Tuesday, September 13, 2022
SYSTEMIC DRUG THERAPY
SYSTEMIC DRUG THERAPY
SYSTEMIC DRUG THERAPY
SURGICAL THERAPY
SKIN SURGICAL TECHNIQUES
PSYCHOTHERAPY
PREVENTIVE MEDICINE
MUSIC THERAPY
LOCAL DRUG THERAPY
Pharmacy: What is it?
DEPARTMENT OF PHARMACY PRACTICE IN HOSPITAL
DEPARTMENT OF PHARMACY PRACTICE IN HOSPITAL
DEFINITION:
“The practice of pharmacy within the hospital under the supervision of a professional
the pharmacist is known as hospital pharmacy”
WHAT THE HOSPITAL PHARMACY DOES?
Predicting demand
Identifying trustworthy vendors
Preparation of sterile or non-sterile preparations
maintenance of Manufacturing records
Quality control of purchased or manufactured products
Distribution of medicaments in the wards
Dispensing of medicaments to out-patients
Implement the pharmacy and therapeutic committee's recommendations
Provide patient counselling
Maintain communication between medical, nursing, and the patient.
Center for medication utilization studies.
AIMS OF HOSPITAL PHARMACISTS' WORK:
1. To improve the quality and efficiency of hospital pharmacy services.
2. To ensure that the prescribed drug is available at a reasonable cost and at the right
time.
3. To organize the pharmacy's policies and put them into action.
4. To perform functions of management of material, purchase, storage of essential
items.
5. To keep track of everything that is received or given out.
6. Advise the patient and anyone associated in their care about the proper use of
medications, as well as any risks, side effects, toxicity, or other negative effects.
7. In order to act as a resource for drug usage data
8. Large and small volume parenterals, which are crucial to patient care, must be
manufactured.
9. To be a member of the pharmacy and therapeutics committee and to help carry out
their recommendations.
10. To plan and participate in educational and research initiatives.
11. To educate the patient's care team about the numerous facets of drug action,
administration, and usage, including: 11.
12. Participate in public health activities to help the general public's health.
13. Involvement with other hospital departments, cooperation, and coordination
INFRASTRUCTURE
Ground floor or first-floor location.
Sufficient space to accommodate patients' sitting needs.
Outpatients' waiting room with Posters on health and cleanliness should be provided, as
should reading material.
Adequate room for routine production of bulk medicines (stock solutions, bulk powders
and ointments etc.) is required.
a chief executive officer's office
Labeling and packaging of drugs area.
Cold storage area
Inquiry wing
Pharmacy store room
The Library
Radio Isotope Dispensing and Storage area
FLOW OF MATERIALS
Requisition or an indent Medications and other supplies are needed for this.
Keep track of stuff you've received.
Distributes medication to in- and out-patients via the outside pharmacy and nursing
station, respectively.
FINANCES
1. The patient's bills are the primary source of payment.
2. Either the patient or a third party pays for the services he or she receives.
3. Research work
4. Endowment money that have been put to use
5. Investing in other ways
6. Payment of general operating expenses by way of gifts or other sources
ROLES AND RESPONSIBILITIES OF HOSPITAL PHARMACIST INDOOR PHARMACISTS
a) Central dispensing area:
1. To ensure that all medications are correctly maintained and delivered.
2. To ensure that the doses prepared are accurate.
3. Keep accurate records.
4. Preparation of bills
5. Coordinate the patient's entire pharmaceutical needs 6.
7. Maintain a high level of professionalism and expertise 8. Maintain open lines of
communication with all pharmacy staff members.
b) Patient care areas
1. To keep in touch with the nurses
2. Taking a closer look at how drugs are administered.
3. Assist the junior pharmacist and direct patients to the appropriate areas:
4. Identifying the medications that were taken into the hospital
5. obtaining a history of the patient's medication
6. Encourage patients to make their own medicinal product choices
7. Follow-up on a patient's complete drug regimen
8. Taking care of patients' mental health issues
9. Assisting in the treatment of cardiac and respiratory emergencies
c) General duties:
1. First, make certain that all medications are handled correctly.
2. Participate in cardiac and pulmonary emergencies
3. to provide training and instruction for pharmacists.
