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临床试验/NCT06037720
NCT06037720尚未招募不适用

Diagnostic Accuracy Study of a Point-of-Care Test for Coagulation Function: CoaguChek System Versus Standard Laboratory Tests in Cardiac Surgery Requiring Cardiopulmonary Bypass

Hospital de Base0 个研究点目标入组 50 人开始时间: 2023年9月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
主要终点
Point-of-care diagnostic method

研究概览

简要总结

Intraoperative coagulopathies in complex procedures are common. For the diagnosis and adequate therapy, laboratory tests are necessary, which can delay the patient's therapy. In this sense, the study aims to evaluate the point-of-care test device for patients undergoing surgeries with cardiopulmonary bypass.

Objective: To analyze the accuracy between the point-of-care diagnostic method and the laboratory test considered the gold standard for checking the INR.

Methodology: Cross-sectional study of diagnostic accuracy with simultaneous testing of the Coaguchek XS device and standard laboratory method in patients undergoing cardiopulmonary bypass to evaluate INR results.

详细描述

Laboratory evaluation of blood clotting is widely used in perioperative medicine, either by conventional technique (prothrombin time - PT/INR, Activated Partial Thromboplastin Time - aPTT, fibrinogen dosage and platelet count) or by the Point of Care method (Thromboelastogram ) - notably in surgical procedures with the possibility of severe volume loss (cardiovascular, oncological, trauma, etc.).

The prothrombin time (PT) is a general assessment of the integrity of the extrinsic and common pathway of coagulation. It determines the time of formation of the fibrin clot. The INR/RNI (International Normalized Ratio) is calculated from the PT and is intended to establish valid comparisons regardless of the type of PT reagent (known as thromboplastin) used by different clinical laboratories. The INR is indicated for evaluating the integrity of the extrinsic (factor VII*) and common pathway (fibrinogen and factors II*, V and X*), and for monitoring the anticoagulant effect of an anti-vitamin K agent (warfarin), capable of inhibiting the synthesis of vitamin K dependent factors (II, VII, IX, X, proteins C and S).

Today, due to its safety, sensitivity and speed, the thromboelastogram is recommended as the method of choice for assessing hemostasis in a surgical setting. However, because it is still not widespread in many centers, mainly due to its high cost, many hospitals are limited to the use of traditional laboratory methods which, despite their undeniable reliability, require more time for their execution and release of results.

In cardiac surgery with cardiopulmonary bypass (CPB), the use of prime solution to fill the CPB circuit results in hemodilution of coagulation factors, with factor I (fibrinogen) being one of the most affected, but not the only one. Each abnormality detected requires a specific action. Thus, the activated clotting time (ACT) is normalized with the administration of protamine. Thrombocytopenia and/or platelet dysfunction, with platelet concentrate infusion. Abnormalities in clotting factors, with administration of the specific factor, eg fibrinogen, either by factor concentrate, cryoprecipitate or plasma. It is at this moment that a quick assessment of hemostasis, in a global and individualized way at the same time, is necessary.

More than a decade ago, devices appeared on the market designed to help patients using warfarin to maintain their anticoagulation within parameters established for each case, providing safety, speed and comfort. Using a reagent strip and a drop of blood, evaluating the INR has become as simple as evaluating capillary blood glucose for diabetic patients. In just a few seconds, INR assessment can show significant changes in the extrinsic coagulation pathway, an important step to help with rapid decision-making in surgical environments. The Coaguchek Device, validated and used for outpatient management of patients using Warfarin, presents valuable characteristics for this purpose (simplicity, speed, safety), also important in the context of intraoperative decision-making. There are few reports in the literature on the use of the Coaguchek device in surgery and on the reliability of the data obtained through its use.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Cross Sectional

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

  • patients over 18 years old
  • admitted to the Hospital de Base of the Federal District for cardiac surgery, who volunteered to participate in the examination both by the traditional method of venous INR examination and by the use of the Coaguchek device and only after signing the TCLE.

排除标准

  • patients who give up the research even after signing the TCLE will be excluded
  • patients who do not meet the aforementioned inclusion criteria
  • patients who refuse to participate in the study
  • patients with kidney, liver, hematological disease or any disease that affects coagulation
  • patients participating in other studies

结局指标

主要结局

Point-of-care diagnostic method

时间窗: During surgery

To analyze the accuracy between the point-of-care diagnostic method and the laboratory test considered the gold standard for verifying the INR.

次要结局

未报告次要终点

研究者

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

Fabricio Tavares Mendonca

MD, MSc, PhD

Hospital de Base

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