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1.
Ann Fr Anesth Reanim ; 33(2): 128-34, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24462574

ABSTRACT

French law allows organ donation after death due to cardiocirculatory arrest. In the Maastricht classification, type III non-heart-beating donors are those who experience cardiocirculatory arrest after the withdrawal of life-sustaining treatments. French authorities in charge of regulating organ donation (Agence de la Biomédecine, ABM) are considering organ collection from Maastricht type III donors. We describe a scenario for Maastricht type III organ donation that fully complies with the ethical norms governing care to dying patients. That organ donation may occur after death should have no impact on the care given to the patient and family. The dead-donor rule must be followed scrupulously: the organ retrieval procedure must neither cause nor hasten death. The decision to withdraw life-sustaining treatments, withdrawal modalities, and care provided to the patient and family must adhere strictly to the requirements set forth in patient-rights legislation (the 2005 Léonetti law in France) and should not be influenced in any way by the possibility of organ donation. A major ethical issue regarding the family is how best to transition from discussing treatment-withdrawal decisions to discussing possible organ retrieval for donation should the patient die rapidly after treatment withdrawal. Close cooperation between the healthcare team and the organ retrieval team is crucial to minimize the distress of family members during this transition. Modalities for implementing Maastricht type III organ donation are discussed here, including the best location for withdrawing life-sustaining treatments (operating room or intensive care unit).


Subject(s)
Critical Care , Ethics Committees , Heart Arrest , Societies, Medical , Terminal Care/ethics , Tissue Donors/classification , Tissue and Organ Procurement/ethics , Airway Extubation , Attitude to Health , Brain Death , Conflict of Interest , Death , Dissent and Disputes , France , Humans , Patient Care Team , Professional-Family Relations , Prognosis , Terminal Care/legislation & jurisprudence , Terminal Care/standards , Third-Party Consent , Tissue and Organ Harvesting/legislation & jurisprudence , Tissue and Organ Harvesting/methods , Tissue and Organ Harvesting/standards , Tissue and Organ Procurement/legislation & jurisprudence , Tissue and Organ Procurement/standards , Withholding Treatment/legislation & jurisprudence
2.
Ann Fr Anesth Reanim ; 32(12): 833-7, 2013 Dec.
Article in French | MEDLINE | ID: mdl-24184168

ABSTRACT

OBJECTIVE: Ventilator-associated pneumonia (VAP) is the most common hospital-acquired infection in intensive care unit (ICU). The aim of the study was to evaluate the follow-up of the guidelines for VAP prevention. STUDY DESIGN: Retrospective, observational and multicenter study. PATIENTS AND METHODS: During one year, all patients with mechanical ventilation over 48 hours were included in the CCLIN-Ouest Network. The demographic characteristics of the patients, the use of specific protocol for VAP prevention and the density of incidence of VAP were recorded. The use of a protocol for preventing VAP (absence, incomplete, complete and care bundle (i.e. complete prevention of VAP with weaning mechanical protocol and sedation protocol)) was collected. RESULTS: 26 ICU with 5742 patients were included. Ten ICU (38%; 2595 patients) had no protocol for VAP prevention, eight ICU (31%; 1821 patients) had an incomplete protocol, five ICU (19%; 561 patients) had a complete protocol and three ICU (12%; 765 patients) had a care bundle. The density of incidence of VAP was 14.8‰ (Interquartile range [IQR]: 10.2-0.1) for no protocol group, 15.6‰ [IQR: 12.6-6.2] for incomplete protocol group, 11.0‰ [IQR: 9.1-14.0] for complete protocol group and 12.9‰ [5-7,7-9,9-12] for care bundle group (P=0.742). CONCLUSIONS: The compliance to prevention of VAP was poor. Proposals for improving practice are discussed.


