Physiological Changes During Pregnancy

The human body undergoes significant physiological changes during pregnancy. The cardiovascular system experiences an increase in stroke volume by 30%, heart rate by 15%, and cardiac output by 40%. However, systolic blood pressure remains unchanged, while diastolic blood pressure decreases in the first and second trimesters, returning to non-pregnant levels by term. The enlarged uterus may interfere with venous return, leading to ankle edema, supine hypotension, and varicose veins.

The respiratory system sees an increase in pulmonary ventilation by 40%, with tidal volume increasing from 500 to 700 ml due to the effect of progesterone on the respiratory center. Oxygen requirements increase by only 20%, leading to over-breathing and a fall in pCO2, which can cause a sense of dyspnea accentuated by the elevation of the diaphragm. The basal metabolic rate increases by 15%, possibly due to increased thyroxine and adrenocortical hormones, making warm conditions uncomfortable for women.

The maternal blood volume increases by 30%, mostly in the second half of pregnancy. Red blood cells increase by 20%, but plasma increases by 50%, leading to a decrease in hemoglobin. There is a low-grade increase in coagulant activity, with a rise in fibrinogen and Factors VII, VIII, X. Fibrinolytic activity decreases, returning to normal after delivery, possibly due to placental suppression. This prepares the mother for placental delivery but increases the risk of thromboembolism. Platelet count falls, while white blood cell count and erythrocyte sedimentation rate rise.

The urinary system experiences an increase in blood flow by 30%, with glomerular filtration rate increasing by 30-60%. Salt and water reabsorption increase due to elevated sex steroid levels, leading to increased urinary protein losses. Trace glycosuria is common due to the increased GFR and reduction in tubular reabsorption of filtered glucose.

Calcium requirements increase during pregnancy, especially during the third trimester and lactation. Calcium is transported actively across the placenta, while serum levels of calcium and phosphate fall with a fall in protein. Ionized levels of calcium remain stable, and gut absorption of calcium increases substantially due to increased 1,25 dihydroxy vitamin D.

The liver experiences an increase in alkaline phosphatase by 50%,

Recommendations for Feeding Low-Birthweight Infants

Low-birthweight infants, those with a birthweight of less than 2,500 g, should be exclusively breastfed for the first six months of life, according to WHO recommendations. If the mother’s milk is not available, donor human milk should be sought. If that is not possible, standard formula milk can be used. There is no difference in the duration of exclusive breastfeeding between low-birthweight and normal-weight infants. Daily vitamin A supplementation is not currently recommended for low-birthweight infants, but very low-birthweight infants should receive daily supplementation of vitamin D, calcium, and phosphorus. Low-birthweight infants who are able to breastfeed should start as soon as possible after birth, once they are clinically stable.

When late decelerations are observed on a CTG, it is considered a pathological finding and requires immediate fetal blood sampling to check for fetal hypoxia and acidosis. A pH level of over 7.2 during labor is considered normal, but if fetal acidosis is detected, urgent delivery should be considered. Despite the reassuring normal fetal heart rate and variability, the presence of late decelerations is a worrisome sign that requires prompt investigation and management.

Cardiotocography (CTG) is a medical procedure that measures pressure changes in the uterus using either internal or external pressure transducers. It is used to monitor the fetal heart rate, which normally ranges between 100-160 beats per minute. There are several features that can be observed during a CTG, including baseline bradycardia (heart rate below 100 beats per minute), which can be caused by increased fetal vagal tone or maternal beta-blocker use. Baseline tachycardia (heart rate above 160 beats per minute) can be caused by maternal pyrexia, chorioamnionitis, hypoxia, or prematurity. Loss of baseline variability (less than 5 beats per minute) can be caused by prematurity or hypoxia. Early deceleration, which is a decrease in heart rate that starts with the onset of a contraction and returns to normal after the contraction, is usually harmless and indicates head compression. Late deceleration, on the other hand, is a decrease in heart rate that lags behind the onset of a contraction and does not return to normal until after 30 seconds following the end of the contraction. This can indicate fetal distress, such as asphyxia or placental insufficiency. Variable decelerations, which are independent of contractions, may indicate cord compression.

Safe Pain Relief Options for Breastfeeding Mothers: A Guide to Medications

Breastfeeding mothers often experience pain and discomfort, and it is important to know which pain relief options are safe to use while nursing. Paracetamol and ibuprofen are considered safe and can be used as first-line medication for analgesia. Codeine and other opiates can be used sparingly as third-line medication, but caution must be taken as some women may be slow metabolizers and it can cause drowsiness and respiratory depression in the infant. Aspirin is contraindicated due to the risk of Reye’s disease and other side-effects. Naproxen is generally safe, but paracetamol and ibuprofen should be the mainstay of analgesia. Tramadol can be used with caution and should be prescribed by a specialist. It is important to advise the woman on the safe use of medication and to monitor for any signs of toxicity in the infant.

Management options for breastfeeding problems in new mothers

Breastfeeding is a common challenge for new mothers, and it is important to provide them with effective management options. The first-line option recommended by NICE guidelines is a one-to-one visit from a health visitor or breastfeeding specialist nurse. This allows for observation and advice on optimal positioning, milk expressing techniques, and pain management during breastfeeding. Information leaflets and national breastfeeding support organisation websites can supplement this training, but they are not as effective as one-to-one observation. Prescribing formula milk may be an option if there is evidence of significant weight loss in the baby. It is important to reassure the mother that establishing a good breastfeeding technique can take time, but active support should be provided to maximise the chances of success.

