The distribution of patients in groups during CT examination on COVID-19.
\r\n\tAtherosclerosis is a systemic disease. Some 60% of patients with peripheral artery disease will have ischaemic heart disease, and 30% have cerebrovascular disease. Within five years of diagnosis, 10-15% of patients with intermittent claudication will die from cardiovascular disease. Therefore, management begins with the identification and modification of risk factors that are common to peripheral artery disease, heart disease, and stroke. Treatment goals include reducing cardiovascular risk and improving functional capacity. Revascularization is indicated for persistent symptoms.
\r\n\tThe main objective of the book is to deal with peripheral arterial disease in the most diverse aspects. Addressing issues such as pathophysiology, signs and symptoms, clinical aspects, treatment, and prognosis.
\r\n\t
In the coming years, due to the introduction of methods of medical diagnostics and treatment using ionizing radiation, the growth of medical exposure of the Russian population expected to continue, especially due to computed tomography (CT). Therefore, it is important to evaluate radiation dose levels and population radiation risks in the form of a possible oncological pathology among the population in the long term after exposure [1, 2, 3, 4, 5, 6, 7, 8].
Estimating the stochastic effects on the basis of a linear non-threshold model,
Due to the widespread use of CT of the chest organs for the diagnosis of COVID-19, including during repeated examinations, this issue is of particular relevance.
The aim of the study was to assess effective radiation doses for chest CT for the diagnosis of Covid-19 and calculate the radiation risk of the effects of this exposure.
We analyzed the results of 1003 CT examinations of the chest performed in patients with suspected COVID-19 during one week in October 2020 in the city diagnostic center. Among these patients were 6.2% children in the ages of 12–14 years old, 15.3% adolescents in the ages of 15–19 years old, 60.1% adults in the ages of 20–64 years old, and 18.4% older persons of ages 65 years and older. The average ages and confidence intervals (p ≤ 0,05) were 13.8 ± 0.20 years old in group 1 (children), 17.1 ± 0.41 years old in group 2 (adolescents); 45.8 ± 1.47 years old in group 3 (adults) (of which 41.8% are of ages 20–45 years old and 58.2% are of ages 46–64 years old); 69.4 ± 1.79 years old in group 4 (older persons). The percentage number of male (female) persons in the groups are 51.6% (48.4%) in group 1, 52.3% (47.7%) in group 2, 46.3% (53.7%) in group 3, 47% (53%) in group 4. The proportion of patients with CT signs of pneumonia and without pathological signs amounted to a total of 54,6% and 45,4%, respectively, for each of the four age groups. The distribution of the patients into groups during CT examination is given in Table 1.
Groups | Age (ears) | Subgroups by patient sex | Number of patients | Proportion of patients with CT signs pneumonia, % | Proportion of patients without CT signs of pathology, % |
---|---|---|---|---|---|
1 | Children (12–14) | 1.1. Men | 32 | 15.6 | 84.4 |
1.2. Women | 30 | 13.3 | 86.7 | ||
1. Total | 62 | 14.5 | 85.5 | ||
2 | Adolescents (15–19) | 2.1. Men | 80 | 26.3 | 73.7 |
2.2. Women | 73 | 21.9 | 78.1 | ||
2. Total | 153 | 24.2 | 75.8 | ||
3 | Adults (20–64) | 3.1. Men | 279 | 55.6 | 44.4 |
3.2. Women | 324 | 71.0 | 29.0 | ||
3. Total | 603 | 63.8 | 36.2 | ||
4 | Older people (65 and older) | 4.1. Men | 87 | 77.0 | 23.0 |
4.2. Women | 98 | 51.0 | 49.0 | ||
4. Total | 85 | 63.2 | 36.8 | ||
Total Sample | 1003 | 54.6 | 45.4 |
The distribution of patients in groups during CT examination on COVID-19.
CT studies of the chest were performed on a Siemens Somatom Emotion 16 scanner (16-slice) using a standard algorithm. The voltage on the tube was 130 kV with automatic modulation of the amperage; the slice thickness was 0.8 mm (pitch 1.4) or 1.5 mm (pitch 1.2). Of each patient, the values of the parameters determining the radiation load were entered into the database CTDIvol (mGy), DLP (mGy*cm) and ED, mSv.
The calculation of the effective dose (ED, mSv) for a single phase CT scan was performed according to the following equation.
