Primary Postpartum Hemorrhage

Recommendation

Strength

1. PREVENTION OF POSTPARTUM HEMORRHAGE

1.1 Risk Assessment:

1.1.1. Risk factors for PPH may present antenatally or intrapartum; care plans must be modified as and when risk factors arise.

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1.1.2. Clinicians must be aware of risk factors for PPH and should take these into account when counselling women about place of delivery.

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1.1.3. Women with known risk factors for PPH should only be delivered in a hospital with a blood bank on site.

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1.1.4. An individualized risk assessment for postpartum hemorrhage should be documented upon arrival to a labor unit and updated throughout labor and delivery.

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1.2 Risk Factors

1.2.1 Consider the following antenatal risk factors for PPH

·       Age > 35

·       Obesity (BMI >35)

·       More than 3 prior births

·       Previous PPH

·       Previous Cesarean section with placenta previa or PAS

·       Previous uterine surgery

·       Presence of uterine fibroid

·       Multiple pregnancy

·       Polyhydramnios

·       Fetal macrosomia

·       Anemia

·       Known coagulopathy or other bleeding disorders

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1.2.2. Consider the following intrapartum risk factors for PPH

·       Oxytocin use in labor

·       Prolonged second stage

·       Prolonged third stage

·       Retained placenta

·       Manual removal of placenta

·       Assisted vaginal birth

·       Cesarean section whether elective or emergency

·       Perineal trauma

·       Uterine rupture

·       General anaesthesia

·       Infection

·       Non-cephalic presentation

·       Precipitate labor

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1.3. Antenatal Risk Management

1.3.1. Antenatal anemia

1.3.1.1. Antenatal anemia should be investigated and treated appropriately as this may reduce the morbidity associated with PPH.

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1.3.2. Maternal blood disorders

 1.3.2.1. Involve specialist physician to:

·       Optimize coagulation profile prior to birth

·       Advise on birth options (e.g. mode of birth)

1.3.2.2. Seek anesthetic opinion regarding options for analgesia during labor and birth

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1.3.3. Abnormal placentation

1.3.3.1. Determine placental site and if abnormal placental adherence is suspected (PAS):

·       Refer to a center equipped for placenta accreta management.

·       Involve multidisciplinary team including urologist, general surgeon, vascular surgeon,  hematologist, senior anaesthetist and ICU specialist in preoperative planning.

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1.4. Intrapartum Risk Management

1.4.1. Management of third stage of labor

The use of uterotonics for prevention of PPH during the third stage of labor

is recommended for all births.

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1.4.2. Cord clamping:

1.4.2.1. Late cord clamping (performed approximately 1 to 3 minutes after birth) is recommended for all births while initiating simultaneous essential newborn care.

1.4.2.2. Early cord clamping (<1 minute after birth) is not recommended unless the neonate is asphyxiated and needs to be moved immediately for resuscitation.

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1.4.3. Controlled cord traction:

1.4.3.1 Consider Controlled cord traction (CCT) as part of active/modified active management of third stage as it may.

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1.4.3.2. Providers employing CCT should only do so after signs of placental separation, and traction should be performed with uterine contraction as these measures reduce the risk of uterine inversion, cord avulsion, and partial detachment of the placenta.

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1.5. Prophylactic Uterotonics:

1.5.1. Oxytocin:

1.5.1.1. In most circumstances, oxytocin is the prophylactic uterotonic of choice.

1.5.1.2 For vaginal birth

·       If vaginal birth with IV access: Oxytocin 10 IU IV injected slowly over 3–5 minutes is recommended in preference to IM

·       If vaginal birth without IV access: Oxytocin 10 IU IM

·       To be transferred ransfer to rational: When compared with IM, IV oxytocin reduces the risk of PPH, need for blood transfusion 60-62 and incidence of retained placenta with no significant difference in side effects (e.g. hypotension and tachycardia) between routes 60,61

