FDG-PET/CT for differentiating between aseptic and septic delayed union in the lower extremity
verfasst von:
Kirsten E. van Vliet, Vincent M. de Jong, M. Frank Termaat, Tim Schepers, Berthe L. F. van Eck-Smit, J. Carel Goslings, Niels W. L. Schep
18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET)/computed tomography (CT) has proven to have a high diagnostic accuracy for the detection of bone infections. In patients with delayed union it may be clinically important to differentiate between aseptic and septic delayed union. The aim of this study was to evaluate the efficacy and to assess the optimal diagnostic accuracy of FDG-PET/CT in differentiating between aseptic and septic delayed union in the lower extremity.
Methods
This is a retrospective study of consecutive patients who underwent FDG-PET/CT scanning for suspicion of septic delayed union of the lower extremity. Diagnosis of aseptic delayed union or septic delayed union was made based on surgical deep cultures following PET/CT scanning and information on clinical follow-up. FDG-uptake values were measured at the fractured site by use of the maximum standardized uptake value (SUVmax). Sensitivity, specificity and diagnostic accuracy of FDG-PET/CT were calculated at various SUVmax cut-off points.
Results
A total of 30 patients were included; 13 patients with aseptic delayed unions and 17 patients with septic delayed unions. Mean SUVmax in aseptic delayed union patients was 3.23 (SD ± 1.21). Mean SUVmax in septic delayed union patients was 4.77 (SD ± 1.87). A cut-off SUVmax set at 4.0 showed sensitivity, specificity and diagnostic accuracy of FDG-PET/CT were 65, 77 and 70% to differentiate between aseptic and septic delayed union, respectively.
Conclusion
Using a semi-quantitative measure (SUVmax) for interpretation of FDG-PET/CT imaging seems to be a promising tool for the discrimination between aseptic and septic delayed union.
Background
Osteomyelitis is an inflammatory process of bone caused by microorganisms. Microorganisms such as Staphylococcus aureus (30%) and coagulase-negative staphylococci (22%) are the most common pathogens found in patients with osteomyelitis; however, poly-microbial cultures are found in 29% of the cases [1, 2].
Diagnosis of osteomyelitis remains difficult due to the absence of clear clinical, radiological and laboratory findings [3]. Laboratory parameters, such as CRP and leukocyte count, lack the sensitivity and specificity to diagnose osteomyelitis [4]. Standard follow-up with conventional radiography has a low sensitivity varying from 43 to 75% and specificity from 75 to 83% to detect osteomyelitis. Positive findings on radiographs are reliable, but indicate a late stage of osteomyelitis since abnormalities are not detectable until 50–75% of the bone matrix is destroyed [5, 6]. This lack of diagnostic accuracy requires an alternative diagnostic approach in trauma patients.
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A previously published meta-analysis showed that 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET)/computed tomography (CT) scan showed the highest diagnostic accuracy (sensitivity 96% and specificity 91%) for suspected osteomyelitis, compared with other imaging modalities, such as bone scintigraphy, leucocyte scintigraphy and MRI [7]. Uptake of FDG is a reflection of cellular glucose metabolism and is semi-quantitatively expressed as the standardized uptake value (SUV). Physiological uptake is present in all tissues of the body and thus in bone as well. Increased FDG-uptake occurs in areas with increased glucose consumption due to increased metabolic activity of the tissue involved or due to the invasion of inflammatory cells [8‐10]. Hybrid PET and CT combines detection of metabolic changes with morphologic information and may therefore be helpful in the assessment of post-traumatic osteomyelitis.
However, the clinical problem is to differentiate between delayed union with and without the presence of osteomyelitis, as increased metabolism and morphologic changes probably will be present in both conditions [11, 12]. Considering the fact that osteomyelitis is almost always accompanied by delayed fracture healing, the term ‘septic delayed union’ can be better used for the condition of bone described in this study. We hypothesize that in case of septic delayed union metabolism will be increased to a higher degree than in the case of aseptic delayed union. Therefore the metabolic activity on FDG-PET/CT, the standardized uptake value (SUVmax), was assessed in a cohort of consecutive patients with suspicion of septic delayed union.
The aim of this study was to evaluate the efficacy and to assess the optimal diagnostic accuracy of FDG-PET/CT in differentiating between aseptic and septic delayed union in the lower extremity.
Methods
Patient population
A retrospective study was performed in a cohort of consecutive patients undergoing FDG-PET/CT scanning for the suspicion of septic delayed union. All patients were selected from an electronic database at our academic Level-1 trauma center from the period March 2010 to October 2014. Patients were excluded if they underwent surgery within 3 months to PET/CT, because it is known that FDG-levels will normalize within approximately 3 months after surgery [9, 13].
