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Sero-prevalence of syphilis and associated factors among pregnant women in Ethiopia: a systematic review and meta-analysis

Systematic Reviews volume 10, Article number: 223 (2021) Cite this article

Abstract

Background

Syphilis remained a major cause of reproductive morbidity and poor pregnancy outcomes in developing countries. Previously, studies showed inconsistent results and failed to show the actual picture of the diseases in Ethiopia. Thus, the aim of this meta-analysis was, first, to determine the updated pooled prevalence of syphilis among pregnant women in Ethiopia and, second, to assess its associated factors.

Methods

A comprehensive search was made on PubMed, Google scholar, Science Direct, and African Journals Online databases to identify relevant articles. A random effects model was used to estimate pooled syphilis prevalence and odds ratio (OR) with the respective 95% confidence intervals (CIs) using STATA 14 statistical software. I2 statistics and Egger’s regression test in conjunction with funnel plot was used to determine heterogeneity and publication bias among included studies respectively.

Result

We identified 13 suitable studies in this analysis. Accordingly, the pooled prevalence of syphilis among pregnant women in Ethiopia was 2.32% (95% CI, 1.68–2.97). Specifically, syphilis prevalence was 2.53% (95% CI, 1.92–3.14%) and 1.90% (95% CI, 0.40–3.40%) as per the treponemal and non-ytreponemal diagnostic test, respectively. On the other hand, regional analysis indicated that 4.06% (95% CI, 2.86–5.26) in Southern Nations Nationalities and Peoples (SNNP), 2.16% (95% CI, 1.57–2.75) in Amhara and 1.46% (95% CI, 0.69–2.23) in Oromia region. Being married (OR, 0.37 (95% CI, 0.12–0.91%)) was less likely to develop syphilis. On the other hand, women with history of multiple sexual partner (OR, 2.98 (95% CI, 1.15–7.70)) and women with history of previous sexually transmitted infection (STI) (OR, 4.88 (95% CI, 1.35–17.62)) have higher risk to develop syphilis. Besides, the pooled syphilis-HIV coinfection was 0.80% (95% CI, 0.60–1.01%).

Conclusion

This study provides evidence of relatively high prevalence of syphilis among pregnant women in Ethiopia. Therefore, it is recommended to further ramping up of current intervention measures to prevent future generations.

Systematic review registration

PROSPERO CRD42020211650

Peer Review reports

Background

Syphilis is a sexually transmitted infection (STI) caused by the spirochete Treponema pallidum, and it continues to be a main public health problem worldwide [1]. It spreads primarily through sexual contact and vertical transmission and can rarely be spread through blood transfusion. Syphilis can be successfully controlled by effective public health measures due to the availability of a sound diagnostic test and effective and economical treatment options [2]. However, if syphilis is left untreated, it can lead to devastating fetal outcomes [3].

Pregnant women are sexually active and are at risk of STI, including syphilis [4]. Globally, 36 million people are infected with syphilis, out of which 2 million are pregnant women. More than half of infected women transmit the infection to their babies resulting in adverse pregnancy outcomes including early fetal death, stillbirth, preterm birth, low birth weight, neonatal death, and congenital infection in infants [5].

Syphilis remained a major cause of reproductive morbidity and poor pregnancy outcomes in developing countries [4]. In sub-Saharan Africa, syphilis sero-prevalence ranges from 4 to 15%, and can cause adverse outcomes in 50–80% of pregnancies [6]. Ethiopia is among the top three sub-Saharan countries with the highest numbers of adverse pregnancy outcomes attributed to syphilis [7]. Furthermore, studies have demonstrated that 21% children born from seropositive mothers in Ethiopia developed signs of syphilis. Besides, stillbirth and abortion rates of syphilis diagnosed women were almost double relative to the general population [8].

Previously established systematic review and meta-analysis conducted on the prevalence of syphilis among pregnant women in Ethiopia includes only five studies with smaller sample size and did not report syphilis prevalence based on the diagnostic test modality. Besides, it failed to demonstrate syphilis-HIV co-infection and predictors of syphilis sero-positivity [9]. Thus, in the absence of concrete and inclusive evidence in STI endemic settings including HIV and syphilis, this systematic review and meta-analysis was conducted to determine the updated pooled prevalence of syphilis among pregnant women in Ethiopia. Moreover, syphilis sero-reactivity associated factors and syphilis-HIV co-infection was also determined in this study to guide public health intervention and control measures.

