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OBSTETRIC EMERGENCY
RED ALERT RED ALERT RED ALERT
Cases of Obstetric Red Alert
Emergencies
 Eclampsia/fits
 Severe Haemorrhage/Hypovolaemic shock
 Obstetric collapse
 Amniotic fluid embolism
 Pulmonary oedema
 Inversion of uterus
 Uterine rupture
 Septicaemic shock
 DIVC
 Shoulder Dystocia
 Cord Prolapse
HYPERTENSIVE DISORDER IN PREGNANCY
 Hypertension in pregnancy is defined as a SBP of ≥ 140 mmHg and/or DBP ≥ 90
mmHg.
 An increase of 15 mmHg diastolic and 30 mmHg systolic BP levels above
baseline BP is no longer recognised as hypertension if absolute values are
below 140/90mmHg.
 Gestational Hypertension
 Hypertension alone, detected for the first time after
20th week. The definition is changed to “transient”
when pressure normalises postpartum.
 Chronic Hypertension
 Hypertension diagnosed prior to 20thweek; or the
presence of hypertension preconception, or de novo
hypertension in late gestation that fails to resolve
postpartum.
PRE-ECLAMPSIA - ECLAMPSIA
 Clinically diagnosed in the presence of de novo hypertension after 20th week, and
1 or more of the following:
 i. Significant proteinuria
 ii. Renal insufficiency – serum creatinine ≥ 90 μmol/L or oliguria
 iii. Liver disease – raised transaminases and/or severe right upper quadrant or
epigastric pain
 iv. Neurological problems – convulsions (eclampsia); hyperrefexia with clonus or
severe headaches, persistent visual disturbances (scotoma)
 v. Haematological disturbances – thrombocytopenia, coagulopathy, haemolysis
 vi. Fetal growth restriction
 This is followed by normalisation of the BP by 3 months postpartum.
SEVERE PRE ECLAMPSIA
 Systolic BP (SBP) of ≥ 170 and/or diastolic BP (DBP) of ≥ 110 mmHg on two occasions
along with significant proteinuria of ≥ 1g/day or
 DBP of ≥ 100 mmHg on 2 occasions with significant proteinuria (1+ on dipstick), with
two or more symptoms and signs of imminent eclampsia, which includes:
 Severe headache
 Visual disturbance
 Epigastric pain and/or vomiting
 Clonus
 Papilloedema
 Liver tenderness
 Abnormal liver enzymes (raised ALT or AST)
 Platelet count < 100,000/cm3
 HELLP syndrome (haemolysis, elevated liver enzymes, low platelets)
 Intrauterine growth restriction (IUGR)
 Pulmonary oedema and/or congestive cardiac failure
ECLAMPSIA
 Defined as tonic-clonic (grand mal) seizure occurring in association with
features of PE.
 May occur antepartum (45%), intrapartum (18 – 19%) or postpartum (36%).
ECLAMPSIA
 All cases of eclampsia should have the baby delivered immediately regardless
of gestation after BP is controlled.
 Sign and symptoms of severe pre eclampsia and eclampsia
 Severe frontal headache
 Vomiting
 Blurring of vision
 Epigastric pain
 Hyper- reflexia
 Severe hypertension
Management
 Initiate Red Alert System
 Give IM MgSO4 5g each buttock or IV MgSO4 4g slow bolus
 Continue the MgSO4 infusion at 1g / hr
 Anti-hypertensive drugs
 Manage patient in lateral position
 Suck out secretions / saliva
 Ix: Hb, platelet, coagulation profile, LFT, BUSE, serum creatinine, serum uric
acid, GXM
 Refer out (district hospital)
MgSO4 Therapy
 IM regime loading dose
 MgSo4 im deep intra-muscular 5g in each buttock (total 10g).
 IM regime maintenance dose
 MgSo4 IM deep intra-muscular injection 2.5g in each buttock every 4 hours
 IV regime loading dose
 MgSO4 iv 4 gm (diluted to 20 ml with NS) slow intravenous over 10-15 minutes,
 MgSO4 iv infusion 1g / hour.
