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1.
Eur Heart J ; 22(13): 1128-35, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11428853

ABSTRACT

BACKGROUND: Primary therapies in acute myocardial infarction (thrombolysis and angioplasty) have inherent limitations which may be overcome by combining them. So far, no trial has demonstrated a clinical benefit in combining mechanical and pharmacological treatment strategies. METHODS: From January 1995 to December 1999, out of 1010 patients admitted to our institution for acute myocardial infarction, 148 had received pre-hospital full dose thrombolysis within 12 h of onset. One hundred and thirty-one patients were included and underwent immediate angioplasty and stenting when suitable, independent of the infarct-artery patency (TIMI grade flow 0-3). In-hospital outcome was assessed and clinical information was collected for a mean (+/-SD) of 2+/-1 years. RESULTS: Ninety-minute angiography revealed a patent (TIMI grade 3) infarct artery in 65 patients (49%). Immediate angioplasty was performed in 119 patients (91%) with stent implantation in 114 (96%). Angioplasty achieved TIMI 2, 3 flow in 98%, and complete patency (TIMI 3 flow) in 92%. Six other patients underwent deferred revascularization (surgery in one patient, angioplasty in five) and six received medical treatment. Stent thrombosis and reinfarction occurred in three patients (2.3%). In-hospital death occurred in six patients (4.6%), including four patients presenting with cardiogenic shock. Major bleeding was observed in 2.3% of cases. No patient had emergency surgery. Freedom from death and reinfarction at 2 years was 90% and freedom from death, reinfarction and target vessel revascularization was 83%. CONCLUSION: A strategy of combined reperfusion using full dose pre-hospital thrombolysis and immediate angioplasty with stent implantation in a non-selected acute myocardial infarction population is safe and achieves high and early patency rates. This preliminary experience suggests that a combined strategy in acute myocardial infarction may have a significant impact on both early and long-term outcomes.


Subject(s)
Angioplasty, Balloon, Coronary , Fibrinolytic Agents/therapeutic use , Myocardial Infarction/therapy , Myocardial Reperfusion , Stents , Thrombolytic Therapy , Combined Modality Therapy , Coronary Angiography , Female , Follow-Up Studies , Humans , Male , Middle Aged , Myocardial Infarction/epidemiology , Risk Factors , Time Factors , Treatment Outcome
2.
Arch Mal Coeur Vaiss ; 93(1): 21-6, 2000 Jan.
Article in French | MEDLINE | ID: mdl-11227714

ABSTRACT

The aim of this study was to assess the results of revascularisation by angioplasty and stenting in octogenarians in the acute phase of myocardial infarction. One hundred and four patients over 80 years of age were identified between January 1995 and April 1995 out of 906 patients admitted within 24 hours of the onset of myocardial infarction. The average age was 85 +/- 4 years with a female predominance (63.4%) and a high incidence of cardiogenic shock (28.8%). Ninety eight patients underwent angioplasty with coronary stenting in 81 patients (82.6%) within 39 +/- 35 min of hospital admission. A primary success was obtained in 96% of cases with restitution of TIMI 3 flow in 83.6% of cases. Hospital mortality was 26.5%, highly influenced by the presence of cardiogenic shock (60.7% versus 12.8% without shock). Univariate analysis showed cardiogenic shock (p < 0.0001) and ejection fraction (p = 0.009) to be predictive of mortality, and a tendency in favour of TIMI 3 flow (p = 0.07) and stent implantation (p = 0.09). Complications were rare: 1% of minor cerebrovascular accidents and 4% of vascular complications. There were no cases of emergency bypass surgery and only one patient had a recurrence of ischaemia at 30 days. The authors conclude that the results at 1 month in a high risk group of octogenarians seem to be in favour of an invasive management with coronary stenting in the acute phase of myocardial infarction.


Subject(s)
Angioplasty, Balloon , Myocardial Infarction/therapy , Myocardial Revascularization/methods , Stents , Aged , Aged, 80 and over , Female , Humans , Male , Prospective Studies , Risk Factors , Treatment Outcome
3.
Clin Intensive Care ; 6(2): 57-61, 1995.
Article in English | MEDLINE | ID: mdl-10150800

ABSTRACT

OBJECTIVE: To evaluate psychological status in consecutive survivors of ICU who needed mechanical ventilation (MV). DESIGN: Prospective study. SETTING: Twenty-four bed intensive care unit. PATIENTS: Fifty-four mechanically ventilated patients were considered for the study; 43 patients were included, but 11 refused or were unable to fill in the form. INTERVENTIONS: A 32-question form was filled out by the patients 48-96 hours after weaning from mechanical ventilation. MEASUREMENTS AND MAIN RESULTS: The mean characteristics of the patients were: age 51.6 years, simplified acute physiologic score (SAPS) 14, organ system failure (OSF) 1.57, OMEGA score 277, length of stay 29 days, length of mechanical ventilation 14 days. Thirty-three required sedation, 30 analgesia, 20 paralysis. The results were as follows: Pain: 13 suffered intolerable pain with a mean intensity of pain during care of 3.5/10. Comfort: 25 felt an inability to communicate, 18 were bothered by noise and 15 by light, while nine feared to be abandoned by staff. Sleep disorders: 28 remember dreaming with a personal judgement about these dreams (0 = pleasant, 10 = nightmare) of 7.6/10; 17 noticed increasing sleep disorders during their stay. Anxiety: 22 felt diffuse anxiety disorder and 16 described intense fear of dying at least once. Mood: 38 felt physical depression and 18 intellectual depression. Delirium or confusion: 33 had delirium or a confused state at the time of weaning and nine suffered hallucinations. Nine correctly appreciated their length of stay and 18 knew the date when they were interviewed. CONCLUSIONS: These results showed that psychological status is poor in ventilated ICU patients, which should be considered in their care.


Subject(s)
Critical Illness/psychology , Respiration, Artificial/psychology , Adult , Affect , Aged , Aged, 80 and over , Confusion/psychology , Female , Humans , Male , Middle Aged , Pain/psychology , Prospective Studies , Severity of Illness Index , Sleep Wake Disorders/psychology , Stress, Psychological/psychology , Surveys and Questionnaires
4.
Chest ; 104(3): 889-98, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8365306

ABSTRACT

Mortality of the adult respiratory distress syndrome (ARDS) remains high and could be increased by pulmonary barotrauma induced by positive-pressure mechanical ventilation. Extracorporeal CO2 removal combined with low-frequency positive-pressure ventilation (ECCO2R-LFPPV) has been proposed to reduce lung injury while supporting respiratory failure. Use of this technique in 23 patients resulted in the following: a dramatic and highly significant increase of PaO2 obtained rapidly with ECCO2R-LFPPV, allowing subsequent reduction in inspired oxygen fraction; a reduction of the risk of barotrauma evidenced by a significant decrease in pressures and insufflated volumes; a survival rate of 50 percent. Bleeding was the only complication related to the technique and was the cause of death in four patients. This method allowed improvement in gas exchange along with reduction of the risk of barotrauma caused by the ventilator.


Subject(s)
Barotrauma/prevention & control , Carbon Dioxide/blood , Extracorporeal Circulation , Lung Injury , Oxygen/blood , Positive-Pressure Respiration , Respiratory Distress Syndrome/therapy , Adolescent , Adult , Barotrauma/etiology , Extracorporeal Circulation/adverse effects , Extracorporeal Membrane Oxygenation , Female , Hemodynamics , Humans , Male , Middle Aged , Positive-Pressure Respiration/adverse effects , Respiratory Distress Syndrome/blood , Respiratory Distress Syndrome/physiopathology
5.
Leuk Lymphoma ; 10(4-5): 317-21, 1993 Jul.
Article in English | MEDLINE | ID: mdl-8220129

