postpartum haemorrhage, dr jeevan

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  • 7/31/2019 Postpartum Haemorrhage, Dr Jeevan

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    Definition

    Qualitative definition:

    Vaginal bleeding in excess of 500 ml after child birth.

    But practically it is difficult to assess.

    Clinical definition:Any amount of bleeding from or into the genital tract following child

    birth which adversely affect the general condition of patient

    evidenced by rise in pulse rate and falling blood pressure.

    (Systolic BP < 90 mmHg and pulse > 110/min.)

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    Epidemiology

    According to the data of 1998, PPH found to

    be major culprit for maternal death in Nepal.

    About 47% of the maternal death was caused

    by PPH.

    A recent survey done in 10 districts of Nepalshows that PPH causes 19% of the maternal

    death

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    Types of PPH

    Primary:

    Bleeding within 24 hrs postpartum

    Secondary:

    Bleeding beyond 24 hrs till puerperium(6

    weeks).

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    Note:

    Every healthy non anaemic women canhave catastrophic blood loss

    Bleeding may occur at a slow rate overseveral hours and condition may not be

    recognised until the woman suddenly enters

    shock

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    Causes of primary PPH

    4 Ts

    Tone

    Trauma

    Tissue Remnant

    Thrombin

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    A. Reduced Tone (70%)

    With separation of placenta uterine sinuses

    which are torn cannot be compressed

    effectively due to imperfect contraction and

    retraction of uterus

    Risks: Grand Multipara

    Over distension of uterus

    Malnutrition and anaemia

    Prolonged labour

    Malformed uterus

    Uterine fibroid

    precipitate labour ( reduced adaptation / genital trauma)

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    B. Trauma (20%)

    Trauma to genital tract.

    Cervix , vaginal wall, perineal tear can occur

    Occurs more often with increased

    instrumentation, difficult labour

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    C. Tissue Retained (10%)

    Bits of placenta / membrane

    Blood clots

    Primarily interfere in uterine contraction

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    D. Thrombin (

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    Prevention of PPH

    PPH cannot always be prevented . However

    incidence and its magnitude can be reduced

    substantially.

    Antenatal:

    Improvement of health status

    High risk patient screening and counselling

    Blood grouping

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    Intranatal:

    Slow delivery of baby. Baby should be pushed out not pulled out Active management of third stage of labour which includes: inj.

    oxytocin 10U IM stat, CCT to be done after placental separationonly and fundal massage

    Examination of placenta and membrane should be routinely done

    Oxytocin infusion should be continued at least one hour after

    delivery in those cases in which labour is induced or augmented by

    oxytocin

    Exploration of birth canal especially following difficult labour or

    instrumental delivery

    Observation of patient for about 2 hours before sending her to

    ward.

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    Management of PPH

    Shout for extra help. urgently mobilise all

    personnel available

    Counsel mother and her relatives about the

    condition gravity

    Rapid evalutation of general condition bymeasuring pulse, BP, Temperature and

    respiratory rate

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    Management of PPH

    If patient has following features, the patient is

    considered to have gone into shock:

    Systolic BP: < 90 mmHg

    Pulse: > 100/min

    Pallor

    Unconciousness

    Cold clammy Periphery

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    Management of PPH

    Management of shock:

    Basic principles of shock are: Maintain Airway , Breathing and circulation

    Oxygen

    positioning

    Open IV line ( 2 lines) by large bore canula

    and infuse fluid (NS or RL) fast.

    Catheterisation and input/output charting

    Send blood for Hb%, Blood grouping and cross

    matching

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    Management of PPH

    Uterine massage should be done

    if well contracted

    Examine cervix, vagina and perinium for traumaif present repair.

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    Management of PPH

    If uterine atony is there then following steps

    have to be carried out

    Step 1.

    Uterine massage

    Inj. Oxytocin 10 U IM stat if not given earlier

    and Inj. Oxytocin 10-20 U in 500ml Rl/NS @

    40-60 drops/min Examine expelled placenta and membrane

    Bladder catheterisation if not done earlier

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    Management of PPH

    Step 2.

    Exclude coexisting injured/traumatic site in the

    birth canal

    Continue Oxytocin drip

    Misoprostol 600 microgram per rectally

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    Management of PPH

    Step 3.

    Bimanual compression / Aortic compression

    Tight intrauterine packing under anaesthesia

    Step 4.

    Surgery

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    Continuous care following

    control of PPH

    Vitals should be monitored every 15 min in 1st hour then

    every 30 min in 2nd hour and 4 hourly in next 24 hours.

    Breast feeding

    Hb. done after 24 hours If haemoglobin is below 7 gm/dl and vitals of the patient is

    unstable, blood transfusion should be done or referred.

    Iron tablet should be given for 6 months

    Albendazole given if was not given earlier. Nutritional counselling

    Discharged only after 24 hours of control of PPH

    During discharge counselling to be done regarding FP

    and danger signs.

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    Secondary PPH

    Bleeding usually occurs between 8th and 14th

    day of delivery

    The causes of late post partum are

    Retained bits of cotyledon or membrane(commonest)

    Infection and separation of slough over a

    deep cervico vaginal tear Endometritis and subinvolution of placental

    site due to delay healing process

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    Conclusion:

    The commonest cause of PPH is uterine atony

    Tone of the uterus can be regained by simple

    measures like fundal massage and oxytocin

    infusion primarily.All said and done to prevent from catastrophe

    the essentials are:

    Intelligent anticipation Skilled supervision

    Prompt detection

    Effective institution of therapy

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