Continuing professional development (CPD) for healthcare
professionals is an important strategic instrument for improving health. The
Department of Health identifies CPD as a way of maintaining standards of care;
improving the health of the nation; and recruiting, motivating, and retaining
high quality staff. To this end, direct NHS spending on continuing professional
development in 1999-2000 was about £1bn. If we regard CPD as any method to
improve health professionals’ skills the total resources devoted to it are
probably much greater, particularly with the recent increased participation in
response to the need for re-certification and revalidation. To ensure the
maximum gain from participation in CPD, these resources must be used
efficiently.
To assess the efficiency of participating in CPD, economic
criteria are needed. Resources for health care are scarce, and money spent on
CPD could otherwise be used for direct patient care. These opportunity costs are
explicitly considered in the economic methods of cost benefit analysis and costs
effectiveness analysis. Casebeer et al highlighted the need for economic
evaluation of CPD activities, but they emphasised the use of cost benefit
analysis, which requires monetary values to be assigned to measures of
effectiveness. Cost benefit analysis is generally used to ascertain whether an
intervention should be undertaken. Cost effectiveness analysis is used to decide
which interventions (out of a number of alternatives) should be undertaken.
However, cost effectiveness analysis in education research is
rare. The quality of such research is also often poor: Clune found that only 1%
of 541 “cost-effectiveness” studies of elementary and secondary education
between 1991 and 1996 could be considered reliable, with strong design and
analysis. In contrast, economic evaluation of healthcare technologies is
increasing, and the methods for making such analysis are rapidly evolving.
There is a sizeable literature on the effectiveness of CPD
interventions (over 100 randomised controlled trials are thoroughly reviewed by
Davis et al), but the evidence on the cost effectiveness of CPD has not been
systematically investigated. In this article we therefore investigate the
quantity and quality of the evidence on the cost effectiveness of CPD for
healthcare professionals.
The literature that assesses the cost effectiveness of CPD
interventions in health care. A literature search showed that economic
evaluations of CPD are rare. It is impossible to draw any feasible conclusions
regarding the cost effectiveness of different modes of CPD for healthcare
professionals.
The external validity of the existing studies may be impaired for many
reasons. This raises concerns over the extent to which the results can be
generalised and used to inform policy. Both costs and technologies change over
time, along with differences in input prices and technologies across settings
(and especially across countries). Also, the studies mainly focused on
intermediate rather than final outcomes: any effects of CPD on patient health
therefore have to be inferred from changes in the behaviour of physicians.
Interpreting the results is difficult since uniform methods
of costing or analysis are not applied. The “ingredients” included in costs
analysis are not identified in a standard form: development costs and the
opportunity costs of the participants needed to be included. In addition, the
resource implications of an educational intervention (such as for additional
screenings) would need to be included in a cost benefit analysis but not in a
cost effectiveness analysis. Often, the evidence seemed to be directed at both
forms of analysis, despite these analyses being methodologically and purposively
distinct.
Overall the literature on the effectiveness of CPD continues
to expand, but effectiveness is not a sufficient criterion for implementation.
For scarce resources to be devoted to CPD, the relative cost effectiveness of
different educational interventions must be established, and those offering the
most value for money must be implemented. An investment in high quality
evaluations would therefore reap health benefits for the public and ease policy
makers’ decisions about resource allocation.
Cost effectiveness analysis must be applied to studies of
educational effectiveness, and this should be possible with the methods detailed
by Levin and McEwan or Drummond and Jefferson. At present, notwithstanding the
substantial resource commitment to CPD, evidence on the cost effectiveness of
CPD is completely inadequate.
The hot flush (or flash) is the most characteristic
manifestation of the climacteric. The climacteric can be defined as all the
physiological and pathological events that directly follow the onset of reduced
ovarian function, both before and after the last menstrual period (the
menopause).
The aetiology of the hot flush is complex and is still
uncertain but is probably caused by lability in the thermoregulatory centre of
the hypothalamus induced by falling oestrogen and progesterone levels.
Instability of the thermoregulatory centre leads to sudden, transient and
erratic peripheral vasodilation in the skin blood vessels with a concomitant
sensation of flushing and a measurable increase in skin temperature. Hot flushes
can occur with differing severity and at different frequency during the day or
night. At night, these changes may be recognised and referred to as night
sweats. Together, hot flushes and night sweats are described as vasomotor
symptoms
A Cochrane Collaboration examined double-blind,
randomised, placebo-controlled trials of oral HRT therapy for at least three
months duration were chosen.
Study participants totalled 2,511. Trial duration ranged from
three months to three years. There was a significant reduction in the weekly hot
flush frequency for HRT compared to placebo. This was equivalent to a 77%
reduction in frequency for HRT relative to placebo.
Symptom severity was also significantly reduced compared to
placebo. Withdrawal for lack of efficacy occurred significantly more often on
placebo therapy. Withdrawal for adverse events, commonly breast tenderness,
oedema, joint pain and psychological symptoms, was not significantly increased
for HRT therapy. In women who were randomised to placebo treatment, a 51%
reduction in hot flushes was observed between baseline and end of study.
Oral HRT is highly effective in alleviating hot flushes and
night sweats. Therapies purported to reduce such symptoms must be assessed in
blinded trials against a placebo or a validated therapy. Withdrawals due to
side-effects were only marginally increased in the HRT groups despite the
inability to tailor HRT in these fixed dose trials. Comparisons of hormonal
doses, product types or regimens require analysis of trials with these specific
"within study" comparisons.
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