García-Cruz Edgar, Villalobos-Pedroza Montserrat, Antonio-Villa Neftali Eduardo, Manzur-Sandoval Daniel, Navarro-Martínez Daniel Alejandro, Barrera-Real Axel J, Mier Y Terán-Morales Elisa, Angulo-Cruzado Stephanie Teresa, García-González Naybeth Ediel, Cervantes-Salazar Jorge Luis, Benita-Bordes Antonio, Díaz-Gallardo Linda Guieniza, Quiroz-Martinez Victor Alejandro, Sauza-Sosa Julio César, Montalvo-Ocotoxtle Isis Guadalupe, Ferrer-Saldaña Jeyli Estrella, Lazcano-Díaz Emmanuel A, Ávila-Vanzzini Nydia, Baranda-Tovar Francisco Martín
Adult Congenital Heart Disease Clinic, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Int J Cardiol Congenit Heart Dis. 2024 Jan 19;15:100492. doi: 10.1016/j.ijcchd.2024.100492. eCollection 2024 Mar.
Latin American registries of clinical and demographic profiles of ACHD are scarce. International guidelines classify disease complexity with different approaches. With these two regards, a registry was carried out to examine factors associated with mortality and to compare severity classifications in our population.
Cross-sectional study conducted on ACHD between 2018 and 2022 to evaluate clinical and demographic characteristics and to assess the agreement between the 2020 ESC Guidelines and 2018 AHA/ACC Guidelines for the Management of Adults with Congenital Heart Disease using the method. Binomial logistic regression models were used to examine correlates of mortality. 3459 patients were included [56 % women, median age 34 years (IQR 24-50)]; 83.41 % were alive and 4.11 % died. The subjects had the following characteristics: 74.18 % were in NYHA I FC, 87.30 % had SVEF ≥50 %, 18.42 % developed arrhythmias, 58.92 % were surgically repaired, 7.05 % received palliative management, and 0.03 % were in heart transplant protocol. The agreement between ESC and AHA/ACC complexity classifications was low (43.29 %) in moderate ACHD, and high (83.10 %) in severe disease. Mortality was higher in patients with NYHA III-IV FC, arrhythmias and under palliative care.
This study found that ESC and AHA/ACC complexity classifications have limited concordance in categorizing moderate complexity CHD. Reparative procedures had lower mortality odds than palliative care.
拉丁美洲关于先天性心脏病(ACHD)临床和人口统计学特征的登记资料匮乏。国际指南采用不同方法对疾病复杂性进行分类。基于这两点,开展了一项登记研究,以检查与死亡率相关的因素,并比较我们研究人群中的严重程度分类。
于2018年至2022年对ACHD患者进行横断面研究,以评估临床和人口统计学特征,并使用 方法评估2020年欧洲心脏病学会(ESC)指南和2018年美国心脏协会(AHA)/美国心脏病学会(ACC)成人先天性心脏病管理指南之间的一致性。采用二项逻辑回归模型检查死亡率的相关因素。纳入3459例患者[56%为女性,中位年龄34岁(四分位间距24 - 50岁)];83.41%存活,4.11%死亡。受试者具有以下特征:74.18%处于纽约心脏协会(NYHA)心功能分级I级,87.30%左心室射血分数(LVEF)≥50%,18.42%发生心律失常,58.92%接受手术修复,7.05%接受姑息治疗,0.03%进入心脏移植程序。ESC和AHA/ACC复杂性分类在中度ACHD中的一致性较低(43.29%),在重度疾病中较高(83.10%)。NYHA心功能分级III - IV级、有心律失常和接受姑息治疗的患者死亡率较高。
本研究发现,ESC和AHA/ACC复杂性分类在对中度复杂性先天性心脏病进行分类时一致性有限。修复性手术的死亡几率低于姑息治疗。