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与HeartMate左心室辅助装置相比,Jarvik 2000引发的感染较少。

The Jarvik 2000 is associated with less infections than the HeartMate left ventricular assist device.

作者信息

Siegenthaler M P, Martin J, Pernice K, Doenst T, Sorg S, Trummer G, Friesewinkel O, Beyersdorf F

机构信息

Department of Cardiovascular Surgery, Albert-Ludwigs University Freiburg, Germany.

出版信息

Eur J Cardiothorac Surg. 2003 May;23(5):748-54; discussion 754-5. doi: 10.1016/s1010-7940(03)00073-3.

Abstract

OBJECTIVES

Device-related infections remain a considerable problem of left-ventricular support. We compared the device-related-infections between the HeartMate left ventricular assist device (LVAD) and the Jarvik 2000 permanent LVAD, a device with a novel retroauricular power-supply.

METHODS

Between December 2000 and September 2002 we implanted the HeartMate-vented, electrical-system in 11 patients and the permanent Jarvik 2000 in six patients. Total support time was 1626 patient-days (HeartMate, 26-271 days) versus 1246 patient-days (Jarvik 2000, 8-411 days). As potential risk factors for infection we analyzed age, preoperative hospital-days, total protein, cardiac index, maximal oxygen uptake, use of inotropes, LVAD risk-score-index and Aaronson-Mancini-score, intubation time, and intensive care unit stay. We used the Center of Disease Control definitions for surgical site infections.

RESULTS

HeartMate-patients were younger than Jarvik 2000 patients (46+/-13 versus 58+/-6 years, P=0.056), there were no other differences in the risk factors. Four HeartMate-patients needed late (>or=48 h) surgical revisions for bleeding/hematomas versus no revisions in the Jarvik 2000 patients. In the HeartMate-patients, there were seven (64%) driveline-infections, five (45%) device-pocket infections, and three (27%) bloodstream-infections, or 0.43 device-related infections/100 patient-days. Infections occurred early (34+/-31 days). Three patients required urgent transplantation due to bloodstream infection. There were no adverse outcomes in the HeartMate-group due to infection. In the Jarvik 2000 patients, there was one driveline-infection (16%) after 270 days of support (0.08 device-related infections/100 patient-days), significantly less than in the HeartMate-group (P=0.044). Driveline infections resolved with antibiotics and local wound care in the Jarvik 2000 patient, but only in one of seven HeartMate-patients.

CONCLUSIONS

Implantation of the Jarvik 2000 is associated with less device-related infections than the HeartMate-LVAD. The power-supply of the permanent Jarvik 2000 is suitable for long-term mechanical support.

摘要

目的

与装置相关的感染仍是左心室辅助支持的一个重大问题。我们比较了HeartMate左心室辅助装置(LVAD)和Jarvik 2000永久性LVAD(一种具有新型耳后电源的装置)之间与装置相关的感染情况。

方法

在2000年12月至2002年9月期间,我们为11例患者植入了HeartMate通风电气系统,为6例患者植入了永久性Jarvik 2000。总支持时间为1626患者日(HeartMate,26 - 271天),而Jarvik 2000为1246患者日(8 - 411天)。作为感染的潜在风险因素,我们分析了年龄、术前住院天数、总蛋白、心脏指数、最大摄氧量、血管活性药物的使用、LVAD风险评分指数和Aaronson - Mancini评分、插管时间以及重症监护病房停留时间。我们采用疾病控制中心关于手术部位感染的定义。

结果

HeartMate患者比Jarvik 2000患者年轻(46±13岁对58±6岁,P = 0.056),在风险因素方面无其他差异。4例HeartMate患者因出血/血肿需要进行晚期(≥48小时)手术修正,而Jarvik 2000患者无需修正。在HeartMate患者中,有7例(64%)发生了驱动线感染,5例(45%)发生了装置袋感染,3例(27%)发生了血流感染,即每100患者日有0.43例与装置相关的感染。感染发生较早(34±31天)。3例患者因血流感染需要紧急移植。HeartMate组未因感染出现不良结局。在Jarvik 2000患者中,1例在支持270天后发生了驱动线感染(16%)(每100患者日0.08例与装置相关的感染),明显少于HeartMate组(P = 0.044)。Jarvik 2000患者的驱动线感染通过抗生素和局部伤口护理得以解决,但在7例HeartMate患者中只有1例如此。

结论

与HeartMate LVAD相比,植入Jarvik 2000与较少的与装置相关的感染相关。永久性Jarvik 2000的电源适用于长期机械支持。

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