Dengue, caused by a mosquito-borne arboviral infection, is endemic to many countries across the world and poses major public health threat to various states in India1-3. Under the National Vector Borne Disease Control Programme, case detection, management and vector control remain as important strategies for prevention and transmission of dengue virus4. Most people with dengue virus infection develop a febrile illness which is usually self-limited. Rarely, they may progress to severe illness with rapid onset of symptoms due to leaky capillaries associated with reduced platelet count, bleeding and hepatic dysfunction. Treatment is usually symptomatic based on clinical manifestation, including fluid replacement and blood component therapy3,4.
Pregnant women in endemic areas are prone to dengue infection and in recent years, concerns have been expressed regarding maternal and foetal consequences5-10. The changes associated with dengue infection such as increase in pro-inflammatory cytokines, capillary leakage due to increased vascular permeability, bleeding tendency secondary to thrombocytopenia and hepatic dysfunction can result in increased incidence of adverse pregnancy outcomes11-13. Earlier studies reported an increase in pre-term delivery, stillbirths and low-birth weight (LBW) in pregnancies complicated with dengue infection, while recent investigations suggested no or little increased risk12. We aimed to study the maternal and perinatal outcomes in pregnant women who presented with fever and diagnosed to have dengue infection and compared them against women who did not have dengue during pregnancy.
Material & Methods
This was a retrospective observational study conducted at the women and children hospital attached with the Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India. Women admitted with fever during pregnancy and undergoing test for dengue infection during January 2015 to December 2018, were identified from admission registers maintained at the antenatal and labour wards, and the dengue report registers at the Microbiology department. The diagnosis of dengue was made using the clinical symptoms with confirmatory laboratory testing [either NS1 antigen or immunoglobulin M (IgM) antibody] as per the national guidelines laid down by the National Vector Diseases Control Programme of India 20084. Those detected with dengue infection were considered as cases. The control group included pregnant women who were admitted with fever during the study period and tested negative for dengue. The study was approved by the Institute Ethics Committee and since the data were extracted from medical records, a waiver of consent was accorded (JIP/IEC/2019/169). All procedures performed in this study were done with the ethical standards set by the Scientific Advisory Committees and Institute Ethical Committees (IEC) - Human Studies, based on the 1964 Helsinki declaration and its later amendments as well as ethical guideline issued by the Indian Council of Medical Research.
The sample size was calculated using the nMaster2.0 software (CMC Vellore, India) based on the study by Friedman et al14. Using a two-sided alpha error of five per cent, power of 80 per cent and dengue positive to dengue negative case ratio of 1:4, a minimum of 55 pregnant women with dengue infection (dengue positive) and 220 pregnant women without dengue (dengue negative) were needed for the present study to detect a difference of about nine per cent in the occurrence of stillbirth between the groups. However, we included all pregnant women with fever who got admitted and tested positive on dengue serology during the study period.
Using a predesigned proforma, the details of the cases and controls were extracted from the medical records. Information was collected on demographic details, symptoms at presentation and clinical profile. Details of microbiological testing, haematological and biochemical investigations and treatment modalities such as transfusion of blood products, need for intensive care admission and mechanical ventilation were retrieved. Obstetric details such as gestational age at delivery, mode of delivery and neonatal outcomes including birthweight and neonatal and maternal morbidity were also collected.
Outcomes of interest were pre-term birth, stillbirth and LBW babies. Other complications such as miscarriage, pre-term premature rupture of membranes, intrauterine growth restriction, need for transfusion, rates of thrombocytopenia, etc., were also studied. The diagnosis of ascites was done on ultrasonographic examination. Small for gestation age was defined as the estimated foetal weight <10th percentile for the gestational age13. Pre-term birth was defined as those delivering before completion of 37 wk of pregnancy15 and LBW as defined as birth weight <2500 g irrespective of gestational age16. Based on the viability of the foetus in the institution, stillbirth was defined as a baby born with no signs of life at or after 28 wk of gestational age or with a birth weight of 1000 g17,18 and the pregnancy losses before the cut-off of gestational age for foetal viability or that of birth weight were considered a miscarriage in the study.
Statistical analysis: Data was analyzed using STATA 15.0 (Stata Corp., College Station, Texas, USA). While summary statistics for continuous variables were expressed either as mean with standard deviation or median with range, findings on categorical variables were presented as frequencies and percentages. Association between continuous variables with outcomes were tested with Student’s t test or Mann-Whitney U test depending on the normality distribution of the variables or otherwise. Association of categorical variables with outcomes was assessed, depending on the frequency of the events, using Chi-squared test (if the frequency of the vents were more than 5) or Fisher’s exact test (when the frequency of the events was <5); P values of < 0.05 was considered statistically significant.
