We conducted a retrospective chart review of 193 patients admitted during a
3-month period to determine the frequency of and potential risk factors as
sociated with thrombocytopenia, and the association of acquired thrombocyto
penia with length of stay in a surgical-trauma intensive care unit (SICU) a
nd mortality. All records were reviewed beginning 24 hours after admission.
Patients were followed for the duration of SICU stay or until death. Data
collected and analyzed as potential risk factors for thrombocytopenia were
age, gender, admitting diagnosis, classification (trauma, surgical, medical
), APACHE II score, medical history, all scheduled drugs with start and sto
p dates, select laboratory values, arterial or central line placement, and
complications. Thrombocytopenia occurred in 25 (13%) patients. These patien
ts were more likely (p<0.05) than those without thrombocytopenia to have th
e following potential risk factors: presence of a central or arterial line
(76% vs 46%, p<0.025), nonsurgical diagnosis (60%;, vs 37%, p<0.05), diagno
sis of sepsis (p<0.001), and administration of phenytoin (p<0.01), piperaci
llin (p<0.005), imipenem-cilastatin (p<0.001), and vancomycin (p<0.005). A
longer SICU stay (mean 21 vs 4.5; days, p<0.05) and increased mortality (16
% vs 4%, p<0.05) were significantly associated with thrombocytopenia. Cefaz
olin administration was significantly associated with nonthrombocytopenia (
p<0.05). Factors not associated with thrombocytopenia were age, gender, and
administration of histamine(2)-receptor antagonists, heparin, enoxaparin,
penicillins, ceftazidime, ceftriaxone, chloramphenicol, and amphotericin B.
A central or arterial line was the only factor associated with the develop
ment of thrombocytopenia in a multiple linear regression analysis (p=0.0003
, multiple r=0.2580). Thrombocytopenia is not a common occurrence in the SI
CU, but is associated with a longer SICU stay and increased mortality.