The CTDIvol values were entered into the database from the CT scanner console. Then, the DLP was calculated by the formula:
The procedure for registering the indicator “irradiated length (cm)” was as follows. Previously, the X-ray technician performed an X-ray (tomogram) of the chest. Then the region of interest (ROI) was installed on the CT scanner console in accordance with the Recommendations of EUR16262, 1999 [10]: Volume of investigation (routine chest) - from lung apex to the base of the lungs. The length of this area (irradiated length) was measured individually in each patient. In this area, a CT scan was subsequently performed and, accordingly, the patient was irradiated. DLP was calculated for this zone.
In our study, for the chest the “irradiated length” (Median, 25th and 75th percentile) was (cm): 31.3 (30.1–33.4) - in children, 34.7 (32.6–36.6) - in adolescents, 36.6 (34.9–38.7) - in adults, 33.3 (31.6–36.8) – for persons 65 years and older.
Then, using the DLP, the effective doses was estimated according to the formula [11]:
To calculate the effective dose (ED, mSv) the chest KED DLP conversion factor (mSv*mGy−1 *cm−1) used was KED DLP = 0.012 for both the children group (12–14 years old) and the adolescent group (15–19 years old) and KED DLP = 0.016 for the subjects older than 19 years [12, 13].
The method of calculating the risk of radiation consequences is based on the analysis of the frequency of leukemia and other oncological diseases, hereditary disorders in subsequent generations in the population after irradiation of people during the atomic explosions in Hiroshima and Nagasaki, the Marshall Islands, after gamma irradiation of patients with cancer and after incidents and accidents at nuclear reactors. Several hundred publications with this information were summarized in ICRP Publication 103, 2007 [11], and the risks of these consequences in persons of different genders and ages were calculated depending on the radiation dose received. In our study, calculations of radiation risk are carried out according to the National Methodological Recommendations [14] as follows:
where
R is the radiation risk per 100,000 population at an exposure dose of ED, mSv;
ED - effective dose, mSv;
r - risk indicator for exposure of 1 mSv (mSv−1).
A risk indicator for exposure of 1 mSv used, lifetime cancer risk of radiation is 5.5 * 10−5 mSv−1 for the entire population regardless of age and sex. However, in this study r (risk indicator) were used, taking into account the age and sex of patients (Table 2) in accordance with the National Methodological Recommendations [14]. These values were calculated for the Russian population (mortality and morbidity data for 2008) using risk models and ICRP calculation methods [11, 15]. When calculating Radiation risk level, the scales listed in Table 3 were used.
Age, years | Man | Woman | Age, years | Man | Woman |
---|---|---|---|---|---|
0–4 | 5,6*10−5 | 2,2*10−4 | 45–49 | 2,9*10−5 | 4,9*10−5 |
5–9 | 5,0*10−5 | 1,8*10−4 | 50–54 | 2,6*10−5 | 4,1*10−5 |
10–14 | 4,6*10−5 | 1,4*10−4 | 55–59 | 2,1*10−5 | 3,4*10−5 |
15–19 | 4,4*10−5 | 1,0*10−4 | 60–64 | 1,7*10−5 | 2,7*10−5 |
20–24 | 4,0*10−5 | 8,1*10−5 | 65–69 | 1,3*10−5 | 2,0*10−5 |
25–29 | 3,8*10−5 | 7,1*10−5 | 70–74 | 9,5*10−6 | 1,3*10−5 |
30–34 | 3,6*10−5 | 6,3*10−5 | 75–79 | 6,4*10−6 | 7,9*10−6 |
35–39 | 3,4*10−5 | 5,6*10−5 | 80–84 | 4,3*10−6 | 4,6*10−6 |
40–44 | 3,3*10−5 | 5,7*10−5 | 85+ | 2,1*10−6 | 1,3*10−6 |
Lifetime risk of death ratios, taking into account harm from reduced quality of life, calculated [14] per 1 mSv effective dose for medical diagnostic chest irradiation.
Radiation risk levels | Radiation risk | |
---|---|---|
Values | Values per 100,000 people | |
NEGLIGIBLE | <10−6 (less than 1 case per 1,000,000 people) | < 0.1 |
MINIMUM | 10−6–10−5 (1 to 10 cases per 1,000,000 people) | 0.1–1 |
VERY LOW | 10−5–10−4 (1 to 10 cases per 100,000 people) | 1–10 |
LOW | 10−4–10−3 (1 to 10 cases per 10,000 people) | 10–100 |
MODERATE | 10−3–3*10−3 (1 to 3 cases per 1,000 people) | 100–300 |
The radiation risk levels (individual lifetime risk) to a patient’s health associated with medical exposure during diagnostic studies or treatment procedures [14].
