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    INFECTION

    Dr. Mehrunnisa Umar Assistant Professor

    Department of Medicine

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    An Observation

    In developed countries infection continues to beone of the most common causes of disease anddeath, particularly in children.

    Infections like pneumonia, diarrhoea, malaria,tuberculosis, and conditions like malnutrition etc.have bad effects on health and growth of nation.

    Vaccination and control of vectors transmittingdiseases has significant effect but diseases tend toreappear.

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    Microbiology

    Microbiology is the science of studying the microbes

    Variety in the genes of microbes explain behavior aswell as how microbes are helpful and/or problematicto us.

    These teeny, tiny dots that we may not even be ableto see with the highest power of our microscopes,are sometimes able to kill us.

    Keep in mind that humankind has also been able toharness the power of the microbial world for ourbenefit using their versatility and success atadaptation.

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    Microbiology

    Given that pathogenic microbes are ubiquitous, whyaren't we sick all the time?

    This is because;

    Species and individual defense mechanisms

    Artificial immunity through immunizations and herdimmunity.

    Public health measures enacted to interrupt naturaltransmission cycles.

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    A complex interaction b/w bacteria & host

    Bacteria must overcome obstacles before diseaseoccurs

    They must enter the host successfully and colonizetissue and then damage host tissue, and grow in thatlocation.

    Microorganisms enter the body, for example, throughrespiratory tract, cuts or wounds, insect bites andconsumption of contaminated food.

    Additionally, hospital procedures involving catheters,intravenous therapy or transplantation increase thechances of microorganisms entering a patients body.

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    Effects of Infection on Human Body

    Acute EffectsFever, lethargy, weakness, catabolism,WBC, anaemia,Inflammation (five signs)Mental disorientation

    Shock Septicaemia, bleedingOrgan Failure

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    Effects of Infection on Human Body

    Chronic EffectsWeight loss, wastingPhysical retardation in childrenMalnutrition

    Chronic damage to organs

    Post infection syndrome - fatigue

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    Effects of Infection on Human Body

    Immune mediatedSkin rashes and nodulation

    Arthritis e.g. RA, RF,SerositisNeuropathy herpes

    Haematological immune damagesNephritis strep

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    Effects of Infection on Human Body

    Toxic (Toxin Mediated)Erythematous strep rashesSTSSToxic diarrhoeasToxic membrane diphtheria

    Bacterial toxins clostridia (tetanus,botulism), diphtheria

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    Pathogenecity - Pathology

    Pathogenicity is the ability to destroy tissueand cause a physiological or anatomicalchange and, eventually disease.

    MECHANISMS OF PATHOGENESISMicroorganisms cause disease by certainbasic mechanisms:

    Invasion of tissue

    Production of toxins

    Virulence

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    Defense Mechanism Of The HumanBody

    The body resists infection and disease in anumber of ways through nonspecificresponses and specific responses.

    Four nonspecific defenses in the body

    Skin

    Mucous membranes

    Phagocytosis

    Inflammation

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    Defense Mechanism Of The HumanBody

    HUMORAL IMMUNITY Antibodies are highly specific protein molecule

    Antibody mediated defenses include:

    Antitoxins,

    Bacteriolytic antibodies, Antibodies plus complement,Opsonizing antibodies

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    Defense Mechanism Of TheHuman Body

    CELL MEDIATED IMMUNITY

    Specific immune response provided by T-

    lymphocytes

    Cell-mediated defenses include:

    Cytotoxic T-lymphocytes,K & NK cells,

    Activated macrophages

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    Host Microbe Interaction

    Host: Any organism that harbors a microbe is a host.

    Mutualism: A relationship between a host and microbewhere they both benefit each other.

    Commensalisms: a relationship between host and microbewhere one benefits and the other is neither harmed nor helped.

    Parasitism: a relationship between host and microbewhere one benefits and the other is harmed.

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    Disease: When an organism can't carry

    out normal cell function, results in adisturbance in state of health.

    Not just microbes that cause thesemalfunctions, but when microbes arethe cause, it's called infectious disease.Infection means the multiplication of apathogenic microbe in a host.

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    Bacterial Diseases

    Infection:During this stage the bacteria are introduced into the bodytissues

    Incubation:During this stage the bacteria multiply in numbers, at timeseven before the body defense mechanism could come intoaction.

    Prodromal Phase: During prodrome the symptoms of disease begin to appear.

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    Clinical Phase:Characteristic clinical features of agiven disease

    Resolution Phase:When diagnosed and appropriatetreatment with antibiotic is instituted,resolution is expected.

