of 36 months [31]. The peak of the functional and anatomical efficacy of the Iluvien IV insert has been observed between 6 and 11 months post-injection [32][33]. Being a non-biodegradable implant, floaters have been complained about by some patients after Iluvien implant [32][33].
The Fluocinolone Acetonide in diabetic Macular Edema (FAME) study [30], a 3-year, randomized, sham injection-controlled, double-masked, multicenter clinical trial, led to the FDA approval, in 2014, of the FAc 0.19 mg IV implant (IluvienTM) for the treatment of DME in patients who were previously treated with steroids and did not have a clinically significant IOP elevation, excluding patients with confirmed or suspected ocular or periocular infections, patients with glaucoma and CRD ≥ 0.8, and patients with known hypersensitivity to any component of the implant [29][32].
In 2014, the EMA approved the Iluvien IV implant for the treatment of vision impairment associated with non-infectious uveitis or chronic DME insufficiently responsive to other available therapies [29][32].
The official product label in Europe recommends retreatment after at least 1 year and does not recommend the simultaneous treatment of both eyes.

3. Pharmacology of Intravitreal Corticosteroids Used for the Treatment of DME

a
Water solubility: DEX is the one that is the most water soluble, which implies increased bioavailability but rapid elimination. For these reasons, it is available commercially as a sustained-release biodegradable implant [15]. Fac is 50% less water soluble than DEX but still requires a sustained-release delivery system to maintain an efficient IV concentration of the drug over time. TA has low water solubility, and it is available as an IV injectable suspension [15]. Sustained IV inserts have the advantage of reducing the frequency of IV injections, with a subsequent decrease in complications related to repeated IV injection procedures, higher patient compliance, and lower healthcare costs [15].
b
Intravitreal pharmacokinetics: Human studies analyzing aqueous humor samplings have demonstrated that the 4 mg TA IV injection has a mean elimination half-time of 15.4 ±1.9 days [34].
Animal studies (monkeys and rabbits) have shown that the Ozurdex IV implant has the highest rate of drug release during the first 2 months, followed by a prolonged lower level of release, with IV DEX levels not more detectable 6 months after the implant [28]. Moreover, DEX was detected in the plasma only in a small percentage of samples (12%) [28], suggesting a high systemic safety profile of the Ozurdex IV insert.
Human studies have demonstrated that, after the Iluvien IV implant, FAc was detectable in the aqueous humor at 36 months, and that the plasma levels of FA were always below the limits of quantification [31].
In comparison with both IV TA injection and FAc implant, Ozurdex IV insert has been demonstrated to provide extremely higher doses of steroids delivered into the vitreous body and the retina during the first 2 months of therapy. Conversely, the Iluvien insert was projected to release a sustained low concentration of steroids for a long period of time. Studies in rabbits have calculated that the vitreous maximum concentration after the IV injection of 4 mg TA, DEX 0.7 mg, and FAc 0.59 mg implants were 460 ng/mL, 1300 ng/mL, and 18 ng/mL, respectively [15]. The Ozurdex implant represents, therefore, a pulse administration of a high dose of CSs, which is a therapeutic modality successfully used to treat important inflammatory or autoimmune diseases, such as acute optic neuritis [1][2]. Moreover, the well-known phenomenon of reduced responsiveness to steroid treatment over time, likely related to the downregulation of the glucocorticoid receptors, is alleviated by a pulse dosing of CSs, as provided by the Ozurdex insert [15].

4. Clinical Efficacy and Safety Profile of Intravitreal Corticosteroids Used in DME Treatment

a
Triamcinolone acetonide (TA)
RCTs failed to demonstrate the non-inferiority of IVTA in comparison with IV sham injections [35], macular laser photocoagulation [22], or anti-VEGF agents [19] so TA did not receive approval for DME treatment.
In particular, the DRCR.net Protocol B, a 3-year RCT including CIDME 840 eyes randomized to receive IV injections of TA 1 mg or 4 mg or focal/grid laser photocoagulation, demonstrated that IVTA was associated with lower VA gain and higher risk of IOP rise and cataract development than laser [22].
The DRCR.net Protocol I, a 5-year RCT including CIDME 854 eyes randomized to receive sham injection + prompt laser, 4 mg IVTA injection + prompt laser, or ranibizumab injection + prompt or deferred laser, showed that the VA gain was significantly higher in both ranibizumab groups (comparable between ranibizumab and TA in pseudophakic eyes), with lower local side effects [19].
IVTA has been widely used off-label with different dosages and intervals between administrations, showing to be an effective and relatively inexpensive method for DME management [36].
TA intravitreal injection has shown a clear time-limited therapeutic effect, with clinical efficacy for approximately 3 months [35][36][37][38].
The cumulative incidence of OHT after IVTA injections ranges between 13% and 50% [19][22][35][36][37][38][39][40][41]. The time required for the IOP elevation after a TA injection is 1–8 weeks, IOP reaches the peak value in 2–16 weeks, remains elevated for 1–9 months, and returns to pre-treatment values after 4–9 months [42]. The majority of cases of steroid-induced IOP rise post-IVTA (95–97% of cases) can be managed with ocular hypotensive drugs, whereas a minority of cases should receive glaucoma surgery [8][19][35].
The incidence of cataract extraction requirement after IVTA injections ranges between 10% and 83%, with a higher incidence in younger patients [19][22][35][36][37][38][39][40][41].
As compared to the anti-VEGF agents, IVTA provided lower functional results when both phakic and pseudophakic eyes were considered [19][39][40][41][43], and there was similar VA gain in pseudophakic eyes, where the confounding factor of the cataract development is excluded [19]. The morphological outcomes were comparable or lower than those related to the anti-VEGF agents [19][39][41][44].
The functional and anatomical outcomes of the association of IVTA with macular laser [45] or with anti-VEGF [44][46] were comparable to those obtained with macular laser or anti-VEGF as monotherapy and were linked to a higher risk of IOP rise and cataract development.
In conclusion, although IVTA has shown to be effective in DME management, its short duration of action and the high incidence of IOP elevation and cataract development, especially in younger patients, have limited its use in favor of other approved intravitreal CSs. More recently, TA administered as supra-choroidal [26][47] and sub-tenon injections [25] in DME eyes has shown promising although time-limited results.
b
Dexamethasone
The registration study “MEAD” [27] was a 3-year, randomized, multicenter, masked, sham-controlled clinical trial including 1048 CIDME eyes (25% eyes were treatment-naïve) randomized to receive 0.7 mg or 0.35 mg DEX implant or sham procedure. Re-treatment was allowed no more often than every 6 months. The study demonstrated that both 0.7 mg and 0.35 mg DEX implants were significantly more effective than sham in improving VA and decreasing macular edema, although approximately 25% of eyes developed an IOP, 1.5% required glaucoma surgery, and 50–60% of phakic eyes required cataract surgery. The MEAD study demonstrated that the high-dose DEX insert provided the best benefit/risk ratio and led to the approval of the DEX 0.7 mg implant (Ozurdex) [27].
Another RCT [48] and numerous real-world studies [49][50][51][52] have demonstrated the effectiveness of the Ozurdex IV implant in DME treatment.
Published studies about Ozurdex implants having at least 24–36 months of follow-up reported a BCVA gain ranging between +2.8 and +9.6 letters [27][51][53][54]. The BCVA improvement was higher in pseudophakic eyes, where the confounding factor of the cataract development could be excluded [27][55][56]. The long-term functional response to Ozurdex seems to be predictable on the basis of the BCVA gain at 3 months post-injection [57]. Although the registration MEAD study allowed re-injections after 6 months, 35% of patients in the real-life studies required a re-injection between 3 and 5 months [49][58][59].
The Ozurdex IV implant has shown better functional and morphological results in treatment-naïve and in recent DME eyes [52][53][58][59][60], as well as when it was administered at need as opposed to a fixed regimen of 5 or 6 months of interval between re-injections [58][61]. The incidence of IOP elevation after the Ozurdex intravitreal implant ranges from 8% and 38% of cases [27][48][49][50][51][52][55][56][58][62][63][64][65]. Previous studies found that the IOP elevation after DEX implants was highly predictable, with the IOP peak occurring between 6 to 8 weeks post-op and returning to baseline values by around 3 to 4 months post-op [8][27][62][65]. Patients should, therefore, undergo a safety visit 6–8 weeks after the Ozurdex implant in order to evaluate the therapeutic response to the drug and to measure the IOP. Repeated injections of Ozurdex implants were not found to have any cumulative effect on the IOP [65].
The majority of cases of IOP elevation after the Ozurdex implant were generally transient and successfully managed with topical treatment, whereas filtration surgery was needed in 0–1.7% of cases [27][48][49][58][62][65], and the surgical options include trabeculectomy, shunts implant, and minimally invasive glaucoma surgery [66].
Cataract development or progression in phakic eyes after 0.7 mg DEX implant was 68% in the approval MEAD study [27], whereas real-life studies reported a lower incidence, ranging between 0% and 50%, due to the predominant selection of pseudophakic eyes [48][49][50][51][55][56][58][64][65][67]. The incidence of cataract development after Ozurdex varies depending on follow-up duration and type of treated pathology and seems to be directly correlated with the number of Ozudex implants [51][53][65].
Both RCTs and real-world studies showed that the Ozurdex implant is associated with high systemic safety, with systemic side effects involving less than 1% of patients, with the most frequent being hypertension worsening [27][58][65][68].
When compared to the macular focal/grid laser photocoagulation for CIDME management, Ozurdex has shown comparable functional results and better anatomical outcomes [50].
In general, the comparison of the Ozurdex IV implant and anti-VEGF in DME eyes has shown that Ozurdex is associated with the following:
-
lower BCVA gain [55][56][68], which became comparable to anti-VEGF when pseudophakic eyes were analyzed separately [55][56][63];
-
better anatomical results, i.e., higher ability in reducing the macular edema, that did not translate directly into better BCVA improvements [55][63][68][69][70][71][72], which may be likely due to the cataract development;
-
comparative better results in naïve than in non-naïve eyes, whereas the outcomes in the two groups appear similar in anti-VEGF studies [53];
-
better results in chronic and persistent DME eyes and in eyes with moderate-severe DME (CRT > 410 microns) [72][73]
-
better outcomes in real-life studies than in interventional studies [74]: the possibility of retreating at an earlier stage and the higher number of naïve (2/3 of treatment-naïve eyes in anti-VEGF studies vs. 1/5 in the Ozurdex studies), or short duration DME eyes with better baseline VA in the real-life studies, may explain these differences (on the other hand, systematic review and meta-analysis studies have demonstrated that IV anti-VEGF showed better anatomical and functional results in RCTs compared to the observational studies, likely because fewer injections are administered in the observation studies than those suggested by the RCTs [53][68][74], and VA gain seems to be strictly related to the number of the IV injections, at least during the first year of therapy [75][76]);
-
higher risk of OHT, glaucoma, and cataracts and lower risk of serious systemic adverse events [55][56][63][67][68][71];
-
lower number of required IV injections [53][55][56][68]: the comparison of the results of the MEAD study (Ozurdex pivotal study) [27] and RESTORE study (ranibizumab pivotal study) [77] showed that the VA gain observed in pseudophakic eyes receiving 0.7 mg DEX in the MEAD study (6 letters over 3 years with 4–5 implants) was comparable to that achieved in the RESTORE study by eyes receiving a mean of 7 ranibizumab injection/year
-
lower treatment costs, including medications, OCT, FA, and surgical procedures. The global cost of a 1-year therapy with Ozurdex is approximately one-half of that with anti-VEGF, which is mainly related to the significantly lower frequency of IV injections, even when the costs of the cataract and glaucoma surgeries are added [78].
