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1.
Ann Cardiol Angeiol (Paris) ; 69(5): 219-226, 2020 Nov.
Article in French | MEDLINE | ID: mdl-32800321

ABSTRACT

INTRODUCTION: Coronary heart disease is the leading cause of morbidity and mortality in nonagenarians, whose numbers have doubled in twenty years. In the absence of recommendations, the place of coronary invasive strategy in this population remains a therapeutic challenge and its interest as well as its risks are poorly established. The aim of our study was to evaluate the safety of coronary invasive practice in the nonagenarian population for all indications. POPULATION AND METHODS: This was a monocentric case-control study conducted from January 1, 2010 to May 30, 2019. The patients included were all nonagenarians who had undergone coronary angiography at the centre hospitalier de Troyes during this period. For each patient included, two controls matched on sex, date of procedure and procedure were drawn at random. The main judgment criterion was the occurrence of immediate per- or post-procedure complications during the stay in which the procedure was performed. The main secondary outcome measures were average length of stay, occurrence of intercurrent events during the stay (nosocomial infections, confusional syndrome), and loss of autonomy. RESULTS: In all, 59 nonagenarians and 118 controls were included in our study. We identified 30.5% major complications in the nonagenarians versus 10.2% in the controls (P=0.001; OR=0.26 [0.1-0.6]), with a significant difference in the occurrence of cardiogenic shock (P=0.04), heart failure (P=0.02) and ventricular rhythm disorders (P=0.04). Post-procedure acute renal failure was greater in the nonagenarians (P=0.02; OR=0.20 [0.05-1.57]). The mean length of stay was on average twice as long in the nonagenarians. CONCLUSION: Nonagenarian patients are subject to more complications when undergoing coronary invasive procedures compared to patients under 75.


Subject(s)
Myocardial Revascularization/adverse effects , Postoperative Complications/etiology , Age Factors , Aged, 80 and over , Case-Control Studies , Female , Humans , Male , Postoperative Complications/epidemiology , Retrospective Studies
2.
Clin Microbiol Infect ; 25(10): 1246-1252, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31055167

ABSTRACT

OBJECTIVES: The aim was to describe the impact of infective endocarditis (IE) on functional, cognitive and nutritional statuses, and to estimate the influence of these parameters on surgical management and mortality. METHOD: This was a prospective study over 13 months in 14 French hospitals, including patients ≥75 years of age with definite or possible IE. A comprehensive geriatric assessment (CGA) was performed during the first week of hospitalization, including a retrospective estimation of functional status 2 months before hospitalization, and 3 months after. RESULTS: A total of 120 patients were included (mean age 83.1 ± 5.0 (75-101) years). IE was associated with a dramatic impairment of functional status between 2 months prior hospitalization and the first geriatric evaluation (90.8% able to walk vs. 35.5% (p < 0.0001), ADL (Activities in Daily Living) 5.0 ± 1.7 vs. 3.1 ± 2.1 (p < 0.0001)). The 19 operated patients (15.8%) had less comorbidities (cumulative illness rating scale geriatric 10.8 ± 8.2 vs. 15.3 ± 7.1 (p 0.0176)), better functional (ADL 5.9 ± 0.4 vs. 4.9 ± 1.8 (p 0.0171) and nutritional (mini nutritional assessment 20.4 ± 5.0 vs. 17.3 ± 6.2 (p 0.0501)) statuses than non-operated patients. Among all infectious, cardiac and geriatric parameters, body mass index (HR 0.9, range 0.8-1, p 0.05) and ADL at the time of the first evaluation (HR 0.7, range 0.6-0.9, p 0.002) were the sole independent predictors of the 3-month (32.5%) and 1-year mortality (42.5%). Three months later, the 57 assessed patients only partially recovered their ADL (3.7 ± 1.9 vs. 5.3 ± 1.4 2 months prior hospitalization and 4.6 ± 1.9 at the first CGA; p < 0.0001). CONCLUSION: Functional and nutritional abilities are crucial components that can be accurately explored through a CGA when managing IE in oldest patients.


