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1.
Diagn Interv Imaging ; 101(9): 507-517, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32094095

ABSTRACT

Magnetic resonance imaging (MRI) has become the reference imaging for the management of a large number of diseases. The number of MR examinations increases every year, simultaneously with the number of patients receiving a cardiac electronic implantable device (CEID). A CEID was considered an absolute contraindication for MRI for years. The progressive replacement of conventional pacemakers and defibrillators by MR-conditional CEIDs and recent data on the safety of MRI in patients with "MR-nonconditional" CEIDs have progressively increased the demand for MRI in patients with a CEID. However, some risks are associated with MRI in CEID carriers, even with "MR-conditional" devices because these devices are not "MR-safe". A specific programing of the device in "MR-mode" and monitoring patients during MRI remain mandatory for all patients with a CEID. A standardized patient workflow based on an institutional protocol should be established in each institution performing such examinations. This joint position paper of the Working Group of Pacing and Electrophysiology of the French Society of Cardiology and the Société française d'imagerie cardiaque et vasculaire diagnostique et interventionnelle (SFICV) describes the effect and risks associated with MRI in CEID carriers. We propose recommendations for patient workflow and monitoring and CEID programming in MR-conditional, "MR-conditional nonguaranteed" and MR-nonconditional devices.


Subject(s)
Cardiology , Defibrillators, Implantable , Pacemaker, Artificial , Electronics , Humans , Magnetic Resonance Imaging
2.
Ann Cardiol Angeiol (Paris) ; 64(2): 63-7, 2015 Apr.
Article in French | MEDLINE | ID: mdl-25702240

ABSTRACT

UNLABELLED: Clinically discovering a systolic murmur is frequent among the young military population. When this murmur does not sound benign, a transthoracic echocardiography (TTE) is made to detect any cardiopathy, which could cause sudden cardiac death. The aim of this study was to evaluate the interest of systematic TTE in the assessment of any cardiac systolic murmur (CSM) among militaries. METHODS: We ran a retrospective monocentric study in the "Clermont-Tonnerre" military hospital in Brest. We included all patients sent for TEE, aged 15 to 30 years old, from the 1st January 2010 until the 31st July 2013. RESULTS: Two hundred and eighty TTES assessing CSM were performed. We found 28/280 (10%) echocardiographic abnormalities: 13 were bicuspid aortic valves (4.6%), 6 were ventricular septal defects (2.15%), 3 were atrial septal defects (1.07%), 4 were mild mitral regurgitations (1.43%), one mild pulmonary stenosis (0.35%) and one aortic stenosis (0.35%). No hypertrophic cardiomyopathy was found. Concerning military expertise, 11 (3.92%) patients among these 28 with abnormal TEE were considered unfit for work or "fit for work with limitations". CONCLUSION: Assessing a cardiac systolic murmur with TEE lead to the diagnosis of a cardiomyopathy in 10% of the case. This study enhances the importance of systematic TEE when a CSM is detected in the young military, in order to determine if those soldiers can still fulfill their military duty.


Subject(s)
Echocardiography , Heart Diseases/complications , Heart Diseases/diagnostic imaging , Military Medicine , Military Personnel , Systolic Murmurs/diagnostic imaging , Systolic Murmurs/etiology , Adolescent , Adult , Aortic Valve/abnormalities , Aortic Valve/diagnostic imaging , Bicuspid Aortic Valve Disease , Diagnosis, Differential , Echocardiography/methods , Female , France/epidemiology , Heart Auscultation , Heart Diseases/epidemiology , Heart Septal Defects, Atrial/diagnostic imaging , Heart Septal Defects, Ventricular/diagnostic imaging , Heart Valve Diseases/diagnostic imaging , Humans , Male , Military Personnel/statistics & numerical data , Mitral Valve Insufficiency/diagnostic imaging , Palpation , Predictive Value of Tests , Retrospective Studies , Sensitivity and Specificity
3.
Int J Sports Med ; 35(7): 551-8, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24258471