The mean and median values of effective doses in the formed groups were close, the assessment of the data according to Kolmogorov–Smirnov test for normality and Shapiro–Wilk’s W test showed that the nature of their distribution is close to normal. The measured data were expressed as the average ± confidence interval (X ± CI) at p ≤ 0.05, as well as median (Me, 25th and 75th percentile). The significance of differences between the groups according to Student t-criterion, P value<0.05 was considered for statistical significance. STATISTICA statistical software (version 10.0; Stat Soft. Inc., United States) was used for analysis.
The average effective doses to patients with a single CT scan in the formed groups as illustrated in Table 4 and Figure 1A were 2.59 ± 0.19 mSv in group 1 (children 12–14 years old), 3.23 ± 0.17 mSv in group 2 (adolescents 15–19 years old), 3.43 ± 0.08 mSv in group 3 (adults 19–64 years old) and 3.28 ± 0.19 mSv in group 4 (older persons – 65 years and older).
Groups | Age (years) | Subgroups by sex | ED, Me (25th; 75th percentile), mSv* | ED, X ± CI, mSv* | Radiation risk | |||
---|---|---|---|---|---|---|---|---|
Cases, per 100,000 people | Level | |||||||
Calculating | Values | Criteria interval | ||||||
1 | Children (12–14) | Men | 2.65 (2.45; 2.96) | 2.92 ± 0.30 | ED*4.6 | 13.4 | 10–100 | LOW |
Women | 2.17 (1.88; 2.46) | 2.23 ± 0.16 | ED*14.0* | 31.2 | 10–100 | LOW | ||
Total | 2.46 (2.13; 2.70) | 2.59 ± 0.19 | ED*9.3* | 24.1 | 10–100 | LOW | ||
2 | Adolescents (15–19) | Men | 3.38 (3.01; 3.88) | 3.50 ± 0.23 | ED*4.4 | 15.4 | 10–100 | LOW |
Women | 2.51 (2.37; 3.15) | 2.93 ± 0.23 | ED*10.0 | 29.3 | 10–100 | LOW | ||
Total | 3.13 (2.37; 3.60) | 3.23 ± 0.17 | ED*7.2 | 23.3 | 10–100 | LOW | ||
3 | Adults (20–64) | Men | 3.69 (3.05; 4.10) | 3.61 ± 0.08 | ED*3.1 | 11.2 | 10–100 | LOW |
Women | 3.27 (2.42; 3.77) | 3.28 ± 0.13 | ED*5.3 | 17.4 | 10–100 | LOW | ||
Total | 3.39 (2.72; 3.93) | 3.43 ± 0.081,2 | ED*4.2 | 14.4 | 10–100 | LOW | ||
4 | Older people (65 and older) | Men | 3.15 (2.57; 3.90) | 3.30 ± 0.23 | ED*0.7 | 2.3 | 1–10 | VERY LOW |
Women | 3.26 (2.05; 4.20) | 3.26 ± 0.30 | ED*0.9 | 2.9 | 1–10 | VERY LOW | ||
Total | 3.21 (2.51; 3.90) | 3.28 ± 0.193,4 | ED*0.8 | 2.6 | 1–10 | VERY LOW |
Effective doses and their compliance with radiation risk levels in patient groups with a single CT scan of the chest on COVID-19.
Significance of differences mean values ED (X) between groups (p ≤ 0,05) 11 and 3, 22 and 3, 31 and 4, 42 and 4.
Average doses, mSv (A), and radiation risk values by age groups of patients (B) with a single, double and triple computed tomography of the chest. On the ordinate axis: (A) – average effective dose and confidence intervals (p ≤ 0.05), mSv; (B) – values of radiation risk per 100,000 people; on the abscissa: age groups. Legend: number of CT scans of the patient,
These doses are comparable with the ED values shown in the report [16] on the evaluation of DRLs for adult CT in European countries and in studies of other authors [17, 18, 19]. The DRLs for CT of adult chest organs in European countries were: 4.7–6.31 mSv in Netherlands [11, 14], 5.1–5.95 mSv in Germany [16, 18], 6.8 mSv in Austria [16], 5.95–10.4 mSv in Great Britain [16, 19], 7.31 mSv in Finland [16], 8.5–10.5 in Denmark [16], as well as 7.65 mSv in Australia [20].
In our earlier study [21], with standard protocols on different CT scanners, the values of the ED were in the ranges of 2.4–6.04 mSv and 8.4–15.33 mSv, for a single-phase and multiphase with contrast CTs, respectively. The use of low-dose protocols (tube voltage from 80 to 100 kV with automatic modulation of current) made it possible to reduce the ED to 1.6 mSv, when applying the iterative reconstruction algorithm MBIR for single-phase CTs and to 4.41 mSv when applying the iterative reconstruction algorithm ASIR for multiphase CTs [22].
