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Dive into the research topics where Urs B. Schaad is active.

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Featured researches published by Urs B. Schaad.


Clinical Infectious Diseases | 2000

Acute Community-Acquired Diarrhea Requiring Hospital Admission in Swiss Children

Bettina Essers; André P. Burnens; Francesco M. Lanfranchini; Stefano G. E. Somaruga; Rodo O. von Vigier; Urs B. Schaad; Christoph Aebi; Mario G. Bianchetti

In order to ascertain the prevalence of agents that cause childhood diarrheal illness, stool specimens of 312 consecutive children with community-acquired diarrhea requiring admission were evaluated. Pathogens were detected in 166 (53%) of the 312 children (>/=2 pathogens in 28 children): Rotavirus (n=75), Salmonella spp. (n=37), Campylobacter spp. (n=24), Shigella spp. (n=5), Giardia spp. (n=4), Yersinia spp. (n=2), Aeromonas spp. (n=15), Cryptosporidium (n=15), enteropathogenic Escherichia coli (n=13), enterotoxigenic E. coli (n=7), and enterohemorrhagic E. coli (n=5). In conclusion, acute childhood diarrheal illness pathogens, such as Aeromonas, Cryptosporidium, and diarrheagenic E. coli, account for a large proportion of patients with a microbiologically positive stool specimen.


Pediatric Infectious Disease Journal | 1997

Oral ciprofloxacin vs. intravenous ceftazidime plus tobramycin in pediatric cystic fibrosis patients: comparison of antipseudomonas efficacy and assessment of safety with ultrasonography and magnetic resonance imaging

David A. Richard; Sanda Nousia-Arvanitakis; Veronika Sollich; Barbara Hampel; Bernd Sommerauer; Urs B. Schaad

BACKGROUNDnMore data on the efficacy and safety of ciprofloxacin in pediatric cystic fibrosis patients are needed.nnnMETHODSnOne hundred eight pediatric cystic fibrosis patients (ages 5 to 17 years) with acute bronchopulmonary exacerbations entered a randomized multicenter trial designed to compare the safety and efficacy of antipseudomonas therapy with oral ciprofloxacin (15 mg/kg twice daily; maximum dosage 750 mg twice daily) or intravenous ceftazidime plus tobramycin (CAZ/TM) for 14 days.nnnRESULTSnClinical improvement was observed in 93% of patients treated with oral ciprofloxacin and in 96% of those receiving parenteral therapy. Transient suppression of Pseudomonas aeruginosa was achieved in 63% of patients at the end of the course of iv CAZ/TM therapy and in 24% receiving ciprofloxacin. Ultrasound examination and nuclear magnetic resonance imaging scans showed no evidence of cartilage toxicity in any of the ciprofloxacin-treated patients. Musculoskeletal adverse events were reported with similar frequency in the two groups of patients (7% in the group receiving ciprofloxacin therapy and 11% in the IV CAZ/TM group). The only sustained musculoskeletal symptom was a case of synovitis in a patient receiving parenteral CAZ/TM.nnnCONCLUSIONnCiprofloxacin thus appears to be safe and effective for use in young patients with bronchopulmonary exacerbation of cystic fibrosis.


Pediatric Infectious Disease Journal | 2012

Antibiotic therapy for pediatric community-acquired pneumonia: do we know when, what and for how long to treat?

Susanna Esposito; Robert Cohen; Javier Diez J.D. Domingo; Oana Falup O.F. Pecurariu; David Greenberg; Ulrich Heininger; Markus Knuf; Irja Lutsar; Nicola Principi; Fernanda Rodrigues; Mike Sharland; Vana Spoulou; George A. Syrogiannopoulos; Vytautas Usonis; Anne Vergison; Urs B. Schaad

