2019年8月31日星期六

Liver Function analysis-quantum magnetic resonance analyzer



(Liver Function) Analysis Report Card

Name: Example(Female) Sex: Female Age: 34
Figure: 170cm, 62kg Testing Time: 31/08/2019 10:16

 
 
 
Actual Testing Results
Testing Item Normal Range Actual Measurement Value Testing Result
Protein Metabolism 116.34 - 220.621 153.709
Energy Production Function 0.713 - 0.992 .945
Detoxification Function 0.202 - 0.991 .533
Bile Secretion Function 0.432 - 0.826 .549
Liver Fat Content 0.097 - 0.419 .381
 
Reference Standard:
  Normal(-)   Mildly Abnormal(+)
  Moderately Abnormal(++)   Severely Abnormal(+++)
 
Protein Metabolism: 116.34-220.621(-) 90.36-116.34(+)
  60.23-90.36(++) <60.23(+++)
 
Energy Production Function: 0.713-0.992(-) 0.475-0.713(+)
  0.381-0.475(++) <0.381(+++)
 
Detoxification Function: 0.202-0.991(-) 0.094-0.202(+)
  0.043-0.094(++) <0.043(+++)
 
Bile Secretion Function: 0.432-0.826(-) 0.358-0.432(+)
  0.132-0.358(++) <0.132(+++)
 
Liver Fat Content: 0.097-0.419(-) 0.419-0.582(+)
  0.582-0.692(++) >0.692(+++)
 
 
Parameter Description
Protein Metabolism:
Protein in food is digested and absorbed by the intestinal tract to be sent to the liver for conversion and reorganization, different types of amino acids are metabolized to manufacture a variety of proteins for the need of cells according to the body's need. In addition, the liver will decompose the useless protein into amino acids, and then the amino acids are further changed into urea to be excreted by the kidney or intestinal tract.
Energy Production Function:
After carbohydrates are digested, the liver will carry out powdered sugar metabolism to produce energy for the need of cells and then convert overmuch powdered sugar into glycogen for storage. After fatty foods are digested, the liver will further convert fat into energy.
Detoxification Function:
Food will produce some toxins in the digestive process and the metabolism process. The liver as well as detoxifying enzymes carry out detoxification to decompose the hazardous substances (alcohol and ammonia) into harmless substances (such as urea, water and carbon dioxide) to be excreted out of the body.
Bile Secretion Function:
Bile is the end product of metabolism in the liver, which has the role of fat digestion and promotes the body to absorb fat-soluble vitamins A, D, E and K. The overmuch bile will be sent to gallbladder for standby.
Liver Fat Content:
If the liver fat content is more than 5% of wet weight or over 1 / 3 liver cells of per unit area on liver biopsy have lipid droplets under a microscope, the liver is called as a fatty liver. The fatty liver is also known as liver fatty degeneration which refers to fat accumulation in liver cells due to a variety of causes. When a healthy person takes in meals with reasonable ingredients, the liver fat content accounts for 5% of the weight of liver. B-US can detect the fatty liver with over 30% of liver fat content.
The fatty liver is divided into obese fatty liver, alcoholic fatty liver, diabetes fatty liver which are the three common causes of fatty liver. In addition, there are nutritional disorder fatty liver, drug-induced fatty liver, acute fatty liver of pregnancy and so on. What are the symptoms of fatty liver? The person with mild fatty liver can have no any discomfort. The patients with moderate or severe fatty liver can have loss of appetite, fatigue, nausea, vomiting, abdominal distension, diarrhea, liver pain, left shoulder and back pain and swollen and other symptoms. The hepatomegaly can be found by a medical examination, and a few livers have mild jaundice and spider angioma. Abnormal liver function, triglycerides and cholesterol increase can be found by a laboratory test. Early diagnosis and prompt treatment can effectively control the further development of fatty liver, so fat deposition in the liver can fade.
 

 
The test results for reference only and not as a diagnostic conclusion.