ABSTRACT

The study objective was to identify prognostic factors associated with survival in patients treated for acute leukemias who developed invasive aspergillosis (IA) during induction therapy. This retrospective analysis involved 21 patients treated in two hematologic centers over a six-year period. All were treated in protective isolated rooms with high-dose amphotericin B as soon as fungal infection was suspected. Ten (45%) of the twenty-one patients died. There was no statistical difference between the patients who survived and those who died in relation to the mean time of onset of IA or the total and mean daily dose of amphotericin B. On the other hand a favourable outcome correlated strongly with complete leukemic remission (p < 0.0001): all but one of the patients with objective residual leukemia died of IA, whereas all those who achieved complete hematological remission survived. In conclusion, it seems that the main vital prognostic factor in these leukemic patients with IA was the achievement of complete remission. We were unable to control IA in 10 of 11 patients with refractory leukemia, regardless of neutropenic status, despite early administration of high-dose amphotericin B. All the patients who achieved complete remission were successfully treated with amphotericin B.


Subject(s)
Aspergillosis/mortality , Leukemia/complications , Lung Diseases, Fungal/mortality , Acute Disease , Adolescent , Adult , Aged , Amphotericin B/therapeutic use , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Aspergillosis/complications , Aspergillosis/drug therapy , Humans , Leukemia/drug therapy , Leukemia/mortality , Lung Diseases, Fungal/complications , Lung Diseases, Fungal/drug therapy , Middle Aged , Neutropenia/chemically induced , Neutropenia/complications , Patient Isolation , Prognosis , Remission Induction , Retrospective Studies , Risk Factors , Survival Analysis , Treatment Outcome
6.
Eur J Med ; 2(3): 143-7, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8261054

ABSTRACT

OBJECTIVES: An open clinical study was conducted in the haematological department of an intensive care unit to investigate cure of staphylococcal septicaemia in neutropenic central venous catheter carriers without removal of the line. METHODS: Thirteen neutropenic patients with a central venous catheter were investigated. These patients were under treatment for haematological malignancies and had at least 2 blood cultures positive for Staphylococcus aureus or coagulase-negative staphylococcus. Antibiotherapy including vancomycin was given through the catheter. Each case was re-evaluated on day 3 of treatment. The catheter was removed if blood cultures remained positive or if clinical signs of bloodstream infection persisted or worsened. RESULTS: Clinical recovery was obtained in ten patients and bacterial eradication in twelve. Three patients died from septic shock: two deaths were not related to staphylococcal septicaemia; one death was due to a staphylococcal septic shock which occurred within a few hours of admission, despite of prompt removal of the central venous catheter. CONCLUSIONS: With appropriate antibiotherapy, leaving the central venous catheter in place would appear possible in cases of staphylococcal septicaemia. Response to treatment, however, must be carefully monitored.


Subject(s)
Catheterization, Central Venous , Neutropenia/complications , Sepsis/drug therapy , Staphylococcal Infections/drug therapy , Adult , Catheterization , Humans , Middle Aged , Vancomycin/administration & dosage
7.
Intensive Care Med ; 19(5): 279-84, 1993.
Article in English | MEDLINE | ID: mdl-8408937

ABSTRACT

OBJECTIVE: To evaluate the bacteriology of early aspiration pneumonia using a protected specimen brush and quantitative culture techniques, and whether penicillin G is adequate as initial treatment pending culture results. PATIENTS AND METHODS: 52 patients (of which 45 required mechanical ventilation) meeting usual clinical criteria for aspiration pneumonia were prospectively included. On admission, patients were given intravenous penicillin G and a protected specimen brush was performed < or = 48 h after. RESULTS: Cultures of the brush were negative (< 10(3) CFU/ml) in 33 patients (1 had blood cultures positive with S. pneumoniae) and positive (> or = 10(3) CFU/ml) for S. pneumoniae in 2 patients. Seventeen patients had a positive culture (> or = 10(3) CFU/ml) for at least one penicillin G resistant microorganism, with a total of 20 organisms (S. aureus: 6; H. influenzae: 2; Enterobacteriaceae: 8; P. aeruginosa: 3; C. albicans: 1). In 4 of these patients, a penicillin-sensitive pathogen was also recovered in significant concentrations (S. pneumoniae: 2; Streptococcus sp.: 2). These 17 patients with a resistant pathogen did not differ from the 35 other patients with respect to need for ventilatory support and mortality rate. By contrast, they were older (61.1 +/- 21.9 vs. 42.9 +/- 18.8 years; p < 0.005) and required longer mechanical ventilation (6.1 +/- 4.6 vs. 3.5 +/- 2.7 days; p < 0.03) and hospitalization (11.2 +/- 8.8 vs. 6.7 +/- 4.7 days; p < 0.02). Of 17 patients 12 with penicillin G resistant organisms versus 0/35 without, were in-hospital patients and/or had a digestive disorder (p < 0.001). CONCLUSION: The broad range of offending organisms seen in early aspiration pneumonia precludes use of any single empiric regimen, making protected specimen brush mandatory in many patients. Nevertheless, the involvement of S.pneumoniae in a notable proportion of our patients suggests that routine penicillin prophylaxis after early aspiration (at least in most patients with community-acquired aspiration) is warranted given the potential severity of pneumococcal sepsis in such patients.