Based on the risk indicator value for exposure of 1 mSv with age and sex (Table 3) were calculations radiation risk values and radiation risk levels after chest CT radiation per 100,000 exposed persons (Table 4). The maximum radiation risk values for a single CT were observed (Figure 1B) in groups of children (24.1*10−5) and adolescents (23.3*10−5). As can be seen in Figure 2B, the radiation risk values for a single CT were 31.2*10−5 in women children (12–14 years old) and 29.3*10−5 in women adolescents (15–19 years old), which exceeds the risk values for men in these groups by 2.3 and 1.9 times, respectively. For the group of adult patients the average risk was 14.4*10−5, (11.2*10−5) in men and 17.4*10−5 in women, which is 1.6 times higher than in men. Nevertheless, all these risk values are in the range of 10*10−5–100*10−5, which corresponds to the level LOW. For the group of older age patients, the radiation risk was 2.6*10−5, which corresponds to the leval rang of 1*10−5–10*10−5, VERY LOW.
Average doses for a single CT scan (A), radiation risk values for a single (B), twice repeated (C) and triple (D) CT, distribution by levels of radiation risk by age groups and depending on the sex of patients. On the ordinate axis: (A) – average effective dose and confidence intervals (p ≤ 0.05), mSv; (B–D) – values of radiation risk per 100,000 people; on the abscissa axis: age groups. Legend:
We have compared the calculations with estimates of radiation risks in other studies.
For example, when planning the limits of exposure of astronauts [23], the risk of oncological diseases and genetic effects are rather low: 0.2*10−6 for leukemia, 0.2*10−6 for other types of malignant neoplasms, and 0.05*10−6 for genetic effects, per year per dose of additional irradiation of 1 mSv. Spontaneous incidence are 50*10−6 for leukemia, 1000–2000*10−6 for other types of malignant neoplasms and 8000*10−6 for genetic effects per year.
In publication 103 of the ICRP [11], new views of the ICRP on the principles and approaches to ensuring radiation safety, are formulated in comparison with the previous document - Publication 60 of the ICRP [15]. Epidemiological data obtained since the publication of Publication 60 of the ICRP served as a reason for revising the values of the nominal risk factors per unit dose for radiogenic cancers and hereditary effects (Table 5).
Irradiated population | Malignant neoplasms | Hereditary effects | Total | |||
---|---|---|---|---|---|---|
Publ. 103 | Publ. 60 | Publ. 103 | Publ. 60 | Publ. 103 | Publ. 60 | |
Whole population | 5.5 | 6.0 | 0.2 | 1.3 | 6.0 | 7.3 |
Adults | 4.1 | 4.8 | 0.1 | 0.8 | 4.0 | 5.6 |
Children | 6.9 | 7.2 | 0.3 | 1.8 | 8.0 | 9.0 |
KAdults/ Children | 1.68 | 1.5 | 3.0 | 2.25 | 2.0 | 1.61 |
As we can see, the new risk values in Publication 103 are slightly lower as those specified in Publication 60. But, at the same time, for children compared with adults, they were increased in terms of Malignant neoplasms from 1.5 to 1.68, for hereditary defects from 2.25 to 3.0, and in the total number of negative effects from 1.61 to 2.0. Our results are comparable to these guidelines.
I.A. Tsalafoutas, G.V. Koukourakis [24] emphasize that stochastic negative effects can be caused even by small doses of radiation, and give the following example of calculating the risk associated with radiation during CT. The assumption of a 5% probability of risk per 1 Sv (1,000 mSv) for the occurrence of cancer or hereditary effects means that the examination, which leads to patient exposure in ED = 10 mSv (typical for CT of the abdomen and pelvis), implies 0.05% chance of such risks. That is, for every 10,000 patients, who underwent CT with a dose of 10 mSv, five people can be expected, to develop cancer or hereditary effects as the result of radiation.
There was calculation individual of effective dose and risk of malignancy based on Monte Carlo simulations after whole body CT [25]. The Excess Relative Risk (ERRMC), as a measurement of the exceeding risk of an exposed person compared to a non-exposed person, calculated using the solid cancer mortality in the United States as baseline (female: 17,500/100,000; male: 22,100/100,000).
