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INterest of the Negative Predictive Value of Integrons in Choosing a Narrow-spectrum Empirical anTibiotic Treatment vs Usual Empirical Antibiotic Treatment for Urinary Tract infectionS in the PEDiatric Emergency Department (INVICTUS PED)

U

University of Limoges (UL)

Status

Terminated

Conditions

Urinary Tract Infections in Children

Treatments

Procedure: usual practice
Procedure: integron research

Study type

Interventional

Funder types

Other

Identifiers

NCT05066854
87RI20_0029 (INVICTUS PED)

Details and patient eligibility

About

INVICTUS PED primary objective is to show the non-inferiority of an empirical antibiotic therapeutic management guided by the early detection of integrons in the urine, compared to a usual empirical antibiotic treatment, for the recovery of children admitted to the pediatric emergency department (ED) with a non-severe urinary tract infection (UTI) with fever

Full description

Urinary tract infections with fever are common in children and require primary health care management. Because of the risk of immediate evolution to a systemic infection with long-term renal scars, empirical antibiotic treatment is recommended. The French Group for Pediatric Infectious Diseases (GPIP) recommends the use of third-generation cephalosporins (3GC) targeting enterobacteria, which are mainly involved in UTI and increasingly resistant to antibiotics through the production of extended-spectrum β-lactamases. However, use of 3GC is a well-known risk factor for resistant germs selection and one of the main guideline to fight antibiotic resistance, which is an important public health issue, is to reduce their use. Integrons are genetic elements involved in the spread of antibiotic resistance in enterobacteria. Preliminary studies showed that integron search using polymerase chain reaction (PCR) directly on urine samples had a great NPV (>98%) for trimethoprim-sulfamethoxazole (SXT). The hypothesis is that, in children presenting to the pediatric ED with non-severe UTI with fever, absence of integron in their urine could allow prescribing an empirical antibiotic treatment with SXT without decreasing the chance of recovery, thus decreasing the use of 3GC.

Two strategies is compare: i) In the control group: empirical antibiotic treatment according to the usual practice of each center, in line with the GPIP guidelines, ii) in the experimental group: empirical antibiotic treatment chosen depending on the results of the integron search with PCR. When PCR is positive, treatment according to usual practice; when PCR is negative, treatment with SXT.

Two follow-up visits, by phone, will be planned: at H48 (+ 24h), when the empirical antibiotic treatment is assessed based on the urine culture and antimicrobial susceptibility test (AST) results, and on D30 (+/- 2 days) at the end of the follow-up.

Enrollment

36 patients

Sex

All

Ages

3 months to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children above 3 months old and under 18 years old
  • Consultation in a participating pediatric emergency department
  • Suspicion of UTI with fever (Fever ≥ 38°C and urine dipstick test positive for leukocytes and/or nitrites)
  • First episode of UTI with fever
  • Written informed consent of the holders of parental authority
  • Affiliated to Social Security

Exclusion criteria

  • Criteria of severity:

    • Severe infection with severe sepsis or septic shock
    • Dehydration ≥ 10%
    • Fever ≥ 38°C > 4 days (96h)
    • Indication of surgical or interventional drainage
  • Complication risk factors:

    • Any anatomic or functional defect of the urinary tract (other than low-grade VUR and calyceal dilation < 10 mm)
    • Repetition of UTI with fever ≤ than 6 months since the previous episode
    • Repetition of UTI with fever and anatomic or functional defect of the urinary tract
    • Pregnancy
    • Severely immunocompromised patient
    • Severe chronic renal failure defined as a clearance < 30 mL/min/1.73 m2
    • Severe liver failure
  • 3GC allergy

  • Contra-indication to SXT:

    • G6PD deficiency
    • Treatment with methotrexate
    • Allergy to sulfonamide
  • Antibiotic treatment within 48h before admission

  • Empirical antibiotic treatment not recommended

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Integron research
Experimental group
Description:
Empirical antibiotic treatment chosen based on the results of the integron search: * when PCR is negative, patients will receive SXT (30 mg/kg/j of sulfamethoxazole and 6 mg/kg/j of trimethoprim) * when PCR is positive or uninterpretable for integrons, patients will receive an empirical antibiotic treatment based on the usual practice of each center according to the GPIP guidelines.
Treatment:
Procedure: integron research
Usual practice
Other group
Description:
Empirical antibiotic treatment based on the usual practice of each center according to the GPIG guidelines.
Treatment:
Procedure: usual practice

Trial contacts and locations

4

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Central trial contact

Christine LAGUILLE, MD

Data sourced from clinicaltrials.gov

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