(A) NURSING PROCESS - PHARMA Flashcards

1
Q

It’s used by nurses for the appropriate delivery
of patient care and drug administration.

➢ The nurse has supporting role to administer
proper care/medication administration.

➢ Nurses have many important tasks, yet drug
administration is the number one priority, about
40% of the nurse’s time is spent administering
medication

➢ drug administration (top of the list)

A

NURSING PROCESS IN PHARMACOLOGY

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2
Q

NURSING PROCESS

A

ASSESSMENT
DIAGNOSIS
PLANNING
IMPLEMENTATION
EVALUATION

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3
Q

ASSESSMENT

A

COLLECTION

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4
Q

DIAGNOSIS

A

ANALYSING COLLECTED DATA

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5
Q

PLANNING

A

GENERATE SOLUTION/PLAN

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6
Q

IMPLEMENTATION

A

TAKING ACTIONS/IMPLEMENT PLAN

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7
Q

EVALUATION

A

ASSESSING OUTCOMES

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8
Q

PATIENT PROBLEM

A

DIAGNOSIS

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9
Q

Holistic view rather than disease model
➢ Include preventive, primary, acute and chronic
health care among all ill patients
➢ Organizing patient’s HEALTH PROBLEM
➢ Then taking necessary actions by using the
nursing process

A

CONCEPT

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10
Q

Gathers info (subjective and objective data)
➢ Nurse perform complete systemic assessment,
adding on query related to illness and drug
regimen
➢ Info can be from patients, relative, health
provider and medical records

A

ASSESSMENT

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11
Q

Provided verbally by patients or thru fam
members, friends and other sources
➢ Nurse can ask open ended questions
▪ Current health hx/fam hx
▪ Symptoms or even signs he/she
experienced
▪ Discussion of his health concern,
medications/SE, OTC remedies used,
nutritional supplements, herbal medicines,
contraception
* Attitude and beliefs about taking Rx
* Allergies
* Financial barriers
* Tobacco use, alcohol/caffeine
* Caregiver and support system
(compliance/SE monitoring/notifiers)

A

SUBJECTIVE

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12
Q

➢ What nurses directly observe from the
consultation period
➢ Collecting data from personal senses (hearing,
seeing, smell, touch)
➢ Provide additional information about the
symptom
▪ Target organ most likely to be affected
▪ PE, VS, Patient’s body language
➢ Correlation with laboratory work-ups reviewed

A

OBJECTIVE

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13
Q

➢ Based on analysis of the assessment
➢ Determines the type of care the patient shall
receive
➢ Nurse formulates the patient problem which
will guide on the development of plan of care
➢ Ex: of common patient problem related to drug
therapy:
▪ abdominal pain
▪ Vivid dreams\confusion
▪ Decrease adherence
▪ Hesitancy

A

PATIENT PROBLEM

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14
Q

➢ Data are used to set goals and plans
➢ Goals: patient centered, realistic, specific, with time
frames, measurable for achievement and
reevaluation
➢ Development of nursing intervention that will be
both acceptable to patient and nurse
➢ Ex:
▪ the patient will independently administer the
prescribed doses per day of insulin after 4th
session of instruction
▪ The patient will prepare medication recording
sheet after second session of instruction

A

PLANNING

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15
Q

➢ Part of nursing process, where nurses provide
EDUCATION, DRUG ADMINISTRATION,
PATIENT CARE AND OTHER INTERVENTION
necessary to assist the patient in accomplishing the
establish medication goal
➢ Nurse’s role: administering medications and
monitoring its effectiveness

A

IMPLEMENTATION

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16
Q

➢ Patient teaching/when to learn/where to learn, is it
conducive (comfortable and quiet)
➢ ▪ Know obstacles:
▪ pain must first be relieved,
▪ Language barrier
▪ Age (young or elderly)
➢ Patient teaching is very important to patient’s
recovery (both parents and relatives or caregivers)
*side effects
➢ General information shall be provided on how to
take the drug
▪ Written information or instruction shall be
provided (Patient teaching card)
* Name of drug
* Reason for taking the Rx
* Time sched when to take the medicines
* Possible side effects/adverse events
* Notification of HCP if side effects
occur
* Health care provider’s telephone
number
* Warning information (pregnant, not to
take with alcohol)