 IV regime maintenance dose
 MgSO4 5 gm (10mls) in 40mls DS, infuse at 10ml/hour (infusion rate 1g / hour).
 25 gm MgSO4 at 2ml/hour
ANTI-HYPERTENSIVES INTRAVENOUS /
INFUSION DOSAGE – DURING HYPERTENSIVE
CRISIS
 Labetalol
 BOLUS (acute hypertension)
 Give 5 mg IV bolus (over 2 min). If 5 mg not effective then double the dose every
10 min. (10 mg, 20 mg, 40 mg). Maximum bolus dose is 40 mg.
 BP measure immediately before, and 5 minutes and 10 minutes after initial
dose.
 Maximum effect within 5 minutes of each injection.
 MAXIMUM TOTAL CUMULATIVE DOSE OF 300MG
LABETALOL
 INFUSION
 Drop-mat Infusion pump.
 Labetalol hydrochloride 200 mg + 160 mL DS / NS / D5% (resultant 200 mL)
 Infusion rate is 0.5mg/min (30mls/hr) to 2 mg/min (120mls/hr).
 Adjusted by 0.5 mg/min every 15 minutes according to BP response.
 Maximum infusion dose at 30 drops/min. If BP still not well-controlled despite at
maximum dosage, to consult Specialist.
 Syringe pump
 iv Labetalol 200 mg in 50 mls N/Saline, start at 20 mg/h (or 4 mls/h) and increase
every 30 min, stop infusion if rate exceed 150 mg/h (or 30 mls/h)).
TREATMENT FOR HYPERTENSION
 Exact level BP at which to start treatment is controversial, but generally
treat if SBP > 140 – 160 mmHg and DBP > 90 – 110 mmHg.
 Treatment is mandatory if BP is ≥ 160/110.
 Oral α-methyldopa (longest safety data – preferable especially during 1st and
2nd trimester) and labetalol (late 2nd and 3rd trimester, if not
contraindicated) are the first line of treatment, followed by Nifedipine.
 Addition of another anti-hypertensive should only be done after the first
antihypertensive has been maximized.
ANTEPARTUM HEMORRHAGE
 Definition: Bleeding from the genital tract after 22 weeks of pregnancy to
delivery of foetus
 Common Causes :
 Placenta praevia
 Abruptio placenta
 Local causes
 Indeterminate APH
 DO NOT PERFORM VE / SPECULUM EXAMINATION UNTIL YOU HAVE EXCLUDE
PLACENTA PRAEVIA
MANAGEMENT
 RESUSCITATION
 -estimated amount of blood loss
 Mild : 2 pads soaked or 200ml or less
 Severe : > 2 pads soaked or > 200ml.
 Mild APH - 1 IV line and GXM 2 units of blood
 Massive APH - 3 IV lines and GXM 4 units of blood
 -use branula size 16 and below
 -transfuse immediately and accordingly
 Oxygen 7L/min via mask.
 CBD insertion – if indicated, monitor urine output.
Quantify bleeding objectively by
using these measurements:
1 pad = 125ml,
1 gallipot = 250ml,
1 kidney dish = 1Litre,
1 sarong = 500ml.
MANAGEMENT
 B. Blood investigation
 Hb, platelet, BT, CT, BUSE, PT, APTT, INR, GXM
 C. Perform Ultrasound Scan
 D. Monitoring -close observation of mother (BP, PR, Pad Charts) and foetus
(CTG).
 E. Definitive treatment - Decision on clinical diagnosis and proceed
accordingly
 DO NOT USE TOCOLYTIC IN THE PRESENCE OF PER-VAGINAL BLEEDING
PLACENTA PREVIA
 Features of bleeding: painless, recurrent, always revealed
 General condition: Proportional to blood loss
 Abdomen: soft, relaxed, malpresentation is common, presenting part high
 Foetal heart sound: usually present
 Admission and Referral
 All placenta praevia major should be managed as in patient from 32 weeks
onwards.
 All bleeding placenta praevia should be admitted at any gestational age.
