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CLINICAL OBSTETRICS AND GYNECOLOGY

Volume 45, Number 1, 165–169


© 2002, Lippincott Williams & Wilkins, Inc.

Management of
Diabetes in Pregnancy
JOSE L. GONZALEZ, MD
Division of Maternal Fetal Medicine, Department of Obstetrics and
Gynecology, School of Medicine, University of New Mexico,
Albuquerque, New Mexico

Management of the diabetic pregnant pa- ance, and appropriate timing and mode of
tient has changed dramatically during the delivery.
last 80 years. Since 1920 when insulin was Management of patients with diabetes
discovered until today when researchers are during pregnancy is guided to obtain target
talking about genetic manipulation, stem plasma glucose concentrations. Most inves-
cells, and pancreatic islet capsules, provid- tigators agree that fasting plasma glucose
ers of health care during pregnancy face the concentrations should be kept under 95
dilemma of choosing adequate therapies for mg/dL and postprandial levels under 120
individual patients. It is the task of the ob- mg/dL. In 1991 Jovanovic-Peterson et al1
stetrician to balance the need for extra fuel published that the glucose value 1 hour after
by the fetus with complications associated a meal is the most predictive of fetal macro-
with excessive maternal blood glucose. somia. Other investigators have used differ-
Key elements in the management of preg- ent laboratory tools to manage patients with
nancies complicated with diabetes include a diabetes during pregnancy such as serum he-
balance of diet, exercise, and medications. moglobin A1C levels. This test is not rou-
Important factors in the clinical manage- tinely used to follow glucose levels since it
ment of patients with diabetes include fre- only reflects average values without taking
quent contact with the providers, psycho- into consideration peaks in plasma glucose
logic and social support, prenatal diagnosis concentrations after meals.
and counseling, fetal surveillance, and ad- Patients with glucose intolerance during
equate postpartum follow-up. Several areas pregnancy need specific diet instructions. A
of controversy exist, including when and typical diet includes three meals with three
how to screen populations for diabetes, snacks during the day. The diet is often
which glycemic levels reduce fetal compli- based on 30 kcal/kg of actual weight. This
cations without affecting maternal compli- recommendation has to be modified in pa-
tients who are obese or underweight. Distri-
bution of calories usually consists of ap-
Correspondence: Jose L. Gonzalez, MD, University of proximately 40–50% carbohydrates, 20%
New Mexico, 2211 Lomas Blvd. NE, ACC4, Department
of Obstetrics and Gynecology, Albuquerque, NM 87131. protein, and 30–40% fat. If dietary manipu-
E-mail: jlgonzalez@salud.unm.edu lation does not provide adequate metabolic

CLINICAL OBSTETRICS AND GYNECOLOGY / VOLUME 45 / NUMBER 1 / MARCH 2002

165
166 GONZALEZ

control, as reflected by abnormally high TABLE 2. Guidelines for Continuous


plasma glucose concentrations, then medi- Insulin Infusion During
cal therapy with meticulous capillary blood Pregnancy
glucose self-monitoring is necessary. Blood Insulin
Glucose Dosage Fluids
(mg/100 mL) (U/hour)* (125 mL/hour)
Insulin Therapy <100 0.5 D5/Ringer’s lactate
100–140 1.0 D5/Ringer’s lactate
FORMULATIONS 141–180 1.5 Normal saline
Exogenous insulin lowers blood glucose 181–220 2.0 Normal saline
levels in all types of diabetes. Optimal >220 2.5 Normal saline
therapy, should approximate physiologic in- * as 25 U regular insulin in 250 ml normal saline with intrave-
sulin delivery, which may be difficult. There nous line flushed before IV administration is started.
are many insulin formulations (Table 1).
These insulin products differ in their onset,
peak, and duration of action. Rapid or pran-
insulin are not routinely used during preg-
dial insulins are used to cover the glucose
nancy. When two different insulins are
excursions after meals. Subcutaneous regu-
drawn into the same syringe, care must be
lar insulin has been prescribed most often.
taken to avoid cross-contamination of bottles.
Insulin Lispro, a semisynthetic insulin mol-
ecule that maintains the activity of regular
insulin, offers the advantage of being ab- MAINTENANCE THERAPY
sorbed more quickly. Initial concerns re- The actual patient’s body weight is used to
garding development or progression of dia- calculate the daily insulin dose. During the
betic retinopathy with the use of insulin Lis- first trimester the recommendation is 0.5
pro have not been supported by recent U/kg. In the second trimester 0.75 U/kg is
studies.2 Intermediate-acting insulins, like recommended, while 1.0 U/kg is recom-
neutral Hagedorn, offer an extended release mended in the third trimester.3 Postpartum,
from a subcutaneous site. Long acting insu- the patient should be placed on her prepreg-
lins are used to suppress the hepatic produc- nancy dose or 50% of the last total daily dose
tion of glucose. Ultralente is an example of a before delivery.
long acting insulin that produces a nearly Insulin therapy during pregnancy usually
constant level of circulating insulin when involves a combination of usually two insu-
given subcutaneously once or twice daily. lin formulations to more closely resemble
Almost all insulins used in adults are pre- what the normal human pancreas does.
pared as 100 U/mL. Being less immuno- Methods and timing of insulin administra-
genic, human insulin is preferred over bo- tion are as important as the insulin dose in
vine insulin. Commercially prepared mix- avoidance of hyperglycemia. Shown in Fig-
tures of regular and neutral Hagedorn ure 1 are three examples of individualized
programs. None is clearly most preferred.
TABLE 1. Insulin Formulations
An alternative for patients with type 1
diabetes is the use of insulin pumps.4 These
Onset Peak Duration calibrated pumps deliver insulin in a pattern
Lispro 15–20 min 1–2 hrs 4 hrs that most closely resembles physiologic in-
Regular 30–60 min 2–4 hrs 4–6 hrs sulin secretion. Advantages to the pump in-
NPH 1–2 hrs 5–7 hrs 10–12 hrs clude basal rates of insulin that reduce the
Lente 1–2 hrs 10–12 hrs 14–18 hrs risk of hyperglycemia, decrease in the inci-
Ultralente 1–2 hrs none 20–24 hrs dence of the ‘dawn’ phenomenon (fasting
Lantus 1–2 hrs none 20 hrs
hyperglycemia) by reducing maternal hypo-
Management of Diabetes in Pregnancy 167

