Loewy John, Loewy Amanda, Kendall Edward J
Department of Medical Imaging, Humber River Regional Hospital, 2115 Finch Ave W, Toronto, ON, Canada M3N 1N1.
Radiographics. 2004 Sep-Oct;24(5):1257-67; discussion 1267-8. doi: 10.1148/rg.245045014.
The presence of an implanted pacemaker is widely regarded as an absolute contraindication to magnetic resonance (MR) imaging; however, this viewpoint is based largely on safety concerns in the 1982-1996 period. Since 1996, changes in pacemaker electronics including decreased ferromagnetic content, increased sophistication of the circuitry, and onboard computer capabilities suggest that the absolute contraindication of MR imaging for pacemaker patients should be reconsidered. In addition, there are now data from prospective trials of 232 patients with demand pacemakers who underwent MR imaging at 0.5-1.5 T. Although a variety of pacemaker parameters were evaluated before, during, immediately after, and 3 months after MR imaging, no significant pacemaker changes were identified. No patients reported abnormal sensations such as pacemaker movement or irregular heartbeats even at direct questioning. These results suggest that peripheral locations such as the brain and knee may be considered for MR imaging. Thus, pacemaker patients should be assessed individually for their suitability for MR imaging, which may be performed safely under defined conditions.
植入式起搏器的存在被广泛视为磁共振(MR)成像的绝对禁忌症;然而,这一观点很大程度上基于1982年至1996年期间的安全担忧。自1996年以来,起搏器电子元件的变化包括铁磁性含量降低、电路复杂性增加以及机载计算机功能增强,这表明对于起搏器患者,磁共振成像的绝对禁忌症应重新考虑。此外,现在有来自232名按需起搏器患者的前瞻性试验数据,这些患者在0.5 - 1.5T的磁场下接受了磁共振成像。尽管在磁共振成像前、成像期间、成像后立即以及成像后3个月对各种起搏器参数进行了评估,但未发现起搏器有显著变化。即使直接询问,也没有患者报告有诸如起搏器移动或心跳不规则等异常感觉。这些结果表明,大脑和膝盖等外周部位可考虑进行磁共振成像。因此,对于起搏器患者是否适合进行磁共振成像应进行个体评估,在特定条件下可以安全地进行磁共振成像检查。