Intramuscular cobinamide versus saline for treatment of severe hydrogen sulfide toxicity in swine

Autor: Joseph K. Maddry, Allyson A. Arana, Philippe Haouzi, Gerry R. Boss, Sari B. Mahon, Thomas F. Gibbons, Vikhyat S. Bebarta, Norma Garrett, Matthew Brenner, Patrick Ng, Tara B. Hendry-Hofer
Rok vydání: 2019
Předmět:
hydrogen sulfide toxicity
Swine
Apnea
Hydrogen sulfide
medicine.medical_treatment
Treatment outcome
Antidotes
resuscitation
Kaplan-Meier Estimate
Hydrogen sulfide poisoning
Toxicology
Injections
Intramuscular

Article
Injections
Vaccine Related
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Natural gas
Biodefense
medicine
Animals
Organic matter
030212 general & internal medicine
Hydrogen Sulfide
Saline
Lung
chemistry.chemical_classification
Intramuscular
business.industry
Prevention
030208 emergency & critical care medicine
General Medicine
Pharmacology and Pharmaceutical Sciences
Cobinamide
Survival Analysis
Treatment Outcome
chemistry
Environmental chemistry
Toxicity
Administration
Administration
Intravenous

Female
Cobamides
Saline Solution
Hypotension
business
Intravenous
Zdroj: Clinical toxicology (Philadelphia, Pa.), vol 57, iss 3
Popis: INTRODUCTION: Hydrogen sulfide (H(2)S) is found in petroleum, natural gas, and decaying organic matter. Terrorist groups have attempted to use it in enclosed spaces as a chemical weapon. Mass casualty scenarios have occurred from industrial accidents and release from oil field sites. There is no FDA approved antidote for sulfide poisoning. We have previously reported that intravenous cobinamide is effective for sulfide poisoning. A rapid-acting antidote that is easy to administer intramuscularly (IM) would be ideal for use in a prehospital setting. In this study, we assessed survival in sulfide-poisoned swine treated with IM cobinamide. METHODS: Eleven swine (45–55 kg) were anesthetized, intubated, and instrumented with continuous femoral and pulmonary artery pressure monitoring. After stabilization, anesthesia was adjusted such that animals ventilated spontaneously with a FiO(2) of 0.21. Sodium hydrosulfide (NaHS, 8mg/mL) was infused intravenously at 0.9 mg/kg.min until apnea or severe hypotension. Animals were randomly assigned to receive cobinamide (4 mg/kg), or no treatment at the apnea/hypotension trigger. The NaHS infusion rate was sustained for 1.5 min post trigger, decreased to 0.2mg/kg.min for 10 min, and then discontinued. RESULTS: The amount of NaHS required to produce apnea or hypotension was not statistically different in both groups (cobinamide: 9.0 mg/kg ±6.1; saline: 5.9 mg/kg ±5.5; mean difference: −3.1, 95% CI: −11.3, 5.0). All of the cobinamide treated animals survived (5/5), none of the control (0/6) animals survived (p
Databáze: OpenAIRE