The role of Point-of-Care Ultrasound of pupil for pupillometry in subarachnoid hemorrhage

iRadiology Pub Date : 2024-01-29 DOI:10.1002/ird3.52
Priyanka Modi, Sanjeev Bhoi, Pallavi Sinha, Savan Pandey
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Neurological examination was limited due to altered sensorium: No neck rigidity; sensory functions, all cranial nerves, and cerebellar signs were not assessed; motor examination: power could not be assessed; B/L upper and lower limbs tone were decreased; B/L upper and lower limbs reflexes were normal; and B/L Plantar flexion were present. Her laboratory parameters were sodium 146.4 mmol/L, potassium 4.53 mmol/L, chloride 119.3 mmol/L, total bilirubin 55.23 μmol/L, creatinine 90.17 μmol/L, urea 8391.61 μmol/L, and INR 1.127.</p><p>A linear probe (frequency of 7–12 MHz) of Point-of-Care Ultrasound (POCUS) systems was utilized for pupillometry. There was anisocoria of 0.7 mm (the size of right and left pupils were 4.2 and 3.5 mm, respectively, Figure 1a,b). The bilateral pupil during direct light stimulation revealed briskly reactive pupils with rebound dilatation (Video 1a,b). 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Some clinicians suggest that infrared pupillary scan findings, such as anisocoria of greater than 3 mm and reduced light reflexes, are predictive of an expanding mass lesion in the brain [<span>1</span>]. However, portable infrared pupillometers are not widely available. On the other hand, POCUS, a simple, objective, and quick imaging tool with an additional advantage of recording, is increasingly available for emergency imaging needs [<span>2</span>].</p><p>The raised intracranial pressure, sequelae of acute nontraumatic SAH, may cause compressive optic neuropathy and papilledema. Complications of compressive optic neuropathy and papilledema can cause relative afferent pupillary defect (RAPD), etc. Also, cerebral vasospasm following acute nontraumatic SAH, a severe complication, occurs in about 75% of patients surviving initial bleeding and leads to delayed cerebral ischemia in 17%–40% of patients. 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引用次数: 0

Abstract

A 60-year-old woman presented to the emergency department, previously diagnosed in other hospital with acute subarachnoid hemorrhage (SAH) involving left proximal Sylvian and anterior interhemispheric sinuses. On presentation, her airway was patent, pulse rate was 86 beats per minute, blood pressure was 112/76 mmHg, respiratory rate was 18 beats per minute, SpO2 was 99% on room air, Glasgow Coma Score was 11 (E3V3M5), and pupils were bilaterally (B/L) mid-dilated, reactive to light, and afebrile to touch. Neurological examination was limited due to altered sensorium: No neck rigidity; sensory functions, all cranial nerves, and cerebellar signs were not assessed; motor examination: power could not be assessed; B/L upper and lower limbs tone were decreased; B/L upper and lower limbs reflexes were normal; and B/L Plantar flexion were present. Her laboratory parameters were sodium 146.4 mmol/L, potassium 4.53 mmol/L, chloride 119.3 mmol/L, total bilirubin 55.23 μmol/L, creatinine 90.17 μmol/L, urea 8391.61 μmol/L, and INR 1.127.

A linear probe (frequency of 7–12 MHz) of Point-of-Care Ultrasound (POCUS) systems was utilized for pupillometry. There was anisocoria of 0.7 mm (the size of right and left pupils were 4.2 and 3.5 mm, respectively, Figure 1a,b). The bilateral pupil during direct light stimulation revealed briskly reactive pupils with rebound dilatation (Video 1a,b). However, the bilateral pupil during consensual light stimulation revealed a normal reactive pupil with no rebound dilatation (Video 1c,d). The patient was managed conservatively and referred to another hospital. She had decompression craniectomy on further deterioration of GCS. She died after 1 month due to infective complications of surgery.

Intracranial pressure can be raised due to any supratentorial mass lesion or head trauma. A common problem in the emergency department is how to decide when operative decompression is urgently required in them. Although computed tomography scans are standard tests for definitive diagnosis of brain stem compression, it is inconvenient to use to monitor for the requirement of surgical intervention. In addition, a more precise assessment of the pupil by manual examination is problematic due to large inter-examiner variability. Hence, there are no specific manual pupillary assessment findings for diagnosing brain stem compression. Some clinicians suggest that infrared pupillary scan findings, such as anisocoria of greater than 3 mm and reduced light reflexes, are predictive of an expanding mass lesion in the brain [1]. However, portable infrared pupillometers are not widely available. On the other hand, POCUS, a simple, objective, and quick imaging tool with an additional advantage of recording, is increasingly available for emergency imaging needs [2].