2019年8月13日星期二

Cardiovascular and Cerebrovascular Analysis-quantum magnetic analyzer



(Cardiovascular and Cerebrovascular) Analysis Report Card

Name: Example(Female) Sex: Female Age: 34
Figure: 175cm, 65kg Testing Time: 12/08/2019 10:16

 
 
 
Actual Testing Results
Testing Item Normal Range Actual Measurement Value Testing Result
Blood Viscosity 48.264 - 65.371 58.072
Cholesterol Crystal 56.749 - 67.522 69.058
Blood Fat 0.481 - 1.043 .92
Vascular Resistance 0.327 - 0.937 1.413
Vascular Elasticity 1.672 - 1.978 1.864
Myocardial Blood Demand 0.192 - 0.412 .399
Myocardial Blood Perfusion Volume 4.832 - 5.147 4.947
Myocardial Oxygen Consumption 3.321 - 4.244 5.581
Stroke Volume 1.338 - 1.672 1.219
Left Ventricular Ejection Impedance 0.669 - 1.544 1.862
Left Ventricular Effective Pump Power 1.554 - 1.988 1.682
Coronary Artery Elasticity 1.553 - 2.187 1.724
Coronary Perfusion Pressure 11.719 - 18.418 16.63
Cerebral Blood Vessel Elasticity 0.708 - 1.942 1.505
Brain Tissue Blood Supply Status 6.138 - 21.396 12.688
 
Reference Standard:
  Normal(-)   Mildly Abnormal(+)
  Moderately Abnormal(++)   Severely Abnormal(+++)
 
Blood Viscosity: 48.264-65.371(-) 65.371-69.645(+)
  69.645-73.673(++) >73.673(+++)
 
Cholesterol Crystal: 56.749-67.522(-) 67.522-69.447(+)
  69.447-74.927(++) >74.927 (+++)
 
Blood Fat: 0.481-1.043(-) 1.043-1.669(+)
  1.669-1.892(++) >1.892(+++)
 
Vascular Resistance: 0.327-0.937(-) 0.937-1.543(+)
  1.543-1.857(++) >1.857(+++)
 
Vascular Elasticity: 1.672-1.978(-) 1.672-1.511(+)
  1.511-1.047(++) <1.047(+++)
 
Myocardial Blood Demand: 0.192-0.412(-) 0.412-0.571(+)
  0.571-0.716(++) >0.716(+++)
 
Myocardial Blood Perfusion Volume: 4.832-5.147(-) 4.177-4.832(+)
  4.029-4.177(++) <4.029(+++)
 
Myocardial Oxygen Consumption: 3.321-4.244(-) 4.244-5.847(+)
  5.847-6.472(++) >6.472(+++)
 
Stroke Volume: 1.338-1.672(-) 0.647-1.338(+)
  0.139-0.647(++) <0.139(+++)
 
Left Ventricular Ejection Impedance: 0.669-1.544(-) 1.544-2.037(+)
  2.037-2.417(++) >2.417(+++)
 
Left Ventricular Effective Pump Power: 1.554-1.988(-) 1.076-1.554(+)
  0.597-1.076(++) <0.597(+++)
 
Coronary Artery Elasticity: 1.553-2.187(-) 1.182-1.553(+)
  0.983-1.182(++) <0.983(+++)
 
Coronary Perfusion Pressure: <8.481(+++) 8.481-11.719(++)
  18.418-21.274(++) >21.274(+++)
 
Cerebral Blood Vessel Elasticity: 0.708-1.942(-) 0.431-0.708(+)
  0.109-0.431(++) <0.109(+++)
 
Brain Tissue Blood Supply Status: 6.138-21.396(-) 3.219-6.138(+)
  1.214-3.219(++) <1.214(+++)
 