There was calculation individual of Effective Dose and estimation of organ-specific additional Lifetime Attributable Risk (LAR) of cancer mortality after Whole Body Computed Tomography based on Monte Carlo simulations and report VII about Biologic Effects of Ionizing Radiation (BEIR VII). Considering the effective doses of 1.48 ± 0.15 mSv for the lungs, the LAR for mortality from lung cancer [n / 100,000] was 13.25 ± 4.24.
In our study, it was shown that with a single chest CT scan in patients with suspected COVID-19, additional (to a spontaneous level) cases of oncological pathology per 100,000 people may occur: 24.1 cases in children, 23.3 cases in adolescents, 14.4 cases in adults, 2.6 cases in older persons.
The average effective dose will increase in proportion to the increase in the number of CTs performed on the patient from 2.6–3.4 mSv with a single CT scan to the calculated values of 7.8–10.3 mSv with three times CTs. This will lead to a threefold increase in radiation risks to levels per 100,000 people may occur (Figure 1B): 72.3 cases in children, 69.8 cases in adolescents, 43.2 cases in adults, 7.9 cases in older persons. Due to the increased post-radiation risks in children; сcurrently, both the European and the American Society of Pediatric Radiology do not recommend the use of CT to diagnose COVID-19 pneumonia in children. CT is indicated only for severe, where concurrent pathology need to be excluded.
In men, the average radiation doses in the four age groups were slightly higher than in women (Figure 2A). However, with an increase in the number of CT scans from one (Figure 2B) to two (Figure 2C) and up to three (Figure 2D) in females, the increase in the calculated radiation risk compared to men is more significant, especially in women children (in 2.3 times) and among women adolescent (in 1.9 times). The radiation risk in men and women in all subgroups by age up to 65 years remains at the LOW level (10*10−5–100*10−5), and in the older subgroup at the WERY LOW level (1*10−5–10*10−5). However, with a three-fold CT scan in groups of children and adolescents, the radiation risk in women approaches the border of the MODERATE level (100*10−5–300*10−5), and in the old group to the border of the LOW level (10*10−5–100*10−5).
By evaluating the lung irradiation with the doses used in the ongoing clinical trials to treat COVID -19 patients, our data shows that a radiation dose 0.5 Gy provides an acceptable Risk Identification Checklist (RIC) estimate (LAR 1%), irrespective of sex and age at exposure [26]. However, a promising direction is the use of modern CT scanners, which allow the use of low-dose algorithms for CT diagnostics [27], while significantly reducing the radiation exposure to patients.
Because the study established effective radiation doses for chest CTs of patients with the diagnosis of COVID-19, the radiation risks for a single, double and triple chest CTs in different age and sex of patients were calculated. It has been found, that the radiation risk due to a single, double and triple chest CTs for patients under 65 years old is LOW, and for 65 years old and older patents is VERY LOW. Taking into account the radiation risk during CT is necessary to reduce the long-term consequences of radiation exposure on the population.
The study was performed without external funding.
The authors declare no conflict of interest.
The study was approved by the local ethics committee.
ASIR | Adaptive Statistical Iterative Reconstruction |
CT | Computed tomography |
CTDIvol | Computed tomography dose index |
DLP | Dose length product |
DRLs | Diagnostic reference levels |
ED | Effective doses |
ICRP | International Commission on Radiological Protection |
LAR | Lifetime Attributable Risk |
MBIR | Model-Based Iterative Reconstruction |
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Her research interests include archaea metabolism, enzymes purification and characterization, gene regulation, carotenoids and bioplastics production, antioxidant\ncompounds, waste water treatments, and brines bioremediation.\nRosa María’s other roles include editorial board member for several journals related\nto biochemistry, reviewer for more than 60 journals (biochemistry, molecular biology, biotechnology, chemistry and microbiology) and president of several organizing committees in international meetings related to the N-cycle or respiratory processes.",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",slug:"ana-isabel-flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",slug:"christian-palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",slug:"francisco-javier-martin-romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",slug:"sukru-beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",biography:"Dr. Şükrü Beydemir obtained a BSc in Chemistry in 1995 from Yüzüncü Yıl University, MSc in Biochemistry in 1998, and PhD in Biochemistry in 2002 from Atatürk University, Turkey. 