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DIABETIC PREGNANCY JOINT CLINIC

Antenatal Clinic
Mater Dei University Hospital, Malta
Tel: 25454479

   
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07/09/2010

Visits to this Site:   8591125

 

- Antenatal Management
 
GUIDELINES FOR THE MANAGEMENT OF DIABETES IN PREGNANCY
A National Clinical Guideline recommended for use in Malta based on the St. Vincent Declaration

prepared by
C. Savona-Ventura
MD, DScMed, FRCOG, Accr.Cert.OG, MRCPI
Consultant Obstetrican i/c Diabetic Pregnancy Joint Clinic


Department of Health
Malta
2000
[Revised 2007]
 

The St. Vincent Declaration aim for pregnancy is: "To achieve pregnancy outcome in the diabetic woman that approximates that of the non-diabetic woman". This can be achieved by a dedicated Pregnancy Diabetes Clinic, where a specialist team including a named physician(s) and a named obstetrician(s) should see all pregnant diabetic women in a combined clinic in a hospital with a neonatal intensive care unit. A routine busy antenatal clinic cannot give the same standards of care given by a dedicated clinic.

The Diabetic Pregnancy Joint Clinic was restructured in October 1998, after the criteria of referral and management were reviewed by the Department of Obstetrics & Gynaecology and the Diabetes Clinic. The Diabetic Pregnancy Joint Clinic is managed jointly by the Obstetric Department [Prof. C. Savona-Ventura] and the Diabetes Clinic. Consultations with the dietitian would be arranged after the first visit and subsequently if deemed necessary.
The scope of the Diabetic Pregnancy Joint Clinic is to ensure that all diabetic women have:

  • Tight control of diabetes during pregnancy
  • Education about treatment of hypoglycaemia and avoidance of ketoacidosis
  • Access to a specialist team
  • Quality ultrasound scanning to assess gestation and fetal growth
  • Fetal monitoring, particularly if at very high risk
  • Regular examination of fundi and assessment of renal function.
Criteria for Referral to Clinic

All patients who are diagnosed to suffer from any form of significant carbohydrate intolerance during their pregnancy should be referred to the Diabetic Pregnancy Joint Clinic. These patients include:

  • Pre-existing Diabetes Mellitus/I.G.T. who have become pregnant;
  • Gestational Diabetes Mellitus [oGTT 2-hr blood glucose value >=11.0 mmol/l];
  • Mild Gestational DM [oGTT 2-hr blood glucose value 8.6-10.9 mmol/l].

Pre-Conception Care

All patients with pre-existing diabetes should ensure that they enter pregnancy in an optimum state of health and metabolic control. This help prevent congenital anomalies and deterioration of maternal diabetic complications. Pre-conception care was sought in only 29% of our patients; there has however been a minimal change in malformation rates since 1983-1986 [6.8%] -> 1999-2004 [4.7%].

  • Check for and treat any proliferative retinopathy found in 8.2% of our patients - deteriorating retinopathy in 5.1%
  • Assess kidney function - deteriorating nephropathy in 1.02% of our patients
  • Assess thyroid function
  • Blood pressure control
  • Stop ACE inhibitors; change to methyldopa, apresoline, nifedipine
  • Start folic acid - 400 mcg/day - three months before pregnancy
  • Cardiac evaluation
  • Neurological evaluation
  • Review hypoglycaemic agents being used
  • Stop smoking

Contraindication to pregnancy include:

  1. Severe nephropathy
  2. Uncontrolled hypertension
  3. Unmanageable retinopathy
  4. Active coronary disease

Clinic Management policies

The precise roles of different members of the diabetes pregnancy care team cannot be clearly defined as all members of the team are involved, each adding their own contribution. It is planned that patients will be seen by the Diabetic Team at specific times during their pregnancy in line with the standard schedule given to antenatal patients and in harmony with the routine antenatal care being given to these patients either in the Hospital Antenatal Clinic or by their private specialists.

Visits will be scheduled for:

  • 12-14 weeks
  • 20-22 weeks
  • 28-30 weeks
  • 34 weeks
  • 36 weeks
  • 38 weeks and
  • 6 weeks postpartum.