Subject(s)
Bronchoscopes , Community-Acquired Infections/drug therapy , Community-Acquired Infections/microbiology , Cross Infection/drug therapy , Cross Infection/microbiology , Penicillin G/therapeutic use , Pneumonia, Aspiration/drug therapy , Pneumonia, Aspiration/microbiology , Specimen Handling/instrumentation , Adult , Age Factors , Aged , Asepsis/instrumentation , Community-Acquired Infections/diagnosis , Community-Acquired Infections/epidemiology , Comorbidity , Cross Infection/diagnosis , Cross Infection/epidemiology , Digestive System Diseases/epidemiology , Drug Resistance, Microbial , Female , Hospital Mortality , Humans , Infusions, Intravenous , Length of Stay/statistics & numerical data , Male , Middle Aged , Penicillin G/pharmacology , Pneumonia, Aspiration/diagnosis , Pneumonia, Aspiration/epidemiology , Prognosis , Prospective Studies , Respiration, Artificial/statistics & numerical data
8.
Am Rev Respir Dis ; 146(2): 295-9, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1489115

ABSTRACT

The management of patients with unilateral pneumonia and severe hypoxemia often represents a therapeutic challenge. Mechanical ventilation with the diseased lung uppermost may improve gas exchange, but it is not devoid of adverse effects. No hemodynamic measurements have been reported in patients ventilated in this manner; therefore, whether or not the improvement in PaO2 is counterbalanced by hemodynamic deterioration remains unknown. Almitrine bismesylate is a drug that seems able to improve gas exchange in patients with chronic obstructive pulmonary disease or the adult respiratory distress syndrome. The increase in PaO2 after its administration has been attributed to an improvement in ventilation-perfusion relationships. Its use has never been reported during unilateral pneumonia with severe hypoxemia. We therefore compared its effects with those of lateral position in eight consecutive mechanically ventilated patients with unilateral pneumonia. Blood gas and hemodynamic measurements were performed both at maintenance FIO2 and at an FIO2 of 1.0. Almitrine (1 mg/kg over 1 h) had no effect on PaO2 under either FIO2 condition. Cardiac output remained unchanged, but mean pulmonary artery pressure increased from 22.5 +/- 1.2 to 26.5 +/- 1.3 mm Hg (p < 0.02). By contrast, lateral position had striking effects on PaO2, which increased from 100 +/- 14 mm Hg in supine position to 156 +/- 23 mm Hg (p < 0.01) when the abnormal lung was placed uppermost at maintenance FIO2 and from 207 +/- 21 (supine) to 300 +/- 28 mm Hg (lateral) (p < 0.01) at FIO2 1.0.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Almitrine/therapeutic use , Bacterial Infections/therapy , Hypoxia/therapy , Pneumonia/therapy , Posture , Adult , Almitrine/administration & dosage , Almitrine/pharmacology , Bacterial Infections/complications , Bacterial Infections/physiopathology , Blood Gas Analysis , Female , Hemodynamics/drug effects , Humans , Hypoxia/etiology , Hypoxia/physiopathology , Male , Middle Aged , Oximetry , Pneumonia/complications , Pneumonia/physiopathology , Prospective Studies , Pulmonary Gas Exchange/drug effects , Ventilation-Perfusion Ratio/drug effects
9.
Intensive Care Med ; 18(6): 364-7, 1992.
Article in English | MEDLINE | ID: mdl-1281849

