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Thromboelastography (TEG) and Clopidogrel Withdrawal Time in Elderly Patients With Hip Fracture

Not Applicable
Conditions
Hip Fracture
Interventions
Procedure: Thrombelastograph and surgical timing
Registration Number
NCT04165538
Lead Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Brief Summary

In the elderly patients with hip fracture, some often take antiplatelet drugs such as clopidogrel due to the ischemic cardiovascular or cerebrovascular diseases. In traditional practice, these patients often need to stop medication for 5-7 days before surgery. But on the other hand, delayed surgery will lead to a significant increase in fracture related complications. Therefore, the appropriate time for drug withdrawal is particularly important in this population.

Thromboelastography is a monitoring method that can accurately judge the anticoagulation status of patients. We hope to use thromboelastography to guide the time of drug withdrawal, shorten the time of drug withdrawal as much as possible, and reduce the incidence of fracture related complications without increasing the risk of massive hemorrhage.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
140
Inclusion Criteria
  • hip fracture and operation
  • taking clopidogrel for more than one week before injury, with or without taking aspirin at the same time
Exclusion Criteria
  • high energy injury (such as traffic accident, falling from height), bilateral hip fracture, multiple fractures or injuries, pathological fracture
  • malignant tumor patients
  • hormone users
  • patients with recent active bleeding or bleeding ulcer
  • primary or secondary coagulation dysfunction or depression caused by other reasons than taking antiplatelet drugs (for example, taking warfarin)
  • patients with other acute or unstable diseases requiring delayed surgery (acute heart failure, myocardial infarction, cerebral infarction, cerebral hemorrhage, severe pulmonary infection, deep vein thrombosis or pulmonary embolism, etc.)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
TEG groupThrombelastograph and surgical timing-
Primary Outcome Measures
NameTimeMethod
Estimated red blood cell lossFrom admission when the first blood routine will be obtained to discharge when the last blood routine will be obtained, up to postoperative day 7.

The amount of red blood cell loss estimated by blood routine changes

Secondary Outcome Measures
NameTimeMethod
Blood transfusionFrom admission when the first blood routine will be obtained to discharge when the last blood routine will be obtained, up to postoperative day 7.

Red blood cell infusion volume

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