Of course the scheduled visits will depend on the stage of pregnancy that diagnosis is made. It is thus envisaged that patients with pre-existing disorders would attend all the scheduled visits, whereas patients diagnosed during the pregnancy would attend for visits scheduled during the last trimester. Interim antenatal visits are generally carried out by the attending Specialist Obstetrician unless the clinical condition requires more frequent metabolic follow-up.

There is no need for routine admission in early or late pregnancy, other than when diabetic or obstetric complications of pregnancy are present. However admission may be necessary for those patients with gestational carbohydrate metabolism problems who find it difficult to self-assess their blood glucose levels.

Referral to the Diabetic Pregnancy Joint Clinic will further ensure that these patients are reviewed in the postpartum period, and long-term metabolic advice given accordingly.

It is to be emphasized that the overall responsibility for the patient care and management will remain that of the original attending Specialist Diabetologist and Specialist Obstetrician.

The role of the Joint Clinic is to facilitate and organize regular metabolic and obstetric assessments, including investigations to assess carbohydrate metabolism, renal function, and fetal growth and well-being.

It must be emphasized that the visit regimen proposed above by the Diabetes Pregnancy Joint Clinic is not a comprehensive antenatal regimen since further interim visits to the attending Specialist Obstetrician and diabetologist should be scheduled. In addition, monitoring for fetal well-being in the last month of pregnancy may need to be done more frequently (even twice weekly) that the regimen proposed herein.

 
Targets in Antenatal Care

  • Avoid destroying the normal experience of pregnancy through over zealous application of medical technology.
  • The routine admission of patients in early or late pregnancy is not essential, especially when the patient is undertaking self-monitoring of blood glucose regularly and reliably.
  • All pregnant diabetic women should be seen in a dedicated multidisciplinary combined clinic. The Specialist Team should include a named physician(s) and named obstetrician(s) with a special interest in diabetic pregnancy. These consultants should lead a team and liaison with the dietitian, the diabetes teaching nurse/midwife, and other specialists [neonatologist, ophthalmologist] as required. It is not acceptable for women to have to go to separate clinics on different days.
  • The precise role of the different members of the diabetes pregnancy care team cannot be clearly defined as all members of the team are involved, each adding their own contribution.

*Optimisation of diabetic control

All women should carry out regular blood glucose monitoring. The frequency can be individualized, but pre-prandial testing four times a day - before breakfast, before lunch, before evening meal and before late night snack - is recommended. Occasionally it may be desirable to suggest some post-prandial or night tests. Self-monitoring of blood glucose with a reliable system is the optimum, but this may not be suitable for those women diagnosed as diabetic for the first time late in pregnancy.

The target blood glucose should be as close to normal as possible, while avoiding hypoglycaemia. Each individual should therefore be encouraged to run their blood glucose levels at between 4 and 7 mmol/l [Fasting blood glucose 3.5-5.3 mmol/l or 60-100 mg/dl; 2-hour Post-prandial blood glucose 5.0-7.0 mmol/l or 90-125 mg/dl].

 
  • Fasting BG                <5.3 mmol/l

  • 1 hr post-prandial        7.8 mmol/l

  • 2 hr post-prandial      6.7 mmol/l

  • Mean BG            5.8 mmol/l
 

Long-term control can also be assessed regularly during pregnancy by measuring glycated haemoglobin (<7.0%) or fructosamine, aiming to achieve levels within the normal non-diabetic range.

Insulin regimens should be individualized. It is usually preferable to use human insulin in the form of multiple injections of short acting insulin with long or intermediate acting insulin at night. Alternately, twice daily, short and intermediate acting insulin may be appropriate. In GDM, pharmacological treatment should ideally be introduced if the fasting or pre-meal blood glucose levels consistently exceed 5.5 mmol/l, definitely if the value exceeds 7.0 mmol/l. Recent research has confirmed the safety and clinical efficacy of glibenclamide during pregnancy. Metformin use is still under investigation but appears promising.