Switching from anti-VEGF therapy to Ozurdex in cases of persistent and unresponsive DME has shown to be helpful [64][79], providing better functional and anatomical results and higher cost-effectiveness in cases of “early switch”, i.e., after non-adequate response to 3-monthly anti-VEGF injections [64][80].
As compared with the anti-VEGF agents as monotherapy, the association therapy of Ozurdex plus anti-VEGF has provided a BCVA gain similar [63] or better in the presence of high levels of OCT inflammatory biomarkers [67], with better anatomical results, and higher risks of IOP elevation and cataract development [63][67].
c
Fluocinolone acetonide
The registration study Fluocinolone Acetonide in diabetic Macular Edema (FAME) [30] was a 3-year, randomized, sham injection-controlled, double-masked, multicenter clinical trials including 956 patients with persistent DME despite macular laser (median duration of DME of 3 years) randomized to receive intravitreal inserts releasing 0.2 µg/day or 0.5 µg/day FAc or sham injection. Re-treatment was allowed no more often than every 12 months. FAc-treated eyes showed significantly higher VA gain and CRT reduction as compared with sham, with better results in chronic DME cases, although they were associated with an IOP rise in approximately 35% of eyes, needing glaucoma surgery in 4.8–8.1% of cases, and required cataract surgery in 40–50% of phakic eyes. The mean number of FAc re-treatments was 1.3 over 3 years. FAc-treated eyes required adjunctive therapies, such as laser, IVTA, or anti-VEGF intravitreal injections, in more than 50% of cases. The FAME study demonstrated that the low-dose FAc insert provided the best benefit/risk ratio as compared with the high-dose one and allowed for the FDA approval of the 0.2 µg/day (0.19 mg) FAc intravitreal implant (Iluvien TM) [30].
The clinical efficacy of the Iluvien intravitreal insert has been demonstrated by other RCTs and several real-life observational studies [81][82][83][84][85][86][87][88][89] and confirmed by systematic reviews, meta-analyses, and expert panels [90][91][92].
Published studies with the FAc implant with at least 36 months of follow-up reported a VA gain ranging between 3.6 and 11 letters [30][33][81][82][83][84][85][86][87][88][89].
Iluvien has shown higher effectiveness in chronic (>3 years duration) DME eyes [30] and has provided both functional and anatomic improvements in DME eyes with persistent DME and refractory to previous therapies with laser, anti-VEGF, or other intravitreal steroids (TA or DEX) [81][83][85][86][88][92][93][94].
Moreover, real-world studies with long follow-up showed that the long-active FAc implant was able to provide a long-lasting stabilization of the functional and, more importantly, of the anatomical outcomes, with decreased CRT variation for up to 3 years [82][84][86][89]. These results are crucial because reduced anatomical fluctuations have been associated with better functional improvements, whereas greater macular thickness variability in DME patients has been linked with neural damage and poorer visual outcomes [95][96].
Furthermore, with scheduled follow-ups every 4 months during the 36 months post-implant and a mean of 1.1 insert/3 years, Iluvien required a significantly lower frequency of treatment and check-up visits as compared with both anti-VEGF and other intravitreal steroids (TA and DEX), with a significant saving of time for diabetic patients, who are frequently pluri-medicated and poor-compliant, and a saving of costs for the public health system [97].
In steroid-responders, the IOP increase after the FA implant generally occurs within 2–4 weeks, reaches the peak at 24–48 weeks and returns to baseline values 9–12 months after implantation [8].
The approval study FAME reported that the 0.2 µg/d FAc insert was associated with an IOP rise ≥ 10 mmHg and the need for glaucoma surgery in 34% and 4.8% of cases, respectively (FAME). A post hoc analysis of the FAME study demonstrated that all glaucoma surgeries occurred in eyes with no history of a steroid challenge before the FAc implant [98], so that the FDA approved the IV FAc insert “in patients who have been previously treated with a course of corticosteroids and did not have a clinically significant rise in intraocular pressure”.
In real-world observational studies, the percentages of IOP-related side effects attributable to Iluvien appeared significantly lower than those reported by the FAME pivotal study [33]. Iluvien intravitreal implant was associated with a mean risk of post-operative IOP elevation of 20%, depending on the different definitions of IOP rise, with a risk of steroid-induced glaucoma of 0–10% [81][82][83][84][85][86][87][88][89][90][91][92][99] and a mean requirement of glaucoma surgeries of 0.6%, ranging from 0% to 4.3% [90][91], whereas a minority of cases should receive glaucoma surgery, including trabeculectomy, shunts implant, and minimally invasive glaucoma surgery [98].
This discrepancy between clinical trials and real-world data can be explained considering that, in clinical practice, almost only patients previously treated with intravitreal steroids without post-operative IOP elevation were selected [84][85][87][89].
Cataract development after 0.2 µg/d FAc implant was 82% in the FAME study, whereas in real-world studies, the incidence is limited by the prevalent selection of pseudophakic eyes, ranging between 40–65% of cases [81][82][83][84][85][86][87][88][89][90][91][92]. Phakic patients should expect to have cataract surgery planned between 13 and 18 months post-FAc injection [33].
Previous studies have shown that, although a single 3-year FAc implant was used in more than two-thirds of cases [30][90][91], additional treatments, such as laser photocoagulation, anti-VEGF, or intravitreal steroids achieving an acutely higher concentration, such as the TA or DEX implant, are required in the 33–75% of cases during the 3-year duration of the FAc implant [30][84][86][87][88][89][90][92]. On the other hand, when the FAc IV insert is considered as an additional therapy, it has been shown to significantly reduce the need for IV pharmacotherapy in DME eyes [33][82][89]. These supplementary treatments may represent a limitation and confounding factor in the evaluation of the Iluvien IV implant efficacy.
More recently, the suprachoroidal delivery of fluocinolone acetonide (IluvienR) implant in eyes with chronic DME has provided promising results in improving visual function and reducing the incidence of steroid-induced cataract and glaucoma [100].

5. When to Choose Intravitreal Corticosteroids for DME Treatment (Early Switch from Anti-VEGF or First-Line Therapy)

Subgroups of DME patients who can benefit from therapy with intravitreal steroids should include the following:
a
Patients unresponsive to anti-VEGF therapy: Previous RCTs [18][19][20][21] have demonstrated that approximately 40–65% of patients showed persistent DME despite adequate anti-VEGF therapy. It is important to note that the current literature does not provide a univocal definition of “poor-response” or “non-response” to treatment, so highly heterogeneous guidelines on when and how to switch or stop the different therapeutic approaches in DME have been proposed. The most commonly used definition of persistent or refractory DME after intravitreal pharmacotherapies is a VA gain of <5 letters and/or a CST reduction of <20% on OCT as compared to baseline [29][101].
The reason for the heterogeneous response to the anti-VEGF therapy is not yet fully understood and may be related to differences in VEGF gene polymorphism and expression, patient age, glycemic control, DR severity, and DME duration [102]. Studies have shown that DME patients with high serum and aqueous humor levels of VEGF will show a good response to anti-VEGF, whereas patients with low to normal VEGF levels and higher levels of inflammatory biomarkers do not adequately respond to anti-VEGF treatments [103] and may likely benefit from IV CSs that have been demonstrated to modulate several inflammatory pathways.
Moreover, considering that the final response to anti-VEGF therapy seems to be predictable after 3 to 6 injections and to be independent of the number of injections [20][104], the evaluation of the response after 3–6 IV injections could be appropriate to decide to try an alternative therapy.
According to the current Euretina guidelines, intravitreal CSs are considered a second-line option restricted to anti-VEGF non-responders or patients who have reached a plateau (persistent DME and VA < 5/10) after 3–6 anti-VEGF injections, depending on the response of each single patient [29].
b
Non-compliant patients or patients unable to maintain frequent follow-up visits: DME patients are often working, aging, or in poor health, requiring, therefore, frequent health care visits, and may thus have difficulties adhering to frequent office visits or monthly injection protocols. Approximately 60% of DME patients are poor or noncompliant with intravitreal therapy [105].
Previous RCTs have shown that anti-VEGF therapy requires a rigorous injection schedule to provide favorable outcomes [20][21][106][107], with heavy burdens for both patients and caregivers, and the VA gain is directly related to the number of anti-VEGF injections, especially in the first years of treatment [76][108]. On the other hand, patients receiving anti-VEGF therapy in real-life studies are frequently undertreated because intensive treatment with anti-VEGF is harder to maintain in clinical practice than in clinical trials and reaches poor visual outcomes [53][74].
Non-compliant patients could, therefore, benefit from therapy with intravitreal slow-release steroids, aiming to avoid suboptimal visual function improvement because of a sub-dosing anti-VEGF therapy.
c
Patients with recent arterial thromboembolism (ATE) events: The relationship between IV anti-VEGF injections and the risk of ATEs is still debated [109], and it was not clarified by the majority of the RCTs in which patients with recent ATEs were excluded from the study [21][106][107]. On the other hand, real-world studies and systematic reviews have reported a link between anti-VEGF therapy and several systemic side effects, including deterioration of systemic hypertension, renal dysfunction, gastrointestinal perforation, stroke, myocardial infarction, and thromboembolic events [110][111].
As suggested by several international guidelines, in patients with DME and a history of stroke or myocardial infarction it could be more prudent to use intravitreal CSc as first-line treatment rather than anti-VEGF agents [29][101][112][113][114][115][116].
d
Pregnant or breastfeeding women: DME can progress rapidly during pregnancy, especially in DM type 1 [117][118][119], so the management in pregnancy could be a challenge. The use of anti-VEGF in pregnancy is not recommended because of its potential negative effects on the angiogenesis of developing embryos or fetuses, and several case series have demonstrated a correlation between anti-VEGF IV injections given at the first five weeks of gestation and miscarriages or pre-eclampsia [120]. Although a close observation is suggested in the majority of cases, focal laser photocoagulation or intravitreal Ozurdex implant should be considered as the first-line treatment for DME in pregnancy, when therapy is considered to be necessary [29][101][112][113][114][115][116].
Intravitreal TA [121] and DEX [122] have been already used in the treatment of DME in pregnancy, with no reported side effects.
e
Presence of chronic DME: In cases of chronic edema, anti-VEGF has demonstrated poor efficacy [20][102][123], whereas IV CSs have shown efficacy in persistent DME unresponsive to anti-VEGF therapy [27][30][37][73][81][83][85][86][88][92][93][94].
