Chen Li-Ju, Hsiao Fei-Yuan, Shen Li-Jiuan, Wu Fe-Lin Lin, Tsay Woei, Hung Chien-Ching, Lin Shu-Wen
Graduate Institute of Clinical Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
School of Pharmacy, National Taiwan University, Taipei, Taiwan.
PLoS One. 2016 Jul 27;11(7):e0158407. doi: 10.1371/journal.pone.0158407. eCollection 2016.
Existing data regarding the risk of hemorrhagic events associated with exposure to hypoprothrombinemia-inducing cephalosporins are limited by the small sample size. This population-based study aimed to examine the association between exposure to hypoprothrombinemia-inducing cephalosporins and hemorrhagic events using National Health Insurance Research Database in Taiwan.
A nationwide nested case-control study.
National Health Insurance Research database.
We conducted a nested case-control study within a cohort of 6191 patients who received hypoprothrombinemia-inducing cephalosporins and other antibiotics for more than 48 hours. Multivariable conditional logistic regressions were used to calculate the adjusted odds ratio (aOR) and 95% confidence interval (CI) for hemorrhagic events associated with exposure to hypoprothrombinemia-inducing cephalosporins (overall, cumulative dose measured as defined daily dose (DDD), and individual cephalosporins).
Within the cohort, we identified 704 patients with hemorrhagic events and 2816 matched controls. Use of hypoprothrombinemia-inducing cephalosporins was associated with increased risk of hemorrhagic events (aOR, 1.71; 95% CI, 1.42-2.06), which increased with higher cumulative doses (<3 DDDs, aOR 1.62; 3-5 DDDs, aOR 1.78; and >5 DDDs, aOR 1.89). The aOR for individual cephalosporin was 2.88 (95% CI, 2.08-4.00), 1.35 (1.09-1.67) and 4.57 (2.63-7.95) for cefmetazole, flomoxef, and cefoperazone, respectively. Other risk factors included use of anticoagulants (aOR 2.08 [95% CI, 1.64-2.63]), liver failure (aOR 1.69 [1.30-2.18]), poor nutritional status (aOR 1.41 [1.15-1.73]), and history of hemorrhagic events (aOR 2.57 [1.94-3.41]) 6 months prior to the index date.
Use of hypoprothrombinemia-inducing cephalosporins increases risk of hemorrhagic events. Close watch for hemorrhagic events is recommended when prescribing these cephalosporins, especially in patients who are at higher risk.
现有关于暴露于可致低凝血酶原血症的头孢菌素类药物相关出血事件风险的数据因样本量小而受限。这项基于人群的研究旨在利用台湾地区国民健康保险研究数据库,探讨暴露于可致低凝血酶原血症的头孢菌素类药物与出血事件之间的关联。
一项全国性巢式病例对照研究。
国民健康保险研究数据库。
我们在一组6191例接受可致低凝血酶原血症的头孢菌素类药物及其他抗生素治疗超过48小时的患者中进行了巢式病例对照研究。采用多变量条件逻辑回归计算与暴露于可致低凝血酶原血症的头孢菌素类药物(总体、以限定日剂量(DDD)衡量的累积剂量以及个别头孢菌素类药物)相关的出血事件的调整优势比(aOR)和95%置信区间(CI)。
在该队列中,我们识别出704例出血事件患者和2816例匹配对照。使用可致低凝血酶原血症的头孢菌素类药物与出血事件风险增加相关(aOR为1.71;95%CI为1.42 - 2.06),且随着累积剂量增加而增加(<3 DDDs,aOR 1.62;3 - 5 DDDs,aOR 1.78;>5 DDDs,aOR 1.89)。个别头孢菌素类药物的aOR分别为:头孢美唑2.88(95%CI为2.08 - 4.00),氟氧头孢1.35(1.09 - 1.67),头孢哌酮4.57(2.63 - 7.95)。其他风险因素包括使用抗凝剂(aOR 2.08 [95%CI为1.64 - 2.63])、肝功能衰竭(aOR 1.69 [1.30 - 2.18])、营养状况差(aOR 1.41 [1.15 - 1.73])以及在索引日期前6个月有出血事件史(aOR 2.57 [1.94 - 3.41])。
使用可致低凝血酶原血症的头孢菌素类药物会增加出血事件风险。在开具这些头孢菌素类药物时,建议密切关注出血事件,尤其是在高危患者中。