Medical treatments that can be used for postpartum haemorrhage caused by uterine atony include oxytocin, ergometrine, carboprost, and misoprostol. However, only oxytocin/ergometrine is commonly used to promote smooth muscle contraction in uterine blood vessels, which can help reduce the risk of postpartum haemorrhage. Prostaglandin E2 is typically used to initiate labour, while indomethacin and salbutamol can be used as tocolytics. Mifepristone is commonly used in medical abortion.

Understanding Postpartum Haemorrhage

Postpartum haemorrhage (PPH) is a condition where a woman experiences blood loss of more than 500 ml after giving birth vaginally. It can be classified as primary or secondary. Primary PPH occurs within 24 hours after delivery and is caused by the 4 Ts: tone, trauma, tissue, and thrombin. The most common cause is uterine atony. Risk factors for primary PPH include previous PPH, prolonged labour, pre-eclampsia, increased maternal age, emergency Caesarean section, and placenta praevia.

In managing PPH, it is important to involve senior staff immediately and follow the ABC approach. This includes two peripheral cannulae, lying the woman flat, blood tests, and commencing a warmed crystalloid infusion. Mechanical interventions such as rubbing up the fundus and catheterisation are also done. Medical interventions include IV oxytocin, ergometrine, carboprost, and misoprostol. Surgical options such as intrauterine balloon tamponade, B-Lynch suture, ligation of uterine arteries, and hysterectomy may be considered if medical options fail to control the bleeding.

Secondary PPH occurs between 24 hours to 6 weeks after delivery and is typically due to retained placental tissue or endometritis. It is important to understand the causes and risk factors of PPH to prevent and manage this life-threatening emergency effectively.

The Sites of Haematopoiesis in the Fetus and Adult

Haematopoiesis, the process of blood cell formation, occurs in various sites throughout fetal development and in adults. The dominant site of haematopoiesis changes as the fetus develops and bones are formed. Here are the different sites of haematopoiesis and their significance:

Bone Marrow: From four months into childhood and adulthood, bone marrow becomes the primary source of hematopoiesis. Red blood cells and immune effector cells are derived from pluripotent haematopoietic cells, which are first noted in blood islands of the yolk sac. By 20 weeks, almost all of these cells are produced by the bone marrow.

Yolk Sac: Haematopoiesis begins in the yolk sac and in angiogenic cell clusters throughout the embryonic body. This involves the formation of nucleated red blood cells, which differentiate from endothelial cells in the walls of blood vessels. Yolk sac haematopoiesis peaks at about one month and becomes insignificant by three months.

Liver: By the sixth week, the fetal liver performs haematopoiesis. This peaks at 12-16 weeks and continues until approximately 36 weeks. Haematopoietic stem cells differentiate in the walls of liver sinusoids. In adults, there is a reserve haematopoietic capacity, especially in the liver.

Spleen: The spleen is a minor site of haematopoiesis, being active between the third and sixth months.

Lymph Nodes: Lymph nodes are not a significant site of haematopoiesis.

In patients with certain conditions, such as haemolytic anaemia or myeloproliferative disease, hepatic haematopoiesis may be reactivated, leading to hepatomegaly. Understanding the different sites of haematopoiesis is important for understanding blood cell formation and certain medical conditions.

When a pregnant woman with a confirmed DVT is suspected of having a PE, the first step is to immediately administer LMWH to avoid any delay in treatment. PE during pregnancy can be life-threatening for both the mother and the foetus, causing hypoxia and even cardiac arrest. Thrombolysis is not recommended during pregnancy as it can lead to severe haemorrhage in the placenta and foetus. Apixaban is not approved for use during pregnancy and may have teratogenic effects. Similarly, warfarin is not safe during pregnancy and can cause congenital malformations and haemorrhage in the placenta. While a CTPA can be diagnostic, waiting for the scan can be risky for the mother and baby. Therefore, LMWH should be started without delay, and further investigations can be carried out to confirm or rule out a PE.

Investigation of DVT/PE during Pregnancy

Guidelines for investigating deep vein thrombosis (DVT) and pulmonary embolism (PE) during pregnancy were updated in 2015 by the Royal College of Obstetricians. For suspected DVT, compression duplex ultrasound should be performed if there is clinical suspicion. In cases of suspected PE, an ECG and chest x-ray should be performed in all patients. If a woman presents with symptoms and signs of DVT, compression duplex ultrasound should be performed. If DVT is confirmed, no further investigation is necessary, and treatment for venous thromboembolism (VTE) should continue. The decision to perform a ventilation/perfusion (V/Q) scan or computed tomography pulmonary angiography (CTPA) should be made at a local level after discussion with the patient and radiologist.

When comparing CTPA to V/Q scanning in pregnancy, it is important to note that CTPA slightly increases the lifetime risk of maternal breast cancer (up to 13.6%, with a background risk of 1/200 for the study population). Pregnancy makes breast tissue particularly sensitive to the effects of radiation. On the other hand, V/Q scanning carries a slightly increased risk of childhood cancer compared to CTPA (1/50,000 versus less than 1/1,000,000). It is also important to note that D-dimer is of limited use in the investigation of thromboembolism during pregnancy as it is often raised in pregnant women.