    At times the disease complicates andthe patient may be killed by the diseaselike in severe pneumonia

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    Fever

    FEVER is a Diagnostic ClueIt is an essential host defense mechanismAssociated with or without localizing signsIt can be due to Infection, inflammation or neoplasm

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    Fever

    MONOKINES LYMPHOKINES CYTOKINES

    FEVER

    ENDOGENOUS PYROGENS

    InfectionsToxinsInflammationImmunologic

    responses

    MACROPHAGES ENDOTHELIUM

    HYPOTHALAMIC ENDOTHELIUM

    THERMOREGULATORY NEURONSElevated Thermostat

    MacrophagesEndotheliumLymphocytesOther cells

    Behavioral changes

    CORTEX

    PGE2 and otherArachidonicAcid metabolites

    PG

    +

    + PG

    Peripheral efferents

    Muscle contraction

    Heat production

    Vasomotor center

    Sympathetic chain

    casoconstriction

    Heat conservation

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    Fever

    Range 36.8 + 0.4 o C (98.2 + 0.7 o F)

    Lowest at 6 A.M. 37.2 o C (98.9 o F)

    Peak at 4 - 6 P.M. 37.7o

    C (998.9o

    F)

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    Fever Development

    It is controlled increase in body temperatureover normal values

    It is regulated in the same manner as normaltemperature but the thermostat is set at adifferent (higher) level

    Factors that are responsible for setting of thethermostat at a higher level are called

    `Pyrogens`.

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    Fever Development

    PYROGENS:

    Substances (chemicals, toxins or drugs) thatcan cause fever are called pyrogens

    May be exogenous (outside the host) or endogenous (produced by the host)

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    Fever Development

    PYROGENS:

    Exogenous pyrogensLlipopolysacchride found in the outer

    membrane of Gram -ve organisms.Lipteichoic acidPeptidoglycans

    Act primarily by inducing formation of endogenous pyrogens or sometimes acting

    directly on the endothelial cells in the brain.

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    Fever Development

    PYROGENS:

    Endogenous pyrogens are polypeptidesproduced by a variety of host cells, usuallymonocytes and macrophages. They include:

    Interleukin-1 Interleukin - 1 Tumour necrosis factor (TNF )Interferon (IFN) Interleukin 6

    .

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    Fever Development

    PYROGENS:

    Endogenous pyrogens are polypeptidesproduced by a variety of host cells, usuallymonocytes and macrophages. They include:

    Interleukin-1 Interleukin - 1 Tumour necrosis factor (TNF )Interferon (IFN) Interleukin 6

    .

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    Fever

    EFFECTS OF FEVER ON THE BODY:

    BENEFITS:

    Improves survival in animalsImproves inflammatory responses to illness inhumans

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    Fever

    EFFECTS OF FEVER ON THE BODY:

    COSTS:Each one degree Celsius rise in temperature

    increases oxygen consumption by 13%.Increase in caloric and fluid requirement asmore heat and fluid is lost from the body infebrile condition.

    Pyrogens accelerate muscle breakdown.Mental acuity and concentration is reduced.There may be state of delirium to coma.In children, fits may be present.

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    Fever- Patterns

    o Intermittent type temp return to normal onceduring most days

    o

    Remittent type

    temp do not return to normaleach day

    o

    Sustained/Continuous temp do not vary more than 1

    degree F /day

    o Relapsing - recurrent over days to weeks

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    Classical PUO

    1. FEVER MORE THAN 101 F2. MORE THAN 3 WEEKS3. CAUSE NOT DIAGNOSED AFTER ONE WEEK OF

    INTENSIVE HOSP INVESTIGN

    TYPES OF PUO ACUTE,NOSOCOMIAL,HIV ASSOCIATEDNEUTROPENIC PUO

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    PUO causes

    INFECTIONS 30%MALIGNANCY 20%CONNECTIVE TISSUE D- 15 %OTHERS 20 %UNDIAGNOSED 15 %

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    FEVER - Common Clues

    RESPIRATORY SYMPTOMS URTI ,LRTI,TB,URINARY SYMPTOMS UTI,APN,CYSTITISABDOMINAL SYMPTOMS ABSCESS,ACUTEABDOMENARTHRITIS SYMPTOMS RA,SLE,ASTRAVEL HISTORY

    DIETARY HISTORY

    OCCUPATIONAL HISTORY

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    TRAVEL History

    MALARIA ENDEMIC AREASDENGUE FEVER - Eg )SINGAPOREVIRAL FEVERSTYPHOIDTUBERCULOSISSCHISTOSOMIASIS

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    D ietary & Occupational History

    BIRDS PSITTACOSIS

    ANIMALS CONTACT- TOXOPLASMOSIS (CAT),

    BRUCELLOSIS,LEPTOSPIROSIS (RAT)

    UNCOOKED MEAT/SEA FOOD/ -

    HEPATITIS

    A & E,SALMONELLA

    UNPASTEURIZED MILK

    SALMONELLA,TB,BRUCELLOSIS

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    Drug fever

    All drugs can produce Drug INDUCED fever exceptDIGOXINBradycardia, hypotension, Skin rash, pruritus +,

    Eosinophiliaeg) pencillin, sulpha, ATT

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    THERE IS NO SUBSTITUTEFOR OBSERVING THE PATIENT,

    TALKING TO HIM ANDTHINKING ABOUT HIM.