Previous studies have reported that Ozurdex induced a significant VA gain if administered in eyes with chronic DME resistant to anti-VEGF [72][73].
The Iluvien approval study FAME showed that FAc intravitreal implant was more effective in patients having DME for more than 3 years as compared to patients with more recent DME [30]. Moreover, in real-life studies, Iluvien has demonstrated the ability to increase BCVA and reduce macular thickness in DME patients with persistent DME after treatment with IV anti-VEGF and CSc (TA or Ozurdex) [81][83][85][86][88][92][93][94];
f
Presence of hard exudates (HE) at the center of the fovea: This represents a major complication of DME because it can cause severe central visual loss and it is a negative predictive factor for visual outcomes [124][125]. A post-hoc analysis of the RCT Bevordex study comparing Ozurdex implants every 4 months and monthly bevacizumab injections showed that Ozurdex was associated with greater regression of the HE at 12 months [56]. These results suggest the preferential use of DEX over anti-VEGF in eyes with foveal hard exudates.
g
Associated OCT features of inflammation: Many OCT features, biomarkers of a high level of retinal inflammation and/or chronic DME, seem to be able to predict a poor or suboptimal responsiveness to anti-VEGF treatment, suggesting, therefore, the use of CSs as first-line therapy or an early switch to CS-therapy [126], which include the presence of large intra-retinal para-foveal cysts, a CRT > 410 µm, a large extension of the disorganization of the inner and outer retinal layers, a higher amount of hyper-reflective foci (HRFs), and the presence of a sub-foveal serous retinal detachment (SRD) [126]. In particular, a greater level of HRF seems to be one of the most important predictors for a better response to CS than to anti-VEGF [127]. OCT biomarkers in DME are proposed in order to identify in general good or poor responders to various treatments and to guide the decision to switch to other treatment options, allowing for a more personalized treatment with better visual outcomes [126][128].
h
Need for cataract surgery: DM patients are at higher risk of developing or deteriorating DME after cataract surgery and have a higher incidence of post-surgery macular edema, the so-called Irvine–Gass syndrome (IGS) [129]. Previous authors have reported that 22% of diabetic patients and 30% of patients with DR developed or worsened DME within 1 year after cataract surgery [129]. The results of the anti-VEGF therapy in cases of post-cataract surgery DME or of IGS are inconclusive [130], whereas IV CSs have shown promising outcomes.
The off-label IV or sub-tenon administration of TA has been shown to prevent the development or increase of DME in diabetic patients after cataract surgery [131].
Ozurdex has been shown to be effective in preventing the onset or deterioration of DME and the IGS post-cataract surgery in diabetic patients when administered 2–4 weeks before, concurrently, or post-cataract surgery [132][133].
i
Vitrectomized eyes: The vitreous body serves as a reservoir of IV-injected drugs. The study of the efficacy of the anti-VEGF agents in vitrectomized eyes has been proven to be time-limited [134], whereas TA [135][136], Ozurdex [137], and Iluvien [138] have been shown to be effective in vitrectomized eyes and can be considered the first choice in vitrectomized eyes in suitable cases.

6. When to Avoid Intravitreal Corticosteroids/Prefer Anti-VEGF Agents for DME Treatment

a
History of glaucoma or OHT: IOP rise and glaucoma are the most frequent and important side effects of the IV CSs. An IOP elevation (IOP > 25 mmHg or IOP rise ≥ 10 mmHg) has been reported in 13–50% of cases with IVTA [19][22][42], in 8–38% after Ozurdex [62][65], and in 8–34% after Iluvien [86][89].
Patients with a higher risk of developing IOP elevation after IV steroid therapy are those with OHT, glaucoma, or previous steroid-associated IOP elevation [8][10].
For patients receiving IVTA, the topical CSs challenge had a positive predictive value of 100% and a negative predictive value of 60% [139], so that the utility of the topical CS challenge before the CS intravitreal administration of a different type of CS remains unclear [8].
Considering the Ozurdex IV implant, significant risk factors for post-injection IOP elevation have been demonstrated to be younger age, male sex, type 1 DM, history of uveitis, or preexisting glaucoma treated with two or three hypotensive agents [62]. In particular, glaucomatous patients treated with one, two, or three ocular hypotensive agents had, respectively, 37%, 50%, and 100% risk of being high CS-responders, i.e., of developing an IOP elevation of >15 mmHg after the first Ozurdex injection [62].
Based on the results of the approval FAME study [30], Iluvien has been approved by the FDA explicitly for the treatment of patients who were non-steroid-responders [29][101][114]. Indeed, the absence of IOP elevation after a prior steroid IV injection has been shown to have a positive predictive value ranging between 80% and 100% for a very low risk of IOP increase after the Iluvien implant [82][89][99], whereas eyes showing IOP elevation after Ozurdex had a 20-fold increased risk of developing an OHT after the Iluvien implant [85].
In consideration of all these clinical data, following the current guidelines, IVCS is not indicated in cases of advanced glaucoma treated with two or more anti-glaucomatous agents, and it is allowed in cases of OHT or early to moderate stable glaucoma well controlled with mono-therapy [29][101][114].
On the other hand, anti-VEGF therapy has been associated with an increased risk of persistent IOP rise requiring IOP-lowering treatment in only 5–10% of cases [111] and should be used as first-line DME treatment, especially in OHY and glaucomatous patients.
b
Phakic patients with transparent crystalline: The intravitreal CS treatment has been associated with a high rate of cataract development or progression, particularly in the second year of treatment [19][22][27][30][35][58][65][89][90][91][92]. The incidence of cataract development or progression has been reported to range between 10% and 83% for TA [19][22][35], between 0% and 68% for DEX [27][58][65], and between 40% and 82% for FAc [30][89][90][91][92], whereas it was between 0 and 15.4% after anti-VEGF injections in real-life studies [111].
Considering the cataractogenic effects of IV steroids, they are not suggested in children and young adults and subjects with transparent crystalline affected by DME.
c
History of active or past ocular and periocular infections such as herpes or toxoplasmosis [101]. The CSs have a strong immunosuppressive action, so they can exacerbate all types of infections, and case reports of reactivation of ocular herpetic infection [4] or of acute retinal necrosis [9] after Ozurdex IV implant have been described.
d
Aphakia, absence or interruption of the posterior capsule, large iridectomy: All these conditions are associated with the risk of the implant migration into the anterior chamber, which has been described both for Ozurdex [140] and for Iluvien [141]. The migration of the implant into the anterior chamber can lead to localized or diffuse corneal edema due to endothelial cell loss, which may be related to the chemical toxicity of the implant components or to the mechanical trauma of the rigid device in contact with the cornea [140][141].
e
Presence of DME associated with advanced DR or with PDR: Previous studies have shown that both IV anti-VEGF (ranibizumab and aflibercept) [18][142] and IV CSs (TA, Ozurdex, and Iluvien) [22][143][144] used for the treatment of DME were able to simultaneously reduce the risk of DR progression and PDR development. The five-year outcomes of the Bevordex study showed that patients receiving anti-VEGF (bevacizumab) were less likely to develop PDR than those receiving Ozurdex [56], suggesting that anti-VEGF may be superior to CSs because of its greater anti-angiogenic effect. Anti-VEGF agents are currently considered the first-line treatment option in eyes with DME associated with PDR [29][101][112][113][114][115][116].

7. Summary of the Efficacy and Safety of the Intravitreal Corticosteroid in DME Management

a
Global efficacy and safety profile of intravitreal steroids: The Cochrane Library systematic review published in 2020, including 10 RCTs (4505 eyes) and evaluating the efficacy and safety of IV steroids (TA, DEX, and FAc) as monotherapy for the treatment of DME, concluded that “IV steroids probably are more effective than sham treatment or control, with levels of evidence higher for FAc, lower for DEX and lowest for TA, providing small VA gain (1 ≤ Snellen line) in most studies; they probably are less effective than anti-VEGF in improving BCVA; they are associated with increased risk of cataract development and progression (20% in the control groups and 50–60% in the steroid groups), and may be therefore indicated in pseudophakic eyes; they are associated with IOP elevation (5% in control groups and 30% in steroids groups), need of IOP-lowering medications (1% in control groups and 33% in steroids groups), and need of glaucoma surgery (<1% of controls and 2% in patients treated with steroids); the need of glaucoma surgery is probably higher with FAc)” [145].
b
Comparison of the efficacy profile amongst TA, DEX and FAc: A direct comparison amongst TA, DEX, and FA has not yet been performed either in RCTs nor in large real-life studies. Moreover, having a different pharmacokinetic, they should probably not simply be compared but instead utilized in different selected cases. TA and DEX can be considered as an attack treatment, because, once injected, they immediately release an important dose of drug into the vitreal cavity [15]. On the other hand, the FAc implant can be defined as a background therapy because it delivers low concentrations of FAc into the eye for approximately 36 months [15]. The FAc implant aims to stabilize DME and should be injected preferably in DME eyes that respond to steroid therapy [33].
The “CONSTANT analysis” study has compared the effectiveness of Ozurdex and Iluvien for the treatment of DME found in their pivotal clinical trials and the MEAD [27] and FAME study [30], respectively, by calculating the area under the curve provided by the average letters gained across the entire treatment period (3 years) [146]. The results showed that, as compared with Ozurdex, Iluvien provided better long-term VA outcomes (5.2 vs. 3.5 letters/day, respectively) and a higher reduction of the CRT, with a lower treatment burden. Possible limitations of the MEAD study are that patients could be retreated with the Ozurdex no more often than every 6 months [27] and that cataract surgeries were performed with delay, between months 18 and 30, whereas in the FAME study, the median time of cataract extraction was 18 months [30].
Considering the results of the real-life studies, a small single-center retrospective study comparing the efficacy of Ozurdex and TA 2 mg in eyes with persistent DME after anti-VEGF treatment showed similar functional and anatomical results in the two groups [147]. Moreover, both Ozurdex and Iluvien have been shown to be effective in treating DME in patients previously unsuccessfully treated with TA [93][148]. Finally, the switch from Ozurdex to Iluvien has provided good functional and morphological results in chronic refractory DME eyes [85][87].
c
Comparison of the safety profile amongst TA, DEX, and FAc: The risk for steroid-induced OHT or SIG seems to be higher for FA, lower for TA, and lowest for DEX [8]. Furthermore, Ozurdex [27] is associated with a lesser risk of cataract development as compared with IVTA [22] or Iluvien [30]. These differences may be related to their different gene regulation pattern at the level of the human trabecular meshwork cell lines; moreover, DEX is less lipophilic than TA and FA, with less accumulation in the trabecular meshwork and lens, explaining the reduced incidence of IOP elevation and cataract with Ozurdex [149].
Finally, compared with other CS, DEX is associated with fewer systemic side effects [8].
d
Comparison between intravitreal steroids and anti-VEGF: The review of the literature suggests that both IV anti-VEGF agents and steroids are effective in DME treatment, although further pieces of evidence are needed to determine the comparative efficacies of these treatments [150][151].
