Evidence map›Paper›PMID 40198642›Full record

Observational studyPloS one2025

Impact of Ginkgo biloba drug interactions on bleeding risk and coagulation profiles: A comprehensive analysis.

Ngo Thi Quynh Mai, Nguyen Viet Hieu, Tran Thi Ngan, Tran Van Anh, Pham Van Linh, Nguyen Thi Thu Phuong

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

6 authors.

Ngo Thi Quynh MaiFaculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Nguyen Viet HieuFaculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Tran Thi NganFaculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.ORCID https://orcid.org/0000-0003-4514-713X
Tran Van AnhFaculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Pham Van LinhDepartment of Pathology and Immunology, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Nguyen Thi Thu PhuongFaculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.ORCID https://orcid.org/0000-0003-0523-0852

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This retrospective observational study was conducted to investigate the prevalence and clinical implications of drug interactions involving Ginkgo biloba extract on bleeding risk and coagulation profiles. Our analysis utilized data from patients admitted to Hai Phong International Hospital between January 2022 and December 2023. Inclusion criteria consisted of patients aged 18 years and above, those prescribed Ginkgo biloba extract alone or in combination with other medications, and the availability of complete medical records, including medication history, laboratory tests, and clinical outcomes. Out of 2,647 prescriptions meeting the inclusion criteria, 342 exhibited drug interactions with a prevalence rate of 12.94%. Notably, Ginkgo biloba extract frequent interacts with antiplatelets, anticoagulants, and nonsteroidal anti-inflammatory drugs, with Clopidogrel and Aspirin exhibiting the highest prevalence rates of 2.61% each. However, interactions with anticoagulants including direct oral anticoagulants and acenocoumarol, were not statistically significant in our analysis. Omeprazole was a frequently interacting drug (2.34%) of mild severity. Among the 747 patients analyzed for bleeding disorders, 31 (4.15%) exhibited bleeding symptoms. Correlation analysis indicated a strong association between clinical bleeding and abnormal coagulation results (OR, 1.75; p <  0.001). Moreover, significant correlations were found between Ginkgo biloba extract drug interactions and the bleeding risk (OR: 1.08, p <  0.001) and abnormal coagulation (OR: 1.49, p <  0.001). The severity of Ginkgo biloba extract drug interactions did not correlate with bleeding risk (OR: 1.01, p =  0.767) but influenced abnormal coagulation test results (OR: 0.813, p =  0.019). Specific medications, including clopidogrel, aspirin, celecoxib, loxoprofen, nifedipine, and omeprazole, were significantly associated with the risk of bleeding and abnormal coagulation (p <  0.05). Interactions with ticagrelor, etoricoxib, insulin, omeprazole, and domperidone were associated with abnormal coagulation tests without affecting the reported bleeding. These findings underscore the critical need of evaluating potential interactions involving Ginkgo biloba extract drug interactions in clinical pratice, particularly when assessing bleeding risk and managing coagulation.

Indexed as

Blood CoagulationGinkgo bilobaHemorrhageHerb-Drug InteractionsPlant ExtractsAdultAgedAnticoagulantsAnti-Inflammatory Agents, Non-SteroidalDrug InteractionsFemaleGinkgo ExtractHumansMaleMiddle AgedPlatelet Aggregation InhibitorsAnticoagulantsAnti-Inflammatory Agents, Non-SteroidalGinkgo biloba extractGinkgo ExtractPlant ExtractsPlatelet Aggregation Inhibitors

Identifiers

PMID40198642
PMCPMC11991284

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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.