Because of the declining incidence of anaerobic bacteremia, the predic
table sites of anaerobic infection and the increasing importance of ae
robic isolates (eg; yeasts), the practice of routinely culturing half
the volume of blood collected anaerobically has been questioned. We ha
ve assessed the yield of routine anaerobic blood cultures in our clini
cal setting. Blood culture isolates from November 1994 through October
1995 at Auckland (AKH) and Green Lane/National Women's Hospitals (GL/
NWH) were recorded. The medical records of patients with anaerobic bac
teremia were examined. For the three month period April to June 1996,
all positive blood cultures were analysed with respect to which bottle
(aerobic or anaerobic or both) was positive. For the period November
1994 to October 1995, 5.6% and 5.3% of blood cultures at AKH and GLH r
espectively were positive. At AKH and GLH anaerobes constituted 0.16%
and 0.19% of all blood cultures and 3.1% and 3.5% of all positive bloo
d cultures respectively. Twentyone of 25 (84%) significant anaerobes w
ere from patients in whom anaerobic infection was predictable. More is
olates were recovered from aerobic than anaerobic bottles, 178 versus
71, p<0.001. Aerobic culture also recovered more pathogens (76 versus
38, p<0.001 more yeasts (10 versus 0) and more Pseudomonas spp. (10 ve
rsus I) than did anaerobic culture. Only obligate anaerobes were isola
ted more frequently in anaerobic bottles (5 versus 0, p=0.03). Most in
stances of anaerobic bacteremia occurred in patients where anaerobes c
ould be expected. We conclude that routine use of two aerobic bottles
with clinically directed use of anaerobic blood culture bottle is an a
ppropriate and effective approach in our setting.