A Practical Approach :: Targeted Tuberculin Skin Testing
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The Msinga Experience Lessons Learnt from South Africa 2005–2009 Contents
TUBERCULOSIS MDR/XDR The Msinga Experience Lessons learnt from South Africa 2005–2009 Contents Summary 2 Introduction 4 The MDR/XDR TB epidemic 7 Addressing MDR/XDR TB 10 Turning the tide 15 MDR/XDR TB cases decrease 17 The way forward 20 Endnotes 21 Published in partnership with Umzinyathi District Management January 2009 TUBERCULOSIS MDR/XDR The Msinga Experience Lessons learnt from South Africa 2005–2009 © Pg-images/Dreamstime.com 1 Factors behind the decline in drug resistant TB in Msinga: Summary • The commitment of the Umzinyathi health district management team ensured that TB control was placed at the top of Drug resistant tuberculosis has emerged as a serious public the district’s agenda and that adequate resources health issue around the world. Recent global estimates put were allocated to tackle the number of reported cases for 2006 at close to half a the disease. million. This represents 4.8 percent of all notified TB cases • The management of TB worldwide. An estimated 1.5 million people died from TB in patients was aggressively 2006. addressed by providing In 2006, an outbreak of a deadly and almost incurable refresher training for form of TB was reported in Msinga, Umzinyathi district, a nurses and introducing remote and rural part of KwaZulu-Natal province in South appointment diaries to Africa. The extensively drug-resistant TB or ‘XDR TB’ as it track patients. became known largely occurred among HIV-infected • An increase in the nurse- people, in particular those with terminal AIDS. to-patient ratio also played Patients who were co-infected with XDR TB and HIV an important role in improv- stood little chance of survival. -
The T-SPOT.TB Test Frequently Asked Questions
General tuberculosis information T-SPOT.TB Test description and Frequently asked performance questions T-SPOT.TB Test performance characteristics T-SPOT.TB advantages over tuberculin skin test T-SPOT.TB test results T-SPOT.TB methodology Screening control programs Contact investigations References References Table of contents General tuberculosis information Tuberculosis: Definition, infection and disease 1. What is the scale of the TB problem? 2. How is TB spread? 3. What is TB infection (Latent Tuberculosis Infection “LTBI” or “latent TB”)? 4. What is TB disease (“active TB”)? 5. Are certain groups of individuals at an increased risk of exposure to Mycobacterium tuberculosis? 6. Are certain individuals at an increased risk of progressing from latent TB infection to TB disease? 7. How important is treatment for TB disease? 8. Why is the treatment period for TB disease so long? 9. How important is treatment for TB infection (“LTBI” or “latent TB”)? TB detection 10. Is there a test for the detection of TB infection (“LTBI” or “latent TB”)? • Tuberculin Skin Test (TST) • Interferon-Gamma Release Assays (IGRA) 11. Is there a test for the detection of TB disease (“active TB”)? 12. What are the limitations of the TST? Bacille Calmette-Guérin (BCG) vaccination 13. What is the BCG vaccination? T-SPOT.TB test description and performance 14. What is the intended use of the T-SPOT.TB test? 15. Why does the T-SPOT.TB test measure interferon-gamma? 16. Does the T-SPOT.TB test differentiate between latent TB infection and TB disease? 17. What data is there to support the T-SPOT.TB test in clinical use? 18. -
Faqs 1. What Is a 2-Step TB Skin Test (TST)? Tuberculin Skin Test (TST