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He is a member of the Turkish Biochemical Society, American Chemical Society, and German Genetics society. Dr. Ekinci published around ninety scientific papers, reviews and book chapters, and presented several conferences to scientists. He has received numerous publication awards from several scientific councils. 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Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. 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She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. 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He received his Ph.D. in Molecular Biology with his thesis “Genetic variability of the tick-borne encephalitis virus in natural foci of Novosibirsk city and its suburbs.” His primary field is molecular virology with research emphasis on vector-borne viruses, especially tick-borne encephalitis virus, Kemerovo virus and Omsk hemorrhagic fever virus, rabies virus, molecular genetics, biology, and epidemiology of virus pathogens.",institutionString:"Russian Academy of Sciences",institution:{name:"Russian Academy of Sciences",country:{name:"Russia"}}},{id:"310962",title:"Dr.",name:"Amlan",middleName:"Kumar",surname:"Patra",slug:"amlan-patra",fullName:"Amlan Patra",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/310962/images/system/310962.jpg",biography:"Amlan K. Patra, FRSB, obtained a Ph.D. in Animal Nutrition from Indian Veterinary Research Institute, India, in 2002. He is currently an associate professor at West Bengal University of Animal and Fishery Sciences. He has more than twenty years of research and teaching experience. He held previous positions at the American Institute for Goat Research, The Ohio State University, Columbus, USA, and Free University of Berlin, Germany. His research focuses on animal nutrition, particularly ruminants and poultry nutrition, gastrointestinal electrophysiology, meta-analysis and modeling in nutrition, and livestock–environment interaction. He has authored around 175 articles in journals, book chapters, and proceedings. Dr. Patra serves on the editorial boards of several reputed journals.",institutionString:null,institution:{name:"West Bengal University of Animal and Fishery Sciences",country:{name:"India"}}},{id:"53998",title:"Prof.",name:"László",middleName:null,surname:"Babinszky",slug:"laszlo-babinszky",fullName:"László Babinszky",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/53998/images/system/53998.png",biography:"László Babinszky is Professor Emeritus, Department of Animal Nutrition Physiology, University of Debrecen, Hungary. He has also worked in the Department of Animal Nutrition, University of Wageningen, Netherlands; the Institute for Livestock Feeding and Nutrition (IVVO), Lelystad, Netherlands; the Agricultural University of Vienna (BOKU); the Institute for Animal Breeding and Nutrition, Austria; and the Oscar Kellner Research Institute for Animal Nutrition, Rostock, Germany. In 1992, Dr. Babinszky obtained a Ph.D. in Animal Nutrition from the University of Wageningen. His main research areas are swine and poultry nutrition. He has authored more than 300 publications (papers, book chapters) and edited four books and fourteen international conference proceedings.",institutionString:"University of Debrecen",institution:{name:"University of Debrecen",country:{name:"Hungary"}}},{id:"201830",title:"Dr.",name:"Fernando",middleName:"Sanchez",surname:"Davila",slug:"fernando-davila",fullName:"Fernando Davila",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/201830/images/5017_n.jpg",biography:"I am a professor at UANL since 1988. My research lines are the development of reproductive techniques in small ruminants. We also conducted research on sexual and social behavior in males.\nI am Mexican and study my professional career as an engineer in agriculture and animal science at UANL. Then take a masters degree in science in Germany (Animal breeding). Take a doctorate in animal science at the UANL.",institutionString:null,institution:{name:"Universidad Autónoma de Nuevo León",country:{name:"Mexico"}}},{id:"309250",title:"Dr.",name:"Miguel",middleName:null,surname:"Quaresma",slug:"miguel-quaresma",fullName:"Miguel Quaresma",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309250/images/9059_n.jpg",biography:"Miguel Nuno Pinheiro Quaresma was born on May 26, 1974 in Dili, Timor Island. He is married with two children: a boy and a girl, and he is a resident in Vila Real, Portugal. He graduated in Veterinary Medicine in August 1998 and obtained his Ph.D. degree in Veterinary Sciences -Clinical Area in February 2015, both from the University of Trás-os-Montes e Alto Douro. He is currently enrolled in the Alternative Residency of the European College of Animal Reproduction. He works as a Senior Clinician at the Veterinary Teaching Hospital of UTAD (HVUTAD) with a role in clinical activity in the area of livestock and equine species as well as to support teaching and research in related areas. He teaches as an Invited Professor in Reproduction Medicine I and II of the Master\\'s in