1.5.1.3. For CS birth:

·       Oxytocin 5 IU IV over 1–2 minutes

·       Monitor for hemodynamic impact

·       Avoid rapid IV bolus administration

1.5.1.4. If cardiovascular compromise exists (e.g. hypovolemia, shock, cardiac disease), use caution with IV administration. Rational it may result in transient hemodynamic instability 61, 65

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1.5.2. Ergometrine:

1.5.2.1 Ergometrine can be given IM or, in life-saving circumstances, as a slow IV injection.

1.5.2.2. Ergometrine should not be used in patients with essential or gestational hypertension, or in patients on HIV protease inhibitors.

1.5.2.3. Though undisputedly extremely effective, potential adverse effects limit ergometrine to a second-line agent.

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1.5.3. Carbetocin:

1.5.3.1. Routinely use oxytocin in preference to carbetocin if vaginal birth and cold-chain storage of oxytocin can be guaranteed (e.g. hospital setting).

1.5.3.2. If vaginal birth and cold-chain storage of uterotonics cannot be guaranteed:

·       Carbetocin is an effective alternative uterotonic

·       IM is preferred route of administration

1.5.3.2. If CS birth under regional anesthetic: IV carbetocin may be considered as a cost effective uterotonic

1.5.3.3. If CS birth under general anesthetic: Carbetocin is not recommended due to insufficient evidence.

1.5.3.4. If used: used as a single dose only, not for repeated use

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1.5.4. Misoprostol:

1.5.4.1. Not recommended if alternative injectable uterotonics are available

1.5.4.2. Use only if no other injectable uterotonic is available (e.g. due to unexpected birth in low resource setting or if storage conditions for uterotonics are inadequate).

1.5.4.3. The dose is 600 micrograms orally or sublingual single dose immediately after birth

1.5.4.4. If in a low resource setting with limited PPH treatment capability, consider use if:

·       an injectable uterotonic has been administered AND

·       continued bleeding is anticipated and/or blood loss is estimated to be greater than or equal to 350 mL  

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1.6. Tranexamic Acid (TXA) For Prophylaxis in High Risk Women

1.6.1. Tranexamic acid can be used as a prophylactic agent as an adjunct to uterotonics in patients at high risk for postpartum hemorrhage.

1.6.2. Use TXA within 3 hours of birth of the baby in a fixed dose of 1 g in 10 mL IV over 10 minutes (100 mg/min i.e. 1 ml /minute)

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1.7. Immediate Postpartum Risk Management

1.7.1. Uterine massage:

Sustained uterine massage is not recommended as an intervention to prevent PPH in women who have received prophylactic oxytocin.

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1.7.2. Uterine tonus assessment:

Postpartum abdominal uterine tonus assessment for early identification of uterine atony is recommended for all women.

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1.7.3. Nipple stimulation & breast feeding:

Nipple stimulation and/or early breastfeeding may increase uterine activity but has not been shown to reduce bleeding or incidence of PPH.

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1.7.4. Observation for women with risk factors in the first 2 hours postpartum:

·       Vital signs: Respiratory rate, pulse rate, and blood pressure, every 15-30 minutes in the first hour and every 30 minutes in the second hour.

·       Blood Loss every 15-30 minutes by visualizing the labia and perineum and be alert for slow steady trickle.

·       Temperature every 30 minutes

·       Uterine tonus assessment

·       Urine output: after the first 2 hours

·       After the first 2 hours continue as clinically indicated

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2. RECOGNITION OF PPH

2.1. General Principles In Diagnosis of PPH

2.1.1 Early recognition of postpartum hemorrhage (before deterioration in vital signs) is recommended and should be the goal in order to improve outcomes.

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2.1.2. Clinical signs and symptoms of hypovolemia should be included in the assessment of PPH. However, clinicians should be aware that the signs of hypovolemic shock become less sensitive in pregnancy.