Abruptio Placenta
 Features of bleeding: painful, revealed, concealed or mixed
 General condition: out of proportion in concealed type
 Abdomen: tense, tender and woody, head engaged
 Foetal heart sound: usually absent particularly in concealed type
 Common presentation: preterm 30-35 weeks with elevated BP
POST PARTUM HEMORRHAGE
 DEFINITION: Bleeding from or into the genital tract of > 500ml following
delivery
 1. Type Primary PPH - <24 hours after delivery
 2. Secondary PPH - >24 hours after delivery
 Causes of Primary PPH(4T‟s)
 i. Tone; Atonic Uterus
 ii. Trauma :Trauma to genital tract
 iii. Thrombin: Coagulation defects
 iv. Tissue: Retained products of conception
 Referred Cases From Home Delivery/ District Hospital
 1. Assess blood loss
 2. Check vital signs
 3. No exploration to be done until blood is transfused (at
least 2 units of blood). Proceed to OT for exploration under
GA after transfusion.
 4. MO in district hospital should transfuse 1-2 litres of blood
first in their hospital in all cases of home/ hospital delivery
before transferring the patient.
 5. If patient are still oozing after exploration, transfer
patient to hospital with Specialist and trigger Red Alert
System
 6. Prophylaxis against PPH
 Gravida 5 and above, twin pregnancies, polyhydramnios and prolonged 1st and 2nd
stage should have IV drip with 40U of pitocin/ pint DS at 20drops/min for 6 hours
after 3rd stage of labour.
 7. If local causes, catch bleeder and pack vagina with roller gauze/ pads (up
to 3 pads rolled up into vagina). – remember to inform referral hospital.
 8. All cases of PPH > 800mls or if BP low with systolic < 90, pulse rate >
120/min, please alert Specialist stat via Red Alert.
MATERNAL COLLAPSE IN PREGNANCY AND
THE PEURPERIUM
 Maternal collapse is defined as an acute
event involving the cardiorespiratory
systems and/or brain, resulting in a
reduced or absent conscious level (and
potentially death), at any stage in
pregnancy and up to six weeks after
delivery.
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx
OBSTETRIC EMERGENCY EDITED.pptx

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OBSTETRIC EMERGENCY EDITED.pptx

  • 1. OBSTETRIC EMERGENCY RED ALERT RED ALERT RED ALERT
  • 2. Cases of Obstetric Red Alert Emergencies  Eclampsia/fits  Severe Haemorrhage/Hypovolaemic shock  Obstetric collapse  Amniotic fluid embolism  Pulmonary oedema  Inversion of uterus  Uterine rupture  Septicaemic shock  DIVC  Shoulder Dystocia  Cord Prolapse
  • 3. HYPERTENSIVE DISORDER IN PREGNANCY  Hypertension in pregnancy is defined as a SBP of ≥ 140 mmHg and/or DBP ≥ 90 mmHg.  An increase of 15 mmHg diastolic and 30 mmHg systolic BP levels above baseline BP is no longer recognised as hypertension if absolute values are below 140/90mmHg.
  • 4.  Gestational Hypertension  Hypertension alone, detected for the first time after 20th week. The definition is changed to “transient” when pressure normalises postpartum.  Chronic Hypertension  Hypertension diagnosed prior to 20thweek; or the presence of hypertension preconception, or de novo hypertension in late gestation that fails to resolve postpartum.
  • 5. PRE-ECLAMPSIA - ECLAMPSIA  Clinically diagnosed in the presence of de novo hypertension after 20th week, and 1 or more of the following:  i. Significant proteinuria  ii. Renal insufficiency – serum creatinine ≥ 90 μmol/L or oliguria  iii. Liver disease – raised transaminases and/or severe right upper quadrant or epigastric pain  iv. Neurological problems – convulsions (eclampsia); hyperrefexia with clonus or severe headaches, persistent visual disturbances (scotoma)  v. Haematological disturbances – thrombocytopenia, coagulopathy, haemolysis  vi. Fetal growth restriction  This is followed by normalisation of the BP by 3 months postpartum.
