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David Horne, MD, MPH

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Title: David Horne, MD, MPH


1
You want me to take how many months of
medication? Advising your patient on risks vs.
benefits of LTBI treatment
  • David Horne, MD, MPH
  • Division of Pulmonary and Critical Care
  • Harborview Medical Center
  • University of Washington

2
Outline
  • LTBI Definition, Guideline History
  • Risks Progression to Active TB
  • Risks Treatment
  • Cost vs. Benefit
  • Discussing with your patient
  • Caveat examples use TST isoniazid

3
What is Latent TB Infection?
  • Evidence of prior exposure to Mtb, based on
    interrogation of T cells, without clinical,
    radiographic or microbiologic evidence of active
    disease
  • latency should not imply dormancy of Mtb
    without metabolic activity
  • TB historically 2-state condition active TB or
    latent infection

Spectrum ???
4
TB Outcomes after Exposure
  • Dogma ? Lifetime risk of reactivation TB 5-10
  • Patient May be substantial over- or
    under-estimate of risk

Small NEJM 2001
5
LTBI Screening Treatment Balance
  • Only 10 of individuals with positive LTBI test
    will progress to active TB
  • Adverse effects related to treatments
  • Poor completion rates
  • 70 of TB cases in U.S. due to reactivation
  • LTBI treatment is effective

6
LTBI Screening Recommendations A History
  • Isoniazid - introduced in 1952 for treatment of
    active TB
  • In 1955, use expanded to include treatment of
    LTBI
  • Campaign for widespread prophylaxis instituted
    (genl popln screening)
  • Early 1970s, liver injury deaths due to
    isoniazid hepatotoxicity
  • 1974, ATS recommended restricting prophylaxis to
    lt 35 years of age unless increased risk for
    activation
  • Ensuing years, further decrease in INH use among
    young individuals
  • 2000 Guidelines -Targeted Tuberculin Testing 
  • INH-related morbidity lower than believed
  • Focus on testing/treatment of individuals at high
    risk of progression to active TB

7
LTBI recommendations
  • Targeted tuberculin testing for LTBI identifies
    persons at high risk for developing TB who would
    benefit by treatment of LTBI, if detected.
  • 2000 ATS Guidelines, Targeted Tuberculin Testing
    and Treatment of LTBI

8
Targeted Testing (2000 Guidelines)
  • Recent Infection with M. tuberculosis
  • Close contacts
  • Recent immigrants from areas with high TB rates
    (lt 5 years)
  • Known converters
  • Children younger than 5 years
  • Homeless, IVDU, institutional setting exposures
  • Increased Risk for Progression
  • HIV infection
  • CXR suggestive of old TB (fibrotic)
  • Medical conditions diabetes, silicosis,
    dialysis, cancer, underweight
  • Medically immunosuppressed

9
Targeted Testing Broad Identification
  • 22 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, CXR normal
  • Same person, but 42 years of age immigrated 3
    years prior
  • Same person, but 72 years of age immigrated 3
    years prior

10
Updated Risk Estimates for Active TB
11
Risk of TB Comparing Estimates
RR Estimates, ATS Guidelines 10-25
2-4 30 2-5
12
Risk Active TB Age
Horsburgh, NEJM 2004 350
13
Risk of Active TB
14
Risk of Active TB Immigration
  • Targeted Testing includes recent (lt 5 years)
    immigrants from areas with high TB rates
  • New arrivals from high-incidence countries
    hypothesized to arrive with high-risk early
    latency because of ongoing exposure
  • High TB rates immediately after arrival assumed
    to indicate that reactivation risk declines with
    time in US
  • U.S. TB cases 63 among foreign born (2012)

15
U.S. TB Cases Different Trends by Birth
16
TB Case Rates Remain Elevated in Foreign Born for
Years after Immigration
Cain JAMA 2008
17
Changes in Reactivation Risk Among Immigrants
  • To address marked difference between 1st year and
    subsequent years following immigration, Walter et
    al looked at immigration from Philippines
  • Separated out those who had abnormal immigration
    CXR and developed TB in 1st year (presumed active
    inactive TB)
  • Among those with normal CXRs There was no
    decline in TB reactivation over 9-year period
    (32/100,000)

