Next Lesson - Physiology of the Fetus
Contents
Abstract
- Gestational diabetes is a condition of pregnancy relating to insulin resistance (the body's cells respond poorly to insulin) that usually goes away after birth. It increases the risk of macrosomia (a larger than normal baby) and, rarely, fetal death (stillbirth). Treatment is diet and exercise changes, with metformin (a tablet that lowers blood glucose) or insulin added if blood glucose targets are not met, or insulin straight away if the fasting plasma glucose (blood glucose after fasting) at diagnosis is 7.0 millimoles per litre (mmol/L) or more. Risk factors include a BMI of 30 kg/m² or more, a first-degree relative (such as a parent, brother or sister) with diabetes, a previous baby weighing 4.5 kg or more, previous gestational diabetes, and an ethnicity with a high prevalence of diabetes.
- Pre-eclampsia involves new hypertension after 20 weeks of pregnancy, together with at least one of: new proteinuria (protein in the urine), maternal organ dysfunction or uteroplacental dysfunction (the placenta not working properly). It can first present after birth. Risk factors include age 40 years or over, a BMI of 35 kg/m² or more, high blood pressure or pre-eclampsia in a previous pregnancy, a family history of pre-eclampsia, and some existing conditions such as chronic hypertension, kidney disease, autoimmune disease or diabetes. Management includes antihypertensives (drugs that lower blood pressure) and appropriately timed birth, followed by continued maternal monitoring.
Core
Gestational diabetes is a condition characterised by episodes of hyperglycaemia (high blood glucose) during pregnancy due to insulin resistance (the body's cells respond poorly to insulin). Gestational diabetes usually goes away after birth. Pregnancy normally makes the mother's cells less responsive to insulin, and the pancreas normally makes extra insulin to compensate. Gestational diabetes develops when the pancreas cannot make enough extra insulin. Women who already have insulin resistance, for example with obesity, are more likely to develop gestational diabetes. NICE advises assessing the risk at the booking appointment (the first appointment with a midwife or doctor in pregnancy). The assessment uses the risk factors listed below, not blood tests such as fasting glucose or HbA1c (a measure of average blood glucose over the past 2 to 3 months). Women with a risk factor are offered testing.
Clinical implications of gestational diabetes can be serious and include:
- Miscarriage and congenital malformation (a structural problem present from birth) are recognised risks of diabetes that was already present before pregnancy, particularly when blood glucose is high in early pregnancy. In gestational diabetes the malformation risk is only slightly raised, probably because some women have undiagnosed type 2 diabetes. NICE therefore advises measuring HbA1c when gestational diabetes is diagnosed, to find women who may already have type 2 diabetes. Good glycaemic control (keeping blood glucose within target) reduces these risks.
- Increased incidence of macrosomia (a larger than normal baby). Macrosomia increases risk of shoulder dystocia which is an obstetric emergency (an emergency in childbirth; obstetrics is the care of women in pregnancy and birth). Shoulder dystocia is when the shoulders of the baby get stuck in the birth canal. This can lead to significant fetal morbidity and mortality. There can also be a risk to the mother of postpartum haemorrhage (heavy bleeding after birth) and perineal tears (tears of the perineum, the area between the vagina and anus). Brachial plexus injury (damage to the nerves that supply the arm) to the baby is also possible.
- Increased risk of hypertensive disorders of pregnancy (conditions with high blood pressure in pregnancy). These include gestational hypertension (new high blood pressure after 20 weeks of pregnancy, without significant protein in the urine and without the other features of pre-eclampsia listed below) and pre-eclampsia.
- Increased risk of developing Type 2 Diabetes Mellitus (T2DM) after delivery.
Diagnosis of gestational diabetes is by a 75 g oral glucose tolerance test (a fasting blood test, then a 75 g glucose drink, then a second blood test 2 hours later). Gestational diabetes is diagnosed if the fasting plasma glucose is 5.6 millimoles per litre (mmol/L) or more, or the 2 hour plasma glucose is 7.8 mmol/L or more. Women with a risk factor (listed below) are offered this test at 24 to 28 weeks of pregnancy. Women who have had gestational diabetes before are offered either early self-monitoring of blood glucose or the test as soon as possible after booking. They are then offered a second test at 24 to 28 weeks if the first is normal.
- Dietary modification, similar to initial management of T2DM, focusing on balanced meals and controlled carbohydrate intake (for example regular meals, low glycaemic index starchy foods that release sugar slowly, and fewer sugary foods and drinks).
- Regular exercise, such as walking for 30 minutes after a meal.
- Referral to a dietitian (a specialist in food and nutrition)
- Self-monitoring of blood glucose with finger-prick tests, usually fasting and 1 hour after each meal. NICE advises target levels below 5.3 mmol/L fasting and below 7.8 mmol/L 1 hour after meals.
- Medicines: if the fasting plasma glucose at diagnosis is below 7 mmol/L, diet and exercise changes are tried first. Metformin (a tablet that lowers blood glucose) is offered if targets are not met within 1 to 2 weeks, and insulin is added if targets are still not met. Insulin is offered instead if metformin cannot be used or is not acceptable to the woman. If the fasting plasma glucose at diagnosis is 7.0 mmol/L or more, insulin (with or without metformin) is offered straight away, with diet and exercise changes. Immediate insulin, with or without metformin, can also be considered if the fasting plasma glucose is 6.0 to 6.9 mmol/L and there are complications such as macrosomia or hydramnios (too much amniotic fluid, the fluid around the baby).
- Ultrasound scans of fetal growth and amniotic fluid volume (the fluid around the baby) every 4 weeks from 28 to 36 weeks, to look for macrosomia.
