HELLP! Caring for the Critically Ill Pregnant Patient · 2019-09-27 · • Associated with HELLP...
Transcript of HELLP! Caring for the Critically Ill Pregnant Patient · 2019-09-27 · • Associated with HELLP...
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HELLP! Caring for the Critically Ill Pregnant Patient
Stephen LapinskyMount Sinai Hospital, Toronto
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Disclosures
I have no relevant conflicts of interest
I will discuss “off-label” use of medications, as many are not approved in for use in pregnancy
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Objectives
“Acute Care Hematology & More…”
HELLP
TMAPLT
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Case presentation• 21 year old G3P2, presents at 36 weeks gestation
• Nausea, RUQ pain and tenderness
• BP 145/88, HR 108, afebrile, neuro intact
• Labs: Hgb 105 g/L, WBC 8.8, PLT 120,000, Creat 88 umol/L (1.0 mg/dL)
• AST 220 ALT 410 Bili 68 umol/L LDH 880
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Normal physiological changes in pregnancy
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Hematological changes in pregnancy
• Hemoglobin: - RBC mass increases- plasma volume increases more
• White blood cells: - neutrophils increased by physiological stress- sometimes further increase related to delivery
• Platelets: - gestational thrombocytopenia (incr clearance & dilution)- generally > 70 x109/L
• Coagulation: - procoagulant state- INR no change, PTT may be shortened (4 sec)- fibrinogen levels increased
Hgb drop 10 – 20 g/L
ECOG 2016; 206:259
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• Renal: - decreased creatinine & urea by 25% (incr GFR)
• Electrolytes: - complex water balance (dilution, decr osmotic thresholdfor ADH release, placental vasopressinase)
- slight decr Na, more with preeclampsia, oxytocin infusion
• Liver: - slight fall in AST, ALT, bilrubin, albumin- increase in Alk Phos and sometimes LDH
Biochemical changes in pregnancy
Teasdale and Morton, Obstet Med 2018, online May 24th
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Case presentation• 21 year old G3P2, presents at 36 weeks gestation
• Nausea, RUQ pain and tenderness
• BP 145/88, HR 108, afebrile, neuro intact
• Labs: Hgb 105 g/L, WBC 8.8, PLT 120,000, Creat 88 umol/L (1.0 mg/dL)
• AST 220 ALT 410 Bili 68 umol/L LDH 880
HUS
TTP
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Preeclampsia HELLP AFLP TTP HUS APLA
Timing after 20 wks 3rd trim 3rs trim 2/3 trim Post-P any
HTN +++ + + ± ++ ±
MAHA + ++ ± ++ + ±
Low PLT + ++ ± +++ ++ ++
Coagulop ± + +++ ± ± ++
Liver ± ++ +++ + - ±
Renal ± ± + ++ +++ -
Neuro ++ ± ± +++ + ±
ADAMTS13 N N N <10% >30% N
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Gestational thrombocytopenia
• Thrombocytopenia in the absence of other abnormalities
• During 2nd and 3rd trimester
• Usually > 70,000
• Resolution within days to 2 months postpartum
• No fetal thrombocytopenia
• May recur in subsequent pregnancies
• May be difficult to differentiate from ITP
Obstet Med. 2016 Mar;9(1):15-20.
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Preeclampsia• hypertension• proteinuria• after 20 weeks gestation
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placental ischemia
impaired trophoblastic invasiveness
abnormal implantation
genetics
prostaglandins
nitric oxidecoagulation
activationinflammatory response
endothelial abnormality
diffuse vasospasm
Preeclampsia - Etiology
sFlt1 (from fetal side of placenta) blocks VEGF and PlGF
maternal endothelial effects
Cerdeira et al, BJOG. 2018 Oct;125(11):1389-1395
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Preeclampsia – other reasons for ICU
• pulmonary edema
• intracranial hemorrhage
• acute renal failure
• cerebral edema
• hypertensive crisis
• eclampsia (seizure)
• hepatic (HELLP syndrome)
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Preeclampsia• Affects about 6% of all pregnancies
• In addition to hypertension:- renal - neurological- hepatic - hematological
• 50% will have PLT < 150 x109/L
• Associated with HELLP syndrome
• Treatment:- blood pressure control- seizure prophylaxis with MgSO4- manage organ dysfunction- appropriately timed delivery
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HELLP syndrome
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• Hemolytic anemia
• Elevated Liver enzymes
• Low Platelets
4 to 12% of preeclampsia
Occasionally presents post-partum
HELLP syndrome
Differential:
Weinstein, Am J Obstet Gynecol. 1982;142:159-67.
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• Hepatic:• Abdominal pain, nausea,
vomiting• Elevated AST, ALT• Intrahepatic hemorrhage
• Coagulopathy:• Thrombocytopenia• DIC: 38% • Hemorrhage
• Hemolysis:• Microangiopathic anemia
• Other:• Renal failure• ARDS
HELLP syndrome
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HELLP - Management
Delivery !
Treat
Preeclampsia
Blood
products
Monitor liver
Plasmapheresis
if > 72 hr postpartum
TTP ?
Steroids?Am J Obstet Gynecol. 2003;189:830-4.
