The Challenges and Pitfalls in Diagnosing or Misdiagnosing Tuberculosis: Are the Days of the TB Skin Test Over?

Theodore F. Them, MD, MS, PhD, MPH, FACOEM

Chief, Section of Occupational & Environmental Medicine Guthrie Clinic, Ltd Sayre, Pennsylvania

Roy F. Chemaly, MD, MPH, FIDSA, FACP

Professor of Medicine Director, Infection Control Section Director, Antimicrobial Stewardship Program University of Texas – MD Anderson Cancer Center Houston, Texas

Objectives

• • • • By the end of this presentation, the attendee should be able to: Explain the consequences of misdiagnosing active or latent TB. Describe the currently available tests and their place in TB diagnosis. Recognize the limitations of different TB screening strategies. Discuss how certain patient populations might benefit from the use of an IGRA in place of the TST for TB screening. 2

Tuberculosis Testing

• • • Currently 2 methods are available for the detection of M. tuberculosis infection in the US: Mantoux tuberculin skin test (TST) Interferon-gamma release assays (IGRAs) CDC guidelines 1 allow the use of IGRAs or the TST for screening healthcare workers 3

Issues Affecting TST Utility

1 • • •

False-Positive Results

– Foreign-born persons (BCG vaccinated) account for 64.6% of all TB cases in US – – Exposure to other mycobacteria Unknown cause

False-Negative Results

– Immunosuppression • AIDS • • Cancer Anti-TNF • Transplant

Noncompliance

– Failure to return for TST interpretation 1. Centers for Disease Control and Prevention. MMWR. 2014. 4

Tuberculin Skin Test (TST) vs Interferon-Gamma Release Assays (IGRAs) • • • • • •

TST

2 visits required (minimum) Method: injection into skin Results affected by BCG Results in 48−72 hours Subjective results Can cause booster phenomenon • • • • • •

IGRAs

1 visit required Method: blood draw Results not affected by BCG Next-day results Objective results Does not cause booster phenomenon 5

Commercially Available IGRAs

• • • • • • • • • • • •

QuantiFERON ® -TB Gold 1

ELISA technology Measures IFN-γ release “One and done” PI sensitivity: 88.2% PI specificity: 99.1% “Real-world” specificity: 98%−98.9% 3,4 3 specialized tubes Provides qualitative results Sample stability: 16 hours No FDA-approved borderline category Can be run in hospital lab Available nationally through reference laboratories (eg, Quest) 1. QuantiFERON-TB Gold Package Insert. Cellestis, Inc. Valencia, CA. Doc. No. US05990301L, March 2013.

2. T-SPOT.TB Package Insert. Marlborough, MA: Oxford Immunotec; 2010. 3. Schablon A, et al. BMC Infect Dis. 2011;(11):245-252. 4. Pai M, et al. Ann Intern Med. 2008;149(3):177-184. • • • • •

The T-SPOT ® .TB Test 2

ELISPOT technology Enumerates effector T cells “One and done” PI sensitivity: 95.6% PI specificity: 97.1% • • • “Real-world” specificity: 98.9%−99.1% 1 standard tube 5,6 Provides quantitative and qualitative results • FDA-approved borderline category • • Sample stability: 32 hours Can be run in hospital lab • Available nationally through Oxford Diagnostic Laboratories ® 5. Wang SH, et al. Scand J Infect Dis. 2010;42(11-12):845-850. 6. Bienek DR, et al. Int J Tuberc Lung Dis. 2009;13(11):1416-1421.

T-SPOT and Oxford Diagnostic Laboratories are registered trademarks of Oxford Immunotec, Ltd.

QuantiFERON is a registered trademark of Cellestis, Inc.

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QuantiFERON® TB Gold

QuantiFERON is a registered trademark of Cellestis, Inc.

Blood Collection for QFT

®

Testing

1 • Collection tubes include: – Nil control (grey cap) – – TB antigen (red cap) Mitogen control (purple cap) • • Tubes require shaking (10 times each) to mix blood with antigens coated on the inside of the tubes, but too much shaking could cause aberrant results.

Blood in collection tubes must be incubated for 16−24 hours at 37°C within 16 hours of collection.

2,3 1.

2.

QuantiFERON-TB Gold Package Insert. Cellestis, Inc. Valencia, CA. Doc. No. US05990301L, March 2013.

Herrera V, et al. J Clin Microbiol. 2010;48(8):2672-2676. 3.

Doberne D, et al. J Clin Microbiol. 2011;49(8):3061-3064.

QFT is a registered trademark of Cellestis, Inc.

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The T-SPOT

®

. TB Test

T-SPOT is a registered trademark of Oxford Immunotec, Ltd.

Blood Collection for T-SPOT

®

.TB

1 • • • Standard phlebotomy techniques Uses a standard lithium or sodium heparin tube Less sensitive to preanalytical variables than QFT – Time from collection to analysis – No specialized tubes needed – No specific order of draw – – No shaking of tubes No incubation required – Specimens maintained at room temperature for up to 32 hours 1. T-SPOT.TB Package Insert. Marlborough, MA: Oxford Immunotec; 2013.

T-SPOT is a registered trademark of Oxford Immunotec, Ltd.

