* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Pathogenesis
Harm reduction wikipedia , lookup
Diseases of poverty wikipedia , lookup
Hygiene hypothesis wikipedia , lookup
Focal infection theory wikipedia , lookup
Forensic epidemiology wikipedia , lookup
Transmission (medicine) wikipedia , lookup
Compartmental models in epidemiology wikipedia , lookup
Eradication of infectious diseases wikipedia , lookup
HIV and pregnancy wikipedia , lookup
Public health genomics wikipedia , lookup
Infection control wikipedia , lookup
Fundamentals of Tuberculosis 2 No. of Cases Reported TB Cases United States, 1981-2001 28000 26000 24000 22000 20000 18000 16000 14000 12000 10000 1981 1985 1989 1993 Year 1997 2001 3 TB Case Rates, United States, 2001 D.C. < 3.5 (year 2000 target) 3.6 - 5.6 > 5.6 (national average) Rate: cases per 100,000 4 Trends in TB Cases in Foreign-born Persons, United States, 1986-2001 Percentage No. of Cases 10,000 60 50 8,000 40 30 20 6,000 4,000 2,000 10 0 0 1986 1988 1990 1992 No. of Cases 1994 1996 1998 2000 Percentage of Total Cases 5 Cases per 100,000 TB Case Rates in U.S.-born vs. Foreignborn Persons, United States, 1991-2001 40 30 20 10 0 1991 1993 1995 U.S. Overall 1997 U.S.-born 1999 Foreign-born Note: Case rates for 2000 and 2001 based on an extrapolation from the March 2000 U.S. Census Bureau Current Population Reports. 2001 6 Completion of TB Therapy United States, 1993-1999 100 80 60 40 20 0 1993 1994 Completed 1995 1996 1997 1998 Completed in 1 yr or less Note: Persons with initial isolate resistant to rifampin and children under 15 years old with meningeal, bone or joint, or miliary disease excluded. 1999 7 TB in the United States • From 1953 to 1984, reported cases decreased by approximately 5.6% each year • From 1985 to 1992, reported cases increased by 20% • 25,313 cases reported in 1993 • Since 1993, cases are steadily declining Transmission & Pathogenesis of TB • Caused by Mycobacterium tuberculosis • Spread person to person through the airborne particles that contain M. tuberculosis, called droplet nuclei • Transmission occurs when an infectious person coughs, sneezes, laughs, or sings • Prolonged contact needed for transmission • 10% of infected persons will develop TB disease at some point in their lives 8 9 Common Sites of TB Disease • • • • • • Lungs (85% of all cases) Pleura Central nervous system Genitourinary system Bones and joints Disseminated (miliary TB) 10 Not Everyone Exposed Becomes Infected Probability of transmission depends on: - How Contagious - Kind of Environment - Length of Exposure 11 Development of TB Disease • 10% of infected persons will develop TB disease at some point in their lives • Certain conditions increase the risk that TB infection will progress to disease 12 Factors Contributing to the Increase in TB Cases • HIV epidemic • Increased immigration from high-prevalence countries • Transmission of TB in congregate settings (e.g., correctional facilities, long-term care) • Deterioration of the public health care infrastructure 13 Factors That Increase the Risk of TB Disease Once Infected • • • • HIV infection Substance abuse (especially drug injection) Recent infection with M. tuberculosis Chest radiograph findings suggestive of previous TB (in a person inadequately treated) • Low body weight (10% or more below the ideal) • Certain Medical Conditions, such as….. 14 Medical Conditions that Increase the Risk of TB Disease • • • • • • • • • Diabetes mellitus Silicosis Cancer of the head and neck Hematologic and reticuloendothelial diseases End-stage renal disease Intestinal bypass or gastrectomy Chronic malabsorption syndromes Prolonged corticosteroid therapy Other immunosuppressive therapy 15 Groups at High Risk for TB Exposure • Close contacts of a person with infectious TB • Foreign-born persons from areas where TB is common • Residents of congregate settings • Persons who inject drugs • Locally identified high-burden groups, such as farm workers or homeless persons • Children 16 Clinical Manifestations of TB • • • • • • • Chest pain Productive prolonged cough