REVIEW
ARTICLE
GLYBURIDE
AS TREATMENT IN GESTATIONAL DIABETES MELLITUS
Background: Insulin was primary
choice in Gestational Diabetes Mellitus (GDM) treatment which diet intervention no longer give any significant
responses. Sulfonilurea rarely used in pregnant women with GDM because its
teratogenic and neonatal hypoglycemia effects. Since 2000, some
studies reported successful treatment use glyburide.
Method: Reviewed articles reported glyburide as treatment in
GDM.
Results: GDM in pregnant women could be
treated with Glyburide because its safety although there are no significant
difference between glyburide and insulin macrosomia risk (baby born more than 4000
gram weight); lung
complication; and neonatal hipoglycemic. Beside the
safety reason, glyburide has lower price than insulin. This
cost model can be used by health professional to choose the medicine which has
equality in effect.
Conclusion: Glyburide could be used as therapeutic and costly effective
alternative treatment than insulin in GDM therapy.
Keywords: Gestational Diabetes Mellitus (GDM); insulin; glyburide
INTRODUCTION
Diabetes mellitus
in pregnancy in medical terms is called gestational diabetes mellitus. Diabetes mellitus may only take place during pregnancy but can
also continue though it was no longer pregnant. The
disease is present in approximately 1% of women of reproductive age and 1-2% of
them will suffer from gestational diabetes. Diabetes
mellitus (DM) is a group of metabolic diseases with hyperglycemia
characteristic (increased blood sugar levels ) that occurs cause abnormalities
in insulin secretion, insulin action or both.
Classification of DM with Pregnancy
by Pyke:
Class 1 : Gestational diabetes, which is diabetes that arises during
pregnancy and disappears after childbirth.
Class II : Pregestasional diabetes, namely ranging
from pre-pregnancy diabetes and continued after
pregnancy.
Class III : Pregestasional diabetes
accompanied by complications of the disease blood vessels such as retinopathy, nephropathy, a disease of blood hunters pelvic and peripheral blood vessels.
Mayor of women
with DM controlled with diet and exercise, but 30% - 40% of them require pharmacological therapy. The principle arrangement of blood sugar levels in pregnant
women with diet therapy is, or with additional insulin if therapy diet alone is
not enough. Insulin therapy is effective for dealing with gestational diabetes
but it is not comfortable and relatively expensive. Handling with sulfonilurea
not recommended for pregnant women because of the the risk of defects in the
fetus and neonatal risk hipoglicemia. However,
some studies , glyburide and glipizide are drugs commonly used today. Glyburide or also known as glibenclamide in the treatment of
gestational diabetes mellitus proven effective, safe, and inexpensive addition
to insulin.
Glyburide is
currently classified as category B by the FDA for use in pregnant women, which
means that there is no evidence of risk in humans. In 2001, the American
College of Obstetricians and Gynecologists (ACOG) recommends that careful
in applying oral agents to handle DM Gestational. particular agency is aware
that further studies need to be done for safety criteria for diabetes drugs. In
2004, ACOG reported that 13% of obstetricians 1400 America use these glyburide
as first-line therapy in case of failure of a dietary intervention pad GDM
women diagnosed.
Use of total
glyburide during pregnancy based on shared
pathophysiology of GDM and type 2 diabetes.
Class of drugs sulfonilurea has been used to treat type
2 diabetes for decades involving pa n pancreatic function in lowering blood
sugar levels by inhibiting
effluks potassium through adenosine 5'-triphosphate (ATP). This action causes depolarization cellular and stimulate insulin from the pancreas. effect u all This drug is an m k eningkat insulin secretion. Medication sulfonilurea reduce glucose toxicity and
increase insulin secretion after a meal, thus reducing postprandial hyperglicemia. Research has show that, these drugs also can increase sensitivity of peripheral tissues to insulin.
effluks potassium through adenosine 5'-triphosphate (ATP). This action causes depolarization cellular and stimulate insulin from the pancreas. effect u all This drug is an m k eningkat insulin secretion. Medication sulfonilurea reduce glucose toxicity and
increase insulin secretion after a meal, thus reducing postprandial hyperglicemia. Research has show that, these drugs also can increase sensitivity of peripheral tissues to insulin.
The purpose of
writing this article is to determine the safety glyburide on gestational diabetes and able to conclude that glyburide is
choices therapy GDM safe,
effective and in expensive.
METHOD
In this article,
the data used is obtained by reviewing electronic scientific articles related
to gestational diabetes mellitus (diabetes that occurs during pregnancy), its
handling, its effectiveness in terms of both effect and cost.
The data is taken
from several websites that provide scientific journals related to gestational
diabetes keyword: Gestational
Diabetes Mellitus; insulin; glyburide in the search field (search).
