Kidney Transplant Service, Division of Nephrology, Department of Medicine, University of California-San Francisco, San Francisco, CA 94143, USA.
Transplantation. 2012 Dec 15;94(11):1117-23. doi: 10.1097/TP.0b013e31826ec74e.
BK polyomavirus (BKV) infection remains a significant cause of nephropathy and graft loss. Fluoroquinolones inhibit BKV replication in vitro, and small studies suggest in vivo benefit. A strategy of fluoroquinolone prophylaxis directed specifically against BKV has not been formally tested against a control group in kidney transplant recipients.
We retrospectively compared the impact of a change in antibiotic prophylaxis practice from no BKV prophylaxis (Group 1, n=106, July-December 2009) to BKV prophylaxis with ciprofloxacin 250 mg twice daily for 30 days (Group 2, n=130, January-June 2010) on the rate of BKV infection during the first 12 months after kidney transplantation.
Baseline demographics, transplant characteristics, induction immunosuppression, and 1-year incidence of acute rejection were similar between groups. Group 1 had fewer patients on maintenance corticosteroids (65.1% vs. 83.2%, P=0.002). At 3 months, Group 1 had a significantly higher risk of developing BK viremia (0.161 vs. 0.065, P=0.0378) and viruria (0.303 vs. 0.146, P=0.0067) compared with Group 2, but this difference disappeared at 12 months for both viremia (0.297 vs. 0.261, P=0.6061) and viruria (0.437 vs. 0.389, P=0.5363). Adjusting for the difference in steroid use did not change the results. There was a trend toward higher incidence of biopsy-proven BKV nephropathy in Group 1 (4.7% vs. 0.8%, P=0.057).
Thirty-day ciprofloxacin prophylaxis in kidney transplant recipients is associated with a lower rate of BKV infection at 3 months but not at 12 months. The long-term effectiveness and optimal duration of fluoroquinolone prophylaxis against BKV infection remain unknown.
BK 多瘤病毒(BKV)感染仍然是肾病和移植物丢失的重要原因。氟喹诺酮类药物在体外抑制 BKV 的复制,并且一些小型研究表明其具有体内益处。针对 BK 病毒的氟喹诺酮类药物预防策略尚未在肾移植受者的对照组中进行正式测试。
我们回顾性比较了改变抗生素预防方案对肾移植后 12 个月内 BKV 感染率的影响,方案从没有 BKV 预防(第 1 组,n=106,2009 年 7 月至 12 月)改为环丙沙星 250mg,每日两次,持续 30 天(第 2 组,n=130,2010 年 1 月至 6 月)。
两组患者的基线人口统计学、移植特征、诱导免疫抑制和 1 年急性排斥反应发生率相似。第 1 组服用维持性皮质类固醇的患者较少(65.1%比 83.2%,P=0.002)。第 1 组在 3 个月时发生 BK 病毒血症的风险显著更高(0.161 比 0.065,P=0.0378)和病毒尿症(0.303 比 0.146,P=0.0067),但在 12 个月时,病毒血症(0.297 比 0.261,P=0.6061)和病毒尿症(0.437 比 0.389,P=0.5363)的差异消失。调整类固醇使用的差异后,结果没有改变。第 1 组活检证实的 BKV 肾病发生率呈上升趋势(4.7%比 0.8%,P=0.057)。
肾移植受者使用环丙沙星 30 天预防可降低 3 个月时 BKV 感染率,但 12 个月时则不然。氟喹诺酮类药物预防 BKV 感染的长期效果和最佳持续时间仍不清楚。