Methods and materials

Reporting and study protocol registration

This review was conducted according to the requirements of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement [10] (Additional file 1). This study was registered in International Prospective Register of Systematic Reviews (PROSPERO) database with protocol number, CRD42020211650.

Search strategy and information sources

An inclusive literature search was made from September 1 to 30, 2020, on PubMed, Google scholar, Science Direct, and African Journals Online databases based on Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement [10]. The following key words were used for PubMed database searching: [“Syphilis” or “Treponema pallidum” AND (magnitude OR prevalence OR seroprevalance) AND “pregnant women” OR “pregnant” AND “Ethiopia”]. In addition, literatures and reference lists of relevant articles were also retrieved to find additional studies.

Inclusion and exclusion criteria

All articles fulfilling the following conditions were screened and subsequently assessed for eligibility. Published studies conducted only in Ethiopia and reporting prevalence of syphilis among pregnant women, published in English language up to the end of September 2020. Studies with a clear description of participants’ involved and state the number of participants tested for syphilis, and articles with a clear number and/or prevalence of syphilis cases were also considered. Nevertheless, citations without abstracts and/or full-text, review articles, conference abstracts, editorials, duplicate studies, commentaries, trend analyses, studies which include non-pregnant women and those which do not report syphilis prevalence were excluded from the review. Similarly, given the known synergy between HIV and syphilis [11], studies conducted prior to HIV antiretroviral availability (before January 2005 in Ethiopia) [12] were also excluded as this would affect syphilis prevalence.

Outcome of interest

The primary outcome of this study was the prevalence of syphilis among pregnant women. Moreover, the results have been stratified by diagnostic test (treponemal vs non-treponemal testing) and different geographical regions in Ethiopia. Secondly, we have also determined factors associated with syphilis sero-positivity: marital status (married vs not cohabiting; not cohabiting involves: single, widowed, and divorced), previous STI (present vs absent), and previous history of multiple sexual partner (present vs absent). In addition, the prevalence of syphilis-HIV co-infection was also determined.

Study selection, quality assessment, and data extraction

The title and abstract of studies were screened after removing duplicates. Full-text review was conducted for articles found to be relevant by tittle and abstract to identify potential articles for inclusion in this meta-analysis.

The quality of included studies was evaluated by using Joanna Brigg’s Institute (JBI) quality assessment checklist for prevalence studies [13]. Based on the JBI checklist, studies with a quality score of 50% and above were considered high quality and involved in the analysis. Extracted data includes the following descriptive information: author and publication year, study area/region, study period, laboratory methods employed to diagnose syphilis, sample size, and prevalence of syphilis. In addition, prevalence of syphilis by marital status, presence/absence of previous history of multiple sexual partner, and history of previous STI were extracted whenever reported. Two independent reviewers (HG and DG) were involved in study selection, quality assessment, and data extraction. Disagreement between the reviewers was solved by discussion.

Statistical methods and analysis

Data were entered into Microsoft Excel and then exported to STATA 14 statistical software for further analysis. The I2 values of 25, 50, and 75% was considered low, medium, and high heterogeneity, respectively [14]. In pooled prevalence analysis and 95% confidence intervals (CIs), the random effects model (DerSimonian-Laird method) [15] was used. The overall and subgroup analysis of random effects model with 95% CIs were calculated and demonstrated using a forest plot. Nevertheless, for studies with small (near 0) or large (near 1) prevalence, the inverse variance method was not stable and hence, we used Freeman Tukey arcsine methodology to address stabilizing variances as evidenced elsewhere [12, 16, 17]. Syphilis-HIV co-infection and the effect of selected predictor variables including marital status, previous history of multiple sexual partner, and previous history of STI on syphilis prevalence was analyzed using separate categories of meta-analysis.

The existence of publication bias was determined using funnel plot and Egger’s regression test. In Egger’s test, p < 0.05 was considered statistically significant [18]. The effect of each study on the overall pooled prevalence was determined by using sensitivity analysis. Sensitivity test eliminates each study step by step in the analysis to indicate the pooled effect sizes and related heterogeneity attributed by each individual study.

Result

Study selection

A comprehensive combined literature search generated a total of 936 possible articles, of which 20 were chosen sensibly for detailed full-text assessment and 13 studies were found to be appropriate for consideration in the meta-synthesis (Fig. 1).

