This document provides information about blood transfusion in obstetrics. It discusses the risks of blood transfusion, problems specific to pregnancy, indications for transfusion including anaemia and obstetric hemorrhage, estimating blood loss, management of hemorrhage, and controversies regarding transfusion such as choice of fluids and need for cross-matching in emergencies. The document aims to guide appropriate transfusion practice for reducing maternal mortality from conditions like postpartum hemorrhage.
Blood transfusion in obstetric haemorrhageWafaa Benjamin
Blood transfusion may be a life-saving procedure but it is not without risk.
Obstetric conditions associated with the need for blood transfusion (whether emergency or not) may lead to morbidity and mortality if not managed correctly.
Adverse events associated with transfusion are increasingly important:
So, strict adherence to correct sampling, cross-match and administration procedures is therefore of paramount importance, even in an emergency.
Blood transfusion in obstetric haemorrhageWafaa Benjamin
Blood transfusion may be a life-saving procedure but it is not without risk.
Obstetric conditions associated with the need for blood transfusion (whether emergency or not) may lead to morbidity and mortality if not managed correctly.
Adverse events associated with transfusion are increasingly important:
So, strict adherence to correct sampling, cross-match and administration procedures is therefore of paramount importance, even in an emergency.
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This presentation describes in detail about managing Rh negative pregnancy- to identify and manage Rh non-isommunized and Rh isoimmunized pregnancies, with recent advances
review the evidence (RCT & meta-analyses) concerning the best practices in contemporary Recurrent Pregnancy Loss and Thrombophilia depending on Eshre guideline 2017 and other EBM sources.
Fetal growth restriction (FGR), formerly called intrauterine growth restriction (IUGR), refers to a condition in which an unborn baby is smaller than it should be because it is not growing at a normal rate inside the womb.
Mild FGR usually doesn't cause long-term problems. In fact, most babies who have it catch up in height and weight by age 2. But severe FGR can seriously harm a baby before and after birth. The extent of the problems depends on the cause and how severe the growth restriction is. It also depends on what point in the pregnancy it starts.
This presentation describes in detail about managing Rh negative pregnancy- to identify and manage Rh non-isommunized and Rh isoimmunized pregnancies, with recent advances
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June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
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- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
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- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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2. CONTENTS
INTRODUCTION
1. RISKS
2. SPECIFIC TO PREGNANCY
3. REDUCING RISK
4. GENERAL PRINCIPLES
ABOUBAR ELNASHAR
5. INDICATIONS
1. Anaemia
2. OBS Hge
1. Causes
2. Estimation
3. Management
4. Controversies
5. How much & when to
stop
6. Blood components
SUMMARY
3. INTRODUCTION
Obstetric hge:
major cause of maternal mortality
in the UK: 3rd leading
In Egypt: 1st leading
Postpartum hge
25% of all pregnancy-related deaths.
ABOUBAR ELNASHAR
4. Blood transfusion
one of 8 essential components to reduce maternal
mortality rates.
As ‘too little, too late’.
Women at high risk of losing 1000 ml:
should deliver in a setting where
blood transfusion
intensive care facilities are available.
Life-saving procedure
ABOUBAR ELNASHAR
5. In developing countries
Availability of blood transfusion depends on
Infrastructure
Economics
Social and religious taboos
Practices
: transfusion practices vary from those in
the developed countries
ABOUBAR ELNASHAR
6. 1. RISKS OF BLOOD TRANSFUSION
1. Transfusion-transmitted infections
2. Immunological sequelae:
red cell alloimmunisation.
3. The major risk: ‘incorrect blood component’.
Strict adherence to:
correct sampling
cross-match
Administration procedures:
paramount importance, even in an emergency.
ABOUBAR ELNASHAR
7. 2. PROBLEMS SPECIFIC TO THE PREGNANCY
1. Physiological changes in pregnancy
a. Haemodilution
Increase in
red cell mass (20-30%)
plasma volume (50%):
patient stay haemodynamically stable with
the normal blood loss during delivery.
b. Decrease in platelet levels:
gestational thrombocytopenia.