  • 6. SEVERE PRE ECLAMPSIA  Systolic BP (SBP) of ≥ 170 and/or diastolic BP (DBP) of ≥ 110 mmHg on two occasions along with significant proteinuria of ≥ 1g/day or  DBP of ≥ 100 mmHg on 2 occasions with significant proteinuria (1+ on dipstick), with two or more symptoms and signs of imminent eclampsia, which includes:  Severe headache  Visual disturbance  Epigastric pain and/or vomiting  Clonus  Papilloedema  Liver tenderness  Abnormal liver enzymes (raised ALT or AST)  Platelet count < 100,000/cm3  HELLP syndrome (haemolysis, elevated liver enzymes, low platelets)  Intrauterine growth restriction (IUGR)  Pulmonary oedema and/or congestive cardiac failure
  • 7. ECLAMPSIA  Defined as tonic-clonic (grand mal) seizure occurring in association with features of PE.  May occur antepartum (45%), intrapartum (18 – 19%) or postpartum (36%).
  • 8. ECLAMPSIA  All cases of eclampsia should have the baby delivered immediately regardless of gestation after BP is controlled.  Sign and symptoms of severe pre eclampsia and eclampsia  Severe frontal headache  Vomiting  Blurring of vision  Epigastric pain  Hyper- reflexia  Severe hypertension
  • 9. Management  Initiate Red Alert System  Give IM MgSO4 5g each buttock or IV MgSO4 4g slow bolus  Continue the MgSO4 infusion at 1g / hr  Anti-hypertensive drugs  Manage patient in lateral position  Suck out secretions / saliva  Ix: Hb, platelet, coagulation profile, LFT, BUSE, serum creatinine, serum uric acid, GXM  Refer out (district hospital)
  • 10. MgSO4 Therapy  IM regime loading dose  MgSo4 im deep intra-muscular 5g in each buttock (total 10g).  IM regime maintenance dose  MgSo4 IM deep intra-muscular injection 2.5g in each buttock every 4 hours  IV regime loading dose  MgSO4 iv 4 gm (diluted to 20 ml with NS) slow intravenous over 10-15 minutes,  MgSO4 iv infusion 1g / hour.  IV regime maintenance dose  MgSO4 5 gm (10mls) in 40mls DS, infuse at 10ml/hour (infusion rate 1g / hour).  25 gm MgSO4 at 2ml/hour
  • 11. ANTI-HYPERTENSIVES INTRAVENOUS / INFUSION DOSAGE – DURING HYPERTENSIVE CRISIS  Labetalol  BOLUS (acute hypertension)  Give 5 mg IV bolus (over 2 min). If 5 mg not effective then double the dose every 10 min. (10 mg, 20 mg, 40 mg). Maximum bolus dose is 40 mg.  BP measure immediately before, and 5 minutes and 10 minutes after initial dose.  Maximum effect within 5 minutes of each injection.  MAXIMUM TOTAL CUMULATIVE DOSE OF 300MG
  • 12. LABETALOL  INFUSION  Drop-mat Infusion pump.  Labetalol hydrochloride 200 mg + 160 mL DS / NS / D5% (resultant 200 mL)  Infusion rate is 0.5mg/min (30mls/hr) to 2 mg/min (120mls/hr).  Adjusted by 0.5 mg/min every 15 minutes according to BP response.  Maximum infusion dose at 30 drops/min. If BP still not well-controlled despite at maximum dosage, to consult Specialist.  Syringe pump  iv Labetalol 200 mg in 50 mls N/Saline, start at 20 mg/h (or 4 mls/h) and increase every 30 min, stop infusion if rate exceed 150 mg/h (or 30 mls/h)).
  • 13. TREATMENT FOR HYPERTENSION  Exact level BP at which to start treatment is controversial, but generally treat if SBP > 140 – 160 mmHg and DBP > 90 – 110 mmHg.  Treatment is mandatory if BP is ≥ 160/110.  Oral α-methyldopa (longest safety data – preferable especially during 1st and 2nd trimester) and labetalol (late 2nd and 3rd trimester, if not contraindicated) are the first line of treatment, followed by Nifedipine.  Addition of another anti-hypertensive should only be done after the first antihypertensive has been maximized.
