547 Risk Factors for the Recurrence of Gestational Diabetes

547 Risk Factors for the Recurrence of Gestational Diabetes

424 SPO Abstracts 547 January 1992 Am J Obstet Gynecol RISK FACTORS FOR THE RECURRENCE OF GESTATIONAL DIABETES F.L Gaudier", M.G. Pois!", J.e. Hau...

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424 SPO Abstracts

547

January 1992

Am J Obstet Gynecol

RISK FACTORS FOR THE RECURRENCE OF GESTATIONAL DIABETES F.L Gaudier", M.G. Pois!", J.e. Hauth, D. Corbett" The University of Alabama Hospitals, Birmingham

549

(n=47)

Race (Black) Family History Index Pregnancy Macrosomia (;,,4OOOg) Glucose values (mg/dl) Screening Test (1 hr value plasma) GTT - Fasting 1 hour 2 hour 3 hour Required Insulin Subsequent pregnancy BMI ;,,35 Pre-pg wt. (kg) WI. gain in pg (kg) Newborn wt. (gm) BMI

= Body

Non-Recurrent

(n=43)

Program, University of COlorado Health Sciences Center, Denver, COlorado FIXed minidose warfarin may be effective prophylaxis for venous

thrombosis in hii!b risk patients. COmplete anticoagulation with warfarin in the second and ihird tnmester of pregnancy may lead to fetal and maternal bleeding complications. Parenteral bepann by subcutaneous injection or infusion pump is inconvenient, p'ainful and associated with coml1hcations of bleeding, thrombocytoP."nia, ana osteoporosis. The following patient offered the opportunity to study the usefulness and safety of minidose warfarin in late prejtnancy. Oise ReJ1Ort: A 28 year old para 1 with antithrombin III deficiency suffered a right subclavian vein tlirombosis at 18 weeks gestation and was

P

treated with mtravenous heparin with resolution. Subcutaneous heparin was

79% 57.4%

84% 46.5%

0.55 0.30

23%

7.5%

0.05

189:t50

168:t39

0.04

110:t25 228:t43 225:t60 163:t54 69%

99:t22 205:t35 184:t38 158:t42 31%

0.42 0.Q1 0.0004 0.63 0.04

34.1% 83.4:t23.2 10.9:t5.7 3479+732

10.0% 75.0:t22.9 13.1:t7.0 3359:t680

0.01 0.09 0.11 0.42

substituted for prophylactic th~y but was unsuccessful in prolonginJl the partial thromlxiplastic time (yq) to any degree. A continuous 1Orusion pump was reqwred to assure adequate ~OPllyiaxiS' but the patient was unreceptive to prolonged therapy oT this e. Minidose warfarin (1 mg a day) was offered as an alternative at 32 wee gestation. Maternal and felal blOOd samnles were analv
548 HblAc PREDICTS PREGNANCY MORBIDITY IN DIABETICS.

R. Figueroa, U. Verma, F. Wiltshire~ N. Tejani. Dept. of Ob/Gyn, NY Med. ColI., Valhalla, NY. Objective To evaluate the correlation on initial HbAlc and adverse outcome in diabetic pre~ nancies. Study design Medical records of 174 pregnancies in diabetic women were reviewed. ~ formation obtained was initial HbAlc value and gestational age (92 wks., ~20 wks., S24 wks.,>24 wl9% - ~12% and HbAlc >12%. Data was analyzed using ANOVA and t-tests. Results Compared to pregnancies with normal outcome, HWUc was higher in pregnancies with major congenital malformations (10.2% vs 7.3%; p""O.OI), spontaneous abortions (13.3% vs 7.3%; p(.OO5), and when all adverse outcomes were considered (10.9% vs 7.3%, p(.OO5). A HWUc of> 12% at 92 wks. gestation predicted a 100% morbidity. TABLE ADVERSE PREGNANCY OUTCOME (CUMULATIVE NI1M.)

GA (Weeks) "12 '20

ALL ~ 24 11/13 11/16 )12% 6/6 iO/ll 5/20 7/27 2/8 3/17 ? 9% ~12% 3/27 11/131 0/6 2/18 !: 9% Conclusions HbAlc is a reliable predictor of adverse pregnancy outcome.

36 Week Maternal Fetal

PT

12.3 sec.

14.3 sec.

12.3 sec.

n

87%

23%

91%

24%

VII

159%

48%

195%

52%

IX

115%

15%

194%

15%

X

121%

22%

152%

37%

''hvoer''

"normal"

"nonnal"

Sonoclot

Mass Index

1.0 mco/mI O.09mcolml /mI Warfarin . 9>nduSlon: Fix..,j.! nurudose warfann id not result

We conclude that women with a prior history of GDM are at increased risk for recurrence. These patients may benefH from earlier screening for glucose intolerance in their subsequent pregnancies and especially those who are obese, had fetal macrosomia, or required insulin during their previous pregnancies.

HbAlc

WARFARIN FOR PROPHYLAXIS OF DISEASE IN PREGNANCY: A SAFE

~,r.:~t~c';?"~ ~Jo~e~,S~l&':"'Pr~s~cp,,'$§l?'i:NR·p~~';[.?t~

We evaluated the recurrence of gestational diabetes mellitus (GDM) by identifying ninety women with a pregnancy complicated by glucose intolerance and whose subsequent pregnancy was managed at our institution. Forty-seven (52%) of the patients had a recurrence of GDM in their subsequent gestation. Recurrent

FIXED MINIDOSE nIROMBOEMBOLIC

13.4 sec.

"normal" 10


sJgmficant abnormalities of maternal-fetal coagulation. Some Vitamin de~ndent

¥Z.

factors in the fetus were mildly depressed. Efficacyof minidose

warfarin in pregnancy requires further investigation, though this case study

suggests that tfie fetus is not at increased risK of hemorrfiage.

551

LONG-TERM HEALTH OF CHILDREN OF INSULIN DEPENDENT WOMEN J.E. Converse", Dept of OB/GYN, University of Wisconsin, Madison, WI, M.S. Cranley", School of Nursing, University of Buffalo, Buffalo, NY, and L.B. Curet, Dept of OB/GYN, University of New Mexico, Albuquerque, NM A retrospective, descriptive study was designed to investigate the health status of children born to insulin dependent diabetic mothers (IDDM). The relationship of the child's health to the maternal obstetrical course was also examined. The convenience sample consisted of 80 children born to 56 predominately married, middle-class, medically insured IDDM mothers who received obstetrical services from a midwestern university perinatal center from the years of 1971 to 1987. The children ranged in age from 7 months to 16 years. Three children had died, 2 in infancy and I in childhood. Conclusion: The results showed that in comparison to general population national health statistics, the children in this study had two to four times greater incidences of child health conditions related to medical, neurological, and developmental problems at birth, in the neonatal period, and throughout childhood. The greater the number of maternal health risk factors, the earlier the infant was born, and the more health problems the child had at birth and in childhood. The differences in child health were not related to the trimester in which prenatal care began with the perinatal program nor correlated with maternal hyperglycemia and elevated glycosylated hemoglobin.