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Table 1 An overview of validity of various tests (and combinations thereof) used in the diagnosis of infective uveitides

From: Diagnostic techniques for inflammatory eye disease: past, present and future: a review

 

Infective agent

Assay

n (patients in studies)

Validity*

Reference

Ruokuonen et al.

Rubella (in FHI)

Aqueous IgG

63

100.0%

[35]

Aqueous PCR

20

10.0%

Suzuki et al.

Rubella (in FHI)

GWC (> 3)

14

71.4%

[36]

Aqueous PCR

9

22.2%

Quentin et al.

Rubella (in FHI)

AI (≥ 1.5)

52

100.0%

[37]

Aqueous PCR

28

17.9%

Ang et al.

TB

IGRA (T-SPOT.TB)

162

Sp 75.0%, Sen 36.0%

[48]

TST

 

Sp 51.1%, Sen 72.0%

TST + T-SPOT.TB

 

OR 2.16 (95% CI, 1.23-3.80)

De Groot-Mijnes et al.

HSV

PCR / GWC +

13

46.2%

[50]

 

GWC +

 

46.2%

VZV

PCR / GWC +

16

62.5%

 

GWC +

 

25.0%

Toxoplasma

PCR / GWC +

25

28.0%

 

GWC +

 

64.0%

Kiljstra et al. / Rothova et al.

Toxoplasma

GWC

22-30

72.7%-93.3%

[53, 54]

Talabani et al.

Toxoplasma

PCR + immunoblotting

54

Sen 73%

[55]

GWC + immunoblotting

 

Sen 70%

PCR + GWC

 

Sen 80%

PCR + GWC + immunoblotting

 

Sen 85%

Villard et al.

Toxoplasma

ELISA

19

Sp 85%

[56]

Immunoblotting

19

Sp 85%

PCR

18

Sp 100%

Dabil et al.

CMV, VZV, HSV, Toxoplasma

Multiplex PCR

21

85.7%

[61]

Multiplex PCR

 

71.4% (loss of <1 log sensitivity)

  1. *Most studies are cohort studies and do not represent robust outcomes of validation.
  2. Values stated are positive rates of detection unless otherwise specified.
  3. FHI Fuchs’ heterochromic iridocyclitis, GWC Goldmann-Witmer Coefficient, PCR polymerase chain reaction, AI antibody index, TB Tuberculosis, IGRA interferon-gamma release assays, TST tuberculin skin test, Sp specificity, Sen sensitivity, OR odds ratio, HSV herpes simplex virus, VZV varicella zoster virus.