The document discusses various vaccines including BCG, oral polio, DPT, measles, hepatitis B, tetanus toxoid, and rabies. It defines key terms like vaccine, toxoid, and immunity. For each vaccine, it describes aspects like dosage, administration method, schedule, storage requirements, effectiveness, complications and contraindications. The aim is to educate on different vaccine types and their proper use to induce immunity against diseases.
This ppt contains all the information about the Immunizing agents - Vaccines, Immunoglobulines and Antisera. It is useful for students of the medical field learning Preventive and social medicine, Swasthavritta (Ayurved), and everyone who is interested in knowing about it
Immunization is one of the best public health intervention to prevent morbidity as well as mortality. it also help in prevention of malnutrition in young children.still developing countries are trying hard to make it universal. in india lot of changes have taken place in the immunization schedule and number of newer vaccines have been incorporated. still the awareness as well as acceptability is not universal . this presentation is very basic and will help students as well as teachers. we all have to join hands to make it universal
describing the case definitions, prevalence,modes of transmission,clinical features and presentations,treatment and prevention as a whole of common infectious diseases- small pox,chicken pox, measles, rubella
This ppt contains all the information about the Immunizing agents - Vaccines, Immunoglobulines and Antisera. It is useful for students of the medical field learning Preventive and social medicine, Swasthavritta (Ayurved), and everyone who is interested in knowing about it
Immunization is one of the best public health intervention to prevent morbidity as well as mortality. it also help in prevention of malnutrition in young children.still developing countries are trying hard to make it universal. in india lot of changes have taken place in the immunization schedule and number of newer vaccines have been incorporated. still the awareness as well as acceptability is not universal . this presentation is very basic and will help students as well as teachers. we all have to join hands to make it universal
describing the case definitions, prevalence,modes of transmission,clinical features and presentations,treatment and prevention as a whole of common infectious diseases- small pox,chicken pox, measles, rubella
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
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Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
2. Definitions
VACCINE-suspension of attenuated live or
killed microorganisms administered to
induce immunity
TOXOID-modified bacterial toxin,now non-
toxic,which stimulates formation of
antitoxins
IMMUNITY-resistance of a body to the effects
of a deleterious agent, such as pathogenic
microorganism
3. Types Of Vaccines
Live Attenuated Vaccines
Inactivated Vaccines
Toxoids
Sub-Unit Vaccines
Conjugate Vaccines
DNA Vaccines
4. BCG Vaccine
Calmette and Guerin, two French scientists
began attenuating avirulent strain of M.Bovis
on 1906.
After 230 subcultures over a period of 13
years, they were able to evolve a strain
known as bacilli Calmette Guerin or BCG.
The WHO has recommended the ‘Danish
1331’ strain for the production of BCG
vaccine.
5. AIM
The aim of BCG vaccination is to induce a
benign, artificial primary infection which will
stimulate an acquired resistance to possible
subsequent infection with virulent tubercle
bacilli.
6. Types of Vaccine
There are 2 types of BCG vaccine.
1) The liquid (fresh) vaccine
2) The freeze-dried vaccine
The freeze-dried vaccine is more stable
preparation than liquid vaccine.
Present day vaccines are distributed in the
freeze-dried form
7. Dosage
For vaccination,the usual strength is 0.1 mg
in 0.1 ml volume.
The dose for newborn aged below 4 weeks is
0.05ml.
( This is because the skin of the newborn is
rather thin and intradermal injection with full
dose 0.1ml might penetrate into deeper tissue
and give rise to local abscess formation and
enlarged regional lymph nodes.
8. Administration
The vaccine is injected intradermally using a
‘Tuberculin’ syringe
The site of injection should be just
above the insertion of the deltoid
muscle
A satisfactory injection should produce a
wheal of 5mm in diameter.
9. Age
BCG should be administered very early in
infancy either at birth ( for institutional
deliveries) or at 6 weeks of age.
BCG administration early in life provides a
high level of protection,particularly against
the severe forms of childhood tuberculosis
and tuberculous meningitis.
10. Complications
Prolong severe ulceration at site of
vaccination.
Suppurative lymphadenitis.
Osteomyelitis.
Disseminated BCG infection.
Death
11. Protective Value
The duration of protection is from 15 to 20
years.
Studies have shown that the range of
protection offered by BCG varied from 0 to
80 % in different parts of the world.