ABSTRACT

Several studies have demonstrated that endothelial function is impaired following a dive even without decompression sickness. During this study we determined the effect of decompression sickness on endothelium-dependent and independent vasoreactivity. For this purpose twenty-seven male Sprague-Dawley rats were submitted to a simulated dive up to 1,000 kPa absolute pressure and divided into 3 groups: safe diving without decompression sickness or dives provoking mild or severe sickness. A fourth control group remained at atmospheric pressure. Endothelium-dependent and independent vasomotion was assessed ex vivo by measuring isometric tension in rings of abdominal aorta and mesenteric arteries. Dose-response curves were obtained with phenylephrine, acetylcholine and sodium nitroprusside. Acetylcholine-induced relaxation was measured in the presence of L-NAME, indometacin or both of them at once.Contraction was significantly decreased after each protocol compared with the control rats. Additionally, the response in animals from the severe group was significantly different from that of the safe and mild groups. Dose response curves for acetylcholine alone and in the presence of inhibitors remained unchanged. We did not observe differences in endothelium-dependent vasodilation after diving or in the presence of decompression sickness. Contractile response to phenylephrine was progressively impaired with increased decompression stress. These results may indicate smooth muscle injury.


Subject(s)
Decompression Sickness/physiopathology , Endothelium, Vascular/physiology , Vasoconstriction/physiology , Vasodilation/physiology , Acetylcholine/pharmacology , Animals , Catecholamines/blood , Disease Models, Animal , Diving/adverse effects , Dose-Response Relationship, Drug , Enzyme Inhibitors/pharmacology , Hydrocortisone/blood , Indomethacin/pharmacology , Male , NG-Nitroarginine Methyl Ester/pharmacology , Nitroprusside/pharmacology , Phenylephrine/pharmacology , Rats, Sprague-Dawley , Vasoconstriction/drug effects , Vasoconstrictor Agents/pharmacology , Vasodilation/drug effects , Vasodilator Agents/pharmacology
4.
J Sports Med Phys Fitness ; 48(2): 246-51, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18427421

ABSTRACT

AIM: Exercise training is known to improve endothelium-dependent relaxation in the coronary and skeletal muscle arteries. However, the effects of exercise training on peripheral nonworking tissue, including microcirculation, are still unclear. Therefore, we investigated the effect of chronic and regular aerobic exercise on cutaneous microvascular endothelial function in rats. METHODS: We assessed the effect of physical training on skin microcirculation in 7 sedentary (SED) and 21 training rats (Wistar-Kyoto), submitted to a treadmill training protocol (15 m/min; 15% incline; 60 min/day; 8 weeks). Training rats were divided into 3 groups, exercising 1 day/week (Ex1), 3 days/week (Ex3) or 5 days/week (Ex5). Cutaneous blood flow was recorded before the beginning of the training protocol, after 4 weeks and at the end of the training program. Hyperemic response (RH) was the flow reaction obtained after sudden release of the garrot. For data analysis, cutaneous vascular conductance (CVC) was indexed as cutaneous blood flow divided by mean arterial blood pressure (in millimeters of mercury, mmHg) and normalized to baseline values. RESULTS: At baseline, CVC was not different among groups (SED or training) at 3 steps of experimental protocol. The hyperemic stimulus significantly increased normalized CVC only in group Ex3 after 4 weeks (P<0.006) and 8 weeks (P<0.006). CONCLUSION: Exercise training exerts a generalized effect on the vasculature by increasing endothelial function in vessel beds different from those perfusing actively working muscle. However, some differences exist since training at a frequency of 3 bouts weekly only modifies cutaneous microcirculation.


