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ORIGINAL RESEARCH |
From the Department of Obstetrics and Gynecology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Address reprint requests to: Melinda B. McFarland, MD Department of Obstetrics and Gynecology The University of Texas Health Science Center at San Antonio 7703 Floyd Curl Drive San Antonio, TX 78284-7836 E-mail: mcfarland{at}uthscsa.edu
| Abstract |
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Methods: Women with GDM were treated with dietary therapy for 4 weeks. Each measured her blood glucose using a memory-based reflectance glucometer, and those in poor glycemic control (mean glucose exceeding 105 mg/dL) after 4 weeks of dietary therapy were prescribed insulin. Women were stratified by fasting plasma glucose value of 3-hour glucose tolerance tests (GTTs).
Results: Women with fasting glucose at or below 95 mg/dL were significantly more likely to achieve good glycemic control after 2 weeks of dietary therapy than were those with values above 95 mg/dL whose control did not improve during the study. Receiver operating characteristic (ROC) analysis determined that fasting values of GTT between 91 and 95 mg/dL best predicted that insulin would be needed for good glycemic control.
Conclusion: Women with GDM should be prescribed dietary therapy alone for at least 2 weeks before they are prescribed insulin. In those with fasting glucose above 95 mg/dL, insulin may be prescribed after 1 week of dietary therapy, or at diagnosis.
The criteria for prescribing insulin for women with gestational diabetes mellitus (GDM) remain controversial. An ACOG Technical Bulletin1 states that all women with diagnoses of gestational diabetes should be prescribed dietary therapy. Insulin should be prescribed when fasting plasma glucose exceeds 105 mg/dL, or 2-hour postprandial levels exceed 120 mg/dL.2 However, duration of dietary therapy is not specified.
Surveys of obstetricians and maternal-fetal subspecialists in practice3 and training4 show the need for clarification of treatment guidelines. These surveys found that practitioners had widely varied management practices for insulin prescription. For example, ACOG recommends1 that fasting and 2-hour postprandial blood glucose levels should be monitored "at least weekly." However, ACOGs criteria were devised before the widespread use of more frequent blood glucose self-monitoring, which was used by 44% of practitioners4 for women with gestational diabetes treated with diet and by 76% of practitioners prescribing insulin.
Longitudinal ultrasonographic studies5,6 found that accelerated growth in fetuses of diabetic mothers might occur early in the third trimester, by 2830 weeks gestation. Most cases of GDM are diagnosed during this time, so it is important that quick, effective treatment of GDM be given to avoid fetal consequences. It is important to know how much time is needed to achieve good glycemic control with diet alone and to develop predictors for failure of dietary therapy alone at diagnosis. We sought to determine how much time it takes for dietary therapy alone to effect good glycemic control in GDM and whether the need for insulin could be predicted at diagnosis.
| Materials and Methods |
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Women with histories of diabetes outside pregnancy or those with fasting glucose levels on the 3-hour GTT above 140 mg/dL were excluded. Subjects were prescribed diets for 4 weeks, after which those in poor glycemic control, defined as mean blood glucose exceeding 105 mg/dL, were prescribed insulin therapy. According to our protocol, women with weekly mean glucose levels above 200 mg/dL at any time during the study were prescribed insulin immediately.
Caloric assignment was calculated based on actual weight at diagnosis. Obesity was defined by BMI, calculated by prepregnancy weight (kg) divided by height (m, squared). Maternal height was measured at first prenatal visit. Prepregnancy weight was taken from records or by subject reports if records were not available. Obese women (BMI at least 27) received 25 kcal/kg of actual body weight, those with BMI 2026 received 30 kcal/kg, and those with BMI less than 20 received 35 kcal/kg.
Nutrients were distributed as follows: 5055% carbohydrates, 2025% protein (minimum 75 g per day), and 2025% fat (less than 10% saturated fat). Energy was distributed as follows: breakfast 20%, lunch 25%, supper 25%, postmeal snacks 5% each, and bedtime snack 15%. All women received extensive dietary counseling by a registered dietician, with emphasis on developing diets consistent with their living situations and cultural norms. Subjects recorded all intake in diaries, which were reviewed on at least one other occasion by a dietician, who provided appropriate counseling. The importance of dietary compliance was reinforced by the obstetric care provider and a diabetes nurse-educator at each weekly clinic visit. All women checked for morning ketonuria daily, and caloric intake was adjusted as necessary during the clinic visits.
Subjects were instructed to monitor their blood glucose using memory reflectance meters seven times daily, including fasting, preprandial, 2-hour postprandial, and bedtime readings. The overall mean, fasting, preprandial, and postprandial averages were calculated using all values for the specified week of treatment.