Subject(s)
Endocarditis/mortality , Endocarditis/pathology , Geriatric Assessment , Aged , Aged, 80 and over , Comorbidity , Endocarditis/surgery , Female , France , Hospitalization/statistics & numerical data , Humans , Male , Nutritional Status , Prospective Studies , Survival Analysis
3.
Diabetes Metab ; 32(3): 262-9, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16799404

ABSTRACT

AIM: Lipoprotein lipase (LPL) is a key enzyme of lipid metabolism, and its genetic polymorphism may be a candidate for modulating lipid parameters in type 2 diabetic subjects (D2). METHODS: In a group of 404 type 2 diabetic patients, aged 59.5+/-10.8y, BMI=28.9+/-5.3 kg/m2, HbA1c=8.2+/-1.9%, we studied the H and P polymorphisms at the LPL locus detectable with the restriction enzymes HindIII and PvuII. Patients were separated into 229 males (17H1H1, 84H1H2, 128H2H2 and 51P1P1, 110P1P2, 68P2P2) and 175 females (16H1H1, 69H1H2, 90H2H2 and 51P1P1, 85P1P2, 39P2P2), and compared on the basis of their lipid parameters and their macrovascular complications. RESULTS: Triglyceride (TG) and HDL-cholesterol(c) concentrations differed between patients with and without coronary heart disease (CHD) (3.44+/-2.09 and 1.96+/-1.40 mmol/l for TGs and 1.05+/-0.24 and 1.34+/-0.40 mmol/l for HDL-c, P<0.001). HDL-c concentrations were lower in male H2H2 and P2P2 subjects (P<0.001), and TG levels were higher in male H2H2 and P2P2 subjects (P<0.0001 for Hind III and P<0.05 for PvuII). Allele frequency of the HindIII and PvuII restriction site was similar to those reported in other Caucasian populations and the presence of the H2/P2 variants was significantly higher in CHD patients. The prevalence of CHD in this population was 18% but was 29% in H2H2 and 38% in P2P2 subjects (P<0.02). CONCLUSION: Thus, HindIII and PvuII polymorphisms seem to exert a modulating role on lipid profile particularly in male D2, contributing to increase the risk of macrovascular events.


Subject(s)
Diabetes Mellitus, Type 2/enzymology , Diabetes Mellitus, Type 2/genetics , Diabetic Angiopathies/genetics , Lipids/blood , Lipoprotein Lipase/genetics , Polymorphism, Genetic , Aged , Coronary Disease/enzymology , Coronary Disease/epidemiology , Coronary Disease/genetics , DNA-Cytosine Methylases , Diabetes Mellitus, Type 2/complications , Diabetic Angiopathies/enzymology , Diabetic Angiopathies/epidemiology , Female , Humans , Lipoproteins/blood , Male , Middle Aged , Multivariate Analysis , Risk Factors , Site-Specific DNA-Methyltransferase (Adenine-Specific) , Triglycerides/blood
4.
Thromb Haemost ; 83(4): 540-4, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10780313

ABSTRACT

The PFA-100 (Dade) is a new functional whole blood analyzer, the accuracy and reliability of which have been evaluated in von Willebrand disease and during acetyl salicylate acid therapy. This new test has the advantages of rapidity and simplicity. It may be useful to monitor new antiplatelet agents, such as GPIIb/IIIa receptor antagonists. The objective of this study was to assess the PFA-100 in comparison with aggregometry and with the percentage of blockaded receptors GPIIb/IIIa during and after c7E3 Fab infusion in fifteen patients undergoing PTCA. Our results showed a change of closure time values from normal to abnormal within a small margin of flow cytometric values (60-75% of blockaded receptors), and moreover a variable platelet response to long-term low dose aspirin treatment in agreement with aggregometry. No influence with heparin was observed. In conclusion, this study shows that PFA-100 may be helpful in the decision making for additional antiaggregant therapy before PTCA or in monitoring long-term GPIIb/IIIa receptor antagonist treatment.


Subject(s)
Angioplasty, Balloon, Coronary , Antibodies, Monoclonal/pharmacology , Immunoglobulin Fab Fragments/pharmacology , Platelet Aggregation Inhibitors/pharmacology , Platelet Aggregation/drug effects , Platelet Function Tests/instrumentation , Abciximab , Adenosine Diphosphate/pharmacology , Antibodies, Monoclonal/adverse effects , Antibodies, Monoclonal/therapeutic use , Anticoagulants/adverse effects , Anticoagulants/pharmacology , Anticoagulants/therapeutic use , Blood Cell Count , Collagen/pharmacology , Epinephrine/pharmacology , Equipment Design , Female , Hemoglobins/analysis , Hemorrhage/chemically induced , Heparin/adverse effects , Heparin/pharmacology , Heparin/therapeutic use , Humans , Immunoglobulin Fab Fragments/adverse effects , Immunoglobulin Fab Fragments/therapeutic use , Male , Microcomputers , Middle Aged , Platelet Aggregation Inhibitors/administration & dosage , Platelet Aggregation Inhibitors/therapeutic use , Pulmonary Embolism/blood
5.
Thromb Haemost ; 81(6): 869-73, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10404759

