Table 1.
Demographic and clinical characteristics of the per-protocol study population (n=203).
Age; months Mean ± SD (range) | 40±36 (3–144) |
Gender (male: female;%) | 57.6: 42.4 |
Stool frequency; number of watery stools in previous 24 hours Mean ±SD (range) | 7.7±5.0 (3–30) |
Vomiting frequency; number of episodes in previous 24 hours Mean ±SD (range) | 3.2±3.6 (0–20) |
Nausea (% patients) | 59.1 |
Abdominal pain (% patients) | 49.3 |
Dehydration (% patients) | 25.6 |
Fever (% patients) | 35.0 |
Antibacterial therapy (% patients) | |
Ceftriaxone | 9.9 |
Cefuroxime | 4.9 |
Ampicillin-sulbactam + amikacin, azithromycin, clarithromycin or metronidazole | 4.0 |
Metronidazole | 3.4 |
Ceftriaxone-metronidazole | 3.0 |
Amoxicillin-clavulanic acid | 2.5 |
Ampicillin-sulbactam | 2.5 |
Cefdinir + amoxicillin-clavulanic acid or metronidazole | 1.0 |
Cefixime | 1.0 |
Cefuroxime-metronidazole | 1.0 |
Cefdinir | 0.5 |
Cefixime, ceftriaxone | 0.5 |
Ceftazidime | 0.5 |
Piperacillin, vancomycin, fluconazole | 0.5 |
Other | 1.0 |