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RecruitingNCT07134751FISSUpdated Apr 2, 2026

Febrile Infants Swedish Study

An observational study in Febrile Illness Acute, Meningitis, Bacterial and Urinary Tract Infection (Diagnosis), sponsored by Region Skane. Recruiting at 11 sites in Sweden. Open to participants aged Up to 60 Days. Per ClinicalTrials.gov, last updated 2026-04-02.

Sponsored by Region Skane · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
Up to 60 Days
Sex
All
01

Study summary

Approximately one million febrile infants aged ≤60 days present annually to pediatric emergency departments (PEDs) in Europe and the United States. Although fewer than 5% are diagnosed with meningitis or bacteremia (invasive bacterial infections - IBIs), and 10-15% with urinary tract infections (UTIs), current guidelines recommend extensive diagnostic evaluations, hospitalization, and empirical treatment with broad-spectrum parenteral antibiotics. This approach may contribute to medical overuse, with implications for patient care, healthcare resource utilization, and environmental sustainability.

The Febrile Infants Swedish Study (FISS) is a prospective observational study conducted across 11 PEDs in Sweden. All febrile infants aged ≤60 days presenting to participating sites will be eligible. A new clinical guideline for the management of infants with fever without source (FWS) will be implemented in 7 PEDs, while 4 PEDs will continue with current standard practice and serve as a comparison group.

The study is expected to run for approximately two years and aims to recruit a minimum of 2,500 febrile infants

Read the detailed description

BACKGROUND

Each year, around one million febrile infants aged ≤60 days present to pediatric emergency departments (PEDs) in Europe and the United States. Previous studies report that 2-5% of these infants are diagnosed with meningitis or bacteremia (invasive bacterial infections - IBIs) and 10-15% with urinary tract infections (UTIs). Due to the potential severity of these infections, current guidelines recommend comprehensive diagnostic evaluations, hospitalization, and empirical treatment with broad-spectrum antibiotics. Consequently, an estimated 800,000 infants undergo these interventions annually without confirmed SBI.

These practices may have unintended consequences. Lumbar punctures can be painful, stressful, and time-consuming, with unsuccessful attempts linked to longer hospital stays. Early antibiotic exposure has been associated with increased risks of chronic conditions and reduced vaccine response and contributes to antimicrobial resistance. Hospitalization may lead to complications, disrupt breastfeeding, and impose financial and emotional burdens on families. Routine testing can result in overdiagnosis and medical overuse. Additionally, healthcare delivery has environmental implications, with each hospital bed-day generating significant waste and energy consumption.

Current guidelines rely on binary thresholds for biomarkers such as CRP and procalcitonin. They also lack consideration of clinical context, such as the infant's condition or fever characteristics, resulting in a uniform approach that may not suit individual cases.

There is a need for more individualized, evidence-based guidelines that integrate clinical and laboratory findings to support risk stratification and informed decision-making. Guidelines that reduce unnecessary interventions may improve care, optimize resource use, and lessen environmental impact.

The Febrile Infants Swedish Study (FISS) aims to evaluate a new clinical guideline.

PRIMARY AIM

To evaluate the new guideline for the management of infants aged ≤60 days and compare to current praxis.

SECONDARY AIMS

  • To collect clinical data (height/duration of fever, gestational age, birth weight, clinical symptoms/signs, laboratory results, diagnoses) which will enable the improvement of the guideline and the development of a more individualized management guideline.
  • To describe adherence to the new guideline and variation between the study sites in the management of febrile infants aged ≤60 days.

STUDY DESIGN

This will be a multicenter prospective observational study in 11 PEDs in Sweden. All febrile infants presented to the study PEDs will be considered as eligible for the study. The new guideline will be implemented as the PEDs standard management protocol for infants aged ≤60 days with FWS in 7 PEDs (Lund, Malmö, Helsingborg, Kristianstad, Ystad, Örebro, Sachsska-Stockholm). In 4 PEDs (Uppsala, Gothenburg, Jönköping, and Karolinska-Stockholm), the management of febrile infants aged ≤60 days will continue according to current praxis and these PEDs will participate in this study as a control group

STUDY POPULATION

All febrile infants aged ≤60 days brought to any of the study PEDs will be considered eligible for the study.

INCLUSION CRITERIA

  1. Age ≤60 days.
  2. Temperature ≥38.0 C measured either at home or at the PED.

DEFINITIONS

Fever Without a Source (FWS): Defined as a body temperature ≥38°C, measured either at home or in the pediatric emergency department (PED), without an identifiable focus of infection following medical history and physical examination.

Serious bacterial infection (SBI) is defined as a Urinary Tract Infection (UTI), bacteremia, or bacterial meningitis.

Urinary tract infection (UTI) is defined as urine dipstick positive for leukocyte esterase or nitrite and a urine culture with growth of (1) any amount of a single pathogen in samples obtained by suprapubic aspiration; (2) ≥10,000 colony- forming units (cfu)/ml of a single pathogen in samples obtained by a 'clean catch' method or catheterization.

Bacteremia is defined as growth of a bacterial pathogen in a blood culture. The presence of coagulase- negative staphylococci, Propionibacterium spp, Bacillus cereus spp, micrococci, alpha haemolytic streptococci and diphtheroids were considered contaminants, unless indicated otherwise because of clinical or laboratory parameters.

