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Low vs. high haemoglobin trigger for transfusion in vascular surgery: protocol for a randomised trial.
Møller, A; Nielsen, H B; Wetterslev, J; Pedersen, O B; Hellemann, D; Shahidi, S.
Affiliation
  • Møller A; Trial site: Department of Anaesthesia and Intensive care, Slagelse Hospital, Slagelse, Denmark.
  • Nielsen HB; Nordic Bioscience, Biomarkers & Research - ProScion, Herlev, Denmark.
  • Wetterslev J; Department of Anaesthesia, Abdominalcentre, Rigshospitalet, Copenhagen, Denmark.
  • Pedersen OB; Copenhagen Trial Unit, Centre for Clinical Intervention Research, Department 7812, Rigshospitalet, Copenhagen, Denmark.
  • Hellemann D; Department of Clinical Immunology, Naestved Sygehus, Naestved, Denmark.
  • Shahidi S; Trial site: Department of Anaesthesia and Intensive care, Slagelse Hospital, Slagelse, Denmark.
Acta Anaesthesiol Scand ; 61(8): 952-961, 2017 Sep.
Article in En | MEDLINE | ID: mdl-28782109
ABSTRACT

BACKGROUND:

In patients with cardiovascular disease, guidelines for administration of red blood cells (RBC) are mainly based on studies outside the vascular surgical setting with the recommendation to use a haemoglobin (hb) trigger-level lower than by guidelines from The European Society for Vascular Surgery. Restricting RBC transfusion may affect blood O2 transport with a risk for development of tissue ischaemia and postoperative complications.

METHODS:

In a single-centre, open-label, assessor blinded trial, 58 vascular surgical patients (> 40 years of age) awaiting open surgery of the infrarenal aorta or infrainguinal arterial bypass surgery undergo a web-based randomisation to one of two groups perioperative RBC transfusion triggered by hb < 8 g/dl or hb < 9.7 g/dl. Administration of fluid follows an individualised strategy by optimising cardiac stroke volume and near-infrared spectroscopy determines tissue oxygenation. Serious adverse event rates are myocardial injury (troponin-I ≥ 45 ng/l or ischaemic electrocardiographic findings at day 30), acute kidney injury, death, stroke and severe transfusion reactions. A follow-up visit takes place 30 days after surgery and a follow-up of serious adverse events in the Danish National Patient Register within 90 days is pending.

DISCUSSION:

This trial is expected to determine whether a RBC transfusion triggered by hb < 9.7 g/dl compared with hb < 8 g/dl results in adequate separation of postoperative hb levels, transfusion of more RBC units and maintains a higher tissue oxygenation. The results will inform the design of a multicentre trial for evaluation of important postoperative outcomes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vascular Surgical Procedures / Blood Transfusion / Hemoglobins Type of study: Clinical_trials / Guideline / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Acta Anaesthesiol Scand Year: 2017 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vascular Surgical Procedures / Blood Transfusion / Hemoglobins Type of study: Clinical_trials / Guideline / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Acta Anaesthesiol Scand Year: 2017 Document type: Article Affiliation country:
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