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TRANSCRIPT
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POSTPARTUM
HEMORRHAGELaura Noble B.A., RRT, AA
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Postpartum Hemorrhage
Case Presentation Definition Epidemiology
Preventative Measures Etiology Management Replacement Therapy
What Can We Do As AnesthesiaAssistants? Case summary
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Case Review
Healthy 32 yr old G3P2
22 weeks pregnant for induction of labourof fetus with a fetal anomaly
Mallampati IV Vaginal delivery with retained placenta
Heavy bleeding
Systolic BP ~60mmHg
Transferred to OR
Dx: Postpartum Hemorrhage
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DEFINITION
Blood loss >500mL for a vaginal delivery
Blood loss >1000mL for a caesarian section
10% decrease in hematocrit
Requires a blood transfusion Primary PPH is within 24 hours after birth
Secondary PPH is 24 hours to 6 weeks after birth
Primary PPH involves heavier bleeding and is
more likely to result in maternal morbidity andmortality
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PHYSIOLOGICAL CHANGESIN PREGNANCY
Blood volume increases by 50%
Red blood cells only increase 20-30%
Uterine blood flow is 600ml/min Hypercoaguable state
Upper airway edema
Decrease in FRC Oxygen consumption increase by 20%
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EPIDEMIOLOGY
Major cause of maternal death worldwide
PPH can occur in 10-18% of all births
3% of vaginal deliveries will result insevere PPH
25% of all maternal deaths are caused by
severe hemorrhage
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PREVENTATIVE MEASURES
Active management of the third stage oflabour
Oxytocin with delivery of baby
Prophylactic oxytocin decreases PPH by 40%
Deliver placenta with controlled cord tractionand inspect for completeness
Palpate uterus and inspect lower genital tract
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ETIOLOGY
Remember the 4 Ts:
1. Tone
2. Tissue3. Trauma
4. Thrombin
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1. TONE
Uterine Atony
Boggy uterus
Most common cause of PPH
70% of all PPH
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Risk Factors for Uterine Atony
Uterine over distension(polyhydramnious,large baby, multiples)
Uterine exhaustion(precipitous labour,
prolonged/augmented labour, high parity)
Infection(prolonged rupture of membranes,fever)
Anatomical distortion of the uterus
(uterine abnormality, fibroids, placenta previa)
Exposure to specific drugs (NTG, Volatileagents, Beta agonists)
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2. TISSUE Retained products Abnormal placenta (placenta accreta, increta or
percreta)
Previous uterine surgery
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3. TRAUMA
Lacerations of cervix, vagina,perineum or C/S incision site
Hematomas
Uterine rupture
Uterine inversion
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Risk Factors for Trauma
Precipitous delivery
Operative delivery
Assisted delivery (forceps, vacuum)
Previous uterine surgery
Fundal placenta
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4. THROMBIN
Abnormal coagulation
Very rare
Usually identified before delivery
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Risk Factors for Thrombin
Pre-existing Von Willebrands Hemophilia Idiopathic thrombocytopenia (ITP)
History of blood clots
Acquired in pregnancy Pre-eclampsia HELLP Amniotic fluid embolus
Medication (aspirin, heparin)
Antepartum hemorrhage
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MANAGEMENT OF PPH
Communication!!!!
Call for HELP!!
Determine etiology (four Ts)
Vital signs
Large bore I.Vs
Blood work
Oxygen
OR
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Dont Panic!
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Management for Tone
1. Multidisciplinary team work
2.