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Methods
Suspicion of septic delayed union was based on clinical signs, mostly unexplained pain. The diagnosis aseptic or septic delayed union was made based on surgical deep cultures after PET/CT scanning. Aseptic delayed union was defined as two negative deep cultures or a negative clinical follow-up of 1 year. Septic delayed union was defined as at least one positive deep culture out of two samples or a positive clinical follow-up of 1 year. The presence of a sinus tract or pus was diagnosed as septic delayed union (Table 1).
Table 1
Patients’ characteristics
Patient no./sex/age (years)
Fracture site
Culture
Final diagnosis
1/M/29
Tibia
Negative
Aseptic delayed union
2/M/47
Tibia
Positive
Septic delayed union
3/M/63
Tibia
No culture
Aseptic delayed union
4/F/51
Tibia
Positive
Septic delayed union
5/F/74
Calcaneus
Positive
Septic delayed union
6/M/51
Calcaneus
Positive
Septic delayed union
7/M/25
Femur
Positive
Septic delayed union
8/F/34
Tibia
Negative
Aseptic delayed union
9/F/23
Femur
No culture
Aseptic delayed union
10/M/18
Tibia
Positive
Septic delayed union
11/F/30
Calcaneus
Negative
Aseptic delayed union
12/F/73
Tibia
No culture
Aseptic delayed union
13/M/47
Calcaneus
Negative
Aseptic delayed union
14/M/31
Tibia
No culture
Septic delayed union
15/M/39
Tibia
No culture
Aseptic delayed union
16/M/42
Tibia
Negative
Aseptic delayed union
17/F/64
Calcaneus
Positive
Septic delayed union
18/M/33
Tibia
Negative
Aseptic delayed union
19/M/57
Tibia
Positive
Septic delayed union
20/M/47
Tibia
No culture
Septic delayed union
21/M/60
Tibia
Positive
Septic delayed union
22/M/68
Tibia
Positive
Septic delayed union
23/M/70
Tibia
No culture
Septic delayed union
24/M/49
Tibia
Negative
Aseptic delayed union
25/F/56
Calcaneus
Positive
Septic delayed union
26/M/41
Tibia
Positive
Septic delayed union
27/F/39
Tibia
Negative
Aseptic delayed union
28/M/25
Femur
Positive
Septic delayed union
29/M39
Femur
Positive
Septic delayed union
30/M/55
Tibia
Negative
Aseptic delayed union
For the assessment of FDG-uptake in the bone we used the maximum standardized uptake value (SUVmax), which is a semi-quantitative measure for FDG-uptake. The region of interest (ROI) was determined by identifying the affected region on CT. SUVmax in this region was determined on the transaxial PET images using Hermes Hybrid PDR v 1.4B (HERMES Medical Solutions AB, Stockholm, Sweden). FDG-uptake values in normal contralateral bone were measured as well. The ROI was drawn on transaxial CT images around the cortex and superimposed on the corresponding PET image were SUVmax was calculated. The normal contralateral bone was used as a reference. In patients with bilateral fractures, comparisons with the contralateral site were omitted.
For the efficacy of FDG-PET/CT to differentiate between aseptic and septic delayed union, we calculated the sensitivity, specificity and diagnostic accuracy at various SUVmax cut-off points.
PET/CT scanning
Each patient underwent 18F-FDG-PET-CT on a Philips Gemini-16 TOF PET-CT scanner (Philips Healthcare, Eindhoven, The Netherlands). Based on BMI a dose of 180-400 MBq18F-FDG was administered intravenously. Before administration of the radio-tracer patients fasted for at least 6 h and serum glucose level was checked to be < 10 mmol/l. Patients had bed rest from 15 min before till 30 min after administration of FDG in a room of at least 23 °C. FDG-PET-CT imaging started 60 min ± 10 min post injection.
Images were acquired with a low-dose PET-CT protocol (CT: 120 kV, 60mAs, 16 × 1.5 collimation, 0.813 pitch; PET: 2 min/bed position) and reconstructed with standard Philips time-of-flight reconstruction software (3D LOR OSEM).
Transverse, coronal and sagittal image reconstructions were performed with and without attenuation correction.
Statistical analysis
The statistical analysis was performed using SPSS, v.20 (SPSS for windows, version 20; SPSS®Inc., Chicago, Illinois, USA). Normality of continuous data was tested with the Shapiro–Wilk and Kolmogorov–Smirnov test and by inspecting the frequency distributions (histograms). Homogeneity of variance was tested using the Levene’s test.
Descriptive analysis was performed to assess baseline characteristics, medians and percentiles (non-parametric data) and means and standard deviations (parametric data) were calculated. Differences were assessed using the Student’s T test (parametric data) or the Mann–Whitney U test (non-parametric data). Categorical data were compared using the Chi-square test. P value < 0.05 was taken as the threshold of statistical significance.