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2.1.4. Consider initiation of response to PPH when there is excessive bleeding in the first 24 hours post birth, judged clinically, or through estimation of blood loss volume (> 500 ml after VD or 1000ml after CS), or changes in the hemodynamic state.

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2.2 Visual Assessment of The Amount of Postpartum Blood Loss

2.2.1. Visual estimation of blood loss is always subjective and can be imprecise and often leads to underestimation of large volumes or overestimation of small volumes

2.2.2. When conducting visual assessment of blood loss, consider the volume, nature and speed of blood loss.

2.2.3. Simulated scenarios and pictorial guides may improve staff accuracy  

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2.3. Quantitative Measurement of The Amount of Postpartum Blood Loss

2.3.1 Consider that quantitative measurement, provides a more accurate assessment of blood loss when compared with visual estimation.

2.3.2. Consider measurement of blood loss by blood collection drapes for vaginal deliveries,5,10 or the weighing of swabs and weigh blood-soaked items (e.g. linen, pads, swabs, drapes) to quantify volume.5,60 If weighing, 1 gram is equivalent to 1 mL blood loss.

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2.4. Diagnosis of PPH & Assessment of Hemodynamic Compromise

2.4.1. PPH can be minor (500–1000 ml blood loss) or major (more than 1000 ml blood loss). The condition becomes worse if the patient lost >2000 mL of blood.

2.4.2. Diagnose minor PPH (blood loss 500-1000 mL) if there are: 

·       Normal blood pressure

·       Mild increase in heart rate (but <100 beats/minute)

·       Palpitation

·       Lightheadedness

2.4.3. Diagnose major PPH (blood loss from 1000-2000 mL) if there are: 

·       Drop of blood pressure below the original average of the patient

·       Tachycardia (≥ 100 beats/minute)

·       Sweating

·       Weakness

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2.4.4. Signs of hemodynamic compromise are a late indicator of PPH and may not be evident until large volumes of blood are lost (e.g. up to 25% of total blood volume or greater than 1500 mL).

2.4.5. Don’t wait for the following to diagnose major PPH as blood loss is already >2000 mL and the condition would be severe enough to be of poorer prognosis:

·       Systolic blood pressure drops below 70-80 mmHg 

·       Tachycardia (120-140 beats/minute)

·       Restlessness, confusion and pallor

·       Oliguria

2.4.6. Conversely, compromise may occur earlier in women with:

·       Gestational hypertension with proteinuria

·       Anemia

·       Dehydration

·       Small stature

·       Cardiac disease

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3. RESPONDING TO AND MANAGEMENT OF PPH

3.1. General Principles In Responding To PPH

3.1.1. Bleeding after labor is an emergency and responding to it should not be delayed and should start as early as possible and goes hand in hand with the rest of management (Communication with the patient, senior staff, resuscitation investigation, and monitoring).

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3.1.2. Use an approach that involves maintaining hemodynamic stability while simultaneously identifying and treating the cause of blood loss.

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3.1.3. The urgency and measures undertaken to resuscitate and arrest hemorrhage need to be tailored to the amount of blood loss (which is usually underestimated), the patient general condition, and the degree of shock.

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3.1.4 The GDG recommends adoption of the EMOTIVE bundle (Early detection, Massage, Oxytocics, Tranexamic acid, IV fluids, Examination & Escalation) as the standard first-response protocol for all cases of postpartum hemorrhage. Initiate all components within 15 minutes of PPH diagnosis to ensure rapid, standardized, and evidence-based management, with ongoing monitoring and escalation as needed, see Appendix II.

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3.2. Communication And Multidisciplinary Care:

3.2.1. Communication with the patient and her birthing partner is important, and clear information of what is happening should be given from the outset.