ABSTRACT

A quantitative flow cytometry assay was used to evaluate the ex vivo kinetics of c7E3 Fab platelet effect in 16 patients undergoing PTCA treated with abciximab and compared with aggregometry assay. Immunolabeling of platelets was directly assessed on whole blood, using in parallel two monoclonal antibodies (Mabs) raised against GPIIIa, Mab1, the binding of which is inhibited by c7E3 Fab, and Mab2, the binding of which is not affected by c7E3 Fab. We found a severe and sustained inhibition of both GPIIb/IIIa receptors and platelet functions. The inter-individual variation in response to abciximab was low. A significant transient increase at H24 and H48 in the binding of Mab2 was found as an unexpected result, and confirmed in vitro. Results demonstrate that flow cytometry is a reliable method in agreement with aggregation. In addition, our results show that it is a standardized tool and a time-saving technique.


Subject(s)
Antibodies, Monoclonal/administration & dosage , Anticoagulants/administration & dosage , Blood Platelets , Immunoglobulin Fab Fragments/administration & dosage , Platelet Glycoprotein GPIIb-IIIa Complex/analysis , Abciximab , Aged , Angioplasty, Balloon, Coronary , Female , Flow Cytometry/methods , Humans , Intraoperative Complications/prevention & control , Male , Middle Aged
6.
Am J Cardiol ; 77(14): 1252-4, 1996 Jun 01.
Article in English | MEDLINE | ID: mdl-8651110

ABSTRACT

We found a significant ABD-assisted right ventricular hypokinetic regression after thrombolytic therapy in acute pulmonary embolism but could not demonstrate a linear relation between improvement in early right ventricular function and angiography.


Subject(s)
Myocardial Contraction , Pulmonary Embolism/physiopathology , Thrombolytic Therapy , Ventricular Dysfunction, Right , Aged , Coronary Angiography , Echocardiography , Female , Humans , Male , Middle Aged , Plasminogen Activators/therapeutic use , Prospective Studies , Pulmonary Embolism/drug therapy , Recombinant Proteins/therapeutic use , Urokinase-Type Plasminogen Activator/therapeutic use
7.
Diagn Mol Pathol ; 9(3): 145-50, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10976721

ABSTRACT

The reliability of the Hybrid Capture II (HC-II; Digene, Silver Spring, MD, U.S.A.) assay was tested in detecting 18 human Papillomavirus (HPV) types for the screening of cervical lesions. Cytology, HPV testing, colposcopy, and biopsy were used to monitor 204 women with normal smears at the first entry. The median follow-up was 15 months (range, 4-27 months). The primary endpoint was clinical progression defined as the presence of a cervical intraepithelial lesion at the biopsy. In the patient population of 204 HPV-infected women, 81 (39.7%) had a persistent HPV infection at two or three examinations with a final histologic diagnosis of 14 high-grade and 13 low-grade squamous intraepithelial lesions (SIL) within 4 to 22 months. Women with regressive HPV infection did not develop any lesion during the same period. The evaluation of the viral load of high-risk HPV by the HC-II did not represent a sensitive approach to predict the persistence or the apparition of high-grade lesions. Thus, persistent high-risk HPV infection detected with HC-II represents a reliable tool to select populations at risk for the development of high-grade cervical lesions.


Subject(s)
Carcinoma, Squamous Cell/virology , Cervix Uteri/virology , DNA, Viral/isolation & purification , Nucleic Acid Hybridization , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , Reagent Kits, Diagnostic , Tumor Virus Infections/virology , Uterine Cervical Dysplasia/virology , Uterine Cervical Neoplasms/virology , Uterine Cervicitis/virology , Vaginal Smears , Adolescent , Adult , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/etiology , Chronic Disease , Colposcopy , Disease Progression , Female , Follow-Up Studies , Humans , Mass Screening , Middle Aged , Reproducibility of Results , Risk Factors , Sensitivity and Specificity , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/etiology , Viral Load , Uterine Cervical Dysplasia/etiology
8.
Cancer Chemother Pharmacol ; 43(3): 227-32, 1999.
Article in English | MEDLINE | ID: mdl-9923553