Subject(s)
Critical Care/methods , Pneumonia, Ventilator-Associated/prevention & control , Aged , Clinical Protocols , Conscious Sedation , Female , Follow-Up Studies , France/epidemiology , Guideline Adherence , Health Care Surveys , Humans , Incidence , Intensive Care Units , Male , Middle Aged , Surveys and Questionnaires , Ventilator Weaning
5.
Intensive Care Med ; 37(5): 796-800, 2011 May.
Article in English | MEDLINE | ID: mdl-21369807

ABSTRACT

PURPOSE: To determine whether procalcitonin (PCT) levels could help discriminate isolated viral from mixed (bacterial and viral) pneumonia in patients admitted to the intensive care unit (ICU) during the A/H1N1v2009 influenza pandemic. METHODS: A retrospective observational study was performed in 23 French ICUs during the 2009 H1N1 pandemic. Levels of PCT at admission were compared between patients with confirmed influenzae A pneumonia associated or not associated with a bacterial co-infection. RESULTS: Of 103 patients with confirmed A/H1N1 infection and not having received prior antibiotics, 48 (46.6%; 95% CI 37-56%) had a documented bacterial co-infection, mostly caused by Streptococcus pneumoniae (54%) or Staphylococcus aureus (31%). Fifty-two patients had PCT measured on admission, including 19 (37%) having bacterial co-infection. Median (range 25-75%) values of PCT were significantly higher in patients with bacterial co-infection: 29.5 (3.9-45.3) versus 0.5 (0.12-2) µg/l (P < 0.01). For a cut-off of 0.8 µg/l or more, the sensitivity and specificity of PCT for distinguishing isolated viral from mixed pneumonia were 91 and 68%, respectively. Alveolar condensation combined with a PCT level of 0.8 µg/l or more was strongly associated with bacterial co-infection (OR 12.9, 95% CI 3.2-51.5; P < 0.001). CONCLUSIONS: PCT may help discriminate viral from mixed pneumonia during the influenza season. Levels of PCT less than 0.8 µg/l combined with clinical judgment suggest that bacterial infection is unlikely.


Subject(s)
Bacterial Infections/diagnosis , Calcitonin/blood , Influenza A Virus, H1N1 Subtype , Influenza, Human/diagnosis , Pneumonia/diagnosis , Protein Precursors/blood , Adult , Bacterial Infections/blood , Bacterial Infections/physiopathology , Biomarkers , Calcitonin Gene-Related Peptide , Female , France , Humans , Influenza, Human/physiopathology , Influenza, Human/virology , Male , Middle Aged , Pneumonia/physiopathology , Pneumonia/virology , Retrospective Studies , Sensitivity and Specificity , Severity of Illness Index
6.
Eur Respir J ; 37(2): 364-70, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20595153

ABSTRACT

Survival rates vary significantly between intensive care units, most notably in patients requiring mechanical ventilation (MV). The present study sought to estimate the effect of hospital MV volume on hospital mortality. We included 179,197 consecutive patients who received mechanical ventilation in 294 hospitals. Multivariate logistic regression models with random intercepts were used to estimate the effect of annual MV volume in each hospital, adjusting for differences in severity of illness and case mix. Median annual MV volume was 162 patients (interquartile range 99-282). Hospital mortality in MV patients was 31.4% overall, 40.8% in the lowest annual volume quartile and 28.2% in the highest quartile. After adjustment for severity of illness, age, diagnosis and organ failure, higher MV volume was associated with significantly lower hospital mortality among MV patients (OR 0.9985 per 10 additional patients, 95% CI 0.9978-0.9992; p = 0.0001). A significant centre effect on hospital mortality persisted after adjustment for volume effect (p < 0.0001). Our study demonstrated higher hospital MV volume to be independently associated with increased survival among MV patients. Significant differences in outcomes persisted between centres after adjustment for hospital MV volume, supporting a role for other significant determinants of the centre effect.


