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Table 2 Reference population mean and Study Participants C min and C max by antiretroviral drug

From: Factors affecting antiretroviral pharmacokinetics in HIV-infected women with virologic suppression on combination antiretroviral therapy: a cross-sectional study

     

C min

C max

Antiretroviral agent*

Reference

Dose (mg)

Freq

N

Population mean (ug/mL)

Study participants median (IQR)

Population mean (ug/mL)

Study participants median (IQR)

Atazanavir**

[33]

400

QD

9

273

214 (95–373)

3152

1870 (979–2950)

Atazanavir** boosted with ritonavir

[33]

300

QD

18

862

835 (663–1220)

5233

3430 (2670–4450)

Lopinavir boosted with ritonavir

[34]

400

BID

16

5500

6660 (4360–7710)

9800

8420 (7240–11600)

Lopinavir boosted with ritonavir

[34]

800

QD

4

1700

6445 (2452–8260)

11800

11685 (7403–14900)

Efavirenz

[35]

600

QD

16

1768

1680 (1180–3450)

4072

3235 (2330–5180)

Nevirapine

[36]

200

BID

11

3730

5270 (3380–7190)

5740

5510 (4810–7860)

Nevirapine

[36]

400

QD

8

2880

5995 (2590–7275)

6690

6400 (4838–9380)

  1. QD, once daily; BID, twice daily; IQR, interquartile range.
  2. *Nucleos(t)ide backbone: of 9 participants on Atazanavir 400 mg QD, all 9 were taking Abacavir/3TC; of 18 participants on Atazanavir/ritonavir 300 mg/100 mg QD, 11 were taking Abacavir/3TC, 3 Tenofivir/FTC, 3 Tenofivir/3TC and 1 Zidovudine/3TC; of 16 participants on Lopinavir/ritonavir 400 mg/100 mg BID, 7 were taking Zidovudine/3TC, 6 Abacavir/3TC, 1 Tenofivir/FTC, 1 Tenofivir/3TC and 1 was on PI monotherapy; of 4 participants on Lopinavir/ritonavir 800 mg/200 mg QD, 2 were taking Tenofivir/FTC, 1 Abacavir/3TC, 1 Didanosine/3TC; of 16 participants on Efavirenz 600 mg QD, 5 were taking Tenofivir/FTC, 5 Abacavir/3TC, 5 Zidovudine/3TC, 1 Tenofovir/3TC; of 11 participants on Nevirapine 200 mg BID, 7 were taking Zidovudine/3TC, 4 Abacavir/3TC; of 8 participants on Nevirapine 400 mg/ QD, 4 were taking Abacavir/3TC, 1 Tenofivir/FTC, 1 Zidovudine/3TC, 1 Tenofivir/3TC, 1 Didanosine/3TC.
  3. ** Of the 27 particpants taking Atazanavir or Atazanvir/ritonavir, none were taking any gastric acid suppression medication.