Incidence of abnormal coagulation and its correlation with iv fluids, blood components transfusion in orthopedic trauma patients
Not Applicable
- Conditions
- Health Condition 1: S00-T88- Injury, poisoning and certain other consequences of external causes
- Registration Number
- CTRI/2019/03/017946
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age 18 years to 65 years having orthopaedic trauma
2. Either sex
3. ASA -I, II and III
Exclusion Criteria
1. Patient refusal
2. Age less than 18 years and more than 65 years
3. ASA- IV or more
4. Patients with existing head injury
5. Patients with existing vascular injury
6. Patients who is taking anticoagulant and/or antiplatelet drugs
7. Patients with unstable haemodynamics requiring vasopressor or inotropic
supports
8. Patients with sepsis
9. Patients with chronic liver diseases
10. Patients with known hypercoagulable status
11. Patients with gravid uterus
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To observe the incidence of inadvertent perioperative coagulopathy in orthopaedic trauma patients. <br/ ><br>Timepoint: Perioperative period, 72 hours postoperative and 30 days postoperative.
- Secondary Outcome Measures
Name Time Method Association of coagulopathy with surgery duration, surgical blood loss, IV fluid and blood components transfusion.Timepoint: Perioperative period;Relationship between coagulopathy and survival rateTimepoint: 72 hours postoperative and 30 days postoperative.