The 30-Year Outcome for Patients After Myocardial Infarction Due to Coronary Artery Lesions Caused By Kawasaki Disease

2010 ◽  
Vol 32 (2) ◽  
pp. 176-182 ◽  
Author(s):  
Etsuko Tsuda ◽  
Takuya Hirata ◽  
Osamu Matsuo ◽  
Tadaaki Abe ◽  
Hisashi Sugiyama ◽  
...  
Circulation ◽  
2015 ◽  
Vol 131 (suppl_2) ◽  
Author(s):  
Masanori Abe ◽  
Makoto Watanabe ◽  
Ryuji Fukazawa ◽  
Shunichi Ogawa

Introduction: An important complication of Kawasaki disease (KD) is myocardial ischemia and acute myocardial infarction which occurs by thrombosis in coronary aneurysms and severe stenosis. The most characteristic features of coronary artery lesions (CALs) are dilation or aneurysm in acute stage and stenosis after convalescence stage. As these lesions exist singly or multiply in one coronary branch or multiple branches, coronary hemodynamics can be complicated. Ordinal methods have less potential for detection of these diseased states. Recently, Fusion imaging from coronary CT angiography (CTA) /SPECT has been thought good method for evaluation of location and severity of myocardial damages in adults. Therefore, we evaluate CALs, ischemia, and infarction after KD by Fusion imaging. Patients and Method: Seventeen patients (16 males and 1 female, age10 to 34 y) were subject. Eight patients had coronary artery bypass grafting (CABG). These tests were performed 8 to 30 years after onset of KD. CTA are performed by 64-slice-CT (LightSpeed VCT:GE Healthcare) ,and SPECT (Infinia:GE) by Tc-tetrofosmin was performed at rest and at stress after infusing adenosine. CTA and SPECT images were fused by the software (CardIQ Fusion:GE). Results and findings: In all cases, we had enough good images to detect the location of CALs and the area of ischemia. 1) Fusion images showed that no patient had significant stenotic findings at the anastomosis of bypass-graft at least several years after CABG. 2) Coronary native small branches arose from giant aneurysm were occluded by thrombosis and sub-aneurysmal lesions were infracted which were not detected by ordinal method. 3) Minimum sized myocardial ischemic lesions along to the normal visual epicardial coronary artery were detected and were suspected the existence of abnormal micro-coronary circulation caused by fibrous plaque or micro-thrombosis. 4) Collateral arteries at the stenotic and/or occluded lesions with or without ischemia were clearly detected by Fusion method. conclusion: Fusion images can visualize morphologically and functionally complicated CALs, myocardial ischemia ,and myocardial infarction after KD. Also, we can realize that peripheral coronary vessels are damaged with myocardial ischemia.


2003 ◽  
Vol 53 (1) ◽  
pp. 178-178
Author(s):  
Yasuhiko Mori ◽  
Hiroshi Katayama ◽  
Tatsuo Shimizu ◽  
Toshio Shimizu ◽  
Kenichi Okumura ◽  
...  

2019 ◽  
Vol 34 (10) ◽  
pp. 1571-1579
Author(s):  
Wataru Tamaki ◽  
Etsuko Tsuda ◽  
Syuji Hashimoto ◽  
Tamami Toyomasa ◽  
Mikiya Fujieda

2021 ◽  
Vol 13 (1) ◽  
pp. 12
Author(s):  
A. Boutaleb ◽  
D. Hamraoui ◽  
K. Bouayed

Author(s):  
Maoling Yang ◽  
Qiongfei Pei ◽  
Jing Zhang ◽  
Haobo Weng ◽  
Fengchuan Jing ◽  
...  

Author(s):  
Hongying Shi ◽  
Fengfeng Weng ◽  
Chen Li ◽  
Zengyou Jin ◽  
Junyong Hu ◽  
...  

