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Mother-to-child transmission of human immunodeficiency virus in aten years period

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Reproductive Health20118:35

https://doi.org/10.1186/1742-4755-8-35

Received: 20 June 2011

Accepted: 30 November 2011

Published: 30 November 2011

Abstract

Objectives

to evaluate mother-to-child transmission (MTCT) rates and related factors in HIV-infected pregnant women from a tertiary hospital between 2000 and 2009.

Subjects and method

cohort of 452 HIV-infected pregnant women and their newborns. Data was collected from recorded files and undiagnosed children were enrolled for investigation. Statistical analysis: qui-square test, Fisher exact test, Student t test, Mann-Whitney test, ANOVA, risk ratio and confidence intervals.

Results

MTCT occurred in 3.74%. The study population displayed a mean age of 27 years; 86.5% were found to have acquired HIV through sexual contact; 55% were aware of the diagnosis prior to the pregnancy; 62% were not using HAART. Mean CD4 cell-count was 474 cells/ml and 70.3% had undetectable viral loads in the third trimester. HAART included nevirapine in 35% of cases and protease inhibitors in 55%; Zidovudine monotherapy was used in 7.3%. Mean gestational age at delivery was 37.2 weeks and in 92% by caesarian section; 97.2% received intravenous zidovudine. Use of AZT to newborn occurred in 100% of them. Factors identified as associated to MTCT were: low CD4 cell counts, elevated viral loads, maternal AIDS, shorter periods receiving HAART, other conditions (anemia, IUGR (intra uterine growth restriction), oligohydramnium), coinfecctions (CMV and toxoplasmosis) and the occurrence of labor. Use of HAART for longer periods, caesarian and oral zidovudine for the newborns were associated with a decreased risk. Poor adhesion to treatment was present in 13 of the 15 cases of transmission; in 7, coinfecctions were diagnosed (CMV and toxoplasmosis).

Conclusion

Use of HAART and caesarian delivery are protective factors for mother-to-child transmission of HIV. Maternal coinfecctions and other conditions were risk factors for MTCT.

Keywords

  • Viral Load
  • Zidovudine
  • Prenatal Care
  • Toxoplasmosis
  • Bacterial Vaginosis

Introduction

Epidemiologic surveys show that HIV transmission patterns have changed, shifting the epidemic towards the poorer, those living in non-urban areas and women. Increasing heterosexual transmission is responsible for the ever growing rates of infected women. Considering that 85% of infected women are within their reproductive years, the risk of mother-to-child transmission (MTCT) is significant [1].

In Brazil, a sentinel study (Estudo Sentinela-Parturiente) has shown that the prevalence of HIV infection among pregnant women is 0.41% and that HIV testing for pre-natal care is performed in only 62.3% of patients [2]. Out of 63 countries analyzed by UNAIDS, Brazil provides antiretroviral therapy for 50 to 75% of infected pregnant women [1]. MTCT rates were evaluated in a large multicentric study that found 8.6% of newborn infection in 2000 and 7.1% in 2001 [3].

Several factors have been implicated in MTCT of HIV, including: advanced maternal AIDS-related illness, elevated viral loads (VL), breastfeeding, route of delivery, other infectious and obstetrics conditions and low CD4 cell counts during pregnancy [47]. Furthermore, viral subtype [8], viral concentration in maternal genital fluids [9, 10] and genetic factors were also identified [11]. Short duration of antiretroviral therapy during the course of pregnancy, problems regarding adhesion to treatment [12] and coinfecctions such hepatitis C virus [13], genital herpes [14], cytomegalovirus [15], syphilis [16], toxoplasmosis [17, 18] and recreational drug abuse [19] further increase the risk of MTCT.

The beneficial role of antiretroviral therapy in decreasing the risk of MTCT of HIV has been largely documented, since ACTG 076 protocols were published [20]. The use of highly active antiretroviral therapy (HAART) prior to conception and its earlier initiation in the course of pregnancy was also associated with lower rates of transmission [12].

