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Research Article

Performance of clinical scoring systems in acute organophosphate poisoning

, , , , , & show all
Pages 850-854 | Received 24 Jun 2013, Accepted 30 Aug 2013, Published online: 26 Sep 2013
 

Abstract

Introduction. Clinical scoring systems are used to predict mortality rate in hospitalized patients. Their utility in organophosphate (OP) poisoning has not been well studied. Methods. In this retrospective study of 396 patients, we evaluated the performance of the Acute Physiology and Chronic Health Evaluation (APACHE) II score, the Simplified Acute Physiology Score (SAPS) II, Mortality Prediction Model (MPM) II, and the Poisoning Severity Score (PSS). Demographic, laboratory, and survival data were recorded. Receiver operating characteristic (ROC) curves were generated, and the area under the curve (AUC) was calculated to study the relationship between individual scores and mortality rate. Results. The mean (standard deviation) age of the patients was 31.4 (12.7) years, and at admission, their pseudocholinesterase (median, interquartile) level was 317 (222–635) U/L. Mechanical ventilation was required in 65.7% of the patients and the overall mortality rate was 13.1%. The mean (95% confidence interval) scores were as follows: APACHE-II score, 16.4 (15.5–17.3); SAPS-II, 34.4 (32.5–36.2); MPM-II score, 28.6 (25.7–31.5); and PSS, 2.4 (2.3–2.5). Overall, the AUC for mortality was significantly higher for APACHE-II (0.77) and SAPS-II (0.77) than the PSS (0.67). When patients were categorized, the AUCs were better for WHO Class II (0.71–0.82) than that for Class I compounds (0.60–0.66). For individual compounds, the AUC for APACHE-II was highest in quinalphos (0.93, n = 46) and chlorpyrifos (0.86, n = 38) and lowest in monocrotophos (0.60, n = 63). AUCs for SAPS-II and MPM-II were marginally but not significantly lower than those for APACHE-II. The PSS was generally a poorer discriminator compared to the other scoring systems across all categories. Conclusions. In acute OP poisoning, the generic scoring systems APACHE-II and SAPS-II outperform the PSS. These tools may be used to predict the mortality rate in OP poisoning.

Acknowledgments

The authors wish to acknowledge the contributions of Mr. J Jerobin, Dr. A Nair and Dr. A. Bennett in collecting patient data.

Declaration of interest

The authors report no declarations of interest. The authors alone are responsible for the content and writing of the paper.

This project was supported by the South Asian Clinical Toxicology Research Collaboration which is funded by the Wellcome Trust International Collaborative Research Grant (GR071669MA).

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