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1.
Eur J Clin Microbiol Infect Dis ; 36(9): 1651-1660, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28409290

ABSTRACT

Viral meningitis is mainly caused by non-polio enteroviruses (NPEV). Large-scale data on the clinical characteristics between different outbreaks within the same region are lacking. This study aimed to analyse a possible influence of the circulating NPEV genotype on the disease outcome of affected children. A retrospective cohort study analysing two major outbreaks of NPEV meningitis in Germany in 2008 and 2013 was conducted in cooperation with the National Reference Centre for Poliomyelitis and Enteroviruses (NRC PE) and five German children's hospitals. A total of 196 patients with laboratory-confirmed NPEV meningitis were enrolled. In 2008, children with NPEV meningitis had significantly higher fever and showed more behavioural changes and less back pain. To better define typical findings in echovirus 30 (E-30) meningitis, patients were split into the following three groups: E-30 positive patients, patients with "Non E-30" infection and patients with "Untyped" NPEV infection. E-30 positive patients were significantly older and their disease course was more acute, with early admission to but also early discharge from hospital. E-30 positive patients showed a significantly higher rate of headache and meningism, and a lower rate of diarrhoea and clinically defined septicaemia when compared to the others. Regarding laboratory testing, E-30 positive patients presented with significantly elevated peripheral blood neutrophil counts when compared to patients with "Non E-30" or "Untyped" NPEV infection. In conclusion, E-30 meningitis in children shows a characteristic pattern of clinical features. To further characterise NPEV strains worldwide, continuous surveillance and typing of NPEV strains causing central nervous system disease is warranted.


Subject(s)
Disease Outbreaks , Enterovirus B, Human , Enterovirus , Meningitis, Viral/epidemiology , Meningitis, Viral/virology , Child , Child, Preschool , Enterovirus/classification , Enterovirus B, Human/classification , Female , Germany/epidemiology , History, 21st Century , Humans , Male , Meningitis, Viral/diagnosis , Meningitis, Viral/history , Patient Admission/statistics & numerical data , Retrospective Studies , Serogroup , Symptom Assessment
2.
Allergol Select ; 1(1): 21-27, 2017.
Article in English | MEDLINE | ID: mdl-30402598

ABSTRACT

Food allergens are frequent causes of anaphylaxis. In particular in children and adolescents they are the most frequent elicitors of severe allergic reactions, and in adults food allergens rank third behind insect venom and drugs. Since July 2006 severe allergic reactions from Germany, Austria, and Switzerland are collected in the anaphylaxis registry. Currently 78 hospitals and private practises are connected. From July 2006 until February 2009 1,156 severe allergic reactions were registered. Among children and adolescents (n = 187, age range from 3 months to 17 years) food allergens were the most frequent triggers, comprising 58% of cases. In the adult group (n = 968, 18 - 85 years) food allergens were in the third position (16.3%) behind insect venom and drugs. In children legumes (31%) and in particular peanuts were frequently responsible food allergens, followed by tree nuts (25%) with hazelnut being the most frequent elicitor. In adults fruits (13.4%) most often induced severe food-dependent anaphylaxis, but also animal products (12.2%); among these most frequently crustaceans and molluscs. Cofactors were often suspected in food-dependent anaphylaxis, namely in 39% of the adult group and in 14% of the pediatric group. In adults drugs (22%) and physical activity (10%) were reported to be the most frequent cofactors, in children physical activity was suspected in 8.7% and drugs in 2.6%. Concomitant diseases like atopic dermatitis, allergic asthma, or allergic rhinoconjunctivitis were reported in 78% of children and adolescents and in 67% of the adults. In conclusion, food-induced anaphylaxis, its cofactors and concomitant diseases are age-dependent. The data offers to identify risk factors of anaphylaxis.

