Table 5.
Parameters | Deceased patients (n = 13) | Surviving patients (n = 136) |
---|---|---|
Gender (n (female, %)) | 12 (92) | 118 (87) |
Age (median, range) | 43.8 (24.3–72.2) | 42.0 (13.6–72.2) |
Follow-up time (median, range) | 4.1 (0.5–8.6) | 6.2 (0.4–12.0) |
SLE duration (median, range) | 6.3 (0.1–29.5) | 4.2 (0.0–42.1) |
Antiphospholipid syndrome (n, %) | 6 (46) | 43 (32) |
SLEDAI-2K (median, range) | 8 (2–24) | 5 (0–34) |
SDI (median, range) | 1 (0–5) | 1 (0–11) |
NPSLE phenotype (n, %) | ||
Inflammatory | 4 (31) | 44 (32) |
Ischemic | 5 (39) | 52 (38) |
Combined | 4 (31) | 40 (29) |
NPSLE syndrome (n, %) | ||
Aseptic meningitis | 0 (0) | 5 (4) |
Cerebrovascular disease | 8 (62) | 77 (57) |
Demyelinating syndrome | 0 (0) | 0 (0) |
Headache | 0 (0) | 10 (7) |
Movement disorder (chorea) | 1 (8) | 4 (3) |
Myelopathy | 0 (0) | 13 (10) |
Seizure disorders | 0 (0) | 15 (11) |
Acute confusional state | 0 (0) | 7 (5) |
Anxiety disorder | 0 (0) | 1 (1) |
Cognitive dysfunction | 4 (31) | 45 (33) |
Mood disorder | 2 (15) | 12 (9) |
Psychosis | 2 (15) | 6 (4) |
AIDPa | 0 (0) | 0 (0) |
Autonomic disorder | 0 (0) | 1 (1) |
Mononeuropathy | 0 (0) | 1 (1) |
Myasthenia gravis | 0 (0) | 0 (0) |
Neuropathy, cranial | 1 (8) | 6 (4) |
Plexopathy | 0 (0) | 1 (1) |
Polyneuropathy | 1 (8) | 6 (4) |
Other | 3 (23)a | 25 (18) |
aOther NP symptoms in deceased major NPSLE patients: cerebral vasculitis (n = 2), mononeuritis multiplex (n = 1).AIDP: acute inflammatory demyelinating polyneuropathy; NPSLE: neuropsychiatric systemic lupus erythematosus; SDI: SLICC damage index; SLE: systemic lupus erythematosus; SLEDAI-2K: systemic lupus erythematosus disease activity index 2000.