Lacrimal scintigraphy BNMS Guidelines.

PURPOSE: The purpose of this guideline is to assist specialists in Nuclear Medicine and Radionuclide Radiology in recommending, performing, interpreting and reporting the results of lacrimal scintigraphy (also known as Dacroscintigraphy). This guideline will assist individual departments to formulate their own local protocols. This does not aim to be prescriptive regarding technical aspects of individual camera acquisitions, which need to be developed in conjunction with the local experts in medical physics. There are numerous radiological techniques to assess the physiology of the lacrimal system. This guideline will describe the application of a drop of radiotracer into each eye and consecutive imaging to demonstrate the level of impaired drainage, with the possibility of quantifying such impairment. This guideline is a recent and updated version of a previously published guideline on the British Nuclear Medicine Society website in 2018 [1].

Transcriptional upregulation of c-MET is associated with invasion and tumor budding in colorectal cancer.

c-MET and its ligand HGF are frequently overexpressed in colorectal cancer (CRC) and increased c-MET levels are found in CRC liver metastases. This study investigated the role of the HGF/c-MET axis in regulating migration/invasion in CRC, using pre-clinical models and clinical samples. Pre-clinically, we found marked upregulation of c-MET at both protein and mRNA levels in several invasive CRC cells. Down-regulation of c-MET using RNAi suppressed migration/invasion of parental and invasive CRC cells. Stimulation of CRC cells with rh-HGF or co-culture with HGF-expressing colonic myofibroblasts, resulted in significant increases in their migratory/invasive capacity. Importantly, HGF-induced c-MET activation promoted rapid downregulation of c-MET protein levels, while the MET transcript remained unaltered. Using RNA in situ hybridization (RNA ISH), we further showed that MET mRNA, but not protein levels, were significantly upregulated in tumor budding foci at the invasive front of a cohort of stage III CRC tumors (p < 0.001). Taken together, we show for the first time that transcriptional upregulation of MET is a key molecular event associated with CRC invasion and tumor budding. This data also indicates that RNA ISH, but not immunohistochemistry, provides a robust methodology to assess MET levels as a potential driving force of CRC tumor invasion and metastasis.

Radionuclide Imaging of Cardiovascular Infection.

Owing to expanding clinical indications, cardiac implantable electronic devices (CIEDs) are being increasingly used. Despite improved surgical techniques and the use of prophylactic antimicrobial therapy, the rate of CIED-related infection is also increasing. Infection is a potentially serious complication, with clinical manifestations ranging from surgical site infection and local symptoms in the region of the generator pocket to fulminant endocarditis. The utility of radionuclide imaging as a stand-alone noninvasive diagnostic imaging test in patients with suspected endocarditis has been less frequently examined. This article summarizes the recent advances in radionuclide imaging for evaluation of patients with suspected cardiovascular infections.

The assessment of time-of-flight on image quality and quantification with reduced administered activity and scan times in 18F-FDG PET.

OBJECTIVES: The last decade has seen considerable technological innovations in PET detectors with the availability, among other advances, of time-of-flight (TOF). TOF has been shown to increase the signal-to-noise ratio (SNR), which should allow for a reduction in acquired counts while maintaining image quality. METHODS: Fifty-eight patients referred for routine F-flurodeoxyglucose ((18)F-FDG) oncology PET studies were included in this study. Patients with weight below or above 100 kg were prescribed 350 or 400 MBq of (18)F-FDG, respectively. Listmode data were acquired for 2.5 min per bed position and reconstructed with ordered-subset expectation maximization (OSEM) reconstruction. TOF reconstruction was performed on reduced-count data, with two levels of reduction (-20 and -40% for patients <100 kg and -16 and -30% for patients >100 kg) achieved by clipping the listmode data. Liver SNR, mediastinum mean standardized uptake value (SUV(mean)), and lesion maximum standardized uptake value (SUV(max)) were measured in all images. All images were visually assessed as adequate or suboptimal. RESULTS: No significant difference was seen in mediastinum SUV(mean) or lesion SUV(max) when comparing reduced-count TOF with full-count OSEM images. Compared with the original OSEM images, liver SNR was higher for TOF images using the more conservative -20% reduction of counts (P < 0.001, Wilcoxon's signed-rank test), whereas no significant statistical difference was seen with -40% reductions. CONCLUSION: Incorporation of TOF allows for a reduction in acquired counts; this method has been implemented at our institution, with administered activity reduced for all patients to 280 MBq and a reduction in scan times for all but the largest patients. This has significantly reduced the patient radiation dose and improved scanner flexibility and throughput.

Unilateral adrenal metastasis from non­small-cell lung cancer demonstrating very high FDG uptake with a standardized uptake value in excess of sixty.

We report the case of a 52-year-old man who presented with a 2-week history of dyspnea and wheeze. CT scan of the chest showed a large soft-tissue lesion in the right main bronchus extending into the trachea. Pathologic examination of endoscopic tracheal biopsies showed features consistent with a non­small-cell lung carcinoma. 18F-FDG PET/CT showed very high uptake of FDG in the bronchial tumor (high standardized uptake values: 25.1) and unexpected very intense uptake in the left adrenal gland (high standardized uptake values: 62.5). Laparoscopic adrenalectomy was performed, and subsequent histopathological examination confirmed metastatic non­small-cell carcinoma in the adrenal gland. Although adrenal malignancies are generally metabolically active, such high uptake of FDG within a metastatic lesion has not been reported previously.

