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Effectiveness of Intraoperative Cell Salvage in Aseptic Revision Total Hip Arthroplasty.

Effectiveness of Intraoperative Cell Salvage in Aseptic Revision Total Hip Arthroplasty: a Single-center Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05237830
Enrollment
140
Registered
2022-02-14
Start date
2011-01-01
Completion date
2022-01-31
Last updated
2022-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Revision of Total Hip Arthroplasty

Brief summary

Intraoperative cell salvage is an important measure of patient blood management but its effectiveness in patients undergoing revision total hip arthroplasty remains unclear. Over the last decade, we have used intraoperative cell salvage systematically in this group of patients. However, since the use of cell salvage has a cost and requires additional resources, we decided to retrospectively investigate its usefulness in this particular indication.

Interventions

PROCEDUREUse of Cell Salvage in revision of total hip arthroplasty

The effective use of the cell saver was defined as the ability to re-transfuse at least 125 mL of re-suspended red blood cells with a hematocrit of 60 %.

Sponsors

University of Liege
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Eligible patients were adults undergoing elective aseptic revision of hip arthroplasty at the department of orthopedic surgery of the University Hospital of Liege between 01 January 2011 and 31 December 2020.

Exclusion criteria

* Patients undergoing revision for infection or with local malignancies were excluded from this study.

Design outcomes

Primary

MeasureTime frameDescription
Cell savage useduring the surgical procedureThe primary outcome was the proportion of patients in whom the cell saver was effectively used (%)

Secondary

MeasureTime frameDescription
Re-infusedduring the surgical procedureTotal volume of re-suspended blood re-infused (mL)
Hemoglobinduring the surgical procedurePost-operative hemoglobin level (g/dL)
Allogenic Transfusion7 daysThe need for allogenic blood transfusion (unit)
Aspirated bloodduring the surgical procedureThe total volume of blood aspirated into the reservoir (mL)
Fluidduring the surgical procedureThe total amount of fluid infused (mL)

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026