Subject(s)
Microcirculation , Physical Conditioning, Animal , Skin/blood supply , Animals , Laser-Doppler Flowmetry , Male , Rats , Rats, Inbred WKY
5.
Arch Mal Coeur Vaiss ; 100(6-7): 514-8, 2007.
Article in French | MEDLINE | ID: mdl-17893633

ABSTRACT

The object of this study was to assess the cardiovascular tolerance and efficacy of early nicotine substitution therapy in 100 patients admitted to the Coronary Care Unit for acute coronary syndromes (ACS). The files of the first 100 consecutive patients having received nicotine substitution therapy immediately after an ACS were consulted retrospectively and a questionnaire was sent to all patients. A reply was obtained in 90% of cases. In this series, there was a 7% rate of cardiovascular events in the days following hospital discharge, comparable to previously reported results. The smoking relapse rate at six months after the ACS was 38.9%, a percentage which was less than in previously reported series. Although consultations to help stop smoking and nicotine substitution did not seem to have significant benefits in this study, the authors recommend continuing and improving the management of coronary patients who smoke.


Subject(s)
Coronary Disease/complications , Nicotinic Agonists/therapeutic use , Smoking Prevention , Angina Pectoris, Variant/complications , Angina, Unstable/complications , Coronary Artery Bypass , Female , Humans , Male , Middle Aged , Myocardial Infarction/complications , Patient Education as Topic , Recurrence , Retrospective Studies , Smoking Cessation/methods , Stents , Surveys and Questionnaires
6.
Heart ; 92(1): 58-61, 2006 Jan.
Article in English | MEDLINE | ID: mdl-15845613

ABSTRACT

OBJECTIVE: To analyse coronary stents with multislice spiral computed tomography (MSCT) in comparison with coronary angiography. PATIENTS AND METHODS: 310 patients referred for conventional coronary angiography underwent MSCT on the next day (16 x 0.75 mm cross section, 420 ms rotation, 110 ml contrast agent intravenously at 4 ml/s). Two independent blinded reviewers analysed the MSCT. RESULTS: 143 patients had previous stenting (232 stents) and 190 (82%) of the 232 stents were detected. Intrastent lumen was interpretable in 126 (64%) of the detected stents. Lumen interpretability depended on stent diameter: for stent diameter > 3 mm, 81% of lumens were interpretable, as against 51% with < or = 3 mm stent diameter (p < 0.001). Restenosis detection likewise depended on stent diameter: with small stents (< or = 3 mm), sensitivity and specificity of MSCT were 54% and 100%, respectively; positive and negative predictive values were 100% and 94%. For stents with > 3 mm diameter, corresponding values were 86%, 100%, 100%, and 99%. CONCLUSION: 16 slice MSCT allows analysis of in-stent lumen in about half of all stented angioplasties. It performs better when stent diameter is more than 3 mm and may offer a non-invasive alternative to conventional coronary angiography for monitoring stented coronary arteries. Technical progress may improve interpretability and hence increase the yield of MSCT in this application.


Subject(s)
Coronary Restenosis/diagnostic imaging , Stents , Tomography, Spiral Computed/methods , Aged , Coronary Angiography/methods , Female , Humans , Male , Sensitivity and Specificity
7.
Int J Sports Med ; 26(10): 822-6, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16320164

ABSTRACT

We undertook this study to determine whether long-term high intensity exercise would modify cutaneous endothelial-dependent vasodilation. We compared a group of 9 highly trained windsurfers (mean age: 24.5 +/- 1.6 years) to a control group of 8 sedentary individuals (22.9 +/- 0.4 years, NS). Laser Doppler was used to measure cutaneous blood flow in the resting state (baseline), during post-occlusive hyperaemia (endothelium-dependent vasodilation), and local heating to 42 degrees C. Lipid profile was similar in both groups. Resting heart rate was significantly lower in windsurfers. Baseline cutaneous vascular conductance (CVC) values were similar in both groups (0.059 +/- 0.016 and 0.051 +/- 0.009). During reactive hyperaemia, normalized peak CVC value was significantly higher in the windsurfers group (1775.4 +/- 286.9 and 826.4 +/- 121.7 % baseline CVC; p = 0.01). Normalized peak CVC value in response to local heating (42 degrees C) was not significantly different between both groups (2359.4 +/- 346.1 and 1467.7 +/- 282.6 % baseline CVC). Endothelium-dependent vasodilation in cutaneous microcirculation is significantly enhanced in the forearm skin of highly trained windsurfers when compared to sedentary controls.


