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Elektronisk udgave - Sundhedsstyrelsen

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28<br />

sin; tranexamic acid; erythropoietin; hemodilution; autotransfusion;<br />

cell salvage; device; or blood transfusion; autologous. An extensive<br />

EMBASE search was done as well. All the titles and abstracts were<br />

examined for studies evaluating the efficacy of the technologies for<br />

minimizing perioperative blood use. The manufacturers of the drugs<br />

were asked to identify any articles or reports on this subject. The references<br />

of all relevant randomized trials, reports, review articles,<br />

and previous meta-analyses (40, 41) were searched for other potentially<br />

useful trials.<br />

Only randomized trials in which the technologies were compared<br />

with a concurrent control, and which described the proportion of<br />

patients receiving at least one unit of allogeneic red blood cells were<br />

included. (Studies on autotransfusion/CS in cardiac surgery were limited<br />

to the evaluation of autotransfusion/CS initiated after coming<br />

off cardiopulmonary bypass.) Studies were included irrespective of<br />

whether they were full publications, abstracts or letters to the editor;<br />

used placebo or open-label controls; or were published in English<br />

or non-English journals. Because they have been shown to lead<br />

to biased estimates of treatment effect (42, 43), articles that were<br />

described as randomized, but in which clinicians could have been<br />

aware of which treatment the patient would receive (e.g. allocation<br />

by chart number, birth date, etc.) were excluded. Duplicate publications,<br />

studies of children, non-elective surgery, and trials in which<br />

patients were randomized postoperatively were excluded.<br />

Data from the studies were independently abstracted onto study<br />

data forms by two individuals. Disagreements were resolved by consensus.<br />

Except for the meta-analysis of ANH, no attempt was made<br />

to conceal the identity of the author or the medium of publication.<br />

The primary outcome measure was the proportion of patients receiving<br />

at least one unit of allogeneic packed red blood cells. A range<br />

of other relevant data were abstracted 13 . The methodological quality<br />

of the studies was reported using the Jadad scale (44). The Jadad<br />

scale contains questions about three items: the process of randomization,<br />

double blinding, and the description of withdrawals. Tests<br />

for heterogeneity were performed for each meta-analysis, and if positive,<br />

the studies that appeared to be the major contributors to the<br />

13 Other data abstracted from the studies were the the dose of medication used for pharmeceutical agents; the volume of blood<br />

withdrawn for ANH; the type of surgery (primary or re-operation), peri-operative myocardial infarction, re-operation because of<br />

bleeding and pre-operative use of aspirin for cardiac surgery; the route of administration (intravenous or subcutaneous) and the<br />

total dose (low (1800 units/kg)) of erythropoietin; the intra and post-operative transfusion thresholds<br />

reported (hemoglobin >100 g/l, 80-100 g/l or

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