Duch J M, Yee J
Department of Medicine, Wright-Patterson Medical Center, Wright-Patterson Air Force Base, OH 45433-5529, USA.
Am J Kidney Dis. 2001 Jan;37(1):149-153. doi: 10.1016/s0272-6386(01)80069-x.
Intraperitoneal (IP) administration of either streptokinase (SK) or urokinase (UK) has assumed an adjunctive role to antibiotic therapy in selected patients with relapsing peritonitis. In these circumstances, bacteria may be protected from antibiotics through sequestration in either fibrinous structures or biofilms within the lumen of the peritoneal dialysis (PD) catheter or the peritoneal cavity. In some cases, it appears that disruption of these sheltered microenvironments by thrombolytic agents facilitated eradication of the offending organism and obviated the need for catheter removal, replacement, or interim hemodialysis. Although IP SK has been generally well tolerated as additive therapy in relapsing peritonitis, sporadic reports of significant complications, such as abdominal pain, fever, and severe hypotension, have precluded its more widespread acceptance. The only other thrombolytic agent used in this setting, UK, is presently unavailable because of a manufacturing shortfall. Therefore, adjunctive thrombolytic therapy for relapsing peritonitis is currently restricted. To circumvent these limitations, we devised an IP tissue plasminogen activator (tPA) protocol to eliminate recurring infection in a patient undergoing chronic ambulatory PD. After a third episode of peritonitis caused by Enterobacter cloacae, treated twice previously with an adequate antibiotic regimen, we instilled 6 mL of tPA (1 mg/mL) into the PD catheter for a 2-hour dwell time. The treatment was well tolerated and, in conjunction with a third course of antibiotic therapy, has produced an infection-free interval of 8 months.
对于部分复发性腹膜炎患者,腹腔内注射链激酶(SK)或尿激酶(UK)已成为抗生素治疗的辅助手段。在这种情况下,细菌可能通过在腹膜透析(PD)导管腔内或腹腔内的纤维蛋白结构或生物膜中隔离而免受抗生素的作用。在某些情况下,溶栓剂破坏这些受保护的微环境似乎有助于根除致病微生物,从而无需拔除导管、更换导管或进行临时血液透析。虽然腹腔内注射SK作为复发性腹膜炎的辅助治疗通常耐受性良好,但关于严重并发症(如腹痛、发热和严重低血压)的零星报道使其未能得到更广泛的接受。在此情况下使用的唯一其他溶栓剂UK,目前因生产短缺而无法获得。因此,目前复发性腹膜炎的辅助溶栓治疗受到限制。为了克服这些限制,我们设计了一种腹腔内注射组织型纤溶酶原激活剂(tPA)的方案,以消除一名接受持续性非卧床腹膜透析患者的反复感染。在由阴沟肠杆菌引起的第三次腹膜炎发作后,患者此前已接受过两次足够疗程的抗生素治疗,我们将6 mL tPA(1 mg/mL)注入PD导管,保留2小时。该治疗耐受性良好,并且与第三个疗程的抗生素治疗一起,产生了8个月的无感染期。