Last Portion of Class (Minamata Disease -) Flashcards

1
Q

Where did Minamata Disease first occur?

A

A fishing community on the West coast of Japan in Minamata Bay in the 1950s -> first saw it in animals in 1952 and then children among the first sufferers in 1956.
- a wide variety of seafood was harvested from Minamata Bay: oysters and clams.

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2
Q

What was the timeline of Minamata Disease?

A
  • In 1908 they built a chemical fertilizer factor Chisso Corporation factory in Minamata.
  • In the1920s and 30s, they greatly started to produce fertilizer from this company.
  • From 1932, Chisso started to use mercury in its products. -> from 1932 to 1968, Chisso dumped methyl mercury (a waste by-product) into Minamata Bay.
  • In 1952, residents of Minamato started noticing concerning signs in animals.
  • Feral cats who ate fish scraps from docks of Minamata Bay started exhibiting weird pyschological signs
    • Ran into rocks, jumped into the sea and drowned, seizing
    • Most of the cats in the fishing village ended up dying
  • Soon after, people started showing alarming symptoms as well
    • Delusions, tremors, delirium
  • Children among first sufferers in 1956.
    Researchers tested sediments at the mouth of the wastewater canal in 1959 and found up to 2 kg of mercury per ton of sediment—enough to be economically viable to mine.
    Second outbreak in Niigata on Agano River in 1964-65. (like Chisso factory, also used mercury catalyst)
    1968 → 12 years after discovery of the disease → Chisso stops production with the product → compensation for ppl
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3
Q

What did people of the Minamato Bay area first think Minamata disease was?

A

Thought it was a new contagious disease (bc it was highly localized): an “epidemic of an unknown disease of the central nervous system.”

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4
Q

What were the symptoms of Minamata Disease?

A
  • People reported loss of sensation, difficulties seeing, hearing and swallowing.
  • Followed by severe convulsions, coma and death.
  • Mortality rate of 30% among those who got it
  • Epidemiologically studies showed not contagious disease but rather due to seafood
    • Suspected it was heavy metal poisoning
    • Hypothesized it was mercury poisoning
  • Mercury bioaccumulates → doens’t get flushed out of your body: neurological effects
  • Found it high in pregnant women → miscarriages and found cerebral palsy in children
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5
Q

Who was Hajime Hosokawa?

A
  • Chisso factory doctor
    • Did an experiment on feeding waste water to a cat
    • Him and company knew way before it started in the population how dangerous the disease was
  • Some of the 138 plaintiffs in the first Minamata disease damages case against the Chisso Corp. leave Kumamoto District Court on March 20, 1973… FINISH NOTES
  • Really just was acute mercury poisoning
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6
Q

What was the case of mercury poisoning in Canada?

A
  • Grassy Narrows → pulp company dumped waste water into river
  • Mercury contamination found in Freshwater fish
    • When they realized there were elevated mercury levels in the fish, they closed the sports fishing industry and commercial fishing industry there
  • Annishinaabe also relied on fish in their diet
    • Closing of factory → economic consequences → more turned to eating the fish
    • Solicited medical tests to see if they’re being exposed
    • 1973 → found that their hair samples had 12x the normal amount of mercury; and 50x more (elevated) levels of mercury in their blood
    • Speaking difficulties, similar symptoms to those in Minamata
  • Since 1970s → efforts to address mercury poisoning in Ontario
    • Japanese came over to suggest methods to test them
    • Found it was the pulp mill leading to mercury contamination
    • But a lot of that mercury remains in the environment
    • But help for these problems remain elusive in many respects
    • Not just mercury poisoning, but advocated by other sources of heavy metals/contamination in the waterways
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7
Q

What was the deal about New Environmental Diseases?

A
  • Not as deadly as infectious pathogens.
  • Many came about in the context of new technologies and compounds applied to industrial production.
  • Novel chemicals, new uses of old substances, found their way into human bodies in many different ways
    • Workplaces
    • Households
    • Wider environment
  • In case of Minamata → new technologies using chemicals that disemminated into the wider environment
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8
Q

What were the first Polio vaccines?

A
  • Sabin vaccine was available in 1962
    • More successful in the long run bc you could administer it much more easily (could drink it) → went into the gut → most effective (bc polio is an intervirus)
    • Easier to administer in rural areas because it required less sterile equipment and got rid of fear of vaccine
    • Much weaker version of the virus → passed it through tissue cultures to weaken it → ppl ingest it → goes into gut → ppl pass it in stool as well → in places with poor sanitation other ppl would be exposed to it as well which would achieve wider coverage (weak version evoke an immune reaction in them)
  • Salk vaccine was the injected vaccine and first one available in 1985
  • Global vaccine campaigns were highly successful
    • Number of polio cases falls dramatically with Salk vaccine (first) and then with the Sabine vaccine in 1980s
  • By May 1988 they eradicated smallpox
    • Next major goal was to eradicate polio globally
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9
Q

What were the results of the Global Polio Eradication Initiative?

