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One-year clinical experience on the use of Nintedanib in systemic sclerosis
被引:0
作者:
Magnani, Luca
[1
]
Spinella, Amelia
[2
]
Testoni, Sofia
[1
,2
]
Lumetti, Federica
[2
]
Scelfo, Chiara
[3
]
Dardani, Lucia
[1
]
Bajocchi, Gianluigi
[1
]
Clini, Enrico
[4
]
Salvarani, Carlo
[1
,2
]
Giuggioli, Dilia
[2
,5
]
机构:
[1] AUSL IRCCS Reggio Emilia, Rheumatol Unit, Reggio Emilia, Italy
[2] Univ Modena & Reggio Emilia AOU Modena, Scleroderma Unit, Rheumatol, VIA POZZO 71, I-41100 Modena, Italy
[3] AUSL IRCSS Reggio Emilia, Pneumol Unit, Reggio Emilia, Italy
[4] Univ Modena & Reggio Emilia, Dept Med & Surg Sci Children & Adult, Resp Dis Unit, Pneumol, Reggio Emilia, Italy
[5] Univ Modena & Reggio E, Policlin Modena, Dept Med & Surg Sci Children & Adult, Rheumatol Unit, Via Pozzo 71, I-41100 Modena, Italy
来源:
RESPIROLOGY CASE REPORTS
|
2023年
/
11卷
/
06期
关键词:
autoimmunity;
fibrosis;
interstitial lung disease;
rare disease;
systemic sclerosis;
CLASSIFICATION;
SCLERODERMA;
D O I:
10.1002/rcr2.1120
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
We reviewed 11 patients with systemic sclerosis-related ILD who were referred to our Scleroderma Unit from January 2020 to January 2021 and started Nintedanib. Non-specific interstitial pneumonia (NSIP) was prevalent (45%), usual interstitial pneumonia (UIP) and UIP/NSIP pattern were both 27%. Only one patient had a history of smoking. Eight patients were on mycophenolate mofetil (MMF), eight were treated with corticosteroids (mean dose 5 mg/day of Prednisone or equivalent), and three were on Rituximab. The mean modified British Council Medical Questionnaire (mmRC) decreased from 3 to 2.5. Two patients had to reduce their daily dose to 200 mg/day for severe diarrhoea. Nintedanib was generally well tolerated.
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