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Published on: March 24, 2017
Infectious Disease Provider Perspectives on Shorter Tuberculosis Treatment Regimens
Aliya Moreira1,2, Dana Hassneiah1,2, Susan E Beekmann3
1Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Infectious disease physicians prefer shorter tuberculosis treatment regimens, but newer guideline-recommended options show low uptake. Barriers include concerns about effectiveness and toxicities of new tuberculosis drugs.
Area of Science:
- Infectious Diseases
- Pulmonology
- Clinical Practice Guidelines
Background:
- Current guidelines recommend shorter rifamycin-based regimens (≤4 months) for tuberculosis infection.
- Newer all-oral regimens include 6-month options for drug-resistant tuberculosis (bedaquiline, pretomanid, linezolid [BPaL/BPaL-M]) and a 4-month regimen for drug-susceptible disease (rifapentine, isoniazid, moxifloxacin [HPMZ]).
- Implementation of these updated tuberculosis treatment regimens often lags behind guideline recommendations.
Purpose of the Study:
- To assess current tuberculosis treatment practices among infectious disease clinicians.
- To identify barriers hindering the adoption of newly recommended tuberculosis treatment regimens.
Main Methods:
- A survey was distributed to 1501 North American adult infectious disease physician members of the IDSA's Emerging Infections Network.
- Quantitative analysis of survey responses (percentages) and qualitative analysis of open comments were performed.
Main Results:
- Ninety-three percent of 349 respondents favored ≤4-month tuberculosis treatment regimens.
- Low adoption rates were observed for HPMZ (1% use, 5% experience) and BPaL/BPaL-M (39% intended use, 40% unsure).
- Key barriers included concerns regarding treatment toxicities (HPMZ, linezolid), drug interactions, and medication availability.
Conclusions:
- Infectious disease physicians prioritize shorter tuberculosis treatment durations but exhibit low uptake of newer guideline-recommended regimens.
- Concerns about effectiveness and treatment toxicities impede the implementation of novel tuberculosis therapies.
- Optimizing implementation requires enhanced adverse effect management, monitoring, and shared decision-making strategies.
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