Previous studies have shown that intravitreal CSs (TA and DEX) can provide similar VA improvements as anti-VEGF therapy, at least in pseudophakic eyes, where cataract progression does not limit functional performances [19][55][56][63]. A recent systematic review and meta-analysis, including 138 real-life observational studies representing more than 40,000 DME eyes treated with IV pharmacological agents or laser in the last decade, found that these therapies led generally to VA gain in real-world practice, with comparable results for anti-VEGF and CS (mean VA gain at 12 months of +4.6 letters for anti-VEGf and +4.4 letters for steroids) and significantly lower results associated with laser (+2.1 letters at 1-year follow-up), and that the clinical outcomes of the IV pharmacotherapies were significantly less impressive than those obtained in the RCTs, which was likely due to under-treatment and study population characteristics [54].
Other authors have recently underlined that both IV CSs and anti-VEGF do not result in a completely dry macula in approximately 50% of cases and that, because of their different mechanisms of action, the response can be better with one treatment compared to the other due to the disease and patient characteristics [152].
A new comprehensive review and meta-analysis conducted by the American Academy of Ophthalmology investigating efficacy and safety of the IV pharmacological therapy for DME reported that both anti-VEGF and CSs are similarly effective for DME treatment, with higher ocular side effects (cataract and IOP elevation) associated with CSs, especially in predisposed patients [153].
As already underlined, IV steroids are associate with high risk of IOP rise (0–35%) and cataract development (0–80%) [19][22][27][30][35][36][37][40], whereas these complications affect ≤ 15% of anti-VEGF-treated eyes [111].
On the other hand, IV CSs have shown high systemic safety, with ATEs incidence comparable to that found in controls [19][27][30], whereas IV anti-VEGF agents have been associated with significantly increased risk of systemic side effects and ATEs [110][111].
Moreover, IV CSs have shown to be more effective than anti-VEGF in cases of chronic and persistent or recurrent DME [27][30][72][73][81][83][85][86][88][92][93][94], where anti-VEGF have demonstrated poor efficacy in these cases [20][102][123].
Finally, as compared with anti-VEGF therapy, IV sustained-release CSs are associated with a significantly lower number of IV injections and check-up visits [55][56][82][89], which may reduce the injection-related complications [154] and improve patient compliance and reduce the costs for the public health system [78][97].
e
Rationale of the association of intravitreal steroids and anti-VEGF agents: These drugs have different mechanisms of action and could theoretically work well in combination. A systematic review and meta-analysis of the Cochrane Library published in 2018, which included 8 RCTs for a total of 817 eyes (the majority of which using bevacizumab plus TA), showed that the combination of IV anti-VEGF and steroids does not appear to provide additional visual benefit compared to monotherapy, exposing the patients to the potential side effects of both agents, such as cataract, glaucoma, stroke, and heart attack [155].

References

  1. Adcock, I.M.; Mumby, S. Glucocorticoids. Handb. Exp. Pharmacol. 2017, 237, 171–196.
  2. Kapugi, M.; Cunningham, K. Corticosteroids. Orthop. Nurs. 2019, 38, 336–339.
  3. Jonas, J.B.; Söfker, A. Intraocular injection of crystalline cortisone as adjunctive treatment of diabetic macular edema. Am. J. Ophthalmol. 2001, 132, 425–427.
  4. Jusufbegovic, D.; Schaal, S. Quiescent herpes simplex keratitis reactivation after intravitreal injection of dexamethasone implant. Retin. Cases Brief Rep. 2017, 11, 296–297.
  5. Nicholson, B.P.; Atchison, E.; Idris, A.A.; Bakri, S.J. Central serous chorioretinopathy and glucocorticoids: An update on evidence for association. Surv. Ophthalmol. 2018, 63, 1–8.
  6. Araki, T.; Ishikawa, H.; Iwahashi, C.; Niki, M.; Mitamura, Y.; Sugimoto, M.; Kondo, M.; Kinoshita, T.; Nishi, T.; Ueda, T.; et al. Central serous chorioretinopathy with and without steroids: A multicenter survey. PLoS ONE 2019, 14, e0213110.
  7. Kačmar, J.; Cholevík, D. Corticosteroid Induced Posterior Subcapsular Cataract. Czech Slovak Ophthalmol. 2019, 74, 226–232. (In English)
  8. Roberti, G.; Oddone, F.; Agnifili, L.; Katsanos, A.; Michelessi, M.; Mastropasqua, L.; Quaranta, L.; Riva, I.; Tanga, L.; Manni, G. Steroid-induced glaucoma: Epidemiology, pathophysiology, and clinical management. Surv. Ophthalmol. 2020, 65, 458–472.
  9. Ulavíková, Z.; Anwarzai, J.; Krásnik, V. Acute retinal necrosis after intravitreal dexamethasone implant. A case report. Cesk. Slov. Oftalmol. 2022, 78, 144–148. (In English)
  10. Armaly, M.F.; Becker, B. Intraocular pressure response to topical corticosteroids. Fed. Proc. 1965, 24, 1274–1278.
  11. Yoshimura, T.; Sonoda, K.-H.; Sugahara, M.; Mochizuki, Y.; Enaida, H.; Oshima, Y.; Ueno, A.; Hata, Y.; Yoshida, H.; Ishibashi, T. Comprehensive analysis of inflammatory immune mediators in vitreoretinal diseases. PLoS ONE 2009, 4, e8158.
  12. Daruich, A.; Matet, A.; Moulin, A.; Kowalczuk, L.; Nicolas, M.; Sellam, A.; Rothschild, P.-R.; Omri, S.; Gélizé, E.; Jonet, L.; et al. Mechanisms of macular edema: Beyond the surface. Prog. Retin. Eye Res. 2018, 63, 20–68.
  13. Zhang, J.; Zhang, J.; Zhang, C.; Zhang, J.; Gu, L.; Luo, D.; Qiu, Q. Diabetic Macular Edema: Current Understanding, Molecular Mechanisms and Therapeutic Implications. Cells 2022, 11, 3362.
  14. Zhang, X.; Wang, N.; Schachat, A.P.; Bao, S.; Gillies, M. Glucocorticoids: Structure, signaling and molecular mechanisms in the treatment of diabetic retinopathy and diabetic macular edema. Curr. Mol. Med. 2014, 14, 376–384.
  15. Whitcup, S.M.; Cidlowski, J.A.; Csaky, K.G.; Ambati, J. Pharmacology of Corticosteroids for Diabetic Macular Edema. Investig. Ophthalmol. Vis. Sci. 2018, 59, 1–12.
  16. Fogli, S.; Del Re, M.; Rofi, E.; Posarelli, C.; Figus, M.; Danesi, R. Clinical pharmacology of intravitreal anti-VEGF drugs. Eye 2018, 32, 1010–1020.
  17. Sohn, H.J.; Han, D.H.; Kim, I.T.; Oh, I.K.; Kim, K.H.; Lee, D.Y.; Nam, D.H. Changes in aqueous concentrations of various cytokines after intravitreal triamcinolone versus bevacizumab for diabetic macular edema. Am. J. Ophthalmol. 2011, 152, 686–694.
  18. Reddy, R.K.; Pieramici, D.J.; Gune, S.; Ghanekar, A.; Lu, N.; Quezada-Ruiz, C.; Baumal, C.R. Efficacy of Ranibizumab in Eyes with Diabetic Macular Edema and Macular Nonperfusion in RIDE and RISE. Ophthalmology 2018, 125, 1568–1574.
  19. Diabetic Retinopathy Clinical Research Network; Elman, M.J.; Aiello, L.P.; Beck, R.W.; Bressler, N.M.; Bressler, S.B.; Edwards, A.R.; Ferris, F.L., 3rd; Friedman, S.M.; Glassman, A.R.; et al. Randomized trial evaluating ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema. Ophthalmology 2010, 117, 1064–1077.e35.
  20. Bressler, N.M.; Beaulieu, W.T.; Glassman, A.R.; Blinder, K.J.; Bressler, S.B.; Jampol, L.M.; Melia, M.; Wells, J.A., 3rd. Diabetic Retinopathy Clinical Research Network Persistent Macular Thickening Following Intravitreous Aflibercept, Bevacizumab, or Ranibizumab for Central-Involved Diabetic Macular Edema With Vision Impairment: A Secondary Analysis of a Randomized Clinical Trial. JAMA Ophthalmol. 2018, 136, 257–269, Erratum in JAMA Ophthalmol. 2018, 136, 601.
  21. Glassman, A.R.; Wells, J.A., 3rd; Josic, K.; Maguire, M.G.; Antoszyk, A.N.; Baker, C.; Beaulieu, W.T.; Elman, M.J.; Jampol, L.M.; Sun, J.K. Five-Year Outcomes after Initial Aflibercept, Bevacizumab, or Ranibizumab Treatment for Diabetic Macular Edema (Protocol T Extension Study). Ophthalmology 2020, 127, 1201–1210.
  22. Diabetic Retinopathy Clinical Research Network (DRCR.net); Beck, R.W.; Edwards, A.R.; Aiello, L.P.; Bressler, N.M.; Ferris, F.; Glassman, A.R.; Hartnett, E.; Ip, M.S.; Kim, J.E.; et al. Three-year follow-up of a randomized trial comparing focal/grid photocoagulation and intravitreal triamcinolone for diabetic macular edema. Arch Ophthalmol. 2009, 127, 245–251.
  23. Hauser, D.; Bukelman, A.; Pokroy, R.; Katz, H.; Len, A.; Thein, R.; Parness-Yossifon, R.; Pollack, A. Intravitreal triamcinolone for diabetic macular edema: Comparison of 1, 2, and 4 mg. Retina 2008, 28, 825–830.
  24. Yilmaz, T.; Weaver, C.D.; Gallagher, M.J.; Cordero-Coma, M.; Cervantes-Castaneda, R.A.; Klisovic, D.; Lavaque, A.J.; Larson, R.J. Intravitreal triamcinolone acetonide injection for treatment of refractory diabetic macular edema: A systematic review. Ophthalmology 2009, 116, 902–911; quiz 912–913.
  25. Ogura, Y.; Shimura, M.; Iida, T.; Sakamoto, T.; Yoshimura, N.; Yamada, M.; Ishibashi, T. Phase II/III Clinical Trial of Sub-Tenon Injection of Triamcinolone Acetonide (WP-0508ST) for Diabetic Macular Edema. Ophthalmologica 2019, 241, 161–169.
  26. Nawar, A.E. Effectiveness of Suprachoroidal Injection of Triamcinolone Acetonide in Resistant Diabetic Macular Edema Using a Modified Microneedle. Clin. Ophthalmol. 2022, 16, 3821–3831.
  27. Boyer, D.S.; Yoon, Y.H.; Belfort, R., Jr.; Bandello, F.; Maturi, R.K.; Augustin, A.J.; Li, X.-Y.; Cui, H.; Hashad, Y.; Whitcup, S.M.; et al. Three-Year, randomized, sham-controlled trial of dexamethasone intravitreal implant in patients with diabetic macular edema. Ophthalmology 2014, 121, 1904–1914.