ABSTRACT

PURPOSE: To determine the effects of amifostine on an isolated perfused rat-heart model and its protective activity with regard to cardiotoxic doxorubicin perfusion. METHODS: Langendorff constant-pressure isolated rat-heart preparations were used to analyze the effects of the drugs during a 40-min period of perfusion after a 20-min stabilization interval. The first study was conducted with amifostine alone (controls and 10(-6), 10(-5), and 10(-4) M amifostine; n=6 in each group). The second study was conducted with amifostine and doxorubicin (controls, 2.5 x 10(-5) M doxorubicin, 2.5 x 10(-5) M doxorubicin and 10(-5) M amifostine, and 2.5 x 10(-5) M doxorubicin and 10(-4) M amifostine; n=4 in each group). RESULTS: Amifostine had no significant effect on hemodynamic parameters at 10(-6), 10(-5), and 10(-4) M concentrations. However. amifostine increased the coronary flow expressed as a percentage+/-SEM of the baseline flow as follows: 82+/-4% for controls, 95+/-6% for 10(-6) M amifostine, (P=0.13), 111+/-4% for 10(-5) M amifostine (P < 0.01), and 104+/-3% for 10(-6) M amifostine (P < 0.01). When we commenced an amifostine perfusion 20 min in advance of and then during a 40-min perfusion with doxorubicin, at a cardiotoxic concentration of 2.5 x 10(-5) M the left ventricular pressures (LVDP, expressed as percentages +/-SEM of the baseline LVDP before doxorubicin) were 55+/-3% for the doxorubicin controls, 68+/-2% for doxorubicin with 10(-5) M amifostine (P=0.05), and 80+/-3% for doxorubicin with 10(-4) M amifostine (P < 0.01). Whether this protective effect might be related to the known free-radical-scavenging activity of amifostine remains to be determined. CONCLUSION: On a Langendorff-type model of rat heart, 10(-5) and 10(-4) M amifostine alone induced a coronary dilation and, when associated with a cardiotoxic concentration of 2.5 x 10(-5) M doxorubicin, 10(-5) and 10(-4) M amifostine displayed a cardioprotective effect.


Subject(s)
Amifostine/pharmacology , Antibiotics, Antineoplastic/antagonists & inhibitors , Doxorubicin/antagonists & inhibitors , Heart/drug effects , Animals , Antibiotics, Antineoplastic/toxicity , Coronary Circulation/drug effects , Creatine Kinase/metabolism , Doxorubicin/toxicity , In Vitro Techniques , Male , Myocardial Contraction/drug effects , Myocardium/enzymology , Oxygen Consumption/drug effects , Rats , Rats, Wistar
9.
Oncol Rep ; 5(2): 363-6, 1998.
Article in English | MEDLINE | ID: mdl-9468558

ABSTRACT

Chronic malignant pleural effusion may be treated by instillating products in the pleural space to induce pleurodesis. We used intrapleural doxycycline at doses greater than 2000 mg in 16 malignant pleural effusion (14 patients). Patient survival ranged from 1 day to 19.5 months. Mean drainage duration was 7.5 days (range, 5-10 days). Pain (moderate n=7; severe n=2) was the most frequent side-effect with hypotension (moderate n=3; severe n=1). Five cases were not evaluable at one month because of death during the month following treatment (n=3) or during treatment (n=2). At one month follow-up, success was defined as no pleural effusion (n=5), partial response as minimal effusion (n=4) and we considered that treatment had failed if pleural drainage was necessary (n=2). Five patients died within one month and 5 had more than 3 months survival (4 without recurrence).


Subject(s)
Anti-Bacterial Agents/administration & dosage , Doxycycline/administration & dosage , Pleural Effusion, Malignant/therapy , Pleurodesis , Adult , Aged , Anti-Bacterial Agents/adverse effects , Doxycycline/adverse effects , Female , Follow-Up Studies , Humans , Male , Middle Aged , Neoplasms/complications , Pleural Effusion, Malignant/etiology , Recurrence , Sclerotherapy , Survival Analysis , Treatment Outcome
10.
Oncol Rep ; 8(6): 1327-31, 2001.
Article in English | MEDLINE | ID: mdl-11605059

ABSTRACT

Drainage of malignant pleural effusions (MPE) by thoracocenthesis and subsequent pleurodesis is an established means of symptomatic relief in terminally-ill patients, but the optimal therapy remains unclear. Among many sclerosing agent, talc is the most widely used, but its intrapleural administration and dosage have not been clearly determined. To assess the efficacy of using talc slurry with high dose (8 g) as a sclerosing agent instilled into the pleural space at the patient bedside, we carried out a study in 31 patients suffering from symptomatic MPE, followed until death or up to 1 year with radiographs. Patients were evaluated for immediate tolerance (31 patients), and for efficacy and long-term tolerance (27 patients) of the talc therapy. We have shown, that pleurodesis was satisfactory in 22/27 patients (81.4%). This result appeared comparable with other series. Moreover, we observed a long-lasting efficacy: within 6 months and within 12 months after talc instillations, 20/20 patients and 9/9 patients respectively were symphysed with efficacy. Complications related to talc (8 g) were rare and moderate (pain, fever). Taking into account some technical aspects of talc instillation for good performance of the therapy, we recommend this method as the optimal route of administration.


