Harper Katharine D, Incavo Stephen J
Washington DC VA Medical Center, Washington, DC.
Houston Methodist Hospital, Houston, Texas.
JBJS Essent Surg Tech. 2024 May 22;14(2). doi: 10.2106/JBJS.ST.22.00071. eCollection 2024 Apr-Jun.
Vancomycin is a prophylactic antibiotic with bactericidal activity against methicillin-resistant that is commonly used in total joint replacement surgery. In total knee arthroplasty (TKA), intraosseous infusions administered following tourniquet inflation have demonstrated improved local vancomycin concentrations with decreased systemic absorption. This administration method results in no adverse reactions locally, as well as equivalent or lower systemic complications compared with other vancomycin administration methods. Intraosseous infusion of prophylactic surgical antibiotics has been shown to be more effective than intravenous administration, with the potential for reduction in surgical site infections.
After the operative extremity has been prepared and draped in the usual sterile fashion, the limb is elevated and the tourniquet is inflated to 250 mm Hg. Prior to incision, an intraosseous vascular access system (Arrow EZ IO; Teleflex) is inserted with a power driver into the tibial tubercle region. The desired volume of the medication is injected into the tibia. The device is removed and then inserted into the anterior distal femur, centrally, just proximal to the patella. Following this, the desired volume of the medication is injected into the femur. The device is then removed, and the TKA proceeds according to the surgeon's standard technique.
Alternative administration methods for vancomycin include other invasive methods and noninvasive delivery. Intravenous delivery is the most traditional form of medication delivery. Additional alternatives include noninvasive placement of antibiotic powder into the wound and localized soft-tissue injections of desired medications.
Opting to administer antibiotics and other medications intraosseously (rather than intravenously) has shown improved compliance with the golden-hour rule of preoperative antibiotics (especially for vancomycin), lower incidences of acute kidney injury or adverse systemic effects, and improved local tissue concentrations of all medications delivered.
Expected outcomes include improved local tissue concentrations with decreased systemic concentrations of vancomycin and with no reported local or systemic adverse reactions, as well as the potential for improved infection prevention. Literature regarding the use of intraosseous infusion during TKA has been thorough and very well received. A prospective, randomized study by Young et al. evaluated local and systemic concentrations of vancomycin following intraosseous versus intravenous administration. The authors found that low-dose intraosseous vancomycin resulted in tissue concentrations equal to or superior to those of systemic administration, also noting that the administration route reduced the infiltration time of the vancomycin without systemic complications. Local concentrations at the knee were found to be 5 to 9 times greater with intraosseous infusion in patients with a body mass index of >35 kg/m as compared with the use of intravenous administration, with no adverse reactions systemically. Local concentrations in this patient population were also found to be comparable to those observed in patients with a lower body mass index. A recent study assessing the use of intraosseous vancomycin showed that local concentrations of vancomycin were maintained even if the procedure continued beyond the point of tourniquet deflation, with mean concentrations being 5 times higher locally at the end of the procedure in the intraosseous versus the intravenous group. A separate study showed no adverse systemic reactions and no incidents of acute kidney injury among patients receiving intraosseous vancomycin. An additional study showed that intraosseous administration of vancomycin decreased the incidence of postoperative joint infections compared with traditional intravenous administration. Newer studies assessing the use of intraosseous infiltration have begun to focus on the delivery of other medications, not just antibiotics. At our institution, we have examined the benefits of intraosseously administrated morphine, which has shown a significant decrease in pain and opioid consumption up to 2 weeks postoperatively.
You may run into issues with the medication delivery due to the amount of resistance you encounter. If resistance is too great, you may first attempt to readjust the intraosseous needle depth to improve flow. If resistance is still high, you may consider downsizing to a 30-cc syringe in order to better infiltrate the medication.Note that if you downsize your syringe, you will require more time to infiltrate the desired amount of fluid. An additional way to save time is to open multiple syringes and have them prefilled with your desired medication so that they may be handed off once completed rather than needing to be refilled.A hemostat or pickup may be applied underneath the cuff of the intraosseous needle in order to help remove the needle from the bone. This step is sometimes required because the intraosseous handpieces do not have multidirectional trigger capabilities, and removing the needle can require an upward force to be applied.The use of midline locations allows the small incisions you make for intraosseous infusion to be incorporated into your larger knee incision, with no additional morbidity to the patient.Consider utilizing the medial and/or lateral femoral condyles as landmark locations for infusion if your patient is large. Alternatively, recent literature has shown nearly equivalent results with just the tibial infusion, so you may consider discontinuing the femoral intraosseous infusion if there are consistent issues with successfully initiating the medication delivery.
