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Tuberculosis most commonly affects the lungs. Common symptoms of active lung TB are:
- A persistent cough of more than two weeks that brings up phlegm and blood at times
- Breathlessness, which is usually mild to begin with and gradually gets worse
- Lack of appetite and weight loss
- A high temperature of 38ºC (100.4ºF) or above
- Extreme tiredness or fatigue
- Night sweats
- Chest pains
- Less commonly TB infection can occure in other organs of the body, as :
Lymph nodes , bones and joints, digestive system, nervous system, bladder and reproductive system. This is known as extra pulmonary TB. Symptoms of extra pulmonary TB vary according to organ/system affected. Extra pulmonary TB is more common in people with a weakened immune system, such as those with HIV.
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CAUSES:-
The main cause of TB is Mycobacterium tuberculosis, a small, aerobics, non motile bacillus. TB spread when a person with an active TB infection in their lungs coughs or sneezes and someone else inhales the expelled droplets containing TB bacteria.
Risks factors: The most common risk factor associated with TB is HIV and other conditions that impair the immune system.
Other factors include:
- Tobacco use
- Malnutrition
- Alcoholism
Symptomatic Diagnosis: Coughing for more than 2 weeks, loss of weight, loss of appetite, fever and night sweats, fatigue are common symptoms of tuberculosis. If someone has these symptoms, one should seek medical advice to check whether it is tuberculosis.
Blood tests
- Sputum examination- Samples of mucous and phlegm are checked for the presence of bacteria.
- Chest X-ray: This uses radiation to create an image of lungs. In TB infection, there are changes in the structure of lungs, which of lungs, are visible on the X-ray.
- Drug susceptibility testing: It provides a definitive diagnosis of drug- resistant TB.
- CBNAAT (Cartridges Based Nucleic Acid Amplification Test): CBNAAT is used for early diagnosis of MDR-TB and TB in high risk population such as presumptive TB cases in PLHIV (people living with HIV), EP-TB (extra-pulmonary TB) and pediatric populations. The CB NAAT machines have been placed at most of the districts in the country at headquarter or Medical College, ART Center or major Pediatric hospitals.
For TB of extra pulmonary sites. Diagnosis includes:
- Computerized tomography (CT) scan: A series of X-rays of body is taken at slightly different angles and a computer puts the images together to create a detailed picture of the inside of body.
- Magnetic resonance imaging (MRI) scan: A magnetic field and radio waves are used to produce detailed images of the inside of body.
- Ultrasound scan: High-frequency sound waves create an image of part of the inside of the body.
- Urine tests
- Biopsy: A small tissue sample is taken from the affected site and tested for the presence of disease.
For new TB cases, the treatment in intensive phase (IP) consists of four drugs FDCs- Isoniazid (INH), Rifampicin, Pyrazinamide and Ethambutol (HRZE) in daily doses (as per four weight band categories) for eight weeks and in continuation phase three drugs FDCs with Rifampicin, Isoniazid, and Ethambutol (HRE) are continued for 16 weeks.
For previously treated cases of TB, the intensive phase is of 12 weeks, where injection streptomycin is given for eight weeks along with four drugs FDCs (INH, Rifampicin, Pyrazinamide and Ethambutol) in daily doses (as per weight bands) and after eight weeks streptomycin is stopped, the four drugs FDCs (INH, Rifampicin, Pyrazinamide and Ethambutol) are continued for another four weeks. In continuation phase FDCs containing Rifampicin, INH, and Ethambutol are given for another 20 weeks as daily doses.
The continuation phase in both new and previously treated cases may be extended by 12-24 weeks in certain forms of TB like skeletal, disseminated TB based on clinical decision of the treating physician.
Patients eligible for retreatment should be referred for a rapid molecular test or drug susceptibility testing to determine at least rifampicin resistance, and preferably also isoniazid resistance status. On the basis of the drug susceptibility profile, a standard first-line treatment regimen (2HRZE/4HR) can be repeated if no resistance is documented; and if rifampicin resistance is present, shorter regimen for MDR-TB (multi drug resistant TB) regimen should be prescribed according to WHO’s recent drug resistant TB treatment guidelines.
RNTCP has introduced a new drug bedaquiline for MDR-TB under conditional access programme in 2016 across six sites, with a country wide scale up plan in 2017-2020.
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PREVENTION:-
With the objective to prevent emergence of TB in susceptible population various measures are indicated:
a) Air borne infection control measures-TB infection control is a combination of measures aimed at minimizing the risk of TB transmission in community, hospitals and other settings. Various infection control measures are:
- Early diagnosis, and proper management of TB patients.
- Health education about cough etiquettes and proper disposal of sputum by patient. Cough etiquette means covering nose and mouth when coughing or sneezing. This can be done with a tissue, or if the person doesn’t have a tissue they can cough or sneeze into their upper sleeve or elbow, but they should not cough or sneeze into their hands. The tissue should then be safely disposed of.
- Houses should be adequately ventilated.
- Proper use of air borne infection control measures in health care facilities and other settings.
B) Contact tracing-Since transmission can occur from index case to the contact any time (before diagnosis or during treatment) all contacts of TB patients must be evaluated. These groups include:
- All close contacts, especially household contacts
- In case of paediatric TB patients, reverse contact tracing for search of any active TB case in the household of the child must be undertaken.
- Particular attention will be paid to contacts with the highest susceptibility to TB infection
C) Isoniazid preventive therapy- Preventive therapy is recommended to Children < 6 years of age, who are close contacts of a TB patient. These children should be evaluated for active TB by a medical officer/ pediatrician and after excluding active TB he/she should be given INH preventive therapy.
In addition to above, INH preventive therapy will be considered in following situation: -
- For all HIV infected children who either had a known exposure to an infectious TB case or are Tuberculin skin test (TST) positive (>=5mm induration) but have no active TB disease.
- All TST positive children who are receiving immunosuppressive therapy (e.g. Children with nephrotic syndrome, acute leukemia, etc.).
- A child born to mother who was diagnosed to have TB in pregnancy will receive prophylaxis for 6 months, provided congenital TB has been ruled out. BCG vaccination can be given at birth even if INH preventive therapy is planned.
Close contacts of index cases with proven DR-TB (drug resistant TB) will be monitored closely for signs and symptoms of active TB as isoniazid may not be prophylactic in these cases.
D) BCG vaccination- It is provided at birth or as early as possible till one year of age. BCG vaccine has a protective effect against meningitis and disseminated TB in children.
E) Addressing social determinants of TB like poverty, malnutrition, urbanization, indoor air pollution, etc. requires inter departmental/ ministerial coordinated activities.
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1 Comments
Thank you for the right information
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