Abstract
Background
We piloted a randomised controlled trial (RCT) comparing pregnancy outcomes among women with booking gestational diabetes (GDM) receiving immediate or deferred treatment.
Methods
Consecutive, consenting women < 20 weeks gestation, with GDM risk factors attending the hospital book-in clinic, completed an oral glucose tolerance test (OGTT). Clinicians were blinded to OGTT results. Women fulfilling World Health Organisation GDM criteria were randomised to either clinic referral /ongoing treatment (Treated Group n = 11), or no treatment (No Treatment Group n = 10). Women without ‘Booking GDM’ (‘Decoys’ n = 58) and those in the No Treatment Group had a repeat OGTT at 24–28 weeks (with GDM treated if diagnosed). Midwives and mothers were asked to complete surveys and attend focus groups before and after the study respectively regarding their experiences and expectations of the study protocol.
Results
Sufficient women completed each step of the RCT. Gestation at OGTT was late at 18 ± 2 weeks with Treated and No Treatment groups largely similar. At 24–28 weeks gestation, GDM was present in 8/9 (89%) in the No Treatment group and 11/56 (20%) Decoys. NICU admission was highest in the Treated group (36% vs 0% p = 0.043), largely due to small for gestational age, and Large for Gestational Age babies greatest in the No Treatment group (0% vs 33% p = 0.030).
Conclusion
An RCT deferring ‘Booking GDM’ treatment is feasible. Most women with untreated ‘Booking GDM’ in mid 2nd trimester had GDM at 24–28 weeks. Early treatment may have both benefits and harms. A full RCT is needed.
Trial registration
Australia New Zealand Clinical Trials Registry ACTRN12615000974505. Registered 17th May 2015; URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=369100&isReview=true Retrospectively Registered.
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Find the latest articles, discoveries, and news in related topics.Background
Gestational diabetes mellitus (GDM) increases the risk of obstetric and neonatal complications, with future risks to mother and baby [1,2,3]. Two randomised controlled trials (RCTs) of GDM management from 24 to 28 weeks gestation, among women without pre-existing diabetes, showed significant reductions in the risk of both macrosomia and pre-eclampsia/Pregnancy Induced Hypertension [4, 5].
It has been recommended that women with possible undiagnosed diabetes are identified early in pregnancy and treated [6, 7]. However, during the screening process, a significant proportion of women are identified as below the biochemical criteria for ‘Diabetes in Pregnancy’, yet fulfilling criteria for GDM at 24–28 weeks gestation. Fasting glucose can be higher at the beginning of pregnancy [8], with one Chinese study reporting that many women with ‘early GDM’ did not have GDM when the oral glucose tolerance test (OGTT) was repeated at 24–28 weeks [8]. This has led to calls not to use the 24–28 week GDM criteria earlier in pregnancy [9]. However, this has left a void, with no recommendations on the next management steps for women with lesser degrees of hyperglycaemia early in pregnancy.
The Treatment of BOoking Gestational diabetes Mellitus (ToBOGM) Study is a randomised controlled trial (RCT) developed to test whether women with ‘hyperglycaemia’ at booking (Booking GDM), should be treated to avoid GDM complications, or whether earlier treatment increases other pregnancy complications. We now report on the findings of the ToBOGM pilot RCT investigating recruitment, proportion with ‘GDM’ at booking, blinding procedures, uptake of heel-prick glucose and outcome measures to facilitate power calculations.
Methods
The primary aim of this pilot study was to test the protocol for a larger scale RCT of either immediate or deferred treatment for Booking GDM. Clinic midwives at the Campbelltown Hospital Book-in clinic (i.e. first antenatal clinic attendance) assessed the need of all pregnant women for early testing for Diabetes in Pregnancy, based upon GDM Risk factors [10]. Women are referred for a 75 g, 3 point, 2 h oral glucose tolerance test (OGTT) as per local policy. Between July 20th 2015 and April 7th 2016, consecutive pregnant women at 4 to 19 + 6 weeks gestation, with a singleton pregnancy, aged ≥18 years and referred for an OGTT were invited to participate. Exclusions were inability to understand English, or a presence of a major active medical disorder. Consenting women completed questionnaires at baseline, 24–28 and 34–38 weeks and attended a study OGTT appointment. Other data were extracted from the clinical notes.
