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SAMJ: South African Medical Journal

On-line version ISSN 2078-5135
Print version ISSN 0256-9574

SAMJ, S. Afr. med. j. vol.106 n.2 Pretoria Feb. 2016

http://dx.doi.org/10.7196/SAMJ.2016.V106I2.9903 

RESEARCH

 

Thrombocytopenia during pregnancy in women with HIV infection receiving no treatment

 

 

H M Sebitloane

MB ChB, FCOG (SA); MMed Department of Obstetrics and Gynaecology, School of Clinical Medicine, College of Health Sciences, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa

Correspondence

 

 


ABSTRACT

BACKGROUND: Thrombocytopenia (TCP) complicates 5 - 8% of pregnancies. Most cases of TCP are gestational, and the condition is usually mild and occurs in the latter part of pregnancy. Apart from pregnancy-associated medical complications such as pre-eclampsia, HIV infection is a recognised cause of TCP, and a relatively high prevalence of TCP during pregnancy would be expected in a setting with a high antenatal seroprevalence of HIV.
METHODS: This was a sub-analysis of the data from a prospective trial in which the incidence of postpartum sepsis in HIV-infected women was compared with that in HIV-uninfected women. Women who were considered at low risk and eligible for vaginal delivery were recruited at 36 weeks' gestation, and followed up for 6 weeks after delivery. Full blood counts and CD4 counts of HIV-infected women were obtained at baseline and repeated 6 weeks after delivery.
RESULTS: The prevalence of TCP was 5.3% during pregnancy and 1.2% 6 weeks after delivery. The prevalence was similar among HIV-infected (6.0%) and HIV-uninfected women (4.7%) (p=0.292). Among the HIV-infected women, who were not receiving antiretroviral therapy (mean CD4 cell count of 453 cells/
μL), there was no significant association between immunosuppression and the severity of TCP.
CONCLUSIONS: Most of the TCP seen during pregnancy is of the gestational variety, and in this study HIV infection did not increase its prevalence or its severity.


 

 

Thrombocytopenia (TCP) (platelet count <150 x 109/L) during pregnancy often causes anxiety among both patients and healthcare practitioners. It occurs in 5 - 8% of pregnancies, the prevalence depending on whether it is associated with medical disorders or not.[1,2] Gestational TCP (gTCP), also known as incidental or benign TCP of pregnancy, accounts for approximately 80% of all cases of TCP occurring in pregnancy[1] and typically develops in the late second or third trimester when physiological haemodilution leads to an increased mean platelet volume and subsequent accelerated consumption. Women with gTCP are usually asymptomatic, their low platelet count being detected as part of routine antenatal screening. Fetal TCP is usually mild and transient, requiring no intervention.[3] A history of gTCP is sometimes obtained, as there is the potential for it to recur. A recurrence rate of 13.6% was noted in a series of 22 cases,[4] while among 37 patients with gTCP, Ruggeri et al.[3] reported 100% recurrence in 4 women who had repeat pregnancies.[3] gTCP is usually mild (platelet count 100 - 150 x 109/L), and although the minimum threshold has never been established, counts of <70 x 109/L are uncommon.[5] Severe TCP (<50 x 109/L) is rare, occurring in <0.1% of pregnancies.[6] In these cases, pathological causes of increased destruction or utilisation of platelets such as pre-eclampsia/eclampsia, the HELLP syndrome (haemolysis, elevated liver enzymes and low platelet count), and microangiopathies such as thrombotic thrombocytopenic purpura, (auto)immune thrombocytopenic purpura, haemolytic uraemic syndrome and haemolysis are likely. Viral infections such as viral hepatitis and infection with cytomegalovirus and HIV may also cause TCP.

