Literature DB >> 36006594

The Case for Early and Universal Screening for Gestational Diabetes Mellitus: Findings from 9314 Pregnant Women in a Major City in Nigeria.

Rosemary Ogu1,2, Omosivie Maduka3,4, Vetty Agala5,2, Precious Obuah6, Faithwin Horsfall7,2, Esther Azi8,2, Cecilia Nwibubasa9,2, Ufuoma Edewor5,2, Ibimonye Porbeni10,2, Osita John1, Ngozi Orazulike1,2, Dango Kalio7, Kenneth Okagua7, Clement Edet8,9, Agiriye Harry8,9, Henry Ugboma1, Claribel Abam2.   

Abstract

INTRODUCTION: Risk-based screening has been replaced by universal screening as the recommended course of care for gestational diabetes mellitus (GDM). As of 2016, no state in Nigeria had implemented a policy of universal screening for GDM. This research aimed to assess findings from a universal screening programme and its implication for scaling up universal and early screening for GDM.
METHODS: This was a descriptive cross-sectional study conducted in Rivers State Nigeria between February 2017 and January 2020. Multistage sampling was used to recruit 9314 pregnant women from 30 primary, secondary, and tertiary health facilities in the state. An interviewer-administered structured questionnaire was used by trained healthcare workers to collect socio-demographic, obstetric and medical information. All study participants had a plasma glucose test on their first hospital visit and a diagnosis made using the World Health Organization (WHO) criteria. Data obtained was analysed using the IBM Statistical Package for Social Sciences (SPSS) version 23.
RESULTS: Most women [5683 (61.0%)] were aged 25-34 (mean 29.60 ± 5.64) years. The prevalence of GDM in this study was 5.2% with a prevalence of GDM in the first, second and third trimesters of 4.9%, 4.2% and 6.7%, respectively. The prevalence of GDM among persons with a family history of diabetes was 13.2% (97 persons) while 4.6% (391 persons) without family history were diagnosed with GDM. Gestational age, family history of diabetes and age group were found to be significant predictors of GDM among the study participants after adjusting for confounding variables.
CONCLUSION: The practice of universal screening was useful in identifying GDM in 1 out of 20 pregnant women in the study sample. Screening at all trimesters was useful in identifying GDM. There is an urgent need to scale up early and universal screening for GDM across sub-Saharan Africa.
© 2022. The Author(s).

Entities:  

Keywords:  Gestational diabetes mellitus; Pregnancy; Universal screening

Year:  2022        PMID: 36006594      PMCID: PMC9500119          DOI: 10.1007/s13300-022-01307-y

Source DB:  PubMed          Journal:  Diabetes Ther        ISSN: 1869-6961            Impact factor:   3.595


Key Summary Points

Introduction

The prevalence of gestational diabetes mellitus (GDM) in pregnancy has steadily increased parallel to the increase in the prevalence of overweight, obesity and type II diabetes mellitus among women [1]. GDM poses a threat to the health and safety of mothers and children with negative outcomes such as macrosomia, unexplained foetal deaths in offspring and risk of type II diabetes in mothers [2]. Adequate diagnosis and management of hyperglycaemia are, therefore, necessary to prevent and control these untoward outcomes [3]. Early detection of GDM is expected to lead to early management and subsequently result in better pregnancy outcomes [4, 5]. A risk-based screening had been the traditional approach to identifying GDM. It entails a review of risk factors like overweight or obesity, family history of diabetes, previous obstetric history of big babies, a previous incident of hyperglycaemia in pregnancy or a previous history of poor obstetric outcomes [2-5]. The main argument for risk-based screening is that subjecting all pregnant women to screening for hyperglycaemia is not cost-effective. Unfortunately, the challenge with risk-based screening is its low sensitivity for the detection of GDM. This means that many cases of GDM and hyperglycaemia in pregnancy go undetected with continued negative consequences for mother and baby [4, 6–10]. Risk-based screening has long been replaced by universal screening as the recommended course of care by the International Federation of Gynaecology and Obstetrics (FIGO), International Diabetes Federation (IDF) and the World Health Organization (WHO) strongly recommend universal screening. The international recommendations also state that screening should occur during the first encounter between a pregnant woman and the antenatal clinic [8, 9]. Unfortunately, as of 2016, no state in Nigeria was implementing a policy of universal screening for GDM even though this has been recognized as best practice since 2013. In addition, risk-based screening is routinely practised at 28 weeks of gestation in Nigeria [10, 11]. The Medical Women’s Association of Nigeria (MWAN) is a non-governmental organization and professional body of female medical and dental doctors with a focus on improving health outcomes for women and children. In 2016, MWAN Rivers obtained support from the World Diabetes Foundation (WDF) to pilot access and advocacy interventions for the control of gestational diabetes mellitus (GDM) in Rivers State, Niger Delta Region of Nigeria. One of these interventions is the implementation of universal screening for GDM. This research aimed to assess findings from the project’s universal screening programme and its implication for scaling up universal and early screening for hyperglycaemia across the country and the rest of sub-Saharan Africa.