The preferred method for diagnosing gestational diabetes is still the oral glucose tolerance test.

Gestational diabetes is a common medical disorder affecting around 4% of pregnancies. Risk factors include a high BMI, previous gestational diabetes, and family history of diabetes. Screening is done through an oral glucose tolerance test, and diagnostic thresholds have recently been updated. Management includes self-monitoring of blood glucose, diet and exercise advice, and medication if necessary. For pre-existing diabetes, weight loss and insulin are recommended, and tight glycemic control is important. Targets for self-monitoring include fasting glucose of 5.3 mmol/l and 1-2 hour post-meal glucose levels.

Breastfeeding women can safely take sertraline or paroxetine as their preferred SSRIs. These medications are known to have minimal to low levels of exposure to infants through breast milk, and are not considered harmful to them. Therefore, if a mother is diagnosed with postnatal depression and requires antidepressant treatment, she should not be advised to stop breastfeeding.

Understanding Postpartum Mental Health Problems

Postpartum mental health problems can range from mild ‘baby-blues’ to severe puerperal psychosis. To screen for depression, healthcare professionals may use the Edinburgh Postnatal Depression Scale, which is a 10-item questionnaire that indicates how the mother has felt over the previous week. A score of more than 13 indicates a ‘depressive illness of varying severity’, with sensitivity and specificity of more than 90%. The questionnaire also includes a question about self-harm.

‘Baby-blues’ is seen in around 60-70% of women and typically occurs 3-7 days following birth. It is more common in primips, and mothers are characteristically anxious, tearful, and irritable. Reassurance and support from healthcare professionals, particularly health visitors, play a key role in managing this condition. Most women with the baby blues will not require specific treatment other than reassurance.

Postnatal depression affects around 10% of women, with most cases starting within a month and typically peaking at 3 months. The features are similar to depression seen in other circumstances, and cognitive behavioural therapy may be beneficial. Certain SSRIs such as sertraline and paroxetine may be used if symptoms are severe. Although these medications are secreted in breast milk, they are not thought to be harmful to the infant.

Puerperal psychosis affects approximately 0.2% of women and requires admission to hospital, ideally in a Mother & Baby Unit. Onset usually occurs within the first 2-3 weeks following birth, and features include severe swings in mood (similar to bipolar disorder) and disordered perception (e.g. auditory hallucinations). There is around a 25-50% risk of recurrence following future pregnancies. Paroxetine is recommended by SIGN because of the low milk/plasma ratio, while fluoxetine is best avoided due to a long half-life.

Causes of Second-Trimester Miscarriage: Incomplete Fusion of Paramesonephric Ducts and Other Factors

Second-trimester miscarriage can have various causes, including a septate or bicornuate uterus, cervical incompetence, and antiphospholipid syndrome or systemic lupus erythematosus. One possible reason for a septate or bicornuate uterus is incomplete fusion of the paramesonephric ducts. However, other factors such as low maternal serum progesterone or a failure of migration of gonadotropin-releasing hormone (GnRH)-secreting neurones from the olfactory placode can also contribute to second-trimester miscarriage. It is important to consider all possible causes when investigating recurrent pregnancy loss.

Management of Breast Conditions: Understanding the Different Treatment Options

Breast conditions can present with a variety of symptoms, and it is important to understand the appropriate management for each. Here are some common breast conditions and their corresponding treatments:

1. Fungal infection of the nipples: This is characterized by bilateral symptoms and signs of nipple thrush. Treatment involves applying a topical miconazole 2% cream to the affected nipples after every feed for two weeks. The infant should also be treated with miconazole cream in the mouth.

2. Paget’s disease of the nipple: This is a form of in situ carcinoma that warrants urgent referral to the Breast team under the 2-week wait pathway. Symptoms include unilateral erythema, inflammation, burning pain, ulceration, and bleeding.

3. Breast cellulitis or mastitis: This is associated with the breast itself and is characterized by unilateral engorgement, erythematosus skin, and tenderness. Treatment involves oral flucloxacillin.

4. Eczema of the nipple: This affects both nipples and presents with a red, scaly rash that spares the base of the nipple. Treatment involves avoiding triggers and using regular emollients, with a topical steroid cream applied after feeds.

5. Bacterial infection of the nipples: This is treated with a topical antibacterial cream, such as topical fusidic acid.

Understanding the appropriate management for each breast condition is crucial in providing effective treatment and improving patient outcomes.

A study conducted in Norway in 2006 revealed that singleton pregnancies conceived through assisted fertilization had a six-fold higher risk of placenta praevia compared to naturally conceived pregnancies. The risk of placenta previa was also nearly three-fold higher in pregnancies following assisted fertilization for mothers who had conceived both naturally and through assisted fertilization. This abnormal placental placement is believed to be linked to the abnormal ovarian stimulation hormones that occur during IVF. Additionally, the incidence of placenta praevia is associated with previous caesarean sections, multiparity, and previous gynaecological surgeries, while the incidence of other options given increases with the number of previous caesarean sections.

Understanding Placenta Praevia

Placenta praevia is a condition where the placenta is located wholly or partially in the lower uterine segment. It is a relatively rare condition, with only 5% of women having a low-lying placenta when scanned at 16-20 weeks gestation. However, the incidence at delivery is only 0.5%, as most placentas tend to rise away from the cervix.

