• Steffen T Simon, Irene J Higginson, Claudia Bausewein, Caroline J Jolley, Sabrina Bajwah, Matthew Maddocks, Carolin Wilharm, Adejoke O Oluyase, Anne Pralong, and BETTER-B Consortium.
• University of Cologne, Faculty of Medicine and University Hospital, Department of Palliative Medicine, Cologne, Germany.
• Palliat Med. 2024 Sep 12: 26921632412709452692163241270945.

BackgroundSevere and refractory chronic breathlessness is a common and burdensome symptom in patients with advanced life-limiting disease. Its clinical management is challenging because of the lack of effective interventions.AimTo provide practice recommendations on the safe use of pharmacological therapies for severe chronic breathlessness.DesignScoping review of (inter)national guidelines and systematic reviews. We additionally searched for primary studies where no systematic review could be identified. Consensus on the recommendations was reached by 75% approval within an international expert panel.Data SourcesSearches in MEDLINE, Cochrane Library and Guideline International Network until March 2023. Inclusion of publications on the use of antidepressants, benzodiazepines, opioids or corticosteroids for chronic breathlessness in adults with cancer, chronic obstructive pulmonary disease, interstitial lung disease or chronic heart failure.ResultsOverall, the evidence from eight guidelines, 14 systematic reviews and 3 randomised controlled trials (RCTs) on antidepressants is limited. There is low quality evidence favouring opioids in patients with chronic obstructive pulmonary disease, cancer and interstitial lung disease. For chronic heart failure, evidence is inconclusive. Benzodiazepines should only be considered for anxiety associated with severe breathlessness. Antidepressants and corticosteroids should not be used.ConclusionManagement of breathlessness remains challenging with only few pharmacological options with limited and partially conflicting evidence. Therefore, pharmacological treatment should be reserved for patients with advanced disease under monitoring of side effects, after optimisation of the underlying condition and use of evidence-based non-pharmacological interventions as first-line treatment.

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