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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 156 (1997), S. 423-427 
    ISSN: 1432-1076
    Keywords: Key words Teicoplanin  ;  Neonatal infections  ;  Sepsis  ; Gram-positive
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Gram-positive bacteria, notably coagulase negative staphylococci, have become an important cause of infection in neonates. Furthermore, many of these pathogens are now resistant to multiple antibacterial agents. Teicoplanin, a glycopeptide antibiotic, is active against a broad range of Gram-positive pathogens, including methicillin-resistant staphylococci. It has advantages over vancomycin in terms of tolerability, with a lower propensity to cause nephrotoxicity and anaphylactoid-like reactions, and in terms of ease of administration and monitoring requirements. The clinical utility of teicoplanin in neonates with Gram-positive infections has been investigated in several noncomparative studies. Clinical and bacteriological response rates in 173 neonates treated with teicoplanin 8–10 mg/kg intravenously or intramuscularly once daily after a loading-dose regimen of 10–20 mg/kg per day have ranged from 80%–100% and 83%–100%, respectively. Few adverse events related to teicoplanin have been reported in this patient population. Conclusion Teicoplanin (8–10 mg/kg) administered intravenously or intramuscularly once daily after a loading-dose regimen of 15–20 mg/kg per day appears to be an effective and well tolerated treatment for Gram-positive infections in neonates.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 158 (1999), S. 955-957 
    ISSN: 1432-1076
    Keywords: Key words Chromosome deletion ; Chromosome 3 ; Partial monosomy 3p ; AbbreviationDQ developmental quotient
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A boy with monosomy for the distal part of the short arm of chromosome 3 is described. The clinical features this patient has in common with the previously reported cases include pre- and post-natal growth delay, microcephaly, craniofacial dysmorphism and mental retardation. In addition, minor abnormalities not previously reported were observed, such as snapping thumbs, dorsiflected big toes, connecting anterior and posterior fontanelles at birth, nasolacrimal duct stenosis and double urethral meatus. Conclusion These five new clinical findings may help in further delineation of the syndrome and allow its early recognition. A complete revision of clinical findings published in literature is reported.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-198X
    Keywords: Key words Multicystic dysplastic kidney ; Turner syndrome ; Literature review
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Renal malformations occur in 33%–70% of cases of Turner syndrome (chromosome 45 and variants). We describe two cases of multicystic dysplastic kidney in Turner syndrome. A literature review of renal abnormalities in Turner syndrome shows the frequency of cystic disease to be 1.76%. In multicystic dysplastic kidney, diagnostic investigation of the contralateral kidney, including voiding cystourethrography, is necessary in view of the high incidence of associated diseases (15%–20% of cases, vesicoureteric reflux) and other anomalies.
    Type of Medium: Electronic Resource
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