|
1. |
Premature Closure of the Foramen Ovale and Ductus Arteriosus in a Fetus With Transposition of the Great Arteries |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 65-66
Mary Donofrio,
Preview
|
PDF (653KB)
|
|
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
2. |
CirculationElectronic PagesMarch 19, 2002 |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1269-1269
James Willerson,
Preview
|
PDF (173KB)
|
|
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
3. |
Oral Anticoagulation for Acute Coronary Syndromes |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1270-1274
Marc Brouwer,
Freek Verheugt,
Preview
|
PDF (936KB)
|
|
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
4. |
Successful Treatment of Amiodarone-Induced Thyrotoxicosis |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1275-1277
Faizel Osman,
Jayne Franklyn,
Michael Sheppard,
Michael Gammage,
Preview
|
PDF (545KB)
|
|
摘要:
Background—Amiodarone-induced thyrotoxicosis (AIT) is a difficult management problem about which there are little published data. We examined whether continuing amiodarone or differentiating AIT into 2 subtypes affected outcome.Methods and Results—The type and duration of antithyroid treatment and response were recorded in a consecutive series of 28 cases. Comparisons were made between those in whom amiodarone either was continued or stopped and between those with either possible type 1 or type 2 AIT. Of the 28 cases, 5 had spontaneous resolution of AIT; 23 received carbimazole (CBZ) alone as first-line therapy. Eleven achieved long-term euthyroidism off CBZ or on a maintenance dose. Five became hypothyroid and required long-term thyroxine. Five relapsed after stopping CBZ treatment and were rendered euthyroid with either long-term CBZ (n=3) or radioiodine (n=2). Four were intolerant of CBZ and received propylthiouracil (PTU), with good effect in 3. One was resistant to thionamide alone (CBZ then PTU) and responded to adjunctive steroids. No difference in presentation or outcome was noted between those in whom amiodarone was continued or stopped or between possible type 1 or type 2 AIT.Conclusions—Continuing amiodarone has no adverse influence on response to treatment of AIT. First-line therapy with a thionamide alone is appropriate in iodine-replete areas, thus avoiding potential complications of other drugs. Differentiating between 2 possible types of AIT does not influence management or outcome.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
5. |
Local Expression of Interleukin-1 Receptor Antagonist by Plasmid DNA Improves Mortality and Decreases Myocardial Inflammation in Experimental Coxsackieviral Myocarditis |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1278-1281
Byung-Kwan Lim,
Seong-Choon Choe,
Jae-Ok Shin,
Seong-Hyun Ho,
Jong-Mook Kim,
Seung-Shin Yu,
Sunyoung Kim,
Eun-Seok Jeon,
Preview
|
PDF (1297KB)
|
|
摘要:
Background—The inflammatory cytokines have an important role in the pathogenesis of viral myocarditis. Inerleukin-1 (IL-1) is one of the major cytokines that modulate the outcome of viral infection. Among the methods for in vivo gene transfer, direct injection of plasmid DNA is one that is simple and feasible. In this study, we expressed human IL-1 receptor antagonist (hIL-1Ra) in the mouse heart by direct injection of a novel plasmid vector and evaluated its effects on coxsackieviral (CVB3) myocarditis.Methods and Results—A plasmid vector expressing hIL-1Ra (total 40 &mgr;g/mouse) was injected into the heart apex of 8-week-old inbred female Balb/C mice (day 3). On day 0, mice (IL-1Ra-CVB3, n=35) were infected intraperitoneally with 104PFU of CVB3; control mice (pCK-CVB3, n=15) were injected with empty vector on day −3 and infected on day 0. hIL-1Ra was expressed in the heart, reached its peak on day 5, and persisted for 2 weeks. The 14-day survival rate of IL-1Ra-CVB3 was higher (77%) than that of controls (30%,P<0.01). Myocardial virus titers on day 3 were lower in IL-1Ra-CVB3 mice. Myocardial inflammation on day 7 and fibrosis on day 14 were markedly decreased in IL-1Ra-CVB3.Conclusion—These results showed that direct injection of the expression plasmid vector into the heart was an effective method to transfer the cytokine gene in vivo, and expressed IL-1Ra in the heart can modulate the deleterious effect of the host immune response in viral myocarditis.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
6. |
Catheter-Based Endomyocardial Injection With Real-Time Magnetic Resonance Imaging |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1282-1284
Robert Lederman,
