Evidence map›Paper›PMID 30538421›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2018

Safety of high-dose intravitreal triamcinolone acetonide as low-cost alternative to anti-vascular endothelial growth factor agents in lower-middle-income countries.

Hammouda Hamdy Ghoraba, Mahmoud Leila, Sameh Mohamed Elgouhary, Emad Eldin Mohamed Elgemai, Haithem Mamon Abdelfattah, Hashem Hammouda Ghoraba, Mohamed Amin Heikal

Open access · goldAbstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Hammouda Hamdy GhorabaDepartment of Ophthalmology, Faculty of Medicine, Tanta University, Tanta, Egypt.
Mahmoud LeilaRetina Department, Research Institute of Ophthalmology, Giza, Egypt, mahmoudleila@yahoo.com.
Sameh Mohamed ElgouharyDepartment of Ophthalmology, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Emad Eldin Mohamed ElgemaiDepartment of Retina, Magrabi Eye Hospital, Tanta, Egypt.
Haithem Mamon AbdelfattahDepartment of Retina, Magrabi Eye Hospital, Tanta, Egypt.
Hashem Hammouda GhorabaDepartment of Retina, Magrabi Eye Hospital, Tanta, Egypt.
Mohamed Amin HeikalDepartment of Ophthalmology, Faculty of Medicine, Benha University, Benha, Egypt.
Benha University · EGTanta University · EGDamanhour University · EGMenoufia University · EGResearch Institute of Ophthalmology · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of this study was to evaluate the safety of high-dose intravitreal triamcinolone acetonide (IVTA) as affordable low-cost alternative to anti-vascular endothelial growth factor (anti-vascular endothelial growth factor [anti-VEGF] agents) in lower-middle-income countries. PATIENTS AND

methodsThis was a retrospective interventional non-comparative case series. The study recruited patients who received 20 mg IVTA for treating various retinal and optic nerve diseases over the past 5 years. Main outcome measure was assessment of complications secondary to high-dose IVTA. The crosstabs procedure was used to display the interaction between the variables tested. The ANOVA test was used to analyze the differences among group means.

resultsThe study included 207 eyes of 168 patients. The main indication for high-dose IVTA were diabetic macular edema 64%, and macular edema secondary to retinal vein occlusion 19%. The mean follow-up period post-injection was 22 months. Mean number of injections was 1.3. Cataract developed in 54% of eyes. Glaucoma developed in 18.5% of eyes. Glaucoma surgery for intractable glaucoma attributed to high-dose IVTA was needed in 1% of eyes. Endophthalmitis and retinal detachment developed in one patient each.

conclusionHigh-dose IVTA is a safe and cost-effective alternative to anti-VEGF agents. Cataract formation and intraocular pressure rise do not pose major adverse effects when weighed against the risk of vision loss due to inability to afford anti-VEGF treatment.

Indexed as

cost-effectiveness of anti-VEGFhigh-dose IVTAICER of anti-VEGF per QALY

Identifiers

PMID30538421
PMCPMC6263217
OpenAlexW2903448212

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.