Results
During the study period, of the 408 pregnant women with fever, 91 women (22.3%) diagnosed as having dengue infection were included as cases, and the remaining 317 (dengue negative) were included as controls. Among those tested positive for dengue, 59 (64.8%) had IgM antibody and the remaining (32, 35.2%) were positive for NS1 antigen. Baseline characteristics at the time of presentation were compared and are shown in Table I. Ascites on ultrasound examination was noted in 11 (12%) among the patient group compared to 19 (6%) among controls (P=0.056); whereas pleural effusion was observed in one (1.1%) and five (1.6%) in both the groups, respectively.
Table I: The baseline characteristics of the study population
Six maternal deaths were recorded among patient group, with five of them due to dengue shock syndrome and one due to dengue haemorrhagic fever. No maternal death occurred in the control group. Thrombocytopaenia occurred more among pregnant women with dengue compared to controls. Requirement of platelet transfusion (n=8, 8.7% vs. n=13, 4.2%, P=0.084) and packed red cell transfusion (n=13, 14.1% vs. n=42, 13.4%, P=0.861) were similar in both the groups. Table II shows obstetrics complications, labour and delivery characteristics among the study population.
Table II: The obstetrics complications, labour and delivery characteristics of the study population
Foetal and neonatal outcomes in the study population is shown in Table III. The proportion of pregnant women experiencing pre-term birth was higher among those who had dengue infection compared to the controls (32.1% vs. 22.7%) as was the findings on stillbirth (9.1% vs. 3.4%). Occurrence of LBW and small for gestational age babies were lower among pregnant women with dengue than among the controls. The risk of stillbirth was 2.67 [95% confidence interval (CI) 1.09, 6.57] times higher among the cases than the controls. Risk of LBW (risk ratio 1.13, 95% CI 0.87, 1.45) and pre-term birth (Risk ratio 1.33, 95% CI 0.89, 1.97) was similar among cases and controls.
Table III: The foetal and neonatal outcomes in the study population
Discussion
Earlier studies reported varying range of occurrence of adverse perinatal events in women developing dengue in pregnancy5-10,12,14,19,20. In 2008, Tan et al20 in a study from Malaysia reported no difference in pregnancy outcomes between women who experienced dengue while pregnant and those who did not. The same group of authors subsequently in a prospective study observed the risk of miscarriage [adjusted odds ratio (OR) 4.2] to be increased among those who developed dengue infection during pregnancy. A systematic review by Paixão et al12 highlighted about the increased risk of various foetal adverse outcomes, such as the risks of LBW (OR=1.41) and pre-term birth (OR=1.71); the review considered data from 292 women with dengue infection during pregnancy.
Physiological changes in pregnancy such as being in a procoagulant state and the haemodilution may delay the manifestation of severe diseases following dengue infection, such as haematocrit increase or thrombocytopenia. Moreover, pregnancy-related complications such as haemolysis elevated liver enzymes low platelet (HELLP) syndrome or preeclampsia can make early recognition of dengue complications difficult12. In dengue infection, pro-inflammatory mediators such as interleukin-6 and tumour necrosis factor-∞ can result in uterine contractions and pre-term birth21. Furthermore, thrombocytopaenia resulting in increased bleeding tendency and increased endothelial permeability can result in pathological changes in the placenta evidenced by stromal oedema, syncytial knots and chorangiosis, resulting in dysfunction and hypoxia. These changes, in turn, can negatively affect transfer of nutrients to the growing foetus in the womb across placenta, which can cause foetal growth restriction or in severe cases, can lead to stillbirth21,22. In the present study, occurrence of stillbirth was significantly higher among those who had dengue infection during pregnancy compared to those pregnant women who had fever but not due to dengue, whereas pre-term birth or foetal growth restriction, even though occurred in higher proportion in pregnant women with dengue, were not significantly different compared to controls.
Being a hospital record based study, the present investigation focused on pregnant women presenting to hospital with fever. Those who had a miscarriage or milder symptoms who may not have reached the hospital at the time of dengue infection may have been excluded from the study affecting the strength of association of dengue infection with various outcomes. Even though all women who presented with fever and had undergone dengue testing were included, we could not complete the recruitment based on 1:4 ratio (case : control), which can be considered as another limitation of the study. The lower event rates and the low number of controls precluded us from performing multivariate analysis for studying the association of various factors with adverse pregnancy outcomes.
Dengue, an endemic arbovirus infection in many Indian States and the subcontinent, poses a challenging public health problem, particularly when it occurs during pregnancy as it can lead to both maternal and foetal morbidity as well as mortality. In this investigation, occurrence of maternal mortality, stillbirths, pre-term birth and thrombocytopaenia were found to be high among pregnant women with dengue compared to the control. Larger prospective multicentric studies are required to assess the strength of association between dengue infection and various adverse pregnancy outcomes, which would help formulate appropriate monitoring and treatment strategies.
