Evidence map›Paper›PMID 35225525›Full record

ArticleIndian journal of ophthalmology2022

Secondary developmental glaucoma in eyes with congenital aphakia.

Swathi Vallabh Badakere, Simranjeet Aulakh, Divya Sree Ramya Achanta, Raghava Chary, Sirisha Senthil, Sunita Chaurasia, Muralidhar Ramappa, Deepak P Edward

Open access · diamondAbstract read
In one paragraph

Article in Indian journal of ophthalmology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Genetics of the anterior segment dysgenesis.Taiwan journal of ophthalmology
    Review
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

8 authors at 2 institutions in 2 countries.

Swathi Vallabh BadakereAhalia Foundation Eye Hospital, Palakkad, Kerala, India.
Simranjeet AulakhJasti V Ramanamma Children's Eye Care Center, Hyderabad, Telangana, India.
Divya Sree Ramya AchantaCentre for Rare Eye Diseases and Ocular Genetics; The Cornea Institute; Jasti V Ramanamma Children's Eye Care Center, Hyderabad, Telangana, India.
Raghava CharyVST Glaucoma Center, L V Prasad Eye Institute, Hyderabad, Telangana, India.
Sirisha SenthilJasti V Ramanamma Children's Eye Care Center; VST Glaucoma Center, L V Prasad Eye Institute, Hyderabad, Telangana, India.
Sunita ChaurasiaCentre for Rare Eye Diseases and Ocular Genetics; The Cornea Institute; Jasti V Ramanamma Children's Eye Care Center, Hyderabad, Telangana, India.
Muralidhar RamappaCentre for Rare Eye Diseases and Ocular Genetics; The Cornea Institute; Jasti V Ramanamma Children's Eye Care Center, Hyderabad, Telangana, India.
Deepak P EdwardDepartment of Ophthalmology and Visual Sciences and Pathology, University of Illinois Eye and Ear Infirmary, Chicago, United States.
L V Prasad Eye Institute · INUniversity of Illinois Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo describe the clinical spectrum and management of glaucoma in congenital aphakia.

methodsThe demographics and clinical spectrum of eyes with congenital aphakia with and without glaucoma were compared, and management outcomes of congenital aphakia cases with glaucoma were studied retrospectively between April 2000 and June 2020.

resultsThere were a total of 168 eyes (84 subjects) with a diagnosis of congenital aphakia, of which 29 eyes of 18 subjects were diagnosed with glaucoma. Corneal opacity was the presenting complaint in 26/29 eyes with glaucoma and 139/139 eyes without glaucoma. The (interquartile range (IQR)) horizontal corneal diameterwas 10.5mm (IQR, 9.0-12.5) and 8mm (IQR, 5-10) in eyes with and without glaucoma (P = 0.01), respectively. The median (IQR) axial length was 17.5mm (IQR, 13.5-19.5) and 15mm (IQR, 14-16) mm in eyes with and without glaucoma (P = 0.03), respectively. Nineteen eyes with glaucoma had adequate intraocular pressure (IOP) control with one medication. Three eyes underwent transscleral diode cyclophotocoagulation and maintained IOP without medications. Three eyes underwent trabeculectomy and trabeculotomy, trabeculectomy followed by penetrating keratoplasty, and trabeculectomy, respectively, of which two eyes became phthisical. At the last follow-up, the median (IQR) IOP was 14 mm Hg (IQR, 14-17) Hg. The median(IQR) follow-up duration was 4.53 months (IQR, 2.03- 48.06).

conclusionOne-fifth of the eyes with congenital aphakia had secondary developmental glaucoma. The corneal diameter and axial lengths were higher in the eyes with glaucoma compared to eyes without glaucoma. Medical management is the preferred short-term mode of IOP control. Transscleral cyclophotocoagulation may be preferred over surgical intervention.

Indexed as

AphakiaGlaucomaTrabeculectomyCiliary BodyFollow-Up StudiesHumansIntraocular PressureRetrospective StudiesTreatment OutcomeClinical spectrum of glaucomacongenital aphakiasecondary developmental glaucoma

Identifiers

PMID35225525
PMCPMC9114612
OpenAlexW4214577541

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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.