  28. Chang-Lin, J.-E.; Attar, M.; Acheampong, A.A.; Robinson, M.R.; Whitcup, S.M.; Kuppermann, B.D.; Welty, D. Pharmacokinetics and pharmacodynamics of a sustained-release dexamethasone intravitreal implant. Investig. Ophthalmol. Vis. Sci. 2011, 52, 80–86.
  29. Schmidt-Erfurth, U.; Garcia-Arumi, J.; Bandello, F.; Berg, K.; Chakravarthy, U.; Gerendas, B.S.; Jonas, J.; Larsen, M.; Tadayoni, R.; Loewenstein, A. Guidelines for the Management of Diabetic Macular Edema by the European Society of Retina Specialists (EURETINA). Ophthalmologica 2017, 237, 185–222.
  30. Campochiaro, P.A.; Brown, D.M.; Pearson, A.; Chen, S.; Boyer, D.; Ruiz-Moreno, J.; Garretson, B.; Gupta, A.; Hariprasad, S.M.; Bailey, C.; et al. Sustained delivery fluocinolone acetonide vitreous inserts provide benefit for at least 3 years in patients with diabetic macular edema. Ophthalmology 2012, 119, 2125–2132.
  31. Campochiaro, P.A.; Nguyen, Q.D.; Hafiz, G.; Bloom, S.; Brown, D.M.; Busquets, M.; Ciulla, T.; Feiner, L.; Sabates, N.; Billman, K.; et al. Aqueous levels of fluocinolone acetonide after administration of fluocinolone acetonide inserts or fluocinolone acetonide implants. Ophthalmology 2013, 120, 583–587.
  32. Fusi-Rubiano, W.; Blow, R.R.; Lane, M.; Morjaria, R.; Denniston, A.K. Iluvien™ (Fluocinolone Acetonide 0.19 mg Intravitreal Implant) in the Treatment of Diabetic Macular Edema: A Review. Ophthalmol. Ther. 2018, 7, 293–305, Erratum in Ophthalmol. Ther. 2020, 9, 205.
  33. Kodjikian, L.; Bandello, F.; de Smet, M.; Dot, C.; Zarranz-Ventura, J.; Loewenstein, A.; Sudhalkar, A.; Bilgic, A.; Cunha-Vaz, J.; Dirven, W.; et al. Fluocinolone acetonide implant in diabetic macular edema: International experts’ panel consensus guidelines and treatment algorithm. Eur. J. Ophthalmol. 2022, 32, 1890–1899.
  34. Audren, F.; Tod, M.; Massin, P.; Benosman, R.; Haouchine, B.; Erginay, A.; Caulin, C.; Gaudric, A.; Bergmann, J.-F. Pharmacokinetic–pharmacodynamic modeling of the effect of triamcinolone acetonide on central macular thickness in patients with diabetic macular edema. Investig. Ophthalmol. Vis. Sci. 2004, 45, 3435–3441.
  35. Gillies, M.C.; Simpson, J.M.; Gaston, C.; Hunt, G.; Ali, H.; Zhu, M.; Sutter, F. Five-year results of a randomized trial with open-label extension of triamcinolone acetonide for refractory diabetic macular edema. Ophthalmology 2009, 116, 2182–2187.
  36. Aceves-Franco, L.A.; Sanchez-Aguilar, O.E.; Barragan-Arias, A.R.; Ponce-Gallegos, M.A.; Navarro-Partida, J.; Santos, A. The Evolution of Triamcinolone Acetonide Therapeutic Use in Retinal Diseases: From Off-Label Intravitreal Injection to Advanced Nano-Drug Delivery Systems. Biomedicines 2023, 11, 1901.
  37. Zając-Pytrus, H.M.; Kaczmarek, R.; Strońska-Lipowicz, D.; Pomorska, M.; Misiuk-Hojło, M. Theeffects and safety of intravitreal triamcinolone injections in the treatment of diabetic macular edema. Adv. Clin. Exp. Med. 2017, 26, 45–49.
  38. Sorrentino, F.S.; Bonifazzi, C.; Parmeggiani, F. Diabetic macular edema: Safe and effective treatment with intravitreal triamcinolone acetonide (Taioftal). PLoS ONE 2021, 16, e0257695.
  39. Rodrigues, M.W.; Cardillo, J.A.; Messias, A.; Siqueira, R.C.; Scott, I.U.; Jorge, R. Bevacizumab versus triamcinolone for persistent diabetic macular edema: A randomized clinical trial. Graefes Arch. Clin. Exp. Ophthalmol. 2020, 258, 479–490.
  40. Abdel-Maboud, M.; Menshawy, E.; Bahbah, E.I.; Outani, O.; Menshawy, A. Intravitreal bevacizumab versus intravitreal triamcinolone for diabetic macular edema–Systematic review, meta-analysis and meta-regression. PLoS ONE 2021, 16, e0245010.
  41. Zhu, Y.; Li, J.; Yu, S.; Mao, B.; Ying, J. Clinical Comparative Study of Intravitreal Injection of Triamcinolone Acetonide and Aflibercept in the Treatment of Diabetic Retinopathy Cystoid Macular Edema. Emerg. Med. Int. 2022, 2022, 1348855.
  42. Jain, S.; Thompson, J.R.; Foot, B.; Tatham, A.; Eke, T. Severe intraocular pressure rise following intravitreal triamcinolone: A national survey to estimate incidence and describe case profiles. Eye 2014, 28, 399–401.
  43. Kriechbaum, K.; Prager, S.; Mylonas, G.; Scholda, C.; Rainer, G.; Funk, M.; Kundi, M.; Schmidt-Erfurth, U.; Diabetic Retinopathy Research Group. Intravitreal bevacizumab (Avastin) versus triamcinolone (Volon A) for treatment of diabetic macular edema: One-year results. Eye 2014, 28, 9–15; quiz 16.
  44. Soheilian, M.; Garfami, K.H.; Ramezani, A.; Yaseri, M.; Peyman, G.A. Two-year results of a randomized trial of intravitreal bevacizumab alone or combined with triamcinolone versus laser in diabetic macular edema. Retina 2012, 32, 314–321.
  45. Zhang, L.; Chen, X. Efficacy and safety of triamcinolone acetonide injection combined with laser photocoagulation in the treatment of diabetic macular edema: A systematic review and meta-analysis. Ann. Palliat. Med. 2021, 10, 12467–12477.
  46. Arain, M.A.; Muzaffar, W.; Farooq, O.; Azhar, M.N. Combined Intravitreal Triamcenolone Acetonide and Bevacizumab for Refractory Diabetic Macular Edema. J. Coll. Physicians Surg. Pak. 2018, 28, 603–606.
  47. Barakat, M.R.; Wykoff, C.C.; Gonzalez, V.; Hu, A.; Marcus, D.; Zavaleta, E.; Ciulla, T.A. Suprachoroidal CLS-TA plus Intravitreal Aflibercept for Diabetic Macular Edema: A Randomized, Double-Masked, Parallel-Design, Controlled Study. Ophthalmol. Retin. 2021, 5, 60–70.
  48. Callanan, D.G.; Gupta, S.; Boyer, D.S.; Ciulla, T.A.; Singer, M.A.; Kuppermann, B.D.; Liu, C.-C.; Li, X.-Y.; Hollander, D.A.; Schiffman, R.M.; et al. Dexamethasone intravitreal implant in combination with laser photocoagulation for the treatment of diffuse diabetic macular edema. Ophthalmology 2013, 120, 1843–1851.
  49. Lam, W.-C.; Albiani, D.; Yoganathan, P.; Chen, J.C.; Kherani, A.; Maberley, D.; Oliver, A.; Rabinovitch, T.; Sheidow, T.G.; Tourville, E.; et al. Real-world assessment of intravitreal dexamethasone implant (0.7 mg) in patients with macular edema: The CHROME study. Clin. Ophthalmol. 2015, 9, 1255–1268.
  50. Heng, L.Z.; Sivaprasad, S.; Crosby-Nwaobi, R.; Saihan, Z.; Karampelas, M.; Bunce, C.; Peto, T.; Hykin, P.G. A prospective randomised controlled clinical trial comparing a combination of repeated intravitreal Ozurdex and macular laser therapy versus macular laser only in centre-involving diabetic macular oedema (OZLASE study). Br. J. Ophthalmol. 2016, 100, 802–807.
  51. Malclès, A.; Dot, C.; Voirin, N.; Agard, E.; Vié, A.-L.; Bellocq, D.; Denis, P.; Kodjikian, L. Real-life study in diabetic macular edema treated with dexamethasone implant: The reldex study. Retina 2017, 37, 753–760.
  52. Rosenblatt, A.; Udaondo, P.; Cunha-Vaz, J.; Sivaprasad, S.; Bandello, F.; Lanzetta, P.; Kodjikian, L.; Goldstein, M.; Habot-Wilner, Z.; Loewenstein, A.; et al. A Collaborative Retrospective Study on the Efficacy and Safety of Intravitreal Dexamethasone Implant (Ozurdex) in Patients with Diabetic Macular Edema: The European DME Registry Study. Ophthalmology 2020, 127, 377–393.
  53. Kodjikian, L.; Bellocq, D.; Mathis, T. Pharmacological Management of Diabetic Macular Edema in Real-Life Observational Studies. BioMed Res. Int. 2018, 2018, 8289253.
  54. Mehta, H.; Nguyen, V.; Barthelmes, D.; Pershing, S.; Chi, G.C.; Dopart, P.; Gillies, M.C. Outcomes of Over 40,000 Eyes Treated for Diabetic Macula Edema in Routine Clinical Practice: A Systematic Review and Meta-analysis. Adv. Ther. 2022, 39, 5376–5390.
  55. Callanan, D.G.; Loewenstein, A.; Patel, S.S.; Massin, P.; Corcóstegui, B.; Li, X.-Y.; Jiao, J.; Hashad, Y.; Whitcup, S.M. A multicenter, 12-month randomized study comparing dexamethasone intravitreal implant with ranibizumab in patients with diabetic macular edema. Graefes Arch. Clin. Exp. Ophthalmol. 2017, 255, 463–473.
  56. Cornish, E.E.; Teo, K.Y.; Gillies, M.C.; Lim, L.L.; Nguyen, V.; Wickremasinghe, S.; Mehta, H.; McAllister, I.L.; Fraser-Bell, S. Five-year outcomes of eyes initially enrolled in the 2-year BEVORDEX trial of bevacizumab or dexamethasone implants for diabetic macular oedema. Br. J. Ophthalmol. 2022, 107, 79–83.
  57. Al-Khersan, H.; Hariprasad, S.M.; Chhablani, J. Dex Implant Study Group. Early Response to Intravitreal Dexamethasone Implant Therapy in Diabetic Macular Edema May Predict Visual Outcome. Am. J. Ophthalmol. 2017, 184, 121–128.
