June 3, 2015

Clinically relevant subgroups in COPD and asthma


Eur Respir Revvol. 24 no. 136 283-298
  • Neil Barnes6

  • +Author Affiliations
    1. 1Clinical and Experimental Medicine, University of Birmingham, Queen Elizabeth Hospital Birmingham, Birmingham, UK
    2. 2Dept of Respiratory Medicine, Birmingham Heartlands Hospital, Birmingham, UK
    3. 3Dept of Pulmonology, Semmelweis University, Budapest, Hungary
    4. 4Respiratory Medicine, CHU Sart-Tilman B35, Liege, Belgium
    5. 5Service of Allergology and Clinical Immunology, UHC “Mother Teresa”, Tirana, Albania
    6. 6GlaxoSmithKline, Stockley Park West, Uxbridge, UK
    1. Alice M. Turner, Clinical and Experimental Medicine, University of Birmingham, Queen Elizabeth Hospital Birmingham, Mindelsohn Way, Birmingham, B15 2WB, UK. E-mail: a.m.wood@bham.ac.uk

    2. Abstract
    As knowledge of airways disease has grown, it has become apparent that neither chronic obstructive pulmonary disease (COPD) nor asthma is a simple, easily defined disease. In the past, treatment options for both diseases were limited; thus, there was less need to define subgroups. As treatment options have grown, so has our need to predict who will respond to new drugs. To date, identifying subgroups has been largely reported by detailed clinical characterisation or differences in pathobiology. These subgroups are commonly called “phenotypes”; however, the problem of defining what constitutes a phenotype, whether this should include comorbid diseases and how to handle changes over time has led to the term being used loosely.

    Clinical asthma phenotyping: A trial for bridging gaps in asthma management

    Logo of wjcpLink to Publisher's site

    World J Clin Pediatr. 2015 May 8; 4(2): 13–18.
    Published online 2015 May 8. doi:  10.5409/wjcp.v4.i2.13
    PMCID: PMC4438436

    Abstract:
    Asthma is a common disease affecting millions of people worldwide and exerting an enormous strain on health resources in many countries. Evidence is increasing that asthma is unlikely to be a single disease but rather a series of complex, overlapping individual diseases or phenotypes, each defined by its unique interaction between genetic and environmental factors.

    June 1, 2015

    Thresholds in chemical respiratory sensitisation

  • Stella A. Cochranea
  • Josje H.E. Artsb
  • Colin Ehnesc
  • Stuart Hindled
  • Heli M. Hollnageld
  • Alan Poolee
  • Hidenori Sutof
  • Ian Kimberg

  • Abstract
    There is a continuing interest in determining whether it is possible to identify thresholds for chemical allergy. Here allergic sensitisation of the respiratory tract by chemicals is considered in this context. This is an important occupational health problem, being associated with rhinitis and asthma, and in addition provides toxicologists and risk assessors with a number of challenges.
  • Masticatory Changes in Oral Breath Secondary to Allergic Rhinitis: Integrative Review

    Logo of iaorl
    Abstract
    Introduction The III Brazilian Consensus on Rhinitis (2012) defines allergic rhinitis as a nasal mucosa inflammation, mediated by immunoglobulin E, after exposure to allergens.

    May 30, 2015

    Predictors of treatment with antibiotics and systemic corticosteroids for acute exacerbations of asthma and chronic obstructive pulmonary disease in primary care

    Research article

    Highly Accessed

    Open AccessSalwan Al-ani1*Mark Spigt12Johanna Laue1 and Hasse Melbye1


    Abstract
    Background
    Antibiotic and oral corticosteroid prescribing rate in patients suffering from acute exacerbations of chronic obstructive pulmonary disease (COPD) or asthma in general practice are only sparsely described. Our aim was to identify predictors for such prescribing when results from CRP testing, spirometry, and pulse oximetry are available.

    Lies, damned lies, and marketing: an editor’s lament

    Article Abstract
    Authors: Lawrence Grouse

    Abstract

    Many of the articles published in the ICC COLUMN have emphasized the plight that respiratory patients around the world have in obtaining satisfactory access to appropriate medications and health care. Two main problems have been identified. The first involves the high costs that prevent many patients from obtaining care (1). The second involves the difficulty to determine whether or not new medications, diagnostic procedures, and treatments actually do benefit patient outcomes. This paper provides an editor’s perspective on how the marketing activities of proprietary organizations make it difficult to assess published clinical research that is intended to determine the value of treatments.

    May 27, 2015

    Whistles and wheezes: don't miss diseases

    • Problem solving in clinical practice
    Editor's Choice
    1. K Huxstep
    +Author Affiliations
    1. Department of PaediatricsBroomfield HospitalChelmsford, UK

    Abstract

    Upper airway obstruction (UAO) in infants and children has a broad spectrum of presentations including benign self-resolving conditions, from mild croup, to critical life-threatening conditions which, though uncommon now, require prompt recognition and effective multidisciplinary collaborative management to achieve a good outcome. The aim of this article is to highlight the diagnostic and management difficulties in acute UAO in paediatric patients and encourage a problem-solving approach.

    This Article


    1. All Versions of this Article:
      1. archdischild-2013-304604v1
      2. 100/3/132 most recent

    Prolonged efficacy of the 300IR 5-grass pollen tablet up to 2 years after treatment cessation, as measured by a recommended daily combined score

    Open Access
    Research


    Alain Didier1*Hans-Jørgen Malling2Margitta Worm3Friedrich Horak4 and Gordon L Sussman5

    Abstract
    Background
    The 300IR (index of reactivity) 5-grass pollen tablet has favorable short-term and sustained clinical efficacy in patients with grass pollen-induced allergic rhinoconjunctivitis (ARC). Here, we report maintenance of efficacy and safety over 2 years following treatment discontinuation.

    European medicines agency guideline for biological medicinal products: a further step for a safe use of biosimilars

    Open Access
    Editorial


    Carlo Agostini1*Giorgio Walter Canonica2 and Enrico Maggi3

    Clinical and Molecular Allergy 2015, 13:3  doi:10.1186/s12948-015-0010-3
    The electronic version of this article is the complete one and can be found online at:http://www.clinicalmolecularallergy.com/content/13/1/3
    This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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