 
Parameter Description
Blood Viscosity(N): The basic indicator of Hemorheology refers to the internal friction among blood molecules.
Hyperviscosity state: Namely, the viscosity of blood is high, and blood flow is affected. Therefore, high blood pressure patients with high viscosity are prone to have cerebrovascular accidents, such as stroke and other phenomena; coronary heart disease patients with high viscosity are prone to have myocardial infarction and so on.
The blood flow in the blood vessels is in a laminar flow state, which is stratified flow. The flow velocity close to the vessel wall is slower, and the flow velocity is fastest in the middle. Thus, the larger the shear rate is, the greater the slope is, the greater the shear stress is, the faster the flow velocity is, and the lower the N is. The smaller the shear rate is, the lower the slope is, the smaller the shear stress is, the lower the flow velocity is, and the higher the N is.
Cholesterol Crystal:
(1) Increase is seen in primary high cholesterol blood, the aura of mild atherosclerosis, blood stagnation type chest pain, phlegm congestion type chest pain, etc.
(2) Reduction is seen in decreased immunity, malnutrition, cardiac insufficiency, Qi and Yin deficiency type chest pain, Yang Qi deficiency type chest pain, etc.
Blood Fat:Blood fat abnormity is divided into primary abnormity and secondary abnormity.
1. Primary Hyperlipoproteinemia: refers to hyperlipoproteinemia caused by the possibility of unknown cause related to certain environmental factors (including diet, nutrition, drugs, etc.), or gene mutations.
2. Secondary Hyperlipoproteinemia: refers to hyperlipidemia caused by certain systemic diseases or drugs, such as hyperlipidemia caused by diabetes, hypothyroidism, nephrotic syndrome, chronic renal failure and acute renal failure and so on.
(1) Increase is seen in idiopathic hyperlipidemia, atherosclerosis, blood stagnation type chest pain, etc.
(2) Reduction is seen in ferrite decreased immunity, the Qi and Yin deficiency type chest pain, etc.
(3) Decline is seen in decline of cerebral arterial oxygen content and mild ischemic cerebrovascular disease aura.
Vascular Resistance:
Increase is in direct proportion to the length of blood vessels, and is in inverse proportion to the caliber of blood vessels. The increase of vascular resistance is seen in mildly elevated systolic and diastolic blood pressure, mild hypertension, insomnia with deficiency of both heart and spleen, phlegm-heat internal confusion type insomnia, etc.
Decline is seen in mildly declined systolic and diastolic blood pressure, mild hypotension, Yin deficiency and Huo exuberance type insomnia, etc.
Vascular Elasticity:refers to the expansion extent of arterial vascular elasticity during systolic ejection.
Influence Factors: (1) The size of SV. The greater the SV is, the greater the FEK is. (2) Emptying rate. The faster the emptying rate is, the smaller the FEK is. (3) Bad vascular elasticity.
The SV is not low, the emptying rate is not fast, and the FEK is also small, so it is possible to determine the possibility of hardening of blood vessels. It should not determine the possibility by a single parameter. The increase of vascular elasticity is seen in the mildly elevated systolic blood pressure, the mildly reduced diastolic blood pressure, the mildly increased pulse press and slightly higher blood pressure. The decline is seen in mildly atherosclerosis, coronary heart diseases, blood stagnation type chest pain, Yang Qi deficiency type chest pain, etc.
Myocardial Blood Demand:The blood demand per minute of coronary artery perfusion of heart.
Myocardial Blood Perfusion Volume:The actual blood demand per minute of coronary artery perfusion of heart.
Myocardial Oxygen Consumption:The milliliter value of oxygen consumption of heart per minute.
Influence Factors: Three aspects
(1) Heart rate: the heart rate is fast, and the HOV is great.
(2)(2) Myocardial contractility: the cardiac contractility is strong, and the HOV is great.
(3) Myocardial contraction time: the longer the contraction time is, the greater the HOV is.
Thus, low oxygen consumption and high cardiac work are the best state.
Stroke Volume:The blood volume output by the heart in beat each time.
Influence Factors: Five aspects
(1) The effective circulating blood volume (BV): when the blood volume is insufficient, the returned blood volume is little, and the SV is reduced.
(2) The weakening of myocardial contractility: the contractility is low, and the pressure is low, so the ejected blood volume is less.
(3) The extent of ventricular filling: In range of myocardial elasticity, the greater the degree of filling is, the stronger the retraction is, and the SV is increased. The normal heart chamber capacity is 173ml, but not all of the blood is ejected. The blood volume in the left ventricle is about 60% -70% of the total capacity, being about 125ml or so. Usually, the Chinese people's average SV is 80-90ml.
(4) The size of peripheral vascular resistance (PR). The PR is large, and then the SV is reduced; the PR is small, and then the SV is increased.
(5) Ventricle wall movement.
When the ventricle is contracted, the cardiac muscle is in coordinated movement. If the myocardial contraction is not coordinated, the SV is reduced. For instance, some patients with myocardial infarction have part of infarction, so the myocardial contractility is inconsistent and the SV is reduced. However, under normal circumstances, the ventricle wall movement can not be abnormal.
Left Ventricular Ejection Impedance:reflects the indicators of resistance status of the left ventricular outflow channel.
Influence Factors:
(1) The fact whether the outflow channel has lesion. The aortic stenosis and other conditions can make VER increased.
(2) The outflow channel has no lesion, while the emptying rate of aortic blood is slow, so VER is increased.
