Article Text

Download PDFPDF
Are all patients that count included in palliative care studies?
  1. Pål Klepstad1,2 and
  2. Marianne Jensen Hjermstad3,4
  1. 1Department of Circulation and Medical Imaging, Faculty of Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway
  2. 2Department of Anaesthesiology and Emergency Medicine, St. Olavs Hospital, Trondheim, Norway
  3. 3Department of Oncology, Regional Centre for Excellence in Palliative Care, Oslo University Hospital, Oslo, Norway
  4. 4Faculty of Medicine, European Palliative Care Research Centre, Norwegian University of Science and Technology (NTNU), Trondheim, Norway
  1. Correspondence to Dr Pål Klepstad, Department of Intensive Care, St Olav University Hospital, Trondheim 7006, Norway; pal.klepstad{at}ntnu.no.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

The famous quote from Albert Einstein that ‘Everything that can be counted does not necessarily count; everything that counts cannot necessarily be counted’1 can perhaps be paraphrased to ‘Every patient that can be included does not necessarily count, every patients that counts cannot necessarily be included’. The study by Stone et al2 published in this issue of BMJ Supportive & Palliative Care highlights this. Stone et al demonstrated that in a carefully planned, non-interventional study with rather simple assessments, less than one-tenth of the patients admitted to the relevant units were included. The actual result from this observation is that the study may reflect the situation for a minor group of the patients only. This raises obvious concerns about the generalisability of findings from the study to those patients met in everyday clinical practice.

Stone et al should be recommended for reporting these data. There is reason to believe that these difficulties are under-reported in the Results section of many publications. Difficulties in recruitment and access to patients, and poor compliance are factors that are most likely under-communicated in the planning and conduction of studies and in the interpretation of the research.

What are the obstacles related to inclusion and what can be done in order to increase the number of included patients, thereby improving the generalisability of study results? The study by Stone et al categorised the patients who failed to be included into three categories. The first category included those who were ineligible for inclusion. Some reasons were nothing to be done with, …

View Full Text

Footnotes

  • Competing interests None.

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

Linked Articles