Clinical Chemistry Flashcards

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1
Q

A branch of medical science that involves the analysis of chemical components of body fluids.

A

Clinical Chemistry

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2
Q

The development of scientific research in medicine and the emergence of organic & physiological chemistry.

A

Two Main Origins of Clinical Chemistry

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3
Q

Made possible by significant contributions from biology and natural philosophy.

A

Development of Clinical Chemistry

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4
Q

A Greek physician considered as the “Father of Medicine” and author of the Hippocratic oath (as introduced in Module 1). He started the belief that diseases are caused by imbalances of humors in the body. This belief sparked an interest among early physicians to observe body fluids.

A

Hippocrates

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5
Q

He introduced the anatomic approach of disease process and explained diseases in terms of localized pathologic anatomy, rather than as attributable to an imbalance of the humors diffused throughout the system.

A

Giovanni Morgagni

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6
Q

He is considered to be the “Father of Modern Chemistry”. He recognized and named two elements, oxygen and hydrogen. He discovered the role of oxygen in the process of combustion and that respiration is a slow combustion process. He started the belief that chemical analysis is a refined type of dissection that sparked a renewal of interest in the examination of body fluids.

A

Antoine Laurent Lavoisier

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7
Q

They believed that living organisms contain a “vital force” that was the very essence of life. They also believed that processes within living organisms were unique and could not be duplicated in the laboratory. To them, in vitro synthesis of “organic” compounds is impossible and denied that chemistry has a role in physiology.

A

Vitalists

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8
Q

Believed that animals are no more than “machines” and that life could be explained fully by chemical and physical principles and properties alone.

A

Mechanists

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9
Q

Believed that man is not unique. The believe that there is continuity between man and the animals as attested by Darwin’s publication “Origin of Species” which is considered to be the foundation of evolutionary biology.

A

Darwinists

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10
Q

He was successful in isolating urea from urine samples. He also believed that chemical laboratories should be located near the wards, where chemical analysis of urine excretions of the sick could be carried out.

A

Antoine Francois de Fourcroy

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11
Q

He was able to synthesize urea in vitro by evaporating an isomeric solution of ammonium cyanate proving that “organic” substances could be synthesized in vitro without any “vital force” in a living organism. This created a bridge between the “organic” and “inorganic” worlds. In doing so, he gave the first proof that vitalism is wrong.

A

Friedrich Wohler

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12
Q

He was able to synthesize organic compounds such as ethanol, formic acid, and benzene in vitro via chemical treatments of inorganic compounds.

A

Marcellin Berthelot

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13
Q

He discovered that glycogen was formed by the liver which contradicted the vitalism belief that only plants can produce complex compounds.

A

Claude Bernard

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14
Q

He was the first to observe that urea and albumin concentration in plasma decreases as their concentration increases in the urine of the patient.

A

John Bostock

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15
Q

Credited as the first to make the true connection between chemistry and medical practice and was a vitalist. However, he advocated the benefits to be derived from the application of chemistry to physiology in the treatment of diseases. Also, he favored the study of physics and chemistry by medical students.

A

William Prout

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16
Q

He stressed the practical diagnostic value of chemistry and urged medical school curriculum to use English as the medium of instruction.

A

Henry Bence Jones

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17
Q

“Chemical studies are relevant to clinical medicine.”

“It is in the blood that we must look for many important
modifications in connection with disease.”

A

Thomas Hodgkin

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18
Q

Century when an average medical student or average practitioner barely had a nodding acquaintance with chemistry and could not use a microscope.

A

19th Century

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19
Q

The Hospital recognized the powerful aid that the science of medicine
“has received from the study of organic chemistry and knowledge and use of the microscope”, thus authorizing the purchase of a microscope at a cost not to exceed 50 US dollars.

A

Massachusetts General Hospital, 1847

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20
Q

The position of a “Chemist-Microscopist” was established.

A

Massachusetts General Hospital, 1851

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21
Q

He proposed that the American hospitals must employ clinical chemists to advance their ability to differentiate between the physiologic and the pathologic.

A

Otto Knut Folin

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22
Q

Scientists who determined reference intervals of chemicals/ analytes. They correlated variations/ abnormal values with pathologic conditions. They also elucidated metabolic pathways in health and disease.

A

Otto Knut Folin and Donald Dexter Van Slyke

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23
Q

He invented a volumetric gas-measuring apparatus for the determination of carbon dioxide concentration.

A

Donald Dexter van Slyke

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24
Q

Developed a method for the production of a protein-
free filtrate that can be used for determining blood sugar.

A

Otto Knut Folin and Hsien Wu

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25
Q

He developed the alkaline picrate method for the determination of creatinine concentration.

A

Max Jaffe

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26
Q

pioneered by Otto Knut Folin after his development of the Duboscq apparatus. Involves the observation of the intensity of colored product after chemical reactions.

A

Colorimetry

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27
Q

Measurement of light absorbance at selected wavelengths.

A

Spectrophotometry

28
Q

The first attempt to automate instruments. This is a continuous-flow instrument that reacted specimen and reagents to produce a measurable color density.

A

Auto-Analyzer

29
Q

The second attempt towards automation. Introduced by Norman Anderson which was the first clinical analyzer to incorporate a computer.

A

Centrifugal Analyzer

30
Q

Capable of performing multiple tests analyzed one after another on a given clinical specimen.

