HELLP Syndrome as a

separate entity

Dr. Mohammed Abdalla

EGYPT, Domiat G. Hospital

HELLP Syndrome
may it be a
separate
entity?
yes

 HELLP, a syndrome characterized by

hemolysis, elevated liver
enzyme levels and a low platelet
count, is an obstetric complication that
is frequently misdiagnosed at initial
presentation. Many investigators
consider the syndrome to be a variant of
preeclampsia,

but it may be a separate entity.

In some cases , HELLP symptoms are

the first warning of preeclampsia and
the condition is misdiagnosed as
hepatitis, idiopathic thrombocytopenic
purpura, gallbladder disease, or thrombotic
thrombocytopenic purpura.

Epidemiology and Risk Factors

HELLP syndrome 0.2 to 0.6 % of all pregnancies.
Preeclampsia 5 to 7 % of all pregnancies.
Superimposed HELLP syndrome develops in 4 to 12

percent of women with preeclampsia or eclampsia.

Maternal mortality has been estimated to be as high as 2-

24%
Perinatal mortality is equally high, ranging from 9 39 %.

.Wolf JL. Liver disease in pregnancy. Med Clin North Am 1996

Etiology and Pathogenesis

The hemolysis in HELLP syndrome is
a microangiopathic hemolytic anemia.
Red blood cells become fragmented as
they pass through small blood vessels
with endothelial damage and fibrin
deposits.
The peripheral smear may reveal
spherocytes, schistocytes, triangular
cells and burr cells.
increase in Bilirubin and lactic dehydrogenase
levels.

Etiology and Pathogenesis

The elevated liver enzyme
levels in the syndrome are thought
to be secondary to obstruction of
hepatic blood flow by fibrin
deposits in the sinusoids. This
obstruction leads to periportal
necrosis and, in severe cases,
intrahepatic hemorrhage,
subcapsular hematoma formation or
hepatic rupture.

Etiology and Pathogenesis

The thrombocytopenia has been
attributed to increased consumption
and/or destruction of platelets.
With platelet activation, thromboxane A and
serotonin are released, causing vasospasm,
platelet agglutination and aggregation, and further
endothelial damage.

Clinical Presentation
90%of patients present with generalized
malaise,
65 % with epigastric pain,
30 % with nausea and vomiting,
31 percent with headache.

All are nonspecific symptoms

Because of the variable

nature of the clinical
presentation, the
diagnosis of HELLP
syndrome is generally
delayed for an
average
of eight
days.
Usually
presented
by complications

In one retrospective chart

review of patients with
HELLP syndrome, only
two of 14 patients entered
the hospital with the
correct diagnosis.

Because early diagnosis of this

syndrome is critical, any
pregnant woman who presents
with malaise or a viral-type
illness in the third trimester
should be evaluated with a
complete blood cell count and
liver function tests.

Clinical Presentation
The physical examination may be normal in patients
with HELLP syndrome.

1- right upper quadrant tenderness 90 %

2- Edema is not a useful marker
3- Hypertension and proteinuria may be
absent or mild.

Clinical Presentation
SYMPTOMS

Clinical Presentation

signs

Diagnosis
There is agreement among most of the
authors that, the diagnosis requires the
concurrence of hemolysis, elevated liver
enzymes, and low platelet count. However,
there is obviously still a lack of consensus
on the laboratory parameters and their
cutoff values used to diagnose
Martin JN Jr, Rinehart BK, May WL, Magann EF, Terrone DA,
Blake PG.

Laboratory Diagnostic Criteria for

HELLP syndrome
Haemolysis
Abnormal peripheral smear : spherocytes,
schistocytes, triangular cells and burr cells
Total Bilirubin level > 1.2 mg/dL
Lactate dehydrogenase level > 600U/L

Elevated liver function test result

Serum aspartate amino transferase level > 70U/L
Lactate dehydrogenase level >600 U/L

Low platelet count

Platelet count < 150 000/mm3

Platelet count
appears to be the
most reliable
indicator of the
presence of HELLP
syndrome

Clinical utility of strict diagnostic

criteria for the HELLP
the use of strict diagnostic criteria in
the definition of the HELLP
syndrome allows for greater
prediction of complication rates.
and define the cases that are
Eligible to conservative
management

Classification
based on the number of
abnormalities

full HELLP

partial HELLP

syndrome

syndrome

considered
for delivery
within 48
hours

candidates
for more
conservative
management

Audibert F, Friedman SA, Frangieh AY, Sibai BM. Am J Obstet Gynecol 1996;
. 175:460-4

Classification
on the basis of platelet
count
class I, less than 50,000 per mm3
class II, 50,000 to less than 100,000 per mm3
class III, 100,000 to 150,000 per mm3

Management
Delivery
Corticosteroids
Magnesium sulphate

Hypotensive drugs
Blood products

The treatment approach should be based on the

estimated gestational age and the condition of
the mother and fetus.
Prolongation of pregnancy, in theory, may be
favourable for the foetus whereas it remains
controversial whether maternal condition is
further deteriorated by expectant management

Visser W, Wallenburg HC. Temporising management

of severe pre-eclampsia with and without the HELLP
syndrome. Br J Obstet Gynaecol 1995;102:111-7

Eligibility to conservative
management

hypertension is controlled at less

than 160/110 mm hg,

Oliguria responds to fluid
management .
Elevated liver function values are not
associated with right upper quadrant
or epigastric pain.
Class II III .(platelet count).>50000

 The Cochrane Library holds two

protocols which when complete
may summarize evidence to date on
the use of corticosteroids for
HELLP syndrome . and
interventionist versus expectant
management of severe preeclampsia before term.