There are several factors associated with placenta praevia, including multiparity, multiple pregnancy, and embryos implanting on a lower segment scar from a previous caesarean section. Clinical features of placenta praevia include shock in proportion to visible loss, no pain, a non-tender uterus, abnormal lie and presentation, and a usually normal fetal heart. Coagulation problems are rare, and small bleeds may occur before larger ones.

Diagnosis of placenta praevia should not involve digital vaginal examination before an ultrasound, as this may provoke severe haemorrhage. The condition is often picked up on routine 20-week abdominal ultrasounds, but the Royal College of Obstetricians and Gynaecologists recommends the use of transvaginal ultrasound for improved accuracy and safety. Placenta praevia is classified into four grades, with grade IV being the most severe, where the placenta completely covers the internal os.

In summary, placenta praevia is a rare condition that can have serious consequences if not diagnosed and managed appropriately. It is important for healthcare professionals to be aware of the associated factors and clinical features, and to use appropriate diagnostic methods for accurate grading and management.

The cardiotocogram shows late decelerations and foetal bradycardia, indicating the need for immediate delivery. Instrumental delivery is not possible and oxytocin and vaginal prostaglandin are contraindicated. The safest approach is an emergency caesarian section.

Cardiotocography (CTG) is a medical procedure that measures pressure changes in the uterus using either internal or external pressure transducers. It is used to monitor the fetal heart rate, which normally ranges between 100-160 beats per minute. There are several features that can be observed during a CTG, including baseline bradycardia (heart rate below 100 beats per minute), which can be caused by increased fetal vagal tone or maternal beta-blocker use. Baseline tachycardia (heart rate above 160 beats per minute) can be caused by maternal pyrexia, chorioamnionitis, hypoxia, or prematurity. Loss of baseline variability (less than 5 beats per minute) can be caused by prematurity or hypoxia. Early deceleration, which is a decrease in heart rate that starts with the onset of a contraction and returns to normal after the contraction, is usually harmless and indicates head compression. Late deceleration, on the other hand, is a decrease in heart rate that lags behind the onset of a contraction and does not return to normal until after 30 seconds following the end of the contraction. This can indicate fetal distress, such as asphyxia or placental insufficiency. Variable decelerations, which are independent of contractions, may indicate cord compression.

Obesity is the only factor among the given options that has been linked to miscarriage. Other factors such as heavy lifting, bumping your tummy, having sex, air travel, and being stressed have not been associated with an increased risk of miscarriage. However, factors like increased maternal age, smoking in pregnancy, consuming alcohol, recreational drug use, high caffeine intake, infections and food poisoning, health conditions, and certain medicines have been linked to an increased risk of miscarriage. Additionally, an unusual shape or structure of the womb and cervical incompetence can also increase the risk of miscarriage.

Miscarriage: Understanding the Epidemiology

Miscarriage, also known as abortion, refers to the expulsion of the products of conception before 24 weeks. To avoid any confusion, the term miscarriage is often used. According to epidemiological studies, approximately 15-20% of diagnosed pregnancies will end in miscarriage during early pregnancy. In fact, up to 50% of conceptions may not develop into a blastocyst within 14 days.

Recurrent spontaneous miscarriage, which is defined as the loss of three or more consecutive pregnancies, affects approximately 1% of women. Understanding the epidemiology of miscarriage is important for healthcare providers and patients alike. It can help to identify risk factors and provide appropriate counseling and support for those who have experienced a miscarriage. By raising awareness and promoting education, we can work towards reducing the incidence of miscarriage and improving the overall health and well-being of women and their families.

To prevent bacterial sepsis in newborns, maternal intravenous antibiotic prophylaxis should be provided to women who have previously given birth to a baby with early- or late-onset GBS disease. GBS is a common cause of sepsis in newborns, particularly in preterm infants with a birth weight of less than 1500 g. GBS is a commensal of the female genital tract and can cause urinary tract infections, septic abortion, and postpartum endometritis in mothers. In newborns, GBS can cause early or late infection, and antibiotics should be administered if signs of sepsis are present at birth.

Group B Streptococcus (GBS) is a common cause of severe infection in newborns. It is estimated that 20-40% of mothers carry GBS in their bowel flora, which can be passed on to their infants during labor and lead to serious infections. Prematurity, prolonged rupture of membranes, previous sibling GBS infection, and maternal pyrexia are all risk factors for GBS infection. The Royal College of Obstetricians and Gynaecologists (RCOG) has published guidelines on GBS management, which include not offering universal screening for GBS to all women and not offering screening based on maternal request. Women who have had GBS detected in a previous pregnancy should be offered intrapartum antibiotic prophylaxis (IAP) or testing in late pregnancy and antibiotics if still positive. IAP should also be offered to women with a previous baby with GBS disease, women in preterm labor, and women with a fever during labor. Benzylpenicillin is the preferred antibiotic for GBS prophylaxis.