Michael Guttman,
Dana Peters,
Richard Thompson,
Jonathan Sorger,
Alexander Dick,
Venkatesh Raman,
Elliot McVeigh,
Preview
|
PDF (605KB)
|
|
摘要:
Background—We tested the feasibility of targeted left ventricular (LV) mural injection using real-time MRI (rtMRI).Methods and Results—A 1.5T MRI scanner was customized with a fast reconstruction engine, transfemoral guiding catheter–receiver coil (GCC), MRI-compatible needle, and tableside consoles. Commercial real-time imaging software was customized to facilitate catheter navigation and visualization of injections at 4 completely refreshed frames per second. The aorta was traversed and the left ventricular cavity was entered under direct rtMRI guidance. Pigs underwent multiple injections with dilute gadolinium-DTPA. All myocardial segments were readily accessed. The active GCC and the passive Stiletto needle injector were readily visualized. More than 50 endomyocardial injections were performed with the aid of rtMRI; 81% were successful with this first-generation prototype.Conclusion—Percutaneous endomyocardial drug delivery is feasible with the aid of rtMRI, which permits precise 3-dimensional localization of injection within the LV wall.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
7. |
Randomized Trial of a Distal Embolic Protection Device During Percutaneous Intervention of Saphenous Vein Aorto-Coronary Bypass Grafts |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1285-1290
Donald Baim,
Dennis Wahr,
Barry George,
Martin Leon,
Joel Greenberg,
Donald Cutlip,
Unsal Kaya,
Jeffrey Popma,
Kalon Ho,
Richard Kuntz,
Preview
|
PDF (1406KB)
|
|
摘要:
Background—Stents provide effective treatment for stenotic saphenous venous aorto-coronary bypass grafts, but their placement carries a 20% incidence of procedure-related complications, which potentially are related to the distal embolization of atherosclerotic debris. We report the first multicenter randomized trial to evaluate use of a distal embolic protection device during stenting of such lesions.Methods and Results—Of 801 eligible patients, 406 were randomly assigned to stent placement over the shaft of the distal protection device, and 395 were assigned to stent placement over a conventional 0.014-inch angioplasty guidewire (control group). The primary end point—a composite of death, myocardial infarction, emergency bypass, or target lesion revascularization by 30 days—was observed in 65 patients (16.5%) assigned to the control group and 39 patients (9.6%) assigned to the embolic protection device (P=0.004). This 42% relative reduction in major adverse cardiac events was driven by myocardial infarction (8.6% versus 14.7%,P=0.008) and “no-reflow” phenomenon (3% versus 9%,P=0.02). Clinical benefit was seen even when platelet glycoprotein IIb/IIIa receptor blockers were administered (61% of patients), with composite end points occurring in 10.7% of protection device patients versus 19.4% of control patients (P=0.008).Conclusions—Use of this distal protection device during stenting of stenotic venous grafts was associated with a highly significant reduction in major adverse events compared with stenting over a conventional angioplasty guidewire. This demonstrates the importance of distal embolization in causing major adverse cardiac events and the value of embolic protection devices in preventing such complications.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
8. |
Angiogenic Gene Therapy (AGENT) Trial in Patients With Stable Angina Pectoris |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1291-1297
Cindy Grines,
Matthew Watkins,
Greg Helmer,
William Penny,
Jeffrey Brinker,
Jonathan Marmur,
Andrew West,
Jeffery Rade,
Pran Marrott,
H. Hammond,
Robert Engler,
Preview
|
PDF (1276KB)
|
|
摘要:
Background—The angiogenic response to myocardial ischemia can be augmented in animal models by gene transfer with the use of a replication defective adenovirus (Ad) containing a human fibroblast growth factor (FGF) gene.Methods and Results—The objectives of the Angiogenic GENe Therapy (AGENT) trial were to evaluate the safety and anti-ischemic effects of 5 ascending doses of Ad5-FGF4 in patients with angina and to select potentially safe and effective doses for subsequent study. Seventy-nine patients with chronic stable angina Canadian Cardiovascular Society class 2 or 3 underwent double-blind randomization (1:3) to placebo (n=19) or Ad5-FGF4 (n=60). Safety evaluations were performed at each visit and exercise treadmill testing (ETT) at baseline and at 4 and 12 weeks. Single intracoronary administration of Ad5-FGF4 seemed to be safe and