A

NURSE RESPONSIBILITIES

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17
Q

➢ Give instructions on what SE will be expected
➢ what will help minimize it
➢ Eg: change in the color of urine/stool, counsel on
dizziness after intake, orthostatic hypotension etc

A

SIDE EFFECTS

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18
Q

➢ Perform assessment of patient’s motor skills and
abilities so as to provide modifications that will be
necessary which will be added in the teaching plan
➢ ROUTE
➢ Use of drug cards

A

SELF ADMINISTRATION

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19
Q

➢ Advise on food to include and to avoid
➢ Many foods interact with certain medications
▪ Can decrease drug absorption, increase risk
of toxicity or create other problems

A

DIET

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20
Q

OTHER IMPORTANT NURSING CONSIDERATIONS: DECS

A

➢ Drug allergies
➢ Expiration
➢ Cultural beliefs/ religious
➢ Additional:
▪ Flexibility of timing schedule (WORK
SCHEDULE ETC)
▪ Use of pill box if with multiple drugs or
recording sheet
▪ Evaluation of understanding re: regimen in
a regular basis
▪ Empower patients re responsibility to take
their pill
▪ ID patients with risk of noncompliance

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21
Q

➢ Determine if whether goals has been met through
improvement of complaint and evaluation of
objective data

A

EVALUATION

22
Q

PROCESS OF BRINGING A NEW
PHARMACEUTICAL DRUG TO THE MARKET

A

DRUG DEVELOPMENT

23
Q

DRUG DEVELOPMENT PROCESS

A

BASIC RESEARCH
PRE-CLINICAL
CLINICAL STUDIES (3 PHASES)
APPROVAL
POST-CLINICAL

24
Q

PHARMACEUTICAL RESEARCH

A

FDA AND BFAD

25
Q

➢ Done prior to the implementation of the clinical
trials (using human subjects)
➢ Determine TOXIC and PHARMACOLOGICAL
efficacy through/using ANIMAL TESTING in a
laboratory
➢ Able to determine genotoxicity (damage genetic
information in a cell in addition to drug absorption,
distribution, metabolism and excretion

A

PRE-CLINICAL TRIALS

26
Q

: help to establish guidelines in
including women/minorities in clinical trials and that to
be included in appropriate numbers in National Institute
of Health -supported researches

A

NIH REVITALIZATION

27
Q

➢ Multidisciplinary team approach (nurses,
physician, pharmacologist, statistician and
➢ research associates)
➢ Required to ENSURE SAFETY and QUALITY in
all phases of the clinical trial

A

HUMAN EXPERIMENTATION

28
Q

Small group of people /First time to
evaluate safety (dosage range) and side
effects

A

PHASE 1

29
Q

Larger group to see if its effective,
further evaluate safety (used in larger
group)

A

PHASE 2

30
Q

Large group confirm
EFFECTIVENESS, MONITOR SIDE
EFFECTS, COMPARE WITH COMMONLY
USED KNOWN TREATMENTS/Collect
information that will allow the drug to be used
safely

A

PHASE 3

31
Q

Drug effect studies after it has been
marketed (effects in various population,
assess side effects associated with LONG
TERM USE

A

PHASE 4

32
Q

CORE ETHICAL PRINCIPLES/GUIDELINES FOR RESEARCH INVOLVING HUMANS

A
  1. RESPECT FOR PERSON
  2. BENEFICENCE
  3. JUSTICE
33
Q
  1. RESPECT FOR PERSON
    ➢ Incorporates at least two ethical convictions
A
  1. SHOULD BE TREATED AS AUTONOMOUS AGENTS
  2. PERSONS WITH DIMINISHED AUTONOMY ARE ENTITLED TO PROTECTION
34
Q

The principle of respect for persons thus divides
into two separate moral requirements:

A

the requirement to acknowledge autonomy and the
requirement to protect those with diminished
autonomy.

