Efficacy of 7 Days Versus 14 Days of Antibiotic Therapy for Acute Pyelonephritis in Kidney Transplant Recipients, a Multicentre Randomized Non-inferiority Trial.

Status: Recruiting
Location: See all (9) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Infections are a major cause of morbidity and mortality in solid organ transplant recipients. In kidney transplant recipients (KTR) urinary tract infection (UTI) represent 45-72% of all infections, and 30% of all hospitalizations for sepsis. Acute transplant pyelonephritis are the most common complications occurring in more than 20% of patients, mainly in the first year after transplantation. They are associated with an increased risk of acute kidney rejection and long-term kidney graft dysfunction. Gram-negative bacteria, mainly E. coli, account for more than 70% of UTI in KTR. As those infections are favoured by urinary tract modifications/defects and immunosuppression, they are often recurrent and necessitate repeated courses of antibiotics. Selective pressure due to antibiotic consumption, along with frequent hospital admissions and immunosuppression, are well known risk factors for the development of antibiotic resistant infections. Multidrug (MDR)- or extensively (XDR)- drug resistant Enterobacteriaceae including ESBL- or carbapenemase-producing organisms, are thus increasingly observed in transplant units and represent a global threat as very few new antibiotics are expected in the next decade. One main strategy to limit antimicrobial resistance is to reduce the duration of antibiotic treatment. A 7 day-course is recommended for simple acute pyelonephritis (APN) treated with fluoroquinolones or parenteral B-lactams, prolonged up to 10 or 14 days in the presence of underlying disease at risk of complications. Most KT teams treat patients between 14-21 days as recommended by American guidelines. However, the need to extend treatment duration in immunosuppressed patients is a poorly defined concept and the optimal duration of treatment for APN in KTR is not known as these patients are excluded from most studies. As there is an urgent need to reduce antibiotic consumption in this population at high risk of developing infections due to resistant pathogens, the hypothesis is that a 7 day-treatment is sufficient to cure APN with good clinical response after 48h of treatment in KTR and is as effective as 14 days.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \>18 years KTR

• APN defined by: fever (T°≥38°C) (with or without clinical signs and/or symptoms of UTI) and pyuria (≥10\^4 white blood cells/mL or ≥10/mm3) and positive urine culture (uropathogen ≥10\^3 CFU/mL susceptible to the empirically administrated antibiotic)

• No confirmed or suspected febrile non urinary bacterial infection

• No urologic/renal complication at baseline imaging (abscess, obstruction...)

• Favourable early response to antibiotic treatment:48 to 60 hours after the first dose of antibiotic effective against the causative uropathogen) defined by: T°\<38°C and improvement (or resolution) of signs and/or symptoms of urinary tract infection if present at diagnosis

• Written informed consent

Locations
Other Locations
France
CHU Bordeaux
NOT_YET_RECRUITING
Bordeaux
Hôpital Foch
NOT_YET_RECRUITING
Boulogne-billancourt
CHU Mondor
RECRUITING
Créteil
CHU Lyon
NOT_YET_RECRUITING
Lyon
CHU Nantes
RECRUITING
Nantes
CHU Kremlin-Bicêtre
NOT_YET_RECRUITING
Paris
CHU Necker
RECRUITING
Paris
CHU Saint Louis
RECRUITING
Paris
CHU Toulouse
NOT_YET_RECRUITING
Toulouse
Contact Information
Primary
Matthieu Lafaurie, MD
matthieu.lafaurie@aphp.fr
142494117
Backup
Jérôme Lambert, Pr
jerome.lambert@u-paris.fr
142499742
Time Frame
Start Date: 2024-02-22
Estimated Completion Date: 2027-08-22
Participants
Target number of participants: 470
Treatments
Experimental: 7 day-duration antibiotic treatment
Active_comparator: 14 day-duration antibiotic treatment
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov