Skip to main content
BMC Infectious Diseases logoLink to BMC Infectious Diseases
. 2019 Nov 27;19:997. doi: 10.1186/s12879-019-4587-x

Dengue infection during pregnancy in Burkina Faso: a cross-sectional study

Kongnimissom Apoline Sondo 1,2,, Adama Ouattara 1,3, Eric Arnaud Diendéré 2, Ismaèl Diallo 1, Jacques Zoungrana 4, Guelilou Zémané 2, Léa Da 2, Arouna Gnamou 2, Bertrand Meda 5, Armel Poda 4, Hyacinthe Zamané 1,3, Ali Ouédraogo 1,3, Macaire Ouédraogo 4, Blandine Thieba/Bonané 1,3
PMCID: PMC6880640  PMID: 31771564

Abstract

Background

Dengue fever is prevalent in the world; in recent years, several outbreaks occurred in West Africa. It affects pregnant women. We aimed to assess the consequences of dengue fever on pregnant women and their fetuses during dengue epidemic in Burkina Faso.

Methods

We conducted a cross-sectional study from November 1, 2015 to January 31, 2017 in 15 public and private health facilities in Ouagadougou, using secondary data. Immunochromatographic rapid test Duo detecting specific antibodies, immunoglobin M/G and /or dengue non structural antigen1 virus was used to diagnose dengue cases.

Results

Out of 399 (48%) women registered during the study period, 25 (6%) were pregnant. The average age of pregnant women was 30 years, with 18 and 45 years as extremes. The main symptoms were fever (92%) and headache (92%). Nine patients (36%) had severe dengue characterized by bleeding (16%), neurological symptoms (16%) and acute respiratory distress (8%). Eight (32%) of the 25 women had early miscarriage and 8 (32%) women gave birth to viable fetuses. Among those with viable babies, 5 (20%) presented post-partum hemorrhage and 3 (12%) presented early delivery. The main fetal complications included 3 cases of acute fetal distress (12%). One case of maternal death (4%) and 4 cases of neonatal mortality (44.5%) were notified.

Conclusion

Dengue fever occurring during pregnancy increases maternal and neonatal mortality. Its severe complications require specific monitoring of pregnant women until delivery.

Keywords: Dengue fever, Pregnant woman, Burkina Faso

Background

Dengue is an arboviral infection transmitted by mosquitos of the genus Aedes [1, 2]. The incidence of dengue has increased by a factor of 30 over the past 5 decades, with the emergence of many new affected countries [2]. About 2.5 billion people live in endemic areas and an estimated 50 million people are infected each year [13]. The disease can affect anyone but pregnant women are more at risk. The most common clinical symptom of dengue is fever that can cause abortion or early delivery. Dengue-related thrombocytopenia increases the risk of bleeding during pregnancy or at delivery, and therefore leads to higher maternal mortality rate.

Studies on the reciprocal influence between dengue and pregnancy are quite rare. The fetal consequences of dengue are neither well understood nor well documented [4]. Few data on dengue during pregnancy exist. Authors reported some cases in Asia, Europe or Latin America [1, 5, 6]. In sub-Saharan Africa, it was urgent to assess the extent of the disease. In Burkina Faso as in other sub-Saharan countries, dengue cases have been reported since 2013, with an outbreak in 2016. The objective of this survey was to describe the socio-epidemiological, clinical, biological aspects, and the evolution of dengue during pregnancy in Ouagadougou.

Methods

This was a descriptive cross-sectional study involving 15 health facilities in the city of Ouagadougou: 4 District hospitals and 3 Teaching hospitals with packages of healthcare services corresponding to the secondary and tertiary levels of the health pyramid in Burkina Faso. In addition, eight private health facilities were selected according to their capacity of diagnosing dengue to be part of the study. We obtained the authorization of the General Director of Healthcare in Ouagadougou for data collection. The diagnosis of dengue was performed using rapid diagnostic tests (RDTs), which are immuno-chromatographic tests detecting Non Structural Antigen 1 (NS1Ag) and immune-globulin M and G (IgM and IgG). We used the World Health Organization classification of dengue (WHO 2009) to classify the women according to the severity of dengue.

The study population consisted of all the patients (male and female) diagnosed with dengue in these healthcare centers from November 1, 2015 to January 31, 2017, using dengue RDTs.

The sample consisted of all the pregnant women treated for dengue in these healthcare centers. The inclusion criteria were the positivity of the NS1 antigen and/or IgM and/or IgG. Isolated IgG positivity was considered a serological scar of dengue but we could not titrate this antibody.

