Abstract

The prognostic value of copeptin in subarachnoid hemorrhage (SAH) has been reported, but the prognosis was largely affected by the initial clinical severity. Thus, the previous studies are not very useful in predicting delayed cerebral ischemia (DCI) in poor-grade SAH patients. Here, we first investigated the feasibility of predicting DCI in poor-grade SAH based on consecutive measurements of plasma copeptin. We measured copeptin levels of 86 patients on days 1, 3, 5, 7, 9, 11, and 13 using ELISA. The primary outcome was the association between consecutive copeptin levels and DCI development. The secondary outcomes were comparison of copeptin with C-reactive protein (CRP) in predicting DCI. Additionally, we compared the prognostic value of transcranial Doppler ultrasonography (TCD) with copeptin using TCD alone to predict DCI. Increased copeptin (OR = 1.022, 95% CI: 1.008–1.037) and modified Fisher scale IV (OR = 2.841; 95% CI: 0.998–8.084) were closely related to DCI. Consecutive plasma copeptin measurements showed significant differences between DCI and non-DCI groups (p < 0.001). Higher CRP and DCI appeared to show a correlation, but it was not statistically significant. Analysis of copeptin changes with TCD appeared to predict DCI better than TCD alone with AUCROC differences of 0.072. Consecutive measurements of plasma copeptin levels facilitate the screening of DCI in poor-grade SAH patients.

Highlights

  • Delayed cerebral ischemia (DCI) is a clinical condition caused by ischemia resulting in secondary or delayed neurological deterioration in patients with aneurysmal subarachnoid hemorrhage (SAH) [1,2]

  • 86 patients were included in the analysis (Figure 1) including 56 patients who underwent simple coiling or stent-assisted coil embolization (SACE) and 30 patients treated with additional external ventricular drainage (EVD) or craniotomy with hematoma removal after coil embolization

  • Copeptin levels were significantly increased in patients with cerebroin the emergency room

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Summary

Introduction

Delayed cerebral ischemia (DCI) is a clinical condition caused by ischemia resulting in secondary or delayed neurological deterioration in patients with aneurysmal subarachnoid hemorrhage (SAH) [1,2]. Compared to good-grade SAH, it is difficult to detect DCI early in patients with poor-grade SAH because they usually receive intubation and mechanical ventilation or therapeutic coma for increased intracranial pressure (IICP) and neurological changes are difficult to diagnose. Transcranial Doppler ultrasonography (TCD) has a high sensitivity of 90% (95% confidence interval [CI]: 77–96%) and a negative predictive value of 92% (95% CI: 83–96%) in detecting DCI due to arterial vasospasm [1]. In addition to TCD, a sensitive and robust plasma marker is necessary to predict DCI early in patients with poor-grade SAH who are at an elevated risk of DCI and poor neurologic outcomes

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