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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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