CAISM/UNICAMP has been involved in the treatment and care of HIV-infected pregnant women since 1988. A historical cohort of HIV infected pregnant women has shown reduction of MTCT rates from 32.3% in 1990 to 2.9% in 2000. The greatest decline was observed after the introduction of the complete recommendations of ACTG 076 protocol. At that time, there were no reported cases of MTCT in pregnant women treated with HAART [21].

The objectives of this study were to evaluate mother-to-child transmission of HIV and related factors, to describe clinical and epidemiological profile of HIV infected pregnant women in a specialized prenatal care facility from 2000 to 2009 and to identify possible consequences of maternal infection to the newborn infant.

Subjects and method

Observational and analytical study, with a historical cohort constituted by a population of 452 HIV-infected pregnant women in the period of 2000 to 2009 receiving care at the institution. The women were retrospectively selected from clinical records and from the epidemiologic surveillance system. A specific form was developed for data gathering and the EPINFO program was used for data analysis. The following variables were analyzed: epidemiologic characteristics of the women (age, formal education, parity, planned pregnancy), clinical characteristics (previous use of HAART, previous diagnosis of HIV, CD4 cell count, viral load, regimens of antiretroviral treatment, maternal coinfecctions and gestational problems) and characteristics of the newborn (birth weight, birth length, Capurro, Apgar scores, neonatal morbidity and use of oral zidovudine).

All newborns exposed to HIV were referred to the Pediatric Immunodeficiency Service at the same University. In the few cases, where a final diagnosis of HIV infection in the newborn was not possible due to loss of follow up, the main caretaker was contacted by phone or mail. Research protocol was previously approved by the Institution Review Board (Project number 459/2004).

Statistical analysis was conducted regarding demographic and epidemiologic characteristics of the women, prenatal care, use of antiretroviral therapy, delivery and newborn. Data was analyzed through proportions distributions and means, comparatively between groups of HIV-infected and non-infected children. The specific effect of several different interventions was analyzed through their individual risk ratios (RR). Possible associations between each variable were further tested with qui-square test or Fisher's exact test. The association between continuous variables was tested through student t test (parametric data), Mann-Whitney test (non-parametric data) and ANOVA. The 95% confidence interval and the level of significance of 0.05 were used. Data was analyzed with the statistical program SAS version 9.1.

The association between maternal and perinatal variables and MTCT was evaluated with qui-square test, Fisher's exact test and calculation of risk ratio and confidence intervals to 95%. Multivariate analysis was performed according to the COX model for proportional risks (adjusted risk ratio). However, due to problem during mathematical convergence related to the actual absolute number of positive outcomes (mother-to-child transmission events), results in this front could not be measured.

The study protocol was approved by the Internal Review Board (IRB) of the Center for Women's Integrated Healthcare (CAISM), Department of Obstetrics and Gynecology, University of Campinas (UNICAMP) and by the IRB of the School of Medical Sciences of the same institution (approval letter #459/2004).

Results

Between 2000 and 2009, 26.668 deliveries occurred in the institution and 452 were from HIV-infected pregnant women, corresponding to a prevalence of 1.69% of all deliveries. Figure 1 shows excluded cases in the final analysis, performed with 401 infants. Data referring to multiple gestations were not replicated. The analysis comprised 392 gestation events.
Figure 1
Figure 1

Mother-to-child transmission in HIV pregnant women from 2000 to 2009.

Characteristics of pregnant women, prenatal care and delivery

The characteristics of pregnant women are presented in Table 1. The majority of them (243 in 389-62.5%) was not on antiretroviral therapy when they got pregnant. Among women already using antiretroviral drugs, the most common combination was two nucleoside reverse transcriptase inhibitors (NRTI) and one protease inhibitor (PI) or one non-nucleoside reverse transcriptase inhibitor (NNRTI). Ninety percent of women (295 in 328) reported good adhesion (95% or more of all HAART had been taken as prescribed, in two occasions) to treatment during pregnancy [22].
Table 1

Characteristics of HIV-infected pregnant women from 2000 to 2009

Characteristics

  
 

N

%

Age

  

