Overview

Fixed-dose Amikacin for Elderly UTI

Status:
Not yet recruiting
Trial end date:
2021-12-01
Target enrollment:
0
Participant gender:
All
Summary
Aminoglycosides are broad-spectrum antibiotics, effective against gram-negative bacteria. Aminoglycosides urine concentration exceeds that of the plasma by up to a hundred. Their efficacy is dependent on their level above minimal inhibitory concentration (MIC); however high levels are associate with nephrotoxicity. Therefore aminoglycosides have a narrow therapeutic rang. The correlation between administrated dose and blood drug levels is hard to predict. Amikacin is a highly effective aminoglycoside, highly effective against extended spectrum beta lactamase (ESBL) bacteria. Older patients suffer from more urinary tract infection (UTIs), and have a higher frequency of infection with resistant bacteria, mainly among frail nursing home residents. Our goal is to prove that fixed low dose amikacin in the elderly patient in non-inferior to weight-adjusted treatment. Study design: A randomized prospective, open label, non-inferiority trial Study participants will be 65 years or older, who were admitted to the medical ward due to a UTI will be assigned to one of the following study arms: 1. Intervention arm: in which patients will receive a fixed dose of amikacin, 500 mg, once a day. 2. Comparator arm: in which patients will receive a weight adjusted dose of amikacin (15 mg/kg adjusted body weight) and continue in adjusted intervals according plasma concentrations, using the Barnes Jewish Hospital nomogram. All participants will be followed up with: 1. Amikacin blood levels 6-14 hours following first administration, used for dose adjustment according to the nomogram. Peak amikacin blood levels, 30- 60 minutes following first or second administration. 2. Urine analysis and culture upon admission to the emergency department (ER). In patients with indwelling urinary catheters, cultures will be taken following replacement with a new catheter. 3. Broad serum biochemistry, complete blood count, C-reactive protein and blood cultures will be taken upon admission to the ER, two days after recruitment and at least once every three days following that, as long as the patient is receiving amikacin. Duration of amikacin treatment will be according to the attending physician's clinical judgment; however, it will not be shorter than 72 hours since first dose. Total duration of amikacin treatment will not exceed 10 days. Total treatment for UTI will not fall short of seven days of antibiotics (either amikacin or any suitable alterative according to blood and/or urine cultures).
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rabin Medical Center
Treatments:
Amikacin
Criteria
Inclusion Criteria:

1. A clinical diagnosis of UTI according to: pyuria, along with a new complaint of
dysuria, urgency or frequency of urination, or lower abdominal pain or discomfort; AND
one of the following: systemic fever, flank pain, tenderness over the costo-vertebral
angle, rigors and chills, vomiting.

2. Patients with moderate to severe cognitive impairment, who are unable to give reliable
anamnesis, or those with permanent indwelling urinary catheter for 24 hours or more,
will be considered as suffering from UTI is they present with systemic fever, pyuria
and the lack of a more probable infectious cause.

3. Patients who can give informed consent or those with a legal guardian who can consent
on their behalf.

4. Patients who received a single dose of any antimicrobial drug prior to recruitment,
including amikacin.

-

Exclusion Criteria:

1. Creatinine clearance < 40 mL/sec according to the Cockcroft-Gault equation

2. A known sensitivity to aminoglycosides

3. A known neuromuscular pathology (including myasthenia gravis).

4. Polycystic kidney disease

5. A urine or blood culture positive for amikacin resistant bacteria in the 30 days prior
to recruitment.

6. Clinical suspicion of prostatitis, epididymitis or orchitis.

7. Hemodynamical instability (mean arterial pressure of 65 mmHg or under).

8. More than one dose of antimicrobial treatment that is adequate for classical UTI
bacteria, unless a bacterial culture shows resistance to said treatment.

9. Immunosuppressed patients; steroidal treatment will be allowed.

-