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Table 1 Baseline demographic and clinical characteristics of eligible HIV-1-infected patients

From: Virological failure of staggered and simultaneous treatment interruption in HIV patients who began Efavirenz-based regimens after allergic reactions to nevirapine

  

EFV-based regimens

 
 

Available data (n)

Simultaneous Interruptiona

Staggered Interruptionb

Controlsc

p valued

Total number, n

559

161

82

316

 

Mean age, years (SD)

559

41.8 (8.3)

39.4 (9.4)

43.0 (8.4)

0.003

Female, %

559

39.1

59.8

33.9

<0.001

Mean body weight, kilograms (SD)

556

54.9 (9.2)

54.8 (9.8)

56.9 (12.4)

0.091

History of previous major opportunistic infections, %

556

40.6

35.4

51.9

0.007

History of previous allergic reactions to other drugs (exclude NVP), %

555

32.7

30.9

11.4

<0.001

Median duration of previous NVP-based regimens, days (IQR)

234

14 (11,27)

14 (12, 30)

 

0.574

Median baseline of CD4 cell count, cells/uL (IQR) e

543

69 (24, 140)

90 (26, 167)

47 (13, 132)

0.006

Baseline plasma HIV-1 RNA >100,000 copies/ml, % e

258

69.6

77.4

76.0

0.595

Baseline EFV-based regimens

     

-Once-daily regimen,%

556

0.6

2.5

13.7

<0.001

-OBRs

559

    

D4T/3TC, %

 

93

73

58

 

AZT/3TC, %

 

6

24

23

 

TDF/3TC, %

  

2

11

 
  1. Note: AZT = Zidovudine; D4T = Stavudine; EFV = Efavirenz; IQR = Interquartile range; NVP = Nevirapine; OBRs = Optimized background regimens; SD = Standard deviation; TDF = Tenofovir; 3TC = Lamivudine.
  2. aHIV-1-infected patients who simultaneously discontinued all drugs in NVP-based regimens when they experienced allergic reactions to NVP-based regimens.
  3. bHIV-1-infected patients who discontinued NVP first but continued use of the other NRTIs for a few days when they experienced allergic reactions to NVP-based regimens.
  4. cHIV-1-infected patients who were naïve to antiretroviral therapy and were never exposed to NVP before beginning EFV-based regimens.
  5. dp-value represents the difference between the three groups (Simultaneous interruption, Staggered interruption, and Control).
  6. eThese results would be included if they were examined within 6 months before starting EFV-based regimens.