< 20

35

8.9

20 a 29

234

59.7

≥ 30

123

31.4

Caucasian race

234

59.7

Number of pregnancies

  

1-2

177

45.2

≥ 3

215

54.9

Fixed sexual partner

263

76.9

Planned pregnancy

73

21.8

Use of contraceptive method

214

62.9

Previous HIV-infected child

30

10.6

HIV diagnosis

  

Before pregnancy

215

55.1

During pregnancy

170

43.6

Sexual contact transmission

262

86.5

CDC classification

  

1

102

26.2

2

161

41.4

3

72

18.5

Not classified

54

13.9

First CD4 > 350 cel/ml (for NAIVE)

137

39.1

VL < 50(copies/ml) after HAART

93

53.1

Efavirenz exposition

41

10.5

Total

392

100

(#) The numbers are different because of lack of informations from some patients

The mean number of prenatal visits was 7 (ranging from 1 to 18). Mean gestational age at the beginning of prenatal care was 18.1 weeks (ranging from 3 to 38). The majority of women (273 in 392-69.6%) presented at least one obstetric complication: preterm labor (14.5%), intrauterine growth restriction (6.1%) and chronic or gestational hypertension (5.1%) among others. Two hundred ninety nine in 392 (76.3%) had also at least one other infectious complication: bacterial vaginosis (32.9%), urinary tract infection (27%) and papilomavirus/intracervical neoplasia (22.7%) were the most prevalent. Resistance testing was performed only in 14 of 392 pregnant women (3.6%) by clinical indication (good adhesion and elevated viral load after two months of therapy). These patients were found to be carrying multiresistant HIV.

Prophylactic antiretroviral therapy (maternal CD4 > 350 for naive) was used in 39.1% (137 in 350). Only eleven in 392 women (2.8%) did not use antiretroviral therapy during pregnancy by late diagnosis; 41 in 384 (10.5%) were exposed to efavirenz. Zidovudine monotherapy was used by 28 in 384 women (7.3%) and in 21 patients, it was maintained until birth. ART combinations used are presented in Table 2. Mean CD4 cell-count was 474 cells/ml. Mean duration of antiretroviral therapy during pregnancy was 142.4 days. After HAART with PI, 66 pregnant women (71.7%) had undetectable viral loads. Three hundred and seventy in 380 cases (97.4%), intravenous zidovudine was used during labor and delivery.
Table 2

Association between HAART combinations during pregnancy and newborn infection

Newborn infection

With

Without

P*

RR

IC 95%

 

N

%

n

%

   

Antiretroviral therapy

    

0.0478

  

AZT Monotherapy

3

14.3

18

85.7

 

1.00

 

NRTI+NRTI

0

0.0

14

100

 

NC

 

NRTI+NRTI+NVP

5

3.9

124

96.1

 

0.27

0.07-1.05

NRTI+NRTI+NFV

3

2.3

125

97.7

 

0.16

0.04-0.63

NRTI+NRTI+LPV/R

1

1.6

63

98.4

 

0.11

0.01-0.99

Other PI regimens

1

4.3

22

95.7

 

0.30

0.03-2.70

(#) Missed information for 13 cases in 392 gestation events

(##) NC: not calculated

(###) No antiretroviral: 11 cases; 2 cases with newborn infection

Mean gestational age at birth was 37.2 weeks. In 92% (357 in 388) of cases, delivery was conducted by caesarean section, mainly indicated by HIV infection.

Characteristics of the newborns

Of 401 newborns, 208 (52.9%) were female. Mean birth weight was 2820 g and mean birth age by the method of Capurro was 37.6 weeks. Seventy nine children were premature (24%) and 87 (21.96%) had low birth weight. Neonatal use of oral zidovudine in the hospital was confirmed in 100% of cases.

Twenty one children presented with major congenital malformations among 48 in 393 (12.2%) presenting with any malformation: 9 cases of cardiac anomaly, 7 cases of genital tract malformations and 5 cases of urinary tract malformations. The remaining cases comprised minor malformation such as supernumerary finger, auricular appendage, among others.