RESPONSIBILITIES OF AN OUTPATIENT PHARMACIST
This is where the bulk of the products are sold.
a) Central dispensing area:
1. To make certain that all medications are correctly maintained and administered.
2. To ensure that the doses prepared are accurate.
3. Keep accurate records.
4. Preparation of invoices
5. Maintains a clean and orderly pharmacy.
b) Patient care areas
1. The pharmaceutical regions should be inspected on a regular basis.
2. Recognize the medications that have been delivered into the hospital.
3. The tracking of medications
4. Offer guidance to the patients.
c) General responsibilities:
1. First, make certain that all medications are handled correctly.
2. Participate in cardio-pulmonary emergencies
3. The next phase is to provide training and instruction for pharmacists.
4. Coordinate outside service's overall pharmacological needs.
HEALTH CARE SERVICES MANAGEMENT
FAMILY MEDICAL CARE
HEALTH-CARE COSTS
HEALTH-CARE COSTS
Providing
health care comes at a high cost to the national economy, and that cost has
been rising rapidly in countries like the United States, Germany, and Sweden;
in Britain, the rise has been slower. Both industrialized and developing
countries have expressed serious concern about this development. A large part
of this fear stems from the absence of consistent data to support the idea that
more health care spending will result in better health. Countries in the
developing world are pushing to replace the health-care system that developed
under European colonialism with one that is more affordable and more suited to
their needs.
For both
private and public health-care delivery systems, rising costs have prompted a
review of policies and a search for more cost-effective ways to accomplish
their objectives. Despite the money spent, health services aren't always used
efficiently by those who need them, and the results might vary greatly from
community to community, despite the expenditures. There was a 24% drop in
deaths in Britain's most wealthier areas between 1951 and 1971 compared to a
16% drop in the most impoverished areas of society. More than only the quality
of medical care affects one's ability to stay healthy. Well-being encompasses
all of the above, in addition to adequate living and working conditions and
enough access to social services.
IN THE
DEVELOPING NATIONS:
Culturally,
socially and economically, developing countries differ greatly from developed
countries, but they all have a low average income per person and huge
percentages of their populations living below the poverty line. The majority of
their inhabitants reside in rural areas, despite the fact that most have a
small elite class that lives mostly in the city. During the mid- and late-20th
century, pockets of slums appeared in urban areas in emerging and some
developed countries due to an increase in rural peoples and immigrants. In the
21st century, improved, cheaper construction methods allowed for the production
of inexpensive homes in highly crowded areas like New York City and cities in
India, reducing some of the city's housing woes. Some cities are simply too
congested to keep public health under check, though. Thousands of urban and
rural poor die each year from avoidable and curable diseases, generally linked
to inadequate hygiene and sanitation, contaminated water supplies,
malnutrition, vitamin deficiency, and chronic preventable infections, due to a
lack of even the simplest steps. In the 1980s, life expectancy at birth for men
and women in Africa was roughly one-third lower than in Europe, and infant
mortality in Africa was about eight times higher than in Europe. These and
other deprivations are reflected in the findings. As a result, emerging countries
place a great focus on expanding primary health care.
Lacking
adequate resources, developing countries have often been unable to establish or
implement the plans necessary to offer basic services at the village or urban
poor level. They are. Health care systems that work in one country may not work
in another, and this is becoming increasingly apparent. Research has shown that
a country's unique circumstances, people, culture, philosophy, and economic and
natural resources all have a role in providing high-quality health care.
More and
more developing countries are promoting services that use less highly qualified
primary health care workers who may be deployed more broadly in order to cover
the widest possible range of people. Undernutrition, infection,
gastrointestinal illnesses, and respiratory symptoms are some of the most
pressing medical issues in the developing world, all of which may be traced
back to factors like poverty, ignorance, and poor hygiene. It's not difficult
to recognize and treat them in most cases. Preventive measures, on the other
hand, are usually easy and inexpensive. There is no need for specialized
training in most circumstances; the phrase "primary health worker"
encompasses all nonprofessional members of the healthcare team.
IN
DEVELOPED NATIONS:
Health care
providers in the industrialized world face a distinct set of challenges than
those in developing countries. While many diseases that once ravaged the Third
World have been eliminated or are easily curable, many others remain
unaffected. Environmental and public health threats have been reduced or
eliminated. A wide range of social services, varied in quality, have been made
available. Public monies are available to help pay for medical expenses, and
private insurance policies are also an option. In spite of this, governments
have a finite amount of money to spend on health care, and the rising expense
of modern medicine means that many people will be unable to afford effective
treatment. The growing need for more money for health education and prevention
initiatives targeted at the poor raises the overall cost of modern medical
care.
What is PHARMACOTHERAPY |
PHARMACOTHERAPY
Basic characteristics
·
How drugs are absorbed into the body and distributed?
