Evidence map›Paper›PMID 40597840›Full record

ArticleBMC ophthalmology2025

Exudative retinal detachment and hypertensive choroidopathy in a patient with suspected HELLP syndrome: a case report.

Muzi Li, Jinfeng Qu

Abstract readCase Reports
In one paragraph

Article in BMC ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

2 authors.

Muzi LiDepartment of Ophthalmology, Peking University People's Hospital, Beijing, China.
Jinfeng QuDepartment of Ophthalmology, Peking University People's Hospital, Beijing, China. drbari@163.com.

Funding

Beijing Natural Science Foundation 7232192
6 · The paper itself

Abstract

backgroundThe HELLP syndrome is a serious complication in pregnancy, characterized by haemolysis, elevated liver enzymes and low platelet count. We report a patient who was unaware of pregnancy presenting initially with bilateral visual loss and exudative retinal detachment and was diagnosed with HELLP syndrome during work-up. CASE PRESENTATION: A female patient, unaware of her pregnancy, presented with painless, severe bilateral vision loss and exudative retinal detachment. Multimodal imaging of her fundus revealed hypertensive choroidopathy and retinopathy. During systemic work-up, she was found to be 26 weeks pregnant and was diagnosed with HELLP syndrome based on laboratory abnormalities. Her vision fully recovered within 4 months following urgent pregnancy termination and blood pressure control.

conclusionsThis case highlights the importance of obtaining a thorough medical history and considering pregnancy-related complications in the differential diagnosis for reproductive-age women with acute vision loss. Prompt diagnosis and treatment of this condition are essential for the recovery of patients' visual outcome.

Indexed as

Choroid DiseasesHELLP SyndromeRetinal DetachmentAdultFemaleFluorescein AngiographyFundus OculiHumansPregnancyVisual AcuityHELLP syndromeHypertensive retinopathyMalignant hypertensionSevere preeclampsiaVisual impairment

Identifiers

PMID40597840
PMCPMC12210448

What OpenQuestion holds

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Registered trials

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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.