Thirty four in 382 children (8.9%) presented at least one other illness during neonatal period (12 cases of pneumonia, 10 cases of hepatitis C, 6 cases of candidiasis and toxoplasmosis, 4 cases of cytomegalovirus infection, hepatitis B and urinary tract infection, 3 cases of meningitis and sepsis, 2 cases of syphilis and one case of rubella, varicela and tuberculosis).

Factors associated with mother-to-child transmission of HIV

MTCT of HIV occurred in this cohort in 3.74% of cases. Risk factors identified for transmission were: low CD4 cell count, maternal AIDS-related illness, reduced time on HAART, obstetric and infectious concurring illnesses, presence of labor, neonatal coinfecctions, low birth weight, newborns small for gestational age, fail to complete postnatal prophylactic use of oral AZT and maternal and newborn anemia.

Any concurring AIDS-related illness during prenatal care enhanced the risk of transmission in around 5 times; maternal anemia (hemoglobin level under 11 g/dl) increased the risk of transmission in 4 times and also in cases of intrauterine growth restriction. Ovular infection elevated the risk in more than 21 times; neurotoxoplasmosis by itself increased it in more than 7 times (Table 3).
Table 3

Maternal factors associated and mother-to-child transmission of HIV

VARIABLES

MTCT

With

MTCT

Without

P*

RR

IC 95%

 

N

%

n

%

   

AIDS-related illness

    

0.0748

  

Yes

2

14.3

12

85.7

 

4.87

1.19-19.93

No

11

2.9

364

97.1

 

1.00

 

First CD4 (cel/ml)

    

0.0029

  

≥ 350

1

0.5

212

95.5

 

1.00

 

< 350

8

5.8

129

94.2

 

12.44

1.57-98.35

Time using HAART

    

0.0632

  

15 days or longer

11

3.1

342

96.9

 

1.00

 

Less than 15 days

2

16.7

10

83.3

 

5.35

1.33-21.53

Ovular infection

    

0.0035

  

Yes

2

66.7

1

33.3

 

21.61

8.15-57.29

No

12

3.1

377

96.9

 

1.00

 

Neurotoxoplasmosis

    

0.0127

  

Yes

1

25

3

75

 

7.46

1.26-44.23

No

13

3.4

375

96.6

 

1.00

 

Route of delivery

    

0.0190

  

Vaginal

4

12.9

27

87.1

 

1.00

 

Caesarean

10

2.8

347

97.2

 

0.22

0.07-0.65

Labor

    

0.0088

  

Yes

6

9.8

55

90.2

 

4.54

1.58-13.04

No

7

2.2

316

97.8

 

1.00

 

Time after ruptured membranes

    

0.5936

  

Less than 4 hours

2

11.1

16

88.9

 

1.00

 

> 4 hours

3

8.1

34

91.9

 

0.73

0.13-3.99

No

10

 

328

    

IV AZT

    

0.3126

  

Yes

12

3.5

362

96.5

 

0.35

0.05-2.40

No

1

10.0

9

90

 

1.00

 

Anemia (Hb level < 11 g/dl)

    

0.0254

  

Yes

4

11.8

30

88.2

 

4.21

1.40-12.72

No

10

2.8

348

97.2

 

1.00

 

(#) The numbers are different because of lack of informations from some patients

First CD4 cell count during prenatal care was different among cases associated with transmission of HIV (219.1 cells/ml) and those not associated with it (480.9 cells/ml) (p = 0.002). Values lower than 350 cells/ml increased the risk of MTCT in more than 12 times (Table 3).

During gestation, use of HAART constituted protective factor against MTCT of HIV, with difference attributed to the mean duration of use in days among cases of transmission (93.2 days) and those without transmission (144.2 days) (p = 0.0121). HAART use for less than 15 days prior to delivery determined and increased risk of transmission of more than 5 times (Table 3). The use of antiretroviral drugs during pregnancy was not associated with low birth weight (p = 0.0808) or premature birth (p = 0.43).

Caesarean operation has shown protection in the order of 80% against MTCT of HIV. In the other, delivery occurring after the onset of labor determined an increased risk of almost 5 times for transmission of HIV (Table 3).

