Bailleul Amaury, Fulgencio Jean-Pierre, Vimont Sophie, Mordelet Cécile, Ray Benoit, Lassel Ludovic, Lapidus Nathanaël, Quesnel Christophe, Garnier Marc
Sorbonne Université, AP-HP, GRC29, DMU DREAM, Hôpital Tenon, Service d'Anesthésie-Réanimation et Médecine Périopératoire - 4 rue de la Chine, 75020 Paris, France.
Département de Bactériologie, Hôpital Saint-Antoine, AP-HP, Sorbonne Université, - 184 rue du Faubourg Saint-Antoine, 75012 Paris, France; Sorbonne Université, INSERM UMR S_1155, Hôpital Tenon, Paris, France.
Infect Dis Now. 2023 Oct;53(8):104766. doi: 10.1016/j.idnow.2023.104766. Epub 2023 Aug 3.
Totally implantable venous access ports (TIVAP) are devices mainly used to deliver antineoplastic chemotherapies, of which the insertion may be complicated by TIVAP-related infection (TIVAP-RI). This study aims to provide data on the risk factors for TIVAP-RI and its influence on patient prognosis.
Prospective observational study including adult patients with solid tumors, in whom a TIVAP was inserted to deliver antineoplastic chemotherapy between January 2018 and October 2019. Factors associated with TIVAP-RI and one-year mortality were determined using multiple logistic regressions.
More than a thousand (1014) patients were included, among whom 48 (4.7%) presented with TIVAP-RI. Gram-positive cocci and Gram-negative bacilli represented 51% and 41% of the pathogens isolated, respectively. Young age (odds ratio [OR] 0.67; 95% Confidence Interval [0.53-0.83] per 10-year increase), WHO performance status ≥ 1 (OR 3.24 [1.52-7.79]), chemotherapy administration in the month before TIVAP placement (OR 2.26 [1.17-4.26]), and radiation therapy of the homolateral chest wall (OR 3.28 [1.51-6.67]) were independently associated with TIVAP-RI occurrence. During the year following TIVAP insertion, 287 (28%) patients died. TIVAP-RI was not associated with one-year mortality (OR 1.56 [0.75-3.19]).
TIVAP insertion in adult patients with solid tumors is associated with a low infection rate, which did not influence one-year mortality. In addition to young age and impaired health status, TIVAP insertion in the month following initiation of the antineoplastic chemotherapy and TIVAP insertion in an irradiated area are two newly reported preventable TIVAP-RI risk factors.
完全植入式静脉通路导管(TIVAP)主要用于输注抗肿瘤化疗药物,其置入过程可能并发与TIVAP相关的感染(TIVAP-RI)。本研究旨在提供TIVAP-RI的危险因素及其对患者预后影响的数据。
前瞻性观察性研究,纳入2018年1月至2019年10月期间因输注抗肿瘤化疗药物而置入TIVAP的成年实体瘤患者。采用多因素logistic回归分析确定与TIVAP-RI及1年死亡率相关的因素。
共纳入1000多名(1014例)患者,其中48例(4.7%)发生TIVAP-RI。分离出的病原体中,革兰氏阳性球菌和革兰氏阴性杆菌分别占51%和41%。年龄较小(每增加10岁,比值比[OR]为0.67;95%置信区间[0.53-0.83])、世界卫生组织体能状态≥1(OR为3.24[1.52-7.79])、在TIVAP置入前1个月内进行化疗(OR为2.26[1.17-4.26])以及同侧胸壁放疗(OR为3.28[1.51-6.67])与TIVAP-RI的发生独立相关。在TIVAP置入后的1年内,287例(28%)患者死亡。TIVAP-RI与1年死亡率无关(OR为1.56[0.75-3.19])。
成年实体瘤患者置入TIVAP的感染率较低,且不影响1年死亡率。除年龄较小和健康状况受损外,在抗肿瘤化疗开始后的1个月内置入TIVAP以及在放疗区域置入TIVAP是两个新报道的可预防的TIVAP-RI危险因素。