  58. Bucolo, C.; Gozzo, L.; Longo, L.; Mansueto, S.; Vitale, D.C.; Drago, F. Long-term efficacy and safety profile of multiple injections of intravitreal dexamethasone implant to manage diabetic macular edema: A systematic review of real-world studies. J. Pharmacol. Sci. 2018, 138, 219–232.
  59. Castro-Navarro, V.; Cervera-Taulet, E.; Navarro-Palop, C.; Monferrer-Adsuara, C.; Hernández-Bel, L.; Montero-Hernández, J. Intravitreal dexamethasone implant Ozurdex® in naïve and refractory patients with different subtypes of diabetic macular edema. BMC Ophthalmol. 2019, 19, 15.
  60. Zarranz-Ventura, J.; Romero-Núñez, B.; Bernal-Morales, C.; Velazquez-Villoria, D.; Sala-Puigdollers, A.; Figueras-Roca, M.; Copete, S.; Distefano, L.; Boixadera, A.; García-Arumi, J.; et al. Differential response to intravitreal dexamethasone implant in naïve and previously treated diabetic macular edema eyes. BMC Ophthalmol. 2020, 20, 443.
  61. Sarao, V.; Veritti, D.; Furino, C.; Giancipoli, E.; Alessio, G.; Boscia, F.; Lanzetta, P. Dexamethasone implant with fixed or individualized regimen in the treatment of diabetic macular oedema: Six-month outcomes of the UDBASA study. Acta Ophthalmol. 2017, 95, e255–e260.
  62. Malclès, A.; Dot, C.; Voirin, N.; Vié, A.-L.; Agard, E.; Bellocq, D.; Denis, P.; Kodjikian, L. Safety of intravitreal dexamethasone implant (ozurdex): The SAFODEX study. Incidence and Risk Factors of Ocular Hypertension. Retina 2017, 37, 1352–1359.
  63. Maturi, R.K.; Glassman, A.R.; Liu, D.; Beck, R.W.; Bhavsar, A.R.; Bressler, N.M.; Jampol, L.M.; Melia, M.; Punjabi, O.S.; Salehi-Had, H.; et al. Effect of Adding Dexamethasone to Continued Ranibizumab Treatment in Patients With Persistent Diabetic Macular Edema: A DRCR Network Phase 2 Randomized Clinical Trial. JAMA Ophthalmol. 2018, 136, 29–38.
  64. Martínez, A.H.; Delgado, E.P.; Silva, G.S.; Mateos, L.C.; Pascual, J.L.; Villa, J.L.; Vicente, P.G.; Almeida-González, C.-V. Early versus late switch: How long should we extend the anti-vascular endothelial growth factor therapy in unresponsive diabetic macular edema patients? Eur. J. Ophthalmol. 2020, 30, 1091–1098.
  65. Rajesh, B.; Zarranz-Ventura, J.; Fung, A.T.; Busch, C.; Sahoo, N.K.; Rodriguez-Valdes, P.J.; Sarao, V.; Mishra, S.K.; Saatci, A.O.; Mirete, P.U.; et al. Safety of 6000 intravitreal dexamethasone implants. Br. J. Ophthalmol. 2020, 104, 39–46.
  66. Pérez-Sarriegui, A.; Casas-Llera, P.; Díez-Álvarez, L.; Contreras, I.; Moreno-López, M.; Figueroa, M.; González-Martín-Moro, J.; Muñoz-Negrete, F.; Rebolleda, G. Phaco-non-penetrating deep sclerectomy in ocular hypertension secondary to dexamethasone intravitreal implant. Arch. Soc. Esp. Oftalmol. 2018, 93, 580–585.
  67. Kaya, M.; Atas, F.; Kocak, N.; Ozturk, T.; Ayhan, Z.; Kaynak, S. Intravitreal Ranibizumab and Dexamethasone Implant Injections as Primary Treatment of Diabetic Macular Edema: The Month 24 Results from Simultaneously Double Protocol. Curr. Eye Res. 2023, 48, 498–505.
  68. He, Y.; Ren, X.-J.; Hu, B.-J.; Lam, W.-C.; Li, X.-R. A meta-analysis of the effect of a dexamethasone intravitreal implant versus intravitreal anti-vascular endothelial growth factor treatment for diabetic macular edema. BMC Ophthalmol. 2018, 18, 121.
  69. Shah, S.U.; Harless, A.; Bleau, L.; Maturi, R.K. Prospective randomized subject-masked study of intravitreal bevacizumab monotherapy versus dexamethasone implant monotherapy in the treatment of persistent diabetic macular edema. Retina 2016, 36, 1986–1996.
  70. Comet, A.; Gascon, P.; Ramtohul, P.; Donnadieu, B.; Denis, D.; Matonti, F. INVICTUS: Intravitreal anti-VEGF and dexamethasone implant comparison for the treatment of diabetic macular edema: A 12 months follow-up study. Eur. J. Ophthalmol. 2021, 31, 754–758, Erratum in Eur. J. Ophthalmol. 2020, 31, NP158.
  71. Patil, N.S.; Mihalache, A.; Hatamnejad, A.; Popovic, M.M.; Kertes, P.J.; Muni, R.H. Intravitreal Steroids Compared with Anti-VEGF Treatment for Diabetic Macular Edema: A Meta-Analysis. Ophthalmol. Retin. 2023, 7, 289–299.
  72. Chi, S.-C.; Kang, Y.-N.; Huang, Y.-M. Efficacy and safety profile of intravitreal dexamethasone implant versus antivascular endothelial growth factor treatment in diabetic macular edema: A systematic review and meta-analysis. Sci. Rep. 2023, 13, 7428.
  73. Pacella, F.; Romano, M.R.; Turchetti, P.; Tarquini, G.; Carnovale, A.; Mollicone, A.; Mastromatteo, A.; Pacella, E. An eighteen-month follow-up study on the effects of Intravitreal Dexamethasone Implant in diabetic macular edema refractory to anti-VEGF therapy. Int. J. Ophthalmol. 2016, 9, 1427–1432.
  74. Veritti, D.; Sarao, V.; Soppelsa, V.; Lanzetta, P. Managing Diabetic Macular Edema in Clinical Practice: Systematic Review and Meta-Analysis of Current Strategies and Treatment Options. Clin. Ophthalmol. 2021, 15, 375–385.
  75. Holekamp, N.M.; Campbell, J.; Almony, A.; Ingraham, H.; Marks, S.; Chandwani, H.; Cole, A.L.; Kiss, S. Vision Outcomes Following Anti–Vascular Endothelial Growth Factor Treatment of Diabetic Macular Edema in Clinical Practice. Am. J. Ophthalmol. 2018, 191, 83–91, Erratum in Am. J. Ophthalmol. 2018, 194, 192.
  76. Ciulla, T.A.; Pollack, J.S.; Williams, D.F. Visual acuity outcomes and anti-VEGF therapy intensity in diabetic macular oedema: A real-world analysis of 28 658 patient eyes. Br. J. Ophthalmol. 2021, 105, 216–221.
  77. Mitchell, P.; Bandello, F.; Schmidt-Erfurth, U.; Lang, G.E.; Massin, P.; Schlingemann, R.O.; Sutter, F.; Simader, C.; Burian, G.; Gerstner, O.; et al. The RESTORE study: Ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema. Ophthalmology 2011, 118, 615–625.
  78. Gascon, P.; Borget, I.; Comet, A.; Carton, L.; Matonti, F.; Dupont-Benjamin, L. Costs comparison of treating diabetic macular edema with aflibercept, ranibizumab or dexamethasone at 1 year in France (INVICOST study). Eur. J. Ophthalmol. 2021, 32, 1702–1709.
  79. Busch, C.; Zur, D.; Fraser-Bell, S.; Laíns, I.; Santos, A.R.; Lupidi, M.; Cagini, C.; Gabrielle, P.-H.; Couturier, A.; Mané-Tauty, V.; et al. Shall we stay, or shall we switch? Continued anti-VEGF therapy versus early switch to dexamethasone implant in refractory diabetic macular edema. Acta Diabetol. 2018, 55, 789–796.
  80. Ruiz-Moreno, J.M.; Ruiz-Medrano, J. Early-switch versus late-switch in patients with diabetic macular edema: A cost-effectiveness study. Graefes Arch. Clin. Exp. Ophthalmol. 2023, 261, 941–949.
  81. Peto, T. An overview of the clinical outcomes of the fluocinolone acetonide 190 µg intravitreal implant clinical evidence study in the United Kingdom (ICE-UK). Curr. Med. Res. Opin. 2017, 33 (Suppl. S2), 3–4.
  82. Eaton, A.; Koh, S.S.; Jimenez, J.; Riemann, C.D. The USER Study: A Chart Review of Patients Receiving a 0.2 µg/day Fluocinolone Acetonide Implant for Diabetic Macular Edema. Ophthalmol. Ther. 2019, 8, 51–62.
  83. Augustin, A.J.; Bopp, S.; Fechner, M.; Holz, F.; Sandner, D.; Winkgen, A.-M.; Khoramnia, R.; Neuhann, T.; Warscher, M.; Spitzer, M.; et al. Three-year results from the Retro-IDEAL study: Real-world data from diabetic macular edema (DME) patients treated with ILUVIEN® (0.19 mg fluocinolone acetonide implant). Eur. J. Ophthalmol. 2020, 30, 382–391.
  84. Rehak, M.; Busch, C.; Unterlauft, J.-D.; Jochmann, C.; Wiedemann, P. Outcomes in diabetic macular edema switched directly or after a dexamethasone implant to a fluocinolone acetonide intravitreal implant following anti-VEGF treatment. Acta Diabetol. 2020, 57, 469–478.
  85. Cicinelli, M.V.; Rosenblatt, A.; Grosso, D.; Zollet, P.; Capone, L.; Rabiolo, A.; Lattanzio, R.; Loewenstein, A.; Bandello, F.; Nassisi, M.; et al. The outcome of fluocinolone acetonide intravitreal implant is predicted by the response to dexamethasone implant in diabetic macular oedema. Eye 2021, 35, 3232–3242, Erratum in Eye 2021, 35, 3459.
  86. Bailey, C.; Chakravarthy, U.; Lotery, A.; Menon, G.; Talks, J. Medisoft Audit Group Extended real-world experience with the ILUVIEN® (fluocinolone acetonide) implant in the United Kingdom: 3-year results from the Medisoft® audit study. Eye 2022, 36, 1012–1018.
  87. Baillif, S.; Staccini, P.; Weber, M.; Delyfer, M.-N.; Le Mer, Y.; Gualino, V.; Collot, L.; Merite, P.-Y.; Creuzot-Garcher, C.; Kodjikian, L.; et al. Management of Patients with Diabetic Macular Edema Switched from Dexamethasone Intravitreal Implant to Fluocinolone Acetonide Intravitreal Implant. Pharmaceutics 2022, 14, 2391.