Walter AJRCCM 2014
18
Durable Reactivation Risk Differs by Region of
Origin
Cain AJRCCM 2007
19
Seattle-King County Experience
PHSKC Annual Report on TB, 2010
20
Risk of Active TB - Summary
  • Major Risk Factors include
  • Age
  • HIV
  • CXR upper lobe fibronodular disease
  • Moderate Risk
  • Recent Conversion
  • Among immigrants risk varies by region of origin
    and may persist

21
Treatment Risks
  • Of INH adverse effects, drug-induced liver injury
    (DILI) most feared
  • Significant transaminase elevation 0.1-0.6
  • RFs age, EtOH, ethnicity
  • USPHS study from 1970s still quoted 20 - 34
    years 0.3, 35-49 1.2, 50 64 2.3, gt65
    years 4.6
  • Seattle study 0.28 of gt65 years
  • 2004-0817 severe adverse events associated with
    INH
  • 5 died, 5 liver txpestimated 291,000-433,000
    treated annually
  • Other LTBI regimens likely safer than INH

22
Cost-Benefit the Societal Perspective
  • Older studies have supported screening and
    treatment of LTBI as cost-effective for all risk
    groups (e.g. Rose Arch Int Med 2000)
  • Recent study using revised estimates of LTBI
    progression, completion rates of LTBI identified
    cost effectiveness for certain risk groups (Linas
    AJRCCM 2011)

23
Cost-Benefit the Societal Perspective
24
Assessing your patients risk
25
Individual Risk Stratification Online TST/IGRA
Interpreter www.tstin3d.com
26
TB Risk Estimates tstin3d.com
  • 22 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, CXR normal?5.8 lifetime risk
  • 42 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, CXR normal?3.8 lifetime risk
  • 42 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, DM (Hgb A1c 7.9)? 10.6 lifetime risk
  • 42 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, CXR shows stable RUL fibronodular
    changes ? 47.6 lifetime risk
  • 73 y/o Filipino woman, immigrated 3 years ago
    TST 15mm, CXR normal? 0.7 lifetime risk

27
Risk Estimates - tstin3d.com
  • May overestimate individual risk of TB
    progression
  • Assumes baseline annual risk of TB 0.1 in
    healthy persons
  • If patient is recent close contact, then risk of
    TB is 5 for the first 2 years and 0.1
    thereafter
  • Horsburgh differences
  • Same baseline risk, lower risks following new
    conversion by age group
  • Lower risks for progression in co-existing
    conditions
  • May overestimate INH DILI risk

28
Shared Decision Making Risk Stratification
Advising Your Patient
  • At what level of risk for TB progression should
    you recommend LTBI Treatment?
  • No guideline recommendations
  • Some experts use cut-offs of 3 risk or 5 risk
  • Based on USPHS study estimated risk of
    age-related INH toxicity (50 64 2.3, gt65
    years 4.6 percent)
  • Remember Seattle study, 0.28 of gt65 years

29
Shared Decision Making
  • Firm cut-off will not be appropriate for all
    situations
  • Individual costs involve more than DILI
  • Discuss with patient using available tools
  • Patients need to be motivated to actually
    complete treatment
  • Completion rates lt 50 in many series

30
In Summary
  • Risk for progression to active TB varies by
    patient factors
  • Age of patient important in calculating life-time
    risk
  • Duration of risk following immigration likely
    longer than previously stated region of origin
    may impact risk

31
In Summary
  • Better tools are available for risk assessment
    and may aid clinicians and patients in
    considering LTBI treatment
  • To treat or not to treat? Have a discussion
  • Alternative Regimens are increasingly popular
    improved completion rates
  • LTBI guidelines overdue for update

32
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