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Karen Dickinson a Cochrane Injuries Group, Child
Health Monitoring Unit, Department of Epidemiology and Public Health,
Institute of Child Health, London WC1N 1EH, b Child Health Monitoring Unit, Department of
Epidemiology and Public Health, Institute of Child Health
Correspondence to: I Roberts ian.roberts{at}ich.ucl.ac.uk
Objective:
To assess whether trials in head injury are large enough to avoid moderate random errors and designed to avoid moderate biases.
Design:
All randomised controlled trials on the
treatment and rehabilitation of patients with head injury published
before December 1998 were surveyed. Trials were identified from
electronic databases, by hand searching journals and conference
proceedings, and by contacting researchers. Data were extracted on the
number of participants, quality of concealment of allocation, use of blinding, loss to follow up, and types of participants, interventions, and outcome measures.
Results:
279 reports were identified, containing
information on 208 separate trials. The average number of participants
per trial was 82, with no evidence of increasing size over time. The total number of randomised participants in the 203 trials in which size
was reported was 16 613. No trials were large enough to detect reliably a 5% absolute reduction in the risk of death or disability, and only 4% were large enough to detect an absolute reduction of 10%.
Concealment of allocation was adequate in 22 and inadequate or unclear
in 25 of the 47 (23%) in which it was reported. Of 126 trials
assessing disability, 111 reported the number of patients followed up,
and average loss to follow up was 19%. Of trials measuring disability,
26 (21%) reported that outcome assessors were blinded.
Conclusions:
Randomised trials in head injury are too
small and poorly designed to detect or refute reliably moderate but clinically important benefits or hazards of treatment. Limited funding
for injury research and unfamiliarity with issues of consent may have
been important obstacles.
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