Fig. 1
figure1

PRISMA flow chart for the studies screened, reviewed and included

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Characteristics of included studies

Among the 13 studies [19,20,21,22,23,24,25,26,27,28,29,30,31] included in the meta-analysis, a total of 17,656 pregnant women were screened for syphilis in three different regions of Ethiopia. Regional distribution of studies revealed that eight [19,20,21,22,23,24, 26, 29] from Amhara, two [25, 28] from Southern Nations Nationalities and Peoples (SNNP) and three [27, 30, 31] from Oromia region. In spite of that, there was no any study from other regions of Ethiopia fulfilling the inclusion criteria. Except a single prospective cohort study [27] which was conducted in Assela, Oromia region; all included records were cross-sectional studies with study participants ranging from 181 [31] to 4346 [30] and conducted from 2005 to 2019. Different diagnostic tests were employed for screening syphilis; six studies [19,20,21,22, 25, 31] used treponema pallidum hemagglutination assay (TPHA), three studies [24, 28, 29] used venereal diseases research laboratory (VDRL), two studies [26, 30] employed rapid plasma reagin (RPR) test, and one study [27] used syphilis rapid immunoassay, while the other one [23] used Immuno-chromatography test strips (ICS test). As per the established literature, the TPHA, syphilis rapid immunoassay and ICS test constitute the treponemal test while the VDRL and RPR are non-treponemal diagnostic tests [32].

Out of 17,656 pregnant women screened for syphilis, 416 were found positive. Out of 416 seropositive women, 172 were from SNNP, 183 were from Amhara, and 61 were from Oromia (Table 1).

Table 1 Summary characteristics of studies included in the meta-analysis
Full size table

Prevalence of syphilis among pregnant women

The pooled prevalence of syphilis among pregnant women in Ethiopia from the random effects model was 2.32% (95% CI, 1.68–2.97; I2 = 98.9%; Eggers test, p = 0.14). Subgroup analysis based on the diagnostic test employed indicated that 2.53% (95% CI, 1.92–3.14%) and 1.90% (95% CI, 0.40–3.40%) syphilis prevalence using treponemal and non-treponemal test, respectively (Fig. 2). As graphically demonstrated in the symmetrical funnel plot, there was no evidence of publication bias within included studies (Fig. 3). Moreover, this was also assured by Egger’s test (p = 0.14). In addition, the sensitivity analysis clearly indicated that the influence of individual studies on the summary effect estimate was not significant. Consequently, the pooled effect size estimate of syphilis among pregnant women in Ethiopia was steady and reliable when analyzed by omitting one study at a time (Table 2).

Fig. 2
figure2

Pooled prevalence estimate (ES) of syphilis among pregnant women in Ethiopia

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Fig. 3
figure3

Funnel plot, evaluating the existence of publication bias for pooled syphilis prevalence

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Table 2 Sensitivity analysis
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Syphilis prevalence in different regions of Ethiopia

The prevalence of syphilis based on the geographical regions of Ethiopia was 4.06% (95% CI, 2.86–5.26) in SNNP, 2.16% (95% CI, 1.57–2.75) in Amhara, and 1.46% (95% CI, 0.69–2.23) in Oromia region (Table 3).

Table 3 Summary estimate for syphilis prevalence in different regions of Ethiopia
Full size table

Pooled prevalence of syphilis-HIV co-infection among pregnant women

The overall pooled prevalence of syphilis-HIV co-infection among pregnant women in this meta-analysis was 0.80% (95% CI, 0.60–1.01; I2 = 95.2%) (Fig. 4).

Fig. 4
figure4

Pooled prevalence estimate (ES) of syphilis-HIV co-infection among pregnant women in Ethiopia

Full size image

Factors associated with syphilis sero-positivity

The association of syphilis sero-positivity with marital status, previous history of multiple sexual partner and previous history of STI was quantified using OR. The odds of having syphilis are almost three times higher in pregnant women who had history of multiple sexual partners than those who had no such partner, OR 2.98 (95% CI, 1.15–7.70). Pregnant women who had previous history of STI were more than four times more likely to develop syphilis than women who had no such history, OR 4.88 (95% CI, 1.35–17.62), whereas married women had 63% lower risk of having syphilis compared to those who are not cohabiting (single, widowed, divorced), OR 0.37 (95% CI, 0.12–0.91) (Table 4).