2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
K.M.Z Mohd Saad Jalaluddin

Abstract Background Drug-coated balloon has been widely used to treat In-Stent Restenosis as recommended by ESC/EACT coronary intervention guideline. However, trials of effectiveness of DCB in treating de novo lesions in diabetic patients are limited. This study will highlight the impact of DCB in diabetic patients with only de novo lesions against non-diabetic patients. Aim To compare the outcomes of Paclitaxel Drug Coated Balloon (DCB) in Diabetic and non-diabetic patients with only de novo coronary artery disease. Methods A retrospective, single center study was conducted from January 2016 till December 2018. All diabetic and non-diabetic patients underwent angioplasty to only de novo coronary artery lesions were included in the study. Patients' baseline characteristic, angiographic data, post procedural and 12 months follow-up outcomes including major adverse coronary artery event (MACE), target lesion revascularization (TLR) and myocardial infarction (MI) are compared. Results A total of 1257 patients (726 diabetic and 531 non-diabetic patients) with total 1385 de novo coronary artery lesions (791 lesions in diabetic group and 594 lesions in non-diabetic group) were included in this study. Mean age for non-diabetic group was 57.6±10.6 years and diabetic group was 59.6±9.6 years with male predominance (91.1% in non-diabetic group, n=484 and 79.2% in diabetic group, n=575). Majority of diabetic group has hypertension (83.7%, n=608 vs 58.6%, n+311), chronic renal failure (10.3%, n=75 vs 1.9%, n=10), documented coronary artery disease (55.6%, n=404 vs 47.5%, n=252) and previous coronary angioplasty 39.5%, n=287 vs 28.8%, n=153). Adequate pre-dilatation was done in both groups (98.5%, n=585 in non-diabetic group and 99.4%, n=786 in diabetic group; p=0.000). Mean DCB diameter and length were almost similar in both groups. Mean residual stenosis after DCB was 11.15±16.9% in non-diabetic group and 13.13±13.4% in the diabetic group (p=0.008). 74.6% of non-diabetic group (n=396) and 77.1% of diabetic group (n=560) were on double antiplatelet therapy for 12 months. 86.8% (n=461) of non-diabetic and 88.4% (n=642) of diabetic patients were available for follow up. MACE events were significantly higher (p=0.000) in diabetic group (4.3%, n=31) as compare to non-diabetic group (0.6%, n=3). Target lesion revascularization (TLR) and myocardial infarction (MI) was also significantly higher in diabetic group (TLR 1.4%, N=10 vs 0.6%, n=3, p=0.049; MI 2.6%, n=19 vs 0.4%, n=2, p=0.002). Conclusion Treating de novo coronary lesions in diabetic patients with DCB associated with significantly higher MACE events, target lesion revascularization and myocardial infarction. Diabetic patients appear to have a greater volume of atherosclerotic plaque and increased propensity for atherosclerotic plaque rupture. Funding Acknowledgement Type of funding source: None


1996 ◽  
Vol 39 (3) ◽  
pp. 534-535 ◽  
Author(s):  
Shoko Kanekura ◽  
Isao Kitajima ◽  
Junichiro Nishi ◽  
Masao Yoshinaga ◽  
Koichiro Miyata ◽  
...  

Rheumatology ◽  
2018 ◽  
Vol 58 (5) ◽  
pp. 770-775 ◽  
Author(s):  
Jong Gyun Ahn ◽  
Yoonsun Bae ◽  
Dongjik Shin ◽  
Jiho Nam ◽  
Kyu Yeun Kim ◽  
...  

Abstract Objectives Kawasaki disease (KD) is an acute systemic vasculitis of unknown aetiology that affects infants and young children. Recent reports of elevated serum high mobility group box 1 (HMGB1) level during the acute phase of KD and its relationship to poor response to IVIG treatment suggest a possible association of HMGB1 polymorphisms with KD. We investigated the association between the polymorphisms of the HMGB1 gene, KD susceptibility, coronary artery lesions, and KD response to IVIG treatment. Methods Whole genome sequencing of the HMGB1 gene was performed to identify causative variants. Two tagging single nucleotide polymorphisms of the HMGB1 gene were selected using linkage disequilibrium analysis. The tagging single nucleotide polymorphisms were genotyped using the TaqMan Allelic Discrimination assay in a total of 468 subjects (265 KD patients and 203 controls). Results The HMGB1 single nucleotide polymorphisms were not associated with KD susceptibility. However, in KD patients, there was a significant association of rs1412125 with coronary artery lesions formation in the recessive model (GG vs AA + GA: odds ratio = 4.98, 95% CI = 1.69–14.66, P = 0.005). In addition, rs1412125 was associated with IVIG resistance in the recessive (GG vs AA + GA: odds ratio = 4.11, 95% CI = 1.38–12.23, P = 0.017) and allelic models (G vs A: odds ratio = 1.80, 95% CI = 1.06–3.06, P = 0.027). Conclusion The rs1412125 in HMGB1 might be a risk factor for the development of coronary artery lesions and IVIG resistance in KD patients.


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