(3) The entire vascular resistance is large.
Left Ventricular Effective Pump Power:reflects the contraction strength of effective stroke of blood of the left ventricle.
Normally, the people: 1.8 kilograms. Pump power is low, and contraction is not good, so myocardial fibers may have problems. Pump power is high, and contractility is good, so the ejected blood volume is much.
Influence Factors: Four aspects
(1) The extent of ventricular filling: In range of elasticity, the greater the degree of filling is, the stronger the contractility is; the degree of filling and the contractility are in direct proportion. If out of the limit, the myocardial expansion is large, but the contractility is reduced. Thus, the proper degree of filling is a factor influencing the contractility.
(2) The effective circulating blood volume (returned blood volume BV): The returned blood volume is little, the filling is insufficiency, and the contractility is small; the returned blood volume is much, the filling is better, and the contractility is strong.
(3) The functional status of myocardium itself: The fact whether the myocardium has lesion. For instance, myocarditis. Myocardial cells are damaged, and myocardial elasticity is reduced, so the contractility is lowered.
(4) The normal degree of blood and oxygen supply of myocardium itself: The blood and oxygen supply is insufficient, so the contractility is lowered. Myocardial Oxygen Consumption: the milliliter value of oxygen consumption of heart per minute.
Coronary Artery Elasticity:
The source of power of life is the heart, and the blood nourishing the body constantly flows under her impetus. However, she also demands the nourishing of blood. Coronary artery, namely three blood vessels respectively located in the heart, can supply blood and oxygen to her. The coronary artery is the artery special for supplying blood to the heart. If cholesterol and other substances are accumulated in the blood vessels, the vascular cavity will be narrower or be blocked and the blood flow will be smooth and then be blocked to cause cardiac ischemia and a series of symptoms which are coronary heart disease, namely coronary atherosclerosis. Coronary heart disease is also called as coronary atherosclerotic heart disease. The excessive fat deposition results in atherosclerosis and weakened elasticity. The mortality of human on cardiovascular and cerebrovascular diseases induced on the arterial vessel wall has exceeded 1 / 2 of the total mortality of population.
Dangerous factors making the elasticity of coronary artery weakened: high blood fat, smoking, diabetes, obesity, high blood pressure, lack of physical activity, Psychological overstrain, family history of coronary heart disease, oral contraceptive, etc.
Coronary Perfusion Pressure:the pressure of coronary artery of heart in blood supply is influenced by diastolic blood pressure and left atria pressure.
Part of myocardial ischemia, insufficient myocardial blood supply and entire myocardial ischemia can lead to myocardial infarction.
Cerebral Blood Vessel Elasticity:
The brain artery or the neck artery controlling the brain has lesion, which leads to disorder of intracranial blood circulation and damage of brain tissue. The elasticity of hardened brain blood vessels is weakened, and the vessel cavity is narrowed, so it is easy to form cerebral thrombosis. After the patients with cerebral arteriosclerosis excessively drink, the blood pressure will be suddenly elevated, the blood vessels will ruptured, so it is prone to form cerebral hemorrhage. After load drinking of alcohol, the concentration of alcohol in blood can reach its peak in a half hour. The alcohol can not only directly stimulate the blood vessel wall to make it lose its elasticity but also stimulate the liver to promote the synthesis of cholesterol and triglyceride,thus leading to atherosclerosis and cerebral atherosclerosis. Cerebrovascular disease can be divided into acute cerebrovascular disease and chronic cerebrovascular disease according to their process. The acute cerebrovascular disease includes trans ient ischemic attack, cerebral thrombosis,cerebral embolism, hypertensive encephalopathy, cerebral hemorrhage, subarachnoid hemorrhage, etc. The chronic cerebrovascular disease includes cerebral arteriosclerosis, cerebrovascular dementia, cerebral artery steal syndrome, Parkinson's disease, etc. The cerebrovascular disease which is known generally refers to the acute cerebrovascular disease. It often endangers the human life due to acute incidence, so it is easy to cause the attention. The chronic cerebrovascular disease is easy to be ignored by people due to its long course.
Brain Tissue Blood Supply Status:
Brain tissue blood supply mainly depends on the brain artery or the neck artery controlling the brain. Cerebrovascular diseases can be divided into two categories according to their nature, one is the ischemic cerebrovascular disease and the other one is the hemorrhagic cerebrovascular disease. There are many cases about the ischemic cerebrovascular disease in clinic, the patients account for 70% ~ 80% of all patients with cerebrovascular disease. Due to cerebral arteriosclerosis and other reasons, the vessel cavity of brain artery is narrowed, the blood flow is reduced or completely blocked, the brain blood circulation is disordered, and the brain tissue is damaged,so a series of symptoms occur. The hemorrhagic cerebrovascular disease is mainly caused by long-term high blood pressure, congenital cerebral vascular malformation and other factors.Due to blood vessel rupturing, blood spilling, oppression on brain tissue and blocked blood circulation, the patients often show increased intracranial pressure, disorientation and other symptoms. Thus, the patients account for about 20% ~ 30% of all patients with cerebrovascular disease.
 


