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Published on: October 29, 2020
Ciprofloxacin-induced Q-T interval prolongation
John P Knorr1, Mersedeh Moshfeghi, Mary C Sokoloski
1Albert Einstein Medical Center, Philadelphia, PA 19141, USA. knorr.john@gmail.com
Insights
A pediatric patient with Crohn's disease experienced Q-T interval prolongation after starting ciprofloxacin. The condition resolved after discontinuing the antibiotic, highlighting a potential drug-induced cardiac side effect.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Gastroenterology
Background:
- Crohn's disease is a chronic inflammatory condition.
- Prolonged Q-T interval can lead to serious cardiac arrhythmias.
- Identifying iatrogenic causes of Q-T prolongation is crucial in pediatric care.
Observation:
- A 16-year-old boy with a history of Crohn's disease presented with an acute flare and perirectal abscess.
- Treatment with intravenous ciprofloxacin was initiated.
- Within 48 hours, the patient developed bradycardia and a prolonged Q-T interval (486 msec).
Findings:
- The patient's Q-T interval normalized within seven days of discontinuing ciprofloxacin.
- No further cardiac anomalies were observed.
- This suggests ciprofloxacin as a potential cause of Q-T interval prolongation in this patient.
Implications:
- This case highlights a potential adverse effect of ciprofloxacin in pediatric patients.
- Clinicians should monitor for Q-T interval prolongation in pediatric patients receiving ciprofloxacin, especially those with underlying conditions.
- Further investigation into fluoroquinolone-induced cardiotoxicity in children may be warranted.
Purpose:
A case of Q-T interval prolongation in a pediatric patient with no known risk factors for the development of a long Q-T syndrome is reported.
Summary:
A 16-year-old boy arrived at a children's hospital reporting mucous diarrhea that had lasted two weeks, light-headedness with two blackouts on the day before his arrival to the hospital, and a 4.3-kg weight loss over the previous three weeks. He had a 3.5-year history of Crohn's disease and had been hospitalized for two months with a diagnosis of colitis with cryptitis. He was admitted for the treatment of an acute flare of Crohn's disease and a perirectal abscess. The patient was started on i.v. ciprofloxacin 400 mg twice daily and metronidazole 500 mg every six hours. The selected agents provided adequate empirical coverage of the suspected organisms and would not be contraindicated with the patient's allergy to penicillin. Within 48 hours of administration of ciprofloxacin, the patient became bradycardic. The cardiology service was consulted, and an electrocardiogram showed a mildly prolonged Q-T interval (corrected Q-T interval, 486 msec) and low heart rate (42 beats/min). Antimicrobial therapy was changed to ampicillin and then to linezolid. The patient's Q-T interval normalized within seven days of ciprofloxacin discontinuation. The patient had no further cardiac anomalies. Two weeks later, he was discharged on linezolid and aztreonam for the treatment of his abscess and was responding to treatment.
Conclusion:
A pediatric patient with Crohn's disease and colitis with cryptitis developed a prolonged Q-T interval within 48 hours of treatment with ciprofloxacin.
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