Understanding Post-Partum Haemorrhage: Types and Management

Post-partum haemorrhage (PPH) is a common complication of childbirth that can lead to serious maternal morbidity and mortality. There are two types of PPH: primary and secondary. Primary PPH occurs within 24 hours of delivery and is further classified as major or minor based on the amount of blood loss. Major PPH is defined as bleeding from the genital tract with an estimated blood loss of >1000mls, while minor PPH is defined as blood loss <1000mls within 24 hours of delivery. The most common cause of primary PPH is uterine atony. Secondary PPH, on the other hand, occurs from 24 hours until 12 weeks post-partum and is characterized by abnormal bleeding from the genital tract. Any bleeding from 24 hours until 36 hours post-partum with blood loss >500mls is considered secondary PPH.

Management of PPH centers around adequate resuscitation, bimanual uterine compression to stimulate contraction, and the use of IV oxytocin. While obstetric haemorrhage is no longer a major cause of maternal death in developed countries, it remains a significant problem in developing countries. Understanding the types and management of PPH is crucial in preventing maternal morbidity and mortality.

The patient is likely suffering from obstetric cholestasis, which can increase the risk of premature birth and stillbirth. The main symptom is severe itching, and elevated serum bile acids are typically present. Liver function tests, including bilirubin levels, may not be reliable. The most effective treatment is ursodeoxycholic acid (UDCA), which is now mostly synthetic. While antihistamines and topical menthol creams can provide some relief, UDCA is more likely to improve outcomes.

Intrahepatic Cholestasis of Pregnancy: Symptoms and Management

Intrahepatic cholestasis of pregnancy, also known as obstetric cholestasis, is a condition that affects approximately 1% of pregnancies in the UK. It is characterized by intense itching, particularly on the palms, soles, and abdomen, and may also result in clinically detectable jaundice in around 20% of patients. Raised bilirubin levels are seen in over 90% of cases.

The management of intrahepatic cholestasis of pregnancy typically involves induction of labor at 37-38 weeks, although this practice may not be evidence-based. Ursodeoxycholic acid is also widely used, although the evidence base for its effectiveness is not clear. Additionally, vitamin K supplementation may be recommended.

It is important to note that the recurrence rate of intrahepatic cholestasis of pregnancy in subsequent pregnancies is high, ranging from 45-90%. Therefore, close monitoring and management are necessary for women who have experienced this condition in the past.

Eclampsia: Diagnosis and Treatment Options

Eclampsia is a serious complication of pregnancy that requires prompt diagnosis and treatment. It is a multisystem disorder characterized by hypertension, proteinuria, and edema, and can lead to seizures and coma if left untreated. The definitive treatment for eclampsia is delivery of the fetus, which should be undertaken as soon as the mother is stabilized.

Seizures should be treated with magnesium sulfate infusions, while phenytoin and diazepam are second-line treatment agents. Pregnant women should be monitored for signs of pre-eclampsia, which can progress to eclampsia if left untreated.

While it is important to rule out other intracranial pathology with CT imaging of the brain, it is not indicated in the treatment of eclampsia. Hydralazine or labetalol infusion is the treatment of choice for hypertension in the setting of pre-eclampsia/eclampsia.

Following an eclamptic episode, around 50% of patients may experience a transient neurological deficit. Therefore, prompt diagnosis and treatment are crucial to prevent serious complications and ensure the best possible outcome for both mother and baby.

A cut-off of 110 g/L should be used in the first trimester to determine if iron supplementation is necessary. This is because pregnancy causes a high-volume, low-pressure state which can dilute the blood and lower haemoglobin levels. Therefore, a lower cut-off is used compared to the canonical 115 g/L. In women after delivery, the cut-off is haemoglobin lower than 100 g/L, while in women during the second and third trimesters, it is haemoglobin lower than 105 g/L. Haemoglobin lower than 115 g/L is the cut-off for non-pregnant women, while haemoglobin lower than 120 g/L is never used as a cut-off for iron replacement therapy as it is within the normal range.

During pregnancy, women are checked for anaemia twice – once at the initial booking visit (usually around 8-10 weeks) and again at 28 weeks. The National Institute for Health and Care Excellence (NICE) has set specific cut-off levels to determine if a pregnant woman requires oral iron therapy. These levels are less than 110 g/L in the first trimester, less than 105 g/L in the second and third trimesters, and less than 100 g/L postpartum.

If a woman’s iron levels fall below these cut-offs, she will be prescribed oral ferrous sulfate or ferrous fumarate. It is important to continue this treatment for at least three months after the iron deficiency has been corrected to allow the body to replenish its iron stores. By following these guidelines, healthcare professionals can help ensure that pregnant women receive the appropriate care to prevent and manage anaemia during pregnancy.

Neonatal Seizures: Likely Causes and Differential Diagnosis

Neonatal seizures can be a cause of concern for parents and healthcare providers. The most common cause of neonatal seizures is hypoglycaemia, which can occur in neonates born to mothers with gestational diabetes. Hypoglycaemia can lead to significant morbidity and mortality if left untreated. Other possible causes of neonatal seizures include hypoxic ischaemic encephalopathy, neonatal sepsis, intracranial haemorrhage, and benign familial neonatal seizures. However, in the absence of prematurity or complicated delivery, hypoglycaemia is the most likely cause of neonatal seizures in a term baby born to a mother with gestational diabetes. Diagnosis and treatment should be prompt to prevent long-term complications.