Methods

Study Design

The study was a descriptive cross-sectional survey.

Study Area and Study Sites

This study was carried out in Rivers State Nigeria. Rivers State is in the oil-rich zone of Nigeria, called the Niger Delta Region. The study was carried out in health facilities across the primary, secondary and tertiary levels of health administration in all senatorial districts of the state.

Study Population

The study recruited all pregnant women who were receiving antenatal care from the selected health facilities in Rivers State, Niger Delta Region, from February 2017 to January 2020. During this period a total of 9314 women with completed data entry forms were studied.

Sampling Technique

Sampling was done using a multi-stage technique. The first stage (stratified sampling) involved selecting one local government area (LGA) per senatorial district via a simple random sampling method from the listing of the LGAs in each senatorial district in the state. Two LGAs (Obio-Akpor and Port Harcourt LGA) were then purposively included in the sample because they make up the capital city of Rivers State and host the two tertiary institutions in the state. The second stage involved selecting health facilities from the primary and secondary levels via simple random sampling. This was done using the list of health facilities (both private and public) obtained from the Rivers State Primary Healthcare Management Board and the Rivers State Hospitals Management Board as the sampling frame. A total of 28 primary and secondary health facilities and the two tertiary health facilities in the state were included in the study. The final stage involved recruiting all women attending antenatal clinics (ANC) in the selected facilities.

Study Instrument and Data Collection

An interviewer-administered structured questionnaire was used by trained healthcare workers to collect information from the women attending ANC. This questionnaire was in both paper and Open Data Kit (ODK) format and addressed socio-demographic characteristics such as age, education and marital status; obstetric and medical history included trimester, parity, history of diabetes and history of hypertension. Monitoring and evaluation were periodically carried out with twice-monthly site visits and monthly data collection, analysis and review.

Screening Protocol

All pregnant women visiting the selected facilities were screened on their first hospital visit. Those with normal results were re-screened at the 24th–28th weeks of pregnancy. Screening of blood glucose was done via capillary blood with the Accu-Check Active (Model: GB) Roche Glucometer. All measurements of blood glucose were done in mmol/l. At least five health workers per facility (laboratory technologists, nurses, and medical doctors) were trained on data collection and use of glucometers for screening. A pregnant woman was determined to have a positive screening test for GDM if the fasting plasma glucose was ≥ 5.1 mmol/l or if the random plasma glucose was ≥ 8.5 mmol/l in line with WHO criteria. Anyone with a positive screening test had venous blood collected for laboratory confirmation [12, 13].

Data Analysis

The data collected were entered into Microsoft Excel Worksheet 2016 version and were analysed using the IBM Statistical Package for Social Sciences (SPSS) version 23. All descriptive statistics were reported as frequency and proportions for categorical variables and as means with standard deviations for continuous variables. Chi-square test of association and logistic regression were carried out to determine associations and predictors of GDM. The results were presented as odds ratio (95% confidence interval). The level of significance (α) set at 0.05; p value < 0.05 was statistically significant.

Ethical Considerations

Ethical approval was obtained from the University of Port Harcourt Teaching Hospital (ADM/90S.II/VOLXI/396) while permission to conduct the study was obtained from all the contributing institutions, the Rivers State Primary Health Care Management Board, Rivers State Hospitals Management Board, the University of Port Harcourt Teaching Hospital (UPTH) and the Rivers State University Teaching Hospital. All participants were informed of the benefits and risks of the study. They were assured of voluntary withdrawal from the study, confidentiality and anonymity of their data. Written informed consent to participate was obtained from all study participants and the study was conducted in accordance with the Declaration of Helsinki.