Serotype 2 of dengue virus (DENV-2) was identified by Polymerase chain reaction (PCR) in the Pastor Institute of Dakar, as the causal agent of the epidemic during the study period [7].

The diagnosis of malaria was performed using malaria RDTs Histidine Rich Protein 2 and / or blood smears.

The data were collected from the consultation records, laboratories and the clinical records of the patients. The collected data were analyzed using EPI INFO version 3.5.

Results

Socio-epidemiological characteristics of pregnant women

In this study, 835 patients were screened for dengue, using rapid diagnostic tests (RDTs). Among them, there were 399 women (48%), including 25 (6.5%) pregnant women. Sixty-eight percent of the pregnant women were between the ages of 25 and 35 years. The average age of pregnant women was 30 years with 18 and 45 years as extremes, and 92% of pregnant women lived in Ouagadougou. Forty four percent (44%) had university degrees and 36% high school level. Thirty-wo percent (32%) were public and private sectors workers. Students accounted for 24%, as did housewives, and 20% of women were informal sector workers. Dengue frequency distribution during the study period showed a peak in October with 10 cases (40%), which corresponds to the peak in all the patients. Eight cases (32%) were notified in November 2016 (Fig. 1).

Fig. 1.

Fig. 1

Distribution of dengue cases in pregnant women by month

Clinical and biological characteristics of pregnant women

Among the pregnant women diagnosed with dengue, 8 were in their first trimester of pregnancy, 8 in their second trimester and 9 in their third trimester.

The reported clinical symptoms were fever (92%), asthenia (64%) and painful symptoms (84%) including headaches (92%), arthralgia (72%) and lumbago/myalgia (64%). Hemorrhagic signs (32%) included epistaxis (24%) and metrorrhagia (16%). Four women (16%) presented neurological symptoms such as consciousness disorders (coma stage I = 1 case and coma stage II = 3 cases). Two cases of malaria-dengue co-infection were notified. The clinical characteristics of women are shown in Table 1.

Table 1.

Distribution of cases according to clinical aspects

Clinical aspects Frequency (%)
Stage of pregnancy
 First trimester 08 (32)
 Second trimester 08 (32)
 Third trimester 09 (36)
Clinical signes
 Fever 23 (92)
 Painfull signs 21 (84)
  Headaches 23 (92)
  Arthralgia 18 (72)
  Myalgia 16 (64)
  Abdominal pain 12 (48)
  Retro-orbicular pain 04 (16)
 Asthenia 16 (64)
 Vomiting 14 (56)
 Hemorrhagic signs 08 (32)
  Epistaxis 06 (24)
  Metrorrhagia 04 (16)
  Gingivorragia 03 (12)
 Othera 04 (16)
 Neurologics signs 04 (16)
  Comatose stage II 02 (8)
  Comatose stage I 02 (8)
 Jaundice 03 (12)
 Hépatomegaly 03 (12)
 Dyspnea 02 (8)
 Oligoanuria 02 (8)
 Plasma leak (pleurisy) 01 (4)
 Lithiasis 01 (4)

a = Hematemesis, hematuria, melena, hemorrhagic at the injection site

Twenty-one of the 25 pregnant women (84%) had early dengue with positive NS1Ag. Sixteen pregnant women (64%) presented with primary dengue and 6 others (36%) with secondary dengue fever. Three patients were carriers of IgG alone.

Fifteen pregnant women (52%) had anemia with hemoglobin level less than 10 g/dl. Two of them were transfused with packed red blood cells. Thrombocytopenia defined as platelet count less than 150,000 / mm3, was observed in 12 patients (48%). Six of them had platelet count less than 50,000 / mm3 and 5 women received transfusion of platelets. Six women (24%) had elevated levels of aspartate aminotransferase (ASAT) ranging from 2 to 15 times the normal value. Two patients had a serum creatinine higher than 120 μmol/l.

Sixteen women (64%) had dengue fever with warning signs while 9 women (36%) had severe dengue fever, according to the 2009 WHO classification.

Maternal and fetal consequences

In mothers

Maternal complications were present in 6 cases. There was early delivery in 3 cases (12%) and intra partum hemorrhage in 5 cases (20%). Three women gave birth vaginally while 3 others underwent caesarean section. Two women expelled macerated fetuses. Seventeen women were always pregnant while they were discharged, and 8 women gave birth, with one of them having twins. A death was recorded in a context of liver failure and postpartum hemorrhage, which stands for 4% of lethality. Lethality was 12.5% among those who gave birth.