A
  • The eradication campaign has been in many respects highly successful
    • Types 2 and 3 thought to no longer exist in nature
    • Number of cases globally has declined dramatically (about 90% since beginning of campaign)
  • Still is number 1 serotype out there:
    • WPV1
    • cVDPV: vaccine-derived virus → arises from mutation of the live virus in the vaccine
      • In some instances, once it is excreted in the ppls stool it is mutated into a more severe version that causes paralysis and death.
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10
Q

What diseases have been successfully eradicated?

A
  • Smallpox: the only human disease to have been successfully eradicated from nature.
  • Rinderpest: Animal disease successfully eradicated (2011)
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11
Q

What was the history of Smallpox and Vaccines?

A
  • Earliest vaccine developed.
    -> Sabin oral vaccine in 1962
    -> Salk vaccine was the first injected one available in 1985.
  • Had thought would confer lifelong immunity, but soon realized would need boosters.
  • Compulsory vaccination programs often targeted at children.
    Epidemics would prompt new vaccination programs often targeted at children.
    Mandatory smallpox vaccine campaigns would be enforced by saying their child could not go to school unless they were vaccinated.
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12
Q

What was the smallpox vaccination campaign like in the Phillipines?

A
  • San Jose College Manila University 1887
  • Smallpox had long been a problem in the Philipines, under Spanish rule they had a pretty good health program
    • Quarantines
  • Spanish disseminated vaccine lymph for 1806 on.
  • Phillipines had public health department from 1883
  • Provisions for isolation and quarantine
  • By 1898 there were 122 regular vacunadores (vaccinators) working in provinces and major towns.
    • Vaccinators usually weren’t paid well, so not much motivation to vaccinate people.
  • Problem with early vaccination campaigns → vaccination/virus very weak → hard to get it work
  • In other instances, vaccines were contaminated with bacteria → more issues, opposition
  • Spanish-American War (1898) → public health system collapse → America took over public health system
    • Established separated hospitals for smallpox, leprosy, etc.
    • Established a smallpox vaccination campaign
  • 103,931 vaccinations in Phillipines 1899
  • In 1902 → teams would enter the most crowded houses (with army) and lead ppl out of the house 1 by 1 and anyone who did not have smallpox scars would be vaccinated.
    • Colonial force
    • Carried out on ppl seen as below the ppl in power
  • 18 million by 1914
  • 1929-30, endemic smallpox eradicated
  • Vaccination programs helped establish colonial apparatus.
  • Epidemics were persisting even as smallpox was being locally eradicated around the globe.
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13
Q

What helped in the eradication of smallpox due to vaccination campaigns?

A
  • Epidemic persisted even with compulsory vaccination.
  • Highly visible symptoms that enabled quick identification of disease (unlike TB for example)
  • No reservoir in other animals (unlike plague)
    -> Human disease
  • Only transmitted between humans - no vectors involved (unlike malaria, influenza) -> why smallpox eradication was seen as a possibility.
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14
Q

What was Russian Smallpox Eradication like?

A
  • Russia had a long history of large-scale vaccination campaigns. Central medical authorities worked with local governing bodies to distribute vaccines.
  • Soviet government imposed compulsory vaccination of the entire population in April 1919.
  • Effective technique for rapid vaccine production and widespread dissemination.
  • Successfully eliminated smallpox between 1936 and 1938.
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15
Q

When did new attention to Global Health happen?

A
  • In the wake of WWII.
  • World Health Organization (WHO) created in 1948.
  • USA smallpox free in 1949.
  • In Cold War context: Disease eradication offered possibilities for ‘technical cooperation’ between the USA and USSR.
  • For WHO offered opportunities for it to asserts its role in the post-war world.
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16
Q

Who was Viktor Zhdanov (1914-1987)?

A
  • Soviet deputy minister instrumental in persuading WHO to approve global smallpox eradication campaign.
  • If you have enough people that are immune, then the virus can’t find a host and dies out.
  • But challenge was you could not vaccinate everyone, everywhere, all at once.
    -> Eg. India -> everywhere so spread out.
  • Costs were seen as prohibitive.
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17
Q

What was Smallpox eradication like in Nigeria?

A
  • In December 1966 there was an occasion of a new mode of pursuing eradication.
    -> Team faced with a smallpox epidemic in an area -> took what limited supplies they had -> identified new cases, isolated them, and traced ppl who had been in contact with those cases and vaccinated them. -> just those who had been in touch.
  • Within 5 months, the chain of transmission had been broken even tho less than 5% of the population had been vaccinated.
  • Led WHO to focus more on containment instead of mass vaccination. -> identifying, and finding contacts. -> led to surveillance and containment strategy.
    -> Also in India where ir found great success.
  • As much about administration and control as it is medical expertise.
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18
Q

When was the last case of smallpox?

A

October 1977.
- Ali Maow Maalin (1954-2013) living in Mogadishu, Somalia. Last known “natural” smallpox cases before eradication of the virus. Maalin went on to lead polio vaccination campaigns in Somalia.
- Since 1984 there are only two locations globally where variola virus is officially stored and handled under WHO supervision.
-> No more natural smallpox, only captivated/captured smallpox in Russian and US.

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19
Q

Who was Janet Parker?