Financial support & sponsorship: Author (SK) acknowledges the Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), for providing support through the Golden Jubilee Short-Term Research Award for under graduates (JIP/UGRMC/GJ-STRAUS/2019/20).
Conflicts of Interest: None.
References
1. World Health Organization. Dengue and Severe Dengue Available from:
https://www.who.int/news-room/fact-sheets/detail/dengue-and-severe-dengue accessed on January 27, 2022.
2. Hadinegoro SR. The revised WHO dengue case classification:does the system need to be modified?
Paediatr Int Child Health 2012;32:33–8.
3. Ganeshkumar P, Murhekar MV, Poornima V, Saravanakumar V, Sukumaran K, Anandaselvasankar A, et al. Dengue infection in India:A systematic review and meta-analysis. PLoS Negl Trop Dis 2018;12:e0006618.
4. . National Vector Borne Disease Control Program, Directorate of Health Services. Dengue Available from:
https://nvbdcp.gov.in/index1.php?lang=1&level=1&sublinkid=5776&lid=3690 accessed on January 27, 2022.
5. Leite RC, Souza AI, Castanha PM, Cordeiro MT, Martelli CT, Ferreira AL, et al. Dengue infection in pregnancy and transplacental transfer of anti-dengue antibodies in north east, Brazil. J Clin Virol 2014;60:16–21.
6. Singla N, Arora S, Goel P, Chander J, Huria A. Dengue in pregnancy:An under-reported illness, with special reference to other existing co-infections. Asian Pac J Trop Med 2015;8:206–8.
7. 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:e2217.
8. Nascimento LBD, Siqueira CM, Coelho GE, Siqueira JB Júnior. Dengue in pregnant women:Characterization of cases in Brazil, 2007-2015. Epidemiol Serv Saude 2017;26:433–42.
9. Agarwal K, Malik S, Mittal P. A retrospective analysis of the symptoms and course of dengue infection during pregnancy. Int J Gynaecol Obstet 2017;139:4–8.
10. Kariyawasam S, Senanayake H. Dengue infections during pregnancy:Case series from a tertiary care hospital in Sri Lanka. J Infect Dev Ctries 2010;4:767–75.
11. Marinho PS, Cunha AJ, Amim Junior J, Prata-Barbosa A. A review of selected arboviruses during pregnancy. Matern Health Neonatol Perinatol 2017;3:17.
12. Paixão ES, Teixeira MG, Costa MDCN, Rodrigues LC. Dengue during pregnancy and adverse fetal outcomes:A systematic review and meta-analysis. Lancet Infect Dis 2016;16:857–65.
13. World Health Organization. Physical status:The use and interpretation of anthropometry. Report of a WHO Expert Committee. World Health Organ Tech Rep Ser 1995;854:1–452.
14. Friedman EE, Dallah F, Harville EW, Myers L, Buekens P, Breart G, et al. Symptomatic Dengue infection during pregnancy and infant outcomes:A retrospective cohort study. PLoS Negl Trop Dis 2014;8:e3226.
15. World Health Organization. WHO recommendations on interventions to improve preterm birth outcomes. Geneva: WHO;2015.
16. World Health Organization. WHA global nutrition targets 2025:Low birth weight policy brief. Geneva: WHO;2014.
17. World Health Organization. ICD-10 international statistical classification of diseases and related health problems. Geneva: WHO;2004.
18. Aminu M, van den Broek N. Stillbirth in low- and middle-income countries:Addressing the 'silent epidemic'. Int Health 2019;11:237–9.
19. Nascimento LB, Siqueira CM, Coelho GE, Siqueira JB Jr. Symptomatic dengue infection during pregnancy and livebirth outcomes in Brazil, 2007-13:A retrospective observational cohort study. Lancet Infect Dis 2017;17:949–56.
20. Tan PC, Soe MZ, Si Lay K, Wang SM, Sekaran SD, Omar SZ. Dengue infection and miscarriage:A prospective case control study. PLoS Negl Trop Dis 2012;6:e1637.
21. Vidal MS Jr, Lintao RCV, Severino MEL, Tantengco OAG, Menon R. Spontaneous preterm birth:Involvement of multiple feto-maternal tissues and organ systems, differing mechanisms, and pathways. Front Endocrinol (Lausanne) 2022;13:1015622.
22. Rathore SS, Oberoi S, Hilliard J, Raja R, Ahmed NK, Vishwakarma Y, et al. Maternal and foetal-neonatal outcomes of dengue virus infection during pregnancy. Trop Med Int Health 2022;27:619–29.