well tolerated with no immediate adverse events. Fever of <1-day duration occurred in 3 patients in the highest-dose group. Transient, asymptomatic elevations in liver enzymes occurred in 2 patients in lower-dose groups. Serious adverse events during follow-up (mean, 311 days) were not different between placebo and Ad5-FGF4. Overall, patients who received Ad5-FGF4 tended to have greater improvements in exercise time at 4 weeks (1.3 versus 0.7 minutes,P=NS, n=79). A protocol-specified, subgroup analysis showed the greatest improvement in patients with baseline ETT ≤10 minutes (1.6 versus 0.6 minutes,P=0.01, n=50).Conclusions—Results show evidence of favorable anti-ischemic effects with Ad5-FGF4 compared with placebo, and it appears to be safe. Angiogenic gene transfer with Ad5-FGF4 shows promise as a new therapeutic approach to the treatment of angina pectoris.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
9. |
Effect of Azithromycin Treatment on Endothelial Function in Patients With Coronary Artery Disease and Evidence ofChlamydia pneumoniaeInfection |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1298-1303
Nikhil Parchure,
Emmanouil Zouridakis,
Juan Kaski,
Preview
|
PDF (1098KB)
|
|
摘要:
Background—It has been suggested that infection withChlamydia pneumoniae(CPn) can trigger inflammatory mechanisms that may in turn impair vascular endothelial function. The aim of the present study was to assess whether treatment with the macrolide antibiotic azithromycin improves endothelial function in patients with coronary artery disease and antibodies positive toCPn.Methods and Results—We carried out a randomized, prospective, double-blind, placebo-controlled trial in 40 male patients (mean age, 55±9 years) with documented coronary artery disease and positiveCPn-IgG antibody titers. After baseline evaluation, patients were randomized to receive either azithromycin or placebo for 5 weeks. Flow-mediated dilation (FMD) of the brachial artery and E-selectin, von Willebrand factor, and C-reactive protein (CRP) levels were assessed at study entry and at the end of the treatment period. Our results showed that patients who received azithromycin had a significant improvement in FMD (mean change, 2.1±1.1%;P<0.005). In contrast, FMD was not significantly changed in the placebo group (mean change, −0.02±0.2%,P=0.64). Azithromycin therapy also resulted in a significant decrease of E-selectin and von Willebrand factor levels. CRP levels were not significantly altered by treatment with either azithromycin or placebo. Beneficial effects of azithromycin treatment were independent from the presence of low (<1:32) or high (≥1:32)CPnantibody titers.Conclusions—Our findings indicate that treatment with azithromycin has a favorable effect on endothelial function in patients with documented coronary artery disease and evidence ofCPninfection irrespective of antibody titer levels. Whether these favorable actions of antibiotic treatment will translate into a beneficial effect on atherogenesis and cardiac events needs further investigation.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
10. |
Effects of Long-Term Biventricular Stimulation for Resynchronization on Echocardiographic Measures of Remodeling |
|
Circulation: Journal of the American Heart Association,
Volume 105,
Issue 11,
2002,
Page 1304-1310
Leslie Saxon,
Teresa De Marco,
Jill Schafer,
Kanu Chatterjee,
Uday Kumar,
Elyse Foster,
Preview
|
PDF (1285KB)
|
|
摘要:
Background—Long-term ventricular resynchronization therapy improves symptom status. Changes in left ventricular remodeling have not been adequately evaluated.Methods and Results—Fifty-three patients with systolic heart failure and bundle-branch block underwent implantation of biventricular stimulation (BVS) devices as part of a randomized trial. Echocardiograms were acquired at randomization and at 6-week intervals until completion of 12 weeks of continuous BVS. There were no changes in heart rate or QRS duration after 12 weeks of BVS. Serum norepinephrine values did not change with BVS. After 12 weeks of BVS, left atrial volume decreased. Left ventricular end-systolic and end-diastolic dimensions and left ventricular end-systolic volume also decreased after 12 weeks of BVS. Sphericity index did not change. Measures of systolic function, including left ventricular outflow tract and aortic velocity time integral and myocardial performance index, improved.Conclusions—Long-term resynchronization therapy results in atrial and ventricular reverse remodeling and improved hemodynamics.
ISSN:0009-7322
出版商:OVID
年代:2002
数据来源: OVID
|
|