Evidence map›Paper›PMID 34588225›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2022

Evaluation of amikacin dosing schedule in critically ill elderly patients with different stages of renal dysfunction.

Saeideh Ghaffari, Ali Mohammad Hadi, Farhad Najmeddin, Bita Shahrami, Mohammad-Reza Rouini, Atabak Najafi, Mojtaba Mojtahedzadeh

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In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Saeideh GhaffariTehran University of Medical Sciences, Tehran, Iran.
Ali Mohammad HadiDepartment of Clinical Pharmacy, University of Basra, Basra, Iraq.
Farhad NajmeddinDepartment of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Bita ShahramiDepartment of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad-Reza RouiniTehran University of Medical Sciences, Tehran, Iran.
Atabak NajafiDepartment of Anesthesiology and Critical Care, Tehran University of Medical Sciences, Tehran, Iran.
Mojtaba MojtahedzadehDepartment of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran mojtahed@sina.tums.ac.ir.ORCID 0000-0003-2160-9301
Tehran University of Medical Sciences · IRUniversity of Basrah · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAmikacin is still a widely used aminoglycoside for the treatment of life-threatening infections. The pharmacokinetic parameters of this antibiotic may be altered in critically ill conditions. Moreover, in the elderly population, pathophysiological changes affect these pharmacokinetic variables, making it difficult to predict the appropriate dose and dosing schedule for amikacin. This study aimed to characterise the pharmacokinetics of amikacin in critically ill elderly patients with renal dysfunction, and to evaluate if the available dose adjustment schedules dependent on renal function would be appropriate for empirical dosing.

methodsCritically ill patients aged >60 years with a creatinine clearance of >20 mL/min in need of treatment with amikacin were randomly enrolled. All the patients received approximately 25 mg/kg amikacin. The patients were then divided into three groups according to the stages of their renal dysfunction based on creatinine clearance, and the optimum time to re-dosing was calculated for each group. The pharmacokinetic parameters of the patients were calculated and estimated as population pharmacokinetic data.

resultsOf 30 patients, only 20% attained the target peak levels of amikacin of >64 mg/L. In addition, the mean volume of distribution was 0.47 L/kg. There was a poor correlation between amikacin clearance and creatinine clearance. The difference in amikacin half-life was not statistically significant among any of the stages of renal impairment.

conclusionsThe initial dosing of amikacin in critically ill elderly patients should not be reduced, even in the context of renal impairment. Regarding the dose adjustment in renal impairment, dosing intervals estimation, no decision can be made based on the creatinine clearance and the first dose individualisation method in terms of the two-sample measurements may be considered as an appropriate strategy.

Indexed as

AmikacinKidney DiseasesAgedAnti-Bacterial AgentsCritical IllnessHalf-LifeHumansMiddle AgedAmikacinAnti-Bacterial Agentsaminoglycosidecritical illnesselderlypharmacokineticsrenal impairmenttherapeutic drug monitoring

Identifiers

PMID34588225
PMCPMC8899630
OpenAlexW3204000051

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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.