A
  • Last known person to die from smallpox in September 1978.
  • She contacted the disease from a medical research laboratory.
  • Debate about decisions to continue to keep the variola virus.
    -> Some said we should eliminate it from nature forever (didn’t need the virus for vaccine production bc vaccine is made from cowpox) -> some said we should keep it to compare it when new disease occur.
    -> Ethical argument: just bc its harmful to humans doesn’t mean we should eradicate it. -> own right to existence.
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20
Q

What were the 2 big themes of the post-war period in terms of disease?

A

global disease control and emerging pathogens.
-> In late 20th c. had a new sense of emerging pathogens due to increased surveillance of disease.

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21
Q

Review: Smallpox: Vaccination to Eradication compared to TB

A
  • Epidemics persisted even with compulsory vaccination
  • Highly visible symptoms that enabled quick identification of disease.
    (unlike TB, for example)
    • TB eradication is hard bc its hard to control the disease when you can’t tell who has it
  • No reservoir in other animals
    (Unlike plague)
  • Only transmitted between humans - no vectors involved
    (unlike malaria, influenza)
    • mosquitos
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22
Q

What was Malaria Eradication like in the post-war period?

A
  • Vector-borne disease, do you eradicate the parasite? Or the vector? Or both?
    • vector: anopheles mosquito
  • Intersection of the history of pesticides (DDT) with the history of anti-malaria medicine.
  • WW2 - Pacific theatre and globally, malaria and typhus major sources of illness.
    • major cause of death
    • spread by mosquitos and lice
    • and by time of WWII researchers knew they were the critters involved
  • Insecticidal value of dichloro-diphenyl-trichloroethane (DDT) identified in 1939.
    • and becomes available as a highly effective pesticide
    • applied significantly during the war to control typhus and malaria
    • Widespread spraying of homes in Siciliy, Italy to prevent spread of malaria
      • effective bc it did kill mosquitos
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23
Q

What were the downsides of using DDT to deal with Malaria?

A
  • DDT is a persistent organic pollutant (POP)
  • Resistanct to breakdown through usual chemical and biological processes
  • Persists in the environment and can be transported long distance, including tavelling up food chains
    • Bioaccumulates
    • Harms of DDT are largely environmental harms → bc it biomagnifies and bioaccumulates → significant harm to bird population, good and bad insects → killed lots of birds
  • Also was being detected in human bodies and correlation to some degree to cancer
  • By 1970 DDT is banned is US except when used to control malaria-carrying mosquitos
  • Still used around the world to control malaria around the world
  • Toxicity of DDT to humans and other creatures is one problem of it
  • Other is evolving pesticide resistance of infects and other pests
  • 19th-20th c. → backfired → pesticide and antibiotic resistance
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24
Q

Charles Darwin and Natural Selection in reference to Disease

A

Natural selection - if there were natural variations in organisms that were beneficial to survival then those who had those characteristics, passed them on to their offspring → creatures with those characteristics more likely to prevail.

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25
Q

What was the evolutionary problem that occurred when dealing with malaria using DDT?

A

millions of flies could come from two successful flies breeding → rapid evolution
- Bc of the scale of insect reproduction you can have evolutionary change in a matter of years.
- A few individuals where resistant to the insecticide → survived spraying → reproduced → if the resistance was inheritable, it carried on to their offspring → natural selection
- By 1970s, they were already talking about the resistance to insecticides in insect populations to DDT
- Can see this in the increase of bed bugs and cockroaches in the present
- Reason we are seeing more of these pests is climate change but more than that it is bc the arsenal we had to get rid of these creatures, these creatures have evolved resistance to them.
- Malaria is the oldest and with tuberculosis, cumulatively deadliest human disease.
- Kills between 1 and 2.7 million people each year.
- Most are in Africa between 1 and 5yrs
- History of treatment has included efforts to treat effects on human body and to control mosquitoes

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26
Q

What is Quinine and what is it used for?

A
  • Available from 16th c.
  • From cinchona bark
  • Impedes growth and reproduction of malarial parasites (plasmodia) in red blood cells
    • (but if elsewhere in body, parasite could reinfect blood)
  • Cinchona plant found in Peru.
  • Component of tonic water → used it in India to help treat malaria
    • Tied up in colonial history
    • Cinchona native to the Americas → but planted in India to try and stop spread of malaria
  • Part of the challenge is that quinine cannot be synthesized
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27
Q

What Synthetic Anti-Malaria drugs were used?

A

Atabrine and cholorquine developed in 1930s.
-> Atabrine -> stops malaria plasmodium from reproducing in the human body. -> negative side effects: turn you bright yellow, made people feel really ill and didn’t work right away. -> have to take multiple doses.
-> chloroquine - not as many side effects as atabrine
- Troops not fond of atabrine: turned them yellow, made them sick, took forever to work.
- Chloroquine not used until 1946.

28
Q

What was the 1955 WHO malaria eradication campaign like?

A
  • Relied on DDT and insecticide spraying to control the vectors
  • Alongside distribution of chloroquine to control the parasite
  • Saved 15-25 million lives
  • Eradicated the disease in wealthy nations (in Europe and Australia)
  • Significant drop in cases like India
  • Campaign floundered by 1960s (ended in 1969)
    • due to chloroquine resistance in parasites
29
Q

What was Chloroquine Resistance like during the 1960s?

