Evidence map›Paper›PMID 28399831›Full record

ArticleBMC ophthalmology2017

Characteristics of cases needing advanced treatment for intractable Posner-Schlossman syndrome.

Kazuichi Maruyama, Yuko Maruyama, Sunao Sugita, Kazuhiko Mori, Yu Yokoyama, Shiho Sanuki-Kunimatsu, Hiroko Nakagawa, Shigeru Kinoshita, Manabu Mochizuki, Toru Nakazawa

Open access · goldAbstract read
In one paragraph

Article in BMC ophthalmology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Long-term prognosis for glaucoma in patients with Posner-Schlossman syndrome.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. The genetic contribution ofAnnals of translational medicine · 2019
    Article
  14. Observational
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

10 authors at 3 institutions in 1 country.

Kazuichi MaruyamaDepartment of Ophthalmology and Visual Science, Tohoku University Graduate School of Medicine, Sendai, Japan. maruyama-k@oph.med.tohoku.ac.jp.
Yuko MaruyamaDepartment of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Sunao SugitaRIKEN Center for Development Biology, Kobe, Japan.
Kazuhiko MoriDepartment of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Yu YokoyamaDepartment of Ophthalmology and Visual Science, Tohoku University Graduate School of Medicine, Sendai, Japan.
Shiho Sanuki-KunimatsuDepartment of Ophthalmology and Visual Science, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroko NakagawaDepartment of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Shigeru KinoshitaDepartment of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Manabu MochizukiDepartment of Ophthalmology, Tokyo Medical and Dental University, School of Medicine, Tokyo, Japan.
Toru NakazawaDepartment of Ophthalmology and Visual Science, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kyoto Prefectural University of Medicine · JPTohoku University · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Posner-Schlossman syndrome (PSS), which is characterized by recurrent unilateral attacks of ocular hypertension. Surgical treatment is sometimes necessary because intraocular pressure (IOP) cannot be controlled with anti-glaucoma medications. To identify the clinical features of Posner-Schlossman syndrome (PSS) indicative of the need for intraocular pressure (IOP)-controlling surgery.

methodsThis study was a retrospective case-series analysis of the clinical charts of 33 patients diagnosed with PSS, who underwent surgery to control IOP or received medication only. Various clinical factors were compared between the surgical and medication groups.

resultsThe surgical group had a higher corneal endothelial cell (CEC) density loss (p < 0.05), higher maximum IOP (p < 0.01), greater visual field loss (p < 0.01) and higher positive number for cytomegalovirus (CMV) (p < 0.001) than the non-surgical group. Eighteen of the 33 patients had a high CEC reduction ratio. Of these 18, 16 required glaucoma surgery.

conclusionsPSS patients with a higher CEC reduction ratio, higher maximum IOP, greater visual field loss and higher positive number for CMV in the aqueous humor tended to be more likely to require progressive treatment, such as glaucoma surgery.

Indexed as

FemaleFiltering SurgeryFollow-Up StudiesHumansIntraocular PressureMaleMiddle AgedOcular HypertensionRecurrenceRetrospective StudiesSyndromeTreatment OutcomeVisual FieldsCorneal endothelial cell (CEC) densityGlaucoma surgeryIntraocular pressure (IOP)Polymerase chain reaction (PCR)Posner–Schlossman syndrome (PSS)

Identifiers

PMID28399831
PMCPMC5387341
OpenAlexW2606841115

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.