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Platelet transfusions
are indicated for the prevention and treatment
of hemorrhage in patients with thrombocytopenia
or platelet function defects. Their main use
is in the prevention of bleeding in patients
with hematologic malignancies who have marrow
failure caused by their disease or treatment.
For such patients
it has become accepted clinical practice to
tranfuse platelets when platelet levels are
very low. Ever since in the early 1960's a clear
relationship between hemorrhage and platelet
count was documented in patients with acute
leukemia, the threshold for platelet transfusions
has been debated (1).
These early studies
suggested a threshold of 20,000 / mm3,
and an NHI consensus conference published in
1987 supported this level for most patients,
although it was also concluded that lower levels
were safe for patients in stable condition (2,3).
More recent studies,
however, have shown that a threshold platelet
level of 10,000 / mm3
in stable patients is equally safe. This lower
threshold level will result in nearly 25% fewer
platelet transfusions than the 20,000 / mm3
level. Consequently, this lower threshold will
also result in lower cost, and less exposure
to donor blood products (4).
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Perhaps thresholds below
10,000 / mm3
are safe for stable patients, but the poor reproducibility
of automated platelet counts below 10,000 /
mm3 makes the
study of this topic difficult (5).
For patients with
fever, active bleeding or invasive procedures,
platelet thresholds higher than 10,000 / mm3
may well be indicated.
IBMT policies
stipulate the transfusion of platelets for the
following indications in patients with bone-marrow
failure:
- stable patients with
platelet counts less than 10,000 / mm3
- patients with platelet
counts less than 20,000 / mm3
and signs of hemorrhagic diathesis
- patients with platelet
counts less than 50,000 / mm3
and massive bleeding
- patients with platelet
counts less than 50,000 / mm3
who have to undergo major surgery
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| (1)
Gaydos LA, et al. N Engl J Med 266: 905, 1962.
(2) Freireich EJ. Transfusion 6:50 , 1966. (3)
JAMA 257: 1777, 1987. (4) Rebulla P, et al. N
Engl J Med 337: 1870, 1997. (5) Beutler E. Blood
81: 1411, 1993. |