Bleeding in the 1st Trimester

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Bleeding in the first trimester of pregnancy is not an uncommon event but is a source of anxiety for mothers.

– The reasons for this can range from idiopathic to serious conditions like an ectopic pregnancy.

– In addition, it can also be due to gynaecological conditions like ectropion, trauma and polyps

 

If a woman has bleeding in the first trimester, management depends on the gestational age and her symptoms:

If <6 weeks gestation:

– Expectant management. Advise woman to repeat pregnancy test after 7-10 days

– If this is positive then return to the clinic

– If the test is negative this means that the woman has miscarried

 

If >6 weeks gestation or any pain/tenderness:

– Immediate referral for assessment for ultrasound scan

 

At assessment, it is likely that the woman will have her blood tests taken for b-hCG and an ultrasound scan

– The scan may reveal various things like an ectopic, miscarriage or a healthy viable pregnancy

 

Pregnancy of Unknown Location

If scan is inconclusive however, this is known as a pregnancy of unknown location.

– In this case, take 2 serum hCG measurements 48 hours apart.

 

If hCG decreases >50%:

– It is most likely is that pregnancy will miscarriage.

– Therefore, take urine pregnancy test after 14 days which will most likely come back negative

– If still positive, she needs review in assessment unit again

 

If hCG increases >63%:

– Most likely is that this is a healthy intrauterine viable pregnancy

– Therefore, offer transvaginal ultrasound between 7-14 days later

 

If hCG change is between <50%  and >63%:

– This suggests could be due to ectopic pregnancy

– Therefore, refer to early pregnancy assessment service within 24 hours and repeat ultrasound scan

 

Miscarriage

This is a term used to describe expulsion of the products of conception before 24 weeks gestational age

– About 1/5 of diagnosed pregnancies will result in miscarriage in the early stages

– It should be suspected if there is a positive urine pregnancy test and bleeding in first trimester

 

Cause:

– During first trimester, usual cause is chromosomal abnormality (most common is trisomy 16)

– During second trimester, most common cause is an incompetent cervix (risk from cervical surgery)

 

Miscarriage can be divided into several types:

Diagnosis:

Transvaginal ultrasound is used:

– If no heartbeat seen but there is a visible foetal pole, use the crown rump length (CRL) to estimate gestation:

– At a CRL of 7mm, you should normally be able to detect heartbeat.

– If CRL <7mm –> cannot diagnose miscarriage at this stage so repeat scan after 1 week, then diagnose

– If CRL >7mm and no heart rate –> suggests that miscarriage has occurred

 

If no heartbeat seen and no visible foetal pole, you can measure the gestational mean sac diameter (MSD):

– If MSD <25mm –> can’t diagnose miscarriage at this stage so repeat scan after 1 week, then diagnose

– If MSD >25mm –> diagnose miscarriag

 

Management:

This depends on the type of miscarriage:

 

i)Threatened:

– If heavy bleeding admit to hospital and observe

– If light reassure and refer back to midwife

– Take blood test for hCG (48 hours apart) to check status of the baby

 

ii) Inevitable, incomplete or missed:

– 1st line is expectant (watch and wait for 1-2 weeks)

– If infection, risk of haemorrhage or previous miscarriage, then do medical or surgical management

– Medical = Vaginal misoprostol (acts to contract and dilate cervix to expel the fetus)

– Surgical = Manual vacuum aspiration or surgical management in operating theatre

 

iii) Complete:

– Discharge to GP as the miscarriage has already occurred

 

N.B. You must give anti-D prophylaxis to women presenting at any stage of miscarriage who are:

– Rhesus negative with pregnancy >12 weeks or a pregnancy that is managed surgically

 

Recurrent miscarriage

This is the occurrence of 3 or more consecutive pregnancies that end in miscarriage of the fetus before 24 weeks

– This requires prompt investigation to search for an underlying cause. This can be split into 3 types of investigations used to detect chromosomal abnormalities, blood problems, and anatomical causes.

 

Investigations:

Blood tests:

– Thrombophilia screen

– Antiphospholipid antibodies (lupus anticoagulant, anticardiolipin/anti-B2 glycoprotein)

– Hormonal Profile

– Blood glucose tests

– Thyroid function tests

 

Imaging:

– Pelvic Ultrasound used to detect any structural abnormalities

 

Karyotyping:

– This is used to determine whether there are any chromosomal abnormalities:

 

Cytogenic analysis:

– This can be performed on the products of conception (POC)

 

Parental peripheral blood karyotyping:

– This can be performed when analysis of the POC shows  an unbalanced structural chromosomal abnormality

 

Management:

– This involves managing the underlying condition

– If the underlying condition is irreversible, consider IVF or adoption

– Ensure that you also give psychological support to the couple

 

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