<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors></authors><secondary-authors><author><style face="normal" font="default" size="100%">Pedersen, Torje</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">IDEAL—Lowering CHD Risk with High-Dose Statins</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2005-12-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">27-27</style></pages><abstract><style  face="normal" font="default" size="100%">The IDEAL (Incremental Decrease in Clinical Endpoints Through Aggressive Lipid Lowering) Trial compared high and low doses of statins over a five-year time period. The primary endpoint was a composite of heart attack, coronary heart disease death, or cardiac arrest with resuscitation. Secondary endpoints included the primary events plus unstable angina that required hospitalization, coronary artery bypass graft (CABG), or percutaneous coronary intervention (PCI).</style></abstract><number><style face="normal" font="default" size="100%">1</style></number><volume><style face="normal" font="default" size="100%">5</style></volume></record></records></xml>