Subject(s)
Pleural Effusion, Malignant/therapy , Pleurodesis , Sclerosing Solutions/administration & dosage , Talc/administration & dosage , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged
11.
Anticancer Res ; 23(1A): 405-9, 2003.
Article in English | MEDLINE | ID: mdl-12680240

ABSTRACT

BACKGROUND: Our purpose was to determine the effects of amifostine, a cytoprotective agent, on doxorubicin tolerance and cardiotoxicity in rats. MATERIALS AND METHODS: Male Wistar rats were treated every other day with an intraperitoneal injection of amifostine or saline 30 minutes before intraperitoneal injection of doxorubicin or saline. Weight change was recorded, and contractile function was evaluated after 11 injections by means of the isolated heart. RESULTS: Weight evolution and cardiac function were significantly improved by 7 and 20 mg/kg amifostine (p < 0.001) but not by 50 mg/kg. The final weight were: controls 349 +/- 16 g; doxorubicin alone 258 +/- 54 g; with amifostine: 7 mg/kg 314 + 28 g; 20 mg/kg 312 +/- 32 g; 50 mg/kg 250 +/- 34 g. Left ventricular developed pressure were: controls 137 +/- 15 mmHg; doxorubicin alone 119 +/- 20 mmHg; with amifostine: 7 mg/kg 140 +/- 20 mmHg; 20 mg/kg 137 +/- 25 mmHg; 50 mg/kg 124 +/- 20 mmHg. CONCLUSION: Seven and 20 mg/kg amifostine protected rats from the toxicity of doxorubicin at the cumulative dose of 18 mg/kg during a 12-day treatment, with regard to weight loss and heart contraction.


Subject(s)
Amifostine/pharmacology , Antibiotics, Antineoplastic/toxicity , Doxorubicin/toxicity , Heart/drug effects , Animals , Body Weight/drug effects , Drug Interactions , In Vitro Techniques , Male , Myocardial Contraction/drug effects , Rats , Rats, Wistar , Ventricular Function, Left/drug effects
12.
Int J Cardiol ; 47(3): 273-80, 1995 Jan 06.
Article in English | MEDLINE | ID: mdl-7721504

ABSTRACT

We studied prospective recording of clinical, electrocardiographic, Doppler and echographic parameters in 32 patients with proven pulmonary embolism, matched with 32 patients with clinically suspected pulmonary embolism and normal perfusion scan or angiography. Thirty-seven per cent of cases and 16% of control subjects had clinical signs of right ventricular overload; S1-Q3-T3 ECG pattern was found in 11 cases and one control. Other clinical and ECG parameters did not reach significant difference. Echographic septum motion was abnormal in 42% of cases and 9% of controls (P < 0.05), end-diastolic right ventricular diameter was > 25 mm in 67% of cases and 11% of controls, ratio of end-diastolic right over left ventricular diameters increased over 0.6 in 67% of cases and 11% of controls, while Doppler examination found tricuspid regurgitant peak flow velocity > 2.5 m/s in 84% of cases vs. 10% of controls. According to these parameters, Doppler-echocardiography was normal in 6% of cases and 87% of control subjects (P < 0.001 for each). In suspected pulmonary embolism, our study shows that Doppler-echocardiography may be both sensitive and specific in emergency conditions and help the decision making for further invasive investigations.


Subject(s)
Echocardiography, Doppler , Pulmonary Embolism/diagnostic imaging , Acute Disease , Adult , Aged , Angiography , Case-Control Studies , Electrocardiography , Female , Humans , Logistic Models , Male , Middle Aged , Prospective Studies , Pulmonary Embolism/diagnosis , Sensitivity and Specificity
13.
J Invasive Cardiol ; 11(7): 416-20, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10745564

ABSTRACT

This study assesses the feasibility and safety of immediate sheath removal after coronary angioplasty with the use of 6 French (Fr) guiding catheters by the femoral route and weight-adjusted low-dose heparin (100 IU/kg). We prospectively evaluated such a strategy among a single-center cohort of 261 consecutive patients undergoing routine percutaneous transluminal coronary angioplasty (PTCA). Immediate sheath withdrawal was performed in cases when post-PTCA residual coronary stenosis was less than 30%, with or without stenting. One hundred eighty-two (70%) of the enrolled patients were eligible for immediate sheath removal. When compared with non-eligible patients (sheath removal 4 hours or more post-PTCA), we observed a reduction of hematoma occurrence (15% vs. 30%; p < 0.01), time to manual hemostasis of the puncture site (13.8 +/- 7 vs. 19.7 +/- 12 minutes; p < 0.0001), and time to hospital discharge (2.2 +/- 1.9 vs. 2.8 +/- 1.8 days; p < 0.02), while ischemic event rate was similar (1 vs. 2 non-Q wave myocardial infarction; 2 vs. 1 repeat PTCA for out-of-lab acute vessel closure). In conclusion, a good angiographic result at completion of PTCA using a 6 Fr sheath, even without stenting, makes an immediate sheath removal feasible at no increased risk and with a potential reduction in minor bleeding complications.


