THE VACCINATION DEBATE: Sorting Through the Bias and Fear Edwin Hofmann-Smith, PhD, ND Natural Childbirth and Family Clinic 10360 NE Wasco, Portland, OR 97220 503 252 8125 Public Health Point of View Vaccination protects the individual AND OTHERS, potentially eliminates epidemics Measles: 1/1000 death rate (pneumonia, encephalitis, nerve damage, etc.) Cost of doctors, hospitals, etc. greater than cost of vaccines Risks of vaccination less than risk of disease One of the “greatest achievements of medicine/public health”. Smallpox, polio, diphtheria, measles, rubella, mumps, tetanus, all practically eliminated Public health perspective Pregnant mom picked up pertussis, her newborn got it, spent next five weeks in NICU, permanent lung damage Child picks up measles in Switzerland, exposes plane full of people, many quarantined, some cases, no epidemic Individual family’s perspective Risk of disease may be minimal (since there are no epidemics) Risk of vaccination is underestimated by officialdom Don’t trust the vaccine authorities Can control exposure (hep B, HPV) Our situation isn’t typical, we eat healthy, use homeopathy, BIAS A preference or an inclination, especially one that inhibits impartial judgment Helps us understand why there is such a wide divergence of opinions For instance, did you believe the cigarette manufacturers when they say smoking doesn’t cause cancer? BIAS: vaccine manufacturers Obvious, everybody knows this There are safeguards regarding conflict of interest, but revolving door is reality Like military-industrial complex Donate much money to political campaigns, lobbyists, media Regulators get captured by regulatees. (It’s an axiom.) BIAS: media Advertising dollars are extremely persuasive When was the last time you heard of a media outlet go against both government and advertisers? BIAS: CDC/Federal Government Vaccines for Children Program: Federal government supplies vaccines for free if clinic agrees to vaccinate according to the standard schedule Tends to keep pediatricians in lock-step BIAS: Vaccine Injury Compensation Program Vaccine injury table - compensation only for accepted injuries with specific timing after vaccination Large cost to program if additional injury added to table Adversarial program - litigant must prove causation Poling case - autism and seizures, “mitochondrial defect” BIAS: scientific method Hard to prove causation for adverse effects Hard to prove causation if effect is delayed, infrequent, subtle, not obviously related to disease Publication bias Funding bias Adverse effects research is a tough road BIAS: Public health officers Vaccination is one of the “greatest achievements of medicine” Federal grants to states’ public health departments based on vaccination rates Keeps public health departments motivated to push vaccination BIAS: pediatric community Don’t want to think that what they do every day could be harming (some) kids Vaccinations are an integral part of practice, keep numbers up Vaccine objectors are seen as uninformed “conspiracy theorists” “Don’t worry, they’re completely harmless” VACCINE APPROVAL Try to balance cost of development with safety Very brief followup in safety trials Autoimmune and other adverse effects may take weeks to months to develop. Generally look for immediate adverse effects, then rely on post-marketing surveillance Vaccine adverse events reporting system Reporting is required for serious effects Anyone can report Rate of reporting is between 1 and 10% Vaccine safety datalink Some managed care organizations report data on adverse effects, etc. First hard evidence of an adverse effect from mercury (thimerasol) Quickly advised removal of thimerosal “SAFE” “The U.S. Food and Drug Administration defines a safe product as ‘one that has acceptable risks, given the magnitude of the benefit expected in a specific population and within the context of alternatives available.’ Determining what degree of risk is 'acceptable' is a particular challenge for regulators and policy-makers” (and parents) BIAS: Fear Unknown contaminants Stories of adverse effects have “legs”, not even necessarily true Internet sites - no peer review, have “ax to grind” Consequences are huge: lifetime of care for disabled child Personal knowledge of vaccine-injured child Mechanisms of adverse effects Autoimmunity Microglial activation Unintended contamination: virus, DNA/RNA, enzymes (hypothesized) Chemical toxicity: mercury/thimerosal, aluminum, formaldehyde ASD and Developmental Disabilities 1/110 current rate of autism spectrum (CDC) 13% with developmental disabilities ASD lifetime cost of care is $3.2 million Medical care cost about 5 times more than normal kids About 700,000 with ASD 50 - 60% of their parents believe illness was triggered by vaccination ASD causation Doctors treating ASD estimate 20-50% have clear-cut vaccine injury. Most parents blame vaccination. MMR is worst one Can be multiple illness/antibiotics Gut flora probably involved in some Some have bizarre immunological abnormality Family history: autoimmune, neurological Neurodevelopmental Disorders: Etiology Mercury? - rates not dropping Aluminum - not much research Autoimmune - auto-antibodies not found in convincing frequency, no delay in some cases Gut connection Microglial activation Hannah Poling case Multiple ear infections (food allergy, antibiotics, immune dysfunction?) Tympanostomy tubes At 19 months, “We need to catch her up on her vaccinations”. Got 9 vaccines. Prompt and profound decline Mitochondrial defect Mitochondrial dysfunction Mitochondria as cellular “batteries” They generate free radicals, also soak up free radicals by antioxidants Free radicals damage the mitochondria Genetic mitochondrial dysfunction? Unlikely. Nitric oxide generates free radicals Microglial/excitotoxin hypothesis for ASD Proposed in 2003 by Russell Blaylock, MD Microglia and astrocytes become activated when the systemic immune system becomes activated Secrete inflammatory chemicals (cytokines), excitotoxins (glutamate and quinolinic acid), free radicals and lipid peroxidation products (damage mitochondria) Similar to nitric oxide mechanism of CFS, etc. Can get stuck “on” Nitric oxide and chronic disease The proven mechanism of chronic fatigue syndrome, multiple chemical sensitivities, post-traumatic stress disorder, gulf war syndrome, etc. (Martin Pall) Over production of nitric oxide (eg. in inflammation) leads to damaging free radicals, etc. and can lead to positive feedback loop. Overproduction can be local. Autism has damage notably in cerebellum and frontal cortex. Vitamin D hypothesis Vitamin D has effects on about 10% of human genes Rise in autism parallels recommendation of sun avoidance More prevalent in dark-skinned, etc. Pregnant women should get 4000 IU per day, babies 800IU/day Aluminum toxicity The calculated body burden of aluminum from vaccinations exceeds that from dietary sources, however, it is below the minimal risk level equivalent curve after the brief period following injection. In young children, vaccines with aluminium hydroxide caused significantly more erythema and induration than plain vaccines (odds ratio 1·87) and significantly fewer reactions of all types (0·21) Aluminum toxicity Impairs mercury excretion Impairs glutathione synthesis Maximum dose per vaccine (850 mcg) not based on safety studies Vaccines with aluminum: DTaP, Hib, Prevnar, Hep B, Hep A, HPV US Recommended Vaccines Hep B (3 doses); Polio (4 doses) DTaP (5 doses); Rotavirus (3 doses) Hib (3 or 4 doses); Pneumococcus (4 doses) Varicella (2 doses); MMR (2 doses) Hepatitis A (2 doses) Total doses - 28 Total vaccines 42 Japanese schedule 2004 Polio: 3 shots starting around 3 months DTaP: 3 shots starting around 3 months Measles, rubella: age 1 Japanese encephalitis: 4 shots BCG: 3 shots starting at 4 mo. Total doses - 14 Total vaccines - 21 Timing Immune system not mature till 1 year of age Maternal antibodies protect against disease in the infant and inhibit antibody response, last about 6 months Breast feeding protects against some diseases like Hib and PC Hepatitis B Childhood infection: usually asymptomatic but 2590% risk of chronicity Chronic infection: liver cancer, cirrhosis Common in Asia, Africa, Eastern Europe, Pacific Islanders, Central America, and the Carribean Transmitted by contact with blood, semen and vaginal secretions Vaccination added in 1991 Chronic Acute Hepatitis B vaccine Risk of autoimmunity Extremely low risk of disease - very weak justification for vaccination Not recommended Pertussis (whooping cough) Increasing d/t lower vaccination rates Newborns not protected (lack of