FAQs 1. What is a 2-step TB skin test (TST)? Tuberculin Skin Test (TST) is a screening method developed to evaluate an individual’s status for active Tuberculosis (TB) or Latent TB infection. A 2-Step TST is recommended for initial skin testing of adults who will be periodically retested, such as healthcare workers. A 2 step is defined as two TST’s done within 1month of each other. 2. What is the procedure for 2-step TB skin test? Both step 1 and step 2 of the 2 step TB skin test must be completed within 28 days. See the description below. STEP 1 Visit 1, Day 1 Administer first TST following proper protocol A dose of PPD antigen is applied under the skin Visit 2, Day 3 (or 48-72 hours after placement of PPD) The TST test is read o Negative - a second TST is needed. Retest in 1 to 3 weeks after first TST result is read. o Positive - consider TB infected, no second TST needed; the following is needed: - A chest X-ray and medical evaluation by a physician is necessary. If the individual is asymptomatic and the chest X-ray indicates no active disease, the individual will be referred to the health department. STEP 2 Visit 3, Day 7-21 (TST may be repeated 7-21 days after first TB skin test is re ad) A second TST is performed: another dose of PPD antigen is applied under the skin Visit 4, 48-72 hours after the second TST placement The second test is read. -
Prior Tuberculin Skin Testing Does Not Boost Quantiferon-TB Results in Paediatric Contacts
REFERENCES 4 Aaron SD, Vandemheen KL, Fergusson D, et al. Tiotropium 1 Suissa S, Ernst P, Vandemheen KL, Aaron SD. in combination with placebo, salmeterol, or fluticasone– Methodological issues in therapeutic trials of COPD. Eur salmeterol for treatment of chronic obstructive pulmonary Respir J 2008; 31: 927–933. disease: a randomized trial. Ann Intern Med 2007; 146: 2 Sin DD, Wu L, Anderson JA, et al. Inhaled corticosteroids 545–555. 5 Wedzicha JA, Calverley PM, Seemungal TA, et al. The and mortality in chronic obstructive pulmonary disease. prevention of chronic obstructive pulmonary disease exacer- Thorax 2005; 60: 992–997. bations by salmeterol/fluticasone propionate or tiotropium 3 Calverley PM, Anderson JA, Celli B, et al. Salmeterol and bromide. Am J Respir Crit Care Med 2008; 177: 19–26. fluticasone propionate and survival in chronic obstructive pulmonary disease. N Engl J Med 2007; 356: 775–789. DOI: 10.1183/09031936.00030508 Prior tuberculin skin testing does not boost QuantiFERON-TB results in paediatric contacts To the Editors: children were evaluated with TST and QFT-GIT. At the first visit, 63 (77.8%) contacts were QFT-GIT negative, eight (9.9%) We read with interest the paper by LEYTEN et al. [1], which were QFT-GIT positive and 10 (12.3%) had an undetermined appeared in the June 2007 issue of the European Respiratory QFT-GIT. Of those initially negative children, only one became Journal (ERJ). LEYTEN et al. [1] showed that prior tuberculin skin QFT-GIT positive after TST. The mean IFN-c antigen-specific 1 tests (TST) do not induce false-positive QuantiFERON -TB production did not change 11 weeks after skin testing (ESAT-6/ Gold in-tube (QFT-GIT) assay results when evaluated in the CFP-10/TB7.7 difference -0.030 IU?mL-1,p50.281). -
Tuberculosis in Infants Less Than 3 Months Ofage
Archives of Disease in Childhood 1993; 69: 371-374 371 Tuberculosis in infants less than 3 months of age Arch Dis Child: first published as 10.1136/adc.69.3.371 on 1 September 1993. Downloaded from H S Schaaf, R P Gie, N Beyers, N Smuts, P R Donald Abstract identified from a register of cases proved by The clinical and radiological features in 38 culture. infants less than 3 months of age with A history of contact with adult pulmonary tuberculosis proved by culture are tuberculosis, the presenting symptoms and described and may aid early diagnosis of their duration, and clinical features such as this often fatal condition. Respiratory lymphadenopathy, respiratory signs, and the symptoms, cough in 33 (87%) and tachyp- presence of hepatosplenomegaly were noted. noea in 31 (82%), were the commonest Tuberculin testing was either by Mantoux test presenting symptoms. Twenty five infants 5 units purified protein derivative or Tine test (66%) had hepatomegaly and 20 (53%) (Lederle) with an induration of > 15 mm or a splenomegaly. Mantoux testing gave an confluent reaction respectively being regarded induration of >15 mm in three of 17 (18%) as significant. infants. In a further five a Tine test gave The chest radiographs of 27 (71%) of the 38 confluent response. Chest radiography in infants were assessed systematically by a panel 27 infants showed miliary tuberculosis in consisting of all the authors. Particular seven (26%) and hilar or paratracheal attention was paid to the presence of miliary adenopathy in 14 (52%) and 10 (37%) tuberculosis, the presence of hilar or para- respectively. -