Children who were considered to be small for gestational age had an increased risk of almost 5 times for HIV infection. Mean values of birth weight was different in cases of transmission of HIV (2416 grams) and those without (2836 grams) (p = 0.0392). Low birth weight was associated with an increase of 3 times or more in the risk of transmission. Children who did not receive oral zidovudine in the neonatal period had an increased risk of acquiring HIV of more than 35 times. Neonatal infections were significantly associated with mother-to-child transmission of HIV. Toxoplasmosis increased the risk in almost 24 times and cytomegalovirus infection in more than 15 times (Table 4). Table 5 shows characteristics of HIV infected newborn and table 6 shows the mother-to-child-transmission rate year by year. The tendency is to a lower rate in the last years.
Table 4

Neonatal factors associated with mother-to-child transmission of HIV

VARIABLES

With

Without

P*

RR

IC 95%

 

N

%

n

%

   

Birth weight

    

0.0270

  

≥ 2500 g

8

2.8

301

97.2

 

1.00

 

< 2500 g

7

8.0

80

92

 

3.11

1.16-8.33

Birth Weight in comparison to gestational age (GA)

    

0.0110

  

Adequate forGA

10

2.9

332

97.1

 

1.00

 

Small for GA

5

13.2

33

86.8

 

4.50

1.62-12.48

Oral AZT

    

0.0010

  

Yes

11

2.8

381

97.2

 

1.00

 

No

2

100

0

0

 

35.64

19.90-63.81

Neonatal pathology

    

0.0047

  

Yes

5

14.7

29

85.3

 

5.67

2.01-15.96

No

9

2.6

338

97.4

 

1.00

 

Congenital Toxoplasmosis

    

< 0.0001

  

Yes

4

66.7

2

33.3

 

23.94

10.63-53.93

No

11

2.8

384

97.2

 

1.00

 

Pneumonia

    

0.0076

  

Yes

3

25.0

9

75

 

8.10

2.63-25.02

No

12

3.1

377

97.9

 

1.00

 

Congenital CMV

    

0.0075

  

Yes

2

50.0

2

50

 

15.27

5.00-46.63

No

13

3.3

384

96.7

 

1.00

 

Hepatitis B

    

1.0000

  

Yes

0

0.0

4

100

 

NC

 

No

15

3.8

382

96.2

   

Syphilis

    

1.0000

NC

 

Yes

0

0.0

2

100

   

No

15

3.8

384

96.2

   

Anemia (hb < 13,5 g/dl)

    

0.0051

  

Yes

8

8.7

84

91.3

 

5.83

1.58-21.46

No

3

1.5

198

98.5

 

1.00

 

IUGR (intra uterine growth restriction)

    

0.0470

  

Yes

3

12.5

21

87.5

 

4.18

1.25-14.00

No

11

3.0

357

97

 

1.00

 

Hepatitis C

    

1.0000

  

Yes

0

0.0

10

100

 

NC

 

No

15

3.8

376

96.2

   

(#) The numbers are different because of lack of informations from some patients

(##) NC: not calculated

Table 5

Charateristics of HIV infected newborns.