ClassFasting/preprandial Blood Glucose2 hour postprandial Blood GlucoseManagment
A1always <5.3 mmol/l always <6.7 mmol/lDiet only
A25.3-7.0 mmol/l6.7-7.0 mmol/lDiet +/- pharmacological Rx
B1>7.0 mmol/l>7.0 mmol/lDiet + Insulin
 

Glibenclamide should be started at 2.5 mg daily with the dose increased every 4-5 days to a maximum of 20 mg/day. If control is not achieved, then the sulphonylurea should be replaced by insulin.

Insulin regimens should be individualized. It is usually preferable to use human insulin in the form of multiple injections of short acting insulin with long or intermediate acting insulin at night. Alternately, twice daily, short and intermediate acting insulin may be appropriate.

Estimation of insulin requirements can be gauged after metabolic daily blood glucose profiles have been obtained. The initial requirements can follow the administration of a short-acting insulin according to a sliding scale, the dose depending of the blood glucose level. The daily requirements can then be assessed and managed by the introduction of intermediate acting insulin.

Sliding Insulin Dose: The use of a sliding plain insulin dosage to correct for elevations in blood glucose levels is recommended whenever the normal regimen prescribed to the patient is not sufficient to maintain optimum control.

 
Blood Glucose levelsInsulin Dose
10.0-12.2 mmol/l
(180-220 mg/dl)
4 units
12.2-13.3 mmol/l
(220-240 mg/dl)
6 units
13.3-15.6 mmol/l
(240-280 mg/dl)
8 units
15.6-16.7 mmol/l
(280-300 mg/dl)
10 units
16.7-18.9 mmol/l
(300-340 mg/dl)
12 units
>18.9 mmol/l
(>340 mg/dl)
14 units
 

Dietary advice is essential for optimal diabetic control during pregnancy. All women who have diabetes should have regular access to a dietitian. Dietary advice should be individualized on the basis of the woman's weight, home blood glucose monitoring, lifestyle and personal circumstances. Food intake should be adequate to maintain maternal and fetal nutrition. An energy prescription of 30-35 kcal/kg pre-pregnant ideal body weight is recommended, though this should be flexible to correct for any alteration in activity levels. Those women whose body weight exceeds 120% of their ideal body weight may require a lower energy intake per kg in order to limit their weight gain during pregnancy. Frequent small meals may facilitate improved blood glucose control.

Complex carbohydrates should provide about 50% of the total calories. This should be distributed in the form of 10-gram exchanges as regular main meals and snacks throughout the day. Levels of dietary fiber of 30-50g per day should be advised. Foods rich in antioxidants - fresh fruits and vegetables - may have aa role in reducing malformations. All foods containing refined sugars, eg cakes, ice cream, sweets, soft drinks, should be strictly avoided preferably by all pregnant women irrespective of their carbohydrate metabolism status.

Folate supplements (4 mg/day) should be routinely prescribed preconceptionally and in the first trimester to reduce the risk of neural tube defects. Exercise helps maintain control and women should be encouraged to walk for about 30 minutes per day.

 
*Screen for diabetic complications

There should be a regular screening for ophthalmic and renal disorders each trimester of pregnancy with regular retinal examinations and measurement of renal function. The blood pressure should be assessed regularly throughout pregnancy in view of the increased risk of the development of pregnancy-induced or gestational hypertension in these patients.

 
*Antenatal Obstetric Surveillance

There are no good data that demonstrate superiority of one type of surveillance program over another. There are wide variations between centers that share good and similar outcome results. Obstetric review in diabetics should be carried out every 2-4 weeks until 28 weeks, then every 2 weeks until 34-36 weeks and then weekly depending on the severity of the metabolic disorder. This can be done in conjunction with the regular attending obstetrician through the use of their joint Antenatal/Diabetic co-operation card.

CLINICAL ASSESSMENT remains critically important. This requires regular assessment of fundal height correlated to gestational age, fetal well-being through fetal heart auscultation, blood pressure measurement, body weight, urine analysis for glucose and protein, and assessment of fetal presentation and engagement in the last trimester.

