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1.
J Eur Acad Dermatol Venereol ; 20(10): 1194-6, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17062030

ABSTRACT

BACKGROUND: Onychodystrophy is a major manifestation of onychomycosis. However, nail trauma may also result in onychodystrophy. The fifth toenail, due to its location, suffers repeated friction/pressure trauma from shoes. OBJECTIVE: To test the hypothesis that treatment failure of fifth toenail onychomycosis is not a marker of treatment failure of other toenails with onychomycosis. METHODS: Fifty patients who had fifth toenail deformity (with or without onychomycosis) and onychomycosis of the other toenails were treated with oral terbinafine, 250 mg/day, for 4 months. RESULTS: Forty-three patients completed the study. Before the study, 26/43 (61%) had callus lateral to the fifth toe (suggesting mechanical pressure in that area). Twenty-one/43 (49%) of the fifth toenails had onychomycosis. At the end of the treatment period, only 4/21 (19%) of the fifth toenails (with initial onychomycosis), compared with 12/21 (57%) of the other toenails, were completely cured (CC). Out of the whole group (n=43), the clinical cure rate of the fifth toenail was 4/43 (9%) and for the other toenails, 20/43 (47%) (P<0.05). The mycological cure rates were 11/21 (52%) for the fifth toenail and 25/43 (58%) for the other toenails. Callus lateral to the fifth toe was associated with a poor clinical result (P<0.01). CONCLUSIONS: Clinical improvement of the fifth toenail after systemic antifungal therapy is less favourable and does not correspond with the clinical cure of the other toenails, mostly because of mechanical factors. Therefore, patients should be told to adjust their expectations as to the visual results of their antifungal treatment.


Subject(s)
Antifungal Agents/administration & dosage , Foot Dermatoses/drug therapy , Nails/pathology , Naphthalenes/administration & dosage , Onychomycosis/drug therapy , Antifungal Agents/pharmacokinetics , Humans , Nails/injuries , Nails/microbiology , Naphthalenes/pharmacokinetics , Pressure , Shoes , Terbinafine , Treatment Outcome
2.
Phys Med Biol ; 49(19): 4543-61, 2004 Oct 07.
Article in English | MEDLINE | ID: mdl-15552416

ABSTRACT

Monte Carlo simulation is an essential tool in emission tomography that can assist in the design of new medical imaging devices, the optimization of acquisition protocols and the development or assessment of image reconstruction algorithms and correction techniques. GATE, the Geant4 Application for Tomographic Emission, encapsulates the Geant4 libraries to achieve a modular, versatile, scripted simulation toolkit adapted to the field of nuclear medicine. In particular, GATE allows the description of time-dependent phenomena such as source or detector movement, and source decay kinetics. This feature makes it possible to simulate time curves under realistic acquisition conditions and to test dynamic reconstruction algorithms. This paper gives a detailed description of the design and development of GATE by the OpenGATE collaboration, whose continuing objective is to improve, document and validate GATE by simulating commercially available imaging systems for PET and SPECT. Large effort is also invested in the ability and the flexibility to model novel detection systems or systems still under design. A public release of GATE licensed under the GNU Lesser General Public License can be downloaded at http:/www-lphe.epfl.ch/GATE/. Two benchmarks developed for PET and SPECT to test the installation of GATE and to serve as a tutorial for the users are presented. Extensive validation of the GATE simulation platform has been started, comparing simulations and measurements on commercially available acquisition systems. References to those results are listed. The future prospects towards the gridification of GATE and its extension to other domains such as dosimetry are also discussed.


Subject(s)
Computer Simulation , Software , Tomography, Emission-Computed, Single-Photon/methods , Monte Carlo Method , Reproducibility of Results , Thermodynamics
3.
Laryngoscope ; 103(1 Pt 1): 33-41, 1993 Jan.
Article in English | MEDLINE | ID: mdl-8421417

ABSTRACT

The efficacy and safety of a once-a-day antibiotic in the treatment of sinusitis was studied. Two randomly assigned groups were treated with either once-a-day cefixime, a third generation cephalosporin, or amoxicillin three times a day. One hundred and fourteen patients were evaluated with antral punctures, microbiologic evaluation, and radiographic studies. Cultures revealed 40% gram-negative organisms, 48% gram-positive, and 12% anaerobes. The most common bacteria were Haemophilus influenzae, Streptococcus pneumoniae, Staphylococcus aureus and viridans group streptococci. Ninety-four percent of the cefixime group were cured compared with 96% of the amoxicillin group. Staphylococcus resistance was a problem in both groups, necessitating an occasional change to amoxicillin-clavulanate potassium in the amoxicillin group. Once-a-day antibiotics offer the potential for improved compliance in the treatment of sinusitis. Cefixime offers an additional benefit of covering beta-lactamase producing strains of bacteria which are increasing in incidence and resistant to many penicillins.


