US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary

R. Andrés Floto, Kenneth N. Olivier, Lisa Saiman, Charles L. Daley, Jean‐Louis Herrmann, Jerry A. Nick, Peadar G. Noone, Diana Bilton, Paul A. Corris, Ronald L. Gibson,

Thorax · 2015 · 460 citations · 151 references

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TL;DR

Non‑tuberculous mycobacteria are ubiquitous environmental organisms that cause chronic pulmonary infection, posing a major threat to cystic fibrosis patients but remaining difficult to diagnose and treat. A panel of 19 experts from the US Cystic Fibrosis Foundation and the European Cystic Fibrosis Society convened to develop consensus recommendations for screening, investigation, diagnosis, and management of NTM‑associated pulmonary disease in cystic fibrosis. They employed PICO methodology and systematic literature reviews to draft recommendations, then refined them through consensus and public consultation within the CF communities. The resulting pragmatic, evidence‑based recommendations aim to optimize management of this challenging condition.

Abstract

Non-tuberculous mycobacteria (NTM) are ubiquitous environmental organisms that can cause chronic pulmonary infection, particularly in individuals with pre-existing inflammatory lung disease, such as cystic fibrosis (CF). Pulmonary disease (PD) caused by NTM has emerged as a major threat to the health of individuals with CF, but remains difficult to diagnose and problematic to treat. In response to this challenge, the US Cystic Fibrosis Foundation (CFF) and the European Cystic Fibrosis Society (ECFS) convened a panel of 19 experts to develop consensus recommendations for the screening, investigation, diagnosis and management of NTM-PD in individuals with CF. PICO (population, intervention, comparison, outcome) methodology and systematic literature reviews were employed to inform draft recommendations, which were then modified to achieve consensus and subsequently circulated for public consultation within the USA and European CF communities. We have thus generated a series of pragmatic, evidence-based recommendations as an initial step in optimising management for this challenging condition.

References

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