 The antenatal administration of dexamethasone (Decadron) in a

high dosage of 10 mg intravenously every 12 hours has been

shown to markedly improve the laboratory abnormalities associated

with HELLP syndrome.

Steroids given antenatally do not prevent the typical

worsening of laboratory abnormalities after delivery.
However, laboratory abnormalities resolve more
quickly in patients who continue to receive steroids
postpartum.

Magann EF, Bass D, Chauhan SP, Sullivan DL, Martin RW, Martin JN Jr. Am
.J Obstet Gynecol 1994;171:1148-53

 Corticosteroid therapy should be

instituted in patients with HELLP
syndrome who have a platelet count of
less than 100,000 per mm3 .And should
be continued until liver function
abnormalities are resolving and the
platelet count is greater than 100,000 per
mm3

Magann EF, Perry KG Jr, Meydrech EF, Harris RL, Chauhan

SP, Martin JN Jr. Am J Obstet Gynecol 1994;171:1154-8.

Intravenously administered
dexamethasone appears to be more
effective than intramuscularly
adminstered betamethasone for the
antepartum treatment of mothers with
HELLP syndrome.
(Am J Obstet Gynecol 2001;184:1332-9.).

Administration of glucocorticoids
increases the use of regional anesthesia
in women with antepartum HELLP
syndrome who have thrombocytopenia.

(Am J Obstet Gynecol 2002;186:475-9.).

 Patients treated with

dexamethasone exhibit longer time
to delivery; This facilitates maternal
transfer to a tertiary care center and
postnatal maturity of fetal lungs

(Am J Obstet Gynecol 2002;186:475-9.).

Patients with HELLP

syndrome should be
treated prophylactically
with magnesium sulfate
to prevent seizures,
whether hypertension is
present or not.

 Antihypertensive therapy
should be initiated if blood pressure
is consistently greater than 160/110
mm hg despite the use of
magnesium sulfate. The goal is to
maintain diastolic blood pressure
between 90 and 100 mm hg.

The most commonly used

antihypertensive agent has
been

hydralazine
Labetolol
Nifedipine

Between 38 -93 % of patients

with HELLP syndrome receive
some form of blood product.
Patients with a platelet count
greater than 40,000 per mm3 are
unlikely to bleed.

Patients who undergo cesarean section

should be transfused if their platelet count

is less than 50,000 per mm3 ,
Prophylactic transfusion of platelets at
delivery does not reduce the incidence of
postpartum hemorrhage or hasten
normalization of the platelet count. .
Patients with DIC should be given fresh
frozen plasma and packed red blood cells.

Pain relief with intravenous narcotics

and local anesthesia is acceptable but

certainly not optimal for pain control.
Epidural anesthesia has been
controversial but it is the technique of
choice when it can be accomplished
safely. Insertion of an epidural catheter is
generally safe in patients with a platelet
count greater than 100,000 per mm3.
General anesthesia can be used when
regional anesthesia is considered unsafe.

Portis R, Jacobs MA, Skerman JH, Skerman EB. HELLP syndrome (hemolysis, elevated
liver enzymes, and low platelets) pathophysiology and anesthetic considerations. AANA
. J 1997;65:37-47

Complications

Complications
The mortality rate for women with HELLP

syndrome is approximately 1.1 %

From 1 to 25 % of affected women develop
serious complications such as DIC, placental
abruption, adult respiratory distress syndrome,
hepatorenal failure, pulmonary edema,
subcapsular hematoma and hepatic rupture.
A significant percentage of patients receive
blood products.

Sibai BM, Ramadan MK, Usta I, Salama M, Mercer BM, Friedman SA. Maternal
morbidity and mortality in 442 pregnancies with hemolysis, elevated liver enzymes,
. and low platelets (HELLP syndrome). Am J Obstet Gynecol 1993;169:1000-6

Complications
Infant morbidity and mortality rates range
from 10 to 60 %, depending on the severity of
maternal disease.
Infants affected by HELLP syndrome are
more likely to experience intrauterine growth
retardation and respiratory distress
syndrome.

Dotsch J, Hohmann M, Kuhl PG. Neonatal morbidity and mortality

associated with maternal haemolysis, elevated liver enzymes and low
. platelets syndrome. Eur J Pediatr 1997;156:389-91

Complications

take home
Once the diagnosis of HELLP
syndrome has been established, the
best markers to follow are the
maternal lactate dehydrogenase
level and
the maternal platelet count

take home
The laboratory abnormalities in
HELLP syndrome typically
worsen after delivery and then
begin to resolve by three to four
days postpartum.
Martin JN Jr, Blake PG, Perry KG Jr, McCaul JF, Hess LW, Martin RW.
The natural history of HELLP syndrome: patterns of disease progression
. and regression. Am J Obstet Gynecol 1991;164(6 pt 1):1500-9

take home
The incidence of hemorrhagic
complications is higher when
platelet counts are < 40,000
per mm3

take home
Patients with HELLP syndrome who
complain of severe right upper
quadrant pain, neck pain or shoulder
pain should be considered for hepatic
imaging regardless of the severity of
the laboratory abnormalities, to assess
for subcapsular haematoma or rupture

take home
Patients with HELLP
syndrome should be
routinely treated with
corticosteroids.