Table 4 Summary estimate of OR for syphilis sero-positivity associated factors
Full size table

Discussion

Syphilis is one of the easily preventable and treatable sexually transmitted infections but continued to exert a high burden worldwide especially in sub-Saharan Africa where resources are scarce. Therefore, prevention and control of syphilis among pregnant women using appropriate intervention measures is crucial for the emergence of syphilis free generation. For that, determining the actual burden of syphilis infection and antenatal care (ANC) follow-up screening plays a great role in early diagnosing and treatment of syphilis, and prevention of its vertical transmission. This study aimed to determine the updated pooled prevalence and factors associated to syphilis positivity, and the pooled syphilis-HIV co-infection among pregnant women in Ethiopia.

This meta-analysis showed that the overall pooled prevalence of syphilis among pregnant women in Ethiopia was 2.32% (95% CI, 1.68–2.97). The pooled prevalence was two times higher than the recent nationwide HIV/syphilis sentinel reports among ANC attendees in Ethiopia (1.1%) [33]. The variation in syphilis prevalence between this meta-analysis and the sentinel survey might be due to the rough estimate nature of the sentinel report that might underrepresent the actual burden of the diseases. Contrastingly, previous meta-analysis reported higher prevalence of syphilis among pregnant women in Ethiopia, 3.67% [9] relative to this study. This might be because of the previous meta-analysis includes studies with higher syphilis prevalence conducted in the pre-antiretroviral therapy availability. However, given the known synergy between HIV and syphilis [11], we have excluded studies conducted prior to HIV antiretroviral availability in this meta-analysis. Besides, the diseases dynamics may change overtime and impact the observed prevalence [34]. Partly, it may be due to the difference in the number of included studies (5 studies in earlier meta-analysis and 13 articles in this study), indicating the sample size may impact the prevalence.

On the other hand, the pooled prevalence in this meta-analysis was comparable with the report from a countrywide surveillance of HIV/syphilis prevalence among pregnant women attending ANC in Tanzania (2.5%) [35]. The similarity in syphilis prevalence in Ethiopia and Tanzania might be partly due to the WHO’s increased focus and prioritization of antenatal syphilis (in conjunction with HIV and hepatitis B virus) screening for better intervention measures. Besides, combination rapid HIV/syphilis tests are now used to a greater degree in ANC which may also result in increased syphilis testing/diagnoses in different countries of the world to indicate the actual picture of the diseases in various settings.

As shown in subgroup analysis, this study indicated relatively higher prevalence of syphilis using treponemal diagnostic test modality 2.53% (95% CI, 1.92–3.14%) compared to the non-treponemal test 1.90% (95% CI, 0.40–3.40%). This could be due to reactivity to a treponemal test implies infection but it does not determine whether the infection is recent or remote or whether it has been treated or not [32]. Thus, it suggests that treponemal tests stay positive for decades after treatment and may not always indicate active infection. On the other hand, non-treponemal tests have a high false-positive rate and are difficult to interpret on their own [32]. Therefore, considering the difficulty of syphilis diagnosis, the results have to be interpreted with care.

Regional analysis showed a higher and lower prevalence of syphilis in SNNP (4.06%) and in Oromia (1.46%) respectively. Higher syphilis prevalence in SNNP might be attributed to the risky socio-cultural practices such as polygamy is more practiced in SNNP [36] relative to other regions of Ethiopia. Partly, it might be due to the difference in the number of studies included in each category.

In addition, pooled estimate of syphilis-HIV co-infection was also assessed. Consequently, the overall pooled prevalence was 0.80% (95% CI, 0.60–1.01%). A comparable result (0.73%) was obtained from Republic of Congo [37]. While a study in Tanzania reported lower (0.3%) prevalence [35], another study from Rwanda indicated higher (1.2%) prevalence [38] of syphilis-HIV co-infection relative to the findings of this study. The difference in prevalence of syphilis-HIV co-infection might be attributed to the variation in level of implementation and integration of STI prevention and control measures in different countries.

