Complications in pregnancy and maternal medicine Flashcards

1
Q

Pre-eclampsia

A

Pre-eclampsia refers to new high blood pressure (hypertension) in pregnancy with end-organ dysfunction, notably with proteinuria (protein in the urine).

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2
Q

When does pre-eclampsia usually occur?

A

After 20 weeks gestation

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3
Q

Triad of pre-eclampsia

A

HTN
proteinuria
oedema

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4
Q

Pregnancy-induced HTN

A

Pregnancy-induced hypertension or gestational hypertension is hypertension occurring after 20 weeks gestation, without proteinuria.

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5
Q

Chronic HTN

A

Chronic hypertension is high blood pressure that exists before 20 weeks gestation and is longstanding. This is not caused by dysfunction in the placenta and is not classed as pre-eclampsia.

BP >140/90mmHg on 2 occasions >4 hours apart

Single reading of diastolic BP >110mmHg

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6
Q

Causes of pre-eclampsia

A

Multifactorial

Genetic (FH)

Poor placentation

Immunological (poorly developed gestational immune tolerance)

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7
Q

High risk-factors for pre-eclampsia

A

Pre-existing hypertension

Previous hypertension in pregnancy

Existing autoimmune conditions (e.g. systemic lupus erythematosus)

Diabetes

Chronic kidney disease

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8
Q

Moderate-risk factors for pre-eclampsia

A

Older than 40

BMI > 35

More than 10 years since previous pregnancy

Multiple pregnancy

First pregnancy

Family history of pre-eclampsia

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9
Q

aspirin for pre-eclampsia prophylaxis

A

12 weeks until birth

one high risk factor or >3 moderate risk factors

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10
Q

dalteparin in pre-eclampsia

A

Give Dalteparin if anti-phospholipid syndrome or other pro-coagulant disorders

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11
Q

symptoms of pre-eclampsia

A

Headache

Visual disturbance or blurriness

Nausea and vomiting

Upper abdominal or epigastric pain (this is due to liver swelling)

Oedema

Reduced urine output

Brisk reflexes

Reduced fetal movement

Bleeding

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12
Q

signs of pre-eclampsia

A

HTN

Proteinuria

Non-dependent oedema

Hyper-reflexia/ clonus

Fetal growth restriction

Oligohydraminos

Abnormal fetal Doppler

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13
Q

maternal investigations pre-eclapmsia

A

Platelet count

Renal function: U&E and eGFR

LFT

DIC: coagulation profile in severe cases or thrombocytopenia

Level of proteinuria (PCR, 24 hour collection)

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14
Q

fetal investigations pre-eclampsia

A

Growth velocity (fetal growth ultrasound)

Fetal wellbeing (CTG, amniotic fluid volume, fetal Doppler)

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15
Q

diagnosis of pre-eclampsia

A

The NICE guidelines (2019) advise a diagnosis can be made with a:

Systolic blood pressure above 140 mmHg

Diastolic blood pressure above 90 mmHg

Cuff at heart level

Korotkoff phase V should be used

PLUS any of:
Proteinuria (1+ or more on urine dipstick)

Organ dysfunction (e.g. raised creatinine, elevated liver enzymes, seizures, thrombocytopenia or haemolytic anaemia)

Placental dysfunction (e.g. fetal growth restriction or abnormal Doppler studies). Low PIGF

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16
Q

Proteinuria pre-eclampsia

A

Urine protein:creatinine ratio (above 30mg/mmol is significant)

Urine albumin:creatinine ratio (above 8mg/mmol is significant)

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17
Q

management gestational HTN

A

Treating to aim for a blood pressure below 135/85 mmHg

Admission for women with a blood pressure above 160/110 mmHg

Review medication if blood pressure stays below 110/70

Urine dipstick testing at least weekly

Monitoring of blood tests weekly (full blood count, liver enzymes and renal profile)

Monitoring fetal growth by serial growth scans

PlGF testing on one occasion

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18
Q

pre-eclampsia scoring systems

A

Scoring systems are used to determine whether to admit the woman (fullPIERS or PREP‑S)

Gestation

Severity of maternal disease

Speed of progression (fulminating pre-eclampsia)

Presence of complications (HELLP)

Fetal wellbeing

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19
Q

pre-eclampsia management

A

Blood pressure is monitored closely (at least every 48 hours)

