Literature DB >> 21104409

Endpoints in respiratory diseases.

Fernando Maria de Benedictis1, Roberto Guidi, Silvia Carraro, Eugenio Baraldi.   

Abstract

A wide range of outcome measures or endpoints has been used in clinical trials to assess the effects of treatments in paediatric respiratory diseases. This can make it difficult to compare treatment outcomes from different trials and also to understand whether new treatments offer a real clinical benefit for patients. Clinical trials in respiratory diseases evaluate three types of endpoints: subjective, objective and health-related outcomes. The ideal endpoint in a clinical trial needs to be accurate, precise and reliable. Ideally, the endpoint would also be measured with minimal risk and across all ages, easy to perform, and be inexpensive. As for any other disease, endpoints for respiratory diseases must be viewed in the context of the important distinction between clinical endpoints and surrogate endpoints. The association between surrogate endpoints and clinical endpoints must be clearly defined for any disease in order for them to be meaningful as outcome measures. The most common endpoints which are used in paediatric trials in respiratory diseases are discussed. For practical purposes, diseases have been separated into acute (bronchiolitis, acute viral-wheeze, acute asthma and croup) and chronic (asthma and cystic fibrosis). Further development of endpoints will enable clinical trials in children with respiratory diseases with the main objective of improving prognosis and safety.

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Year:  2010        PMID: 21104409     DOI: 10.1007/s00228-010-0922-2

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  41 in total

Review 1.  Biomarkers and surrogate endpoints: preferred definitions and conceptual framework.

Authors: 
Journal:  Clin Pharmacol Ther       Date:  2001-03       Impact factor: 6.875

Review 2.  Holding chambers (spacers) versus nebulisers for beta-agonist treatment of acute asthma.

Authors:  C J Cates; J A Crilly; B H Rowe
Journal:  Cochrane Database Syst Rev       Date:  2006-04-19

3.  Surrogate endpoints in clinical trials: definition and operational criteria.

Authors:  R L Prentice
Journal:  Stat Med       Date:  1989-04       Impact factor: 2.373

4.  Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis.

Authors:  A L Quittner; S Sweeny; M Watrous; P Munzenberger; K Bearss; A Gibson Nitza; L A Fisher; B Henry
Journal:  J Pediatr Psychol       Date:  2000-09

Review 5.  Eosinophil cationic protein (ECP): molecular and biological properties and the use of ECP as a marker of eosinophil activation in disease.

Authors:  P Venge; J Byström; M Carlson; L Hâkansson; M Karawacjzyk; C Peterson; L Sevéus; A Trulson
Journal:  Clin Exp Allergy       Date:  1999-09       Impact factor: 5.018

6.  Variation in the distribution of patient-reported outcomes based on different definitions of defining asthma severity.

Authors:  Steven R Erickson; Duane M Kirking
Journal:  Curr Med Res Opin       Date:  2004-12       Impact factor: 2.580

Review 7.  Bronchiolitis.

Authors:  Rosalind L Smyth; Peter J M Openshaw
Journal:  Lancet       Date:  2006-07-22       Impact factor: 79.321

Review 8.  Respiratory medicines for children: current evidence, unlicensed use and research priorities.

Authors:  A R Smyth; A Barbato; N Beydon; H Bisgaard; K de Boeck; P Brand; A Bush; B Fauroux; J de Jongste; M Korppi; C O'Callaghan; M Pijnenburg; F Ratjen; K Southern; D Spencer; A Thomson; H Vyas; A Warris; P J Merkus
Journal:  Eur Respir J       Date:  2009-10-19       Impact factor: 16.671

9.  Development of the asthma control test: a survey for assessing asthma control.

Authors:  Robert A Nathan; Christine A Sorkness; Mark Kosinski; Michael Schatz; James T Li; Philip Marcus; John J Murray; Trudy B Pendergraft
Journal:  J Allergy Clin Immunol       Date:  2004-01       Impact factor: 10.793

10.  Clinical evaluation and treatment of acute asthma exacerbations in children.

Authors:  L Indinnimeo; F Bertuola; R Cutrera; F M De Benedictis; P Di Pietro; M Duse; P Gianiorio; G Indirli; S La Grutta; M La Rosa; R Longhi; S Miceli Sopo; P Miglioranzi; M Miraglia Del Giudice; F Monaco; D Radzik; S Renna; D Snijders; S Zampogna; A Barbato
Journal:  Int J Immunopathol Pharmacol       Date:  2009 Oct-Dec       Impact factor: 3.219

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  4 in total

Review 1.  Novel end points for clinical trials in young children with cystic fibrosis.

Authors:  Shannon J Simpson; Lauren S Mott; Charles R Esther; Stephen M Stick; Graham L Hall
Journal:  Expert Rev Respir Med       Date:  2013-06       Impact factor: 3.772

2.  Which outcomes should be used in future bronchiolitis trials? Developing a bronchiolitis core outcome set using a systematic review, Delphi survey and a consensus workshop.

Authors:  A Rosala-Hallas; Ashley P Jones; Paula R Williamson; Emma Bedson; Vanessa Compton; Ricardo M Fernandes; David Lacy; Mark David Lyttle; Matthew Peak; Kentigern Thorburn; Kerry Woolfall; Clare Van Miert; Paul S McNamara
Journal:  BMJ Open       Date:  2022-03-09       Impact factor: 2.692

3.  Development and content validation of a self-completed, electronic Pediatric Asthma Symptom Diary.

Authors:  Marci Clark; Carla Romano; Oyebimpe Olayinka-Amao; Diane Whalley; Rebecca Crawford; Purnima Pathak; Caterina Brindicci; Kristin Garg; Kattayoun Kordy; Francois Everhard; Francesco Patalano; Zach Roesler; Thomas Sutton; Oskar Göransson; Ross Landles; Christel Naujoks; Jessica Marvel; Dorothy L Keininger
Journal:  J Patient Rep Outcomes       Date:  2022-03-20

Review 4.  Choosing primary endpoints for clinical trials of health care interventions.

Authors:  Charlie McLeod; Richard Norman; Edward Litton; Benjamin R Saville; Steve Webb; Thomas L Snelling
Journal:  Contemp Clin Trials Commun       Date:  2019-11-12
  4 in total

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