Recombinant tissue plasminogen activator reduces incidence of catheter malfunction and bacteremia

Lilit A Sargsyan MD, Risheng Xu DO, Alicia Romero MD, Brett W. Stephens MD, Donald A Molony MD
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Only one study, however, has previously evaluated recombinant tissue plasminogen activator (rt-PA) as a locking solution for primary prevention of catheter failure rather than as a treatment of existing/suspected thrombosis. In addition, line-related sepsis constitutes up to 75% of deaths from infection among this population,<span>2</span> and infection risk increases in the presence of partial or complete thrombosis.<span>3</span></p><p>In this month's literature watch, we review a study by Hemmelgarn and colleagues designed to evaluate whether rt-PA administered once weekly as locking solution in substitution for the scheduled dose of heparin is superior to the current customary care of locking catheters with heparin only after each dialysis session, in preventing catheter malfunction (primary outcome) and infection (secondary outcome).</p><p>The ideal study design to investigate whether one intervention is superior to another is a randomized clinical trial (RCT) with masked allocation and determination of outcomes. The study by Hemmelgarn and colleagues represents a well-designed RCT with random allocation of the patients and full masking (blinding) of group assignment, in which the investigators evaluate whether a protocol including 1 mg of rt-PA as a locking solution used once a week in place of 5,000 U of heparin is superior to heparin alone in preventing catheter malfunction and bacteremia.</p><p>Participants were recruited from 11 Canadian hemodialysis centers within 2 weeks of a newly inserted hemodialysis catheter. Patients were excluded from the study if their catheters at baseline failed to function adequately, defined as a blood flow of at least 300 mL/min during the dialysis sessions immediately prior to randomization. Masked random treatment allocation in a 1:1 ratio was performed centrally with the use of a permuted-block design stratified according to center and catheter status (first ever catheter for patient or not). Catheter malfunction and catheter-related bacteremia episodes by pre-defined criteria were documented. Analysis of outcomes was conducted on an intention-to-treat basis. Additionally, a cost assessment of maintaining future catheter patency was conducted.</p><p>Although the study was originally designed for an enrollment of 340 patients to ensure 80% power to detect approximately a 34% reduction in the incidence of catheter malfunction with rt-PA once weekly, due to lower than expected enrollment, only 225 patients were enrolled. Despite a smaller size, the study did show a significant reduction in the primary outcome because of a higher than expected baseline risk and higher than expected risk reduction with treatment. The strengths of the study included masked allocation, pre-defined inclusion and exclusion criteria, and clinically relevant pre-defined primary and secondary outcomes. Additionally, there were no significant differences in baseline characteristics of both groups, indicating the success of the blocked stratified randomization schema used. Finally, the study had excellent follow-up with robust ascertainment of the outcomes. The single limitation of this study (smaller than expected study size) does not invalidate the overall findings but does reduce the precision of the final estimates of effect size or benefit.</p><p>The current study by Hemmelgarn and colleagues demonstrates that the use of rt-PA as a locking solution for central venous catheters in place of heparin for one out of every three hemodialysis sessions decreases significantly the incidence of hemodialysis catheter malfunction and bacteremia. Hemmelgarn and colleagues demonstrated a reduction in events of hemodialysis catheter malfunction of 14.8%. If this reflects the true absolute risk reduction, than a number needed to treat (NNT) of seven patients to prevent one catheter malfunction episode can be expected. Similarly, locking hemodialysis catheters once weekly with rt-PA reduced episodes of catheter-related bacteremia by 0.97 episodes per 1,000 patient days, resulting in an NNT of approximately three patients treated for 1 year to prevent one episode of bacteremia.</p><p>Several clinically important questions are not addressed by this robust RCT. Most importantly, this study does not determine whether additional benefit or risk can be obtained with larger or more frequent rt-PA doses.<span>4</span> If infection risk is reduced, a reduction in mortality might also be anticipated. The current study was insufficiently powered and of insufficient duration to determine whether the reduced incidence of the primary or secondary outcomes resulted in improved survival. There were five deaths among patients receiving customary care and three in the experimental rt-PA group. There was no difference between the groups in total or in serious adverse events. Adverse events were experienced by 70% versus 68.7% of patients in the rt-PA and heparin-only groups, respectively. Significant intracranial bleeding episodes were observed in the customary care (heparin-only) group only.</p><p>The authors also explored to some degree the cost differences of the two strategies and noted that for an incremental cost for rt-PA of $13,956 (Canadian dollars) one would expect to prevent one episode of catheter-related bacteremia. This apparent benefit did not include considerations of substantial potential improvements in patient quality of life, and it is likely that when expressed in terms of patient-centered outcomes such as QOL, the intervention might be even more clearly cost effective. 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引用次数: 0

Abstract

Hemmelgarn B, Moist L, Lok C, et al. Prevention of dialysis catheter malfunction with recombinant tissue plasminogen activator. N Engl J Med. 2011;364:303-312.

