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1.
J Integr Bioinform ; 8(3): 176, 2011 Sep 15.
Article in English | MEDLINE | ID: mdl-21926439

ABSTRACT

Many real applications have the imbalanced class distribution problem, where one of the classes is represented by a very small number of cases compared to the other classes. One of the systems affected are those related to the recovery and classification of scientific documentation. Sampling strategies such as Oversampling and Subsampling are popular in tackling the problem of class imbalance. In this work, we study their effects on three types of classifiers (Knn, SVM and Naive-Bayes) when they are applied to search on the PubMed scientific database. Another purpose of this paper is to study the use of dictionaries in the classification of biomedical texts. Experiments are conducted with three different dictionaries (BioCreative, NLPBA, and an ad-hoc subset of the UniProt database named Protein) using the mentioned classifiers and sampling strategies. Best results were obtained with NLPBA and Protein dictionaries and the SVM classifier using the Subsampling balancing technique. These results were compared with those obtained by other authors using the TREC Genomics 2005 public corpus.


Subject(s)
Classification/methods , Data Mining/methods , Dictionaries as Topic
2.
Arch Pediatr ; 9(8): 805-9, 2002 Aug.
Article in French | MEDLINE | ID: mdl-12205790

ABSTRACT

UNLABELLED: The perinatal manifestations of the long QT syndrome are rare, but early diagnosis and therapy are necessary to prevent sudden death. CASE REPORTS: A long QT syndrome was diagnosed in two neonates who presented with foetal bradycardia. In one case, a mutation in the gene KCNQ1 was identified, and a long QT syndrome was diagnosed in the mother and two brothers of the neonate. On beta-blocker therapy, one infant became free of long QT syndrome related symptoms, but a sudden death of the second infant occurred. CONCLUSION: The long QT syndrome should be considered in the differential diagnosis of foetal bradycardia. Early treatment of the neonate and his family may prevent ventricular arrhythmias and sudden death.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Bradycardia/etiology , Long QT Syndrome/congenital , Potassium Channels, Voltage-Gated , DNA Mutational Analysis , Death, Sudden, Cardiac , Diagnosis, Differential , Electrocardiography , Fatal Outcome , Female , Humans , Infant, Newborn , KCNQ Potassium Channels , KCNQ1 Potassium Channel , Long QT Syndrome/diagnosis , Long QT Syndrome/drug therapy , Pedigree , Potassium Channels/genetics
3.
Presse Med ; 29(16): 1451-4, 2000 Sep 16.
Article in French | MEDLINE | ID: mdl-11039084

ABSTRACT

BACKGROUND: Subgaleal hemorrhage results from a pericranial effusion of blood subsequent to neonatal trauma. This exceptional situation compared with other pericranial effusion conditions in the neonate may be life-threatening. CASE REPORTS: We report the obstetrical and neonatal data in 5 cases of subgaleal hemorrhage observed in our unit over an 8-year 8-month period. We detail one particularly demonstrative case which illustrates the potentially serious course of certain clinical presentations. DISCUSSION: Subgaleal hemorrhage is a clinical diagnosis. Signs of hemorrhagic shock are associated with hemostasis disorders in the more severe forms of the condition. The main risk factor is instrumental delivery with suction. Careful monitoring is required.


Subject(s)
Birth Injuries , Extraction, Obstetrical/adverse effects , Hematoma/etiology , Scalp , Apgar Score , Birth Injuries/therapy , Emergencies , Female , Follow-Up Studies , Hematoma/therapy , Humans , Infant, Newborn , Male , Time Factors , Vacuum Extraction, Obstetrical/adverse effects
4.
Acta Biotheor ; 45(3-4): 237-50, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9436298

