SLCOG Clinical Practice Guideline

Management of Primary Postpartum Haemorrhage

Guideline 16June 2022Obstetric emergencies1 tables3 figures
Open source PDF

1. Introduction

The aim of this guideline is to provide evidence-based recommendations in the management of primary postpartum haemorrhage (PPH). This is the commonest direct cause of maternal death globally and in Sri Lanka. The objective of this guideline is to ensure anticipation, prevention, early detection and timely and appropriate management of PPH.

2. Definition

For the purpose of this guideline PPH is defined as blood loss of 500 ml or more from the genital tract within 24 hours of the birth of a baby. Blood loss of over 1000 ml is defined as major PPH. Major can be further sub-divided into moderate (1001-2000 ml) and severe >2000 ml.

In a woman with lower body mass (e.g. <60 Kg) a lower level of loss of blood volume may be clinically significant.

Since blood volume differs between persons, blood loss must be individualized.

The loss of 40% or more of the blood volume is life threatening and will be defined as a massive obstetric haemorrhage. Blood volume = 100ml/Kg

Irrespective of the loss of blood volume, appearance of cardiovascular instability (i.e. tachypnea, altered mental status, tachycardia and hypotension) signifies possibility of major obstetric hemorrhage.

3. Prevention of Postpartum Haemorrhage

Active management of the third stage of labour is the cornerstone of prevention of primary PPH.

Postpartum care observations should be recorded on a MEOWS chart for early detection of patients needing further care.

Minimizing risk:

PPH occurs most often in women without risk factors. Therefore, the blood group and level of haemoglobin of every woman who goes into labor must be known.

a Consultant Obstetrician and Gynaecologist, Colombo North Teaching Hospital, Ragama, Sri Lanka

b Consultant Obstetrician and Gynaecologist, Castle Street Hospital for Women, Colombo 8, Sri Lanka

c Professor in Obstetrics and Gynaecology, Department of Obstetrics and Gynaecology, University of Colombo, Sri Lanka

d Consultant Obstetrician and Gynaecologist, Colombo North Teaching Hospital, Ragama, Sri Lanka

e Consultant Obstetrician and Gynaecologist, Colombo North Teaching Hospital, Ragama, Sri Lanka

Women with known risk factors associated with PPH, as listed in Box 1. Should be advised to deliver in a specialist obstetric unit under extra vigilance. Of these, Abruptio placenta, Placenta praevia and Morbidly adherent placentae are especially at higher risk.

Box. 1 Risk Factors for PPH

Risks existing prior to labour

Risk factors during Labor

Good practices:

4. Management of Primary PPH

In Sri Lanka usual practice has been to commence treatment when there is continuing bleeding despite uterine massage irrespective of the amount of blood lost.

It is recommended that this practice be continued.

4.1. Identification of severity of haemorrhage

Clinicians should be aware that the visual estimation of post partum blood loss is inaccurate and that clinical signs and symptoms should be included in the assessment of PPH.

Shock index (SI)- (Heart rate/Systolic Blood Pressure) as an effective predictor for PPH SI <0.9 provides reassurance, whereas SI ≥1.7 indicates a need for urgent attention in haemorrhage. (BJOG. 2015; 122(2): 268-75. doi: 10.1111/1471-0528.13206.)

Call for help:

Who should be informed when the woman presents with PPH?

However, in the absence of a MO any staff member could inform.

a. The obstetric middle grade,

b. The anesthetic middle grade; Where available, the early involvement of the anesthetic team, even while the patient is still in the labor room is recommended.

c. Inform theatre

d. Alert MO blood bank

e. Alert Consultant Obstetrician

f. Alert Consultant Anaesthetist

g. Transfusion medicine specialist / Haematologist

h. Alert the head of the institution

In a hospital clear instruction to telephone operator how to convey such message should be given by the administration to alert the stipulated staff as stated above. The telephone operator should document the list of staff informed and submit it to the ward to be attached to the Bed Head Ticket.

Communication with the mother

Maintain a calm atmosphere.

Keep the mother (and labor companion/family) informed and reassure the mother regularly where feasible.

4.2. Documentation: It is important to record: to be done later once the mother is stable

4.2.1. Measures for minor PPH: Blood loss 500-1000ml without clinical shock

4.2.2. PPH of more than blood loss 1000ml/ active bleeding/ signs of shock

Resuscitation

blood. O-ve O+ve group-specific uncross matched cross-matched.

Figure from Management of Primary Postpartum Haemorrhage
Figure from the source guideline

4.5.1. Establish a cause for the bleeding – Four T’s, Tone, Tissue, Trauma, Thrombin

4.5.3.1. Management of Atonic Haemorrhage

Before transferring the patient it’s important to do the following;

Resort to hysterectomy without delay if other measures appear to be failing.

4.5.3.2. Management of Traumatic PPH

Manage only in theatre under suitable anaesthesia and exposure

1. Exclude high vaginal and cervical tears before suturing episiotomy.

2. Examine for paravaginal and broad ligament haematomata with a combined per vaginal and per rectal examination.

4. Paravaginal hematomas of more than 5 cm diameter will usually require surgical evacuation. A bleeding point is usually present and must be looked for. In cases where it is difficult to control bleeding, a Foley catheter with its balloon inflated may be left in the cavity. Packing of the vagina may also be useful.

5. Cervical tears must be identified by systematic inspection of the cervix using Green- Armytage forceps and sutured.

6. In case of multiple tears with venous oozing, it may be better to insert a balloon catheter into the vagina or to pack the vagina with moistened vaginal packs than to try to suture all the tears.

7. Vasopressin soaked pack (1 vial: 200ml diluted saline).

Rupture of the uterus

4.5.3.3. Coagulopathy causing PPH

Death in utero, Abruptio placentae, severe Pre- Eclampsia, HELLP syndrome, Sepsis, Amniotic fluid embolism, Acute fatty liver, primary immune Thrombocytopenia, Von Willebrand’s disease etc.

Special Situations

4.5.4. Debriefing