In fetuses and newborns

Fetal complications were observed in 6 cases including 3 cases (12%) of fetal distress and 3 cases (12%) of prematurity. Four cases of neonatal deaths (44.5%) were notified, 3 of which were due to prematurity and one case to neonatal infection. Women and fetal consequences are summarized in Table 2.

Table 2.

Maternal and perinatal outcomes

Item Frequency (%)
Mother outcome
 Death 1 (4)
 Exit without medical advice 1 (4)
 Maternal death (n = 8: known outcome) 1 (12,5)
Pregnancy outcome
 Normal pregnancy 17 (56)
 Delivery a 8 (36)
 Normal vaginal delivery (living newborn) 3 (12)
 Preterm delivery (macerated dead fetus) 2 (8)
 Caesarean section 3 (12)
 Living newborns (n = 9 birth) 5 (55.5)
 Dead (n = 9 birth) 4 (44.5)
 Death in-utero 2 (8)
 Perinatal death 2 (4)
Maternal complications 6 (24)
 Hemorrhagic deliveryb 5 (20)
 Preterm delivery 3 (12)
 Dynamic dystocia 2 (8)
Fetal complications 5 (20)
 Fetal distress 3 (12)
 Prematurity 3 (12)
 Néonatal infections 2 (8)

a = Eight deliveries with 9 children: one twin birth

bdelivery bleeding (4) and parietal hematoma after cesarean section = 1

Discussion

During the study period, 25 pregnant women were infected by dengue virus in Ouagadougou. The monthly epidemiological curve showed a maximum number of cases in October and November. The proportion of pregnant women with dengue was probably underestimated during our study as we only described the cases present in our database and as the survey was conducted in facilities not frequented by all pregnant women. Dengue surveillance should be instituted in pregnant women in order to distinguish it from malaria, since the two diseases share many common symptoms. The patients’ average age was 30 years, close the result of a descriptive survey conducted in Rio de Janeiro [8], and lower than the results found in other series in French Guiana [9] and Malaysia [5]. The disparity in the age of pregnant women could be justified by the fact that the average age of first maternity differs from one country to another, by sociocultural differences, and development level differences.

Unlike the common situation in developing countries where most of women suffering from infectious diseases are unemployed, housewives or farmers, most of pregnant women in our series were public and private sectors workers. Therefore, most of them could afford for the rapid diagnostic test cost (15 to 25 euros). This fact shows that pregnant women from low socioeconomic categories (housewives, farmers, unemployed) suffering from dengue but unable to afford for RDTs cost could not be diagnosed. The dengue frequency in pregnant women was underestimated, regarding the 2016 dengue outbreak in the city of Ouagadougou [7].

Out of the 25 pregnant women infected by dengue in our study, 84% were at phase of viremia. In Colombia, a reverse situation was observed in two studies with an acute viremic phase of 29.9 and 27.3% [6, 10]. In our context, dengue diagnosis was performed early compared to other authors’ results because of the epidemic context. About 9 cases of probably secondary dengue were observed, showing that these patients had caught a previous infection by dengue virus; that could explain the high proportion of severe mother and child complications (24 and 20% respectively). On the other hand, this high proportion of complications in Sub Saharan Africa contrasts with the results reported by some authors who suggested that being black was a protective factor and could explain the low proportions of severe dengue notified in African series [7, 11, 12].

In our study, the reported cases showed an upward distribution according to the trimester of pregnancy, with a doubling of the number of cases from the 1st to the 3rd trimester. Similar findings were reported in Colombia [13]. However, some authors reported higher infection frequency during the first trimester of pregnancy (45.4%) [10]. Carles in French Guiana found a higher incidence of the infection during the second trimester (40.9%) [14]. The period of occurrence of dengue seems to determine the types of complications, to the point that pregnant women infected during their first trimester had higher risk of miscarriage [3, 15]. When the infection occurred during the last trimester, the risk of low birth weight, premature labor and vertical transmission seemed to be higher [3, 8, 13, 16]. However other factors could explain the low birth weight as well as the prematurity. In our series, the evolution and the outcome of the pregnancies of women infected in their first and second trimester were not taken into account. However, out of 9 women in their third trimester of pregnancy, we observed 8 deliveries during the acute stage of dengue, with delivery bleeding 5/25 (20%) and prematurity 3/8 (12%). Almost half (45.5%) of the 9 newborns died. In the literature, there is a high percentage of threating preterm delivery, as shown in series conducted in Malaysia (50%) [5] and French Guiana (55%) [13]. A study in Cuba reported a risk of preterm delivery 3.7 times higher than in our series [17]. A specific management of pregnant women with dengue fever, especially in the last trimester, could reduce the risk of prematurity and prevent the risk of bleeding during delivery.