3.
Eur J Clin Microbiol Infect Dis ; 31(11): 3173-82, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22850740

ABSTRACT

A prospective clinical study was performed to correlate nasopharyngeal carriage of bacteria with the type of lower respiratory tract infections (LRTI) in hospitalised children. To determine bacterial load in nasopharyngeal aspirates (NPA) we used semiquantitative culturing and quantitative TaqMan-PCR for those pathogens difficult to culture. Specimens and clinical data were obtained from 311 children between 0 and 16 years of age with LRTI during the period of 2006-2008. The most common detected potentially pathogenic colonisers were Haemophilus influenzae (32.1 %), Moraxella catharralis (26.7 %), Staphylococcus aureus (17.7 %) and Streptococcus pneumoniae (16.7 %). As expected S. aureus was the most common coloniser in children less than 4 months of age, whereas H. influenzae detection peaked in older children. Co-colonisation with other bacterial pathogens were more often observed in children with S. aureus (46 %) and S. pneumoniae (49 %) than in those with H. influenzae (30 %) or M. catharralis (27 %). Children with S. aureus co-colonisation had higher levels of C-reactive-protein, received antibiotics more frequently and stayed longer in hospital than those with S. aureus single colonisation. In contrast, children with H. influenzae, M. catharralis or S. pneumoniae colonisation suffered more often from pneumonia than children with S. aureus colonisation. Coloniser specific analysis of bacterial quantity revealed no significant reduction of the bacterial carriage from the first to the second NPA. No correlation of a high bacterial load and occurrence of pneumonia could be detected. In conclusion, clinical characteristics in children with LRTIs are associated with a specific bacterial set of colonisers detected in the nasopharynx rather than on their quantity.


Subject(s)
Bacteria/classification , Bacteria/isolation & purification , Bacterial Infections/pathology , Carrier State/microbiology , Nasopharynx/microbiology , Respiratory Tract Infections/pathology , Adolescent , Bacterial Infections/microbiology , Bacterial Load/methods , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Polymerase Chain Reaction/methods , Prospective Studies , Respiratory Tract Infections/microbiology
4.
Eur J Pediatr ; 159 Suppl 2: S70-3, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11043148

ABSTRACT

UNLABELLED: Phenylketonuria treatment policies vary not only between different countries worldwide, but also within one country. Recommendations and guidelines for phenylketonuria should deal with the following subjects: 1. What is the target age to start dietary phenylalanine restriction under newborn-screening conditions? 2. At which plasma phenylalanine concentration should phenylalanine restriction be initiated? 3. Which are the recommended plasma phenylalanine concentrations at different ages? 4. What is the recommended frequency of monitoring phenylalanine in plasma? Statements from the following countries are presented: Czech Republic, Denmark, France, Germany, Great Britain, Hungary, Ireland, Poland, Slovakia and the United States. CONCLUSION: Due to the lack of internationally accepted guidelines, management of phenylketonuria still varies between different countries. Our efforts should focus on the formulation of internationally acceptable and accepted recommendations for the treatment of patients with phenylketonuria at different ages.


Subject(s)
Phenylketonurias/diet therapy , Practice Guidelines as Topic , Adolescent , Adult , Aging/blood , Child , Child, Preschool , Data Collection , Europe , Humans , Infant , Infant, Newborn , Phenylalanine/administration & dosage , Phenylalanine/blood , Phenylketonurias/blood , Time Factors , United States
7.
Eur J Pediatr ; 153(4): 267-70, 1994 Apr.
Article in English | MEDLINE | ID: mdl-8194561

ABSTRACT

We report on a boy who developed proximal renal tubular acidosis with loss of carnitine at the age of about 6 months. A few months later he began to suffer from progressive muscular weakness and neurological disturbances. Blood biochemistry showed elevated lactate and beta-hydroxybutyrate with increased lactate/pyruvate and beta-hydroxybutyrate/acetoacetate ratios. A high urinary excretion of lactate and citric acid cycle intermediates was found. These results indicated a defect of the mitochondrial respiratory chain. Analysis of biopsy material from skeletal muscle revealed low activities of all respiratory chain complexes. In muscle and fibroblasts cytochrome c-oxidase (complex IV) was absent. Despite high dose multi-vitamin therapy the boy died at the age of 30 months from central respiratory failure. At autopsy the neuropathological diagnosis of Leigh disease was made.


Subject(s)
Acidosis, Renal Tubular/etiology , Cytochrome-c Oxidase Deficiency , Leigh Disease/complications , Acidosis, Renal Tubular/metabolism , Brain Diseases/etiology , Brain Diseases/metabolism , Electron Transport Complex IV/metabolism , Fatal Outcome , Humans , Infant , Leigh Disease/blood , Leigh Disease/metabolism , Male , Mitochondrial Myopathies/etiology , Mitochondrial Myopathies/metabolism , Oxidoreductases/deficiency
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