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Consideration of IGRA Logistics

Phlebotomy Steps

Collection tubes Tubes drawn in specific order Blood volume Shake collection tubes Purge tube with butterfly Sample stability

QuantiFERON ® -TB Gold 1

3 specialized tubes Required; Nil, TB antigen, mitogen

T-SPOT ® .TB Test 2

Standard tube N/A 1 mL (0.8−1.2 mL); under- or overfilling outside the 0.8- to 1.2-mL range may lead to erroneous results Required; shake the tubes up and down 10 times Fill 6-mL tube Not required Required when a butterfly needle is used Specimens must be incubated as soon as possible but within 16 hours Not required Up to 32 hours 1. QuantiFERON-TB Gold Package Insert. Cellestis, Inc. Valencia, CA. Doc. No. US05990301L, March 2013.

2. T-SPOT.TB Package Insert. Marlborough, MA: Oxford Immunotec; 2010.

T-SPOT is a registered trademark of Oxford Immunotec, Ltd. QuantiFERON is a registered trademark of Cellestis, Inc.

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Targeted Testing High-Risk Populations for TB

Targeted TB Testing

• • • • • • Close contacts of persons known or suspected to have TB disease Foreign-born from areas of high incidence TB disease America, Africa, Asia, Eastern Europe, and Russia) (Latin Persons who travel to areas with a high prevalence of TB disease Residents and employees of high-risk congregate settings (correctional facilities, long-term care facilities, homeless shelters) Healthcare workers who serve clients or patients who are at increased risk for TB disease Specific populations defined locally as having increased incidence of latent M-TB (possibly including medically underserved, low-income populations, or persons who abuse drugs or alcohol) 13

TB in the US: 2012 Data

1 • • • 9588 new TB cases in US (case rate of 3.0) TB rate among foreign born (FB) was 13x higher than US-born 4 states account for one half of all reported cases: – California – – – Texas New York Florida 1. Centers for Disease Control and Prevention. www.cdc.gov/mmwr/preview/mmwrhtml/mm6211a2.htm?s_cid=mm6211a2_e . 14

TB in the US: 2013 Data¹

• • • • • TB population statistics: 54.2% of 6172 FB persons with TB originated from Mexico, Philippines, India, Vietnam, and China 6.8% reported as HIV+ 5.7% reported being homeless in past year 3.9% confined to correctional facility at time of diagnosis Every 100 contacts not treated will lead to 3 new cases of TB in 1−2 years.

1 1. Centers for Disease Control and Prevention. Trends in Tuberculosis – United States, 2013. MMWR. 2014.

Screening TB Contacts: Acceptance of Diagnosis 1 • • • • The results of this study: Grinsdale J, et al. Int J Tuberc Lung Dis. 2011;15(12):1614–1619. Contacts tested with QFT were more likely to complete evaluation (64% vs 56%).

Infected contacts started (89% vs 72%) and completed (70% vs 53%) LTBI treatment more often in group tested with QFT.

Positive QFT results, but not positive TST results, correlated with the intensity, proximity, and duration of TB exposure.

1.

.

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Clinical Implications with Suboptimal Testing: Employee Health Case

Case Study

• • 41-year-old male Indian nurse who started work at a Cancer Center September 2012. Was referred with a diagnosis of pneumonia. PMHx: February 2012, he started having a cough with off and on sputum production. He was diagnosed with bronchitis and received 2 courses of azithromycin with no improvement. • Referred to a pulmonologist had chest x-ray done in March 2012 and a PPD skin test, which were both negative ; received cefuroxime and later on Levaquin with no improvement. • At that point, he was diagnosed with possible asthma, and was started on inhaled steroids. • His cough got a little bit better initially and started to get worse again.

Case Study

• • December 2012: Worsening cough and hemoptysis now. Saw another pulmonologist in February 2013 for a second opinion. No chest x-ray was done. Was prescribed another course of an antibiotic with no improvement.

Case Study

• Past Social History: – Born and raised in India. He immigrated to Canada in 2005 and then moved to the US few years later. – Working since September 2012 as a nurse on the Stem Cell Transplant Units. – Exposure to an active case of TB 35 years ago when he was a child (his uncle had active TB). – The patient had multiple PPD skin tests, which were negative. He received the BCG vaccine as well. – He is married and he has 2 kids (9-month-old and 6 year-old).

Case Study

• • May 2013: He went back to India for a vacation. He saw an internist who did a Ziehl Neelsen stain on 3 sputum specimens, which came back positive for AFB. His chest x-ray showed bilateral infiltrates. After return to the USA had a positive Quantiferon -TB test done.

May 2013; before therapy October 2013; while on therapy

Testing Special Patient Populations Using IGRAs

Issues Affecting LTBI Diagnosis 1

• • LTBI is difficult to diagnose in immunocompromised patients.

• Risk for progression to active TB is greater in immunocompromised patients.

No gold standard exists to diagnose LTBI.

– TST performs particularly poorly in immunocompromised patients because of an increased likelihood for false-negative results.

1. Redelman-Sidi G, et al. Am J Respir Crit Care Med. 2013;188(4):422-431.

Advantages of IGRAs

• • • • Results are numerical and thus less subject to reader bias. No need for a follow-up visit for reading of results.

Not affected by BCG vaccination status as they use TB-specific antigens that are not present in BCG.

Whatever test for TB you use, understand the variables that affect test results, so that you can manage them and get the most accurate results possible.