Multimodality imaging approach to left ventricular dysfunction in diabetes: an expert consensus document from the European Association of Cardiovascular Imaging.

peer reviewedHeart failure (HF) is among the most important and frequent complications of diabetes mellitus (DM). The detection of subclinical dysfunction is a marker of HF risk and presents a potential target for reducing incident HF in DM. Left ventricular (LV) dysfunction secondary to DM is heterogeneous, with phenotypes including predominantly systolic, predominantly diastolic, and mixed dysfunction. Indeed, the pathogenesis of HF in this setting is heterogeneous. Effective management of this problem will require detailed phenotyping of the contributions of fibrosis, microcirculatory disturbance, abnormal metabolism, and sympathetic innervation, among other mechanisms. For this reason, an imaging strategy for the detection of HF risk needs to not only detect subclinical LV dysfunction (LVD) but also characterize its pathogenesis. At present, it is possible to identify individuals with DM at increased risk HF, and there is evidence that cardioprotection may be of benefit. However, there is insufficient justification for HF screening, because we need stronger evidence of the links between the detection of LVD, treatment, and improved outcome. This review discusses the options for screening for LVD, the potential means of identifying the underlying mechanisms, and the pathways to treatment

Radiotherapy delivery during motion

This paper discusses the 3D dosimetric consequences of radiotherapy delivery during two kinds of motion, (i) the respiratory motion by the patient and (ii) the motion by the gantry while rotating around the patient. Respiratory motion primarily compromises treatments in the thorax and abdomen regions. Several strategies to reduce respiratory motion effects have been developed or are under development. The organ motion could for instance be measured and incorporated in the treatment planning, or adapted to by using respiratory gating and tumour-tracking delivery techniques. Gantry motion is involved in various forms of intensity-modulated arc-therapy techniques. The purpose is to increase the modulation by simultaneously varying the MLC positions, the rotation speed of the gantry, and the dose rate during the treatment. The advantage of these techniques is the increased possibility to deliver a high absorbed dose to the target volume while minimizing the dose to normal tissues. However, the dosimetric uncertainties associated with motion, small fields and steep dose gradients, has to be evaluated in detail, and this requires adequate true 3D dose-verification tools

Dosimetric verification of breathing adapted radiotherapy using polymer gel

In radiation therapy patient movement caused by respiration can be a major challenge to the ambition to deliver a high absorbed dose to the target volume while minimizing the dose to normal tissues. Large respiratory motion requires increased margins, which implies an increased risk of morbidity from late toxicity. It is therefore important to take respiratory motion into account when treating targets in the thorax region. The aim of this study was to investigate the feasibility of using a 3D gel dosimeter for dose verification of breathing adapted radiotherap

RapidArc™ treatment verification using polymer gel dosimetry

The aim of this study was to verify a novel volumetric arc therapy technique, RapidArc". Polymer gel dosimetry system was used to measure the advanced inhomogeneous 3D dose distribution produced using the technique RapidArc". A preclinical installation of the novel beam delivery approach was set up on a linear accelerator at Rigshospitalet in Copenhagen. A prostate treatment plan was delivered to a 1.3 l nPAG gel phantom using one single arc rotation from 200 to 160 degrees, and a target dose of 3.3 Gy. Magnetic resonance imaging of the gel was carried out using the 1.5 T scanner and MATLAB was used for image processing and 3D rendering. The difference in relative absorbed dose between the treatment planning system (TPS) and gel measurement was calculated voxel by voxel within the 80% and the 95% isodose volume, respectively. Measurements agreed well with the TPS within the treated volume. Within both isodose volumes 90% of the voxels showed a deviation less or equal to 5%. This study shows that the 3D gel dosimetry system is a useful tool for dose verification of advanced treatment delivery techniques

Feasibility study using MRI and two optical CT scanners for readout of polymer gel and Presage (TM)