Subject(s)
Hospital Mortality , Intensive Care Units/statistics & numerical data , Respiration, Artificial , Adult , Aged , Aged, 80 and over , Critical Illness/mortality , Critical Illness/therapy , Diagnosis-Related Groups/statistics & numerical data , Female , Humans , Male , Middle Aged , Respiration, Artificial/statistics & numerical data , Severity of Illness Index , Survivors/statistics & numerical data , Treatment Outcome
7.
Med Mal Infect ; 40(5): 296-8, 2010 May.
Article in French | MEDLINE | ID: mdl-19616908

ABSTRACT

BACKGROUND: Peripheral blood stem cell transplantation is a frequent option, especially for patients with hematological malignancies. CASE REPORTS: A first patient received this treatment for acute myeloblastic leukemia, the second for Richter's syndrome (follicular lymphoma). In both cases, allograft (unrelated donor, non myeloablative conditioning) was followed by graft versus host disease (GVH) requiring an immunosuppressive treatment. Respectively 15 and three months after graft, these two patients presented with multiple organ failure including very severe hepatic dysfunction. The diagnosis was made according to positive blood PCR, positive BAL, and hepatic histological findings. DISCUSSION: Adenoviruses, frequent in pediatrics, can be responsible for extremely severe infections among immunocompromised adults. T lymphocyte depletion plays a key role. CONCLUSION: Adenoviral infections can be fatal among immunocompromised patients. Diagnostic improvement should lead to early treatment, which however, remains to be clearly defined.


Subject(s)
Adenovirus Infections, Human , Multiple Organ Failure , Adenovirus Infections, Human/etiology , Adult , Humans , Immunocompromised Host , Male , Middle Aged , Multiple Organ Failure/etiology
8.
J Phys Chem B ; 110(51): 25916-25, 2006 Dec 28.
Article in English | MEDLINE | ID: mdl-17181240

ABSTRACT

Multiwalled carbon nanotubes (MWCNTs) were grown on the fibers of a commercial porous carbon paper used as carbon-collecting electrodes in fuel cells. The tubes were then covered with Pt nanoparticles in order to test these gas diffusion electrodes (GDEs) for oxygen reduction in H2SO4 solution and in H2/O2 fuel cells. The Pt nanoparticles were characterized by cyclic voltammetry, transmission electron microscopy, and X-ray photoelectron spectroscopy. The majority of the Pt particles are 3 nm in size with a mean size of 4.1 nm. They have an electrochemically active surface area of 60 m2/g Pt for Pt loadings of 0.1-0.45 mg Pt/cm2. Although the electroactive Pt surface area is larger for commercial electrodes of similar loadings, Pt/MWCNT electrodes largely outperform the commercial electrode for the oxygen reduction reaction in GDE experiments using H2SO4 at pH 1. On the other hand, when the same electrodes are used as the cathode in a H2/O2 fuel cell, they perform only slightly better than the commercial electrodes in the potential range going from approximately 0.9 to approximately 0.7 V and have a lower performance at lower voltages.

9.
Ann Fr Anesth Reanim ; 25(11-12): 1111-8, 2006.
Article in French | MEDLINE | ID: mdl-17029679

ABSTRACT

OBJECTIVE: The Standard Mortality Ratio (SMR), comparing the observed in-hospital mortality to the predicted, may measure the intensive care units (ICU) performance. STUDY DESIGN: Multicentric retrospective national study. METHODS: A probability model using a severity score such SAPS II calculated the predicted mortality rate. A national French study has been undertaken to compare the SMR of ICUs and looked for explanation. RESULTS: One hundred six units, 34 were medical (32%), 18 surgical (17%) and 57 medical/surgical (51%) participated to the study. Forty-six ICUs (43%) were located in teaching hospitals. The SMR of the 87,099 stays was 0.84 (0.82-0.85). The SMR of ICUs varied from 0.41 to 1.55. Ten units had a SMR>0.85, which suggested a low performance. They had more stays for cardiovascular failures, as compared with others. The best units (SMR<0.82) had more stays for drug overdose. The SMR increased with the number of organ failures, from 0.47 with zero failure to 1.11 with 4 or more organ failures. The stays with cardiovascular failure, either unique or associated, had a higher SMR. The 7935 stays with a drug overdose had a SMR of 0.12 (0.10-0.14), which suggested a bad calibration of the model in theses cases. CONCLUSION: The case mix must be taken in account when comparing the ICUs performance by the mean of SMR, particularly when the units admitted a lot of drug overdoses.


