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The impact on therapeutic approach after coronary computed tomography in a heart transplant patient population
Session:
Comunicações Orais - Sessão 14 - Transplante cardíaco
Speaker:
Ana Amador
Congress:
CPC 2023
Topic:
H. Interventional Cardiology and Cardiovascular Surgery
Theme:
26. Cardiovascular Surgery
Subtheme:
26.8 Cardiovascular Surgery - Transplantation
Session Type:
Comunicações Orais
FP Number:
---
Authors:
Ana Amador; João Calvão; Catarina Martins da Costa; André Cabrita; Catarina Marques; Ana Pinho; Luís Santos; Cátia Oliveira; Mariana Vasconcelos; Sandra Amorim; Filipe Macedo
Abstract
<p style="text-align:justify"><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Background.</span></span></strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif"> Although coronary angiography (CA) remains the goldstandard for coronary allograft vasculopathy (CAV) screening, coronary computed tomography (CCT) has been used as non-invasive alternative. There is sparse data regarding how the CCT findings impact subsequent medical approach.</span></span></span></span></p> <p style="text-align:justify"><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Methods.</span></span></strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif"> From January 2021 to April 2022, we prospectively included heart transplant (HT) recipients who performed CCT for CAV detection at a university hospital centre. Clinical, CCT and CA data were collected. </span></span></span></span></p> <p style="text-align:justify"><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Results.</span></span></strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif"> We included 38 patients (pts), 23 (60.5%) men with mean age of 58±14 years. The main cause of transplantation was familial dilated cardiomyopathy (42.1%), followed by ischemic cardiopathy (31.6%). Median graft duration was 10 years (IQR 9) and 65.8% had previous rejection. At CCT time, 97.4% of pts had LEVF ≥60%, 89.5% pts had ≥1 cardiovascular risk factor (CVRF), 18.4% had peripheral arterial or cerebrovascular disease (PA/CVD), 94.7% pts took anti-thrombotics (86,8% anti-platelets and 7.9% anticoagulants) and all took anti-lipids (71.0% statins, 5.3% ezetimib, 26.7% both). </span></span></span></span></p> <p style="text-align:justify"><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Median calcium score was 17 (IQR 231) and 32 pts completed CCT: 7, 24 and 1 patients had ISHLT-CAV classification of 0, 1 and 2, respectively. Most patients (37.5%) had both calcified and hypodense plaques and median number of affected segments was 2 (IQR 3). </span></span></span></span></p> <p><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">The remained 6 pts had extensive coronary calcification and a CA was performed: 3, 1 and 2 had ISHLT-CAV classification of 1, 2 and 3, respectively. Four (10.5%) pts needed additional ischemia testing: the one with CAV3 and both the pts with CAV2; also one pt with CAV1 but suboptimal quality of CCT images. </span></span></span></span></p> <p><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">CCT also detected cardiac thrombus and pulmonary nodules in 2 and 4 pts, respectively. </span></span></span></span></p> <p><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Findings in CCT lead to therapeutic changes in 10 (26.3%) pts – all had changes in anti-lipids. One pt also changed anti-thrombotics and anti-hypertensive (aspirin to warfine due to cardiac thrombus and titulation of amlodipine) and other pt with CAV1 with hypondense plaques and 21 years of graft switched immunosuppressant to everolimus. Therapeutic changes were associated with diabetes after HT (p=0,043), but there were no significant associations with other CVRF, sex, age, previous PA/CVD, ischemic etiology, graft duration, plaque characteristics, calcium score, CAV classification nor previous rejection. However, our small sample size may not have the power to expose such associations.</span></span></span></span></p> <p><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">During the mean follow up of 12,2±4,2 months, there were no deaths, PCI, ACS, ventricular arrythimias or stroke. 3 pts had de novo rejection (1 humoral, 1 celular and 1 both) – the last one, evolved from CAV1 to CAV3 and was submitted to a new heart transplant. </span></span></span></span></p> <p><span style="font-size:12pt"><span style="font-family:"Times New Roman",serif"><strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Conclusions: </span></span></strong><span style="font-size:11.0pt"><span style="font-family:"Calibri",sans-serif">Therapeutic changes (mainly anti-lipids) occurred in about 25% of pts after CCT, and were only associated with diabetes after HT. More studies are needed to access how CCT may guide therapy according to plaque burden. </span></span></span></span></p>
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