Receiver operating characteristic (ROC) curves were generated to determine predictability of fasting plasma glucose of GTT for poor glycemic control by mean blood glucose exceeding 105 mg/dL or the ACOG criterion of fasting glucose exceeding 105 mg/dL or postprandial glucose exceeding 120 mg/dL. For analysis, women were stratified by fasting values of GTT (at most 95 mg/dL versus above 95 mg/dL). Categoric data were analyzed with Fisher exact and
2 tests using Bonferroni inequality to adjust P values for multiple comparisons when the overall
2 statistic was significant. Continuous data were analyzed by one-way analysis of variance for repeated measures using the Bonferroni t test ad hoc to determine multiple comparisons when the F statistic was significant. P < .05 was statistically significant. Logistic regression analysis was used to assess the effect various factors had on the need for insulin.
| Results |
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Logistic regression analysis was done using need for insulin as the dependent variable. Independent variables used were maternal weight, BMI, weight gain during study, gestational age at diagnosis, all values of GTT, and the number of abnormal values of GTT. The fasting (P = .01), 1-hour (P = .04), and 3-hour (P = .001) values of the GTT and the number of abnormal values (P = .03) were associated with need for insulin. The other independent variables were not significant risk factors.
| Discussion |
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Attaining good glycemic control is the cornerstone of managing women with gestational diabetes.10 Women with poor control have a higher incidence of fetal macrosomia,11 with resultant birth trauma, and other metabolic complications. Ultrasonographic studies5,6 found that such fetal overgrowth might have begun already before diagnosis; therefore, the time to prevent related morbidity is limited, and the decision to prescribe insulin should be quick.
It is still controversial which women with GDM will benefit from insulin. Some investigators12,13 found benefit in prophylactic insulin in all women with GDM. Although an ACOG Technical Bulletin1 recommends prescribing insulin if fasting glucose levels exceed 105 mg/dL or 2-hour postprandial levels exceed 120 mg/dL, two single readings (fasting or postprandial) in 1 week might not adequately show the level of glucose control in women receiving no additional monitoring. Conversely, prescribing insulin based on two elevated readings in women showing otherwise good control, by intensified monitoring, might result in overtreatment.
We found that a fasting glucose level between 91 and 95 mg/dL can predict the need for insulin for good glycemic control. We also identified a subset of women with fasting glucose not more than 95 mg/dL who will benefit from dietary therapy alone. Such therapy should be continued for at least 2 weeks because significant improvement in glycemic control can be achieved during that time. Almost 60% of women with fasting glucose above 95 mg/dL failed to achieve good glycemic control even after 4 weeks of dietary therapy. Subjects in this group weighed more and had GDM diagnosed at earlier gestational ages (ostensibly because of risk factors), possibly indicating more severe disease. Because these women did not improve their glycemic control significantly given a longer treatment period, a shorter (1-week) trial of dietary therapy appears to be adequate. Consideration might be given to immediate insulin prescription in this subset, particularly if GDM is diagnosed late in gestation, or to a longer trial of dietary therapy if women show nearoptimal glycemic control early in treatment with diet alone.
| Footnotes |
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Received May 21, 1998. Received in revised form November 16, 1998. Accepted December 3, 1998.
| References |
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2. Metzger BE. Summary and recommendations of the Third International Workshop-Conference on Gestational Diabetes Mellitus. Diabetes 1991;40(Suppl 2):197201.[Abstract]
3. Landon MA, Gabbe SG, Sachs L. Management of diabetes mellitus and pregnancy: A survey of obstetricians and maternal-fetal specialists. Obstet Gynecol 1990;75:63540.
4. Owen J, Phelan ST, Landon MB, Gabbe SG. Gestational diabetes survey. Am J Obstet Gynecol 1995;172:61520.[Medline]
5. Ogata ES, Sabbagha R, Metzger BE, Phelps RL, Depp R, Freinkel N. Serial ultrasonography to assess evolving fetal macrosomia. JAMA 1980;243:24058.[Abstract]
6. Langer O, Kozlowski S, Brustman L. Abnormal growth patterns in diabetes in pregnancy: A longitudinal study. Israel J Med Sci 1991;27:51623.[Medline]
7. National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes 1979;28:103957.[Medline]
8. Langer O, Anyaegbunam A, Brustman L, Divon MY. A prospective randomized study: Management of women with one abnormal glucose tolerance test value reduces adverse outcome in pregnancy. Am J Obstet Gynecol 1989;161:5939.
9. Langer O, Brustman L, Anyaegbunam A, Mazze R. The significance of one abnormal glucose tolerance test value on adverse outcome in pregnancy. Am J Obstet Gynecol 1987;157:75863.[Medline]
10. Langer O. Management of gestational diabetes. Clin Perinatol 1993;20:60317.[Medline]
11. Langer O, Rodriguez DA, Xenakis EM, McFarland MB, Berkus MD, Arredondo F. Intensified versus conventional management of gestational diabetes. Am J Obstet Gynecol 1994;170:103647.[Medline]
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