Evidence map›Paper›PMID 42371622›Full record

Trial reportJAMA network open2026

Procalcitonin to Guide 7 vs 14 Days of Antibiotics in Bloodstream Infections: A Secondary Analysis of the BALANCE Trial.

Rayoun Ramendra, Julie K Wright, Kevin C Kain, Bridget Kim, Hridesh Mishra, Kathleen Zhong, Pierre Aslanian, Alex Carignan, John Conly, Michael Detsky and 18 more

Erratum issuedAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Rayoun RamendraDivision of Infectious Diseases, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Julie K WrightDivision of Infectious Diseases, Department of Medicine, University Health Network, Toronto, Ontario, Canada.
Kevin C KainDivision of Infectious Diseases, Department of Medicine, University Health Network, Toronto, Ontario, Canada.
Bridget KimDivision of Infectious Diseases, Department of Medicine, University Health Network, Toronto, Ontario, Canada.
Hridesh MishraDivision of Infectious Diseases, Department of Medicine, University Health Network, Toronto, Ontario, Canada.
Kathleen ZhongDivision of Infectious Diseases, Department of Medicine, University Health Network, Toronto, Ontario, Canada.
Pierre AslanianMedicine, Centre Hospitalier de l'Université de Montréal, Université de Montréal, Montreal, Quebec, Canada.
Alex CarignanDepartment of Microbiology and Infectious Diseases, Université de Sherbrooke, Quebec, Canada.
John ConlyDepartment of Medicine, University of Calgary and Alberta Health Services, Calgary, Alberta, Canada.
Michael DetskyCritical Care Medicine, Mount Sinai Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Erick DuanDivision of Critical Care, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Gerald EvansDepartment of Medicine (Infectious Diseases), Queen's University, Kingston, Ontario, Canada.
Jan O FriedrichCritical Care and Medicine, Unity Health Toronto-St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Francois LamontagneDepartment of Medicine, Université de Sherbrooke, Quebec, Canada.
Francois LauzierDepartment of Medicine, Université Laval, Quebec, Canada.
Derek R MacfaddenDivision of Infectious Diseases, Ottawa Hospital, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
John MarshallSurgery and Critical Care Medicine, Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.
Lauralyn McIntyreDepartment of Medicine, Ottawa Hospital, University of Ottawa, Ottawa, Ontario, Canada.
John MuscedereDepartment of Critical Care Medicine, Queen's University, Kingston, Ontario, Canada.
Andrew MorrisDepartment of Medicine, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.
Ruxandra PintoSunnybrook Research Institute, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Asgar RishuSunnybrook Research Institute, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Henry T StelfoxDepartment of Critical Care, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Linda R TaggartDivision of Infectious Diseases, Department of Medicine, St Michael's Hospital, Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.
Jennifer TsangDivision of Critical Care, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Alexis F TurgeonDivision of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, Faculty of Medicine, Université Laval, Québec City, Quebec, Canada.
Rob FowlerInterdepartmental Division of Critical Care Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Nick DanemanDivision of Infectious Diseases, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The Bacteremia Antibiotic Length Actually Needed for Clinical Effectiveness (BALANCE) trial showed that 7 days of antibiotics was noninferior to 14 days among patients with bacteremia. However, it is unknown whether patients with high serum procalcitonin (PCT) level at day 7 of therapy would benefit from a prolonged treatment course. Objective: To investigate whether an elevated serum PCT level at day 7 of bacteremia was associated with increased mortality among patients treated with 7 vs 14 days of antibiotics. Design, Setting, and Participants: This cohort study was a planned secondary analysis of the BALANCE trial from 2014 to 2023, a multicenter randomized clinical trial where serum was collected on day 7 of bacteremia and patients were followed up for 90 days after study enrollment. Serum samples were collected from patients 7 days after initiation of antibiotics; PCT levels were later quantified by an antibody-based assay and therefore were not available to clinicians. Data were analyzed from January to June 2025. Intervention: Patients were randomized to receive either 7 or 14 days of antibiotics. Antibiotic selection, dosing, and route were at the discretion of the treating team. Main Outcomes and Measures: The primary outcome was defined as death from any cause within 90 days of the positive index blood culture result. Secondary outcomes included death by any cause while admitted to the ICU, death by any cause while admitted to the hospital, number of days alive and not admitted to the ICU within 28 days of the index positive blood culture, number of days alive and not admitted to hospital within 28 days of the index positive blood culture, and the duration of mechanical ventilation. Results: A total of 125 patients (median age 63, [IQR, 58-79] years; 80 [64.0%] male) were included in this study. Sixty-five participants (52%) had low PCT levels (<250 pg/mL) and 60 (48%) had high PCT levels (≥250 pg/mL) on day 7. The high PCT group was older, had more comorbidities, and had a higher prevalence of community-acquired bacteremia. Ninety-day mortality was higher in the high vs low PCT group: 21.6% (13 of 60) vs 6.2% (4 of 65) (absolute risk difference [ARD] 15.5%; 95% CI, 3.6%-27.5%). Among patients with high PCT level, 90-day mortality was not different among participants with 7 vs 14 days of antbiotics (ARD, -19.9%; 95% CI, -1.7 to 41.7). Conclusions and relevance: In this cohort study, elevated PCT level on day 7 was associated with increased 90-day mortality. However, prolonging antibiotics beyond 7 days was not associated with improved mortality in patients with a residually high PCT level. Seven days of antibiotics appears sufficient for most patients with bloodstream infections independent of day 7 serum PCT level.

Indexed as

Anti-Bacterial AgentsBacteremiaProcalcitoninAgedBiomarkersCohort StudiesDrug Administration ScheduleFemaleHumansMaleMiddle AgedTreatment OutcomeAnti-Bacterial AgentsBiomarkersProcalcitonin

Identifiers

PMID42371622
PMCPMC13316601

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.