TB Policies in 24 Countries a Survey of Diagnostic and Treatment Practices About Médecins Sans Frontières
Out of Step 2015 TB Policies in 24 Countries A survey of diagnostic and treatment practices About Médecins Sans Frontières Médecins Sans Frontières (MSF) is an independent international medical humanitarian organisation that delivers medical care to people affected by armed conflicts, epidemics, natural disasters and exclusion from healthcare. Founded in 1971, MSF has operations in over 60 countries today. MSF has been involved in TB care for 30 years, often working alongside national health authorities to treat patients in a wide variety of settings, including chronic conflict zones, urban slums, prisons, refugee camps and rural areas. MSF’s first programmes to treat multidrug-resistant TB opened in 1999, and the organisation is now one of the largest NGO treatment providers for drug-resistant TB. In 2014, the organisation started 21,500 patients on first-line TB treatment across projects in more than 20 countries, with 1,800 patients on treatment for drug-resistant TB. About the MSF Access Campaign In 1999, on the heels of MSF being awarded the Nobel Peace Prize – and largely in response to the inequalities surrounding access to HIV/AIDS treatment between rich and poor countries – MSF launched the Access Campaign. Its sole purpose has been to push for access to, and the development of, life- saving and life-prolonging medicines, diagnostics and vaccines for patients in MSF programmes and beyond. About Stop TB Partnership The Stop TB Partnership is leading the way to a world without TB, a disease that is curable but still kills three people every minute. Founded in 2001, the Partnership’s mission is to serve every person who is vulnerable to TB and to ensure that high-quality treatment is available to all who need it. -
Health Care Provider Information
Health Care Provider Information NOTE: This page is a resource for Whatcom County clinicians dealing with tuberculosis: recognizing active disease and screening for and treating latent infection. The Whatcom County Health Department provides this as a tool/resource in our collaboration with community clinicians, and we welcome feedback and suggestions for additions and changes that improve its usefulness. (Contact Info) Distinguishing Active TB Disease from Latent Infection TB life cycle/Transmission: Tuberculosis (TB) is a disease caused by bacteria (Mycobacteria tuberculosis, or Mtb) transmitted from people with active pulmonary or laryngeal TB disease as aerosolized particles that are suspended in air. Other people may inhale these infectious particles and become infected with Mtb. In the vast majority of cases, their immune system responds to the infection and walls it off, resulting in a latent tuberculosis infection with no disease (and not contagious). When the infected person is immunosuppressed (e.g., HIV/AIDS) or has an immature immune system (young child), the infection may progress to primary active disease without latency. Immune response: The asymptomatic, noncontagious cases are identified by measuring their immune response to tuberculosis, using a TB skin test (TST) or a blood test (interferon gamma release assay, or IGRA). Progression to disease: About 5% of those with latent infection progress to active tuberculosis disease in the first two years after becoming infected. The risk for progression after that is about 0.1% per year (1% per decade of remaining lifetime). The risk of progression increases with conditions that suppress the immune system. This progression can occur with initial infection (primary disease) or after a latent period (reactivation disease). -
Mdr Tb Exposure Screening and Treatment Recommendations