A

Sequential Multiple Analyzer with Computer (SMAC)

31
Q

Introduced the perfected technology of automated pipetting which is the approach of choice for automation in clinical chemistry laboratories even up to these days.

A

Beckman Astra

32
Q

The Standard of Clinical Laboratories

A

Save Time and Improve Performance by Eliminating Human Errors and Reduce the Risk of Cross Contamination.

33
Q

An unseen side of medical practice and care for many people.

A

Clinical Laboratory Testing

34
Q

Basis for many clinical conclusions that doctors and clinicians make regarding a person’s health.

A

Laboratory Results

35
Q

one of the most commonly performed assays in the Clinical Chemistry section.

A

Blood Sugar Testing

36
Q

Refers to an increased level of blood glucose (blood sugar).

A

Hyperglycemic State

37
Q

Refers to low level of blood glucose (blood sugar).

A

Hypoglycemic State

38
Q

Measures the levels of glucose in the blood at any given point in the day.

A

Random Blood Sugar (RBS)

39
Q

Prohibits the patient to eat and drink any liquids other than water for at least eight hours before collection of blood.

A

Fasting Blood Sugar (FBS)

40
Q

Often requested by physicians for pregnant patients to rule out or confirm diagnosis of Gestational Diabetes Mellitus.

A

Oral Glucose Tolerance Test (OGTT)

41
Q

Reflects the average blood glucose levels of the patient over a three-month period. Also known as Glycated hemoglobin or Glycosylated hemoglobin.

A

HbA1c (Hemoglobin A1c)

42
Q

Involves a combination of tests conducted together to check for any risks of cardiovascular diseases. Include determining the concentrations of (a) fatty acid, (b) cholesterol, and (c) lipoprotein levels.

A

Lipid Profile Tests

43
Q

Simplest form of lipid.

A

Fatty Acids

44
Q

Storage form of fat.

A

Triglycerides

45
Q

A steroid alcohol and is the precursor of hormones, vitamin D, and bile salts.

A

Cholesterol

46
Q

Special particles made up of fats and proteins. Often described as carriers of cholesterol and triglycerides.

A

Lipoproteins

47
Q

Also known as the “bad cholesterol”, transports cholesterol from the liver to peripheral tissues.

A

Low Density Lipoprotein (LDL)

48
Q

Also referred to as the “good cholesterol”. It transports cholesterol from peripheral tissues back to the liver for metabolism. Once transported, cholesterol is then broken down by the liver.

A

High Density Lipoprotein (HDL)

49
Q

Transport exogenous triglycerides (triglycerides coming from diet) to the muscles and adipocytes.

A

Chylomicrons

50
Q

Responsible for transporting endogenous triglycerides.

A

Very Low Density Lipoprotein (VLDL)

51
Q

Laboratory just for the kidneys. Includes Creatinine, Blood Urea Nitrogen (BUN), and Blood Uric acid (BUA) testing.

A

Renal Function Tests

52
Q

A waste product of muscle metabolism that is elevated in impaired renal function.

A

Creatinine

53
Q

A waste product of protein catabolism that is also elevated in cases of kidney diseases.

A

Blood Urea Nitrogen (BUN)

54
Q

Elevation of BUN.

A

Azotemia

55
Q

Azotemia is accompanied by renal failure.

A

Uremia

56
Q

Product op purine nucleic acids. Measured to detect kidney dysfunction, to detect presence of renal stone (renal calculi), and for diagnosis/ monitoring of gout.

A

Blood Uric Acid (BUA)

57
Q

Also referred to as the hepatic panel, are group of blood tests that provide health information about a patient’s liver state. These tests include Bilirubin and liver enzyme tests (AST, ALT, GGT).

A

Liver Function Tests

58
Q

A yellow-colored pigment and is a product of hemoglobin (heme) breakdown. Include determining the levels of total bilirubin (TB), unconjugated/ indirect bilirubin (B1), and conjugated/ direct bilirubin (B2).

A

Bilirubin

59
Q

Formerly called Serum Glutamic Oxaloacetic Transaminase (SGOT).

A

Aspartate aminotransferase (AST)

60
Q

Formerly called Serum Glutamic Pyruvic Transaminase (SGPT).

A

Alanine aminotransferase (ALT)

61
Q

Useful in the diagnosis of chronic alcoholism resulting in liver damage.

A

Gamma-glutamyl transferase (GGT)

62
Q

Liver damage is most likely present if…

A

ALT and AST are found together in elevated amounts in the blood.

63
Q

It includes Troponin test, Myoglobin test, and Cardiac Enzyme tests.

A

Cardiac Function Tests

64
Q

Regulatory proteins in the cardiac muscles. Considered to be the most specific test for myocardial damage. Include Troponin I and Troponin T which are both specific to the myocardium of the heart.

A

Troponins

65
Q

A pigment found in muscle tissues. It is not as specific as troponin because it is found in both skeletal tissues and cardiac tissues.

A

Myoglobin

66
Q

Enumerate the Cardiac Enzyme Markers.

A

Creatine Kinase- MB (CK-MB), Aspartate aminotransferase (AST) and Lactate Dehydrogenase (LDH).

67
Q

What enzyme marker is the most specific to the heart.

A

Creatine Kinase- MB (CK-MB)