A
  • Parasites become resistant to it.
  • By the late 1960s countries with malaria also had drug-resistant parasites.
  • Plasmodium falciparum - most lethal malaria parasite in humans.
  • By late 1950s and early 1960s plasmodium falciparum was resistant to chloroquine in Asia and Latin America.
  • But DDT persists as prevention but not as eradicating malaria.
30
Q

What was the Timeline of Vaccines?

A
  • 1796 - Smallpox
  • 1882 - Rabies
  • 1905-21 - Tuberculosis
  • 1921 - Diptheria
  • 1924 - Tetanus
  • 1930s - Pertussis, Yellow Fever
  • 1945 - Influenza
  • 1955 - Polio
  • 1963 - Measles
  • 1967 - Mumps
31
Q

What was the case of the TB Vaccine in 1905-1921?

A
  • 1905 researchers attempted to make BCG (Bacillus Calmette-Guérin) vaccine → made using an attenuated form of microbacterium bovis.
    • had some success after its introduction in 1921
    • first tested in baby who lived with his grandma in small apartment in Paris → never developed TB
    • problem was concern about effectiveness → hard to know if you were giving vaccine to someone who hadn’t previously been exposed → hard to know if they got TB if it was bc they previously had it or got it after vaccine
    • Lubec Germany disaster → children given BCG vaccine with accidental aggressive TB and 72 of them developed TB and died within a year
  • 251 neonates received three oral BCG doses accidentally contaminated by virulent Mycobacterium tuberculosis; 67 (26.7%) infants died of tuberculosis
32
Q

What were Bacteriostatic Agents and what was their role in the 1930s?

A
  • Prontosil red → first commercial sulphonamide antibacterial, available from 1935 onwards.
  • Sulpha drugs good at slowing and impeding reproduction of bacteria → gave body more of a chance to fight off disease
  • antibiotics could actually kill them tho
33
Q

What was the first Antibiotic and when was it produced?

A
  • “Accidental” discovery of antibiotics by Alexander Fleming at St. Mary’s Hospital in London.
  • Observed mold growing on a plate cultivating staphylococci organism -> staphylococci dissolved.
  • Mold species : Penicillin notatum.
  • By the 1940s -> we able to make enough penicillin to use to treat a mouse -> found it worked.
  • Tested on humans -> worked for the most part until they ran out of it, and did not have enough to treat completely.
  • Penicillin as a treatment for wound infection.
  • Much more effective against staphylococci than sulpha drugs.
  • Worked against a wide range of infections: pneumonia, meningitis, erysipelas, scarlet fever, gonorrhea, syphilis.
  • Most important use was in the potential to treat TB -> streptomyocin.
  • Selman Waksman (1888-1973) and Albert Schatz (1920-2005) -> Developed streptomycin, first used on a TB patient in 1944.
34
Q

What did Discovering TB by Christian W. McMillen highlight?

A
  • If you’re in 1945, you don’t have enough to treat TB
  • By 1955, the same patient, same symptoms → but can actually save this person’s life instead of just making them comfortable and providing them with care
  • Dramatic transformation in treatment of TB and cases that would once be a death sentence
  • Antibiotics become a miracle drug
35
Q

What was the timeline of staphylococcus and humans?

A

(Timeline of development of effective treatments and resistance)
1943: First effective treatments of staphylococcus populations with PENICILLIN -> 1946: Staphylcoccus populations evolved resistance to PENICILLIN.
:late 1950s: Substitute methicillin for penicillin to kill staphylococcus -> 1961: Staphylococcus populations evolved resistance to METHICILLIN.
Early 1980s: Substitute VANCOMYCIN for methicillin. -> 1986: Straphyloccocus populations evolved resistance to VANCOMYCIN.
Mid 1990s: Substitute LINEZOLID (Zyvox) for vancomycin. -> 2001: Staphylococcus populations evolved resistance to LINEZOID.
- By 1961, Kenya’s director of TB services was warning the gov’t that antibiotic-resistance was becoming a problem
- Infrastructure in Kenya to deliver antibiotics were also conditions to create resistance → not enough medicine to fully treat → some parasites would survive → acquire resistance → those who only came once (didn’t have the means to get repeated treatment) → led to more resistant bacteria
- Inadequate drug supplies
- Lengthy treatment regimens
- Poor patient compliance
- All acted to foster increase the problem of drug resistance in Kenya through the 1960s and 1970s.

36
Q

What was the late 20th c. Antibacterial Panacea?

A
  • Started putting antibiotics in everything:
  • Throat lozenges
  • Anti-bacterial deodorant
  • Toothpaste with triclosan in it.
37
Q

What germs have evolved resistance to triclosan in lab settings?

A
  • Escherichia coli (severe intestinal illness)
  • Salmonella enterica (strains of which cause typhoid fever)
  • Pseudomonas aeruginosa (gastroenteritis and urinary tact infections)
  • Staphylococcus auereus (staph infections)
  • 75% of Americans showed triclosan in their urine -> more you use these things, more anti-resistant bacteria
  • Antibiotics were prescribed for minor problems for decades or if physicians were unsure of what was causing illness. -> Leads to multiple drug-resistant TB.
38
Q

What is the % multiple-drug-resistant/RR-TB in New TB Cases?

