Department of Surgery, Division of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Thorac Cardiovasc Surg. 2020 Dec;68(8):669-673. doi: 10.1055/s-0039-1695780. Epub 2019 Sep 6.
We previously identified preparation of the internal mammary artery as a risk factor significantly impairing antibiotic tissue penetration into the presternal subcutaneous tissue. We, therefore, adapted our dosing schema regarding preoperative timing to overcome this risk factor.
Eight patients who underwent coronary artery bypass grafting with a left internal mammary artery and vein grafts were included in this clinical trial. Cefazolin (4 g) was administered twice (3 hours and 1 hour) prior to skin incision and once during skin closure (2 g). Antibiotic concentrations were measured with subcutaneous microdialysis probes on both sternal sides. Results were directly compared with the previously published patient cohort receiving the standard schema (4 g cefazolin prior to skin incision and 2 g during closure).
All patients (7 male, 1 female, 69 ± 7 years, 26.3 ± 3.9 kg/m) survived the perioperative period. Mean area under the curve on the right and left sternal side was 117.0 ± 92.5 μg/mL and 114.5 ± 83.2 μg/mL, respectively ( = 0.95). This was well above the previously measured mean peak tissue concentrations without early preoperative antibiotic administration on the side of mammary artery harvesting (52.4 ± 48.5 μg/mL vs. 13.1 ± 5.8 μg/mL; = 0.039). The %fT > minimal inhibitory concentration (MIC) for and during the first 10 hours in presternal tissue was ≥ 70% but did not differ compared with standard schema.
Early, additional preoperative administration of cefazolin was able to significantly increase peak tissue concentrations during surgery compared with the standard protocol. No difference, however, could be achieved in the percentage of time during which the concentration exceeded the MIC.
我们之前发现,准备内乳动脉是一个显著降低抗生素在胸骨前皮下组织中穿透能力的风险因素。因此,我们调整了术前给药时间的方案,以克服这一风险因素。
本临床试验纳入了 8 名接受冠状动脉旁路移植术(使用左内乳动脉和静脉移植物)的患者。在切开皮肤前 3 小时和 1 小时给予头孢唑林(4g)两次,并在皮肤缝合时给予一次(2g)。使用皮下微透析探针在双侧胸骨侧测量抗生素浓度。结果与接受标准方案(切开皮肤前给予 4g 头孢唑林,缝合时给予 2g)的先前发表的患者队列直接比较。
所有患者(7 名男性,1 名女性,69±7 岁,26.3±3.9kg/m2)均度过围手术期。右侧和左侧胸骨侧的曲线下面积均值分别为 117.0±92.5μg/mL 和 114.5±83.2μg/mL( = 0.95)。这明显高于在未进行早期术前抗生素给药的内乳动脉采集侧测量到的先前平均峰值组织浓度(52.4±48.5μg/mL 比 13.1±5.8μg/mL; = 0.039)。在胸骨前组织中,和的第一个 10 小时内,%fT > 最小抑菌浓度(MIC)的时间为 70%,但与标准方案相比无差异。
与标准方案相比,早期、额外的术前头孢唑林给药可显著增加手术期间的峰值组织浓度。然而,在浓度超过 MIC 的时间百分比方面,无法达到差异。