Procalcitonin in the context of delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage

被引:12
|
作者
Veldeman, Michael [1 ]
Lepore, Daniel [2 ,3 ]
Hoellig, Anke [1 ]
Clusmann, Hans [1 ]
Stoppe, Christian [2 ]
Schubert, Gerrit Alexander [1 ]
Albanna, Walid [1 ]
机构
[1] Rhein Westfal TH Aachen, Rhein Westfal Tech Hsch, Dept Neurosurg, Aachen, Germany
[2] Rhein Westfal TH Aachen, Rhein Westfal Tech Hsch, Dept Intens Care & Intermediate Care, Aachen, Germany
[3] Ctr Hosp Univ Liege, Dept Anesthesia & Intens Care Med, Liege, Belgium
关键词
subarachnoid hemorrhage; delayed cerebral ischemia; procalcitonin; cerebral aneurysm; vascular disorders; C-REACTIVE PROTEIN; MULTIDISCIPLINARY CONSENSUS CONFERENCE; SEPSIS; PREDICTOR; EVENT;
D O I
10.3171/2020.5.JNS201337
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE Aneurysmal subarachnoid hemorrhage (aSAH) initiates a deleterious cascade activating multiple inflammatory processes, which can contribute to delayed cerebral ischemia (DCI). Procalcitonin (PCT) is an established marker for sepsis treatment monitoring, and its time course in the context of DCI after aSAH remains unclear. The aim of this trial was to assess the predictive and confirmative value of PCT levels in the context of DCI. METHODS All patients admitted to the authors' institution with aSAH between 2014 and 2018 were prospectively screened for eligibility. Daily PCT levels were recorded alongside relevant aSAH characteristics. The predictive and confirmative values of PCT levels were assessed using a receiver operating characteristic and area under the curve (AUC) analysis. The course of PCT levels around the DCI event was evaluated in an infection-free subgroup of patients. RESULTS A total of 132 patients with aSAH were included. Early PCT levels (first 3 days post-aSAH) had a low predic-tive value for the development of DCI (AUC 0.661, standard error [SE] 0.050; p = 0.003) and unfavorable long-term outcome (i.e., Glasgow Outcome Scale-Extended scores 1-4; AUC 0.674, SE 0.054; p = 0.003). In a subgroup analysis of infection-free patients (n = 72), PCT levels were higher in patients developing DCI (p = 0.001) and DCI-related cerebral infarction (p = 0.002). PCT concentrations increased gradually after DCI and decreased with successful intervention. In refractory cases progressing to cerebral infarction, PCT levels showed a secondary increase. CONCLUSIONS Early higher PCT levels were associated with the later development of DCI and unfavorable outcome. Analysis of PCT beyond the first couple of days after hemorrhage is hampered by nosocomial infections. In infection-free patients, however, PCT levels rise during DCI and an additional increase develops in patients developing cerebral infarction. Clinical trial registration no.: NCT02142166 (clinicaltrials.gov)
引用
收藏
页码:29 / 37
页数:9
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