ULTRASOUND scanning forms the basis of surveillance of the fetus of the diabetic woman to confirm gestational age, exclude congenital malformations, assess fetal growth, and fetal well-being.

 

Gestational Age Assessment:

An early scan in the first trimester helps confirm the gestational age through the measurement of crown-rump length. A repeat scan at 18-22 weeks gestation further confirms the gestational age through the measurement of biparietal diameter and other criteria.

Congenital Malformations:

An ultrasound scan performed at 18-22 weeks also examines for the presence of congenital anomalies. IT IS ESSENTIAL TO PROMOTE PRECONCEPTIONAL CARE AND GOOD METABOLIC CONTROL PRIOR TO EMBARKING ON A PREGNANCY IN WOMEN WITH PREVIOUSLY EXISTING DM OR THOSE WITH A PAST HISTORY OF GDM.

Fetal Growth Assessment:

Serial ultrasound measurements from the late second trimester onwards. using fetal growth parameters including circumference measurements of the abdomen and head are essential to determine normal fetal growth and identify early asymmetric growth acceleration or deceleration. Fetal weight estimates in cases of suspected macrosomia may help in decision-making about mode of delivery.

Fetal Well-being Assessment:

There is no single reliable test for the assessment of fetal well-being. Attention should be targeted at the particular pathology which is suspected. Women with vascular disease and hypertension may have relatively early onset intrauterine growth retardation. Babies of such mother are at very high risk but standard testing with Doppler and biophysical monitoring is likely to be predictive of intrauterine growth retardation and fetal compromise. Serial fetal biophysical profiles based on a modified Manning Score using ultrasonography and cardiotocography are advised. The modified Manning Score below takes into account the presence of increased liquor volume since this may be a sign of inadequately controlled carbohydrate metabolism. Fetal compromise may result from an imbalance between placental function and fetal metabolic demands, such as occurs in macrosomic babies with polyhydramnios. The predictive power of biophysical monitoring for this type of metabolic-based compromise is of short duration.

MODIFIED MANNING SCORE

FETAL VARIABLENormal
(score = 2)
(test x30 min)
Abnormal
(score = 0)
Fetal breathing1+ episode of 30 sec durationAbsent
Fetal movement3+ discrete body or limb movements<3 movements
Fetal tone1+ episode of active extension-flexionSlow or no extension/flexion
Liqour volume1+ pocket diabeter >1 - <7 cmPockets <1 or >7 cm
CTG2+ reactions of FHR to fetal movement
No FHR reactions to movement
 

The timing of starting and the frequency of testing must depend on the risk assessment. However, once to twice weekly monitoring starting at 36 weeks gestation may be considered a reasonable practice, with an earlier onset in the presence of poor diabetic control, vascular disease, or abnormal fetal growth.

FETAL MOVEMENTS ASSESSMENT during the third trimester by the mother herself may have a role in the management of diabetic pregnancies identified as high risk.

 

ANTENATAL MANAGEMENT
SUMMARY

  • Dietary advice should encourage diets with high levels of complex carbohydrates and soluble fibre and reduced saturated fats. Folic acid supplements should be offered.
  • All women should undertake frequent home blood glucose monitoring, and blood glucose levels should be maintained as near normal as possible.
  • Fasting BG <5.3 mmol/l
  • 1 hr post-prandial <7.8 mmol/l
  • 2 hr post-prandial <6.7 mmol/l
  • Mean BG 5.8 mmol/l
  • HbA1c <7.0%
  • Metabolic control should be assessed by measurement of glycated Haemoglobin; and ketonuria should be searched for if blood glucose is high or in the presence of intercurrent illness.
  •  

  • Fundi, blood pressure and renal function should be assessed.
  • Ultrasound scanning must be made available for assessing gestational age, examining for congenital anomalies and for assessing fetal growth.
  • Maternal monitoring of fetal movement should be encouraged. Fetal monitoring with cardiotocography and biophysical profiles is controversial, but it should definitely be used for high risk pregnancies.
  • antenatal image
     
     
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