2012
DOI: 10.1111/j.1537-2995.2011.03515.x
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Is fresh‐frozen plasma clinically effective? An update of a systematic review of randomized controlled trials (CME)

Abstract: Combined with the 2004 review, 80 RCTs have investigated FP with no consistent evidence of significant benefit for prophylactic and therapeutic use across a range of indications evaluated. There has been little improvement in the overall methodologic quality of RCTs conducted in the past few years.

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Cited by 246 publications
(209 citation statements)
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“…A systematic review of all randomised controlled trials evaluating the clinical use of FFP found no consistent clinical benefit across a range of clinical groups. 8 Meta-analysis of trials in the cardiac section showed no significant difference between the experimental and control arms for the outcome of blood loss (-35.24 ml; 95% confidence interval -84.16-13.68 ml).…”
Section: Will Ffp Improve Clinical Outcomes?mentioning
confidence: 99%
“…A systematic review of all randomised controlled trials evaluating the clinical use of FFP found no consistent clinical benefit across a range of clinical groups. 8 Meta-analysis of trials in the cardiac section showed no significant difference between the experimental and control arms for the outcome of blood loss (-35.24 ml; 95% confidence interval -84.16-13.68 ml).…”
Section: Will Ffp Improve Clinical Outcomes?mentioning
confidence: 99%
“…Approximately, 280 000 units of FFP are issued annually in the UK to adults (93%) and children (7%) [51]. A recent systematic review found no evidence of benefit for prophylactic or therapeutic FFP use across a range of settings -including use in liver disease, cardiac surgery, warfarin anticoagulation reversal, thrombotic thrombocytopenic purpura, burns, shock and head injury [52]. However, despite 80 randomised controlled trials on this topic, the methodological quality of many trials is poor [52].…”
mentioning
confidence: 99%
“…A recent systematic review found no evidence of benefit for prophylactic or therapeutic FFP use across a range of settings -including use in liver disease, cardiac surgery, warfarin anticoagulation reversal, thrombotic thrombocytopenic purpura, burns, shock and head injury [52]. However, despite 80 randomised controlled trials on this topic, the methodological quality of many trials is poor [52]. A large observational study of coagulopathy in ICU (ISOC-1) [53] illustrates the clinical uncertainties surrounding the use of FFP.…”
mentioning
confidence: 99%
“…According to the results of a systematic review of 80 randomized clinical trials, the current guidelines for the administration of FFP are largely empirical. 21 In the United States, FFP at a dose of 10 to 15 mL/kg is used to reverse the warfarin effect; however, there is a paucity of evidence supporting its efficacy. 22 Moreover, FFP transfusion has several disadvantages, that is, (1) a delay in therapeutic effect because of the time required to obtain the ABO blood type and to thaw and transfuse several hundred milliliters of FFP; (2) transfusionassociated circulatory overload, especially in elderly patients with cardiac disease; (3) allergic reactions; (4) infection from exposure to multiple donors; and (5) transfusion-related acute lung injury, the most common cause of transfusionrelated deaths in the United States.…”
Section: Discussionmentioning
confidence: 99%