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Table 2b Clinical characteristics at randomisation not used in minimisation algorithm, and recorded at randomisation

From: Update on the third international stroke trial (IST-3) of thrombolysis for acute ischaemic stroke and baseline features of the 3035 patients recruited

  

No.

(%)

Cardiac rhythm

Sinus rhythm, not AF

2121

(70%)

 

Atrial fibrillation

914

(30%)

Systolic BP at randomisation

< = 140 mmHg

897

(30%)

 

141 to 180 mmHg

1738

(57%)

 

> 180 mmHg

400

(13%)

 

median (interquartile range)

155 (140, 170)

Diastolic BP at randomisation

< = 80 mmHg

1537

(51%)

 

81 to 110 mmHg

1420

(47%)

 

> 110 mmHg

78

(3%)

 

median (interquartile range)

80 (71, 91)

Blood glucose1

< 3.5 mmol/l

7

(0%)

 

3.5-6 mmol/l

532

(18%)

 

6-8 mmol/l

1654

(54%)

 

> 8 mmol/l

559

(18%)

 

not measured (old form)

283

(9%)

 

median (interquartile range)

7.0 (6.0, 8.0)

Probability of being alive and independent at 6 m2

< 0.30

1383

(46%)

 

> = 0.30

1652

(54%)

 

median (interquartile range)

0.35 (0.12, 0.59)

Recruited at a centre with pre-trial experience3

Centres without pre-trial experience

1891

(62%)

 

Centre with pre-trial experience

1144

(38%)

Doctor's opinion of scan at randomisation

Normal

1792

(59%)

 

Possible evidence of recent ischaemic change

701

(23%)

 

Definite evidence of recent ischaemic change

542

(18%)

  1. 1. For the first 282 patients, glucose was not recorded. After patient 282, it was collected at randomisation. Glucose therefore was not available for those 282 patients
  2. 2. Probability calculated with a validated prognostic model from baseline data [14].
  3. 3. Pre-trial experience of thrombolysis is defined as having had a protocol for open label rtPA and had treated at least 3 people in the 12 months before joining the trial; 76 (49%) centres met this criterion.