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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04398238
Other study ID # 346/2020/Oss/IOR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2021
Est. completion date April 4, 2023

Study information

Verified date May 2023
Source Istituto Ortopedico Rizzoli
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective observational study: impact of a peri-operative patient blood management program (PBM) on transfusion rates of patients undergoing elective hip replacement.


Description:

A Patient Blood Management (PBM) program was implemented in year 2019 in our institution: patient scheduled for elective total hip replacement underwent pre-operative screening about one month before surgery, and those with pre-operative hemoglobin < 13 g/dl were screened for possible causes and treatment of anemia. Data from two different time frames, before and after the implementation of the program, were collected to study the change in clinical outcomes such as transfusion rates, length of stay, etc.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date April 4, 2023
Est. primary completion date November 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - undergoing elective hip replacement in the selected time-frame - American Society of Anesthesiology (ASA) status 1-2-3 - age >18 Exclusion Criteria: - patients not undergoing screening as outpatients at pre-operative clinic

Study Design


Intervention

Combination Product:
evaluation by transfusion medicine specialist
screening for anemia causes and treatment: iron/folate/vitamin B12 supplementation, Erythropoietin administration if indicated

Locations

Country Name City State
Italy Sandra Giannone Bologna BO

Sponsors (1)

Lead Sponsor Collaborator
Istituto Ortopedico Rizzoli

Country where clinical trial is conducted

Italy, 

References & Publications (3)

Ellermann I, Bueckmann A, Eveslage M, Buddendick H, Latal T, Niehoff D, Geissler RG, Hempel G, Kerkhoff A, Berdel WE, Roeder N, Van Aken HK, Zarbock A, Steinbicker AU. Treating Anemia in the Preanesthesia Assessment Clinic: Results of a Retrospective Evaluation. Anesth Analg. 2018 Nov;127(5):1202-1210. doi: 10.1213/ANE.0000000000003583. — View Citation

Munoz M, Acheson AG, Auerbach M, Besser M, Habler O, Kehlet H, Liumbruno GM, Lasocki S, Meybohm P, Rao Baikady R, Richards T, Shander A, So-Osman C, Spahn DR, Klein AA. International consensus statement on the peri-operative management of anaemia and iron deficiency. Anaesthesia. 2017 Feb;72(2):233-247. doi: 10.1111/anae.13773. Epub 2016 Dec 20. — View Citation

Rineau E, Chaudet A, Chassier C, Bizot P, Lasocki S. Implementing a blood management protocol during the entire perioperative period allows a reduction in transfusion rate in major orthopedic surgery: a before-after study. Transfusion. 2016 Mar;56(3):673-81. doi: 10.1111/trf.13468. Epub 2016 Jan 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary transfusion rates percentage of patients undergoing hip replacement who receive at least one unit of concentrated red cells during or after surgery from day of surgery till day of discharge, up to 60 days
Secondary minimum hemoglobin minimum hemoglobin reached after surgery from day of surgery till day of discharge, up to 60 days
Secondary hemoglobin at discharge last measured hemoglobin before discharge from hospital from day of surgery till day of discharge, up to 60 days
Secondary length of stay total days of hospital stay from admission to discharge from day of surgery till day of discharge, up to 60 days
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