Morris M, Phares K, Zaccardelli D, Ujhelyi M R
Cardiac Rhythm Disease Management Medtronic Inc, Minneapolis, MN, USA.
J Vasc Access. 2008 Jan-Mar;9(1):20-7.
Catheter failure, either due to dislodgment, occlusion or infection is the leading complication of chronic intravenous drug therapy. Better drug delivery techniques are required to advance life saving therapies that require this delivery method. This study evaluated the chronic performance of a fully implantable drug delivery system that incorporates a novel intravenous catheter. The system was designed to reduce complications associated with intravascular drug delivery including catheter occlusion, breakage, migration, and infection.
Twelve canines were implanted with a novel central venous catheter (Model 10642; Medtronic, Minneapolis, MN) connected to a totally implanted programmable drug pump (Model 8637 SynchroMed II, Medtronic). The drug delivery systems infused saline (n=6) or treprostinil (n=6) (Remodulin; United Therapeutics, Research Triangle Park, NC) for either 12 or 26 weeks at a continuous flow rate of 540 microL/day. Catheter performance was assessed at 0 (implant), 2, 4, 8, 12, 16, 20, and 24 weeks by quantifying delivery pressure, delivery volume and steady state Treprostinil concentrations.
All catheters remained patent and free of complications for the duration of the study. Analysis of pressure waveforms during bolus delivery showed low and unchanged catheter resistance throughout the study. Measurement of pump delivery volume accuracy showed that the delivered volume was statistically similar to the calculated delivery (product of flow rate and elapsed time). Measurement of plasma treprostinil levels showed stable concentrations over the study period. There were no catheter dislodgments or breakage. Pathology showed all catheters free from fibrosis and thrombus and minimal changes to the vascular endothelium.
The Model 10642 vascular catheter along with the SynchroMed II implantable drug delivery system showed promising performance in a chronic animal model.
导管故障,无论是由于移位、堵塞还是感染,都是慢性静脉药物治疗的主要并发症。需要更好的药物输送技术来推进需要这种输送方式的挽救生命的治疗方法。本研究评估了一种包含新型静脉导管的完全可植入药物输送系统的长期性能。该系统旨在减少与血管内药物输送相关的并发症,包括导管堵塞、破裂、移位和感染。
12只犬植入了与完全植入式可编程药物泵(型号8637 SynchroMed II,美敦力公司)相连的新型中心静脉导管(型号10642;美敦力公司,明尼阿波利斯,明尼苏达州)。药物输送系统以540微升/天的连续流速输注生理盐水(n = 6)或曲前列尼尔(n = 6)(瑞莫杜林;联合治疗公司,研究三角园,北卡罗来纳州),持续12周或26周。在0(植入)、2、4、8、12、16、20和24周时,通过量化输送压力、输送体积和稳态曲前列尼尔浓度来评估导管性能。
在研究期间,所有导管均保持通畅且无并发症。推注给药期间压力波形分析显示,在整个研究过程中导管阻力低且无变化。泵输送体积准确性的测量表明,输送体积在统计学上与计算的输送量(流速与经过时间的乘积)相似。血浆曲前列尼尔水平的测量显示在研究期间浓度稳定。没有导管移位或破裂。病理学检查显示所有导管均无纤维化和血栓形成,血管内皮变化极小。
10642型血管导管与SynchroMed II植入式药物输送系统在慢性动物模型中显示出良好的性能。