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有磁共振条件性起搏器和植入式心脏复律除颤器系统的患者行磁共振检查的途径:真 PROMRI 研究结果。

Access to magnetic resonance imaging of patients with magnetic resonance-conditional pacemaker and implantable cardioverter-defibrillator systems: results from the Really ProMRI study.

机构信息

Fondazione Cardimed and C.D.C. I.O.S. MF Group, Pomigliano d'Arco.

Ospedale E.E. Miulli - Acquaviva delle Fonti, Bari.

出版信息

Europace. 2018 Jun 1;20(6):1001-1009. doi: 10.1093/europace/eux118.

DOI:10.1093/europace/eux118
PMID:29016759
Abstract

AIMS

The Really ProMRI study evaluates magnetic resonance imaging (MRI) access for patients with cardiac implantable electronic devices (CIEDs) as well as the performance of magnetic resonance (MR)-conditional leads when undergoing MRI.

METHODS AND RESULTS

Patients either with an MR-conditional pacemaker or implantable defibrillator (ICD) system or with at least a component (device or one or more leads) from an MR-conditional system, were asked to fill in a questionnaire when they were referred to a MR scan. The rate of prescription, denial, or execution of MR examinations was evaluated in a 1-year follow-up visit. In total, 555 patients [median age (interquartile range) 72.2 (62.2-78.6); 72% male] were enrolled, 49% (270) with a pacemaker, 51% (285) with an ICD system. Five-hundred and ten patients completed the follow-up period. A total of 37 MRI referrals were reported in 35 patients, with a consequent event rate of 7.0/100 patient-years (CI, 4.9-9.7). Fourteen were denied, while 23 [66%; (CI, 48-81%)] were performed. The number of patients with MR referrals was not statistically different between pacemaker and ICD groups (21 vs. 14; P = 0.178). The rate of scans performed was higher in the pacemaker subjects (19/23 vs. 4/14, P = 0.003), while it was similar between patients with or without a complete MR-conditional system (19/30 vs. 4/7, P = 0.606).

CONCLUSION

In this study, we reported a 7.0/100 patient-year's event rate of MR prescriptions in CIED patients. Many examinations were denied, despite MR-conditional systems, especially in ICD patients. Regulatory and cultural changes are needed to allow wider access to MR imaging in CIED patients with MR-conditional systems.

摘要

目的

Really ProMRI 研究评估了心脏植入式电子设备 (CIED) 患者的磁共振成像 (MRI) 检查,并评估了 MRI 检查中具有磁共振兼容性的导线的性能。

方法和结果

当被转诊进行 MRI 检查时,患者要么有一个具有磁共振兼容性的起搏器或植入式除颤器 (ICD) 系统,要么至少有一个具有磁共振兼容性系统的部件(设备或一个或多个导线),被要求填写一份问卷。在为期 1 年的随访中,评估了处方、拒绝或执行 MRI 检查的比例。共有 555 名患者(中位数年龄[四分位数间距]72.2[62.2-78.6];72%为男性)入组,49%(270 名)为起搏器患者,51%(285 名)为 ICD 系统患者。510 名患者完成了随访期。共有 35 名患者报告了 37 次 MRI 转诊,因此发生率为 7.0/100 患者年(CI,4.9-9.7)。有 14 次被拒绝,而有 23 次(66%[CI,48-81%])进行了检查。起搏器组和 ICD 组的 MRI 转诊患者数量无统计学差异(21 名与 14 名;P=0.178)。在起搏器患者中,进行扫描的比例更高(19/23 与 4/14,P=0.003),而在具有或不具有完整磁共振兼容性系统的患者中,扫描比例相似(19/30 与 4/7,P=0.606)。

结论

在这项研究中,我们报告了 CIED 患者进行 MRI 检查的 7.0/100 患者年事件发生率。尽管具有磁共振兼容性系统,但仍有许多检查被拒绝,尤其是在 ICD 患者中。需要进行监管和文化变革,以允许具有磁共振兼容性系统的 CIED 患者更广泛地接受磁共振成像检查。

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