Uterine massage
3. Pharmacological management
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2. Uterine Massage
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3. Pharmacologic Managementof Atony
Oxytocin
Egonovine Maleate (Ergot)
Hemabate (15-Methyl prostaglandinF2 alpha)
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Management for Tissue
Inspect placenta for completeness
Manually remove remainder ofplacenta
Abnormal placenta
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Management for Trauma
Suture any lacerations
Inspect uterus for inversion
Correction of uterine inversion- doneunder GA
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Management for Thrombin
Fresh frozen plasma
Platelet transfusion
Cryoprecipitate
Hematology consult
Replace specific coagulation factors
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Surgical Intervention Uterine artery ligation
Uterine balloon inflation
Hysterectomy
Pack uterus
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Interventional Radiology
Uterine artery embolization
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REPLACEMENT THERAPY
Volume replacement options
Blood loss is usually underestimated
May be asymptomatic until blood lossreaches 25-35%
Any patient who is at risk for PPH should
be cross-matched upon arrival to hospital
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WHAT CAN WE DO ASANESTHESIA ASSISTANTS?
Be aware Team work Oxygen Help transport to the OR Monitors I.V. access Retrieve Ergot and Hemabate from the
fridge Blood work
(contd)
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WHAT CAN WE DO ASANESTHESIA ASSISTANTS?
RSI
Difficult airway equipment
Prime the Level 1 rapid infuser Check and hang blood
Warming mechanisms (Hotline, blankets)
Point of care testing Put in/assist with an arterial line, CVP
Be prepared for anything!
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Case Review
Healthy 32 yr old G3P2
1 CS, 1 SVD
22 weeks pregnant for induction of labour
Mallampati IV Retained placenta
Heavy bleeding
Systolic BP ~60mmHg
Transferred to OR
(contd)
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Case Review
GA
RSI with Glide scope
2 18g I.V.s and arterial line inserted Placenta manually removed
Uterotonics given
Bakri balloon and vaginal packing inserted
(Contd)
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Case Review
Interventional Radiology Surgical Hysterectomy Total EBL 10L
Total blood products given:PRBC 21, platelets 6, Cryo 10, FFP 12
N/S 1 litre R/L 4 litres, Voluven 1.5 litres
(Contd)
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Case Review
ICU admission
PCV 10/5, Fi02 0.40
ABG 7.49/31/193/24/10
HgB 84, platelets 122, INR 1.0
Normal electrolytes
Pt extubated the following morning
(contd)
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Case Review
Transferred out of ICU
Minimal pain medication required
Discharged home 3 days later
Patient awareness?
(contd)
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What caused this PPH?
Tissue retained placenta
undiagnosed accreta
Trauma Ruptured uterus
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Questions?
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References
1. Chestnut D. Obstetric Anesthesia. 3rd edition. Philadelphia: Elsevier Mosby; 2004.
1. University of Toronto Department of Anesthesia. CME Module 8: ClinicalManagement of Post Partum Hemorrhage. [online]. 2008 [cited April 5, 2009];[16screens]. Available from URL:http://www.anesthesia.utoronto.ca/edu/cme/courses/m08/m08p04.htm
2. Anderson J, Etches D. Prevention and Management of Postpartum Hemorrhage[online]. March 2007 [cited April 19, 2009]; Available from URL:http://www.aafp.org/afp/20070315/875.html
3. Schurmans N, MacKinnon C, Lane C, Etches D. Prevention and Management ofPostpartum Haemorrhage. SOGC Clinical Practice Guidelines [serial online] 2000April [cited April 19, 2009]; 88:[11 screens]. Available from: URL:http://www.sogc.org/guidelines/public/88E-CPG-April2000.pdf
4. World Health Organization. Prevention of Postpartum Haemorrhage by Activemanagement of Third Stage of Labour: MPS Technical Update. Geneva: WorldHealth Oraganization, 2006.
http://www.anesthesia.utoronto.ca/edu/cme/courses/m08/m08p04.htmhttp://www.anesthesia.utoronto.ca/edu/cme/courses/m08/m08p04.htmhttp://www.aafp.org/afp/20070315/875.htmlhttp://www.aafp.org/afp/20070315/875.htmlhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.sogc.org/guidelines/public/88E-CPG-April2000.pdfhttp://www.aafp.org/afp/20070315/875.htmlhttp://www.anesthesia.utoronto.ca/edu/cme/courses/m08/m08p04.htm -
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