Kariyawasam H H, Pepper J R, Hodson M E, Geddes D M
Department of Cystic Fibrosis, Royal Brompton and Harefield NHS Trust, London, UK.
Respir Med. 2000 Dec;94(12):1161-5. doi: 10.1053/rmed.2000.0943.
Totally implantable venous intravenous access devices (TIVADs) have an essential role in the frequent delivery of antibiotics in cystic fibrosis (CF) patients. This study at the Royal Brompton Hospital (RBH) reports the experience of TIVADs in patients attending the RBH adult CF unit implanted at the RBH and elsewhere over a 13-year period. The case notes of adult CF patients who had undergone TIVAD insertion were reviewed retrospectively. The patients were divided into those who had the insertion carried out at the RBH and those who had the device inserted elsewhere. All devices were cared for the at the RBH. A total of 115 devices in 74 patients were reviewed. The median duration of function of 109 devices was 1429 days (range 2-3989) or 3.9 years, with a total exposure of 91,188 days or 249.8 years. There was no significant difference between devices inserted at the RBH and those inserted elsewhere (P= 0.59). Thirty-four patients had devices installed without complications. Forty patients had complications in 62 devices. The incidence of complications was 34.5% at the devices inserted at RBH and 73.7% elsewhere (P<0.001). Of the 115 devices, mechanical complications occurred in 42 (36%) with a median time of diagnosis of 373 days (range 1-2554), infectious complications occurred in 16 (14%), with a median time of diagnosis of 413 days (range 40-2556) and symptomatic venous thrombosis occurred in four (3.5%). RBH-inserted devices had significantly fewer mechanical complications (P<0.001) compared with those inserted elsewhere. The group as a whole had fewer infectious complications than in most other reported series. We conclude that TIVADs provide effective and long-term intravenous access and have fewer complications if they are inserted and cared for at a centre with special expertise in their insertion and management.
完全植入式静脉输液通路装置(TIVADs)在囊性纤维化(CF)患者频繁输注抗生素方面发挥着重要作用。皇家布朗普顿医院(RBH)的这项研究报告了在13年期间于RBH及其他地方植入TIVADs的RBH成人CF病房患者的使用经验。对接受TIVADs植入的成年CF患者的病历进行了回顾性分析。患者被分为在RBH植入的和在其他地方植入的两组。所有装置均在RBH进行护理。共回顾了74例患者的115个装置。109个装置的中位功能持续时间为1429天(范围2 - 3989天)或3.9年,总暴露时间为91,188天或249.8年。在RBH植入的装置与在其他地方植入的装置之间无显著差异(P = 0.59)。34例患者植入装置后无并发症。40例患者的62个装置出现并发症。在RBH植入的装置并发症发生率为34.5%,在其他地方植入的为73.7%(P<0.001)。在115个装置中,42个(36%)发生机械并发症,中位诊断时间为373天(范围1 - 2554天);16个(14%)发生感染并发症,中位诊断时间为413天(范围40 - 2556天);4个(3.5%)出现有症状的静脉血栓形成。与在其他地方植入的装置相比,在RBH植入的装置机械并发症明显更少(P<0.001)。与大多数其他报道系列相比,该组总体感染并发症较少。我们得出结论,TIVADs提供了有效且长期的静脉通路,并且如果在具有TIVADs植入和管理专业知识的中心进行植入和护理,并发症会更少。