  88. Mathis, T.; Papegaey, M.; Ricard, C.; Rezkallah, A.; Matonti, F.; Sudhalkar, A.; Vartin, C.; Dot, C.; Kodjikian, L. Efficacy and Safety of Intravitreal Fluocinolone Acetonide Implant for Chronic Diabetic Macular Edema Previously Treated in Real-Life Practice: The REALFAc Study. Pharmaceutics 2022, 14, 723.
  89. Singer, M.A.; Sheth, V.; Mansour, S.E.; Coughlin, B.; Gonzalez, V.H. Three-Year Safety and Efficacy of the 0.19-mg Fluocinolone Acetonide Intravitreal Implant for Diabetic Macular Edema: The PALADIN Study. Ophthalmology 2022, 129, 605–613.
  90. Fallico, M.; Maugeri, A.; Lotery, A.; Longo, A.; Bonfiglio, V.; Russo, A.; Avitabile, T.; Furino, C.; Cennamo, G.; Barchitta, M.; et al. Fluocinolone acetonide vitreous insert for chronic diabetic macular oedema: A systematic review with meta-analysis of real-world experience. Sci. Rep. 2021, 11, 4800.
  91. Kodjikian, L.; Baillif, S.; Creuzot-Garcher, C.; Delyfer, M.-N.; Matonti, F.; Weber, M.; Mathis, T. Real-World Efficacy and Safety of Fluocinolone Acetonide Implant for Diabetic Macular Edema: A Systematic Review. Pharmaceutics 2021, 13, 72.
  92. Khoramnia, R.; Peto, T.; Koch, F.; Taylor, S.R.; de Sousa, J.P.C.; Hill, L.; Bailey, C.; Chakravarthy, U.; ILUVIEN Registry Safety Study (IRISS) Investigators Group. Safety and effectiveness of the fluocinolone acetonide intravitreal implant (ILUVIEN): 3-year results from the European IRISS registry study. Br. J. Ophthalmol. 2023, 107, 1502–1508.
  93. Schmit-Eilenberger, V. A novel intravitreal fluocinolone acetonide implant (Iluvien®) in the treatment of patients with chronic diabetic macular edema that is insufficiently responsive to other medical treatment options: A case series. Clin. Ophthalmol. 2015, 9, 801–811.
  94. McCluskey, J.D.; Kaufman, P.L.; Wynne, K.; Lewis, G. Early adoption of the fluocinolone acetonide (FAc) intravitreal implant in patients with persistent or recurrent diabetic macular edema (DME). Int. Med. Case Rep. J. 2019, 12, 93–102.
  95. Starr, M.R.; Salabati, M.; Mahmoudzadeh, R.; Patel, L.G.; Ammar, M.J.; Hsu, J.; Garg, S.; Ho, A.C.; Kuriyan, A.E. Fluctuations in Central Subfield Thickness Associated With Worse Visual Outcomes in Patients With Diabetic Macular Edema in Clinical Trial Setting. Am. J. Ophthalmol. 2021, 232, 90–97.
  96. Wang, V.Y.; Kuo, B.L.; Chen, A.X.; Wang, K.; Greenlee, T.E.; Conti, T.F.; Singh, R.P. Fluctuations in macular thickness in patients with diabetic macular oedema treated with anti-vascular endothelial growth factor agents. Eye 2022, 36, 1461–1467.
  97. Ch’ng, S.W.; Brent, A.J.; Empeslidis, T.; Konidaris, V.; Banerjee, S. Real-World Cost Savings Demonstrated by Switching Patients with Refractory Diabetic Macular Edema to Intravitreal Fluocinolone Acetonide (Iluvien): A Retrospective Cost Analysis Study. Ophthalmol. Ther. 2018, 7, 75–82.
  98. Parrish, R.K., 2nd; Campochiaro, P.A.; Pearson, P.A.; Green, K.; Traverso, C.E. FAME Study Group Characterization of Intraocular Pressure Increases and Management Strategies Following Treatment With Fluocinolone Acetonide Intravitreal Implants in the FAME Trials. Ophthalmic Surg. Lasers Imaging Retin. 2016, 47, 426–435.
  99. Roth, D.B.; Eichenbaum, D.; Malik, D.; Radcliffe, N.M.; Cutino, A.; Small, K.W.; PALADIN Study Group. The 0.19-mg Fluocinolone Acetonide Intravitreal Implant for Diabetic Macular Edema: Intraocular Pressure-Related Effects over 36 Months. Ophthalmol. Retin. 2023, 8, 49–54.
  100. El Rayes, E.N.; Leila, M. Visual function and retinal morphological changes after single suprachoroidal delivery of fluocinolone acetonide (Iluvien®) implant in eyes with chronic diabetic macular edema. Int. J. Retin. Vitr. 2023, 9, 20.
  101. Kodjikian, L.; Bellocq, D.; Bandello, F.; Loewenstein, A.; Chakravarthy, U.; Koh, A.; Augustin, A.; de Smet, M.D.; Chhablani, J.; Tufail, A.; et al. First-line treatment algorithm and guidelines in center-involving diabetic macular edema. Eur. J. Ophthalmol. 2019, 29, 573–584.
  102. Bressler, S.B.; Odia, I.; Maguire, M.G.; Dhoot, D.S.; Glassman, A.R.; Jampol, L.M.; Marcus, D.M.; Solomon, S.D.; Sun, J.K.; Diabetic Retinopathy Clinical Research Network. Factors Associated With Visual Acuity and Central Subfield Thickness Changes When Treating Diabetic Macular Edema With Anti–Vascular Endothelial Growth Factor Therapy: An Exploratory Analysis of the Protocol T Randomized Clinical Trial. JAMA Ophthalmol. 2022, 137, 382–389, Erratum in JAMA Ophthalmol. 2022, 140, 1030.
  103. Kwon, J.-W.; Jee, D. Aqueous humor cytokine levels in patients with diabetic macular edema refractory to anti-VEGF treatment. PLoS ONE 2018, 13, e0203408, Erratum in PLoS ONE 2018, 13, e0207902.
  104. Gonzalez, V.H.; Campbell, J.; Holekamp, N.M.; Kiss, S.; Loewenstein, A.; Augustin, A.J.; Ma, J.; Ho, A.C.; Patel, V.; Whitcup, S.M.; et al. Early and Long-Term Responses to Anti–Vascular Endothelial Growth Factor Therapy in Diabetic Macular Edema: Analysis of Protocol I Data. Am. J. Ophthalmol. 2016, 172, 72–79.
  105. Ehlken, C.; Helms, M.; Böhringer, D.; Agostini, H.T.; Stahl, A. Association of treatment adherence with real-life VA outcomes in AMD, DME, and BRVO patients. Clin. Ophthalmol. 2017, 12, 13–20.
  106. Nguyen, Q.D.; Brown, D.M.; Marcus, D.M.; Boyer, D.S.; Patel, S.; Feiner, L.; Gibson, A.; Sy, J.; Rundle, A.C.; Hopkins, J.J.; et al. Ranibizumab for diabetic macular edema: Results from 2 phase III randomized trials: RISE and RIDE. Ophthalmology 2012, 119, 789–801.
  107. Korobelnik, J.-F.; Do, D.V.; Schmidt-Erfurth, U.; Boyer, D.S.; Holz, F.G.; Heier, J.S.; Midena, E.; Kaiser, P.K.; Terasaki, H.; Marcus, D.M.; et al. Intravitreal aflibercept for diabetic macular edema. Ophthalmology 2014, 121, 2247–2254.
  108. Uludag, G.; Hassan, M.; Matsumiya, W.; Pham, B.H.; Chea, S.; Trong Tuong Than, N.; Doan, H.L.; Akhavanrezayat, A.; Halim, M.S.; Do, D.V.; et al. Efficacy and safety of intravitreal anti-VEGF therapy in diabetic retinopathy: What we have learned and what should we learn further? Expert Opin. Biol. Ther. 2022, 22, 1275–1291.
  109. Virgili, G.; Parravano, M.; Evans, J.R.; Gordon, I.; Lucenteforte, E. Anti-vascular endothelial growth factor for diabetic macular oedema: A network meta-analysis. Cochrane Database Syst. Rev. 2017, 6, CD007419, Update in Cochrane Database Syst. Rev. 2018, 10, CD007419.
  110. Porta, M.; Striglia, E. Intravitreal anti-VEGF agents and cardiovascular risk. Intern. Emerg. Med. 2020, 15, 199–210.
  111. Zehden, J.A.; Mortensen, X.M.; Reddy, A.; Zhang, A.Y. Systemic and Ocular Adverse Events with Intravitreal Anti-VEGF Therapy Used in the Treatment of Diabetic Retinopathy: A Review. Curr. Diabetes Rep. 2022, 22, 525–536.
  112. Puliafito, C.A.; Cousins, S.W.; Bacharach, J.; Gonzalez, V.H.; Holekamp, N.M.; Merrill, P.T.; Ohr, M.P.; Parrish, R.K., 2nd; Riemann, C.D. Forming a Consensus: Data and Guidance for Physicians Treating Diabetic Macular Edema. Ophthalmic Surg. Lasers Imaging Retin. 2016, 47 (Suppl. S4), S4–S15.
  113. Browning, D.J.; Stewart, M.W.; Lee, C. Diabetic macular edema: Evidence-based management. Indian J. Ophthalmol. 2018, 66, 1736–1750.
  114. Amoaku, W.M.; Ghanchi, F.; Bailey, C.; Banerjee, S.; Banerjee, S.; Downey, L.; Gale, R.; Hamilton, R.; Khunti, K.; Posner, E.; et al. Diabetic retinopathy and diabetic macular oedema pathways and management: UK Consensus Working Group. Eye 2020, 34 (Suppl. S1), 1–51, Erratum in Eye 2020, 34, 1941–1942.
  115. Chhablani, J.; Wong, K.M.; Tan, G.S.F.; Sudhalkar, A.M.; Laude, A.F.; Cheung, C.M.G.F.M.; Zhao, P.F.; Uy, H.; Lim, J.; Valero, S.M.; et al. Diabetic Macular Edema Management in Asian Population: Expert Panel Consensus Guidelines. Asia-Pac. J. Ophthalmol. 2020, 9, 426–434.
  116. Giridhar, S.; Verma, L.; Rajendran, A.; Bhend, M.; Goyal, M.; Ramasamy, K.; Rajalakshmi; Padmaja, R.; Natarajan, S.; Palanivelu, M.S.; et al. Diabetic macular edema treatment guidelines in India: All India Ophthalmological Society Diabetic Retinopathy Task Force and Vitreoretinal Society of India consensus statement. Indian J. Ophthalmol. 2021, 69, 3076–3086.
  117. Cloete, L. Diabetes mellitus: An overview of the types, symptoms, complications and management. Nurs. Stand. 2021, 37, 61–66.
  118. Lovic, D.; Piperidou, A.; Zografou, I.; Grassos, H.; Pittaras, A.; Manolis, A. The Growing Epidemic of Diabetes Mellitus. Curr. Vasc. Pharmacol. 2020, 18, 104–109.
