Evidence map›Paper›PMID 37663090›Full record

ArticleOpen forum infectious diseases2023

Antibacterial Utilization for Febrile Illnesses and Laboratory-Confirmed Bloodstream Infections in Northern Tanzania.

Ganga S Moorthy, Deng B Madut, Kajiru G Kilonzo, Bingileki F Lwezaula, Ronald Mbwasi, Blandina T Mmbaga, James S Ngocho, Wilbrod Saganda, John P Bonnewell, Manuela Carugati and 7 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2023. 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
0.5field-weighted citation impact, top 29% 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.

  1. Article
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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

17 authors at 6 institutions in 3 countries.

Ganga S MoorthyDivision of Pediatric Infectious Diseases, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-3191-1117
Deng B MadutDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-4023-3928
Kajiru G KilonzoKilimanjaro Christian Medical Centre-Duke University Collaboration, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0002-0367-5826
Bingileki F LwezaulaDepartment of Medicine, Mawenzi Regional Referral Hospital, Moshi, Tanzania.ORCID https://orcid.org/0000-0003-2909-9705
Ronald MbwasiKilimanjaro Christian Medical Centre-Duke University Collaboration, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0002-2365-5072
Blandina T MmbagaKilimanjaro Christian Medical Centre-Duke University Collaboration, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0002-5550-1916
James S NgochoKilimanjaro Christian Medical Centre-Duke University Collaboration, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0001-6242-9863
Wilbrod SagandaKilimanjaro Christian Medical University College, Tumaini University, Moshi, Tanzania.
John P BonnewellDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-2886-4885
Manuela CarugatiDivision of Infectious Diseases and International Health, Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-3187-5905
Joseph R EggerDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-0862-9511
Julian T HertzDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-7396-4789
L Gayani TillekeratneDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-6012-7271
Michael J MazeCentre for International Health, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0001-8909-1508
Venance P MaroKilimanjaro Christian Medical Centre-Duke University Collaboration, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0003-3838-0312
John A CrumpDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0002-4529-102X
Matthew P RubachDuke Global Health Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-5262-1421
Duke University · USTumaini University · TZDuke Medical Center · USKilimanjaro Christian Medical Centre · TZSt. Francis Referral Hospital · TZUniversity of Otago · NZ

Funding

Partnership for Global Health Research Training Program (Renewal)-Supplement for OBSSR, NCI, NCI-AIDS and NIDCDD43TW010543 · FIC · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Wafaie W Fawzi, DAVIDSON HOWES HAMER · 2017 to 2026
$12.1M
Unified Program for Therapeutics in Children (UPTiC)T32HD094671 · NICHD · DUKE UNIVERSITY · PI Ian J Davis, Kanecia Obie Zimmerman · 2019 to 2026
$2.9M
FIC NIH HHS D43 TW010543NICHD NIH HHS T32 HD094671
6 · The paper itself

Abstract

Background: We describe antibacterial use in light of microbiology data and treatment guidelines for common febrile syndromes in Moshi, Tanzania. Methods: We compared data from 2 hospital-based prospective cohort studies, cohort 1 (2011-2014) and cohort 2 (2016-2019), that enrolled febrile children and adults. A study team member administered a standardized questionnaire, performed a physical examination, and collected blood cultures. Participants with bloodstream infection (BSI) were categorized as receiving effective or ineffective therapy based upon antimicrobial susceptibility interpretations. Antibacterials prescribed for treatment of pneumonia, urinary tract infection (UTI), or presumed sepsis were compared with World Health Organization and Tanzania Standard Treatment Guidelines. We used descriptive statistics and logistic regression to describe antibacterial use. Results: Among participants, 430 of 1043 (41.2%) and 501 of 1132 (44.3%) reported antibacterial use prior to admission in cohorts 1 and 2, respectively. During admission, 930 of 1043 (89.2%) received antibacterials in cohort 1 and 1060 of 1132 (93.6%) in cohort 2. Inpatient use of ceftriaxone, metronidazole, and ampicillin increased between cohorts ( Conclusions: Receipt of antibacterials for febrile illness was common. While guideline-consistent prescribing increased over time, more than one-third of participants with BSI received ineffective antibacterials.

Indexed as

antibacterial useantimicrobial stewardshipfeverguidelinesTanzania

Identifiers

PMID37663090
PMCPMC10468737
OpenAlexW4386027387

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.