Case

Year

PN

visits

Initial CD4

Final CD4

Final VL

ARV

Time ARV

Adhesion

IV

AZT

AZT newborn

Ruptured membran

Route of delivery

Labor

Capurro

Birth Weight

Maternal

Pathology

Neonatal Pathology

Death

01

00

10

< 100

-

-

AZT

112

No

Yes

No

0

Ces

No

41

3370

No

PCP

Yes

02

00

-

-

-

-

AZT

49

No

Yes

Yes

2 h

Vag

Yes

36

2530

No

Toxo

No

03

00

2

-

-

-

AZT

40

No

Yes

Yes

0

Ces

Yes

40

3110

No

Rubella

No

04

01

8

-

-

-

AZT

21

No

Yes

Yes

0

Ces

No

38

3230

No

No

No

05

01

3

289

-

-

Haart

14

No

Yes

No

0

Ces

No

34

2635

No

No

No

06

01

9

11

05

47000

Haart

260

No

Yes

Yes

1 h

Vag

Yes

37

1985

Candid, PCP

Toxo

Yes

07

02

6

315

-

420

AZT

10

No

Yes

Yes

240 h

Vag

Yes

33

1320

Stevens-Johnson, Hep C

No

No

08

02

3

110

-

17000

Haart

255

No

Yes

Yes

0

Ces

No

40

3000

Neurotox

Toxo

No

09

03

5

344

-

< 50

Haart

140

Yes

Yes

Yes

0

Ces

Yes

40

3695

No

No

Yes

10

04

6

424

630

1410

Haart

84

No

Yes

Yes

0

Ces

No

35

1340

No

Oral cand.

No

11

04

5

233

-

-

AZT

135

No

Yes

No

0

Ces

No

33

1705

No

CMV

No

12

05

0

-

-

-

No

0

No

No

No

63 h

Vag

Yes

32

1425

No

No

No

13

06

2

160

-

-

Haart

21

No

Yes

Yes

0

Ces

Yes

39

2790

No

No

No

14

06

1

135

120

38380

Haart

-

No

Yes

Yes

7 h

Ces

Yes

37

2015

No

First gemelar

No

15

08

3

86

146

63

Haart

70

Yes

Yes

Yes

0

Ces

Yes

37

2100

Oral candid

Neurotoxo, CMV, TB

No

Table 6

Mother-to-child transmission of HIV by years of birth

YEAR

With

Without

total

 

N

%

n

%

 

2000

3

13.6

18

86.4

22

2001

3

6.1

46

93.9

49

2002

2

3

65

97

67

2003

1

2.5

39

97.5

40

2004

2

3

40

97

42

2005

1

3.1

31

96.9

32

2006

2

4.4

44

95.7

46

2007

0

0

37

100

37

2008

1

1.9

51

98.1

52

2009

0

0

12

100

12

Total (#)

15

3.7

384

96.3

399

(#) The numbers are different because of lack of information from some patients

Discussion

The present study, analyzing 452 pregnancies from 2000 to 2009, found an HIV MTCT rate of 3.74%, which was above the expected for a reference maternity, in which nationally [23] and internationally accepted standard prophylactic measures are routinely employed in the care of HIV infected pregnant women. However, further studying of the 15 cases of transmission of HIV has shown particular results that explain such numbers. In spite of a multidisciplinary approach to prenatal care, with emphasis in medical (infectious disease specialist and obstetrician) and psychosocial care, the vast majority of mothers had substantial problems regarding adhesion to treatment and regular use of antiretroviral therapy prescribed during the gestation period. As a direct consequence of poor adhesion to treatment, some women reached delivery bearing high viral loads or even unknown values of viral load.

Our results shown several risk factors (low CD4 cell count, maternal AIDS-related illness, reduced time on HAART, obstetric and infectious concurring illnesses, presence of labor, neonatal coinfecctions, low birth weight, newborns small for gestational age, fail to complete postnatal prophylactic use of oral AZT and maternal and newborn anemia) associated with MTCT of HIV, confirming worldwide data on the subject [47, 12, 15, 17, 18].

Women with advanced degrees of imunossupression (CD4 < 350 or AIDS) had a significantly higher risk of transmitting HIV to their newborns, similarly to results found in literature [47, 24].

HAART leads to undetectable viral load more rapidly in the course of treatment [12, 2527]. HAART in comparison to AZT monotherapy was strongly associated with decreased risk of MTCT. Duration of antiretroviral therapy shorter than 15 days was associated with and increased risk, as was demonstrated by international study [12]. It is established that after two weeks of antiretroviral therapy the decrease in maternal viral load would be sufficient to decrease the risk of neonatal infection. Our data found that PI containing regimens were an important factor to protect against MTCT.

Preterm and low birth weight were not observed as complications of HAART use during pregnancy, in agreement with findings of other studies [2831], but as opposite to what was concluded by others [3234]. Thus, our results confirm the safety of antiretroviral drugs during pregnancy.