  • 14.
  • 15. ANTEPARTUM HEMORRHAGE  Definition: Bleeding from the genital tract after 22 weeks of pregnancy to delivery of foetus  Common Causes :  Placenta praevia  Abruptio placenta  Local causes  Indeterminate APH  DO NOT PERFORM VE / SPECULUM EXAMINATION UNTIL YOU HAVE EXCLUDE PLACENTA PRAEVIA
  • 16. MANAGEMENT  RESUSCITATION  -estimated amount of blood loss  Mild : 2 pads soaked or 200ml or less  Severe : > 2 pads soaked or > 200ml.  Mild APH - 1 IV line and GXM 2 units of blood  Massive APH - 3 IV lines and GXM 4 units of blood  -use branula size 16 and below  -transfuse immediately and accordingly  Oxygen 7L/min via mask.  CBD insertion – if indicated, monitor urine output. Quantify bleeding objectively by using these measurements: 1 pad = 125ml, 1 gallipot = 250ml, 1 kidney dish = 1Litre, 1 sarong = 500ml.
  • 17. MANAGEMENT  B. Blood investigation  Hb, platelet, BT, CT, BUSE, PT, APTT, INR, GXM  C. Perform Ultrasound Scan  D. Monitoring -close observation of mother (BP, PR, Pad Charts) and foetus (CTG).  E. Definitive treatment - Decision on clinical diagnosis and proceed accordingly  DO NOT USE TOCOLYTIC IN THE PRESENCE OF PER-VAGINAL BLEEDING
  • 18. PLACENTA PREVIA  Features of bleeding: painless, recurrent, always revealed  General condition: Proportional to blood loss  Abdomen: soft, relaxed, malpresentation is common, presenting part high  Foetal heart sound: usually present  Admission and Referral  All placenta praevia major should be managed as in patient from 32 weeks onwards.  All bleeding placenta praevia should be admitted at any gestational age.
  • 19. Abruptio Placenta  Features of bleeding: painful, revealed, concealed or mixed  General condition: out of proportion in concealed type  Abdomen: tense, tender and woody, head engaged  Foetal heart sound: usually absent particularly in concealed type  Common presentation: preterm 30-35 weeks with elevated BP
  • 20. POST PARTUM HEMORRHAGE  DEFINITION: Bleeding from or into the genital tract of > 500ml following delivery  1. Type Primary PPH - <24 hours after delivery  2. Secondary PPH - >24 hours after delivery  Causes of Primary PPH(4T‟s)  i. Tone; Atonic Uterus  ii. Trauma :Trauma to genital tract  iii. Thrombin: Coagulation defects  iv. Tissue: Retained products of conception
  • 21.  Referred Cases From Home Delivery/ District Hospital  1. Assess blood loss  2. Check vital signs  3. No exploration to be done until blood is transfused (at least 2 units of blood). Proceed to OT for exploration under GA after transfusion.  4. MO in district hospital should transfuse 1-2 litres of blood first in their hospital in all cases of home/ hospital delivery before transferring the patient.  5. If patient are still oozing after exploration, transfer patient to hospital with Specialist and trigger Red Alert System
  • 22.  6. Prophylaxis against PPH  Gravida 5 and above, twin pregnancies, polyhydramnios and prolonged 1st and 2nd stage should have IV drip with 40U of pitocin/ pint DS at 20drops/min for 6 hours after 3rd stage of labour.  7. If local causes, catch bleeder and pack vagina with roller gauze/ pads (up to 3 pads rolled up into vagina). – remember to inform referral hospital.  8. All cases of PPH > 800mls or if BP low with systolic < 90, pulse rate > 120/min, please alert Specialist stat via Red Alert.
  • 23. MATERNAL COLLAPSE IN PREGNANCY AND THE PEURPERIUM  Maternal collapse is defined as an acute event involving the cardiorespiratory systems and/or brain, resulting in a reduced or absent conscious level (and potentially death), at any stage in pregnancy and up to six weeks after delivery.