Subject(s)
Hospital Mortality , Intensive Care Units/statistics & numerical data , Intensive Care Units/standards , Cardiovascular Diseases/mortality , France , Humans , Length of Stay , Retrospective Studies
10.
Rev Med Interne ; 26(10): 824-6, 2005 Oct.
Article in French | MEDLINE | ID: mdl-16084628

ABSTRACT

INTRODUCTION: High dose steroids and intravenous immunoglobulins are the gold treatment of acute immune thrombocytopenic purpura, before splenectomy for severe and refractory forms of the disease. Authors report two cases of severe acute refractory immune thombocytopenia with a dramatic response to plasma exchanges. EXEGESIS: The first case was an idiopathic form, complicated by hemorragic peritoneal effusion. After failure of steroids, intravenous immunoglobulins and splenectomy and 2 courses of rituximab, plasmapheresis normalized in 3 days platelet count. In the second observation, ITP was associated to systemic lupus with antiphospholipids antibodies and multivisceral failure, despite steroids and intravenous immunoglobulins. After 3 plasma exchanges, platelet count was normalized, and the patient is under remission after 24 months follow-up. CONCLUSION: Plasmapheresis must be evaluated as an emergency treatment in refractory forms of acute immune thrombocytopenic purpura.


Subject(s)
Plasmapheresis , Purpura, Thrombocytopenic/therapy , Acute Disease , Adult , Female , Humans , Platelet Count , Purpura, Thrombocytopenic/blood , Remission Induction , Time Factors , Treatment Outcome
11.
Pathol Biol (Paris) ; 52(8): 474-9, 2004 Oct.
Article in French | MEDLINE | ID: mdl-15465267

ABSTRACT

OBJECTIVE: Methicillin resistance and infections caused by methicillin-resistant Staphylococcus aureus represent a growing problem and a challenge for health-care institutions. We evaluated risk factors, morbidity and cost of infections caused by methicillin-resistant (MRSA) and methicillin-susceptible (MSSA) Staphylococcus aureus. DESIGN: We performed an un-matched case-control study in an 20-bed medical intensive care unit from 1994-2001 at Nantes teaching hospital, France. All patients with pneumonia, bacteraemia and urinary MRSA (cases) or MSSA (controls) nosocomial infections were included in the study. RESULTS: Twenty four patients with MRSA infection were compared to 64 patients with MSSA infections. Patients with MRSA infection were older (56 vs. 45 years, P < 0.01), had longer length of stay (47 vs. 35 days, P < 0.05) and were infected later (22 vs. 10 days, P < 0.00001) than patients with MSSA infection. No difference was observed between the two groups according to the Omega index, acute simplify index and mortality. MRSA infections involved extra cost due to antimicrobial treatment (184 vs. 72 Euros, P < 0.005) and length of stay (37,278 vs. 27,755 Euros, P < 0.05). CONCLUSION: Patient infected by MRSA seems to be different from patient infected by MSSA but without consequence on Omega index and mortality. But methicillin-resistance involves extra cost due to antimicrobial treatment and length of stay.


Subject(s)
Cross Infection/epidemiology , Intensive Care Units , Methicillin Resistance , Staphylococcal Infections/epidemiology , Staphylococcus aureus/isolation & purification , Costs and Cost Analysis , Cross Infection/economics , Cross Infection/microbiology , Drug Resistance, Bacterial , Female , France , Humans , Male , Morbidity , Risk Factors , Staphylococcal Infections/economics , Staphylococcus aureus/drug effects
12.
Ann Fr Anesth Reanim ; 23(1): 15-20, 2004 Feb.
Article in French | MEDLINE | ID: mdl-14980319

