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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 4, July/August 2017

226

AFRICA

The high HIV burden in South Africa and the known

prothrombotic nature of HIV has sensitised clinicians to

investigate HIV-infected patients with respiratory symptoms for

PE. The non-specific signs of PE, as well as the added TB disease

burden often confounds the clinical scenario in these patients

and probably results in more patients being imaged.

As the prevalence of HIV increases globally, the trend

towards increased CTPA imaging may result in higher incidence

rates of PE. This is yet to be proven by new studies undertaken

in this decade.

Prevalence of HIV in patients with PE

Major studies published to date have evaluated the relationship

between VTE and HIV by determining the frequency of PE in

HIV-positive hospital populations. Our study differs in that it

examined a population of patients with suspected PE who had

CTPA, and then determined the HIV prevalence in the whole

group as well as in those with proven PE.

More than two-thirds (68%) of the population undergoing

CTPA who were tested for HIV was shown to be infected. This

is the first study, performed at a local South African hospital, to

report on the prevalence of HIV in patients referred for CTPA

with confirmed PE (67%). This increased prevalence reflects the

population demographics of this hospital, which is known to have

the highest HIV burden locally in the Cape metropolitan area,

14

and

is therefore also reflective of the high clinical index of suspicion of

PE in HIV-positive patients presenting to this hospital.

No statistical significance was found in the prevalence of HIV

in patients with and without proven PE. This can be explained by

our small sample size, as there were insufficient data to suggest

a statistically significant association. The known association,

however, has already been proven by larger studies conducted

worldwide.

Pulmonary embolism and TB

Published studies evaluating the relationship between PE and TB

are limited and report the prevalence of VTE in TB populations.

Our study differs in that it determined the TB prevalence in

patients who underwent CTPA for suspected PE, and those with

proven PE.

Forty per cent of patients undergoing CTPA, who were tested

for TB, had microbiological confirmation of TB. We found a

statistically significant association (at the 10% level) between TB

positivity and PE. Additional randomised studies are however

required to confirm a positive association between PE and TB, as

we evaluated only patients with an available TB laboratory result.

Pulmonary embolism and the influence of TB in HIV

We further evaluated the HIV-positive group with confirmed PE

on CTPA to determine the prevalence of TB co-morbidity. We

found an overall 71% prevalence of TB in HIV-positive patients

with proven PE. No statistically significant difference however was

found in the prevalence of TB co-morbidity between HIV-positive

and -negative groups with identified PE. This prevalence was

much higher than the 47% rate of TB infection in HIV-positive

patients who developed DVT during their hospital admissions,

reported previously by Govender

et al

., in South Africa.

15

There is no agreement in the literature as yet as to whether

antiretroviral therapy has a progressive or additive effect

in promoting VTE. Some studies have implicated protease

inhibitors in VTE, while other studies showed no association.

8,16

Only 50% of our patients who were HIV infected and had

PE were on HAART regimens at any time during or prior to the

study. These numbers did not allow for evaluation of the effects of

HAART on severity and extent of PE. Further studies are required

to examine the effects of HAART regimens on VTE severity.

Distribution and severity of PE

No studies in the literature have compared detailed imaging

data with regard to CTPA findings between HIV-positive

and -negative patients. We demonstrated that in HIV-positive

patients, thrombi were most frequently found in the right (82%)

and left lower lobes (86%) of the lung. In the HIV-negative

patients, the most commonly affected lobe of the lung was the

left lower lobe (91%). No statistical difference was, however,

demonstrated in the prevalence of PE between the HIV-infected

and uninfected groups performed per lobe of the lung.

In evaluating the degree of occlusion in the different lobar

arteries/most proximal segments giving origin to the distal

segmental arteries of the lung, we found more extensive PE

HIV status

HIV positive

HIV negative

VI/LV ratio

2.00

1.50

1.00

0.50

0.00

Fig. 6.

Differences between HIV positive and negative

according to RV:LV ratios (

p

=

0.611).

HIV status

HIV positive

HIV negative

PA/AO ratio

2.00

1.50

1.00

0.50

0.00

103

21 61

15

80

18

*

*

Fig. 7.

Differences between HIV positive and negative accord-

ing to PA:AO ratios (

p

=

0.191).