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Table 2 Factors associated with reported adverse events in 228 exposed HCWs/HCSs on HIV post-exposure prophylaxis

From: Adverse events and adherence to HIV post-exposure prophylaxis: a cohort study at the Korle-Bu Teaching Hospital in Accra, Ghana

Characteristic

Adverse events status1

Crude hazard ratio [95 % CI]

p-value

Adjusted hazard ratio [95 % CI]

p-value

Present

Absent

Drug regimen

      

3TC/AZT −28 days

68

7

1.00

 

1.00

 

3TC/AZT-3 days

28

73

0.31 [0.20–0.48]

<0.001

0.30 [0.18–0.48]

<0.001

3TC/AZT/LPV-RTV-28 days

50

2

1.06 [0.74–1.53]

0.752

1.06 [0.65–1.72]

0.817

Gender

     

-

Female

81

50

1.00

   

Male

65

32

1.08 [0.78–1.50]

0.629

  

Type of exposure

     

-

Percutaneous

131

80

1.00

   

Mucocutaneous

15

2

1.42 [0.83–2.43]

0.197

  

Age category (yrs)

     

-

18–30

101

60

1.00

   

31–40

32

18

1.02 [0.69–1.52]

0.921

  

41–50

8

2

1.28 [0.62–2.62]

0.508

  

>51

5

2

1.14 [0.46–2.80]

0.777

  

Risk assessment

      

Low

51

63

1.00

 

1.00

 

Medium

40

16

1.60 [1.06–2.42]

0.027

0.95 [0.61–1.49]

0.885

High

55

3

2.12 [1.45–3.10]

<0.001

0.97 [0.57–1.66]

0.922

Profession

     

-

Nurses

51

31

1.00

   

HCS

14

10

0.94 [0.52–1.69]

0.832

  

Laboratory Staff

15

1

1.51 [0.85–2.68]

0.162

  

Medical Doctors

46

31

0.96 [0.65–1.43]

0.843

  

Ward Attendants

20

9

1.11 [0.66–1.86]

0.695

  
  1. 1N = 228, exposed HCWs/HCSs lost to follow (n = 36) and exposed HCWs/HCSs who truncated their schedule due to source patient testing HIV negative (n = 16) were excluded; 3TC = lamivudine; AZT = zidovudine; LPV-RTV = lopinavir-ritonavir; CI = confidence interval