Johanna A A Damen, Banafsheh Arshi, Maarten van Smeden, Silvia Bertagnolio, Janet V Diaz, Ronaldo Silva, Soe Soe Thwin, Laure Wynants, Karel G M Moons
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These models were evaluated using data contributed to the WHO Global Clinical Platform for COVID-19 from nine LMICs (Burkina Faso, Cameroon, Democratic Republic of Congo, Guinea, India, Niger, Nigeria, Zambia, and Zimbabwe). Model performance was assessed in terms of discrimination and calibration.</p><p><strong>Results: </strong>Out of 144 eligible models, 140 were excluded due to a high risk of bias, predictors unavailable in LIMCs, or insufficient model description. Among 11,338 participants, the remaining models showed good discrimination for predicting in-hospital mortality (3 models), with areas under the curve (AUCs) ranging between 0.76 (95% CI 0.71-0.81) and 0.84 (95% CI 0.77-0.89). An AUC of 0.74 (95% CI 0.70-0.78) was found for predicting ICU admission risk (one model). All models showed signs of miscalibration and overfitting, with extensive heterogeneity between countries.</p><p><strong>Conclusions: </strong>Among the available COVID-19 prognostic models, only a few could be validated on data collected from LMICs, mainly due to limited predictor availability. Despite their discriminative ability, selected models for mortality prediction or ICU admission showed varying and suboptimal calibration.</p>","PeriodicalId":72800,"journal":{"name":"Diagnostic and prognostic research","volume":"8 1","pages":"17"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11656577/pdf/","citationCount":"0","resultStr":"{\"title\":\"Validation of prognostic models predicting mortality or ICU admission in patients with COVID-19 in low- and middle-income countries: a global individual participant data meta-analysis.\",\"authors\":\"Johanna A A Damen, Banafsheh Arshi, Maarten van Smeden, Silvia Bertagnolio, Janet V Diaz, Ronaldo Silva, Soe Soe Thwin, Laure Wynants, Karel G M Moons\",\"doi\":\"10.1186/s41512-024-00181-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>We evaluated the performance of prognostic models for predicting mortality or ICU admission in hospitalized patients with COVID-19 in the World Health Organization (WHO) Global Clinical Platform, a repository of individual-level clinical data of patients hospitalized with COVID-19, including in low- and middle-income countries (LMICs).</p><p><strong>Methods: </strong>We identified eligible multivariable prognostic models for predicting overall mortality and ICU admission during hospital stay in patients with confirmed or suspected COVID-19 from a living review of COVID-19 prediction models. These models were evaluated using data contributed to the WHO Global Clinical Platform for COVID-19 from nine LMICs (Burkina Faso, Cameroon, Democratic Republic of Congo, Guinea, India, Niger, Nigeria, Zambia, and Zimbabwe). Model performance was assessed in terms of discrimination and calibration.</p><p><strong>Results: </strong>Out of 144 eligible models, 140 were excluded due to a high risk of bias, predictors unavailable in LIMCs, or insufficient model description. Among 11,338 participants, the remaining models showed good discrimination for predicting in-hospital mortality (3 models), with areas under the curve (AUCs) ranging between 0.76 (95% CI 0.71-0.81) and 0.84 (95% CI 0.77-0.89). An AUC of 0.74 (95% CI 0.70-0.78) was found for predicting ICU admission risk (one model). All models showed signs of miscalibration and overfitting, with extensive heterogeneity between countries.</p><p><strong>Conclusions: </strong>Among the available COVID-19 prognostic models, only a few could be validated on data collected from LMICs, mainly due to limited predictor availability. 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引用次数: 0
摘要
背景:我们在世界卫生组织(WHO)全球临床平台中评估了预测COVID-19住院患者死亡率或ICU入院率的预后模型的性能,该平台是包括低收入和中等收入国家(LMICs)在内的COVID-19住院患者个人临床数据的存储库。方法:通过对COVID-19预测模型的实时回顾,我们确定了用于预测确诊或疑似COVID-19患者住院期间总死亡率和ICU住院率的合格多变量预后模型。使用来自9个中低收入国家(布基纳法索、喀麦隆、刚果民主共和国、几内亚、印度、尼日尔、尼日利亚、赞比亚和津巴布韦)向世卫组织COVID-19全球临床平台提供的数据对这些模型进行了评估。从判别和校准两个方面对模型性能进行了评估。结果:在144个符合条件的模型中,140个因高偏倚风险、LIMCs中无法获得预测因子或模型描述不充分而被排除。在11,338名参与者中,其余模型在预测住院死亡率(3个模型)方面表现出良好的辨别能力,曲线下面积(auc)范围在0.76 (95% CI 0.71-0.81)和0.84 (95% CI 0.77-0.89)之间。预测ICU入院风险的AUC为0.74 (95% CI 0.70-0.78)(一个模型)。所有模型都显示出校准不当和过拟合的迹象,各国之间存在广泛的异质性。结论:在现有的COVID-19预后模型中,只有少数模型可以根据从中低收入国家收集的数据进行验证,这主要是由于预测器的可用性有限。尽管它们具有判别能力,但所选的死亡率预测或ICU入院模型显示出不同的和次优的校准。
Validation of prognostic models predicting mortality or ICU admission in patients with COVID-19 in low- and middle-income countries: a global individual participant data meta-analysis.
Background: We evaluated the performance of prognostic models for predicting mortality or ICU admission in hospitalized patients with COVID-19 in the World Health Organization (WHO) Global Clinical Platform, a repository of individual-level clinical data of patients hospitalized with COVID-19, including in low- and middle-income countries (LMICs).
Methods: We identified eligible multivariable prognostic models for predicting overall mortality and ICU admission during hospital stay in patients with confirmed or suspected COVID-19 from a living review of COVID-19 prediction models. These models were evaluated using data contributed to the WHO Global Clinical Platform for COVID-19 from nine LMICs (Burkina Faso, Cameroon, Democratic Republic of Congo, Guinea, India, Niger, Nigeria, Zambia, and Zimbabwe). Model performance was assessed in terms of discrimination and calibration.
Results: Out of 144 eligible models, 140 were excluded due to a high risk of bias, predictors unavailable in LIMCs, or insufficient model description. Among 11,338 participants, the remaining models showed good discrimination for predicting in-hospital mortality (3 models), with areas under the curve (AUCs) ranging between 0.76 (95% CI 0.71-0.81) and 0.84 (95% CI 0.77-0.89). An AUC of 0.74 (95% CI 0.70-0.78) was found for predicting ICU admission risk (one model). All models showed signs of miscalibration and overfitting, with extensive heterogeneity between countries.
Conclusions: Among the available COVID-19 prognostic models, only a few could be validated on data collected from LMICs, mainly due to limited predictor availability. Despite their discriminative ability, selected models for mortality prediction or ICU admission showed varying and suboptimal calibration.