Urine dipstick testing is not routinely necessary (the diagnosis is already made)

Ultrasound monitoring of the fetus, amniotic fluid and dopplers is performed two weekly

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20
Q

medical management of pre-eclampsia

A

labetolol first line
nifedipine
methyldopa

IV hydralazine
IV labetalol
IV magnesium sulphate
fluid restriction

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21
Q

severe/fulminating pre-eclampsia

A

Control HTN

Prevent seizures (maternal Mg infusion)

Administer steroids for lung maturation if preterm

Deliver by most appropriate route

Strict fluid balance

HDU care

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22
Q

obstetric emergency pre-eclampsia

A

Seizures occurring in pregnancy or within 10 days of delivery

> 2 of following within 24 hours of seizure

HTN

Proteinuria one ‘plus’ or at least 0.3G/24h

Thrombocytopenia <100,000ul

Raised transaminases

23
Q

pre-eclampsia management after delivery

A

Enalapril (first-line)

Nifedipine or amlodipine (first-line in black African or Caribbean patients

Labetolol or atenolol (third-line)

24
Q

post-natal management of pre-eclampsia

A

May require antihypertensive treatment for 6-12 weeks postnatrally

Increased risk of VTW, particularly in severe proteinuria

If severe PET, may require follow up bloods

Postnatal HTN clinic where appropriate

Discuss contraception before discharge

Discuss implications for future pregnancy

Write to GP with details of treatment, delivery, and aftercare

25
complications of pre-eclampsia | maternal
CNS: Eclampsia Intracranial haemorrhage/ stroke Cortical blindness Renal: Renal tubular necrosis (AKI) Respiratory: Pulmonary oedema Liver: HELLP syndrome Liver capsule haemorrhage Liver rupture Haematological: DIC VTE Placenta: Placental abruption
26
fetal complications of pre-eclampsia
Highest single risk factor for stillbirth (20% of stillbirths) Accounts for 46% of infants born small for gestation age Accounts for 30% of premature infants
27
risk factors for GDM
Previous gestational diabetes Previous macrosomic baby (≥ 4.5kg) BMI > 30 Ethnic origin (black Caribbean, Middle Eastern and South Asian) Family history of diabetes (first-degree relative)
28
OGTT GDM
24-28 weeks 5. 6 fasting 7. 8 2 hours after 75g sugar
29
Pre-pregnancy care GDM
Information about optimum blood glucose control prior to conception Improving general health, reducing obesity Aiming to reduce risks of diabetes embropathy and other adverse pregnancy outcomes for mother and baby All women should be offered pre-pregnancy care T1, T2, previous GDM Aim for HbA1c <40mmol/mol Avoid pregnancy if >86 Offer women with DM/ BMI >27: Weight loss advice Retinal assessment: Advise to defer rapid optimisation of blood glucose control until after retinal assessment Renal assessment: Before discontinuing contraception Medications: Folic acid 5mg/day (3/12 preconception to 3/12 after conception) Aspirin 75mg >12 weeks gestation Assess need for VTE prophylaxis If BMI >35 recommend vitD supplements (Pregnacare) Stop unsafe medications, e.g. statins
30
SAFER GDM
STOP: think ahead, is medication suitable for pregnancy? A1C: on target or too high Folic acid Enjoy Referral early to specialist care
31
Management of GDM
Fasting glucose less than 7 mmol/l: trial of diet and exercise for 1-2 weeks, followed by metformin, then insulin Fasting glucose above 7 mmol/l: start insulin ± metformin Fasting glucose above 6 mmol/l plus macrosomia (or other complications): start insulin ± metformin
32
blood sugar monitoring GDM
Fasting: 5.3 mmol/l 1 hour post-meal: 7.8 mmol/l 2 hours post-meal: 6.4 mmol/l Avoiding levels of 4 mmol/l or below
33
Planning GDM delivery
Delivery 37-38+6 IOL: 37-38+6 Elective CS: 38-39
34
postnatal care GDM
Diabetes improves immediately after birth. Women with gestational diabetes can stop their diabetic medications immediately after birth. They need follow up to test their fasting glucose after at least six weeks. HbA1C at 13 weeks and yearly thereafter due to increased risk of T2DM Lifestyle advice Contraception and need for pre conception care in future Women with existing diabetes should lower their insulin doses and be wary of hypoglycaemia in the postnatal period. The insulin sensitivity will increase after birth and with breastfeeding. Future obesity, metabolic syndrome, diabetes, HTN, CVD