The raised intracranial pressure, sequelae of acute nontraumatic SAH, may cause compressive optic neuropathy and papilledema. Complications of compressive optic neuropathy and papilledema can cause relative afferent pupillary defect (RAPD), etc. Also, cerebral vasospasm following acute nontraumatic SAH, a severe complication, occurs in about 75% of patients surviving initial bleeding and leads to delayed cerebral ischemia in 17%–40% of patients. Ischemic optic neuropathy (ION), which is the result of vascular insufficiency in the optic nerve, is seen in SAH [3, 4]. An RAPD (with paradoxical pupillary dilatation in response to light) is an important sign of optic nerve disease or injury. If present, it confirms the lesion like ION in the pupil pathway on the afferent side. During POCUS study, this RAPD may be seen as an abnormal direct pupillary light reflex in the form of rebound dilatation or hippus and normal contralateral pupillary light reflex prior to the development of any clinically significant loss of vision. Rebound dilation (previously known as pupillary unrest) is defined as “a period of constriction followed by dilation with a change equal to or greater than 2 mm.” Hippus is defined as a “rhythmic pulsation of the pupils of the eyes, as they dilate and constrict within fixed limits” [5]. However, future studies are required to validate this observation.

Priyanka Modi analyzed the data and prepared the first draft of the manuscript. Priyanka Modi, Sanjeev Bhoi, Pallavi Sinha, and Savan Pandey participated in the conception and design of the study; Priyanka Modi constructively revised the manuscript, participated in data collection and organization, participated in and supervised the study throughout. All authors commented on previous versions of the manuscript and approved the final version.

The authors declare no conflicts of interest.

Not applicable.

The patient provided written informed consent at the time of entering this study.

Abstract Image

在蛛网膜下腔出血中利用瞳孔定点超声波测量瞳孔的作用
急诊科接诊了一名60岁的女性患者,她之前在其他医院被诊断为急性蛛网膜下腔出血(SAH),病变累及左侧西尔维安近端和大脑半球窦前部。就诊时,她的呼吸道通畅,脉搏为每分钟86次,血压为112/76 mmHg,呼吸频率为每分钟18次,室内空气中SpO2为99%,格拉斯哥昏迷评分为11(E3V3M5),双侧(B/L)瞳孔中散,对光有反应,触摸无发热。由于感觉改变,神经系统检查受到限制:颈部无僵硬感;未评估感觉功能、所有颅神经和小脑体征;运动检查:无法评估力量;B/L 上肢和下肢张力下降;B/L 上肢和下肢反射正常;B/L 足底屈曲存在。她的化验指标为:钠 146.4 mmol/L、钾 4.53 mmol/L、氯 119.3 mmol/L、总胆红素 55.23 μmol/L、肌酐 90.17 μmol/L、尿素 8391.61 μmol/L、INR 1.127。瞳孔散大0.7毫米(左右瞳孔分别为4.2毫米和3.5毫米,图1a,b)。在直接光刺激时,双侧瞳孔显示为快速反应性瞳孔,并伴有反弹性散大(视频 1a、b)。然而,在双方同意的光刺激下,双侧瞳孔显示为正常反应性瞳孔,无反弹性散大(视频 1c、d)。患者接受了保守治疗,并转诊到另一家医院。由于 GCS 进一步恶化,她接受了减压开颅手术。任何幕上肿块病变或头部外伤都可能导致颅内压升高。急诊科的一个常见问题是如何决定何时急需手术减压。虽然计算机断层扫描是明确诊断脑干受压的标准检测方法,但用于监测是否需要手术干预并不方便。此外,由于检查者之间的差异较大,通过人工检查对瞳孔进行更精确的评估也存在问题。因此,目前还没有诊断脑干受压的特定手动瞳孔评估结果。一些临床医生认为,红外线瞳孔扫描结果,如异位超过3毫米和对光反射减弱,可预测脑部肿块病变的扩大[1]。然而,便携式红外瞳孔仪并不普及。另一方面,POCUS 是一种简单、客观、快速的成像工具,具有记录的额外优势,越来越多地满足急诊成像需求[2]。压迫性视神经病变和乳头水肿的并发症可引起相对传入性瞳孔缺损(RAPD)等。此外,急性非创伤性 SAH 后的脑血管痉挛也是一种严重的并发症,约 75% 的患者在最初出血后存活下来,17%-40% 的患者会导致延迟性脑缺血。缺血性视神经病变(ION)是视神经血管功能不全的结果,也见于 SAH [3,4]。RAPD(瞳孔对光的反应性扩张)是视神经疾病或损伤的一个重要标志。如果出现,则证实传入侧瞳孔通路存在 ION 等病变。在进行 POCUS 检查时,这种 RAPD 可表现为反弹性散大或海马形式的异常直接瞳孔对光反射,而对侧瞳孔对光反射正常,然后才会出现任何临床意义上的视力下降。反跳性扩张(以前称为瞳孔动荡)被定义为 "收缩一段时间,然后扩张,变化等于或大于 2 毫米"。Hippus被定义为 "瞳孔在固定范围内扩张和收缩时的节律性脉动"[5]。然而,还需要今后的研究来验证这一观察结果。普里扬卡-莫迪分析了数据并撰写了手稿初稿。Priyanka Modi、Sanjeev Bhoi、Pallavi Sinha 和 Savan Pandey 参与了研究的构思和设计;Priyanka Modi 对手稿进行了建设性的修改,参与了数据收集和整理,全程参与并指导了研究。所有作者都对手稿的前一版本发表了意见,并批准了最终版本。作者声明没有利益冲突。不适用。患者在参与本研究时提供了书面知情同意书。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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