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国际上用于确定上消化道出血风险的评分系统的开发、验证和比较评估。

Development, Validation, and Comparative Assessment of an International Scoring System to Determine Risk of Upper Gastrointestinal Bleeding.

机构信息

London Digestive Centre, HCA Healthcare UK, London, United Kingdom.

Pragmatic Clinical Trials Unit, Queen Mary University of London, London, United Kingdom.

出版信息

Clin Gastroenterol Hepatol. 2019 May;17(6):1121-1129.e2. doi: 10.1016/j.cgh.2018.09.039. Epub 2018 Sep 27.

Abstract

BACKGROUND & AIMS: The Glasgow-Blatchford score (GBS) and pre-endoscopy Rockall score (pRS) are used in determining prognoses of patients with acute upper gastrointestinal bleeding, but neither predicts outcomes of patients with a high level of accuracy. A scoring system is needed to identify patients at risk of adverse outcomes and patients at low risk of harm.

METHODS

We pooled data from 5 data sets in Canada, the United Kingdom, and Australia on 12,711 patients with acute upper gastrointestinal bleeding. The GBS and pRS were calculated for each patient. We performed multivariable logistic regression modeling of data from 10,639 cases to develop the new scoring system Canada - United Kingdom - Adelaide (CANUKA). We performed area under the receiver operating characteristic analyses to test the ability of CANUKA to identify patients who died or had rebleeding within 30 days, surgical or radiologic intervention to control bleeding, need for therapeutic endoscopy, and transfusion-a poor outcome was defined as 1 or more of these outcomes. Patients at low risk of a poor outcome (safe for management as an outpatient) were identified based on lack of transfusion, rebleeding, therapeutic endoscopy, interventional radiology or surgery, or death. We validated in 2072 patients from a separate cohort compiled from 2 datasets.

RESULTS

In the development data set there was no difference between GBS and pRS in identifying patients who died without 30 days of bleeding (area under the receiver operating characteristic curve [AUROC], 0.67; 95% CI, 0.62-0.72 for GBS; AUROC, 0.70; 95% CI, 0.66-0.74 for pRS; P = .21). The GBS was superior to the pRS in identifying patients with rebleeding, hemostatic interventions, and transfusions. In the validation data set, CANUKA had higher accuracy than the GBS in identifying patients who died within 30 days of bleeding (AUROC, 0.77 vs 0.74; P = .047), but there was no significant difference in the accuracy of these scoring systems in identifying patients who required hemostatic intervention. The GBS more accurately identified patients who required therapeutic endoscopy (AUROC, 0.78; 95% CI, 0.76-0.81 for GBS; AUROC, 0.77; 95% CI, 0.74-0.79 for CANUKA; P = .47). For patients classified as low-risk patients by CANUKA (score ≤1), 96.3% were safely discharged, whereas 16 patients with a GBS ≤1 had an adverse outcome (a 95.3% probability of safe discharge).

CONCLUSIONS

In an international validation analysis of the GBS and pRS for patients with acute upper gastrointestinal bleeding, we found the GBS to more accurately identify those who later required hemostatic interventions and transfusions; the scoring systems identified 30-day mortality or rebleeding with equal levels of accuracy. We developed a scoring system (CANUKA) that had similar performance to the GBS in predicting patient outcomes and it more accurately identifies patients at low risk for adverse outcomes.

摘要

背景与目的

格拉斯哥-布拉奇福德评分(GBS)和内镜前罗克洛尔评分(pRS)用于预测急性上消化道出血患者的预后,但两者都不能准确预测患者的结局。需要一种评分系统来识别有不良结局风险的患者和低风险伤害的患者。

方法

我们汇总了来自加拿大、英国和澳大利亚的 5 个数据集的 12711 例急性上消化道出血患者的数据。为每个患者计算了 GBS 和 pRS。我们对来自 10639 例病例的数据进行了多变量逻辑回归建模,以开发新的评分系统加拿大-英国-阿德莱德(CANUKA)。我们进行了接受者操作特征曲线下面积分析,以测试 CANUKA 识别 30 天内死亡或再出血、手术或放射介入控制出血、需要治疗性内镜检查和输血的患者的能力(不良结局定义为出现 1 种或多种这些结局)。根据是否需要输血、再出血、治疗性内镜检查、介入放射学或手术或死亡,确定低风险不良结局(可作为门诊管理的安全患者)的患者。我们在来自 2 个数据集的 2072 例患者的独立队列中进行了验证。

结果

在开发数据集,GBS 和 pRS 在识别无 30 天内出血死亡的患者方面没有差异(接受者操作特征曲线下面积[AUROC],GBS 为 0.67;95%CI,0.62-0.72;pRS 为 0.70;95%CI,0.66-0.74;P=0.21)。GBS 在识别再出血、止血干预和输血患者方面优于 pRS。在验证数据集,CANUKA 在识别 30 天内出血死亡的患者方面比 GBS 具有更高的准确性(AUROC,0.77 比 0.74;P=0.047),但这些评分系统在识别需要止血干预的患者方面的准确性没有显著差异。GBS 更准确地识别需要治疗性内镜检查的患者(AUROC,0.78;95%CI,0.76-0.81 为 GBS;AUROC,0.77;95%CI,0.74-0.79 为 CANUKA;P=0.47)。对于 CANUKA (评分≤1)分类为低风险的患者,96.3%安全出院,而 16 例 GBS≤1 的患者出现不良结局(95.3%安全出院的可能性)。

结论

在对急性上消化道出血患者的 GBS 和 pRS 进行国际验证分析中,我们发现 GBS 更能准确识别那些随后需要止血干预和输血的患者;这些评分系统对 30 天死亡率或再出血的预测具有相同的准确性。我们开发了一种评分系统(CANUKA),它在预测患者结局方面与 GBS 具有相似的性能,并且更能准确识别低风险不良结局的患者。

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