ABSTRACT

The effects of aprotinin, a broad-based proteinase inhibitor, in the management of hemorrhagic complications during prolonged venovenous extracorporeal CO2 removal in patients with adult respiratory distress syndrome are not evaluated. In two patients, aprotinin infusion was added to heparin to treat bleeding, occurring after few days of bypass and responsible for respiratory and hemodynamic deterioration. After aprotinin infusion (loading dose of 2 x 10(6) kIU followed by a continuous infusion of 5 x 10(5) kIU/h) combined with heparin, bleeding vanished until the end of bypass.


Subject(s)
Aprotinin/therapeutic use , Extracorporeal Membrane Oxygenation/adverse effects , Hemorrhage/drug therapy , Respiratory Distress Syndrome/therapy , Adult , Aprotinin/administration & dosage , Aprotinin/pharmacology , Blood Cell Count , Blood Coagulation Factors/analysis , Drug Therapy, Combination , Female , Hemorrhage/blood , Hemorrhage/etiology , Heparin/administration & dosage , Heparin/therapeutic use , Humans , Infusions, Intravenous , Injections, Intravenous , Respiratory Distress Syndrome/complications , Time Factors
10.
Am Rev Respir Dis ; 143(4 Pt 1): 738-43, 1991 Apr.
Article in English | MEDLINE | ID: mdl-2008985

ABSTRACT

Circuits on mechanical ventilators with cascade humidifiers are routinely changed every day or every other day, although humidifying cascades have been considered unlikely to increase the risk of respiratory infection because they do not generate aerosols. Moreover, changing ventilator tubings every 24 rather than every 48 h increases the risk of ventilator-associated pneumonia. To study the effects of ventilator circuit changes on the rate of nosocomial pneumonia and on patient and circuit colonization, 73 consecutive patients requiring continuous mechanical ventilation for more than 48 h were randomly assigned to either ventilator circuit changes every 48 h (Group 1, n = 38) or no change (Group 2, n = 35). Patients dying or being weaned before 96 h were not analyzed (Group 1 n = 3; Group 2 n = 7; leaving Group 1 n = 35 and Group 2 n = 28; p = 0.13). Ventilator-associated pneumonia was defined as the occurrence during mechanical ventilation or within 48 h after weaning of a new and persistent infiltrate on chest X-ray, purulent tracheal secretions, and a positive culture of a protected brush specimen (greater than or equal to 10(3) cfu/ml). Bacterial colonization was assessed every 48 h by quantitative cultures of pharyngeal swab, tracheal aspirate, humidifying cascade, and expiratory tubing trap. The two groups were similar in terms of age, indication for and duration of ventilation, and severity of illness.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Bacterial Infections/etiology , Cross Infection/etiology , Pneumonia/etiology , Respiration, Artificial/adverse effects , Aged , Bacteria/isolation & purification , Bacterial Infections/microbiology , Cross Infection/microbiology , Equipment Contamination , Female , Humans , Male , Middle Aged , Pharynx/microbiology , Pneumonia/microbiology , Prospective Studies , Respiration, Artificial/methods , Trachea/microbiology
11.
Crit Care Med ; 19(3): 346-51, 1991 Mar.
Article in English | MEDLINE | ID: mdl-1999095

ABSTRACT

OBJECTIVE: To assess the prognosis of patients with hematologic malignancies in acute renal failure who require hemodialysis. DESIGN: Retrospective study. SETTING: ICU. PATIENTS: Forty-three consecutive patients. METHODS: Prognostic analysis using both univariate and multivariate (stepwise regression) methods. RESULTS: Fifteen (35%) patients recovered from acute renal failure and 12 (28%) were discharged from the ICU. The prognosis of patients with acute renal failure linked to sepsis is poorer than the prognosis of the patients with acute renal failure from other etiologies. Only one patient survived in the former group (n = 26) and 11 in the latter group (n = 17); p less than .0001 in multivariate analysis. When accompanied by associated respiratory failure, mortality rate was higher (93% vs. 33%; p less than .0001). The Simplified Acute Physiology Score (SAPS) calculated within the first 24 hr of admission was significantly (p less than .001) related to mortality when the SAPS was greater than or equal to 13. The presence of neutropenia and the type of hematologic malignancy were not related to a worse prognosis. Tolerance to hemodialysis appeared good, and complications were rare.


