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Dive into the research topics where Andreas Pfleger is active.

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Featured researches published by Andreas Pfleger.


Thorax | 2002

Laser acupuncture in children and adolescents with exercise induced asthma

Wilfried Gruber; Ernst Eber; D Malle-Scheid; Andreas Pfleger; Elisabeth Weinhandl; L Dorfer; Maximilian S. Zach

Background: Laser acupuncture, a painless technique, is a widely used alternative treatment method for childhood asthma, although its efficacy has not been proved in controlled clinical studies. Methods: A double blind, placebo controlled, crossover study was performed to investigate the possible protective effect of a single laser acupuncture treatment on cold dry air hyperventilation induced bronchoconstriction in 44 children and adolescents of mean age 11.9 years (range 7.5–16.7) with exercise induced asthma. Laser acupuncture was performed on real and placebo points in random order on two consecutive days. Lung function was measured before laser acupuncture, immediately after laser acupuncture (just before cold dry air challenge (CACh)), and 3 and 15 minutes after CACh. CACh consisted of a 4 minute isocapnic hyperventilation of –10°C absolute dry air. Results: Comparison of real acupuncture with placebo acupuncture showed no significant differences in the mean maximum CACh induced decrease in forced expiratory volume in 1 second (27.2 (18.2)% v 23.8 (16.2)%) and maximal expiratory flow at 25% remaining vital capacity (51.6 (20.8)% v 44.4 (22.3)%). Conclusions: A single laser acupuncture treatment offers no protection against exercise induced bronchoconstriction in paediatric and adolescent patients.


Paediatric Respiratory Reviews | 2013

Management of acute severe upper airway obstruction in children

Andreas Pfleger; Ernst Eber

There are many causes of acute severe upper airway obstruction (UAO) in children. The timing of symptom onset and the presence of fever will help to distinguish infectious from non-infectious conditions. Signs and symptoms from congenital malformations often present at birth but may also develop over time. The most common cause of UAO in children is croup. Choking on a foreign body also occurs relatively frequently. Evaluation of the child with UAO starts with a detailed history followed by a thorough physical examination, including an assessment of severity. Severe airway obstruction will result in respiratory failure. This situation requires an immediate response. A child with partial airway obstruction may initially have an adequate airway. However, this situation can deteriorate rapidly. Therefore, providing supportive care and mobilizing resources for definitive airway management may be the most appropriate interventions.


Journal of Cystic Fibrosis | 2016

Microbial colonization and lung function in adolescents with cystic fibrosis

Andreas Hector; Tobias Kirn; Anjali Ralhan; Ute Graepler-Mainka; Sina Berenbrinker; J. Riethmueller; Michael Hogardt; Marlies Wagner; Andreas Pfleger; Ingo B. Autenrieth; Matthias Kappler; Matthias Griese; Ernst Eber; Peter Martus; Dominik Hartl

With intensified antibiotic therapy and longer survival, patients with cystic fibrosis (CF) are colonized with a more complex pattern of bacteria and fungi. However, the clinical relevance of these emerging pathogens for lung function remains poorly defined. The aim of this study was to assess the association of bacterial and fungal colonization patterns with lung function in adolescent patients with CF. Microbial colonization patterns and lung function parameters were assessed in 770 adolescent European (German/Austrian) CF patients in a retrospective study (median follow-up time: 10years). Colonization with Pseudomonas aeruginosa and MRSA were most strongly associated with loss of lung function, while mainly colonization with Haemophilus influenzae was associated with preserved lung function. Aspergillus fumigatus was the only species that was associated with an increased risk for infection with P. aeruginosa. Microbial interaction analysis revealed three distinct microbial clusters within the longitudinal course of CF lung disease. Collectively, this study identified potentially protective and harmful microbial colonization patterns in adolescent CF patients. Further studies in different patient cohorts are required to evaluate these microbial patterns and to assess their clinical relevance.


European Journal of Pediatrics | 2001

Clinical and histopathological findings in two Turkish children with follicular bronchiolitis

Martin Benesch; Herbert Kurz; Ernst Eber; Eva-Maria Varga; Hubert Göpfrich; Andreas Pfleger; Helmut Popper; Ulrike Setinek-Liszka; Maximilian S. Zach

Abstract We report on two Turkish children who presented with progressive airway obstruction. Open lung biopsy revealed follicular bronchiolitis. The children were treated with systemic steroids and various topical medications. Whereas the respiratory situation of patient 1 required immunosuppressive therapy, the condition of patient 2 stabilised without systemic medication. Conclusion Diagnosis of follicular bronchiolitis should be considered when children present with recurrent respiratory tract infections, progressive dyspnoea, and chronic bronchial obstruction. Children in whom follicular bronchiolitis is suspected should undergo open lung biopsy for confirmation of diagnosis.


