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Revision Total Hip Replacement Arthroplasty and Hematologic Variables

Completed
Conditions
Avascular Necrosis of Hip
Degenerative Hip Joint Disease
Interventions
Other: RTHRA group
Registration Number
NCT02951741
Lead Sponsor
Seoul National University Bundang Hospital
Brief Summary

Revision total hip replacement arthroplasty is a surgery having intra- and postoperative substantial blood loss. The investigators will investigate the relationship between the various hematologic variables and postoperative bleeding volume.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
62
Inclusion Criteria
  • revision total hip replacement
Exclusion Criteria
  • hematologic disease
  • anticoagulant medication
  • American Society of Anesthesiologists physical status 4 and 5

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
RTHRA groupRTHRA grouppatients undergoing revision total hip replacement
Primary Outcome Measures
NameTimeMethod
Change of FIBTEM5 minutes before initiation of anesthesia and 5 minutes after finishing operation

FIBTEM: one of the measurements of the rotational thromboelastometry

Secondary Outcome Measures
NameTimeMethod
Hemoglobinpostoperative day 4
postoperative bleeding volumepostoperative 72 hours
volume of infused fluid during operationPeriod from starting to finishing the operation (During operation, an expected average of 3 hours)

Infused total crystalloid and colloid volume during the operation will be recorded

intraoperative urine outputPeriod from starting to finishing the operation (During operation, an expected average of 3 hours)
transfusion unitsPeriod from starting to finishing the operation (During operation, an expected average of 3 hours) and postoperative first day

Red blood cell

Hematocritpostoperative day 4
Platelet countpostoperative day 4
prothrombin time_international normalized ratiopostoperative day 1
activated partial prothrombin timepostoperative day 1
fibrinogen concentrationpostoperative day 1

Trial Locations

Locations (1)

Seoul National University Bundang Hospital

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Seongnam-si, Gyeonggi-do, Korea, Republic of

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