35
Q
  • Right to refuse to participate in a research
  • Right to withdraw anytime without penalty
A
  • Right to refuse to participate in a research
  • Right to withdraw anytime without penalty
36
Q

➢ Integral part of respect for person
➢ Should have decision of their own
➢ Patient can refuse any or all treatment except
decision will pose threat to others
➢ Right to refuse to participate in a research study
➢ Right to withdraw from study at anytime without
penalty

A

AUTONOMY

37
Q

➢ Roots: Nuremberg Code in 1947 (Right to be
informed and that participation is voluntary,
➢ without coercion
* Need to sign the informed consent
* If with legal age; but if 12-15 years old: needs
assent form
* Children 11 and below: with parents consent
➢ If coercion is suspected, nurses are obligated to
report it promptly
➢ Health care provider need to explain what is
expected; respond to query
➢ Provided with Inclusion and exclusion criteria,
study protocol, study related documentation

A

INFORMED CONSENT

38
Q

INFORMED CONSENT CHECKLIST:

A

➢ Statement that the study involves research
➢ Purpose of the study, explanation
➢ Duration of participation
➢ Id, description of procedures and experiments
➢ Description of reasonable foreseeable
risk/discomfort and benefits
➢ Disclosure of appropriate alternative
procedure/courses of treatment or courses of
treatment if any
➢ Confidentiality records and to what extent
➢ Explanation of any compensation or whether any
medical treatment is available when injury occurs
➢ Contact person to answer when with query
➢ That the participation is voluntary

39
Q

➢ Duty to protect the research subjects from harm
* Ensures risk and possible benefits in
participating to the study were divulge during
orientation
➢ RISK BENEFIT RATIO
* Risk benefit ratio is one of the most complex
problems faced by the researcher
* Benefits > Risk or vise versa
➢ No matter how noble the intentions > calculation of
risk
* Requirement of Dept of Health and Human
Services: Institutional Review Boards

A

BENEFICENCE

40
Q

➢ Selection of research subject shall be FAIR
➢ Research are conducted so that the distribution of
benefits and burden is equitable
* Justice requires the fair and equal distribution
of benefits and risks of participation in a
research study.
* Recruitment and selection of participants must
be done in a fair and equal manner.
* Justice forbids exposing one group of people
to the risks of the research solely for the
benefit of another group. *Community
representatives have the responsibility to ensure
that community participation in a research
study is justified.
➢ Appropriate protections for research participants
(pay special attention to the benefits that the
➢ participants or their communities will receive as a
result of their participation in the research and
➢ advise the research team so that incentives offered
by the research will not influence the decision
➢ to participate.

A

JUSTICE

41
Q

Nurse foremost duty is to care for the patient

A

FLORENCE NIGHTINGALE PRINCIPLE

42
Q

responsible for BOTH the safety of the
subjects/patients and integrity of the research
protocol

A

NURSE

43
Q

➢ Nurse (key creating a culture of
safety/accountability related to controlled
substances
* Verification of orders before administration
* Accounting of all controlled drugs
* Documentation of all discarded/waste
medications; patients record after
administration
* Keep all controlled drugs in a locked storage
area (narcotics under double lock)

A

COMPREHENSIVE DRUG ABUSE PREVENTION AND CONTROL ACT (1970)

44
Q

S2 License is solely given to
any authoritative person who is acknowledged by
law that can prescribe dangerous drugs.
* This group of professionals who can prescribe
regulated drugs are physicians,
veterinarians, and dentists