Subject(s)
Forearm/blood supply , Hyperemia/physiopathology , Microcirculation , Skin/blood supply , Sports/physiology , Adult , Blood Pressure/physiology , Case-Control Studies , Heart Rate/physiology , Humans , Laser-Doppler Flowmetry , Male , Physical Fitness/physiology , Regional Blood Flow/physiology , Rest/physiology , Systole/physiology , Vasodilation/physiology
8.
Presse Med ; 34(18): 1331-6, 2005 Oct 22.
Article in French | MEDLINE | ID: mdl-16269998

ABSTRACT

Physicians can aid their patients' smoking cessation by providing psychological support, advice, behavioral strategies, and drugs. Success depends on appropriate management, including selection of the right moment to begin treatment and an understanding of the development of the withdrawal syndrome, smoking urges, and the possibility of failure. The standard pharmacological treatment for nicotine dependence uses different forms of nicotine substitutes and bupropion, while we await data about other drugs currently under study. The score on the "simplified" Fagerström questionnaire usually determines the initial nicotine dose. Six forms of nicotine substitutes are available. They provide either prolonged nicotine release (transcutaneous patches) that prevents withdrawal symptoms, or rapid release through the buccal and nasal mucosa (chewing gum, suckers, inhalers and nasal sprays) to anticipate the positive effects represented by cigarettes and the urges occurring during withdrawal. The efficacy of these substitutes, widely studied, is approximately twice that of placebo. Their use is no longer contraindicated in patients with heart disease, when necessary. Bupropion should be used in treating nicotine dependence either as a first-line treatment, or if nicotine substitutes (150 mg/d the first week, 300 mg/d thereafter) fail. The combination of bupropion and nicotine substitutes can be considered, either from the outset for heavy or very heavy smokers, or afterwards, if withdrawal symptoms or urges to smoke persist in subjects treated by only one of these two drug classes. One of the new drugs under evaluation is rimonabant, the first representatives of a new class of drugs, selective CB1 endocannabinoid receptor antagonists. Promising results about its use in smoking cessation were released in 2004.


Subject(s)
Antidepressive Agents, Second-Generation/therapeutic use , Bupropion/therapeutic use , Central Nervous System Stimulants/administration & dosage , Dopamine Uptake Inhibitors/therapeutic use , Nicotine/analogs & derivatives , Nicotine/therapeutic use , Nicotinic Agonists/therapeutic use , Polymethacrylic Acids/administration & dosage , Polyvinyls/administration & dosage , Smoking Cessation/methods , Administration, Cutaneous , Adult , Antidepressive Agents, Second-Generation/administration & dosage , Cannabinoid Receptor Antagonists , Cannabinoids/antagonists & inhibitors , Chewing Gum , Child , Humans , Nicotine/administration & dosage , Nicotinic Agonists/administration & dosage , Piperidines/administration & dosage , Piperidines/therapeutic use , Pyrazoles/administration & dosage , Pyrazoles/therapeutic use , Rimonabant , Smoking Cessation/psychology , Surveys and Questionnaires , Time Factors , Tobacco Use Cessation Devices
10.
Arch Mal Coeur Vaiss ; 96(10): 967-72, 2003 Oct.
Article in French | MEDLINE | ID: mdl-14653057

