Evidence map›Paper›PMID 42234767›Full record

Observational studyPloS one2026

Comparing the safety and efficacy of sodium valproate, levetiracetam, and phenytoin in attenuating the severity of agitation in patients with post-traumatic brain injury: An observational study.

Shivani Singh, Raghavendra Nayak, Shivaprakash Gangachannaiah, Ashutosh Bhosale, Reena Sherin Parveen, Varun Kumar S G, Geeta Sundar

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

7 authors.

Shivani SinghDepartment of Pharmacology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Raghavendra NayakDepartment of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Shivaprakash GangachannaiahDepartment of Pharmacology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.ORCID https://orcid.org/0000-0002-6359-4024
Ashutosh BhosaleDepartment of Pharmacy Practice, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, IIndia.
Reena Sherin ParveenDepartment of Pharmacology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Varun Kumar S GDepartment of Applied Statistics and Data Science, Prasanna School of Public Health, Manipal Academy of Higher Education, Manipal, Karnataka, IIndia.ORCID https://orcid.org/0000-0003-0255-726X
Geeta SundarDepartment of Neurosurgery, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe present study aimed to compare the safety and efficacy of sodium valproate, levetiracetam, and phenytoin in agitation control. METHODS AND MATERIAL: This prospective observational study included 189 adult patients with traumatic brain injury (TBI) receiving sodium valproate, phenytoin, and levetiracetam. Agitation was monitored using the Richmond Agitation-Sedation Scale (RASS) at baseline and serially over seven days. The study evaluated the percentage of patients who experienced agitation-relief (A-R) following antiepileptic drugs, along with pattern of adverse events among the three groups.

resultsSodium valproate (sod.v) demonstrated better efficacy with 85.7% of patients achieving A-R compared to 63.5% in levetiracetam (P = 0.016). The median time to achieve A-R was 3 days in sod.v and significantly lesser compared to 4 days in phenytoin (P = 0.04) and 5 days in levetiracetam (P = 0.0001). By day 4, 72% of patients in the sod.v achieved A-R, in contrast to 50% in the phenytoin and 31.7% in the levetiracetam group. The safety profile of sod.v and levetiracetam was more favorable with lesser occurrence of adverse events compared to phenytoin (P = 0.017).

conclusionsTo our knowledge, this is the first pivotal evidence to compare antiepileptics for agitation control in post-traumatic brain injury patients. Our study demonstrated that patients receiving sodium valproate showed relatively greater and earlier improvement in agitation control, with an acceptable safety profile. The study proves the dual benefits of sod.v in post-TBI improving patient outcomes and alleviating mental strain on patients, and their families.

Indexed as

AnticonvulsantsBrain Injuries, TraumaticPhenytoinPiracetamPsychomotor AgitationValproic AcidAdultAgedFemaleHumansLevetiracetamMaleMiddle AgedProspective StudiesTreatment OutcomeYoung AdultAnticonvulsantsLevetiracetamPhenytoinPiracetamValproic Acid

Identifiers

PMID42234767
PMCPMC13232942

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.