3.2.2. Relevant staff with an appropriate level of expertise should be alerted of PPH.

3.2.3. The first-line obstetric and anesthetic staff should be alerted when women present with minor PPH (blood loss 500–1000 ml) without clinical shock

3.2.4. A multidisciplinary team involving senior members of staff should be called to attend to women with major PPH (blood loss of more than 1000 ml) and ongoing bleeding or clinical shock

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3.3. Responding To & Managing Minor PPH

3.3.1. Measures for minor PPH (blood loss 500–1000 ml) without clinical shock:

·       Establish IV access: 2 wide bore IV cannulas (Orange 14G & Grey 16G) are to be inserted. 14G for fluid and blood replacement & 16G for pharmacologic therapy 

·       Urgent venipuncture and obtain 20 ml of blood for:

o   Grouping & cross-matching

o   Full blood count

o   Coagulation screen, including fibrinogen, if available

·       Pulse, respiratory rate and blood pressure recording every 15 minutes

·       Commence warmed crystalloid infusion.

·       If bleeding is rapid and patient continues to bleed, consider starting the full protocol for major PPH.

·       In minor PPH, there are no firm criteria for initiating red cell transfusion. The decision to provide blood transfusion should be based on both clinical and hematological assessment.

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3.4. Identification of The Cause (the 4Ts)

3.4.1. If blood loss after delivery seems increased, start the measures of minor PPH and immediately assess for the Tone of the uterus, the presence of Trauma, any retained Tissue or Thrombin activity.

·       Tone: massage the fundus to see whether the uterus is atonic or well contracted.

·       Tissue: retained placental fragment. Inspect the placenta for a missing part. Also suspect retained placental fragment or pieces of membranes as a cause if there is atonic fundus unresponsive to uterotonics.

·       Trauma: if fundus is well contracted, blood clotting is ok and no placental remnants, explore birth canal for improperly repaired birth tract injuries.

·       Thrombin: The fundus is contracted (may be atonic) and the blood is not clotting.

·       Other unknown causes: if all of the above is normal, assess for uterine rupture/ inversion, concealed bleeding (e.g. vault hematoma, internal hemorrhage after CS) and non-genital causes (e.g. subcapsular liver rupture).

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3.5. Responding To & Managing Major PPH

3.5.1. Full protocol for major PPH (blood loss greater than 1000 ml) and continuing to bleed or clinical shock:

·       A and B: assess Airway and Breathing

·       C – evaluate Circulation

·       Position the patient flat

·       Insert two peripheral cannulas (14 gauge) if not inserted before

·       Immediately draw 20 mL of blood for:

o   Cross-matching (4 units of blood minimum)

o   Full blood count

o   Coagulation screen (PT, INR, aPTT including fibrinogen, if available)

o   Chemistry profile (Serum Creatinine, SGOT, SGPT, Albumin, LDH, Blood Sugar)

·       Keep the woman warm using appropriate available measures

·       Transfuse blood as soon as possible.

·       Until blood is available, infuse up to 3.5 L of warmed crystalloids as Lactated Ringer’s (1–2 mL for every 1 mL of blood loss)²

·       Stop fluid once blood is ready.

·       The best equipment available should be used to achieve rapid warmed infusion of fluids.

·       Special blood filters should not be used, as they slow infusions.

·       If actively bleeding, transfuse early and do not wait unnecessarily for laboratory results and use clinical assessment as the main determinant

3.5.2. Blood transfusion:

·       3.5.2.1. If actively bleeding, transfuse early, do not wait unnecessarily for laboratory results. The clinical picture should be the main determinant of the need for blood transfusion and time should not be unnecessarily spent awaiting laboratory results.

·       3.5.2.2. Packed RBCs:

o   Provide emergency blood (Packed RBCs) with immediate issue of group O, rhesus D (RhD)-negative, with a switch to group-specific blood as soon as feasible.

o   Single Hb/hematocrit estimations may be misleading and can lead to delays in initiating red cell transfusion, serial measurements may be helpful to monitor ongoing progress.