A
  • Drug-resistant TB
  • Not being able to treat TB with multiple-drug-resistant TB
  • Higher in places like Russia, Kazakhstan, etc (over 18% of cases)
39
Q

What was the Timeline of the HIV/AIDS Epidemic

A
  • Cluster of rare diseases that emerged in major US cities: LA, San Francisco, New York
  • Pneumocytis carnii pneumonia -> affected ppl with weakened immune system -> in the lungs
  • CDC issued an MMWR (Morbidity and Mortality Weekly Report) -> important tool for alerting ppl globally of unusual clusters of disease.
  • JUNE 5 1981 -> showed rise in Pneumocystis Pneumonia in 5 healthy, gay men. -> suggests some association between a homosexual lifestyle and the disease (Sex)
  • In JULY (16, 1982) more reports of this type of pneumonia around the world.
  • 1952 -> 15,000 cases of Pneumocystis carnii Pneumonia around the world.
  • What was apparent was those who were falling ill and dying were facing an alarming collapse of their immune systems. -> characteristics: young, gay men dominated (disease)
  • Time when gay men were more visible -> Stonewall riots, politics.
40
Q

What was the Early History of HIV/AIDs in North America?

A
  • 1981- GRID: “Gay Related Immune Deficiency”
  • Other distinct groups
    -> Haitians
    -> Hemophiliacs
    -> Intravenous drug users
  • Cases concentrated in distinct, marginalized populations created stigma and fear.
  • 1982: agree on a name that was not GRID:
  • AIDS: Acquired Immune Deficiency Syndrome
  • More research being done on AIDs -> identified a virus
  • By 1986 it was called HIV -> Human Immunodeficiency Virus (1986)
41
Q

What was the characteristics of HIV/AIDS?

A
  • Weakening of the body’s immune system.
  • Latent period -> could be years or shorter
  • HIV positive -> AIDS (most advanced stage of HIV infection)
  • In the wake of HIV infection, many opportunistic infections could attack the body.
    -> When this happened, it was typically when ppl went from HIV positive to having AIDS.
    -> Eg. toxo (toxoplamosis), cryptococcal meningitis, TB, HCV (hepatitis C virus), HPV and cervical cancer
42
Q

How did HIV/AIDs spread?

A
  • Researchers and public health went to great lengths to emphasize that HIV COULD NOT BE spread through shaking hands, hugging, in restaurants or in restrooms.
  • ONLY passed through EXCHANGE OF BODILY FLUIDS -> BLOOD and SEMEN
    -> sex, re-used needles, blood transfusion.
  • Many public washrooms in the 1980s were equipped with public sensors (became widely adopted) -> avoid touching despite not being a valid way to spread HIV.
43
Q

Number of People Infected with HIV by Region

A
  • Increased cases in Africa
  • BY 1992, 11 million in the Americas infected.
  • By early 1990s, over 5 million people around the world were infected (SEE GRAPH)
  • African American males and Hispanic males were just as likely to get it from drug use as white men getting it from homosexual contact.
  • Heterosexual contact a significant form of transmission as well.
44
Q

What was the state of HIV/AIDS by the Late 1990s?

A
  • In early 1980s, a disease with unknown cause.
    -> ppl used language of the Black Death to refer to it in early years.
  • Naming the disease, identifying the virus. -> more biomedical, scientific.
  • Perceptions of HIV/AIDS as new ‘plague’ persisted.
  • Although now more chronic than acute.
    -> originally was labelled as acute tho.
    -> as treatments were developed in 1990s in particular, AIDS more chronic.
  • From the 1990s onward -> more people living with HIV and managing it AS A CHRONIC DISEASE
45
Q

What was AIDS stigmatization like?

A
  • 4-H disease: Homosexuals, Heroin addicts, Haitians, Hemophiliacs
    -> Like lepers sort of -> stigmatized as sexual deviants, sinners, etc, -> same as Black Death -> sinners and morally bad ppl responsible for Black Death.
    -> Nast nickname for it
    -> eg. Ryan White -> hemophiliac -> got HIV from infected blood products that he had needed to survive in 1984 -> barred from going to school.
  • In winter of 1981-82, 75,000 US tourists visited Haiti; in 1982-83 that number dropped to 10,000
  • Most significant stigmatization: against gay men.
  • JAN 1981 -> Ronald Reagan become president, didn’t talk about it until 5 years into presidency.
  • 1992: Ronald Reagan: joked, downplayed about HIV/AIDS. -> thought it was just a disease for homosexuals primarily. -> less interest in doing anything about it and little regard for young men who were getting it and dying.
  • fear of AIDS led to stoppage of gay men and men working in healthcare, food, getting custody of their children
  • Forced ppl who had been pushed on the margins of society to now interact with systems like the medical system -> but partner could not visit you if you were drying, could no recognize insurance benefits.
    • Gay activists pressured the CDC to change the name of “GRID” to AIDS.
      • 1982 - Gay Men’s Health Crisis (GMHC) founded by Larry Kramer (1935-2020) and others.
      • First AIDS hotline, buddy programme and social hub, That year also saw the first campaigns to promote use of condoms among MSM (men who have sex with men)
  • Didn’t have same response from gov’t CDC to deal with HIV
46
Q

What was ACT UP?

