Thoracic interventional radiology in children.

Abstract:

:Significant technological advancements have been achieved in radiology with the introduction of a branch speciality known as interventional radiology. Radiology has moved into the therapeutic arena, performing minimally invasive diagnostic and therapeutic procedures. The interventional radiologist can treat certain vascular and non-vascular conditions with "keyhole" or perhaps more correctly "pinhole" techniques using catheter-based technology directed under image guidance with X-ray (including computed tomography), ultrasound and magnetic resonance imaging. Interventional radiology can provide new treatment options for children not possible a few years ago.

journal_name

Paediatr Respir Rev

authors

John P

doi

10.1053/prrv.2000.0121

keywords:

subject

Has Abstract

pub_date

2001-06-01 00:00:00

pages

131-44

issue

2

eissn

1526-0542

issn

1526-0550

pii

S1526-0542(00)90121-0

journal_volume

2

pub_type

杂志文章,评审
  • Treatment of interstitial lung disease in children.

    abstract::The treatment of interstitial lung disease in children depends on the nature of the underlying pathology. In approximately 50% of cases a specific aetiology can be found such as: chronic viral infection, an auto-immune process, sarcoidosis or alveolar proteinosis. In the remainder, the process is idiopathic and the pa...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2004.01.004

    authors: Dinwiddie R

    更新日期:2004-06-01 00:00:00

  • Disease-modifying drug therapy in cystic fibrosis.

    abstract::Whilst substantial progress has been made in the treatment of cystic fibrosis, the disease still carries a significant burden in terms of symptoms, requirement for treatment and early mortality. The last decade has witnessed a new era in the development of small molecule drugs targeting the CFTR protein, which for the...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2017.03.008

    authors: Harman K,Dobra R,Davies JC

    更新日期:2018-03-01 00:00:00

  • Hypoxic Challenge Test for airflight in children with respiratory disease.

    abstract::During airflight, cabins are pressurised to 8000ft (2438m) leading to an effective FiO2 of 0.15. This leads to a fall in oxygen saturation in all passengers, and especially those with underlying lung disease. The hypoxic challenge test using a body plethysmograph can predict a need for supplemental oxygen during airfl...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2016.05.002

    authors: Balfour-Lynn IM

    更新日期:2017-01-01 00:00:00

  • Vocal cord dysfunction in children.

    abstract::Vocal cord dysfunction is characterised by paradoxical vocal cord adduction that occurs during inspiration, resulting in symptoms of dyspnoea, wheeze, chest or throat tightness and cough. Although the condition is well described in children and adults, confusion with asthma often triggers the use of an aggressive trea...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2007.05.004

    authors: Noyes BE,Kemp JS

    更新日期:2007-06-01 00:00:00

  • Respiratory viruses in the intensive care unit.

    abstract::Respiratory viruses cause a number of clinical 'syndromes' in the intensive care unit with different viruses being able to produce similar clinical pictures. Our main presenting problems are upper airway (e.g. croup and tracheitis), lower airway with intrapulmonary shunt (e.g. bronchitis and pneumonia), lower airway w...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:

    authors: Roe M,O'Donnell DR,Tasker RC

    更新日期:2003-09-01 00:00:00

  • Cardiac manifestations of neuromuscular disorders in children.

    abstract::Cardiac abnormalities occur in association with many of the neuromuscular disorders that present in childhood. Genetic defects involving the cytoskeleton, nuclear membrane, and mitochondrial function have all been described in patients with skeletal myopathy and cardiac involvement. The most common classes of neuromus...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2009.10.004

    authors: Hsu DT

    更新日期:2010-03-01 00:00:00

  • Diabetes in cystic fibrosis.

    abstract::Cystic fibrosis related diabetes (CFRD) is a common complication of cystic fibrosis, caused by a fall in insulin secretion with age in individuals with pancreatic insufficiency. CFRD is associated with worse clinical status and increased mortality. Treatment of CFRD with insulin results in sustained improvements in lu...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章

    doi:10.1016/j.prrv.2013.02.002

    authors: Bridges N

    更新日期:2013-05-01 00:00:00

  • Ethical aspects of home long term ventilation in children with neuromuscular disease.

    abstract::Increasing numbers of children and young adults are now receiving home ventilation. Whereas in some neuromuscular conditions the outcome and quality of life gains are clear cut; in others eg Spinal Muscular Atrophy Type I there are a few outcome studies with conflicting results and it is more difficult to balance the ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2005.06.003

    authors: Simonds AK

    更新日期:2005-09-01 00:00:00

  • Cough in children: when does it matter?

    abstract::Cough is a common presenting symptom to paediatricians and paediatric respiratory physicians. The causes of chronic cough in childhood are significantly different from those in adults, and a different approach to diagnosis and management is needed. In most cases cause can be identified or a satisfactory label given. T...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2005.11.008

    authors: Massie J

    更新日期:2006-03-01 00:00:00

  • Primary ciliary dyskinesia among Arabs: Where do we go from here?

    abstract::Primary ciliary dyskinesia (PCD), also known as immotile-cilia syndrome, is a rare genetic disease that is inherited in an autosomal recessive manner. Several studies have explored certain aspects of PCD in the Arab world, yet much is still lacking in terms of identifying the different characteristics of this disease....