ABOUBAR ELNASHAR
8. c. Hypercoagulable state
Increase in
coagulation factors:
fibrinogen and factors VII, VIII, and IX
supervening over the increase in the natural
anticoagulants:
Protein A, Protein C, and Antithrombin III.
Fibrinolytic system decreases in activity.
Plasminogen is increased, but its activity is dampened by a
corresponding increase in plasminogen inhibitor type II.
Hypercoagulable state
limit blood loss
can tip the mother into:
DIC and
Pulmonary embolism.
ABOUBAR ELNASHAR
9. 2. Difficulty in assessment of blood loss by
Vital signs:
{increased maternal plasma volume}.
Haemodilution and high cardiac output: large
amount of blood loss in a pregnant female
before the hypotension and fall in Hgb/ Hct
Visual assessment
{large amounts of blood lost may be concealed in
the uterine cavity}.
ABOUBAR ELNASHAR
10. 3. Associated comorbid conditions
PET
Thrombocytopenia
HELLP syndrome
can bring about catastrophic hge.
ABOUBAR ELNASHAR
11. 4. Risk to foetus
While managing acute haemorrhagic emergencies,
the foetus has to be kept in mind, to prevent
Infections
Haemolytic Disease of the Foetus and Newborn
(HDFN) in the current and future pregnancies.
ABOUBAR ELNASHAR
12. 3. REDUCING RISK OF BLOOD TRANSFUSION
1. Optimization of Hb in ANC
Screening
at booking
at 28 w.
at 20–24 w in multiple pregnancies
Diagnosis
1st T. Hb: ≤11.0 g/l
2nd &3rd T. Hb: ≤ 10.5 g/l
Postpartum Hb: ≤ 10.0 g/l
ABOUBAR ELNASHAR
13. Treatment
Inform patient
How to improve dietary iron intake
Factors affecting absorption of dietary iron
Oral iron:
1st TT line.
:if no demonstrable rise in Hb at 2 ws
Check compliance
Further TT
Parenteral iron
indicated when
oral iron is not tolerated
absorbed
patient compliance is in doubt
if the woman is approaching term and there is insufficient time
for oral supplementation to be effective.
ABOUBAR ELNASHAR
14. 2. Active management of the third stage of labour
To minimise blood loss.
Involve
use of uterotonics
early clamping of the cord
controlled cord traction
3. Women at high risk of hge
should be advised to deliver in hospital.
ABOUBAR ELNASHAR
15. 4. GENERAL PRINCIPLES OF BLOOD
TRANSFUSION
1. Consent for blood transfusion
obtained where possible
In an emergency:
information on blood transfusion should be
provided retrospectively.
Document in patient case notes
Reason for transfusion
Consent
ABOUBAR ELNASHAR
16. 2. All women should have
blood group and
antibody status
checked at
Booking
28 w.
Group and screen samples used for provision of blood in pregnancy should be
less than 3 days old.
Transfusion or pregnancy may stimulate the production of unexpected
antibodies against red cell antigens through either a primary or secondary
immune response. To ensure that the specimen used for compatibility testing is
representative of a patient’s current immune status, serological studies should
be performed using blood collected no more than 3 days in advance of the
actual transfusion when the patient has been transfused or pregnant within the
preceding 3 months.
ABOUBAR ELNASHAR
17. In a woman at high risk of emergency transfusion:
Placenta praevia, and with no clinically significant alloantibodies
group and screen samples
should be sent once a week
{exclude or identify any new antibody formation}
keep blood available if necessary.
Close contact with the hospital transfusion
laboratory is essential.
ABOUBAR ELNASHAR
18. 3. Blood product specification in pregnancy&puerperium
ABO-, rhesus D- (RhD-) and K- (Kell-)
compatible red cell units should be transfused.
If clinically significant red cell antibodies are present:
blood negative for the relevant antigen should be
cross-matched before transfusion; close contact with the
transfusion laboratory is essential to avoid delay in transfusion in life-
threatening hge.