Subject(s)
Acute Kidney Injury/therapy , Leukemia/complications , Renal Dialysis , Acute Kidney Injury/complications , Acute Kidney Injury/etiology , Acute Kidney Injury/mortality , Adolescent , Adult , Aged , Female , Humans , Intensive Care Units , Length of Stay , Male , Middle Aged , Retrospective Studies , Sepsis/complications
12.
Arch Intern Med ; 151(2): 310-6, 1991 Feb.
Article in English | MEDLINE | ID: mdl-1992958

ABSTRACT

The study objective was to describe the clinical, biologic, and hemodynamic features of adult overwhelming meningococcal purpura and to examine the prognostic factors by multivariate analysis at the time of admission to the intensive care unit. Thirty-five patients (greater than or equal to 13 years of age) with meningococcal infection, circulatory shock, and generalized purpuric lesions of abrupt onset were recorded in eight intensive care units from 1977 to 1989. The patients were young (mean age, 26.6 years; range, 13 to 68 years) and had been previously healthy. The female-to-male ratio was 3:1. Mortality was 54.3%, with most deaths occurring within the first 48 hours, usually secondary to irreversible shock with multiple organ failure. Ischemic complications (eight cases), prolonged heart failure (seven cases), and secondary septicemia (five cases) were the chief complications among survivors. Initial hemodynamic study after volume loading showed low stroke volume index (mean +/- SD, 29.4 +/- 13 mL/m2) and tachycardia (mean +/- SD, 138 +/- 16 beats per minute), a profile suggesting a greater myocardial depression than usually observed in gram-negative bacillary septic shock. Univariate prognostic analysis showed that four variables at the time of admission were associated with fatal outcome: a plasma fibrinogen level of 1.5 g/L or less, a factor V concentration of 0.20 or less, a platelet count lower than 80 x 10(9)/L, and a cerebrospinal fluid leukocyte count of 20 x 10(6)/L or less. Stepwise regression analysis showed that low fibrinogen level (less than or equal to 1.5 g/L) was the sole adverse prognostic variable (odds ratio = 2, 95% confidence interval, 1.5 to 2.7). Adult overwhelming meningococcal purpura is still associated with high mortality and morbidity. Low fibrinogen level at time of admission may permit early recognition of the most severely ill patients.


Subject(s)
Hemodynamics/physiology , Meningococcal Infections/physiopathology , Purpura/physiopathology , Adolescent , Adult , Aged , Factor V/metabolism , Female , Fibrinogen/metabolism , Humans , Leukocyte Count , Male , Meningococcal Infections/microbiology , Meningococcal Infections/mortality , Meningococcal Infections/therapy , Middle Aged , Multivariate Analysis , Platelet Count , Purpura/microbiology , Purpura/mortality , Purpura/therapy , Retrospective Studies , Survival Rate
13.
Intensive Care Med ; 16(5): 291-7, 1990.
Article in English | MEDLINE | ID: mdl-2212252

ABSTRACT

The course of 260 adults with haematological malignancies admitted to a medical intensive care unit was studied to evaluate the value of life support techniques and to research predictive factors. The overall in the medical intensive care unit (MICU) and hospital mortality rates were respectively 43% (113 patients) and 57% (148 patients). Among survivors, 64% (49 patients) were still alive after 6 months and 44% (35 patients) after 1 year. Among 34 haemodialysed patients, the MICU mortality was 67% (23 patients) and among 111 mechanically ventilated patients 85% (94 patients). Prolonged mechanical ventilation, more than seven days, was performed in 11 of the 17 survivors and did not influence long term survival. No individual predictor of mortality was found comparing survivors and non-survivors. However, SAPS, intractable sepsis and failure of more than one organ system were significantly different in non-survivors (p less than 0.001). Among the 20 patients requiring both mechanical ventilation and haemodialysis, only two left the MICU and both died soon thereafter. We conclude that life support therapy should be initiated in patients with haematological disorders and that prolonged mechanical ventilation is compatible with long term survival. However, the combination of mechanical ventilation and haemodialysis is always associated with a poor prognosis and therefore the use of both techniques simultaneously for one patient is questionable.