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2018.09.002

    authors: Hammoudeh S,Gadelhak W,Janahi IA

    更新日期:2019-02-01 00:00:00

  • Cystic fibrosis: basic science.

    abstract::Advances in the elucidation of cystic fibrosis transmembrane regulator (CFTR) function have resulted in a greater understanding of the relationship between the CF gene defect and clinical disease. The clinical phenotype is influenced by the class of mutation and possibly by other modifier genes. CFTR regulates the vol...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2000.0029

    authors: McAuley DF,Elborn JS

    更新日期:2000-06-01 00:00:00

  • Parental smoking: asthma and wheezing illnesses in infants and children.

    abstract::Parental smoking has an important impact on asthma and wheezing illnesses in infants and children. In utero exposure is associated with impaired lung growth and wheezing illnesses, particularly in preschool children. Exposure to environmental tobacco smoke is associated with increased wheezing illnesses and increased ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2001.0141

    authors: Landau LI

    更新日期:2001-09-01 00:00:00

  • The burden of asthma in children: an Australian perspective.

    abstract::The burden of asthma among children is high in Australia compared with many other countries. Recent data show that 14-16% of children report a diagnosis of asthma that remains a problem. Boys, children under the age of 5 years and urban indigenous children experience a greater burden of asthma than other children. Mor...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2004.11.004

    authors: Poulos LM,Toelle BG,Marks GB

    更新日期:2005-03-01 00:00:00

  • Newborn screening for cystic fibrosis offers an advantage over symptomatic diagnosis for the long term benefit of patients: the motion for.

    abstract::Comprehensive newborn screening for cystic fibrosis has occurred for more than 25 years in some regions and the results of randomised controlled trials reporting the outcomes have been published. Testing protocols for CF have recently been reviewed and the sensitivity and specificity of these protocols are high. In sp...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2008.09.004

    authors: McKay K,Wilcken B

    更新日期:2008-12-01 00:00:00

  • That ICS should be first line therapy for asthma--con.

    abstract::Asthma is a heterogeneous disease and it is therefore unrealistic to expect that inhaled corticosteroids (ICS) would be appropriate first line preventer therapy for all children with asthma. There is good theoretical and clinical trial evidence demonstrating that leukotriene receptor antagonists (LTRAs) are more effec...

    journal_title:Paediatric respiratory reviews

    pub_type: 评论,杂志文章

    doi:10.1016/j.prrv.2011.05.008

    authors: van Asperen PP

    更新日期:2011-12-01 00:00:00

  • Allergic bronchopulmonary aspergillosis in paediatric cystic fibrosis patients.

    abstract::Allergic bronchopulmonary aspergillosis (ABPA) is a severe complication in children, adolescents and adults with cystic fibrosis (CF), the prevalence of which ranges from 6-25%. The disease is the result of the colonisation of the respiratory tract by fungi of the genus Aspergillus, commonly Aspergillus fumigatus, and...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2005.09.003

    authors: de Almeida MB,Bussamra MH,Rodrigues JC

    更新日期:2006-03-01 00:00:00

  • Congenital upper airway obstruction.

    abstract::Most causes of upper airway obstruction are rare in the neonatal period and during infancy. They may, however, cause major respiratory problems either initially or during the first few weeks of life. It is important to recognise these problems at an early stage so that appropriate measures to overcome airway obstructi...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2003.10.001

    authors: Dinwiddie R

    更新日期:2004-03-01 00:00:00

  • What does imaging the chest tell us about bronchopulmonary dysplasia?

    abstract::Bronchopulmonary dysplasia (BPD) is a common complication of preterm birth. Chest imaging is important in making the diagnosis of BPD, and in assessing for complications. More recently computerised tomography (CT) scanning has provided insights in to the pathophysiology of BPD. Studies in infants, young and school age...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2010.05.005

    authors: Wilson AC

    更新日期:2010-09-01 00:00:00

  • Long-term cardio-respiratory consequences of heart disease in childhood.

    abstract::The dynamic interaction between the heart and lungs leads to a degree of respiratory co-morbidity including both restrictive and obstructive airway abnormalities, which may be overlooked in children with congenital and acquired heart disease. The improving imaging techniques of the heart, both foetal and post-natal co...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2007.08.006

    authors: Fitzgerald DA,Sherwood M

    更新日期:2007-12-01 00:00:00

  • A systematic review of studies examining the rate of lung function decline in patients with cystic fibrosis.