In the era of HIV, particularly in South Africa (SA), where the seroprevalence in the antenatal population exceeds 25%, clinicians may not be able to differentiate gTCP from that associated with HIV. TCP has been reported to be present in 5 - 9% of patients who have HIV infection but are asymptomatic, and in 21 - 40% of those with AIDS.[6,7] Although TCP was initially thought to occur early in the course of HIV infection, reports have shown a correlation between TCP and low CD4 counts.[6,7] Moreover, TCP has been shown to correlate with a poorer prognosis and rapid progression to AIDS.[7,8] Transient TCP is a feature of the acute retroviral syndrome seen in primary HIV infection.[9] The two mechanisms involved in HIV-associated TCP are thought to be immune-mediated destruction of platelets (in early infection) and a defect in platelet production (in advanced disease).[8] HIV also directly infects megakaryocytes, causing apoptosis and dysmegakaryopoiesis.[8] Individuals with HIV-associated TCP have a clinical presentation and response to therapy similar to that of idiopathic (immune) thrombocytopenic purpura (ITP).[10] Apart from the severity and the time of onset of TCP in pregnant women with ITP (being more severe and occurring in earlier gestation), there is as yet no diagnostic test to differentiate gTCP from ITP, as circulating antibodies may be found in both conditions.[11]

There are limited data on the prevalence of gTCP in HIV-infected women. In a clinical setting where patients may arrive unbooked and in labour, or without a previous platelet count, it becomes important to establish the role of HIV in TCP.

 

Methods

This was a sub-analysis of data from a prospective longitudinal study aimed at determining the effect of HIV on postpartum infectious morbidity. The cohort comprised HIV-infected (n=675) and HIV-uninfected (n=648) women attending King Edward VIII Hospital, Durban, SA, between 2005 and 2007. Participants were recruited at >36 weeks' gestation. They had to be at low risk with no obstetric morbidities, and eligible for a vaginal delivery. Ethical approval for the parent study was obtained from the University of KwaZulu-Natal BioMedical Research Ethics Committee (Ref. H031/01).

At baseline all women had full blood counts (FBCs), and CD4 counts if HIV-infected. They were reviewed on three occasions in the post-delivery period, and tests were repeated 6 weeks after delivery. TCP was defined as a platelet count of <150 x 109/L. It was regarded as severe if the platelet count was <50 x 109/L.

 

Results

Results were available for 1 311 women (669 HIV-infected and 642 HIV-uninfected) at baseline, and for 897 (461 (68.9%) of the HIV-infected and 436 (67.9%) of the HIV-uninfected) women at 6 weeks. None of the HIV-infected participants received combination antiretroviral therapy (ART), as the standard of care at the time was only single-dose nevirapine. The HIV-infected and HIV-uninfected groups were comparable in terms of age, parity and body mass index (Table 1). The baseline FBC results are also shown in Table 1. HIV-infected women had significantly lower baseline haemoglobin (Hb) concentrations and total white cell counts (WCCs) than HIV-uninfected women. The mean Hb at baseline was 11.1 g/dL for HIV-infected women and 11.7 g/dL for HIV-uninfected women (p<0.001). Twenty-three percent of the women had an Hb of <10.5 g/dL; these comprised 30.1% of the HIV-infected group compared with 16.4% of the HIV-uninfected group (p<0.001). The mean CD4 count of the HIV-infected women was 453 cells/μL at enrolment, increasing by 22% to a mean of 552 cells/μL at 6 weeks postpartum. Women with CD4 counts of <200 cells/μL (11.1% of the HIV-infected population) had a mean CD4 count at enrolment of 129 cells/μL and a mean count of 131 cells/μL 6 weeks after delivery.

 

 

The mean platelet count was 243.2 x 109/L in the HIV-infected group (range 84 - 533) and 247.4 x 109/L in the HIV-uninfected group (range 26 - 597) (p=0.354) (Table 1). The incidence of gTCP was 40/669 (5.9%) in the HIV-infected and 30/642 (4.7%) in the HIV-uninfected women at baseline (relative risk (RR) 1.28; 95% confidence interval (CI) 0.81 - 2.03; p=0.292) (Table 2). The TCP was mild in both groups, with only 3 HIV-uninfected and 4 HIV-infected women in each group having platelet counts of <100 x 109/L.

