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. Author manuscript; available in PMC: 2014 Oct 29.
Published in final edited form as: Cochrane Database Syst Rev. 2004;(1):CD001884. doi: 10.1002/14651858.CD001884.pub2
Methods The pharmacy provided bottles containing placebo or desmopressin (DDAVP) that were identical in appearance. A card drawn at random at the beginning of the operation determined which vial was to be used for the patient. The method used to generate allocation sequences was not described
Participants 83 consecutive patients having open heart surgery were randomly allocated to one of two groups
  1. Desmopressin (DDAVP) group: n = 40.

  2. Placebo group: n = 43.


NB: No patient demographic data were reported.
Interventions
  1. DDAVP group received 0.3 ug/kg of DDAVP diluted in 50 ml of normal saline, given intravenously over 15 minutes after cardiopulmonary bypass had been discontinued, the protamine infused, and the heparin reversal documented by measurement of the activated clotting time.

  2. Placebo group received equivalent volumes of normal saline.

Outcomes Number of patients transfused allogeneic blood (n)
Number of patients transfused fresh frozen plasma (n)
Number of patients transfused platelets (n)
Blood loss (ml)
Amount of autotransfusion (ml)
Number of patients treated with EACA
Notes Quality assessment score (Schulz criteria): 4/7
Transfusion protocol not specified.
Risk of bias
Item Authors’ judgement Description
Adequate sequence generation? Unclear Method of randomisation was not described.
Allocation concealment? Unclear B - Unclear
Blinding?
All outcomes
Yes Double blind.