ABSTRACT

We have measured the change of lung mechanical parameters on isolated rabbit lungs exposed to chlorine gas (Cl2). Experimental results show parallel increase in elastance and resistance of impaired lungs. We tried to determine whether this may be explained by a reduction of the ventilated areas in the lung, consecutive to closure of some airways. We have been tried to simulate these experimental results by studying the effects of various airways occlusions imposed on two concurrent models (symmetrical and dissymmetrical) of the tracheo-bronchial tree. For each model, we successively evaluated the resistance of the normal lung, simulated a partial peripheral airways occlusion and estimated the induced changes in total resistance. Analytical expressions of the "occluded lung" elastance and resistance have been found for the symmetrical model but not for the dissymmetrical model (a graphical approach is proposed). With the symmetrical model, simulated results are comparable to experimental ones when the occlusion level is proximal. Whatever the dissymmetry level (delta) of the fractal tree model, we could not simulate the expected increase in resistance with the observed increase in elastance. We conclude that either the occlusion in non homogeneous or the lung impairment is not only a reduction in ventilated areas.


Subject(s)
Airway Resistance/drug effects , Chlorine/toxicity , Disease Models, Animal , Lung Compliance/drug effects , Respiratory Distress Syndrome/chemically induced , Airway Resistance/physiology , Animals , Blood-Air Barrier/drug effects , Blood-Air Barrier/physiology , Gases , Lung Compliance/physiology , Pulmonary Edema/chemically induced , Pulmonary Edema/physiopathology , Rabbits , Respiratory Distress Syndrome/physiopathology , Respiratory Mechanics/drug effects , Respiratory Mechanics/physiology
5.
Eur J Clin Pharmacol ; 45(2): 123-8, 1993.
Article in English | MEDLINE | ID: mdl-8223832

ABSTRACT

The predictive ability of population pharmacokinetic parameters of tianeptine, obtained from a mixed effect analysis of pre-marketing pharmacokinetic studies, was evaluated using tianeptine plasma concentrations obtained during a large multi-center post-marketing surveillance study. The mean prediction error was 7.8 ng.ml-1 and the root mean square prediction error was 52.1 ng/ml when initial estimates of population pharmacokinetic parameters were used to predict drug concentrations in one half of the post-marketing data. When the population parameters were revised to reflect the data collected in the first half of the post-marketing study, the mean prediction error was reduced to -3.2 ng.ml-1 and the root mean square prediction error was reduced to 29.5 ng.ml-1. These results suggest that population pharmacokinetic parameters obtained from pre-marketing data may not accurately predict drug concentrations in patients receiving the drug in the post-marketing setting. Once the population parameters are updated to reflect data from the post-marketing period, the predictive ability of the data-base increases, but substantial variability in the prediction error remains.


Subject(s)
Antidepressive Agents, Tricyclic/blood , Product Surveillance, Postmarketing , Thiazepines/blood , Adolescent , Adult , Antidepressive Agents, Tricyclic/pharmacokinetics , Female , Humans , Male , Pharmacoepidemiology , Predictive Value of Tests , Thiazepines/pharmacokinetics , Time Factors
6.
Eur J Clin Pharmacol ; 45(2): 173-9, 1993.
Article in English | MEDLINE | ID: mdl-8223841

ABSTRACT

Two thousand three hundred and thirty five plasma concentrations of tianeptine from 112 patients enrolled in nine studies of tianeptine pharmacokinetics performed prior to the marketing of the drug were pooled for analysis using mixed-effect modeling. Studies represented a combination of single dose and multiple dosing at steady-state. Tianeptine plasma concentration time data were fit to a two compartment model with first order absorption using the NONMEM computer program. The results of this analysis suggested that alcoholism is associated with significant increase in clearance (124% increase) and volume of the central compartment (161% increase). The volume of the peripheral compartment is significantly lower in women (31% decrease) and in depressed patients (59% decrease). The population mean (interindividual variability) clearance was equal to 0.17 l.h-1 x kg-1 (28.6%), the volume of central compartment was 0.13 l.kg-1 (60.4%), intercompartmental clearance was 0.07 l.h-1 x kg-1 (30.1%), volume of the tissue compartment was 1.17 l.kg-1 (28.3%), and the absorption rate constant was 0.63 h-1 (21.8%). The residual variability was approximately 30% at concentrations expected during clinical use of the drug. Because of the increased clearance, alcoholic patients would be expected to have significantly reduced concentrations during steady-state dosing. These population parameters provide a basis for developing initial dosing recommendations and for performing bayesian evaluations of drug concentrations obtained in post-marketing studies.