A
  • 1987 - The AIDS Coalition to Unleash Power (ACT UP) formed at the Lesbian and Gay Community Services Centre in New York City.
  • Direct action to get media coverage and forced government to act on HIV crisis.
  • Local, then national and then international organization with many committees and subcommittees.
  • ACT UP’s demands: Access to drugs and clinical trials, research funding.
  • Argued in trials that no one should get a placebo in participating in trials bc a placebo was a death sentence -> a lot of gay men were willing to act in drug trials -> found more success. -> a lot of gay men cooperated with science to forward HIV research.
  • HIV antibody tests available in 1985.
  • AIDS treatment activism initially targeted FDA.
  • Later turned to NIH (National Institutes of Health) - US / global centre for medical research.
47
Q

What was the problem of HIV and Africa and what was the response to it?

A
  • TAG → research on TB and AIDS
    • Treatment Action Group that had its origins in the AIDS activist organization, ACT UP.
    • 2002 → TAG began raising awareness of the impact that tuberculosis (TB) was having on people with HIV in the developing world.
    • In 2007, received a $4,7 million grant to foster increased international advocacy on TB/HIV research and treatment.
48
Q

What was the book “And the Band Played On?”

A
  • Randy Shilts: San Francisco Chronicle journalist who documented early years of HIV epidemic.
  • Best-selling book (1987) and later made-for-tv.
  • Described Air Canada flight Gaetan Dugas as “patient zero”
    -> Dugas gave a lot of information on his partners, who the CDC tracked and thus they also appeared in this study.
  • Dugas was vilified at the time and the years since as being the cause of the epidemic.
    -> Shilts characterized him as promiscuous, immoral
    -> These stories of Dugas show our narratives/feed into them and modern thinking on disease.
    -> In more recent period, we consider moral dimensions being attacked to infections (eg. TB)
    -> And idea in 20th and 21st c. that we are at risk bc of globalization, aviation.
    -> These are narratives of disease, stories we tell that is not always connected to the evidence.
    -> Dugas was not this patient zero who spread the disease through being a flight attendant -> he was one of the gay men who tragically died of the disease and aided in the study of it.
49
Q

Where did HIV/AIDs come from?

A

Haiti/Caribbean (1968)
- Then travelled to New York (1972), Pennsylvania (1969-1973) California (1978 in San Francisco)
- This is a disease that suppresses the immune system.
-> Aided in death by TB, etc.
- M strand HIV-1 (responsible for majority of HIV cases globally and over time)
- Likely emerged c. 1921 in the Congo.
- SIV -> HIV
-> Simian immunodeficiency virus became human immunodeficiency virus
-> started as enzootic disease in chimpanzees (Pan troglodytes) and then became a human disease.
- Hunter or cook exposed to chimpanzee blood containing SIV in central Africa (Spillover)
-> Significant injury leading to this spillover.
-> HIV did not become epidemic this way (chimps infecting humans)
- Rare case of infection managed to spread and multiply (Amplification)
-> amplification - once the spillover has happened, other factors intervene to cause the disease to amplify and spread more widely. -> most likely the case for the epidemic

50
Q

What were the two steps that most likely led to HIV/AIDS epidemic in the 1970s-1980s?

A
  1. SPILLOVER
    - Hunter or cook exposed to chimpanzee blood containing SIV in central Africa
  2. AMPLIFICATION
    - Rare case of infection managed to spread and multiply
    -> once the spillover has happened, other factors intervene to cause the disease to amplify and spread more widely.
51
Q

What was Sleeping Sickness?

A

Major epidemic in Uganda and Congo between 1896 and 1906 killed between 300,000 and 500,000.
- In central Africa in turn of the 20th c. one of the main concerns among colonizers and Africans was sleeping sickness.
- SYMPTOMS: Enlarged lymph nodes, weeks and months of intermittent fever, profound daytime sleepiness, confusion, poor coordination, can last for several months, if untreated, can cause death.
-> Similar to malaria in that parasite is transmitted by a vector and makes the person weak.
- VECTOR: Tstetse fly - (Glossina) feeding on human blood.
- Tsetse flies are vectors of African trypanosomiasis (sleeping sickness) in humans. They carry the parasite Trypanosoma brucei and can infect humans and animals with it when biting them to feed on their blood.

52
Q

What Drugs were there for Sleeping Sickness?

A
  • Bayer 205
  • were administered through intravenous injections → needle used
  • Sleeping sickness first communicable disease for which campaign was put out
53
Q

What was the connection between French Public Health and Sleeping Sickness?

