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2.
Arch Pediatr ; 24(11): 1060-1066, 2017 Nov.
Article in French | MEDLINE | ID: mdl-28988637

ABSTRACT

CONTEXT: Very few studies have evaluated the role of procalcitonin (PCT) in infants with bronchiolitis. AIMS: To describe infants who had both a diagnosis of bronchiolitis at the emergency department and a blood test including PCT, and to compare the characteristics of children according to the PCT value. METHODS: Infants admitted to the Pediatric Emergency Department between 1 January 2014 and 31 December 2014 who had a diagnosis of bronchiolitis and a blood test including PCT were included. The clinical, biological, and radiological characteristics of the infants with PCT <1 or ≥1g/L were compared. RESULTS: One hundred thirty six infants were included. Patients with high PCT (n=20) had a higher temperature (38.5°C, IQR=37.8-38.6 vs. 37.5°C, IQR=37.1-38.2; P<0.01), C-reactive protein (50mg/L, IQR=25-83 vs. 5mg/L, IQR=0-19; P<0.01), and neutrophils (7.8×109/L, IQR=6.0-8.5 vs 4.5×109/L, IQR=2.9-6.6; P<0.01) higher than patients with low PCT (n=116). Presence on the chest x-ray of alveolar condensation did not differ between the two PCT groups. Infants coming from the low-PCT group received fewer antibiotics (14.7% vs 65%; P<0.01). CONCLUSION: In a Pediatric Emergency Department, PCT with a value of 1 or more cannot predict the presence of alveolar condensation on the chest x-ray. It seems to be associated with the antibiotics prescription, even if this could not be proved because of the design of the study.


Subject(s)
Bronchiolitis/blood , Bronchiolitis/diagnosis , Calcitonin/blood , Emergency Service, Hospital , Female , Humans , Infant , Male , Predictive Value of Tests , Retrospective Studies
3.
Clin Drug Investig ; 28(8): 479-85, 2008.
Article in English | MEDLINE | ID: mdl-18598093

ABSTRACT

BACKGROUND AND OBJECTIVES: Darunavir (DRV, TMC114) is a novel protease inhibitor administered in combination with low-dose ritonavir (DRV/r) and is highly active against both wild-type and multidrug-resistant HIV-1 strains. Sildenafil is an oral therapy for erectile dysfunction. Concomitant administration of protease inhibitors and sildenafil increases sildenafil plasma concentrations. The potential for a pharmacokinetic drug interaction exists when sildenafil and DRV/r are co-administered, as these drugs are primarily metabolized by cytochrome P450 (CYP) 3A, and darunavir and ritonavir are CYP3A inhibitors. The primary objective of this open-label, crossover, phase I study was to assess the effect of multiple doses of DRV/r on the pharmacokinetics of sildenafil and its active metabolite N-desmethyl sildenafil. The secondary objective was to assess the short-term safety and tolerability of co-administration of sildenafil and DRV/r. METHODS: Sixteen HIV-negative healthy male subjects were randomized to one of two sequences. In two sessions each subject received treatments A and B. In treatment A, a single dose of sildenafil 100 mg was administered. In treatment B, the subjects received DRV/r 400/100 mg twice daily for 8 days and on day 7 a single dose of sildenafil 25 mg was co-administered. Full pharmacokinetic profiles of sildenafil, N-desmethyl sildenafil, darunavir and ritonavir were determined. Safety and tolerability were also assessed. RESULTS: Sildenafil exposure (area under the plasma concentration-time curve [AUC]) was comparable between the two treatments despite administration of a lower dose of sildenafil (25 mg) with DRV/r than when sildenafil (100 mg) was administered alone. When sildenafil 25 mg was co-administered with DRV/r, the sildenafil maximum plasma concentration (Cmax) was 38% lower compared with Cmax after administration of sildenafil alone at a dose of 100 mg. N-desmethyl sildenafil Cmax and AUC from the time of administration until the last time point with a measurable concentration after dosing (calculated by linear trapezoidal summation [AUClast]) values decreased by approximately 95% when sildenafil 25 mg was co-administered with DRV/r compared with sildenafil 100 mg alone. Combined treatment with DRV/r and sildenafil was generally safe and well tolerated. CONCLUSION: Sildenafil exposure is increased in the presence of DRV/r. In this setting, a dose adjustment for sildenafil is warranted; no more than 25 mg of sildenafil is recommended over a 48-hour period when co-administered with DRV/r.