ABSTRACT

INTRODUCTION: Hospital units report on their inpatient care activity by writing yearly activity reports, which are used by their Medical Information Department (MID) to develop standardized summaries for communication to healthcare authorities. The data are categorized by uniform patient groups and used to describe inpatient care activity and to guide resource allocation. The objective of this study was to evaluate the completeness of activity reports from intensive care units (ICUs) in France. METHODS: Activity reports sent in 1998 and 1999 by French ICUs participating in the study were collected using dedicated abstracting software supplied to the relevant MIDs. Completeness of data in the activity reports was evaluated, with special attention to the SAPSII score, Omega rating of ICU procedures according to the Classification of Medical Procedures, and primary and secondary diagnoses. RESULTS: The 106 ICUs that volunteered for the study reported data on 107,652-hospital stays. Mean age and SAPSII were 55 +/- 21 years and 35 +/- 21 years, respectively. Mean ICU and hospital lengths of stay were 6.2 +/- 12.4 and 16.1 +/- 21.6 days, respectively. Mean ICU and hospital mortality rates were 15% and 19%. The SAPSII and Omega procedures were reported for 81% and 80% of stays, respectively. The SAPSII and Omega procedures were calculated or coded in 94% (100/106) and 96% (102/106) of ICUs, respectively. Mean number of Omega procedures was 4.3+/-3.9. However, only 5% (5/106) of ICUs entered the SAPSII for every stay, and 21% (22/106) of ICUs failed to enter the SAPSII for over 20% of stays. Similarly, 53% (56/106) of ICUs rated no more than five Omega procedures on average per stay. The primary diagnosis was reported for all stays, and the mean number of secondary diagnoses was 3.5 +/- 3.8. In 80% (86/106) of ICUs, no more than five secondary diagnoses were coded on average per stay. CONCLUSION: The analysis of this national database shows that data communicated to the MIDs and therefore to the healthcare authorities, are incomplete regarding SAPSII, ICU procedures, treatment intensity, and diagnoses. This may lead to the underestimation of ICU activity and resource needs, particularly if the SAPSII and selected procedures identified as markers for high-intensity critical care are used in the future.


Subject(s)
Intensive Care Units/statistics & numerical data , Age Factors , Data Collection , Databases, Factual , Documentation , France , Humans , Length of Stay
13.
Presse Med ; 29(2): 76-8, 2000 Jan 22.
Article in French | MEDLINE | ID: mdl-10682031

ABSTRACT

OBJECTIVE: The aim of this study was to assess renal and respiratory tolerance of aerosolized tobramycin in intubated and mechanically ventilated patients with nosocomial pneumonia. PATIENTS AND METHODS: This was a multicenter, randomized, double-blind, placebo controlled study. Thirty-eight mechanically ventilated patients with documented nosocomial pneumonia were included. Patients treated with intravenous betalactam and tobramycin were randomly allocated to receive aerosolized tobramycin (6 mg/kg/day, n = 21) or placebo (n = 17). The aerosol was administered via a pneumatic nebulizer once a day for 5 days. RESULTS: Respiratory tolerance was good in all but two patients. No acute renal failure occurred. By day 10, 7 patients in the tobramycin group (35%) had been extubated versus 3 in the placebo group (18.5%, p = 0.18). By day 28, 6 patients had died (2 in the tobramycin group and 4 in the placebo group, p = 0.23). CONCLUSION: Aerosolized tobramycin was well tolerated in ventilated patients with documented nosocomial pneumonia.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Cross Infection/drug therapy , Pneumonia, Bacterial/drug therapy , Tobramycin/administration & dosage , Adult , Aerosols , Aged , Anti-Bacterial Agents/adverse effects , Creatinine/blood , Data Interpretation, Statistical , Double-Blind Method , Drug Tolerance , Female , Humans , Intubation, Intratracheal , Kidney/drug effects , Male , Middle Aged , Placebos , Respiration/drug effects , Respiration, Artificial , Time Factors , Tobramycin/adverse effects , Treatment Outcome
14.
Intensive Care Med ; 24(10): 1040-6, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9840237