Malfunctioning and infected hemodialysis catheters increase morbidity, mortality, and the cost of care of hemodialysis patients. More than 50% to 70% of hemodialysis catheters will be expected to fail within the first year, with half to two-thirds of these failures attributable to catheter thrombosis.1 Heparin has been shown to be superior to saline as a locking solution in preventing catheter malfunction. Only one study, however, has previously evaluated recombinant tissue plasminogen activator (rt-PA) as a locking solution for primary prevention of catheter failure rather than as a treatment of existing/suspected thrombosis. In addition, line-related sepsis constitutes up to 75% of deaths from infection among this population,2 and infection risk increases in the presence of partial or complete thrombosis.3

In this month's literature watch, we review a study by Hemmelgarn and colleagues designed to evaluate whether rt-PA administered once weekly as locking solution in substitution for the scheduled dose of heparin is superior to the current customary care of locking catheters with heparin only after each dialysis session, in preventing catheter malfunction (primary outcome) and infection (secondary outcome).

The ideal study design to investigate whether one intervention is superior to another is a randomized clinical trial (RCT) with masked allocation and determination of outcomes. The study by Hemmelgarn and colleagues represents a well-designed RCT with random allocation of the patients and full masking (blinding) of group assignment, in which the investigators evaluate whether a protocol including 1 mg of rt-PA as a locking solution used once a week in place of 5,000 U of heparin is superior to heparin alone in preventing catheter malfunction and bacteremia.

Participants were recruited from 11 Canadian hemodialysis centers within 2 weeks of a newly inserted hemodialysis catheter. Patients were excluded from the study if their catheters at baseline failed to function adequately, defined as a blood flow of at least 300 mL/min during the dialysis sessions immediately prior to randomization. Masked random treatment allocation in a 1:1 ratio was performed centrally with the use of a permuted-block design stratified according to center and catheter status (first ever catheter for patient or not). Catheter malfunction and catheter-related bacteremia episodes by pre-defined criteria were documented. Analysis of outcomes was conducted on an intention-to-treat basis. Additionally, a cost assessment of maintaining future catheter patency was conducted.

Although the study was originally designed for an enrollment of 340 patients to ensure 80% power to detect approximately a 34% reduction in the incidence of catheter malfunction with rt-PA once weekly, due to lower than expected enrollment, only 225 patients were enrolled. Despite a smaller size, the study did show a significant reduction in the primary outcome because of a higher than expected baseline risk and higher than expected risk reduction with treatment. The strengths of the study included masked allocation, pre-defined inclusion and exclusion criteria, and clinically relevant pre-defined primary and secondary outcomes. Additionally, there were no significant differences in baseline characteristics of both groups, indicating the success of the blocked stratified randomization schema used. Finally, the study had excellent follow-up with robust ascertainment of the outcomes. The single limitation of this study (smaller than expected study size) does not invalidate the overall findings but does reduce the precision of the final estimates of effect size or benefit.

The current study by Hemmelgarn and colleagues demonstrates that the use of rt-PA as a locking solution for central venous catheters in place of heparin for one out of every three hemodialysis sessions decreases significantly the incidence of hemodialysis catheter malfunction and bacteremia. Hemmelgarn and colleagues demonstrated a reduction in events of hemodialysis catheter malfunction of 14.8%. If this reflects the true absolute risk reduction, than a number needed to treat (NNT) of seven patients to prevent one catheter malfunction episode can be expected. Similarly, locking hemodialysis catheters once weekly with rt-PA reduced episodes of catheter-related bacteremia by 0.97 episodes per 1,000 patient days, resulting in an NNT of approximately three patients treated for 1 year to prevent one episode of bacteremia.

Several clinically important questions are not addressed by this robust RCT. Most importantly, this study does not determine whether additional benefit or risk can be obtained with larger or more frequent rt-PA doses.4 If infection risk is reduced, a reduction in mortality might also be anticipated. The current study was insufficiently powered and of insufficient duration to determine whether the reduced incidence of the primary or secondary outcomes resulted in improved survival. There were five deaths among patients receiving customary care and three in the experimental rt-PA group. There was no difference between the groups in total or in serious adverse events. Adverse events were experienced by 70% versus 68.7% of patients in the rt-PA and heparin-only groups, respectively. Significant intracranial bleeding episodes were observed in the customary care (heparin-only) group only.

