The aim of this study was to evaluate the roles of Ga-67-citrate and Tc-99(
m)-methylene diphosphonate (Tc-99(m)-MDP) planar and single photon emission
tomographic (SPET) imaging in patients with vertebral osteomyelitis. Thirt
y patients (22 females, 8 males) aged 62.7 +/- 16.4 years (mean +/- s) were
enrolled prospectively between May 1995 and May 1998. The patients had bee
n on antibiotics for 7 +/- 4 weeks prior to the study. Histology was availa
ble for all but nine patients with mild infections, who were evaluated by a
combination of magnetic resonance imaging (MRI), clinical and laboratory t
ests. Ga-67-citrate (185 MBq) and three-phase bone (555 MBq Tc-99(m)-MDP) p
lanar and SPET imaging were performed in all patients, together with MRI as
a comparison. In total, 67 infectious foci were detected. Based on histolo
gy, there were four cases of severe, 13 cases of moderate and four cases of
mild osteomyelitis; nine mild infections were also classified by the combi
nation of MRI, clinical and laboratory results. Combined MRI and Ga-67-citr
ate SPET correctly classified all patients; MRI detected all 67 infectious
foci, whereas 67Ga-citrate SPET identified 54 only. False-negative results
were seen with all other modalities, especially in cases of mild and modera
te infection. 67Ga-citrate SPET identified unsuspected cases of endocarditi
s (n = 2), paravertebral abscess (n = 1), subaxillary soft tissue abscess (
n = 1) and rib osteomyelitis (n = 1). For 67Ga-citrate SPET, the target-to-
background ratio was 2.24 +/- 0.31, 1.76 +/- 0.07 and 1.30 +/- 0.18 for sev
ere, moderate and mild osteomyelitis, respectively. Significant differences
were noted between severe and moderate infection (P = 0.0051) and between
severe and mild infection (P < 0.0001); that between moderate and mild infe
ction was non-significant. For Tc-99(m)-MDP planar and SPET imaging, and fo
r planar Ga-67-citrate imaging, there was no correlation with severity. We
conclude that 67Ga-citrate SP:ET is able to identify vertebral osteomyeliti
s and detect additional sites of infection. It can also aid in determining
the severity of infection and, potentially, the response to therapy. ((C) 2
000 Lippincott Williams & Wilkins).