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Phil Alderson a UK Cochrane Centre, NHS
Research and Development Programme, Oxford OX2 7LG, b Child Health Monitoring
Unit, Institute of Child Health, University College, London WC1N 1EH
Correspondence to:
P Alderson palderson{at}cochrane.co.uk
Many systematic reviews are inconclusive and reinforce the
message that there is clinical uncertainty. Phil Alderson and Ian Roberts argue that journals should make a point of publishing such
reviews rather than waiting for reviews that show marked benefit or
harm. Some experts disagree, however, but we failed to persuade them to
commit their views to print.
Studies with dramatic findings make interesting reading.
Journal editors understandably want to publish articles that their readers will enjoy. This is one cause of publication bias, where research with less dramatic results tends to be published in journals with a smaller circulation, if indeed it is published at all. Systematic reviews are no less vulnerable to this bias than other types
of research. Should journals resist this pressure and make a point of
publishing systematic reviews even if all they show is continuing
clinical uncertainty? The answer will depend on the importance we
attach to demonstrating uncertainty in medical practice.
Worldwide, several million people are treated each year for
severe head injury.1 Over a million of them die, and many
more are permanently disabled. In many places, hyperventilation,
mannitol, drainage of cerebrospinal fluid, barbiturates, and
corticosteroids are routinely used in the intensive care management of
severely head injured patients, yet none of these interventions has
been reliably shown to reduce death or disability. Indeed, on the basis of the currently available randomised evidence, it is impossible to
refute either a moderate increase or a moderate decrease in the risk of
death or disability.2 Not surprisingly, use of these
treatments varies widely.3-5 A 1996 survey of treatments for raised intracranial pressure in 44 neurosurgical units in the
United Kingdom and Ireland found that hyperventilation was used in 89%
of units, drainage of cerebrospinal fluid in 69% of units,
barbiturates in 69% of units, and corticosteroids in 14% of
units.3 Given the uncertainty about the effectiveness of these interventions, this variation in practice might be seen as a
large but poorly controlled experiment. Patients taking part in this
experiment enjoy none of the benefits of treatment decisions being
vetted by a research ethics committee. No useful clinical information
will result from their participation. In this instance it is hard to
see how the censoring of clinical uncertainty serves the interests of
current or future patients.
Greater openness about uncertainty would challenge the prevailing
health care culture of uncontrolled experimentation on the many and
controlled experimentation on the few. Reliable answers to many
important therapeutic questions require large scale randomised controlled trials.6 Acknowledging uncertainty is a
prerequisite for such trials, and the "uncertainty principle" can
be used to simplify trial entry criteria and make large trials
possible. According to this principle, a patient can be entered into a
randomised controlled trial if, and only if, the responsible clinician
and the patient are substantially uncertain which of the trial
treatments would be most appropriate. Publication of systematic reviews
showing uncertainty stimulates and facilitates such trials, as in the case of the current Medical Research Council trial of corticosteroids in head injury.7
More trials and larger trials would undoubtedly bring some surprises.
Human albumin solution was widely regarded to be safe and effective in
the fluid management of critically ill patients until a systematic
review of the evidence from randomised trials challenged this. The
review raised clinical uncertainty despite 50 years of use of human
albumin in medicine.8 Uncertainty is the lifeblood of
clinical research, and the censorship of clinical uncertainty can only
pave the way for pallid research agendas reflecting commercial interests.
Reviews are more likely to have dramatic findings if their methods
are weak. Journal prejudice against reviews of research which have
revealed uncertainty may be one reason why the characteristics of
reviews published in the Cochrane Database of Systematic
Reviews differ from those published in print journals. Compared
with Cochrane reviews, samples of reviews published in print journals
have shown more evidence of publication bias9 and less
evidence of methodological rigour.10 For example, failure
to search non-English literature introduces bias because studies with
dramatic results appear preferentially in the English language
literature. If clinical journals prefer reviews with dramatic findings,
they may be creating incentives to do poor quality reviews, which is in
no-one's best interests. These trends may mislead those who think they
have found evidence that they believe should influence clinical practice.
So the uncertainty demonstrated in systematic reviews can help
clarify the options available to clinicians and patients. It can
stimulate more research and better research and so help to resolve
uncertainty. Uncertainty should not be hidden away as an embarrassment.
We should be willing to admit that "we don't know" so that the
evidential base of health care can be improved for future generations.
The censorship of uncertainty is the enemy of evidence based care. The
opportunity cost of the illusion of clinical certainty, whether
measured in terms of clinical trials never conducted, morbidity and
mortality resulting from the use of inappropriate forms of care, or the
health resources squandered, might easily exceed the annual health care
budget. Confidence in the face of ignorance may be the hallmark of a
traditional medical education, but journal editors need not collude in this.
Summary points
Denying uncertainty does not benefit patients and may increase
health service costs
More large scale randomised trials need to be conducted based on the
"uncertainty principle"
Systematic reviews with more dramatic results tend to be
methodologically weaker
Publication bias against reviews which show uncertainty may create
incentives for poor quality reviews
Admitting uncertainty helps clarify treatment options and stimulates
further research

(Credit: SUE SHARPLES)
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Censoring uncertainty does not benefit patients
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Reasons for publication bias
![]()
Benefits of admitting uncertainty
| |
Acknowledgments |
|---|
We thank Iain Chalmers for helpful comments.
| |
Footnotes |
|---|
Competing interests: PA and IR are involved in the Cochrane Collaboration.
| |
References |
|---|
| 1. | Jennett B. Epidemiology of head injury. J Neurol Neurosurg Psychiatry 1996; 60: 362-369[Medline]. |
| 2. |
Roberts I, Schierhout G, Alderson P.
Absence of evidence for the effectiveness of five interventions routinely used in the intensive care management of severe head injury: a systematic review.
J Neurol Neurosurg Psychiatry
1998;
65:
729-733 |
| 3. | Maata B, Menon D. Severe head injury in the United Kingdon and Ireland:a survey of practice and implications for management. Crit Care Med 1996; 24: 1743-1748[CrossRef][Medline]. |
| 4. |
Jeevaratnam DR, Menon DK.
Survey of intensive care of severely head injured patients in the United Kingdom.
BMJ
1996;
312:
944-947 |
| 5. | Ghajar J, Hairi RJ, Narayan RK, Iacono LA, Firlik K, Patterson RH. Survey of critical care management of comatose head-injured patients in the United States. Crit Care Med 1995; 23: 560-567[CrossRef][Medline]. |
| 6. |
Peto R, Baigent C.
Trials: the next 50 years. Large scale randomised evidence of moderate benefits.
BMJ
1998;
317:
1170-1171 |
| 7. | www.crash.ucl.ac.uk |
| 8. |
Cochrane Injuries Group Albumin Reviewers.
Human albumin administration in critically ill patients: systematic review of randomised controlled trials.
BMJ
1998;
317:
235-240 |
| 9. |
Egger M, Davey Smith G, Schneider M, Minder C.
Bias in meta-analysis detected by a simple, graphical test.
BMJ
1997;
315:
629-634 |
| 10. |
Jadad AR, Cook DJ, Jones A, Klassen TP, Tugwell P, Moher M, et al.
Methodology and reports of systematic reviews and meta-analyses: a comparison of Cochrane reviews with articles published in paper-based journals.
JAMA
1998;
280:
278-280 |
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