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Consideration of the feasibility of cash as an alternative modality relies on local-level assessment of capacity, resources, political environment, beneficiary needs and preferences, and lessons learned from previous programs in those areas.
This modality relies on the detection of paramagnetic deoxyhemoglobin within red blood cells, and does not require administration of exogenous tracers.
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Most trauma centers that use FAST as a primary screening modality rely on the assumption that any missed injuries are low-grade lesions without serious clinical consequence [ 24, 25].
Consideration of the feasibility of cash as an alternative to other modalities relies on local-level assessment of capacity, available resources, political environment, beneficiary needs and preferences, and lessons learned from previous programs in those areas.
In the case of X-ray energies used in clinical mammography, phase-contrast and dark-field imaging are capable of overcoming these limitations as image formation in these modalities relies on the intrinsically enhanced electron density contrast and small-angle scattering capability of the tissue, respectively [ 8– 10].
While these modalities rely on sensors and devices situated in the environment, there is a need for new modalities that enhance the mobile experience.
However, both modalities rely on size-related and morphological criteria to differentiate between benign and malignant lymph nodes, decreasing the sensitivity for detection of small metastases.
Current cross-sectional imaging modalities rely on insensitive size and morphologic criteria and, thus, lack the desired accuracy for characterizing lymph nodes [ 26].
As current imaging modalities rely on detection of increased hepatic arterial supply, it is not difficult to see how well-differentiated HCC or high-grade dysplastic nodules can be misdiagnosed.
Thus, fVII-tPDT as a localised therapy is different in the mechanism of action from Icon immunotherapy, which is a systemic modality and relies on host immune functions through NK cell- and complement-mediated cytotoxicity (Hu and Li, 2010).
With limitations of imaging modalities, targeting largely relies on indirect methods.
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