·       3.5.2.2. Transfusion of FFP:

o   Administration of FFP should be guided by coagulation profile test results and whether bleeding is continuing.

o   But if coagulation profile results are not available and bleeding is continuing, after 4 units of red blood cells, 4 units of FFP should be infused until test results are known.

o   If coagulation profile results are not available, early FFP should be considered for conditions with a suspected coagulopathy, such as placental abruption or amniotic fluid embolism, or where detection of PPH has been delayed.

o   If prothrombin time/activated partial thromboplastin time is more than 1.5 times normal and hemorrhage is ongoing, more units of FFP are likely to be needed to correct coagulopathy.

·       3.5.2.3. Clinicians should be aware that these blood components must be ordered as soon as a need for them is anticipated, as there will always be a short delay in supply because of the need for thawing.

3.5.3. Cryoprecipitate For Fibrinogen Replacement

·       A plasma fibrinogen level of greater than 2 g/l should be maintained, if test is available, during ongoing PPH.

·       Cryoprecipitate should be used for fibrinogen replacement.

·       Physician should be aware that fibrinogen below 3 g/l and especially below 2 g/l is associated with progression of bleeding, increased RBC and blood component requirements, and the need for invasive procedures.

3.5.4. Transfusion of platelets

·       During PPH, platelets should be transfused when the platelet count is less than 75 × 10⁹/l (75000 / mm³) based on laboratory monitoring.

·       The platelets should ideally be group compatible. RhD-negative women should receive RhD-negative platelets.

3.5.5. Use Continued Resuscitation with lab-guided replacement to maintain the following lab parameters:

·       Hb greater than 8 gm%

·       Platelet count greater than 50 × 109 /l (50000/mm³)

·       Prothrombin time (PT) less than 1.5 times normal

·       Activated partial thromboplastin time (APTT) less than 1.5 times normal 

·       Fibrinogen level greater than 2 g/l.

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3.5.5. Tranexamic acid (TXA)

3.5.5.1. Tranexamic acid can be used in all patients as an adjunct to uterotonics in the setting of postpartum hemorrhage regardless of whether the bleeding is due to genital tract trauma or other causes.

3.5.5.2. Give TXA as early as possible, ideally within 3 hours of birth, in a fixed dose of 1 g in 10 mL (100 mg/mL) IV at 1 mL per minute (i.e., over 10 minutes).

3.5.5.3. A second dose of 1 g IV may be administered if bleeding continues after 30 minutes of the first dose or for bleeding that stops but restarts within 24 hours of completing the first dose.

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4. MONITORING AND INVESTIGATIONS IN MAJOR PPH

4.1 Immediate venipuncture (20 ml) for:

·       Cross-matching (4 units of Packed RBCs minimum)

·       FBC

·       Coagulation screen (PT, INR, aPTT including fibrinogen, if available)

·       Chemistry profile (Serum Creatinine, SGOT, SGPT, Albumin, LDH, Blood Sugar)

·        Repeat as necessary

4.2 Continuous pulse, blood pressure and respiratory rate recording (preferably using oximeter, electrocardiogram and automated blood pressure recording when available) and Monitor temperature every 15 minutes.

4.3.         Foley’s catheter to monitor urine output

4.4.         Documentation of fluid balance, blood, blood products and procedures.

4.5.         Consider transfer to intensive therapy unit once the bleeding is controlled or monitoring at high dependency unit on delivery suite, if appropriate.

4.6.         Consider objective scoring system for monitoring as the MEOWS Score (see Appendix II)

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5. ROLE OF THE ANESTHETIST IN THE MANAGEMENT OF PPH

The management of PPH requires a multidisciplinary approach: Allow the anesthetist to play a crucial role in maintaining hemodynamic stability and, in determining and administering the most appropriate method of anesthesia.

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6. PAIN MANAGEMENT

Consider pain relief requirements during initial resuscitation and all subsequent treatments

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7. PHARMACOLOGICAL AND MECHANICAL STRATEGIES IN MANAGEMENT OF PPH

7.1. Clinicians should be prepared to use a combination of pharmacological, mechanical and surgical methods to arrest PPH. These methods should be directed towards the causative factor.