ABSTRACT

The authors carried out a retrospective study of short and long-term mortality after aortic valve replacement and assessed the quality of life by the IRIS scale in patients over 75 years of age operated for severe aortic stenosis at the University Hospital of Brest between June 1990 and March 1995. The hospital files of 110 consecutive patients (71 women, 39 men; average age 78 +/- 2 years, range 75-85 years) were studied. The pre- per- and postoperative data was studied. Each survivor was contacted by telephone during the year 2000 and a health and IRIS quality of life questionnaire was sent to them. Precise information about patients who had died was obtained from the family and/or medical practitioner. In the preoperative period, 30.9% of patients had left ventricular failure. The average aortic valve surface area was 0.53 +/- 0.12 cm2. Of the patients who underwent coronary angiography (60%), one third had significant coronary lesions. Coronary artery bypass surgery was associated with aortic valve replacement in 10% of cases. Biological prostheses were used in 108 patients. The operative mortality was 8.2%. One year, 5 year and 10 year survival rates were 89.9%, 75.5% and 33.3% respectively. Of the survivors, 16.7% were in institutional care and 83.3% lived at home. A total of 77.8% were readmitted to hospital, about half of them for cardiac problems. Cardiac treatment was prescribed for 97% of patients. The quality of life questionnaire was completed by 35 patients: the quality of life was better than average in nearly 83% of these patients. Aortic valve replacement for aortic stenosis in patients over 75 years of age improves life expectancy which is almost the same as that of the normal population of the same age, and improves the quality of life by restoring functional autonomy, enabling the majority of them to live in their own houses most of the time.


Subject(s)
Aortic Valve Stenosis/mortality , Aortic Valve Stenosis/surgery , Quality of Life , Age Factors , Aged , Aged, 80 and over , Female , Humans , Male , Patient Readmission , Postoperative Complications/epidemiology , Retrospective Studies
11.
Arch Mal Coeur Vaiss ; 96 Spec No 4: 7-12, 2003 May.
Article in French | MEDLINE | ID: mdl-12852280

ABSTRACT

Syncope is a common symptom of clinical practice which raises the problem of the differential diagnosis of other causes of loss of consciousness and a logical diagnostic strategy to avoid systematic prescription of expensive, invasive and often valueless investigations. The aim of this article is to propose a diagnostic procedure for syncopes in adults based on recent recommendations and the value of currently available diagnostic tests.


Subject(s)
Syncope/diagnosis , Diagnosis, Differential , Humans , Incidence , Medical History Taking , Physical Examination , Syncope/etiology
12.
Europace ; 5(2): 207-11, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12633648

ABSTRACT

UNLABELLED: Left ventricular-based pacing is an established method for treatment of congestive heart failure in patients with ventricular dyssynchrony. The transvenous epicardial approach is the method of choice to pace the left ventricle. AIMS: To evaluate short and long-term stability and pacing and sensing performance of an S-shaped non-steroid unipolar lead. METHODS: Forty-eight procedures were performed in 43 consecutive patients (mean age: 70+/-8 years, 32 males) with severe congestive heart failure. The left ventricular lead was placed into a coronary sinus tributary. Pacing and sensing thresholds and pacing impedance were measured at implant, 1 and 6 months. RESULTS: The mean procedure time was 90.0+/-35.5 min. Pacing thresholds at implant, 1 and 6 months were 1.1+/-0.8 V, 1.9+/-1.3 V and 1.9+/-1.5 V respectively. In 7 patients, lead implantation was unsuccessful. One of them had a successful second attempt. Lead revision was performed in 5 patients for loss of capture. CONCLUSION: The S-shaped unipolar lead evaluated in this study provides stable long-term position and pacing thresholds. Recent improvement of this S-shaped lead model will hopefully reduce the rate of implantation failures and acute dislodgements.


Subject(s)
Heart Failure/complications , Heart Failure/therapy , Pacemaker, Artificial , Ventricular Dysfunction, Left/etiology , Ventricular Dysfunction, Left/therapy , Ventricular Fibrillation/etiology , Ventricular Fibrillation/therapy , Aged , Electrocardiography , Female , Follow-Up Studies , Heart Failure/physiopathology , Humans , Male , Middle Aged , Outcome Assessment, Health Care , Sensitivity and Specificity , Time Factors , Ventricular Dysfunction, Left/physiopathology , Ventricular Fibrillation/physiopathology
13.
Europace ; 4(2): 155-8, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12135247

ABSTRACT

This is a case-report of two patients with superior vena cava syndrome related to pacemaker leads. Both patients were treated successfully using intravenous stenting.