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Sensitivity, specificity and diagnostic accuracy to differentiate between septic delayed union and aseptic delayed union were calculated for different SUVmax uptake values. The accuracy of PET/CT for diagnosing septic delayed union at various SUVmax cut-off points were plotted in a receiver operating characteristic (ROC) curve, in which the test characteristics of sensitivity and specificity were calculated to discriminate between aseptic and septic delayed union.
Results
Thirty patients were included, 21 men and 9 women with a mean age of 46 years (range 18–74); 4 patients had a femur fracture, 20 patients a tibial fracture, and 6 patients a calcaneal fracture. Final diagnosis demonstrated a total of 13 aseptic delayed unions and 17 septic delayed unions (Fig. 1; Table 2). Two patients had bilateral fractures. Of 28 patients, contralateral normal bones were measured as well.
Fig. 1
Flowchart of methods: all patients were divided into aseptic or septic delayed union based on surgical deep cultures or clinical follow-up
Table 2
Summary of patients’ characteristics and SUVmax
Patients’ characteristics and SUVmax
No. of patients
30
Sex (M/F)
21/9
Mean age (years)
46 (range 18–74)
Aseptic delayed union
Septic delayed union
No. of fractures
13
17
Location of fracture:
Femur
1
3
Tibia
10
10
Calcaneus
2
4
SUVmax:
Mean
3.23
4.77
P value
SD
1.21
1.87
0.016
×
Fourteen patients in the septic delayed union group had positive perioperative culture. Bacteria found in the bacteriological cultures were mostly anaerobic bacteria, such as Enterococcus, Escherichia, Fusobacterium and Clostridium and Staphylococcus bacteria or a combination of these bacteria.
Standardized uptake values
Aseptic delayed union patients had a mean of SUVmax 3.23 (SD ± 1.21). Septic delayed union patients had a mean of SUVmax 4.77 (SD ± 1.87). SUVmax in aseptic delayed union was significantly lower compared to septic delayed union (P value 0.016). Contralateral normal unaffected bones had a mean of SUVmax 0.76 (SD ± 0.26).
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The efficacy of FDG-PET/CT to discriminate between aseptic and septic delayed union at various SUVmax cut-off points were plotted into a ROC curve (Fig. 2). Sensitivity, specificity and diagnostic accuracy of FDG-PET/CT were 0.65, 0.77 and 70.0, respectively and an AUC of 0.747, with a cut-off SUVmax set at 4.0 (Table 3).
Fig. 2
The efficacy of FDG-PET/CT to discriminate between aseptic and septic delayed union at various SUVmax cut-off points. Lines cross approximately at SUVmax 4.0 which corresponds with a sensitivity of 65% and specificity of 77%
Table 3
Efficacy of FDG-PET/CT to differentiate between aseptic and septic delayed union at SUVmax cut-off points
SUVmax cut-off
Septic delayed union (n = 17)
Aseptic delayed union (n = 13)
True positive
True negative
False positive
False negative
Sensitivity
Specificity
Diagnostic accuracy
> 3.0
13
5
8
4
0.76
0.38
0.60
> 4.0
11
10
3
6
0.65
0.77
0.70
> 5.0
5
12
1
12
0.29
0.92
0.57
×
Discussion
This retrospective study showed that aseptic delayed union is characterized by a lower metabolic activity than septic delayed union. Integrating this metabolic activity, expressed as SUVmax in the interpretation of the images helps in the differentiation of both conditions. In this study of 30 delayed union fractures, 13 aseptic delayed unions had a mean SUVmax of 3.23 and 17 septic delayed unions had a mean SUVmax of 4.77, which is a significant difference (P value 0.016). Normal contralateral bones had a mean SUVmax of 0.76.
For the use of the FDG-PET/CT scan as a diagnostic tool, it is essential to weight the importance of discriminating and excluding septic delayed union from aseptic delayed union in trauma patients. Higher sensitivity may lead to unnecessary surgery, while higher specificity could cause undertreatment of septic delayed union. A cut-off SUVmax set at 4.0 indicates an approximately equal and acceptable sensitivity and specificity of 65 and 77%, respectively. SUVmax set at 3.0 indicates a good sensitivity of 76%, but simultaneously gains at the expanse of the specificity reducing to 38%. Higher SUVmax of 5.0 has an excellent specificity of 92%, but has a very poor sensitivity of 29% in contrast. Therefore, in our opinion a SUVmax set at 4.0 is the best cut-off point for the use of this diagnostic tool.