RESULTS AND DISCUSSION
Clinical experience
pe ngoba tan with glyburide for GDM has progressed. Since 2000, several studies have shown that
glyburide is ernatif alt effective when compared with insulin to achieve
adequate glycemic control in women with GDM. however,
it should be noted that the differences in the criteria of glycemic control may
affect the results. In addition, differences in
population (ethnic and geographic location), sample size, method, dose of the
drug could significantly affect the results.
Despite the
concerns about the significant teratogenic effects and the possibility of baby
makrosomia associated with the use of oral hypoglycemic medications during
pregnancy, especially sulfonylurea class, Elliott
et al. Showed that only a few of glyburide
was detected capable placental aspirated tested in vitro perfusion model. And
than, based on observations of Langer et al, concluded that glyburide
did not detect on the umbilical cord / placenta and there was no significant
difference between glyburide and insulin except on the reduction of maternal
hypoglycemia episodes on premises glyburide (2%) compared to insulin (20%).
To determine
whether glyburide distributed into breast milk in women with a history of GDM
have done research, where study previously with two first-generation
sulfonylureas, tolbutamide and chlorpropamide
showed that his transfer there is significant
drug into breast milk. In nonrandomized
controlled observation study conducted on sulfonilurea second generation, glyburide and glipizide in breast milk, suggesting that
glyburide not found in breast milk and blood glucose on all infants Breastfed normaly.
A study randomized
controlled trial to glyburide versus
insulin showed that treatment with glyburide can
provide a relatively safe alternative of insulin
therapy. According Glyburide including the FDA
category B drug for use in pregnant women, which means that there is no
evidence of risk in humans. Then retrospective trials have shown up
even wa 20% of GDM patients, especially pretreatment with substantial hyperglycemia, likely to require adjuvant or alternative therapy with insulin. At a later study showed
that treatment with glyburide compared with insulin resulted in lower sugar
levels and higher percentage of the 'excellent glycemic control' with
fewer hypoglycemic episodes.
Most physicians
assume that cost is one of the aspects to
consider in deciding which nursing care they created.
The cost of becoming a more important factor when
physicians must choose drugs with similar effectiveness.
Glyburide
significantly cheaper than insulin. Analysis /
cost model can be useful for physicians in deciding the selection of drugs,
especially drugs that have the same properties. It is described by Goetzl
et al, that glyburide significantly cheaper than insulin for the treatment of gestational diabetes can save
the cost of treatment.
CONCLUSION
Given the effects
/ risks of drug entry into the placenta and can harm the fetus glyburide a
synthetic drug can be recommended for women with diabetes during pregnancy.
Since 2000, several studies have shown that glyburide
is an effective alternative to insulin to achieve adequate glycemic control in women with GDM. however, it
should be noted that the difference of control glycemic criteria may affect the
results. Further more, differences in
populations (ethnic and geographic location), sample size, method, drug dose
significantly affect the results.
A study randomized controlled trial to glyburide versus insulin showed that treatment with glyburide can provide a relatively safe alternative of insulin therapy. Further
retrospective trials have shown that up to
20% of GDM patients, especially with pretreatment substantially hyperglycemia likely to require adjuvant or alternative therapy with insulin.
Some studies
also show that glyburide is not found in the umbilical cord / placenta and
showed that glyburide not found in breast milk and blood glucose levels in all
breastfed infants is normal. Additionally, glyburide significantly cheaper than
insulin that can be used as a consideration in deciding the selection of drugs,
especially drugs that have the same efficacy.
REFERENCES
Elliott, B. D, Langer O, Schenker, S, Johnson, R. F., 1991,
insignificant transfer of glyburide across the human placenta Occurs. Am J Obstet Gynecol 165:807 - 812.
Goetzl, L., and Wilkins, I., 2002, Glyburide Compared to
Insulin for the Treatment of Gestational Diabetes Mellitus: A Cost Analysis, Journal of Perinatology, 22: 403-406.
Langer, O., Conway, DL, Berkus MD, Xenakis, EMJ, Gonzales, O.,
2000, A Comparison Of Glyburide And Insuli n In Women With Gestational Diabetes Mellitus, T he
Massachusetts Medical Society, Vol ume 343.
Moore, TR, 2007, Glyburide for the Treatment of Gestational
Diabetes, Diabetes
Care, Volume 3.
Trojnar, AK,
Marciniak, B., Gorzelak, have done, BL, Trojnar, M., Oleszczuk, J., 2008, Glyburide
for the treatment of gestational diabetes mellitus, Medical University of Lublin,
Staszica 16, Pharmacological Reports, 60, 308-318.
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