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Erythropoietin And/Or Iron Sucrose For Perioperative Anemia Management In Hip and Knee Arthroplasty

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Unknown

Conditions

Anemia, Iron Deficiency

Treatments

Drug: Iron sucrose
Drug: rHuEPO

Study type

Observational

Funder types

Other

Identifiers

NCT03917394
EPO-retro-cohort-PUMCH

Details and patient eligibility

About

Perioperative anemia is very common in patients undergoing total hip arthroplasty (THA) and total knee arthroplasty (TKA). This study retrospectively analyzes the use of rHuEPO and iron sucrose in patients undergoing total hip and knee arthroplasty in order to observe the short-term efficacy and safety of rHuEPO and iron sucrose.

Full description

This study aims to explore whether short-term use of rHuEPO and iron sucrose can improve postoperative anemia and promote postoperative rehabilitation after hip and knee arthroplasty. According to different therapies of perioperative anemia , included subjects would be divided into rHuEPO monotherapy group, iron sucrose monotherapy group, rHuEPO combined with iron sucrose group and control group (without rHuEPO and iron sucrose).

Enrollment

780 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients who underwent hip or knee arthroplasty between May 1, 2012 (included) and December 31, 2015 in Peking Union Medical College Hospital
  2. Age ≥ 18 years, sex unlimited

Exclusion criteria

  1. Patients with serious absence of clinical data

  2. Patients with rHuEPO contraindication

    1. Patients with uncontrolled severe hypertension
    2. Patients allergic to this product and other mammalian cell derivatives, or to human serum albumin
    3. Co-infected patients
  3. Patients definitely allergic to iron sucrose injection

  4. Patients with coagulation dysfunction

Trial design

780 participants in 4 patient groups

rHuEPO monotherapy group
Description:
rHuEPO was administrated during hospitalization period.
Treatment:
Drug: rHuEPO
iron sucrose monotherapy group
Description:
Iron sucrose was administrated during hospitalization period.
Treatment:
Drug: Iron sucrose
rHuEPO combined with iron sucrose group
Description:
rHuEPO combined with iron sucrose was administrated during hospitalization period.
Treatment:
Drug: rHuEPO
Drug: Iron sucrose
control group
Description:
Subjects didn't be administrated with rHuEPO and/or iron sucrose during hospitalization period.

Trial contacts and locations

1

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Central trial contact

Wei Wang, PhD; Rui Wang, Master

Data sourced from clinicaltrials.gov

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