TY - JOUR
T1 - Importance of Blood Glucose Management Before 18F-FDG PET/CT in 322 Patients with Bacteremia of Unknown Origin
AU - Pijl, Jordy P
AU - Glaudemans, Andor W J M
AU - Gheysens, Olivier
AU - Slart, Riemer H J A
AU - Kwee, Thomas C
N1 - © 2023 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2023/8
Y1 - 2023/8
N2 - We investigated the effects of blood glucose levels on the performance of
18F-FDG PET/CT for detecting an infection focus in patients with bacteremia.
Methods: A total of 322 consecutive patients with bacteremia who underwent
18F-FDG PET/CT between 2010 and 2021 were included. Logistic regression analysis was performed to evaluate the association between finding a true-positive infection focus on
18F-FDG PET/CT and blood glucose level, type of diabetes, and use of hypoglycemic medication. C-reactive protein, leukocyte count, duration of antibiotic treatment, and type of isolated bacteria were considered as well.
Results: Blood glucose level (odds ratio, 0.76 per unit increase;
P = <0.001) was significantly and independently associated with
18F-FDG PET/CT outcome. In patients with a blood glucose level between 3.0 and 7.9 mmol/L (54-142 mg/dL), the true-positive detection rate of
18F-FDG PET/CT varied between 61% and 65%, whereas in patients with a blood glucose level between 8.0 and 10.9 mmol/L (144-196 mg/dL), the true-positive detection rate decreased to 30%-38%. In patients with a blood glucose level greater than 11.0 mmol/L (200 mg/dL), the true-positive detection rate was 17%. In addition to C-reactive protein (odds ratio, 1.004 per point increase;
P = 0.009), no other variables were independently associated with
18F-FDG PET/CT outcome.
Conclusion: In patients with moderate to severe hyperglycemia,
18F-FDG PET/CT was much less likely to identify the focus of infection than in normoglycemic patients. Although current guidelines recommend postponing
18F-FDG PET/CT only in cases of severe hyperglycemia with glucose levels greater than 11 mmol/L (200 mg/dL), a lower blood glucose threshold seems to be more appropriate in patients with bacteremia of unknown origin and other infectious diseases.
AB - We investigated the effects of blood glucose levels on the performance of
18F-FDG PET/CT for detecting an infection focus in patients with bacteremia.
Methods: A total of 322 consecutive patients with bacteremia who underwent
18F-FDG PET/CT between 2010 and 2021 were included. Logistic regression analysis was performed to evaluate the association between finding a true-positive infection focus on
18F-FDG PET/CT and blood glucose level, type of diabetes, and use of hypoglycemic medication. C-reactive protein, leukocyte count, duration of antibiotic treatment, and type of isolated bacteria were considered as well.
Results: Blood glucose level (odds ratio, 0.76 per unit increase;
P = <0.001) was significantly and independently associated with
18F-FDG PET/CT outcome. In patients with a blood glucose level between 3.0 and 7.9 mmol/L (54-142 mg/dL), the true-positive detection rate of
18F-FDG PET/CT varied between 61% and 65%, whereas in patients with a blood glucose level between 8.0 and 10.9 mmol/L (144-196 mg/dL), the true-positive detection rate decreased to 30%-38%. In patients with a blood glucose level greater than 11.0 mmol/L (200 mg/dL), the true-positive detection rate was 17%. In addition to C-reactive protein (odds ratio, 1.004 per point increase;
P = 0.009), no other variables were independently associated with
18F-FDG PET/CT outcome.
Conclusion: In patients with moderate to severe hyperglycemia,
18F-FDG PET/CT was much less likely to identify the focus of infection than in normoglycemic patients. Although current guidelines recommend postponing
18F-FDG PET/CT only in cases of severe hyperglycemia with glucose levels greater than 11 mmol/L (200 mg/dL), a lower blood glucose threshold seems to be more appropriate in patients with bacteremia of unknown origin and other infectious diseases.
U2 - 10.2967/jnumed.122.264839
DO - 10.2967/jnumed.122.264839
M3 - Article
C2 - 37414447
SN - 0161-5505
VL - 64
SP - 1287
EP - 1294
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 8
ER -