ReviewJournal of inflammation research2026
A Narrative Review of Recent Developments in Aspirin Therapy After Desensitization in NSAIDs-Exacerbated Respiratory Disease.
Review in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
NSAID-exacerbated respiratory disease (N-ERD) is characterized by asthma, chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP), and intolerance to NSAIDs (including aspirin). In N-ERD, CRSwNP often remains refractory to standard medical and surgical treatment, necessitating escalation. Aspirin therapy after desensitization (ATAD) is an established option for CRSwNP in N-ERD, but its use is limited by adverse effects, non-response, and safety issues associated with aspirin desensitization. This narrative review focuses on newer developments in ATAD for N-ERD, including shortened desensitization schedules, lower aspirin maintenance doses, and use of intranasal preparations of aspirin such as intranasal lysine-aspirin. The developments in use of biomarkers for distinguishing the different underlying endotypes and phenotypes of N-ERD, and subsequent potential for individualization of treatment are also discussed. The availability of biologics for the treatment of CRSwNP may provide further treatment escalation options in N-ERD patients who do not tolerate or respond to ATAD; however, there is an absence of direct comparative evidence for ATAD versus biologics. Further, the conjunctive use of ATAD and biologics provides an interesting avenue of research. Finally, following a discussion of the recent advancements in ATAD and biologics in N-ERD, clinical recommendations for treatment options and pathways are made.
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