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

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05597540
Collaborator
(none)
470
2
50

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Short antibiotic treatment
  • Drug: Usual antibiotic treatment
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
470 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Randomized double blind trial
Primary Purpose:
Treatment
Official Title:
Efficacy of 7 Days Versus 14 Days of Antibiotic Therapy for Acute Pyelonephritis in Kidney Transplant Recipients, a Multicentre Randomized Non-inferiority Trial.
Anticipated Study Start Date :
Nov 1, 2022
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: 7 day-duration antibiotic treatment

Drug: Short antibiotic treatment
7 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

Active Comparator: 14 day-duration antibiotic treatment

Drug: Usual antibiotic treatment
14 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

Outcome Measures

Primary Outcome Measures

  1. Clinical cure day 30 [at day 30]

    Clinical cure and microbiological eradication and no additional antibiotic treatment since the end of antibiotic treatment up to the main evaluation at day 30. Clinical cure is defined as fever <38°C and no symptoms of Urinary Tract Infection (UTI). Microbiological eradication is defined as uropathogen ≤ 10.3 CFU/mL in urine culture.

Secondary Outcome Measures

  1. Clinical cure day 90 [at day 90]

    Clinical cure and microbiological eradication and no additional antibiotic treatment since the end of antibiotic treatment up to the main evaluation at day 90. Clinical cure is defined as fever <38°C and no symptoms of Urinary Tract Infection (UTI). Microbiological eradication is defined as uropathogen ≤ 10.3 CFU/mL in urine culture.

  2. Clinical cure day 180 [at day 180]

    Clinical cure and microbiological eradication and no additional antibiotic treatment since the end of antibiotic treatment up to the main evaluation at day 180. Clinical cure is defined as fever <38°C and no symptoms of Urinary Tract Infection (UTI). Microbiological eradication is defined as uropathogen ≤ 10.3 CFU/mL in urine culture.

  3. Incidence of relapse/recurrence day 30 [at day 30]

    Relapse or recurrence of the Urinary Tract Infection

  4. Incidence of relapse/recurrence day 90 [at day 90]

    Relapse or recurrence of the Urinary Tract Infection

  5. Incidence of adverse event [at day 180]

    Incidence of adverse events imputable to antibiotic treatment

  6. MDRD [at day 90 and day 180]

    Modification of Diet in Renal Disease (MDRD) Study equation. Froissart M, Rossert J, Jacquot C, Paillard M, Houillier P. Predictive performance of the modification of diet in renal disease and Cockcroft-Gault equations for estimating renal function. J Am Soc Nephrol 2005;16(3):763-73.

  7. CKD [at day 90 and day 180]

    CKD-EPI (Chronic Kidney Disease EPIdemiology collaboration, Levey, 2009) A New Equation to Estimate Glomerular Filtration Rate. Andrew S. Levey, MD; Lesley A. Stevens, MD, MS; Christopher H. Schmid, PhD; Yaping (Lucy) Zhang, MS; Alejandro F. Castro III, MPH; Harold I. Feldman, MD, MSCE; John W. Kusek, PhD; Paul Eggers, PhD; Frederick Van Lente, PhD; Tom Greene, PhD; and Josef Coresh, MD, PhD, MHS, for the CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration). Annals of Internal Medicine 2009;150(9):604-613

  8. Hospital length of stay [at day 180]

    Hospitalisation length stay defined by the delay between the date of inclusion and the date of hospital discharge

  9. Antibiotic consumption [at day 180]

    Antibiotic consumption (indication, dose and duration) throughout the follow-up will be recorded.

  10. Rectal carriage [at day 14 and day 30]

    Rectal carriage of antibiotic resistant bacteria at the end of treatment and at day 14 and day 30

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 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) and positive urine culture (single 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...)

  • Early response after 48h of antibiotic treatment defined by: T°<38°C and improvement or complete resolution of any symptoms and/or signs of UTI if present at baseline 48 to 60 hours after the first administration of effective antibiotic.

  • Written informed consent

Exclusion Criteria:
  • Severe or complicated conditions

  • Any rapidly progressing disease or immediately life-threatening illness, including, but not limited to, septic shock, current or impeding respiratory failure, acute heart or liver failure

  • Admission or stay in intensive care unit at baseline

  • Obstruction of the urinary tract

  • Renal, perinephric or prostatic abscess

  • Dual antibiotic therapy (prophylactic antibiotic such as cotrimoxazole allowed) (only 1 dose of aminoside is allowed before randomization)

  • First month post transplantation

  • Current indwelling catheter (including bladder catheter, ureteral stents, percutaneous nephrostomy tubes)

  • Prior inclusion in this study

  • current participation to another interventional study

  • Neurogenic bladder

  • Enterocystoplasty

  • Immunodeficiency or immunosuppressive therapy not related to kidney transplantation including hematologic malignancy, cancer, asplenia, neutropenia<500 PNN/mm3

  • Pregnancy, breastfeeding

  • Hypersensitivity or previous severe adverse drug reaction to the antibiotic therapy

  • Unable or unwilling, in the judgment of the investigator, to comply with the protocol

  • Life expectancy<1 month

  • Patient under legal guardianship or without healthcare coverage

  • Homeless patient

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT05597540
Other Study ID Numbers:
  • APHP200020
First Posted:
Oct 28, 2022
Last Update Posted:
Oct 28, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 28, 2022