Conventional Antibiotic Prophylaxis Versus Add-On 5 Days Levofloxacin Before Percutaneous Nephrolithotomy

Sponsor
Mansoura University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03178292
Collaborator
(none)
300
1
2

Study Details

Study Description

Brief Summary

To evaluate whether 5 days of levofloxacin before percutaneous nephrolithotomy (PCNL) in reducing upper urinary tract infection and urosepsis after PCNL.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Percutaneous nephrolithotomy (PCNL) is a minimally invasive procedure for removal of large volume upper urinary tract stones. Although PCNL is effective and yielding high stone-free rates, complications rates range from 18.30% to 83% with sepsis has been reported in 0.3% to 7.6% of cases result in the most common cause of perioperative mortality in PCNL patients.

Urosepsis after PNL is an important and potentially catastrophic complication. The overall incidence of fever (25%), bacteremia (23%), endotoxemia (34%) and septicemic shock occurs in 0.3%-2.5% of patients. Urosepsis and shock result from the intravasation of bacteria or endotoxins into bloodstream, which in turn increases with prolonged surgery, degree of hydronephrosis, bacterial load in the renal pelvis, and presence of infected stones.

Charton et al., concluded that without antibiotic prophylaxis 35% of patient suffered urinary tract infection a post-PCNL, although preoperative urine showing no growth. In a prospective but nonrandomized assessment of PCNL patients receiving oral ciprofloxacin, intravenous ciprofloxacin, or no antimicrobial treatment found postoperative urinary tract infection to occur in 17%, 0%, and 40% of patients, respectively. Mariappan et al., stated that midstream urine (MSU) culture does not represent upper tract infection in patients with obstructing stones. Also, stone and pelvic urine cultures are better predictors of upper tract infection and urosepsis in such cases.

Antibiotic prophylaxis has been recommended (Level of evidence: IIb, III) for patients subjected to PCNL to avert these infectious complications, as profiled in an American Urological Association (AUA) Best Practice Policy Statement. They also recommend antibiotic prophylaxis before shock wave lithotripsy and ureteroscopy with high level (Level of evidence: Ia and Ib, respectively) due to presence of meta-analysis and large randomised controlled trial.

The optimal timing, dosing, and duration of a prophylactic antibiotic regimen for PCNL procedures has also been a point of discussion. The AUA best practice policy statement currently recommends that a one-time dose on the day of the procedure is sufficient. The EAU guidelines are less definitive in concluding that a short course is adequate but that the "length of time is to be determined." Mariappan and colleagues in a prospective non-randomised trial found that 52 patients who had dilated collecting systems, stone burden greater than 2 cm, and no confounding factors predisposing to UTIs who received a 1-week course of ciprofloxacin before PCNL had a 3-fold lower risk of postoperative UTI and SIRS than 46 patients who received standard perioperative antibiotics on the day of surgery.

Bag and colleagues prospectively randomized 101 patients with greater than 2.5-cm kidney stones and/or hydronephrosis with sterile preoperative urine cultures to a 7-day course of nitrofurantoin versus no antibiotics before PCNL and found a statistically significant lower rate of postoperative SIRS (19% vs 49%), endotoxemia (18% vs 42%), positive result on kidney urine culture (0% vs 10%), and positive result on stone culture (8% vs 30%) in the arm receiving nitrofurantoin.

Although these two small series support a week of preoperative antibiotics before PCNL, larger, prospective, randomized studies are needed to better elucidate the risks and benefits of empiric antibiotics

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Conventional Antibiotic Prophylaxis Versus Add-On 5 Days Levofloxacin Before Percutaneous Nephrolithotomy (PCNL)
Anticipated Study Start Date :
Jun 15, 2017
Anticipated Primary Completion Date :
Jun 15, 2017
Anticipated Study Completion Date :
Jun 15, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Levofloxacin

Levofloxacin 500 mg daily for 5 days

Drug: Levofloxacin
Levofloxacin 500Mg daily for 5 days
Other Names:
  • Levofloxacin 500Mg
  • Placebo Comparator: Placebo

    Placebo tab daily for 5 days

    Drug: Placebo
    Placebo Oral Tablet daily for 5 days
    Other Names:
  • placebo Oral Tablet
  • Outcome Measures

    Primary Outcome Measures

    1. Upper urinary tract infection and systemic inflammatory response syndrome (SIRS) after PCNL by Criteria for SIRS established by the American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference [1 year]

      SIRS if patient has Two or more of the 4 SIRS criteria

    Secondary Outcome Measures

    1. difference between culture and sensitivity of Preoperative urine (MSU) and intraoperative renal pelvic urine and extracted stone. [1 year]

      Preoperative urine (MSU),intraoperative renal pelvic urine and extracted stone culture and sensitivity.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Stones ≥ 2.5 cm and/or hydronephrosis

    • Sterile mid urine stream

    Exclusion Criteria:
    • Patients with a stent, nephrostomy tube or indwelling catheter

    • Uncontrolled Diabetes mellitus

    • Renal failure

    • Fever before surgery

    • Concomitant bladder stone or tumour

    • Patients with active UTI

    • Contralateral renal/ureteric stone

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Urology and Nephrology Center Mansoura Aldakahlia Egypt 35516

    Sponsors and Collaborators

    • Mansoura University

    Investigators

    • Study Chair: Ahmed Shoma, MD, Urology and Nephrology center
    • Study Director: Nasr Eltabey, MD, Urology and Nephrology center
    • Principal Investigator: Mahmoud Laimon, Msc, Urology and Nephrology center
    • Principal Investigator: Muhamad Abdullateef, Msc, Urology and Nephrology center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Abdelwahab Hashem, Urology Msc, Oncology fellow at Urology and Nephrology Center, Principal Investigator, Mansoura University
    ClinicalTrials.gov Identifier:
    NCT03178292
    Other Study ID Numbers:
    • Ab-PCNL
    First Posted:
    Jun 6, 2017
    Last Update Posted:
    Jun 6, 2017
    Last Verified:
    May 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 6, 2017