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7.2. When uterine atony is perceived to be a cause of the bleeding, then a sequence of pharmacological and mechanical measures (in the form of uterine massage and urinary bladder catheterization) should be instituted until the bleeding stops.

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7.3 Stopping the bleeding should not be delayed and should start as early as possible and goes hand in hand with the rest of management above (Communication and multidisciplinary approach, Resuscitation, Investigation, and Monitoring)

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7.4. The most common cause of primary PPH is uterine atony. The initial management of PPH should, therefore, involve measures to stimulate myometrial contractions. Thus, mechanical and pharmacological measures should be instituted/administered as needed.

7.5.         Palpate the uterine fundus and rub it to stimulate contractions and expel its contents (‘rubbing up the fundus’)

7.6.         Ensure that the bladder is empty (Foley catheter & leave in place)

7.7 First line pharmacological therapy for uterine atony (Oxytocin):

·       Give oxytocin 5 IU IV over 1-2 minutes (even if had the prophylactic dose before). The dose may be repeated, only once, after five minutes but consider the maximum dose for IV oxytocin which is 10 IU IV.

·       Rapid IV bolus administration may cause hypotension, tachycardia, arrhythmia and myocardial ischemia.

·       Continue with oxytocin IV infusion 40 IU in 500 mL of either 0.9% sodium chloride (saline) or compound sodium lactate (Ringer’s lactate) at a rate of 5-10 IU/hour via:

o   Using ordinary IV line about adjust it to deliver 20-40 drop/minute

o   Infusion pump, if available, equals to 62.5–125 mL per hour

o   Minimum infusion duration is 2 - 4 hours; use clinical judgement.

·       Oxytocin infusion may be a safer alternative to a bolus dose of oxytocin in some women (e.g. major cardiovascular disorders)

·       If the patient had induction of labor (IOL) with oxytocin, you may use the same infusion but at increased rate.

·       If IV access unavailable or delayed, oxytocin 10 IU IM can be administered

·       If carbetocin has already been given, consider non-oxytocin uterotonic instead

7.8 Supplemental therapy if no adequate response: give the following:

7.8.1.   Ergometrine maleate:

o   0.25 - 0.5 mg IV over 1-2 minutes (dilute 250 micrograms in 5 mL 0.9% sodium chloride) that may be repeated every 5 minutes to a maximum of 1 mg

o   It is contraindicated with retained placenta, severe hypertension, pre-eclampsia, eclampsia severe/persistent sepsis, renal, hepatic, vascular, or cardiac disease

7.8.2.   Misoprostol:

·       Consider misoprostol if alternative uterotonics unavailable or contraindicated (e.g. asthma, hypertension) or if bleeding not effectively controlled with oxytocin.

·       Give 800 mcg sublingual (rapid onset of action with side effects more likely)

·       Or 1000 mcg per rectum (slow absorption but prolonged effect)

·       Consider clinical circumstances when determining optimal route

·       Side effects: Hyperthermia is a common side effect (>38 C is common) and malignant hyperthermia > 40 C has been reported in 1 - 14% of cases

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8. SURGICAL TREATMENTS OF PPH

8.1. If pharmacological measures fail to control the hemorrhage, surgical interventions should be initiated sooner rather than later and the most experienced, anesthetist and obstetrician should be called to be involved in the management.

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8.2. Transfer the patient to the operative theatre flat with high-flow oxygen and perform an examination under anesthesia for the exclusion of the presence of remnants (to be evacuated if present) and dealing with any birth tract injuries if found

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8.3. Bimanual Compression: The use of bimanual uterine compression is recommended as a temporary measure until appropriate care is available for the treatment of PPH due to uterine atony after vaginal delivery

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8.4. Intrauterine balloon tamponade:

·       If bimanual compression has been effective consider the use of intrauterine balloon tamponade (e.g. Bakri Balloon) as balloon is an appropriate first-line ‘surgical’ intervention for most women where uterine atony is the only or main cause of hemorrhage after the success of bimanual uterine compression.