FIG. 1. Examples of three individualized programs for administering in-


sulin subcutaneously each day. These programs include a combination of
regular and neutral Hagedorn insulin (A), Lispro and neutral Hagedorn in-
sulin (B), and Lispro and ultralente insulin (C).

glycemia, and improved patient compliance pump dose is often calculated based on 80%
since the patient does not constantly have to of the total daily dose requirement. This to-
inject insulin. Other advantages include in- tal dose of regular insulin is divided into
creased contact with health care providers 60% being given continuously and 40% be-
and greater flexibility with lifestyle. Disad- ing administered in boluses before meals to
vantages of the pump include cost of the de- cover the carbohydrate load.
vice, infection at the needle insertion site,
and pump malfunction that may produce hy- INTRAVENOUS THERAPY
perglycemia and ketoacidosis. These factors Ketoacidosis is fortunately uncommon in
make the insulin pump an alternative only closely regulated type 1 diabetic patients but
for patients who are very compliant with may result from profound hyperglycemia
blood glucose self-monitoring. The insulin and ketosis. Along with the appropriate re-
168 GONZALEZ

placement of fluids and electrolytes and the and Jackson6 published in 1986 did not re-
infusion of bicarbonate, insulin administra- veal any adverse perinatal outcomes when
tion is necessary. The desired goal is a serum patients with gestational diabetes were
glucose level of less than 300 mg/dL with no treated with oral hypoglycemics. Piacqua-
urinary ketone bodies. The author usually dio et al 7 demonstrated an increase in
begins regular insulin as a 10 to 20 U of in- congenital malformations of Mexican-
travenous bolus plus 0.15 U/kg/h of constant American women treated during early preg-
intravenous infusion. The dose is increased nancy with oral hypoglycemic agents. In
hourly if serum glucoses do not fall despite 1994, Denno and Sadler8 found no embryo-
adequate fluid therapy. As acidosis is re- toxicity associated with use of these medica-
versed, the insulin dose is decreased to 5 to tions in an animal model.
10 U every 2 to 4 hours. Once satisfactory Glyburide, a sulfonylurea that does not
control is achieved, only subcutaneous regu- cross the placenta, is appealing because of
lar insulin is required using a sliding scale its apparent safety to the fetus. Presumed
dose regimen. When the patient is eating, in- mechanisms of action include an increase in
termediate acting insulin may be started. the secretion of insulin and some effect pe-
The intrapartum management of diabetes ripherally to increase insulin receptor sensi-
is similar to the management of a woman tivity. A recent randomized study by Langer
with diabetes about to undergo surgery. et al9 revealed that glucose levels in gesta-
Monitoring of the blood glucose level by tional diabetic patients could also be con-
finger stick or venipucture every hour is vi- trolled using glyburide. The need to treat
tal, because strict glucose control (less than with insulin, rather than glyburide, for inad-
100 mg/dL) is desired to avoid maternal hy- equate glucose control was observed in only
perglycemia or hypoglycemia. Uncon- 4% cases. There were no maternal or neona-
trolled maternal blood glucose levels during tal complications. Further investigation at
the intrepartum period may result in neona- other institutions is necessary.
tal hypoglycemia with the potential for tem-
porary or permanent neuronal damage.5 In-
trapartum blood glucose control is achieved
by using intravenous infusion of dextrose Areas of Ongoing
solutions with minimal or no insulin Investigation
therapy. Continuous intravenous infusion of Several alternative therapies are being ex-
regular insulin or Lispro is preferred since plored for the management of patients with
the rapid onset and short duration of action diabetes during pregnancy. These include
make them ideal to titrate the therapy. A the possibility of pancreatic islet transplan-
constant intravenous infusion pump should tation,10 embryonic stem cells that could dif-
be used for this. ferentiate into insulin producing tissue, and
gene therapy.
In addition to glyburide, other hypoglyce-
Oral Hypoglycemic Agents mic agents may be considered as alterna-
Oral hypoglyemic drugs include agents with tives for the treatment of patients with ges-
differing chemistries and mechanisms of ac- tational diabetes. Medications that increase
tion. Sulfonylurea, biguanide, alpha-glu- the receptor-sensitivity to insulin may be
cosidase inhibitors, and thiazolidinedione more appropriate, since this is the main
drugs are indicated in the management of problem in gestational diabetes. Metformin,
nonpregnant adults with type 2 diabetes. a biguanide oral hypoglycemic agent, has
Oral hypoglycemics have been proposed as been used in patients with infertility and
alternative modalities in the treatment of polycystic ovaries.11 Preliminary findings
gestational diabetes. Studies from Coetzee in small groups of patients have reported fa-
Management of Diabetes in Pregnancy 169

