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(Stroke. 2004;35:2211.)
© 2004 American Heart Association, Inc.
Comments, Opinions, and Reviews |
From the Department of Clinical Neurosciences, Western General Hospital, Edinburgh, UK.
Correspondence to Dr Charles P. Warlow, Department of Clinical Neurosciences, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK. E-mail cpw@skull.dcn.ed.ac.uk
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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"We should deliver an exact neurology, or doctrine of the nerves" and "without the perfect knowledge of the nerves the doctrine of the brain and its appendix would be left wholly lame and imperfect."
Of course, his pharmacopoeia was primitive in the extreme and he had no reliable way of proving that any treatment interventions worked, unless they had a very obvious and immediate effect. But these days we have the most remarkable tool to evaluate our interventions, the randomized controlled trial, although it is not yet 60 years since the first trial in the modern era was published in the BMJ on October 30, 1948, of streptomycin for pulmonary tuberculosis3 (Figure 1). It was conducted in the UK just after World War II when the supply of the antibiotic was so limited that Austin Bradford Hill, the statistician, was able to persuade clinicians to use randomization between the new treatment and control as a form of fair rationing and to construct 2 groups of patients who were so similar in their prognosis at baseline that any definite difference in their outcome must be because of the new treatment.
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