To understand the process of FDG-uptake in case of abnormal bone healing, one should take into account the dynamics of normal bones and uncomplicated fracture healing expressed by FDG-uptake. In our first study, we therefore determined the FDG uptake in normal bones. We concluded that normal FDG uptake of the long bones of the lower extremity have a SUVmean < 0.5 and a SUVmax < 0.8 [14]. Two studies have described the patterns of physiological FDG-uptake in bones during uncomplicated fracture healing. Zhuang et al. demonstrated in 37 patients that FDG-uptake may be normal within 12 weeks following fracture [15]. Shon et al. reported a study of four patients with uncomplicated fracture healing that FDG-uptake normalized within 8 weeks [16]. These two studies confirm that FDG-uptake of physiological bone healing will normalize in time based on visual assessment of the PET image. Unfortunately, no studies have been published defining the FDG-uptake pattern, let alone SUV measures, in the process of complicated fracture healing. In the setting of complicated fracture healing such as aseptic delayed fracture healing and septic delayed union, reasons for increased metabolism results into poor differentiation between the origin of increased FDG-uptake. In our study we included patients with delayed fracture healing to differentiate septic delayed union from aseptic delayed union.
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Some discrepancies were found in the rates of diagnostic accuracy parameters between this study and previous studies. Schiesser et al. described a sensitivity, specificity and diagnostic accuracy of 100, 87.5 and 95% respectively for detection of osteomyelitis. This study included soft tissue infections as well, which could explain the higher diagnostic accuracy. Noteworthy, one of the false-positive cases described in this study turned out to be a delayed union [17]. Winter et al. found a sensitivity, specificity and diagnostic accuracy of 100, 86 and 93% respectively for detection of osteomyelitis in the peripheral skeleton. Two of four false positive findings were related to recent surgery within the previous 6 months [13].
Hartmann et al. used visual assessment and found a sensitivity, specificity and diagnostic accuracy of 100, 85 and 91% respectively for detection of osteomyelitis in the peripheral skeleton. FDG-uptake was expressed into intensity of greyscale and was graded into a five-point scale [18]. Wenter et al. also used visual assessment in addition to SUV measurements and found a sensitivity, specificity and diagnostic accuracy of 85, 86 and 86% respectively [19]. In our opinion, the visual scoring of FDG-uptake is less objective than the use of SUVs and may be more sensitive to inter- and even intraobserver differences. Therefore we call for an unbiased predictive SUV cut-off point to differentiate between normal bone uptake, uncomplicated fracture healing, aseptic delayed union and septic delayed union.
Guhlmann et al. did use SUV measurements for FDG-uptake for diagnosing osteomyelitis. This study found a very high sensitivity, specificity and diagnostic accuracy; 100, 92 and 97%. The high diagnostic accuracy found in this study can be explained by the long follow-up of patients in whom ongoing bone healing can be excluded and the risk for more fulminant osteomyelitis increases. Mean SUV found in peripheral fractures with osteomyelitis was 3.6 (SD 2.0), which approaches the SUV found in our study; SUVmax 4.77 [20]. However, it is not consistent to compare these results with our results, because it is unclear if they used SUVmean of SUVmax to calculate the FDG-uptake.
Overall it can be stated that in previous studies a higher diagnostic accuracy of FDG-PET/CT for detecting osteomyelitis has been found compared to our diagnostic accuracy for detecting septic delayed union. This can be explained by differences in patient population and the different methods to quantify FDG-uptake.
Our data demonstrate that FDG-PET/CT is able to differentiate between aseptic and septic delayed union in the lower extremities in trauma patients by using the cut-off SUVmax set at 4.0. These findings broaden the domain in which FDG-PET/CT can provide additional information for guiding surgical therapy into an earlier and clinical relevant detection period. Early diagnosis has an obvious advantage for guiding surgical treatment which will lead to reduced morbidity compared to an unrecognized septic delayed union.
A larger prospective cohort study is needed to establish the distribution pattern of FDG-uptake during fracture healing in order to develop a diagnostic window for FDG-PET/CT in septic delayed union after trauma and osteosynthesis.
Limitations and strengths
Drawback of this study is its retrospective design with all its known sources of bias and the small number of patients included due to low prevalence of septic delayed unions. Moreover, we have just one assessment of FDG-uptake in time and therefor nothing can be concluded about the dynamics of the process.
The strength of our study is that there has been limited research about the FDG-uptake in fractures of the lower extremity, while this information could be important in early detection of septic delayed union after post-traumatic treatment to prevent the bone from (irreversible) damage. Another important aspect of the use of an objective measure such as SUV is the reduction of interobserver discrepancies in the assessment of septic delayed union.
Conclusion
Using a semi-quantitative measure (SUVmax) for interpretation of FDG-PET/CT imaging seems to be a promising tool for the discrimination between aseptic and septic delayed union. To use the FDG-PET/CT as a diagnostic tool, larger prospective studies with multiple measurements in the course of fracture healing should be executed.
Compliance with ethical standards
Conflict of interest
All authors mentioned above, declare that they have no conflict of interest.
Funding
There is no funding source.
Ethical approval
Ethical approval and informed consent are not applicable, due to the retrospective study design.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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