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Therapeutics |
Clinical impact ratings IM/Ambulatory care






Cardiology 





Neurology 





Endocrine 





Key Words: cerebrovascular disorders cholesterol (LDL) coronary disease drug delivery systems heptanoic acids pyrroles
| The first 150 words of the full text of this article appear below. |
METHODS
Design:
randomised controlled trial.
Allocation:
{concealed*}
.
Blinding:
blinded (clinicians, patients, and endpoints adjudication committee).*
Follow up period:
median 4.9 years.
Setting:
256 sites in 14 countries across 4 continents.
Patients:
10 001 patients 3575 years of age (mean age 61 y, 81% men) who had clinically evident CHD (defined as previous myocardial infarction or coronary revascularisation, or previous or current angina with objective evidence of CHD), low density lipoprotein cholesterol (LDL-C) concentration 130250mg/dl (3.46.5 mmol/l), and triglyceride concentration
600 mg/dl (6.8 mmol/l). LDL-C concentration was required to be <130 mg/dl (3.4 mmol/l) during an 8 week run in period with atorvastatin, 10 mg/day.
Intervention:
atorvastatin, 80 mg/day (n = 4995) or atorvastatin, 10 mg/day (n = 5006), with target mean LDL-C concentrations 75 mg/dl (1.9 mmol/l) and 100 mg/dl (2.6 mmol/l), respectively.
Outcomes:
cerebrovascular events, including fatal or non-fatal stroke and transient ischaemic attack (TIA) (predefined secondary outcome).
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Walter Reed Army Medical Center, Washington, DC, USA
Relevant Article
Evid. Based Med. 2007 12: 63-64.
(in )
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