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Among these 55 groups, replies were obtained from 18 groups.
Following a reminder, an additional 36 replies were obtained.
In total, replies were obtained from 447 (71%) of the establishments.
Efficacy was assessed retrospectively by sending postal questionnaires during a different time period to another sample of patients who had sequentially received this therapy until 50 usable replies were obtained, this occurred after sending out 55 questionnaires (91% response rate).
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A reminder was sent after 2 weeks if no reply was obtained.
No reply was obtained from Giantonni or Sutherland; it was assumed that these studies also used sterile non-coated catheterisation.
In reply to a survey, a reasonable (44%) response was obtained, which represented surgeons working in both community and academic institutions.
While response rate was low – only 19.5% of individuals replied – responses were obtained from 102 organisations.
When 15 positive replies in each group were obtained, the recruitment was closed.
The data were obtained via a mailed reply-paid questionnaire survey undertaken in August-September 2012. August-September 2012
Patients' views were obtained from written responses to a postal questionnaire (136 replies).
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