Veterinary Medicine degree at UTAD. Currently, he holds the position of Chairman of the Portuguese Buiatrics Association. He is a member of the Consultive Group on Production Animals of the OMV. He has 19 publications in indexed international journals (ISIS), as well as over 60 publications and oral presentations in both Portuguese and international journals and congresses.",institutionString:"University of Trás-os-Montes and Alto Douro",institution:{name:"University of Trás-os-Montes and Alto Douro",country:{name:"Portugal"}}},{id:"38652",title:"Prof.",name:"Rita",middleName:null,surname:"Payan-Carreira",slug:"rita-payan-carreira",fullName:"Rita Payan-Carreira",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRiFPQA0/Profile_Picture_1614601496313",biography:"Rita Payan Carreira earned her Veterinary Degree from the Faculty of Veterinary Medicine in Lisbon, Portugal, in 1985. She obtained her Ph.D. in Veterinary Sciences from the University of Trás-os-Montes e Alto Douro, Portugal. After almost 32 years of teaching at the University of Trás-os-Montes and Alto Douro, she recently moved to the University of Évora, Department of Veterinary Medicine, where she teaches in the field of Animal Reproduction and Clinics. Her primary research areas include the molecular markers of the endometrial cycle and the embryo–maternal interaction, including oxidative stress and the reproductive physiology and disorders of sexual development, besides the molecular determinants of male and female fertility. She often supervises students preparing their master's or doctoral theses. She is also a frequent referee for various journals.",institutionString:null,institution:{name:"University of Évora",country:{name:"Portugal"}}},{id:"283019",title:"Dr.",name:"Oudessa",middleName:null,surname:"Kerro Dego",slug:"oudessa-kerro-dego",fullName:"Oudessa Kerro Dego",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/283019/images/system/283019.png",biography:"Dr. Kerro Dego is a veterinary microbiologist with training in veterinary medicine, microbiology, and anatomic pathology. Dr. Kerro Dego is an assistant professor of dairy health in the department of animal science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. He received his D.V.M. (1997), M.S. (2002), and Ph.D. (2008) degrees in Veterinary Medicine, Animal Pathology and Veterinary Microbiology from College of Veterinary Medicine, Addis Ababa University, Ethiopia; College of Veterinary Medicine, Utrecht University, the Netherlands and Western College of Veterinary Medicine, University of Saskatchewan, Canada respectively. He did his Postdoctoral training in microbial pathogenesis (2009 - 2015) in the Department of Animal Science, the University of Tennessee, Institute of Agriculture, Knoxville, Tennessee. Dr. Kerro Dego’s research focuses on the prevention and control of infectious diseases of farm animals, particularly mastitis, improving dairy food safety, and mitigation of antimicrobial resistance. Dr. Kerro Dego has extensive experience in studying the pathogenesis of bacterial infections, identification of virulence factors, and vaccine development and efficacy testing against major bacterial mastitis pathogens. Dr. Kerro Dego conducted numerous controlled experimental and field vaccine efficacy studies, vaccination, and evaluation of immunological responses in several species of animals, including rodents (mice) and large animals (bovine and ovine).",institutionString:"University of Tennessee at Knoxville",institution:{name:"University of Tennessee at Knoxville",country:{name:"United States of America"}}},{id:"251314",title:"Dr.",name:"Juan Carlos",middleName:null,surname:"Gardón",slug:"juan-carlos-gardon",fullName:"Juan Carlos Gardón",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/251314/images/system/251314.jpeg",biography:"Juan Carlos Gardón Poggi received University degree from the Faculty of Agrarian Science in Argentina, in 1983. Also he received Masters Degree and PhD from Córdoba University, Spain. He is currently a Professor at the Catholic University of Valencia San Vicente Mártir, at the Department of Medicine and Animal Surgery. He teaches diverse courses in the field of Animal Reproduction and he is the Director of the Veterinary Farm. He also participates in academic postgraduate activities at the Veterinary Faculty of Murcia University, Spain. His research areas include animal physiology, physiology and biotechnology of reproduction either in males or females, the study of gametes under in vitro conditions and the use of ultrasound as a complement to physiological studies and development of applied biotechnologies. Routinely, he supervises students preparing their doctoral, master thesis or final degree projects.",institutionString:"Catholic University of Valencia San Vicente Mártir, Spain",institution:null},{id:"125292",title:"Dr.",name:"Katy",middleName:null,surname:"Satué Ambrojo",slug:"katy-satue-ambrojo",fullName:"Katy Satué Ambrojo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/125292/images/system/125292.jpeg",biography:"Katy