CMV seronegative red cell
Platelet components:
should be provided for elective transfusions during
pregnancy.
ABOUBAR ELNASHAR
19. 5. INDICATIONS OF BLOOD TRANSFUSION IN
OBSTETRICS
I. Anaemia of pregnancy and Haemoglobinopathies
II. Obstetric hge
III. Surgeries where significant blood loss is expected.
ABOUBAR ELNASHAR
20. I. BLOOD TRANSFUSION FOR ANAEMIA
Antepartum anaemia
responsible for 15% of maternal mortality.
Early correction:
avoids the need for transfusion
reduces maternal mortality.
The decision for transfusion
should not be made on the basis of Hgb alone
Healthy&clinically stable women do not require
blood transfusion even with Hb of <7 g/dl.
ABOUBAR ELNASHAR
21. Indications: Cochrane SR, 2007
1. Hb <6 g/dl
there are <4 ws for delivery
2. Hb is <7 g/dl
in labour or
in immediate postpartum period, if there is
previous history of bleeding or
patient is prone for bleeding due to some
medical condition.
3. Hb is 7 g/dl
continued bleeding or
at risk of further significant hge or
presenting with severe symptoms that need
immediate correction (cardiac decompensation).
ABOUBAR ELNASHAR
22. 4. Sickle disease and thalassaemia
severe situations
{prophylactic transfusion:
increases in costs
number of hospitalizations
risk of alloimmunisation}.
ABOUBAR ELNASHAR
23. II. BLOOD TRANSFUSION FOR OBSTETRIC
HAEMORRHAGE
The leading cause of maternal mortality
13% in developed countries
33% in Africa.
[WHO, 2006]
may occur before or after delivery
>80% of cases occur postpartum
[McLintock , James, 2011]
ABOUBAR ELNASHAR
24. 1. Causes Of Obstetric Haemorrhage
Early pregnancy
Abortions
Ectopic pregnancy
Later pregnancy
Antepartum haemorrhage
Placenta praevia, placental abruption
bleeding from vaginal or cervical lesions
Primary postpartum haemorrhage
Tone (uterine atony)
Tissue (retained products)
Trauma (cervical and genital tract damage during delivery)
Thrombin (coagulation disorder)
Secondary postpartum haemorrhage
Uterine atony
retained products
genital tract trauma,
uterine inversion ABOUBAR ELNASHAR
25. 2. Estimation Of Blood Loss
1. Visual assessment:
Inaccurate
clinicians can underestimate blood loss by 50%.
PPH
>500 ml after VD and
>1000 ml after CS, do not adequately reflect the
clinical response of the patient.
Massive hge
1000-1500 ml
50% blood volume loss within 3-h or
rate of loss of 150 ml/min.
ABOUBAR ELNASHAR
26. 2. HCT
Immediate Hct will not reflect actual blood loss.
Even blood loss of 1000 ml will reflect a fall
in Hct of only 3% in the 1st h.
3. Urine output
sensitive to changes in blood volume
can give an early indication of changes in renal
perfusion and hence perfusion of other organs.
4. Pulse Oximetry
an imperfect tool in the haemodynamically
unstable patient.
ABOUBAR ELNASHAR
27. More accurate methods:
1. Weighing packs:
Hospital keeps scales in delivery rooms to weigh lap sponges &
other materials to estimate blood loss.
1kg soaked swabs: 1000ml
2. Comparing visual estimation of blood loss with the
use of a collector bag
soda can hold about 350 cc of blood
concluded that the latter did not significantly reduce the risk of severe
PPH.
ABOUBAR ELNASHAR
28. 3. Written guidelines
Maximum capacity of Swab
Small (10x10cm): 60ml
Medium (30x30 cm): 140ml
Large (45x45 cm): 350ml
Floor spill
50 cm diameter: 500ml
75 cm diameter: 1000ml
100 cm diameter: 1500ml
Vaginal PPH
Limited to bed only unlikely to exceed 1000ml
Spilling from bed to floor likely to exceed
1000ml
ABOUBAR ELNASHAR
30. 3. Management Of Obstetric Haemorrhage
Multidisciplinary approach to massive blood loss yields
the best results.