In our study, we recorded only 3 cases of Caesarean section out of the eight deliveries. Most of the studies reported as many cases of Caesarean section as natural deliveries; for instance, Alvarenga and Leon reported 50 and 53.8% respectively [8, 18]. Considering the high risk of bleeding in pregnant women with dengue, caesarean section practice would reduce the incidence of postpartum bleeding.

We recorded one maternal death out of 25 cases. Maternal mortality is significant in most studies: 17/78 in Sudan, 2/13 in Rio de Janeiro, and 3/16 in South Asia [5, 8, 19]. The recorded case of death in our series occurred in a context of complications, similarly to the situation reported by Machado in Brazil who found that pregnant women were 3.4 times more susceptible to catch severe dengue, and that dengue-related mortality in pregnant women was higher than in non-pregnant women [20, 21]. Therefore, any pregnant woman diagnosed with dengue must be considered as having a high risk of developing severe dengue. Such women require rigorous medical surveillance.

Conclusion

Our study showed that pregnant women are at high risk of complications when they catch dengue fever. The usual bleeding during delivery may be aggravated by this disease. On the other hand, some of the complications noted in this study cannot be exclusively attributed to dengue fever. Nevertheless, these complications should be taken into account in order to prevent the risk of bleeding and preterm delivery.

Acknowledgements

We thank the regional director of health of Ouagadougou for having authorized this study, the heads of the facilities included in the studies, (public and private health facilities in Ouagadougou city), and all those who took part in the study. This research was presented at the 6th Congress of the African Society of Infectious Pathology in Dakar (Senegal 2017).

Abbreviations

ASAT

Aspartate aminotransferase

IgG

Immunoglobin G

IgM

Immunoglobin M

NS1Ag

Non Structural Antigen 1

PCR

Polymerase Chain Reaction

RDTs

Rapid Diagnostic Tests

WHO

World Health Organization

Authors’ contributions

SKA, OA, DEA and ID designed the study, wrote the research protocol, collected and analyzed data, and wrote the manuscript. ZG, GA, DL and ZH collected data. ZJ, PA, and MB provided the bibliography. OA, TBB and OSM directed the study, gave a critical reading and final correction of the article. All authors read and approved the final manuscript.

Funding

The study did not receive any funding. Not applicable.

Availability of data and materials

The data used during the study are available from the corresponding author.