Pharmacokinetics is the study of how pharmaceuticals travel
through the body, including absorption, distribution, tissue localization,
biotransformation, and excretion. Pharmacodynamics refers to the study of how
medications work and the impact they have on the body. Absorption and
distribution in the body are prerequisites for a drug's effectiveness.
Intestinal absorption of drugs taken orally can vary widely, with some taking
longer to be absorbed than others. It is possible to decrease the rate of
absorption of even the most rapidly absorbed medications such that they can
remain effective for up to 12 hours or more. Intravenous or intramuscular
administration of drugs circumvents absorption issues, however, accurate dosage
calculations are still essential.
The same medicine can have various effects on different
people. Drug metabolism and excretion may be slower in the elderly due to
decreased renal and liver function. As a result of these and other reasons,
elderly patients typically require lesser doses of medication.
The existence of the disease, nutrition, heredity, and the
presence of other medicines in the system can all influence a person's response
to medication. In addition, just as everyone's tolerance for pain differs, so
does the body's reaction to the medication. In certain cases, bigger doses are
required, while in other cases persons who are extremely sensitive to
medications experience negative effects at lower amounts than others.
As intestine motility and gastric acidity decline with age,
infants and children may absorb nutrients at different rates than adults.
Premature newborns, who have less fat tissue and a higher proportion of water
in their bodies, may have a distinct pattern of drug distribution. During
childhood, metabolic rates, which influence pharmacokinetics, are substantially
higher. Children's medication dosages are typically based on their weight (in
milligrams per kilograms) or their surface area (in square centimeters)
(milligrams per square meter). Children of the same age can have a broad range
of sizes, which makes it difficult to determine how much a medicine should be
given depending on the child's age. For children, drug dosages may be
considerably different from those for adults because they are not miniature
adults.
Taking several drugs, some of which may be incompatible with
others, makes the elderly particularly vulnerable to the side effects of
pharmaceuticals, and this makes them more likely to have drug interactions that
are harmful to their health. Gastric acid production and arteriosclerosis
restrict the arteries, reducing blood flow to the digestive tract and other
organs, as we get older. It is a good example of the principle that should
guide all drug therapy—drugs should be administered in the lowest effective
dose, especially because adverse effects rise with concentration—in
prescription medication to the elderly. Elderly people often have poorer
tolerance for small side effects, which younger people may not even notice, due
to illness or frailty.
Repeated dosages of medication ensure that the amount
delivered and the amount excreted or metabolized are equivalent. Because of
individual differences, it may be difficult to identify the correct dosage for
some medications. If the therapeutic window (i.e., the concentration above
which the medicine is hazardous and below which it is useless) is relatively
limited, assessing the plasma level of the drug may be informative. It is
common practice to keep an eye on the blood levels of drugs like phenytoin,
digitalis, and lithium, which are used to treat bipolar disorder and treat
seizures, in order to assure their safety.
INDICATIONS FOR USE
In order to alleviate symptoms, treat infection, lower the
risk of future sickness, and destroy targeted cells, such as in the
chemotherapeutic treatment of cancer, medications are used. There may be
no need for a medicine at all in some cases. As vital as deciding which drug to
take, it is also crucial to recognize that there is no effective medication out
there. In situations where more than one drug is beneficial, doctors choose the
one that is most effective and least harmful to patients. A new medicine may
promise better results, but it may also be more expensive and unpredictable.
In addition to the organs and systems to which it is
explicitly addressed, every medication has many functions. Patients may also
have idiosyncratic effects (abnormal reactions unique to that individual) and
allergic reactions to some treatments, which are further indications of the
need to pick drugs carefully and avoid their use altogether when simpler
procedures can be implemented instead. Consider the widespread notion that
antibiotics such as penicillin may treat viral infections, which simply isn't
true. Antibiotics should only be used when absolutely necessary, as new
antiviral medications are now being developed. There is a growing number of
drug-resistant organisms that need to be countered by cautious use of these
substances.
The risk of drug interactions, which can reduce a drug's
effectiveness, rises when it is taken in excess. It is possible that a drug's
presence in the stomach or intestines will affect the absorption of another.
Tetracycline's absorption is decreased by antacids, which generate insoluble
complexes. The interfering effects of one medicine on another are of increasing
consequence. If a drug inhibits the metabolism of another drug, it permits the
drug to accumulate in the body, increasing the risk of toxicity in the absence
of a reduction in the dosage. Many medicines that require microsomal enzymes in
the liver to be digested are increased in quantities after taking Cimetidine, a
medication used to treat peptic ulcers. If the other medicine is warfarin, this
inhibition can be dangerous. If the dosage is not lowered, bleeding may occur.