Subject(s)
Critical Care/standards , Hematologic Diseases/therapy , Neoplasms/therapy , Adult , Cause of Death , Evaluation Studies as Topic , Female , Hematologic Diseases/complications , Hematologic Diseases/mortality , Humans , Life Support Care/standards , Male , Middle Aged , Neoplasms/complications , Neoplasms/mortality , Neutropenia/epidemiology , Neutropenia/etiology , Prognosis , Renal Dialysis/standards , Respiration, Artificial/standards , Survival Rate
14.
Ann Med Interne (Paris) ; 141(6): 519-25, 1990.
Article in French | MEDLINE | ID: mdl-2285205

ABSTRACT

Between 1974 and 1988, 7 myocardial infarctions occurred in 6 (4 men, 2 women) out of 400 systemic lupus erythematosus patients. Their ages at the onset of lupus ranged from 13 to 44 years (m = 26). Four had renal involvement. Control of lupus in all 6 patients required high-dose steroids (at least 1 mg/kg/d of prednisone). Myocardial infarction occurred 4 to 19 years after the onset of lupus (m = 13). One patient died of cardiogenic shock. When the infarction occurred, only one patient was undergoing a lupus flare, while the disease was quiescent or slightly active in the 5 others. One patient had no risk factors for atheroma but had been taking steroids for 10 years. Among the other 4, one had hypertension, another had hyperlipidemia and 3 were smokers; they had been on steroids for 2, 4, 11 and 13 years. Coronary angiogram showed occlusion in all 4, but atheroma in only 2 patients. Lupus anticoagulant was present in 3 of these 4 patients. The mechanisms responsible for coronary occlusion in lupus patients are probably complex and interwoven. In addition to "classical" factors (i.e., vasculitis or steroid-induced atheroma), other factors, such as antiphospholipid antibodies and/or smoking, may play an important thrombogenic role.


Subject(s)
Lupus Erythematosus, Systemic/complications , Myocardial Infarction/etiology , Adult , Female , Fibrinolytic Agents/therapeutic use , Humans , Lupus Erythematosus, Systemic/mortality , Male , Middle Aged , Myocardial Infarction/drug therapy , Myocardial Infarction/mortality
20.
Intensive Care Med ; 14 Suppl 2: 488-91, 1988.
Article in English | MEDLINE | ID: mdl-3403793

ABSTRACT

Using a rapid computerized thermodilution method, we examined the evolution of right ventricular performance in 23 patients with septic shock. Nine survived the episode of septic shock. The other 14 patients died of refractory circulatory shock. Significant right ventricular systolic dysfunction, defined as decreased ejection fraction (-39%) and right ventricular dilation (+38%) was observed in all patients with septic shock. However, in the survivors, increased right ventricular preload may prevent hemodynamic evidence of right ventricular pump failure by utilizing the Frank-Starling mechanism to maintain stroke volume. Conversely, in the nonsurvivors, right ventricular dysfunction was more prononced two days after the onset of septic shock, leading to a fall in stroke. In the last patients, a decrease in contractility appears to be the major factor accounting for decreased right ventricular performance, as evidenced by the marked increase in end-systolic volume (+27%) without significant change in pulmonary artery pressure, during the later stage of septic shock. The observed right ventricular pump failure then appears associated with an alteration in diastolic mechanical properties of this ventricle, as suggested by a leftward displacement of the individual pressure-volume curves.


Subject(s)
Heart/physiopathology , Shock, Septic/physiopathology , Stroke Volume , Adult , Blood Pressure , Cardiac Output , Heart Ventricles/physiopathology , Humans , Middle Aged , Pulmonary Artery/physiopathology , Thermodilution/methods
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