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Review
. 2015 Mar;11(1):26-38.
doi: 10.1183/20734735.015414.

Real-world research and its importance in respiratory medicine

Affiliations
Review

Real-world research and its importance in respiratory medicine

David Price et al. Breathe (Sheff). 2015 Mar.

Abstract

Educational aims: To improve understanding of: The relative benefits and limitations of evidence derived from different study designs and the role that real-life asthma studies can play in addressing limitations in the classical randomised controlled trial (cRCT) evidence base.The importance of guideline recommendations being modified to fit the populations studied and the model of care provided in their reference studies.

Key points: Classical randomised controlled trials (cRCTs) show results from a narrow patient group with a constrained ecology of care.Patients with "real-life" co-morbidities and lifestyle factors receiving usual care often have different responses to medication which will not be captured by cRCTs if they are excluded by strict selection criteria.Meta-analyses, used to direct guidelines, contain an inherent meta-bias based on patient selection and artificial patient care.Guideline recommendations should clarify where they related to cRCT ideals (in terms of patient populations, medical resources and care received) and could be enhanced through inclusion of evidence from studies designed to better model the populations and care approaches present in routine care.

Summary: Clinical practice requires a complex interplay between experience and training, research, guidelines and judgement, and must not only draw on data from traditional or classical randomised controlled trials (cRCTs), but also from pragmatically designed studies that better reflect real-life clinical practice. To minimise extraneous variables and to optimise their internal validity, cRCTs exclude patients, clinical characteristics and variations in care that could potentially confound outcomes. The result is that respiratory cRCTs often enrol a small, non-representative subset of patients and overlook the important interplay and interactions between patients and the real world, which can effect treatment outcomes. Evidence from real-life studies (e.g. naturalistic or pragmatic clinical trials and observational studies encompassing healthcare database studies and cohort studies) can be combined with cRCT evidence to provide a fuller picture of intervention effectiveness and realistic treatment outcomes, and can provide useful insights into alternative management approaches in more challenging asthma patients. The Respiratory Effectiveness Group (REG), in collaboration with the European Academy of Allergy and Clinical Immunology (EAACI) and the European Respiratory Society (ERS), is developing quality appraisal tools and methods for integrating different sources of evidence. A REG/EAACI taskforce aims to help support future guideline developers to avoid a one-size-fits-all approach to recommendations and to tailor the conclusions of their meta-analyses to the populations under consideration.

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Conflict of interest statement

Conflict of interest: Outside of the submitted work, D. Price reports Board Membership for Aerocrine, Almirall, Amgen, AstraZeneca, Boehringer Ingelheim, Chiesi, Meda, Mundipharma, Napp, Novartis, and Teva; consultancy fees from Almirall, Amgen, AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Meda, Mundipharma, Napp, Novartis, Pfizer, and Teva; grants from the UK National Health Service, British Lung Foundation, Aerocrine, AstraZeneca, Boehringer Ingelheim, Chiesi, Eli Lilly, GlaxoSmithKline, Meda, Merck, Mundipharma, Novartis, Orion, Pfizer, Respiratory Effectiveness Group, Takeda, Teva, and Zentiva; support for lectures/speaking engagements from Almirall, AstraZeneca, Boehringer Ingelheim, Chiesi, Cipla, GlaxoSmithKline, Kyorin, Meda, Merck, Mundipharma, Novartis, Pfizer, SkyePharma, Takeda, and Teva; for manuscript preparation from Mundipharma and Teva; payment for travel/accommodations/meeting expenses from Aerocrine, Boehringer Ingelheim, Mundipharma, Napp, Novartis, and Teva; funding for patient enrolment or completion of research from Almirall, Chiesi, Teva, and Zentiva, unrestricted funding for investigator-initiated studies from Aerocrine, AKL Ltd, Almirall, Boehringer Ingelheim, Chiesi, Meda, Mundipharma, Napp, Novartis, Orion, Takeda, Teva and Zentiva. In addition, D. Price has a patent for AKL Ltd and has shares in AKL Ltd which produces phytopharmaceuticals, and owns 80% of Research in Real Life Ltd, and its subsidiary social enterprise Optimum Patient Care. Outside of the submitted work, G. Brusselle reports personal fees from Astra Zeneca, Boehringher-Ingelheim, Chiesi, GlaxoSmithKline, Novartis, Pfizer, Almirall and Mundipharma. Outside of the submitted work, N. Roche reports grants and personal fees from Boehringer Ingelheim; grants and personal fees from Novartis; and personal fees from Teva, GlaxoSmithKline, AstraZeneca, Chiesi, Mundipharma and Almirall.

Figures

Figure 1
Figure 1
Studies have shown that classical efficacy RCTs exclude about 90% for a) asthma and 95% for b) COPD routine care populations due to strict inclusion and exclusion criteria. a) For asthma clinical-trial patients criteria included: visual analogue scale (VAS) <2; historical reversibility in FEV 12% within the last 12 months; absence of significant co-morbidity; nonsmoker or if previous smoker (XS) a smoke burden <10 pack-years; regular use of ICS; symptomatic asthma (defined as either the use of short acting β2-agonist daily or nocturnal awakening due to asthma at least once a week). b) For COPD clinical-trial patients criteria included: VAS >7.5, absence of significant co-morbidity; smoker (S) or XS; a smoke burden of >15 pack-years; no history of hay fever indicating presence of atopy. Reproduced from [5] with permission from the publisher.
Figure 2
Figure 2
Integrated research framework, bounded by population and ecology of care axes running from highly selected to managed care populations (Y-axis) and from highly interventional to observational study design approaches (X-axis). Adapted from [10] with permission from the publisher.
Figure 3
Figure 3
Long-term adherence to ICS. Short-term cRCTs will miss the interaction between real-life adherence and treatment outcomes. Reproduced from [20] with permission from the publisher.
Figure 4
Figure 4
The COMPACT study demonstrated the difference in outcomes associated with management of only lower airways inflammation (budesonide) compared with systemic (upper and lower airways) inflammation management (montelukast) in asthmatic patients without (a) and with (b) rhinitis. Reproduced from [31, 32] with permission from the publishers.
Figure 5
Figure 5
Mean (95% CI) difference between non-smokers and smokers with asthma, Suggesting alternatives to higher-dose ICS may be required. *: p≤0.01 for smokers versus non-smokers. Reproduced from [36] with permission from the publisher.

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