ACOG:
The CMQCC protocol
Step-by-step checklist format
Based on the staging of obstetric hge
RCOG
Therapeutic and monitoring guidelines for minor and
major postpartum hge
While there are some individual variations, the broad
outlines remain the same. ABOUBAR ELNASHAR
31. The 4 mainstay of management of hge:
1. Rapid resuscitation with crystalloids:
restore and maintain the circulating blood
volume
prevent tissue and organ hypo-perfusion.
2. Blood transfusion in acute hge:
maintain tissue oxygenation
reversal or prevention of coagulopathy using
appropriate blood components.
ABOUBAR ELNASHAR
32. 3. Prevention& treatment of
hypothermia,
acidosis
hypocalcaemia:
optimal function of transfused coagulation factors.
4. Simultaneously, the cause of bleeding should be
Identified
controlled, by
medical means
surgery or
invasive radiography.
ABOUBAR ELNASHAR
33. Major PPH >1000 ml or ShockMinor PPH <1000 ml
&Compensated
Airway, Breathing& Circulation
O2 by mask at 10–15 L/M
14-gauge cannula x2
Blood component rapidly
Packed RBC: Fresh frozen plasma:
Platelets= 6:4:1
Until blood is available: IV up to 3.5 L
crystalloid lactated Ringer (± one L of it
is colloid)
Keep patient& infusions warm
IV access one 14-
gauge cannula
Crystalloid infusion:
1-1.5 L lactated Ringer
ABOUBAR ELNASHAR
34. 4. Controversies For Transfusion In Obstetrics
1. Colloids or Crystalloids:
have no advantage over Crystalloids
high cost
(The SAFE trial and the CRISTAL trial)
Crystalloids
rapidly equilibrate with the extracellular fluid
only 20% remains in circulation after 1st h.
The accepted average ratio of Colloid: Crystalloid is
1:1.5.
ABOUBAR ELNASHAR
35. Crystalloid:
NS
D5NS can be given
Ringer
Hartmann
Ringer=lactated Ringer
Nacl: 6.5 g,
Kcl:0.42 g,
Ca cl: 0.25 g,
1 mol of Na bicarbonate
is dissolved in 1 liter of distilled water
Colloids:
Human albumin,
Hydroxyethylstarch (HES)
Dextran
Mannitol
Haemaccel
ABOUBAR ELNASHAR
Hartmann solution= compound
sodium lactate
NaCl
KCl
CaCl dihydrate
Na lactate
36. 2. Whole blood or blood component?
superior to PRBCs or combined transfusions in
preventing acute tubular necrosis and other
complications.
replaces many coagulation factors
its plasma expands blood volume.
exposing the patient to fewer donors.
The availability of fresh warm blood in developing countries
could provide an alternative to more expensive and infra
structure-dependent blood components.
ABOUBAR ELNASHAR
37. 3. To cross-match or not to cross-match?
The chances of a clinically significant red cell
antibody being missed in a patient with a negative
antibody screen (false negative) are
1-4/10,000.
Given that the chance of adverse consequences is
small, in cases of acute massive hge, it appears
reasonable to transfuse blood without
type-and-screened red blood cells.
[Rege et al, 2014]
ABOUBAR ELNASHAR
38. 5. Blood Transfusion: How Much& When To Stop?
The decision for blood transfusion
Hb≤6.0 g/dl
almost always required
Hb≥10.0 g/dl
rarely required
Hb is normal but acute hge
Required
Single Hb/ hct
±misleading
±:delay initiating red cell transfusion
Serial measurements helpful
ABOUBAR ELNASHAR
39. Goals of management of massive blood loss:
Most protocols recommend maintaining a target
Hct of 21-24%.
Restrictive transfusions and liberal transfusions were of equivalent
value in critically ill patients while relatively stable patients undergoing
liberal transfusions had a higher 30-day mortality.