OGTT results were sent to one investigator (DS). Women with Diabetes In Pregnancy (fasting ≥7.0 and/or 2 h ≥ 11.1 mmol/l) were referred immediately to the clinic for treatment. Women below the 24–28 week GDM [4] criteria (fasting ≥5.1 and/or 1 h ≥ 10.0 mmol/l and/or 2 h ≥ 8.5 mmol/l), were advised that they did not require referral to the clinic (‘decoys’). Such decoys blinded the obstetric team as to whether women involved in ToBOGM were controls or women without ‘hyperglycaemia’. Women fulfilling criteria for GDM were randomised to either referral to the clinic (Treated) or were advised (using identical letters to the ‘decoys’) that they did not require referral to the clinic (No Treatment). The participant, as well as midwifery, obstetric, diabetes clinic, and research staff were kept blinded to all numeric results and only knew if a woman had been referred for GDM treatment. Randomisation to either immediate or deferred treatment was undertaken using an electronic randomiser (SPSS Version 22.0, IBM, USA), stratified as either low risk (fasting 5.1–5.2 mmol/l, 1 h 10–10.5 mmol/l and /or 2 h 8.5–8.9 mmol/l) or high risk (based upon the IADPSG 2 fold excess risk of adverse outcomes at 24–28 weeks gestation [6]: fasting 5.3–6.9 mmol/l, 1 h ≥ 10.6 mmol/l and /or 2 h 9.0–11.0 mmol/l).
All women receiving treatment for GDM received group education, were taught to self-monitor blood glucose and saw a dietitian. Fasting and 2 h post-prandial glucose targets were < 5.3 mmol/l and < 6.8 mmol/l respectively [5]. Where glucose thresholds were exceeded on more than two occasions with no obvious cause, women were offered medication (metformin or insulin treatment). Only women not referred to clinic attended a 24–28 week OGTT, and were referred for treatment if GDM was diagnosed.
All women were asked for their baby to provide a heel prick glucose 1–2 h after birth. Venous umbilical cord blood was drawn into EDTA tubes for assessing a range of metabolites and assessing the adipo-insular axis. Glucose, triglyceride and 3-beta hydroxy butyrate were measured in a single International Organization for Standardization accredited laboratory. Plasma insulin and C-peptide levels were measured using a sandwich chemiluminescence immunoassay (Liaison XL, Diasorin, Saluggia, Italy). Leptin and adiponectin measurements were determined using a radioimmunoassay kit (Merck Millipore, Darmstadt Germany).
Qualitative assessment
Midwives at Campbelltown Hospital completed a survey prior to the pilot study commencing. An additional one hour focus group was conducted with a group of midwives (n = 6) at the conclusion of the pilot study, to examine their experience of taking part in the RCT. A survey was also completed by mothers who were booked into the clinic at Campbelltown Hospital for antenatal care. A group of mothers (n = 4) also took part in a focus group at the conclusion of the pilot study. The midwife and the mothers’ surveys both contained demographic questions, closed ended questions about knowledge of GDM and open ended questions about expectations and experiences of the pilot study protocol. In the focus groups, the midwives and mothers were asked about their expectations and experiences of GDM and the study protocol. The focus groups were audio recorded and transcribed verbatim. Focus group transcripts and open ended interviews were analysed using thematic analysis [11]. This involved reading through the qualitative data, developing a coding frame based on commonality of responses across participants, leading to identification of themes that captured expectations and experiences of GDM and involvement in the study. The themes included acceptability, unacceptability, concerns, absence of concerns, and importance of mothers consent.
Statistics
As a pilot, limited by funding, a target was set to randomise 20 women with GDM at booking, with an expectation, based upon a prior study [12], that 100 women would need to be consented to meet this target. Mean and standard deviations are reported for continuous variables, and number and percentages are reported for categorical variables. Geometric mean is used for non-normally distributed biochemical measurements [13]. All tests are 2 tailed. Analyses were undertaken using SPSS Version 22.0 (IBM, USA) with proportions compared using Chi squared test and continuous variables compared using Analysis of Variance. The study was approved by the South Western Sydney Local Health District Ethics committee (reference 15/LPOOL/14).
