Discuss the importance of adult vaccination, immunization updates and resources, adult immunization practice and Seize opportunities in adult immunization and discussion
Healthy Mothers Healthy Babies
2014 Annual Meeting & Conference
October 7th, 2014
Presented by: Carol E. Hayes, CNM, MN, MPH
American College of Nurse Midwives representative to CDC Advisory Committee on Immunization Practice (ACIP)
Healthy Mothers Healthy Babies
2014 Annual Meeting & Conference
October 7th, 2014
Presented by: Carol E. Hayes, CNM, MN, MPH
American College of Nurse Midwives representative to CDC Advisory Committee on Immunization Practice (ACIP)
Immunization is one of the best public health intervention to reduce mortality and morbidity caused by vaccine preventable diseases. in this part i am going to describe regarding cold chain ,frequently ask questions regarding vaccines and how to manage acute and life threatening adverse reactions at most peripheral level
Safety Of the Influenza vaccine In pregnancy Lifecare Centre
Dr. Sharda jain,Life care centre
Safety of Inactivated Influenza Vaccines – WHO –SAGE position paper ,
The study found no evidence of increased RR or HR for
Major birth defects,
spontaneous abortion, or
Small for gestational age infants in pregnant women vaccinated with trivalent or monovalent influenza vaccine .
KCR features in the newest Pharma Voice, June 2017, top industry publication. Andrzej Piotrowski, MD, Ph.D., Medical Monitor at KCR, commented on malaria treatment and research.
Child vaccination program in India is carried under the Universal Immunization Programme. It consists of various vaccines to be administered at various ages. Some of the popular vaccines are BCG, Oral Polio Vaccine, Measles Vaccine, DPT Vaccine, Tetanus Toxoid, Hepatatis B, etc.
via : https://www.itsu.org.in
Immunization is one of the best public health intervention to reduce mortality and morbidity caused by vaccine preventable diseases. in this part i am going to describe regarding cold chain ,frequently ask questions regarding vaccines and how to manage acute and life threatening adverse reactions at most peripheral level
Safety Of the Influenza vaccine In pregnancy Lifecare Centre
Dr. Sharda jain,Life care centre
Safety of Inactivated Influenza Vaccines – WHO –SAGE position paper ,
The study found no evidence of increased RR or HR for
Major birth defects,
spontaneous abortion, or
Small for gestational age infants in pregnant women vaccinated with trivalent or monovalent influenza vaccine .
KCR features in the newest Pharma Voice, June 2017, top industry publication. Andrzej Piotrowski, MD, Ph.D., Medical Monitor at KCR, commented on malaria treatment and research.
Child vaccination program in India is carried under the Universal Immunization Programme. It consists of various vaccines to be administered at various ages. Some of the popular vaccines are BCG, Oral Polio Vaccine, Measles Vaccine, DPT Vaccine, Tetanus Toxoid, Hepatatis B, etc.
via : https://www.itsu.org.in
Published in Living Well Magazine (March/April 2016 edition), BiondVax's CEO considers whether flu prevention will be possible through the M-001 universal flu vaccine.
This presentation is about the relevance of vaccine as a public health tool against vaccine preventable diseases and the need to accelerate the development of vaccines against malaria and other diseases of global health importance in developing countries such as Nigeria.
Immunization, or immunisation, is the process by which an individual's immune system becomes fortified against an infectious agent (known as the immunogen).
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
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.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
2. At the end of this presentation, participants will be
able to:
1.Discuss the importance of adult vaccination
2.Be aware of immunization updates and resources
3.Discuss adult immunization practice
4.Seize opportunities in adult immunization and
discussion
Learning ObjectivesLearning Objectives
3. Impact of Vaccine Preventable Diseases in PeopleImpact of Vaccine Preventable Diseases in People
4. ““WHEN MEDITATING OVER A DISEASE, IWHEN MEDITATING OVER A DISEASE, I
NEVER THINK OF FINDING A REMEDY FOR IT,NEVER THINK OF FINDING A REMEDY FOR IT,
BUT, INSTEAD, A MEANS OF PREVENTION.”BUT, INSTEAD, A MEANS OF PREVENTION.”
LOUIS PASTEURLOUIS PASTEUR
5.
6. Diseases for Which Vaccination isDiseases for Which Vaccination is
Routinely RecommendedRoutinely Recommended
7. Other Diseases for Which Vaccines areOther Diseases for Which Vaccines are
Used in Special SituationsUsed in Special Situations
8. Ten Great Public Health AchievementsTen Great Public Health Achievements
1900 - 19911900 - 1991
9.