Screening and Treatment Recommendations for People Exposed to Multidrug Resistant TB All people at increased risk of tuberculosis (TB) infection should be screened for TB infection per United States Preventive Services Task Force [1] and Centers for Disease Control and Prevention guidelines [2]. This document provides specific guidance for screening and post- screening management of all people who have been identified through public health investigations as having been exposed to multidrug resistant tuberculosis (MDR TB). Recommendations for symptomatic contacts, children less than 5 years of age and those who are highly immunocompromised (see step 1B) are different from other groups. Step 1: Initial Screening A. Assess contacts for symptoms of active TB disease ▪ Cough lasting 3 weeks or longer ▪ Contacts reporting cough of less than 3 weeks duration at the time of screening should have follow-up to determine if the cough has resolved. If they have a persistent cough for greater than or equal to 3 weeks, further evaluation is indicated. ▪ Hemoptysis (coughing up blood) ▪ Chest pain ▪ Night sweats ▪ Fevers or chills ▪ Unintentional weight loss ▪ Loss of appetite ▪ Fatigue B. Obtain a medical history including prior TB screening and TB treatment information ▪ Contacts with prior positive tuberculin skin test (TST) or interferon-gamma release assay (IGRA) results (documentation of previous testing is recommended) do not need a new TST or IGRA performed; they should be considered to have a positive TB screening test. In the event a person with a past positive TST or IGRA has a new TST or IGRA performed and it is negative, the significance of the new screening test is uncertain. -
Chapter 5 Diagnosis of Latent Tuberculosis Infection (LTBI)
Chapter 5 Diagnosis of Latent Tuberculosis Infection (LTBI) CONTENTS Introduction ............................................. 5.2 Purpose................................................................ 5.2 Policy ................................................................... 5.2 Tuberculosis Classification System ..... 5.3 High-Risk Groups ................................... 5.4 Diagnosis of Latent Tuberculosis Infection ........................... 5.5 Interferon gamma release assays ........................ 5.5 Selecting a TB screening Test ............................. 5.6 Mantoux tuberculin skin testing ........................... 5.7 Candidates for Mantoux tuberculin skin testing ........................................................... 5.8 Administration of the tuberculin skin test ........... 5.11 Measurement of the tuberculin skin test ........... 5.13 Interpretation of the tuberculin skin test ............. 5.14 Human immunodeficiency virus screening ........ 5.16 Follow-up activities ............................................. 5.16 Chest radiography .............................................. 5.16 Resources and References ................. 5.19 NEVADA TUBERCULOSIS PROGRAM MANUAL Diagnosis of Latent Tuberculosis Infection 5 . 1 R e v i s e d A P R I L 2 0 1 8 Introduction Purpose Use this section to understand and follow national and Nevada State guidelines to do the following: ▪ Classify patients with latent TB infection (LTBI). ▪ Diagnose LTBI. In the 2005 guideline “Controlling Tuberculosis in the United States: -
Tuberculin Testing: Its Basis, Methods, and Comparative Results
Tuberculin testing: Its basis, methods, Tuberculin test and comparative results DOUGLAS P. HAGEN, D.O. Kirksville, Mo. Several procedures for administering test has converted to positive. Several methods tuberculin for skin testing of performing tuberculin skin tests will be re- viewed, and the results of the methods will be are reviewed. The Mantoux test is compared. considered the most accurate, in that the test dose can be measured Basis for tuberculin testing accurately, the equipment and During the first infection with the tubercle materials required are available readily, bacillus, the host acquires hypersensitivity to the organism. Hypersensitivity can be induced and the reactions can be read by the whole tubercle bacillus alone or a and recorded quantitatively. Its chief combination of the wax fraction of the or- disadvantage is the skill required ganism containing a lipopolysaccharide and to administer the test. Multiple-puncture tuberculoprotein but