ABSTRACT

OBJECTIVE: To assess the incidence and to evaluate the feasibility of inter-unit continuous surveillance of intensive care unit (ICU)-acquired infections. DESIGN: Prospective multicentre, longitudinal, incidence survey. SETTING: Five ICUs in university hospitals in western France. PATIENTS: All patients admitted to the ICU during two 3-month periods (1994-1995). MEASUREMENTS AND RESULTS: The main clinical characteristics of the patients, ICU-acquired infections, length of exposure to invasive devices and the micro-organisms isolated were analysed. The study included 1589 patients (16970 patient-days) and the infection rate was 21.6 % (13.1 % of patients). The ventilator-associated pneumonia rate was 9.6 %, sinusitis 1.5 %, central venous catheter-associated infection 3.5 %, central venous catheter-associated bacteraemia 4.8 %, catheter-associated urinary tract infection 7.8 % and bacteraemia 4.5 %. The incidence density rate of ICU-acquired infections was 20.3% patient-days. Ventilator-associated pneumonia and sinusitis rates were 9.4 and 1.5% ventilation-days, respectively. Central venous catheter-associated infection and central venous catheter-associated bacteraemia rates were 2.8 and 3.8% catheter-days, respectively. The catheter-associated urinary tract infection rate was 8.5% urinary catheter-days and the bacteraemia rate 4.2% patient-days. Six independent risk factors for ICU-acquired infection were found by stepwise logistic regression analysis: absence of infection on admission, age > 60 years, length of stay, mechanical ventilation, central venous catheter and admission to one particular unit. A total of 410 strains of micro-organisms were isolated, 16.8 % of which were Staphylococcus aureus (58.0% methicillin-resistant). CONCLUSION: This prospective study using standardised collection of data on the ICU-acquired infection rate in five ICUs identified six risk factors. It also emphasized the difficulty of achieving truly standardised definitions and methods of diagnosis of such infections.


Subject(s)
Cross Infection/epidemiology , Infection Control/organization & administration , Intensive Care Units/statistics & numerical data , Interinstitutional Relations , Catheters, Indwelling/adverse effects , Cross Infection/etiology , Feasibility Studies , Female , France , Hospitals, University/organization & administration , Hospitals, University/statistics & numerical data , Humans , Incidence , Length of Stay/statistics & numerical data , Logistic Models , Male , Middle Aged , Prospective Studies , Respiration, Artificial/adverse effects , Risk Factors
15.
Ann Intern Med ; 129(3): 182-9, 1998 Aug 01.
Article in English | MEDLINE | ID: mdl-9696725

ABSTRACT

BACKGROUND: Acinetobacter baumannii is an important opportunistic pathogen that is rapidly evolving toward multidrug resistance and is involved in various nosocomial infections that are often severe. It is difficult to prevent A. baumannii infection because A. baumannii is ubiquitous and the epidemiology of the infections it causes is complex. OBJECTIVE: To study the epidemiology of A. baumannii infections and assess the relation between fluoroquinolone use and the persistence of multidrug-resistant clones. DESIGN: Three case-control studies and a retrospective cohort study. SETTING: A 20-bed medical and surgical intensive care unit. PATIENTS: Acinetobacter baumannii was isolated from 45 patients in urine (31%), the lower respiratory tract (26.7%), wounds (17.8%), blood (11.1%), skin (6.7%), cerebrospinal fluid (4.4%), and sinus specimens (2.2%). One death was due to A. baumannii infection. MEASUREMENTS: Antimicrobial resistance pattern and molecular typing were used to characterize isolates. The incidence of A. baumannii infection and the use of fluoroquinolones were calculated annually. RESULTS: Initially, 28 patients developed A. baumannii infection. Eleven isolates had the same antimicrobial susceptibility profile, genotypic profile, or both (epidemic cases), and 17 were heterogeneous (endemic cases). A surgical procedure done in an emergency operating room was the main risk factor for epidemic cases, whereas previous receipt of a fluoroquinolone was the only risk factor for endemic cases. The opening of a new operating room combined with the restriction of fluoroquinolone use contributed to a transitory reduction in the incidence of infection. When a third epidemiologic study was done, previous receipt of a fluoroquinolone was again an independent risk factor and a parallel was seen between the amount of intravenous fluoroquinolones prescribed and the incidence of endemic infection. CONCLUSION: Epidemic infections coexisted with endemic infections favored by the selection pressure of intravenous fluoroquinolones.


