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Testing for sepsis in primary care

Testing for sepsis in primary care: diagnostic and prognostic study investigating the potential benefits of point-of-care testing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON20451
Enrollment
350
Registered
2018-02-09
Start date
2018-06-23
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Interventions

The study is diagnostic and prognostic without an intervention. The following variables are obtained for the development of a clinical decision tool: Age
temperature
blood pressure
heart rate
respiratory rate
oxygen saturation
rigors
acute clinical deterioration
C-reactive protein
procalcitonin

Sponsors

UMC Utrecht
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Adult patients (>18 years) 2)Home visit by a general practitioner from an out-of-hours service 3)Acutely ill patients with fever, confusion or general deterioration or otherwise suspected of a serious infection.

Exclusion criteria

Exclusion criteria: 1) No informed consent 2) Non-infectious cause of the acute complaints, e.g. stroke or myocardial infarction. 3) Hospitalisation less than 7 days before the home visit. 4) Condition that requires secondary care assessment in case of any signs of systemic infection (eg chemotherapy with possible neutropenia). 5)Terminal illness or other reason not to refer the patient to a hospital despite presence of a life-threatening condition.

Design outcomes

Primary

MeasureTime frame
The primary outcome is diagnosis of sepsis within 72 hours of inclusion. The reference standard is an expert panel assessment (following the SEPSIS-3 definitions)

Secondary

MeasureTime frame
Severity of sepsis 30-day mortality Hospital and ICU admission within 72 hours and length of hospital stay. Cost-effectiveness

Contacts

Public ContactFeike Loots

UMC Utrecht, div. Julius Center

F.J.Loots-2@umcutrecht.nl+31(0)6 24284896

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)