Results
Figure 1 includes the numbers invited (607), consented (100), and randomised (22). One woman randomised to No Treatment decided to withdraw from the trial and was referred to the GDM clinic and treated. Of the 128 eligible women, 100 (78.1%) consented and 79 (61.7%) entered the study. The randomisation process was adhered to, 88% of babies had the heel prick test and other outcomes were available for 96% of women/babies.
Table 1 compares the Treated and No Treatment groups, and ‘any booking GDM’ with the decoys. Compared with decoys, women with booking GDM had higher baseline BMI, serum insulin, leptin and 3 beta hydroxyl butyrate concentrations and lower adiponectin levels. At baseline, 4/21 (19%) with booking GDM, were diagnosed at the low and 17/21 (81%) at the higher glycaemic stratum; 17/21 (81%) had an elevated fasting glucose level with or without a higher post load glucose. Treated women had a higher systolic blood pressure than No Treatment women at baseline. Among the remaining women randomised to No Treatment, 8/9 (89%) had GDM on the 24–28 week OGTT while 11/56 (19.6%) had developed GDM in the decoy group. There were no differences between the Treated and No Treatment group for gestational age at delivery. Babies of women in the No Treatment group were more likely to have a large for gestational age (LGA) baby (p = 0.03), but babies of women in the Treated group were more likely to be admitted to NICU (p = 0.043: three small gestational age (SGA), one of whom was < 37 weeks). The only stillbirth was in the No Treatment group with placental abruption (not considered to be due to delayed treatment). Compared with women with booking GDM, decoys had more gestational weight gain (p = 0.001) and were less likely to be induced (p = 0.001).
The characteristics of midwives and women participating in the survey and focus groups are shown in Additional file 1: Table S1 and Additional file 2: Table S2. Of the women, one was a participant in the pilot study, one was currently pregnant but did not have GDM, one had recently had a baby and did not have GDM, and one had GDM in a previous pregnancy. All were familiar with the OGTT testing in pregnancy. Tables 2 and 3 describe the qualitative responses of midwives and antenatal women respectively from the open ended survey questions and focus groups. Overall, the midwives’ and the mothers responded positively to the study procedures. Respondents gave feedback on the importance of informed consent throughout all stages of the study. Most women reported preferring face-to-face initial contact. There were some concerns around the ethics of delaying treatment. The heelprick glucose was widely accepted. In the focus group, the midwives talked about the need to have a researcher dedicated to the study in the clinic, so that the study did not impact on their workload.
Discussion
We have shown that our study protocol was feasible, requiring few changes. Randomisation and each step of the protocol were implemented with no significant problems. Both the mothers interviewed and the midwives were generally positive about the procedures, although there was some concern over the delay in treatment for women allocated to the No Treatment condition. In spite of this, most eligible women consented to the RCT and were able to enter the study.
Our overall capture rate for the heel prick was over 80%, higher than the 71.25% in HAPO [14]. Those not captured included three premature births that occurred at a neighbouring hospital, a stillbirth, and the remainder not collected due to participants being discharged early and lost to follow-up. We hope to improve the heel-prick capture rate through providing more information to midwives and by providing participants with leaflets/bags with the study logo so that midwives are aware of their involvement in the study and the importance of capturing the heel-prick.
Although small, our study is the first to show that early GDM treatment could be associated with a play off between a reduced LGA rate but an increased NICU admission rate (largely associated with SGA for those treated from booking). SGA/fetal undernutrition can be a consequence of overtreatment [15], or insufficient gestational weight gain [16], with putative long term consequences [17]. Hypertension and smoking (and potentially metformin treatment [18]) can also contribute to reduced fetal growth and in the main trial, it will be important to assess any interaction between these characteristics, fetal gender and outcomes from early GDM treatment. Our study reminds us that we do not know the optimal glycaemic targets early in pregnancy and that we should be cautious. Our study is also the first to challenge the finding that 33–66% of women early in pregnancy might not have GDM on repeat fasting glucose testing [8]. As 89% of untreated women in our study had GDM at both 18 weeks and 24–28 weeks gestation, there is a case for using the 24–28 week criteria from the middle of the second trimester.