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    FEVER & MYALGIA VIRAL FEVERS LEUCOPENIA &THROMBOCYTOPENIA

    INFLUENZA URTI SYMPTOMS

    POLYMYOSITIS PROXIMAL M WEAKNESS,MUSCLE PAIN & TENDERNESS, CPK HIGH

    MENINGOCOCCAL INFECTION -Rash

    SEPSIS

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    Fever & Night Sweats

    TUBERCULOSISLYMPHOMA

    ABSCESSBRUCELLOSISINFECTIVE ENDOCARDITISALCOHOL WITHDRAWAL SYNDROME

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    FEVER Brady, Tachycardia

    RELATIVE BRADYCARDIA

    TYPHOID FEVERMALARIAMENINGITISLEPTOSPIROSISVIRALDRUG FEVER

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    RELATIVE TACHYCARDIA

    TOXINS

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    Fever & Eyes

    EYE PAIN

    TEMPORAL ARTERITIS WATERY EYES- PANDRY EYES SLE,RA

    SC Hemorrhages SBECONJUNCTIVITIS TB,SLECONJUNCTIVAL SUFFUSION-LEPTOSPIROSISUVEITIS- TB,SLE,SARCOIDOSIS

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    FEVER WITH JAUNDICE

    LEPTOSPIROSIS RENAL FAILURE +HEPATITIS-DRUGS (ATT) ,VIRAL

    ALCOHOLIC HEPATITISCIRRHOSIS OF LIVERHEPATOMA

    VIRAL FEVERSMALARIA

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    GENERALIZED LYMPHADENOPATH LEUKEMIA ALL , CLLLYMPHOMA MEDIASTINAL INVOLVEMENT

    HIV INFECTION

    ORAL CANDIDIASIS,THIN BUILTTOXOPLASMOSIS-WITH LIVER,SPLEENDISSEMINATED TUBERCULOSIS WITH LIVER

    ,SPLEENBRUCELLOSIS-WITH LIVER,SPLEEN

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    FEVER WITH HEPATOSPLENOMEGALY

    MALARIATYPHOIDLYMPHOMALEUKEMIADISSEMINATED TBINFECTIVE ENDOCARDITISBRUCELLOSISKALA AZAR

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    FEVER WITH MENTAL CONFUSION

    MENINGITISMENINGISM- TYPHOIDHIVBRUCELLOSISCNS NEOPLASMS

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    LOCAL TENDERNESS

    TONGUE - RELAPSING FEVERTRAPEZIUS SUB DIAPHRAGMATICABSCESSSTERNAL METASTASIS, PRE LEUKEMIASPINAL BRUCELLOSIS,TYPHOID,SBE,OM

    THIGH - POLYMYOSITIS,BRUCELLOSISCALF POLYMYOSITIS, RMSF

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    FEVER - ARDS

    SARS INFECTIONCEREBRAL MALARIA (P FALCIPARUM )HANTA VIRUS INFECTIONSEPSIS

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    HIGH ESR

    TBTEMPORAL ARTERITISCARCINOMALYMPHOMASABSCESSMYELOPROLIFERATIVE DISORDER

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    FEVER & LOW PLATELETS DENGUE FEVERVIRAL FEVERSLEUKEMIALYMPHOMAMYELOPROLIFERATIVE DISORDER

    DRUG FEVERSLEHIV INFECTION

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    CHEST X-RAY DIAGNOSIS

    TB-ANY FORMLYMPHOMAS-MEDIASTINAL INVOLVEMENTSARCOIDOSIS BHLPNEUMONIASAUTOIMMUNE DISEASES

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    DIAGNOSTIC TESTS ANA,ANTI DS DNA SLEBONE SCAN-OSTEOMYELITIS,METASTASISECHO HEART ATRIAL MYXOMA,IE,PCITIS

    SMEAR TEST + VE MALARIA,ELISA IGM AB -LEPTOSPIRAVIRAL CULTURE + INEBV,CMV INFECTIONS

    BLOOD CULTURE + INIE,SEPSIS,AGGLUTININ TEST + INSALMONELLA ,BRUCELLOSIS

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    ULTRA SOUND

    HEPATOMAABSCESSHYPERNEPHROMA (PHYSICIAN S TUMOUR)LYMPHOMAPELVIC TUMORS

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    Blood cultures for aerobic and anaerobic pathogens.

    maximum 6 sets of blood cultures are required.

    Urine culture

    Cultures of sputum

    Stool Cultures

    Perform cultures for - Bacteria,- Mycobacteria, and- Fungi

    Cultures:

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    Serologies are most helpful if paired samples show asignificant, usually 4-fold, increase of antibodies specificto an infectious microorganism.

    Brucellosis, CMV, infectious mononucleosis, HIV,amebiasis, toxoplasmosis, and chlamydial diseases arediagnosed by serology.

    These diagnostic tests are of limited value in mostpatients with FUO, but they are appropriate for evaluation of the above illnesses in the correct clinicaland epidemiological setting.

    Serologies

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    THANK YOU

    ALL WE KNOW IS STILL INFINITELYLESS THAN ALL THAT REMAINS UNKNOWN

    -WILLIAM HARVEY -