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A simplified approach to the pooled analysis of calibration of clinical prediction rules for systematic reviews of validation studies

机译:一种简化的方法,用于对临床预测规则的校准进行汇总分析,以进行验证研究的系统评价

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Objective: Estimating calibration performance of clinical prediction rules (CPRs) in systematic reviews of validation studies is not possible when predicted values are neither published nor accessible or sufficient or no individual participant or patient data are available. Our aims were to describe a simplified approach for outcomes prediction and calibration assessment and evaluate its functionality and validity. Study design and methods: Methodological study of systematic reviews of validation studies of CPRs: a) ABCD2 rule for prediction of 7 day stroke; and b) CRB-65 rule for prediction of 30 day mortality. Predicted outcomes in a sample validation study were computed by CPR distribution patterns (“derivation model”). As confirmation, a logistic regression model (with derivation study coefficients) was applied to CPR-based dummy variables in the validation study. Meta-analysis of validation studies provided pooled estimates of “predicted:observed” risk ratios (RRs), 95% confidence intervals (CIs), and indexes of heterogeneity (I2) on forest plots (fixed and random effects models), with and without adjustment of intercepts. The above approach was also applied to the CRB-65 rule. Results: Our simplified method, applied to ABCD2 rule in three risk strata (low, 0–3; intermediate, 4–5; high, 6–7 points), indicated that predictions are identical to those computed by univariate, CPR-based logistic regression model. Discrimination was good (c-statistics =0.61–0.82), however, calibration in some studies was low. In such cases with miscalibration, the under-prediction (RRs =0.73–0.91, 95% CIs 0.41–1.48) could be further corrected by intercept adjustment to account for incidence differences. An improvement of both heterogeneities and P-values (Hosmer-Lemeshow goodness-of-fit test) was observed. Better calibration and improved pooled RRs (0.90–1.06), with narrower 95% CIs (0.57–1.41) were achieved. Conclusion: Our results have an immediate clinical implication in situations when predicted outcomes in CPR validation studies are lacking or deficient by describing how such predictions can be obtained by everyone using the derivation study alone, without any need for highly specialized knowledge or sophisticated statistics.
机译:目的:当预测值既未发布也不可访问,或者没有足够的参与者或患者数据时,无法在验证研究的系统评价中评估临床预测规则(CPR)的校准性能。我们的目的是描述一种用于结果预测和校准评估的简化方法,并评估其功能和有效性。研究设计和方法:对CPR验证研究进行系统评价的方法研究:a)ABCD2规则,用于预测7天卒中; b)CRB-65规则,用于预测30天死亡率。通过CPR分布模式(“衍生模型”)计算出样本验证研究中的预期结果。作为确认,在验证研究中将逻辑回归模型(具有推导研究系数)应用于基于CPR的虚拟变量。验证研究的荟萃分析提供了“有预测和可观察”风险比(RR),95%置信区间(CI)和森林样地(固定和随机效应模型)异质性指数(I2)的合并估计(有或没有)调整截距。上述方法也适用于CRB-65规则。结果:我们的简化方法应用于三个风险层次的ABCD2规则(低,0–3;中,4–5;高,6–7点),表明预测与基于CPR的单变量logistic计算的预测相同回归模型。辨别力很好(c统计量= 0.61-0.82),但是,某些研究的校正率很低。在这种校准不正确的情况下,可以通过截距调整来校正发生率差异,从而进一步纠正预测不足(RRs = 0.73–0.91,95%CIs 0.41–1.48)。观察到异质性和P值均得到改善(Hosmer-Lemeshow拟合优度检验)。更好的校准和改进的合并RR(0.90–1.06),更窄的95%CI(0.57–1.41)。结论:当描述CPR验证研究的预测结果缺乏或不足时,我们的结果具有直接的临床意义,方法是描述每个人仅使用衍生研究就可以获得这样的预测,而无需高度专业的知识或复杂的统计数据。

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