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PREVENTIVE PEDIATRICS Ma. Philomena G. Lopez, MD

Department of Pediatrics

* with notes from the lecture. If anything, just refer to the book. 

PREVENTIVE PEDIATRICS ENCOMPASSES:

1. health supervision of infants, children and adolescents

2. frequent concerns during health visits 3. future challenges

A. Health Supervision of Infants, Children and Adolescents  Guidelines must be made to prevent morbidities to:

o childhood injuries o educational failures o child abuse and neglect o family violence o teenage pregnancy o media influence o obesity

o risk behaviors (tobacco, alcohol, drugs)  Principles of Health Supervision

o health promotion

o establish partnership with each child and the family

o establish communication:

- demonstrate respect and empathy - listen to concern of patients

- use nonjudgmental questions to promote dialogue

- establish relationship with children by communicating directly to them  Periodic Health Supervision Visits

o history and physical examination o screening tests

o immunizations

o surveillance of developmental milestones o observe parent-child interaction

o anticipatory guidance and counseling B. Frequent concerns during health visits

 child’s behavior  parenting

 common issues on growth and development  TEETHING:

o there is no correlation between teething and diarrhea. During teething, child bites at a lot of thing that might be a source of the infection

o 8 or 9 mo old has no teeth? Is it normal? o Not related to development of infection, fever

and mood disturbances

 SLEEP PROBLEMS (night terror vs. nightmares) o Nightmares

- more common

- vivid, exciting scary events - the child can recall the dream o Night terror

- not common, 10-15 mins

- frightening circumstances, also vivid, exciting and scary

- child cannot recall the dream  TOILET TRAINING

o Must start when the child is ready, not at less than 2 y/o

o Readiness – when the child is able to

communicate that he wants to go to the toilet

 TEMPER TANTRUMS

o Although temper tantrums maybe normal, physician must investigate the presence of family violence or parental depression, since it may contribute to temper tantrums

 DISCIPLINE

o Approach with firmness and consistency o Positive – (reinforcement) remove prize if

child did not perform well

o Negative – verbal rather than soank C. Future challenges in Preventive Pediatrics

o new immunizations

o improved screening tests / tools o tobacco use

o violence O OBESITY:

- overweight - BMI 85th to 95th %ile - obese - BMI > 95th %ile

o early hypertension o hypercholesterolemia o media influence on behaviors o parental health needs o literacy promotion

o reducing cardiovascular diseases

- starting 3 y/o: blood pressure monitoring every visit

- if high risk: can take BP at less than 3 y/o - encourage child to participate in active

physical activity

- starting 2 y/o: educate parents on appropriate use of dietary fats PROCEDURES FOR PREVENTIVE PEDIATRIC HEALTH CARE A. General Procedures

 Hereditary / Metabolic Screening o Congenital Hypothyroidism o Congenital Adrenal Hyperplasia o Galactosemia

o Glucose 6-phosphate dehydrogenase deficiency (G6PD Deficiency) o Homocystinuria

o Phenylketonuria

 if positive, can offer treatment as early as possible

 Immunization  Tuberculin test

o Ag = PPD; 5TU commonly used

o Inject 0.1 ml @ volar surface, read result in 42-72 hrs  measure induration.

o Interpret: 0-4 = negative 5-9 = equivocal

10mm & above = positive  Iron supplementation

o Start at 6 mos o If high risk: 1-4 mos  Vitamin A supplementation

o 6-11 mos = 100,000 units o 12-24 mos = 200,000 units  Deworming

o 1/year from 2 years old onwards B. Procedures for patients at risk

 Hearing screening  prior to discharge

 Hemoglobin/hematocrit  1yr up; 10-19 adolescent  Urinalysis  1-2/year; detect UTI