maternal antibody) Ordinary cough for a week then paroxysmal Serious in babies: pneumonia, seizures, pulmonary hypertension Pertussis vaccine Start 3 - 6 months depending on exposure, etc. Follow general recommendations: one shot at a time, not when sick or if gut is unhealthy, family history of neurological or autoimmune diseases, silicea 200C as preventive. Don’t repeat if reaction to first shot. Recommended Diphtheria Bacteria cause sore throat and liberate a toxin Very rare except some foreign countries Recommended because can’t get pertussis vaccine without it. Available as DTaP, Tdap, etc. Tetanus Anaerobic bacterium found in soil, manure Infection due to dirty wound causes generalized muscle spasm Recommended: DTaP, Tdap Can’t get pertussis vaccine without it Polio Disease eradicated from the Western Hemisphere, Europe, etc. No risk of disease Vaccine is now relatively safe but not needed. Disease may be eradicated world-wide in future Can vaccinate later before foreign travel Haemophilus influenza type B Bacterium is normal flora for nose and throat. Can become invasive and cause meningitis, pneumonia, cellulitis, epiglottis, etc. Now rare due presumably to vaccination Largely prevented by maternal antibody and breast feeding Hib: not recommended Have seen some neurological reactions, but none permanent Risk of disease very low Strep. pneumoniae (Prevnar) More than 90 separate strains exist Causes pneumonia, otitis media, sinusitis, sepsis, septic arthritis, meningitis, etc. Vaccine is directed against the 13 worst strains Now other strains are causing more disease (serotype replacement) and Staph carriage is increased Prevnar: not recommended Risk of disease is very low in the absence of specific risk factors like immune dysfunction Breast feeding is protective Serotype replacement Vaccine is relatively reactogenic Rotavirus Almost all kids get this by the time they’re 5 years old Vomiting 12 to 18 hours, then usually diarrhea Self limited 37 deaths per year in US Rotavirus vaccine Live virus vaccine Rotarix (GlaxoSmithKline) contains parts of a pig virus that doesn’t make pigs sick Rota Teq (Merck) contains parts of a pig virus that kills baby pigs Increase in intussusception with Rota Teq Not recommended Hepatitis A Fecal-oral transmission Very common in third world, rare in US Usually asymptomatic in kids but more severe in adults No chronic state Vaccine relatively safe but not recommended unless a high risk group Measles Measles: 1/1000 death rate, neurological damage Virtually eliminated in US d/t vaccine Drop in vaccination rate associated with many-fold increase in cases Measles vaccine MMR is the most common vaccine trigger of autism, but usually was given with other vaccines and kid was already sick Recommended to support public health effort Give after age 2 - 3 Give 50 - 75,000 IU vitamin A, good vitamin D status, healthy, not with other vaccines Mumps Relatively mild disease Self limited Vaccine: can’t get it without measles and rubella Recommended after age 2 Rubella If pregnant mom contracts it in first trimester, fetus gets it and might die or have severe birth defects Our public health approach - vaccinate all kids. Prevents epidemics. Successful. Essentially eradicated from US Rubella vaccine 15% of adolescent and adult women will get acute arthrisis, usually transient Worse with wild virus infection Can’t get it without M and M Recommend: start after age 2 Don’t re-vaccinate if seronegative as adult Varicella Zoster (Chickenpox) Epidemics among young children Occasional severe disease Susceptibles like immuno-suppressed, chemotherapy at risk for severe disease Carrier state with 30% getting shingles later Exposure to children with chickenpox boosts immunity CHICKENPOX (VARICELLA) Disease is usually mild but virus persists Asymptomatic re-activation of vaccine virus Risk of shingles later in life less with vaccine? Likely. Shingles vaccine necessary because less boosting of immunity from epidemics. Risk of “serious” reaction to vaccine is 0.03 to 0.3% Chickenpox vaccine program Best information says, shingles less frequent and milder after vaccination than wild disease Live virus, slight risk of mild disease after shot Risks less after shot than from disease Recommend after age two or three with usual preventive for live virus