Subject(s)
Acinetobacter Infections/epidemiology , Acinetobacter Infections/microbiology , Acinetobacter/drug effects , Anti-Infective Agents/pharmacology , Cross Infection/epidemiology , Cross Infection/microbiology , Acinetobacter/classification , Acinetobacter/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Drug Resistance, Multiple , Female , Fluoroquinolones , Humans , Male , Middle Aged , Opportunistic Infections/epidemiology , Opportunistic Infections/microbiology , Retrospective Studies
16.
AJNR Am J Neuroradiol ; 19(4): 641-7, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9576648

ABSTRACT

PURPOSE: The purpose of this study was to determine the utility of spiral CT in the diagnosis of brain death. METHODS: Spiral CT was evaluated prospectively in 14 brain-dead patients and in 11 healthy subjects. A two-phase protocol was used. Twenty seconds after intravenous injection of a nonionic iodinized contrast medium, the CT table was drawn through the gantry at a rate of 10 mm/s while scanning was in progress. The second scanning phase was started automatically a mean of 54 seconds later, using the same parameters. Opacification or absence of opacification of carotid, vertebral, and basilar arteries and intracerebral veins was ascertained for each image in both phases. The diagnosis of brain death was confirmed by elecroencephalography (n = 7), angiography (n = 5), or both (n = 2). Statistical analysis with the Fisher exact test enabled us to compare the brain-dead patients with the healthy control subjects. RESULTS: In brain death, the pericallosal and terminal arteries of the cortex did not opacify during the two phases of spiral CT, whereas the superficial temporal arteries were always visible. The internal cerebral veins, the great cerebral vein, and the straight sinus did not opacify, whereas the superior ophthalmic veins were visible on both sides 13 times. For each vessel type, specificity was 100% for nonvascular opacification criteria on the right and left sides. CONCLUSION: Two-phase spiral CT can demonstrate the absence of intracerebral blood flow in brain death.


Subject(s)
Brain Death/diagnostic imaging , Tomography, X-Ray Computed/methods , Adolescent , Adult , Cerebral Angiography , Child , Electroencephalography , Female , Humans , Male , Middle Aged , Subtraction Technique
17.
J Infect Dis ; 171(1): 232-6, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7798671

ABSTRACT

Animal study results have suggested a role in sepsis for human interleukin for DA1.a cells/leukemia inhibitory factor (HILDA/LIF). HILDA/LIF and interleukin-6 (IL-6) levels were prospectively studied by serial ELISAs in 34 septic patients. HILDA/LIF was detected in 11 of 34 patients at plasma levels of 100-37,000 pg/mL. Peak HILDA/LIF levels correlated with increased temperature and creatinine and IL-6 and with decreased arterial CO2 (P < .05). Multivariate analysis showed that shock and decreased arterial CO2 accounted for 75% of peak HILDA/LIF plasma variations (R2 = .753). Fatal outcome was most often associated with detectable HILDA/LIF (> 56 pg/mL) and peak IL-6 plasma levels > 850 pg/mL (sensitivity, 83%; specificity, 87%), but both (at respective levels of > 480 and > 850 pg/mL) were associated with fatal outcome. HILDA/LIF was detected in septic patients exhibiting shock, and its levels correlated with higher mortality and shorter survival.


Subject(s)
Growth Inhibitors/blood , Lymphokines/blood , Shock, Septic/immunology , Systemic Inflammatory Response Syndrome/immunology , APACHE , Adult , Aged , Aged, 80 and over , Analysis of Variance , Enzyme-Linked Immunosorbent Assay , Female , Humans , Interleukin-6/blood , Leukemia Inhibitory Factor , Male , Middle Aged , Prognosis , Shock, Septic/mortality , Survival Analysis , Systemic Inflammatory Response Syndrome/mortality
18.
Bone Marrow Transplant ; 13(1): 19-26, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8019449

