PMTCT, and National's - Health Systems Trust
PMTCT, and National's - Health Systems Trust
PMTCT, and National's - Health Systems Trust
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Current Status of Infant Testing<br />
Currently National DOH Guidelines for infant testing in <strong>PMTCT</strong> pilot sites indicate that an<br />
ELISA test should be performed at age 12 months. Previously HIV antibody assays were being<br />
performed between 9-12 months but this has shown to generate a large number of false<br />
positives particularly when testing at around 9 months, due to persistence of maternal HIV<br />
antibodies.<br />
A study conducted at King Edward Hospital (KZN) site of the PETRA study showed HIV ELISA<br />
test specificity at 9 months <strong>and</strong> 12 months of only 59% <strong>and</strong> 89% respectively 1 . The low specificity<br />
at 9 months suggested the change in policy to delay the rapid test to 1 year (with a repeat<br />
test at 15 months in the event of a positive result). Provincial departments have been asked<br />
to stop testing at 9 months <strong>and</strong> to ensure that the 1 st antibody HIV test is performed on a child<br />
1 year or older. Despite this recommendation, some provinces such as the Western Cape<br />
continue to test infants at 9 months.<br />
Some experts think that a rapid test at 12 months may still be too early 5 . A study conducted<br />
at the Coronation Hospital in Gauteng showed that 40% of HIV uninfected children tested HIV<br />
ELISA positive at 12 months of age with a lab based ELISA test 4 . Delaying testing further,<br />
however, may be impractical <strong>and</strong> result in further loss to follow up.<br />
Problems with the Current Testing Protocol<br />
The delay of 1 year in being able to make a reasonably accurate diagnosis in infants has the<br />
following repercussions:<br />
• Unacceptable rates of loss to follow up (in some provinces >50%)<br />
• Inability to adequately evaluate the effectiveness of the <strong>PMTCT</strong> programme<br />
• Inability to provide appropriate clinical <strong>and</strong> social support to families<br />
• Immeasurable emotional costs to families waiting for the HIV status of an infant<br />
• Direct <strong>and</strong> indirect costs of providing co-trimoxazole to HIVnegative babies<br />
• Large numbers (70-94%) of HIV negative babies treated as HIV positive for the first<br />
year of life.<br />
Advantages of Earlier Testing<br />
There are numerous benefits to performing early nucleic acid testing of HIV exposed infants,<br />
which clearly have enormous social implications <strong>and</strong> will affect management of HIV in these<br />
children, their families, <strong>and</strong> society. Using earlier NAT would have the following benefits:<br />
• Reduction in the loss to follow up<br />
By offering testing of infants at 6 weeks this would provide some incentive for mothers to<br />
adhere to this follow up visit <strong>and</strong> they may be more willing to disclose their status in order<br />
for their infant to be tested. Women who learn that their infants are positive at this early<br />
stage may be more motivated to return for frequent clinic visits in order to maintain the<br />
health of their infants <strong>and</strong> to benefit from ongoing care.<br />
• Improved monitoring of the effectiveness of the <strong>PMTCT</strong> programme<br />
Earlier testing of infants would enable the National Department of <strong>Health</strong> to have more<br />
accurate records of HIV transmission rates in which to evaluate programme effectiveness.<br />
This is an important monitoring tool as unacceptably high vertical transmission rates may<br />
be due to problems in other aspects of the programme such as poor uptake of nevirapine,<br />
inappropriate obstetric practices or poor infant feeding counselling.<br />
• Reducing the numbers of children requiring long term follow up by 90%<br />
The HIV status of infants could be tested at a 6 week visit <strong>and</strong> HIV uninfected children<br />
discharged from specific HIV follow up as early as 10-14 weeks of age with certain provisos.<br />
Only HIV infected children (about 10% of the total HIV exposed, non breastfed children)<br />
would require specific further follow up <strong>and</strong> prophylaxis for opportunistic infections.<br />
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