not by tuberculoprotein techniques need minimal skill alone. The reaction that occurs when an anti- for administration and false negative gen to tuberculosis is introduced intradermally provides a valuable testing procedure for both reactions are rare. However, the epidemiologic and case finding purposes. tuberculins are not well standardized, Tuberculin testing material is basically of the dose of tuberculin two types, old tuberculin (OT) and purified retained in the skin is unknown, and protein derivative (PPD). Old tuberculin is false positive reactions may a concentrated filtrate of broth in which tu- occur. Because of the variables affecting bercle bacilli have grown for 6 weeks. Cultures of Mycobacterium tuberculosis are heat-ster- the dose, quantitative measures ilized. -
Faqs for Health Professionals Quantiferon®-TB Gold Plus
FAQs for Health Professionals QuantiFERON®-TB Gold Plus Sample to Insight Contents Questions and answers 4 About TB 4 What is latent TB? And how is it different from active TB disease? 4 What is the meaning of ‘remote’ or ‘recent’ TB infection and can QFT distinguish between remote and recent infection? 5 Why is latent TB infection important? 5 How should screening for TB and LTBI be prioritized? 5 Is latent TB contagious? 7 Doesn’t everybody in high-incidence countries have latent TB? 7 About QFT-Plus 8 What is QFT-Plus? 8 What is the intended use of QFT-Plus? 8 How does QFT-Plus differ from QFT 9 What is the benefit of detecting immune responses from CD8 T cells 10 Why not have only CD8 T cell response in TB2 instead of CD4 and CD8? 10 Has TB7.7 been removed? Why? 10 Why the fourth tube? 10 In what clinical situations can QFT-Plus be used? 11 Can QFT-Plus distinguish between active TB and LTBI? 12 How does it work? 12 Why measure interferon-gamma? 12 How does QFT-Plus differ from the TST? 12 How long does it take to get QFT-Plus results? 13 Does a prior TST influence a QFT-Plus result? 14 What is the minimum time necessary to wait between exposure to M. tuberculosis and QFT-Plus testing? 14 Why do you include a positive control? How does this work? 14 What approvals does QFT-Plus have? 14 What is the evidence supporting QFT and QFT-Plus? 15 2 QuantiFERON-TB Gold Plus FAQ for Health Professionals 09/2017 Sensitivity and specificity of QFT-Plus 15 Why is it important to have a test with high specificity? 15 QFT-Plus procedure 17 What -
Robert Koch from Obscurity to Glory to Fiasco
Robert Koch From Obscurity to Glory to Fiasco Martin Dworkin Professor Emeritus, MicroBiology University of Minnesota Article Number: 1 Date of publication: October 5, 2011 Follow this and additional works at: http://purl.umn.edu/148010 Recommended Citation: Dworkin, Martin (2013). Robert Koch From Obscurity to Glory to Fiasco, Journal of Opinions, Ideas, and Essays. October 5.2011 Article #1. Available at http://purl.umn.edu/148010. Submissions will be accepted from any member of the University of Minnesota community. Access will be free and open to all. ROBERT KOCH: FROM OBSCURITY TO GLORY TO FIASCO Martin Dworkin Department of Microbiology University of Minnesota The Early Years Nunquam otiosus (21) Robert Koch was born in 1843 in Clausthal, Germany, a small mining city in Lower Saxony. His father was a mining engineer and Robert was one of eleven surviving children. During his early education he decided to become a teacher but always had an inclination toward natural science. Shortly after entering the University of Gottingen, one of Germany’s leading universities, his interactions with such great scientists as Henle, Wohler, and Meissner convinced him that natural science was to be his destiny. However, practical considerations led him to study medicine. While it became quickly clear that he had a talent for experimentation, Koch was a practical man and his impending marriage to Emmy Fraatz made it clear that a steady source of income was a reality. After completing his medical studies in 1866, Koch took and passed the state medical examination and became licensed to practice medicine. During the next six years he had five different positions as a practicing physician.