 Lead tests  not done routinely; only for suspected patients

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ANTICIPATORY GUIDANCE  injury prevention

 nutrition and eating behaviors  developmental expectations  oral health

 parental health and relationships  environmental exposures  media education  school problems  sexuality and puberty

 family violence and substance abuse LEVELS OF PREVENTION

A. Primary Prevention

 measures directed at avoiding disorders before they begin, often with a special emphasis on those who are at increased risk to develop a condition or disease

 eg:

o chlorination and fluoridation of water o immunization

o mother’s classes

o counseling parents of toddlers about keeping poisons and drugs out of reach of children o pasteurization

B. Secondary Prevention

 measures in which the condition or precursor is identified early and effective treatment instituted for remediation of condition before progression or for elimination of precursors

 eg:

o treatment with antibiotics for streptococcal sore throat

o screening for lead levels

o screening for scoliosis among adolescents

C. Tertiary prevention

 measures are directed in ameliorating or halting disabilities from the established diseases  eg:

o chest physiotherapy for a child with cystic fibrosis

o physical therapy for patients with Rheumatoid arthritis or with cerebral palsy

ROLES OF PEDIATRICIANS IN PROTECTING CHILDREN’S HEALTH AT ALL THREE LEVELS:

 as direct providers of clinical prevention services  as coordinators of services

 as leaders in developing community based programs  as advocates for child health

IMMUNIZATION  Ultimate goal: eradication of disease  Immediate goal: prevention of disease  TYPES OF PROTECTION INDUCED:

o Complete protection for life o Partial protection (booster doses) A. GOALS CAN BE ACHIEVED IN 2 WAYS:

 ACTIVE IMMUNIZATION

o Involves administration of all or part of a microorganism or a modified product of that microorganism (toxoid, purified antigen, antigen produced by genetic engineering) to evoke an immunologic response mimicking that of the natural infection but which usually presents little or no risk to the recipient  administration of microorganism or toxoid, purified antigen so the body can produce antibody against it

 PASSIVE IMMUNIZATION

o the administration of preformed antibody to a recipient for the prevention and

amelioration of infectious diseases o types of prodcucts:

- Normal (standard) human Ig for general use  gammaglobulin --> little

protection from measles, HepaA - Specific Human Ig  HepaB, rabies, VZ  for immediate protection

 Igs are short-lived – 3mos  supplement antibodies

 Vaccination – administration of vaccine or toxoid (inactivated toxin) for prevention of disease B. ACTIVE IMMUNIZATION

 live attenuated viral vaccine  more reactions Measles

MMR OPV Varicella

 Inactivated viral vaccine  less reactions Flu vaccine

Hep A IPV

Hep B (recombinant DNA)

 Detoxified exotoxin (Toxoid)  local reaction diphtheria

tetanus

 Purified protein antigens acellular pertussis, Hep B

 Whole cell pertussis vaccine DTP

 Inactivated acellular pertussis vaccine DTaP

 Capsular polysaccharide Typhoid

 Protein conjugated polysaccharide vaccine Hib

Pneumococcal

 Live attenuated bacterial vaccine BCG (Bacille Calmette Guerin)

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C. Contraindications to ALL LIVE VACCINES:  immunocompromised patients

o patients with HIV, malignancy, aplastic anemia, nephritic syndrome, in chemotherapy and prolonged steroid, pregnant

 patients given immunoglobulins and blood products for the past 3 months

o blood has small amounts of IgG which can interfere with globulin production

 pregnancy and possibility of getting pregnant within 3 months

 household contacts of immunocompromised patients o give OPV via IM instead

o Baby may pass out virus in the stool – may spread bacteria and affect the

immunocompromised patient

D. Simultaneous administration of Multiple Vaccines  no contraindications for multiple vaccines routinely

recommended

 immune response to one vaccine generally does not interfere with other vaccines

o must administer at different sites, using different syringes at the right route  There should be an interval of 28 days between

administration of live vaccines

 After 7th birthday, Td is recommended for both primary and booster vaccination

o Td – tetanus diptheria

 Interchangeability of Vaccine Products is allowed for primary and booster doses

E. Lapsed immunizations

 in general, intervals between vaccine doses that exceed those that are recommended do not

adversely affect the immunologic response, provided immunizations series is completed

o if immunization status is not known  treat it as the start of the immunization again