- Timing of birth: women with gestational diabetes are advised to give birth no later than 40 weeks plus 6 days. Induction of labour (starting labour artificially) or caesarean section (an operation to deliver the baby through the abdomen) is offered if they have not given birth by then. Earlier birth is considered if there are maternal or fetal complications.
- After birth: glucose-lowering medicines are stopped immediately. A fasting plasma glucose test is offered 6 to 13 weeks after the birth to exclude diabetes. If it is normal, an HbA1c test is offered every year, because of the raised risk of type 2 diabetes.
- Maternal BMI of 30 kg/m² or more
- A first-degree relative (such as a parent, brother or sister) with diabetes
- Previous baby weighing 4.5 kg or more (macrosomia)
- Previous gestational diabetes
- An ethnicity with a high prevalence of diabetes: South Asian, Black, African-Caribbean or Middle Eastern origin
Pre-eclampsia is a potentially serious multisystem disorder (a disorder that can affect many organs). Pre-eclampsia is defined by new hypertension after 20 weeks of pregnancy in a woman whose blood pressure was previously normal (normotensive). Hypertension here means a systolic blood pressure of 140 mmHg or more, or a diastolic blood pressure of 90 mmHg or more. At least one other new feature must also be present: proteinuria (protein in the urine), maternal organ dysfunction (for example kidney, liver, nervous system or blood problems) or uteroplacental dysfunction (the placenta not working properly), such as fetal growth restriction (the baby growing more slowly than expected). Proteinuria is not essential when the other diagnostic features are present. Pre-eclampsia can also first present after birth.
The pathophysiology of pre-eclampsia (how the disease develops) is complex and incompletely understood. Inadequate remodelling of the maternal spiral arteries (the small arteries in the wall of the uterus that supply the placenta) means that they do not widen as they normally should in early pregnancy. This can contribute to placental hypoperfusion and dysfunction (poor blood flow to the placenta, which then works poorly). Placental factors acting on the maternal circulation contribute to systemic endothelial dysfunction (damage to the cells lining blood vessels throughout the body), vasoconstriction and increased vascular permeability (leakier blood vessels). This produces hypertension and can injure several organs; injury to the endothelium of the glomeruli (the filters in the kidney) can cause proteinuria. Reduced uteroplacental perfusion can also impair fetal growth.
- Often no symptoms at first: raised blood pressure and protein in the urine are usually picked up at routine checks in pregnancy
- Severe headache that does not go away with simple painkillers
- Visual disturbances (blurred vision or flashing lights)
- Hyperreflexia (overactive reflexes)
- Sudden swelling of the face, hands or feet (oedema)
- Seizures (fits): in a woman with pre-eclampsia these are called eclampsia, a serious complication rather than an early symptom
- Right upper quadrant pain (severe pain just below the ribs on the right, from liver involvement)
- Vomiting
- Maternal age 40 years or over
- Maternal obesity (BMI of 35 kg/m² or more at the first appointment in pregnancy)
- High blood pressure or pre-eclampsia in a previous pregnancy, or a family history of pre-eclampsia
- Existing conditions: chronic hypertension (high blood pressure that is present before 20 weeks of pregnancy), chronic kidney disease, autoimmune disease (the immune system attacks the body's own tissues) such as systemic lupus erythematosus or antiphospholipid syndrome, or type 1 or type 2 diabetes
- A first pregnancy, more than 10 years since the last pregnancy, or a multi-fetal pregnancy (more than one baby, such as twins)
Risk factors matter because they identify who is advised to take aspirin 75 mg to 150 mg daily from 12 weeks of pregnancy until the birth. This applies to women at high risk (previous hypertensive disease in pregnancy, chronic kidney disease, autoimmune disease, diabetes or chronic hypertension). It also applies to women with more than one moderate risk factor (a first pregnancy, age 40 years or over, more than 10 years since the last pregnancy, a BMI of 35 kg/m² or more, a family history of pre-eclampsia, or a multi-fetal pregnancy).
- Birth and delivery of the placenta address the placental component of pre-eclampsia. Timing depends on gestation (how many weeks pregnant the woman is) and on the condition of the mother and baby. From 37 weeks, birth is started within 24 to 48 hours. Before 37 weeks (preterm), the woman is monitored closely unless there are signs that justify planned early birth. These signs include blood pressure that cannot be controlled, worsening liver, kidney or blood test results, or ongoing severe neurological features. A senior obstetrician (a doctor who specialises in pregnancy and childbirth) is involved in the decision. The disorder can persist or first present after birth, so treatment and monitoring must continue as clinically indicated.
- Antihypertensives (drugs that lower blood pressure). Labetalol (a beta blocker, which slows the heart and lowers blood pressure) is offered first. Nifedipine (a calcium channel blocker, which relaxes the walls of blood vessels) is offered if labetalol is not suitable, and methyldopa (which acts on the brain to lower blood pressure) if neither is suitable. Treatment is offered if blood pressure stays above 140/90 mmHg, and to all women with severe hypertension (systolic blood pressure over 160 mmHg or diastolic blood pressure over 110 mmHg). The aim is a blood pressure of 135/85 mmHg or less.
- Intravenous (into a vein) magnesium sulfate, a drug that prevents and treats fits, is given in critical care to women with severe hypertension or severe pre-eclampsia who have had an eclamptic fit (a fit caused by eclampsia). It is also offered, with antenatal corticosteroids (steroids given before birth to help the baby's lungs mature), when early birth is planned for preterm pre-eclampsia, if indicated.
Edited by: Dr. Ben Appleby
Reviewed by: Dr. Thomas Burnell and Dr. Marcus Judge
Quiz
- 5024


