Evidence map›Paper›PMID 34138408›Full record

ArticleInternational journal of clinical pharmacy2021

Timeliness of administration of amoxicillin-clavulanic acid and meropenem in a large tertiary care centre.

Astrid Van Wilder, Luk Bruyneel, Charlotte Decock, Nel Ten Haaf, Willy E Peetermans, Yves Debaveye, Kris Vanhaecht, Isabel Spriet

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of clinical pharmacy, 2021. 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

8 authors.

Astrid Van Wilder *Leuven Institute for Healthcare Policy, KU Leuven - University of Leuven, Kapucijnenvoer 35, Leuven, Belgium. astrid.vanwilder@kuleuven.be.ORCID http://orcid.org/0000-0001-7475-4890
Luk Bruyneel *Leuven Institute for Healthcare Policy, KU Leuven - University of Leuven, Kapucijnenvoer 35, Leuven, Belgium.ORCID http://orcid.org/0000-0003-1209-692X
Charlotte DecockLeuven Institute for Healthcare Policy, KU Leuven - University of Leuven, Kapucijnenvoer 35, Leuven, Belgium.
Nel Ten HaafLeuven Institute for Healthcare Policy, KU Leuven - University of Leuven, Kapucijnenvoer 35, Leuven, Belgium.
Willy E PeetermansDepartment of Internal Medicine, University Hospitals Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-6974-8493
Yves DebaveyeDepartment of Intensive Care Medicine, University Hospitals Leuven, Leuven, Belgium.
Kris VanhaechtLeuven Institute for Healthcare Policy, KU Leuven - University of Leuven, Kapucijnenvoer 35, Leuven, Belgium.ORCID http://orcid.org/0000-0001-5636-4792
Isabel SprietPharmacy Department, University Hospitals Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0001-6342-0676

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background For amoxicillin-clavulanic acid and meropenem to be effective, concentrations must exceed the minimum inhibitory concentration of infecting pathogens. Objective To retrospectively evaluate time windows between both scheduled prescription and administration and reconstitution-preparation and end of administration of intravenous amoxicillin-clavulanic acid and meropenem prescriptions. Setting 37 hospital wards at a tertiary hospital, Belgium. Method All adult hospital stays with at least one amoxicillin-clavulanic acid or meropenem administration in 2018 were reviewed. Time windows were deemed acceptable if < 30 min between prescription and administration and < 90 or < 150 min between reconstitution-preparation and end of administration for amoxicillin-clavulanic acid and meropenem, respectively. Main outcome measure Time windows between prescription and administration and between reconstitution-preparation and administration. Results For 50 273 administered prescriptions, both time windows were acceptable in 53.7% of first dose and 56.4% of follow-up dose administrations. 43.7% of first doses did not respect the time window between reconstitution-preparation and administration (2.8%) or between prescription and administration (40.9%). These discrepancies equalled 11.1% and 26.3% for follow-up doses, respectively. Large variation across hospital wards was observed. After the first five consecutive administrations, 93.1% of patients had not received their antibiotics within the time windows allowed. The most striking predictor of timely administration with respect to both prescription and reconstitution-preparation time was prescription synchronisation with nursing administration rounds. Conclusion For amoxicillin-clavulanic acid and meropenem, timeliness of reconstitution-preparation and administration was appropriate in approximately half of administrations. Evaluating and safeguarding the timeliness of antibiotic administration should be considered an important aspect of antibiotic stewardship.

Indexed as

AmoxicillinAmoxicillin-Potassium Clavulanate CombinationAdultAnti-Bacterial AgentsClavulanic AcidHumansMeropenemRetrospective StudiesTertiary Care CentersAmoxicillinAmoxicillin-Potassium Clavulanate CombinationAnti-Bacterial AgentsClavulanic AcidMeropenemAnti-bacterial agentsDrug prescriptionsElectronic prescribingPractice patternsTime factors

Identifiers

What OpenQuestion holds

Textmetadata
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.