Table 3 Pooled mean estimates for hepatitis C virus (HCV) antibody prevalence stratified by populations’ and subpopulations’ risk of exposure to HCV infection in Egypt.

From: Characterizing hepatitis C virus epidemiology in Egypt: systematic reviews, meta-analyses, and meta-regressions

 

Studies

Samples

Prevalence

Effect size

Heterogeneity measures

Total N

Total N

Range (%)

Mean (%) (95% CI)

Q (p-value)*

τ 2**

I² (confidence limits)ǂ

Prediction interval (%)ǁ

All populations

General population

264

1,677,404

0.0–57.6

11.9 (11.1–12.6)

38,386.8 (p < 0.0001)

0.0257

99.3% (99.3–99.3%)

3.5–24.0

Populations at high risk

57

7,459

8.8–100

55.6 (49.4–61.7)

1,437.3 (p < 0.0001)

0.2079

96.1% (95.5–96.6%)

13.1–93.6

Populations at intermediate risk

45

9,427

0.0–90.0

14.3 (10.3–18.8)

1,436.2 (p < 0.0001)

0.1553

96.9% (96.4–97.4%)

0–51.0

Populations with liver-related conditions

72

47,214

4.3–100

56.0 (50.4–61.6)

7,777.2 (p < 0.0001)

0.2199

99.1% (99.0–99.2%)

12.8–94.2

Special clinical populations

34

5,542

0.5–96.1

35.0 (27.3–43.1)

1206 (p < 0.0001)

0.2256

97.3% (96.8–97.7%)

1.5–81.8

General population (populations at low risk)

Blood donors

116

1,566,669

0.0–38.0

10.4 (9.6–11.2)

24,513.7 (p < 0.0001)

0.0180

99.5% (99.5–99.6%)

3.6–20.0

  Family replacement

15

262,535

3.8–14.6

7.1 (5.9–8.3)

1,931.7 (p < 0.0001)

0.0080

99.3% (99.1–99.4%)

2.8–13.1

  Voluntary

27

1,025,535

0.7–27.2

5.4 (4.4–6.5)

9,700.4 (p < 0.0001)

0.0133

99.7% (99.7–99.8%)

1.3–12.2

Pregnant women

14

12,700

2.3–19.0

9.0 (6.0–12.6)

455.0 (p < 0.0001)

0.0405

97.1% (96.2–97.8%)

0.4–26.1

Children

10

3,408

0.0–38.0

6.4 (2.9–11.1)

171.6 (p < 0.0001)

0.0604

94.8% (92.2–96.5%)

0–28.2

Egyptian expatriate workers undergoing mandatory pre-employment screening and Egyptians living abroad

23

9,168

0.0–38.4

14.4 (9.3–20.4)

1137.0 (p < 0.0001)

0.0349

98.1% (97.7–98.4%)

0–50.4

Other general populations

101

85,459

0.0–57.6

14.3 (12.3–16.4)

6472.6 (P < 0.0001)

0.0192

98.5% (98.3–98.6%)

0.9–38.3

Populations at high risk

Hemodialysis patients

26

4,915

10.0–100.0

65.5 (56.5–74.1)

809.1 (p < 0.0001)

0.2119

96.9% (96.2–97.5%)

18.9–98.6

Thalassemia patients

21

1,812

8.8–82.0

46.3 (34.9–57.9)

484.0 (p < 0.0001)

0.2710

95.9% (94.7–96.8%)

2.9–93.9

Multi-transfused patients

6

449

15.2–81.6

42.9 (24.5–62.3)

80.5 (p < 0.0001)

0.2144

93.8% (89.1–96.5%)

0–98.3

Other populations at high risk

4

283

13.0–63.0

57.5 (36.8–76.9)

34.6 (p < 0.0001)

0.0393

91.3% (80.9–96.1%)

0.0–100

Populations at intermediate risk

Healthcare workers

10

3,402

0.0–42.1

8.4 (3.7–14.8)

274.4 (p < 0.0001)

0.0891

96.7% (95.4–97.7%)

0–37.9

Diabetic patients

6

1,384

12–60.3

24.7 (6.0–50.4)

415.1 (p < 0.0001)

0.4330

98.8% (98.3–99.1%)

0–100

Household contacts of HCV infected persons

13

2,339

0–46.0

13.7 (7.6–21.1)

260.2 (p < 0.0001)

0.1197

95.4% (93.6–96.7%)

0–49.3

Hospitalized patients

6

401

0–90.0

15.9 (0–57.8)

411.1 (p < 0.0001)

1.221

98.8% (98.3–99.1%)

0–100

Other populations at intermediate risk

10

1,547

8.4–41.4

15.2 (11.3–19.4)

39.5 (p < 0.0001)

0.0234

77.2% (58.1–87.6%)

4.2–31.0

Populations with liver-related conditions

Hepatocellular carcinoma patients

22

5,553

30.0–95.2

74.0 (67.1–80.3)

506.2 (p < 0.0001)

0.1071

95.9% (94.7–96.8%)

39.4–97.2

Liver disease patients

28

34,727

16.4–100

65.6 (60.9–70.2)

1121.2 (p < 0.0001)

0.0582

97.6% (97.1–98.0%)

40.3–87.0

Liver cirrhosis patients

2

130

56.0–75.4

66.0 (45.9–83.6)

5.50 (p = 0.0190)

0.0172

81.8% (23.1–95.7%)

0.0–100

Viral hepatitis patients

14

5,992

4.3–78.7

18.1 (11.4–25.8)

360.8 (p < 0.0001)

0.1152

96.4% (95.1–97.3%)

0–54.2

Non-Hodgkin’s lymphoma patients

6

812

7.4–50.6

35.3 (17.5–55.4)

149.6 (p < 0.0001)

0.2378

96.7% (94.7–97.9%)

0–96.8

Special clinical populations

Special clinical populations

34

5,542

0.5–96.1

35.0 (27.3–43.1)

1,206 (p < 0.0001)

0.2256

97.3% (96.8–97.7%)

1.5–81.8

  1. *Q: the Cochran’s Q statistic, a measure assessing the existence of heterogeneity in effect size. **τ2: the estimated between-study variance in the double arcsine transformed proportions of the true effect sizes. The back-transformed τ2 was not calculated as the methodology to do so is not currently available. ǂI²: a measure assessing the magnitude of between-study variation that is due to differences in effect size across studies rather than chance. Prediction interval: estimates the 95% interval in which the true effect size in a new HCV study will lie.
  2. **Abbreviation: CI, confidence interval.