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Plague. Dr Navya N Assistant Professor Department Of Community Medicine. SPECIFIC LEARNING OBJECTIVES. To understand the epidemiology of plague disease To understand the clinical features of plague To understand the prevention and control of plague. INTRODUCTION. Zoonotic disease
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Plague Dr Navya N Assistant Professor Department Of Community Medicine
SPECIFIC LEARNING OBJECTIVES • To understand the epidemiology of plague disease • To understand the clinical features of plague • To understand the prevention and control of plague
INTRODUCTION • Zoonotic disease • Causative organism – Yersinia Pestis • One of the oldest diseases known to man • Exits in natural foci – transmitted- infected flea bites
INTRODUCTION • Many forms - enzootically, epizootically, sporadically and in epidemics • Endemic in many parts of the world • Widely distributed in the tropics and subtropics • In SEAR, natural foci of plague- India, Indonesia, Myanmar and possibly in Nepal
PLAGUE PANDEMICS • Justinian plague: Sixth century-100 million victims • Black Death: 14th century - 50 million deaths. • 3rd pandemic: Hong Kong in 1894 • This pandemic resulted in 13 million deaths in India
PROBLEM STATEMENT • Plague outbreaks continued to occur- decreasing frequency • Globally in 2013 – 783 cases- human plague – 126 deaths • In India – 2004- localized outbreaks – bubonic plague – 8 cases, 3 deaths- Dangud village- Uttarkashi
AGENT FACTORS • Gram - negative , non motile, coccobacillus • Bipolar staining with special stains – Wayson’s stain • Reclassified as Enterobacteriaceae • Non sporulating, non - lactose fermenting
RESERVOIR OF INFECTION • Wild rat (Tatera Indica) • Field mice • Gerbils • Disease -Maintained and spread by resistant species of wild rodents (Rodents immune to plague)
SOURCE OF INFECTION • Infected rodents and flea • Case of pneumonic plague
PLAGUE VECTORS • Xenopsyllacheopis(Oriental rat flea; worldwide) • Oropsyllamontanus(United States) • Nosopsyllusfasciatus(Nearly worldwide) • Xenopsyllabrasiliensis(Africa & India) • Xenopsyllaastia(Indonesia and Southeast Asia) • Xenopsyllavexabilis(Pacific Islands)
TRANSMISSION • Flea bite (78%) • Direct animal contact (20%) − Tissues, body fluids, scratches, bites − Enters through break in skin • Aerosol (2%) • Human cases − April-November (93%) − Increased activity of fleas and hosts
BLOCKED FLEA • Flea- ingest upto 0.5 cu.mm of blood- 5000 plague bacilli. • Plague bacilli multiply enormously- gut of rat flea- may block the proventriculus- no food - blocked flea • Blocked flea- eventually faces starvation and dies as it is unable to obtain blood meal. • A blocked flea is an efficient transmitter of plague • A partially blocked flea is more dangerous then a completely blocked flea because it can live longer
HOST FACTORS • AGE and SEX : all ages and both sexes • HUMAN ACTIVITIES : activities – increases flea-man contact • MOVEMENT OF PEOPLE : cargo, sea or land • IMMUNITY : no natural immunity
ENVIRONMENTAL FACTORS • SEASON : north india – September – may South- no definite plague season • TEMPERATURE AND HUMIDITY : 20-25 deg C humidity – 60% • RAINFALL : heavy rainfall – flood the burrows – protective factor • URBAN and RURAL AREAS • HUMAN DWELLINGS
PLAGUE IN RODENTS • Primarily a disease of rodents • Infection is maintained- natural foci of the disease in wild rodent colonies • Enzootic (maintenance) hosts • Epizootic (amplification) hosts
PLAGUE IN RODENTS • Enzootic hosts: • Relatively mild illness and low mortality rates. • Voles and mice • Epizootic hosts: • High susceptibility and high mortality. • Mice, rats, voles, gerbils, ground squirrels and marmots • Rats have historically been a primary carrier
URBAN PLAGUE • Infected fleas or rodents move to urban area • Commensal (domestic) rodents infected • Rapid die off • Fleas seek new host − Domestic cats or humans • Poverty, filth, homelessness
HUMAN PLAGUE -CLINICAL FEATURES • Bubonic Plague • Septicaemic Plague • Pneumonic Plague
BUBONIC PLAGUE • Mode of entry: Flea bite • IP: 2-6 days • Infection spreads to the regional lymph nodes • Headache, chills, fever, malaise and pain in the affected regional lymph nodes • Buboes: Inflammation and swelling in one or several nodes (Axillary and supraclavicular) • Mortality – untreated – 50-60% and treated - <5%
SEPTICAEMIC PLAGUE • Invades and continues to multiply in the bloodstream. • Secondary to bubonic plague or without detectable lymphadenopathy. • DIC, multiple organ failure and ARDS • Complications : Plague pneumonia, plague meningitis and hepatic or splenic abscesses • Mortality – untreated 100%
PNEUMONIC PLAGUE • IP: 1-3 days • Least common-most dangerous and fatal form • Primary – Inhalation of infected droplets – Y Pestis • Secondary complication of septicaemic plague • Chills, fever, headache, body pains, weakness and chest discomfort. • Person to person spread possible • Death if specific antibiotic therapy is not begun within 18 - 24 hours of onset
PREVENTION & CONTROL • Early diagnosis & Treatment • Chemoprophylaxis • Control of fleas • Control of rodents • Vaccination • Surveillance • Health education
DIAGNOSIS • Demonstrate the bacilli • Blood, sputum & aspirates from suspected buboes • Gram, Giemsa, Wright, or Wayson stain • Supportive but not confirmatory
DIAGNOSIS • Cultures: Specific phage lysis • 4 fold in titre to the Yersiniapestis F1 antigen by passive haemagglutination test • Dipstick PHTs • ELISAs for detecting IgM and IgG antibodies
PREVENTION AND CONTROL • Early diagnosis and treatment • Notification: • Antibiotics: Streptomycin drug of choice – IM -2 divided doses – 7-10 days ( 30mg/kg/BW) • Others - Tetracycline, gentamycin • cephalosporins are NOT effective • Isolation • Disinfection
Plague Prophylaxis • Close contacts of cases- pneumonic plague • Persons suspected to have had direct contact with body fluids or tissues of - infected mammal in previous six days • Tetracycline and Chloramphenicol
FLEA INDICES (Multiplication of this index by 100 gives the percentage index)
RODENT AND FLEA CONTROL • Isolate infected animals −Limit number of people in contact, Personal protection- Surgical mask, gloves, eye protection • Flea control−Most effective method to break the chain of transmission (Rodent-flea-man) −Insecticidal spraying (DDT and BHC), malathion −Indoor spraying, Rat burrows- insufflated- insecticidal dusts
VACCINATION • For prevention, not the control of the human plague • Formalin killed vaccine is used. • 1 week prior to anticipated outbreak • 2 doses- SC - interval of 7-14 days • Immunity develops within 7 days • Booster dose to given every 6 months
PREVENTION AND CONTROL • Public health education −Notification of dead rats and suspected plague case • Surveillance • Epidemiological investigation −To determine source of infection −Distribution −Prevalence −Potential spread to human population