Week 1 Flashcards

1
Q

Adaptation

A

A change that allows for the subject to get used to new situation or environment

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2
Q

Allostasis

A

The ability of the brain to strategize and monitors multiple things to meet future challenges

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3
Q

Epidemiology

A

The study of if the distribution, manifestation, and determinants of health and diseases in different groups

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4
Q

Etiology

A

The causes or manner of causes of a disease or condition

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5
Q

Health promotion

A

Process by integrating environmental and social intervention in that increases control and improvement over people’s health

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6
Q

Homeostasis

A

Steady state in the body, defines the “norm” of a person

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7
Q

Laterogenic

A

Illness causes by medical examination or treatment

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8
Q

Idiopathic

A

Any disease that arises randomly and unknown cause

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9
Q

Primary prevention

A

Intervening before an illness occurs

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10
Q

Secondary prevention

A

Aims to reduce impact of diseases or injuries that have already occurred

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11
Q

Tertiary prevention

A

Soften impact of ongoing illness which has lasting effects

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12
Q

Pathogenesis

A

Development of disease

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13
Q

Pathophysiology

A

A disorder in function due to disease

Interaction between the change of normal physiology impacted by a pathology

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14
Q

Pharmacology

A

Branch of medicine concerned with uses, effects, and modes of action of drugs

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15
Q

Pharmacodynamics

A

Branch of pharmacology that focuses on effects and mechanisms (of action) of the drug

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16
Q

Physiological

A

The functioning of a living organism or body part

17
Q

Risk factor

A

Higher chance of developing a disease

18
Q

Steady state

A

Stable condition that does not change overtime

Or when change in one direction is balanced by a change in the other direction

19
Q

Stressors

A

Internal or external factor that creates potential for physiologic, emotional, cognitive, or behavioural changes

20
Q

What amount of water is recommended for taking pills/tablets

A

8Ounces/1 glass/240 mL

21
Q

Phases of drug activity

A
  1. Pharmaceutical
    2.pharmacokinetic
    3.pharmacodynamic
22
Q

What is the pharmaceutical phase

A

-this phase is when the drug is being prepped for absorption
Dissolved

23
Q

What is the Pharmacokinetic phase

A

This phase is when the drug is being transported from the site of admin to the circulation fluid

To be absorbed, distributed, biotranformed, and then excreted

24
Q

Types of drug coatings

A

Regular
Buffered or enteric polymers
Gelatin
Etc

25
Q

What is absorption? And how is solutes transported?

A

-movement of drugs from admin site to circulating fluid (determines time for effect of drug to occur)

-transportation of solutes depend on the: route of admin, nature of the drug.
Transportation method include passive transport or through facilitated, active transport, or pinocytosis

26
Q

Sites of absorption ?

A

-parenteral, enteral, topical (inc. mucosal), pulmonary

27
Q

Factors the affect absorption?

A

-circulation to site of admin
-absorbing membrane’s thickness and size
-drug composition
-solubility of drug (soluble drugs absorbs faster)
-route of admin
-ph of environment
-drug formulation
-dosage
- drug to drug interaction
Food-drug interaction
Acid drug absorbed best in acid
Basic drug is absorbed best in base

Alteration if ph of body tissues can impact absorption

28
Q

What can you do to increase absorption?

A

Massage site
Select more vascular site
Ambulate after admin
Alter ph
Increase temp at site

More concentration = rapid absorption

29
Q

Principles of ionization

A

Ionic: charged electrically. As a drug becomes more ionized, becomes more water soluble

Non-ionized: not charged. As a drug becomes more non-ionized it becomes more lipid soluble

Cell membranes are generally composed of more fat/ lipid

30
Q

What is drug ionization?

A

Acids are absorbed in acids because they are non ionized
Base are absorbed in bases because they are non ionized
Acid in a basic environment is ionized and therefore less able to absorb across membrane.

Why does this happen? Because drugs work best when they Self absorb in their own environment this enables them to be nonionized therefore more lipid soluble. When it is ionized it is more water soluble and cells are made up of more fat/lipid therefore hydrophobic. Need to use specialized transport

31
Q

What is the distribution phase ?

A

When drug moves from blood or circulating fluid to site of action

32
Q

How is medication distributed

A

Drugs are transported in body via blood
Greater blood flow to an area = higher concentration of drug being delivered
Lipid soluble agents are distributed throughout entire body tissues because there is no barrier

33
Q

How is the drug transported in the blood? What can’t it do while being transported?

A

It is transported by binding on to plasma proteins, when it binds it forms drug protein complexes. Drug binding does not allow for crossing capillary membranes as well as distribution of drug

34
Q

How is the process of distribution affected?

A

Blood supply
Drugs affinity to receptors
Ionization of drugs
Plasma protein binding (unbound drug will give desired effect)

35
Q

What’re the causes of uneven drug distribution

A

Plasma protein binding/tissue binding

Some drugs bind readily or reversible with certain tissues such as fat or bone. Fat and bone stores the drugs.

Elderly and obese people have a higher ratio of fat which means the action will be prolonged

diazepam is stored in fat

36
Q

What is metabolism (bio transformation) and where does it occur

A

Breaks down the drug so that it can be more easily removed from the body by forming water soluble metabolites, occurs in the liver

It is the process by which the structure (and function) of drugs, nutrients, vitamins, and minerals is altered

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