Tuberculosis
Tuberculosis
REMEMBER!!!!
TUBERCULOSIS IS INITIALLY ASYMPTOMATIC
EPIDEMIOLOGY
• According to the World Health Organization (WHO), nearly 2 billion people—one third of
the world's population—have been exposed to the tuberculosis pathogen.
• annually, 8 million people become ill with tuberculosis, and 2 million people die from the
disease worldwide
• Tuberculosis is the world's greatest infectious killer of women of reproductive age and the
leading cause of death among people with HIV/AIDS
Etiology
-poverty and overcrowding
-energy-protein malnutrition
-multivitamin deficiency vit A, D and C
-presence of debilitating diseases
-
CHILDREN BELOW 5 YEARS OLD- due to inadequate level of immunity
Pathophysiology of Tuberculosis
Precipitating Factors:
Predisposing Factors:
• Age
- Occupation (e.g Health Workers)
• Immunosuppression - Repeated close contact w/ infected persons
• Prolonged corticosteroid therapy - Indefinite substance abuse via IV
• Systemic Infection:
• - recurrence of infectio
Diabetes Mellitus
End-stage Renal Disease
HIV or AIDS infection
Bad Prognosis
DEATH
Mode of transmission
• Direct or indirect contact with infected persons usually by respiratory discharges
• Use of contaminated utensils
• Direct inoculation of the pathogen
• Rarely, through skin lesions
• Drinking cow’s milk containing Mycobacterium bovis
Sources of infection:
• SPUTUM of persons with TB is the usual source of the microorganism
• Blood
• Saliva
Quantitative Classification of TB
• Minimal
• Moderately Advanced
• Far Advance classifications Minimal
• Moderately Advanced
• Far Advance classifications
Clinical Classification
▪ Inactive TB
-symptoms of tuberculosis are absent
-sputum negative
-no evidence of cavity on x-ray
• Active
-Tuberculin test is positive
-x-ray on chest is progressive
-symptoms due to lesions are present
-sputum and gastric contents are positive
• Activity not determined
-no suitable period of observation
-no lab data
Clinical Manifestations
• Afternoon rise of temperature
• Night sweating
• Malaise and weight loss
• Cough, dry to productive
• Dyspnea, hoarseness of voice
• Occasional chest pain
• Sputum positive for AFB
•
HEMOPTYSIS
►SPITTING OF BLOOD OR BLOOD STAINED SPUTUM
►PATHOGNOMONIC SIGN OF TUBERCULOSIS
DIAGNOSTIC PROCEDURES
• SPUTUM ANALYSIS FOR AFB -(CONFIRMATORY)
PURPOSE:
To determine the presence of microorganism
NURSING KEYPOINTS:
• 10-15 ml
• A.M.
• Gargle with water
• Instruct patient to take several deep breaths and then cough deeply
DIAGNOSTIC PROCEDURES
a. CHEST X-RAY
b. Mantoux test (Tubirculin Test)
• Screening test for TB
• Indicator for (+) exposure to TB pathogen
• (+) interpretation parameters:
5mm induration 10mm induration 15mm induration
(+) HIV, AIDS patients (+) immigrants and pediatric (+) general population
patients
REMEMBER!!!!!!!!!!!
• RESULT IS READ 48-72 HRS
• BCG MAY CAUSE FALSE
POSITIVE RESULT
• MANTOUX TEST IS USED TO DETERMINE EXPOSURE TO TB, NOT ACTIVE INFECTION
c. TINE TEST (OT)
• a multiple puncture tuberculin skin test
• This test uses a small "button" that has four to six short needles coated with TB antigens
• The test is read by measuring the size of the largest papule
• A negative result is the presence of no papules
d. HEAF TEST aka 6-prick test (LT)
• diagnostic skin test performed to determine TB exposure
• Given to pedia patients
• After a negative result BCG may be offered
• The test is read between 2 and 7 days later
Result:
Negative - No indurations, maybe 6 minute
puncture scars
Grade 1 - 4-6 papules
(also considered negative)
Grade 2 - Confluent papules form
indurated ring (positive)
Grade 3 - Central filling to form disc (positive)
Grade 4 - Disc >10 mm with or without blistering (strongly positive)
MODALITIES OF TREATMENT
1.Short course chemotherapy may be given through a six-month treatment with Isoniazid(INH),
Rifampicin, Pyrazinamide(PZA), and Ethambutol.
ISONIAZID + VITAMIN B6
REMEMBER!!!!!!!!!
INTAKE OF DRUGS
2-4WEEKS AFTER, THE PATIENT IS NO LONGER CONTAGIOUS
MODALITIES OF TREATMENT
1.Short course chemotherapy may be given through a six-month treatment with Isoniazid(INH),
Rifampicin, Pyrazinamide(PZA), and Ethambutol.
2. Patients with drug resistance may be given with second line drugs such as capreomycin, streptomycin,
cycloserin, amikacin, and quinolone drugs
3. WHO recommends “Direct Observed Therapy” (DOT) to prevent noncompliance. The healthworker
insures that the patient takes his/her drugs.
4. If the medicine is taken correctly, the patient becomes resistant to anti-TB drugs and this is very
dangerous because if the disease recurs it becomes hard to treat the second time around.
5. Relapsing patients usually become resistant to individual drugs (INH, Rifampicin, Ethambutol PZA).
Elements of DOTS
1. Political commitment with increased and sustained financing
2. Case detection through quality-assured bacteriology
3. Standardize treatment with supervision and patient support
4. An effective drug supply and management system
5. Monitoring and evaluation system, and impact measurement.