IO = intraosseousMRSA = methicillin-resistant RCT = randomized controlled trialsIV = intravenousBMI = body mass indexOR = operating room.
万古霉素是一种预防性抗生素,对耐甲氧西林金黄色葡萄球菌具有杀菌活性,常用于全关节置换手术。在全膝关节置换术(TKA)中,止血带充气后进行骨内输注已证明可提高局部万古霉素浓度,并减少全身吸收。与其他万古霉素给药方法相比,这种给药方法不会导致局部不良反应,全身并发症相当或更低。骨内输注预防性手术抗生素已被证明比静脉给药更有效,有可能降低手术部位感染的发生率。
在以常规无菌方式准备好手术肢体并铺好手术巾后,抬高肢体并将止血带充气至250 mmHg。在切开前,使用动力驱动器将骨内血管通路系统(Arrow EZ IO;泰利福公司)插入胫骨结节区域。将所需体积的药物注入胫骨。取出该装置,然后将其插入股骨远端前方、髌骨近端中央。之后,将所需体积的药物注入股骨。然后取出该装置,TKA按照外科医生的标准技术进行。
万古霉素的替代给药方法包括其他侵入性方法和非侵入性给药。静脉给药是最传统的药物给药形式。其他替代方法包括将抗生素粉末无创放置在伤口中以及对所需药物进行局部软组织注射。
选择骨内(而非静脉内)给药抗生素和其他药物已显示出更好地遵守术前抗生素黄金时间规则(尤其是对于万古霉素)、急性肾损伤或全身不良反应发生率更低,以及所输送的所有药物在局部组织中的浓度更高。
预期结果包括万古霉素局部组织浓度提高,全身浓度降低,且无局部或全身不良反应报告,以及预防感染的可能性提高。关于TKA期间使用骨内输注的文献很全面且广受认可。Young等人进行的一项前瞻性随机研究评估了骨内给药与静脉给药后万古霉素的局部和全身浓度。作者发现低剂量骨内万古霉素导致的组织浓度等于或高于全身给药,还指出给药途径减少了万古霉素的浸润时间且无全身并发症。与静脉给药相比,体重指数>35 kg/m²的患者采用骨内输注时膝关节局部浓度高5至9倍,且无全身不良反应。该患者群体的局部浓度也与体重指数较低的患者相当。最近一项评估骨内万古霉素使用的研究表明,即使手术持续到止血带放气后,万古霉素的局部浓度仍能维持,骨内组与静脉组相比,手术结束时局部平均浓度高5倍。另一项研究表明,接受骨内万古霉素治疗的患者无全身不良反应和急性肾损伤事件。另一项研究表明,与传统静脉给药相比,骨内给予万古霉素可降低术后关节感染的发生率。评估骨内浸润使用的最新研究已开始关注其他药物的输送,而不仅仅是抗生素。在我们机构,我们研究了骨内给予吗啡的益处,结果显示术后长达2周疼痛和阿片类药物消耗量显著减少。
由于遇到的阻力大小,你可能在药物输送方面遇到问题。如果阻力过大,你可以首先尝试重新调整骨内针的深度以改善流速。如果阻力仍然很高,你可以考虑换成30毫升注射器以更好地浸润药物。请注意,如果更换注射器,浸润所需体积的液体将需要更多时间。另一种节省时间的方法是打开多个注射器并预先装满所需药物,以便完成后可以直接交接而无需重新装填。可以在骨内针的套管下方应用止血钳或镊子,以帮助从骨中取出针。这一步有时是必需的,因为骨内手持件没有多向触发功能,取出针可能需要向上施加力。使用中线位置可使你为骨内输注所做的小切口纳入较大的膝关节切口中,而不会给患者带来额外的发病率。如果患者体型较大,可以考虑将股骨内侧和/或外侧髁作为输注的标志位置。或者,最近的文献表明仅进行胫骨输注也能得到几乎相同的结果,因此如果在成功开始药物输送方面一直存在问题,你可以考虑停止股骨骨内输注。
IO = 骨内;MRSA = 耐甲氧西林金黄色葡萄球菌;RCT = 随机对照试验;IV = 静脉内;BMI = 体重指数;OR = 手术室