首页> 外文期刊>European Journal of Surgical Oncology: The Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology >Totally implantable venous access port systems and risk factors for complications: a one-year prospective study in a cancer centre.
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Totally implantable venous access port systems and risk factors for complications: a one-year prospective study in a cancer centre.

机译:完全植入的静脉通路系统和并发症危险因素:在癌症中心进行的为期一年的前瞻性研究。

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摘要

BACKGROUND: Totally Implantable Venous Access Port Systems (TIVAPS) are widely used in oncology, but complications are frequent, sometimes necessitating device removal and consequently delays in chemotherapy. The aim of this study was to investigate possible risk factors for morbidity. METHODS: A total of 815 consecutive cancer patients (median age: 56.2 years [0.8-85.2]; 522 female) were enrolled in this observational, single-centre study between May 2nd 2006 and April 30th 2007. TIVAPS implantation involved principally cephalic or external jugular vein access. Patients were followed up for one year unless the device was removed earlier. RESULTS: The overall morbidity rate was 16.1% (131/815). Complications necessitated device removal in 55 patients a mean of 3.7 months [0.2-12.0] after implantation. These comprised TIVAPS-related infection (19), port expulsion (14), catheter migration (6), venous thrombosis (5), mechanical problems (3), skin disorders (2), pain (2), drug extravasation (2) infection unrelated to TIVAPS (1) and inflammation (1). No patient died during the study. The factor most strongly predictive of complications was the interval between insertion and first use of the TIVAPS, ranging from 0 to 135 days (median: 8.0 days). The morbidity rate was 24.4% when this interval was 0-3 days, 17.1% when it was 4-7 days and 12.1% when it exceeded 7 days (p < 0.01; Chi(2) test). The median interval was 6 days (0-53) and 8 days (0-135), respectively, in patients with and without complications (p < 0.001). CONCLUSION: To reduce complications, an interval of at least 8 days between placement of the TIVAPS and its first use may be advisable.
机译:背景:完全可植入的静脉通路系统(TIVAPS)在肿瘤学中被广泛使用,但是并发症很常见,有时需要移除器械,因此延迟了化疗。这项研究的目的是调查可能的发病风险因素。方法:在2006年5月2日至2007年4月30日期间,共有815名连续癌症患者(中位年龄:56.2岁[0.8-85.2]; 522名女性)参加了该观察性单中心研究。TIVAPS植入主要涉及头侧或外向颈静脉通路。对患者进行了为期一年的随访,除非较早取出该设备。结果:总发病率为16.1%(131/815)。并发症导致需要在植入后平均3.7个月[0.2-12.0]的55例患者中移除器械。这些包括与TIVAPS相关的感染(19),端口驱逐(14),导管迁移(6),静脉血栓形成(5),机械问题(3),皮肤疾病(2),疼痛(2),药物外渗(2)与TIVAPS(1)和炎症(1)无关的感染。研究期间没有患者死亡。最能预测并发症的因素是TIVAPS插入与首次使用之间的间隔,范围为0至135天(中位数:8.0天)。在此间隔为0-3天时,发病率为24.4%;在4-7天时,发病率为17.1%;超过7天时,发病率为12.1%(p <0.01; Chi(2)测试)。有和没有并发症的患者的中位间隔分别为6天(0-53)和8天(0-135)(p <0.001)。结论:为减少并发症,建议放置TIVAPS与首次使用之间至少间隔8天。

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