vorable outcomes with continued use of this al. Is insulin Lispro associated with the de-
drug during pregnancy. velopment or progression of diabetic retro-
Another area of interest is the develop- pathy during pregnancy? Am J Obstet Gy-
ment of noninvasive glucose monitoring de- necol. 2000;183:1162–1165.
vices as an alternative to performing mul- 3. Jovanovic L. Role of diet and insulin treat-
tiple finger sticks. These noninvasive glu- ment of diabetes in pregnancy. Clin Obstet
Gynecol. 2000;43:46–55.
cose monitor devices could dramatically
4. Gabbe S. New concepts and applications in
change the lifestyle of patients with diabetes the use of insulin pump during pregnancy. J
in pregnancy. Matern Fetal Med. 2000;9:42–45.
5. Halamek LP, Stevenson DK. Neonatal hy-
poglycemia, part II: Pathophysiology and
Summary therapy. Clin Ped. 1998:37:11–16.
Pregnancies complicated with diabetes are 6. Coetzee EJ, Jackson WPU. The manage-
best managed using a multidisciplinary team ment of noninsulin dependent diabetes dur-
approach to individualize diet and insulin ing pregnancy. Diabetes Res Clin Pract.
regimens. The combination of rapid and in- 1986;1:281–287.
termediate acting insulins more closely re- 7. Piacquadio K, Hollingsworth DR, Murphey
sembles what happens physiologically with H. Effects of in utero exposure to oral hypo-
the pancreatic secretion of insulin. In pa- glycemic drugs. Lancet. 1991;338:866–
tients with type 1 diabetes, the insulin pump 869.
is an alternative if she is highly motivated 8. Denno KM, Sadler TW. Effects of the bi-
and compliant with frequent monitoring guanide class of oral hypoglycemic agents
on mouse embryo-genesis. Teratology.
blood glucose levels. In gestational diabetes,
1994;49:260–266.
oral hypoglycemic agents like glyburide
9. Langer O, Conway DL, Berkus MD, et al. A
may be alternative therapies. More studies comparison of glybuide and insulin in
are needed to determine if any oral hypogly- women with gestational diabetes mellitus. N
cemic agent is safest and most effective in Engl J Med. 2000;343:1134–1138.
controlling maternal hyperglycemia. 10. Hunter SK. Present and future perspectives
of the use of free or encapsulated pancreatic
islet cell trasplantation on a treatment of
References pregnancy complicated with Type I diabe-
1. Jovanovic-Peterson L, Peterson CM, Reed tes. J Matern Fetal Med. 2000;9:46–51.
GF, et al. NiHCD Diabetes in early preg- 11. Gluek CJ, Phillips H, Cameron D, et al. Con-
nancy study. Maternal port prandial glucose tinuing metformin thoughout pregnancy in
level and infant birth weight: The diabetes in women with polycystic ovary syndrome ap-
early pregnancy study. Am J Obstet Gyne- plies to safety reduce first trimester sponta-
col. 1991;164:103–111. neous abortion: a pilot study. Fertil Steril.
2. Buchbinder A, Miodounik M, McElvy S, et 2001;75:46–52.

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