Subject(s)
Angioplasty, Balloon, Coronary/instrumentation , Body Weight , Device Removal , Heparin/administration & dosage , Myocardial Ischemia/therapy , Aged , Cohort Studies , Coronary Artery Bypass/adverse effects , Coronary Disease/therapy , Dose-Response Relationship, Drug , Feasibility Studies , Female , Heparin/therapeutic use , Humans , Male , Middle Aged , Myocardial Ischemia/etiology , Prospective Studies , Registries , Time Factors
14.
Arch Mal Coeur Vaiss ; 92(9): 1229-33, 1999 Sep.
Article in French | MEDLINE | ID: mdl-10533672

ABSTRACT

The authors report the case of a large mycotic right coronary aneurysm detected at echocardiography in a 45 year old patient with AIDS. Although emergency surgery was planned, the patient died of rupture of the aneurysm with cardiogenic shock and sudden pericardial tamponade. This case underlines the diagnostic value of echocardiography, by the transthoracic approach for para-cardiac masses and with the transoesophageal probe for accurate localisation and demonstration of the coronary origin. In this case, the CT scan was less useful than transthoracic echocardiography. Coronary angiography confirmed the strongly suggestive echocardiographic diagnosis and helped decide management strategy. Atheromatous coronary aneurysms may be treated by stenting but mycotic aneurysms require surgical management.


Subject(s)
Acquired Immunodeficiency Syndrome/complications , Aneurysm, Infected/diagnostic imaging , Coronary Aneurysm/diagnostic imaging , Aneurysm, Infected/complications , Aneurysm, Infected/microbiology , Coronary Aneurysm/complications , Echocardiography , Echocardiography, Transesophageal , Fatal Outcome , Humans , Male , Middle Aged , Mycobacterium avium/isolation & purification
15.
Arch Mal Coeur Vaiss ; 88(9): 1291-9, 1995 Sep.
Article in French | MEDLINE | ID: mdl-8526709

ABSTRACT

The aim of this study was to evaluate the results of systematic use of 6 French guiding catheters in conventional balloon coronary angioplasty without any restriction of indications apart from coronary lesions necessitating other techniques such as atherectomy. Therefore, after a learning period, 200 consecutive procedures performed between November 1993 and June 1994 for the treatment of 234 lesions were analysed prospectively. Fifty-one patients had stable and 70 unstable angina. In 79 cases, the angioplasty was performed on the culprit lesion of a myocardial infarction. An angiographic success was obtained for 206 lesions or 88% of cases which increased to 95% after exclusion of attempted recanalisation. There were 3 cases of damage to the ostium and 7 patients underwent implantation of a stent with the same catheter for occlusive or threatening dissection. There were 10 ischaemic complications (5%) (7 non-Q wave infarctions, 2 Q wave infarctions, 1 aorto-coronary bypass, no deaths) and 8 local complications at the site of arterial catheterisation during the hospital period. These results demonstrate the feasibility of coronary angioplasty with wide lumen 6 French guiding catheters and show that they amy be used in first intention for all conventional balloon angioplasty procedures.


Subject(s)
Angioplasty, Balloon, Coronary/instrumentation , Coronary Disease/therapy , Adult , Aged , Aged, 80 and over , Equipment Safety , Evaluation Studies as Topic , Feasibility Studies , Female , Humans , Male , Middle Aged , Prospective Studies
16.
Arch Mal Coeur Vaiss ; 88(11 Suppl): 1723-8, 1995 Nov.
Article in French | MEDLINE | ID: mdl-8815832

