Key takeaways:
- High quality of life and angina burden have been related after CT or invasive angiography for CAD prognosis.
- Girls skilled small variations in high quality of life outcomes and chest ache charges vs. males.
Lengthy-term outcomes after CT or invasive coronary angiography to diagnose CAD have been related, with comparable enchancment in most high quality of life measures and angina signs, researchers reported.
Minor variations in some QOL measures and charges of angina have been reported in ladies vs. males, in line with a prespecified secondary evaluation of the DISCHARGE trial revealed in JAMA Cardiology.

“Chest ache signs and QOL in sufferers with suspected CAD usually enhance inside 6 to 12 months after preliminary diagnostic analysis, each in sufferers with and with out a confirmed prognosis of CAD. These advantages have been demonstrated in trials evaluating the effectiveness of cardiac CT with customary of care or useful testing methods,” Nina Rieckmann, PhD, of the Institute of Public Well being at Charité – Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin in Berlin, and colleagues wrote. “To our information, no massive multicenter trial has in contrast QOL and chest ache in sufferers present process CT vs. invasive coronary angiography as first-test methods. Invasive procedures are sometimes extra anxiety-provoking for sufferers, and procedure-related issues could affect sufferers’ subsequent QOL.”
The DISCHARGE trial
DISCHARGE was a randomized trial evaluating CT vs. invasive coronary angiography as preliminary diagnostic methods for guiding the remedy of three,561 sufferers with steady chest ache and intermediate pretest chance of obstructive CAD (imply age, 60 years; 56% ladies).
As Healio beforehand reported, danger for main opposed CV occasions was related after CT in contrast with the invasive technique to diagnose chest ache, and sufferers skilled fewer procedure-related issues with the CT technique.
For the current evaluation of DISCHARGE, researchers assessed the affect on QOL and angina signs following obstructive CAD rule-in or rule-out by way of CT or invasive imaging methods.
The first QOL end result was Euro QOL 5-dimensions descriptive system (EQ-5D-3L) visible analog scale (EQ-5D-3L-VAS) and SF-12 bodily element rating (SF-12-PCS) at a median 3.5-year follow-up. The first prespecified chest ache end result was angina.
Outcomes of DISCHARGE secondary evaluation
At baseline, there was no important distinction in QOL measured by any rating. All major measures of QOL improved considerably for each teams at 3.5 years, except for the Hospital Anxiousness and Despair Scale-Anxiousness (HADS-A) subscale, which was a secondary outcomes measure and solely improved within the diagnostic CT group (imply change, 0.2; 95% CI, 0.4 to 0; P = .04).
Girls had decrease baseline and follow-up QOL rating vs. males however confirmed higher enhancements in EQ-5D-3L-VAS rating (1.9; 95% CI, 3.4 to 0.5; P = .009), SF-12-PCS rating (1.4; 95% CI, 2.1 to 0.7; P < .001), and HADS-A rating (0.3; 95% CI, 0.0-0.7; P = .04), in line with the examine.
Angina charges at a median follow-up of three.5 years have been related between diagnostic CT and invasive methods, however ladies assigned to invasive coronary angiography skilled larger charges vs. males (10.2% vs. 6.2%; P = .007).
“This examine informs the method of shared decision-making about imaging checks in sufferers whose chest ache has an intermediate chance of obstructive CAD,” the researchers wrote. “Regardless of first-test technique, feminine sufferers had considerably bigger enhancements in subjective well being, bodily functioning and nervousness in contrast with male sufferers at 3.5 years. … Our findings assist the idea of the so-called gender paradox, through which females presenting with steady chest ache and suspected CAD usually report extra signs however have much less extreme myocardial ischemia and obstructive coronary artery illness in contrast with males, though we acknowledge that we didn’t measure complete symptom burden within the DISCHARGE trial.”