Besides, the association between pregnant women with and without previous history of multiple sexual partner and syphilis sero-positivity was measured in this study. Accordingly, pregnant women with previous history of multiple sexual partners were 2.98 times more likely to get syphilis infection compared to women without such partner. This was consistent with previously established evidences [39,40,41,42] and could be attributed to the fact that people with multiple sexual partner has higher risk of getting STI including syphilis. This study also showed that pregnant women with previous history of STI were 4.88 times at higher risk of developing syphilis relative to pregnant women without such history. This is in line with the findings from Malawi [43] and China [44]; this could be partly due to lack of behavioral change and other prevention interventions that resulted in maintaining risky behaviors among women who had history of previous STI.

On the other hand, this meta-analysis also demonstrated that married women had 63% lower risk of developing syphilis compared to those who are not cohabiting (single, widowed, divorced). This was comparable with earlier studies conducted in rural Tanzania [45] and three sub-Saharan countries [46]. This might be due to the tendency of non-cohabiting women to practice high-risk sexual behaviors like having multiple sexual partners. Partly, this could be because of women in ANC are sexually active age groups, suggesting that if they are non-cohabiting they may have high-risk sexual behaviors.

Limitations

Given the difficulty of syphilis diagnosis, most of the included studies used treponemal diagnostic test alone which may impact the prevalence report. Some regions in the country were not represented in this study due to lack of established original studies in the area. Furthermore, all included studies were facility based. Thus, interpretation of findings has to be with due consideration of these limitations.

Conclusions

This review provides evidence of relatively high prevalence of syphilis among pregnant women. This study also assessed the burden of syphilis-HIV co-infection and determinants of syphilis sero-reactivity in Ethiopia. Therefore, it is recommended to further ramping up of current intervention measures, like routine screening of all ANC women and integration of syphilis testing and treatment to the already established HIV prevention program in the country. Further, nationwide studies involving all regions are needed to assess the magnitude and determinant factors for syphilis among pregnant women in Ethiopia.

Availability of data and materials

Any data related to this manuscript will be accessible by requesting the corresponding author.

Abbreviations

ANC:

Antenatal care

CI:

Confidence interval

HIV:

Human immunodeficiency virus

ICS test:

Immuno-chromatography test

OR:

Odds ratio

RPR:

Rapid plasma reagin

SNNP:

Southern Nations Nationalities and Peoples of Ethiopia

STI:

Sexually transmitted infection

TPHA:

Treponema pallidum hemagglutination assay

VDRL:

Venereal diseases research laboratory

References

  1. 1.

    Kojima N, Klausner JD. An update on the global epidemiology of syphilis. Curr Epidemiol Rep. 2018;5(1):24–38.

    PubMed  PubMed Central  Article  Google Scholar 

  2. 2.

    Khan S, Menezes GA, Dhodapkar R, Harish BN. Seroprevalence of syphilis in patients attending a tertiary care hospital in Southern India. Asian Pac J Trop Biomed. 2014;4(12):995–7.

    Article  Google Scholar 

  3. 3.

    Peeling RW, Hook EW III. The pathogenesis of syphilis: the Great Mimicker, revisited. J Pathol. 2006;208(2):224–32.

    CAS  PubMed  Article  Google Scholar 

  4. 4.

    Tiruneh M. Seroprevalence of multiple sexually transmitted infections among antenatal clinic attendees in Gondar Health Center Northwest Ethiopia. Ethiopian Med J. 2008;46(4):359–66.

    Google Scholar 

  5. 5.

    Organization WH. The global elimination of congenital syphilis: rationale and strategy for action. 2007.

    Google Scholar 

  6. 6.

    Gloyd S, Chai S, Mercer MA. Antenatal syphilis in sub-Saharan Africa: missed opportunities for mortality reduction. Health Policy Plan. 2001;16(1):29–34.

    CAS  PubMed  Article  Google Scholar 

  7. 7.

    Kuznik A, Habib AG, Manabe YC, Lamorde M. Estimating the public health burden associated with adverse pregnancy outcomes resulting from syphilis infection across 43 countries in sub-Saharan Africa. Sex Transm Dis. 2015;42(7):369.

    PubMed  PubMed Central  Article  Google Scholar 

  8. 8.

    Naeye R, Tafari N, Marboe C, Judge D. Causes of perinatal mortality in an African city. Bull World Health Organ. 1977;55(1):63.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Tesfaye B: Gestational syphilis in Ethiopia, meta-analysis and systemic review. In: 30th EPHA Annual Conference: 2019;2019.

