Keywords
TTP - severe preeclampsia - multidisciplinary team - autoantibodies
Thrombotic thrombocytopenic purpura (TTP) is a rare, severe life-threatening emergency
characterized by microangiopathic hemolytic anemia, thrombocytopenia, acute renal
insufficiency, altered mental status, and fever. It exists in both congenital and
acquired forms and is associated with the absence or severe depletion of von Willebrand
factor cleaving protease known as a disintegrin and metalloproteinase with thrombospondin-like
repeats (ADAMTS-13).[1]
[2] A deficiency in this protease can be congenital or the result of an acquired auto
antibody to ADAMTS-13 and can lead to extensive platelet adhesion and clumping and
possibly secondary end-organ damage. Plasma-based therapy containing replacements
of ADAMTS-13 was a major advancement for treatment of TTP. Today, high-dose intravenous
methylprednisolone and plasma exchange are the mainstay treatments. Pregnancy can
precipitate the disease in first-time patients or can exacerbate its recurrence. However,
if TTP occurs for the first time during pregnancy, it may mimic other severe conditions
such as severe preeclampsia. Rather than plasma exchange, preeclampsia only responds
to delivery of infant.
The incidence of TTP in pregnancy is 1 in 25,000[3] compared with the 5 to 8% incidence of preeclampsia.[4] Consequently, TTP may be easily overlooked by obstetric providers. Once diagnosed,
however, all of the hospital's resources including maternal transport service, internal
medicine service, critical care team, laboratory, blood bank, hospital educators,
and neonatology and hematology services should be recruited.
We present a patient with TTP with inhibitors against ADAMTS-13 complicated by severe
preeclampsia with headache who was successfully treated with corticosteroids, plasma
exchange therapy, delivery, and liberal use of the hospital resources.
Case Report
This was a 28-year-old G6, P1041 at 32.2 weeks who presented to the clinic for a routine
prenatal visit and a known history of TTP secondary to ADAMTS-13 deficiency. The patient
had been extensively educated by the staff about the potential effects of her disease
on her pregnancy and was keeping a log of her weight and blood pressures along with
a fetal movement chart. She had gained 20 pounds in 3 weeks, had a 6/10 headache,
300 mg/dL protein, and blood pressure of 155/109. All of her previous visits were
characterized by normal urine dips and blood pressure, and home blood pressures had
been normal. At this time, she was receiving plasmapheresis and 50 mg of methylprednisolone
three times weekly. Her platelet count had decreased from 100,000 to 76,000/μL, and
lactate dehydrogenase was 330 IU/L, an increase from 100 IU/L. She was admitted with
a diagnosis of severe preeclampsia with thrombocytopenia and hemolysis with possible
acute TTP episode. Internal medicine and hematology oncology departments were consulted
and the neonatal intensive care unit was notified. The laboratory, blood bank, and
medical critical care team were called about the patient. Her liver enzymes returned
as normal, fibrinogen was 439 mg/dL, international normalized ratio was 0.9, and reticulocyte
count was 4.44%. There was no laboratory evidence of renal involvement. Magnesium
sulfate was started; she was given betamethasone for lung maturation, and neurology
consultation was requested. No parenteral antihypertensive medication was required
as her blood pressures fluctuated between 130/80 and 160/113. No abnormalities were
found on the fetal ultrasound, and fetal surveillance was normal. Over the next 24
hours, her headache worsened and a multispecialty conference with the medical team,
neonatology, maternal-fetal medicine, anesthesia, and nursing departments was held.
The consensus was that the patient had an acute episode of TTP with superimposed severe
preeclampsia. A cesarean delivery under general anesthesia was performed obtaining
a 3 pound, 7 ounce infant. She received 2 U of packed red blood cells and one pack
of platelets. During her postpartum course, she underwent plasmapheresis and received
methylprednisolone every other day for 1 week and received magnesium sulfate for 24
hours. Her platelets were 96,000/μL when she developed a febrile postpartum endometritis
requiring parenteral antibiotics. On postoperative day 15, the patient was discharged
in stable condition with platelets in the 100,000s.
Discussion
Laboratory values may not help in differentiating the two conditions because many
of the characteristic laboratory features of both severe preeclampsia and TTP are
similar. Furthermore, the usefulness of ADAMTS-13 serum activity level is limited
in diagnosing TTP in pregnancy, as it appears to decrease as a physiological response
to pregnancy and preeclampsia.
Treatment protocols for both conditions separately are standardized. Plasma exchange,
even in pregnancy, is the current gold standard to prevent and treat autoantibody-driven
ADAMTS-13-deficient TTP. Plasma exchange therapy has consistently reduced the mortality
from 90 to ~25%.[2] Our patient did not immediately receive plasmapheresis because the decision to intervene
with plasma exchange is based upon the severity of thrombocytopenia and microangiopathic
hemolytic anemia and presence of neurological abnormalities and renal failure. Although
there may be some anecdotal evidence[5] that delivery is an optional therapy for an acute episode of TTP in pregnancy, it
is not universally accepted.
There are newer approaches to treat TTP. Rituximab, a monoclonal antibody against
mature B cells, is currently being used to treat TTP because treatments for TTP should
be immunomodulatory. It acts to reduce immunoglobulin G antibodies against ADAMTS-13[6] and may be one of the safest adjunct therapies for the continuation of pregnancy.
Our case also illustrates the importance of proper and timely use of hospital resources
and of maintaining a designated service that is ultimately responsible for the coordination
of care. Complex life-threatening conditions that are managed by a multidisciplinary
team can result in unfocused and ineffective care that delays definitive management.
Our patient benefitted not only from the clinical input of her consultants, but also
from the structure of the care plan. The obstetric team remained the designated captain
of the ship. The patient and her family were extensively counseled and notes of the
content left on her chart to avoid any confusion that could occur when nurse or resident
rounds were made later by team members who were not present during the initial family
counseling.