The sudden collapse that occurred shortly after the rupture of membranes suggests the possibility of amniotic fluid embolism. The patient’s condition is too severe to be attributed to a simple vasovagal event. While amniotic fluid emboli can indirectly cause myocardial infarctions, it is difficult to diagnose a primary myocardial infarction without any mention of preceding chest pain. Typically, occult bleeding and hypovolemic shock would develop gradually. Although postural orthostatic tachycardia syndrome is more prevalent in women of reproductive age, it would not cause the significant hypotension observed in this case.

Amniotic fluid embolism is a rare but serious complication of pregnancy that can result in a high mortality rate. It occurs when fetal cells or amniotic fluid enter the mother’s bloodstream, triggering a reaction that leads to various signs and symptoms. While several risk factors have been associated with this condition, such as maternal age and induction of labor, the exact cause remains unclear. It is believed that exposure of maternal circulation to fetal cells or amniotic fluid is necessary for the development of an amniotic fluid embolism, but the underlying pathology is not well understood.

The majority of cases of amniotic fluid embolism occur during labor, but they can also occur during a cesarean section or in the immediate postpartum period. Symptoms of this condition include chills, shivering, sweating, anxiety, and coughing, while signs may include cyanosis, hypotension, bronchospasms, tachycardia, arrhythmia, and myocardial infarction. Diagnosis is primarily clinical and based on exclusion, as there are no definitive diagnostic tests available.

Management of amniotic fluid embolism requires a multidisciplinary team and critical care unit. Treatment is mainly supportive, focusing on addressing the patient’s symptoms and stabilizing their condition. Given the high mortality rate associated with this condition, prompt recognition and management are crucial for improving outcomes.

Types of Miscarriage: Understanding the Differences

Miscarriage is a devastating experience for any woman. It is important to understand the different types of miscarriage to help manage the situation and provide appropriate care. Here are the different types of miscarriage and their characteristics:

Inevitable Miscarriage: This occurs when the products of conception are being passed vaginally, and the cervical os is open. It is an inevitable event.

Complete Miscarriage: This occurs when all the products of conception have been passed, and the cervical os is closed.

Threatened Miscarriage: This is characterised by vaginal bleeding and cramps, but the patient is not passing tissue vaginally. The uterus is of the right size for dates, and the cervical os is closed.

Septic Miscarriage: This occurs when there are retained products of conception in the uterus or cervical canal, leading to infection. The cervical os is likely to be open.

Missed Miscarriage: This is when the fetus dies in utero but is not expelled from the uterus. The uterus is small for dates, and the cervical os is closed.

Understanding the different types of miscarriage can help healthcare providers provide appropriate care and support to women experiencing this difficult event.

Pregnant women with a BMI greater than 30 kg/m2, regardless of their medical history, should receive a high dose of 5mg folic acid to prevent neural tube defects. Iron supplementation may be necessary for those with iron-deficiency anemia, but it is not currently indicated for this patient. Low-dose folic acid supplementation may be appropriate for non-obese pregnant women. Vitamin B12 supplementation is necessary for those with a deficiency, but it is not currently indicated for this patient. Vitamin D supplementation may be necessary for those with a deficiency, but it is not currently indicated for this patient unless she has risk factors such as dark skin and modest clothing.

Folic Acid: Importance, Deficiency, and Prevention

Folic acid is a vital nutrient that is converted to tetrahydrofolate (THF) in the body. It is found in green, leafy vegetables and plays a crucial role in the transfer of 1-carbon units to essential substrates involved in the synthesis of DNA and RNA. However, certain factors such as phenytoin, methotrexate, pregnancy, and alcohol excess can cause a deficiency in folic acid. This deficiency can lead to macrocytic, megaloblastic anemia and neural tube defects.

To prevent neural tube defects during pregnancy, it is recommended that all women take 400mcg of folic acid until the 12th week of pregnancy. Women at higher risk of conceiving a child with a neural tube defect should take 5mg of folic acid from before conception until the 12th week of pregnancy. Women are considered higher risk if they or their partner has a neural tube defect, they have had a previous pregnancy affected by a neural tube defect, or they have a family history of a neural tube defect. Additionally, women with certain medical conditions such as coeliac disease, diabetes, or thalassaemia trait, or those taking antiepileptic drugs, or who are obese (BMI of 30 kg/m2 or more) are also considered higher risk.

In summary, folic acid is an essential nutrient that plays a crucial role in DNA and RNA synthesis. Deficiency in folic acid can lead to serious health consequences, including neural tube defects. However, taking folic acid supplements during pregnancy can prevent these defects and ensure a healthy pregnancy.

To prevent neural tube defects, it is recommended that women who are at risk start taking folic acid before conception. The standard dose of 0.4mg should be taken daily until 13 weeks of pregnancy. It is important to start taking folic acid before conception because the neural tube is formed within the first 28 days of embryo development. If a woman waits until after her missed period, any defects may already be present. Women who are at an increased risk of neural tube defects, such as those who have had a previous child with NTD, diabetes mellitus, are on antiepileptic medication, are obese (with a body mass index over 30 kg/m²), are HIV positive and taking co-trimoxazole, or have sickle cell disease, should take an increased dose of 5mg folic acid.

Folic Acid: Importance, Deficiency, and Prevention

Folic acid is a vital nutrient that is converted to tetrahydrofolate (THF) in the body. It is found in green, leafy vegetables and plays a crucial role in the transfer of 1-carbon units to essential substrates involved in the synthesis of DNA and RNA. However, certain factors such as phenytoin, methotrexate, pregnancy, and alcohol excess can cause a deficiency in folic acid. This deficiency can lead to macrocytic, megaloblastic anemia and neural tube defects.