  10. 10.

    Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097.

    PubMed  PubMed Central  Article  Google Scholar 

  11. 11.

    Kenyon CR, Osbak K, Chico RM. What underpins the decline in syphilis in Southern and Eastern Africa? An exploratory ecological analysis. Int J Infect Dis. 2014;29:54–61.

    PubMed  Article  Google Scholar 

  12. 12.

    Geremew D, Endalamaw A, Negash M, Eshetie S, Tessema B. The protective effect of isoniazid preventive therapy on tuberculosis incidence among HIV positive patients receiving ART in Ethiopian settings: a meta-analysis. BMC Infect Dis. 2019;19(1):1–9.

    Article  Google Scholar 

  13. 13.

    JB I. The Joanna Briggs Institute critical appraisal tools for use in JBI systematic reviews checklist for prevalence studies. North Adelaide: The Joanna Briggs Institute; 2017.

    Google Scholar 

  14. 14.

    Huedo-Medina TB, Sánchez-Meca J, Marín-Martínez F, Botella J. Assessing heterogeneity in meta-analysis: Q statistic or I2 index? Psychol Methods. 2006;11(2):193.

    PubMed  Article  PubMed Central  Google Scholar 

  15. 15.

    DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  16. 16.

    Fazel S, Khosla V, Doll H, Geddes J. The prevalence of mental disorders among the homeless in western countries: systematic review and meta-regression analysis. PLoS Med. 2008;5(12):e225.

    PubMed  PubMed Central  Article  Google Scholar 

  17. 17.

    Geremew D, Melku M, Endalamaw A, Woldu B, Fasil A, Negash M, Baynes HW, Geremew H, Teklu T, Deressa T. Tuberculosis and its association with CD4+ T cell count among adult HIV positive patients in Ethiopian settings: a systematic review and meta-analysis. BMC Infect Dis. 2020;20:1–10.

    Article  CAS  Google Scholar 

  18. 18.

    Sterne JA, Egger M, Smith GD. Investigating and dealing with publication and other biases in meta-analysis. BMJ (Clinical research ed). 2001;323(7304):101–5.

    CAS  Article  Google Scholar 

  19. 19.

    Assefa A. A three year retrospective study on seroprevalence of syphilis among pregnant women at Gondar University Teaching Hospital Ethiopia. Afr Health Sci. 2014;14(1):119–24.

    PubMed  PubMed Central  Article  Google Scholar 

  20. 20.

    Biadgo B, Hassen A, Getaneh M, Tesfa H, Jaleta KN, Eshetu T, Kasew D, Melku M. Syphilis and human immunodeficiency virus infections among pregnant women attending antenatal care clinic of Gondar family guidance association, Northwest Ethiopia: implication for prevention of mother to child transmission. Reprod Health. 2019;16(1):27.

    PubMed  PubMed Central  Article  Google Scholar 

  21. 21.

    Endris M, Deressa T, Belyhun Y, Moges F. Seroprevalence of syphilis and human immunodeficiency virus infections among pregnant women who attend the University of Gondar teaching hospital, Northwest Ethiopia: a cross sectional study. BMC Infect Dis. 2015;15:111.

    PubMed  PubMed Central  Article  Google Scholar 

  22. 22.

    Melku M, Kebede A, Addis Z. Magnitude of HIV and syphilis seroprevalence among pregnant women in Gondar, Northwest Ethiopia: a cross-sectional study. HIV/AIDS (Auckland, NZ). 2015;7:175–82.

    Google Scholar 

  23. 23.

    Tareke K, Munshea A, Nibret E. Seroprevalence of syphilis and its risk factors among pregnant women attending antenatal care at Felege Hiwot Referral Hospital, Bahir Dar, northwest Ethiopia: a cross-sectional study. BMC Res Notes. 2019;12(1):69.

    PubMed  PubMed Central  Article  Google Scholar 

  24. 24.

    YidegYitbarek G, Ayele BA. Prevalence of syphilis among pregnant women attending antenatal care clinic, Sede Muja District, South Gondar, Northwest Ethiopia. J Pregnancy. 2019;2019:1584527.

    Google Scholar 

  25. 25.

    Amsalu A, Ferede G, Assegu D. High seroprevalence of syphilis infection among pregnant women in Yiregalem hospital southern Ethiopia. BMC Infect Dis. 2018;18(1):109.