10. MYTH:MYTH: Disease rates have droppedDisease rates have dropped
due to factors other than vaccinationdue to factors other than vaccination
•• Better living conditions (less crowded housing, better nutrition, etc.)Better living conditions (less crowded housing, better nutrition, etc.)
have had an impact on disease rates. BUT, the only real decrease in ahave had an impact on disease rates. BUT, the only real decrease in a
VPD has occurred after the introduction of a vaccine to prevent it.VPD has occurred after the introduction of a vaccine to prevent it.
•• This is also true for newer vaccines like Hib (1987) and varicellaThis is also true for newer vaccines like Hib (1987) and varicella
(1995), which were introduced during times of modern hygiene.(1995), which were introduced during times of modern hygiene.
•• When some developed countries (U.K., Sweden, Japan) stopped usingWhen some developed countries (U.K., Sweden, Japan) stopped using
DTP vaccine, their pertussis rates jumped dramatically.DTP vaccine, their pertussis rates jumped dramatically.
•• Several recent outbreaks of measles, pertussis, and varicella in theSeveral recent outbreaks of measles, pertussis, and varicella in the
U.S. have been traced to pockets of unvaccinated children in statesU.S. have been traced to pockets of unvaccinated children in states
that allow personal belief exemptions. When vaccinationthat allow personal belief exemptions. When vaccination
rates go down, disease rates go uprates go down, disease rates go up.
13. RESOURCES FOR IMMUNIZERSRESOURCES FOR IMMUNIZERS
NACI – National Advisory Committee on Immunizations
(Canada)
PHAC – Public health Agency of Canada (Canada)
CATMAT - Committee to Advise on Tropical Medicine and
Travel
Canadian Immunization Guide (Canada)
Immunize Canada (Canada)
IPAC – Infection Prevention and control Canada (Canada)
ICID – International Centre for Infectious Diseases
(Canada)
CRNNS – College of Registered Nurses Nova Scotia
(Canada)
- Care Directives: Guidelines for Registered Nurses
- Immunization Guidelines for Registered Nurses
Nova Scotia Communicable Disease Prevention and
Control (Canada)
Nova Scotia Immunization Manual (Canada)
ICPNS – Infection Prevention and Control Nova Scotia
(Canada)
Canadian Pediatric Society (Canada)
CDC – Centre for Disease Control (United States)
WHO – World Health Organization (International)
14. NACI is a national advisory committee of experts in the fieldsNACI is a national advisory committee of experts in the fields
of pediatrics, infectious diseases, immunology, medicalof pediatrics, infectious diseases, immunology, medical
microbiology, internal medicine and public health.microbiology, internal medicine and public health.
The Committee reports to the Assistant Deputy Minister ofThe Committee reports to the Assistant Deputy Minister of
Infectious Disease Prevention and Control, and works withInfectious Disease Prevention and Control, and works with
staff of the Centre for Immunization and Respiratorystaff of the Centre for Immunization and Respiratory
Infectious Diseases of the Public Health Agency of Canada toInfectious Diseases of the Public Health Agency of Canada to
provide ongoing and timely medical, scientific and publicprovide ongoing and timely medical, scientific and public
health advice.health advice.
NACI makes recommendations for the use of vaccinesNACI makes recommendations for the use of vaccines
currently or newly approved for use in humans in Canada,currently or newly approved for use in humans in Canada,
including the identification of groups at risk for vaccine-including the identification of groups at risk for vaccine-
preventable diseases for whom vaccination should bepreventable diseases for whom vaccination should be
targeted.targeted.
NACI knowledge syntheses, analyses and recommendationsNACI knowledge syntheses, analyses and recommendations
on vaccine use in Canada are included in published literatureon vaccine use in Canada are included in published literature
reviews, statements and updates. NACI recommendations arereviews, statements and updates. NACI recommendations are
also published in thealso published in the Canadian Immunization Guide.
