Collecting data on cancer

BMJ 1994; 308 doi: 10.1136/bmj.308.6931.791a (Published 19 March 1994)
Cite this as: BMJ 1994;308:791.2

Access to the full text of this article requires a subscription or payment. Please log in or subscribe below.

  1. I Bassnett,
  2. A M Pollock,
  3. M Gill
  1. Camden and Islington Health Authority, London NW1 2LJ
  2. Department of Public Health Sciences, St George's Hospital Medical School, London SW17 0RE
  3. Brent and Harrow Health Authority, Harrow, Middlesex HA1 3UJ.

    EDITOR, - Few people would disagree with S J Karp's plea for improving the collection of data on patients with cancer.1 The case Karp makes for the clinical oncology information network, however, is unconvincing. One justification claimed for the network is that three studies came to erroneous conclusions in auditing the outcomes of care because they used data for cancer registries.*RF 2-4* This is incorrect; Karp has misunderstood the studies' design.

    All three studies were …

    Access to the full text of this article requires a subscription or payment

    Article access

    Article access for 1 day

    Purchase this article for £20 $30 €32*

    The PDF version can be downloaded as your personal record

    * Prices do not include VAT

    THIS WEEK'S POLL