To prevent neural tube defects during pregnancy, it is recommended that all women take 400mcg of folic acid until the 12th week of pregnancy. Women at higher risk of conceiving a child with a neural tube defect should take 5mg of folic acid from before conception until the 12th week of pregnancy. Women are considered higher risk if they or their partner has a neural tube defect, they have had a previous pregnancy affected by a neural tube defect, or they have a family history of a neural tube defect. Additionally, women with certain medical conditions such as coeliac disease, diabetes, or thalassaemia trait, or those taking antiepileptic drugs, or who are obese (BMI of 30 kg/m2 or more) are also considered higher risk.

In summary, folic acid is an essential nutrient that plays a crucial role in DNA and RNA synthesis. Deficiency in folic acid can lead to serious health consequences, including neural tube defects. However, taking folic acid supplements during pregnancy can prevent these defects and ensure a healthy pregnancy.

It should be noted that a significant percentage of women who experience threatened miscarriages will ultimately miscarry. Additionally, it is crucial to consider the possibility of an ectopic pregnancy in pregnant patients who present with both pain and bleeding.

Miscarriage is a common complication that can occur in up to 25% of all pregnancies. There are different types of miscarriage, each with its own set of symptoms and characteristics. Threatened miscarriage is painless vaginal bleeding that occurs before 24 weeks, typically at 6-9 weeks. The bleeding is usually less than menstruation, and the cervical os is closed. Missed or delayed miscarriage is when a gestational sac containing a dead fetus is present before 20 weeks, without the symptoms of expulsion. The mother may experience light vaginal bleeding or discharge, and the symptoms of pregnancy may disappear. Pain is not usually a feature, and the cervical os is closed. Inevitable miscarriage is characterized by heavy bleeding with clots and pain, and the cervical os is open. Incomplete miscarriage occurs when not all products of conception have been expelled, and there is pain and vaginal bleeding. The cervical os is open in this type of miscarriage.

Category 2 caesarean sections are performed when there is a non-immediate life-threatening emergency concerning the mother or the baby. This may include an abnormality detected by cardiotocography that requires an emergency caesarean section within 75 minutes of the decision being made. It is not immediately life-threatening to either the mother or the baby.

Category 1 caesarean sections are performed in immediately life-threatening situations, such as haemodynamic instability of the mother.

Category 3 caesarean sections are not immediately life-threatening to the mother but are necessary for the non-immediate life-threatening condition of the baby, such as distress.

Category 4 caesarean sections are elective and may be chosen by the mother or recommended based on past medical history.

Caesarean Section: Types, Indications, and Risks

Caesarean section, also known as C-section, is a surgical procedure that involves delivering a baby through an incision in the mother’s abdomen and uterus. In recent years, the rate of C-section has increased significantly due to an increased fear of litigation. There are two main types of C-section: lower segment C-section, which comprises 99% of cases, and classic C-section, which involves a longitudinal incision in the upper segment of the uterus.

C-section may be indicated for various reasons, including absolute cephalopelvic disproportion, placenta praevia grades 3/4, pre-eclampsia, post-maturity, IUGR, fetal distress in labor/prolapsed cord, failure of labor to progress, malpresentations, placental abruption, vaginal infection, and cervical cancer. The urgency of C-section may be categorized into four categories, with Category 1 being the most urgent and Category 4 being elective.

It is important for clinicians to inform women of the serious and frequent risks associated with C-section, including emergency hysterectomy, need for further surgery, admission to intensive care unit, thromboembolic disease, bladder injury, ureteric injury, and death. C-section may also increase the risk of uterine rupture, antepartum stillbirth, placenta praevia, and placenta accreta in subsequent pregnancies. Other complications may include persistent wound and abdominal discomfort, increased risk of repeat C-section, readmission to hospital, haemorrhage, infection, and fetal lacerations.

Vaginal birth after C-section (VBAC) may be an appropriate method of delivery for pregnant women with a single previous C-section delivery, except for those with previous uterine rupture or classical C-section scar. The success rate of VBAC is around 70-75%.

As a medical student, you may not be required to interpret fetal CTGs, but you should have a basic understanding of their purpose and key features. A CTG measures fetal heart rate and uterine contractions and is used when there are risk factors for fetal hypoxia. While CTGs are not specific and can lead to increased medical intervention, changes in fetal heart rate should be taken seriously as they indicate fetal distress.

To interpret a CTG, you can use the mnemonic DR C BRA VADO. DR stands for defining the patient’s risk factors for being on a CTG monitor, while C refers to counting the number of contractions in 10 minutes. BRA stands for baseline rate and variability, with a normal fetal baseline rate being 110-160 beats per minute and variability ranging from 5 to 25 beats per minute. A refers to accelerations, which are rises in fetal heart rate, and D refers to decelerations, which are reductions in fetal heart rate. Late decelerations, which are slow to recover, are particularly concerning as they indicate fetal hypoxia.

As a medical student, it is important to be aware of terminal bradycardia and terminal decelerations, which are indicators for emergency caesarean section. Other changes in CTG features are usually investigated with fetal scalp blood sampling and an ABG to check for acidosis. The NICE guidelines provide a useful table for interpreting CTG features and determining appropriate management, ranging from normal care to urgent intervention.

