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Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
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Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
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Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model

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Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model
Journal Article

Development of a histopathology scoring system for the pulmonary complications of organophosphorus insecticide poisoning in a pig model

2020
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Overview
Organophosphorus (OP) insecticide self-poisoning causes over 100,000 global deaths annually. Around a third of patients are intubated and up to half of these can die. Post-mortem analysis of OP poisoned patients' lungs reveals consolidation, edema and hemorrhage, suggesting that direct or indirect lung damage may contribute to mortality. The lung injury caused by these formulated agricultural preparations is poorly characterised in humans, and a valid histopathology scoring system is needed in a relevant animal model to further investigate the disease and potential treatments. We conducted two pilot studies in anesthetized minipigs, which are commonly used for toxicological studies. In the first, pigs were given 2.5 mL/kg of either OP (n = 4) or saline (n = 2) by gavage and compared with positive controls (iv oleic acid n = 2). The second study simulated ingestion followed by gastric content aspiration: mixtures of OP (n = 3) or saline (n = 2) (0.63-0.71mL/kg) were placed in the stomach, and then small volumes of the gastric content were placed in the lung. At post-mortem examination, lungs were removed and inflation-fixed with 10% neutral buffered formalin. Samples (n = 62) were taken from cranial and caudal regions of both lungs. Two experienced lung histopathologists separately scored these samples using 8 proposed features of damage and their scores related (Kendall rank order). Two elements had small and inconsistent scores. When these were removed, the correlation increased from 0.74 to 0.78. Eight months later, a subset of samples (n = 35) was re-scored using the modified system by one of the previous histopathologists, with a correlation of 0.88. We have developed a reproducible pulmonary histopathology scoring system for OP poisoning in pigs which will assist future toxicological research and improve understanding and treatment of human OP poisoning.