Evidence map›Paper›PMID 41574403›Full record

ArticleJournal of clinical pharmacology2026

Clinical Impact of Adjusted Valproic Acid Level in Patients with Hypoalbuminemia: A Single-Center Cohort Study.

Renad Bin Naheet, Khalid Al Sulaiman, Khuld Aloufi, Abdullah F Alharthi, Mashael AlFaifi, Lama Nazer, Mohammad Shawaqfeh, Abdulmajeed M Alshehri, Mohammed Abutaleb, Abdulaziz Alarifi and 12 more

Abstract read
In one paragraph

Article in Journal of clinical pharmacology, 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

22 authors.

Renad Bin NaheetPharmaceutical Care Department, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Khalid Al SulaimanPharmaceutical Care Department, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.ORCID https://orcid.org/0000-0002-5547-2043
Khuld AloufiPharmaceutical Care Department, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Abdullah F AlharthiDepartment of Clinical Pharmacy, College of Pharmacy, Shaqra University, Al-Dawadmi Campus, Al-Dawadmi City, Riyadh, Saudi Arabia.
Mashael AlFaifiPharmaceutical Care Department, King Saud Medical City, Riyadh, Saudi Arabia.
Lama NazerDepartment of Pharmacy, King Hussein Cancer Center, Amman, Jordan.
Mohammad ShawaqfehCollege of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdulmajeed M AlshehriPharmaceutical Care Department, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Mohammed AbutalebPharmaceutical Care Department, King Fahad Central Hospital, Jazan, Saudi Arabia.ORCID https://orcid.org/0000-0002-5300-5900
Abdulaziz AlarifiKing Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
Asma A AlshehriPharmaceutical Care Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Ahmad H Al-AniDepartment of Pharmacy Practice, College of Pharmacy, AlMaarefa University, Dariyah, Riyadh, Saudi Arabia.
Omar SaggafDepartment of Pediatrics, Dr. Soliman Fakeeh Hospital, Jeddah, Saudi Arabia.
Ramesh VishwakarmaNorwich Clinical Trial Unit, Norwich Medical School, University of East Anglia, Norwich, UK.
Maryam AlharbiAl Rayyan Medical Collages, Medinah, Saudi Arabia.
Delael AlnaserDepartment of Pharmacy, Medical Services in Public Security, Ministry of Interior, Riyadh, Saudi Arabia.
Saud AlrashdiDepartment of Pharmacy, Medical Services in Public Security, Ministry of Interior, Riyadh, Saudi Arabia.
Abdulaziz A JalyDepartment of Pharmacy, Jazan University Hospital, Jazan, Saudi Arabia.
Farhan AleneziKing Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
Moayad AlkhlewiKing Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
Abdulelah AlanaziHealthcare Delivery Services Department, Alahsa Health Cluster, Ministry of Health, Al Ahsa, Saudi Arabia.
Ohoud AljuhaniDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID https://orcid.org/0000-0002-8078-564X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Valproic acid (VPA) is highly protein-bound, thereby impacting its free fraction and clearance in hypoalbuminemia. There is limited data on VPA use in such patients. Thus, this study evaluates the impact of adjusted VPA concentration (aVPAc) in predicting effectiveness and adverse effects compared to total VPA (tVPA) levels in hypoalbuminemic patients. A retrospective cohort study involved adult patients with seizures or epilepsy between January 1, 2016, and December 31, 2022. The levels of tVPA and aVPA (adjusted for albumin) were compared using receiver operating characteristic curves, and AUC differences were assessed using the DeLong method. Safety endpoints included hepatotoxicity, hyperammonemia, hyponatremia, and thrombocytopenia, while effectiveness endpoints were seizure occurrence, status epilepticus, and the use of additional antiepileptic medications during hospitalization. Of the 1621 screened patients, 71 with hypoalbuminemia received VPA. An aVPAc threshold of 154.19 mg/dL demonstrated higher sensitivity (86%) but lower specificity (47%) for predicting hepatotoxicity compared to a tVPA threshold of 67.53 mg/dL (sensitivity: 71%, specificity: 72%). Although aVPAc yielded a comparable negative predictive value (96% vs 95%), tVPA showed superior positive predictive value (25% vs 18%) and a higher Youden index (0.43 vs 0.33), indicating better overall discriminatory performance; however, these findings did not achieve statistical significance. In contrast, an aVPAc threshold of 188 mg/dL showed a sensitivity of 100% and a specificity of 82% for predicting hyperammonemia, which is superior to the tVPA threshold of 74.32 mg/dL that has a sensitivity of 40% and a specificity of 88%. The aVPAc also achieved a higher Youden index of 0.82 compared to 0.28 for tVPA. Adjusted VPA concentrations showed greater sensitivity than tVPA in predicting hepatotoxicity and hyperammonemia, suggesting potential utility for ruling out these adverse effects in hypoalbuminemic patients. Further research with a larger sample size is needed to validate these findings.

Indexed as

AnticonvulsantsHypoalbuminemiaValproic AcidAdultAgedChemical and Drug Induced Liver InjuryCohort StudiesEpilepsyFemaleHumansMaleMiddle AgedRetrospective StudiesSeizuresAnticonvulsantsValproic Acidadjusted levelhepatotoxicityhyperammoniahypoalbuminemiathrombocytopeniatotal levelsvalproic acid

Identifiers

PMID41574403
PMCPMC13501342

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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.