Evidence map›Paper›PMID 41727741›Full record

ArticleClinical case reports2026

Wernicke-Korsakoff Syndrome a Rare Complication of Hyperemesis Gravidarum: Case Report.

Ayush Neupane, Anil Shahi, Bishaka Adhikari

Abstract read
In one paragraph

Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Ayush NeupaneDepartment of Internal Medicine Chitwan Medical College Bharatpur Nepal.
Anil ShahiDepartment of Internal Medicine Chitwan Medical College Bharatpur Nepal.ORCID https://orcid.org/0009-0001-7901-8216
Bishaka AdhikariDepartment of Internal Medicine Chitwan Medical College Bharatpur Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperemesis gravidarum-induced Wernickes-Korsakoff syndrome (WKS) is an uncommon but potentially devastating disorder in pregnancy characterized by oculomotor abnormalities, cerebellar dysfunction, and either an altered mental state or mild memory impairment. However, most cases may not display the full spectrum of clinical abnormalities, we report a 34-year-old woman at 15 weeks of gestation who presented with all typical features of WKS, which includes worsening confusion, an unsteady gait, visual symptoms, and episodes of disorientation after two months of relentless vomiting. Clinical evaluation revealed dehydration, horizontal nystagmus, early papilledema, and biochemical evidence of malnutrition. MRI confirmed the diagnosis of WE. She responded to high-dose intravenous thiamine, electrolyte replacement, nutritional support, and ICU-level care. Neuropsychiatric symptoms, including impaired concentration, recent memory loss, and hallucinations, gradually resolved. She was discharged in stable condition after 26 days and demonstrated significant recovery with a normal fetal scan at follow-up. This case highlights the timely need for multidisciplinary treatment modalities and high-dose thiamine supplementation in pregnant women with severe hyperemesis to prevent irreversible neurological injury.

Indexed as

hyperemesis gravidarumthiamineWernickes–Korsakoff syndrome

Identifiers

PMID41727741
PMCPMC12916254

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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.