 
The test results for reference only and not as a diagnostic conclusion.

2019年8月7日星期三

keep more body health-bioplasm 9d nls analyzer


http://www.bioplasm-nls.com

New medical technologies have been developing very quickly in the last decades. A significant success was achieved in treatment of oncological and oncohematological diseases. Development of transplantology increases chances of oncologic patients for recovery. However application of cytostatic and immune suppressing medications, ensuring functioning of transplantates, leads to severe decreasing of immunity and appearance of complications in a form of opportunistic infections. Besides, group of infections development risk includes patients suffering from acquired immune deficiency syndrome (AIDS), complications after abdominal surgical interventions, major severe burns, and premature newborns or newborns subjected to aggressive medical therapy within the first days of life (parenteral feeding and massive antibacterial therapy). Among contributive risk factors of invasive mycoses development are intake of antibiotic with a wide spectrum for more than two weeks, total intravenous nutrition, continuous artificial lung ventilation, shock, preceding mycotic infections.
Results of 8124 autopsies show that incidence of mycotic infections in clinics of Frankfurt on the Main has increased from 2.2% in 1978 to 5.3% in 2004. This increase happened mainly due to aspergillus infection, incidence of which has increased 10 times within this period of time.
A peculiarity of aspergillus infection course is a variety of its clinical manifestations. Therapists single out invasive and non-invasive aspergillosis.
Invasive pulmonary aspergilliosis (IPA) is the most severe form of the disease, when dissemination of the process into other organs (CNS, parenchymatous organs of abdominal cavity) is possible. Often the first symptom of invasive mycotic infection is a fever, refractory to broad-spectrum antibiotics. Absence of a result at treatment with antibacterial preparations at clinical picture of acute pneumonia in patients with expressed immune suppression must be regarded as a possibility of IPA development. When such clinical manifestations are registered diagnostic maneuvers must be fulfilled. Speed and intensity of IPA manifestations depend on degree of immune suppression. IPA signs reveal themselves distinctly after granulocytopaenia, Sometimes IPA diagnosis may be made basing on results of a biopsy only, but a risk of haemorrhagic complications in patients with hemoblastoses may be one of barriers for biopsy.

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