Evidence map›Paper›PMID 28485312›Full record

Trial reportChinese medical journal2017

Pharmacokinetic and Pharmacodynamic Efficacies of Continuous versus Intermittent Administration of Meropenem in Patients with Severe Sepsis and Septic Shock: A Prospective Randomized Pilot Study.

Hui-Ying Zhao, Jian Gu, Jie Lyu, Dan Liu, Yi-Tong Wang, Fang Liu, Feng-Xue Zhu, You-Zhong An

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Chinese medical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07681544 (Meropenem Dosing in Critically Ill Patients), which is not on this map. Cited by 34 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 8 pooled it
2.7field-weighted citation impact, top 11% 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.

NCT07681544 nacompletednot on this mapstarted 2024, after this paper: background citation

Meropenem Dosing in Critically Ill Patients: Early Evaluation of Plasma Concentrations and Minimum Inhibitory Concentration

TypeinterventionalSponsorHospital Italiano de Buenos AiresRan2024 to 2025Enrolled26ConditionsEmpirical Antimicrobial Therapy, Critically Ill, Meropenem, Pharmacokinetics and PharmacodynamicsArmsBlood extraction
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 8 syntheses or guidelines pooled it, 66 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

8 authors at 2 institutions in 1 country.

Hui-Ying ZhaoDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Jian GuDepartment of Pharmacy, Peking University People's Hospital, Beijing 100044, China.
Jie LyuDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Dan LiuDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Yi-Tong WangDepartment of Pharmacy, Peking University People's Hospital, Beijing 100044, China.
Fang LiuDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Feng-Xue ZhuDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
You-Zhong AnDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing 100044, China.
Peking University People's Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe antibiotic meropenem is commonly administered in patients with severe sepsis and septic shock. We compared the pharmacokinetic, clinical, and bacteriological efficacies of continuous infusion of meropenem versus intermittent administration in such patients.

methodsPatients admitted to the Intensive Care Unit (ICU) with severe sepsis or septic shock who received meropenem were randomly assigned to either the continuous (n = 25) or intermittent groups (n = 25). The continuous group received a loading dose of 0.5 g of meropenem followed by a continuous infusion of 3 g/day; the intermittent group received an initial dose of 1.5 g followed by 1 g for every 8 h. Clinical success, microbiological eradication, superinfection, ICU mortality, length of ICU stay, and duration of meropenem treatment were assessed. Serial plasma meropenem concentrations for the first and third dosing periods (steady state) were also measured.

resultsClinical success was similar in both the continuous (64%) and intermittent (56%) groups (P = 0.564); the rates of microbiological eradication and superinfection (81.8% vs. 66.7% [ P = 0.255] and 4% vs. 16% [ P = 0.157], respectively) showed improvement in the continuous group. The duration of meropenem treatment was significantly shorter in the continuous group (7.6 vs. 9.4 days; P= 0.035), where a better steady-state concentration was also achieved. Peak and trough concentrations were significantly different between the continuous and intermittent groups both in the first (Cmax: 19.8 mg/L vs. 51.8 mg/L, P= 0.000; Cmin: 11.2 mg/L vs. 0.5 mg/L, P= 0.000) and third dosing periods (Cmax: 12.5 mg/L vs. 46.4 mg/L, P= 0.000; Cmin: 11.4 mg/L vs. 0.6 mg/L, P= 0.000). For medium-susceptibility pathogens, continuous infusion concentrations above the minimal inhibitory concentration were 100%, which was better than that in the intermittent group.

conclusionsContinuous infusion of meropenem provides significantly shorter treatment duration and a tendency for superior bacteriological efficacy than intermittent administration. Continuous infusion may be more optimal against intermediate-susceptibility pathogens.

Indexed as

AgedAged, 80 and overAnti-Bacterial AgentsFemaleHumansIntensive Care UnitsMaleMeropenemMiddle AgedPilot ProjectsProspective StudiesSepsisShock, SepticThienamycinsAnti-Bacterial AgentsMeropenemThienamycins

Identifiers

PMID28485312
PMCPMC5443018
OpenAlexW2612714554

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.