Our study has the strength of obstetrician blinding and the use of decoys, to avoid confounding of the NICU admission and LSCS rates. The use of quantitative and qualitative measures is also a strength. The study only tests the use of the IADPSG/WHO criteria [6, 7] and not other criteria for GDM. Weaknesses include the higher baseline systolic blood pressure and the small sample size. The latter prevents the identification of the impact of any specific management issues such as the use of metformin or treatment compliance. The late clinic booking of women was a major impediment to recruitment and we have tested the benefits/harms with a mid-second, not a first trimester GDM diagnosis. Most (48%) of the exclusions were due to this late booking, which was due to local clinic processes (now rectified). For the main study, we have negotiated with the antenatal clinic to expedite the booking of women with risk factors for GDM, to avoid delays and hopefully recruit before 12–14 weeks gestation. Such earlier recruitment is more likely to directly answer the question about the benefits/risks of treatment in the first trimester raised by both Zhu et al. [8] and Sweeting et al. [19]. The latter showed that the group with the poorest pregnancy outcome were diagnosed before 12 weeks. Women diagnosed with GDM between 13 and 23 weeks had outcomes more similar to those diagnosed > 24 weeks. The study would have recruited the target number of women quicker if an early OGTT had been requested universally. However, the study followed the national guideline to use risk factor screening to assess who should proceed to an early OGTT.
Conclusion
In conclusion, we have completed the first RCT of whether GDM, defined by 24–28 week criteria, should be treated at booking. Our surveys and interviews of mothers and midwives, along with the successful completion of the study highlights its feasibility. Although a small study, the findings suggest that there may be a play off between reducing macrosomia and increasing fetal undernutrition, a finding warranting a larger RCT. A full trial is urgently required.
Abbreviations
- EDTA:
-
Ethylenediaminetetraacetic acid
- GDM:
-
Gestational diabetes mellitus
- IADPGS/WHO:
-
International association of diabetes and pregnancy study group/world health organisation
- LGA:
-
Large gestational age
- NICU:
-
Neonatal intensive care unit
- OGTT:
-
Oral glucose tolerance test
- RCT:
-
Randomised controlled trial
- SGA:
-
Small gestational age
- ToBOGM:
-
Treatment of booking gestational diabetes mellitus
References
Metzger BE, Coustan DR. Summary and recommendations of the fourth international workshop conference on gestational diabetes mellitus. Diabetes Care. 1998;21(Suppl 2):B161–7.
Cheung NW, Byth K. The population health significance of gestational diabetes. Diabetes Care. 2003;26(7):2005–9.
Buchanan TA, Xiang AH. Gestational diabetes mellitus. J Clin Investig. 2005;115(3):485–91.
Crowther CA, Hiller JE, Moss JR, McPhee AJ, Jeffries WS, Robinson JS. Effect of treatment of gestational diabetes on pregnancy outcomes. New England J Med. 2005;352(24):2477–86.
Landon MB, Spong CY, Thom E, Carpenter MW, Ramin SM, Casey B, Wapner RJ, Varner MW, Rouse DJ, Thorp JM Jr, Sciscione A. A multicenter, randomized trial of treatment for mild gestational diabetes. New England J Med. 2009;361(14):1339–48.
IADPSG Consensus Panel. International Association of Diabetes and Pregnancy Study Groups (IADPSG) recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676–82.
WHO. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. WHO/NMH/MND/13.2, 2013. Available at http://apps.who.int/iris/bitstream/10665/85975/1/WHO_NMH_MND_13.2_eng.pdf. Last accessed February 2014.
Zhu WW, Yang HX, Wei YM, Yan J, Wang ZL, Li XL, Wu HR, Li N, Zhang MH, Liu XH, Zhang H. Evaluation of the value of fasting plasma glucose in the first prenatal visit to diagnose gestational diabetes mellitus in China. Diabetes Care. 2013;36(3):586–90.
McIntyre HD, Sacks DA, Barbour LA, Feig DS, Catalano PM, Damm P, McElduff A. Issues with the diagnosis and classification of hyperglycemia in early pregnancy. Diabetes Care. 2016;39(1):53–4.
Nankervis A, McIntyre HD, Moses R, Ross GP, Callaway L, Porter C, Jeffries W, Boorman C, De Vries B, McElduff A. For the Australasian Diabetes in Pregnancy Society. ADIPS consensus guidelines for the testing and diagnosis of gestational diabetes mellitus in Australia and New Zealand. 2014 http://adips.org/downloads/2014ADIPSGDMGuidelinesV18.11.2014_000.pdf Accessed 1 Feb 2017.