Subject(s)
Pacemaker, Artificial/adverse effects , Stents , Superior Vena Cava Syndrome/etiology , Superior Vena Cava Syndrome/therapy , Adult , Aged , Aged, 80 and over , Electrodes, Implanted/adverse effects , Female , Humans , Male
14.
Eur Heart J ; 23(10): 815-20, 2002 May.
Article in English | MEDLINE | ID: mdl-12009722

ABSTRACT

AIMS: Syncope is a frequent and potentially dangerous symptom. The epidemiological data are based on series mainly collected 20 years ago in the U.S.A. and do not adequately assist in the management of patients admitted now for this symptom in Europe. METHODS AND RESULTS: To evaluate prospectively the epidemiological aspects and the management of the patients admitted in the emergency department of an adult university hospital for a 'verified' syncope, charts of all the patients consecutively admitted between June 1999 and June 2000 were systematically reviewed by a member of the cardiology staff. Those with a loss of consciousness were selected and those with a definite syncope were included in the study group and followed until they were discharged from the hospital. Among the 37,475 patients who presented to the emergency department, 454 (1.21%) had a definite syncope. For 296 it was the first episode and 169 (mean age 43+/-23 years) were discharged straight away; 285 (mean age 66+/-19 years; P<0.0001) were admitted to internal medicine (n=151), cardiology (n=65), neurology (n=44), endocrinology (n=14) and surgery (n=11) services. In 75.7% of all the patients a diagnosis was reported but it was inadequate to explain a syncopal episode in 56 cases (16.3%). Management differed by department: 36% of the patients had 'neurological' investigations mainly in internal medicine and neurology. Except in cardiology very few had 'cardiological' investigations particularly tilt test and electrophysiological studies (5%). CONCLUSION: Syncope is a frequent symptom but its cause often remains unknown partly due to inadequate management. Precise and simple guidelines are urgently needed.


Subject(s)
Patient Admission , Syncope/therapy , Adult , Age Factors , Aged , Aged, 80 and over , Female , France/epidemiology , Humans , Length of Stay , Male , Middle Aged , Prospective Studies , Recurrence , Syncope/epidemiology , Time Factors , Treatment Outcome
15.
J Am Coll Cardiol ; 38(7): 1966-70, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11738301

ABSTRACT

OBJECTIVE: The purpose of this study is to report prospectively the results of six-month follow-up of permanent left ventricular (LV) based pacing in patients with severe congestive heart failure (CHF) and left bundle branch block (LBBB). BACKGROUND: Left ventricular pacing alone has been demonstrated to result in identical improvement compared to biventricular pacing (BiV) during acute hemodynamic evaluation in patients with advanced CHF and LBBB. However, to our knowledge, the clinical outcome during permanent LV pacing alone versus BiV pacing mode has not been evaluated. METHODS: Pacing configuration (LV or BiV) was selected according to the physician's preference. Patient evaluation was performed at baseline and at six months. RESULTS: Thirty-three patients with advanced CHF and LBBB were included. Baseline characteristics of LV (18 patients) and BiV (15 patients) pacing groups were similar. During the six-month follow-up period, seven patients died three BiV and four LV). In the surviving patients at 6 months, 8 of 14 patients in the LV group and 9 of 12 in the BiV group were in New York Heart Association class I or II (p = 0.39). No significant difference was observed between the two groups in terms of objective parameters except for LV end-diastolic diameter decrease (-4.4 mm in BiV group vs. -0.7 mm in LV group; p = 0.04). CONCLUSION: At six-month follow-up, a trend toward improvement was observed in objective parameters in patients with severe CHF and LBBB following LV-based pacing. The two pacing modes (LV and BiV) were associated with almost equivalent improvement of subjective and objective parameters.