Subject(s)
Antidepressive Agents, Tricyclic/pharmacokinetics , Thiazepines/pharmacokinetics , Administration, Oral , Adult , Aged , Aged, 80 and over , Alcoholism/metabolism , Antidepressive Agents, Tricyclic/administration & dosage , Antidepressive Agents, Tricyclic/blood , Databases, Factual , Female , Humans , Male , Metabolic Clearance Rate , Middle Aged , Models, Biological , Thiazepines/administration & dosage , Thiazepines/blood
7.
Br J Psychiatry Suppl ; (15): 66-71, 1992 Feb.
Article in English | MEDLINE | ID: mdl-1389025

ABSTRACT

Alcohol interferes with the central metabolism of the catecholamines and especially with indolamines (5-HT). Thus, the use of an antidepressant such as tianeptine, whose main neurochemical effect is to increase the reuptake of 5-HT, seems to be particularly indicated for the continued treatment of depressed patients after alcohol withdrawal. This study evaluated the therapeutic efficacy and acceptability during long-term administration of tianeptine in depressed patients (major depressive episode or dysthymic disorder) in a multicentre trial, after withdrawal from alcohol abuse or dependence. The results relate to 130 depressed patients, who abstained from alcohol and received treatment for a year. Only one patient dropped-out because of side-effects, and medication was interrupted in 5% of subjects because of alcoholic relapses. Prescribed in the long term, tianeptine did not produce orthostatic hypotension, changes in bodyweight, or alterations in the ECG. All changes found in haematological and biochemical investigations suggested an improvement in patients' physical state. This, and other studies, indicate that tianeptine appears to have the potential to be a safe antidepressant, which might be particularly useful in those patients who are susceptible to the side-effects of psychotropic drugs.


Subject(s)
Alcoholism/rehabilitation , Antidepressive Agents, Tricyclic/administration & dosage , Depressive Disorder/drug therapy , Ethanol/adverse effects , Substance Withdrawal Syndrome/drug therapy , Thiazepines/administration & dosage , Adolescent , Adult , Aged , Alcoholism/psychology , Antidepressive Agents, Tricyclic/adverse effects , Depressive Disorder/psychology , Female , Follow-Up Studies , Humans , Long-Term Care , Male , Middle Aged , Personality Inventory , Recurrence , Substance Withdrawal Syndrome/psychology , Thiazepines/adverse effects
8.
Br J Psychiatry Suppl ; (15): 61-5, 1992 Feb.
Article in English | MEDLINE | ID: mdl-1389024

ABSTRACT

Tianeptine is a new tricyclic compound whose principal action is to increase the reuptake of serotonin. In a multicentre trial in which 380 depressed patients were treated for one year, tianeptine produced a significant reduction in the MADRS scores from day 14, with a sustained reduction maintained for up to 12 months; other measures of efficacy (HRSA, HSCL, and CGI) also reflected the improvement. Only 11% of patients withdrew because of recurrence of depression and 2% because of side-effects, which were mainly drowsiness, irritability, and gastrointestinal disturbance. Apart from a minor reduction in heart rate, unaccompanied by any conduction changes, no clinically relevant changes in vital signs or laboratory tests were seen. Seven subjects who attempted suicide by tianeptine overdose had favourable outcomes, in spite of also taking other psychotropic drugs or alcohol. No evidence of tolerance or withdrawal symptoms was seen after treatment was stopped. These results suggest that tianeptine has the potential to provide safe antidepressant activity in both the acute and chronic phases of treatment.