Community-acquired pneumonia (CAP) is a common cause of morbidity among children in developed countries and accounts for an incidence of 10-40 cases per 1000 children in the first 5 years of life. Given the clinical, social and economic importance of CAP, there is general agreement that prompt and adequate therapy is essential to reduce the impact of the disease. The aim of this discussion paper is to consider critically the available data concerning the treatment of uncomplicated pediatric CAP and to consider when, how and for how long it should be treated. This review has identified the various reasons that make it difficult to establish a rational approach to the treatment of pediatric CAP, including the definition of CAP, the absence of a pediatric CAP severity score, the difficulty of identifying the etiology, limited pharmacokinetic (PK)/pharmacodynamic (PD) studies, the high resistance of the most frequent respiratory pathogens to the most widely used anti-infectious agents and the lack of information concerning the changes in CAP epidemiology following the introduction of new vaccines against respiratory pathogens. More research is clearly required in various areas, such as the etiology of CAP and the reasons for its complications, the better definition of first- and second-line antibiotic therapies (including the doses and duration of parenteral and oral antibiotic treatment), the role of antiviral treatment and on how to follow-up patients with CAP. Finally, further efforts are needed to increase vaccination coverage against respiratory pathogens and to conduct prospective studies of their impact.Community-acquired pneumonia (CAP) is a common cause of morbidity among children in developed countries and accounts for an incidence of 10–40 cases per 1000 children in the first 5 years of life. Given the clinical, social and economic importance of CAP, there is general agreement that prompt and adequate therapy is essential to reduce the impact of the disease. The aim of this discussion paper is to consider critically the available data concerning the treatment of uncomplicated pediatric CAP and to consider when, how and for how long it should be treated. This review has identified the various reasons that make it difficult to establish a rational approach to the treatment of pediatric CAP, including the definition of CAP, the absence of a pediatric CAP severity score, the difficulty of identifying the etiology, limited pharmacokinetic (PK)/pharmacodynamic (PD) studies, the high resistance of the most frequent respiratory pathogens to the most widely used anti-infectious agents and the lack of information concerning the changes in CAP epidemiology following the introduction of new vaccines against respiratory pathogens. More research is clearly required in various areas, such as the etiology of CAP and the reasons for its complications, the better definition of first- and second-line antibiotic therapies (including the doses and duration of parenteral and oral antibiotic treatment), the role of antiviral treatment and on how to follow-up patients with CAP. Finally, further efforts are needed to increase vaccination coverage against respiratory pathogens and to conduct prospective studies of their impact.


The Quinolones (Third Edition) | 2000

Chapter 15 – Use of the Quinolones in Pediatrics

Urs B. Schaad

Publisher Summary nThe use of fluoroquinolones in children has been limited because of their potential to induce arthropathy in juvenile animals. This extraordinary form of age-related drug toxicity has been demonstrated with all the fluoroquinolones tested so far, which has led to various restrictions. Their use has been considered to be contraindicated in children, in growing adolescents, and during pregnancy and lactation. However, since the mid-1980s, many children have received treatment with fluoroquinolones, particularly ciprofloxacin, as they are the only oral antimicrobials with potential activity against the multiple resistant and difficult-to-treat infections such as Pseudomonas aeruginosa infections in children with cystic fibrosis, complicated urinary tract infections, and enteric infections. Many investigators have also reported their experience in the use of ciprofloxacin and other fluoroquinolones on “compassionate use”-based protocols. The results indicate that prolonged therapy with the fluoroquinolones is effective and well tolerated in pediatric patients, with no significant evidence of arthropathy, bone abnormalities, or other serious adverse events. The excellent antibacterial and pharmacodynamic properties of some of the latest quinolones such as gatifloxacin, gemifloxacin, moxifloxacin, and des-F(6)-quinolone indicate that these agents might become alternatives for the treatment of childhood bacterial central nervous system (CNS) and respiratory tract infections.