    abstract::A systematic review was performed (i) to describe the reported overall rate of progression of CF lung disease quantified as FEV1%predicted decline with age, (ii) to summarise identified influencing risk factors and (iii) to review methods used to analyse CF lung disease progression data. A search of publications provi...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2016.03.002

    authors: Harun SN,Wainwright C,Klein K,Hennig S

    更新日期:2016-09-01 00:00:00

  • CFTR modulator therapy in patients with cystic fibrosis and an organ transplant.

    abstract::CFTR modulators are a class of drugs which directly target the defective CFTR protein in cystic fibrosis (CF), improving its function with resultant clinical improvements. Currently these drugs are confined to people with a limited selection of genetic mutations. New modulators are in development which will lead to th...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2018.04.003

    authors: Mitchell RM,Jones AM,Barry PJ

    更新日期:2018-06-01 00:00:00

  • Gene and cell therapy for cystic fibrosis.

    abstract::Since the discovery of the CF gene over a decade ago, several groups worldwide have explored the potential of gene therapy, the insertion of a normal copy of the gene into the respiratory epithelium. Both viral and synthetic gene transfer agents have been designed to this end, although problems with repeat application...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2006.04.214

    authors: Davies JC

    更新日期:2006-01-01 00:00:00

  • Urban air pollution and respiratory infections.

    abstract::Public awareness of the impact of air quality on health is increasing worldwide. Indoor and outdoor air pollutants impair children's growing lungs, and increase the risk of respiratory infections. In many cities, children face indoor air pollution from fuels used for cooking and heating, as well as outdoor pollution f...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2014.03.001

    authors: Brugha R,Grigg J

    更新日期:2014-06-01 00:00:00

  • Atelectasis: mechanisms, diagnosis and management.

    abstract::The term atelectasis describes a state of collapsed and non-aerated region of the lung parenchyma, which is otherwise normal. This pathological condition is usually associated with several pulmonary and chest disorders and represents a manifestation of the underlying disease, not a disease per se. Atelectasis may occu...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2000.0059

    authors: Peroni DG,Boner AL

    更新日期:2000-09-01 00:00:00

  • Children and the global tuberculosis situation.

    abstract::The current global strategy for control of tuberculosis, Directly Observed Treatment, Short-course (DOTS) focuses, as a priority, on the management of patients with sputum smear positive tuberculosis. As tuberculosis in children is rarely sputum smear positive, this has led many to believe that children are not import...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/s1526-0542(04)90027-9

    authors: Enarson DA

    更新日期:2004-01-01 00:00:00

  • Differences in the clinical and genotypic presentation of sickle cell disease around the world.

    abstract::Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in malaria endemic regions. Cardiopulmonary complications are major causes of morbidity and mortality. Hemoglobin SS (Hb SS) represents a large proportion of SCD in the Americas, United Kingdom, and certain regions of Afric...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2013.11.003

    authors: Saraf SL,Molokie RE,Nouraie M,Sable CA,Luchtman-Jones L,Ensing GJ,Campbell AD,Rana SR,Niu XM,Machado RF,Gladwin MT,Gordeuk VR

    更新日期:2014-03-01 00:00:00

  • Local mucociliary defence mechanisms.

    abstract::The lung is continually at risk of exposure to noxious environmental agents and respiratory pathogens. An elaborate series of defence mechanisms have been developed to protect the airways from these insults. The lower respiratory tract is protected by local mucociliary mechanisms that involve the integration of the ci...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1053/prrv.2000.0009

    authors: Chilvers MA,O'Callaghan C

    更新日期:2000-03-01 00:00:00

  • Use of steroids in the perinatal period.

    abstract:INTRODUCTION:Corticosteroids can be used prenatally to mature the fetal lungs and postnatally to treat or prevent chronic lung disease (CLD). Randomised controlled trials have been performed to evaluate the benefits and risks of perinatal corticosteroid therapy. METHODS:Systematic reviews of randomised controlled tria...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/s1526-0542(04)90057-7

    authors: Halliday HL

    更新日期:2004-01-01 00:00:00

  • Chylothorax: diagnosis and management in children.

    abstract::Chylothorax is the accumulation of chyle in the pleural space, as a result of damage to the thoracic duct. Chyle is milky fluid enriched with fat secreted from the intestinal cells and lymphatic fluid. Chylothorax in children, is most commonly seen as a complication of cardiothoracic surgery but may occur in newborns ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2009.06.008

    authors: Soto-Martinez M,Massie J

    更新日期:2009-12-01 00:00:00

  • Regulation of bacterial trafficking in the nasopharynx.

    abstract::Bacterial 'colonisation' of the nasopharynx by potential bacterial pathogens is frequent in early childhood and is frequent as part of a dynamic process in which the microbiota of the oral and nasopharynx are established. New understanding recognizes this process is evolving and that competition and likely regulation ...

    journal_title:Paediatric respiratory reviews

    pub_type: 杂志文章,评审

    doi:10.1016/j.prrv.2012.04.001

    authors: Pelton SI

    更新日期:2012-09-01 00:00:00