Shah P, Shah V
Department of Paediatrics, Mount Sinai Hospital, Rm 775A, 600 University Avenue, Toronto, Ontario, Canada.
Cochrane Database Syst Rev. 2005 Jul 20(3):CD002772. doi: 10.1002/14651858.CD002772.pub2.
Peripherally placed percutaneous central venous catheters (PCVC) are used in neonates to provide long-term vascular access. Major complications associated with these catheters include mechanical complications (catheter thrombosis, occlusion or dislodgement) and infection. Strategies to prevent catheter thrombosis and occlusion include the use of heparin. Systematic review has revealed that heparin is effective in prolonging the umbilical arterial catheter stay in neonates. However, heparin is known to be associated with complications such as bleeding and thrombocytopenia which may result in serious long-term sequelae.
The primary objective is to assess the effectiveness of heparin for prevention of catheter related thrombosis. The secondary objectives are to assess the effectiveness of heparin on catheter occlusion, duration of catheter patency, catheter related sepsis and complications associated with the use of heparin.
A literature search was performed using the following databases: MEDLINE (1966-February 2005), EMBASE (1980-February 2005), CINAHL (1982-February 2005) and the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 1, 2005) and abstracts from the annual meetings of the Society for Pediatric Research/American Pediatric Society and Pediatric Academic Societies published in Pediatric Research (1991-2005). No language restrictions were applied.
Selection criteria applied to the clinical trials were: the population had to be neonates, intervention had to be heparin infusion compared to placebo or no treatment for prevention of any of the complications related to peripherally placed PCVC, the trial had to be randomized or quasi-randomized and at least one of the primary or secondary outcomes reported.
The methodological quality of included trials was assessed using criteria for masking of randomization, masking of intervention, completeness of follow-up and masking of outcome measurement. Data on relevant outcomes were extracted and the effect size was estimated by calculating relative risk (95% CI), risk difference (95% CI) and weighted mean difference (95% CI).
Two randomized trials on the use of heparin for peripherally placed PCVC were identified . One trial (Kamala et al) of 66 neonates of adequate methodology met the eligibility criteria. There was no statistically significant differences in the incidence of thrombosis (RR 0.79, 95% CI 0.35, 1.79), occlusion (RR 0.63, 95% CI 0.22), catheter related sepsis (RR 0.89, 95% CI 0.06, 13.57), extension of intraventricular hemorrhage (RR 0.87, 95% CI 0.25, 3.03), mortality (RR 0.59, 95% CI 0.18, 1.90) or duration of catheter patency (WMD 1.50 days, 95% CI -1.35 days, 4.35 days) between heparin and no heparin groups. Another trial (Betremieux et al) was excluded due to several methodological issues: 1. randomization was at the time of umbilical catheter placement rather than later PCVC placement 2. multiple PCVC were used in some infants, with reported results based on number of catheters rather than infants.
Prophylactic use of heparin for prevention of complications related to peripherally placed PCVC has been examined in only one randomized controlled clinical trial that was eligible for inclusion in this review. No significant differences in the incidence of thrombosis, occlusion, sepsis, mortality and duration of catheter patency were observed. With the current state of knowledge, routine use of heparin for this purpose can not be recommended. Implication for research: Increasing survival of extremely low birth weight infants may be accompanied by prolonged intravenous access for nutrition. Well designed randomized controlled trials of sufficient power to determine the benefits and risks of continuous infusion of heparin in neonates with peripherally inserted PCVC are warranted.
外周置入的经皮中心静脉导管(PCVC)用于新生儿以提供长期血管通路。与这些导管相关的主要并发症包括机械性并发症(导管血栓形成、堵塞或移位)和感染。预防导管血栓形成和堵塞的策略包括使用肝素。系统评价显示肝素在延长新生儿脐动脉导管留置时间方面有效。然而,已知肝素与出血和血小板减少等并发症相关,这些并发症可能导致严重的长期后遗症。
主要目的是评估肝素预防导管相关血栓形成的有效性。次要目的是评估肝素对导管堵塞、导管通畅持续时间、导管相关败血症以及与肝素使用相关的并发症的有效性。
使用以下数据库进行文献检索:MEDLINE(1966年 - 2005年2月)、EMBASE(1980年 - 2005年2月)、CINAHL(1982年 - 2005年2月)以及Cochrane对照试验中心注册库(CENTRAL,Cochrane图书馆,2005年第1期),以及发表于《儿科研究》(1991年 - 2005年)的儿科研究协会/美国儿科学会和儿科学术协会年会摘要。未设语言限制。
应用于临床试验的入选标准为:研究对象必须是新生儿,干预措施必须是肝素输注,与安慰剂或不治疗相比,用于预防与外周置入PCVC相关的任何并发症,试验必须是随机或半随机的,并且至少报告一项主要或次要结局。
使用随机化掩盖、干预掩盖、随访完整性和结局测量掩盖的标准评估纳入试验的方法学质量。提取相关结局的数据,并通过计算相对风险(95%可信区间)、风险差异(95%可信区间)和加权平均差异(95%可信区间)来估计效应大小。
确定了两项关于肝素用于外周置入PCVC的随机试验。一项有66例新生儿的试验(Kamala等人)方法学充分,符合入选标准。肝素组和非肝素组在血栓形成发生率(相对风险0.79,95%可信区间0.35,1.79)、堵塞发生率(相对风险0.63,95%可信区间0.22)、导管相关败血症发生率(相对风险0.89,95%可信区间0.06,13.57)、脑室内出血扩展发生率(相对风险0.87,95%可信区间0.25,3.03)、死亡率(相对风险0.59,95%可信区间0.18,1.90)或导管通畅持续时间(加权平均差异1.50天,95%可信区间 - 1.35天,4.35天)方面无统计学显著差异。另一项试验(Betremieux等人)因几个方法学问题被排除:1. 随机化是在脐导管置入时进行,而非后来的PCVC置入时;2. 一些婴儿使用了多个PCVC,报告结果基于导管数量而非婴儿数量。
仅在一项符合本综述纳入标准的随机对照临床试验中研究了预防性使用肝素预防外周置入PCVC相关并发症的情况。在血栓形成、堵塞、败血症、死亡率和导管通畅持续时间的发生率方面未观察到显著差异。基于目前的知识水平,不推荐为此目的常规使用肝素。对研究的启示:极低出生体重儿存活率的提高可能伴随着静脉营养通路使用时间的延长。有必要进行设计良好、有足够效力的随机对照试验,以确定持续输注肝素对接受外周插入PCVC新生儿的益处和风险。