12. Contraindications
Should not be given to people suffering from
1) Generalised eczema
2) Infective dermatitis
3) Hypogammaglobulinaemia
4) Deficient Immunity
5) Leukemia
6) Lymphoma
7) General malignant diseases
8) In pregnancy.
13. Oral Polio Vaccine
Oral polio vaccine was described by Sabin in
1957.
It contains live attenuated virus types 1, 2 and
3 grown in primary monkey kidney or human
diploid cell cultures.
For administrative convenience the Trivalent
(TOPV) vaccine is given.
14. Dosage
• The dose is 2 drops.
WHO recommends that vaccinators use
dropper supplied with the vial of oral polio
vaccine as this is the most direct and effective
way to deliver the correct drop size.
15. Administration
The back of the child is tilted and gently squeeze
the cheek or pinch the nose to make the mouth
open.
The drop is allowed to fall on
the child’s tongue from the
dropper.
The OPV induces both local and systemic
immunity.
16. Advantages of OPV
Does not require the use of highly trained
personnel.
Induces both humoral and intestinal immunity.
Antibody is quickly produced in a large
proportion of vaccines.
The vaccinee excretes the virus and so infects
others who are also immunised
thereby
(i) Useful in controlling epidemics
(ii) relatively inexpensive.
18. Contraindications
Live vaccine is not usually given to
immunocompromised individuals.
Leukemia
Malignancy
On corticosteroids therapy
19. Storage
Sterilised vaccine should be kept at +4oc for a
year and at +25oc for a month
Non-sterilised vaccine should be kept at -20oc
in deep freeze.
20. DPT Vaccine
It gives protection against 3 diseases
1) Diphtheria
2)Pertusis
3)Tetanus
The vaccine is a toxoid preparation of 2 types
1)Plain
2) Absorbed
Has a protective efficacy of 85%
21. Dosage and Administration
0.5ml is available
Administrated in deep intramuscular
injection in upper and outer aspect of thigh.
23. Adverse Reaction
Fever
Mild local reactions
Pain
Swelling
Induration at site of injection
Neurological complications (encephalitis)
Encephalopathy
Convulsion
Reye’s syndrome
24. Contraindications
Severe reaction to previous dose like:
Collapse
Shock
Persistent screaming
Convulsions
Other neurological and anaphylactic
reactions
25. Measles Vaccine
Only live attenuated vaccines are
recommended for use.
Presented as a freeze-dried product.
Before use, the vaccines is reconstituted with
sterile diluent.
26. Dosage
0.5ml single dose given subcutaneously at 9
months old.
Suspected contacts are
immunised with vaccine
within 3 days of exposure
27. Storage
Kept at 20-80C in dark, refrigerated in freeze
compartment.
The vaccine in sensitive to sunlight, hence it
is kept in coloured vials.
29. Reactions
When injected, the attenuated virus
multiplies and induces a mild ‘measles’
illness (fever and rash) 5-10 days after
immunization
Fever may last for 1-2 days and rash 1-3 days.
30. Immunity
It develops within 11-12 days after vaccination
and usually persists for life
33. Hepatitis B Vaccine
The recombinant hepatitis B vaccine was
introduced in 1986.
The active substance in recombinant
hepatitis B vaccine is HBsAg.
34. Dosage
Adult dose is 10-20 mcg initially (depending
on formulation) and again at 1 and 6 months.
Children under 1o yrs of age should be given
half of the adult dose at the same time
intervals.
35. Administration
For greatest reliability of absorption, the
deltoid muscle is preferred for injection as
gluteal injection often results in deposition of
vaccine in fat rather than muscle.
36. Advantages
All children and adolescent aged less than 18 yrs and
not previously vaccinated should receive the vaccine.
Indicated for certain groups at high risk of
contracting HBV infection. E.g.
High risk sexual behaviour
Partner
Household contacts of HBsAg positive persons
Injecting drug users
Person who frequently required blood transfusions
Recipient of solid organ transplantation
Health care workers dealing with HBV patients
International travellers to endemic countries
40. Dosage and Schedule
A primary course of immunisation consists of
2 doses given at interval of 1-2 months.
1st booster at 1 yr after the initial 2 doses.
2nd booster given 5 yrs after 3rd dose.
In pregnancy, 2 doses are given:
1st at 16-2o weeks
2nd at 20-24 weeks
44. Rabies Vaccine
Against the rabies virus.
Prevention by
1) post exposure prophylaxis
2) pre exposure prophylaxis
3) Post exposure treatment of persons who
have been vaccinated previously.