Results

The most represented age bracket was the age category 25–34 years with 5683 (61.0%) participants. The mean age of participants was 29.60 ± 5.64 years. Married women constituted 8743 (93.9%) of the sample while 5370 (57.7%) participants had secondary school education (Table 1). Among the participants, 5048 (54.5%) had one to two children, while 2037 (22.0%) had at least three. Most study participants were screened during the second (4576, 49.1%) and third trimester (3518, 37.8%), respectively (Table 1). Only 1.3% of study participants had type 2 diabetes, while 7.9% had a family history of diabetes and 9.9% had a family history of hypertension (Table 2).
Table 1

Socio-demographic and obstetric characteristics

VariablesFrequency (n = 9314)Per cent (%)
Age in years
 15–24182719.6
 25–34568361.0
 35–44173318.6
 ≥ 45710.8
 Mean age29.60 ± 5.64 years
Marital status
 Single5135.5
 Married874393.8
 Divorced/separated430.5
 Widow150.2
Educational status
 No formal education1571.7
 Primary5315.7
 Secondary537057.6
 Tertiary325635.0
Parity
 0222923.9
 1–2504854.2
 ≥ 3203721.9
Gestational age
 First trimester122013.1
 Second trimester457649.1
 Third trimester351837.8
Table 2

Past medical and family history of study participants

VariablesFrequency (n)Per cent (%)
Diabetes status (n = 9314)
 Diabetic1191.3
 Not diabetic919598.7
Family history of diabetes (n = 9314)
 Yes7337.9
 No858192.1
Diabetic close relative (n = 733)
 Father37751.4
 Mother33145.2
 Sibling253.4
Known hypertensive (n = 9314)
 Yes1601.7
 No915498.3
Family history of hypertension (n = 9314)
 Yes92910.0
 No838590.0
Relative with hypertension (n = 929)
 Father34537.1
 Mother56260.5
 Sibling222.4
Socio-demographic and obstetric characteristics Past medical and family history of study participants The prevalence of GDM in this study was 5.2%. Almost half of the study participants were screened during the second trimester [4382 (47.1%)], while the first trimester had the lowest number of participants screened (1160, 12.5%). The prevalence of GDM was highest among participants screened in the third trimester (234, 6.7%) and lowest among those screened in the second trimester (194, 4.2%). The prevalence of GDM among persons with a family history of diabetes was 13.2% (97 persons) while 4.6% (391 persons) were diagnosed with GDM despite a negative family history of diabetes (Table 3).
Table 3

Stage of pregnancy, family history of diabetes and GDM prevalence GDM status (n = 9314)

VariableNormal (%)GDM positive (%)Total
Trimester (weeks)
 First trimester (0–13)1160 (95.1)60 (4.9)1220 (100.0)
 Second trimester (14–26)4382 (95.8)194 (4.2)4576 (100.0)
 Third trimester (27–40)3284 (93.3)234 (6.7)3518 (100.0)
Family history of diabetes
 Yes636 (86.8)97 (13.2)733 (100.0)
 No8190 (95.4)391 (4.6)8581 (100.0)
Total8826 (94.8)488 (5.2)9314 (100.0)
Stage of pregnancy, family history of diabetes and GDM prevalence GDM status (n = 9314) There was a significantly higher proportion of persons with GDM who had tertiary education compared with persons without GDM (x2 = 15.64; p = 0.001), a significantly higher proportion of persons with GDM in the third trimester of pregnancy compared to persons in other trimesters (x2 = 23.60; p < 0.001) and a significantly higher proportion of persons with a positive family history of diabetes among those with GDM compared to those without (x2 = 102.40; p < 0.001) (Table 4). Gestational age, family history of diabetes and age group were found to be significant predictors of GDM (p < 0.001) among the study participants after adjusting for confounding variables (Table 5).
Table 4

Association among socio-demographics, family history, gestational age and prevalence of GDM among study participants

