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Anemia of Inflammation and Deficiency Anemia

Anemia of Inflammation and Deficiency Anemia in Critically Ill Patients; Biological Markers

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04071067
Acronym
AIDA
Enrollment
1000
Registered
2019-08-28
Start date
2020-01-01
Completion date
2021-07-01
Last updated
2019-08-28

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

Conditions

Anemia, Iron Deficiency, Anemia of Chronic Disease

Brief summary

Critical patients which requiring admission to intensive care (IT) are a special group of patients. In these patients the prevalence of anemia reported in studies is 75%. This prevalence is similar to that in the retrospective observational study conducted in our intensive care unit(ICU). Of the 783 patients included in the study, 551 (73.37%) had anemia on admission. Frequently anemia is present on discharge from ICU or hospital and may persist for an average of 11 weeks. Some studies have reported the presence of anemia as far as 6 months after discharge. It is widely accepted that anemia has a negative impact on rehabilitation and quality of life, but the treatment can not be exclusively based on blood products due to the risks associated with transfusion. Alternative treatments such as injectable iron or erythropoietin should be considered. The Transfusion Management Initiative Group recently issued recommendations on perioperative anemia. Similar recommendations for ICU have not yet been developed in Romania. The current study has two main purposes. The first to adopt the perioperative anemia diagnostic algorithm and adapt it to anemic patients on ICU; the second to identify patients with mixed anemia (inflammatory and iron deficient anemia) who can benefit from treatment with iron.

Interventions

None listed

Sponsors

Iuliu Hatieganu University of Medicine and Pharmacy
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients admitted to ICU ICU stay \>48hours

Exclusion criteria

* Refusal to participate in the study * Allergy to iron products * Anemia requiring massive transfusion in the last 7 days * Treatment of iron products in the last 7 days * Chronic renal failure with GFR \<30mL / min or on dialysis * Metabolism of iron * Pregnant or lactation patients * Rheumatic diseases * Inflammatory bowel diseases * Hematological pathologies * Impossibility of performing laboratory tests within 72 hours of admission

Design outcomes

Primary

MeasureTime frame
Number of transfusions during ICU stayUp to 3 months of hospital stay
Change in hemoglobin levels during ICU stay21 days: day 0=point 1; day 7=point 2; day 14=point 3; day 21 =point 4;

Secondary

MeasureTime frame
Number of hours of mechanical ventilation during hospital stayUp to 3 months
Days spent in hospitalUp to 3 months
Days spent on ICUUp to 3 months of hospital stay
Change in hemoglobin level during hospital stayUp to 3 months: week 3=point 1; week 6=point 2; week 9=point 3; week 12=point4

Other

MeasureTime frameDescription
Change in hepcidin levelsDays 0, 3, 7, 14, 21Hepcidin is a peptide produced by the liver. It acts by binding to ferroportin, the sole exporter of iron. The hepcidin-ferroportin complex is sequestrated in the cytosol of cells followed by its degradation. Ferroportin degradation prevents iron from being exported from the cell.

Countries

Romania

Contacts

Primary ContactRobert Szabo, Resident MD
robsz11@yahoo.com0040755628255

Outcome results

None listed

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