ABSTRACT

In general, there are two types of right heart thrombi diagnosed by echocardiography: mobile and non-mobile thrombi, more often located in the atrium than in the ventricle and a potential source of pulmonary embolism. However, they differ in several points: clinical context, clinical and echocardiographic presentations, embolic potential, prognosis and treatment. The result of peripheral venous thrombosis, mobile thrombus it is usually diagnosed during echocardiographic investigation of pulmonary embolism. The appearances are often that of serpentine thrombus floating in the right heart chambers associated with signs of acute cor pulmonale. It is a marker of imminent and often fatal embolism as it completes a previous and usually severe pulmonary embolism; the mortality is over 40%. It is a contra-indication for pulmonary angiography because of the risk of embolism and a therapeutic emergency. Some groups advocate surgical embolectomy and others thrombolysis. Its precise frequency in the acute stage of pulmonary embolism and its treatment remain to be determined by a prospective, multicentre clinical trial. The adherent non-mobile thrombus is usually implanted on the free wall of the right atrium or the interatrial septum. Its formation, in situ, is due to stasis secondary to decompensated congenital or acquired cardiac disease or to the presence of an intracardiac foreign body such as a pacing wire. It is less likely to cause pulmonary embolism. It decreases or disappears with anticoagulant therapy and the outcome is usually good. The differential diagnosis between a mobile thrombus and a Chiari network, or between an adherent thrombus and a vegetation on a intracardiac pacing wire may be difficult and requires transoesophageal echocardiography. The investigation of pulmonary embolism requires systematic echocardiography, one of the objectives of which is to search for right sided thrombi.


Subject(s)
Echocardiography, Doppler , Heart Diseases/diagnostic imaging , Pulmonary Embolism/etiology , Thrombosis/diagnostic imaging , Anticoagulants/therapeutic use , Atrial Function, Right , Diagnosis, Differential , Embolectomy/methods , Emergencies , Heart Atria , Heart Diseases/complications , Heart Diseases/mortality , Heart Diseases/therapy , Humans , Prognosis , Pulmonary Embolism/mortality , Pulmonary Embolism/therapy , Thrombolytic Therapy , Thrombosis/complications , Thrombosis/mortality , Thrombosis/therapy
17.
Arch Mal Coeur Vaiss ; 86(7): 1039-45, 1993 Jul.
Article in French | MEDLINE | ID: mdl-8291939

ABSTRACT

The objectives of this report were to analyse clinical presentation, echocardiographic features and diagnostic and therapeutic problems posed by an unusual form of thrombo-embolic disease: mobile right heart thrombosis. Systematic echocardiography in 170 cases of severe pulmonary embolism identified mobile right thrombi in 12 cases. The auscultatory findings were abnormal in 6 cases, 3 showing signs of tricuspid obstruction. Two-dimensional echocardiography showed an extremely mobile right atrial mass, sometimes prolapsing across the tricuspid valve, which was variously spheric, ovoid or worm-like; dilatation of the right heart chambers and echocardiographic signs of cor pulmonale were observed in all cases. The differential diagnosis with other embolic masses of the right atrium and, above all, with well-developed Chiari networks, may be difficult and requires transoesophageal echocardiography. Pulmonary angiography is contra-indicated because of the risk of embolism. Embolectomy under cardiopulmonary bypass was carried out in 8 patients, immediately after echocardiography in 6 cases. The thrombus was recovered from the right atrium in 6 cases and from the pulmonary artery in 2 cases: there was one operative death. Medical treatment was administered to 3 inoperable patients. The clinical and echocardiographic outcome was good in 2 of these but the third patient died; autopsy revealed thrombi in the right atrium and pulmonary artery. One patient died before any treatment could be given and autopsy showed the thrombus in the pulmonary artery. These results confirm the extreme instability of this type of thrombus and the risk of death due to its embolism.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Echocardiography , Heart Diseases/diagnostic imaging , Pulmonary Embolism/complications , Thrombosis/diagnostic imaging , Adult , Aged , Aged, 80 and over , Atrial Function, Right , Diagnosis, Differential , Embolectomy/methods , Emergencies , Female , Heart Atria , Heart Diseases/etiology , Heart Diseases/therapy , Humans , Male , Middle Aged , Pulmonary Embolism/therapy , Thrombosis/etiology , Thrombosis/therapy
18.
Arch Mal Coeur Vaiss ; 94(10): 1038-44, 2001 Oct.
Article in French | MEDLINE | ID: mdl-11725708

