University of Missouri, Kansas City, USA.
Children's Mercy Hospital, Kansas City, MO, USA.
Spine Deform. 2021 Jul;9(4):1191-1196. doi: 10.1007/s43390-020-00273-4. Epub 2021 Jan 18.
Case series.
The use of topical hemostatic agents is common in spinal deformity surgery. While beneficial, emerging case data shows gelatin-containing agents causing intra-operative complications. We present two patients who developed anaphylaxis after injection of these gelatin-containing hemostatic agents into the vertebral body using manual pressure. In the literature, while anaphylactic reactions associated with the use of animal-derived gelatin has been implicated; the risk of injecting these products into the closed vascular cavity of the vertebral body with subsequent embolization into systemic circulation bears emphasis. This report is to meant to make the surgical team aware of the risks of injecting hemostatic agents using manual pressure into the vertebral body and to highlight a plausible mechanism for the phenomenon.
Two children with spinal deformity undergoing posterior spinal fusion procedures with the use of gelatin-containing hemostatic agents injected into the vertebral body through the pedicle are described.
Both patients had gelatin-containing hemostatic agent solution injected under manual pressure through the vertebral pedicle to prevent excessive bleeding. Anaphylaxis occurred soon thereafter, resulting in emergent cessation of the surgery and initiation of medical resuscitation. In both cases, tryptase levels obtained just after the event were elevated.
Patients with an allergy to or prior history of exposure to zoologic products undergoing spine surgery may be at risk of anaphylaxis if the gelatin-containing hemostatic agent is injected under manual pressure into the closed space of the vertebral body. This allows rapid entry into the venous circulation. We recommend that the surgeon perform a thorough history of a patient's allergies and use extreme caution when injecting these topical hemostatic products into the vertebral body.
IV.
病例系列。
在脊柱畸形手术中,局部止血剂的使用很常见。虽然有一定益处,但新出现的病例数据表明,含明胶的制剂会导致术中并发症。我们报告了两例患者,他们在使用手动压力将含明胶的止血剂注入椎体后,出现了过敏反应。在文献中,虽然与使用动物源性明胶相关的过敏反应已被牵涉;但将这些产品注入椎体的封闭血管腔内,随后栓塞到体循环中,风险值得强调。本报告旨在使手术团队意识到使用手动压力将止血剂注入椎体的风险,并强调这种现象的一种合理机制。
描述了两例接受后路脊柱融合术的脊柱畸形儿童,在手术中通过椎弓根将含明胶的止血剂注入椎体。
两名患者均通过椎弓根手动加压注入含明胶的止血剂溶液以防止过度出血。此后不久即发生过敏反应,导致紧急停止手术并开始进行医疗复苏。在两种情况下,事件发生后获得的类胰蛋白酶水平均升高。
在接受脊柱手术的对动物制品过敏或有过敏史的患者,如果将含明胶的止血剂通过手动压力注入椎体的封闭空间,可能会发生过敏反应。这会使它迅速进入静脉循环。我们建议外科医生对患者的过敏史进行彻底评估,并在将这些局部止血产品注入椎体时极其小心。
IV。