Obstetric Emergencies

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OBSTETRIC

EMERGENCIES

PGY1 Education Program

Wednesday 26 th September and 3 rd October 2012

Dr Wendy Carseldine

Teaching Fellow, Maternity and Gynaecology

OVERVIEW

Hypertension in Pregnancy

Post-partum haemorrhage

Shoulder dystocia

Maternal collapse

HYPERTENSION IN PREGNANCY

Pre-existing hypertension

Hypertension prior to 20 weeks gestation

Must be investigated before labelled essential

Pregnancy induced hypertension

After 20 weeks gestation

Pre-eclampsia

Multi-system disorder unique to pregnancy

Hypertension + involvement

Renal

Haematological

Liver

Neurological

Pulmonary oedema

IUGR

Placental abruption

HYPERTENSION IN PREGNANCY

Crises in pre-eclampsia

HELLP: Complicate up to 20% of pre-eclampsia

Pulmonary oedema

Placental abruption

Cerebral haemorrhage

Cortical blindness

DIC

Renal failure

Hepatic rupture

Unusual causes of HT in pregnancy

Phaeochromocytoma

Renal artery stenosis

Coarctation of the aorta

HYPERTENSION IN PREGNANCY:

HISTORY

Symptoms

Headache, visual disturbance

RUQ/epigastric pain

Nausea and vomiting

Severe oedema

Signs

Hypertension

Proteinuria

RUQ tenderness

Hyper-reflexia, clonus

IUGR +/- FDIU

Placental abruption

HYPERTENSION IN PREGNANCY:

INVESTIGATIONS

Bloods

FBC

EUC

LFT

Uric acid

Co-ags

Urine

Protein creatinine ratio

24 hour protein collection

Ultrasound

Fetal growth

AFI

Fetal dopplers

HYPERTENSION IN PREGNANCY:

TREATMENT

Prevention

Aspirin

Clexane

Antihypertensive treatment

Oral agents

Labetalol

Methyldopa

Clonidine

Nifedipine

IV agents

Hydralazine

Labetalol

Diazoxide

HYPERTENSION IN PREGNANCY:

TREATMENT

Seizure prevention

MgSO

4

Loading dose

Infusion for 24 hours

Delivery

Risk of prematurity

Risk of disease development

POST-PARTUM HAEMORRHAGE

Every minute, at least one woman dies from complications related to pregnancy or childbirth, 529 000 women a year.

Five direct complications account for more than 70% of maternal deaths: haemorrhage (25%), infection (15%), unsafe abortion (13%), eclampsia (12%), and obstructed labour (8%).

PPH

Incidence: 5-15%

Definitions

>500 mL blood loss during or after childbirth or enough to cause haemodynamic compromise

Severe >1000 mL

Primary: first 24 hours

Secondary: from 24 hours to 6 weeks postpartum

PPH: RISK FACTORS/CAUSES (THE 4

‘T’S)

Tone (70%)

Prolonged 3 rd stage

Over distended uterus (polyhydramnious, twins, macrosomia)

Exhausted uterus (rapid labour, prolonged 1 st or 2 nd stage, high parity, dystocia/augmentation with Syntocinon)

Infection

Drug induced

Uterine anomalies (fibroids, structural)

Trauma (20%)

Episiotomy, perineal tear

Caesarean section

Uterine rupture

Uterine inversion

Tissue (10%)

Retained placenta/cotyledon

Abnormal placenta (accreta or increta)

Coagulopathy (1%)

Pre-existing

Pregnancy acquired (pre-eclampsia, infection, DIC secondary to FDIU)

PPH: PREVENTION

Identification of risk factors

Appropriate antenatal and intrapartum management

Delivery in a unit with rapid access to blood and blood products

Abnormal placentation

All women should have an antenatal ultrasound for placental location

Recognition of placenta praevia or abnormally adherent placentation

Active management of the 3 rd stage of labour

Prophylactic oxytocin (reduce risk by 50%)

Early cord clamping, controlled cord traction

Provide appropriate information to women requesting physiological 3 rd stage

PPH: MANAGEMENT

Communication

Team: midwives, obstetric staff, anaesthetist,

Haematology lab, blood bank, haematologist

Porters for patient transport and delivery of blood/specimens

Nominate a team member to record events

Use of Massive Transfusion Protocol

JHH: x7700

PPH: MANAGEMENT

ABC

Assess Airway

Assess breathing

Oxygen by mask (10-15 l/min)

Evaluate circulation

2 x large IV access (at least 16g cannula), consider arterial line

Rapid IVF initial resuscitation (Normal saline, gelofusine)

Keep patient warm (also warmed IVF)

Transfuse blood ASAP (Packed RBC, FFP,

Platelets, Cryoprecipitate)

Consider Recombinant fVIIa

PPH: MANAGEMENT

Monitoring and Investigation

Venepuncture

X-match, FBC, Coagulation profile, EUC, LFT

Observations

BP, HR, RR, O2 Sat, Temp

Insert IDC to monitor urine output and contract uterus

Thromboembolic prophylaxis once bleeding controlled

Estimate blood loss

Weigh if large volume

PPH: MANAGEMENT

Transfer to theatre

Examination under anaesthetic (GA/regional)

Atony

Mechanical (bimanual compression, empty bladder)

Pharmacological (Syntocinon, Ergometrine, Misoprostol/Cervagem,

Prostin F2  )

Balloon tamponade (Bakri)

Laparotomy: B-Lynch Suture, uterine artery/internal iliac artery ligation, hysterectomy

Artery embolisation (radiology)

Trauma

Examine uterus (rupture), cervix, vagina, vulva, perineum

Apply pressure and surgical repair

Correct inversion

Tissue

Examination of placenta

Manual removal (digital or curettage) of retained products

Coagulopathy

Correction directed by laboratory testing

PPH: MANAGEMENT

Once bleeding is controlled

Consider ICU/HDU care

Ongoing review and laboratory testing

Debriefing and counselling to woman, family and staff

Remember next pregnancy prevention/active management

SHOULDER DYSTOCIA

Incidence: 2%

Risk Factors

Maternal obesity

Macrosomia

Post-dates pregnancy

Diabetes

Assisted delivery

SHOULDER DYSTOCIA:

MANAGEMENT

Get help

Consider episiotomy

McRoberts manoeuvre

Suprapubic pressure

Constant

Rocking

Delivery of the posterior arm

Consider use of infant feeding tube

Internal manoeuvres

Last resort

Zavanelli

Fracture the fetal clavicle

Symphysiotomy

MATERNAL COLLAPSE

PPH

Cardiac arrest

Amniotic fluid embolism

Thromboembolic disease

Puerperal sepsis

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