 

 

Among the HIV-infected women, TCP occurred at all ranges of CD4 counts and was not associated with immunosuppression (CD4 count <200 cells/μL). On the contrary, TCP occurred with increasing frequency with increasing CD4 counts (Table 2). The non-parametric test showed a low correlation of 0.062. Three participants (all HIV-infected) were found to have puerperal sepsis (endometritis), their infection resolving on first-line antibiotics.

For 461 HIV-infected women and 436 HIV-uninfected women, both the baseline and 6 weeks post-delivery platelet measurements were available. Eleven women had TCP at the 6-week assessment (6 HIV-infected women (1.3%) and 5 HIV-uninfected women (1.2%)) (p=0.881) (Table 3). TCP had persisted from the antenatal period in 3 women in each HIV group (total 6); the remainder (3 HIV-infected and 2 HIV-uninfected women) were new cases of TCP. The correlation between platelet counts and CD4 counts at baseline and 6 weeks for the 11 women with TCP in the postpartum period is shown in Table 4. Of the 3 HIV-infected women with persistent TCP after the first assessment, only 1 (patient 3) was immunosuppressed according to the CD4 count. Of the 3 who had developed TCP for the first time in the postnatal period, only 1 (patient 4) was immunosuppressed.

 

 

Discussion

gTCP develops in up to 5% of all pregnancies in the third trimester.[1] In the present study the overall prevalence of TCP during pregnancy was 5.3%, and there was no statistical difference in the prevalence between women with and without HIV infection. Mandelbrot et al.[11] found a comparable prevalence of TCP among HIV-infected pregnant women of 3.2%; however, these authors associated >80% of cases of TCP with HIV-positive status despite the study having no HIV-uninfected controls. In the present study, the prevalence of severe TCP (<50 x 109/L) was very low despite half of the patients being HIV-infected. In a study of patients of unknown HIV status, with a sample size comparable to the present study, Dwivedi et al.[12] reported an overall prevalence of TCP of 8%, 4% of cases being severe, and attributed this to the high prevalence of anaemia in their patients.[12]

There are several reasons why the TCP in the women in the present study was probably gestational: (i) the prevalence rates are comparable to those reported in other series;[1,2](ii) in most of the women with TCP who had two readings (22/26 HIV-infected women and 18/21 HIV-uninfected women), the platelet counts returned to normal in the postpartum period; and (iii) most of the women had mild TCP, in keeping with previous reports on gTCP.[1,2] Of the women with TCP at 6 weeks, low platelet counts had been detected in the antenatal period in 3 in each HIV group, and their TCP was mild (>100 x 109/L), a feature not in keeping with ITP. One woman (patient 7 in Table 4) who had antenatal and post-delivery platelet counts of 81 x 109/L and 92 x 109/L, respectively, may in fact have had ITP, although it has been reported that it may take as long as 12 weeks after delivery for platelet counts to recover,[13] and follow-up in the present study did not extend beyond 6 weeks. ITP could also have been responsible for the new development of TCP in 2 HIV-uninfected participants, as no other explanation could be found. Classic ITP occurs in the second or third decade of life,[3] and complicates 1/1 000 - 10 000 pregnancies.[12] In a report of 117 patients with TCP at term, Subbiah et al.[14] found 41% of cases to be gestational and 26% to be due to ITP. However, this was a selected high-risk group and does not represent the general obstetric population.

The development of new-onset TCP in 3 HIV-infected women could have been related to their HIV status. In the first case (patient 4 in Table 4), TCP was probably due to defect ive production of platelets. This woman was severely immunocompromised and had a low Hb and total WCC both at baseline and 6 weeks after delivery. She was not receiving any ART, in the context of Dominguez et al.'s[10] finding that untreated HIV-infected thrombocytopenic individuals had lower platelet turnover than those treated with zidovudine. The TCP in the other 2 women was probably immune-mediated HIV-associated TCP, since both had relatively high CD4 counts. Immunologically competent HIV-infected individuals (as opposed to those who are immunosuppressed) would be expected to produce more antiplatelet antibodies, leading to increased platelet destruction; among 41 HIV-infected individuals with TCP, platelet destruction was more prominent in patients with high CD4 counts.[10] It could be argued that the TCP in the HIV-infected participants (patients 1 - 3 in Table 4) that was detected both in the antenatal period and at 6 weeks was also immunologically induced. If that is so, the prevalence of HIV-related TCP during pregnancy in the present study would be 0.9%, and while low platelet counts occurred mainly among women with CD counts of >200 cells/μL, the TCP was mild. While other studies have reported a relationship between the severity of the HIV infection and the occurrence or severity of TCP,[7] this was not confirmed in the present study. Ambler et al.[15] documented similar findings in a population of highly active antiretroviral therapy (HAART) recipients.