A
  • Similar to US in Philippines
  • In 1920s, Cameroun Francais (now part of Cameroon), French physicians sought to control sleeping sickness at a population level.
  • Implemented Jamot doctrine, designed by physician Eugene Jamot.
  • Mobile teams to visit each villages, take blood samples to detect disease and treat infected on the spot using glass syringes.
  • Mobility prioritized over disinfection.
    -> Eg. didn’t have time to boil the syringes -> just rinsed with water
    -> Even tho they knew the importance of sanitation at this point
    -> Mobile teams worked in facilities without electricity.
  • Methods used were effective in treating sleeping sickness.
  • Had started specific mobile disease teams trying to identify diseases like malaria, TB, leprosy and treat them.
54
Q

How did Amplification of HIV happened in Africa?

A
  • Using improperly sterilized syringes across Africa to treat diseases like sleeping sickness.
  • Through public health programs for a variety of diseases (sleeping sickness, yaws, syphilis, leprosy, malaria, TB)
  • Spread of sexually transmitted infections in rapidly growing cities.
  • Part of a process of urbanization and industrialization in colonial context.
  • Camps and cities became sights of STIs bc men were brought in to do construction on railroad (11 men to every woman)
    -> Spread diseases -> sb with multiple concurrent partners
55
Q

What was Amplification of HIV at mid-century (1950s) like?

A
  • Non-sterile needles and syringes used in public health programs in central and western Africa
  • Led to “inoculation hepatitis” -> transmission of Hepatitis B during inoculation for some reason.
    -> HIV transmitted this way as well.
  • Virus is also more infective in those recently infected
    -> Multiple concurrent partners increases chances of infection
    -> So too would a public health campaign.
56
Q

How did HIV spread between 1920 and 1961?

A
  • Following railway routes and waterways -> spreads from smaller communities into larger communities
  • Eg, from Kinshasa to Mbuji-Mayi (Katanga)
  • In the case of the Congo, the Congo civil war by colonial powers -> in Katanga refugees from there further spread disease
  • UN intervened, sending in peacekeepers.
    -> Recruited teachers and doctors to come work in the Congo after the civil war.
    -> Ppl displaced from their homes and international workers
    -> Haitians (4500) came in the 1960s to the Congo.
  • Thought that while in the Congo some of these Haitians contracted HIV and went home to Haiti.
    -> Link between Haiti and the Congo is thought to help spread the disease across the Pacific.
    -> Spread takes place largely in the wake of the Congo civil war and in the global movement of people.
    -> Greater inter-continental migration and of internationals in the area.
  • In the 1970s Haiti became a place where they started producing/manufacturing a lot of blood products.
    -> Helped circulate HIV if there were parts of it in the blood products, and tourism -> how it travelled back to the US.
57
Q

What was the Scale of HIV in Africa?

A
  • Dwarfs the scale of HIV in other parts of the world.
  • HIV had been circulating in the sub-Saharan Africa for decades before it was big in the US/spread to the US.
  • When it appears in the US in the early 1980s, it was “discovered” but not really -> just drew attention to it -> diagram shows the scale of the disease after they knew what they were looking for.
  • Eg. Botswana: HIV prevalence of over 25% for those aged 15-49; same in Lesotho
  • Most severe in Southern Africa even now
  • Most important mode of HIV in Africa is through heterosexual contact.
    -> Led to decline in life-expectancy -> fallen below 20 years.
    -> In some instances, death rates exceed birth rates.
    -> Economic impacts -> exists in cities.
    -> Synergistic effects between HIV and other diseases (Weakens immune system -> eg. TB -> high mortality from TB -> opportunistic infections)
  • Speaks to the way the TB and HIV epidemics are interrelated.
    x- Especially global impacts
    • ppl living with HIV are up to 20 times more likely to fall ill with TB
    • TB is the leading cause of death among people living with HIV
    • In 2017, approximately 300 000 people died from AIDS-related TB.
  • Because of synergistic effects with other disease, syphilis and TB are two of the most significant opportunistic infections that have followed the HIV pandemic.
58
Q

What was Legionnaires’ Disease?

A
  • Outbreak of unknown sickness occurred following annual conference of Pennsylvania State American Legionnaires
  • Met in Philadelphia, July 1976
  • Immediately after conference ended, 182 ppl fell sick and 29 died.
  • Tiredness, chest pains, lung congestion, and fever.
  • Generated a lot of conspiracy theories
  • Pair of CDC scientists identified cause of outbreak as previously unknown genus of bacteria they named Legionella
  • Linked to two previous outbreaks of respiratory disease
    • Not as serious as the Philadelphia case
    • were in a hospital and private health centre
59
Q

Legionella Bacteria

A
  • Found in freshwater (puddles to rivers) and soil
  • At least 50 different species of Legionella but strain identified in Philadelphia: Legionella pneumophilia [small army of organisms that love the lungs] is most virulent to humans.
  • Initial flu-like symptoms, fever, deep cough,, sometimes delirium, and kidney damage → illness develops into pneumonia
  • 5% to 30% mortality, can treated by antibiotics
  • Pathogen does not pass from person-to-person, it is spread from a shared environmental source
    • most effective if the water has been aerosolized
  • Most common point of infection: when a person breathes in Legionella-laden water than has aerosolized from a contaminated source
    Increasingly found in buildings with new technologies that rely on freshwater to heat and cool.
60
Q

Where does Legionella Thrive?