Acta Paediatrica | 2010

Evidence for fluid volume depletion in hyponatraemic patients with bacterial meningitis

Mario G. Bianchetti; Hr Thyssen; R. Laux-End; Urs B. Schaad

Since the mechanisms underlying hyponatraemia in meningitis are poorly understood, we retrospectively reviewed the records of 187 paediatric patients with bacterial meningitis treated at the Department of Pediatrics, University of Bern, Switzerland, between 1982 and 1994. The degree of dehydration calculated from naked weight on admission and at 5 days was consistently (by 2.8 × 10−2) and significantly more pronounced in 30 hyponatraemic (plasma sodium 130 mmoll−1 or less) than in 157 normonatraemic patients (plasma sodium 131 mmoll−1 or more). Furthermore, a tendency towards reduced sodium excretion was noted in hyponatraemic patients. The results suggest that in bacterial meningitis hyponatraemia is mostly induced by clinically latent fluid volume depletion.


European Journal of Paediatric Neurology | 1998

Acute encephalitis in Swiss children: aetiology and outcome.

Tobias Iff; Filippo Donati; Franco Vassella; Urs B. Schaad; Mario G. Bianchetti

Since published data on the course and prognosis of encephalitis in Central Europe is limited, we retrospectively evaluated 104 children with either acute strict sense encephalitis (n = 80) or acute cerebellar ataxia (n = 24) treated at the Department of Pediatrics, University of Bern, Switzerland, between 1980 and 1991. Of the 80 patients with strict sense encephalitis, four (5%) died acutely and 28 (36%) of 78 followed up had sequelae - eight patients with severe, six with moderate and 14 with mild sequelae. Young age and seizures were shown to correlate with poor outcome. Among the 24 patients with acute cerebellar ataxia, there was no fatal outcome and none developed severe residua, but six had mild and one had moderate sequelae. Initial cerebrospinal fluid white cell count was significantly higher in these children with sequelae compared with those without any sequelae after acute cerebellar ataxia.


Acta Paediatrica | 1997

Screening for complement deficiency in bacterial meningitis

T Ernst; Pj Späth; C Aebi; Urs B. Schaad; Mario G. Bianchetti

Seventy‐seven children with bacterial meningitis were screened for complement deficiency. Both the classical and the alternate pathways were normal in 75 patients. Transiently reduced total haemolytic activity of the classical pathway was documented in a boy with meningococcal meningitis. Total haemolytic activity of both the classical and the alternate pathways were reduced in another patient with pneumococcal meningitis: individual complement components determination indicated predominant activation of the alternate pathway.


European Journal of Pediatrics | 1995

Mycobacterium genavense invasive infection in two children with AIDS: Long-term followup

Didier Reymond; Peter Birrer; Urs B. Schaad

Mycobacterium genavense is a rare cause of opportunistic infection in immunocompromised hosts. Follow up of two cases ofM. genavense invasive infection in children with haemophilia A and AIDS are presented. One patient died 18 months after diagnosis ofM. genavense infection of an indirectly related cause, probably ofPneumocystis carinii pneumonia. The second patient still attends our outpatient clinic and the infection is under control. Both presented with abdominal lymphomas and pain and a wasting syndrome. A combination of several drugs against atypical mycobacteria is used for treatment.


European Journal of Pediatrics | 1995

Current concepts of bacterial meningitis

Urs B. Schaad

ConclusionsAs reflected in the relevant milestones, there has undoubtedly been considerable knowledge gained in recent years on diagnosis and management of bacterial meningitis. Future research aims at specific anti-inflammatory measures, optimal treatment of meningitis caused by penicillin-resistant pneumococci, routine in vitro screening of new agents for potential neurotoxicity, and immunogenic, safe and protective conjugate vaccines for young infants. Hence, challenges remain.


Fems Immunology and Medical Microbiology | 2006

Antibody responses induced by long‐term vaccination with an octovalent conjugate Pseudomonas aeruginosa vaccine in children with cystic fibrosis

Adrian Zuercher; Michael P. Horn; John U. Que; Anna Ruedeberg; Martin H. Schoeni; Urs B. Schaad; Paul Marcus; Alois B. Lang

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Ulrich Heininger

Boston Children's Hospital

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Ulrich Heininger

Boston Children's Hospital

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C Aebi

University of Basel

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