Title: Anaemia
1Anaemia Thrombocytopenia in Pregnancy
- Giselle Kidson-Gerber
- Haematology Registrar
- Prince of Wales Hospital
2Anaemia in pregnancy
3Physiological changes in normal pregnancy
- RBC dilution with rise in blood volume and plasma
volume - Definition of anaemia in pregnancy
- T1, T3 Hb lt 110g/L
- T2 Hb lt 105g/L
- Return to normal within 1 week post-partum, if
normal iron stores
4Potential consequences of moderate to severe
anaemia
- Maternal
- Fatigue, dyspnoea, syncope, chest pain
- Mortality (esp lt 50g/L)
- Foetal (esp lt 60g/L)
- Impaired mental development if low iron stores
- Low birth weight
- Preterm labour
- Perinatal death
- Low amniotic fluid volume
- Spontaneous miscarriage
- Placental Hypertrophy
5Common causes of anaemia in pregnancy
6Preconception
- Assess nutrition status
- Full blood count
- Investigate if anaemia present
- Correct anaemia prior to conception
- Haemoglobinopathy screening
7Investigations
- FBC, with MCV, blood film
- Fe studies ferritin esp.
- Folate (RCF stores) B12 levels
- Reticulocyte count
- UEC, LFT, Coagulation studies
- Haemoglobinopathy screening
8Iron deficiency anaemia
- Most common cause in Western countries
- Increased iron requirements during pregnancy,
- especially multiple pregnancies
- Replace Ferrous sulfate 325mg tds (105mg
elemental Fe) - Anaemia corrects in 4 - 6 weeks
- Stores replaced in 4 - 6 months
- Dietary advice
- Once replete
- Ongoing supplement 30 - 60mg elemental iron
daily - Monitor, including whilst breastfeeding
9Iron therapies
10Folic Acid deficiency
- 2nd most common cause of anaemia in pregnancy
- Increased requirements for mother and foetus
- Red cell folate measure more reflective of
tissue stores over past months - Supplement all 200 - 500mcg/d
- (greater if haemolysis)
- Replacement 1000mcg/d
11Haemoglobinopathies Practical significance
- Major haemoglobinopathy in mother
- Rare
- Specialist obstetric haematology care
- Haemoglobinopathy traits in mother
- Silent risk foetus
- Transfusion-dependent anaemia or sickle cell
disease - Barts disease/hydrops foetalis maternal foetal
morbidity - Dependent on maternal and paternal genotype
- Importance of appropriate timely screening
12Difficulties with detection of haemoglobinopathy
traits
- Patient asymptomatic
- Patient unaware of carrier status
- Difficult to detect in laboratory
- May have normal Hb or MCV
- Haemoglobinopathy screening does not
detect all cases - Iron deficiency can mask indicator of
thalassaemia trait
13Haemoglobinopathies
14Screening
- Why? - Detect foetus at risk of major
haemoglobinopathy - Who? - At risk ethnic groups, ? all
- (Southern Europe, Middle East, Africa, Asia,
Indian subcontinent) - - Mother partner
- When? - Ideally preconception
- - Limited timeframe for Ix intervention
- What? - FBC Hb, MCV
- - HbEPG (includes HPLC, HbH bodies)
15Full blood count
- Simple
- Limitations
- ? MCV may not detect - a thalassaemia trait
- sickle trait - ? Hb may not detect - ß thalassaemia trait
- - a thalassaemia trait - sickle
trait - Iron deficiency must be excluded as cause of low
MCV
16HbEPG Hb Electrophoresis
- Separates different haemoglobins according to
charge - Alkaline acid gels
- Known position of haemoglobin bands
-
HbF
HbA
HbS
HbA2,C,E
HbS trait
Control
Normal
ß thalassaemia trait
HbE trait
HbE disease
17HPLC High Performance Liquid Chromatography
- Separate according to elution time
- Quantify of different haemoglobins present
- Iron deficiency lowers HbA2
Normal
HbS trait
HbS band 39
HbA predominant haemoglobin 88
HbA 50
18When to refer or ask for help
- Positive result
- Unexplained anaemia
- Uncertain what investigations to perform
- Uncertain how to interpret investigations
- Complex area!
- Variation in conditions and test results
- Specialist services are available DNA testing
is readily available should be accessed when
there is doubt
19DNA testing
- Confirm results or clarify unclear results
- Test mother partner
- Foetus
- If have a known mutation in both parents
- Usually gives definitive genotype, although not
100 predictive of phenotype - Formal genetic counselling prior
- Must be organised EARLY in pregnancy
- - ideally preconception.