ABSTRACT

We investigated T cell receptor (TCR) alpha/beta and gamma/delta repertoire reconstitution after autologous and allogeneic bone marrow transplantation (BMT) in humans using 13 monoclonal antibodies directed at constant and variable regions of the TCR. The TCR gamma/delta repertoire was studied kinetically during the first month and then 1 year post-BMT whereas alpha/beta peripheral blood T lymphocytes (PBTL) were studied within the first 3 months and 1 year post-BMT. Through these two studies, we found 7 of 26 patients with over-represented TCR gamma/delta subsets during the early period post-BMT. Moreover, during this period the V gamma 9V delta 2 frequency among gamma/delta T cells was found to be higher than among normal donors. Study on TCR alpha/beta T cells also revealed abnormally expanded V-specific subset (5 of 10 patients within 3 months following BMT) demonstrating that repertoire alteration early after BMT is a general phenomenon concerning potentially all T cell subsets. More surprisingly, the alpha/beta T cell repertoire was also found to be altered late after BMT (7 of 15 patients after 1 year post-BMT presented one or more overepresented alpha/beta TCR subset). These alterations of TCR combinatorial diversity should be taken into account in understanding the immunological status of patients after BMT.


Subject(s)
Bone Marrow Transplantation/immunology , T-Lymphocyte Subsets/immunology , Adolescent , Adult , Child , Female , Gene Expression , Humans , Leukemia/genetics , Leukemia/immunology , Leukemia/surgery , Leukocyte Count , Lymphoma/genetics , Lymphoma/immunology , Lymphoma/surgery , Male , Middle Aged , Neoplasms/genetics , Neoplasms/immunology , Neoplasms/surgery , Phenotype , Receptors, Antigen, T-Cell, alpha-beta/genetics , Receptors, Antigen, T-Cell, gamma-delta/genetics
19.
Pediatr Pulmonol ; 8(4): 268-72, 1990.
Article in English | MEDLINE | ID: mdl-2371075

ABSTRACT

The precise diagnosis of lower respiratory tract infection in the critically ill newborn remains a difficult challenge. The bronchoscopic protected specimen brush (PSB) is a reliable method in intubated adults. Because the bronchoscopic procedure is not generally available for young children, Zucker proposed a blind technique for introducing the PSB into the distal airways. His results were promising but were not compared with any bacteriologic reference method. Therefore, we wanted to evaluate this technique in comparison with the open lung biopsy (OLB) when it could be ethically accomplished. Eleven PSB were collected simultaneously with an OLB. The sensitivity of the PSB procedure was 100%, its specificity 88%, its positive predictive value 66%, and its negative predictive value 100%. There were no complications secondary to the PSB procedure. In this short study, the PSB procedure using a blind technique is safe and feasible to obtain uncontaminated specimens in intubated and ventilated newborns, and is largely accurate in identifying the bacterial etiologic agent of lower respiratory tract infection.


Subject(s)
Bacterial Infections/diagnosis , Bronchoscopes , Pneumonia/diagnosis , Respiration, Artificial , Bacterial Infections/pathology , Biopsy/methods , Humans , Infant , Infant, Newborn , Lung/pathology , Pneumonia/pathology , Predictive Value of Tests , Prospective Studies , Specimen Handling , Trachea/microbiology
20.
Agressologie ; 31(8 Spec No): 503-4, 1990.
Article in French | MEDLINE | ID: mdl-2089970

ABSTRACT

A prospective study was carried out in a medical and surgical ICU to determine the incidence of nosocomial urinary tract infection (NUTI) and to identify the most important risk factors. Over a 6 month period, 180 patients were included. All had an indwelling catheter. Six risk factors were studied: age, sex, illness (medical, surgical, trauma), hospital or extra-hospital origin, simplified acute physiology score and length of bladder catheterization. Forty three patients developed a NUTI. Length of bladder catheterization was the only significant different risk factor in infected and non-infected patients. Kaplan Meir analysis was used to determine time to development of NUTI. The risk rose from 19% for 5 day long catheterization to 50% for 14 day long catheterization.


Subject(s)
Cross Infection/epidemiology , Urinary Catheterization , Urinary Tract Infections/epidemiology , Adult , Catheters, Indwelling , Female , Humans , Incidence , Intensive Care Units , Male , Prospective Studies , Risk Factors , Time Factors
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