Repeated pulse of methylprednisolone and cyclophosphamide with continuous dexamethasone therapy for patients with severe paraquat poisoning
- PMID: 16424716
- DOI: 10.1097/01.ccm.0000195013.47004.a8
Repeated pulse of methylprednisolone and cyclophosphamide with continuous dexamethasone therapy for patients with severe paraquat poisoning
Abstract
Objective: Paraquat is widely used in the world, and all treatments for paraquat poisoning have been unsuccessful. Many patients have died of paraquat poisoning in developing countries. A novel anti-inflammation method was developed to treat severe paraquat-poisoned patients with >50% to <90% predictive mortality: initial pulse therapy with methylprednisolone (1 g/day for 3 days) and cyclophosphamide (15 mg/kg/day for 2 days), followed by dexamethasone 20 mg/day until Pao2 was >11.5 kPa (80 mm Hg) and repeated pulse therapy with methylprednisolone (1 g/day for 3 days) and cyclophosphamide (15 mg/kg/day for 1 day), which was repeated if Pao2 was <8.64 kPa (60 mm Hg).
Design: Randomized controlled trial.
Setting: Academic medical center in Taiwan.
Patients: Twenty-three paraquat-poisoned patients with >50% and <90% predictive mortality assessed by plasma paraquat levels were prospectively and randomly assigned to the control and study groups at a proportion of 1:2.
Interventions: The control group received conventional therapy and the study group received the novel repeated pulse treatment with long-term steroid therapy.
Measurements and main results: We measured patient mortality during the study period. There was not a different distribution of basal variables between the two study groups. The mortality rate (85.7%, six of seven) of the control group was higher than that of the study group (31.3%, five of 16; p = .0272).
Conclusions: The novel anti-inflammatory therapy reduces the mortality rate for patients with severe paraquat poisoning.
Comment in
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Randomized control trial of immunosuppression in paraquat poisoning.Crit Care Med. 2007 Jan;35(1):330-1; author reply 331. doi: 10.1097/01.CCM.0000251817.82117.7D. Crit Care Med. 2007. PMID: 17197797 No abstract available.
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