- Option of prenatal genetic diagnosis with IVF
20Take home message
- Evaluate anaemia PRIOR to pregnancy
- Determine cause of low MCV
- Replace iron, if deficient
- Low threshold for haemoglobinopathy screening and
referral
21Thrombocytopenia in pregnancy
22Thrombocytopenia
- Physiological thrombocytopenia in normal
pregnancy - Average decrease in platelet count of 10
- Occurs mostly in 3rd trimester
- Due to haemodilution or accelerated destruction
- Normalises 24 -72 hours post-partum
- Complicated Thrombocytopenia
- Up to 10 of pregnancies
- Mild - 100 - 150 x 109/L
- Moderate - 50 - 100 x 109/L
- Severe - lt 50 x 109/L
23Causes of Thrombocytopenia in Pregnancy
- Pregnancy-specific
- Increased destruction
- Gestational
- Preeclampsia
- HELLP
- Acute Fatty Liver of Pregnancy
- Disseminated intravascular coagulopathy
- Non-pregnancy-specific
- Increased destruction
- Idiopathic thrombocytopenic purpura (ITP)
- Microangiopathies TTP, HUS, DIC
- SLE, Antiphospholipid syndrome
- Drug-induced
- Viral infections HIV, HCV, EBV, CMV
- Hypersplenism
- Decreased production
- Bone Marrow Disease
- Nutritional deficiency
- Liver disease
- Congenital thrombocytopenia
24Causes of Thrombocytopenia in Pregnancy
- Pregnancy-specific
- Increased destruction
- Gestational
- Preeclampsia
- HELLP
- Acute Fatty Liver of Pregnancy
- Disseminated intravascular coagulopathy
- Non-pregnancy-specific
- Increased destruction
- Idiopathic thrombocytopenic purpura (ITP)
- Microangiopathies TTP, HUS, DIC
- SLE, Antiphospholipid syndrome
- Drug-induced
- Viral infections HIV, HCV, EBV, CMV
- Hypersplenism
- Decreased production
- Bone Marrow Disease
- Nutritional deficiency
- Liver disease
- Congenital thrombocytopenia
25Causes of Thrombocytopenia in Pregnancy
- Pregnancy-specific
- Increased destruction
- Gestational
- Preeclampsia
- HELLP
- Acute Fatty Liver of Pregnancy
- Disseminated intravascular coagulopathy
- Non-pregnancy-specific
- Increased destruction
- Idiopathic thrombocytopenic purpura (ITP)
- Microangiopathies TTP, HUS, DIC
- SLE, Antiphospholipid syndrome
- Drug-induced
- Viral infections HIV, HCV, EBV, CMV
- Hypersplenism
- Decreased production
- Bone Marrow Disease
- Nutritional deficiency
- Liver disease
- Congenital thrombocytopenia
26Causes of Thrombocytopenia in Pregnancy
- Pregnancy-specific
- Increased destruction
- Gestational
- Preeclampsia
- HELLP
- Acute Fatty Liver of Pregnancy
- Disseminated intravascular coagulopathy
- Non-pregnancy-specific
- Increased destruction
- Idiopathic thrombocytopenic purpura (ITP)
- Microangiopathies TTP, HUS, DIC
- SLE, Antiphospholipid syndrome
- Drug-induced
- Viral infections HIV, HCV, EBV, CMV
- Hypersplenism
- Decreased production
- Bone Marrow Disease
- Nutritional deficiency
- Liver disease
- Congenital thrombocytopenia
27Clinical approach
- Symptoms, bleeding history
- Prenatal platelet count
- Gestation
- Previous pregnancies
- Associated features
- Co-morbidities
28Gestational Thrombocytopenia
- Occurs in 5-8 of all pregnancies
- 75 of all pregnancy-associated thrombocytopenia
- ? Mechanism haemodilution, accelerated plt
turnover, trapping or destruction at placenta - Maternal haemorrhage risk not increased
- Foetal thrombocytopenia risk not increased
29Gestational Thrombocytopenia
- Clinically - asymptomatic
- - normal pre-natal platelet count
- - occurs in late T2 in T3
- - normalises post-partum
-
- Mild thrombocytopenia
- Platelet count gt 70 x109/L (usually gt 100)
- Anti-platelet antibodies do not reliably
distinguish from ITP - Diagnosis of exclusion
30Idiopathic Thrombocytopenic Purpura (ITP)
- 5 of pregnancy-associated thrombocytopenia, 0.1
of pregnancies - Concern maternal and foetal haemorrhage
- Clinically - any trimester
- - prenatal thrombocytopenia
- - bleeding history
- Especially likely to be ITP if
- Platelet count lt50 x109/L
- T1
- History of auto-immune disease
31Idiopathic Thrombocytopenic Purpura (ITP)
- Maternal haemorrhage risk increased,
- relates to platelet count
- Platelet count lt 20 risk of spontaneous bleeding
- Platelet count gt 50 aim for NVD
- Platelet count gt 70 for epidural (variable,
anaesthetist preference) - Foetal thrombocytopenia
- due to trans-placental passage of maternal
IgG - 10-20 platelet count lt 50 x109/L
- 5 platelet count lt 20 x109/L 25-50 develop
bleeding - Best predictor sibling
- Check cord platelet count at delivery, nadir day
2-3. - Therapeutic options monitor only, IVIg,
prednisone, (splenectomy)
32Summary of approach to thrombocytopenia in
pregnancy
- Exclude pre-eclampsia syndromes
- BP, UA, symptoms, FBC, UEC, LFT, Uric Acid
- Exclude non-pregnancy-related medical causes,
usually have specialist involved already - When to refer
- Known history of ITP
- Unknown cause platelet count is
- lt130 x 109/L in T1 T2
- lt100 x 109/L in T3
- Otherwise monitor FBC monthly
33