Elektronisk udgave - Sundhedsstyrelsen
Elektronisk udgave - Sundhedsstyrelsen
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