    PubMed  PubMed Central  Article  Google Scholar 

  26. 26.

    Mulu A, Kassu A, Tessema B, Yismaw G, Tiruneh M, Moges F, Wondmikun Y, Nishikawa T, Ota F. Seroprevalence of syphilis and HIV-1 during pregnancy in a teaching hospital in northwest Ethiopia. Jpn J Infect Dis. 2007;60(4):193.

    PubMed  Google Scholar 

  27. 27.

    Schönfeld A, Feldt T, Tufa TB, Orth HM, Fuchs A, Mesfun MG, Pfäfflin F, Nordmann T, Breuer M, Hampl M, et al. Prevalence and impact of sexually transmitted infections in pregnant women in central Ethiopia. Int J STD AIDS. 2017;0(0):1–8.

    Google Scholar 

  28. 28.

    Ageru TA, Abiso TL. Sero-prevalence of HIV and syphilis infection among pregnant mothers attended labor ward at Wolaita Sodo University Teaching Referral Hospital: a five-year retrospective study (2012–2016). Am J Health Res. 2018;6(3):67–73.

    Article  Google Scholar 

  29. 29.

    Zinabie S, Belachew E, Yidenek T, Lewetegn M, Asfaw T. Sero-prevalence of syphilis and HIV and associated factors in pregnant women attending antenatal care clinics in Debre Berhan Public Health Institutions, Ethiopia. Am J Biomed Life Sci. 2018;6(3):56–62.

    Article  Google Scholar 

  30. 30.

    Wubete M, Mohammed M, Mengistu M, Mekonnen R: Prevalence of syphilis among pregnant women attending antenatal clinic of Bulchana Health Center, Shashemene, West Arsi Zone, Ethiopia. Int J Med Biomed Stud. 2019;3(2). https://www.semanticscholar.org/paper/PREVALENCE-OF-SYPHILIS-AMONG-PREGNANT-WOMEN-CLINIC-Wubete-Mohammed/7115c1b8f8b4498198653a6776f9b4458c33c309.

  31. 31.

    Fikadu B, Gebrish S, Asfaw T. Sero-prevalence of syphilis among pregnant women attending Antenatal Care Clinic at Jimma Univeristy specialized Hospital, Ethiopia. J Med Medical Sci. 2019;10(1):1–5.

    Google Scholar 

  32. 32.

    Henao-Martínez AF, Johnson SC. Diagnostic tests for syphilis: new tests and new algorithms. Neurology. 2014;4(2):114–22.

    PubMed  PubMed Central  Google Scholar 

  33. 33.

    Ababa A: Report on the 2014 round antenatal care based sentinel HIV surveillance in Ethiopia. Ethiop Public Heal Instititute 2015. https://ephi.gov.et/wp-content/uploads/2014/09/2014roundANCbasedHIVsurveillancereport.pdf.

  34. 34.

    Korenromp EL, Mahiané SG, Nagelkerke N, Taylor MM, Williams R, Chico RM, Pretorius C, Abu-Raddad LJ, Rowley J. Syphilis prevalence trends in adult women in 132 countries–estimations using the spectrum sexually transmitted infections model. Sci Rep. 2018;8(1):1–10.

    CAS  Article  Google Scholar 

  35. 35.

    Manyahi J, Jullu BS, Abuya MI, Juma J, Ndayongeje J, Kilama B, Sambu V, Nondi J, Rabiel B, Somi G. Prevalence of HIV and syphilis infections among pregnant women attending antenatal clinics in Tanzania, 2011. BMC Public Health. 2015;15(1):501.

    PubMed  PubMed Central  Article  Google Scholar 

  36. 36.

    Tesfay GH. Note on: the adverse effects of polygamy on the rights of women: a case study in Gedeo and Sidama Zones. Haramaya Law Rev. 2017;6:91–110.

    Google Scholar 

  37. 37.

    Niama RF, Bongolo NCL, Kombo ESB, Yengo R, Mayengue PI, Kosso E-BM, Louzolo I, Macosso L, Dzeret G, Babeaux ASPD: Syphilis and HIV infections among pregnant women attending antenatal clinics in Republic of Congo. Pan Afr Med J 2017;28(1). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681004/.

  38. 38.

