Evidence map›Paper›PMID 42872236›Full record

ArticleOpen forum infectious diseases2026

Omitting the Eradication Phase of Treatment of Adults with Melioidosis: A Pilot, Single-Center Randomized Controlled Trial.

Simon Smith, James Stewart, Enzo Binotto, Jennifer Ho, Trent Yarwood, Valerie Nancarrow, Julian Harris, John Wood, Thomas Ragh, Christopher Reilly and 3 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. 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

13 authors.

Simon SmithDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.ORCID https://orcid.org/0000-0002-7770-3738
James StewartDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.ORCID https://orcid.org/0000-0002-1774-8619
Enzo BinottoDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
Jennifer HoDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.ORCID https://orcid.org/0000-0003-2676-5530
Trent YarwoodDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.ORCID https://orcid.org/0000-0002-9783-2764
Valerie NancarrowDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
Julian HarrisDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
John WoodDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
Thomas RaghDepartment of Pharmacy, Cairns Hospital, Cairns, Queensland, Australia.
Christopher ReillyDepartment of Pharmacy, Cairns Hospital, Cairns, Queensland, Australia.
Emily ShielDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
Elizabeth CatchpooleDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.
Josh HansonDepartment of Medicine, Cairns Hospital, Cairns, Queensland, Australia.ORCID https://orcid.org/0000-0002-1423-3839

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Contemporary Australian guidelines for the management of melioidosis recommend a longer duration of intravenous antibiotics during the intensive phase of treatment; recurrent disease is now far less common. A high rate of adverse drug reactions (ADRs) to the currently recommended minimum of 3 months of oral trimethoprim/sulfamethoxazole (TMP/SMX) eradication therapy questions the incremental value of this phase of treatment. Methods: In this pilot, single-center, open-label randomized controlled trial, adults with culture-confirmed melioidosis received either prolonged intravenous intensive-phase therapy followed by oral eradication-phase therapy with TMP/SMX (standard therapy) or prolonged intravenous intensive-phase therapy alone (short-course therapy). The primary outcome was culture-confirmed recurrence at 2 years. Secondary outcomes included clinical (culture-unconfirmed) recurrence and ADRs to TMP/SMX. Results: Among 33 participants, 5 had culture-confirmed recurrence: 0/16 in the standard therapy group and 5/17 (29%) in the short-course therapy group. One participant (6%) in the standard therapy group had clinical recurrence. An ADR to TMP/SMX occurred in 13/16 (81%) in the standard therapy group, necessitating TMP/SMX cessation in 7/13 (44%), hospitalization in 5/13 (38%), and intensive care unit admission in 1/13 (8%). Conclusions: Prolonged intravenous antibiotics alone will cure many patients with melioidosis; however, some still require oral eradication therapy. The potential for recurrence of life-threatening melioidosis must be balanced against the high rate of significant ADRs to high-dose TMP/SMX. This necessitates a greater understanding of the individuals at highest risk of recurrence and determination of the optimal dosing and duration of eradication therapy in those who need it.

Indexed as

adverse reactionsBurkholderia pseudomalleidisease managementdrug-related side effectsdrug therapymelioidosis

Identifiers

PMID42872236
PMCPMC13660701

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.