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Correspondence
Letter in response to Tashkin et al: limited generalisability of uplift findings to clinical practice
  1. Steven Walker1,2,
  2. James Fingleton1,2,3,
  3. Mark Weatherall2,4,
  4. Richard Beasley1,2,3,4
  1. 1 Medical Research Institute of New Zealand, Wellington, New Zealand
  2. 2 Capital & Coast District Health Board, Wellington, New Zealand
  3. 3 Victoria University of Wellington, Wellington, New Zealand
  4. 4 University of Otago Wellington, Wellington, New Zealand
  1. Correspondence to Professor Richard Beasley, Medical Research Institute of New Zealand, Private Bag 7902, Wellington 6242, New Zealand; Richard.Beasley{at}mrinz.ac.nz

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We appreciate the comments made by Tashkin et al 1 regarding the limited generalisability of the Understanding Potential Long-term Impacts on Function with Tiotropium (UPLIFT) findings.2 In response, the sample we studied was not designed to be representative of the general chronic obstructive pulmonary disease (COPD) population, but rather the subgroup of patients with severe COPD who are likely to be at greatest risk of serious cardiovascular events. Second, the derived data presented from the Canadian database analysis do not correspond to the UPLIFT inclusion criteria. The UPLIFT study excluded patients with cardiac arrhythmias deemed unstable or life-threatening, or that required either intervention or a change in drug therapy in the last 12 months.3 In contrast, the Canadian data related to arrhythmias requiring hospital admission in the last 6 months.1 Third, the cardiovascular and renal comorbidity exclusion criteria in UPLIFT were not used in major long-term COPD trials evaluating LABAS±ICS, such as the landmark TOwards a Revolution in COPD Health study, which had no specific cardiovascular or renal comorbidity exclusion criteria.4

In our view, the efficacy/safety profile of a COPD medication can only be determined if those patients who are at greatest risk of serious adverse events are studied. If this has not been done, then failing to list the characteristics of patients who were excluded from trial participation in the medication data sheet is unsatisfactory. We propose that the tiotropium data sheet5 is amended to state that the favourable efficacy/safety profile of tiotropium HandiHaler established in the UPLIFT study applies only to patients without recent cardiovascular or renal comorbidity, as these patients were excluded from the study.

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Footnotes

  • Contributors SW and JF undertook the data collection that was analysed by MW. All authors contributed to both the drafting of the manuscript and this letter.

  • Competing interests RB has been a member of the GlaxoSmithKline (NZ) advisory board, consulted for Cytos Biotechnology and Pharmaxis, received research grants from AstraZeneca, Cephalon, Chiesi, Genentech, GlaxoSmithKline and Novartis, and payment for lectures or support to attend meetings from Boehringer Ingelheim, GlaxoSmithKline, Novartis, Nycomed and Otsuka Pharmaceuticals. JF has received payment for lectures or support to attend meetings from AstraZeneca, Boehringer Ingelheim and Novartis. SW and MW have no competing interests to declare.

  • Provenance and peer review Not commissioned; internally peer reviewed.

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  • PostScript
    D P Tashkin N Metzdorf C Hallmann I Leimer T Lee M Decramer