Braun V, Clarke V. Using thematic analysis in psychology. Qual Res Psychol. 2006;3:77–101.
Simmons D, Devlieger R, van Assche A, Jans G, Galjaard S, Corcoy R, Adelantado JM, Dunne F, Desoye G, Harreiter J, Kautzky-Willer A, Damm P, Mathiesen ER, Jensen DM, Andersen L, Lapolla A, Dalfrà MG, Bertolotto A, Wender-Ozegowska E, Zawiejska A, Hill D, Snoek FJ, Jelsma JG, van Poppel MN. Effect of physical activity and/or healthy eating on GDM risk: the DALI lifestyle study. J Clin Endocrinol Metab 2016, Dec 9 :jc20163455. [Epub ahead of print].
Kingman A, Zion G. Some power considerations when deciding to use transformations. Stat Med. 1994;13:769–83.
The HAPO Study Cooperative Research Group. Hyperglycemia and adverse pregnancy outcomes. New England J Med. 2008;358:1991–2002.
Langer O, Levy J, Brustman L, Anyaegbunam A, Merkatz R, Divon M. Glycemic control in gestational diabetes mellitus: how tight is tight enough; small for gestational age versus large for gestational age? Am J Obstet Gynecol. 1989;161(3):646–53.
Catalano PM, Mele L, Landon MB, Ramin SM, Reddy UM, Casey B, Wapner RJ, Varner MW, Rouse DJ, Thorp JM, Saade G. Inadequate weight gain in overweight and obese pregnant women: what is the effect on fetal growth? Am J Obstet Gynaecol. 2014;211(2):137.e1–7.
Hales CN, Barker DJ. Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis. Diabetologia. 1992;35(7):595–601.
Lindsay RS, Loeken MR. Metformin use in pregnancy: promises and uncertainties. Diabetologia. 2017;60(9):1612–9.
Sweeting AN, Ross GP, Hyett J, Molyneaux L, Constantino M, Harding AJ, Wong J. Gestational diabetes mellitus in early pregnancy: evidence for poor pregnancy outcomes despite treatment. Diabetes Care. 2016;39(1):75–81.
Acknowledgements
We would like to thank staff members at Campbelltown Hospital and participating women for their involvement in the study. We thank Raiyomand Dalal, Western Sydney University/Campbelltown Hospital, Campbelltown, Australia, and Wah Cheung, Westmead Hospital, Sydney for their work as the Safety Monitoring Board, and Alex Hawkey for assisting with the focus group interviews. We thank the ToBOGM Collaboration for their contribution to the development of the protocol.
Author contributions
DS designed the study, performed the final statistical analysis, interpretation of results, and drafted the manuscript. JN was involved in the acquisition of data, recruitment, and contributed to drafting the manuscript. CP undertook the focus groups and the qualitative analyses. LV assisted with the initial statistical analysis, interpretation of results and drafting the manuscript. JU and JP helped design the qualitative aspects of the study, and commented on the manuscript. AR and RR provided consultation regarding the study design, and contributed to drafting the manuscript. All authors have read and approved the final manuscript. DS is guarantor.
Funding
This study was funded by Western Sydney University. The funders had no role in any aspect of the trial.
Availability of data and materials
The datasets obtained and/or analyzed during the current study are not publicly available due to confidentiality consent of the study but can be obtained from the corresponding author on reasonable request.
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All authors declare they have no competing interest.
Ethics approval and consent to participate
The study was approved by the South Western Sydney Local Health District (SWSLHD) Ethics committee (Reference number 15/LPOOL/14). Written consent was obtained by all participants prior to participating in the study.
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Additional files
Additional file 1:
Table S1. Characteristics of Survey and focus group participants: Midwives (DOCX 13 kb)
Additional file 2:
Table S2. Characteristics of Survey and focus group participants: antenatal women (DOCX 14 kb)
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Simmons, D., Nema, J., Parton, C. et al. The treatment of booking gestational diabetes mellitus (TOBOGM) pilot randomised controlled trial. BMC Pregnancy Childbirth 18, 151 (2018). https://doi.org/10.1186/s12884-018-1809-y
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DOI: https://doi.org/10.1186/s12884-018-1809-y