- Case report
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Vitreous opacities after intravitreal triamcinolone injection- a case report
© The Author(s). 2018
- Received: 2 September 2017
- Accepted: 11 June 2018
- Published: 20 June 2018
We report occurrence of peculiar tiny white thread like vitreous opacities after intravitreal triamcinolone injection. These persisted without any change for over a year. We ascribe them to aggregation of triamcinolone crystals due to the purification methods.
Seven patients (8 eyes) with macular edema developed tiny whitish thread like opacities in the vitreous 2–3 months after undergoing an intravitreal injection of triamcinolone acetonide preparation containing benzyl alcohol as preservative. These opacities persisted unchanged for more than a year. The follow up ranged from 91 to 425 days. Vitreous tap was done in one patient which was negative for infection. All patients initially showed improvement but needed re-treatment for recurrence. One patient developed steroid induced rise in intraocular pressure. Microscopic examination of the drug revealed large string like aggregates of triamcinolone crystals.
We hypothesize the possibility of aggregation of triamcinolone crystals into string like structures probably due to the purification methods used during manufacture which led to these thread like opacities in the vitreous.
- Intravitreal injections
- Vitreous opacities
- Macular edema
Intravitreous triamcinolone acetonide (IVTA) has found widespread application for a variety of posterior segment pathologies which cause macular edema. Its therapeutic efficacy has been well demonstrated in clinical trials [1–3]. And its cost effectiveness has made IVTA a widely used agent. Several drug-related and injection-related complications have been reported ranging from localized subconjunctival hemorrhage at the site of injection to serious sight threatening problems . Triamcinolone acetonide is a long acting steroid which is available as a suspension of crystals in benzyl alcohol. The particulate nature of the drug and the lack of preservative free formulation can give rise to deposits on the retina and in the vitreous cavity. The triamcinolone crystals appear as shiny white deposits in the vitreous and have been reported to last for more than 120 days after injection . We report the occurrence of peculiar small thread like opacities in the vitreous which persisted for over a year after the IVTA injection.
We examined seven patients (8 eyes, one bilateral) out of total 15 patients who had received IVTA injection from September 2015 to September 2016. The study adhered to the tenets of the Helsinki Declaration and was approved by the institutional review board of Medical Research Foundation, Chennai. Written informed consent was obtained from every patient. All patients underwent pre-injection detailed eye examination including best corrected visual acuity, intraocular pressure evaluation and fundus evaluation including macular optical coherence tomography. Triamcinolone acetonide, 0.05 ml (2 mg), (Kenacort, Abbott healthcare private limited, Mumbai, India containing triamcinolone acetonide 40 mg and benzyl alcohol 0.9% w/v as preservative in aqueous base) was withdrawn from the vial and injected directly intravitreally through the pars plana using a 26 gauge needle. The preservative free triamcinolone was not available to us. One eye received 4 mg IVTA. The injections were performed in the operation theatre with complete aseptic precautions. Before the injection a drop of topical lignocaine and a drop of 5% betadine was instilled in the eye. After injection betadine eye drops were applied and eye was patched for half an hour. No pre or post injection antibiotics were used. All the patients were examined the day after and again 3 days later to rule out increased intraocular pressure or any suspected intraocular infection. Thereafter all the patients were examined at monthly interval or depending upon the therapeutic response. As per the routine protocol, all the patients underwent vision check, refraction, slit lamp examination, IOP measurement by applanation tonometer, pupillary dilation followed by retinal evaluation with indirect ophthalmoscopy and an optical coherence tomography scanning.
Demographic details, indications and the number of days the vitreous opacities were seen to be persisting after the triamcinolone acetonide injection in the vitreous
Follow up of vitreous opacities in days
PE + IOL + IVTA
Steroid induced glaucoma
Steroid induced glaucoma
Various types of vitreous opacities can occur after IVTA injection. The triamcinolone acetonide, a low water soluble suspension, itself remains in the vitreous as white crystalline deposits. These can cause visual disturbances. On ultrasonography, they appear as clump like, point like, pseudo-membranous or as fine opacities in the subhyaloid space . Triamcinolone is broken down into soluble metabolites 6 betahydroxy triamcinolone acetonide, 21carboxy triamcinolone acetonide, 21carboxy 6beta hydroxy triamcinolone acetonide. These generally clear spontaneously in about 30–60 days.
Both infectious and non-infectious types of endophthalmitis have been reported to occur following IVTA . Bacterial endophthalmitis can occur with vitreous exudates, conjunctival injection, hypopyon and pain. This requires prompt treatment with intravitreal antibiotics. Often times the crystals of triamcinolone can migrate to the anterior chamber giving an appearance of a hypopyon .
An endophthalmitis-like reaction also has been reported following IVTA, wherein dense vitreous haze was seen occluding the vision but without the signs of classic infectious endophthalmitis . This haze was seen to clear spontaneously over a few days. The reason for this was not clear but was thought to be due to spraying of the steroid inside the vitreous cavity while forcible injection through the small gauge needle which might have been jammed.
The preservative or the vehicle used for the triamcinolone preparation may also cause a toxic reaction. In animal studies, severe reaction leading to retinal necrosis has been seen due to the preservatives in various preparations of depot steroids . In vitro studies have shown toxic effects of benzyl alcohol on human retinal pigment epithelial cells . It is recommended to use the preservative free formulation or minimize the amount of preservative in the injection by keeping the injection standing for half an hour after it has been withdrawn in the syringe and then use only the sedimented crystals after discarding the supernatant fluid containing the preservative.
Silicone oil droplets have also been seen after an intravitreal injection. In the SCORE study , 33% of eyes treated with 1 mg of triamcinolone and 12% of eyes treated with 4 mg of triamcinolone had silicone oil droplets. However, this was due to the use of syringes with staked on needles. The problem disappeared following the change to syringes with luer lock needles.
Till now, there are no reports of such thread like tiny opacities as seen in our case series. A vitreous tap in one patient was negative and ruled out infection. Also, the fact that these patients were comfortable and in fact reported visual improvement with no change whatsoever in the number or appearance of these opacities, rule out the possibility of infection.
In conclusion, seven patients are reported with development of tiny thread like vitreous opacities after an intravitreal injection of triamcinolone preparation with preservative. These opacities seem to be harmless, causing no visual disturbance or any other symptoms. However, they were seen to persist without any change for over a year.
Availability of data and materials
The data reported in the article can be found in the table which is included as part of the manuscript.
DR, VR have contributed towards concept and design of the manuscript, analysis and interpretation of data, revising the manuscript critically. HS has contributed towards acquisition and analysis of data, drafting of the manuscript and revising it. All authors have read and approved the final manuscript.
Ethics approval and consent to participate
The institutional review board of Medical Research Foundation approved the study and written informed consent was obtained from all participants.
Consent for publication
Written informed consent was obtained from every patient for publication of this case report and any accompanying images. All copies of the written consent are available for review by the Editor of this journal.
DR has received research grant from Novartis Healthcare for another study. None of the other authors have any competing interests to report.
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