    Françoise N, Bosco MJ, Bellancille N, Théoneste N. HIV/AIDS and syphilis sero-prevalence among pregnant women attending antenatal care center in Rwanda. Am J Lab Med. 2020;5(4):83.

    Article  Google Scholar 

  39. 39.

    Yahya-Malima KI, Evjen-Olsen B, Matee MI, Fylkesnes K, Haarr L. HIV-1, HSV-2 and syphilis among pregnant women in a rural area of Tanzania: prevalence and risk factors. BMC Infect Dis. 2008;8(1):75.

    PubMed  PubMed Central  Article  Google Scholar 

  40. 40.

    Mutagoma M, Remera E, Sebuhoro D, Kanters S, Riedel DJ, Nsanzimana S: The prevalence of syphilis infection and its associated factors in the general population of Rwanda: a national household-based survey. J Sexually Transmitted Dis 2016;2016. https://www.hindawi.com/journals/jstd/2016/4980417/.

  41. 41.

    Macêdo VCd, Lira PICd, Frias PGd, Romaguera LMD, Caires SdFF, Ximenes RAdA. Risk factors for syphilis in women: case-control study. Rev Saude Publica. 2017;51:78.

    PubMed  PubMed Central  Google Scholar 

  42. 42.

    Sombie I, Meda N, Cartoux M, Tiendrebeogo S, Ouangre A, Yaro S, Ky-Zerbo O, Dao B, Van de Perre P, Mandelbrot L. Seroprevalence of syphilis among women attending urban antenatal clinics in Burkina Faso, 1995–8. Sexually Transm Infect. 2000;76(4):314–6.

    CAS  Article  Google Scholar 

  43. 43.

    Kwiek JJ, Mwapasa V, Alker AP, Muula AS, Misiri HE, Molyneux ME, Rogerson SJ, Behets FM, Meshnick SR. Socio-demographic characteristics associated with HIV and syphilis seroreactivity among pregnant women in Blantyre, Malawi, 2000–2004. Malawi Med J. 2008;20(3):80–5.

    PubMed  PubMed Central  Article  Google Scholar 

  44. 44.

    Zhou H, Chen XS, Hong FC, Pan P, Yang F, Cai YM, Yin YP, Peeling RW, Mabey D. Risk factors for syphilis infection among pregnant women: results of a case-control study in Shenzhen China. Sex Transm Infect. 2007;83(6):476–80.

    PubMed  PubMed Central  Article  Google Scholar 

  45. 45.

    Todd J, Munguti K, Grosskurth H, Mngara J, Changalucha J, Mayaud P, Mosha F, Gavyole A, Mabey D, Hayes R. Risk factors for active syphilis and TPHA seroconversion in a rural African population. Sexually Transm Infect. 2001;77(1):37–45.

    CAS  Article  Google Scholar 

  46. 46.

    Potter D, Goldenberg RL, Read JS, Wang J, Hoffman IF, Saathoff E, Kafulafula G, Aboud S, Martinson FE, Dahab M. Correlates of syphilis seroreactivity among pregnant women: the HIVNET 024 Trial in Malawi, Tanzania, and Zambia. Sex Transm Dis. 2006;33(10):604.

    PubMed  PubMed Central  Article  Google Scholar 

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Acknowledgements

We thank the authors of individual studies included in this meta-analysis.

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Author information

Affiliations

  1. Department of Public Health, College of Health Sciences, Debre Markos University, Debre Markos, Ethiopia

    Habtamu Geremew

  2. Department of Immunology and Molecular Biology, School of Biomedical and Laboratory Sciences, University of Gondar, P.o.Box: 196, Gondar, Ethiopia

    Demeke Geremew

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  1. Habtamu Geremew
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  2. Demeke Geremew
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Contributions

HG and DG: Conceived and designed the study, reviewed literatures, extracted and analyzed data, interpreted results, and drafted the manuscript. Both authors have read and approved the final manuscript.

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Correspondence to Demeke Geremew.

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Geremew, H., Geremew, D. Sero-prevalence of syphilis and associated factors among pregnant women in Ethiopia: a systematic review and meta-analysis. Syst Rev 10, 223 (2021). https://doi.org/10.1186/s13643-021-01786-3

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Keywords

  • Syphilis
  • Aero-prevalence
  • Pregnant women
  • Meta-analysis
  • Ethiopia

Systematic Reviews

ISSN: 2046-4053