Abstract:Background
The objective of this study was to investigate the clinical feasibility of near-infrared spectroscopy (NIRS) for the detection of delayed cerebral ischemia (DCI) in patients with poor-grade subarachnoid hemorrhage (SAH) treated with coil embolization.
Methods
Cerebral regional oxygen saturation (rSO
2
) was continuously monitored via two-channel NIRS for 14 days following SAH. The rSO
2
levels according to… Show more
“…In general, continuous lumbar drainage was maintained until 7 days after the treatment. Nimodipine (Samjin Pharmaceutical, Seoul, South Korea) was administered intravenously at a dose of 20 μg/kg/h to prevent cerebral vasospasm ( Park et al, 2021 ).…”
Section: Methodsmentioning
confidence: 99%
“…The H-H grade was divided into two groups: lower H-H (I, II, and III) and higher H-H group (IV and V), and likewise Fisher grade was divided into a low grade (Fisher grades I and II) and high grade (Fisher grades III and IV) ( Kim et al, 2018 ). Severe cerebral vasospasm was defined as a decrease in vessel diameter of over 70% compared with baseline computed tomography angiography or magnetic resonance angiography ( Park et al, 2021 ). This study was approved by the Institutional Review Boards (IRB No: 2016-31, 2018-6, and 2019-06).…”
BackgroundTo assess the association of haptoglobin (Hp) phenotype with neurological and cognitive outcomes in a large cohort of patients with subarachnoid hemorrhage (SAH).MethodsThis prospective multicenter study enrolled patients with aneurysmal SAH between May 2015 and September 2020. The Hp phenotype was confirmed via Western blots. The relative intensities of α1 in individuals carrying Hp2-1 were compared with those of albumin. Multivariable logistic and Cox proportional-hazard regression analyses were used to identify the risk factors for 6-month and long-term outcomes, respectively.ResultsA total of 336 patients including the phenotypes Hp1-1 (n = 31, 9.2%), Hp2-1 (n = 126, 37.5%), and Hp2-2 (n = 179, 53.3%) were analyzed. The Hp phenotype was closely associated with 6-month outcome (p = 0.001) and cognitive function (p = 0.013), and long-term outcome (p = 0.002) and cognitive function (p < 0.001). Compared with Hp1-1 as the reference value, Hp2-2 significantly increased the risk of 6-month poor outcome (OR: 7.868, 95% CI: 1.764–35.093) and cognitive impairment (OR: 8.056, 95% CI: 1.020–63.616), and long-term poor outcome (HR: 5.802, 95% CI: 1.795–18.754) and cognitive impairment (HR: 7.434, 95% CI: 2.264–24.409). Long-term cognitive impairment based on the Hp phenotype was significantly higher in patients under 65 years of age (p < 0.001) and female gender (p < 0.001). A lower relative α1/albumin intensity (OR: 0.010, 95% CI: 0.000–0.522) was associated with poor outcome at 6 months but not cognitive impairment in patients with SAH expressing Hp2-1.ConclusionHp2-2 increased the risk of poor neurological outcomes and cognitive impairment compared with Hp1-1. For Hp2-1, higher relative α1 intensities were related to 6-month favorable outcomes.