A
  • Air conditioners, cooling towers, evaporative condenser, steam turbines, showers, hot tubs, humidifiers, decorative fountains, and even a grocery store produce mister
  • Pretty tolerant of chlorine and other disinfectants
  • If equipment turned off for a period of time, bacteria can proliferate, and then when turned on → send a greater number of bacteria out into the air.
  • Eg. in the Bellevue-Stratford Hotel, Philadelphia November 1976 where the convention/meeting happened.
61
Q

What are Emergent Disease?

A
  • New, newly discovered, resurgent organisms that are causing illness
    • Legionnaires bacteria was not newly, but newly discovered as a cause of disease
    • Resurgent organisms → things we thought had been dealt with but have become more prevalent in terms of global health (eg. typhoid)
  • Conceptual dates from early 1990s → recognition that late 20th c. have conditions for global spread of emergent disease
  • These conditions include:
    • Human population encroachment into isolated area
      • Habitat destruction
      • Humans are moving into biodiverse habitats → diversity of viruses, bacteria → more opportunities for spillover (eg. that led to HIV)
    • Constantly evolving organisms
    • Accelerating transportation linkages and global trade
      • makes our world much more inter-connected
      • eg. thinking of steamships and plague travelling
      • shorten the time it takes to get from place to place → increase the chance that the pathogen makes the journey as well
      • non-controlled organisms become global threats
  • Legionnaires:
    • What is big about it is Conditions of wealth can bring in disease as well
    • Air conditioning was a luxury and part of a luxurious environment → can create new conditions for pathogens to thrive
62
Q

What is Ebola?

A
  • Filoviridae - Filoviruses
  • Severe hemorrhagic fever in humans and nonhuman primates (4 of the species)
  • Filoviridae virus family includes marburgvirus and ebolavirus
  • 5 species of ebolavirus
  • Zaire, Bundibugyo, Sudan, Restone and Tai Forest
    • Tai forest outbreak in animals
      Ebola Virus Disease
  • 21 days (incubation period)
  • Symptoms
    • Fever, muscle pain, headache, sore throat (early stages)
      • difficult to distinguish from malaria or typhoid fever
    • Vomiting, diarrhea, rash, stomach pain
    • Unexplained bleeding or bruising (internal like in stools or external → bleeding of the gums)
63
Q

Treatments of Ebola?

A
  • Medical care significantly improves survival
  • Rehydration with oral and intravenous fluids
    • ppl usually dying from low blood pressure due to fluid loss
  • Treatment of specific symptoms
  • Two vaccines, initially trialed in 2015 and licensed in 2019 and 2020.
64
Q

When was the first outbreak of Ebola?

A

1976
- 2 outbreaks: Nzara, South Sudan and Yambuku, Democratic Republic of Congo
- Mabalo Lokela, village school headmaster first to fall ill in Yambuku
- After his death, his contacts also started falling ill and dying → panic in village
- Minister of Health required quarantine zone in whole region → schools closed
- Outbreak lasted 26 days (2 week quarantine)
- Then it disappeared → effective medical, sterilization practices, protective clothing, quarantine

65
Q

What happened with Ebola in 2014/2016?

A
  • Largest and most complex ebola outbreak since ebola discovered
  • First started in New Guinea then spread to Liberia, Sierra Leone
  • More limited access to healthcare in urban centres as compared to rural
  • Lack of clarity about how to prevent its spread
  • Ebola has significant impacts on healthcare workers
    • Bc they are working closely with bodily fluids of victims
    • More healthcare workers who suffered
    • About 10% of those who died in 2014/2016 were healthcare. workers
  • Role of non-governmental organizations: MSF
    • Significant role in providing healthcare to countries globally in terms of ebola outbreaks
    • Posed problems:
      • Local healthcare workers could not be evacuated to get healthcare
      • International workers working with MSF could be evacuated → part of MSF’s obligations (duty of care) to employees to provide for them
      • Needed to evacuate a Norwegian doctor → were eventually able to evacuate him → but bc of that many countries started to refuse to let their ppl work with MSF bc they needed to know their ppl could be evacuated if they fell ill with ebola
    • They help to offset the disparities in global health
      • Eg. if a country has a weak healthcare system.
66
Q

Ebola and Spillovers?

A
  • Fruit bats are thought to be natural Ebola virus host, but reservoir HAS YET TO BE CONFIRMED
  • Spillovers when bats or primates are eaten.
  • Great apes (forillas, chimpanzees, orangutans) and other animals (antelope, porcupines, monkeys) are all susceptible to Ebola and can transmit the virus to humans.
  • Fruit bats are easier to catch bc they’re quite big → have a fair bit of meat on them so make a good meal
  • Will find deaths of animals in the forest → a bunch that have died → shows outbreak in animals before

How do you Get Ebola virus?

  • Direct contact with
    1. Body fluids of a person who is sick with or has died from Ebola
    2. Objects contaminated with the virus (needles, )
    3. Infected fruit bats or primates
    4. Possibly from contact with semen from a man who has recovered from Ebola