A

S2 PRESCRIPTION

45
Q

➢ This Act, consisting of 15 sections
➢ Declares the policy to promote, require and ensure
the production of adequate supply, use and
acceptance of drugs (including for animal use)
identified by their generic names.
➢ Its objectives are: to PROMOTE, ENCOURAGE
AND REQUIRE THE USE OF GENERIC
TERMINOLOGY IN THE IMPORTATION,
MANUFACTURE, DISTRIBUTION,
MARKETING, ADVERTISING
AND PROMOTION, PRESCRIPTION AND
DISPENSING OF DRUGS; to ensure the
ADEQUATE SUPPLY OF DRUGS WITH
GENERIC NAMES AT THE LOWEST
POSSIBLE COST;
➢ To encourage the extensive use of drugs with
generic names through a national system of
procurement and distribution; to emphasize the
scientific basis for the use of drugs; and to promote
drug safety by minimizing duplication in
medications and/or use of drugs with potentially
adverse drug interactions.

A

GENERIC ACT OF 1988 (RA 6675)

46
Q

➢ Generally: Nurses cannot prescribe or administer
drugs WITHOUT A HEALTH PROVIDER
ORDER
➢ License revocation if found to administer without
order
➢ Can be prosecuted for giving the wrong
drug/dosage/ omitting a drug dose or giving a drug
by a wrong route

A

NURSE PRACTICE ACTS

47
Q

➢ Worldwide, estimated as >10% of all drugs
available are counterfeit/fake
➢ May contain incorrect ingredient, insufficient
amount of active ingredient, no active
➢ ingredient, contain impurities and
contaminants/distributed in fake packaging
➢ Nurse to instruct patients to report any differences
in taste or appearance of the drug or
➢ its packaging

A

DRUG COUNTERFEITING (>10%)

48
Q

must be approved by FDA BEFORE
THEY CAN BE MARKETED
➢ Non proprietary; universally accepted
➢ Not owned by any drug company
➢ Given in “Lower case letters”

A

GENERIC NAME

49
Q

➢ Proprietary name
➢ Chosen by drug company, usually a registered
trademark
➢ Always begin with a capital letter

A

BRAND NAME

50
Q

➢ Over-the-counter medicine, also known as OTC or
nonprescription medicine, refers to medicine that
you can buy without a prescription.
➢ Nonprescription or OTC drugs are medicines the
FDA determines are safe and effective for use
without a doctor’s prescription
➢ OTCs often do more than just relieve aches, pains,
and itches. Some can prevent diseases like tooth
decay [2], cure diseases like athlete’s foot [3], and
help manage recurring conditions like vaginal yeast
infections [4] or migraines [5].
➢ ***It is the US Food and Drug Administration
(FDA) that determines whether medicines are
prescription or nonprescription.
➢ The term prescription refers to medicines that are
safe and effective when used under a doctor’s care,

A

NON-PRESCRIPTION DRUGS

51
Q

OTCs- In 2002, the FDA standardized the OTC
labeling to provide consumers with better information
And describe benefit and risk associated with taking this
OTD

A

➢ Vitamins
➢ Colds prep
➢ Analgesic
➢ Antacids
➢ Laxatives
➢ Antihistamines
➢ Sleep aids
➢ Nasal Sprays
➢ Weight control drugs
➢ Drugs for dermatitis/fungal infection
➢ Fluoride toothpaste
➢ Corn and callus removal products
➢ Herbal Products

52
Q

NURSING CONSIDERATIONS RELATED TO
OVERTHE-COUNTER DRUGS (ADVISE
AMONG PATIENTS)

A

➢ Always read instructions on the label (if not
understood-ask pharmacist)
* Do not use medicines without label
➢ Do not take OTC drugs in higher doses or longer
than label states
➢ Re side effects (though relatively uncommon)
➢ Every person is different, hence responses can also
be different
➢ Drugs may interact with each other/ food/
alcohol/may have effect in other health problem
➢ Throw away expired medicines (throw discolored,
old or those that lost its label)
➢ Children: do not guess amount to be given/ if
instructed to be in ml use ml graduated cups/ follow
➢ age limits
* Always use child resistant cap and relock
* No medicines with alcohol