GET THE APP

Segmenting Multiple Lesions in Medical Images
..

International Journal of Sensor Networks and Data Communications

ISSN: 2090-4886

Open Access

Editorial - (2022) Volume 11, Issue 5

Segmenting Multiple Lesions in Medical Images

Kristin David*
*Correspondence: Kristin David, Department of Architecture DIDA, University of Florence, Italy, Email:
Department of Architecture DIDA, University of Florence, Italy

Received: 12-May-2022, Manuscript No. sndc-22-73316; Editor assigned: 14-May-2022, Pre QC No. P-73316; Reviewed: 19-May-2022, QC No. Q-73316; Revised: 25-May-2022, Manuscript No. R-73316; Published: 30-May-2022 , DOI: 10.37421/2090-4886.2022.11.162
Citation: David, Kristin. “Segmenting Multiple Lesions in Medical Images.” J Sens Netw Data Commun 11 (2022): 162.
Copyright: © 2022 David K. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Editorial

It is an area of study that combines computer science, information engineering, electrical engineering, physics, mathematics, and medicine. In this area, computational and mathematical tools are developed to address issues with medical pictures and their application to clinical treatment and biological research. Data is often given in integral form at each sample point, such as signed and unsigned short (16-bit), though forms ranging from unsigned char (8-bit) to 32-bit float are not unheard of. Depending on the modality, the specific significance of the data at the sample point may vary. For instance, a CT acquisition collects radio density values, while an MRI acquisition may collect T1 or T2-weighted images. Image acquisition with regular time steps may or may not be possible during longitudinal, time-varying acquisitions. Fan-like pictures produced by modalities like curved-array ultrasonography are also frequent and must be processed using various representational and computational strategies.

In long-term investigations, the same subject is frequently pictured. Both the picture analysis and the statistical modelling can take this information into account [1]. In the process of segmenting and analysing individual time points in a longitudinal image, common data, typically from a within-subject template, is used to inform and regularise these procedures. By reducing measurement noise, this regularisation aims to improve statistical power and sensitivity. At the same time, excessive regularisation must be avoided to maintain constant effect sizes [2]. Intense regularisation, for instance, can result in great testretest reliability but reduces the capacity to identify any real adjustments and group differences. A trade-off that maximises noise reduction at the expense of minimal effect size loss frequently needs to be sought after. The introduction of bias during the processing of longitudinal images is another frequent problem. Longitudinal data analysis typically necessitates the use of specialised statistical tools, such as repeated measure ANOVA or the more potent linear mixed effects models. It is also useful to think about how the signal is distributed spatially [3]. The connection between between-subject measures of cortical thickness over time and within a neighbourhood on the cortical surface, for instance, can be utilised to boost statistical power. Additionally, time-toevent analysis, also known as survival analysis, is frequently used to examine longitudinal data and identify key variables. The quantification and fusion of structural or functional information that is accessible at the point and time of picture acquisition has traditionally been a focus of medical image computing.

The underlying anatomical, physical, or physiological processes might be thought of in this manner as being quantitatively sensed. However, there has been an increase in interest in the predictive assessment of disease or therapy progress over the past few years. Consequently, picture-based modelling, whether it is of a biomechanical or physiological type, can broaden the potential of image computation by shifting its focus from a descriptive to a predictive one [4]. Since they offer tools and techniques to photograph, quantify, and combine structural and functional information about the human being in vivo, medical imaging and image computing play an increasingly significant role in this context. The adaptation of general computational models to represent particular themes is one of these two major research fields, opening the door to personalised computational models. Imaging can be used to individually tailor general computational models in three complimentary ways. The evaluation and validation of such models in people and animal models, as well as their translation into the clinical setting with both diagnostic and therapeutic applications, all depend heavily on imaging. In this particular situation, molecular, biological, and pre-clinical imaging provide more information and an improved understanding of the fundamental structure and function of molecules, cells, tissues, and animal models that may, when appropriate, be extrapolated to human physiology. There are many scientific and clinical domains where image-based VPH/Physiome models can be applied [5].

In general, they have the potential to develop into novel virtual imaging methods. Based on the integration of observable but occasionally sparse and inconsistent multimodal pictures and physiological measurements, a greater number of, frequently non-observable, parameters will be effectively imaged in silico. The measurements will be interpreted using computational models in a way that is consistent with the underlying biophysical, biochemical, or biological laws governing the physiological or pathological processes that are the subject of the study. In the end, these investigative tools and systems will improve our comprehension of disease processes, the evolution of diseases naturally, and the impact of pharmacological and/or therapeutic interventions on the course of a disease. Cross-fertilization between imaging and modelling goes beyond the physiologic interpretation of measurements. The development of predictive imaging, which enables the understanding, planning, and optimization of such interventions in silico, is made possible by the combination of image-based patient-specific modelling, models of medical equipment, and models of pharmaceutical therapy.

Conflict of Interest

None.

REFERENCES

  1. AlOthman, Abdulaziz Fahad, Abdul Rahaman Wahab Sait and Thamer Abdullah Alhussain. “Detecting Coronary Artery Disease from Computed Tomography Images Using a Deep Learning Technique” Diagnostics 12 (2022): 2073.
  2. Google Scholar, Crossref       

  3. Albahlal, Abdullah, Hassan Al Dhibi, Sami Al Shahwan and Rajiv Khandekar, et al. “Sympathetic ophthalmia following diode laser cyclophotocoagulation.” Br J Ophthalmol 98 (2014): 1101-1106.
  4. Google Scholar, Crossref, Indexed at

  5. Bertolotto, Michele, Lorenzo E. Derchi, Paul S. Sidhu and Giovanni Serafini, et al. “Acute segmental testicular infarction at contrast-enhanced ultrasound: early features and changes during follow-up.” AJR Am J Roentgenol  4 (2011): 834-841.
  6. Google Scholar, Crossref, Indexed at

  7. Patel, Sarju S., Emilio M. Dodds, Laura V. Echandi and Cristobal A. Couto, et al. “Long- term, drug-free remission of sympathetic ophthalmia with high-dose, short-term chlorambucil therapy.” Ophthalmology 121 (2014): 596-602.
  8. Google Scholar, Crossref, Indexed at

  9. Yang, Tian, Shengfu Chen, Xiaolong He and Huaizu Guo, et al. “How to convincingly measure low concentration samples with optical label-free biosensors.” Sensors Actuators B Chem 306 (2020): 127568.
  10. Google Scholar, Crossref

Google Scholar citation report
Citations: 343

International Journal of Sensor Networks and Data Communications received 343 citations as per Google Scholar report

International Journal of Sensor Networks and Data Communications peer review process verified at publons

Indexed In

 
arrow_upward arrow_upward