35
risk to neonate when mother has GDM
``` neonatal hypoglycaemia polycythaemia (raised Hb) jaundice (raised bilirubin) congenital heart disease cardiomyopathy spina bifida, anencephaly caudal regression/ sacral agenesis ```
36
obstetric cholestasis maternal risks
Vit k deficiency Increased risk of PPH
37
obstetric cholestasis fetal risks
Perinatal mortality is increased up to 11% Fetal distress Meconium Pre-term labour Intracranial haemorrhage Stillbirth
38
obstetric cholestasis presentation
Fatigue Dark urine Pale, greasy stools Jaundice Skin trauma from intense scratching Insomnia and malaise
39
Ix for pruritis
Women presenting with pruritus should have liver function tests and bile acids checked. Viral screen: Hep A,B and C EBV and CMV Liver autoimmune screen: Chronic active hepatitis and primary biliary cirrhosis Anti-smooth muscle and antimitochondrial antibodies USS abdomen- liver and gallstones Obstetric cholestasis will cause: Abnormal liver function tests (LFTs), mainly ALT, AST and GGT Raised bile acids
40
management of obstetric cholestasis
``` ursodeoxycholic acid emollients antihistamine vitK monitor LFTs planned delivery after 37 weeks ```
41
Procoagulant pathophysiological changes in pregnancy:
Hypercoagulable state Increase in fibrinogen and factors VIII, IX, X Concentration of endogenous anticoagulants decreases Additional risk is present for at least 6 weeks post-partum Venous stasis in lower limbs Trauma of pelvic veins at the time of delivery
42
risk factors for VTE in pregnancy
Smoking Parity ≥ 3 Age > 35 years BMI > 30 Reduced mobility Multiple pregnancy Pre-eclampsia Gross varicose veins Immobility Family history of VTE Thrombophilia Paraplegia IVF pregnancy
43
obstetric risk factors for VTE
Multiple pregnancy PET CS Prolonged labour >24 hours Mid-cavity or rotational operative delivery Still birth Preterm birth PPH >1L
44
new onset reversible risk factors VTE
Bone fracture Surgical procedure in pregnancy and puerperium Hyperemesis, dehydration OHSS/ ART Immobility >3 days Long haul travel >4 hours Current systemic infection
45
when to start VTE prophylaxis
28 weeks if there are three risk factors First trimester if there are four or more of these risk factors Up to 6 weeks post natally ``` Hospital admission Surgical procedures Previous VTE Medical conditions such as cancer or arthritis High-risk thrombophilias Ovarian hyperstimulation syndrome ```
46
DVT diagnosis
Gold standard is venography with fetal shield Doppler ultrasound of leg veins is a good alternative: Direct imaging of clot Repeat day 3 and 7 Lack of compressability of vein
47
PE diagnosis
CXR ECG abg Oxygen sats
48
VTE prophylaxis
LMWH | enoxaparin, dalteparin, tinzaparin
49
mechanical prophylaxis VTE
intermittent pneumatic compression with equipment that inflates and deflates to massage the legs Anti-embolic compression stockings
50
DVT presentation
Calf or leg swelling Dilated superficial veins Tenderness to the calf (particularly over the deep veins) Oedema Colour changes to the leg >3cm difference between the calves
51
PE presentation
Shortness of breath Cough with or without blood (haemoptysis) Pleuritic chest pain Hypoxia Tachycardia (this can be difficult to distinguish from the normal physiological changes in pregnancy) Raised respiratory rate Low-grade fever Haemodynamic instability causing hypotension
52
suspected PE pathway
Clinical assessment Perform CXR and ECG Test FBC, U&E, LFTs Commence LMWH (unless treatment is contraindicated) Duplex USS for S/S of DVT VQ scan of CXR normal CTPA if CXR abnormal
53
CTPA vs VQ
CTPA is the test for choice for patients with an abnormal chest xray CTPA carries a higher risk of breast cancer for the mother (minimal absolute risk) VQ scan carriers a higher risk of childhood cancer for the fetus (minimal absolute risk)