A wide range of other medications are also impacted, including
antihypertensives (like calcium channel blockers), antiarrhythmics (like
quinidine), and anticonvulsants (like phenytoin) (e.g., phenytoin). The
excretion of one drug may be reduced by the excretion of another. Penicillin's
elimination is decreased when probenecid is given with it, which raises the
blood level of the antibiotic as a result. The combination between quinidine
and digoxin, a medication used to treat heart failure, can impede the drug's
clearance, elevating the concentration to potentially lethal levels. Toxic
effects can also be caused by the combination of two medications, despite the fact
that either one on its own would be beneficial.
When a patient is being treated by more than one doctor, it
is possible that one of those doctors is unaware of the medications that the
other has given. It is not uncommon for a doctor to give medication to
alleviate a side effect of another medication. It's better to stop taking the
first medication than to start taking another one that has unknown negative
effects. Most often, a recently started medication is suspected as the cause of
a new symptom before any other possibilities are explored. Patients should
notify their doctors of any new medications they are taking and speak with
their pharmacists about the possibility of nonprescription medications
interfering with any prescription medications they are currently taking.
Patients who have a personal physician who checks all of their medications,
prescription and over-the-counter, should do so.
The Food and Drug Administration (FDA) oversees the safety
and efficacy of prescription pharmaceuticals in the United States (FDA). New
pharmaceuticals are approved, indications are identified, formal labelling is
put in place, and adverse responses are monitored. Methods of manufacture are
also approved. Submission and approval by the FDA are required before INDs can
be tested in humans. Clinical studies must be completed before an NDA can be
filed and a medication can become available for sale. Normally, this takes
years, but if the drug helps people with life-threatening illnesses when
existing treatments don't, it may be approved faster. An unapproved medicine
can be prescribed to a single patient with the authorization of a physician. A
patient may be given emergency usage or compassionate use if there is no
alternative treatment option available and the patient's life is in danger. If
a life-threatening emergency warrants it, the FDA may also approve the
acquisition of medications from foreign nations that are not currently
available in the United States. Participating in a clinical trial is another
way to get your hands on an experimental medicine. An "open study,"
in which the investigator is not "blinded" and knows which subjects
and controls are being studied, increases the probability that the patient will
be given a placebo instead of a medicine that works. Food, over-the-counter
medications, and cosmetics are all subject to "truth in advertising"
regulations by the Federal Trade Commission (FTC).
Other countries and governmental bodies have similar drug
regulation agencies. Like the FDA in the United States, the Chinese government
has its own regulatory agency for pharmaceuticals, medical devices, and
cosmetics. Medicines are approved by the European Medicines Agency, which also
oversees the scientific evaluation of medicines and keeps tabs on the safety and
efficacy of those sold within the European Union's member countries.
As a result of the limited patient population, it is not
economically feasible for pharmaceutical companies to go through the lengthy
and expensive regulatory and marketing processes required for treatments for
rare diseases. The Orphan Drug Act of 1983, enacted in the United States to
encourage the development of treatments for uncommon diseases, makes these
medications available to the public.
The term "controlled substance" refers to drugs
that can lead to addiction and abuse. Their production, prescription, and
dispensing are all subject to DEA regulation in the United States. Based on
their misuse potential and physical and psychological dependence, controlled
substances are classified into five schedules. There is no recognized medical
purpose for any of the medications included in Schedule I, which includes
heroin and other narcotics with a high potential for misuse. Narcotics like
opium and cocaine as well as stimulants like amphetamines fall under the
category of Schedule II substances because of the great potential for abuse and
dependence they carry. Barbiturates, sedatives, and preparations containing
only a small amount of codeine are all included in Schedule III, as is a small number
of stimulants and depressants. Some sedatives, antianxiety medications, and
nonnarcotic analgesics are included in Schedule IV because of their low abuse
and dependence potential. Even more so than schedule IV substances, Schedule V
pharmaceuticals have a lesser potential for abuse. A prescription is not
required for some medications, such as cough syrups and antidiarrheal
medications having a little quantity of codeine in them. Any restricted
substance prescribed by a physician must have a DEA registration number on
file. It is not possible to replenish a patient's supply of schedule II
medicines without a fresh prescription in several states, where special
triplicate prescription forms are necessary. Countries and international
territories like the European Union, where the European Drug Enforcement Agency
(EDA) is in charge of combating illegal drug usage and trafficking.
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