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Efficacy and safety of short- versus standard-course ceftriaxone therapy in children with pneumonia: A randomized
Mei Lv1, Yang Yang1, Liyun Fang1
1Department of Pediatrics, Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xian, Shaanxi, 710018, China.
Insights
Short-course ceftriaxone sodium (5-7 days) and standard-course (7-14 days) show similar efficacy for pediatric bacterial pneumonia. Short-course reduces hospital stay and adverse events, while standard-course lowers recurrence.
Area of Science:
- Pediatric Infectious Diseases
- Pharmacology
- Clinical Trials
Background:
- Pediatric bacterial pneumonia affects 30-40% of cases.
- Ceftriaxone sodium is a common treatment, but optimal duration is debated.
Purpose of the Study:
- Compare efficacy, inflammatory markers, and safety of short-course vs. standard-course ceftriaxone sodium.
- Evaluate therapeutic outcomes in pediatric pneumonia patients.
Main Methods:
- Prospective, single-center, randomized controlled trial.
- 200 children (1-14 years) randomized to 5-7 days (short-course) or 7-14 days (standard-course) of ceftriaxone sodium.
- Primary outcome: overall response rate; secondary outcomes: symptom relief, hospital stay, recurrence, adverse events, inflammatory markers.
Main Results:
- Overall efficacy and symptom relief were comparable between groups.
- Short-course significantly reduced hospital stay and adverse events (P<0.05).
- Standard-course showed lower recurrence rates and superior inflammatory marker normalization by day 5 (P<0.05).
Conclusions:
- Both short- and standard-course ceftriaxone sodium demonstrate similar overall efficacy.
- Short-course is suitable for mild pneumonia with rapid inflammatory response.
- Standard-course is preferred for severe cases or delayed inflammation to prevent relapse.
Background:
Pediatric bacterial pneumonia (30-40% of cases) is commonly treated with ceftriaxone sodium, but optimal duration (traditional 7-14 days vs. short 5-7 days) remains controversial.
Objectives:
To compare therapeutic efficacy, inflammatory marker dynamics and safety of short- vs. standard-course ceftriaxone sodium in pediatric pneumonia.
Methods:
This prospective, single-center, single-blind, phase randomized controlled trial randomized 200 children (1-14 years) 1:1 to short-course (5-7 days) or standard-course (7-14 days) ceftriaxone sodium. The primary outcome was overall response rate; secondary outcomes included symptom relief time, hospital stay, recurrence, adverse events, and changes in lung function and inflammatory markers.
Results:
Symptom relief time and overall efficacy were comparable between groups (P>0.05). Short-course ceftriaxone sodium reduced hospital stay and adverse events (P<0.05), while standard-course lowered recurrence rate and achieved superior inflammatory marker normalization by day 5 (P<0.05).
Conclusion:
Short- and standard-course ceftriaxone sodium have similar overall efficacy. A short-course is suitable for mild cases with a prompt inflammatory response, while a standard-course is preferred for severe cases or delayed inflammation to prevent relapse.
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