18.10.3
Application for HIV drug resistance testing
Clinical HIV Guidelines, 5th Edition, 2022. Chapter 18, Continuing ART.
Clinical description
- Patients on DTG- and PI-based regimens who don’t re-suppress below 1000 copies/ml after an
initial high VL despite good adherence need a genotype sample for resistance testing.
- Contact the National HIV drug resistance (HIVDR) Expert Committee (either through DHA or
sending an email to 3rdlineart@lighthouse.org.mw) for a copy of the HIVDR testing application form (see Form 1 on page 135 in the Appendix). You can also access the application form from the DHA website https://dms.hiv.health.gov.mw or through your district ART coordinator.
- Follow the instructions on the application form and ensure that the application form is completely
filled before sending it to the expert committee.
- The expert committee will advise if a genotype sample needs to be collected. Genotyping is only
possible if the current VL is 1000+ and will be more reliable from 5000+.
- The genotype result can only be interpreted correctly if the patient has been taking their ARVs
consistently for 2-3 months before the sample was collected.
- Maintain the current regimen until genotyping results are available.
- Follow the regimen recommendations from the National HIVRDR expert committee.
Check doses against the printed guideline and your clinical judgement before treating a patient. Spotted an error? Report it from the contact links below.
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