ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
Hyperemesis gravidarum revisited: from GDF15 biology to precision multimodal therapy.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Real-world pharmacological treatment of patients with hyperemesis gravidarum in 9 cities of China from 2019 to 2024: a cross-sectional analysis.Frontiers in pharmacology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hyperemesis gravidarum (HG) is a severe and potentially life-threatening form of nausea and vomiting in pregnancy, characterized by intractable vomiting, dehydration, electrolyte imbalance, nutritional deficiencies, and significant weight loss. Despite being a leading cause of early pregnancy hospitalization, its management remains inconsistent and often empirical. Emerging evidence suggests a paradigm shift in the understanding of HG pathophysiology, moving beyond traditional hormonal theories toward an integrated model involving genetic susceptibility and metabolic signaling pathways, particularly Growth Differentiation Factor 15 (GDF15) and RYR2-related mechanisms. This narrative review critically synthesizes current evidence regarding the evolving biological basis of HG and evaluates established and emerging therapeutic strategies. A multimodal, stepwise approach remains the cornerstone of management. First-line pharmacotherapy includes doxylamine-pyridoxine, followed by dopamine antagonists or 5-HT3 receptor antagonists such as metoclopramide and ondansetron, which demonstrate reassuring safety profiles in large cohort studies. Corticosteroids may be considered in refractory cases. Early correction of dehydration, electrolyte disturbances, and thiamine deficiency is essential to prevent complications such as Wernicke's encephalopathy. Nutritional support, preferably through enteral tube feeding rather than parenteral nutrition, should be prioritized when oral intake is inadequate. Integrating biological insights with standardized, compassionate, and multidisciplinary care may improve clinical outcomes and reduce the substantial physical and psychological burden associated with HG.
Indexed as
Identifiers
41942591What OpenQuestion holds
Registered trials
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.