Key result
Prolonged acoustic cardiography electromechanical activation time identifies post-anthracycline systolic dysfunction with ~88% sensitivity.
Why the study?
The usefulness of echocardiography and acoustic cardiography to monitor patients undergoing anthracycline chemotherapy was investigated to assess the need for serial echocardiographies.
Does acoustic cardiography accurately identify systolic dysfunction in patients undergoing anthracycline chemotherapy?
Cohort (n=187)
Does acoustic cardiography accurately identify systolic dysfunction in patients undergoing anthracycline chemotherapy?
Acoustic cardiography provides high sensitivity and specificity for detecting early systolic dysfunction in patients undergoing anthracycline chemotherapy, potentially streamlining monitoring algorithms.
May support acoustic cardiography for detecting anthracycline-related systolic dysfunction; leaves open its role in monitoring algorithms pending prospective validation.
BACKGROUND: Investigate the usefulness of echocardiography and acoustic cardiography to monitor patients exposed to anthracycline chemotherapy. HYPOTHESIS: Serial echocardiographies to monitor systolic function may not be neccessary in all patients undergoing anthracycline chemotherapy. METHODS: In a prospective study, consecutive patients undergoing anthracycline-containing chemotherapy were evaluated with echocardiography and acoustic cardiography at baseline, after completion of chemotherapy, and after a median follow-up of 3.8 years. Systolic dysfunction was defined as a left ventricular ejection fraction≤50%. RESULTS: A total of 187 patients (83% female) with a mean age of 55±14 years underwent chemotherapy for breast cancer (73%), malignant lymphoma (23%), and sarcoma (4%). None of the patients had systolic dysfunction at baseline. Patients were treated with doxorubicin 276±74 mg/m2 or epirubicin 317±55 mg/m2. After chemotherapy, 170 (91%) had normal systolic function, 8 (4%) developed systolic dysfunction, and 9 (5%) had died. Of those 8 patients with systolic dysfunction, 4 (50%) improved to normal systolic function, 1 (13%) remained unchanged, and 3 (37%) died. Patients with normal systolic function after chemotherapy had a mortality rate of 3.5%, and 1.8% developed late systolic dysfunction. Acoustic cardiography-derived percent electromechanical activation time>12.4% had a sensitivity of 88% and a specificity of 84% to identify patients with systolic dysfunction (area under the receiver operating characteristic curve 0.87). CONCLUSIONS: Patients with systolic dysfunction early after anthracycline treatment had worse outcome. Acoustic cardiography was able to identify these patients with a high sensitivity and specificity. Based on the findings of this study, we propose a simple algorithm to monitor patients undergoing anthracycline-containing chemotherapy.
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Toggweiler et al. (2012) conducted a cohort in Patients undergoing anthracycline chemotherapy (n=187). Anthracycline chemotherapy was evaluated on Systolic dysfunction (left ventricular ejection fraction ≤50%). Acoustic cardiography-derived percent electromechanical activation time >12.4% identified systolic dysfunction after anthracycline chemotherapy with 88% sensitivity and 84% specificity (AUC 0.87).
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