Subject(s)
Anti-HIV Agents/pharmacology , HIV Protease Inhibitors/administration & dosage , Phosphodiesterase Inhibitors/pharmacokinetics , Piperazines/pharmacokinetics , Ritonavir/pharmacology , Sulfonamides/pharmacology , Sulfones/pharmacokinetics , Adolescent , Adult , Anti-HIV Agents/administration & dosage , Area Under Curve , Cross-Over Studies , Darunavir , Drug Administration Schedule , Drug Interactions , HIV Protease Inhibitors/pharmacology , Humans , Male , Middle Aged , Phosphodiesterase Inhibitors/administration & dosage , Phosphodiesterase Inhibitors/adverse effects , Phosphodiesterase Inhibitors/blood , Piperazines/administration & dosage , Piperazines/adverse effects , Piperazines/blood , Purines/administration & dosage , Purines/adverse effects , Purines/blood , Purines/pharmacokinetics , Ritonavir/administration & dosage , Sildenafil Citrate , Sulfonamides/administration & dosage , Sulfones/administration & dosage , Sulfones/adverse effects , Sulfones/blood
4.
Ann Biol Clin (Paris) ; 66(2): 175-82, 2008.
Article in French | MEDLINE | ID: mdl-18390427

ABSTRACT

Plasma bilirubin testing is crucial to prevent the occurrence of neonatal kernicterus. Haemolysis may occur during sampling and interfere with bilirubin determination. Moreover, lipidic infusions may induce plasma lipemia and also interfere with bilirubin measurement. We evaluated the interference of haemolysis and lipemia with three methods of total and direct bilirubin measurement adaptated on an Advia 1650 analyser (Siemens Medical Solutions Diagnostics) : Synermed (Sofibel), Bilirubin 2 (Siemens) and Bilirubin Auto FS (Diasys). The measurement of total bilirubin was little affected by haemolysis with all three methods. The Bilirubin 2 (Siemens) method was the less sensitive to haemolysis even at low bilirubin levels. The measurement of conjugated bilirubin was significantly altered by low heamoglobin concentrations for Bilirubin Auto FS(R) (30 microM or 0,192 g/100 mL haemoglobin) and for Synermed (60 microM or 0,484 g/100 mL haemoglobin). In marked contrast, we found no haemoglobin interference with the Direct Bilirubin 2 reagent which complied with the method validation criteria from the French Society for Biological Chemistry. The lipemia up to 2 g/L of Ivelip did not affect neither the measurement of total bilirubin for all three methods nor the measurement of conjugated bilirubin with the Diasys and Siemens reagents. However, we observed a strong interference starting at 0,5 g/L of Ivelip with the Synermed reagent. Our data suggest that both Siemens and Diasys methods allow to measure accurately total and conjugated bilirubin in hemolytic and lipemic samples, nevertheless, the Siemens methodology is less affected by these interferences.


Subject(s)
Bilirubin/blood , Blood Chemical Analysis/methods , Hemolysis , Hyperbilirubinemia, Neonatal/diagnosis , Jaundice, Neonatal/prevention & control , Lipids/blood , Biliverdine/blood , Blood Specimen Collection , Data Interpretation, Statistical , Humans , Infant, Newborn , Nephelometry and Turbidimetry , Reproducibility of Results , Sensitivity and Specificity
5.
Rev Med Brux ; 11(3): 54-8, 1990 Mar.
Article in French | MEDLINE | ID: mdl-2320799

ABSTRACT

In order to evaluate the clinical evolution of ethmoïditis with orbital complications in children and the frequency of surgical treatment, the authors reviewed the clinical findings, evolution, complications and treatment on 74 children with acute ethmoïditis. The antibiotics heal the majority of children (69 cases) until the stage of periorbital cellulitis. The abscesses which are more frequent in older children require surgical drainage.


Subject(s)
Ethmoid Sinusitis/complications , Orbital Diseases/etiology , Abscess/etiology , Adolescent , Anti-Bacterial Agents/therapeutic use , Cellulitis/etiology , Child , Child, Preschool , Ethmoid Sinusitis/drug therapy , Humans , Infant , Retrospective Studies , Thrombophlebitis/etiology
6.
Acta Otorhinolaryngol Belg ; 43(2): 169-75, 1989.
Article in French | MEDLINE | ID: mdl-2603703

ABSTRACT

The authors describe the evolution of a mucocele of the sphenoïdal sinus to a reversible retrobulbar neuritis. They discuss the surgical treatment by trans-antro-ethmoïdal way.


Subject(s)
Blindness/etiology , Mucocele/complications , Optic Neuritis/etiology , Sphenoid Sinus/surgery , Humans , Male , Middle Aged , Mucocele/surgery , Optic Neuritis/complications
8.
Acta Otorhinolaryngol Belg ; 40(4): 635-43, 1986.
Article in French | MEDLINE | ID: mdl-3099538

ABSTRACT

Malignant external otitis is a progressive Pseudomonas infection starting in the external auditory canal. It tends to occur in the elderly diabetic patient and to invade cartilage, bone, nerves and adjacent soft tissues. Aggressive medical management and surgical debridement is curative in most cases as it appears in the case reported in the following communication.


Subject(s)
Otitis Externa/surgery , Pseudomonas Infections , Aged , Anti-Bacterial Agents/therapeutic use , Combined Modality Therapy , Debridement , Female , Humans , Otitis Externa/drug therapy , Otitis Externa/etiology , Pseudomonas aeruginosa , Skin Transplantation
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