Subject(s)
Antidepressive Agents, Tricyclic/administration & dosage , Depressive Disorder/drug therapy , Thiazepines/administration & dosage , Adolescent , Adult , Aged , Aged, 80 and over , Alcoholism/psychology , Alcoholism/rehabilitation , Antidepressive Agents, Tricyclic/adverse effects , Depressive Disorder/psychology , Female , Follow-Up Studies , Humans , Long-Term Care , Male , Middle Aged , Personality Inventory , Thiazepines/adverse effects
9.
Presse Med ; 20(37): 1828-36, 1991 Nov 14.
Article in French | MEDLINE | ID: mdl-1836615

ABSTRACT

Tianeptine is a new tricyclic antidepressant. Double blind studies comparing tianeptine with imipramine and amitriptyline have shown the effectiveness of tianeptine's antidepressor action, its properties of non-specific symptoms related to behaviour disorders (anxiety, inhibition ...) and its action on somatic complaints expressed by depressed patients. Tianeptine is an effective antidepressant in cases of depression with anxiety or alcoholism and also leads to good therapeutic response in cases of dysthemia. In depressions with melancholy and endogenous criteria, the expected percentage of responding patients has been observed with tianeptine. A reinforcement of the therapeutic effect has been demonstrated after 6 months of treatment. Its excellent clinical and parclinical acceptability, especially in long term treatment of patients at risk such as elderly depressed patients or alcoholic patients, makes tianeptine a first intention antidepressant.


Subject(s)
Anxiety Disorders/drug therapy , Depressive Disorder/drug therapy , Psychoses, Alcoholic/complications , Thiazepines/therapeutic use , Amitriptyline/therapeutic use , Antidepressive Agents/therapeutic use , Antidepressive Agents, Tricyclic/therapeutic use , Anxiety Disorders/complications , Depressive Disorder/complications , Double-Blind Method , Humans , Placebos , Thiazepines/adverse effects
10.
Presse Med ; 20(37): 1844-52, 1991 Nov 14.
Article in French | MEDLINE | ID: mdl-1836617

ABSTRACT

An open multicenter study of the efficacy and acceptability of tianeptine, a new antidepressant structurally related to tricyclic antidepressants, was conducted by 36 gerontologists. There were 228 patients in the study; 140 were treated for one year. The patients' overall MADRS score started to decrease on day 14 and continued to decline to month 3. An improvement in depression was again observed near the end of the treatment period from month 9 to month 12. This pattern of improvement was also found with the HARS, the first item on the CGI scale and the Zung self-evaluation scale. These findings demonstrate the beneficial effect of long-term treatment in depressed elderly patients. Ten patients (4.4 percent) dropped out because of side effects: mainly drowsiness, anxiety or gastrointestinal disorders. The benefit/risk ratio (CGI, item 3), an expression of treatment effectiveness and acceptability, was very satisfactory even in these elderly patients. Regularly performed laboratory tests and clinical examinations (including weight and blood pressure) revealed no significant changes. Finally, somatic disorders, essentially cardiovascular and neurological diseases often occurring in depressed patients, remained remarkably quiescent throughout the entire treatment period.


Subject(s)
Depressive Disorder/drug therapy , Thiazepines/therapeutic use , Aged , Aged, 80 and over , Analysis of Variance , Antidepressive Agents, Tricyclic/administration & dosage , Antidepressive Agents, Tricyclic/therapeutic use , Blood Pressure Determination , Body Weight , Cardiovascular Diseases/blood , Cardiovascular Diseases/complications , Depressive Disorder/blood , Depressive Disorder/complications , Electrocardiography , Female , Follow-Up Studies , Humans , Male , Thiazepines/administration & dosage
11.
Presse Med ; 20(37): 1858-63, 1991 Nov 14.
Article in French | MEDLINE | ID: mdl-1836619

ABSTRACT

The cardiovascular effects of tianeptine were assessed by a specific placebo-controlled trial in healthy volunteers and by heart rate, blood pressure and electrocardiogram data analyses in five studies enrolling depressed patients. In two of these studies the effects of tianeptine were compared to those of amitriptyline. The three other studies were performed as open, long-term trials (up to one-year treatment) in large populations of patients (more than 3,300 patients). The findings show that tianeptine does not modify heart rate, blood pressure, conduction or ventricular function. Tianeptine was well tolerated in depressed patients and induced no significant changes at the current dosage in treatment periods from three-months to one-year even in elderly patients, patients with cardiovascular abnormalities or alcoholic patients. Fewer cases of orthostatic hypotension were observed than with other antidepressants. Suicide attempts with tianeptine overdosage did not lead to death due to cardiovascular complications.