The aim of this study was to compare the conventional combination of three-dimensional dosimeter (nPAG gel) and readout method (MRI) with other combinations of three-dimensional dosimeters (nPAG gel/Presage (TM)) and readout methods (optical CT scanners). In the first experiment, the dose readout of a gel irradiated with a four field-box technique was performed with both an Octopus IQ scanner and MRI. It was seen that the MRI readout agreed slightly better to the TPS. In another experiment, a gel and a Presage (TM) sample were irradiated with a VMAT field and read out using MRI and a fast laser scanner, respectively. A comparison between the TPS and the volumes revealed that the MRI/gel readout had closer resemblance to the TPS than the optical CT/Presage (TM) readout. There are clearly potential in the evaluated optical CT scanners, but more time has to be invested in the particular scanning scenario than was possible in this study

Tumor-tracking radiotherapy of moving targets; verification using 3D polymer gel, 2D ion-chamber array and biplanar diode array

The aim of this study was to carry out a dosimetric verification of a dynamic multileaf collimator (DMLC)-based tumor-tracking delivery during respiratory-like motion. The advantage of tumor-tracking radiation delivery is the ability to allow a tighter margin around the target by continuously following and adapting the dose delivery to its motion. However, there are geometric and dosimetric uncertainties associated with beam delivery system constraints and output variations, and several investigations have to be accomplished before a clinical integration of this tracking technique. Two types of delivery were investigated in this study I) a single beam perpendicular to a target with a one dimensional motion parallel to the MLC moving direction, and II) an intensity modulated arc delivery (RapidArc®) with a target motion diagonal to the MLC moving direction. The feasibility study (I) was made using an 2D ionisation chamber array and a true 3D polymer gel. The arc delivery (II) was verified using polymer gel and a biplanar diode array. Good agreement in absorbed dose was found between delivery to a static target and to a moving target with DMLC tracking using all three detector systems. However, due to the limited spatial resolution of the 2D array a detailed comparison was not possible. The RapidArc® plan delivery was successfully verified using the biplanar diode array and true 3D polymer gel, and both detector systems could verify that the DMLC-based tumor-tracking delivery system has a very good ability to account for respiratory target motion

MAGIC-type polymer gel for three-dimensional dosimetry: intensity-modulated radiation therapy verification.

A new type of polymer gel dosimeter, which responds well to absorbed dose even when manufactured in the presence of normal levels of oxygen, was recently described by Fong et al. [Phys. Med. Biol. 46, 3105-3113 (2001)] and referred to by the acronym MAGIC. The aim of this study was to investigate the feasibility of using this new type of gel for intensity-modulated radiation therapy (IMRT) verification. Gel manufacturing was carried out in room atmosphere under normal levels of oxygen. IMRT inverse treatment planning was performed using the Helios software. The gel was irradiated using a linear accelerator equipped with a dynamic multileaf collimator, and intensity modulation was achieved using sliding window technique. The response to absorbed dose was evaluated using magnetic resonance imaging. Measured and calculated dose distributions were compared with regard to in-plane isodoses and dose volume histograms. In addition, the spatial and dosimetric accuracy was evaluated using the gamma formalism. Good agreement between calculated and measured data was obtained. In the isocenter plane, the 70% and 90% isodoses acquired using the different methods are mostly within 2 mm, with up to 3 mm disagreement at isolated points. For the planning target volume (PTV), the calculated mean relative dose was 96.8 +/- 2.5% (1 SD) and the measured relative mean dose was 98.6 +/- 2.2%. Corresponding data for an organ at risk was 34.4 +/- 0.9% and 32.7 +/- 0.7%, respectively. The gamma criterion (3 mm spatial/3% dose deviation) was fulfilled for 94% of the pixels in the target region. Discrepancies were found in hot spots the upper and lower parts of the PTV, where the measured dose was up to 11% higher than calculated. This was attributed to sub optimal scatter kernels used in the treatment planning system dose calculations. Our results indicate great potential for IMRT verification using MAGIC-type polymer gel