Normal (%)GDM (%)Chi-square (p value)
Age group (years)
 15–241751 (19.8)76 (15.6)14.7 (0.002)*
 25–345395 (61.1)288 (59.0)
 35–441615 (18.3)118 (24.2)
 ≥ 4565 (0.7)6 (1.2)
Education
 No formal147 (1.7)10 (2.0)15.64 (0.001)*
 Primary503 (5.7)28 (5.7)
 Secondary5129 (58.1)241 (49.4)
 Tertiary3047 (34.5)209 (42.8)
Marital status
 Single486 (5.5)27 (5.5)2.0 (0.57)
 Married8286 (93.9)457 (93.6)
 Separated41 (0.5)2 (0.4)
 Divorced13 (0.1)2 (0.4)
Gestational age
 1st trimester1160 (13.1)60 (12.3)23.60 (< 0.001)*
 2nd trimester4382 (49.6)194 (39.8)
 3rd trimester3284 (37.2)234 (48.0)
Family history of diabetes
 Yes636 (7.2)97 (19.9)102.40 (< 0.001)*
 No8190 (92.8)391 (80.1)

*p < 0.05

Table 5

Predictors of GDM among study participants

VariableCOR (95% CI)p valueAOR (95% CI)p value
Family history of DM
 Yes3.2 (2.5–4.0) < 0.0013.14 (2.50–4.00) < 0.001*
 No (reference)
Age group (years)
 15–34 years1.45 (1.18–1.80)0.0011.35 (1.10–1.70)0.006*
 35 years and above (reference)
Marital status
 Not married0.96 (0.66–1.40)0.830.88 (0.60–1.29)0.52
 Married (reference)
Education
 Secondary/tertiary1.06 (0.76–1.50)0.731.18 (0.84–1.67)0.35
 None/primary (reference)
Trimester at screening
 First and second trimester1.56 (1.30–1.87) < 0.0011.54 (1.28–1.85) < 0.001*
 Third trimester
(Reference)

COR crude odds ratio, AOR adjusted odds ratio

*Significant associations

Association among socio-demographics, family history, gestational age and prevalence of GDM among study participants *p < 0.05 Predictors of GDM among study participants COR crude odds ratio, AOR adjusted odds ratio *Significant associations

Discussion

The major findings from this project revealed that 1 in 20 women had GDM, GDM was prevalent in all trimesters of pregnancy, and women with a positive family history of diabetes were three times more likely to develop GDM. This study also found that screening women before 20 weeks of gestation and screening persons without positive family history provided a good yield of persons with GDM. While a 2001 study in a tertiary institution in the south-south of Nigeria recorded a GDM prevalence of 0.3% [14], a recent systematic review and meta-analysis of GDM studies in Nigeria carried out between 2008 and 2019 demonstrated a prevalence ranging between 0.7 and 35.6% with a pooled prevalence of 11.0% for the country and 5.5% in the south-south [15]. Even studies in the same geographical region have taken a wide range of values depending on the study design, diagnostic criteria used and the time of the study [10, 16–18]. What is clear however is that there has been a steady increase in the prevalence of gestational diabetes. This increase has been attributed to increased exposure to risk factors, better diagnostic tools and better screening policies [15, 19]. This underscores the need for strategic, universally acceptable interventions for prevention, early detection and treatment of GDM [20]. Our intervention, which models the WHO and FIGO recommendations for universal screening, provided such interventions [21]. It is common knowledge that the risk of GDM is higher among persons with a family history of diabetes. Our study corroborates this by determining a three-fold increase in the risk of GDM among those with a family history of diabetes compared to those without. However, the prevalence of GDM among persons without a family history of diabetes was close to the study population prevalence. If risk-based screening had been employed almost 1 in 20 persons found to have GDM may have been missed. This finding negates the risk-based screening strategy still employed in Nigeria even in the light of the evidence and international guidelines that favour universal screening [6, 10, 13]. Guidelines indicate 24–28 weeks of gestation as the recommended time to screen for GDM [15]. Our study found the highest yield of GDM prevalence to be in the third trimester of pregnancy. However, we also found significant yield in the first and second trimesters, respectively. This supports the philosophy of early screening. Screening pregnant women at first contact with repeat screening during the second or third trimester ensures that no one with GDM is missed [22]. The strengths of this study lie in its large sample size and a robust collection of data from 30 health care facilities across primary, secondary and tertiary levels over 3 years. The study is, however, limited to one state in the country and using capillary plasma glucose as a screening tool. Though the sensitivity of plasma glucose is lower than that of venous blood glucose, the international consensus is that it is acceptable in resource-poor settings as first screening and even diagnosis [13, 23].

