Dear Colleague Letters

June 7, 2019

Dear Colleagues:

TB Medication

CDC is anticipating a nationwide shortage of Aplisol beginning in June 2019 and potentially lasting for 10 months. Attached for your reference is a copy of the official CDC Health Advisory Notice that was issued yesterday, June 6 to ensure rapid and broad awareness of this shortage.

We have provided colleagues in the CDC Info call center with scripts to help answer inquiries from the public; specifically, if a clinician calls for advice, it will include guidance to contact their state or local TB control programs to better understand how their jurisdiction is responding to the shortage.

FDA has informed us that they will post updates on Aplisol availability to their websiteexternal icon as information becomes available from the manufacturer.

Sincerely,

/Philip LoBue/
Philip LoBue, MD, FACP, FCCP Director
Division of Tuberculosis Elimination
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention Centers for Disease Control and Prevention
Centers for Disease Control and Prevention

 

This is an official
CDC HEALTH ADVISORY

Distributed via the CDC Health Alert Network
June 6, 2019, 1130 ET (11:30 AM ET)
CDCHAN-00420

Nationwide Shortage of Tuberculin Skin Test Antigens:
CDC Recommendations for Patient Care and Public Health Practice

 Summary
The Centers for Disease Control and Prevention (CDC) is expecting a 3 to 10 month nationwide shortage of APLISOL®, a product of Par Pharmaceuticals. APLISOL® is one of two purified-protein derivative (PPD) tuberculin antigens that are licensed by the United States Food and Drug Administration (FDA) for use in performing tuberculin skin tests. The manufacturer notified CDC that they anticipate a supply interruption of APLISOL® 5 mL (50 tests) beginning in June 2019, followed by a supply interruption of APLISOL® 1 mL (10 tests) in November 2019. The expected shortage of APLISOL® 1 mL (10 tests) could occur before November 2019, if demand increases before then. The 3-10 month timeframe for the nationwide shortage is the manufacturer’s current estimate and is subject to change.

To monitor the status of this supply interruption, visit FDA’s “Center for Biologics Evaluation and Research (CBER)-Regulated Products: Current Shortages” webpage: https://www.fda.gov/vaccines- blood-biologics/safety-availability-biologics/cber-regulated-products-current-shortagesexternal icon.

Background
Two types of immunological methods are used for detecting Mycobacterium tuberculosis infection: tuberculin skin tests (TSTs) and interferon-gamma release assay (IGRA) blood tests. TSTs and IGRAs are used for diagnosing latent TB infection and may aid in diagnosing TB disease. Additional evaluation and testing is necessary to distinguish between latent TB infection and TB disease, and to determine the correct treatment (1). When findings, such as chest radiography and mycobacterial cultures, are sufficient for confirming or excluding the TB diagnosis, the results from a TST or an IGRA blood test might not be needed (1). Most TB cases in the United States are diagnosed with a set of findings including results from one of these tests.

Two FDA-approved PPD tuberculin antigens are available in the United States for use in performing TSTs: TUBERSOL® and APLISOL®. In controlled studies, the concordance between the two products is high (2).

When TB disease is strongly suspected, specific treatment should be started regardless of results from TST or an IGRA blood test (3,4).

Recommendations
CDC recommends three general approaches to prevent a decrease in TB testing capability because of the expected shortage of APLISOL®.

  • Substitute IGRA blood tests for TSTs. Clinicians who use the IGRA blood tests should be aware that the criteria for test interpretation are different from the criteria for interpreting TSTs (3).
  • Substitute TUBERSOL® for APLISOL® for skin testing. In cross-sectional studies, the two skin test products give similar results for most patients.
  • Prioritize allocation of TSTs, in consultation with state and local public health authorities. Prioritization might require the deferment of testing some persons. CDC recommends testing only for persons who are at risk of TB (5-7). High-risk groups for TB infection include:
    • People who are recent contacts exposed to persons with TB disease;
    • People born in or who frequently travel to countries where TB disease is common;
    • People who currently or used to live in large group settings, such as homeless shelters or correctional facilities;
    • People with weaker immune systems, such as those with certain health conditions or taking certain medications that may alter immunity; and
    • Children, especially those under age 5, if they are in one of the risk groups noted

While overall test concordance is high, switching between PPD skin test products or between TSTs and blood tests in serial testing may cause apparent conversions of results from negative to positive or reversions from positive to negative. This may be due to inherent inter-product or inter-method discordance, rather than change in M. tuberculosis infection status (3,8). Clinicians should assess test results based on the person’s likelihood of infection and risk of progression to TB disease, if infected (1).

In settings with a low likelihood of TB exposure, the deferment of routine serial testing should be considered in consultation with public health and occupational health authorities. Annual TB testing of health care personnel is not recommended unless there is a known exposure or ongoing transmission (8).

References

  1. Lewinsohn, David M., et al. “Official American Thoracic Society/Infectious Diseases Society of America/Centers for Disease Control and Prevention clinical practice guidelines: diagnosis of tuberculosis in adults and children.” Clinical Infectious Diseases 64.2 (2017): e1-e33. https://academic.oup.com/cid/article/64/2/e1/2629583external icon
  2. Villarino ME, Burman W, Wang Y, et Comparable specificity of 2 commercial tuberculin reagents in persons at low risk for tuberculous infection. JAMA. 1999;281(2):169–171. http://dx.doi.org/10.1001/jama.281.2.169external icon
  3. Centers for Disease Control and Prevention. Updated guidelines for using interferon gamma release assays to detect Mycobacterium tuberculosis infection — United States, 2010. MMWR 2010;59(RR- 5): 1-25. http://www.cdc.gov/mmwr/PDF/rr/rr5905.pdfpdf icon
  4. Nahid, Payam, et al. “Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America clinical practice guidelines: treatment of drug- susceptible tuberculosis.” Clinical Infectious Diseases 63.7 (2016): e147-e195. https://academic.oup.com/cid/article/63/7/e147/2196792external icon
  5. Centers for Disease Control and Prevention. Targeted tuberculin testing and treatment of latent tuberculosis MMWR 2000;49(RR-6): 1-51. http://www.cdc.gov/mmwr/PDF/rr/rr4906.pdfpdf icon
  6. Centers for Disease Control and Prevention. Guidelines for the investigation of contacts of persons with infectious tuberculosis; recommendations from the National Tuberculosis Controllers Association and CDC, and Guidelines for using the QuantiFERON®-TB Gold test for detecting Mycobacterium tuberculosis infection, United States. MMWR 2005;54(No. RR-15): 1-47. https://cdc.gov/mmwr/pdf/rr/rr5415.pdfpdf icon
  7. US Preventive Services Task Force. Screening for latent tuberculosis infection in adults: US Preventive Services Task Force recommendation statement. JAMA. 2016;316(9):962–969. DOI: http://dx.doi.org/10.1001/jama.2016.11046external icon
  8. Sosa LE, Njie GJ, Lobato MN, et al. Tuberculosis screening, testing, and treatment of U.S. health care personnel: recommendations from the National Tuberculosis Controllers Association and CDC, 2019. MMWR Morb Mortal Wkly Rep 2019;68:439–443. DOI: http://dx.doi.org/10.15585/mmwr.mm6819a3external icon

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Page last reviewed: June 7, 2019