About NACIAbout NACI
http://www.phac-aspc.gc.ca/naci-ccni/
16. Hepatitis A vaccineHepatitis A vaccine New recommendation: Hepatitis A (HA) vaccine may beNew recommendation: Hepatitis A (HA) vaccine may be
administered to persons six months of age and older. 2016-Septemberadministered to persons six months of age and older. 2016-September
Hepatitis A vaccineHepatitis A vaccine New recommendation: For post-exposure prophylaxisNew recommendation: For post-exposure prophylaxis
within 14 days of exposure of susceptible adults 60 years of age and olderwithin 14 days of exposure of susceptible adults 60 years of age and older
who are household or close contacts of a case, Ig may be provided inwho are household or close contacts of a case, Ig may be provided in
addition to HA vaccine. 2016-Septemberaddition to HA vaccine. 2016-September
Hepatitis A vaccineHepatitis A vaccine New recommendation: Immunization with HA vaccineNew recommendation: Immunization with HA vaccine
may be considered for all individuals receiving repeated replacement ofmay be considered for all individuals receiving repeated replacement of
plasma-derived clotting factors. 2016-Septemberplasma-derived clotting factors. 2016-September
Hepatitis A vaccineHepatitis A vaccine New recommendation: For post-exposure prophylaxis ofNew recommendation: For post-exposure prophylaxis of
susceptible individuals with chronic liver disease, Ig should be providedsusceptible individuals with chronic liver disease, Ig should be provided
within 14 days of exposure in addition to HA vaccine. 2016-Septemberwithin 14 days of exposure in addition to HA vaccine. 2016-September
17. Influenza Vaccine Updated recommendation:Influenza Vaccine Updated recommendation: The current evidenceThe current evidence
does not support a recommendation for the preferential use of LAIV indoes not support a recommendation for the preferential use of LAIV in
children and adolescents 2–17 years of age. 2016-Septemberchildren and adolescents 2–17 years of age. 2016-September
Influenza Vaccine New recommendation:Influenza Vaccine New recommendation: egg allergic individuals may beegg allergic individuals may be
vaccinated against influenza using the low ovalbumin–containing livevaccinated against influenza using the low ovalbumin–containing live
attenuated influenza vaccine (LAIV) licensed for use in Canada.attenuated influenza vaccine (LAIV) licensed for use in Canada.
Chapter(s) revised to reflect this change: Contraindications, PrecautionsChapter(s) revised to reflect this change: Contraindications, Precautions
and Concerns and Anaphylactic Hypersensitivity to Egg and Eggand Concerns and Anaphylactic Hypersensitivity to Egg and Egg
Related Antigens. 2016-SeptemberRelated Antigens. 2016-September
Influenza Vaccine New productInfluenza Vaccine New product:: Fluzone® High-Dose influenza vaccineFluzone® High-Dose influenza vaccine
has been approved for use in Canada in adults ≥65 years of age. 2016-has been approved for use in Canada in adults ≥65 years of age. 2016-
MayMay
Influenza Vaccine New recommendation:Influenza Vaccine New recommendation: NACI now includes adults withNACI now includes adults with
neurologic or neurodevelopment conditions among the groups forneurologic or neurodevelopment conditions among the groups for
whom influenza vaccination is particularly recommended. 2016 - Maywhom influenza vaccination is particularly recommended. 2016 - May
18. Human papillomavirus vaccine New recommendation:Human papillomavirus vaccine New recommendation: Gardasil®9 (HPV9Gardasil®9 (HPV9
vaccine) has recently been authorized for use in Canada for the preventionvaccine) has recently been authorized for use in Canada for the prevention
of HPV types 6, 11, 16, 18, 31, 33, 45, 52, and 58 -related cancers andof HPV types 6, 11, 16, 18, 31, 33, 45, 52, and 58 -related cancers and
anogenital warts 2016-Julyanogenital warts 2016-July
Human papillomavirus vaccine New recommendation:Human papillomavirus vaccine New recommendation: Any of the currentlyAny of the currently
authorized HPV vaccines in Canada can be used according to theauthorized HPV vaccines in Canada can be used according to the
recommended HPV immunization schedules. 2016-Julyrecommended HPV immunization schedules. 2016-July
Pneumococcal vaccine New recommendation:Pneumococcal vaccine New recommendation: On an individual basis,On an individual basis,
PNEU-C-13 vaccine may be recommended to immunocompetent adultsPNEU-C-13 vaccine may be recommended to immunocompetent adults
aged 65 years and older not previously immunized against pneumococcalaged 65 years and older not previously immunized against pneumococcal
disease, for the prevention of community acquired pneumonia anddisease, for the prevention of community acquired pneumonia and
invasive pneumococcal disease caused by the 13 pneumococcal serotypesinvasive pneumococcal disease caused by the 13 pneumococcal serotypes
included in the conjugate vaccine. When it is given, it should precedeincluded in the conjugate vaccine. When it is given, it should precede
PNEU-P-23 vaccine. 2016-OctoberPNEU-P-23 vaccine. 2016-October
19. Pneumococcal vaccine New recommendation: If both PCV13 and
PPSV23 are indicated, these vaccines should not be given at the same
visit. For adults age 19–64 who are receiving both vaccines due to a
high-risk condition, the PCV13 should be given first followed by PPSV23
at least 8 weeks later. If PPSV23 has already been given, wait 8 weeks
(for a child) or 1 year (for an adult age 19 years or older) before giving
PCV13 to avoid interference between the 2 vaccines.