Am J Obstet Gynecol. 2001;182:1332-7
Am J Obstet Gynecol.193:1591-8, 2005
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Acute Fatty Liver of Pregnancy
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Clinical Features• onset usually late third trimester• anorexia, vomiting, jaundice• abdominal pain• coagulopathy, encephalopathy, renal failure
uncommon 1 in 15,000 pregnancies
Acute Fatty Liver of Pregnancy
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Clinical Features• onset usually late third trimester• anorexia, vomiting, jaundice• abdominal pain• coagulopathy, encephalopathy, renal failure
uncommon 1 in 15,000 pregnancies
Acute Fatty Liver of Pregnancy
Early reports: fulminant hepatic failure, high mortality
More recently: early recognition, improved outcome
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Diagnosis: Swansea criteria
Ch’ng et al, Gut 2002; 51:876
Acute Fatty Liver of Pregnancy
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• intrahepatic cholestasis of pregnancy
• viral hepatitis
• acetaminophen overdose
Acute Fatty Liver of PregnancyDifferential Diagnosis
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DELIVERY• no reversal without delivery• improvement occurs within 2 to 3 days• gestation usually near term• high incidence of placental damage
Management
Acute Fatty Liver of Pregnancy
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DELIVERY• no reversal without delivery• improvement occurs within 2 to 3 days• gestation usually near term• high incidence of placental damage
Management
Acute Fatty Liver of Pregnancy
supportive specific transplant
as for hepatic
failure
none effective
plasmapheresis?
if deteriorate
after delivery
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- limited case-reports and a case series- no good evidence to support use
Acute Fatty Liver of Pregnancy
specific
none effective
plasmapheresis?
Seyyed Majidi MR, Vafaeimanesh J. Plasmapheresis in acute Fatty liver of pregnancy: an effective treatment. Case Rep Obstet Gynecol. 2013;2013:615975
Jin F, Cao M, Bai Y, Zhang Y, Yang Y, Zhang B. Therapeutic effects of plasma exchange for the treatment of 39 patients with acute fatty liver of pregnancy. Discov Med. 2012 May;13(72):369-73.
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Liver disease in pregnancy - Etiology
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• association with infants with defect in fatty acid oxidation
• 79% of mothers carrying a fetus homozygous for a specific mutation of long chain 3-hydroxyacyl-CoA dehydrogenase had AFLP
• Mutations in LCHAD detected in 19% of women with previous AFLP
• Some association with HELLP syndrome, placental infarcts
• infants are at risk of hyperketotic hypoglycemia and fatty liver
N Engl J Med 1999; 340:1723
JAMA 2002; 288:2163
Liver disease in pregnancy - Etiology
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Liver disease in pregnancy - Etiology
World J Gastroenterol. Dec 14, 2006; 12(46): 7397-7404
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Thrombotic Microangiopathy in Pregnancy
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Thrombotic Microangiopathy in Pregnancy
HELLP TTP aHUS
Pregnancy
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• Differentiating these conditionsHELLP TTP aHUS
Incidence 1-4% 0.001% 0.001%?
Timing after 20 weeks any time 75% postpartum
Blood pressure increased normal increased (renal dis)
Neurological + +++ -
MAHA, PLT + +++ +
Kidney injury + + +++
Liver injury +++ - -
Effect of delivery improves (36hr) none progression
Thrombotic Microangiopathy in Pregnancy
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• Pregnancy associated atypical HUS (p-aHUS)
– OB complications & delivery may precipitate aHUS
– may initially be diagnosed as preeclampsia/HELLP
– Consider if:<20 weeks, no resolution at 72 hr, history of HUS
– Complement gene abnormalities not always identified
Thrombotic Microangiopathy in Pregnancy
Grand’Maison et al. Obstet Med 2018; 11:137
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• Treatment
HELLP TTP aHUS
Delivery Plasmapheresis eculizumab: limited data in pregnancy (case reports)
Supportive Rx FFP FFP, PLEX?
Thrombotic Microangiopathy in Pregnancy
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Preeclampsia HELLP AFLP TTP HUS APLA
Timing after 20 wks 3rd trim 3rs trim 2/3 trim Post-P any
HTN +++ + + ± ++ ±
MAHA + ++ ± ++ + ±
Low PLT + ++ ± +++ ++ ++
Coagulop ± + +++ ± ± ++
Liver ± ++ +++ + - ±
Renal ± ± + ++ +++ -
Neuro ++ ± ± +++ + ±
ADAMTS13 N N >30% <10% >30%
Mechanism abn placentationantiangiogenic factors
type 1 angiotensinIIreceptor Ab?
LCHAD defic in fetus
low ADAMTS13 STECor
C’ active
autoimmune
Rx Delivery Delivery Delivery PLEXimmuno-suppress
Eculizumab HeparinIVIGPLEX
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Management of the Pregnant ICU patient
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Management of the Pregnant ICU patient• Do necessary radiological procedures
- CT abdo/pelvis needs some consideration
• Do not restrict drug therapy- norepinephrine if needed (hypotension is bad)- some chemo/biologics safe, others not (no thalidomide!)
• No changes to ventilation strategy- mild/mod hypercapnia probably OK, maintain reasonable O2
• Left lateral positioning
• Blood for cross-match q 3 days
• Provide adequate nutrition (+ Fe, folate)
• Know resuscitation status of neonate
• Multidisciplinary management: OB, neonatology, OB Medicine
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Prepare the ICU for Emergencies in Pregnancy
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Pregnant patient in the ICU
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