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VACCINE MINIMUM AGE DOSE (number) ROUTE OF ADMINISTRATION MINIMUM INTERVAL BETWEEN DOSES VACCINE DESTROYED BY ADDITIONAL NOTES BCG - 1 Birth; or any time after birth

0.05 ml for NB 0.1 ml for infants (1) Intradermal deltoid R arm Heat sunlight

 live attenuated bacterial vaccine vs TB

 at birth or any time after birth (prior to discharge  48 hrs after normal delivery, 3 days after delivery by cesarean section)

 0.05 ml ID birth – 4 weeks at R upper deltoid;  0.1 ml ID beyond 1 month

 booster dose given at school entry, 0.1 ml ID L upper deltoid

 vaccine stored in amber bottle and in freezer because it is freeze-dried  live bacterial vaccine given as early as possible

 BCG does not prevent primary complex. Instead, it prevents extrapulmonary type TB  contraindications  immunodeficiency states

 Reactions: abscess or ulcer at the site; axillary lymphadenopathy Usual Reactions Accelerated rxns

Induration 2 – 4 weeks 2-3 days Pustule formation 5-7 weeks 5-7 days Scar formation 2-3 months 2-3 weeks

 Usual reaction: 2-4 wks after immunization, erythema on induration, may form pustule which may burst and exude pus and leave a permanent scar. Do not put antibacterial meds

 Accelerated rxn: 2-3 days in duration, there is early formation of pus and scar. It means that the patient has already been exposed to or with TB

 Axillary lymphadenitis  abnormal (investigate prior to injection, patient may have signs and symptoms of TB)

 Not given at buttocks because it has high SC fats

DTP 6 weeks 0.5 ml (3) IM Upper outer portion of thigh 4 weeks Heat Freezing

 Diphtheria, Tetanus & Pertussis  DTaP

o DT are toxoids

o P is acellular pertussis vaccine  DTP or DTwP

o DT are toxoids

o P is killed or inactivated whole cell bacteria  Usual dose: 0.5 ml, no 3 e.g. 6-10-14

 Route and site:

 IM Deep – the whole needle must be embedded; otherwise, antigenic cyst will form.  If at buttocks  can affect sciatic nerve

 Usual Side Effects:

o fever up to 72 hours (low to moderate)  rarely reaches 400C, usually about 38-38.5OC o restlessness and irritability because of pain. Baby is fuzzy, wants to be carried. o local reaction: pain and swelling at the site of injection  May be prevented by

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o change in sensorium: drowsiness, lethargic, stuporous, convulsion, coma o anaphylactic shock

o incessant crying >3 hrs within 48 hours after receiving the vaccine

o continuous high grade fever 39 to 40.5°C and above within 48 hours after vaccination  before giving next dose, investigate baby’s reaction after 1st dose. A serious reaction indicates contraindication to DTP (w/c has whole cell pertussis component). Therefore, give DTaP (w/c is acellular preparation)

 DTP – P100/dose. DTaP – P800/dose

 NOTE: if doses are missed, do not start again from the 1st dose. Give the next dose already.  Contraindications to DTP or DTwP

o high grade fever

o ongoing neurologic illness: seizure disorders

o previous adverse reactions to DTP (as mentioned above)  DTP is not contraindicated but given with precaution in the following:

o a single high temperature <40°C immediately relieved by antipyretics o history of febrile convulsions

POLIO 6 weeks 2 drops (3) PO

Mouth 4 weeks

Easily by Heat (store

in freezer)

 Live attenuated  Two types of vaccines:

