Systemic lupus erythematosus-related acute lung disease

Author:

Triboulet Félicien1,Guérin Emmanuelle12,Boussouar Samia3,Hékimian Guillaume2,Pha Micheline1,Rouvier Philippe4,Mathian Alexis1,Quentric Paul15,Moyon Quentin12,Hié Miguel1,Schmidt Matthieu26,Combes Alain26,Luyt Charles-Edouard26,Amoura Zahir15,Pineton de Chambrun Marc1256ORCID

Affiliation:

1. Service de Médecine Interne 2, Centre de Référence National Lupus Systémique, Syndrome des Anticorps Anti-Phospholipides et Autres Maladies Auto-Immunes Systémiques Rares, Institut E3M, Assistance Publique-Hôpitaux de Paris (APHP), Hôpital La Pitié-Salpêtrière, Sorbonne Université, Paris, France

2. Service de Médecine Intensive-Réanimation, APHP, Hôpital La Pitié–Salpêtrière, Sorbonne Université, Paris, France

3. Département d’Imagerie Cardiothoracique, APHP, Hôpital La Pitié–Salpêtrière, Sorbonne Université, Paris, France

4. Service d’Anatomopathologie, APHP, Hôpital La Pitié–Salpêtrière, Sorbonne Université, Paris, France

5. Centre d’Immunologie et des Maladies Infectieuses (CIMI-Paris), Inserm, Sorbonne Université, Paris, France

6. UMRS_1166-ICAN, Inserm, Institut de Cardiométabolisme et Nutrition (ICAN), Sorbonne Université, Paris, France

Abstract

Introduction Systemic lupus erythematosus (SLE) is non-organ specific autoimmune disease with mainly skin, joint, and kidney involvement. SLE-related acute lung disease (ALD) is rare, poorly investigated and can lead to acute respiratory failure. We conducted a retrospective study aiming to describe clinical features, treatments and outcome of SLE-related APD. Methods We retrospectively included all patients with SLE and ALD admitted from November 1996 and September 2018 to La Pitié-Salpêtrière Hospital, after exclusion of viral or bacterial lung infection, cardiac failure or any other alternate diagnosis. Results During the time of the study, 14 patients with 16 episodes were admitted to our center: female 79%, mean age ± SD at admission 24 ± 11 years. ALD was inaugural of the SLE in 70% cases. SLE main organ involvement were: arthritis 93%, skin 79%, serositis 79%, hematological 79%, kidney 64%, neuropsychiatric 36% and cardiac 21%. 11 episodes required ICU admission for a median time of 8 days. Chest CT-scan revealed mostly basal consolidation and ground-glass opacities. When available, bronchoalveolar lavage mostly revealed a neutrophilic alveolitis with alveolar hemorrhage in 67% cases. Symptomatic respiratory treatments were: oxygen 81%, high-flow nasal canula oxygen 27%, non-invasive ventilation 36%, mechanical ventilation 64% and venovenous extracorporeal membrane oxygenation 18%. SLE-specific treatments were: corticosteroids 100%, cyclophosphamide 56% and plasma exchange 25%. All patients but one survived to ICU and hospital discharge. Two patients had a relapse of SLE-related ALD but none had interstitial lung disease during follow-up. Conclusion Systemic lupus erythematosus-related acute respiratory failure is a severe event, mostly occurring at SLE onset, typical harboring a basal consolidation pattern on chest CT-scan and alveolar hemorrhage on BAL pathological examination. Mortality in our cohort is lower than previously reported but these results needs to be confirmed in further larger studies.

Publisher

SAGE Publications

Subject

Rheumatology

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