Bacterial meningitis is defined by the presence of a cerebrospinal fluid (CSF) culture or a CSF polymerase chain reaction (PCR) test positive for a bacterial pathogen. Cases with indirect clinical or laboratory indications of bacterial meningitis, such as elevated CSF cell count with positive blood culture and negative CSF culture/PCR, especially if antibiotics are given before the lumbar puncture, can be considered as bacterial meningitis,

Invasive bacterial infection (IBI) is defined as bacterial meningitis or bacteremia.

Delayed treated SBI will be regarded in infants with an SBI who did not receive broad-spectrum antibiotics at the initial management.

02

Conditions studied

  • Febrile Illness Acute
  • Meningitis, Bacterial
  • Urinary Tract Infection (Diagnosis)
  • Invasive Bacterial Infection
  • Serious Bacterial Infection
  • Bacteremia
  • Sepsis

Keywords

  • Guidelines
  • Febrile infants
  • Age ≤60 days
  • Management
  • Serious Bacterial Infections
  • Invansive Bacterial Infections
  • Clinical prediction tool
03

Who can participate

Ages eligible
Up to 60 Days
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All febrile infants aged ≤60 days brought to any of the study Pediatric Emergency Departments will be considered eligible for the study.

Eligibility criteria

Inclusion Criteria:

  • Temperature ≥38.0 C (measured either at home or at the pediatric emergency department)
  • Age ≤60 days
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Febrile Infants aged ≤60 days

    Febrile Infants aged ≤60 days who present to the pediatric emergency department

05

What researchers measure

Primary outcomes

  1. The proportion of febrile infants aged ≤60 days with meningitis, bacteremia, and urinary tract infection identified by the new guideline and the proportion of those that received treatment with delay.

    Time frame: 10 days of attendance

Secondary outcomes

  1. The proportion of investigations, antibiotic treatments, and hospitalizations among febrile infants aged ≤60 days who visited the PED.

    Time frame: Day 1

  2. The prevalence of meningitis, bacteremia, and urinary tract infection among febrile infants aged ≤60 days.

    Time frame: 10 days of attendance

  3. Duration and height of the fever, gestational age, birth weight, breastfeeding, clinical signs and symptoms, and laboratory results.

    Time frame: Day 1

06

Study locations

9 of 11 sites recruiting
  • Sahlgrenska University Hospital
    Gothenburg, Sweden
    • Pia Laurin, Senior Consultant · Contact
    • Pia Laurin, Senior Consultant · Principal investigator
    Recruiting
  • Helsingborg Hospital
    Helsingborg, Sweden
    • Kevin Pearsson,, MD, PhD · Contact
    • Kevin Pearsson, MD, PhD · Principal investigator
    Not yet recruiting
  • Ryhov County Hospital
    Jönköping, Sweden
    • Johan Gyllensvärd, Senior Consultant · Contact
    • Johan Gyllensvärd, Senior Consultant · Principal investigator
    Recruiting
  • Kristianstad Central Hospital
    Kristianstad, Sweden
    • Daniel Gedeborg, Senior Consultant · Contact
    • Daniel Gedeborg, Senior Consultant · Principal investigator
    Recruiting
  • Skåne University Hospital
    Lund, Sweden
    • Ioannis Orfanos, Senior Consultant, PhD · Contact
    • Ioannis Orfanos, Senior Consultant, PhD · Principal investigator
    Recruiting
  • Skåne University Hospital
    Malmö, Sweden
    • Jorge Sotoca Fernandez, Senior Consultant, PhD · Contact
    • Jorge Sotoca Fernandez, Senior Consultant PhD · Principal investigator
    Recruiting
  • Örebro University Hospital
    Örebro, Sweden
    • Andreas Ohlin, Associate Professor, MD, PhD · Contact
    • Andreas Ohlin, Associate Professor, MD, PhD · Principal investigator
    Recruiting
  • Karolinska University Hospital
    Stockholm, Sweden
    • Albano de Juan Plaza, Senior Consultant · Contact
    • Albano de Juan Plaza, Senior Consultant · Principal investigator
    Recruiting
  • Sachs' Children and Youth Hospital
    Stockholm, Sweden
    • Tobias Alfvén, Professor, MD, PhD · Contact
    • Tobias Alfvén, Professor, MD, PhD · Principal investigator
    • Samuel Rhedin, Associate professor, MD, PhD · Sub investigator
    Not yet recruiting
  • Uppsala University Hospital
    Uppsala, Sweden
    • Susanne Sütterlin, Senior Consultant, PhD · Contact
    • Susanne Sütterlin, Senior Consultant, PhD · Principal investigator
    Recruiting
  • Ystad Hospital
    Ystad, Sweden
    • Madeleine Touma, MD · Contact
    • Madeleine Touma, MD · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: Yes — Anonymised datasets not containing any personal data will be available after publication upon request

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07134751
Lead sponsor
Region Skane
Responsible party
Orfanos Ioannis (MD, PhD, Senior Consultant Pediatrician, Region Skane) — Principal investigator
First posted
Aug 21, 2025
Start date
Dec 1, 2025
Primary completion
Dec 31, 2027 (estimated)
Completion
Sep 30, 2028 (estimated)
Last update
Apr 2, 2026

Study contacts

Ioannis Orfanos, Senior Consultant
Contact
ioannis.orfanos@med.lu.se
+4646178225

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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