1. Oral Polio Vaccine (OPV) - live attenuated (Sabin)

- 0.5 ml orally; or 2 drops (using multiple dose) Absolute contraindications:

- altered immune states (malignancies [lymphoma, leukemia], therapy with alkylating agents, metaboltes, high dose steroids, radiation, HIV/AIDS) - pregnancy, household contacts of immunocompromised patients Relative contraindication:

vomiting  may just vomit the vaccine; defer vaccination for a few days diarrhea

Adverse Reaction:

- Paralytic Polio Myelitis  very rare, if it happens, recommend IPV

- IPV was recommended to decrease the incidence of Vaccine-associated paralytic polio (VAPP)

2. Inactivated or Killed Polio Vaccine (IPV) - given intramuscularly

 Available products: individual dose 0.5 ml plastic individual pipette & multiple dose  TOPV  trivalent oral polio vaccine. 3 strains: PV1, PV2, PV3

 Other CI  anaphylactic rxns to neomycin, kanamycin, ptertomycin. Anaphylactic rxns to previous dose

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HEP B 6 weeks or at birth Follow manufacturer instructions (3 – 0, 1, 6 mos) IM Anterolateral aspect Thigh 4 weeks Heat Freezing

 0 (at birth), 1 mo old & 6 mo old, 0.5 ml IM  if mother is HBsAg(+):

- give HBIg & Hep B #1 within 12 hours of birth  inject at 2 diff sites using 2 diff synringes

- Hep B #2 at 1 month - Hep B #3 at 6 months of age

 children and adolescent who have not been vaccinated with Hep B may begin series during any visit

 Contraindications: anaphylactic reaction to previous dose  Reactions: pain and swelling at site, fever

 plasma-derived, genetically-engineered, yeast-derived

 given monthly for patients at high risk: dialysis, medical and lab personnel, px receiving regular blood transfusions

MEASLES 9 months 0.5 ml (1)

SC Outer part of the

thigh

Easily by Heat

 live attenuated

 0.5 ml SC  confers lifelong immunity w/ 1 dose

 given at 9 months but may be given as early as 6 months during epidemics  Reactions:

- fever with or without rashes (5-12 days after administration) maculopapular - hypersensitivity reaction

 Contraindication: immunocompromised patients  those taking high dose steroid, blood profucts, Ig during past 2 months

 Relative Contraindication: untreated active tuberculosis

 other contraindications: anaphylactic reaction to kanamycin & neomycin, acute febrile illness, pregnancy BCG - 2 At school entry whether or not child has BCG scar 0.1 ml (1) ID L deltoid Heat Sunlight  Same reactions as BCG -1 TETANUS TOXOID Women of childbearing age 0.5 ml (5) IM Deltoid region TT1 at 1st contact TT2 at least 4 wks after TT1 TT3 at least 6 wks after TT2 TT4 at least 1 yr after TT5 at least 1 yr after Heat Sunlight;

 For those not given primary immunization in infancy and childhood  For women of childbearing age

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G. AMERICAN ACADEMY OF PEDIATRICS  Hepatitis B

o Inactivated viral antigen o Number, minimum interval:

- 1st dose – birth - 2nd dose – 1-4 mos - 3rd dose – 6-18 mos  DTaP

o More expensive, less reactions

o 3 doses; start at 2 months, 2 months apart o 1st DtaP booster: 15-18 months (1 year after

the 3rd dose)

o Booster can be given earlier than 1 year after the 3rd dose of series as long as there is a 6-month interval

o 2nd Booster: 4-6 years o Booster Td: after 10 y/o

- Reaction: very mild fever  Haemophilus influenzae b (Hib)

o Bacterial, severe pneumonia

o polysaccharide protein conjugate  to develop immunity, it has to be imminuty to the polysaccharide

o shots: If given <1yr: 2 doses; If given >1yr: 1 dose only

o 0.5 ml IM

o Hib titer (Hboc) and anti-Hib (PRP-T) given at 2,4,6 months, then 12-15 months

o Contraindications: anaphylaxis by prior dose o Reaction: low grade fever (2%) pain and

