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| Name | Class |
|---|---|
| Hvidovre University Hospital | OTHER |
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The goal of this prospective study is to investigate whether oral antibiotic therapy alone is feasible and safe in clinically stable children aged 4 weeks to 2 months without any past high-risk medical history with a suspected or confirmed urinary tract infection.
All children aged 4 weeks to 2 months with a suspected urinary tract infection will be observed and examined by physicians and nurses as recommended by current guidelines. Children needing empirical antibiotic therapy will be admitted. The remaining will be contacted by phone if the urine culture is positive, and antibiotic therapy will be initiated if a urinary tract infection is still suspected due to persistent symptoms.
Clinically stable (see eligibility criteria) children without any past high-risk medical history (see eligibility criteria) will initiate oral antibiotic therapy. As empirical oral therapy, amoxicillin-clavulanic acid 50 mg/kg/day divided into 3 doses will be used. If the sensitivity pattern is available, a smaller-spectrum antibiotic can be used instead. If these children at any time point become clinically unstable or have a positive blood culture without suspected contamination, parenteral antibiotic therapy will be initiated. As empirical parenteral therapy, gentamicin 5 mg/kg once daily and ampicillin 100 mg/kg/day divided into 3 doses will be used. If the sensitivity pattern is available, another parenteral antibiotic regime can be used instead.
Admitted children can be sent home when they have clinically improved (judged by the physician) and have been hospitalized at least until the ward round the following day. Parents will be informed to contact the pediatric emergency department immediately if the child worsens or does not tolerate the antibiotics.
A physical or virtual follow-up will be conducted on day 3 (approximately 72 hours after treatment initiation) to ensure clinical improvement and treatment adherence. If needed, antibiotic therapy will be changed according to the sensitivity pattern. Children with a negative urine culture will be informed to stop antibiotic therapy.
The duration of antibiotic therapy will be 10 days. All children will undergo a renal ultrasound within the treatment period.
The above recommendations has been implemented as routine care. Hence, no parental consent is needed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Oral antibiotic therapy | Clinically stable (see eligibility criteria) children without any past high-risk medical history (see eligibility criteria) will initiate oral antibiotic therapy. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Oral antibiotic therapy | Drug | Empirical choice: amoxicillin-clavulanic acid 50 mg/kg/day divided into three doses. If the sensitivity pattern is available, another oral antibiotic, preferably smaller-spectrum, can be used instead. Total duration of antibiotic therapy will be 10 days. |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of participants with recurrent urinary tract infection regardless of the pathogen or death of any cause | Within 28 days after end of treatment | |
| Number of days admitted related to urinary tract symptoms | Within 28 days after treatment initiation |
| Measure | Description | Time Frame |
|---|---|---|
| Number of days with antibiotic-related non-serious adverse events. | Data on diarrhea, loss of appetite, and vomiting will be included. | From date of treatment initiation until the date of treatment stop for the baseline infection, assessed up to 14 days |
| Proportion of participants with a recurrent urinary tract infection regardless of the pathogen or death of any cause. |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of participants with a serious adverse event. | Defined as any untoward medical occurrence that results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in persistent or significant disability, or jeopardizes the patient | Within 100 days after treatment initiation |
INCLUSION CRITERIA:
All children who do not receive any empirical antibiotic therapy but have a positive urine culture can be included if the clinical suspicion of urinary tract infection persists.
A positive urine culture is defined as:
EXCLUSION CRITERIA:
Non-Danish civil registration number.
High-risk medical history.
Markedly elevated c-reactive protein indicating bacteremia.
Elevated creatinine.
Oral therapy is not possible (e.g., frequent vomiting or excessive regurgitation).
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All children aged 4 weeks to 2 months who are referred by their primary physician or the medical helpline 1813 (outside the work hours of their primary physician) to one of four pediatric emergency departments in the Capital Region of Denmark with suspected urinary tract infection.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Naqash Sethi, MD | Contact | +4528405083 | naqash.javaid.sethi.02@regionh.dk | |
| Ulrikka Nygaard, Ass. prof, Ph.D. | Contact | +4535459761 | ulrikka.nygaard@regionh.dk |
| Name | Affiliation | Role |
|---|---|---|
| Naqash Sethi, MD | Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark | Principal Investigator |
| Ulrikka Nygaard, Ass. prof, Ph.D. | Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Copenhagen University Hospital Rigshospitalet | Recruiting | Copenhagen | 2100 | Denmark |
Study protocol and statistical analysis plan will be shared. Individual participant data will be shared to facilitate the conduction of research or quality improvement projects.
Beginning 3 months and ending 5 years following article publication.
Primarily for the conduction of research or quality improvement projects.
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| ID | Term |
|---|---|
| D014552 | Urinary Tract Infections |
| ID | Term |
|---|---|
| D007239 | Infections |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| ID | Term |
|---|---|
| D000890 | Anti-Infective Agents |
| ID | Term |
|---|---|
| D045506 | Therapeutic Uses |
| D020228 | Pharmacologic Actions |
| D020164 | Chemical Actions and Uses |
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|
| Within 100 days after end of treatment |
| Proportion of participants with a recurrent infection with a bacterium resistant to the antibiotic given for the baseline infection or an opportunistic infection | Within 100 days after end of treatment |
| Copenhagen University Hospital Herlev | Recruiting | Herlev | 2730 | Denmark |
|
| Copenhagen University Hospital Hillerød | Recruiting | Hillerød | 3400 | Denmark |
|
| Copenhagen University Hospital Hvidovre | Recruiting | Hvidovre | 2650 | Denmark |
|
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |