Sola J E, Stone M M, Wise B, Colombani P M
Department of Surgery, Johns Hopkins University, Baltimore, Maryland.
Pediatr Pulmonol. 1992 Dec;14(4):239-42. doi: 10.1002/ppul.1950140407.
The use of vascular access systems in patients with cystic fibrosis (CF) is well accepted, with lower overall complications and maintenance costs than percutaneous silastic catheters. We report our 6 year experience with 22 infusaports in 15 CF patients. Our patients had indwelling catheters for an average of 539 days per catheter (range, 14-2,224 days). These infusaports were used for home antibiotic therapy, blood sampling, and total parenteral nutrition. The overall complication rate was relatively low, 1 in every 1,483 catheter days. Infectious complications were extremely infrequent at a rate of 1 in 5,929 catheter days. The rate of mechanical complications was 1 in 1,976 catheter days. However, superior vena caval syndrome or deep venous thrombosis was associated with 3 of 22 catheters (13.6%). Due to this high incidence of major thrombotic events with the attendant risk of pulmonary embolism, all patients with CF using infusaports and without evidence of liver disease or bleeding problems receive aspirin prophylaxis.
在囊性纤维化(CF)患者中使用血管通路系统已被广泛接受,与经皮硅橡胶导管相比,其总体并发症和维护成本更低。我们报告了15例CF患者使用22个输液港的6年经验。我们的患者每个导管平均留置539天(范围为14 - 2224天)。这些输液港用于家庭抗生素治疗、采血和全胃肠外营养。总体并发症发生率相对较低,每1483个导管日出现1例并发症。感染性并发症极为罕见,发生率为每5929个导管日出现1例。机械性并发症发生率为每1976个导管日出现1例。然而,22个导管中有3个(13.6%)出现了上腔静脉综合征或深静脉血栓形成。由于重大血栓事件的高发生率以及随之而来的肺栓塞风险,所有使用输液港且无肝病或出血问题证据的CF患者均接受阿司匹林预防治疗。