Subject(s)
Amoxicillin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Bacterial Infections/drug therapy , Cefotaxime/analogs & derivatives , Sinusitis/microbiology , Administration, Oral , Adolescent , Adult , Aged , Amoxicillin/administration & dosage , Amoxicillin/adverse effects , Amoxicillin-Potassium Clavulanate Combination , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/adverse effects , Capsules , Cefixime , Cefotaxime/administration & dosage , Cefotaxime/adverse effects , Cefotaxime/therapeutic use , Clavulanic Acids/administration & dosage , Clavulanic Acids/therapeutic use , Drug Administration Schedule , Drug Therapy, Combination/administration & dosage , Drug Therapy, Combination/therapeutic use , Female , Humans , Male , Middle Aged , Prospective Studies , Remission Induction , Sinusitis/drug therapy , Time Factors
4.
Pediatrics ; 60(1): 14-9, 1977 Jul.
Article in English | MEDLINE | ID: mdl-327422

ABSTRACT

The effects of terbutaline, ephedrine, and placebo on the cardiovascular and pulmonary systems have been compared in 24 asthmatic children. Ephedrine and terbutaline were both found to be effective bronchodilators, with onset of action within 30 minutes. The bronchodilator effect of ephedrine was maintained for three hours, while terbutaline was active for five hours. Terbutaline caused significantly greater improvement in pulmonary functions than did ephedrine. Both terbutaline and ephedrine were associated with clinically insignificant changes in blood pressure and pulse rate. The only significant side effect observed was hand tremor in children receiving terbutaline and this appeared only early in the course of drug treatment. There was no evidence of tolerance to the bronchodilator effect of ephedrine or terbutaline after eight weeks of therapy.


Subject(s)
Asthma/drug therapy , Ephedrine/therapeutic use , Terbutaline/therapeutic use , Adolescent , Blood Pressure/drug effects , Child , Clinical Trials as Topic , Double-Blind Method , Drug Evaluation , Ephedrine/adverse effects , Ephedrine/pharmacology , Humans , Placebos , Pulse/drug effects , Respiratory Function Tests , Terbutaline/adverse effects , Terbutaline/pharmacology
5.
J Allergy Clin Immunol ; 59(2): 109-14, 1977 Feb.
Article in English | MEDLINE | ID: mdl-319139

ABSTRACT

This report concerns the difficulty in distinguishing variation due to drug effects from the spontaneous daily variation in baseline levels of pulmonary function in the evaluation of bronchodilator responsiveness in asthmatic children. Both prospective and retrospective studies were employed to assess the importance of the influence of the baseline level of function from which change is measured on the degree of responsiveness observed. It was found that for baseline levels up to approximately 90% of the predicted normal value, all patients had the capacity to respond significantly to a bronchodilator. However, there was no limit of baseline function below which a significant response did not occur.


Subject(s)
Asthma/drug therapy , Ephedrine/therapeutic use , Terbutaline/therapeutic use , Adolescent , Bronchi/drug effects , Child , Clinical Trials as Topic , Drug Evaluation , Female , Humans , Male , Respiratory Function Tests
6.
JAMA ; 237(6): 553-7, 1977 Feb 07.
Article in English | MEDLINE | ID: mdl-319269

ABSTRACT

Sixteen asthmatic children between the ages of 7 and 13 years, 13 of whom were receiving theophylline orally around-the-clock, were studied for eight weeks in double-blind manner to evaluate efficacy, toxicity, and development of tolerance to the combination of ephedrine sulfate and theophylline. Reactions to the drug combination, assessed by close observation and daily patient questioning by the nursing staff, showed no toxicity or substantial side effects. Pulmonary function was measured hourly for six hours after each morning dose, and the data were analyzed to determine the degree and duration of bronchodilator response. Comparison of data from weeks 1 and 8 showed no evidence of the development of tolerance. Ephedrine is a potent bronchodilator that, in appropriate doses, can be administered safely along with therapeutic doses of theophylline without fear of progressive tolerance or toxicity.


Subject(s)
Asthma/drug therapy , Ephedrine/therapeutic use , Adolescent , Age Factors , Child , Clinical Trials as Topic , Drug Therapy, Combination , Drug Tolerance , Ephedrine/administration & dosage , Ephedrine/adverse effects , Humans , Placebos , Respiratory Function Tests , Theophylline/administration & dosage , Theophylline/therapeutic use
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