Obstetric and infectious complications of pregnancy have also lead to an increase in the risk of newborn HIV infection, in particular: anemia, intrauterine growth restriction and ovular infection. These factors can be symptomatic of compromised placental barrier function, increasing its permeability to HIV [35] and corroborate the importance of referring prenatal care of HIV infected pregnant women to tertiary specialized healthcare centers.

Great controversy still exists regarding the route of delivery in HIV infected pregnant women. Micro transfusions occurring during uterine contractions enhance blood exchanges between mother and fetus and the presence of significant viral load becomes an important factor in newborn HIV infection. Another issue presents itself as plasma viral load does not adequately represent viral concentrations in vaginal fluids [9]. So, even patients with sustained undetectable plasma viral load could still carry substantial viral load in vaginal secretions. Our data pointed out that the presence of labor has significantly increased the risk of MTCT.

This study demonstrated also, in concordance to current literature, a lower rate of MTCT following elective caesarean delivery, including women on potent antiretroviral therapy and with low peripartum plasma viral load [25, 36]. In fact, this has been the standard of care in this healthcare facility since 2005, provided that the patient did not present in advanced labor (elective caesarean delivery). Previous studies discussed the higher post partum morbidity in HIV pregnant women submitted to a caesarean section. However, recent studies did not find this association, leading to a relative safety by performing a caesarean in these women [25].

Premature rupture of membranes followed by vaginal delivery was present in one case of newborn infection, confirming it as a collaborating factor for MTCT [24, 35].

Low birth weight and small for gestational age also had increased risk for MTCT [37]. Among 15 infected newborns, in seven cases low birth weight was a contributing factor. Furthermore, several of these presented with serious infectious complications of the neonatal period. Maternal acute infections can compromise placental barrier, increasing the risk of MTCT. Several studies have demonstrated association, especially with maternal toxoplasmosis [17, 18] and CMV [15], reinforcing the need of exhaustive screening of these infections during prenatal care. Co-infection with hepatitis C occurred in more than 10% of cases, which can also enhance transmission of HIV [13].

There was one case of multiple gestation in which only the first to be born was infected. Although there is no known association between MTCT and multiple pregnancies after the use of HAART, the first newborn is more frequently infected [38].

Postnatal prophylaxis with oral zidovudine has demonstrated to be a significant factor in protection against neonatal HIV infection since ACTG 076 protocol [20], and our findings were similar.

This study demonstrates that MTCT was strongly associated with maternal factors such as the stage of HIV infection, represented by CD4 counts and viral load, use of HAART and route of delivery, and also factors regarding the gestational period, especially the presence of maternal infectious and obstetric complications. Regarding the newborn, use of neonatal zidovudine still poses as an important factor in the protection against HIV transmission.

One limitation of this study was the impossibility of multivariate analysis due to a limited number of infected newborns, which led us to interpretations based solely on risk ratios.

The increasing number of women infected with HIV observed over the past few years alerts to the importance of approaching the issue of MTCT as a serious public health problem. As a direct consequence of this are the emotional losses to these families and also the considerable financial expenses to both the public and private health system for the care and management of an incurable infection.

Our data demonstrate a high rate of MTCT. However it is strongly associated with poor adhesion to treatment of both HIV and concurring illnesses, to the presence of AIDS and other serious diseases. If only the cases in which newborn infection was in fact preventable were to be analyzed separately, it could be concluded that in one single case such scenario was true, in which all standard prenatal measures were implemented successfully leading to undetectable viral load prior to delivery.

The increasing number and complexity of cases reduce the quality of psychosocial and clinical support which, in turn, can influence adhesion to therapy and eventually lead to poor outcomes to the newborn. Thus, it becomes paramount for the HIV-infected pregnant women to be referred to a tertiary care center offering a multiprofessional approach aiming towards good adhesion to treatment and, ultimately, reducing mother-to-child transmission of HIV.

Declarations

Authors’ Affiliations

(1)
Department of Obstetrics and Gynecology, School of Medicine, University of Campinas, Campinas, Brazil
(2)
Centro de Referência DST/Aids de Campinas, São Paulo, Brazil

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© Delicio et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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