McCollough Cynthia H, Zhang Jie, Primak Andrew N, Clement Wesley J, Buysman John R
Department of Radiology, Mayo Clinic College of Medicine, 200 First St SW, Rochester, MN 55905, USA.
Radiology. 2007 Jun;243(3):766-74. doi: 10.1148/radiol.2433060993. Epub 2007 Apr 26.
To prospectively measure the response of a variety of models of implantable cardiac rhythm management devices (ICRMDs) to the radiation delivered by computed tomography (CT), for both maximum and typical dose levels.
Twenty-one ICRMDs (13 pacemakers, eight cardioverter-defibrillators) manufactured by Medtronic (Minneapolis, Minn) were exposed to ionizing radiation from CT systems in both spiral and dynamic acquisition modes at maximum and typical dose levels. Devices were monitored during exposure to check for any operational abnormalities and were interrogated after exposure to check for any residual abnormalities. Total radiation dose and peak dose rate were measured, and the volume CT dose index was recorded.
Oversensing was observed in 20 of 21 devices at maximum doses and in 17 of 20 devices at typical doses. Oversensing most often manifested as inhibition, although it occasionally manifested as tracking or safety pacing. Two devices inhibited for more than 4 seconds in spiral mode at clinical dose levels. Oversensing was transient and ceased as soon as the device stopped moving through the x-ray beam or the beam was turned off. The partial electrical reset (PER) safety feature was activated in two models, InSync 8040 and Thera DR. With the exception of PER, programming was not altered. Effects occurred only if the x-ray beam passed directly over the ICRMD.
CT irradiation at typical clinical doses results in oversensing of ICRMDs in the majority of devices tested, although the identified effects were predominantly transient.
前瞻性地测量多种植入式心脏节律管理设备(ICRMD)对计算机断层扫描(CT)所释放辐射的反应,包括最大剂量和典型剂量水平。
由美敦力公司(明尼阿波利斯,明尼苏达州)生产的21台ICRMD(13台起搏器,8台心脏复律除颤器)在螺旋和动态采集模式下,分别以最大剂量和典型剂量暴露于CT系统的电离辐射中。在暴露过程中对设备进行监测,以检查是否有任何操作异常,并在暴露后进行问询,以检查是否有任何残留异常。测量总辐射剂量和峰值剂量率,并记录容积CT剂量指数。
在最大剂量下,21台设备中有20台出现过感知,在典型剂量下,20台设备中有17台出现过感知。过感知最常表现为抑制,尽管偶尔也表现为跟踪或安全起搏。在临床剂量水平下,有两台设备在螺旋模式下抑制超过4秒。过感知是短暂的,一旦设备停止通过X射线束或束流关闭,过感知就会停止。InSync 8040和Thera DR这两种型号激活了部分电复位(PER)安全功能。除PER外,编程未改变。只有当X射线束直接穿过ICRMD时才会产生影响。
在典型临床剂量下进行CT照射,在大多数测试设备中会导致ICRMD出现过感知,尽管所发现的影响主要是短暂的。