swelling (10-15%)  Inactivated Poliovirus

o 2 doses, etc (refer to table given)  Measles, Mumps, Rubella (MMR) Vaccine

o live attenuated o 0.5 ml SC

o given at 12-15 months; a booster dose is recommended at 4-6 years old

o Reactions: transient

- Measles: fever with or without rashes (5-12 days after administration),

anaphylaxis, swelling of mouth

- Mumps: fever, swelling of parotid gland - Rubella: fever, mild rash, transient

arthritis or arthralgia, post-auricular lymphadenopathy

- German measles: fever (6-14 days after administration), rash, post auricular lymphadenopathy

o Reasons for giving 2 doses of MMR: - only 87-90% of children actually receive

the measles vaccine

- 5% of children who receive the first vaccine won’t develop immunity

- children who had an immune response to the first dose could get a “booster” effect o must not be given to women who are

expecting to be pregnant within 6 months  may develop congenital rubella syndrome o Contraindications: same as measles,

pregnancy within 3 mos

o HIV positivity is not CI in MMR unless severely CI; MMR is not CI if PPD test was done correctly

 Varicella

o live attenuated o 1st dose: 0.5 ml SC

o routinely given 12 months and up but can be given as early as 9 months

o can be given within 5 days of exposure o a patient given Varicella vaccine can also

develop shingles although the incidence is less frequent and less severe as compared to the actual Varicella infection

o Varicella vaccine is designed to prevent moderate to sever cases

o Recommendations:

- single dose for ages 1-12 years - 2 doses 6-10 wks apart in children >13

years

o Safety of Varicella vaccine:

- the virus is so weak that it is not transferred from someone who got the vaccine to another person

- it can be given to children who are living in the home of someone whose immune system is weak

- may also be given to patients whose mother is pregnant

o Reactions:

- may develop few Varicella-like lesions about 1 month after vaccination  deadly in immunocompromised patients.. severe pneumonia, enchepalitis

 CI pregnancy, possible within 1 month  Pneumococcal vaccine

o polysaccharide protein conjugate o 0.5 ml IM

o Indications:

- patients undergoing splenectomy - sickle cell disease

- asplenia - HIV  Flu Vaccine o inactivated vaccine o dose: - 6 – 36 months: 0.25 ml IM or SC - 3 years and above: 0.5 ml IM or SC o should be administered before the start of flu

season  every year, a new strain causes the flu.. determined around June (US)/February (Phils)

o Recommendation:

- prophylaxis in children older than 6 months and adults over 60 years - suffer from disease of cardiovascular

system, metabolic disease, cystic fibrosis, chronic respiratory disease, chronic renal insufficiency

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 Hepatitis A Vaccine

o inactivated viral antigen o given 2 years and above

o not routinely given, only among selected individuals  recall: fecal-oral route transmission of HepaA

o 2 doses:

- first dose: anytime after 2 years - 2nd dose: (booster) 6-12 months after

first dose

o 2-18 years: 0.5 ml IM (720 U) o >19 years: 1 ml IM (1440 U) o Indications:

- persons traveling to areas with high prevalence of Hepatitis A

- occupational hazards

- hemophiliacs – contacts of infected persons

o Reactions: pain and local swelling o CI: anaphylaxis to prior dose

ADDITONAL NOTES:  Combination Vaccine:

DTaP, IPV, Hib, HepB DTaP, IPV, Hib DTaP, IPV

HepA, HepaB (must follow 0,1,6 mos)  Salmonella T. vaccine:

2 preparations:

 alive – oral, 2 years old and above, 3 doses every other day

inactive – 1 dose, 0.5ml IM

 Mild illness w/o fever  safe to give immunization  moderate to severe w/ or w/o fever  contraindicated to give any vaccines

References

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