As this was a retrospective analysis, maternal TCP could not be correlated with neonatal platelet counts. However, the findings are relevant to inform clinical practice, serving as a baseline. In the current era of universal HAART for all pregnant HIV-infected women, it can be expected that HIV-related TCP will be less frequent. While it is recommended that all efforts be made to acquire a baseline Hb and platelet count for all patients who are about to give birth, a fresh sample is not always indicated, as some clinicians have insisted for fear of HIV-related TCP. This causes delay in management and may potentially lead to poor perinatal outcomes.

 

Conclusion

This analysis establishes that TCP in HIV-infected pregnant women is mainly a result of the pregnancy itself, and that HIV-related TCP is rare, even in women not receiving ART. This is reassuring for practitioners managing women who present 'unbooked' in labour and perhaps require emergency caesarean section, but for whom a previous platelet count is unavailable. A baseline FBC, including Hb and platelets, should ideally be obtained as part of antenatal care during the course of pregnancy, but needs to be repeated during labour only in women with pre-eclampsia or obstetric haemorrhage.

 

 

References

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6. Sloand EM, Klein HG, Banks SM, et al Epidemiology of thrombocytopenia in HIV infection. Eur J Haematol 1992;48(3):168-172. [http://dx.doi.org/10.1111/j.1600-0609.1992.tb00591.x]        [ Links ]

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9. Lescale KB, Eddleman KA, Cines DB, et al. Antiplatelet antibody testing in thrombocytopenic pregnant women. Am J Obstet Gynecol 1996;74(3):1014-1018. [http://dx.doi.org/10.1016/S0002-9378(96)70342-3]        [ Links ]

10. Dominguez A, Gamallo G, Gaercia R, et al. Pathophysiology of HIV related thrombocytopenia: An analysis of 41 patients. J Clin Pathol 1994;47(11):999-1003. [http://dx.doi.org/10.1136/jcp.47.11.999]        [ Links ]

11. Mandelbrot L, Schlienger I, Bocigain A, et al. Thrombocytopenia in pregnant women infected with human immunodeficiency virus: Maternal and neonatal outcomes. Am J Obstet Gynecol 1994;171(1):252-257. [http://dx.doi.org/10.1016/0002-9378(94)90478-2]        [ Links ]

12. Dwivedi P, Puri M, Nigam A, Agarwal K. Fetomaternal outcome in pregnancy with severe thrombocytopenia. Eur Rev Med Pharmacol Sci 2012;16(11):1563-1566.         [ Links ]

13. ACOG practice bulletin: Thrombocytopenia in pregnancy. Number 6, September 1999. Int J Gynaecol Obstet 1999;67(2):117-128.         [ Links ]

14. Subbiah M, Kumar S, Kallol KR, Sharma JB, Singh N. Pregnancy outcome in patients with idiopathic thrombocytopenic purpura. Arch Gynecol Obstet 2014;289(2):269-273. [http://dx.doi.org/10.1007/s00404-013-2958-x]        [ Links ]

15. Ambler KL, Vickars LM, Leger CS, et al Immune thrombocytopenia in the HAART era. Adv Hematol 2012(2012), Article ID 910954. [http://dx.doi.org/10.1155/2012/910954]        [ Links ]

 

 

Correspondence:
H M Sebitloane
sebitloanem@ukzn.ac.za

Accepted 14 October 2015.

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