Satué Ambrojo received her Veterinary Medicine degree, Master degree in Equine Technology and doctorate in Veterinary Medicine from the Faculty of Veterinary, CEU-Cardenal Herrera University in Valencia, Spain. She is a Full Professor at the Department of Medicine and Animal Surgery at the same University. She developed her research activity in the field of Endocrinology, Hematology, Biochemistry and Immunology of horses. She is a scientific reviewer of several international journals : American Journal of Obstetrics and Gynecology, Comparative Clinical Pathology, Veterinary Clinical Pathology, Journal of Equine Veterinary Science, Reproduction in Domestic Animals, Research Veterinary Science, Brazilian Journal of Medical and Biological Research, Livestock Production Science and Theriogenology. Since 2014, she has been the Head of the Clinical Analysis Laboratory of the Hospital Clínico Veterinario from the Faculty of Veterinary, CEU-Cardenal Herrera University.",institutionString:"CEU-Cardenal Herrera University",institution:{name:"CEU Cardinal Herrera University",country:{name:"Spain"}}},{id:"309529",title:"Dr.",name:"Albert",middleName:null,surname:"Rizvanov",slug:"albert-rizvanov",fullName:"Albert Rizvanov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/309529/images/9189_n.jpg",biography:'Albert A. Rizvanov is a Professor and Director of the Center for Precision and Regenerative Medicine at the Institute of Fundamental Medicine and Biology, Kazan Federal University (KFU), Russia. He is the Head of the Center of Excellence “Regenerative Medicine” and Vice-Director of Strategic Academic Unit \\"Translational 7P Medicine\\". Albert completed his Ph.D. at the University of Nevada, Reno, USA and Dr.Sci. at KFU. He is a corresponding member of the Tatarstan Academy of Sciences, Russian Federation. Albert is an author of more than 300 peer-reviewed journal articles and 22 patents. He has supervised 11 Ph.D. and 2 Dr.Sci. dissertations. Albert is the Head of the Dissertation Committee on Biochemistry, Microbiology, and Genetics at KFU.\nORCID https://orcid.org/0000-0002-9427-5739\nWebsite https://kpfu.ru/Albert.Rizvanov?p_lang=2',institutionString:"Kazan Federal University",institution:{name:"Kazan Federal University",country:{name:"Russia"}}},{id:"210551",title:"Dr.",name:"Arbab",middleName:null,surname:"Sikandar",slug:"arbab-sikandar",fullName:"Arbab Sikandar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/210551/images/system/210551.jpg",biography:"Dr. Arbab Sikandar, PhD, M. Phil, DVM was born on April 05, 1981. He is currently working at the College of Veterinary & Animal Sciences as an Assistant Professor. He previously worked as a lecturer at the same University. \nHe is a Member/Secretory of Ethics committee (No. CVAS-9377 dated 18-04-18), Member of the QEC committee CVAS, Jhang (Regr/Gen/69/873, dated 26-10-2017), Member, Board of studies of Department of Basic Sciences (No. CVAS. 2851 Dated. 12-04-13, and No. CVAS, 9024 dated 20/11/17), Member of Academic Committee, CVAS, Jhang (No. CVAS/2004, Dated, 25-08-12), Member of the technical committee (No. CVAS/ 4085, dated 20,03, 2010 till 2016).\n\nDr. Arbab Sikandar contributed in five days hands-on-training on Histopathology at the Department of Pathology, UVAS from 12-16 June 2017. He received a Certificate of appreciation for contributions for Popularization of Science and Technology in the Society on 17-11-15. He was the resource person in the lecture series- ‘scientific writing’ at the Department of Anatomy and Histology, UVAS, Lahore on 29th October 2015. He won a full fellowship as a principal candidate for the year 2015 in the field of Agriculture, EICA, Egypt with ref. to the Notification No. 12(11) ACS/Egypt/2014 from 10 July 2015 to 25th September 2015.; he received a grant of Rs. 55000/- as research incentives from Director, Advanced Studies and Research, UVAS, Lahore upon publications of research papers in IF Journals (DR/215, dated 19-5-2014.. He obtained his PhD by winning a HEC Pakistan indigenous Scholarship, ‘Ph.D. fellowship for 5000 scholars – Phase II’ (2av1-147), 17-6/HEC/HRD/IS-II/12, November 15, 2012. \n\nDr. Sikandar is a member of numerous societies: Registered Veterinary Medical Practitioner (life member) and Registered Veterinary Medical Faculty of Pakistan Veterinary Medical Council. 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Master\\\'s degree in Ecology and Biodiversity Conservation at Federal University of Mato Grosso with a scholarship by CAPES/REUNI program: Project \\"Reproductive biology of Melanorivulus punctatus\\". PhD\\\'s degree in Science (Cell and Tissue Biology Area) \n at University of Sao Paulo with scholarship granted by FAPESP; Project \\"Development of morphofunctional changes in ovary of Astyanax altiparanae Garutti & Britski, 2000 (Teleostei, Characidae)\\". She has experience in Reproduction of vertebrates and Morphology, with emphasis in Cellular Biology and Histology. 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