For adults age 65 and older who are receiving both PCV13 and
PPSV23 as part of the routine recommendation, PCV13 should be given
first and PPSV23 at least 8 weeks after .
** In Nova Scotia currently only the PPSV23 vaccine is publically
funded.
20. Varicella vaccine A clarificationVaricella vaccine A clarification on the minimum interval between twoon the minimum interval between two
varicella-containing vaccines has been made in accordance with thevaricella-containing vaccines has been made in accordance with the
information available in the Health Canada approved product monographs.information available in the Health Canada approved product monographs.
NACI considers the minimum interval of 4 weeks to be acceptable inNACI considers the minimum interval of 4 weeks to be acceptable in
exceptional circumstances. If the second dose of varicella-containing vaccine isexceptional circumstances. If the second dose of varicella-containing vaccine is
administered at an interval of less than 4 weeks, it should be repeated. NACIadministered at an interval of less than 4 weeks, it should be repeated. NACI
continues to recommend an interval between two varicella-containingcontinues to recommend an interval between two varicella-containing
vaccines of at least 3 months for children less than 13 years of age and 6vaccines of at least 3 months for children less than 13 years of age and 6
weeks for individuals 13 years of age and older. 2016-Septemberweeks for individuals 13 years of age and older. 2016-September
Varicella vaccine Updated recommendation:Varicella vaccine Updated recommendation: Susceptibility and ImmunitySusceptibility and Immunity
section updated to provide further information about individuals who requiresection updated to provide further information about individuals who require
immunization with varicella vaccine 2016-Septemberimmunization with varicella vaccine 2016-September
Varicella vaccine Updated recommendation:Varicella vaccine Updated recommendation: Varicella immune globulinVaricella immune globulin
recommendations updated to allow for product administration up to 10 daysrecommendations updated to allow for product administration up to 10 days
since last exposure for the purpose of disease attenuation 2016-Septembersince last exposure for the purpose of disease attenuation 2016-September
21. Canadian Immunization GuideCanadian Immunization Guide
http://healthycanadians.gc.ca/healthy-living-vie-saine/immunization-
immunisation/canadian-immunization-guide-canadien-immunisation/index-
eng.php
The Canadian Immunization Guide is a comprehensive resource onThe Canadian Immunization Guide is a comprehensive resource on
immunization. It was developed based on recommendations andimmunization. It was developed based on recommendations and
statements of expert advisory committees, including the:statements of expert advisory committees, including the:
••National Advisory Committee on Immunization (NACI)National Advisory Committee on Immunization (NACI)
••Committee to Advise on Tropical Medicine and Travel (CATMAT)Committee to Advise on Tropical Medicine and Travel (CATMAT)
22. Care Directives: Guidelines forCare Directives: Guidelines for
Registered NursesRegistered Nurses
http://crnns.ca/publication/care-directives-guidelines-for-registered-nurses/
24. Care Directive:
Influenza Vaccine
Indication: For immunization against infection caused by influenza viruses for patients meeting
the criteria per the Canadian Immunization Guidelines.
Adults:
Administer Influenza vaccine 0.5 ml I.M per product monograph.
Children:
Administer Influenza vaccine 0.5 ml I.M. per NACI recommendations.
Schedule: 6 months to 8yrs. Initial vaccine: 2 doses 0.5ml - 4 weeks apart
Prior vaccine: 1 dose 0.5ml
Administer to patients who meet the criteria as per The Canadian Immunization Guide
Evergreen Edition section, Part 4 Active Vaccines: http://www.phac-aspc.gc.ca/publicat/cig-
gci/p04-eng.php
Note: Epinepherine HCl 1:1000 must be available for immediate use in case of anaphylaxis or
hypersensitivity reaction. (See Epinepherine Care Directive)
_______________________ ________________________________
Date Physician Signature
_______________________ ________________________________
Date Clinic Manager Review
Care Directives
25. Care Directive:
Epinephrine HCl – Adrenalin 1:1000
Indication: For the relief of respiratory distress due to bronchospasm to provide rapid relief of
hypersensitivity reaction to vaccines, drugs and other allergens per the Canadian Immunization
Guidelines.
For Adults:
Administer Epinephrine 0.01mg/kg (maximum 0.5ml) I.M. for anaphylaxis.