Conclusion

The practice of universal screening was useful in identifying GDM in 1 out of 20 pregnant women in the study sample. Screening at all trimesters was useful in identifying GDM. There is a need to scale up early and universal screening for GDM across sub-Saharan Africa.
As of 2016, no state in Nigeria was implementing a policy of universal screening for gestational diabetes mellitus (GDM) despite the international guidelines for universal screening for GDM
This research assessed findings from a universal screening programme and its implication for scaling up universal and early screening for GDM
The practice of universal screening was useful in identifying GDM in 1 out of 20 pregnant women in the study sample
Universal screening identified GDM at all trimesters of pregnancy and among women without any family history of diabetes mellitus among the study sample
Risk-based screening would have missed many women with GDM, underscoring the need to scale up early and universal screening for GDM across sub-Saharan Africa
  14 in total

1.  Effect of treatment of gestational diabetes mellitus on pregnancy outcomes.

Authors:  Caroline A Crowther; Janet E Hiller; John R Moss; Andrew J McPhee; William S Jeffries; Jeffrey S Robinson
Journal:  N Engl J Med       Date:  2005-06-12       Impact factor: 91.245

2.  Gestational diabetes mellitus manifests in all trimesters of pregnancy.

Authors:  V Seshiah; V Balaji; Madhuri S Balaji; A Paneerselvam; T Arthi; M Thamizharasi; Manjula Datta
Journal:  Diabetes Res Clin Pract       Date:  2007-02-09       Impact factor: 5.602

Review 3.  Gestational Diabetes Mellitus:current knowledge and unmet needs.

Authors:  Sarah H Koning; Klaas Hoogenberg; Helen L Lutgers; Paul P van den Berg; Bruce H R Wolffenbuttel
Journal:  J Diabetes       Date:  2016-07-28       Impact factor: 4.006

4.  High prevalence of type 2 diabetes and pre-diabetes in adult offspring of women with gestational diabetes mellitus or type 1 diabetes: the role of intrauterine hyperglycemia.

Authors:  Tine D Clausen; Elisabeth R Mathiesen; Torben Hansen; Oluf Pedersen; Dorte M Jensen; Jeannet Lauenborg; Peter Damm
Journal:  Diabetes Care       Date:  2007-11-13       Impact factor: 19.112

5.  Gestational diabetes mellitus.

Authors:  Amanda Bird Hoffert Gilmartin; Serdar H Ural; John T Repke
Journal:  Rev Obstet Gynecol       Date:  2008

6.  Strategies for implementing the WHO diagnostic criteria and classification of hyperglycaemia first detected in pregnancy.

Authors:  Stephen Colagiuri; Maicon Falavigna; Mukesh M Agarwal; Michel Boulvain; Edward Coetzee; Moshe Hod; Sara J Meltzer; Boyd Metzger; Yasue Omori; Ingvars Rasa; Maria Inês Schmidt; Veerasamy Seshiah; David Simmons; Eugene Sobngwi; Maria Regina Torloni; Hui-xia Yang
Journal:  Diabetes Res Clin Pract       Date:  2014-02-25       Impact factor: 5.602

7.  Point: Universal screening for gestational diabetes mellitus.

Authors:  Robert G Moses; N Wah Cheung
Journal:  Diabetes Care       Date:  2009-07       Impact factor: 17.152

8.  Comparison of screening for gestational diabetes mellitus by oral glucose tolerance tests done in the non-fasting (random) and fasting states.

Authors:  Viswanathan Mohan; Manni Mohanraj Mahalakshmi; Balaji Bhavadharini; Kumar Maheswari; Gunasekaran Kalaiyarasi; Ranjit Mohan Anjana; Ram Uma; Sriram Usha; Mohan Deepa; Ranjit Unnikrishnan; Sonak D Pastakia; Belma Malanda; Anne Belton; Arivudainambi Kayal
Journal:  Acta Diabetol       Date:  2014-10-15       Impact factor: 4.280

9.  A systematic review and meta-analysis of the prevalence and determinants of gestational diabetes mellitus in Nigeria.

Authors:  Taoreed Adegoke Azeez; Tamunosaki Abo-Briggs; Ayodeji Sylvester Adeyanju
Journal:  Indian J Endocrinol Metab       Date:  2021-10-26

Review 10.  The urgent need for universally applicable simple screening procedures and diagnostic criteria for gestational diabetes mellitus--lessons from projects funded by the World Diabetes Foundation.

Authors:  Karoline Kragelund Nielsen; Maximilian de Courten; Anil Kapur
Journal:  Glob Health Action       Date:  2012-07-30       Impact factor: 2.640

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