The authors also explored to some degree the cost differences of the two strategies and noted that for an incremental cost for rt-PA of $13,956 (Canadian dollars) one would expect to prevent one episode of catheter-related bacteremia. This apparent benefit did not include considerations of substantial potential improvements in patient quality of life, and it is likely that when expressed in terms of patient-centered outcomes such as QOL, the intervention might be even more clearly cost effective. This study does not address whether similar benefits might be obtained with other catheter locking solutions.5

As long as a substantial number of patients begins hemodialysis with a catheter for hemodialysis access, complications attributable to the catheters will remain significant. The current study provides compelling evidence that a strategy using once weekly rt-PA in place of heparin as a locking solution, which should reduce partial and/or total catheter thrombosis, will result in improved catheter function and reduced risk of infection. Although this strategy is likely to result in a favorable cost effectiveness, the costs of rt-PA will largely be borne by the dialysis units, the benefits will accrue almost entirely to the patient, and therefore, it should be anticipated that there will be additional disincentives for the adoption of this potentially beneficial therapy in an era of bundled payments for dialysis.

重组组织型纤溶酶原激活剂降低导管故障和菌血症的发生率
刘建军,刘建军,刘建军,等。重组组织型纤溶酶原激活剂预防透析导管故障。中华医学杂志。2011;34(4):393 - 394。血液透析导管的故障和感染增加了血液透析患者的发病率、死亡率和护理费用。预计超过50%至70%的血液透析导管将在第一年失效,其中一半至三分之二的失效可归因于导管血栓形成1肝素已被证明优于生理盐水作为锁定溶液在防止导管故障。然而,先前只有一项研究评估了重组组织型纤溶酶原激活剂(rt-PA)作为一种锁定解决方案,用于初级预防导管失效,而不是作为现有/疑似血栓的治疗方法。此外,在这一人群中,静脉相关性败血症占感染死亡人数的75%,并且在存在部分或完全血栓形成时感染风险增加。在本月的文献观察中,我们回顾了Hemmelgarn及其同事的一项研究,该研究旨在评估每周给予一次rt-PA作为锁定溶液替代计划剂量的肝素,在预防导管故障(主要结局)和感染(次要结局)方面是否优于目前每次透析后仅用肝素锁定导管的习惯护理。研究一种干预措施是否优于另一种干预措施的理想研究设计是随机临床试验(RCT),采用掩码分配和确定结果。Hemmelgarn及其同事的研究代表了一项设计良好的随机对照试验,随机分配患者,并对组分配进行了完全掩盖(盲法),在该研究中,研究人员评估了一项方案,包括1mg rt-PA作为锁定溶液,每周使用一次,代替5000 U肝素,在预防导管故障和菌血症方面是否优于单独使用肝素。参与者在新插入血液透析导管的2周内从11个加拿大血液透析中心招募。如果患者的导管在基线时不能充分发挥作用,则将其排除在研究之外,定义为在随机分组之前的透析期间血流量至少为300 mL/min。按1:1的比例进行隐蔽性随机治疗分配,采用排列块设计,根据中心和导管状态分层(患者是否首次使用导管)。根据预先定义的标准记录导管故障和导管相关菌血症发作。结果分析是在意向治疗基础上进行的。此外,还进行了维持未来导管通畅的成本评估。虽然该研究最初设计入组340例患者,以确保80%的检测率,每周一次rt-PA的导管故障发生率降低约34%,但由于入组人数低于预期,仅入组225例患者。尽管规模较小,但该研究确实显示了主要结果的显著降低,因为基线风险高于预期,治疗后的风险降低高于预期。该研究的优势包括隐蔽分配,预定义的纳入和排除标准,以及临床相关的预定义主要和次要结局。此外,两组的基线特征没有显著差异,表明所使用的阻断分层随机化方案是成功的。最后,该研究具有良好的随访和可靠的结果确定。本研究的单一局限性(小于预期的研究规模)并未使整体研究结果无效,但确实降低了对效应大小或益处的最终估计的准确性。Hemmelgarn及其同事目前的研究表明,每三次血液透析中有一次使用rt-PA作为中心静脉导管的锁定溶液来代替肝素,可显著降低血液透析导管故障和菌血症的发生率。Hemmelgarn和他的同事证明了血液透析导管故障事件减少了14.8%。如果这反映了真正的绝对风险降低,那么可以预期需要治疗(NNT) 7例患者以防止一次导管故障。同样,每周用rt-PA锁定一次血液透析导管,每1000患者日减少导管相关菌血症发作0.97次,导致大约3名患者治疗1年以防止一次菌血症发作。几个重要的临床问题没有被这个稳健的随机对照试验解决。最重要的是,这项研究并没有确定更大或更频繁的rt-PA剂量是否会带来额外的益处或风险如果感染风险降低,预计死亡率也会降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dialysis & Transplantation
Dialysis & Transplantation 医学-工程:生物医学
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