For post vaccination anaphylaxis administer in mid-anterolateral aspect of the thigh, not the
deltoid.
Dosing can be repeated twice at 5 - 15 minute intervals to a maximum of 3 doses if symptoms
persist.
All vaccine recipients receiving emergency epinephrine must be transported to hospital
immediately, via ambulance, for evaluation and observation.
Ensure patient remains in a recumbent position following receipt of epinephrine injection and is
monitored closely.
For Children:
Administer dose: Epinephrine 1:1000, 1 mg/ml solution, by age or weight.
Table 1: Dose of epinephrine (1:1000, 1 mg/mL solution), by age or weight
Age WeightTable 1 - Footnote 1
Dose by injection Dose by autoinjector
0 – 6 months Up to 9 kg (20 pounds) 0.01 mg/kg body weight Not applicable
7 - 36 months 9 - 14.5 kg (20 - 32 lb) 0.1 - 0.2 mg Not applicable
37 - 59 months 15 - 17.5 kg (33 – 39 lb) 0.15 - 0.3 mgTable 1 - Footnote 2 Junior dose of 0.15 mg
5 - 7 years 18 - 25.5 kg (40 – 56 lb) 0.2 - 0.3 mgTable 1 - Footnote 2
Junior dose of 0.15 mg
8 - 12 years 26 - 45 kg (57 – 99 lb) 0.3 mgTable 1 - Footnote 2 - If , less than 30 kg (66 lbs) give Junior dose
- If 30 kg or more: Give standard dose
13 years and older 46 + kg (100 + lb) 0.5 mgTable 1 - Footnote 3
Give standard dose of 0.3mg
Adapted from Immunization Action Coalition. Medical Management of Vaccine Reactions in Children and Teens (PDF document) .
Accessed June 2012.
Table 1 - Footnote 1
Rounded weight at the 50th percentile for each age range
Table 1 - Footnote 2
Maximum dose for children 12 years of age and younger
Table 1 - Footnote 3
Maximum dose for adolescents
Administer to patients who meet the criteria described in the Anaphylaxis policy and as per The
Canadian Immunization Guide Evergreen Edition section: Anaphylaxis: Initial Management in
Non-Hospital Settings. http://www.phac-aspc.gc.ca/publicat/cig-gci/
26. Care Directive:
Benadryl® (Diphenhydramine hydrochloride) Administration
Indication: As an optional adjunct to epinephrine per the Canadian Immunization Guidelines.
Administer Benedryl® 50mg P.O. or I/M per product monograph.
May be given as an adjunct to epinephrine to relieve itching, flushing, uticaria, and nasal and
eye symptoms.
Not recommended for infants under 12 months of age.
When given to children, dosage should be determined by weight (1 mg/kg)
Refer to dosing guidelines in Table 2:
Table 2: Dose of diphenhydramine hydrochloride, by age
Age Weight (pounds) Dose of diphenhydramine hydrochloride
12-23 monthsTable 2 - Footnote 1
7-12 kg (15-25 lbs) 6.25 - 12.5 mg
2 to 4 years 12-25 kg (25-55 lbs) 12.5 - 25 mg
5 to 11 years 25-45 kg (55-99 lbs) 25 - 50 mg
12 years and older 45 kg + (99 lbs or more) 50 mg
1
Use with caution in children 12 - 23 months due to risk of sedation or paradoxical excitement.
Administer to patients who meet the criteria described per The Canadian Immunization Guide
Evergreen Edition section: Anaphylaxis: Initial Management in Non-Hospital Settings.
http://www.phac-aspc.gc.ca/publicat/cig-gci/
_______________________ ________________________________
Date Physician Signature
_______________________ ________________________________
Date Clinic Manager Review
27. IMPORTANT RULE:IMPORTANT RULE:
Vaccine doses should not beVaccine doses should not be
administered at intervals less than theadministered at intervals less than the
recommended minimal intervals orrecommended minimal intervals or
earlier than the minimal ages.earlier than the minimal ages.
But there is no maximumBut there is no maximum interval!interval!
And the classic error :And the classic error :
Re‐starting a vaccine seriesRe‐starting a vaccine series
because of a longer‐than recommendedbecause of a longer‐than recommended
interval.interval.
28. Required information toRequired information to
documentdocument
•• Type of vaccine (e.g., MMR or Hib)Type of vaccine (e.g., MMR or Hib)
•• Vaccine name and lot numberVaccine name and lot number
•• Date the vaccination was givenDate the vaccination was given
•• Name, office address, and title of the healthcareName, office address, and title of the healthcare
provider administering the vaccineprovider administering the vaccine