[Hébert et al, 2012]
Hb ≥8 g/dl
Platelet 50x 109/L
PT ≤1.5 times normal
APPT ≤1.5 times normal
Fibrinogen 2g/L
ABOUBAR ELNASHAR
40. The risk of dilutional coagulopathy
needs to be borne in mind when multiple units of
PRBCs and crystalloids/colloids are used.
<10 units of PRBCs rarely need component
replacement
The lowest mortality occurs in the patients where
ratio of plasma and PRBCs is 1:1.
Recommend ratio of PRBC, fresh frozen plasma and
Platelet of 6: 4:1 in cases of massive hge.
ABOUBAR ELNASHAR
41. 6. Management Of Obstetric Haemorrhage With Blood
Components
There should be a clear local protocol on how to
manage major obstetric hge.
The protocol should be updated annually and practised
in ‘skills drills’ to inform and train relevant personnel.
ABOUBAR ELNASHAR
42. 1. Clinicians should familiarise themselves with
mechanical strategies that can be employed to
reduce postpartum blood loss.
rubbing up the fundus
bimanual uterine compression
emptying the bladder to stimulate uterine
contraction
ABOUBAR ELNASHAR
43. 2. Blood components used for obstetric hge
Red cell transfusion
The decision to provide blood transfusion should
be made on clinical and haematological grounds.
almost always required when Hb ≤60 g/l
rarely required when the Hb≥100 g/l.
Patients with acute hge can have normal Hb: cl
evaluation of the patient is extremely important.
ABOUBAR ELNASHAR
44. In an extreme situation and when the blood group is
unknown:
group O RhD-negative red cells should be given
(although they may be incompatible for patients with
irregular antibodies).
Staff working in obstetric units should be aware of the location of the satellite blood
fridge (where available) and should ensure that access is possible for blood collection.
ABOUBAR ELNASHAR
45. FFP
Dose:
12–15 ml/kg for/6 units of red cells during major
obstetric hge.
Subsequent FFP transfusion should be guided by
the results of clotting tests, aiming to maintain PT
and APTT ratios at less than 1.5 x normal.
During bleeding episodes:
Regular full blood counts
coagulation screens (PT, APTT and fibrinogen)
are performed
ABOUBAR ELNASHAR
46. Cryoprecipitate
Dose:
two 5-unit pools should be administered early in
major obstetric hge.
Subsequent transfusion should be guided by
fibrinogen results
aiming to keep levels above 1.5 g/l.
ABOUBAR ELNASHAR
47. Platelets
Aim:
maintain the platelet count above 50 x 109/l in the
acutely bleeding patient.
A platelet transfusion trigger of 75 x 109/l is
recommended to provide a margin of safety.
The platelets should ideally be group compatible.
RhD-negative women should also receive RhD-
negative platelets.
ABOUBAR ELNASHAR
48. SUMMARY
Blood transfusion is an essential component of
obstetric care and at times lifesaving.
Inappropriate transfusions during pregnancy and the
postpartum period expose the mother to the risk of
HDFN.
In the situation of obstetric hge early resuscitation is
done with crystalloids with oxygenation while
simultaneously taking all steps to control bleeding and
reduce the transfusion requirement.
A preplanned, multidisciplinary protocol yields the best
results in the management.
ABOUBAR ELNASHAR
49. The decision to perform a blood transfusion should be
made on both clinical and haematological grounds.
The majority of protocols recommended that Hct be
maintained minimally at 21-24%; however, in actively
bleeding patient, target Hct should be 30%.
To avoid dilutional coagulopathy,replacement with
coagulation factors and platelets may be necessary.
Whole blood may be preferred in acute massive hge,
especially where blood components are not available.
In an extreme situation and when the blood group is
unknown, O RhD negative red cells should be given.
ABOUBAR ELNASHAR
50. ABOUBAR ELNASHAR
You can get this lecture from:
1.My scientific page on Face book:
Aboubakr Elnashar Lectures.
https://www.facebook.com/groups/2277
44884091351/
2.Slide share web site
3.elnashar53@hotmail.com
4.My clinic: Elthwara St. Mansura