ABSTRACT

Left ventricular ejection fraction is a major prognostic factor of ischaemic heart disease. In the early phase of myocardial infarction, part of the myocardium may be stunned and responsible for marked segmental wall dysfunction which is potentially reversible. The authors studied the potential of low dose dobutamine echocardiography to predict secondary improvement of left ventricular systolic function in 21 patients with recent inaugural myocardial infarction without primary angioplasty. All patients were treated and the investigation was carried out up to 20 micrograms/Kg/min of dobutamine without unwanted side-effects or myocardial ischaemia. The detection of viability by this method was associated with improved wall motion of the affected segments in 74% of cases, most of which had benefited from myocardial revascularisation at control echocardiography performed 8 weeks later. If 4 or more segments were estimated to be viable initially, the left ventricular ejection fraction improved to a value comparable to that obtained at a dosage of 20 micrograms/Kg/min of dobutamine. On the other hand, there was no secondary improvement in 76% of segments estimated to be non-viable whether or not they had been revascularised. The sensitivity, specificity, positive and negative predictive values of low dose dobutamine echocardiography for prediction of myocardial recovery after recent infarction were respectively 71, 79, 74 and 76%. The results of this investigation show prognostic value and could be an aid to the decision concerning revascularisation of patients not having undergone primary angioplasty.


Subject(s)
Cardiotonic Agents , Dobutamine , Echocardiography/methods , Myocardial Infarction/complications , Myocardial Ischemia/pathology , Adult , Aged , Female , Humans , Male , Middle Aged , Myocardial Infarction/pathology , Myocardial Ischemia/diagnostic imaging , Prognosis , Systole , Ventricular Function, Left
19.
Arch Mal Coeur Vaiss ; 95(4): 263-8, 2002 Apr.
Article in French | MEDLINE | ID: mdl-12055764

ABSTRACT

The cumulative and definitive nature of chronic cardiotoxicity of anthracyclines requires a preventive strategy of early diagnosis. The authors undertook a prospective study of the association of echocardiography, mitral Doppler and pulsed Doppler tissue imaging of the left ventricular lateral and posterior walls in the context of this problem in 20 patients without cardiac disease undergoing cancer chemotherapy including anthracyclines. Doppler echocardiography was performed before the first session of chemotherapy and at the end of treatment, 6 +/- 4 months later. After a total cumulative dose of 227 +/- 91 mg/m2 of doxorubicine, there were no changes in left ventricular ejection fraction but a significant decrease in mitral E wave velocity (p = 0.04) and in E/A ratio (p = 0.01), suggesting early changes in left ventricular relaxation. The Doppler tissue examination confirmed the presence of radial and longitudinal abnormalities in myocardial relaxation (decreases in myocardial E wave velocities of the posterior and lateral walls of the left ventricle, p = 0.02 and p = 0.01, respectively). The peak velocity of the myocardial systolic wave (Sm) was significantly decreased in the lateral wall (p = 0.02) and approached statistical significance in the posterior wall (p = 0.07). These results suggest concomitant changes in myocardial systolic and diastolic function with moderate doses of anthracyclines. Therefore, pulsed Doppler tissue examination enables earlier detection of left ventricular cardiotoxicity with anthracyclines than classical echocardiographic parameters.


Subject(s)
Anthracyclines/adverse effects , Echocardiography , Heart Diseases/diagnostic imaging , Neoplasms/drug therapy , Adult , Echocardiography/methods , Female , Heart Diseases/chemically induced , Heart Rate , Heart Ventricles/diagnostic imaging , Humans , Male , Mitral Valve/diagnostic imaging , Prospective Studies , Ultrasonography, Doppler/methods , Ultrasonography, Doppler, Pulsed/methods
20.
Arch Mal Coeur Vaiss ; 93(11): 1291-5, 2000 Nov.
Article in French | MEDLINE | ID: mdl-11190457

ABSTRACT

The feasibility and safety of using hydrophilic guide wires were compared with those of standard guide wires for retrograde catheterization of aortic stenosis in a prospective randomised study. The performances of the guide wires were assessed by the time taken to catheterize the aortic valve (minutes) and the duration of radioscopy (minutes: grays). The success of the procedure was defined as presence of the guide in the left ventricle in less than 8 minutes. The two patient groups were comparable with respect to the severity of the aortic stenosis. Two failures of catheterisation were observed in the "standard guide wire" group compared with three failures with the hydrophilic guide wire. The mean catheterisation time of the "standard" group was 2.56 minutes compared with 3.12 minutes with the hydrophilic guide wire (p = 0.35 NS). This result was correlated with the duration of radioscopy and number of groups (respectively p = 0.18 NS and p = 0.5 NS). One case of tamponade and a transient ischaemic cerebral attack were observed in the "standard" group. This study does not show the hydrophilic guide wire to be superior to the standard guide wire for catheterisation of aortic stenosis. However, the hydrophilic guide wires were perfectly innocuous for this procedure.


Subject(s)
Aortic Valve Stenosis/therapy , Cardiac Catheterization/instrumentation , Aged , Cardiac Catheterization/methods , Equipment Design , Female , Humans , Male , Middle Aged , Treatment Outcome
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