·       After insertion, assess blood loss:

·       If bleeding continues, balloon tamponade may be ineffective—review aetiology of PPH, check balloon placement and consider other surgical interventions.

·       If bleeding ceases on insertion, monitor fundal height, uterine cramping and signs of increased blood loss regularly

·       Balloon is left for 6 hours if bleeding stopped and removed in presence of senior staff lest the return of bleeding.

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8.5. If bimanual compression is ineffective or balloon tamponade fail:

·       Consider exploratory laparotomy when less invasive approaches fail to control bleeding. In the setting of a vaginal delivery, it is common to use a midline vertical abdominal incision for laparotomy, to optimize exposure and reduce risk of surgical bleeding. In the setting of cesarean birth, the existing surgical incision may be used.

·       Conservative surgical interventions (compression sutures and/or arterial ligation) may be attempted as a second line, depending on clinical circumstances and available expertise.

·       Timing is critical. Surgical interventions should be initiated sooner rather than later.

·       Weigh benefits of conservative versus aggressive management (hysterectomy)

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8.6 Hemostatic uterine suture (e.g. B-Lynch suture)

·       Judiciously apply aortic compression (below the level of the renal arteries) as a temporary measure

·       Consider B-Lynch compression or other compression suture

·       It is preferable that a laminated diagram of the brace suture technique, as B-lynch suture, be kept in theatre.

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8.7. Arterial ligation: Stepwise arterial ligation for uterine devascularization may be considered depending on clinical circumstances and available expertise:

·       Bilateral uterine artery ligation

·       Bilateral utero-ovarian artery ligation

·       If expertise available, bilateral internal iliac artery ligation

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8.8. Hysterectomy:

8.8.1. Resort to hysterectomy early (sooner rather than later) especially if:

·       Life is threatened (hemodynamic unstable patient),

·       Bleeding continues after use of conservative treatment options

·       blood transfusion is limited or not an option.

·       In cases of placenta accreta or uterine rupture.

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8.8.2.   Subtotal (Supra-Vaginal) hysterectomy is quicker and safer in Major PPH and in packing of the abdomen, use hot packs.

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8.8.3.   Ideally and when feasible, a second experienced clinician should be involved in the decision for hysterectomy.

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8.8.4.   In rare situations in spite of compression, arterial ligation and hysterectomy, bleeding from undefined origin might persist in the pelvis (undefined diffuse venous bleeding or bleeding due to DIC). Tight pelvic packing with radio-opaque packs, done by a senior obstetrician, may be a last resort to be followed by temporarily closing the abdomen, stabilization of the patient condition by multidisciplinary team, then reopening the abdomen again to remove the packs and reassess hemostasis after 24-48 hours.

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9.         RISK MANAGEMENT

9.1.          Training and Preparation

Every maternity unit should have a multidisciplinary protocol for the management of PPH.

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All staff involved in maternity care should receive training in the management of obstetric emergencies, including the management of PPH.

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Training for PPH should be multidisciplinary and multiprofessional including team rehearsals.

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All cases of PPH involving a blood loss of greater than 1500 ml should be the subject of a formal clinical incident review.

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9.2.          Documentation

Accurate documentation of a delivery with PPH is essential.

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9.3.          Consent

If treatment is likely to affect woman’s fertility, prioritize gaining informed consent.

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10.      Postnatal Care

Upon discharge: Educate about signs, symptoms and self-referral regarding persistent or increasing bleeding, infection and risk of secondary PPH, postnatal depression, and venous thromboembolism

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Oral iron supplementation, either alone or in combination with folic acid, may be provided to postpartum women for 6–12 weeks after delivery for reducing the risk of anemia.

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Offer the woman and family debriefing/clinical disclosure by senior team members, preferably by clinicians who were at the event

Offer additional opportunities for discussion/debrief six weeks postpartum

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