Fabrizio D'Ascenzo1, Enrico Cerrato2, Darryn Appleton3, Claudio Moretti1, Andrea Calcagno4, Nayef Abouzaki3, George Vetrovec3, Thibault Lhermusier5, Didier Carrie6, Barbara Das Neves7, Javier Escaned7, Salvatore Cassese8, Adnan Kastrati8, Alessandra Chinaglia4, Riccardo Belli9, Davide Capodanno5, Corrado Tamburino6, Francesca Santilli10, Guido Parodi11, Ahmed Vachiat12, Pravin Manga12, Luigi Vignali13, Massimo Mancone14, Gennaro Sardella14, Francesco Fedele1, James J DiNicolantonio15, Pierluigi Omedè1, Stefano Bonora16, Fiorenzo Gaita1, Antonio Abbate17, Giuseppe Biondi Zoccai18. 1. Division of Cardiology, Città della Salute e della Scienza "Molinette" Hospital, University of Turin, Turin, Italy. 2. Division of Cardiology, Città della Salute e della Scienza "Molinette" Hospital, University of Turin, Turin, Italy; Division of Cardiology, Hospital Clinico San Carlos, Madrid, Spain. 3. VCU Pauley Heart Center, Richmond, VA, USA. 4. Division of Cardiology, Maria VittoriaHospital, Turin, Italy; Division of Infectious Disease, Amedeo di Savoia Hospital, Turin, Italy. 5. Department of Cardiology, Rangueil Hospital, Toulouse, France. 6. Division of Cardiology, Ferrarotto Hospital, University of Catania, Italy. 7. Division of Cardiology, Hospital Clinico San Carlos, Madrid, Spain. 8. Deutsches Herzzentrum, Munich, Germany. 9. Division of Cardiology, Maria VittoriaHospital, Turin, Italy. 10. Division of Cardiology, Università degli Studi 'G. d'Annunzio' Chieti e Pescara, Italy. 11. Division of Cardiology, Università degli Studi 'G. d'Annunzio' Chieti e Pescara, Italy; Division of Cardiology, Careggi Hospital, Florence, Italy. 12. University of Witwatersrand Charlotte Maxeke Johannesburg Academic Hospital, Division of Cardiology. 13. Department of Cardiology, University of Parma, Italy. 14. Department of Cardiovascular and Pulmonary Sciences, Policlinico Umberto I "Sapienza", University of Rome, Italy. 15. Wegmans Pharmacy, Ithaca, NY. 16. Division of Infectious Disease, Amedeo di Savoia Hospital, Turin, Italy. 17. VCU Pauley Heart Center, Richmond, VA, USA. Electronic address: abbatea@yahoo.com. 18. Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy. Electronic address: gbiondizoccai@gmail.com.
Abstract
AIMS: Limited data are available on prognostic indicators for HIV patients presenting with ACS. METHODS AND RESULTS: Data on consecutive patients with HIV infection receiving standard highly active antiretroviral therapy (HAART) presenting with ACS between January 2001 and September 2012 were collected. Cardiac death and myocardial infarction (MI) were the primary end-points. 10,050 patients with ACS were screened, and among them a total of 201 patients (179 [89%] males and a median age of 53 [47-62] years) were included, 48% of them admitted for ST-elevation myocardial infarction and 14% having left ventricular systolic dysfunction (LVSD) at discharge. CD4+ counts less than 200 cells/mm(3) were reported in 18 patients (9%), and 136 patients (67%) were treated with nucleoside-reverse transcriptase inhibitors (NRTI). After a median of 24 months (10-41), 30 patients (15%) died, 12 (6%) for cardiac reasons, 20 (10%) suffered a MI, 29 (15%) a subsequent revascularization, and 7 (3%) a stent thrombosis. Other than LVSD (hazard ratio=6.4 [95% confidence interval [CI]: 1.6-26: p=0.009]), the only other independent predictor of cardiac death was not being treated with NRTI (hazard ratio=9.9 [95% CI: 2.1-46: p=0.03); a CD4 cell count <200 cells/mm(3) was the only predictor of MI (hazard ratio=5.9 [95% CI: 1.4-25: p=0.016]). CONCLUSIONS: HIV patients presenting with ACS are at significantly increased risk for cardiac death if not treated with NRTI, and at significantly increased risk of MI if their CD4 cell count is <200 cells/mm(3), suggesting that the stage of HIV disease (and lack of NRTI treatment) may contribute to cardiovascular instability.
AIMS: Limited data are available on prognostic indicators for HIVpatients presenting with ACS. METHODS AND RESULTS: Data on consecutive patients with HIV infection receiving standard highly active antiretroviral therapy (HAART) presenting with ACS between January 2001 and September 2012 were collected. Cardiac death and myocardial infarction (MI) were the primary end-points. 10,050 patients with ACS were screened, and among them a total of 201 patients (179 [89%] males and a median age of 53 [47-62] years) were included, 48% of them admitted for ST-elevation myocardial infarction and 14% having left ventricular systolic dysfunction (LVSD) at discharge. CD4+ counts less than 200 cells/mm(3) were reported in 18 patients (9%), and 136 patients (67%) were treated with nucleoside-reverse transcriptase inhibitors (NRTI). After a median of 24 months (10-41), 30 patients (15%) died, 12 (6%) for cardiac reasons, 20 (10%) suffered a MI, 29 (15%) a subsequent revascularization, and 7 (3%) a stent thrombosis. Other than LVSD (hazard ratio=6.4 [95% confidence interval [CI]: 1.6-26: p=0.009]), the only other independent predictor of cardiac death was not being treated with NRTI (hazard ratio=9.9 [95% CI: 2.1-46: p=0.03); a CD4 cell count <200 cells/mm(3) was the only predictor of MI (hazard ratio=5.9 [95% CI: 1.4-25: p=0.016]). CONCLUSIONS:HIVpatients presenting with ACS are at significantly increased risk for cardiac death if not treated with NRTI, and at significantly increased risk of MI if their CD4 cell count is <200 cells/mm(3), suggesting that the stage of HIV disease (and lack of NRTI treatment) may contribute to cardiovascular instability.
Authors: Luis M Beltrán; Alfonso Rubio-Navarro; Juan Manuel Amaro-Villalobos; Jesús Egido; Juan García-Puig; Juan Antonio Moreno Journal: Vasc Health Risk Manag Date: 2015-01-06
Authors: Monica M Parks; Eric A Secemsky; Robert W Yeh; Changyu Shen; Eunhee Choi; Dhruv S Kazi; Priscilla Y Hsue Journal: Eur Heart J Qual Care Clin Outcomes Date: 2021-05-03