Cardiotocography (CTG) is a medical procedure that measures pressure changes in the uterus using either internal or external pressure transducers. It is used to monitor the fetal heart rate, which normally ranges between 100-160 beats per minute. There are several features that can be observed during a CTG, including baseline bradycardia (heart rate below 100 beats per minute), which can be caused by increased fetal vagal tone or maternal beta-blocker use. Baseline tachycardia (heart rate above 160 beats per minute) can be caused by maternal pyrexia, chorioamnionitis, hypoxia, or prematurity. Loss of baseline variability (less than 5 beats per minute) can be caused by prematurity or hypoxia. Early deceleration, which is a decrease in heart rate that starts with the onset of a contraction and returns to normal after the contraction, is usually harmless and indicates head compression. Late deceleration, on the other hand, is a decrease in heart rate that lags behind the onset of a contraction and does not return to normal until after 30 seconds following the end of the contraction. This can indicate fetal distress, such as asphyxia or placental insufficiency. Variable decelerations, which are independent of contractions, may indicate cord compression.

In cases where pregnant women experience severe nausea and vomiting leading to ketonuria and dehydration, admission to the hospital should be considered. This is especially true if they have already tried oral anti-emetics without success. Such symptoms are indicative of hyperemesis gravidarum, which can be confirmed by urine dipstick and increased blood urea levels. While pyridoxine is not recommended by the Royal College of Obstetricians and Gynaecologists (RCOG), ondansetron is effective as a second-line option. However, inpatient treatment is necessary. Gastroscopy is unlikely to be helpful at this stage, even if there is a small amount of blood in the vomit, which is likely due to a Mallory-Weiss tear caused by constant retching. Low K+ levels due to vomiting need to be replaced, and anti-emetics are necessary. Therefore, admission to the hospital for IV fluids, anti-emetics, and a trial of a bland diet is the appropriate course of action.

Hyperemesis gravidarum is an extreme form of nausea and vomiting of pregnancy that occurs in around 1% of pregnancies and is most common between 8 and 12 weeks. It is associated with raised beta hCG levels and can be caused by multiple pregnancies, trophoblastic disease, hyperthyroidism, nulliparity, and obesity. Referral criteria for nausea and vomiting in pregnancy include continued symptoms with ketonuria and/or weight loss, a confirmed or suspected comorbidity, and inability to keep down liquids or oral antiemetics. The diagnosis of hyperemesis gravidarum requires the presence of 5% pre-pregnancy weight loss, dehydration, and electrolyte imbalance. Management includes first-line use of antihistamines and oral cyclizine or promethazine, with second-line options of ondansetron and metoclopramide. Admission may be needed for IV hydration. Complications can include Wernicke’s encephalopathy, Mallory-Weiss tear, central pontine myelinolysis, acute tubular necrosis, and fetal growth issues.

If there is evidence of infection or an increased risk of hemorrhage, expectant management is not appropriate for a miscarriage. A patient with first-trimester vaginal bleeding, a dilated cervical os, and an intrauterine sac without fetal cardiac activity is experiencing an inevitable miscarriage. Miscarriages can be managed through expectant, pharmacological, or surgical means. Expectant management involves bed rest, avoiding strenuous physical activity, and weekly follow-up pelvic ultrasounds. This approach is typically recommended for patients with a threatened miscarriage that presents as vaginal bleeding. The threatened miscarriage may resolve on its own or progress to an inevitable, incomplete, or complete miscarriage. However, in this case, the open cervical os and absent fetal cardiac activity indicate that the miscarriage is inevitable, and the fetus is no longer viable. Medical management involves using drugs like misoprostol or methotrexate to medically evacuate retained products of conception in inevitable or incomplete miscarriages. Nevertheless, this patient is experiencing heavy vaginal bleeding, which has caused hypotension and tachycardia, making her hemodynamically unstable. In all cases of early pregnancy loss with hemodynamic instability, urgent surgical evacuation of products of conception is necessary to minimize further blood loss. Dilation and curettage is a common and controlled method of uterine evacuation.

Management Options for Miscarriage

Miscarriage can be a difficult and emotional experience for women. In the 2019 NICE guidelines, three types of management for miscarriage were discussed: expectant, medical, and surgical. Expectant management involves waiting for a spontaneous miscarriage and is considered the first-line option. However, if it is unsuccessful, medical or surgical management may be offered.

Medical management involves using tablets to expedite the miscarriage. Vaginal misoprostol, a prostaglandin analogue, is used to cause strong myometrial contractions leading to the expulsion of tissue. It is important to advise patients to contact their doctor if bleeding does not start within 24 hours. Antiemetics and pain relief should also be given.

Surgical management involves undergoing a surgical procedure under local or general anaesthetic. The two main options are vacuum aspiration (suction curettage) or surgical management in theatre. Vacuum aspiration is done under local anaesthetic as an outpatient, while surgical management is done in theatre under general anaesthetic. This was previously referred to as ‘Evacuation of retained products of conception’.

It is important to note that some situations are better managed with medical or surgical management, such as an increased risk of haemorrhage, being in the late first trimester, having coagulopathies or being unable to have a blood transfusion, previous adverse and/or traumatic experience associated with pregnancy, evidence of infection, and more. Ultimately, the management option chosen should be based on the individual patient’s needs and preferences.