Objectives: To investigate safety and diagnostic value of 1.5-T MRI in carriers of conventional pacemaker (cPM) or conventional implantable defibrillator (cICD). Methods: We prospectively compared cPM/cICD-carriers undergoing MRI (study group, SG), excluding those device-dependent or implanted <6 weeks before enrolment or prior to 01/01/2000, with cPM/cICD-carriers undergoing chest x-ray, CT or follow-up (reference group, RG). Results: 142 MRI (55 cardiac) were performed in 120 patients with cPM (n=71) or cICD (n=71). In the RG 98 measurements were performed in 95 patients with cPM (n=40) or cICD (n=58). No adverse events were observed. No MRI prolonged/interrupted. All cPM/cICD were correctly reprogrammed after MRI without malfunctions. One temporary communication failure was observed in one cPM-carrier. Immediately after MRI, 12/14 device interrogation parameters did not change significantly (clinically negligible changes of battery voltage and cICD charging time), without significant variations for SG versus RG. Three–12 months after MRI, 9/11 device interrogation parameters did not change significantly (clinically negligible changes of battery impedance/voltage). Non-significant changes of three markers of myocardial necrosis. Non-cardiac MRI: 82/87 diagnostic without artefacts; 4/87 diagnostic with artefacts; 1/87 partially diagnostic. Cardiac MRI: in cPM-carriers, 14/15 diagnostic with artefacts, 1/15 partially diagnostic; in cICD-carriers, 9/40 diagnostic with artefacts, 22 partially diagnostic, nine non-diagnostic. Conclusions: A favourable risk-benefit ratio of 1.5-T MRI in cPM/cICD carriers was reported. Key points: • Cooperation between radiologists and cardiac electrophysiologists allowed safe 1.5-T MRI in cPM/cICD-carriers.• No adverse events for 142 MRI in 71 cPM-carriers and 71 cICD-carriers.• Ninety-nine per cent (86/87) of non-cardiac MRI in cPM/cICD-carriers were diagnostic.• All cPM-carrier cardiac MRIs had artefacts, 14 examinations diagnostic, 1 partially diagnostic.• Twenty-three per cent (9/40) of cardiac MRI in cICD-carriers were non-diagnostic.

An eight-year prospective controlled study about the safety and diagnostic value of cardiac and non-cardiac 1.5-T MRI in patients with a conventional pacemaker or a conventional implantable cardioverter defibrillator / P. Lupo, R. Cappato, G. Di Leo, F. Secchi, G.D.E. Papini, S. Foresti, H. Ali, G.M.G. de Ambroggi, A. Sorgente, G. Epicoco, P.M. Cannaò, F. Sardanelli. - In: EUROPEAN RADIOLOGY. - ISSN 0938-7994. - 28:6(2018), pp. 2406-2416. [10.1007/s00330-017-5098-z]

An eight-year prospective controlled study about the safety and diagnostic value of cardiac and non-cardiac 1.5-T MRI in patients with a conventional pacemaker or a conventional implantable cardioverter defibrillator

F. Secchi;G.D.E. Papini;P.M. Cannaò;F. Sardanelli
2018

Abstract

Objectives: To investigate safety and diagnostic value of 1.5-T MRI in carriers of conventional pacemaker (cPM) or conventional implantable defibrillator (cICD). Methods: We prospectively compared cPM/cICD-carriers undergoing MRI (study group, SG), excluding those device-dependent or implanted <6 weeks before enrolment or prior to 01/01/2000, with cPM/cICD-carriers undergoing chest x-ray, CT or follow-up (reference group, RG). Results: 142 MRI (55 cardiac) were performed in 120 patients with cPM (n=71) or cICD (n=71). In the RG 98 measurements were performed in 95 patients with cPM (n=40) or cICD (n=58). No adverse events were observed. No MRI prolonged/interrupted. All cPM/cICD were correctly reprogrammed after MRI without malfunctions. One temporary communication failure was observed in one cPM-carrier. Immediately after MRI, 12/14 device interrogation parameters did not change significantly (clinically negligible changes of battery voltage and cICD charging time), without significant variations for SG versus RG. Three–12 months after MRI, 9/11 device interrogation parameters did not change significantly (clinically negligible changes of battery impedance/voltage). Non-significant changes of three markers of myocardial necrosis. Non-cardiac MRI: 82/87 diagnostic without artefacts; 4/87 diagnostic with artefacts; 1/87 partially diagnostic. Cardiac MRI: in cPM-carriers, 14/15 diagnostic with artefacts, 1/15 partially diagnostic; in cICD-carriers, 9/40 diagnostic with artefacts, 22 partially diagnostic, nine non-diagnostic. Conclusions: A favourable risk-benefit ratio of 1.5-T MRI in cPM/cICD carriers was reported. Key points: • Cooperation between radiologists and cardiac electrophysiologists allowed safe 1.5-T MRI in cPM/cICD-carriers.• No adverse events for 142 MRI in 71 cPM-carriers and 71 cICD-carriers.• Ninety-nine per cent (86/87) of non-cardiac MRI in cPM/cICD-carriers were diagnostic.• All cPM-carrier cardiac MRIs had artefacts, 14 examinations diagnostic, 1 partially diagnostic.• Twenty-three per cent (9/40) of cardiac MRI in cICD-carriers were non-diagnostic.
English
Conventional implantable cardioverter defibrillators; Conventional pacemakers; Image artefacts; Magnetic resonance imaging; Risk-benefit ratio; Radiology, Nuclear Medicine and Imaging
Settore MED/36 - Diagnostica per Immagini e Radioterapia
Articolo
Esperti anonimi
Ricerca applicata
Pubblicazione scientifica
2018
Springer
28
6
2406
2416
11
Pubblicato
Periodico con rilevanza internazionale
scopus
Aderisco
info:eu-repo/semantics/article
An eight-year prospective controlled study about the safety and diagnostic value of cardiac and non-cardiac 1.5-T MRI in patients with a conventional pacemaker or a conventional implantable cardioverter defibrillator / P. Lupo, R. Cappato, G. Di Leo, F. Secchi, G.D.E. Papini, S. Foresti, H. Ali, G.M.G. de Ambroggi, A. Sorgente, G. Epicoco, P.M. Cannaò, F. Sardanelli. - In: EUROPEAN RADIOLOGY. - ISSN 0938-7994. - 28:6(2018), pp. 2406-2416. [10.1007/s00330-017-5098-z]
reserved
Prodotti della ricerca::01 - Articolo su periodico
12
262
Article (author)
no
P. Lupo, R. Cappato, G. Di Leo, F. Secchi, G.D.E. Papini, S. Foresti, H. Ali, G.M.G. de Ambroggi, A. Sorgente, G. Epicoco, P.M. Cannaò, F. Sardanelli...espandi
File in questo prodotto:
File Dimensione Formato  
10.1007_s00330-017-5098-z.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 482.08 kB
Formato Adobe PDF
482.08 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/572280
Citazioni
  • ???jsp.display-item.citation.pmc??? 8
  • Scopus 18
  • ???jsp.display-item.citation.isi??? 15
  • OpenAlex ND
social impact