Subject(s)
Cardiovascular Diseases/chemically induced , Depressive Disorder/drug therapy , Heart/drug effects , Thiazepines/adverse effects , Antidepressive Agents, Tricyclic/adverse effects , Antidepressive Agents, Tricyclic/pharmacology , Antidepressive Agents, Tricyclic/therapeutic use , Blood Pressure Determination , Cardiovascular Diseases/physiopathology , Heart Conduction System/drug effects , Heart Function Tests/drug effects , Heart Rate/drug effects , Humans , Reference Values , Thiazepines/pharmacology , Thiazepines/therapeutic use , Ventricular Function/drug effects
12.
Encephale ; 16(6): 445-52, 1990.
Article in French | MEDLINE | ID: mdl-2101783

ABSTRACT

Tianeptine, a new antidepressant, has a tricyclic molecular structure. Its main biochemical activity consists of an increase in the reuptake of 5 HT both in men and animals, after acute and chronic administration. Tianeptine demonstrated its antidepressive clinical efficacy in several double-blind versus reference drug trials. A multicentre open trial, including depressed patients enabled us to evaluate the safety of tianeptine and to control the maintenance of the therapeutic efficacy in the course of its long-term prescription. Depressed patients included showed a major depressive episode, single (296.22) or recurrent (296.32) without melancholia or psychotic features, or a dysthymic disorder (300.40), according to DSM III criteria. A minimum MADRS score of a least 25, and the informed consent of the patients were required. The dose of tianeptine was 3 tablets per day (12.5 mg/tablet) with the possibility of increasing to 4 or decreasing to 2 tablets per day, depending on the symptomatology. Therapeutic efficacy was evaluated by item 1 and 2 of the Global Clinical Impression (CGI), the Montgomery and Asberg Depression Rating Scale (MADRS), the Hamilton Anxiety Rating Scale (HARS) and the Hopkins Symptom Check-List (HSCL). Clinical and paraclinical safety were evaluated by CGI item 3, standardized ratings of patients' complaints (CHESS 84), interruption for side effects, evaluation of blood pressure, weight, biological parameters, EKGs. This intermediate evaluation concerns the first 170 depressed patients treated over a one-year period as well as the total group of patients included (n = 447).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Antidepressive Agents, Tricyclic/therapeutic use , Depressive Disorder/drug therapy , Thiazepines/therapeutic use , Adult , Aged , Antidepressive Agents, Tricyclic/adverse effects , Depressive Disorder/blood , Female , Humans , Male , Middle Aged , Thiazepines/adverse effects , Time Factors
13.
Clin Neuropharmacol ; 11 Suppl 2: S74-82, 1988.
Article in English | MEDLINE | ID: mdl-2902922

ABSTRACT

Tianeptine is a new antidepressant effective against anxiety accompanying mood disturbances. Its clinical properties have been assessed by double-blind controlled studies (versus imipramine, amitriptyline, nomifensine, viloxazine) in depressed patients fulfilling the diagnostic criteria of the DSM III: single recurrent major depressive episodes without melancholia or psychotic features, and dysthymic disorders. The authors have concluded that tianeptine is effective in depressive disorders as shown both by depression rating scales and subjective impressions of treated patients. This improvement increases regularly with time. Seventy-eight percent of patients were considered to be "responders" at the end of the treatment with tianeptine. Antidepressant activity of tianeptine is equally present in depressive states appearing after withdrawal from alcohol. In depressed patients with anxiety, the results also reveal the efficacy of tianeptine on anxiety symptoms. Tianeptine, in addition, shows a marked action on somatic complaints. These results have been confirmed by open long-term trials, particularly in the elderly. Tianeptine can be placed in a middle position in the bipolar classification, between the sedative and stimulant antidepressants. Its antidepressant and anxiolytic properties and its action on somatic complaints make the drug particularly suitable for the treatment of the entire range of depressive symptomatology.


Subject(s)
Anti-Anxiety Agents/pharmacology , Antidepressive Agents, Tricyclic/pharmacology , Thiazepines/pharmacology , Clinical Trials as Topic , Humans
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