Reduced-count myocardial perfusion SPECT with resolution recovery.

AIM: The aim of this study was to determine whether resolution recovery (RR) iterative reconstruction algorithms can consistently produce diagnostic quality myocardial perfusion SPECT images for the patient population routinely scanned in this department. Reduced-count data were compared with full-count data without RR according to our established protocol. The desired outcome would be to implement the software to allow a reduction in the administered activity for routine myocardial SPECT. METHODS: Half-count SPECT data were derived from full-count datasets for 53 stress and rest routine myocardial SPECT scans on a GE Infinia camera. Full-count data were reconstructed using standard non-RR ordered subset expectation maximization reconstruction, whereas half-count data were reconstructed using Evolution RR software. Myocardial functional values, image quality and report outcomes of the full-count and half-count reports were compared. Sequential full-time and half-time myocardial SPECT acquisitions were performed for 15 stress and rest studies on a Siemens c.cam dedicated cardiac camera. Half-count data were reconstructed using Siemens Flash 3D RR. RESULTS: No degradation in image quality was found when comparing full-count and half-count studies from the Infinia. Ten percent of the half-count studies from the c.cam were considered slightly worse than full-count data. Statistically significant differences in some full-count versus half-count functional values were found but the actual mean differences were not considered clinically significant. No difference was found for 44 out of 53 full-count versus half-count reports, a minor difference for seven out of 53 and a significant difference in two cases. CONCLUSION: RR was found to produce diagnostic image quality for nearly all scans, but it was felt that a reduction of 50% from our standard protocol was too great. A proposed reduction of 33% administered activity was considered acceptable to produce consistently adequate diagnostic images for both manufacturers.

Ultra-fast processing of gigapixel Tissue MicroArray images using high performance computing.

BACKGROUND: Tissue MicroArrays (TMAs) are a valuable platform for tissue based translational research and the discovery of tissue biomarkers. The digitised TMA slides or TMA Virtual Slides, are ultra-large digital images, and can contain several hundred samples. The processing of such slides is time-consuming, bottlenecking a potentially high throughput platform. METHODS: A High Performance Computing (HPC) platform for the rapid analysis of TMA virtual slides is presented in this study. Using an HP high performance cluster and a centralised dynamic load balancing approach, the simultaneous analysis of multiple tissue-cores were established. This was evaluated on Non-Small Cell Lung Cancer TMAs for complex analysis of tissue pattern and immunohistochemical positivity. RESULTS: The automated processing of a single TMA virtual slide containing 230 patient samples can be significantly speeded up by a factor of circa 22, bringing the analysis time to one minute. Over 90 TMAs could also be analysed simultaneously, speeding up multiplex biomarker experiments enormously. CONCLUSIONS: The methodologies developed in this paper provide for the first time a genuine high throughput analysis platform for TMA biomarker discovery that will significantly enhance the reliability and speed for biomarker research. This will have widespread implications in translational tissue based research.

Ultra-fast processing of gigapixel Tissue MicroArray images using high performance computing.

BACKGROUND: tissue MicroArrays (TMAs) are a valuable platform for tissue based translational research and the discovery of tissue biomarkers. The digitised TMA slides or TMA Virtual Slides, are ultra-large digital images, and can contain several hundred samples. The processing of such slides is time-consuming, bottlenecking a potentially high throughput platform. METHODS: a High Performance Computing (HPC) platform for the rapid analysis of TMA virtual slides is presented in this study. Using an HP high performance cluster and a centralised dynamic load balancing approach, the simultaneous analysis of multiple tissue-cores were established. This was evaluated on Non-Small Cell Lung Cancer TMAs for complex analysis of tissue pattern and immunohistochemical positivity. RESULTS: the automated processing of a single TMA virtual slide containing 230 patient samples can be significantly speeded up by a factor of circa 22, bringing the analysis time to one minute. Over 90 TMAs could also be analysed simultaneously, speeding up multiplex biomarker experiments enormously. CONCLUSIONS: the methodologies developed in this paper provide for the first time a genuine high throughput analysis platform for TMA biomarker discovery that will significantly enhance the reliability and speed for biomarker research. This will have widespread implications in translational tissue based research.

Zero ventilation: a transient episode.

A 65-year-old man with known ischemic heart disease and previous coronary artery bypass grafts was admitted having been found collapsed in the street. He was a smoker with a history of alcohol abuse. On clinical examination he was unkempt, febrile, hemodynamically stable, and had no systemic deficits. The O2 saturation on air was 99%, with a po2 of 9.2, and pco2 of 4.0. Ventilation perfusion (VQ) scan was performed to rule out a pulmonary embolism. While in the department he was noted to be dyspneic and generally unwell. The perfusion images showed reduced perfusion to both lower zones more marked on the right. The ventilation study was markedly abnormal on the initial views with no ventilation to the right lung. However, the patient had recurrent episodes of cough with expectoration of sputum before the anterior view was imaged, which subsequently demonstrated ventilation defects in the right mid and lower zones. A repeat ventilation sequence was performed which confirmed these findings in all views. Chest x-ray performed prior to the lung scan was normal.