  119. Lin, K.-Y.; Hsih, W.-H.; Lin, Y.-B.; Wen, C.-Y.; Chang, T.-J. Update in the epidemiology, risk factors, screening, and treatment of diabetic retinopathy. J. Diabetes Investig. 2021, 12, 1322–1325.
  120. Polizzi, S.; Mahajan, V.B. Intravitreal Anti-VEGF Injections in Pregnancy: Case Series and Review of Literature. J. Ocul. Pharmacol. Ther. 2015, 31, 605–610.
  121. Fazelat, A.; Lashkari, K. Off-label use of intravitreal triamcinolone acetonide for diabetic macular edema in a pregnant patient. Clin. Ophthalmol. 2011, 5, 439–441.
  122. Concillado, M.; Lund-Andersen, H.; Mathiesen, E.R.; Larsen, M. Dexamethasone Intravitreal Implant for Diabetic Macular Edema During Pregnancy. Am. J. Ophthalmol. 2016, 165, 7–15.
  123. Sophie, R.; Lu, N.; Campochiaro, P.A. Predictors of Functional and Anatomic Outcomes in Patients with Diabetic Macular Edema Treated with Ranibizumab. Ophthalmology 2015, 122, 1395–1401.
  124. Holekamp, N.M. Overview of diabetic macular edema. Am. J. Manag. Care 2016, 22 (Suppl. S10), S284–S291.
  125. Bandello, F.; Battaglia Parodi, M.; Lanzetta, P.; Loewenstein, A.; Massin, P.; Menchini, F.; Veritti, D. Diabetic Macular Edema. Dev. Ophthalmol. 2017, 58, 102–138.
  126. Munk, M.R.; Somfai, G.M.; de Smet, M.D.; Donati, G.; Menke, M.N.; Garweg, J.G.; Ceklic, L. The Role of Intravitreal Corticosteroids in the Treatment of DME: Predictive OCT Biomarkers. Int. J. Mol. Sci. 2022, 23, 7585.
  127. Terada, N.; Murakami, T.; Uji, A.; Dodo, Y.; Mori, Y.; Tsujikawa, A. Hyperreflective Walls in Foveal Cystoid Spaces as a Biomarker of Diabetic Macular Edema Refractory to Anti-VEGF Treatment. Sci. Rep. 2020, 10, 7299.
  128. Vujosevic, S.; Simó, R. Local and Systemic Inflammatory Biomarkers of Diabetic Retinopathy: An Integrative Approach. Investig. Ophthalmol. Vis. Sci. 2017, 58, BIO68–BIO75.
  129. Jeng, C.-J.; Hsieh, Y.-T.; Yang, C.-M.; Yang, C.-H.; Lin, C.-L.; Wang, I.-J. Development of diabetic retinopathy after cataract surgery. PLoS ONE 2018, 13, e0202347.
  130. Khodabandeh, A.; Fadaifard, S.; Abdollahi, A.; Karkhaneh, R.; Roohipoor, R.; Abdi, F.; Ghasemi, H.; Habibollahi, S.; Mazloumi, M. Role of combined phacoemulsification and intravitreal injection of bevacizumab in prevention of postoperative macular edema in non-proliferative diabetic retinopathy. J. Curr. Ophthalmol. 2018, 30, 245–249.
  131. Tatsumi, T.; Oshitari, T.; Ando, T.; Takatsuna, Y.; Arai, M.; Baba, T.; Sato, E.; Yamamoto, S. Comparison of the Efficacy of Sub-Tenon versus Intravitreal Triamcinolone Acetonide Injection during Cataract Surgery for Diabetic Macular Edema. Ophthalmologica 2018, 241, 17–23.
  132. Fallico, M.; Avitabile, T.; Castellino, N.; Longo, A.; Russo, A.; Bonfiglio, V.; Parisi, F.; Furino, C.; Panozzo, G.; Scorcia, V.; et al. Intravitreal dexamethasone implant one month before versus concomitant with cataract surgery in patients with diabetic macular oedema: The dexcat study. Acta Ophthalmol. 2021, 99, E74–E80.
  133. Furino, C.; Boscia, F.; Niro, A.; D’Addario, M.; Grassi, M.O.; Saglimbene, V.; Reibaldi, M.; Alessio, G. Diabetic macular edema and cataract surgery: Phacoemulsification Combined With Dexamethasone Intravitreal Implant Compared With Standard Phacoemulsification. Retina 2021, 41, 1102–1109.
  134. Lee, S.S.; Ghosn, C.; Yu, Z.; Zacharias, L.C.; Kao, H.; Lanni, C.; Abdelfattah, N.; Kuppermann, B.; Csaky, K.G.; D’Argenio, D.Z.; et al. Vitreous VEGF Clearance is increased after vitrectomy. Investig. Ophthalmol. Vis. Sci. 2010, 51, 2135–2138.
  135. Costa, J.F.; Sousa, K.; Marques, J.P.; Marques, M.; Cachulo, M.L.; Silva, R.; Gomes, N.; Figueira, J. Efficacy and safety of postvitrectomy intravitreal triamcinolone therapy for diabetic macular edema. Eur. J. Ophthalmol. 2016, 26, 485–490.
  136. Watanabe, A.; Tsuzuki, A.; Arai, K.; Gekka, T.; Kohzaki, K.; Tsuneoka, H. Efficacy of Intravitreal Triamcinolone Acetonide for Diabetic Macular Edema After Vitrectomy. J. Ocul. Pharmacol. Ther. 2016, 32, 38–43.
  137. Rezkallah, A.; Malclès, A.; Dot, C.; Voirin, N.; Agard, É.; Vié, A.-L.; Denis, P.; Mathis, T.; Kodjikian, L. Evaluation of efficacy and safety of dexamethasone intravitreal implants before and after vitrectomy in a real-life study. Acta Ophthalmol. 2017, 96, e544–e546.
  138. Pessoa, B.; Coelho, J.; Correia, N.; Ferreira, N.; Beirão, M.; Meireles, A. Fluocinolone Acetonide Intravitreal Implant 190 μg (ILUVIEN®) in Vitrectomized versus Nonvitrectomized Eyes for the Treatment of Chronic Diabetic Macular Edema. Ophthalmic Res. 2017, 59, 68–75.
  139. Breusegem, C.; Vandewalle, E.; Van Calster, J.; Stalmans, I.; Zeyen, T. Predictive value of a topical dexamethasone provocative test before intravitreal triamcinolone acetonide injection. Investig. Ophthalmol. Vis. Sci. 2009, 50, 573–576.
  140. Tsoutsanis, P.; Kapantais, D. Anterior migration of Ozurdex implant: A review on risk factors, complications, and management. Int. J. Retin. Vitr. 2023, 9, 74.
  141. Rishi, P.; Majumder, P.D.; Biswas, J. Anterior Chamber Migration of Fluocinolone Acetonide Intravitreal Implant. JAMA Ophthalmol. 2019, 137, e185931.
  142. Heier, J.S.; Korobelnik, J.-F.; Brown, D.M.; Schmidt-Erfurth, U.; Do, D.V.; Midena, E.; Boyer, D.S.; Terasaki, H.; Kaiser, P.K.; Marcus, D.M.; et al. Intravitreal Aflibercept for Diabetic Macular Edema: 148-Week Results from the VISTA and VIVID Studies. Ophthalmology 2016, 123, 2376–2385.
  143. Wykoff, C.C.; Chakravarthy, U.; Campochiaro, P.A.; Bailey, C.; Green, K.; Cunha-Vaz, J. Long-term Effects of Intravitreal 0.19 mg Fluocinolone Acetonide Implant on Progression and Regression of Diabetic Retinopathy. Ophthalmology 2017, 124, 440–449.
  144. Iglicki, M.; Zur, D.; Busch, C.; Okada, M.; Loewenstein, A. Progression of diabetic retinopathy severity after treatment with dexamethasone implant: A 24-month cohort study the ‘DR-Pro-DEX Study’. Acta Diabetol. 2018, 55, 541–547.
  145. Rittiphairoj, T.; Mir, T.A.; Li, T.; Virgili, G. Intravitreal steroids for macular edema in diabetes. Cochrane Database Syst. Rev. 2020, 11, CD005656.
  146. Zarranz-Ventura, J.; Mali, J.O. Effectiveness of 190 μg Fluocinolone Acetonide and 700 μg Dexamethasone Intravitreal Implants in Diabetic Macular Edema Using the Area-Under-the-Curve Method: The CONSTANT Analysis. Clin. Ophthalmol. 2020, 14, 1697–1704.
  147. Kuley, B.; Storey, P.P.; Pancholy, M.; Wibbelsman, T.D.; Obeid, A.; Regillo, C.; Garg, S. Treatment of Eyes With Diabetic Macular Edema That Had a Suboptimal Response to Antivascular Endothelial Growth Factor Therapy: 2-mg Intravitreal Triamcinolone Acetonide vs. 0.7-mg Dexamethasone Implant. J. Vitr. Dis. 2020, 4, 372–376.
  148. Augustin, A.J.; Kuppermann, B.D.; Lanzetta, P.; Loewenstein, A.; Li, X.-Y.; Cui, H.; Hashad, Y.; Whitcup, S.M.; Ozurdex MEAD Study Group. Dexamethasone intravitreal implant in previously treated patients with diabetic macular edema: Subgroup analysis of the MEAD study. BMC Ophthalmol. 2015, 15, 150.
  149. Thakur, A.; Kadam, R.; Kompella, U.B. Trabecular Meshwork and Lens Partitioning of Corticosteroids: Implications for elevated intraocular pressure and cataracts. Arch. Ophthalmol. 2011, 129, 914–920.
  150. Gurreri, A.; Pazzaglia, A. Diabetic Macular Edema: State of Art and Intraocular Pharmacological Approaches. Adv. Exp. Med. Biol. 2021, 1307, 375–389.
  151. Tatsumi, T. Current Treatments for Diabetic Macular Edema. Int. J. Mol. Sci. 2023, 24, 9591.
  152. Amoaku, W.M.K.; Saker, S.; Stewart, E.A. A review of therapies for diabetic macular oedema and rationale for combination therapy. Eye 2015, 29, 1115–1130.
  153. Ehlers, J.P.; Yeh, S.; Maguire, M.G.; Smith, J.R.; Mruthyunjaya, P.; Jain, N.; Kim, L.A.; Weng, C.Y.; Flaxel, C.J.; Schoenberger, S.D.; et al. Intravitreal Pharmacotherapies for Diabetic Macular Edema: A Report by the American Academy of Ophthalmology. Ophthalmology 2021, 129, 88–99.
  154. Patel, D.; Patel, S.N.; Chaudhary, V.; Garg, S.J. Complications of intravitreal injections: 2022. Curr. Opin. Ophthalmol. 2022, 33, 137–146.
  155. Mehta, H.; Hennings, C.; Gillies, M.C.; Nguyen, V.; Campain, A.; Fraser-Bell, S. Anti-vascular endothelial growth factor combined with intravitreal steroids for diabetic macular oedema. Cochrane Database Syst. Rev. 2018, 4, CD011599.
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