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Table 2 Rates of correct responses to questions about autoimmune encephalitis knowledge

From: Limitations on knowledge of autoimmune encephalitis and barriers to its treatment among neurologists: a survey from western China

Area of knowledge

Question (correct answer) *

Type(s) of AE

Rate of correct responses, %*

Average rate for area of knowledge (%)

Diagnosis

If a patient is negative for AE-related antibodies, a diagnosis of AE can be ruled out. (F)

All types of AE

91.9

74.2

73.5

Patients with AE usually have an elevated number of nucleated cells in cerebrospinal fluid. (F)

72.5

Many patients with AE show obvious brain abnormalities by magnetic resonance imaging. (F)

58.3

The main clinical manifestations of anti-NMDAR encephalitis are psychiatric symptoms, seizures, dyskinesia, and disturbed consciousness. (T)

Anti-NMDAR encephalitis

95.9

88.1

Some patients with anti-NMDAR encephalitis show abnormal delta brushes in electroencephalography. (T)

80.3

The most frequent tumor among patients with anti-GABABR encephalitis is teratoma. (F)

Rare types of AE

37.1

57.9

The main clinical manifestations of anti-IgLON5 encephalitis are parasomnia, sleep disorder, cognitive impairment, and gait abnormality. (T)

74.8

Brain magnetic resonance imaging of some patients with anti-GFAP encephalitis shows linear perivascular enhancement that extends radially from the ventricles. (T)

61.8

Treatment

Immunotherapy is the core treatment for patients with AE. (T)

All types of AE

87.8

76.7

Active tumor removal is recommended for patients with both anti-NMDAR encephalitis and teratoma who develop disturbed consciousness. (T)

Anti-NMDAR encephalitis

65.5

Prognosis

AE usually shows a single course and does not recur. (F)

All types of AE

64.0

61.5

Most patients with anti-NMDAR encephalitis have good long-term functional outcomes. (T)

Anti-NMDAR encephalitis

75.3

More than 80% of patients with GABABR encephalitis have good long-term prognosis and extremely low risk of mortality. (F)

Rare types of AE

31.3

45.2

Patients with anti-LGI1 encephalitis are more likely to show cognitive dysfunction than patients with other types of AE. (T)

59.1

  1. * Possible responses: “true” (T), “false” (F) or “not sure”
  2. AE = autoimmune encephalitis; NMDAR = anti-N-methyl-d-aspartate receptor; GABABR = anti-γ-aminobutyric acid receptor type B; LGI1 = anti-leucine-rich glioma-inactivated 1; GFAP = anti-glial fibrillary acidic protein