Ghada N El-Sarnagawy, Fatma M Elgazzar, Mona M Ghonem
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Demographic, toxicological, and initial clinical characteristics data, as well as laboratory investigation results, were recorded for the included patients. After acute recovery, patients were followed up for six months and categorized into patients with and without DNS.</p><p><strong>Results: </strong>Out of 174 enrolled patients, 38 (21.8%) developed DNS. The initial Glasgow Coma Scale (GCS), carboxyhemoglobin (COHb) level, CO exposure duration, oxygen saturation, PaCO<sub>2</sub>, and pulse rate were significantly associated with DNS development by univariate analysis. However, the constructed nomogram based on the multivariable regression analysis included three parameters: duration of CO exposure, COHb level, and GCS with adjusted odd ratios of 1.453 (95% CI: 1.116-1.892), 1.262 (95% CI: 1.126-1.415), and 0.619 (95% CI: 0.486-0.787), respectively. The internal validation of the nomogram exhibited excellent discrimination (area under the curve [AUC] = 0.962), good calibration, and satisfactory decision curve analysis for predicting the DNS probability.</p><p><strong>Conclusions: </strong>The proposed nomogram could be considered a simple, precise, and applicable tool to predict DNS development in acute CO-poisoned patients.</p>","PeriodicalId":13561,"journal":{"name":"Inhalation Toxicology","volume":" ","pages":"406-419"},"PeriodicalIF":2.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development of a risk prediction nomogram for delayed neuropsychiatric sequelae in patients with acute carbon monoxide poisoning.\",\"authors\":\"Ghada N El-Sarnagawy, Fatma M Elgazzar, Mona M Ghonem\",\"doi\":\"10.1080/08958378.2024.2374394\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Delayed neuropsychiatric sequelae (DNS) are critical complications following acute carbon monoxide (CO) poisoning that can substantially affect the patient's life. Identifying high-risk patients for developing DNS may improve the quality of follow-up care. To date, the predictive DNS determinants are still controversial. Consequently, this study aimed to construct a practical nomogram for predicting DNS in acute CO-poisoned patients.</p><p><strong>Methods: </strong>This retrospective study was conducted on patients with acute CO poisoning admitted to the Tanta University Poison Control Center (TUPCC) from December 2018 to December 2022. Demographic, toxicological, and initial clinical characteristics data, as well as laboratory investigation results, were recorded for the included patients. After acute recovery, patients were followed up for six months and categorized into patients with and without DNS.</p><p><strong>Results: </strong>Out of 174 enrolled patients, 38 (21.8%) developed DNS. 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引用次数: 0
摘要
目的:迟发性神经精神后遗症(DNS)是急性一氧化碳(CO)中毒后的重要并发症,会严重影响患者的生活。识别发生 DNS 的高危患者可提高后续护理的质量。迄今为止,预测 DNS 的决定因素仍存在争议。因此,本研究旨在构建一个实用的提名图,用于预测急性 CO 中毒患者的 DNS:这项回顾性研究针对 2018 年 12 月至 2022 年 12 月期间坦塔大学中毒控制中心(TUPCC)收治的急性 CO 中毒患者。研究记录了纳入患者的人口统计学、毒理学、初始临床特征数据以及实验室检查结果。急性康复后,对患者进行为期六个月的随访,并将其分为有 DNS 和无 DNS 患者:在 174 名登记患者中,38 人(21.8%)出现 DNS。通过单变量分析,最初的格拉斯哥昏迷量表(GCS)、碳氧血红蛋白(COHb)水平、CO 暴露持续时间、血氧饱和度、PaCO2 和脉搏与 DNS 的发生显著相关。然而,基于多变量回归分析构建的提名图包括三个参数:一氧化碳暴露持续时间、一氧化碳血红蛋白水平和 GCS,调整后的奇异比分别为 1.453(95% CI:1.116-1.892)、1.262(95% CI:1.126-1.415)和 0.619(95% CI:0.486-0.787)。提名图的内部验证显示了极好的区分度(曲线下面积 [AUC] = 0.962)、良好的校准性以及令人满意的预测 DNS 概率的决策曲线分析:结论:所提出的提名图可被视为预测急性 CO 中毒患者 DNS 发展的简单、精确和适用的工具。
Development of a risk prediction nomogram for delayed neuropsychiatric sequelae in patients with acute carbon monoxide poisoning.
Objectives: Delayed neuropsychiatric sequelae (DNS) are critical complications following acute carbon monoxide (CO) poisoning that can substantially affect the patient's life. Identifying high-risk patients for developing DNS may improve the quality of follow-up care. To date, the predictive DNS determinants are still controversial. Consequently, this study aimed to construct a practical nomogram for predicting DNS in acute CO-poisoned patients.
Methods: This retrospective study was conducted on patients with acute CO poisoning admitted to the Tanta University Poison Control Center (TUPCC) from December 2018 to December 2022. Demographic, toxicological, and initial clinical characteristics data, as well as laboratory investigation results, were recorded for the included patients. After acute recovery, patients were followed up for six months and categorized into patients with and without DNS.
Results: Out of 174 enrolled patients, 38 (21.8%) developed DNS. The initial Glasgow Coma Scale (GCS), carboxyhemoglobin (COHb) level, CO exposure duration, oxygen saturation, PaCO2, and pulse rate were significantly associated with DNS development by univariate analysis. However, the constructed nomogram based on the multivariable regression analysis included three parameters: duration of CO exposure, COHb level, and GCS with adjusted odd ratios of 1.453 (95% CI: 1.116-1.892), 1.262 (95% CI: 1.126-1.415), and 0.619 (95% CI: 0.486-0.787), respectively. The internal validation of the nomogram exhibited excellent discrimination (area under the curve [AUC] = 0.962), good calibration, and satisfactory decision curve analysis for predicting the DNS probability.
Conclusions: The proposed nomogram could be considered a simple, precise, and applicable tool to predict DNS development in acute CO-poisoned patients.
期刊介绍:
Inhalation Toxicology is a peer-reviewed publication providing a key forum for the latest accomplishments and advancements in concepts, approaches, and procedures presently being used to evaluate the health risk associated with airborne chemicals.
The journal publishes original research, reviews, symposia, and workshop topics involving the respiratory system’s functions in health and disease, the pathogenesis and mechanism of injury, the extrapolation of animal data to humans, the effects of inhaled substances on extra-pulmonary systems, as well as reliable and innovative models for predicting human disease.