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Management of Accidental Paraquat Ingestion in a Child
Emily Horsley1, Claire Chandler2, Claire Wainwright2
1University of Queensland, Queensland Children's Hospital, Brisbane, Queensland, Australia.
Insights
Early intervention with activated charcoal, N-acetylcysteine, continuous renal replacement therapy (CRRT), and pirfenidone is crucial for managing paraquat poisoning in toddlers. This treatment approach can significantly improve outcomes and prevent long-term complications like pulmonary fibrosis.
Area of Science:
- Toxicology
- Pediatric Intensive Care
- Nephrology
Background:
- Paraquat herbicide ingestion poses a significant risk of severe toxicity, particularly in pediatric populations.
- Accidental paraquat poisoning requires prompt and aggressive management in specialized centers.
Observation:
- A 16-month-old child ingested an unknown amount of paraquat, presenting unique management challenges.
- Treatment involved continuous renal replacement therapy (CRRT), activated charcoal, methylprednisolone, N-acetylcysteine, and pirfenidone.
Findings:
- The child experienced transient oral ulcerations and gastrointestinal issues but no respiratory distress.
- Radiographic evidence of interstitial changes prompted pirfenidone use to prevent pulmonary fibrosis.
- Follow-up at 6 months showed no signs of pulmonary fibrosis.
Implications:
- This case underscores the critical importance of early recognition and specialized care for pediatric paraquat poisoning.
- Multimodal treatment strategies, including CRRT and specific antidotes, can mitigate severe outcomes.
- Prompt management is key to preventing irreversible complications such as lung fibrosis.
Aim:
To report on the management of a toddler who had accidental ingestion of an unknown amount of paraquat, with treatment including continuous renal replacement therapy (CRRT), steroids and antifibrinolytics at a tertiary-level health system.
Methods:
A 16-month-old child weighing 10 kg accidentally ingested an unknown amount of Gramoxone containing paraquat. The child was transferred to a tertiary centre Paediatric Intensive Care Unit (PICU) where she was electively intubated and commenced on CRRT at 7 hours and 15 minutes post-ingestion. She was also treated with activated charcoal, methylprednisolone, N-acetylcysteine infusion and pirfenidone. Paraquat blood and urine samples were monitored throughout her PICU admission.
Results:
The child did not exhibit respiratory distress or significant hypoxia during the admission. She developed ulceration of the lips, mouth and tongue on day 2 which improved after 48 hours. Feed intolerance and pneumatosis intestinalis were managed conservatively. Interstitial changes were noted on chest x-ray on day 3 and pirfenidone was initiated to minimise the risk of pulmonary fibrosis. The child was discharged from PICU to the general ward for further observation. At follow-up, there has been no evidence of pulmonary fibrosis up to 6 months post-discharge.
Conclusions:
This case highlights the toxicity of Paraquat and importance of early management and urgent transfer of paraquat poisoning cases to specialised medical centres. Prompt interventions including activated charcoal, N-acetylcysteine, CRRT and pirfenidone can improve patient prognosis and reduce the risk of long-term complications such as pulmonary fibrosis in paediatric paraquat toxicity.
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