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The Volume of Blood Submitted for Culture in Neonates - a Multicentre Quality Improvement Initiative. (VOB4C)

M

Medical University of Warsaw

Status

Enrolling

Conditions

Neonatal Sepsis

Treatments

Other: Bedside blood culture bottles weighing combined with educational interventions.

Study type

Observational

Funder types

Other

Identifiers

NCT04455022
VOB4C TRIAL'20

Details and patient eligibility

About

The study will examine if introducing the practice of checking the volume of blood culture samples in neonates by bedside weighing will improve the sensitivity of the test and increase confidence in negative results affecting the rate of extended antibiotic treatment in neonates with negative blood cultures.

Full description

In the first part of the study (pre-intervention) the actual volumes of blood submitted for culture in neonates from participating neonatal units will be examined for the period of six months. The culture vials will be pre-weighted using precision scale before delivery to the units. After collecting the sample the vials will be weighted again at the time of admission to microbiology laboratory. At the end of the first phase, the results will be revealed to clinical teams and discussed. The sample volume control by using bedside precision scale will be introduced to the participating units along with educational actions to raise the awareness of importance of collecting adequate volume of blood for culture. The minimum volume of blood will be defined as at minimum 1 ml. The paramount role of blood culture in process of ruling out newborn sepsis will be emphasized. In the second phase of the study clinicians in participating centres will have an opportunity of measuring the volume of samples just after collecting. The volumes will also be independently controlled in the microbiology laboratory. The second phase will also last six months. Collected volumes will be compared to results from pre-intervention period. Clinical outcome measured by frequency of antibiotic treatment in newborn patients with negative blood culture will be compared before and after implemented changes. We hypothesize that introducing routine bedside control of the blood volume submitted for culture will result in increase confidence in negative blood culture results and decrease of antibiotic use in newborn population.

Enrollment

600 estimated patients

Sex

All

Ages

Under 4 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any infant in a neonatal ward who has a blood culture collected (either early-onset or late-onset sepsis suspected).

Exclusion criteria

  • There is no exclusion criteria.

Trial design

600 participants in 1 patient group

Any infant who will have a blood culture collected.
Description:
During the study period educational actions will be taken to raise the awareness of importance of collecting adequate volume of blood for culture (posters, leaflets and educational activities). The minimum volume will be defined as at least 1 ml. The paramount role of blood culture in process of ruling out newborn sepsis will be emphasized. The sample volume control by using bedside precision scale will be introduced.
Treatment:
Other: Bedside blood culture bottles weighing combined with educational interventions.

Trial contacts and locations

4

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Central trial contact

Justyna Romańska, MD; Tomasz Wawrzoniak, MD

Data sourced from clinicaltrials.gov

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