Schwarz R E, Groeger J S, Coit D G
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Cancer. 1997 Apr 15;79(8):1635-40.
Long term intravenous access is a common requirement for cancer patients. This analysis was designed to determine device-related morbidity and factors predictive of poor long term outcome for patients with subcutaneous single lumen intravenous access ports.
Six hundred eighty patients who underwent subcutaneous intravenous port placement between June 1987 and May 1989 at Memorial Sloan-Kettering Cancer Center were followed prospectively until port removal, death, or a maximum of 1960 days. Indications for and circumstances of placement, patient diagnoses, patient demographics, and subsequent courses of treatment were recorded, as well as technical and microbiologic device-related complications. Total, device specific, and complication free device durations were calculated.
The median patient age was 52.4 years (range, 1.6-83.9 years). The female-to-male ratio was 1.5 to 1. Cancer diagnoses included solid organ tumors (84%), leukemia (4%), lymphoma (11%), and others (1%). Indications included access for systemic chemotherapy (98%), total parenteral nutrition (0.5%), and others (1.5%). One insertion complication and six insertion failures occurred, without mortality. The estimated mean overall actuarial device specific duration was 1191 days (range, 2-1960 days). Actuarial mean complication free, device specific duration was 952 days. Complications included sepsis (n = 31; 4.4%), site infection (n = 31; 4.4%), and accessibility failures such as thrombosis and leakage (n = 40, 5.7%). Reasons for end of port duration were patient death (72.4%), end of treatment (13.5%), functional failure or intractable infection (11.2%), and others (2.9%). Independent factors correlating with decreased port specific, complication free duration included placement site, age, tumor type, and catheter tip position.
Subcutaneous intravenous access ports in cancer patients are safe and well tolerated. Long term device duration is primarily influenced by patient survival. In this study, 90% of patients alive at 1 year and 70% of patients alive at 4 years had a functional port.
长期静脉通路是癌症患者的常见需求。本分析旨在确定皮下单腔静脉通路端口患者与装置相关的发病率以及预测长期不良结局的因素。
对1987年6月至1989年5月在纪念斯隆凯特琳癌症中心接受皮下静脉端口置入术的680例患者进行前瞻性随访,直至端口移除、患者死亡或最长随访1960天。记录置入的指征和情况、患者诊断、患者人口统计学资料以及后续治疗过程,以及与装置相关的技术和微生物学并发症。计算总的、特定装置的以及无并发症的装置使用时长。
患者年龄中位数为52.4岁(范围1.6 - 83.9岁)。男女比例为1.5比1。癌症诊断包括实体器官肿瘤(84%)、白血病(4%)、淋巴瘤(11%)和其他(1%)。置入指征包括全身化疗通路(98%)、全胃肠外营养(0.5%)和其他(1.5%)。发生1例置入并发症和6例置入失败,无死亡病例。估计平均总体特定装置精算使用时长为1191天(范围2 - 1960天)。无并发症的特定装置精算平均使用时长为952天。并发症包括败血症(n = 31;4.4%)、局部感染(n = 31;4.4%)以及诸如血栓形成和渗漏等通路失败(n = 40,5.7%)。端口使用结束的原因包括患者死亡(72.4%)、治疗结束(13.5%)、功能衰竭或难治性感染(11.2%)以及其他(2.9%)。与特定端口无并发症使用时长缩短相关的独立因素包括置入部位、年龄、肿瘤类型和导管尖端位置。
癌症患者皮下静脉通路端口安全且耐受性良好。长期装置使用时长主要受患者生存情况影响。在本研究中,1年时存活的患者中有90%以及4年时存活的患者中有70%拥有功能正常的端口。