Ethics approval and consent to participate

It is a retrospective study based on data collected from patients’ clinical records, authorized by the regional director of the health of Ouagadougou.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Drumond EF, Machado CJ, Vasconcelos M, France E. Utilisation des SINASC de données secondaires SIM et SIH dans la littérature scientifique brésilienne de 1990 à 2006. Rev Bras Popol Estud. 2009;26:7–19. doi: 10.1590/S0102-30982009000100002. [DOI] [Google Scholar]
  • 2.WHO Dengue: Guidelines for diagnosis, treatment, prevention and control, Geneva, World Health Organization, new edition 2009P 160, Avenue Appia 20, 1211 Geneva 27, Switzerland.
  • 3.Brésil, Ministère de la Santé Secrétariat de la surveillance de la santé . Dengue: diagnostic et prise en charge clinique - adulte et enfant. 4ème Ed Brasilia. 2011. [Google Scholar]
  • 4.Simmons CP, Farrar JJ, van Vinh Chau N, Wills B. Dengue. N Engl J Med. 2012;366:1423–1432. doi: 10.1056/NEJMra1110265. [DOI] [PubMed] [Google Scholar]
  • 5.Ismail NA, Kampan N, Mahdy ZA, Jamil MA, Razi ZRM. Dengue pendant la grossesse. Asie du Sud - J Trop Med santé publique. 2006;37:681–683. [PubMed] [Google Scholar]
  • 6.Restrepo BN, Isaza DM, Salazar CL, Upegui L, Duke CL, Ramirez R, et al. Efectosdel virus de la Dengue pendant el embarazo. Medellin, en Colombie. Infectio. 2002;6:197–203. [Google Scholar]
  • 7.Organisation Mondiale de la Santé. Dengue : Fiche informative version Juillet 2016.[en ligne] http://www.who.int. Consulté le 2 décembre 2016.
  • 8.Alvarenga CF, Silami VG, Brésil P, MEH B, Lapin J, TMR N. Dengue Pendant la grossesse: une étude de treize cas. Am J Infect Dis. 2009;5:298–303. [Google Scholar]
  • 9.Basurko C, Carles C, Youssef M, Guindi WEL. Conséquences de la dengue pendant la grossesse. Eur J Obst et Gynecol Reprod Biol. 2009;147:29–32. doi: 10.1016/j.ejogrb.2009.06.028. [DOI] [PubMed] [Google Scholar]
  • 10.Restrepo BN, Isaza DM, Salazar CL, Ramirez JL, Upegui GE, Ospina M, et al. Dengue en el embarazo: efectos y en el elrecién. Biomédicale. 2003;23:416–423. doi: 10.7705/biomedica.v23i4.1236. [DOI] [PubMed] [Google Scholar]
  • 11.Chacón-Duque JC, Adhikari K, Avendaño E, et al. African genetic ancestry is associated with a protective effect on dengue severity in colombian populations. Epidemiol. EvolGenet Infect Dis. 2014;27:89–95. doi: 10.1016/j.meegid.2014.07.003. [DOI] [PubMed] [Google Scholar]
  • 12.de la C Sierra B, Kourí G, Guzmán MG. Race: a risk factor for dengue hemorrhagic fever. Arch Virol. 2007;152:533–542. doi: 10.1007/s00705-006-0869-x. [DOI] [PubMed] [Google Scholar]
  • 13.Maron SLC, Marlière RCC, Barcellus RC, Barbosa CN, Ramos JRM, Moreira MEL. Rapport de cas: infection de la dengue verticale. J Pediatr. 2008;84:556–559. doi: 10.2223/JPED.1826. [DOI] [PubMed] [Google Scholar]
  • 14.Carles G, Peiffer H. Effets de la fièvre de la dengue Pendant la grossesse en Guyane française. Dis Clin Infect. 2009;28:637–640. doi: 10.1086/515144. [DOI] [PubMed] [Google Scholar]
  • 15.Waduge GNR, Malavige NG, Pradeepan F, Wijeyaratne CN, Fernando S, Seneviratne SL. Pendant la grossesse, les infections de la dengue: une série de cas du Sri Lanka et de l’ examen de la littérature. J Clin Virol. 2006;37:27–33. doi: 10.1016/j.jcv.2006.06.002. [DOI] [PubMed] [Google Scholar]
  • 16.Carles G, Talarmin A, Péneau C, Dengue M, Bertsch C. Dengue et grossesse: étude de 38 Cas en Guyane française. J Gynecol Obst et Biol Reprod (Paris) 2000;29:758–762. [PubMed] [Google Scholar]
  • 17.Barroso RL, Betancourt ID, Saeta YF, Navarro MMM, Guerre GD. Répercussion de la dengue sérotype 3 sur le produit Conception. Rev Gynecol Obstet. 2009;36:42–50. [Google Scholar]
  • 18.Leon RR, MRM R, Huerta ES, Crivelli AP, GFM A. Dengue pendant el embarazo. Cas comunicación GynecolObstetMex. 2007;75:687–690. [Google Scholar]
  • 19.Adam I, Jumaa PM, Elbashir HM, Karsany MS. Maternelle et périnatale résultats de la dengue à Port - Soudan, l’est du Soudan. J Virol. 2010;7:153. doi: 10.1186/1743-422X-7-153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Machado CR, Machado ES, Rohloff RD, Azevedo M, Campos DP, de Oliveira RB, et al. Is pregnancy associated with severe dengue? A review of data from the Rio de Janeiro surveillance information system. PLoS Negl Trop Dis. 2013;7(5):e2217. doi: 10.1371/journal.pntd.0002217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Mota AK, Miranda Filho AL, Saraceni V, Koifman S. Maternal mortality and impact of dengue in Southeast Brazil: an ecological study, 2001–2005. Cad Saude Publica. 2012;28(6):1057–1066. doi: 10.1590/S0102-311X2012000600005. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data used during the study are available from the corresponding author.


Articles from BMC Infectious Diseases are provided here courtesy of BMC

RESOURCES