Hemoptysis Fever, chills, night sweats Easy fatigability Loss of appetite Weight loss 17 TB Diagnostic Tests • Mantoux Tuberculin Skin Test • Chest X-ray • Sputum examination 18 Latent TB Infection (LTBI) • Occurs when person inhales bacteria and it reaches air sacs (alveoli) of lung • Immune system keeps bacilli encapsulated • Person is not infectious and has no symptoms 19 TB Disease • Occurs when immune system cannot keep bacilli contained • Bacilli begin to multiply • Person develops symptoms 20 LTBI vs. TB Disease • LTBI – Asymptomatic – PPD negative – Chest X-ray normal – Sputum negative – Not infectious • TB Disease – Cough, fever, night sweats – PPD positive – Chest X-ray abnormal – Infectious before treatment initiated 21 Targeted Testing • Not everyone should be routinely tested for TB • Testing should be done only if there is an intent to treat 22 Groups to Target with the Tuberculin Skin Test • Persons with or at risk for HIV infection • Close contacts of persons with infectious TB • Persons with certain medical conditions • Persons who inject drugs • Foreign-born persons from areas where TB is common • Medically underserved, low-income populations • Residents of congregate settings • Locally identified high-prevalence groups 23 Performing the Tuberculin Skin Test • Use Mantoux tuberculin skin test • 0.1 ml of 5-TU PPD injected intradermally • Read within 48-72 hours by healthcare worker • Measure transverse diameter of induration • Record results in millimeters of induration 24 Classifying the TST Reaction - 1 >5 mm is positive in • Persons known to have or suspected of having HIV infection • Close contacts of a person with infectious TB • Persons who have a chest radiograph suggestive of previous TB • Persons who inject drugs (if HIV status unknown) 25 Classifying the TST Reaction - 2 > 10 mm is positive in • Person with certain medical conditions, excluding HIV infection • Persons who inject drugs (if HIV negative) • Foreign-born persons from areas where TB is common • Medially underserved, low-income populations • Residents of long-term care facilities • Children younger than 4 years of age • Locally identified high-prevalence groups 26 Classifying the TST Reaction - 3 > 15 mm is positive in • All persons with no known risk factors for TB 27 Classifying the TST Reaction - 4 For persons who may have occupational exposure to TB, the appropriate cutoff depends on: • Individual risk factors for TB • The prevalence of TB in the facility or place of employment 28 BCG Vaccination and Tuberculin Skin Test • There is no reliable method of distinguishing tuberculin reaction caused by BCG from those caused by TB infection • Evaluate all BCG-vaccinated persons who have a positive skin test result for treatment of latent TB infection 29 Anergy • The inability to react to skin tests due to weakened immune system • Do not rule out diagnosis of TB on basis of negative PPD • Consider anergy in non-reactors who: - Are immunocompromised (e.g., HIV+, cancer chemotherapy) - Have overwhelming TB disease 30 Boosting • Some people with history of LTBI lose their ability to react to tuberculin • Baseline test may be negative (immune system “forgets” how to react to TB-like substance) • Another test 1-3 weeks later will be positive (baseline test stimulated/ “boosted” immune system) 31 Two-Step Testing • A strategy for differentiating between boosted reactions and reactions caused by recent infections • 2nd test given 1 - 3 weeks after baseline • Used in many residential facilities for initial skin testing of new employees who will be retested (with single test) on a regular basis 32 Two-Step Testing Baseline PPD test Negative Result Repeat PPD 1-3 weeks later NEGATIVE: POSITIVE: Person probably does not have TB infection This is a “boosted” reaction due to TB infection a long time ago 33 Assessing Infectiousness of a TB Patient • Patients should be considered infectious if they: – Are undergoing cough-inducing procedures – Have sputum smears positive for acid-fast bacilli and: • Are not receiving therapy • Have just started therapy, or • Have a poor clinical or bacterial response to therapy 34 Assessing Infectiousness of a TB Patient • Patients are not considered infectious if they meet all these criteria: – Adequate therapy received for 2-3 weeks – Favorable clinical response to therapy, and – 3 consecutive negative sputum smears results from sputum collected on different days 35 Techniques to Decrease the Possibility of TB Transmission • Instruct patient to: – – – – Cover mouth when coughing or sneezing Wear mask as instructed Open windows to assure proper ventilation Do not go to work or school until instructed by physician – Avoid public transportation – Limit visitors 36 Evaluation for TB • Medical history • Physical examination • Mantoux tuberculin skin test • Chest radiograph • Bacteriologic exam (smear & culture) 37 Symptoms of TB • • • • • • • • • *Productive prolonged cough *Chest pain *Hemoptysis Fever Chills Night sweats Easy fatigability Loss of appetite Weight loss *commonly seen in cases of pulmonary TB 38 Chest X-Ray • Chest X-rays should be done in patients with positive skin test results • Abnormal chest X-ray cannot itself confirm the diagnosis of TB but can be used in conjunction with other diagnostic indicators 39 Sputum Collection • • • • Sputum specimens are essential to confirm TB Mucus from within lung, not saliva Collect 3 specimens on 3 different days Spontaneous morning sputum more desirable than induced specimens • Collect sputum before drug therapy initiated 40 Smear Examination • Strongly consider TB in patients with smears containing acid-fast bacilli (AFB) • Use follow-up smear examinations to assess patient’s infectiousness and response to therapy 41 Cultures • Used to confirm diagnosis of TB • Culture all specimens, even if smear is negative • Initial drug isolate should be used to determine drug susceptibility 42 Treatment of Latent TB Infection • Daily INH therapy for 9 months – Monitor patients for signs and symptoms of hepatitis and neurotoxicity • Alternate regimen – Rifampin for 4 months 43 High Priority Candidates for Treatment of Latent TB Infection Regardless of age Over age 35 - HIV + or suspect - Close contact - Abnormal chest x-ray - Foreign-born - Medically underserved, low-income - Medical conditions - Long term care facilities - Recent converters - Other populations (homeless, HCWs) 44 Treatment of TB Disease • Include four drugs in initial regimen – – – – Isoniazid (INH) Rifampin (RIF) Pyrazinamide (PZA) Ethambutol (EMB) • Adjust regimen when drug susceptibility results are shown • Never add a single drug to a failing regimen • Ensure adherence to therapy 45 Monitoring for Adverse Reactions Instruct patients taking INH, RIF and PZA to report immediately the following: – – – – – – – – nausea loss of appetite vomiting persistently dark urine yellowish skin malaise unexplained fever for 3 or more days abdominal pain 46 Monitoring for Drug Resistance • Primary - Becoming infected with a strain of M. tuberculosis which is already resistant to one or more drugs • Acquired - Becoming infected with a strain of M. tuberculosis which becomes drug resistant due to inappropriate or inadequate drug treatment 47 Barriers to Adherence • • • • • Stigma Extensive duration of treatment Side effects of medications Concerns of toxicity Lack of knowledge of the disease process and necessary treatment 48 Improving Adherence • • • • Case management Directly Observed Therapy (DOT) Patient education Incentives/enablers 49 Directly Observed Therapy (DOT) • Health care worker watches patient swallow each dose of medication • DOT is the best way to ensure adherence • Should be used with all intermittent regimens • Reduces relapse of TB disease and acquired drug resistance 50 Other Measures to Promote Adherence • Develop an individualized treatment plan for each patient • Work with outreach staff from same cultural and linguistic background as patient • Educate patient about TB, medication dosage, and possible adverse reactions • Use incentives and enablers to remove barriers to adherence • Facilitate access to health and social services