Evidence map›Paper›PMID 39433691›Full record

ArticlePharmaceutical research2024

Identification of Patients Who Require Two-Point Blood Sampling for the Peak and Trough Values Rather Than One-Point Blood Sampling for the Trough Value for the Evaluation of AUC of Vancomycin Using Bayesian Estimation.

Ayako Suzuki, Masaru Samura, Tomoyuki Ishigo, Satoshi Fujii, Yuta Ibe, Hiroaki Yoshida, Hiroaki Tanaka, Fumiya Ebihara, Takumi Maruyama, Yukihiro Hamada and 11 more

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

21 authors.

Ayako SuzukiDepartment of Pharmacy, Showa University Fujigaoka Hospital, 1-30 Fujigaoka, Aoba-Ku, Yokohama-Shi, Kanagawa, 227-8501, Japan.
Masaru SamuraDivision of Pharmacodynamics, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-Ku, Tokyo, 105-8512, Japan. masaru.samura@gmail.com.ORCID http://orcid.org/0000-0002-8637-1237
Tomoyuki IshigoDepartment of Pharmacy, Sapporo Medical University Hospital, 291 Nishi 16-Chome, Minami 1-Jo, Chuo-Ku, Sapporo-Shi, Hokkaido, 060-8543, Japan.
Satoshi FujiiDepartment of Pharmacy, Sapporo Medical University Hospital, 291 Nishi 16-Chome, Minami 1-Jo, Chuo-Ku, Sapporo-Shi, Hokkaido, 060-8543, Japan.
Yuta IbeDepartment of Pharmacy, Sapporo Medical University Hospital, 291 Nishi 16-Chome, Minami 1-Jo, Chuo-Ku, Sapporo-Shi, Hokkaido, 060-8543, Japan.
Hiroaki YoshidaDepartment of Pharmacy, Kyorin University Hospital, 6-20-2 Shinkawa, Mitaka-Shi, Tokyo, 181-8611, Japan.
Hiroaki TanakaDepartment of Pharmacy, Kyorin University Hospital, 6-20-2 Shinkawa, Mitaka-Shi, Tokyo, 181-8611, Japan.
Fumiya EbiharaDepartment of Pharmacy, Tokyo Women's Medical University Hospital, 8-1 Kawada-Cho, Shinjuku-Ku, Tokyo, 162-8666, Japan.
Takumi MaruyamaDepartment of Pharmacy, Tokyo Women's Medical University Hospital, 8-1 Kawada-Cho, Shinjuku-Ku, Tokyo, 162-8666, Japan.
Yukihiro HamadaDepartment of Pharmacy, Tokyo Women's Medical University Hospital, 8-1 Kawada-Cho, Shinjuku-Ku, Tokyo, 162-8666, Japan.
Hisato FujiharaDepartment of Pharmacy, Showa University Fujigaoka Hospital, 1-30 Fujigaoka, Aoba-Ku, Yokohama-Shi, Kanagawa, 227-8501, Japan.
Fumihiro YamaguchiDepartment of Respiratory Medicine, Showa University Fujigaoka Hospital, 1-30 Fujigaoka, Aoba-Ku, Yokohama-Shi, Kanagawa, 227-8501, Japan.
Fumio NagumoDepartment of Pharmacy, Yokohama General Hospital, 2201-5 Kuroganecho, Aoba-Ku, Yokohama-Shi, Kanagawa, 225-0025, Japan.
Toshiaki KomatsuDepartment of Pharmacy, Kitasato University Hospital, 1-15-1 Kitasato, Minami-Ku, Sagamihara-Shi, Kanagawa, 252-0375, Japan.
Atsushi TomizawaDepartment of Pharmacy, Kitasato University Hospital, 1-15-1 Kitasato, Minami-Ku, Sagamihara-Shi, Kanagawa, 252-0375, Japan.
Akitoshi TakumaDepartment of Hospital Pharmaceutics, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-Ku, Tokyo, 142-8555, Japan.
Hiroaki ChibaDepartment of Pharmacy, Tohoku Kosai Hospital, 2-3-11 Kokubuncho, Aoba-Ku, Sendai-Shi, Miyagi, 980-0803, Japan.
Yoshifumi NishiCenter for Pharmacist Education, School of Pharmacy, Nihon University, 7-7-1 Narashinodai, Funabashi-Shi, Chiba, 274-0063, Japan.
Yuki EnokiDivision of Pharmacodynamics, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-Ku, Tokyo, 105-8512, Japan.
Kazuaki TaguchiDivision of Pharmacodynamics, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-Ku, Tokyo, 105-8512, Japan.
Kazuaki MatsumotoDivision of Pharmacodynamics, Faculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Minato-Ku, Tokyo, 105-8512, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIt is recommended to adjust the dose of vancomycin (VCM) with a target area under the concentration-time curve (AUC) of 400-600 μg·h/mL. Factors that affect the deviation between AUCs are estimated from the trough value alone and the trough and peak values using practical AUC-guided therapeutic drug monitoring (PAT) for vancomycin. In this study, factors that affect AUC were evaluated.

methodsAUCs were estimated from a single trough value and trough and peak values, and the patients were classified into those who showed a 10% or greater deviation (deviation group) and those in whom the deviation was less than 10% (no-deviation group). Risk factors related to ≥ 10% deviation of AUC were identified by univariate and multivariate analysis.

resultsAs a result of univariate and multivariate analysis of 30 patients in the deviation group and 344 patients in the no-deviation group, a creatinine clearance (CLcr) of ≥ 110 mL/min (odds ratio (OR) = 3.697, 95% confidence interval (CI) = 1.616-8.457, p = 0.002), heart failure with a brain natriuretic peptide (BNP) of ≥ 300 pg/mL (OR = 4.854, 95%CI = 1.199-19.656, p = 0.027), and the concomitant use of angiotensin converting enzyme inhibitor or angiotensin II receptor blocker (ACE-I/ARB) (OR = 2.544, 95%CI = 1.074-6.024, p = 0.034) were identified as risk factors of ≥ 10% deviation of AUC.

conclusionsEstimation of AUC by two-point blood sampling for the trough and peak values rather than one-point blood sampling for the trough value is suggested to improve the prediction accuracy in patients with enhanced renal function, severe heart failure, and patients using ACE-I/ARB.

Indexed as

Anti-Bacterial AgentsArea Under CurveBayes TheoremDrug MonitoringVancomycinAdultAgedAged, 80 and overBlood Specimen CollectionCreatinineFemaleHumansMaleMiddle AgedAnti-Bacterial AgentsCreatinineVancomycinarea under the concentration–time curveone-point samplingtwo-point samplingvancomycin

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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.