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临床试验/NCT05742295
NCT05742295已完成4 期

Preventing Cefoperazone/Sulbactam Induced Coagulopathy in Critically Ill Egyptian Patients: Efficacy of Vitamin K Prophylactic Doses

Helwan University1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2023年2月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
56
试验地点
1
主要终点
Number of Participants with changes in INR level

研究概览

简要总结

Evaluating the effect of prophylactic doses of vitamin K in preventing the adverse effect of cefoperazone/sulbactam induced coagulopathy in critically ill patients.

详细描述

One of the most challenging issues in the intensive care unit is treating multidrug-resistant (MDR) bacterial infections weighing benefit to risk ratio. MDR bacterial infection in ICU is a major public health problem and the main cause of mortality in ICUs in Egypt. A study published in the American Journal of Infection Control pointed out that the prevalence of MDR bacterial infections in the ICU was 54%.

Cefoperazone is a 3rd generation cephalosporin antibiotic covering many Gram-positive and Gram-negative bacteria, sulbactam is a beta-lactamase inhibitor which is used in combination with many antibiotics to overcome beta-lactamase producing bacteria, therefore the combination of cefoperazone/sulbactam has activity against MDR gram-negative bacteria. On the other hand, cefoperazone has been shown to have the adverse effects of inducing coagulopathy which is reported in many case reports and retrospective cohort studies. In most cases, coagulopathy events occur within a few days from the start of using cefoperazone/sulbactam, therefore the ICU staff was obliged to discontinue the antibiotic and choose another alternative leading to increasing the risk of resistant bacteria and treatment failure. Therefore, discontinuing the antibiotic due to its serious adverse events will lead to poor outcomes, more bacterial resistance, and more cost therapeutic plans for treating the infection and managing the severe adverse drug events which have been occurred such as bleeding. There are 2 mechanisms for cefoperazone-induced coagulopathy. The first the mechanism is related to N-methylthiotetrazole (NMTT), a side chain in cefoperazone molecule, which is responsible for the inhibition of a vitamin K-dependent carboxylation process leading to antagonizing blood clotting factors. The the second mechanism is antibiotics, in general, kill the normal flora in the gut which produce vitamin K. This cefoperazone/sulbactam-induced coagulopathy is not found in healthy volunteers or patients with adequate vitamin K activity, therefore, could consider cefoperazone/sulbactam-induced coagulopathy in critically ill patients, as related to nutritional status of these patients specifically with regard to vitamin K. This study aimed at studying the effect of co-administration of prophylactic doses of vitamin k during the administration of cefoperazone/sulbactam to keep the normal daily requirements of vitamin k, therefore preventing coagulopathy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ICU admitted patients on treatment or prophylactic doses of cefoperazone/sulbactam.

排除标准

  • Patients' aged <18 years
  • Pregnancy or breastfeeding women
  • Active bleeding or bleeding disorder
  • Patients having an abnormal baseline coagulation profile.
  • Patients administer total parenteral nutrition with regular vitamin k supplements.
  • Refusal to sign the written informed consent.

研究组 & 干预措施

Intervention group

Experimental

vitamin K is used as a prophylactic dose to prevent cefoperazone/sulbactam coagulopathy.

干预措施: Vitamin K (Drug)

结局指标

主要结局

Number of Participants with changes in INR level

时间窗: During the duration of cefoperazone/sulbactam treatment up to 2 weeks

comparing INR level between baseline INR (before starting the antibiotic) and during the treatment with the antibiotic

次要结局

  • Number of Participants with bleeding incidence(During the duration of cefoperazone/sulbactam treatment up to 2 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hebatallah Ali Abdeen

Clinical pharmacist

Helwan University

研究点 (1)

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