“…In general, continuous lumbar drainage was maintained until 7 days after the treatment. Nimodipine (Samjin Pharmaceutical, Seoul, South Korea) was administered intravenously at a dose of 20 μg/kg/h to prevent cerebral vasospasm ( Park et al, 2021 ).…”
Section: Methodsmentioning
confidence: 99%
“…The H-H grade was divided into two groups: lower H-H (I, II, and III) and higher H-H group (IV and V), and likewise Fisher grade was divided into a low grade (Fisher grades I and II) and high grade (Fisher grades III and IV) ( Kim et al, 2018 ). Severe cerebral vasospasm was defined as a decrease in vessel diameter of over 70% compared with baseline computed tomography angiography or magnetic resonance angiography ( Park et al, 2021 ). This study was approved by the Institutional Review Boards (IRB No: 2016-31, 2018-6, and 2019-06).…”
BackgroundTo assess the association of haptoglobin (Hp) phenotype with neurological and cognitive outcomes in a large cohort of patients with subarachnoid hemorrhage (SAH).MethodsThis prospective multicenter study enrolled patients with aneurysmal SAH between May 2015 and September 2020. The Hp phenotype was confirmed via Western blots. The relative intensities of α1 in individuals carrying Hp2-1 were compared with those of albumin. Multivariable logistic and Cox proportional-hazard regression analyses were used to identify the risk factors for 6-month and long-term outcomes, respectively.ResultsA total of 336 patients including the phenotypes Hp1-1 (n = 31, 9.2%), Hp2-1 (n = 126, 37.5%), and Hp2-2 (n = 179, 53.3%) were analyzed. The Hp phenotype was closely associated with 6-month outcome (p = 0.001) and cognitive function (p = 0.013), and long-term outcome (p = 0.002) and cognitive function (p < 0.001). Compared with Hp1-1 as the reference value, Hp2-2 significantly increased the risk of 6-month poor outcome (OR: 7.868, 95% CI: 1.764–35.093) and cognitive impairment (OR: 8.056, 95% CI: 1.020–63.616), and long-term poor outcome (HR: 5.802, 95% CI: 1.795–18.754) and cognitive impairment (HR: 7.434, 95% CI: 2.264–24.409). Long-term cognitive impairment based on the Hp phenotype was significantly higher in patients under 65 years of age (p < 0.001) and female gender (p < 0.001). A lower relative α1/albumin intensity (OR: 0.010, 95% CI: 0.000–0.522) was associated with poor outcome at 6 months but not cognitive impairment in patients with SAH expressing Hp2-1.ConclusionHp2-2 increased the risk of poor neurological outcomes and cognitive impairment compared with Hp1-1. For Hp2-1, higher relative α1 intensities were related to 6-month favorable outcomes.
“…Although mainly used as an intraoperative monitoring tool in cardiac surgery, near-infrared spectroscopy (NIRS) has gained increasing awareness as a non-invasive modality option within the intensive care unit ( 50 , 51 ). The modality can display regional cerebral oxygen saturation (rSO2) in the frontal lobes and has previously been validated in stroke patients to correlate with cerebral blood flow through perfusion imaging ( 52 ).…”
Aneurysmal subarachnoid hemorrhage is a disease with high mortality and morbidity due in large part to delayed effects of the hemorrhage, including vasospasm, and delayed cerebral ischemia. These two are now recognized as overlapping yet distinct entities, and supportive therapies for delayed cerebral ischemia are predicated on identifying DCI as quickly as possible. The purpose of this overview is to highlight diagnostic tools that are being used in the identification of DCI in the neurocritical care settings.
“…More interestingly, the same 12% cut-off yielded a sensitivity of 94% (95% CI: 73–99%) and a specificity of 71% (95% CI: 53–85%) to detect DCI ( 59 ). Another study on 24 patients presenting with poor grade aSAH reported a sensitivity of 86% (95% CI: 67–98%) and specificity of 86% (95% CI: 67–96%) for DCI detection using a greater than 15% decrease in c-rSO 2 ( 60 ).…”
Delayed cerebral ischemia (DCI) disproportionately affects poor grade aneurysmal subarachnoid hemorrhage (aSAH) patients. An unreliable neurological exam and the lack of appropriate monitoring leads to unrecognized DCI, which in turn is associated with severe long-term deficits and higher mortality. Near Infrared Spectroscopy (NIRS) offers simple, continuous, real time, non-invasive cerebral monitoring. It provides regional cerebral oxygen saturation (c-rSO2), which reflects the balance between cerebral oxygen consumption and supply. Reports have demonstrated a good correlation with other cerebral oxygen and blood flow monitoring, and credible cerebrovascular reactivity indices were also derived from NIRS signals. Multiple critical c-rSO2 values have been reported in aSAH patients, based on various thresholds, duration, variation from baseline or cerebrovascular reactivity indices. Some were associated with vasospasm, some with DCI and others with clinical outcomes. However, the poor grade aSAH population has not been specifically studied and no randomized clinical trial has been published. The available literature does not support a specific NIRS-based intervention threshold to guide diagnostic or treatment in aSAH patients. We review herein the fundamental basic concepts behind NIRS technology, relationship of c-rSO2 to other brain monitoring values and their potential clinical interpretation. We follow with a critical evaluation of the use of NIRS in the aSAH population, more specifically its ability to diagnose vasospasm, to predict DCI and its association to outcome. In summary, NIRS might offer significant potential for poor grade aSAH in the future. However, current evidence does not support its use in clinical decision-making, and proper technology evaluation is required.
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