Subject(s)
Bundle-Branch Block/therapy , Electrocardiography , Heart Failure/therapy , Heart Ventricles/physiopathology , Pacemaker, Artificial , Ventricular Dysfunction, Left/therapy , Aged , Atrial Fibrillation/physiopathology , Atrial Fibrillation/therapy , Bundle of His/physiopathology , Bundle-Branch Block/physiopathology , Female , Follow-Up Studies , Heart Failure/physiopathology , Humans , Male , Prospective Studies , Ventricular Dysfunction, Left/physiopathology
17.
Arch Mal Coeur Vaiss ; 94(7): 665-72, 2001 Jul.
Article in French | MEDLINE | ID: mdl-11494626

ABSTRACT

The aim of this study was to assess the impact of cardiovascular risk factors on the modelling of atherosclerotic coronary arteries. One hundred consecutive patients who underwent coronary angioplasty were studied by endocoronary ultrasonography at the site of dilatation. At the site of the treated stenosis of the dilated arteries there was either compensatory widening or positive modelling (PM), or focal contraction or negative modelling (NM) if the total surface area (TSA) of the artery at the site of dilatation was greater or smaller than the total surface area of the proximal or distal reference segments. PM was observed in 53 cases (53%) and NM in 47 cases (47%). Lesions with NM had smaller TSA (13.7 +/- 5.8 versus 20.8 +/- 6.4 mm2, p < 0.0001) and a smaller atheromatous plaque (11.8 +/- 5.6 versus 19.1 +/- 6.5 mm2, p < 0.0001) than lesions with PM. Cardiovascular risk factors such as hypercholesterolaemia, smoking and hypertension were not predictive of either form of arterial modelling and there was no relationship between the cardiovascular risk factors and the qualitative appearances of the plaque studied.


Subject(s)
Coronary Artery Disease/physiopathology , Coronary Artery Disease/therapy , Coronary Disease/physiopathology , Coronary Disease/therapy , Coronary Vessels/diagnostic imaging , Angioplasty, Balloon, Coronary , Coronary Artery Disease/diagnostic imaging , Coronary Disease/diagnostic imaging , Echocardiography , Female , Humans , Hypercholesterolemia , Hypertension , Male , Middle Aged , Radiography , Risk Factors , Smoking
18.
Eur J Heart Fail ; 3(4): 441-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11511430

ABSTRACT

BACKGROUND: Beneficial effects of left ventricular (LV)-based pacing on acute hemodynamic parameters were reported in several series, but only a few studies examined the long-term effects of this new pacing procedure. AIMS: To assess long-term effects of permanent LV-based pacing on LV function and mitral regurgitation (MR) in patients with refractory congestive heart failure (CHF). METHODS: A prospective evaluation of LV function and MR was performed in 23 patients with severe but stable CHF and left bundle branch block (mean QRS: 186+/-31 ms) by radionuclide and echocardiographic techniques at baseline and 6 months after implantation of a permanent LV-based (LV alone: 13 patients; biventricular: 10 patients) pacemaker programmed either in a DDD mode (sinus rhythm; n=14) or in a VVIR mode (atrial fibrillation; n=9). RESULTS: Compared to baseline, the 6 months follow-up visit demonstrated a significant increase in radionuclide derived LV ejection fraction from 23.3+/-7 to 26.2+/-7% (P<0.01) and in echocardiographic LV fractional shortening from 13+/-4 to 16+/-6% (P<0.05), without any change in cardiac index, a significant decrease in LV end-diastolic diameter (from 73.2+/-6 to 71.2+/-7 mm; P<0.05), end-systolic diameter (from 63.6+/-6 to 60.2+/-8 mm; P<0.05) and color Doppler MR jet area (from 11.5+/-6 to 6.6+/-4 cm(1); P<0.001). A comparison of patients with LV pacing alone and patients with biventricular pacing showed similar beneficial effects of pacing on MR severity in the two subgroups and a non-significant trend for a better improvement of LV function during biventricular pacing. CONCLUSION: Thus, in patients with severe CHF and left bundle branch block, permanent LV-based pacing may significantly improve LV systolic function and decrease MR.


