Evidence map›Paper›PMID 35387377›Full record

ArticleThe Canadian journal of hospital pharmacy2022

Assessment of Intravenous versus Oral Antimicrobials in a Large Regional Health Authority.

Manpreet Dulku, Tina Sekhon, Aaron M Tejani

Abstract read
In one paragraph

Article in The Canadian journal of hospital pharmacy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Using a planetary health lens to quantify intravenous use of bioequivalent antimicrobials when oral administration is feasible.Journal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada · 2026
    Article
  2. Review
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

3 authors.

Manpreet Dulkuis a student in the Entry-to-Practice Doctor of Pharmacy program (Class of 2022), Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia.
Tina Sekhon, BScPharm, ACPR, is a Clinical Pharmacy Specialist, Medication Use Evaluation, with Lower Mainland Pharmacy Services, Burnaby, British Columbia.
Aaron M Tejani, BSc(Pharm), PharmD, is a Medication Use Evaluation Pharmacist with Fraser Health; a researcher and educator with the Therapeutics Initiative, The University of British Columbia; and a Clinical Assistant Professor with the Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Many antimicrobials given by the intravenous (IV) route have oral (PO) formulations with high oral bioavailability. The advantages of using the PO rather than the IV formulation include lower risk of adverse reactions, shorter length of hospital stay, and lower health care costs. Objectives: The primary objective was to determine the proportions of patients who received the IV and PO formulations of antimicrobials with high oral bioavailability. The secondary objectives were to determine the proportion of patients who were eligible to receive PO antimicrobials from the start of treatment, the proportion who qualified for IV-to-PO step-down, and areas of improvement to increase use of PO antimicrobials. Methods: A retrospective chart review was conducted in hospitals in the Fraser Health Authority, British Columbia, between October 18, 2019, and March 5, 2020. Two hundred charts were randomly selected for patients who had received either azithromycin, ciprofloxacin, clindamycin, fluconazole, levofloxacin, linezolid, moxifloxacin, metronidazole, sulfamethoxazole-trimethoprim, or voriconazole. Results: Of the 200 patients, 124 (62.0%) received the PO formulations, while 76 (38.0%) received the IV formulations. Of the 76 patients receiving IV antimicrobials, 39 (51.3%; 95% confidence interval 44.7%-57.9%) were eligible to receive PO antimicrobials from the start of treatment or could have been stepped down from IV to PO administration. Conclusions: More than half of patients who received IV therapy were eligible to receive the PO formulation of antimicrobials known to have high oral bioavailability; relative to earlier studies, this proportion has not improved over time. This finding highlights the need for continued vigilance in encouraging the use of PO rather than IV formulations for hospitalized patients.

Indexed as

antimicrobialsantimicrobiensintravenous therapyintravenous-to-oral step-downoral therapypassage voie intraveineuse voie oralethérapie intraveineusethérapie orale

Identifiers

PMID35387377
PMCPMC8956462

What OpenQuestion holds

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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.