MULTI-PHACET: multidimensional clinical phenotyping of hospitalised acute COPD exacerbations

• Published in: ERJ open research Vol. 7; no. 3; p. 198
• Main Authors: MacDonald, Martin I, Osadnik, Christian R, Bulfin, Lauren, Leahy, Elizabeth, Leong, Paul, Shafuddin, Eskandarain, Hamza, Kais, King, Paul T, Bardin, Philip G
• Format: Journal Article
• Language: English
• Published: England European Respiratory Society 01.07.2021
• Subjects: Original s
• ISSN: 2312-0541; 2312-0541
• DOI: 10.1183/23120541.00198-2021

The generic term "exacerbation" does not reflect the heterogeneity of acute exacerbations of COPD (AECOPD). We utilised a novel algorithmic strategy to profile exacerbation phenotypes based on underlying aetiologies. Patients hospitalised for AECOPD (n=146) were investigated for aetiological contributors summarised in a mnemonic acronym ABCDEFGX (A: airway virus; B: bacterial; C: co-infection; D: depression/anxiety; E: eosinophils; F: failure (cardiac); G: general environment; X: unknown). Results from clinical investigations were combined to construct AECOPD phenotypes. Relationships to clinical outcomes were examined for both composite phenotypes and their specific aetiological components. Aetiologies identified at exacerbation were reassessed at outpatient follow-up. Hospitalised AECOPDs were remarkably diverse, with 26 distinct phenotypes identified. Multiple aetiologies were common (70%) and unidentifiable aetiology rare (4.1%). If viruses were detected (29.5%), patients had longer hospitalisation (7.7±5.6 6.0±3.9 days, p=0.03) despite fewer "frequent exacerbators" (9.3% 37%, p=0.001) and lower mortality at 1 year (p=0.03). If bacterial infection was found (40.4%), patients were commonly "frequent exacerbators" (44% 18.4%, p=0.001). Eosinophilic exacerbations (28%) were associated with lower pH (7.32±0.06 7.36±0.09, p=0.04), higher venous carbon dioxide tension ( ) (53.7±10.5 48.8±12.8, p=0.04), greater noninvasive ventilation (NIV) usage (34.1% 18.1%) but shorter hospitalisation (4 (3-5) 6 (4-9) days, p<0.001) and lower infection rates (41.4% 80.9%, p<0.0001). Cardiac dysfunction and severe anxiety/depression were common in both infective and non-infective exacerbations. Characteristics identified at exacerbation often persisted after recovery. Hospitalised AECOPDs have numerous causes, often in combination, that converge in complex, multi-faceted phenotypes. Clinically important differences in outcomes suggest that a phenotyping strategy based on aetiologies can enhance AECOPD management.