Journal of Cystic Fibrosis | 2015

Short-term effects of physiotherapy on ventilation inhomogeneity in cystic fibrosis patients with a wide range of lung disease severity

Andreas Pfleger; Michael Steinbacher; Gerold Schwantzer; Elisabeth Weinhandl; Marlies Wagner; Ernst Eber

BACKGROUND Lung clearance index (LCI) is increasingly used as a study endpoint for therapeutic interventions in cystic fibrosis (CF) patients. We set out to assess the effect of chest physiotherapy on ventilation inhomogeneity in clinically stable patients with CF lung disease of varying severity. METHODS In 29 CF patients (7.3-43.7 years) N2MBW (nitrogen multiple breath washout), plethysmography, and spirometry measurements were conducted, followed by 30 min of supervised PEP mask chest physiotherapy and repeated measurements 30 min after therapy. RESULTS We observed a mean change in LCI after physiotherapy from 15.00 to 14.80 (range, -4.84 to 3.37; p=0.578). In seven patients, LCI decreased, and in ten patients, LCI increased by ≥1. For the whole group, statistically significant improvements were seen in Reff, FEV1, FVC, and MEF50. CONCLUSIONS By opening up previously poorly ventilated lung regions, physiotherapy may either increase or decrease ventilation inhomogeneity; the short-term effect of physiotherapy on LCI appears to be unpredictable.


European Journal of Pediatrics | 2000

Disseminated cytomegalovirus infection as initial manifestation of hyper-IgM syndrome in a 15-month-old boy

Martin Benesch; Andreas Pfleger; Ernst Eber; Ulrike Orth; Maximilian S. Zach

Abstract We report on the clinical, laboratory, and molecular genetic findings in a 15-month-old boy who initially presented with disseminated cytomegalovirus and concomitant para-influenza virus infection. Hyper-IgM syndrome, suspected on clinical grounds, was confirmed by immunological investigations. In addition, a previously unreported potentially disease-causing mutation in the CD40 ligand gene was detected in this patient. Conclusion The present case illustrates that disseminated cytomegalovirus infection with atypical clinical features should be included in the spectrum of the hyper-IgM syndrome.


Pediatrics International | 2015

Severe primary pulmonary lymphangiectasis in a premature infant: Management and follow up to early childhood

Friedrich Reiterer; Karin Grossauer; Andreas Pfleger; M Häusler; Bernhard Resch; Ernst Eber; Helmut Popper; Berndt Urlesberger

Primary pulmonary lymphangiectasis (PPL) is a rare congenital developmental abnormality of the lung with a generally poor prognosis. Only a limited number of patients with neonatal‐onset PPL have been reported to survive. We present the case of a male preterm infant (gestational age 34 weeks 6 days) with histologically confirmed PPL, complicated by hydrops fetalis, bilateral hydrothorax (treated in utero with pleuro‐amniotic shunts), and immediate respiratory distress at birth. He survived after extensive neonatal intensive care therapy and was discharged home at the age of 7 months. At last follow up he was 3 years 7 months old, still requiring assisted ventilation via tracheostomy, having recurrent episodes of wheezing and had mild global developmental delay. This case demonstrates that survival beyond the neonatal period is possible even with severe PPL but long‐term morbidity may be relevant, and multidisciplinary management and close follow up are essential.


Respiration | 2007

Diffuse Pulmonary Arteriovenous Malformations in a Teenager with Corrected Total Anomalous Pulmonary Venous Drainage

Andreas Pfleger; Andreas Gamillscheg; Helmut Popper; Freyja-Maria Smolle-Jüttner; Maximilian S. Zach

This case report describes a 13-year-old boy with diffuse microvascular pulmonary arteriovenous malformations, in whom total anomalous pulmonary venous drainage had been corrected surgically in the newborn period. Contrast transesophageal echocardiography, cardiac catheterization and a lung perfusion scan suggested, and lung biopsy confirmed the diagnosis in our patient. Treatment with nifedipin was commenced. Conclusion: This case illustrates the diagnostic difficulties with this rare malformation.


Pediatric Pulmonology | 2017

Small airway function before and after cold dry air challenge in pediatric asthma patients during remission

Michael Steinbacher; Andreas Pfleger; Gerold Schwantzer; Stefanie Jauk; Elisabeth Weinhandl; Ernst Eber

We wanted to compare cold dry air challenge (CACh) induced changes in spirometric parameters with changes in nitrogen multiple breath washout (N2MBW) parameters in pediatric asthma patients during clinical remission over the past year (ie, with “inactive asthma”). As N2MBW assesses ventilation heterogeneity we expected to gain detailed information about peripheral airways contribution.


Journal of Pediatric Hematology Oncology | 2006

Gorham-Stout syndrome in a male adolescent-case report and review of the literature.

Andreas Pfleger; Wolfgang Schwinger; Alfred Maier; Josef Tauss; Helmut Popper; Maximilian S. Zach

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Ernst Eber

Medical University of Graz

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Gerold Schwantzer

Medical University of Graz

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Marlies Wagner

Medical University of Graz

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Martin Benesch

Medical University of Graz

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