Faculté de Médecine, Université de Strasbourg (UNISTRA), Strasbourg university hospital, Nouvel Hôpital Civil, Medical intensive care unit, Strasbourg, France.
Department of Medical Oncology, Strasbourg-Europe Cancer Institute (ICANS), Strasbourg, France.
Eur Heart J Acute Cardiovasc Care. 2023 Oct 25;12(10):682-692. doi: 10.1093/ehjacc/zuad072.
Characteristics, management, and outcomes of patients with active cancer admitted for cardiogenic shock remain largely unknown. This study aimed to address this issue and identify the determinants of 30-day and 1-year mortality in a large cardiogenic shock cohort of all aetiologies.
FRENSHOCK is a prospective multicenter observational registry conducted in French critical care units between April and October 2016. 'Active cancer' was defined as a malignancy diagnosed within the previous weeks with planned or ongoing anticancer therapy. Among the 772 enrolled patients (mean age 65.7 ± 14.9 years; 71.5% male), 51 (6.6%) had active cancer. Among them, the main cancer types were solid cancers (60.8%), and hematological malignancies (27.5%). Solid cancers were mainly urogenital (21.6%), gastrointestinal (15.7%), and lung cancer (9.8%). Medical history, clinical presentation, and baseline echocardiography were almost the same between groups. In-hospital management significantly differed: patients with cancers received more catecholamines or inotropes (norepinephrine 72% vs. 52%, P = 0.005 and norepinephrine-dobutamine combination 64.7% vs. 44.5%, P = 0.005), but had less mechanical circulatory support (5.9% vs. 19.5%, P = 0.016). They presented a similar 30-day mortality rate (29% vs. 26%) but a significantly higher mortality at 1-year (70.6% vs. 45.2%, P < 0.001). In multivariable analysis, active cancer was not associated with 30-day mortality but was significantly associated with 1-year mortality in 30-day survivors [HR 3.61 (1.29-10.11), P = 0.015].
Active cancer patients accounted for almost 7% of all cases of cardiogenic shock. Early mortality was the same regardless of active cancer or not, whereas long-term mortality was significantly increased in patients with active cancer.
患有活动期癌症并因心原性休克入院的患者的特征、治疗方法和结局在很大程度上仍不清楚。本研究旨在解决这一问题,并确定各种病因所致大型心原性休克患者队列中 30 天和 1 年死亡率的决定因素。
FRENSHOCK 是一项于 2016 年 4 月至 10 月在法国重症监护病房进行的前瞻性多中心观察性研究。“活动期癌症”定义为在过去数周内诊断出的恶性肿瘤,伴有计划或正在进行的抗癌治疗。在纳入的 772 例患者中(平均年龄 65.7 ± 14.9 岁;71.5%为男性),51 例(6.6%)患有活动期癌症。其中,主要癌症类型为实体癌(60.8%)和血液系统恶性肿瘤(27.5%)。实体癌主要为泌尿生殖系统(21.6%)、胃肠道(15.7%)和肺癌(9.8%)。各组间的既往病史、临床表现和基线超声心动图几乎相同。住院期间的治疗方法存在显著差异:癌症患者接受更多的儿茶酚胺或正性肌力药物(去甲肾上腺素 72%比 52%,P = 0.005 和去甲肾上腺素-多巴酚丁胺联合用药 64.7%比 44.5%,P = 0.005),但机械循环支持较少(5.9%比 19.5%,P = 0.016)。两组患者的 30 天死亡率相似(29%比 26%),但 1 年死亡率差异显著(70.6%比 45.2%,P < 0.001)。多变量分析显示,活动期癌症与 30 天死亡率无关,但与 30 天存活者的 1 年死亡率显著相关[风险比 3.61(1.29-10.11),P = 0.015]。
患有活动期癌症的患者占心原性休克所有病例的近 7%。无论是否患有活动期癌症,早期死亡率均相同,而患有活动期癌症的患者长期死亡率显著增加。