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superinfection/seizures

L'enllaç es desa al porta-retalls
ArticlesAssaigs clínicsPatents
12 resultats

Randomized comparison of sulbactam/cefoperazone with imipenem as empirical monotherapy for febrile granulocytopenic patients.

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In a prospective, randomized, controlled trial, we compared sulbactam/cefoperazone with imipenem as empirical monotherapy for febrile, granulocytopenic patients; 101 patients received sulbactam/cefoperazone (2 g/4 g every 12 hours) and 102 patients received imipenem (500 mg every 6 hours).
BACKGROUND Data on the relative efficacy of β-lactam/β-lactamase inhibitors (BL/BLIs) versus carbapenems are scant. METHODS This is a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing any BL/BLI versus any carbapenem for the treatment of sepsis. The primary outcome
In a randomized multicentre study ciprofloxacin combined with azlocillin was compared with gentamicin and azlocillin for the treatment of febrile episodes in neutropenic patients. In 147 evaluable episodes in 108 patients, 80 patients received ciprofloxacin/azlocillin and 67 received

Respiratory complications following hydrocarbon aspiration in children.

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Accidental hydrocarbon ingestion may lead to aspiration and chemical pneumonitis in children. In this review article, the clinical course of hydrocarbon pneumonitis, chest radiographic abnormalities, complications, and treatment interventions are summarized. Most children remain asymptomatic and

Neonatal Klebsiella pneumonia sepsis and imipenem/cilastatin.

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Efficacy and safety of imipenem/cilastatin in neonatal Klebsiella pneumonia sepsis was investigated in 45 infants compared to 39 control infants on conventional antibiotic regimen. Sensitivity to imipenem was 94% followed by cephoxitin (88%), quinolons (80%), and amikacin (52%) according to

[Ondine's syndrome (alveolar hypoventilation)].

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Ondine's syndrome is a rare condition characterised by alveolar hypoventilation during sleep on account of an abnormality in the automatic control of respiration. The respiration centre does not react adequately to the carbon dioxide tension in the blood required to maintain normal ventilation. We

The Management of Staphylococcal Toxic Shock Syndrome. A Case Report.

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Staphylococcal toxic shock syndrome (TSS) is most frequently produced by TSS toxin-1 (TSST-1) and Staphylococcal enterotoxin B (SEB), and only rarely by enterotoxins A, C, D, E, and H. Various clinical pictures can occur depending on severity, patient age and immune status of the host. Severe forms,
OBJECTIVE To compare the efficacy, toxicity, and cost-effectiveness of double beta-lactam therapy with monotherapy. METHODS A randomized, controlled trial. METHODS Febrile, granulocytopenic patients (429). METHODS Patients were randomly assigned to receive iv cefoperazone (3 g every 12 hours) plus

Imipenem: first of a new class of beta-lactam antibiotics.

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Imipenem, the first of a new class of carbapenem antibiotics, has potent activity against most clinically important species of bacteria, including isolates resistant to other antibiotics. The drug is well distributed to most tissues and fluids after intravenous administration; however, levels in

[A case of acute osteomyelitis and subperiosteal abscess caused by Streptococcus pyogenes, presumably triggered by influenza A virus].

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A feverish 5-year-old girl diagnosed with influenza A virus from a positive rapid influenza type A antigen test, and suffering pain and redness in her left knee had febrile convulsions and was admitted. Her knee pain and redness increased. She was diagnosed with acute osteomyelitis and subperiosteal

Intravenous ciprofloxacin for infections in cancer patients.

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One hundred forty-seven cancer patients were treated with intravenously administered ciprofloxacin, 200 mg every eight hours, as initial therapy for febrile episodes. Thirty patients (20 percent) were neutropenic (less than 1,000 neutrophils/mm3) at the onset of infection. The overall clinical

A sequential study of intravenous and oral fleroxacin in the treatment of complicated urinary tract infection.

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This study enrolled patients with complicated urinary tract infections (UTIs) in a trial to determine the efficacy and safety of sequential therapy with intravenous fleroxacin (first 3 days) followed by oral fleroxacin, for a total course of 7-14 days, both administered at a dosage of 400 mg once a
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