Department of Neurology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
Department of Neurology, Maasstad Hospital, Rotterdam, the Netherlands.
Ann Neurol. 2022 Apr;91(4):521-531. doi: 10.1002/ana.26312. Epub 2022 Feb 21.
This study aimed to validate the Erasmus Guillain-Barré Syndrome Respiratory Insufficiency Score in the International Guillain-Barré Syndrome Outcome Study cohort, and to improve its performance and region-specificity.
We examined data from the first 1,500 included patients, aged ≥6 years and not ventilated prior to study entry. Patients with a clinical variant or mild symptoms were also included. Outcome was mechanical ventilation within the first week from study entry. Model performance was assessed regarding the discriminative ability (area under the receiver operating characteristic curve) and the calibration (observed vs predicted probability of mechanical ventilation), in the full cohort and in Europe/North America and Asia separately. We recalibrated the model to improve its performance and region-specificity.
In the group of 1,023 eligible patients (Europe/North America n = 842, Asia n = 104, other n = 77), 104 (10%) required mechanical ventilation within the first week from study entry. Area under the curve values were ≥0.80 for all validation subgroups. Mean observed proportions of mechanical ventilation were lower than predicted risks: full cohort 10% versus 21%, Europe/North America 9% versus 21%, and Asia 17% versus 23%. After recalibration, predicted risks for the full cohort and Europe/North America corresponded to observed proportions.
This prospective, international cohort study validated the Erasmus Guillain-Barré Syndrome Respiratory Insufficiency Score, and showed that the model can be used in the full spectrum of Guillain-Barré syndrome patients. In addition, a more accurate, region-specific version of the model was developed for patients from Europe/North America. ANN NEUROL 2022;91:521-531.
本研究旨在验证 Erasmus Guillain-Barré 综合征呼吸衰竭评分在国际 Guillain-Barré 综合征结局研究队列中的有效性,并提高其性能和地区特异性。
我们对前 1500 名纳入患者的数据进行了检查,这些患者年龄≥6 岁,且在研究入组前未进行机械通气。还纳入了具有临床变异或轻度症状的患者。结局为研究入组后第一周内进行机械通气。在整个队列以及欧洲/北美和亚洲分别评估模型的性能,包括区分能力(接受者操作特征曲线下面积)和校准(机械通气的观察概率与预测概率)。我们对模型进行了重新校准,以提高其性能和地区特异性。
在 1023 名符合条件的患者(欧洲/北美 n=842,亚洲 n=104,其他 n=77)中,104 名(10%)在研究入组后第一周内需要机械通气。所有验证亚组的曲线下面积值均≥0.80。观察到的机械通气比例平均值低于预测风险:整个队列 10%比 21%,欧洲/北美 9%比 21%,亚洲 17%比 23%。重新校准后,整个队列和欧洲/北美地区的预测风险与观察到的比例相对应。
这项前瞻性的国际队列研究验证了 Erasmus Guillain-Barré 综合征呼吸衰竭评分,表明该模型可用于 Guillain-Barré 综合征患者的全谱。此外,为欧洲/北美地区的患者开发了一种更准确、具有地区特异性的模型版本。