Subject(s)
Cardiac Pacing, Artificial/methods , Heart Failure/therapy , Mitral Valve Insufficiency/therapy , Ventricular Dysfunction, Left/diagnosis , Ventricular Dysfunction, Left/therapy , Adult , Aged , Female , Follow-Up Studies , Heart Failure/complications , Heart Failure/diagnosis , Heart Function Tests , Hemodynamics/physiology , Humans , Male , Middle Aged , Mitral Valve Insufficiency/complications , Mitral Valve Insufficiency/diagnosis , Pilot Projects , Probability , Prospective Studies , Sensitivity and Specificity , Severity of Illness Index , Treatment Outcome , Ventricular Dysfunction, Left/complications , Ventricular Function, Left
19.
Europace ; 3(1): 60-3, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11271954

ABSTRACT

AIMS: Assessment of complications following implantation of transvenous ventricular electrodes to pace the left ventricle. METHODS AND RESULTS: Twenty-eight patients with severe cardiac failure and left bundle branch block were prospectively followed for adverse effects of implantation of a left ventricular transvenous pacing system. Immediate follow-up was associated with loss of left ventricular pacing in nine patients (32%). This was due to lead dislodgement in four cases (corrected by re-operation in three of these cases), and due to increased threshold in five cases (corrected by programming a higher pacing amplitude in all five cases, but with intermittent diaphragmatic contraction in one case). After 1 month, one patient died, one patient with severe coronary heart disease suffered a myocardial infarction, and left ventricular pacing was lost in two patients. Pericardial effusion, new significant ventricular arrhythmias or other adverse effects were not observed. After a mean follow-up of 16 +/- 9.2 months, pacing leads remained stable and no late complications related to the transvenous left ventricular epicardial pacing were observed. CONCLUSION: Placement of a permanent lead in a tributary of the coronary sinus is feasible without serious adverse effects during the first month. The only frequent adverse event was lead dislodgement; a finding which emphasizes the need for development of specially designed leads for this application.


Subject(s)
Cardiac Pacing, Artificial/methods , Catheterization, Peripheral/adverse effects , Heart Failure/therapy , Pacemaker, Artificial/adverse effects , Aged , Bundle-Branch Block/complications , Bundle-Branch Block/mortality , Bundle-Branch Block/physiopathology , Bundle-Branch Block/therapy , Electrocardiography, Ambulatory , Female , Heart Failure/complications , Heart Failure/mortality , Heart Failure/physiopathology , Heart Rate , Heart Ventricles , Humans , Male , Prospective Studies , Survival Rate
20.
Arch Mal Coeur Vaiss ; 94(1): 44-50, 2001 Jan.
Article in French | MEDLINE | ID: mdl-11233480

ABSTRACT

The aim of this study was to evaluate the clinical events occurring after coronary stenting in a series of 318 consecutive patients treated in 1997. Hospital follow-up was by gathering all the data in the hospital record and medium-term follow-up was performed by questionnaire filled with the help of the patient, the attending physician and the referring cardiologist. The primary clinical success rate was 95.6% and the clinical follow-up rate was 98.7%. The follow-up period was at least 16 months (mean 22 +/- 6 months). The restenosis rate was 15% in the remaining population (318-7 deaths and 4 lost to follow-up) and 47% in the population undergoing control coronary angiography. No major clinical cardiac events (death, myocardial infarction or revascularisation) were observed in 80.5% at 1 year and 79% at 22 months. Twenty per cent of the remaining population had no non-invasive paraclinical investigations for myocardial ischaemia after coronary stenting. These results are comparable to those of the literature, indicating excellent feasibility of this technique and the fact that, programmed or not, coronary stenting is a safe procedure confirming its value in what has become everyday practice. Nevertheless, this experience did highlight certain lapses in medical follow-up and patient information.


Subject(s)
Blood Vessel Prosthesis Implantation , Blood Vessel Prosthesis , Coronary Disease/surgery , Stents , Aged , Coronary Angiography , Female , Humans , Male , Middle Aged , Myocardial Infarction , Prognosis , Retrospective Studies , Treatment Outcome
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