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Module 3: Management of Patients on Antiretroviral Therapy ,[object Object]
Objectives ,[object Object],[object Object],[object Object],[object Object],[object Object]
Principles of Antiretroviral Treatment (ART) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Goals of ART ,[object Object],[object Object],[object Object],[object Object]
1. Suppression of HIV Replication ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
2. Immune Reconstitution ,[object Object],[object Object],[object Object],[object Object],[object Object]
3. Clinical Benefits and Improved Quality of Life ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Keys to Achieving Goals of ART ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Patient Preparation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Take-home Messages  about ART ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Take-home Messages  about ART ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Antiretroviral Drugs: Best Practice  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Rationale Behind Standardized ARV Drug Therapy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Standard 1 st  Line Regimen  for Adults and Adolescents ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],or
Standard 2 nd  Line Regimen  for Adults and Adolescents ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],or
For Patients on Non-standard 1 st  line Regimens… ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
A Note On Fixed Dose Combinations (FDCs) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Considerations prior to starting ART ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
When to Start: Early Initiation of Antiretroviral Therapy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
When to Start: Delayed Initiation of  Antiretroviral Therapy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
When to Start ART in Adults and Adolescents ,[object Object],[object Object],[object Object]
When to Start ART in Adults and Adolescents ,[object Object],[object Object],[object Object],[object Object]
Guidance on Clinical Criteria ,[object Object],[object Object],[object Object],[object Object]
Pregnancy and ART ,[object Object],[object Object],[object Object],[object Object],[object Object]
TB/HIV Co-infected Patients ,[object Object],[object Object],[object Object],[object Object],[object Object]
ART and TB  ,[object Object],[object Object]
ART and TB: When to start Start anti-TB treatment Consider clinical status: start ART as appropriate CD4 count not available Start anti-TB treatment Start ART after completion of TB treatment CD4 count 200-350/mm 3 Start anti-TB treatment Start ART after intensive phase CD4 count 100-200/mm 3 Start anti-TB treatment Start ART as soon as possible  CD4 <100/mm 3 Treatment Recommendation CD4 Count
Monitoring Antiretroviral Therapy
Monitoring ART  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Monitoring ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Monitoring ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Monitoring: Indicators of Treatment Success  ,[object Object],[object Object],[object Object],[object Object],[object Object]
Laboratory Monitoring of ART  ,[object Object],[object Object],[object Object]
Laboratory Monitoring of ART  ,[object Object],[object Object],[object Object]
Laboratory Monitoring of ART: CD4 Count ,[object Object],[object Object],[object Object],[object Object],[object Object]
Laboratory Monitoring of ART: Viral Load ,[object Object],[object Object],[object Object],[object Object],[object Object]
Lab Tests: Monitoring For Toxicity  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Lab tests: Follow up ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Summary Schedule of Laboratory Monitoring X X 1 X (if on TDF) X X 6m X X X Fasting lipids & glucose (PIs) X X X X  (if on NVP) X  (if on NVP) X ALT(LFT) X 1 X 1 X 1 X 1 X 1 X Pregnancy test X  (if on TDF X (if on TDF) X  (if on TDF X (if on TDF) X (if on TDF) X Serum Creatinine X X X X  (if on AZT) X  (if on AZT) X CBC + Differential X X X X CD4 24m 18m 12m 3m 1-2 months Baseline Test

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03.02 management of patients on antiretroviral drugs initiat

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  • 28. ART and TB: When to start Start anti-TB treatment Consider clinical status: start ART as appropriate CD4 count not available Start anti-TB treatment Start ART after completion of TB treatment CD4 count 200-350/mm 3 Start anti-TB treatment Start ART after intensive phase CD4 count 100-200/mm 3 Start anti-TB treatment Start ART as soon as possible CD4 <100/mm 3 Treatment Recommendation CD4 Count
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  • 40. Summary Schedule of Laboratory Monitoring X X 1 X (if on TDF) X X 6m X X X Fasting lipids & glucose (PIs) X X X X (if on NVP) X (if on NVP) X ALT(LFT) X 1 X 1 X 1 X 1 X 1 X Pregnancy test X (if on TDF X (if on TDF) X (if on TDF X (if on TDF) X (if on TDF) X Serum Creatinine X X X X (if on AZT) X (if on AZT) X CBC + Differential X X X X CD4 24m 18m 12m 3m 1-2 months Baseline Test

Editor's Notes

  1. Time to the lowest viral load attained depends on potency of drugs, adherence , pre-treatment viral load, , resistance, presence of OIs, drug pharmacokinetics
  2. * e.g pregnant mother in the first trimeatre with TB who requires both anti-TB and ARV treatment to be commenced. Less potent than standard dual class regimens ABC+3TC+AZT (Trizivir TM) Higher failure rates in patients with VL&gt;10 5 , those with prior NRTI use Utility mainly in some cases of treatment simplification/ cases of drug interactions*/ switch for metabolic side effects New studies suggest that this is an area that needs further investigation DART trial CROI 2005 Boston- AZT+TDF+3TC achieved reasonable results in large cohort in Uganda and Zimbabwe. No comparator arm
  3. Much can be learned form the successful National TB programs which have incorporated use of standardized TB regimens. The success of National TB programs has been due to the simplification of treating many patients. In the last half of 2002 the Kenyan ARV task force made recommendations on standardized ARV regimens. The 1 st line regimen consisting of 2 nucleoside analogues namely stavudine and Lamivudine and Non-Nucleoside analogue either Nevirapine or Efavirenz. This first line regime if properly adhered to should be effective for at least 1 year The second line ARV regime is Protease Inhibitor based: Includes 2 Nucleoside analogues (which should not be in the 1 st line regimen) and a protease inhibitor either Kaletra which contains Lopinavir and ritonavir that boosts blood levels of Lopinavir the pother alternative PI is Nelfinavir. If this 2 regimens fail desinging a third is more difficult with a standardized apprach than an individualised one
  4. Alternative; TDF/AZT/Kaletra Nelfinavir can be used in case there is no cold storage for Kaletra. All pharmacies should have a refrigerator
  5. Based on observational studies using both clinical end points as well as surrogate markers (CD4/Viral load) the limitations of available medication CD4 count given greater weight as a determinant of when to start treatment. Outcome best if treatment is started at a CD4 count &gt;200 cells/mm 3 Viral suppression achieved even when treatment started at low CD4 counts Phillips AN JAMA. 2001;286:2560-2567 Hogg et al JAMA 2001;286:2568-2577 Patients started on treatment using WHO GL Symptomatic patients benefit more from treatment than asymptomatic ones taking into account starting CD4 count
  6. All patients with a CD4 count &lt; 200 should be started on treatment.
  7. X1: If clinically indicated Serum Creatinine not needed for standard 1 st line; required more regularly in patients on TDF. Red X are for tests necessitated by those particular drugs. Most patients can be adequately monitored 6 monthly and as clinically indicated