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Safety of human albumin-serious adverse events reported worldwide in 1998-2000 |
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Safety
of human albumin-serious adverse events reported worldwide in 1998-2000( dagger ).
Vincent
JL, Wilkes MM, Navickis RJ. Br
J Anaesth. 2003 Nov;91(5):625-30.
Department
of Intensive Care, Hopital Erasme, Universite Libre de Bruxelles, Route de Lennik 808,B-1070 Brussels,
Belgium. Hygeia Associates, Grass
Valley,
California,
USA.
BACKGROUND:
Previous pharmacovigilance studies have indicated a low rate of adverse events
in patients receiving human albumin. However, the incidence of adverse events is
likely to have been underestimated because of under-reporting. A more accurate
estimate may be possible during a period such as 1998-2000, when awareness
regarding albumin safety was heightened by publication of a meta-analysis.
METHODS: All serious adverse event reports received, and total doses of albumin
distributed worldwide from the beginning of 1998 to the end of 2000 by 10 major
suppliers of therapeutic human albumin were compiled. RESULTS: Distributed
albumin doses totalled 1.62 x 10(7). The total numbers of non-fatal and fatal
serious adverse events reported were 198 and 13, respectively. The incidence of
all reported serious non-fatal and fatal adverse events was 5.28 per 10(6) doses
(CI 1.60-17.4 per 10(6) doses). For non-fatal serious adverse events only, the
observed incidence was 4.65 per 10(6) doses (CI 1.34-16.2 per 10(6) doses). No
patient death was classified as probably related to albumin administration. The
observed incidence of fatal serious adverse events possibly related to albumin
was 0.185 per 10(6) doses (CI 0.0597-0.574 per 10(6)
doses). The observed incidence of all non-fatal and fatal serious adverse events
was significantly higher during the 1998-2000 period as compared with 1990-1997
(incidence rate ratio 4.98; CI 3.94-6.29), probably chiefly as a result of
reduced under-reporting. CONCLUSIONS: Although the observed incidence of adverse
events is likely to be an underestimate, nevertheless both non-fatal and fatal
serious adverse events in albumin recipients appear to be rare. These results
add further support to the excellent safety record of human albumin.
Br
J Anaesth 2003; 91: 625-30
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